CASE - ServiceManual

CASE™ Exercise Testing System Service Manual Version V6.5 2027786-082

Revision F

The information in this manual only applies to the CASE Version Version 6.5. Due to continuing product innovation, specifications in this manual are subject to change without notice.

CASE and MUSE are trademarks owned by GE Medical Systems Information Technologies, a General Electric Company going to market as GE Healthcare. All other marks are owned by their respective owners. © 2007 General Electric Company. All rights reserved. T-2

CASE Exercise Testing System 2027786-082

Revision F

27 July 2007

Contents

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Intro Int rodu duct ctio ionn . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1 Manual Info rmat ion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Revisio Revision n History History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Manua anuall Purpo Purpose se . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Intende Intended d Aud Audienc ience e . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3 Con ven ti on s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4 Styles Styles . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4 Illustrations Illustrations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4 Safet y Info In fo rm ati on . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5 Resp Respon onsibility sibility of the the Man Manufa ufacture cturerr . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5 Genera enerall . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5 Warni ng s, Cauti on s, and Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6 Equi pm ent Sy mbo ls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7 Servi ce Inf orm atio n . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8 Service Service Requ Requirem iremen ents ts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8 Equip Equipm ment ent Identificatio Identification n . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8

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Equip Equ ipmen mentt Overvi Over view ew . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1 General Descr ipt io n . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3 Front Front View View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3 Rear Rear View View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3 As sem bl y Des cr ip ti on s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4 Monitor onitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4 Keyp Keypad ad . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4 Therm Thermal Writer Writer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5 Pow Power Sys System tem . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6 Standard Standard PC Com Components ponents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7 Con nec ti on s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9 Inpu t and Outp ut Co nnec tor s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10 USB A or B . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10 2-10 COM A or or B . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10 2-10 AN ANALOG AND TTL I/O I/O . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10 -10 Ac Acquisiti isitio on Inte Interf rfa ace . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11 -11

Revision F


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DVI . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11 2-11 Motherboa otherboard rd Pow Power er and and I/O . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13

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Instal Ins tallat latio ionn . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1 Inst allat io n Over view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3 As sem bl y . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4 Installing Installing the Monitor onitor Sup Suppo port rt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4 Installing Installing the Releas Release e Han Handle dle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5 Preparing Preparing the NEC NEC Flat Flat Panel Panel Monitor Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6 Preparing Preparing the CHILIN Flat Flat Panel Panel Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7 Mounting ounting the Flat Flat Pan Panel el Mon Monitor itor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8 Routing Routing the Cables Cables to the Conne Connector ctor Panel Panel . . . . . . . . . . . . . . . . . . . . . . . . . . 3-9 Ad Adjus justin ting the the View iewing ing Angle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-10 -10 Installing the Keyb Keyboard oard and the Mous Mouse e . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11 Configuring Configuring the Mouse ouse (PN (PN 2022 2022144 144-001 -001)) . . . . . . . . . . . . . . . . . . . . . . . . . 3-12 Conne Connecting cting the System System Com Components ponents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-12 Preparing Preparing the Acquisition Acquisition Modu Module le . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13 Load Loading ing Writer Pape Paperr . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-14 3-14 Mains Conn Connection, ection, Pow Power er Up, Up, Functiona Functionall Test . . . . . . . . . . . . . . . . . . . . . . 3-15 Netwo rk Inst allat ion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-17 Configure onfigure the Netwo Network rk . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-18 3-18 Dom Domain Configura onfiguration tion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-18 3-18 Workgro orkgroup up Configu Configuration ration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-21 3-21 Centricity entricity Xi Xi Configu Configuration ration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-23 3-23 Save Save Existing Existing Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-24 3-24 Copy Copy Custom ustom Setup Setups s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-24 3-24 Merge Local Local Exam Examination ination Databa Databases ses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-24 Merge Network Networked ed Exam Examination Databa Database se . . . . . . . . . . . . . . . . . . . . . . . . . . 3-25 Merge User User List and and Configu Configured red Repo Reports rts . . . . . . . . . . . . . . . . . . . . . . . . . . 3-26 Copy Copy Sys System tem Configura onfiguration tion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-27 3-27 Finish Finish Data Databa base se Merge erge . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-27 3-27 Install Install CASE CASE Applica Application tion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-28 3-28 Recon econfigure figure the Syste System m . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-28 3-28 Configu Configure re Netw Network ork User User Profile Profile . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-29 3-29 Install Install Option Option Cod Codes es . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-29 3-29 Restore Restore Syste System m Configu Configuration ration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-29 3-29 Restore Restore Custom CustomSettings Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-30 3-30 Installing a Netwo Network rk Printer for all Us Users ers on on This This CASE CASE . . . . . . . . . . . . . . . 3-30 Data In ter fac e wi th MUSE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32 Establish Establish Conn Connection ection to MUS MUSE E . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-32 Read Read MUSE USE Patient Patient Data Data from CASE CASE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33 Configu Configure re Intern Internet et Exp Explore lorerr . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33 3-33 Estab Establish lish a MUSE USE Acc Accou ount nt . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-33 3-33

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Revision F

Config urin g a CASE/Ca CASE/Cardio rdio Soft System wit h the EMR Appl icatio n . . . . . . . . . . 3-34 Before Before You You Beg Begin in . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-35 3-35 Confi Configuring guring a CAS CASE/CardioSo E/CardioSoft ft System wit with h the EMR EMR Appli Application cation . . . . . . . . . . 3-36 Install the Centricity Centricity EMR Application Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-36 Migrate Historical Historical CardioSo CardioSoft ft Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-38 Migrate Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-38 3-38 Metab ol ic Interf Int erf ace . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-39 Com Communication munication Com Commands mands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-39 Serial Serial Port Port Setting Settings s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-39 3-39 Com Command mand String Structure Structure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-40 Share Shared d File File Settings Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-42 3-42 Data Data File File Structu Structure re . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-42 3-42

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InSite InSi te 2.0 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1 Ins tal li ng InSi te 2.0 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3 Pre-Insta Pre-Installation llation Proc Proces ess s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3 Installation Installation Proc Proced edure ure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5 Unin stal lin g InSi te 2.0 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12 Oper ati ng InSi te 2.0 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14 Setting Setting the the Ope Operation ration Mode ode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14 4-14 Restr ict in g Remo te Ac cess . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-15

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Maint enance enan ce . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1 Intro Int ro du ct io n . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3 Requ Required ired Too Tools ls and and Sup Supplies plies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3 Insp ecti on an d Clean in g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4 Visua Visuall Inspec Inspection tion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4 Exterior Exterior Clea Cleaning ning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4 Interior Interior Clean Cleaning ing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4 Elect ric al Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5 Recom Recommended ended Test Test Sche Schedule dule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5 Recom Recommended ended Test Test Equipm Equipment ent . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5 Protective Protective Earth Earth Resistan Resistance ce Test Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5 Leakag Leakage e Current Current Measurem easurement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6 Earth Earth Leaka Leakage ge (AC line) Current Current Test Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6 Enclosu Enclosure re Leaka Leakage ge Current Test Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7 Patient Patient Lea Leaka kage ge Curren Currentt Test Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8 Patient Patient Leakag Leakage e Current, Current, Mains Mains on on Applied Applied Part Part . . . . . . . . . . . . . . . . . . . . . 5-10

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6

Troubleshoo tin g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1 Over vi ew . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3 Trou bl esho oti ng Tool s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4 Service Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4 Service Screen Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5 Diagnostic Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6 Access the Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6 Acquisition Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7 Keypad Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7 Writer Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8 Enter in g a One-Day Pass wo rd . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-9 General Fau lt Iso lati on . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10 Visual Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10 Power-up Self-test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10 General Tr oub lesh oo tin g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-11 Frequ entl y As ked Qu esti ons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-15 Flat Panel Moni tor Prob lems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-22 Prin ter Deb ug gin g . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-24 Usage and Work arou nd o f Ac ro bat 6 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-26

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Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1 Over vi ew . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3 Syst em Bac kup and Res tor e . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4 Saving to Diskette . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4 Saving System Configurations to Diskette . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4 Saving CustomSettings to Diskette . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5 Restoring from Diskette . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-6 Restoring SystemConfiguration from Diskette . . . . . . . . . . . . . . . . . . . . . . . 7-6 Restoring CustomSetups fromDiskette . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7 Recov erin g fr om a CASE BTRV Erro r . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-9 Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-9 Database Rep air fo r CASE / Cardi oSof t . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11 How the Data is Repaired . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11 Supported Modalities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11

4


Revision F

Non-Supported Features . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11 Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11 Password Protection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11 Directory / File Structure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-12 Repair directory structure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-12 Configuring the Repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-13 Using the Repaired Files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-14 Merging Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-15 External Stored Examinations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-15 Examinations with Full Disclosure ECG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-16 Repair Message Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-16 Patient-Filter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-17 Remo te Ser vi ce . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-18 Cont rol li ng Elec tro stat ic Di sch arg e Damage . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-19 Servi ci ng L ig ht A ssem bly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-20 Servi ci ng t he Key pad A ss embl y . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-21 Remov ing the Wor ks urf ace Ass embl y . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-23 Servicin g the Power Dis trib utio n Ass embly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-25 Ac ces si ng th e Dri ves . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-26 Upgr adin g th e Flop py Dr ive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-29 Replac in g th e Flopp y Dri ve / Card Reader . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-37 Servi ci ng t he Pri nt Head . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-44 Writ er Bo ard Fi rmw are Upd ate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-47 Servi ci ng t he I/O Ass embl y . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-49 Config urin g the Ac qui siti on Interf ace Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-51 Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-52

8

System Rebui ld . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1 Over vi ew . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3 CD Image and A ppl icat io n Ins tall atio n . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4 Kit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4 Initial BIOS Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4 Bios Setup —Changing the Boot Sequence . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5 Disk Image Loading . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5

Revision F


5

Final Bios Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . XP Systems —Verify CRT or Flat Panel Display Settings . . . . . . . . . . . . . . . . . Modify CRT Display Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Verify CRT or Flat Panel Display Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . The System Configuration Utility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

8-5 8-6 8-6 8-6 8-7

Conf ig ur e the CASE Sy stem Lan guag e . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8 Set Menus and Dialog Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8 Set Input Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9 Set Regional Standards and Formats . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9 Set Non-Unicode Program Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10 Install Supp lemental XP System Files and XP Securi ty Patches . . . . . . . . . . . . 8-11 Install XP Security Patches . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11 Inst all t he Ap pli cati on . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-12 Opti ons Inst allat ion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-13

9

Upper Level Ass embly . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-1 Upper Level Prod uct Numb ers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3 Field Replac eable Un its . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-4 FRU Lists . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-5 Core FRUs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-5 Cables, Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-10 Keyboards and Mice . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-10 KISS Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-11 Miscellaneous . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-11 Monitors and Cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-11 Power Cords . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-12 Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-12 FRU Diagrams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-13

6


Revision F

Docu ment atio n FRUs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-35

A B C

Abbr eviati ons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-1

Technical Descrip tion . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-1

Electromagnetic Compatibili ty . . . . . . . . . . . . . . . . . . . . .C-1 Elect rom agnet ic Co mp atib il ity (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-3 Guidance and Manufacturer’s Declaration – Electromagnetic Emissions . . . . . . C-3 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity . . . . . . . C-4 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity . . . . . . . C-5 Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-6 Compliant Cables and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-7

D

CASE Files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-1 Direc tor y Str uct ur e and Not es on CASE Files . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-3 Files in Windows system32 directory: . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-3 File name nomenclature of the examination procedure . . . . . . . . . . . . . . . . . . . . D-4 File in the Windows INF directory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-4 Files in the Windows directory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-4

Revision F


7

For your notes

8


Revision F

1

Revision F

Introduction


1-1

For your notes

1-2


Revision F

Introduction: Manual Information

Manual Information Revisi on History Each page of the document has the document part number and revision letter at the bottom of the page. The revision letter identifies the document’s update level. The revision history of this document is summarized in the table below. Table 1. Revision Histor y PN 2027786-082 Revision

Date

Comment

A

5 May 2006

Initial release of this manual; corresponds with CASE software version 6.5

B

2 June 2006





Revised the System Restore instructions to include the “XP Supl Files CASE UPD from V6.01” CD-ROM Corrected the Keypad part number in the FRU list.

C

20 November 2006



ECO 084616, Warning note added on page 1-5, 19” monitor changed on page 9-13

D

04 January 2007



Revision for CASE update to V6.51 / ECO 086172

E

22 February 2007



ECO 086785, update for WIN XP Patch CD and new motherboard

F

27 July 2007



ECO 087386, update new mouse, hard drive and display without stand and cables, Ferrite bead installation, update of equipment symbols description, update of Maintenance chapter/Electrical Safety Tests

Manual Purpos e This manual supplies technical information for service representative and technical personnel so they can maintain the equipment to the assembly level. Use it as a guide for maintenance and electrical repairs considered field repairable. Where necessary the manual identifies additional sources of relevant information and or technical assistance. See the operator manual for the instructions necessary to operate the equipment safely in accordance with its function and intended use.

Intended Audience This manual is intended for the person who uses, maintains, or troubleshoots this equipment.

Revision F


1-3

Introduction: Conventions

Conventions These are the conventions used in the manual:

Styles 







Bold text indicates keys on the function keypad, the keyboard, text to be

entered, or hardware items such as buttons or switches on the equipment. Italicized text indicates software terms that identify menu items, on-screen controls, buttons, or options in various windows. To perform an operation which appears with a plus (+) sign between the names of two keys, you press and hold the first key while pressing the second key once. This is called a keystroke combination. Example: “Press Ctrl + Esc” means to press and hold down the Ctrl key while pressing the Esc key. When instructions are given for typing a precise text string with one or more spaces, the point where the space bar must be pressed is indicated as Space. The purpose is to ensure you press the spacebar when required.

Illustrations All illustrations in this manual are provided as examples only. They may not necessarily reflect your equipment setup or data displayed. In this manual, all names appearing in examples and illustrations are fictitious. The use of any real person’s name is purely coincidental.

1-4


Revision F

Introduction: Safety Information

Safety Information Respons ibil ity of t he Manufacturer GE Medical Systems Information Technologies is responsible for the effects of safety, reliability, and performance only if: Assembly operations, extensions, readjustments, modifications, or repairs are  carried out by persons authorized by GE Medical Systems Information Technologies.  The electrical installation of the relevant room complies with the requirements of the appropriate regulations. 

The equipment is used in accordance with the instructions for use.

General This device is not intended for home use. Contact GE Medical Systems Information Technologies for information before connecting any devices to the equipment that are not recommended in this manual. Parts and accessories used must meet the requirements of the applicable IEC 60601 series safety standards, and/or the system configuration must meet the requirements of the IEC 60601-1-1 medical electrical systems standard. Periodically, and whenever the integrity of the device is in doubt, test all functions. The use of ACCESSORY equipment not complying with the equivalent safety requirements of this equipment may lead to a reduced level of safety of the resulting system. Consideration relating to the choice shall include: use of the accessory in the PATIENT VICINITY; and  evidence that the safety certification of the ACCESSORY has been performed  in accordance to the appropriate IEC 60601-1 and/or IEC 60601-1-1 harmonized national standard. If the installation of the equipment, in the USA, will use 240V rather than 120V, the source must be a center-tapped, 240V, single-phase circuit.

FIRE HAZARD — For continued protection against risk of fire replace fuse only with fuse of same type and rating.

Revision F


1-5

Introduction: Warnings, Cautions, and Notes

Warnings, Cautions, and Notes The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level or seriousness. Familiarize yourself with their definitions and significance. Hazard is defined as a source of potential injury to a person. Term

1-6

Definition

DANGER

Indicates an imminent hazard which, if not avoided, will result in death or serious injury.

WARNING

Indicates a potential hazard or unsafe practice which, if not avoided, could result in death or serious injury.

CAUTION

Indicates a potential hazard or unsafe practice which, if not avoided, could result in minor personal injury or product/property damage.

NOTE

Provides application tips or other useful information to assure that you get the most from your equipment.


Revision F

Introduction: Equipment Symbols

Equipment Symbols CAUTION, consult accompanying documents.

WARNING, dangerous voltage.

Type BF equipment, external defibrillator protected.

Power switch (ON - OFF)

Equipotential

Signal input

Signal output

Fuse

On/Standby

E SSI FI D L A C

C

R

US

MEDICAL EQUIPMENT UL 2601-1 CAN/CSA 601.1 4P41

Classified by Underwriters Laboratories Inc. with respect to electric shock, fire, mechanical and other specified hazards, only in accordance with UL 2601-1, CAN/CSA C22.2 No. 601.1, IEC 60601-1, and, if required, IEC 60601-2-27, IEC 60601-2-30, IEC 60601-2-34, IEC 60601-1-1. This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment.

Revision F


1-7

Introduction: Service Information

Service Information Service Requirements Follow the service requirements listed below. Refer equipment servicing to GE Medical Systems Information  Technologies’authorized service personnel only. Any unauthorized attempt to repair equipment under warranty voids that  warranty. It is the user’s responsibility to report the need for service to GE Medical  Systems Information Technologies or to one of their authorized agents. Failure on the part of the responsible individual, hospital, or institution using  this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards. 

Regular maintenance, irrespective of usage, is essential to ensure that the equipment will always be functional when required.

Equipment Identif ication The Serial Number and Unit ID number tags appear on back of the device in the location shown below.

Serial Number location

1-8


Revision F


Every GE Medical Systems Information Technologies device has a unique serial number for identification.

### ## ## #### # #

A

Revision F

B

C

D

A

Product Code

B

Year Manufactured (00-99) 00 = 2000 01 = 2001 02 = 2002 (and so on)

C

Fiscal Week Manufactured

D

Production Sequence Number

E

Manufacturing Site

F

Miscellaneous Characteristic


E

F

1-9


For your notes

1-10


Revision F

2

Revision F

Equipment Overview


2-1

For your notes

2-2


Revision F

Equipment Overview: General Description

General Description Shown below is a general overview of a CASE system. See the “CASE Operator’s Manual” for details on operating procedures.

Front View Monitor

Paper tray Function keypad Console for keyboard and mouse

Power switch, floppy disk/SD card reader, and CD drive

Acquisition Module Holder

Rear View

Route external device cables through clamps

Access Panel

Equipotential pin, power inlet with fuses, Mains switch

Revision F


2-3

Equipment Overview: Assembly Descriptions

Assembly Descriptions Familiarity with the components of the CASE assembly will aid in troubleshooting the equipment. The CASE consists of the following components.

Monitor The system uses either a 19" or 17” flat panel monitor rated IEC-950 universal AC input.

This monitor has a standard IEC320 power cord and a DVI video connector on a cable for the digital DVI input signal. The monitor displays optimal waveform quality at the system setting of 1280 x 1024 with a 60Hz refresh rate and 16 bit color depth.

Keypad The keypad is designed as a bus powered, low speed USB peripheral using a Cypress MCU.

There is protection from ESD on the PCB as well. The keypad is hot pluggable, and in the CASE system, it relies on a custom software driver running the USB ports on the motherboard under NT 4.

2-4


Revision F


Thermal Writer The thermal writer assembly contains a thermal print head with cue hole sensor, a motor/encoder assembly to drive the platen roller, and an Information Technologies designed PCB to receive scan line data and motor commands from the PC over USB.

The PCB is based on an Cypress high speed USB MCU with an 8051 core. The program is stored on a FLASH memory chip that can be reprogrammed from the host PC. The PCB connects to the thermal print head motor and cue sensor through a 40-pin ribbon harness. A standard type 'B' R/A USB connector provides the link to the PC using any high speed USB A-to-B cable under 5m. The functioning of this USB writer PCB depends on communication with the host PC motherboard USB controller which is under the control of a software driver. A special driver is always needed to communicate with this writer PCB (this driver is built into the application software). Check operation in the CASE system, since full functionality depends on cooperation with the motherboard USB ports and associated software drivers.

Revision F


2-5


Power System AC power comes into the unit through an IEC-320 inlet module that has an equipotential ground stud mounted near it.

The AC power then goes to a power distribution PCB. Its function is to route AC power and isolated AC power to the proper places in the unit. Regular AC power is routed to the medical grade power supplies. Isolated AC power is derived from the isolation transformer, and routed to the IEC-950 CRT monitor. No switching of AC power is needed with inputs from 100–240 VAC since all supplies and the isolation transformer are universal input in the unit.

2-6


Revision F


Standard PC Compon ents PC Subsystem The PC subsystem (A) provides processing, video, and network capability using industry standard PC components.

B

A

Besides on PCB connectors for floppy and IDE drives, the motherboard has an I/O panel arrangement in one corner (per standard ATX designs) that has off PCB connectors.

Acquis it ion/Interface Card This PCB (B) plugs into an expansion slot on the motherboard and provides an interface to the PC that allows CAM-14 acquisition and analog/TTL I/O and needed COM ports.

PS/2 Keyboard A standard 104-key Windows 95 keyboard with PS/2 interface is connected to the PC I/O panel PS/2 keyboard connector.

Revision F


2-7


PS/2 Mouse A standard two-or three-button mouse with PS/2 interface is connected to the PC I/O panel PS/2 mouse connector.

Hard Drive This drive (A) connects to the motherboard primary IDE channel as a master through a standard IDE ribbon cable. Power comes from the power distribution PCB.

A

B

C

Floppy Driv e / SD Card Reader This drive (B) connects to the motherboard floppy channel through a standard floppy ribbon cable and an internal USB cable. Power comes from the power distribution PCB.

CD-R/W Drive This drive (C) connects to the motherboard primary IDE channel as a slave through a standard IDE ribbon cable daisy-chained with the hard drive. Power comes from the power distribution PCB.

2-8


Revision F

Equipment Overview: Connections

Connections Shown below is the CASE rear connector panel. See Chapter 3 of this document and the CASE Operator’s Manual, “B Miscellaneous, Connecting Peripheral Devices,” for information on connecting peripheral devices to the CASE. Analo g I/O

COM 2

Com D

LAN

Com B

LPT 1 Mouse

Com A

CAM 14

Keyboard

Com 1 Treadmill

Video DVI

Com C

USB Ports Stress Keyboard and External Thermal Writer can be connected to either USB Port.

Revision F


2-9

Equipment Overview: Input and Output Connectors

Input and Output Connectors The pin-by-pin descriptions identify the signal names and pin outs for each connector on the unit.

USB A or B Table 1. USB Jack or Plu g Pin

Name

1

Vcc

2

- Data

3

+ Data

4

Ground

COM A or B Table 2. Acquis ition PCB Serial Ports Pin

Name

1

HANDSHAKE OUT

2

HANDSHAKE IN

3

XMIT 422-

4

GND

5

RXD 422-

6

XMIT 422+

7

+12V, 0.5A MAX

8

RXD 422+

SHLD

CHASSIS

7

8

6 4

5

3

2

1 MD1322-007

ANALOG AND TTL I/O Table 3. Acquisiti on PCB Analog and TTL I/O Connector Pin 1

+12V, 300mA MAX

2

CH1OUT

3

TTL-I/O

4

CH2OUT

5

GND

6

CH3OUT

7

AN2IN

8

CH4OUT

9

AN1IN

SHLD

2-10

Name 5

1

9

6

MD1322-010

CHASSIS


Revision F


Acquisition Interface Table 4. Acquisiti on Modul e I/F Pin

Name

1

+12V, 0.5A MAX

2

GND

3

AMTX+

4

AMTX-

5

AMRX+

6

AMRX-

7, 8, 9, 10

N/C

DVI C3 24

C4

C5

C2

17 9

C1

8

1

Table 5. DVI Pin

Revision F

Name

1

T.M.D.S. DATA 2-

2

T.M.D.S. DATA 2+

3

T.M.D.S. DATA 2/4 SHIELD

4

T.M.D.S. DATA 4-

5

T.M.D.S. DATA 4+

6

DDC CLOCK

7

DDC DATA

8

ANALOG VERT. SYNC

9

T.M.D.S. DATA 1‘-

10

T.M.D.S. DATA 1+

11


12

T.M.D.S. DATA 3-


2-11


Table 5. DVI (Continu ed)

2-12

13

T.M.D.S. DATA 3+

14

+5V POWER

15

GND

16

HOT PLUG DETECT

17

T.M.D.S. DATA 0-

18

T.M.D.S. DATA 0+

19


20

T.M.D.S. DATA 5-

21

T.M.D.S. DATA 5+

22

T.M.D.S. CLOCK SHIELD

23

T.M.D.S. CLOCK+

24

T.M.D.S. CLOCK-

C1

ANALOG RED

C2

ANALOG GREEN

C3

ANALOG BLUE

C4

ANALOG HORZ SYNC

C5

ANALOG GROUND


Revision F


Motherboard Power and I/O Table 6. Power Supply Connector Pin

Name

1

+3.3V

2

+3.3V

3

GROUND

4

+5V

5

GROUND

6

+5V

7

GROUND

8

PWRGD (power good)

9

+5VSB (standby for real-time clock)

10

+12V

11

+3.3V

12

-12V

13

GROUND

14

PS-ON# (power supply remote on/off control)

15

GROUND

16

GROUND

17

GROUND

18

-5V

19

+5V

20

+5V

Table 7. PS/2 Keyboard and Mouse Connector Pin

Revision F

Name

1

DATA

2

N/C

3

GROUND

4

+5V (fused)

5

CLOCK

6

N/C


2-13


Table 8. Parallel Port Connector Pin

2-14

Name

1

STROBE #

2

DATA BIT 0

3

DATA BIT 1

4

DATA BIT 2

5

DATA BIT 3

6

DATA BIT 4

7

DATA BIT 5

8

DATA BIT 6

9

DATA BIT 7

10

ACK#

11

BUSY

12

ERROR

13

SELECT

14

AUTO FEED #

15

FAULT #

16

INIT #

17

SLCT IN #

18

GROUND

19

GROUND

20

GROUND

21

GROUND

22

GROUND

23

GROUND

24

GROUND

25

GROUND


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Table 9. Com 1, 2, C and D Conn ectors Pin

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Name

1

DCD #

2

SERIAL IN

3

SERIAL OUT

4

DTR #

5

GROUND

6

DSR #

7

RTS #

8

CTS #

9

RI #


2-15


For your notes

2-16


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3

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Installation


3-1

For your notes

3-2


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Installation: Installation Overview

Installation Overview Installation of the CASE system consists of the following steps: 1. Unpack and inspect the system. Verify that the shipment is complete and undamaged. If the shipment has missing or damaged pieces, stop the installation and contact GE Healthcare. 2. Assemble the system. Refer to “Assembly” on page 3-4 for details. 3.

Connect the CASE to the exercise device. Refer to the installation instructions included with the exercise device for details.

4.

Install and configure InSite 2.0, if applicable. InSite 2.0 is the service option that allows diagnostics for the CASE system. Refer to Chapter 4, “InSite 2.0” for details on installing and configuring InSite 2.

5.

Connect the CASE system to the network, if applicable. Refer to “Network Installation” on page 3-17.

6.

Connect the CASE system to the MUSE system, if applicable. This allows the CASE system to share information with the MUSE system, speeding up data entry and reducing errors. Refer to “Data Interface with MUSE” on page 3-32 for details.

7.

Configure the CASE system for an EMR application, if applicable. By interfacing with an EMR application, the CASE system can be controlled by and transfer data with the EMR application. Refer to “Configuring a CASE/ CardioSoft System with the EMR Application” on page 3-34 for details.

8.

Configure the CASE system for a metabolic interface, if applicable. Refer to “Metabolic Interface” on page 3-39 for details.

After the installation is complete, the CASE system is ready for the user.

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3-3

Installation: Assembly

Assembly After unpacking and inspecting the CASE system, complete the following procedures to put your new CASE into service.

Installing the Monitor Support 1. Lock the wheels. 2. Open rear access panel.

2-10A

Route the light cable through this opening.

27D

3-4

3.

Remove the nuts from the extended screws at the base of the support.

4.

Route the light cable through the indicated opening on the tray.

5.

The light cable and cable guide MUST be routed through the center of the support neck. If your assembly is not in the center, remove the cable guide and insert it in the center of the neck before proceeding. Insert the support screws into the matching holes of the tray.


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6.

Secure the support to the tray using the nuts removed in Step 3 and apply in the order shown below. Front

5 2

3

6

4 1 Back

2-11B

Installing the Release Handle To install the Release Handle follow these steps:

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1.

Insert the Release Handle into the threaded hole and turn clockwise until the handle is bottomed out.

2.

Lift and turn handle to the center position.

3.

Turn handle counter-clockwise to release tension and clockwise to increase tension on the mounting plate.


3-5


Preparing the NEC Flat Panel Monitor To prepare the NEC monitor for mounting on the CASE system follow these steps:

APPROPRIATE CABLE USAGE — The CASE system is configured to operate ONLY with the digital video interface (DVI) cable (2019792-001 CABLE ASSY DVI-D TO DVI-D VIDEO 1.8 m). DO NOT use the VGA cable that is shipped with the flat panel monitor to configure the CASE system. Discard the VGA cable that is shipped with the flat panel monitor.

1.

Remove monitor from its shipping carton.

2.

Place hands on each side of the monitor and lift up to highest position.

3.

Place the monitor face down on a 55 mm thick non-abrasive surface.

55 mm

4.

Remove the stand cover by sliding the top/bottom pieces off the stand as shown below.

5.

Remove the four screws connecting the monitor to the stand. Cover Top

1

3-6

4

3


Cover Bottom

2

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Preparing the CHILIN Flat Panel Monitor To prepare the CHILIN monitor for mounting on the CASE system follow these steps:

APPROPRIATE CABLE USAGE - The CASE system is configured to operate ONLY with the digital video interface (DVI) cable (2019792-001 CABLE ASSY DVI-D TO DVI-D VIDEO 1.8M) that is shipped separately within the CASE shipment, when using the CHILIN monitor. DO NOT use the DVI or VGA cables that may have been delivered in the monitor's accessory box to configure the CASE system. Discard any cables you may find in the monitor's accessory box.

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1.

Remove monitor from its shipping carton. If the monitor is delivered without stand, proceed with step 4.

2.

Place the monitor face down on a non-abrasive surface

3.

Remove the four screws connecting the monitor to the stand. Start with the lower left one, this one is a little bit harder to remove, then to remove the other screws, turn the stand to allow access to the screws.

4.

After mounting the flat panel monitor (see page 3-8) and routing the cables to the connector panel (see page 3-9), connect the monitor to power as described below:

5.

Remove cover at the backside of the monitor.

6.

Connect cables as shown (use bracket to secure the power cord).

7.

Close cover.


3-7


Mounting the Flat Panel Monitor 1.

Remove the CASE neck assembly and flat panel monitor from their packaging.

2.

Lay the flat panel monitor face down on a clean flat surface and fasten the mounting adapter to the back of the monitor display housing with four M4 pan head screws provided.

3.

Partially insert two M4 pan head screws provided into the two top holes of the mounting adapter.

4 - M4 Screws

2 - M4 Screws

4.

3-8

With the Mounting Plate locked in the vertical position, lift the monitor onto the Mounting Plate while guiding the two M4 pan head screws into the slots in the Mounting Plate.


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5.

Insert the two remaining two M4 pan head screws then tighten all four screws.

Routing the Cables to the Connector Panel Cable Feed Through Hole

Cable Clamps

Connector Panel

27E

APPROPRIATE CABLE USAGE — The CASE system is configured to operate ONLY with the digital video interface (DVI) cable (2019792-001 CABLE ASSY DVI-D TO DVI-D VIDEO 1.8 m). DO NOT use the VGA cable that is shipped with the flat panel monitor to configure the CASE system. Discard the VGA cable that is shipped with the flat panel monitor.

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3-9


1.

Remove monitor from its shipping carton.

2.

Guide the cables through the cable clamps to the connector panel.

3.

To lock the clamps, press first on its small tab, then press the large tab. 2 1 2-13A

Adjusting the Viewing Angle To adjust the viewing angle of the monitor, while holding the monitor, lift and turn the release handle counter clockwise. To lock the monitor in place, lift and return the handle to its original position.

3-10


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Installing the Keyboard and the Mouse

2 1 3b

3a

28A

161A

1. Remove the tray liner.

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2.

Open the access door, revealing the access panel.

3.

Guide the keyboard and mouse cables completely through a.

the center opening at the back of the tray, and

b.

the opening at the top of the access panel.

4.

Coil the excess cable in the tray and replace the access panel and the tray liner.

5.

Choose convenient locations for the keyboard and the mouse on the tray.

6.

If the mouse (PN 2022144-001) is sharing a USB connector, add the USB to PS/2 adapter as described in the next section.

7.

Connect the keyboard and mouse cables. See the Reference Diagram inside the back panel for connector locations.

8.

Connect the monitor to the DVI connector. See the Reference Diagram inside the back panel for connector location.


3-11


Configuring the Mouse (PN 2022144-001) For use with the CASE system, connect the PS/2 adapter to the mouse cable. The PS/2 adapter is required, because there is no free USB port for connection of the mouse cable.

Connecting the System Components 1.

Connect the remaining cables to the system components and secure the connections with retaining screws.

2.

When all connections are made, guide the cables through the gap at the top of the closed access panel and secure them with provided cable clamps if necessary.

Cable clamp

Reference diagram

2-15A

A reference diagram of the CASE Exercise Testing System’s back panel, complete with connector labels, is located inside the access door to the back of the unit. Refer to this diagram for information on where to make system connections. Coil the excess cable for storage as shown above. DO NOT squeeze the cables when closing the access panel. See the CASE Operator’s Manual, “B Miscellaneous, Connecting Peripheral Devices,” for information on connecting other devices to the CASE system. 3-12


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Preparing the Acquisition Module

29B

Preparing the acquisition module

There are two sets of lead label stickers for the acquisition module: AHA labeling and IEC labeling. If not already done, select the proper one for your use and apply. 1.

If not already done, connect the patient cable to the base of the acquisition module. To remove the cable from the acquisition module, press in the spring lock located on one side of the patient cable. If not already done, plug the individual lead wires into the acquisition module, observing the lead labels. 

2.

Trace each individual lead wire from its colored connector back to the Acquisition Module label to insure that it is matched to the correct label location. Improper connection will cause inaccuracies in the ECG.

3.

Place the supplied acquisition module holder to the right side of the cart, then place the acquisition module into the holder. The ECG signal input of the CASE Exercise Testing System is isolated and defibrillation-proof only in conjunction with the CAM-14 Acquisition Module (type BF).

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3-13


Loading Writer Paper Verify that the thermal paper is installed properly. 1.

Lift up the paper Compartment Lid and press the paper Release Button. (A stripe appears on the writer paper when only 20 feet of paper are left.) Release Button

Compartment Lid

53A

2.

Place fanfold paper in paper storage compartment.

Storage Compartment 54A

3.

Feed paper (plain side facing roller) under roller assembly until approximately 3–4 inches extend out of the paper storage compartment.

55A

4. 5.

Press the paper release button while moving the roller assembly back into position.

56A

6.

3-14

Release the paper release button to lock the roller assembly into position. Close the paper compartment lid.


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Mains Connection, Power Up, Functional Test Observe the Safety Information section in Chapter 1.

Mains connection (power line connection)

Mains power switch

Potential equalization system connection 34A

Back Panel

Power button

200A

Side Panel

1.

Connect the CASE Exercise Testing System to the power line and fasten with the clamp provided. DO NOT energize the system at this time.

2.

We also recommend connecting the system to the potential equalization system.

3.

Connect all system components to the power line and put them into operation as outlined in the respective operator manuals.

4.

Turn on the mains power switch on the back of the system.

5.

Turn on the CASE Exercise Testing System with the power button on the Side Panel and the Windows operating screen will appear.

6. Login to system. If logged in as Administrator go to Step 7. If logged in as User go to Step 8. 7. Double click on the CASE icon when it appears. 8.

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The Initial Screen will now appear.


3-15


Do not turn off the mains power switch until you have: a. Exited from the application, and b.

Selected Yes from the Do you want to terminate the program and shut down the device dialog box.

Turn off the CASE Exercise Testing System with the Mains power switch on the back of the unit if it is not used for a prolonged period of time. In all other situations, turn it off and on with the power button on the side panel. The power button on the side panel does not disconnect the system from AC power. See the CASE Operator’s Manual for “Putting the System into Service.”

Before using the CASE system for the first time, you should conduct electrical safety tests on the equipment to ensure the safety of the patient and the operator. For information on conducting these tests, refer to “Electrical Safety Tests” on page 5-5. After the electrical safety tests have been successfully completed, you are ready to continue with the installation.

3-16


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Installation: Network Installation

Networ k Installation After connecting the CASE system to the exercise equipment, it is ready to be connected to the network. This section addresses the installation of the system in a CardioSoft network. The following is a high-level outline of the installation procedure. Perform the following installation procedure in the given order.

1.



Before installation, close ALL programs (CASE / CardioSoft) on ALL stations. The CardioSoft server itself must not be used as a CardioSoft station. If an application is open on any system, it may cause failure of installation.



To ensure trouble-free access to the database, install the same software version on all clients/workstations.

Configure the Network Perform this step by choosing one type of network configuration (Domain Configuration or Workgroup Configuration) and follow all of the steps to setup the networking aspect of the installation.

2.

Save Existing Data Perform this step only after all systems have been configured in the network to merge all data from stand-alone systems to the CardioSoft server.

3.

Install CASE Application Perform this step only after all systems have been configured in the network and all of the data has been merged to the CardioSoft server.

4.

Reconfigure the System Perform this step only after the CASE application has been installed at each system to configure each system for customer use. The RadiSys board used with the CASE System is Full Duplex, Intel ICH2 integrated MAC with Intel 82562 PHY IEEE 802.3 10Base-T and 100Base-TX compatible.

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3-17


Configure the Network CASE/CardioSoft can be installed on either a Domain or Workgroup network configuration. A network administrator must determine which configuration to use prior to the network installation. The following table outlines the installation procedures for both network configurations. They are presented side-by-side to call out differences and similarities. Domain Configuration

Workgroup Configuration

Create a Domain user or domain user group to be used by the CASE systems

Create a user or create users and a user group on the server.

Create a shared folder on the server with full control permissions for the domain user or domain user group.

Create a shared folder on the server with full control permissions for the user or user group.

Provide the server name (or IP address) and path to the created shared folder for mapping a drive letter to the folder. Add each CASE system to the Windows NT / Windows 2000 domain. Provide static IPs for each system (if Remote View function will be used). Provide the domain name.

Provide the workgroup name.

Provide TCP/IP configuration settings.

Provide TCP/IP configuration settings.

Proceed only after the network configuration is identified. If you are installing on a Domain configuration, proceed to “Domain  Configuration” on page 3-18. If you are installing on a Workgroup configuration, proceed to “Workgroup  Configuration” on page 3-21. If existing CASE systems can communicate with the MUSE server, the MUSE server access permissions will need to be reconfigured if a new CASE user is created.

Domain Configuration To install CASE on a domain, you first configure the server and then configure each workstation to be added to the network. A domain administrator may have to perform both steps.

Server Configu ration o n a Domain The configuration of the server consists of the following tasks:  

3-18

Set up the domain user Set up a shared folder on a domain server


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Set up a domain user – Do one of the following:

Create a new domain user account Select an existing domain user account  In either case, the account must be designated as a Network User and exist on the domain where the CardioSoft server resides or on a domain that has a trust relationship with the domain where the CardioSoft server resides. 

Set up Shared Folder – The procedure for setting up a shared folder differs

depending on whether you are installing a new CardioSoft server or updating an existing CardioSoft server. New CardioSoft Server

1.

Log in to the server as the domain administrator.

2. Create a directory named cardio on the local drive of the server. 3.

Share the cardio directory and name the share cardio.

4.

Configure the share permissions such that the designated Network User has full control permissions.

Existing CardioSoft Server

Before renaming the old cardio folder, save the system configuration and all custom setups to disk. For additional information, refer to “General Troubleshooting” on page 6-11. 1.

Log in to the server as the domain administrator.

2.

Rename the existing CardioSoft directory cardio to card_old .

3. Create a new directory named cardio on the local drive of the server. 4.

Share the card_old directory and name the share card_old .

5.


6.

Configure the share permissions for both shares such that the designated Network User has full control permissions.

Workstation Configu ration in a Domain Once the server has been configured, you must configure all the systems that will be connected to the CardioSoft network. The workstation configuration consists of the following steps:  

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Adding a CASE system to the domain Configuring the CASE user accounts and network settings


3-19


Add CASE System to Windows NT / Windows 2000 Domain – To add a case

system to the domain, use the following procedures: 1. Boot Boot the the CAS CASE E wit with h the the Network Enabled hardware hardware profile. 2. Log Log in aass loca locall Admi Admini nist stra rato tor. r. 3.

Enabled . Set the def defaul aultt hardw hardware are pro profil filee as as Network Enabled

a.

Open Open System System Prop Propert erties ies by by right right click clicking ing on on My Computer and and selecting Properties.

b.

Hardware Profiles tab. Click the Hardware

c.

Enabled and Select Network Enabled and click the up arrow button.

d.

Click OK to to close the window.

4. Chan Change ge netw networ ork k set setti ting ngs. s. The domain administrator may have to perform these steps. a.

Neighborhood and Open Open net networ work k proper propertie tiess by right right cclic lickin king g on Network Neighborhood and selecting Properties.

b.

Click Change button in Identification tab.

c.

Click Domain radio button.

Domain Name. d. Type ype in desi design gnat ated ed Domain Name

e.

Check Create a computer account in the domain.

f.

Enter Enter the the doma domain in admi adminis nistra trator tor log login in name name..

g. Enter Enter the the domain domain admi adminis nistra trator tor pass passwor word. d. h.

Click OK to to close the window, then click OK to to close the network properties window. window.

i.

If pro promp mpte ted, d, res resta tart rt the the comp comput uter er..

Configure User Accounts and Network Settings on CASE in a Domain – To

configure the user accounts and network settings, use the following procedures: 1.

Log in in to the the CASE CASE as local local Admi Adminis nistra trator tor..

Network User to 2. Add Add the the desi design gnat ated ed Network User to the local Administrator group.

a.

Tools->User Manager. Manager. Open Start Menu->Programs -> Administrator Tools

b.

Double click on Administrators in the Groups section.

c.

Click Add.

d.

Names textbox, type the domain name and username in this In the Add Names form: [Domain Name]\[Network User].

e.

Click OK and and then close the User Manager window. window.

3. Conf Config igur uree the TCP TCP/I /IP P setti setting ngs. s.

3-20

a.

Perform these steps if the Remote View function is used or communication with a MUSE server (Version (Version 5.0a) is needed. Neighborhood and Right cl click on on Network Neighborhood and select Properties.

b.

Click on the Protocols tab.


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c.

Click on TCP/IP Protocol and then click Properties.

d.

Mask , and If using Remote View function, specify the IP Address, Subnet Mask Gateway.

e.

Click on the DNS tab tab and enter the necessary information.

f.

Address tab and enter the necessary information. Click on the WINS Address

4. Log Log oofff th the CAS CASE. E. Repeat the section Workstation Configuration in a Domain for all systems before proceeding.

Workgroup Configuration To install CASE on a workgroup, you first configure the server and then configure each workstation to be added to the network. An administrator may have to perform both steps.

Server Server Configuration in a Workgroup The configuration of the server consists of the following tasks:  

Set up the domain user Set up a shared folder on a domain server

Set up User for a Workgroup – Do one of the following:  

Create a new user account. Select an existing user account.

In both cases, the user must exist on the CardioSoft server and be designated as a Network User . Set up Shared Folder in a Workgroup – The procedure for setting up a shared

folder varies slightly depending on whether the server is new. New CardioSoft Server

1.

Log in in to the the serv server er as the admini administr strato ator. r.

2. Crea Create te a dir direc ecto tory ry name namedd cardio on the local drive of the server.

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3.


4.

Network User has Configure Configure the the share share permis permissions sions such that the design designated ated Network User has full control permissions.


3-21


Existing CardioSoft Server

Before renaming the old cardio folder, save the system configuration and all custom setups to disk. For additional information, refer to “General Troubleshooting” on page 6-1 6-111. 1.

Log in in to the the serv server er as the admini administr strato ator. r.

2.

Rename Rename the the exist existing ing Cardi CardioSo oSoft ft direc director toryy cardio to card_old .

3. Crea Create te a new new dire direct ctor ory y na name medd cardio on the local drive of the server. 4.

Share the card_old directory directory and name the share card_old .

5.


6.

Configure Configure the the share permi permissio ssions ns for both both shares shares such that that the design designated ated Network User Network User has has full control permissions.

Workstation Configuration in a Workgroup Once the server has been configured, you must configure all the systems that will be connected to the CardioSoft network. The workstation configuration consists of the following steps:  

Adding a CASE system to the workgroup Configuring the CASE user accounts and network settings

Add CASE System to Windows NT / Windows 2000 Workgroup – To add a

CASE system to the work group, use the following procedure: Enabled hardware 1. Boot Boot the the CAS CASE E wit with h the the Network Enabled hardware profile.

2. Log Log in aass loca locall Admi Admini nist stra rato tor. r. 3.

Enabled . Set the def defaul aultt hardw hardware are pro profil filee as as Network Enabled

a.

Open Open system system prop propert erties ies by by right right click clicking ing on on My Computer and and selecting Properties.

b.

Hardware Profiles tab. Click the Hardware

c.

Select Network Enabled and and click the up arrow button.

d.

Click OK to to close the window.

4. Chan Change ge netw networ ork k set setti ting ngs. s. a.

Neighborhood and Open Open net networ work k proper propertie tiess by right right cclic lickin king g on Network Neighborhood and selecting Properties.

b.

Click Change button in Identification tab.

c.

Click Workgroup radio button.

d. Type ype in desi design gnat ated ed Workgroup Name.

3-22

e.

Click OK to to close the window, then click OK to to close the network properties window. window.

f.

If pro prompt mpted, ed, restar restartt the the comput computer er..


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Configure User Accounts and Network Settings on a CASE in a Workgroup –

To configure the user accounts and network setting, use the following procedure. 1.

Log in in to the the CASE CASE as local local Admi Adminis nistra trator tor..

Network User . 2. Crea Create te the the desi design gnat ated ed Network User

a.

Administrator Tools->User Manager. Manager. Open Start Menu-> Administrator Tools

b.

Select New User in in the User Menu. Menu.

c.

Enter the exact exact same same user user name name and and password password as the the designate designatedd Network User used used on the CardioSoft server.

d. Unch Unchec eck k the che check ckbo box x label labeled ed Change Password . e.

Never Expires Expires. Chec Check k the the chec checkb kbox ox labe labele ledd Password Never

f.

Click Groups button.

g. Add Add the the desi design gnat ated ed Network User to to the Administrators group. h. 3.

Click OK and and then close the User Manager window. window.

Confi Configur guree the TCP/IP TCP/IP settin settings. gs. Perform these steps if the Remote View function is used or communication with a MUSE server (Version (Version 5.0a) is needed. a.

Right cl click on on Network Neighborhood and and select Properties.

b.

Click on the Protocols tab.

c.

Click on TCP/IP Protocol and then click Properties.

Mask , and d. If us using ing Remo Remote te View View func functio tion, n, speci specify fy the the IP Address, Subnet Mask Gateway.

e.

Click on the DNS tab tab and enter the necessary information.

f.

Click on the WINS Address tab and enter the necessary information.

4. Log Log oofff th the CAS CASE. E. Repeat the section Workstation Configuration in a Workgroup for all systems before proceeding.

Centri Centri city Xi Configur ation When interfacing the CASE to Centricity Xi, data from the CASE will not transfer to the Centricity system until the CASE application is shut down. However, by default, shutting down the CASE application shuts down the entire CASE system. To prevent this, add the following lines to the win.ini file on the CASE system: [Cardio] Mai-NTDown=0

The following table identifies the location of the win.ini file: CA S E V er s i o n

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WIN.INI L o c at i o n

v6 or late laterr

CASE inst instal alla latio tion n dire direct cto ory

prio priorr to v6

Windo indow ws sys syste tem m direct irecto ory


3-23


Save Save Existing Exist ing Data Data This section describes how to back up existing system configurations, custom setups, user lists, custom configured reports, and examination files. Start this section only after the network has been configured on all systems that will be connected to the CardioSoft network. This section must be completed if at least one CASE system added to the CardioSoft network has locally stored examinations. If all systems (CASE \ CardioSoft) and the shared CardioSoft server folder are new, this section can be skipped. This procedure copies the examination files and the custom setups from each CASE system. However, it copies the system configuration, the user list, and any custom configured reports from only one CASE system, which should be designated as the “special station.” If the CardioSoft network existed before this installation began, it is recommended you use one of the CASE systems connected to the existing CardioSoft network as the “special station.”

Copy Custom Setups Copy to diskette the custom setups from every existing CASE system that is not currently connected to the CardioSoft network. The custom setups stored for CASE systems that were already connected to the CardioSys network should already have been copied before the cardio directory on the CardioSoft server was renamed to card_old . Refer to “Saving Custom Settings to Diskette” on page page 7-5 7-5 for for details.

Merge Local Examination Databases The following procedure merges locally stored examinations from the CA SE system to the shared folder on the network server. It should be performed on each CASE system that meets the following criteria:  

Not currently connected connected to the CardioSoft CardioSoft network Has locally stored examinations

Do not perform this procedure for any system that was connected to an existing CardioSoft network. Additional information can be found in “Database Repair for CASE / CardioSoft” on page page 7-1 7-111. Network User . 1. Log Log in tto o th thee CASE CASE as as desi design gnat ated ed Network User

3-24

2.

Map the next next available available drive letter letter (e.g. (e.g. F:\) to the the cardio shared folder on the CardioSoft server.

3.

Copy the CARD_REP.exe program to the local CASE program directory (e.g., D:\Case\).

4.

Launch th the CARD_REP.exe program.


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5.

Change the Master Directory to the CASE program directory (e.g. D:\Case).

6.

Change the Repair Directory drive to the mapped cardio drive letter (e.g. F:\CARD_R0).

7.

Press Start Repair button to run the merge process.

8.

Enter the password, which can be found in “General Troubleshooting” on page 6-11.

9.

After the merge is completed, press Program End .

10. Log off the CASE. Repeat Copy Custom Setups and Merge Local Examination Databases on all systems before proceeding.

Merge Networked Examination Database This procedure merges the local examination databases that were just uploaded to the server with the network examination databases that previously existed in the card_old folder on the server. It should be performed only: a.

IF the CardioSoft server previously existed and had examination data, and

b.

AFTER all of the locally stored examinations have been uploaded from

each CASE workstation to the CASE server. 1.

Log in to the special station CASE as the designated Network User .

2.

Map the next available drive letter (e.g. F:\) to the cardio shared folder on the CardioSoft server if it is not already connected.

3.

Map any available drive letter (e.g. X:\) to the card_old shared folder on the CardioSoft server.

4. Copy the program CARD_REP.exe to the card_old mapped drive (e.g. X:\). 5.

Launch the CARD_REP.exe program from the card_old mapped drive (e.g. X:\).

6.

Change the Master Directory to the mapped drive card_old (e.g. X:).

7.


8.

Press Start Repair button to run the merge process.

9.

Enter the password, which can be found in “General Troubleshooting” on page 6-11.

10. Close the CARD_REP program by pressing Program End . 11. Log off the CASE.

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3-25


Merge User List and Configured Reports This procedure merges any custom configured reports and user list from the special station to the cardio folder on the CASE/CardioSoft server. If no custom reports or user list exists on the special station, this procedure can be skipped. The procedure varies slightly depending on whether the special station had been a stand-alone workstation or part of an existing network. Chose the appropriate procedure and perform all of the steps.

Special Station Was a Stand-Alone Station 1.


2.

If it is not already connected, map the next available drive letter (e.g. F:\) to the cardio shared folder on the CardioSoft server.

3.

Launch the CARD_REP.exe program from the local CASE program directory (e.g. D:\CASE).

4.

Change the Master Directory to the local CASE program folder (e.g. D:\Case).

5.


6.

Press User / Conf. Rep button to run the merge process.

7.

Click Yes.

8.

Close the CARD_REP program by pressing Program End .

9. Log off the CASE.

Special Station Was Connected to Existi ng CardioSoft Network 1.


2.

If it is not already connected, map the next available drive letter (e.g. F:\) to the cardio shared folder on the CardioSoft server.

3.

If it is not already connected, map any available drive letter (e.g. X:\) to the card_old shared folder on the CardioSoft server.

4.

Launch the CARD_REP.exe program from the card_old mapped drive (e.g. X:\).

5.

Change the Master Directory to the mapped drive card_old (e.g. X:).

6.


7.

Press User / Conf. Rep button to run the merge process.

8.

Click Yes.

9.

Close the CARD_REP program by pressing Program End .

10. Log off the CASE.

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Copy System Configuration This procedure copies the system configuration of the special station to diskette. Log on to the special station as a local administrator and follow the directions described in “Saving System Configurations to Diskette” on page 7-4. If the special station was on the CardioSoft network before the installation procedure was started, the system configuration should have already been saved before the cardio folder was renamed to card_old on the CardioSoft server.

Finish Database Merge Perform this task only after the following tasks have been completed: 

All local databases have been merged into the CARD_R0 folder.



The original server database (if it existed) has been merged into the CARD_R0 folder. The user list has been merged into the CARD_R0 folder. The configured reports have been merged into the CARD_R0 folder.

   

The custom setups have been copied to diskette. The system configuration has been copied to diskette.

To finish the database merge, use the following procedure: 1.


2.

Map the next available drive letter (e.g. F:\) to the cardio shared folder on the CardioSoft server if it is not already connected.

3.

Open the CARD_R0 folder on the mapped drive cardio (e.g. F:\CARD_R0).

4. Move all files in the CARD_R0 folder to the root of the mapped drive cardio (e.g. F:\). 5. Delete the empty CARD_R0 folder. 6. Log off the CASE.

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Install CASE Application The following procedure installs the CASE application. The application should be installed on all CASE workstations. Do not install it on the server.



Install the application only after you configure the CardioSoft network (“Configure the Network” on page 3-18) and save the existing data ( “Save Existing Data” on page 3-24)



Install the application on ONLY ONE workstation at a time. Attempting to install it on more than one workstation at the same time may corrupt the installation on ALL workstations.

1.

Log in as the local Administrator.

2.

Map the next available drive letter (e.g. F:\) to the cardio shared folder on the CardioSoft server. Make sure the Reconnect at login box is checked. Also, Connect as should be the designated Network User . If the designated Network User is a domain user, then enter [ Domain Name]\[ Network User ].

3.

Insert the application installation CD into the CD drive and begin the installation. If the installation does not start automatically (wait some seconds), launch setup.exe in directory Disk1 (“E:\Disk1\setup.exe”).

4.

At the Choose Program Directory (local) screen, choose the default, D:\CASE . Click Next .

5.

At the Choose Database Directory screen, select Browse… and browse to the root folder of the mapped drive cardio on the CardioSoft server.

6.

Verify the Path edit box value is the root folder of the mapped network drive (e.g. F:\).

7.

Finish the installation and reboot the system as prompted.

Reconfig ure the Syst em Configuring the system is the last step in the installation process and prepares the CASE workstations. It should be performed only after the application has been installed on ALL workstations.

Do not start the application on any workstation until the all workstations have been reconfigured. Attempting to start the CASE application before all workstations have been configured may corrupt the installation on all workstations.

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Revision F


Configure Network User Profile The following procedure prepares the default Network User profile. 1.

Log in as the local Administrator.

2.

Open the System applet in Control Panel and select the User Profiles tab.

3. Select the local User user profile ([Computer Name]\User) and click the Copy To… button. 4. Browse to the designated Network User profile directory: (C:\winnt40\Profiles\[Network User Name]). 5.

Click OK .

6.

Click OK to close the System applet.

7. Close Control Panel. 8.

Log off.

9.

Log in as Network User. From this point on, the CASE user should login as the designated Network User . Inform the customer of this change.

10. Verify the desktop wallpaper is the GE wallpaper and the mapped drive cardio on the CardioSoft server is connected.

Install Option Codes The following procedure installs option codes, if they are needed. 1.

Start the CASE application if it did not automatically start.

2.

Type in the desired option codes or load them from the provided diskette.

For additional information, refer to “Network Installation” on page 3-17.

Restore System Configuration For any new CASE workstations on the network, do the following: 

Load the system configuration that was copied from the special station as part of the data backup process. For more information, refer to “Restoring System Configuration from Diskette” on page 7-6.



Verify that all settings are correct for each tab in the System Configuration window. Verify the connection from the workstation to the MUSE server was not broken, if the workstation should communicate with MUSE. For more information, refer to “Data Interface with MUSE” on page 3-32.



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Restore Custom Settings For any new CASE workstations on the network, do the following: 



Load the custom settings that were copied from the special station as part of the data backup process. The custom settings can be saved to the CardioSoft server from one CASE system and then copied from the server to each workstation. For more information, refer to “Restoring System Configuration from Diskette” on page 7-6. Verify that the settings are correct for each tab in the Setup window.

Installing a Network Printer for all Users on This CASE Windows NT stores network printer definitions in the users' profile. To avoid multiple installations for each user, install the printer locally and add a new local port with the path of the network printer: This section should only be performed if a network printer is used. 1. Login as local Administrator. 2.

Click Start -> Settings -> Printers.

3.

Double click Add Printer .

4.

Select My Computer and click Next .

5.

Select port LPT2 and click Next .

6.

Select manufacturer and model of the network printer or use an appropriate driver from CD/disk. Click Next .

7.

At the dialog Type in the name of this printer… Click Next .

8.

At the dialog Indicate whether this printer will be shared… Click Next .

9.

At the dialog Would you like to print a test page… select No and click Finish.

10. Click Start -> Settings -> Printers. 11. Right click the installed printer, select Properties, select Ports tab, and click Add Port…

12. Select Local Port in the list and click New Port… 13. Enter the network printer name \\[Printer Server Name]\[Printer Name] to enter the port name and click OK . 14. At the Properties dialog, click OK .

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Installation: Data Interface with MUSE

Data Interface with MUSE Tests on CASE can be transferred to the MUSE database for general accessibility. The tests can be transferred using one of three methods: a.

Save Examinations to a floppy disk and carry it to MUSE

b.

Send Examinations to MUSE using FTP via LAN

c.

Store Examinations on a shared directory located on MUSE via LAN Methods b and c require a network connection with TCP/IP specifications. All methods require that each CASE use its unique Cart number and correct location number to generate a unique filename.

Establis h Connection to MUSE The preferred method for transferring data depends on the version of MUSE with which you wish to transfer data. For MUSE 5.x, the preferred method is FTP. Use the following procedure to establish a connection from the CASE workstation to MUSE: 1.

Specify the FTP account informations on CASE -> System Configuration -> MUSE by enabling “Data transfer via FTP”

2.

Type in the FTP Server (normally the same as the Web Server).

3.

Enter a Username and Password if this information is required for the FTP server.

For MUSE 4.x , the preferred method is a shared directory. Use the following procedure to establish a connection from the CASE workstation to MUSE: 1.

Specify the account informations on CASE -> System Configuration -> MUSE by enabling “Data transfer via shared directory”.

2.

Type in the correct shared directory. You have multiple methods to enter the correct shared directory. If the shared directory has been mapped and configured to reconnect at logon, you can enter the mapped drive letter (e.g., . F:\ ). If the shared directory has not been mapped, you can enter the UNC format in a valid form (e.g., \\SvrName\SharePointName). If no DNS/WINS is installed on the domain server (i.e. you are using RAS), enter the physical IP address of the server and the directory name (e.g., \\123.456.789.255\SharePointName).

3.

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Enter a Username and Password if this information is required for accessing this shared directory.


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Installation: Data Interface with MUSE

Read MUSE Pati ent Data fr om CASE With MUSE v5.0 or above, you can read the MUSE patient data directly from the CASE workstation. This requires the following:     

MUSE v5.0 or above an account on the MUSE server Internet Explorer v6.0 or above Network connection with TCP/IP specifications Acrobat Reader v4.0 or above

Configure Internet Explorer Before you can access MUSE from CASE, you must first configure Internet Explorer using the following procedure: 1.

On the Windows taskbar, select Start -> Settings -> Control Panel.

2. Double-click on “Internet”. 3. Open the “Connection” tab. 4.

If your connection to the LAN does not require access to the proxy server, deactivate “Access via proxy server”. Otherwise, open “Advanced Settings” and configure the proxy settings appropriately.

5. Do one of the following: If the workstation is connected directly to the LAN via an ethernet connection, activate “Connect to Internet via LAN”  If the workstation is connected to the LAN remotely, activate “Connect via modem”. Click “OK” 

6.

Some changes may not take effect until the OS is restarted.

Establish a MUSE Account To select patients from the MUSE database instead of the local database, you need to establish an account on the MUSE server using the following procedure: 1.

Specify the Web account informations on C ASE -> System Configuration -> MUSE by enabling “Request MUSE data”.

2.

Type in Web Server, the Username, and the Password You have multiple methods to enter the Web Server.   

3.

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Internet name convention: http:\\www.myMuseSvr . Intranet name convention: myMuseSvr IP address: 123.456.789.255

Select the correct MUSE site number.


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Installation: Configuring a CASE/CardioSoft System with the EMR Application

Configuring a CASE/CardioSoft System with the EMR Application The CASE/CardioSoft system * can be configured with the EMR application. The process is identical for both new and existing systems with one exception: when configuring an existing system, you must migrate historical data. The general process is outlined below. Details are found on the following pages. 1.

Go through “Before You Begin” on page 3-35.

2.

Install Logician 5.6.3 or higher on each CASE / CardioSoft client. For details, refer to “Configuring a CASE/CardioSoft System with the EMR Application” on page 3-36.

3.

Install the CASE/CardioSoft interface kit. For details, refer to “Install the CASE/CardioSoft Interface Kit.” on page 3-36.

4.

Import the CardioSoft clinical kit to the EMR application using the instructions in the CASE/CardioSoft - EMR Integration Release Notes. For instructions on accessing the release notes, refer to “Acquire CASE/ CardioSoft – EMR Integration Release Notes” on page 3-35.

5.

Configure the CASE/CardioSoft EMR settings. For details, refer to “Configure CASE/CardioSoft EMR Settings” on page 3-36.

6.

If you are configuring an existing CASE/CardioSoft system, migrate historical CASE/CardioSoft data. This is a four-part process. The instructions in the CASE/CardioSoft - EMR Integration Release Notes explain how to:   

configure the cross-reference file, create LinkLogic relationships, and configure the LinkLogic document relationship.

For details, refer to “Migrate Data” on page 3-38.

* The term “CASE/CardioSoft” is used generically to denote whichever system is being configured, CASE or CardioSoft.

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Before You Begin Complete the following checklist to ensure that you are prepared to configure the CASE/Cardiosoft system with the EMR application.



Install CASE/CardioSoft system

The CASE/CardioSoft system must be installed and operational before you configure the CASE/CardioSoft to EMR interface. 





Use the procedures described in the CASE Service Manual for configuring the CASE system. Use the installation procedures described in the CardioSoft Installation Guide for configuring the CardioSoft system. The CASE/CardioSoft database must reside in a shared location, accessible to all users.

GE recommends installing the CASE/CardioSoft database on a separate server from the EMR application. If you install it on the same server, GE recommends that it is on a separate, dedicated hard drive to ensure that file sizes do not hinder performance.



Enable EMR option on CASE/CardioSoft

The following requirements must be met for the EMR Option to be enabled on the CASE/CardioSoft system: 





The CASE/CardioSoft option code for the EMR application must be entered in the System Configuration >> Option Codes tab PRIOR to configuring the EMR application on the CASE/ CardioSoft system. The EMR option must be enabled in the System Configuration >> General. Click For Service Only (service password: helserv) to display the Service Screen . Click Enable EMR Mode.

Acquire permissions for the EMR application web site

You will need a User ID and password to access the EMR application’s support web site. Ask your EMR application manager for this information.



Acquire CASE/CardioSoft – EMR Integration Release Notes

You will need the CASE/CardioSoft EMR Integration Release Notes for EMR-specific instructions for configuring the EMR application. The release notes can be found on the EMR support web site (http://support.medicalogic.com/ ).

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

Install EMR application

The EMR application must be installed and operational before you begin to configure the CASE/CardioSoft to EMR interface. For information on installing the EMR application, go to http://support.medicalogic.com/ , select your version of the product, and then look under Installation Checklists.



Acquire administrator privileges

You will need administrator privileges to both the CASE/CardioSoft system and to the EMR application to complete this configuration. If you do not have administrator privileges, contact your system administrator.



Acquire default provider name

The customer site administrator must designate the default provider for use before migrating historical data from the CASE/CardioSoft system to the EMR application.

Configuring a CASE/CardioSoft System with the EMR Application To configure the system, use the following instructions: 1.

Set up the CASE/CardioSoft in a networked environment. Make sure that the XEMR option code for interfacing to the EMR application is available (in the CASE/CardioSoft system, click System Configuration, then the Option Code tab).

2.

Install Logician 5.6.3 or higher on each CASE/CardioSoft client.

Install the Centri city EMR Appli cation The installation of the Centricity EMR application consists of the following steps: 1.

Install the CASE/CardioSoft Interface Kit. Install the CASE/CardioSoft Interface Kit. This is available for download/ installation on the EMR application support website (http://support.medicalogic.com/ ).

2. Import the Clinical Kits. Follow the instructions in the CASE/CardioSoft - EMR Integration Release Notes to import the CardioSoft clinical kit. 3.

Configure CASE/CardioSoft EMR Settings After importing the CASE/CardioSoft clinical kit into the EMR application, verify on the CASE/CardioSoft system that the EMR settings are configured correctly.

3-36

a.

Launch the CASE/CardioSoft application.

b.

Click System Configuration. The System Configuration window displays.


Revision F


c.

Verify that the EMR tab now is available onscreen.

EMR tab Communication folders

Error logging folder location

CASE/CardioSoft System Confi guration Setup Tab

The Communication Folder locations were determined automatically after the EMR application was installed, using information from the file /CardioSoft/CardioSoft.ini. d.

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The folder for error logging is automatically generated. Verify that the folder location is accurate (i.e., for CardioSoft c:\ cardio\emr_errors, or for CASE: d:\case\emr_errors).


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Migrate Histor ical Cardi oSoft Data If you have been using CASE/CardioSoft prior to integrating with the EMR application, you will need to migrate your existing CASE/CardioSoft data. This migration transfers all of the data. You cannot selectively migrate only certain records. There are four steps to this migration: 1.

Configure the Cross Reference File.

2.

Create LinkLogic Relationships.

3.

Configure the LinkLogic Document Relationship.

4.

Migrate Data.

Follow the detailed instructions in the CASE/CardioSoft - EMR Integration Release Notes to configure the cross reference file, create LinkLogic relationships, and to configure the LinkLogic document relationship (steps 1 – 3 above). Refer to “Migrate Data” below to migrate historical data from the CASE/CardioSoft system to the EMR application.

Migrate Data After completing the instructions in the CASE/CardioSoft - EMR Integration Release Notes, use the following instructions to migrate the CASE/CardioSoft data: 1.

In the CASE/CardioSoft application, click System Configuration.

2.

Select the EMR tab.

3.

In the Data Transfer Via Shared Directory field, click the ellipsis and select the network LinkLogic installation of the ...Data\In folder.

4.

Click OK .

5.

Click Start . A demographics file (.hd) and its related ImageLink files (.ht) are created for every patient in the CASE/CardioSoft database. These files are picked up by LinkLogic and included in the patient’s chart.

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Installation: Metabolic Interface

Metabolic Interface The CASE workstation can communicate with the data acquisition device over the workstation’s serial port. In addition, it can record test data to a shared file on the network. This section describes: the available communication commands the serial port settings

 

the structure of the command string the test data settings the structure of the test data file

  

Communication Commands The stress test module can process the following commands from the serial port: 'E' 'T' 'O' 'H' 'R' 'W' 'S' 'M'

echo on start treadmill stop treadmill stage hold request measurements start pretest start exercise start recovery

Serial Port Setti ngs The default settings for serial port are parity data bits stop bits baud rate handshake

no 8 1 1200 no

You can modify the settings for the serial port by modifying the following values in [CAS_RECORD] section of the cardio.ini file located in the Windows directory. ' Field

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Values

SpiroParity

0 = no parity 1 = even parity 2 = odd parity

SpiroDataBits

0 = 7 data bits 1 = 8 data bits

SpiroStopBits

0 = 1 stop bit 1 = 2 stop bits


3-39


Field

Values

SpiroBaudrate

0 = 300 baud 1 = 600 baud 2 = 1200 baud 3 = 2400 baud 4 = 4800 baud 5 = 9600 baud 6 = 19200 baud 7 = 38400 baud 8 = 56000 baud 9 = 128000 baud

SpiroHandShake

0 = no handshake 1 = XonXoff 2 = hardware handshake 3 = hardware handshake and interpretation of CR and NULL

For example, to configure the serial port for even parity, 7 data bits, 2 stop bits, 9600 baud, and XonXoff, cardio.ini would look like this: [CAS_RECORD] SpiroParity = 1 SpiroDataBits = 0 SpiroStopBits = 1 SpiroBaudrate = 5 SpiroHandShake = 1

Command String Structur e The CASE workstation sends the following string to the serial port every five seconds: [recoxxx34xMxxxx0x%xxx60xxxx4x-999x-999x-999xx-19xxxx1xx-12x]4CCR

Position is very important in this message. Therefore, an x is used to indicate a space. The following table identifies the remainder of the values in the string. Explanatory notes follow the table. Part of string

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Meaning

Value

Notes

[

Beginning

reco

Stage 'Recovery'

xxx34

Speed * 10

3.4

5, 8

xM

Speed designator

MPH

1

xxxx0

Grade * 10

0.0

5

x%

Grade designator

%

2

xxx60

Heart Rate

60 BPM

5

xxxx4

Ectopic Beats per Minute

4

3, 6


5, 10

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Part of string

Meaning

Value

Notes

x-999

BP Measurement NBR

-999

6, 9

x-999

Systolic BP

-999

4, 6

x-999

Diastolic BP

-999

4, 6

xx-19

ST Level [mm]*10

-1.9

6

xxxx1

ST Slope [mV/s]*10

0.1

6

xx-12

ST Integral uV

-12

6, 9

x]

Ending

4C

Checksum

CR

Carriage return

7

1.

Could be 'K' for KPH. Kilometers per hour. If so, SPEED is KPH. Could be 'P' for KPM. Kilopondmeters. If so, SPEED is KPM from Ergo. Could be 'W' for WATTS. Watts. From Ergo.

2.

Could be 'D' dor DEGREES. If so, GRADE is DEGREES.

3.

This is ECTOPIC COUNT for the minute previous.

4.

mmHg

5. If unavailable, pass 0. 6. If unavailable, pass -999. 7.

Right-most 2 ASCII characters of checksum. Checksum includes [, all spaces,] Alpha characters must be Upper Case.

8.

If Ergometer Watts or KPM, SPEED value is not *10.

9.

Not supported in the current version (value = -999)

10. The stage names are fixed as the following table shows:

Phase

Stagenumber

Stagename in the shared file (4 characters)

Pre-Test

1

base

Pre-Test

2

warm warm

Exercise

1

ramp ramp

Recovery

1

reco reco

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Shared File Setti ngs If the stress test module receives the R command ( request measurement , see “Communication Commands” on page 3-39), the CASE workstation will write the stress test data to a shared file named ergospir.dat . By default, the file is stored in c:\temp. You can change that setting by modifying the following fields in the [CAS_RECORD] section of the win.ini file located in the Windows directory. Field

Values

SprioOptionWriteToFile

0 = Do not write to file 1 = Write to file

SpiroDirectory

Valid directory path

For example, if you want the shared file ergospir.dat to be written to a directory called spirapp\data located on the c:\ drive, the entry in win.ini would look like this: [CAS_RECORD] SpiroOptionWriteToFile = 1 SpiroDirectory = C:\SPIROAPP\DATA

Data File Stru ctu re The CASE workstation will write the following data string to the shared file every five seconds or immediately after phase or stage has changed. [recoxxx34xMxxxx0x%xxx60xxxx4x-999x-999x-999xx-19xxxx1xx-12x]4CCR

Position is very important in this message. Therefore, an x is used to indicate a space. The following table identifies the remainder of the values in the string. Explanatory notes follow the table. Part of string

3-42

Meaning

Value

Notes

[

Beginning

reco

Stage 'Recovery'

xxx34

Speed * 10

3.4

5, 8

xM

Speed designator

MPH

1

xxxx0

Grade * 10

0.0

5

x%

Grade designator

%

2

xxx60

Heart Rate

60 BPM

5

xxxx4

Ectopic Beats per Minute

4

3, 6

x-999

BP Measurement NBR

-999

6, 9

x-999

Systolic BP

-999

4, 6

x-999

Diastolic BP

-999

4, 6


5, 10, 11

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Part of string

Meaning

Value

Notes

xx-19

ST Level [mm] * 10

-1.9

6

xxxx1

ST Slope [mV/s] * 10

0.1

6

xx-12

ST Integral uV

-12

6, 9

x]

Ending

4C

Checksum

CR

Carriage return

7

1.

Could be 'K' for KPH. Kilometers per hour. If so, SPEED is KPH. Could be 'P' for KPM. Kilopondmeters. If so, SPEED is KPM from Ergo. Could be 'W' for WATTS. Watts. From Ergo.

2.

Could be 'D' dor DEGREES. If so, GRADE is DEGREES.

3.

This is ECTOPIC COUNT for the minute previous.

4.

mmHg

5. If unavailable, pass 0. 6. If unavailable, pass -999. 7.

Right-most 2 ASCII characters of checksum. Checksum includes [, all spaces,] Alpha characters must be Upper Case.

8.

If Ergometer Watts or KPM, SPEED value is not *10.

9.

Not supported in the current version (value = -999)

10. The stage names are fixed as the following table shows:

Phase

Stagenumber

before Test-Start Pre-Test

Exercise

Recovery

Stagename in the shared fil e (4 characters) chck

1

base

2

warm

...

warm

1

exer

...

exer

1

reco

...

reco

Test finished

stop

If a phase or stage change occurs, the complete string is written immediately.

Revision F


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For your notes

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Revision F

4

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InSite 2.0


4-1

For your notes

4-2


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InSite 2.0: Installing InSite 2.0

Installing InSite 2.0 InSite 2.0 is a remote service solution that provides GE Service with the following two tools: 

GE CASE CardioSoft InSite Service Agent, which 

uploads files from the CardioSoft program directory\InSite\Upload, downloads files to the CardioSoft program directory\InSite\Download, and



watches disk space of the CardioSoft database drive.





VNC Server, which provides remote access service capability provided  GE Service knows the VNC server password, and  GE CASE CardioSoft InSite Service Agent is set to automatic mode.

This document outlines the steps involved in installing InSite 2.0 in CardioSoft, CardioSoft Client, CardioSoft DFT, and CardioSoft WebServer. InSite 2.0 replaces the previous remote service option, which used a MultiTech modem and pcAnywhere to allow access to the CASE/CardioSoft system. When upgrading from an earlier CardioSoft version, uninstall pcAnywhere from the system before proceeding with the installation of InSite 2.0.

Pre-Inst allation Process Before beginning the installation of the GE CASE CardioSoft InSite Service Agent, complete the following steps. During installation, InSite 2.0 will use the information entered and checked in the following steps as default values. This information includes device name, serial number, CardioSoft program directory, CardioSoft database drive, Proxy server address, and proxy server port. Be sure to record this information while completing these steps. 1.

Verify that CardioSoft, CardioSoft Client, CardioSoft DFT, or CardioSoft WebServer are installed.

2. Turn off the PC. 3.

Connect the CAM-USB with CAM14, CAM-USB A/T with CAM14, or CORINA to the PC.

4.

Turn the PC on.

5. Start CardioSoft. 6.

Select System Configuration.

7.

On the General tab, fill out the Institution Name and Address fields ( Name, Street , City).

8.

On the Option Code tab, check the Internal Serial Number .

9. Exit CardioSoft. 10. Start Internet Explorer. Revision F


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11. To use a proxy server, complete the following steps: a.

Select Tools > Internet Options > Connections tab > Settings.

b.

Select the Use a proxy server for your LAN... check box

c.

Enter the proxy server address and port number.

12. Determine whether the proxy server requires authentication (method, user name, password). If a proxy server will be used, please contact your System Administrator for installation details.

If any of the above information is missing or incomplete, DO NOT PROCEED with the installation. Incorrect information provided during the installation may cause the services to function improperly requiring you to uninstall/reinstall InSite 2.0. Obtain ALL of the required information before proceeding.

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Installation Procedure Use the following instructions to install the InSite 2.0 software: 1. Log on to the system. You must have system administrator privileges to perform the installation. 2.

Insert the CD in the CD ROM drive. If autoplay is enabled, the installation will begin immediately. If autoplay is not enabled, use the following instructions to begin the installation routine: a.

Select Start > Run > Browse.

b.

Locate the file X:\CASECardioSoftSAInstall X = CD ROM drive letter, e.g. D:\ or E:\).

c.

Double-click the file name. The following screen appears.

3.

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Click Next> to advance to the next screen.


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4.

Specify the root installation directory for the GE CASE CardioSoft InSite Service Agent and the VNC Server. The default directory is C:\gehc-it\InSite 2.0.

5.

Click Next> to advance to the next screen.

6.

Confirm or modify the default values (use alphanumeric values only). The following table identifies the fields and required values. Use alphanumeric values only. Spaces are not allowed. Device Name

Unique device name for the GE CASE CardioSoft InSite Service Agent. It consists of Product Name, Product Version, Institution Name, and Mac Address. To locate the Mac Address, use the following instructions: a.

From the Start button, select Programs > Accessories > Command Prompt to open a DOS window.

b.

Type the command ipconfig -all | more

c.

Record the value of the Ethernet Adapter Local Area Connection in the Physical Address line without the leading hyphen (-). This is the Mac Address.

4-6

Serial Number

The serial number of the CAM-USB, CAM-USB/AT, or CORINA.

Program Directory

The directory where CardioSoft application is installed.

Database Driver

The drive where the CardioSoft database is installed.


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The GE Service technician will need to know a part of the device name (e.g., the Mac address) or the serial number to locate your PC using InSite 2.0. To ensure that this information is available when needed, record it in the following table: Device Name: Serial Number: CardioSoft Program Directory: CardioSoft Database Drive:

7.

After the fields have been verified or modified, click Next> to advance to the next screen.

8.

Indicate whether the GE CASE CardioSoft InSite Service Agent will connect to the GE enterprise server through a proxy server and click Next> to advance to the next screen. What happens next depends on your response in step 8. 



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If you selected Yes, you must define the proxy settings InSite 2.0 will use. Proceed to step 9. If you selected No, you will be prompted to select whether the CardioSoft InSite Service Agent and VNC Server should start automatically after install. Skip to step 14.


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9.

Enter the proxy server address and port that was recorded during the preinstallation process.

Record the information in the following table for service interventions: Proxy Server Address: Port:

10. Click Next> to advance to the next screen.

11. Indicate whether the GE CASE CardioSoft InSite Service Agent will require authentication. and click Next> to advance to the next screen. What happens next depends on your response to step 11. 



4-8

If you selected Yes, you must specify the authentication settings InSite 2.0 will use. Proceed to step 12. If you selected No, you will be prompted to select whether the CardioSoft InSite Service Agent and VNC Server should start automatically after install. Skip to step 14.


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12. Enter the User Name and Password information required by the proxy server and select the authentication method.

Record the information in the following table for service interventions: User Name: Password:


14. Choose whether the installer should automatically start the VNC Server and CardioSoft InSite Service Agent upon completion. The installer automatically starts these services by rebooting the computer after installation of InSite 2.0. If you choose not to start these services automatically, you will need to start them manually (see “Operating InSite 2.0” on page 4-14).

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4-9



16. Review the installation summary and do one of the following: 



If the summary is incorrect, click to begin the installation. The progress is displayed, as seen below.

When the software has been registered, the following screen appears.

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17. Click OK to continue the installation. When the installation is complete, the following screen appears.

18. Click Finish to exit the installer application. 19. Contact your local GE Service Center to have them verify connection with InSite 2.0. You will need the information recorded during the installation process.

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InSite 2.0: Uninstalling InSite 2.0

Uninstalling InSite 2.0 If GE Services cannot connect to InSite 2.0, it could indicate that incorrect information was entered during the installation. To correct this problem, you will need to uninstall the software, gather the correct information, and re-install the software using the corrected information. Use the following procedure to uninstall InSite 2.0. 1.

From the Windows taskbar, select Start > Settings > Control Panel.

2. Double-click Add/Remove Programs. 3.

Locate GE CASE CardioSoft InSite Service Agent .

4.

Click Change/Remove. The Uninstall Welcome Screen appears.

5.

Click Next . The Uninstall Summary Screen appears.

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InSite 2.0: Uninstalling Uninstalling InS InSite ite 2.0

6.

Click Next . The InSite 2.0 uninstall routine unregisters the WinVNC service and displays the following dialog box.

7.

Click OK . The uninstall routine completes the uninstallation and displays the Uninstall Confirmation Screen.

8.

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Click Finish to complete the installation.


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InSite 2.0: Operating InSite 2.0

Operating Operatin g InSite InSit e 2.0 2.0 InSite 2.0 can be operated in one of two modes: Automatic or Manual. 



Manual The default mode. Requires you to start the GE CASE CardioSoft InSite Service Agent and and the VNCServer services services when they are needed. Automatic Starts the GE CASE CardioSoft InSite Service Agent and and the VNCServer services automatically when the system boots.

Setti Setti ng th e Operation Operation Mode Use the following instructions to switch operating modes. 1.

From From tthe he Window Windowss task taskbar bar,, sele select ct Start > > Settings > Control Panel. The Control Panel opens.

2. Doub Double le--clic click k Administrative Tools. The Administrative Tools window opens. 3. Doub Double le--clic click k Services. The Services window opens, as seen below. A

B

4. Ver Verify ify tha thatt the the GE CASE CardioSoft InSite Service Agent and and VNCServer services exist. The Status column (A) indicates the status of each service. The Startup Type column (B) indicates the currently selected operating mode of the services ( Automatic or Manual). 5. To togg toggle le eith either er the the Status or the Startup Type, right-click the appropriate column for a service and select the appropriate option.

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InSite 2.0: Restri Restricti cting ng Remote Remote Access Access

Restrict str icting ing Remote mot e Access To provide additional security from unauthorized access, you can use the WinVNC Current User Properties window to: 

set a service password (A),



require confirmation prior to granting access to incoming connections (B), and set a confirmation response time, after which an incoming connection will be automatically rejected (C).



A

B

C

During installation of InSite 2.0, a default password is configured and the Display Query Window check box (B) is deselected. Use the following procedure to set these options. 1.

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Display Display the the Windows Windows taskbar taskbar if if it is not not visibl visible. e.


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InSite 2.0: Restri Restricti cting ng Remote Remote Access Access

D

2.

Click the WinVNC icon (D). The WinVNC: Current User Properties window opens. When the content of the blue diamond is red instead of yellow, yellow, a Remote Access Service connection is active. To cancel an active connection, rightclick the icon (D) and select Kill all clients.

3. Chan Change ge the the pas passw swor ord d und under er Incoming Connections (A). Contact GE Service and inform them of the new password: they need the password to access your PC. 4.

Select th the Display Query Window check box (B) and enter the Timeout (B) in seconds. When an incoming connection tries to access your PC, a Query Window will be displayed on your PC for the period of time specified at Timeout (C). This identifies the user name used and the IP from which the connection is being made. You can use this information to verify that it is GE Service attempting to connect.

To accept the connection, click Accept. If you do not accept within the timeout period, the connection is rejected automatically. automatically. To reject the connection, click Reject. 5. To acc accep eptt your your ccha hang nges es on on the the WinVNC: Current User Properties window, click OK.

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5

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Maintenance


5-1

For your notes

5-2


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Maintenance: Introduction

Introduction A regular equipment maintenance program helps prevent unnecessary equipment and power failures and reduces possible health hazards. This chapter contains instructions for the following recommended maintenance:



Inspecting and cleaning the unit Leakage tests to verify the equipment does not propose a health hazard



Ground continuity test to verify all exposed metal is properly grounded



Failure—on the part of all responsible individuals, hospitals or institutions employing the use of this device—to implement the recommended maintenance schedule may cause equipment failure and possible health hazards. The manufacturer does not, in any manner, assume responsibility for performing the recommended maintenance schedule unless an Equipment Maintenance Agreement exists. The sole responsibility rests with the individuals, hospitals, or institutions utilizing the device.

Requi red Tool s and Supplies In addition to a standard set of hand tools, you will need the special tools and items listed below to maintain or repair the unit. Table 1-1. Tools and Suppli es (Continued) 

   

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Leakage Current Tester  120 V (or equivalent)  240 V (or equivalent) Multimeter Isopropyl Alcohol Dust Remover (compressed air) Lint-free Cloth


5-3

Maintenance: Inspection and Cleaning

Inspection and Cleaning Basic maintenance consists of visual inspection and both external and internal cleaning.

Visual Inspectio n Perform a visual inspection of all equipment and peripheral devices daily. Turn off the unit and remove power before making an inspection or cleaning the unit.    

Check the case and display screen for cracks or other damage. Regularly inspect all cords and cables for fraying or other damage. Verify that all cords and connectors are securely seated. Inspect keys and controls for proper operation.  Toggle keys should not stick in one position.  Knobs should rotate fully in both directions.

Exterior Cleaning Clean the exterior surfaces once per month, and more frequently if needed. 

Use a clean, soft cloth and a mild dishwashing detergent diluted in water.



Wring the excess water from the cloth. Do not drip water or any liquid on the equipment, and avoid contact with open vents, plugs, or connectors.



Dry the surfaces with a clean cloth or paper towel.

Interior Cleaning Disassembly To clean the interior, log off the CASE application, shut down the system, turn the power switch to OFF, and unplug the unit from the power outlet. Remove the screws from the CPU access door, then remove the door.

General Check for dust buildup on the surfaces of the interior circuit boards, components, and assemblies. Use commercially available compressed air to blow away accumulated dust. Follow the manufacturer’s directions for use. After reassembly, reconnect the CASE unit to AC power.

Thermal Printhead Clean the thermal printhead every three months, or more often with heavy use. A build-up of thermal paper coating on the printhead can cause light or uneven printing. Use a solution containing alcohol on a nonwoven, nonabrasive cloth such as TechniCloth to wipe off the printhead. Do not use paper toweling, as it can scratch the printhead.

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Maintenance: Electrical Safety Tests

Electrical Safety Tests The suggested electrical safety tests, described below, are based on UL 60601-1 or the international standard IEC 60601-1, as applicable. What follows is a general description of the suggested tests; refer to the governing standard for a more detailed description. Conduct the tests under normal ambient conditions of temperature, humidity, pressure, and line voltage. The leakage currents correspond to 110% of the rated voltage for the test unit. Most Safety Testers take this into account; otherwise, the measured values must be calculated.

Recommended Test Schedule GE recommends that the tests be performed according to the following schedule:  After initial installation. Once every 12 months thereafter as part of a regular maintenance plan.  

Whenever internal assemblies are serviced.

Recommended Test Equipm ent The following equipment is required to conduct the electrical safety tests: 



Safety Tester calibrated to IEC 60601-1. Refer to the device’s user manual for details on calibration and use. To ensure personal safety, refer to the tesing instrument’s user documentation. Testing connector, as described for the individual tests, below

Protective Earth Resis tance Test This test determines whether the device and/or its power cord has a power ground fault. If the device has a power cord, the test measures the impedance between the cord’s protective earth pin and any accessible metal part which is protectively earthed. If the device does not have a power cord, the test measures the impedance between the AC inlet’s protective earth teminal and any accessible metal part which is protectively earthed. Conduct the test both with and without a power cord. To conduct this test, the test circuit must conform to the following values: Hertz

Amperage

Voltage

50 Hz / 60 Hz

25 A

6V

The test fails if the measured value is greater than indicated in the following table:

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IEC 60601-1

UL 60601-1

With Power Cord

200 mOhm

200 mOhm

Without Power Cord

100 mOhm

100 mOhm


5-5


Leakage Current Measurement To perform the suggested measurements, the unit under test has to be separated from any interconnection to a system. If the unit is part of a system, extended tests must be performed in accordance with the governing standard. The following diagram shows the Measuring Circuit [M] required for leakage current. The reading in mV corresponds to mA (leakage current). The Safety Testers generally work with this Measuring Circuit [M] and the displayed values are already converted to leakage current.

Electrical Diagram f or Leakage Current Measurement

Earth Leakage (AC line) Current Test

This test measures leakage current of the device’s internal power supply. The device has to be turned on and off, and connected to your safety-testing equipment. Measurements should be taken under the following conditions (refer to the safety tester diagram):    

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Device in “ON” state Polarity switch NORM and RVS S1 (neutral) closed and open GND switch open


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The test has failed if the measured values are greater than: Polarity: NORM & RVS S1 (neutral): closed GND: open

Polarity: NORM & RVS S1 (neutral): open GND: open

Total tests/combinations: 2


500 µA (IEC)

1,000 µA (IEC & UL)

300 µA (UL)

Enclosure Leakage Current Test This test measures the leakage current from the chassis to the ground during both normal conditions (N.C.) and single fault conditions (S.F.C.). In both cases, use the Safety Tester to measure the leakage current from any exposed conductive part to the ground, as illustrated in the following diagram.

Electrical Diagram fo r Enclos ure Leakage Current Test

Use the following settings on your Safety Tester during normal conditions:

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Switch

Setting

Polarity

NORMand RVS

GND

closed

S1 (neutral)

closed


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Use the following settings on your Safety Tester during single fault conditions: Switch

Setting

Polarity

NORMand RVS

GND

open and closed

S1 (neutral)

closed and open

The test fails if the measured values are greater than indicated in the following table: IEC 60601-1.

UL 60601-1

N.C.

100 µA

100 µA

S.F.C.

500 µA

300 µA

Patient Leakage Current Test This test measures leakage current from the floating input (patient connection) to ground during normal condition (N.C.) and single fault condition (S.F.C.), and depends on a domestic power outlet with 115 or 230 V AC as the source into the floating inputs. In all cases, the leakage current is measured from the floating input to ground: The device has to be turned on and off, and connected to your safety testing instrument.

Electrical Diagram f or Patient Leakage Current Test

For your protection, the following values of resistor R may be used:

5-8

Device Type

Resistence

Line Voltage

Type BF

22 kOhm

120 to 130 V

47 kOhm

220 to 240 V


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During N.C., measurements should be taken under the following conditions (refer to the safety tester diagram:    

Device in “ON” state Polarity switch NORM and RVS GND switch GND closed S1 (neutral) closed

During S.F.C., measurements should be taken under the following conditions (refer to the safety tester diagram):    

Device in “ON” state Polarity switch NORM and RVS GND switch closed, S1 (neutral) open GND switch open, S1 (neutral) closed

The test has failed if the measured values are greater than: N.C.

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S.F.C.

Polarity: NORM & RVS S1 (neutral): closed GND: closed

Polarity: NORM & RVS S1 (neutral): closed | open GND: open | closed



10 µA (IEC & UL)

50 µA (IEC & UL)


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Patient Leakage Current, Mains on Applied Part

PERSONAL SAFETY — MAINS VOLTAGE is applied to floating input (patient connection) and patient cables/test plug conductors and safety tester PATIN JACK. For the protection of the person performing these tests, the following values of resistor R may be used: 

Type BF — 22 kOhm (120 to 130 V)



Type BF — 47 kOhm (220 to 240 V)

Disconnect safety tester from line voltage before connecting patient cable/test plug to device. 

After line voltage has been disconnected, connect the patient cable/test plug to device.

This test performs leakage current tests during single fault conditions (S.F.C.) with line voltage applied to the floating (patient connection) inputs. In all cases, the leakage current is measured from the floating (patient) inputs jack of the device to ground. To setup this leakage current test:

5-10

1.

Disconnect the safety tester from the line voltage

2.

Ground all signal input/output connections (all SIPs/SOPs connected to ground)

3.

Connect the patient cable/test plug to device

4.

Connect the patient cable/test plug to the safety tester

5.

Ensure that the person/tester in not touching the patient cable/test plug or floating (patient) input or device conductive surfaces

6.

Connect safety tester to line voltage —see warning on previous page.


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During S.F.C, measurements should be taken under the following conditions (refer to safety tester diagram):    

Device in “ON” state Polarity switch NORM and RVS S1 (neutral) open GND switch closed

The test has failed if the measured values are greater than: N.C.

S.F.C.

N/A

Polarity: NORM & RVS S1 (neutral): closed GND: closed



N/A

5 mA (IEC & UL)

After completing this test, disconnect the safety tester from line voltage before disconnecting the patient cable/test plug and/or the device.

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5-11


For your notes

5-12


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6

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Troubleshooting


6-1

For your notes

6-2


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Troubleshooting: Overview

Overview This chapter discusses the tools and techniques for troubleshooting problems with the CASE system. The topics include: 

Service Tools  

      

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Service Screen Diagnostic Tests

Entering a One-Day Password General Fault Isolation General Troubleshooting Frequently Asked Questions Flat Panel Monitor Problems Printer Debugging Usage and Workaround of Acrobat 6


6-3

Troubleshooting: Troubleshooting Tools

Troubleshooting Tools CASE provides two groups of tools to help you diagnose issues with the system:  

Service Screen Diagnostic Tests

Each tool is discussed in more detail below.

Serv ice Screen The Service Screen is used to help diagnose issues with the CASE system. It provides access to the system log, key settings, software tests, and service functions. It can be accessed in the General Settings via the “For Service” key. When prompted for a password, enter helserv or case8k , depending on model.

6-4


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Service Screen Description The following table describes the elements of the Service Screen. Element

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Description

Logbook

Displays internal logbook entries of e errors arising during the run period since the last program start. Each entry is time stamped. You can delete the log or save it for future reference.

Active

Activates the entries in the internal logbook. Can only be deactivated until next program start

Delete…

Deletes all entries in internal logbook.

Save as…

Saves all entries of the internal logbook to a text file.

OK or Cancel

Close the Service Screen

Archive Path

Select on a CASE System the path to the archive A: (floppy drive) or E: (CDROM drive). This Archive Path is only displayed if the password case8k was entered.

CORINA time constant (HP filter)

Time Constant for CORINA ECG Acquisition Module. Should be not changed unless requested by customer.

CAM14 High Pass Filter

High Pass Filter for CAM14 ECG Acquisition Module. Should be not changed unless requested by customer.

Research Full Disclosure ECG (in directory \ONL500, \ONL2000)

Should be set to “none”. If you select any other value, the hard disk will fill up quickly: for every Full disclosure ECG a Full disclosure ECG with 500 Samples per second or 2000 Samples per second will be stored.

CAM14 Disable Lead-Fail Bias

Disable Lead-Fail Bias for CAM14 ECG Acquisition Module.

ACQ TEST

Test of the CASE ECG Acquisition Module.

WRTR TEST

Test of the Thermal Writer.

KEYPAD TEST

Test of the CASE function keyboard.

BURN-IN TEST

Burn-In Test for CASE.

LOOPBACK TEST

Loop back test for CASE Serial ports.

Test dictionary…

Compares the Text Strings of the selected language withthe actual selected language of the system configuration.

Service notice…

Service Person can write notice to a file.

Set CAM-USB/CORINA Serial Number…

Set the CAM-USB or the CORINA Serial number of a CAM-USB or CORINA from Service with Serial Number 0.

Delete Network Locks…

All other stations of the network using this server must be stopped before this Network Locks should be deleted.

Save Log Files

Save the Log Files what have been activated from Engineering and send this Log Files please to Engineering.

Format floppy

Formats a floppy disk. CASE Exercise Testing System 2027786-082

6-5


Diagnosti c Tests The diagnostic tests check operation of the acquisition module and board, writer, and keypad. A burn-in test in the menu is for factory production only.

Access the Tests 1. On the startup screen, click System Config. 2.

On the System Configuration screen click For Service Only.

3.

When the Password prompt appears, enter helserv or case 8R.

4. From the bottom of the Service Screen choose the CASE Test Software you want to view

6-6


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Acquisition Test Click ACQ TEST at the bottom of the service screen. The acquisition test screen appears.

The screen displays information about the status of data acquisition.

Keypad Test Click KEYPAD TEST at the bottom of the service screen.

Press each key on the keypad, and watch the interactive screen to be sure all are functioning properly.

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Writer Test Click W RTR TEST at the bottom of the service screen.

The screen provides information about the writer settings. If the printhead or Power Distribution with Writer PCB assembly is replaced, the resistance value must be entered in this screen, then select Recalc and Save. Speed and roller tests can be run from the CASE Writer Utility screen.

6-8


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Troubleshooting: Entering a One-Day Password

Entering a One-Day Password The one-day password is used when the CASE application has been password protected through the User List. The service/service and Administrator/ admin1,3,5,7 username and password only get you to the desktop; they do not allow you to use the CASE application. The one-day password is the only way to access the CASE application when the application has been password protected. The one-day password is made up of 6 characters, starting with today’s YEAR DATE MONTH (with 2-digits for each parameter). 0=r

5=m

1=z

6=f

2=x

7=n

3=v

8=a

4=c

9=s

Example: the six-digit number for January 15, 2002 is 021501. Using the chart above, the password would convert into “rxzmrz”.

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6-9

Troubleshooting: General Fault Isolation

General Fault Isolation Visual Inspectio n A thorough visual inspection of the equipment can save time. Small things— disconnected cables, foreign debris on circuit boards, missing hardware, loose components—can frequently cause symptoms and equipment failures that may appear to be unrelated and difficult to track. Take the time to make all the recommended visual checks (refer to Table 2, “Visual Inspection List,” on page 6-10) before starting any detailed troubleshooting procedures Table 2. Visual Inspection List Ar ea I/O Connectors and Cables

Lo ok fo r t he f ol lo wi ng pr ob lem s



Fraying or other damage Bent prongs or pins Cracked housing Loose screws in plugs

Fuses



Type and rating. Replace as necessary.

Interface Cables



Excessive tension or wear Loose connection Strain reliefs out of place

  

 

Circuit Boards

     

Ground Wires/Wiring

  

Moisture, dust, or debris (top and bottom) Loose or missing components Burn damage or smell of over-heated components Socketed components not firmly seated PCB not seated properly in edge connectors Solder problems: cracks, splashes on board, incomplete feedthrough, prior modifications or repairs Loose wires or ground strap connections Faulty wiring Wires pinched or in vulnerable position

Mounting Hardware



Loose or missing screws or other hardware, especially fasteners used as connections to ground planes on PCBs

Power Source



Faulty wiring, especially AC outlet Circuit not dedicated to system (Power source problems can cause static discharge, resetting problems, and noise.)

 

Power-up Self-test On power-up, the system automatically runs an internal self-test. If all circuits test good, the start up screen displays.

6-10


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Troubleshooting: General Troubleshooting

General Troubleshooting Problem: Stress test driver settings lost. Stress test profiles were changed or newly created and

are no longer there. Solution: The file ERG_PROT_V5AN.DAT (ERG_PROT_ANSI.DAT old name before

V4.2) in the Windows directory was inadvertently deleted or overwritten. A backup of this file should be made after changing profiles so that it can be restored even after a hard disk error (restore file into Windows directory). Problem: Defective data sets in the database. Errors occur during patient selection, but not

when selecting examination options. Solution: Contact technical support for a reorganization tool, which may repair the error in the

database. By activating the REORG procedure you can reorganize defective BTRIEVE files from CASE. This repair procedure may become necessary when the data becomes damaged for some reason or another (e.g. after a power failure). To carry out the repair procedure successfully, CASE must first of all be terminated. There must be sufficient memory space on your hard disk. As a general rule, the following applies: memory space required = twice as much free memory space as the sum of all CASE files with the suffix “BTR”. The original CASE files are still available in the form of “OLD” files after reorganization and should only be deleted when the reorganization has been completed successfully. If the reorganization is unsuccessful, the only option remaining is to retrieve the latest backup data or contact technical support for the Database Repair Tool (CARD_REP). Problem: Error when reading examinations, examinations get lost

Error messages when calling up examinations from the archive or examinations no longer there. Solution: There are two causes, which may lead to the loss of data on hard disks.

One is a read error on the disk; the second is the destructive influence of some viruses. Indications of a defective hard disk sometimes exhibit themselves as reading errors in certain sectors. The number of defective sectors increases with time. Such a hard disk must be replaced.

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6-11


Problem: Patient locked, although only called up from one workstation

A patient in the network is locked, although they are only called up from one workstation. This error only occurs when the program crashes or after switching off the PC without having terminated CASE beforehand. Solution: Please be sure that CASE is not running from any workstation.

Problem: Monitoring stress tests

Attempt to monitor a stress test from two stations at the same time. Solution: None! A stress test currently being performed can be monitored from one station

only at any one time. Problem: Swapping out examinations.

Almost simultaneous swap-out at several stations; examinations are destroyed. Solution: None! Refer to Device Manual.

Problem: Transferring examinations to data media

When an examination is transferred to another data medium, naming a subdirectory with an umlaut (or other special characters), the examination cannot be retrieved. Solution: Create subdirectories without umlauts (or other special characters).

It is not possible to transfer more than 512 examinations into the root directory of a data medium as DOS is only able to manage a maximum of 512 files on this medium. If more examinations are to be transferred, a subdirectory must be created. The number of files there is practically unlimited. Problem: No connection to ergometer Ergoline 900. Solution: Use Version “752” or “M345” with OEM 4 buttons, or Version “236”/“436” in

Program 10 with original 25 button Ergoline. Problem: Modem RAS connection is not started.

In MUSE Settings of System Configuration of CASE is activated “Start Modem connection before transfer”, but the connection is not started. Please do not start manually the Modem RAS connection, when you configure that the application should start the connection. Solution: Terminate the manually started Modem RAS connection.

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Problem: Not enough memory space when compressing examination.

When compressing examination and using a Hard Disk >4.3GB the following message will occur that less than 15% of storage medium is free. Solution: Set the percentage of storage medium in CASE tab System Configuration, button Database to 1% or Disable Check of free disk space with entry

“LOG_DisableFreeCheck=1” in section “[CARDIO]” in the “WIN.INI” file Problem: Reprogramming Serial Number Solution: 1.

2.

Go to the Service Screen and select Service Tool for Corina and CAM-USB v5.0. Select Read Acquisition System Information. Only when the Acquisition System serial number is “0” the Serial Number Programming Mode can be entered.

Problem: On some occasions, the program does not calculate the target load. Solution: To calculate the target load, the program needs to know the patient's gender, date of

birth, height, and weight. In the following situations, the program is not able to calculate the target load: age < 15 years or age > 84 years or height < 50 cm or height > 250 cm or weight < 20 kg or weight > 200 kg or body surface area (men) < 1.6 m 2 or body surface (women) < 1.2 m 2 Problem: OS Message appears: Adobe Acrobat Reader is not installed. Solution: When the message appears, please install the Acrobat Reader from the CASE CD.

1.

You must have system administrator privileges to install the software.

2.

Insert the CASE CD in the CD ROM drive. If the CD drive automatically starts up, close the CASE Installation Screen.

3.

Select Start > Run.

4. In the command line type X:\Disk\Setup Acrobat (X=CD ROM drive letter, e.g. “E” or “D”). 5.

Click OK .

6. Follow the displayed prompts. Symptom: Application seems to lock up at Test End in Exercise Test. If the database is

damaged and the user initiates to store the test, there is a BTRV error message. But this error message may appear behind the acquisition window. The problem is that the user will not see the message box and for him it seems that the system locked up. Solution: Press one of the keys ALT, ESC, RETURN. This will bring the error message into

the foreground

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6-13


Symptom: Application seems to lock up while printing a Post Test Report on the thermal

printer. Solution: Press the key ‘Stop Printing’ on the function keyboard. Delete the print jobs from

the Marquette Thermal printer: Settings / Control Panel / Printer. Problem: InSite 2.0 - No remote access to server. Solution: Check if the remote servicing software “PC Anywhere” is installed on your PC. If it

is installed, please remove it. Problem: By default the CASE system shuts down, when the CASE application is closed. Solution: To prevent the CASE system from shutting down after the application is closed, the

following entry has to be added to your WIN.INI file: [Cardio] Mai_NTDown=0

Depending on the CASE version the file WIN.INI is located in different folders: CASE Version

WIN.INI Location

v6 or later

CASE installation directory

prior to v6

Windows system directory

Problem: Test cannot be opened with the MUSE Browser function, when running Windows

XP on a CASE system. The window that opens is blank and no error message is displayed. Solution: Install the CD Security Patches CASE XP, PN 2034985-001.

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Troubleshooting: Frequently Asked Questions

Frequently Asked Questions Problem: The Remote Test Screen shows vertical red lines or the ECG does not appear

continuously on the remote viewing system over TCP/IP. Solution: Please make the entries for the package size in the TCP/IP protocol in your Stress

Test System (the remote viewing system does not need an additional entry for TCP/ IP). Windows NT 4.0

1.

With the Registry Editor "regedt32.exe", locate the following key: "HKEY_LOCAL_MACHINE\SYSTEM\CurrentControlSet\Services\\Parameters\Tcpip" Where refers to the subkey for a network adapter that TCP/IP is bound to.

2.

Go to EDIT and then to Add Value.

3.

Select Data Type “REG_DWORD”

4.

Enter the Value Name “MTU”, press , and type in Data “200” Hex ("512" in Dec) and press . Now you have an additional line in the right window: MTU:REG_DWORD:0x200

5.

After the change, reboot the system.

Windows 2000

1.

With the Registry Editor “regedt32.exe” please locate and set the following key: MTU Key: HKEY_LOCAL_MACHINE\SYSTEM\CurrentControlSet\Services\Tcpip\Par ameters\Interfaces\ID for Adapter

2.

Go to EDIT and then to Add Value.

3.

Select Data Type “REG_DWORD”

4.

Enter the Value Name “MTU”, press and type in Data “200” Hex (“512” in Dec) and press Now you have an additional line in the right window: MTU:REG_DWORD:0x200

5.

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After the change, reboot the system.


6-15


Problem: When I open an examination, I get an error when reading examinations,

examinations get lost, or I get a Decompression Error. Errors or decompression error messages come up when I call up examinations (also from the archive) or examinations that are no longer there. Solution: There are two main causes which may lead to the loss / corruption of data on hard

disks: 

A read error on the disk, or



The destructive influence of some viruses.

Additionally, a defective hard disk could be the reason. Indications of a defective hard disk sometimes exhibit themselves as reading errors in certain sectors. The number of defective sectors increases with time. Such a hard disk must be replaced. Check the hard disk using SCANDISK or CHKDSK. If the result of the check indicates many lost sectors, replace the disk. If not, restore the system by using the last BACKUP file. Problem: When I start CASE, I get a database error Solution: Close CASE and start “REORG.BAT” file from CASE directory in DATABASE

directory. Problem: PCW130 value will not be displayed in the stress test measurement summary Solution: PCW 130 is not for use in combination with treadmill stress tests.

The stress test must be complete, the weight of the patient must be entered, and a heart rate of 130 must be reached. (ECG equipment must have the capability for a heart rate of 130.) Problem: The modem I use is not in the modem list and brings up an error message at

initialization Solution: Chose modem type User defined and delete “\X1” out of the field Initialization.

After doing this, the error message will disappear. Configure modems type MultiTech only with 14400 baud and 19.2K baud. Use the newer MultiTech 56K with the modified modem type User defined . Problem: Patient selection menu will not fit within the screen Solution: Select SMALL FONTS within the display configuration window.

Problem: Heart Rate removed after transferred from MAC 1200 to CASE Solution: The Heart Rate is calculated from the RR duration. To get the Heart Rate in CASE,

you must have the Measurement Software Option on the MAC 1200, then the RR duration and the Heart Rate can be calculated.

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Problem: Small differences in the measurement values after transferred from MAC 1200 to

CASE. Solution: The protocol used to transfer the data doesn't use the same amplitude unit for the

measurement values from MAC 1200. These values have to be converted when the data is received in CardioSoft and the results may not be exactly the same values. Problem: Integration of CASE in an archiving system by the customer Solution: Customer buys Adobe Acrobat. Adobe Acrobat installs a printer driver to generate

PDF files. These generated PDF files can be sent to the archive system of the customer and the archiving system can view these files with the PDF reader. PDF files can be printed with high quality on a laser printer. These PDF files are better than exported screen shots (such as JPG files). Problem: Proxy Settings from Internet Explorer influence the FTP file transfer to MUSE Solution: If a Proxy Server name is configured, then the intranet MUSE FTP Server Name

must be excluded from the Proxy Server. Problem: The Windows 2000 network displays a BTRV error message when a registered user

tries to invoke CASE. Solution: In the Windows 2000 network, register the user and grant ALL rights. In Windows

2000, the selection of users with limited rights is the default setting. Problem: [11007] Error starting print job on CASE Solution: This Error Message is generated if the print job cannot be started.

Reasons for this error message: No printer is defined as default printer. Problem: If a PDF report with ECG grid is generated with Adobe Acrobat in CASE, the figure

2 is displayed instead of the ECG grid. Solution: 1.

Display Acrobat Distiller from Adobe Acrobat: Start Menu -> Settings -> Printers.

2.

Double-click on Acrobat Distiller and select the menu: Printer -> Document Defaults...

3. Deactivate field Do not send fonts to Distiller on the Adobe PDF Settings tab. 4.

Set field Graphic-> True Type Font to value Download as Softfont on the Advanced tab.

Problem: When transferring data from MAC 1200, the same patient record is created twice. Solution: The function of CardioSys/Soft to automatically assign an incoming resting ECG

from a MAC 1200 to a patient record does not pose any problems.

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6-17


If the patient with the patient ID from MAC 1200 already exists in CardioSys/Soft, the resting ECG will automatically be assigned to this patient. If the patient with the patient ID from MAC 1200 does not exist in the CardioSys/ Soft database, the patient record will be generated and the resting ECG will be assigned to the new patient record. A second patient record with the name displayed in capital letters is generated only when a resting ECG with the same acquisition date and time is transferred a second time. This second resting ECG is assigned to the second patient record and can be deleted. Make sure that you do not unnecessarily transfer resting ECGs more than once. If a new resting ECG is transferred after the resting ECG is sent a second time, the new one will be assigned to the first patient record. Problem: The MUSE Web Server works, but an error message appears when the CASE

patient list is invoked. Solution: A MUSEWeb user account must be created under Windows and assigned to the

MUSE group. The user account must also be created in MUSE. Problem: Metabolic Carts display a higher heart rate than CASE? Solution: During exercise tests, the heart rate is calculated for 30-second tabular data. The

heart rate is averaged over 30 seconds at 5-second intervals and entered in the table. The max. heart rate is derived from the tabular data. If the heart rate is sent to the metabolic cart at 5-second intervals, the value displayed there may be higher than in CASE. Question: Network installation using cardiouser as the domain user does not work. What can

be done? Answer: For CASE to run in the Windows 2000 environment, the registered user must be a

member of the local group of power users. This applies to both local users and domain users. The user must have the right to access the Cardio installation directory and the Temp directory. We assume you have verified the latter requirement. So the user rights are probably the root cause of the problem. Log on to the CASE client as the Administrator (local), and add the user “?Domain?\cardiouser” to the local user group of power users. Repeat this configuration at each CASE client. For multiple users, it is recommended to create a special user group for them on the domain controller and to add this user group to the local user group of main users. To do so, expand the entry Local users and groups in the computer administration and click the Groups folder. In the window at right, click Main User . A dialog opens showing all members of the group. Clicking the Add button opens a second dialog Select user or group . Select the domain from the combo box at the top. Select the user or the group and confirm with Add . Exit with OK .

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Question: How can I run CardioSoftWeb on a Windows 2000 Domain Controller? Answer: For CardioSoftWeb to run on Windows 2000 domain controllers, users

IUSR_ and IWAM_ must be assigned to the group Server Operators after installation. To do so, open the dialog Active Directory Users and Computers via Control Panel -> Administrative Tools. In the dialog at left, select the Domain, under Domain, on the folder Builtin and open the Property Dialog for the Server Operators. Select the Members tab a add the users IUSR_ and IWAM_. Question: What do the spirometry test parameters mean (LF501)?

For SpiroSoft parameters, see users manual. Answer: Designation of Spirometry Test Parameters

Parameter Designation

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IVC [liters]

Inspiratory vital capacity (relaxed)

Inspiratorische Vitalkapazität

EVC [liters]

Expiratory vital capacity (relaxed)

Exspiratorische Vitalkapazität

FEVC [liters]

Forced expiratory vital capacity

Forcierte Exspiratorische Vitalkapazität

FEV1 [liters]

Volume of air exhaled during the 1st second of FEVC

Forciertes exspiratorisches Volumen in 1 Sekunde

PEF [liters/second]

Peak expiratory flow

Max. exspiratorischer Flow

MEF75 [liters/second]

Max. expired flow at 75% FEVC remaining

Forcierter max. exspiratorischer Flow bei 75% Restvolumen FEVC







MMF [liters/second]

Max. mid-expiratory flow (forced) between 25 and 75% of FEVC

Mittlerer Flow bei 25-75% FEVC

FIVC [liters]

Forced inspiratory vital capacity

Forcierte inspiratorische Vitalkapazität


6-19


Parameter Designation FIV1 [liters]

Volume of air inhaled during the 1st second of FIVC

Forciertes inspiratorisches Volumen nach 1 s

PIF [liters/second]

Peak inspiratory flow

Max. inspiratorischer Flow

MIF75 [liters/second]

Max. inspired flow at 75% of inhaled FIVC

Forcierter max. inspirator. Flow bei 75% der inhalierten FIVC


Max. inspired flow at 50% FIVC remaining

Forcierter max. inspirator. Flow bei 50% inhalierten FIVC


Max. inspired flow at 25% FIVC remaining

Forcierter max. inspirator. Flow bei 25% inhalierten FIVC

MVV [liters/second]

Maximal voluntary ventilationof air expired for one minute (indirect, derived from FEV1)

Maximals exspiratorisches Ventilations-Volumen pro Minute (indirekt, abgeleitet von FEV1)

Question: What are the rules for the MILLER spirometry interpretation (LF501)? Answer: 1.

FEV1/IVC ≥ 70% and IVCref/IVC ≥ 70% --> No Respiratory Problem

2.

FEV1/IVC < 70% and IVCref/IVC < 70% --> Combined Respiratory Problem

3.

FEV1/IVC < 70% and IVCref/IVC °› 70% --> Obstruction

4.

FEV1/IVC ≥ 70% and IVCref/IVC < 70% --> Restriction

Question: What are the maximum numbers of objects in the application? Answer: The CASE application has the follow restrictions for data storage:

6-20

Object

Max. number

Message at the screen

Trend

600

Trend memory full, no more trend data can be saved!

ECG strips

50

Memory for ECG Strips is full, no more ECG Strips can be saved!

Arrhy strips (Episode)

20

N/A


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Object

Max. number

Message at the screen

Medians

450

Memory for sample cardiac cycles is full, no more sample cardiac cycles can be saved!

TWA Median

300

TWA memory full, no more TWA data can be stored!

FD ECG

60 min.

N/A


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Troubleshooting: Flat Panel Monitor Problems

Flat Panel Monitor Problems Problem: No picture Solutions:



The signal cable should be completely connected to the monitor computer. Check that the Vacation Switch is in the ON position. Front Power Switch on the monitor and the CASE power switch should be in the ON position. Check the monitor and your computer with respect to recommended settings.



Check the signal cable connector for bent or pushed-in pins.

  

Problem: Power Button does not respond Solutions:





Unplug the power cord of the monitor from the AC outlet to turn off and reset the monitor. Check the Vacation Switch on the left side of the monitor.

Problem: Image Persistence Solution: Image persistence is when a residual or “ghost” image of a previous image remains

visible on the screen. Unlike CRT monitors, LCD monitors, image persistence is not permanent, but constant images being displayed for a long period of time should be avoided. To alleviate image persistence, turn off the monitor for as long as the previous image was displayed. For example, if an image was on the monitor for one hour and a residual image remains, the monitor should be turned off for one hour to erase the image. We recommend that when your CASE is sitting idle for long periods of time, turn OFF the system or the monitor. Problem: Image is unstable, unfocused or swimming is apparent Solutions:

 

 

Signal cable should be completely attached to the computer. Use the OSM (On Screen Manager) Image Adjust controls to focus and adjust display by increasing or decreasing the fine total. When the display mode is changed, the OSM Image Adjust settings may need to be re-adjusted. Check the monitor with respect to recommended signal timings. If your text is garbled, change the video mode to non-interlace and use 60Hz refresh rate.

Problem: LED on monitor is not lit (no green or amber color can be seen) Solution: Power Switch should be in the ON position and power cord should be connected.

6-22


Revision F

Troubleshooting: Flat Panel Monitor Problems

Problem: Display image is not sized properly Solutions:

 

Use the OSM Image Adjust controls to increase or decrease the Coarse total. Check to make sure that a supported mode has been selected on the system being used. (Please consult system manual to change graphics mode.)

Problem: No Video Solutions:

 

Revision F

If no video is present on the screen, turn the Power button OFF and ON again. Make certain the computer is not in a power-saving mode (touch the keyboard or mouse).


6-23

Troubleshooting: Printer Debugging

Printer Debugging Problem: In Windows 2000, some characters overlap the characters that follow them

Select Start > Settings > Printers and select your standard printer. Solution: Select menu “File” the entry “Properties”. Select “General” Tab and press button

“Printing Preferences” and than press button “Advanced”. In the displayed list is in the topic “Document Options” the Entry “Print Optimizations”. This “Print Optimizations” must be disabled. Problem: Printout incomplete Solution: The printer probably has insufficient memory.

Problem: NT 4.0, slowly printing with HP6P, HP2100M, HP4050M (only CardioSoft) Solution: Please replace the original printer driver with “HP Laserjet 5M” from the Windows

Workstation CD ROM. Problem: Laser printer prints numbers instead of grid. Solution: There are three solutions for this issue: 





If you work within a network installation, make sure that CardioSoft is installed on every client that wand’s to work with this software. Open Printer properties menu and change the printer scheduling to “Print direct.” Do the following entries to the WIN.INI, section .[CARDIO] GRA_DontRemoveGrid=1

Another solution can be to disable character sets in the Control Panel: Start ---> Settings ---> Control Panel ---> Regional Options

1.

In Language settings for systems, disable the following character sets:      

2.

6-24

Arabic Hebrew Indic Korean Thai Vietnamese

After changing these settings the system must be rebooted.


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Troubleshooting: Printer Debugging

Problem: Paper out message from a laser printer is displayed delayed Solution: You can reduce the Transmission Retry Timeout to decrease the delay of the displayed Paper out message, but it could cause a timeout message during the

printing of pages with noisy ECG curves. Reduce the Transmission Retry Timeout in Windows Printer Settings (tab Port , button Configure Port...). Problem The error message “Paper Jam” appears when the P2000 is turned off. Solution With the power on, open and close the writer door. This will clear the error message. Prevention This problem occurs only when the P2000 is turned off after the PC has booted. To

prevent this error from occurring, do not turn off the P2000 while the PC is on.

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Troubleshooting: Usage and Workaround of Acrobat 6

Usage and Workaroun d of Acrobat 6 Problems occur if the newer Adobe Acrobat 6.0 Standard (6.0.0 19.05.2003) is used instead of version 5 which is validated for CASE 5.02 and 5.1x. The following workarounds are helpful if customers are not able to get a full Adobe Acrobat 5 version. The proper usage of Acrobat 6 will be established in a future release. Problem When you try to export an examination to a PDF the following error message

occurs: “Adobe Acrobat Distiller” is not installed!”

Workaround Change printer name and adjust printing preferences.

1.

Go to Start --> Settings --> Printers, and change “Adobe PDF” to “Acrobat Distiller”.

2.

In Printing Preferences of the renamed Adobe PDF (right mouse key) uncheck Do not send fonts to “Adobe PDF .

Problem In CardioSoft 5.1x, Acrobat 6 starts with this error message IF the online help

function is invoked the first time: Could Not Connect

Workaround Click OK to quit the message, then click Help button again. Acrobat now shows the

desired location in the Operator’s Manual. Problem: OS Message appears: Adobe Acrobat Reader is not installed Solution: When the message appears, please install the Acrobat Reader V5.1 from the

CardioSoft CD. 1.

You need system administrator privileges to install the software.

2.

Insert the CardioSoft CD in the CD ROM drive. If the CD drive does an automatically start up, close the CardioSoft Installation Screen.

3.

Select Start > Run.

4. In the command line type X:\Disk\Setup Acrobat (X=CD ROM drive letter, e.g. “E” or “D”). 5.

Click OK .

6. Follow the displayed prompts.

6-26


Revision F

7

Revision F

Service


7-1

For your notes

7-2


Revision F

Service: Overview

Overview This chapter describes the general procedures to perform the most common service tasks. These include: 

System Backup and Restore



Software-Related Service  Software Upgrade Instructions Recovering from a CASE BTRV Error  Database Repair for CASE/CardioSoft Hardware-Related Service 



   



Servicing the Power Distribution Assembly Servicing Drive Replacing the Floppy Drive/SD Card Reader Servicing the Print Head Updating the Writer Board Firmware Servicing the I/O Assembly



Configuring the Acquisition Interface Board

    

Revision F

Controlling Electrostatic Discharge Damage Servicing the Light Assembly Servicing the Keypad Assembly Removing the Worksurface Assembly


7-3

Service: System Backup and Restore

System Backup and Restore Backing up the CASE system configuration and settings files ensures that the system can be restored in case of a catastrophic failure or after the hard drive is replaced. The system configuration files and the system setting files are backed up and restored independently of each other.

Saving to Diskette These procedures are used to back up the following information to a high density, 1.44 MB floppy diskette:  

System configurations System settings

You MUST perform these procedures BEFORE replacing the hard drive. You can also use these procedures to save these settings so they can be copied from one unit to another.

Saving System Configurations to Diskette Before saving your system configurations to diskette, manually write down all of your option codes. To access a listing of option codes for this system, choose System Configuration in the CASE application. Choose the Option Code Tab. 1.

From within the CASE application, select the System Configuration icon. The System Configuration window opens.

2.

In the System Configuration window, select the For Service Only icon. You are prompted to enter a password.

3.

Enter the Service Password: helserv The password is case sensitive: be sure to use a lowercase letters.

4.

Select Ok . The Service window opens.

5.

With the Service window open, insert the floppy diskette in Drive A:.

6.

Select Format Floppy. The Format A:\ dialog window opens.

7. Follow these steps: a.

Select Start A warning message appears.

b.

Select Ok . The message Format complete appears.

c.

7-4

Select OK .


Revision F


d.

Select Close. The Format A:\ dialog window closes.

8.

In the Service window, select Ok . The Service Window closes.

9.

Verify the floppy disk is still in Drive A:

10. In the System Configuration window, select the Save icon. A dialog window will appear, asking Is empty disk inserted in drive A:\? 11. Select ok . The message System Configuration successfully stored to disk displays. 12. Select OK to finish saving the system configuration.

Saving Custom Settings to Diskette 1.

At the initial screen within the CASE application, select New Test .

2.

Highlight a test patient and choose the Select icon. The Test Information window opens.

3.

In the Test Information window, select OK .

4.

Select the Custom Setup icon. The Load Settings window opens.

5. Do one of the following:  

6.

If file names are listed under Settings..., skip to step 9. If file names are not listed under Settings..., continue to step 6.

select the Save icon. The Save Settings window opens.

7.

Verify the following settings:  

Drive should be set to Hard Drive. Save As should be set to whatever you want to name the custom setup. Example: Dr. Smith.

Make sure to delete the three dots before entering the name. 8.

In the Save Settings window, select Save. This saves all of your Custom Settings to the file and location specified.

9.

In the Load Settings window, under Drive, select Hard drive.

10. Under Settings select the Custom Setup Name that you want to save to diskette. If you have more than one file name, repeat these steps for each. 11. Select Load . The message Load setting and overwrite current setting? appears. Revision F


7-5


12. Select OK . The message Overwrite test protocols and phases? appears. 13. Select OK. 14. Select the Custom Setup icon. The Load Settings window opens. 15. Select the Save icon. 16. In the Save Settings window, set the Drive selection to Disk Drive A: 17. Select the first “---” in this list. 18. The Save As selection should be set to whatever you would like to name the custom setup. Example: Dr. Smith. Make sure to delete the three dots before entering the name. 19. In the Save Settings window, select Save. You are returned to the Load Settings window. 20. Repeat step 9 through step 17 for each custom setting. 21. After you have saved the last custom setting, select Cancel in the Load Settings window.

Restor ing fro m Diskette These procedures are used to restore the following information from your system back:  

System configurations System settings

You MUST perform these procedures AFTER replacing the hard drive. You can also use these procedures to restore settings from one unit to another.

Restoring System Configuration from Diskette To successfully restore the system configuration from diskette, you will need the list of option codes that were written down prior to replacing the hard drive. 1. Select the icon System Configuration. The System Configuration window opens. 2.

Insert the diskette with backup settings and procedures into the floppy drive.

3.

In the System Configuration window select the LOAD icon. The message Load System Configuration and overwrite current Configuration? appears.

4.

Select OK . The message Is a disk with the System Configuration inserted in drive A:?

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Revision F


5.

Select OK . The message System configuration successfully loaded (software options not loaded, please use option disk to load) appears.

6.

Select OK .

7.

Select the System Configuration icon. The System Configuration window opens.

8.

In the System Configuration window, select the Option Code tab.

9.

On the Option Code tab of the System Configuration window, select the Modify... icon. The message Change Software option, are you sure? appears.

10. Select OK. 11. Enter all of the option codes that you manually wrote down prior to replacing the hard drive.

Option codes are serial number specific and should not be duplicated.

12. After entering the option codes in the System Configuration window, select OK.

Restoring Custom Setups from Diskette 1.

From the initial screen, select New Test.

2.

Highlight a test patient and click on the Select icon. The Test Information window opens.

3.

In the Test Information window, select OK.

4.

Insert the diskette with backup settings and procedures in drive A:.

5.

Select the Custom Setup icon. The Load Settings window opens.

6.

Make the following selections:   

For Drive, select Disk drive A: Highlight the custom file name under Settings Select Load .

The message Load setting and overwrite current settings? appears. 7.

Select OK. The message Overwrite test protocols and phases? appears.

Revision F

8.

Select OK.

9.

Select the Custom Setup icon.


7-7


The Load Settings window opens. 10. Select Save. The Save Settings window opens. 11. Make the following selections:   

For Drive, select Hard drive Select the first “...” on the list. For Save As, delete the three dots and type in the custom setup name again (example: Dr.Smith)

12. Select the Save icon. You return to the Load Settings window. 13. If you need to restore additional custom setups, repeat step 5 through step 12 for each setting BEFORE proceeding to the following step. 14. If you loaded more than one custom setup, select the custom setup under Settings that you would like to use as your default setup. 15. Select Load . The message Load setting and overwrite current settings? appears. 16. Select OK . The message Overwrite test protocols and phases? appears. 17. Select OK .

7-8


Revision F

Service: Recovering from a CASE BTRV Error

Recovering from a CASE BTRV Error Btrieve errors may occur when the CASE attempts to store a patient test. They may indicate an improper system shutdown or facility power interruptions. The Btrieve recovery process that follows is used to reorganize the corrupt database in order to possibly regain access to tests already stored and to allow new tests to be stored until the system can be repaired. For further information on recovering from a CASE BTRV error, contact technical support at the following phone numbers:  

1-800-558-7072 (U.S.) 561-575-5000 (outside of the U.S.)

Procedure Follow these steps: 1.

Log on as Administrator . a.

From the CASE initial screen press Ctrl+Alt+Delete. The Windows NT Security window opens.

b.

In the Windows NT Security window, click on Logoff .

c.

Hold down the Shift key.

d.

Click on OK .

e.

Continue holding down the Shift key until the Logon screen appears.

f.

Logon as:

g.



User name: Administrator



Password : admin1,3,5,7



Click OK .

Wait for the desktop screen to come up (showing the My Computer, Network Neighborhood, etc. icons).

2.

Click on My Computer.

3.

Click on D:

4.

Click on Case.

5.

Click on Database.

6. Double-click on Reorg.bat. 7.

Each time the Press any key to continue message appears, press the space bar. This will occur four times. After you respond to the last message, the Database window opens.

8.

At the bottom left corner of the Database window, select Start > Programs > GE Medical Systems IT > Configure User Auto Logon.

The Configure User Auto-Login window opens and the message Auto-login configured for user is displayed. Revision F


7-9

Service: Recovering from a CASE BTRV Error

9.

Select OK. Some older systems will not have not have this step. If not, proceed with the next step.

10. Restart the computer as normal. 11. Verify the system boots automatically into the CASE initial screen.

7-10


Revision F

Service: Database Repair for CASE / CardioSoft

Database Repair for CASE / CardioSoft GE Healthcare provides a software tool— card_rep.exe —that can repair the patient.btr and examina.btr database files on the following systems: 

CASE (all versions)



CardioSoft (v4.1 and later)

How the Data is Repaired The tool repairs the database by reading the data from the headers of the examination files in the corresponding modality directory and writing a corresponding patient.btr and examina.btr file. The tool does not modify the original data in the CASE\CardioSoft 0 database. Instead, it stores the repaired data in a temporary directory; the operator is responsible for ensuring the repaired data is usable and for moving the data to the database.

Supported Modalities The tool supports the following modalities: 

Exercise Test (v5 and above)



Rest ECG (v5 and above)



Ambulatory Blood Pressure (v5 and above)



Spirometry (v5 and above)



Archived Patient Records (v5 and above)



Late Potentials (prior to v5)

 

STAT ECG (prior to v5) Right-Heart Cath (prior to v5)

Non-Support ed Features The tool does NOT support entries from external programs because those files do not store patient information. Nor does it repair the following data, which are not stored in the examination files:  

Device/Cart Number Examination Sent to MUSE flag

Installation To install the tool, copy it to the CASE\CardioSoft directory so it can use the DLLs located in that system.

Passwor d Protection To use the tool, you must enter the One Day Password, as described in “General Troubleshooting” on page 6-11. Revision F


7-11


Directory / File Structure The following table identifies the directory structure and contents of the CASE/ CardioSoft system. DIRECTORY / Files

Description

CARDIO

Program directory

DATABASE Patient.Btr Examina.Btr Users.Btr Station.Btr Network.Btr

Database directory Btrieve-file: Patients Btrieve-file: Examinations Btrieve-file: Users Btrieve-file: Network-Stations, not used from V5 on Btrieve-file: Network-Locking, temporary files

RESTECG R*.*

Rest ECG directory Examination files

AVER AC*.*

Late Potentials-directory Examination files

SPIR SC*.*

Spirometry - directory Examination files

EMECG N*.*

STAT ECG - directory Examination files

RHK Z*.*

Right-Heart Cath - directory Examination files

HOLTERBP BC*.*

Ambulatory Blood Pressure - directory Examination files

CAS C*.*

Exercise test - directory Examination files

EXTPROG *.*

Directory: Results from external programs Result files

SOUND *.*

Directory: Sound-Files from all modalities Sound Files

ONLINE *.*

Directory: Full disclosure-Files from all modalities Full disclosure Files

NARRATIV *.*

Directory: Configured Reports Configured Reports from all modalities

Repair directory structure The repair directories have fix names from Card_R0 to Card_R9, where any writeable disk-drive can be selected.

7-12


Revision F


Configuri ng the Repair Below is screenshot of the English version of the CASE/CardioSoft Repair Tool. The tool is also available in German.

To use the tool, do the following: 1.

Specify the root directory of the CASE/CardioSoft system. The tool uses this directory to generate the modality directories.

2.

Specify the disk drive and directory where the repaired data will be stored. Verify there is enough disk space.

3.

Select the examination files the tool will use to restore the database.

4.

Click the Settings button and define the following: 



Revision F

Special Settings for handling mismatched patient data. This determines how the tool will handle patient data differences between the examination files and the database. This could happen when the patient data is modified after an examination was made. You have the following options:  Control the Patient data with a dialogue Use always the Patient data from the examination-file   Retain always the Patient data found in the database Update empty fields of the database with valid entries from the  examination-file Special Settings for handling existing examination-data This determines how the tool will respond when the key generated from the examination-file exists in the database. This could happen when examinations are merged from different directories and there are several


7-13


entries for one patient from the same date and time.(year, month, day, hour, minute and second). You have the following options: Ignore the examination: The examination-file will not be copied to the  repair directory Generate a new key and store the examination.  The second of the recording-time will be incremented and a new try is made with this modified key. This option should be used with care, because when Card_Rep is used with the same examination-files more than once, more than one entry will be found in the database.

Using the Repaired Files After the repair is complete, use the View button to review the entries the tool made in the patient.btr and examina.btr files.

After you verify that the files have been repaired to your satisfaction, you need to replace the missing or corrupt database files with the repaired files. You have two methods for doing this. 

7-14

Move the working files to the repair directory using the following procedure: a. Install CASE/CardioSoft on the temporary repair-directory: c:\card_r0 b.

Copy the file uers.btr and the configured reports from the master directory to the temporary directory using the Users/Conf.Rep button.

c.

Delete the master-directory and rename the temporary-directory to the master-directory.


Revision F




Copy the repaired files to the appropriate master directories using the following procedure. a. Delete the contents of these master directories:         

DATABASE\*.BTR RESTECG\*.* ERGOECG\*.* AVER\*.* SPIR\*.* EMECG\*.* RHK\*.* HOLTERBP\*.* CAS\*.*

SOUND\*.* O  NLINE\*.* Copy the files from the corresponding temporary repair directories. 

b. c.

Copy the files examina.btr and patient.btr from the temporary database directory to the master database directory.

Merging Data Card_rep.exe can be used to merge patient and examination data stored in different directories: 1.

Decide which database should be used as a base and copy the whole directory into a repair directory ( c:\Card_Rep0,... c:\Card_Rep9)

2.

Select the directories of the files where the examinations to be merged are stored.

3.

Start Repair and the selected examinations are merged to the repair directory.

Continue with the work described in “Using the Repaired Files” on page 7-14.

External Stor ed Examinations Card_rep.exe can be used to regenerate the database entries for the external stored examinations. The only restriction is that the device where the examinations are stored must be writeable. This is because the repair-procedure requires that the header of each examination file be changed and the file has to be renamed. Before the repair is started, you should back up the directory of the external stored examinations. This would be helpful if the system crashes while all the files are renamed.

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7-15


Examinations with Full Disclosu re ECG When using a directory structure that does not follow the CASE/CardioSoft conventions, there may be problems with examinations that have a Full disclosure ECG. Card_rep.exe assumes that the Online Files are stored in the directory \ONLINE , which is parallel to examinations. When card_rep.exe does not find such a directory, no Online File will be available for that examination. The modalities that may have Online files are Exercise Test, STAT ECG, Right Heart Cath.

To repair Exercise Tests, where the examinations are stored in the directory d:\exercise, make sure that the corresponding online files are stored in d:\online.

Repair Message Codes The following codes are used to indicate the status of the actual examination to be repaired. Code

7-16

English

German

PN

Patient entered new

Patient neu eingetragen

PF

Patient found and identical to the examination-data

Patient gefunden und identisch

PD

Patient found and different to the examination-data, not updated

Patient gefunden, aber unterschiedlich, kein Update

PE

general error

Allgemeiner Fehler

PU

Patient-data different, updated by the user

Patientendaten unterschiedlich, Update durch Benutzer

PM

Patient-data different, empty fields supplemented

Patientendaten unterschiedlich, leere Fehler ergänzt

PR

Patient-data used from the examination-file

Patientendaten aus dem Untersuchungsfile übernommen

EN

Examination entered new

Untersuchung neu eingetragen

EK

Examination entered new, but recording-date modified

Untersuchung neu eingetragen aber Aufnahmedatum modifiziert

EF

duplicate examination-key, examination ignored

doppelter Untersuchungsschlüssel, Untersuchung ignoriert

E0

Error: internal patient-number is zero

Fehler: Patientennummer ist null

EE

general error

Allgemeiner Fehler


Revision F


Patient-Filter You can use a filter to restrict the repair of patient and examination files based on the patient’s name and ID. The filter can include wild cards (*,?). For example: It is possible to set a filter for the patient´s last name. So only patients/examinations according this filter are stored in the new database. The filter-specification can also include wild cards (* ?) for example Meier

selects patients with the last name Meier.

Me*

selects patients beginning with Me followed by any other combination of characters

Me???

selects patients beginning with Me followed by exact 3 other characters.

*xyz*

selects patients containing the substring xyz

The specification for searching can also be extended by the property “Match case”. The filter is set on the “Settings” dialog box.

Revision F


7-17

Service: Remote Service

Remote Service Remote service is available using InSite 2.0. Refer to Chapter 4, “InSite 2.0” for more information.

7-18


Revision F

Service: Controlling Electrostatic Discharge Damage

Controlling Electrostatic Discharge Damage All external connector inputs and outputs of the device are designed with protection from ESD damage. However, if the device requires service, exposed components and assemblies contained within are susceptible to ESD damage from sources including human hands, non-ESD protected work stations, and/or improperly grounded test equipment.

The CASE contains components that are susceptible to electrostatic discharge damage. Observe all static precautions while performing service. Failure to observe these precautions may result in failure of components.

The following guidelines help make a service workstation more resistant to the ESD damage: Discharge any static charge you may have built up before handling  semiconductors or assemblies containing semiconductors. A grounded, antistatic wristband (3M part number 2046 or equivalent) or heel  strap should be worn at all times while handling or repairing assemblies containing semiconductors. Use properly grounded soldering and test equipment. Use a static-free work surface (3M part number 8210 or equivalent) while  handling or working on assemblies containing semiconductors. Do NOT remove semiconductors or assemblies containing semiconductors  from antistatic containers (Velo-stat bags) until absolutely necessary. Make sure power to an assembly is turned off before removing or inserting a  semiconductor. Do NOT slide semiconductors or electrical/electronic assemblies across any  surface. Do NOT touch semiconductor leads unless absolutely necessary.  Semiconductors and electrical/electronic assemblies should be stored only in  antistatic bags or boxes. These guidelines may not guaranty a 100% static-free workstation, but greatly reduce the potential for failure of any electrical/electronic assemblies. 

Revision F


7-19

Service: Servicing Light Assembly

Servicing Light Assembly Log off the CASE application, shut down the system, turn the power switch to OFF, and unplug the unit from the power outlet. To access the light assembly for servicing follow these steps:

7-20

1.

Remove two screws from the light assembly to separate it from the display support.

2.

Remove two screws from the light assembly circuit board to separate it from the lens.

3.

Disconnect the light cable and replace the circuit board.

4.

Reverse the procedure to reassemble.

5.

Reconnect the CASE unit to AC power.


Revision F

Service: Servicing the Keypad Assembly

Servicing the Keypad Assembly Log off the CASE application, shut down the system, turn the power switch to OFF, and unplug the unit from the power outlet. To access the keypad assembly for servicing follow these steps:

Revision F

1.

Remove the keypad overlay to gain access to the keypad assembly locking tabs.

2.

Working from right to left, release the locking tabs. Extract the keypad assembly.


7-21

Service: Servicing the Keypad Assembly

7-22

3.

Disconnect both cables and replace the keypad assembly.

4.


5.



Revision F

Service: Removing the Worksurface Assembly

Removing mov ing the Work Worksur surface face Assembly Log off the CASE application, shut down the system, turn the power switch to OFF, and unplug the unit from the power outlet. To gain access the writer and power supply assemblies, the CASE worksurface must first be removed. Follow these steps to remove the CASE worksurface: 1.

Disconnect Disconnect the the keyboard keyboard and and mouse connec connectors tors from from the I/O I/O drawer drawer and pull pull the cable through the cable guide and remove.

2.

Discon Disconnec nectt the groun ground d wire wire on the write writerr drawer drawer..

Ground Terminal

3.

Remove Remove the 12 mountin mounting g screws screws from from under under the the worksur worksurface. face.

4.

Lift Lift the the worksu worksurfa rface ce up fro from m the the front front..

Lift the front of the workstation only far enough to reach underneath and disconnect the keypad cables. Lifting the workstation any higher could damage the connectors on the keypad board.

Revision F


7-23

Service: Removing the Worksurface Assembly

5.

While While holding holding the fr front ont of the worksu worksurface rface up, up, reach reach underneath underneath it and and carefully carefully disconnect the two keypad cables located near the left of the keypad assembly.

6.

Lift Lift off off the the worksu worksurfa rface ce and and set set it asid aside. e.

The writer paper release button will fall through when the worksurface is lifted. When reassembling the worksurface, the button must be inserted from the top. Release Button

7-24

7.

Revers Reversee the the proce procedur duree to reasse reassembl mble. e.

8.

Reconn Reconnect ect the CASE CASE unit unit to AC powe power. r.


Revision F

Service: Servicing the Power Distribution Assembly

Servicin rvi cing g the Power Dist Distrib ributi ution on Asse Ass embly mbl y The power distribution assembly contains writer power supply, CPU power supply, power distribution board and EMI filter. filter. Log off the CASE application, shut down the system, turn the power switch to OFF, O FF, and unplug the unit from the power outlet. To service the power distribution assembly, follow these steps:

Revision F

1.

Remove Remove the CASE CASE works worksurf urface ace.. Refer Refer to “Removing the Worksurface Assembly” on page page 7-2 7-233.

2.

Remove Remove the two two lock lock nuts and two screws screws holding holding the the writer writer tray tray in place. place. Remove the writer assembly.

3.

Loosen Loosen the two lock lock nuts nuts holding holding the power power supply supply in place. place.

4.

Disconnect Disconnect the cables cables that that are are connected connected to to the power power supply supply assem assembly. bly. Carefully lift the assembly out for service.

5.

Revers Reversee the the proce procedur duree to reasse reassembl mble. e.

6.

Reconn Reconnect ect the CASE CASE unit unit to AC powe power. r. CASE Exercise Testing System 2027786-082

7-25

Service: A Service: Ac ccessing ing the the Driv rives

Ac A c c ess es s i n g t h e Dri Dr i v es To access drives for servicing, follow these steps:

7-26

1.

Back up the configurat configuration ion and and custom custom setti settings ngs as as described described in “Saving to Diskette” on page page 7-4 7-4..

2.

Log of offf the CASE CASE applicat application, ion, shut shut down down the system system,, turn the power power switch switch to to OFF, and unplug the unit from the power outlet.

3.

Lift drive bezel up at the the bottom bottom and pull itit away from from the the CASE chass chassis. is.

4.

Remove Remove the four four lock lock nuts from the drives drives assemb assembly ly front front pan panel. el.

5.

Slide Slide the drives drives assemb assembly ly out out of the CASE assembly. assembly.


Revision F

Service: A Service: Ac ccessing ing the the Driv rives

Do not allow the drive assembly to drop into the unit. 6.

Hang the the drives drives assembly assembly by the the hooks hooks on its side side panels panels to access access connecto connectors rs and individual drive mounting screws.

The drives are now accessible for replacement or upgrade. If you replace the hard drive, restore your system settings (see “Restoring from Diskette” on page page 7-6 7-6). ).

Revision F


7-27

Service: Accessing the Drives

When replacing the hard drive with the 80 GB hard drive (PN 2000714-011), change the jumper to “Master or single drive” as shown in the illustration below.

When you are done servicing the drives, reverse the procedure to reassemble. Reconnect the CASE unit to AC power.

7-28


Revision F

Service: Upgrading the Floppy Drive

Upgrading the Floppy Drive If you are upgrading from an earlier version of CASE, use the following procedure to replace the existing floppy drive with the floppy drive / card reader. 1.

Perform the procedure described in “Accessing the Drives” on page 7-26 to make the drives accessible for upgrade.

2.

Unplug the ribbon cable from the floppy drive.

Unplug ribbon cable

3.

Unplug the power connector from the floppy drive.

Unplug power connector

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7-29


7-30

4.

Unplug the floppy drive ribbon cable (41978-001) from the motherboard inside the CASE and remove it. This cable will no longer be used.

5.

Remove the 2 screws on each side of the floppy drive.

6.

Slide the floppy drive out of the drive assembly.


Revision F


7.

Guide the “tail” of the USB cable through the drive assembly. Then insert the new floppy drive /card reader (2028841-001) into the slot of the drive assembly.

Insert the USB cable through the assembly first.

8.

Secure the floppy drive / card reader with 2 screws on each side of the floppy bracket.

Secure screws on left side...

and on the right side.

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7-31


9.

The USB cable of the floppy drive / card reader must be connected to the USB connector on the motherboard. Use a flashlight if necessary to ensure correct positioning.

Correct position of the USB cable on the motherboard.

10. View into CASE with the USB cable connected to verify the cable is routed away from the fan.

7-32


Revision F


11. Insert the new floppy ribbon cable (2028841-002) into CASE and connect it to the floppy connector on the motherboard. It can be plugged in one position only.

Floppy cable connected to the motherboard

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7-33


12. Connect the “Drive A” connector of the ribbon cable to the floppy drive /SD card reader. Pin 1 (red wire) on the right side

Ribbon cable connected to the floppy drive / SD card reader

!

7-34


Revision F


13. Connect the power connector to the floppy drive.

Power connector connected to the floppy drive

14. Slide the drive assembly into the CASE assembly.

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7-35


15. Secure the drive assembly front panel with the four lock nuts.

16. Attach the drive bezel.

17. Reconnect the CASE unit to AC power. 18. Turn on the power switch and make sure that the internal fan does not touch any cable (makes no noise). 19. Use Windows Explorer to verify that the card reader and floppy disk can be written to and read from. 20. Format a card or floppy disk as necessary.

Formatting a card or floppy disk will erase ALL data previously stored on the medium. Verify that the medium contains no data that you want or need to retain.

7-36


Revision F

Service: Replacing the Floppy Drive / Card Reader

Replacing the Floppy Drive / Card Reader If the floppy drive / card reader fails, use the following procedure to replace the existing drive / reader with a new unit. 1.

Perform the procedure described in “Accessing the Drives” on page 7-26 to make the drives accessible for upgrade.

2.

Unplug the ribbon cable from the drive / reader.

Unplug ribbon cable

3.

Unplug the power connector from the drive / reader.

Unplug power connector

Revision F


7-37


7-38

4.

Unplug the USB cable from the USB connector on the motherboard. If necessary, you may momentarily lift the drive assembly from its resting position to provide additional room to access the USB connector.

5.

Remove the 2 screws on each side of the floppy drive.

6.

Slide the floppy drive out of the drive assembly.


Revision F


7.

Guide the USB cable of the new drive through the drive assembly and insert the new drive / reader into the slot of the drive assembly.

Insert the USB cable through the assembly first.

8.

Secure the floppy drive / card reader with 2 screws on each side of the floppy bracket.

Secure screws on left side...

and on the right side.

Revision F


7-39


9.

The USB cable of the floppy drive / card reader must be connected to the USB connector on the motherboard. Use a flashlight if necessary to ensure correct positioning.

Correct position of the USB cable on the motherboard.

10. View into CASE with the USB cable connected to verify the cable is routed away from the fan.

7-40


Revision F


11. Connect the “Drive A” connector of the ribbon cable to the floppy drive /SD card reader. Pin 1 (red wire) on the right side

Ribbon cable connected to the floppy drive / SD card reader

!

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7-41


12. Connect the power connector to the floppy drive.

Power connector connected to the floppy drive

13. Slide the drive assembly into the CASE assembly.

7-42


Revision F


14. Secure the drive assembly front panel with the four lock nuts.

15. Attach the drive bezel.

16. Reconnect the CASE unit to AC power. 17. Turn on the power switch and make sure that the internal fan does not touch any cable (makes no noise). 18. Use Windows Explorer to verify that the card reader and floppy disk can be written to and read from. 19. Format a card or floppy disk as necessary.

Formatting a card or floppy disk will erase ALL data previously stored on the medium. Verify that the medium contains no data that you want or need to retain.

Revision F


7-43

Service: Servicing the Print Head

Servicing the Print Head Log off the CASE application, shut down the system, turn the power switch to OFF, and unplug the unit from the power outlet. To replace the print head, follow these steps:

7-44

1.

Remove the thermal writer from the worksurface assembly. Refer to “Removing the Worksurface Assembly” on page 7-23 for details.

2.

Press the paper release button to move the print roller away from the print head.

3.

Remove the rubber disk from the slide plate and set it aside.

4.

Disconnect the print head ribbon cable from the print head connector.

5.

Move the slide plate to the right to remove pressure from the print head.


Revision F


6.

Pull back on the brush assembly and lift out the print head.

7.

Before installing the new print head, record the resistance value. If it is different from the original print head resistance value, the writer test will have to be performed when this your CASE is reassembled. Refer to “Writer Test” on page 6-8 for more information. Resistance Value

8.

Insert the new print head while taking care that the printhead brush does not get caught under the printhead.

Incorrect

Revision F


7-45


9.

Move slide plate to the left to lock it in place.

10. Replace the rubber disk that was removed earlier. 11. Connect the print head cable and reassemble the CASE. 12. Reconnect the CASE unit to AC power and turn the power switch ON. 13. Perform the writer test discussed in “Writer Test” on page 6-8 for more information.

7-46


Revision F

Service: Writer Board Firmware Update

Writer Board Firm ware Update Follow this procedure when replacing the Writer/Power Distribution Assembly FRU to ensure the USB Writer board has the latest firmware and correct printhead resistance. 1.

Install the new Writer/Power Distribution Assembly.

2. Boot up the system. One of two things will happen: 



3.

If the CASE has the latest application software, the system boots normally. Skip to step 7. If a firmware update is needed, the Writer Firmware Update Utility runs. Proceed to step 3.

When the Writer Firmware Update Utility is finished, click OK then Exit. If the update doesn't complete, check the USB connections and connections to the board or FRU that was just installed. Then repeat from step 2.

4.

Perform a normal unit shutdown.

5.

After the screen goes completely black, turn off the Mains power switch on the back of the unit.

6.

Wait at least 30 seconds for all capacitors to drain down, then turn on the Mains power switch and press the start button by the floppy drive door.

7.

Check the writer firmware version using the following procedure: a.

On the Windows taskbar, select Start > Control Panel.

b.

Double-click on GEMS-IT USB Devices.

c.

Verify the two numbers under the Revision section for the thermal writer are 2.08 2.08 or higher. If the numbers shown are less than 2.08 2.08, then the update did not work and you must repeat this procedure from the beginning.

d. 8.

Revision F

Close the USB Devices and Control Panel windows.

Reburn the printhead resistance into the writer PCB using the following procedure: a.

On the Windows taskbar, select Start > Run.

b.

Browse to D:\CASE\Diags\writerutil.exe.

c.

Click OK .

d.

Check the printhead in the writer for the indicated printhead resistance label. Refer to “Resistance Value” on page 7-45 for more information.

e.

If the Printhead Resistance value displayed is incorrect, enter the correct number.


7-47

Service: Writer Board Firmware Update

f.

Click the Recalc and Save buttons.

Perform this step regardless of whether you modified the resistance value: it is required to burn the resistance value into the new writer PCB flash.

g. 9.

Close the Case Writer Utility window.

Perform a normal unit shutdown.

10. After the screen goes completely black, turn off the Mains power switch on the back of the unit. 11. Wait at least 30 seconds for all capacitors to drain down, then turn on the Mains power switch and press the start button by the floppy drive door. The unit is now ready for normal operation. 12. Launch the CASE application. 13. Click on the System Config icon. 14. Select For Service Only. The Service window opens. 15. In the Service window, enter the password helserv. 16. Select Launch Writer Tests. For more information, refer to “Writer Test” on page 6-8. 17. Run the test at the speed of 25 mm/second. The first 1mm of the speed test may be distorted at 25mm/s and 50mm/s, due to the new current limiting startup ramp that was put into 2.07 and higher to prevent motor problems. 18. When the test is complete, quit the CASE application. 19. On the Windows taskbar, select Start > Programs > GE Medical Systems IT > Configure User Auto Logon.

The Configure User Auto Logon window opens. 20. Select User and click OK . Some older systems will not have not have this step. If not, proceed with the next step. 21. Perform a normal Windows shutdown.

7-48


Revision F

Service: Servicing the I/O Assembly

Servicing the I/O Assembly Log off the CASE application, shut down the system, turn the power switch to OFF, and unplug the unit from the power outlet. To access the I/O assembly for servicing follow these steps: 1.

Use a screw driver to loosen and open the I/O access drawer located on the back of the unit.

2.

Remove five mounting screws from the I/O drawer rear panel.

Cable clamps – used for external devices, e.g., the CAM-14. Use care not to damage the attached board by pulling on device cables/cords attached here.

MOUNTING SCREWS

3.

Carefully slide out the I/O drawer to gain access to the I/O boards and mother board assembly

When moving the I/O drawer, keep it to the left or press in on circuit board to prevent the side of the chassis from damaging it.

Revision F


7-49

Service: Servicing the I/O Assembly

4.

Hang the drive bay as described in “Servicing the Power Distribution Assembly” on page 7-25 to position I/F cables appropriately when reinserting the I/O drawer assembly back into the CASE chassis.

5.


6.


Shown below is a picture of the interior of the I/O assembly drawer. Floppy Drive

Not Used

Hard Drive & CDRW

Harness Reset Switch Analog I/O

Power Header

Com D

Com C

7-50


Revision F

Service: Configuring the Acquisition Interface Board

Configuring the Acquisition Interface Board After replacing the acquisition interface board, you must configure the board to work with the CASE workstation by specifying the workstation’s unit serial number. This is done with syscfg.exe using the following instructions. 1.

Make sure that you are at the initial CASE application screen.

2.

Hold down the Ctrl key and press Esc. The Start menu opens.

3.

Log on as a service user with the following procedure: a.

Select Start and then Shut Down. The Shut Down Windows window opens.

b.

Select choose Close all programs and log on as a different user .

c.

Press and hold the Shift key.

Do not release the Shift key until the Logon Information window opens.

d.

Select YES . The system reboots and the Logon Information window appears.

e.

Type service for the user name and password. Use all lowercase letters. The system completes the boot process.

4.

On the Windows desktop, right-click Network Neighborhood and select Properties. The Network window opens.

5. Verify that the Computer Name is entered as the unit serial number. 6.

Select Ok to close the Network window and return to the desktop.

7.

On the Windows taskbar, select Start > Run. The Run dialog box opens.

8.

Type syscfg and click OK . The System Configuration window opens. If Windows cannot find the application, you may need to specify the entire path and filename, which is typically c:\hardware\syscfg.exe.

9.

Verify the Unit Serial Number is correct.

10. If the Unit Serial Number is incorrect, enter the correct number. 11. Select Configure.

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7-51

Service: Configuring the Acquisition Interface Board

Some earlier units prompt you to enter the NT License number also. If this prompt displays, enter Certificate of Authenticity or 00000-oem-000000000000. 12. Select Update. 13. When the update is complete, select Exit . 14. On the Windows taskbar, select Start > Programs > GE Medical Systems IT > Configure User Auto Logon.

The Configure User Auto Logon window opens. 15. Select User , and then click OK . Some older systems will not have not have this step. If not, proceed with the next step. 16. Shut down the computer as normal.

Verification After configuring the acquisition interface board, verify its success by running a burn-in test with the following instructions: 1. Launch the CASE application. 2.

Click on the System Config icon.

3.

Select For Service Only. The Service window opens.

4.

In the Service Screen, enter the password helserv.

5. From the bottom of the Service Screen choose Burn-in Test. The burn-in test begins. 6.

Verify that the correct unit serial number is displayed.

7.

Click anywhere on the screen to stop the burn-in test. The message Stop Burn-in test? appears.

8.

7-52

Select Yes.


Revision F

8

Revision F

System Rebuild


8-1

For your notes

8-2


Revision F

System Rebuild: Overview

Overview In the event of a catastrophic system failure or a hard drive replacement, it will be necessary to restore the CASE system. This process consists of the following steps: 1. Apply the CD image. For details, refer to “CD Image and Application Installation” on page 8-4. 2.

Configure the CASE system language. For details, refer to “Configure the CASE System Language” on page 8-8.

3.

Install the supplemental XP system files, if necessary. For details, refer to “Install Supplemental XP System Files and XP Security Patches” on page 8-11.

4. Install the application. For details, refer to “Install the Application” on page 8-12. 5.

Identify the options that were purchased with this installation. For details, refer to “Options Installation” on page 8-13.

Revision F


8-3

System Rebuild: CD Image and Application Installation

CD Image and Application Installation The CD reimaging procedure will completely erase all information on the unit, including patient data. ALL PATIENT DATA WILL BE LOST. For technical support, call the Jupiter Remote On-Line Center at 1-800-558-7044. If you need technical support and you are not in the US, see “How to Reach Us...” at the front of this manual to determine who to contact for technical support for further information on copying patient data prior to CD reimaging.

This procedure describes how to install the CD image and CASE Exercise Testing System application software. Follow all the instructions to ensure your system saves your exercise test settings (user lists, protocols, etc.) and stored tests during the upgrade process. For information on saving system settings, see “General Troubleshooting” on page 6-11.

Kit Check that the following items are in the kit you received. For technical support, call the Jupiter Remote On-Line Center at 1-800-558-7044. If you need technical support and you are not in the US, see “How to Reach Us...” at the front of this manual to determine who to contact for technical support. Description

QTY

Multi Image CD Kit

3

CASE application software CD

1

XP Supl. Files CD (only shipped with V6.5/V6.51)

1

XP Security Patch CD (only shipped with V6.51)

1

InSite 2.0 CD (only shipped with V6.5/V6.51)

1

Initial BIOS Configuration To do the initial setup, complete the following steps:

8-4

1.

Restart the system by left-clicking Start on the task bar, selecting Shut Down, and selecting Restart .

2.

When Loading... appears press the F2 key immediately to enter the BIOS SETUP.


Revision F


Bio s Setup — Changi ng th e Boot Sequence 1.

When asked to Enter Password type system then press Enter. You will then be entered into the BIOS Setup Utility.

2.

Insert the CASE Disk 1 Image CD into the CD-ROM drive.

3.

Press the right-arrow key to select the Boot Menu.

4.

In the Boot Menu, arrow up/down to highlight the desired device, then use the +/- keys of the numeric keypad to move the device order up/down and change so the sequence is as follows:   

ATAPI CDROM Drive Removable Devices Hard Drive

5. With this order set, right arrow to the Exit Menu, highlight Exit Savings Changes, and press Enter. Highlight Yes and press Enter again. The system will reboot. In the BIOS Setup Utility Screen, under the EXIT menu, the text “CMOS Restore Condition (CMOS Corruption)” is displayed. This is a normal condition. No action is required.

Disk Image Loadin g 1.

The CASE Image Utility window will appear on the display along with some warning messages. Press Y in response to the question Do you wish to continue[Y,N]?

2.

Press Y again in response to the question Are you sure? (The existing contents of your hard drive will be lost!) [Y,N]?

Pressing Y to this prompt will erase the contents of your hard drive. All patient data will be lost. 3. When the message Span Volume [1] Done, Insert next media and press Enter to continue appears, insert Disk 2 into the CD-ROM drive and click OK. 4.

When loading is done the message Partition 1 successfully imaged will appear. Remove the CASE Image CD from the CD-ROM drive.

5. Reboot the system by pressing Ctrl+Alt+Delete. When Loading... appears on the screen, press the F2 key immediately to enter the BIOS SETUP.

Final Bios Configu ration

Revision F

1.

When asked, Enter Password, type system. The BIOS Setup Utility opens.

2.

Use the right arrow key to select the Exit Menu.

3.

In the Exit Menu, use the arrow key to select Restore CMOS From Flash.

4.

Press Enter to select. CASE Exercise Testing System 2027786-082

8-5


5.

Press Enter again to confirm.

6. Use the arrow key to highlight Exit Saving Changes. 7.

Press Enter.

8.

Select Yes and press Enter again to reboot the system.

9.

Press Ctrl+Alt+Delete to open the Login window. Log on with your: 

User name: __________



Password : __________



Click OK

10. The System Configuration Utility dialog box appears on the screen.

XP Systems — Verify CRT or Flat Panel Display Settings The XP image installs display settings for a CASE system with a flat panel display. The display settings for a CASE system with CRT are different. If the image is loaded on a CRT system, the display settings need to be modified.

Modify CRT Display Settings To modify display settings on a CRT system: 1.

Right-click My Computer and click Explore.

2.

Click Local Disk (C:) and double-click the Support folder.

3. Right-click the CRT_Settings.inf file and select Install. 4. Restart the system.

Verify CRT or Flat Panel Display Settin gs Verify that the display settings for CRT or Flat Panel are the same as listed in the table below. 1.

Right-click anywhere on the desktop and select Properties from the menu.

2.

Click the Settings tab on the Display Properties box.

3.

Verify the Screen Resolution and Color Quality.

4.

Click the Advanced button.

5.

Click the Monitor tab.

6.

Verify the Screen Refresh Rate.

Color Quality Screen Resolutio n Screen Refresh Rate

8-6

Display Settings for CRT

Display Settings for Flat Panel (19” and 17” )

Medium (16 bit)

Medium (16 bit)

1024 by 768 pixels

1280 by 1024 pixels

85 Hertz

60 Hertz


Revision F


The System Configu ration Utili ty 1.

Enter the serial number for your CASE. This entry is not case sensitive.

2.

Click Configure. The Acquisition Board Firmware Update runs automatically, followed by the New SID utility. When both operations are complete, the CASE restarts automatically.

Do not interrupt this update. Interruption of the Acquisition Board

Firmware Update may damage the Acquisition Board.

3.

After the computer has restarted, press Ctrl+Alt+Delete to enter the Login screen. Logon as:   

Revision F

User name: Administrator Password: admin1,3,5,7 Click OK.


8-7

System Rebuild: Configure the CASE System Language

Configure the CASE System Language The CASE XP image is a single image with the multi-language user interface. All language support is loaded on the image and can be configured as needed. The following 15 languages are supported:  

Chinese (Simplified) Czech



Danish Dutch English French



German

  

   

Hungarian Italian Japanese Norwegian



Polish Portuguese (Brazilian) Russian Spanish



Swedish

  

Four language support settings are needed to change languages on a CASE XP system:    

Language used on operating system menus and dialogs Input Language Regional Standards and Formats Language for Non-Unicode program

Since all but the Non-Unicode Program Language settings in XP apply to the logged-in user, and since most CASE customers use the User account, apply these setting changes while logged in as a User at a minimum.

Set Menus and Dialog Language The CASE system supports multiple languages for its menus and dialogs. This setting sets the language to be used. Applies to logged-in user account only. 1. Double-click on the Set Windows Language icon on the CASE system desktop.

8-8

2.

Click the Languages tab and choose the desired language from the Language used in menus and dialogs drop-down list.

3.

Click OK .


Revision F


CASE 6.5 supports the following languages:                

Chinese (Simplified) Czech Danish Dutch English French German Hungarian Italian Japanese Norwegian Polish Portuguese (Brazilian) Russian Spanish Swedish

Set Input Language The CASE system has a separate keyboard for each supported language. This setting sets the keyboard to be used. Applies to logged-in user account only. 1.

Click the Languages tab and click the Details button.

2.

Click the Settings tab of the Text Services and Input Languages dialog, and select the keyboard language from the Default input language drop-down list.

3.

Click OK .

Set Regional Standards and Formats This sets how dates, times, etc., appear in the operating system. Applies to logged-in user account only. 1. Double-click the Set Windows Language icon on the CASE system desktop. 2.

Revision F

Click the Regional Option tab and select the Language (and Country) where the CASE system is installed.


8-9


Set Non-Unicod e Prog ram Language The CASE application is a non-unicode program, so this setting is needed for languages to appear correctly in the CASE application. Applies to all user accounts. 1. Double-click the Set Windows Language icon on the CASE system desktop. 2.

Click the Advanced tab.

3.

Select the language for the CASE application from the Language for nonUnicode programs dropdown list.

4.

Click OK . A message is displayed stating that the necessary files are installed on the system.

8-10

5.

Click Yes to use the installed files.

6.

Click Yes to restart the system.


Revision F

System Rebuild: Install Supplemental XP System Files and XP Security Patches

Install Supplemental XP System Files and XP Security Patches If you are restoring a CASE system running on a Windows XP platform, you need to update some system files prior to restoring the CASE application. Use the following instructions. If you are upgrading a CASE system running on a Windows NT platform, it is not necessary to update your system files. Skip the following process and proceed to “Install the Application” on page 8-12. If you are upgrading a CASE V6.5 system running on a Windows XP platform, it is not necessary to update your system files. Skip the following process and proceed to “Install XP Security Patches” on page 8-11. 1.

Insert the XP Supl Files CASE UPD from V6.01 CD (2031971-001) into the CDROM drive. Windows will automatically start the upgrade of the system files. The next time the CASE system is started, Windows will check the file system.

2.

When the system files have been installed on the CASE system, remove the CD-ROM from the CD-ROM drive and proceed to “Install the Application” on page 8-12.

1.

Insert the SECURITY PATCHES CASE XP CD (2034985-001) into the CD-ROM drive.

Install XP Security Patches

Windows will automatically start the installation and finally shut down and restart the system. 2.

Revision F

Remove the CD-ROM from the CD-ROM drive and proceed to “Install the Application” on page 8-12.


8-11

System Rebuild: Install the Application

Install the Applic ation To perform the initial setup, complete the following steps: 1.

Load the application CD into the CD-ROM drive. Windows will start the Install Shield Wizard.

2.

When the Case window opens, select Next .

3.

Choose the destination default, D:\CASE and select Next . The program installs automatically.

4.

Choose Program directory (local).

5.

Choose Database directory (local or network): 

Choose D:\CASE for local.



See “Network Installation” on page 3-17 for network instructions.

The program installs automatically and a progress bar appears on the screen showing the upgrade’s percent of completion. 6.

When the Install Shield Wizard is complete, select Yes I want to restart my computer now.

7.

Remove the Application CD and store. The system is now ready for use.

8.

Select Finish and the system will restart.

9.

After the computer has rebooted, press Ctrl+Alt+Delete to enter the Login screen. Logon as: 

User name: Administrator



Password : admin1,3,5,7



Click OK .

The CASE icon will appear on the desktop. After performing the application installation procedure, reload customer options. For more information, refer to “Options Installation” on page 8-13.

8-12


Revision F

System Rebuild: Options Installation

Options Installation Please read this entire procedure before continuing. To enable options complete the following steps: 1. Open the CASE application. 2.

If the Select Patient window appears, select Cancel.

3. From the right task bar select System Configuration. 4.

At the System Configuration window, select the Option Code tab.

5. Insert the Options disk. 6.

Select the Load button at the statement: Change Software Options - Are you sure?

7.

Select OK .

8.

Select the swopt.txt file then select Open.

9.

Select OK .

10. Remove the Options disk from the drive and store. 11. Peel off the backing of the options code label and affix it to the inside of the writer door.

Revision F


8-13

System Rebuild: Options Installation

8-14


Revision F

9

Revision F

Upper Level Assembly


9-1

Upper Level Assembly:

For your notes

9-2


Revision F

Upper Level Assembly: Upper Level Product Numbers

Upper Level Product Numbers The following table identifies the product numbers for the two upper level CASE assemblies. These numbers are presented for reference only. The products cannot be ordered as field replaceable units (FRUs). Product Number

Revision F

Description

2012492-007

CASE Series

2012492-008

CASE with KISS


9-3

Upper Level Assembly: Field Replaceable Units

Field Replaceable Units Some items in a CASE system may not be assigned separate manufacturing part numbers because they are normally part of a larger assembly. Since they are considered field replaceable units (FRUs), they have specific service part numbers so they can be ordered and replaced by service technicians. Contact Tech Support for FRU information for assemblies used on previous configurations. Verify part numbers before ordering service parts (field replaceable units). See the tech memo series for this product for changes or additions to this list. This section presents the FRUs in two ways: 

FRU List This is a series of tables that identify the FRUs by category. Each table includes the associated item numbers and descriptions.



9-4

FRU Diagrams This is a series of CASE design diagrams that callout the locations of various core FRUs. For each callout, a table following the description lists the item number, description, and location.


Revision F


FRU Lists This section lists FRUs in the following categories:        

Core FRUs Cables, Interface Keyboards and Mice KISS Module Miscellaneous Monitors and Cables Power Cords Software

Core FRUs The following table lists the FRUs that are part of the core CASE system. The FR Us are listed sequentially by item numbe. For each FRU, the table includes the item description, the name and page of the design drawing on which the FRU is included, and the number of the callout identifying the location of the FRU on the drawing. Item Number

Item Description

Drawing(s)

Page

Loc Num

4520-306

WASHER LOCK EXIT #6,



Drawing 10, “Worksurface Detail”

9-30

66

4520-008

WASHER FLAT SS #8,



Drawing2, “WorkStation Back”

9-16

103

4528-106

CLAMP CABLE CUSH-.31 ID



9-16 9-26

106



Drawing2, “WorkStation Back” Drawing8, “CPU Top and Back”7

4535-001

TIE WRAP 4.00 LG X .125W



Drawing9, “Power Detail”

9-28

112

4702-023

WHEEL ASSY, FRONT, BRAKE



Drawing3, “WorkStation Side”

9-18

114

4702-022

WHEEL ASSY, BACK, SWIVEL




9-18

115

45000-604

SCREWSEMS PH 6-32X1/4




9-30

93

45000-603

SCREWSEMS PH 6-32 X 3/16 PHIL



Drawing7, “Drives Detail”

9-24

67

45142-002

HINGE INVISIBLE SOSS 101




9-30

64

45177-204

SCREWPH 2-25 X .25LG



Drawing5, “Display Platform Detail” Drawing8, “CPU Top and Back”

9-22 9-26

104

Drawing2, “WorkStation Back” Drawing8, “CPU Top and Back”

9-16 9-26

57





58017-001

BUTTON PPR TRAY MTG CASE 12



70437-005

LABEL SYMBOL GROUND



Drawing8, “CPU Top and Back”

9-26

105

70437-002

LABEL, SYMBOL, EQUIP.



Drawing8, “CPU Top and Back” Drawing 11, “Trays and Holders”

9-26 9-32

110

9-14 9-18 9-33

45



Drawing1, “WorkStation Front” Drawing3, “WorkStation Side” Drawing 12, “Electrical Diagram”




9-16

60



80307-059

WIRE GROUND CASE

 

400040-001

Revision F

PLUG MC EQUIPOTENTIAL


9-5


Item Number

Item Description

Drawing(s)

Page

Loc Num

400041-001

WASHER LOCK SERRATED F/M-6




9-16

59

402019-001

SCREW100FLHD 4-40 X 3/8




9-30

65

404525-001

LABEL BLANK 2 X 3/4




9-26

83

404811-001

TAB .25 FASTON LUG #6 STUD




9-30

74

405655-006

DOOR PAPER ACCESS




9-30

73

406831-001

HANDLE WRITER DOOR




9-30

49

409561-001

WASHER, M2, SS



Drawing 10, “Worksurface Detail” Drawing 11, “Trays and Holders”

9-30 9-32

111

9-14 9-16 9-20 9-22 9-24 9-28

53



Drawing1, “WorkStation Front” Drawing2, “WorkStation Back” Drawing4, “CPU Detail” Drawing5, “Display Platform Detail” Drawing7, “Drives Detail” Drawing9, “Power Detail”



411059-006

SCREWSEMS PH M3-.5X6 ZIN,

    

411153-001

FUSE 8 AMP TYPE T 5X20MM




9-16

85

411324-001

NUT HEX KEPS M4-.7 CLASS 8 ZP



9-14 9-16

54



Drawing1, “WorkStation Front” Drawing2, “WorkStation Back”

412048-002

WASHER LOCK M4 EXT TOOTH



Drawing1, “WorkStation Front”

9-14

81

418277-602

HOLDER-ACQ MODULE CASE



Drawing 11, “Trays and Holders”

9-32

71

418277-601

TRAY PAPER CASE



Drawing 11, “Trays and Holders”

9-32

70

418278-103

KNOB CRT BRCKT CASE



Drawing5, “Display Platform Detail”

9-22

61

418653-031

CABLE USB A TO B 1M WHITE



Drawing 12, “Electrical Diagram”

9-33

42

419783-001

CABLE IDE DUAL 533 MM




9-33

43

419960-002

FUSEDRAWER 2-POLE BLACK




9-16

21

420430-001

INLET IEC320 MODULE W/SW




9-16

76

420697-001

CLIP - RIBBON CABLE CASE




9-14

63

420759-001

SCREWFLATHEAD M6 X 12




9-22

62

420815-001

SCREW82 DEG FLTHD 8-32 X.63 BLK




9-16

56

420860-001

NUT M6 KEPS




9-22

58

421200-001

SCREWTHREADFORMING M3 ZINC



Drawing4, “CPU Detail”

9-20

51

421491-001

EMI FILTER 6A LOW LEAKAGE 250V




9-28

20

700708-001

RIBBON CABLE 10P 170MM




9-33

91

801500-001

CASE 2 CONN PCB




9-20

38

9-6


Revision F


Item Number

Item Description

2000714-010 OR (alternative) 2000714-011

HARD DRIVE, 40 GB

2002599-001

Drawing(s)

Page

Loc Num




9-24

2

PCB CASE ACQ INTFC




9-20

3

2003089-001

WORKSURFACE CASE




9-30

5

2003091-001

TRAY ACCESSORY CASE




9-14

6

2003092-001

BRACKET MTG FLOPPY DRIVE




9-24

7

2003141-007

DISK DRIVECDRW 52X32X52X EIDE W/ROXIO




9-24

75

2003342-001

EXTRUSION DISPLAY SUPPORT




9-22

9

2004060-001

PCB CASE LIGHT BOARD




9-22

10

2004064-001

PCB CASE USB WRITER




9-28

11

2004111-001

BUSHING SNAP HEYCO .875 DIA SHORTY



9-24 9-26 9-28 9-33

48



Drawing7, “Drives Detail” Drawing8, “CPU Top and Back” Drawing9, “Power Detail” Drawing 12, “Electrical Diagram”

HARD DRIVE, 80 GB

 

2004293-001

PAD WORKSURFACE




9-14

72

2004295-001

BEZEL DRIVES W/BUTTON CASE



Drawing1, “WorkStation Front” Drawing3, “WorkStation Side”

9-14 9-18

12



13

2004296-001

TRAY WRITER CASE




9-14

2004297-001

WELDMENT CARD CAGE




9-26

2004417-001

BUTTON WRITER RELEASE




9-14

17

2004508-001

DOOR ACCESS I/O




9-16

18

2004527-001

PANEL ACCESS CABLE




9-30

19

2004540-001

SHIELD EMI CASE SERIES




9-14

22

2004574-001

BRACKET XFMR CASE




9-16

23

2004605-002

ASSY STRESS KEYPAD 22 KEY CASE SERIES




9-30

88

2004769-001

BUSHING INSULATOR SNAP




9-16

108

2004770-001

CLAMP CABLE .187 ID




9-16

107

2004867-001

LENS CLEAR CASE SERIES




9-22

25

2004915-016

LABEL STRESS KEYPAD (PORTUGUESE)




9-30

88

2004960-001

LABEL MAX-2 POWER RATING




9-26

95

2004972-002

HARN LIGHT EXTERNAL CASE



Drawing5, “Display Platform Detail” Drawing 12, “Electrical Diagram”

9-22 9-33

28



Revision F


9-7


Item Number 2004972-001

Item Description

Drawing(s)

HARN LIGHT INTERNAL CASE

Page

Loc Num

Drawing8, “CPU Top and Back” Drawing 12, “Electrical Diagram”

9-26 9-33

27

Drawing9, “Power Detail” Drawing 12, “Electrical Diagram”

9-28 9-33

30

Drawing9, “Power Detail” Drawing 12, “Electrical Diagram”

9-28 9-33

31



 

2004974-001

HARN POWER INLET W/TOROID

 

2004975-001

HARN POWER FILTER



2004976-001

HARN PS1/PS2/PWRDIST




9-33

32

2004977-002

HARN PWRSPLY TO PDBD LONG




9-33

29

2004977-001

HARN PWRSPLY TO PDBD SHORT




9-33

33

2004979-001

ASSY ISOLATION XFMR 150VA 90V265VAC 1:1



9-16 9-26 9-33

34



Drawing2, “WorkStation Back” Drawing8, “CPU Top and Back” Drawing 12, “Electrical Diagram”



2004980-001

HARN RIBBON WRITER




9-33

35

2004981-001

HARN ATX POWER




9-33

36

2004982-001

HARN POWER HARD/FLOPPY DRIVE




9-33

37

2004985-001

ASSY CABLEWITH BRACKET PC SERIAL




9-20

118

2004986-001

HARN RESET SWITCH CASE



9-16 9-33

39



Drawing2, “WorkStation Back” Drawing 12, “Electrical Diagram”

2005897-001

ASSY CABLE GUIDE CASE SERIES




9-14

24

2006194-001

CABLE POWER DISPLAY




9-33

92

2006195-001

HARN POWER CDRW




9-33

90

2006392-001

PLATE CPU SLIDE




9-20

100

2006536-001

LABEL CASE CABLE GUIDE




9-18

97

2006537-001

LABEL CASE DRIVE SETTINGS




9-18

26

2006538-001

LABEL BIOS SETUP CASE




9-30

99

2006539-001

LABEL CASE WORKSURFACE LIGHT




9-26

98

2006581-001

BUSHING SNAP PLASTIC 3.0IN



Drawing2, “WorkStation Back” Drawing 12, “Electrical Diagram”

9-16 9-33

77

Drawing1, “WorkStation Front” Drawing2, “WorkStation Back” Drawing8, “CPU Top and Back”

9-14 9-16 9-26

55

9-14 9-22

78



Drawing1, “WorkStation Front” Drawing5, “Display Platform Detail”




9-16

101



2006582-001

SCR W/WASHER M4X8

  

2006583-001 2006584-001

9-8

CLAMP PUSH MOUNT .75 DIA. GUIDES PUSH MOUNT 8.0IN LG




Revision F


Item Number

Item Description

Drawing(s)

Page

Loc Num

2006585-001

CLIP WIRE ROUTING PUSH MT




9-16

102

2007165-001

KIT FRU WRITER CASE SERIES




9-14

79

2007169-002

KIT, POWER DISTRIBUTION W/O FILTER




9-28

113

2007206-001

WIRE GROUND W/CHOKE




9-33

47

2007786-009

NAMEPLATE 40MM GE LOGO DK BLUE




9-30

87

2007892-002

MAIN CPU BOARD W/SDRAM, BIOS AND CPU ORcompatible/interchangeable FRU SET MOTHERBOARD CASE RADISYS ROHS




9-20

1

2035864-001 2007976-001

COVER PLATE D CONNECTORS




9-20

82

2008051-001

LABEL SERVICE I/O CASE




9-16

86

2008053-001

STANDOFF 10.5MM LG FEMALE M3 THD




9-20

84

2008062-001

ASSY CHASSIS CASE SERIES




9-16

4

2021892-001

ASSY LCD MOUNT, CASE




9-22

15

2026205-015

KIT, KEYPAD ASSEMBLY (POLISH)




9-30

88

2026205-014

KIT, KEYPAD ASSEMBLY (CZECH)




9-30

88

2026205-013

KIT, KEYPAD ASSEMBLY (HUNGARIAN)




9-30

88

2026205-012

KIT, KEYPAD ASSEMBLY (DANISH)




9-30

88

2026205-011

KIT, KEYPAD ASSEMBLY (NORWEGIAN)




9-30

88

2026205-010

KIT, KEYPAD ASSEMBLY (JAPANESE)




9-30

88

2026205-009

KIT, KEYPAD ASSEMBLY (CHINESE)




9-30

88

2026205-008

KIT, KEYPAD ASSEMBLY (RUSSIAN)




9-30

88

2026205-007

KIT, KEYPAD ASSEMBLY (DUTCH)




9-30

88

2026205-006

KIT, KEYPAD ASSEMBLY (ITALIAN)




9-30

88

2026205-005

KIT, KEYPAD ASSEMBLY (SPANISH)




9-30

88

2026205-004

KIT, KEYPAD ASSEMBLY (SWEDISH)




9-30

88

2026205-003

KIT, KEYPAD ASSEMBLY (FRENCH)




9-30

88

2026205-002

KIT, KEYPAD ASSEMBLY (GERMAN)




9-30

88

Revision F


9-9


Item Number

Item Description

Drawing(s)

Page

Loc Num

2026205-001

KIT, KEYPAD ASSEMBLY (ENGLISH)




9-30

88

2028841-010

CABLE PC DISK DRIVE FDD




9-33

41

2028841-008

DISK DRIVE FDD/ CARD READER




9-24

8

1479-005T

PRINTHEAD




9-14

135

CS-1150

PRINTHEAD SCREW




9-14

136

Cables, Interface The following table identifies the FRUs available for connecting the CASE system tothe exercise products. Item Number 700609-001

Item Description CABLE, TREADMILL TO STRESS SYSTEM

Keyboards and Mice The following table identifies the input and navigation devices availble for the CASE system. Item Number

9-10

Item Description

2005125-014

KEYBOARD PC PS/2 104 (CZECH)

2005125-013

KEYBOARD PC PS/2 104 (HUNGARIAN)

2005125-012

KEYBOARD PC PS/2 104 (DANISH)

2005125-011

KEYBOARD PC PS/2 104 (NORWEGIAN)

2005125-007

KEYBOARD PC PS/2 104 (DUTCH)

2005125-006

KEYBOARD PC PS/2 104 (SWEDISH)

2005125-005

KEYBOARD PC PS/2 104 (SPANISH)

2005125-004

KEYBOARD PC PS/2 104 (ITALIAN)

2005125-003

KEYBOARD PC PS/2 104 (GERMAN)

2005125-002

KEYBOARD PC PS/2 104 (FRENCH)

2005125-001

KEYBOARD PC PS/2 104 (USA)

2005125-016

KEYBOARD PC PS/2 104 (PORTUGUESE)

2007023-001 OR (alternative) 2022144-001

MICROSOFT INTELLIMOUSE

2005125-015

KEYBOARD PC PS/2 104 (POLISH)

MICROSOFT OPTICAL MOUSE PS/2 or USB


Revision F


KISS Module The following table identifies the FRUs that are part of the KISS component available for the CASE system. Item Number

Item Description

2008712-001

PUMP INTERNAL KISS CASE

2008713-001

KIT KISS CASE EXTERNAL

2031030-001

SET KISS MULTILEAD FOR GER, ENG, FRE

2031030-002

SET KISS MULTILEAD FOR ITA, SPA, DUT

2031030-003

SET KISS MULTILEAD FOR SWE, DAN, NOR

2031030-004

SET KISS MULTILEAD FOR HUN, CZE, SLA

2031030-005

SET KISS MULTILEAD FOR RUS, POL

Miscellaneous The following table identifies various FRUs that are not part of some other subsystem. Item Number

Item Description

801280-001

CAM-14 PCB

4582-015

STRAIN RELIEF 5/8D 6N3-4

2024039-001

SET UPGRADE ELECTRODES NEHB

2024040-001

SET UPGRADE ELECTRODES A1-A4

2028841-010

FRU CABLE PC DISK DRIVE FDD(

2031549-001

CORE RING FERRITE SAFETY LOCK D=6.6MM

2031549-002

CORE RING FERRITE SAFETY LOCK D=13MM

2031549-003

CORE RING FERRITE SAFETY LOCK D=27.5MM

2024038-001

SET UPGRADE ELECTRODES FRANK

Monitors and Cables The following table identifies the FRUs assocaited with the CASE system’s display subsystem. Item Number

Revision F

Item Description

2019792-001

CABLE ASSY DVI-D TO DVI-D VIDEO

2032323-001

DISPLAY, 19” CHILIN TECH MDC1900

2026400-001

DISPLAY LCD 17" NEC 1770NX


9-11


Power Cords The following table identifies the power cords available for the CASE system. Item Number

Item Description

401855-010

10A, 8FT, AUST

401855-009

10A, 8FT, DANISH

401855-008

10A, 8FT, INDIAN

401855-007

10A, 8FT, SWISS

401855-004

10A, 8FT, ISRAELI

401855-003

10A, 8FT, ITALIAN

401855-002

10A, 8FT, BRITISH

401855-001

10A, 8FT, CONT. EURO

405535-002

15A, 125V, 12FT, USA

Software The following table identifies the software available for the CASE system. Item Number

9-12

Item Description

2022587-010

CD CASE V6.51

2022588-004

KIT IMAGE CASE XP RADISYS V1.2 MULTILANG

2028915-004

CD CASE V6.51 CLIENT

2028918-001

CD CASE CARDIOSOFT INSITE 2.0

2031971-001

XP SUPL FILES UPD FROM V6.01 CD-ROM

2034985-001

CD SECURITY PATCHES CASE XP (only for CASE systems with product code SCF or higher)


Revision F


FRU Diagr ams The diagrams on the following pages identify the various assemblies, components, and FRUs of the CASE 6.5 system. Key FRUs are identified by numbered callouts. The table following each diagram identifies the Item Number and description of each callout in the drawing.

Revision F


9-13


Drawing 1: WorkStation Front

9-14


Revision F


FRUs in Drawing 1, WorkStation Front Loc Num

Revision F

Item Number

Item Description

6

2003091-001

TRAY ACCESSORY CASE

12

2004295-001


13

2004296-001

TRAY WRITER CASE

17

2004417-001

BUTTON WRITER RELEASE

22

2004540-001

SHIELD EMI CASE SERIES

24

2005897-001

ASSY CABLE GUIDE CASE SERIES

45

80307-059

WIRE GROUND CASE

53

411059-006


54

411324-001


55

2006582-001

SCR W/WASHER M4X8

63

420697-001

CLIP - RIBBON CABLE CASE

72

2004293-001

PAD WORKSURFACE

78

2006583-001

CLAMP PUSH MOUNT .75 DIA.

79

2007165-001

KIT FRU WRITER CASE SERIES

81

412048-002

WASHER LOCK M4 EXT TOOTH

135

1479-005T

PRINTHEAD

136

CS-1150

PRINTHEAD SCREW


9-15


Drawing 2: WorkStation Back

FRUs in Drawing 2, WorkStation Back Loc Num

9-16

Item Number

Item Description

4

2008062-001

ASSY CHASSIS CASE SERIES

18

2004508-001

DOOR ACCESS I/O

21

419960-002

FUSEDRAWER 2-POLE BLACK

23

2004574-001

BRACKET XFMR


Revision F


FRUs in Drawing 2, WorkStation Back (Continued) Loc Num

Revision F

Item Number

Item Description

34

2004979-001

ASSY ISOLATION XFMR 150VA 90V-265VAC 1:1

39

2004986-001


53

411059-006


54

411324-001


55

2006582-001

SCR W/WASHER M4X8

56

420815-001

SCREW82 DEG FLTHD 8-32 X.63 BLK

57

58017-001


59

400041-001

WASHER LOCK SERRATED F/M-6

60

400040-001

PLUG MC EQUIPOTENTIAL

76

420430-001

INLET IEC320 MODULE W/SW

77

2006581-001


85

411153-001

FUSE 8 AMP TYPE T 5X20MM

86

2008051-001

LABEL SERVICE I/O CASE

101

2006584-001

GUIDES PUSH MOUNT 8.0IN LG

102

2006585-001

CLIP WIRE ROUTING PUSH MT

103

4520-008

WASHER FLAT SS #8,

106

4528-106


107

2004770-001

CLAMP CABLE .187 ID

108

2004769-001

BUSHING INSULATOR SNAP


9-17


Drawing 3: WorkStation Side

9-18


Revision F


FRUs in Drawing 3, WorkStation Side Loc Num

Revision F

Item Number

Item Description

12

2004295-001


26

2006537-001

LABEL CASE DRIVE SETTINGS

45

80307-059

WIRE GROUND CASE

97

2006536-001

LABEL CASE CABLE GUIDE

114

4702-023

WHEEL ASSY, FRONT, BRAKE

115

4702-022

WHEEL ASSY, BACK, SWIVEL


9-19


Drawing 4: CPU Detail

FRUs in Drawing 4, CPU Detail Loc Num

9-20

Item Number

1

2007892-002

1

2035864-001

Item Description MAIN CPU BOARD W/SDRAM, BIOS AND CPU ORcompatible/interchangeable FRU CASE RADISYS ROHS MOTHERBOARD KIT


Revision F


FRUs FR Us in Drawing 4, CPU CPU Detail Detail (Continued) L o c Nu m 3

Revision F

It e m N u m b e r

It em Des c r i p t i o n

2002599-001

PCB CASE ACQ INTFC

10.

4520-008

WASHER FLAT SS #8

38

801500-001 801500-001

CASE 2 CONN PCB

51

421200-001 421200-001

SCREWTHREAD FORMING FORMING M3 ZINC

53

411059-006 411059-006

SCREWSEMS PH M3-.5X6 M3-.5X6 ZIN,

82

2007976-001 2007976-001

COVER PLATE D CONNECTORS ECTORS

84

2008053-001 2008053-001

STANDOFF STANDOFF 10.5MM 10.5MM LG FEMALE M3 THD

100

2006392-001 2006392-001

PLATE CPU SLIDE

118

2004985-00 -001

ASSY CABLE WITH ITH BRACKET PC SERIAL IAL


9-21


Drawing 5: 5: Display Displ ay Platfor m Detail Detail 117

FRUs in Drawing 5, Display Platform Detail Detail L o c Nu m

9-22

It e m N u m b e r


9

2003342-001 2003342-001

EXTRUSION ALUMINUM CASE

10

2004060-001 2004060-001

PCB CASE LIGHT BOARD

15

2021893-001

ASSY LCD MOUNT, CASE

25

2004867-001 2004867-001

LENS CLEAR CASE SERIES

28

2004972-002 2004972-002

HARN LIGHT LIGHT EXTERNAL EXTERNAL CASE Note: Also order Ferrite bead 2027241001 (117) when replacing Harness Light External CASE. CASE.


Revision F


FRUs FR Us in Drawing 5, Display Display Platform Detail (Continued) (Continued) L o c Nu m

It e m N u m b e r


117

2027241-001

FERRITE BEAD

53

411059-006 411059-006


58

420860-001 420860-001

NUT M6 KEPS

61

418278-103

KNOB CRT BRCKT CASE

62

420759-001 420759-001

SCREWFLATHEAD M6 X 12

78

2006583-001 2006583-001

CLAMP PUSH MOUNT .75 DIA.

104

45177-204 45177-204

SCREWPH 2-25 2-25 X .25LG .25LG

Drawing 6: 6: Ferri Ferri te Bead Install ation

Revision F


9-23


Drawing 7: 7: Drives Detail Detail

FRUs in Drawing 7, Drives Detail Detail

9-24

L o c Nu m

It e m N u m b e r

2

2000714-010 OR (alternative) 2000714-011

It em Des c r i p t i o n HARD DRIVE, 40 GB HARD DRIVE, 80 GB


Revision F


FRUss in Drawing 7, Drives FRU Drives Detail (Continued) (Continued) L o c Nu m

Revision F

It e m N u m b e r


7

2003092-001 2003092-001

BRACKET MTG FLOPPY DRIVE

8

2028 028841841-00 008 8

DISK ISK DRIVE IVE FDD/ CARD READER

48

2004111-001 2004111-001

BUSHING SNAP HEYCO .875 .875 DIA SHORTY SHORTY

53

411059-006 411059-006


67

45000-603 45000-603

SCREWSEMS PH 6-32 X 3/16 3/16 PHIL

75

2003141-00 -007

DISK ISK DRIVE IVE CDRW 52X32X52X EIDE W/ROXIO


9-25


Drawing 8: CPU Top and Back

FRUs in Drawing 8, CPU Top and Back Loc Num 27

9-26

Item Number 2004972-001

Item Description HARN LIGHT INTERNAL CASE


Revision F


FRUs in Drawing 8, CPU Top and B ack (Continued) Loc Num

Revision F

Item Number

Item Description

34

2004979-001


48

2004111-001


55

2006582-001

SCR W/WASHER M4X8

57

58017-001


83

404525-001

LABEL BLANK 2 X 3/4

95

2004960-001

LABEL MAX-2 POWER RATING

98

2006539-001

LABEL CASE WORKSURFACE LIGHT

104

45177-204

SCREWPH 2-25 X .25LG

105

70437-005

LABEL SYMBOL GROUND

106

4528-106


110

70437-002

LABEL, SYMBOL, EQUIP.

116

2004297-001

WELDMENT CARD CAGE


9-27


Drawing 9: Power Detail

9-28


Revision F


FRUs in Drawing 9, Power Detail Loc Num

Revision F

Item Number

Item Description

11

2004064-001

PCB CASE USB WRITER

20

421491-001

EMI FILTER 6A LOW LEAKAGE 250V

30

2004974-001


31

2004975-001

HARN POWER FILTER

40

2005124-001

PWR SPLY SW 75W MED 4 OUTS 5/12/-12/12

44

420025-003

POWER SUPPLY SWIT 75W-15V

48

2004111-001


53

411059-006


80

2005342-001

BRACKET POWER SUPPLIES

112

4535-001

TIE WRAP 4.00 LG X .125W


9-29


Drawing 10: Works urface Detail

9-30


Revision F


FRUs in Drawing 10, Worksurface Detail Loc Num

Item Number

Item Description

5

2003089-001

WORKSURFACE CASE

19

2004527-001

PANEL ACCESS CABLE

49

406831-001

HANDLE WRITER DOOR

64

45142-002

HINGE INVISIBLE SOSS 101

65

402019-001

SCREW100FLHD 4-40 X 3/8

66

4520-306

WASHER LOCK EXIT #6,

73

405655-006

DOOR PAPER ACCESS

74

404811-001

TAB .25 FASTON LUG #6 STUD

87

2007786-009

NAMEPLATE 40MM GE LOGO DK BLUE

88

2026205-015

KIT, KEYPAD ASSEMBLY (POLISH)

2026205-014

KIT, KEYPAD ASSEMBLY (CZECH)

2026205-013

KIT, KEYPAD ASSEMBLY (hUNGARIAN)

2026205-012

KIT, KEYPAD ASSEMBLY (DANISH)

2026205-011

KIT, KEYPAD ASSEMBLY (NORWEGIAN)

2026205-010

KIT, KEYPAD ASSEMBLY (JAPANESE)

2026205-009

KIT, KEYPAD ASSEMBLY (CHINESE)

2026205-008

KIT, KEYPAD ASSEMBLY (RUSSIAN)

2026205-007

KIT, KEYPAD ASSEMBLY (DUTCH)

2026205-006

KIT, KEYPAD ASSEMBLY (ITALIAN)

2026205-005

KIT, KEYPAD ASSEMBLY (SPANISH)

2026205-004

KIT, KEYPAD ASSEMBLY (SWEDISH)

2026205-003

KIT, KEYPAD ASSEMBLY (FRENCH)

2026205-002

KIT, KEYPAD ASSEMBLY (GERMAN)

2026205-001

KIT, KEYPAD ASSEMBLY (ENGLISH)

2004605-002

ASSY STRESS KEYPAD 22 KEY CASE SERIES1

2004915-016-

LABEL STRESS KEYPAD (PORTUGUESE)1

93

45000-604

SCREWSEMS PH 6-32X1/4

99

2006538-001

LABEL BIOS SETUP CASE

111

409561-001

WASHER, M2, SS

1. NOTE: Both 2004605-002 and 2004915-016 are required to replace the keypad on a Portuguese unit.

Revision F


9-31


Drawing 11: Trays and Holders

FRUs in Drawing 11, Trays and Holders Loc Num

9-32

Item Number

Item Description

70

418277-601

TRAY PAPER CASE

71

418277-602

HOLDER-ACQ MODULE CASE


Revision F


Drawing 12: Electrical Diagram

Revision F


9-33


FRUs in Drawing 12, Electrical Diagram Loc Num

9-34

Item Number

Item Description

27

2004972-001

HARN LIGHT INTERNAL CASE

28

2004972-002

HARN LIGHT EXTERNAL CASE

29

2004977-002

HARN PWRSPLY TO PDBD LONG

30

2004974-001


31

2004975-001

HARN POWER FILTER

32

2004976-001

HARN PS1/PS2/PWRDIST

33

2004977-001

HARN PWRSPLY TO PDBD SHORT

34

2004979-001


35

2004980-001

HARN RIBBON WRITER

36

2004981-001

HARN ATX POWER

37

2004982-001

HARN POWER HARD/FLOPPY DRIVE

39

2004986-001


41

2028841-010

CABLE PC DISK DRIVE FDD

42

418653-031

CABLE USB A TO B 1M WHITE

43

419783-001

CABLE IDE DUAL 533 MM

45

80307-059

WIRE GROUND CASE

47

2007206-001

WIRE GROUND W/CHOKE

48

2004111-001


77

2006581-001


90

2006195-001

HARN POWER CDRW

91

700708-001

RIBBON CABLE 10P 170MM

92

2006194-001

CABLE POWER DISPLAY


Revision F

Upper Level Assembly: Documentation FRUs

Documentation FRUs The following table identifies the documentation available for CASE v6.5 and their part numbers.. Part Number

Revision F

Description

2027786-078

CASE Op Manual ENG

2027786-083

CASE Op Manual GER

2027786-086

CASE Op Manual FRE

2027786-089

CASE Op Manual DUT

2027786-092

CASE Op Manual ITA

2027786-095

CASE Op Manual SPA

2027786-098

CASE Op Manual SWE

2027786-101

CASE Op Manual DAN

2027786-104

CASE Op Manual NOR

2027786-107

CASE Op Manual RUS

2027786-110

CASE Op Manual HUN

2027786-113

CASE Op Manual CZE

2027786-116

CASE Op Manual SLA

2027786-120

CASE Op Manual POL

2027786-127

CASE Op Manual JPN

2027786-130

CASE Op Manual CHS

2027786-185

CASE Op Manual POR

2027786-082

CASE Service Manual ENG

2027786-141

CASE CLIENT OP Manual ENG

2027786-144

CASE CLIENT OP Manual GER

2027786-146

CASE CLIENT OP Manual FRE

2027786-148

CASE CLIENT OP Manual DUT

2027786-150

CASE CLIENT OP Manual ITA

2027786-152

CASE CLIENT OP Manual SPA

2027786-154

CASE CLIENT OP Manual SWE


9-35


Part Number

9-36

Description

2027786-156

CASE CLIENT OP Manual DAN

2027786-158

CASE CLIENT OP Manual NOR

2027786-160

CASE CLIENT OP Manual RUS

2027786-162

CASE CLIENT OP Manual HUN

2027786-164

CASE CLIENT OP Manual CZE

2027786-166

CASE CLIENT OP Manual SLA

2027786-168

CASE CLIENT OP Manual POL

2027786-170

CASE CLIENT OP Manual JPN

2027786-172

CASE CLIENT OP Manual CHS

2027786-188

CASE CLIENT OP Manual POR

2027786-143

CASE CLIENT Service Manual ENG

2027786-142

CASE CLIENT Sw.Install.& Upgr.Guide ENG

2027786-145

CASE CLIENT Sw.Install.& Upgr.Guide GER

2027786-147

CASE CLIENT Sw.Install.& Upgr.Guide FRE

2027786-149

CASE CLIENT Sw.Install.& Upgr.Guide DUT

2027786-151

CASE CLIENT Sw.Install.& Upgr.Guide ITA

2027786-153

CASE CLIENT Sw.Install.& Upgr.Guide SPA

2027786-155

CASE CLIENT Sw.Install.& Upgr.Guide SWE

2027786-157

CASE CLIENT Sw.Install.& Upgr.Guide DAN

2027786-159

CASE CLIENT Sw.Install.& Upgr.Guide NOR

2027786-161

CASE CLIENT Sw.Install.& Upgr.Guide RUS

2027786-163

CASE CLIENT Sw.Install.& Upgr.Guide HUN

2027786-165

CASE CLIENT Sw.Install.& Upgr.Guide CZE

2027786-167

CASE CLIENT Sw.Install.& Upgr.Guide SLA

2027786-169

CASE CLIENT Sw.Install.& Upgr.Guide POL

2027786-171

CASE CLIENT Sw.Install.& Upgr.Guide JPN

2027786-173

CASE CLIENT Sw.Install.& Upgr.Guide CHS

2027786-189

CASE CLIENT Sw.Install.& Upgr.Guide POR


Revision F


Part Number 2025521-xxx

22745001

TBD

Revision F

Description KISS MULTILEAD Op. Manual (will be available in 14 languages)

KISS Service Manual

Installation Manual KISS MAC5000 in dif. Languages


9-37


For your notes

9-38


Revision F

Appendix A Abbreviations

Revision F


A-1

A-2


Revision F

Ab br evi ati on s: Standard Abbreviations

Standard Abbreviations A A A-ang A-arh A-coa A-hyp A1 - A4 AAMI ABP ac, AC ACLS A/D Adj AG Ah AHA Al AllRam AllSec AllTrk ALT Alt-Off am, AM AM-1 AM-1M AM-2 AM-3 AM-4 amp Ampl AMU ANA ANLG AnsrTone A/O ASCII ASSY Attn AUG AUST AUSTRALN Auto AutoRhym AUX aVF avg aVL

Revision F

ampere antianginal antiarrhythmic anticoagulants antihypertensive auxiliary leadwires American Association of Medical Instrumentation ambulatory blood pressure alternating current Advanced Cardiac Life Support analog-to-digital adjustable automotive glass ampere hours American Heart Association aluminum all RAM all sector all track alternate alternate offset acquisition module, ante meridiem acquisition module-1 acquisition module-1 modified acquisition module-2 acquisition module-3 acquisition module-4 ampere amplifier ambulatory monitoring unit analog analog answer tone Analog Output American Standard Code for Information Interchange assembly attention August Australian Australian automatic automatic rhythm auxiliary augmented left leg lead average augmented left arm lead

aVR AWG

augmented right arm lead American Wire Gage B

Bd BDGH BetaB BKSP BLK BLU Blvd BP BPM BRIT BRN BSI Btu

board, baud binding head beta blockers backspace black blue boulevard blood pressure beats per minute Britain brown British Standards Institute British thermal unit C

CalcBlk CAPOC CASE Catoprl Cauc Cer CFM CGR Ch, CH C/L CLK Clonid cm cm2 Cmd CMMR CMOS c/o COM1 COM2 ComLink Comp Confrmd Cont, CONT Coumadn CPR CPU CR CRC CRD


calcium blockers Computer Assisted Practice of Cardiology Computer Aided System for Exercise Catopril Caucasian ceramic cubic feet/minute computer graphic record channel center line clock signal Clonidine centimeter square centimeters command number common mode rejection ratio complementary metal-oxide semiconductor in care of communications port 1 communications port 2 communications link composition confirmed Continental, continued Coumadin cardiopulmonary resuscitation central processing unit diode cyclic redundancy check cord

A-3


crt, CRT CSA CTRL

cathode ray tube Canadian Standards Association control

ESD etc, etc. EURO EXP

electrostatic discharge et cetera Europe, European Expanded

D D/A DA dac, DAC DAN Dat/Tim dBm dc, DC DD DDD DEC Del DEMO DES DevId Diag Digital Digitox Digox Digoxin DIP Dirctry Diurt DOB DOS DP DPST DRAM DR/DT DSKTP Dysopyr

digital to analog damping relay digital-to-analog converter Danish date/time decibel (referenced to 1 milliwatt into 600 ohms) direct current double density, day Digital Diagnostic Diskette Digital Equipment Corporation, December delete demonstration designation device identification diagnostic Digitalis Digitoxin digoxin Digoxin-Lanoxin dual in-line package directory diuretics date of birth disk operating system diametral pitch double-pole, single-throw dynamic RAM digital recording/digital transmission desktop Dysopyramide E

E ecg, Ecg, ECG ECO EDIC EEPROM e.g. EGA EMF EMI ENG EOF EPIC EPLD EPROM

A-4

enable, vector electrode site, vector lead electrocardiogram Engineering Change Order Electrocardiograph Digital Information Center electrically erasable programmable ROM for example enhanced graphics adapter electromotive force electromagnetic interference English end of file Electronic Patient Information Chart electrically programmable logic device eraseable, programmable, read-only memory

F F F1-F5 Fax FCC FE FILH FLH FLRAM FR FrntEnd FSK ft Furosem

fuse, Farad, female function keys 1 through 5 facsimile Federal Communications Commission front end fillister head flat head flash RAM French front end frequency shift keying foot, feet Furosemide G

g GB GERM GND GRN GRY

gram, acceleration due to gravity Great Britain German, Germany ground, digital ground (dc common) green gray H

H HDLC Hex, HEX HH HiRes Hr Hydral Hz

high, vector electrode site, vector lead high-level data link control hexagon, hexadecimal hour high-resolution hour Hydralazine Hertz (cycles per second) I

I I, II, III IC ID i.e. IEC in IN inc, inc., INC Info Ins I/O I/P ISA


on, input, vector electrode site limb leads integrated circuit identification that is International Electrotechnical Commission inch input incorporated information insert input/output input industry standard architecture

Revision F


Isosorb IT

Isosorbide Italian, Italy

MMM mm/mV mm/s Modem MOS MPE ms MS-DOS MTBF mtg MTR mux mV mVR

J JAN JIS

January Japan Industrial Standards K

k, K Kb, KB kg, Kg kHz, KHz kV, KV Kyb

kilo, 1000, 1024 kilobyte kilogram kilohertz kilovolt keyboard

N

L L L1 L2 LA lb LCD Lcl Line Ld Grps LED LH Lidoca LL Loc LocPc LogRetry Ltd

N n/a NA NC Nitrate NLQ NMI NMOS No NO norm nS NSR

line level one level two left arm pound liquid crystal display local line lead groups light-emitting diode left hand Lidocaine left leg location Local MAC PC log retry limited

mA MAC mains voltage

max Measure Med MEM MF MHz min Misc mm MM

Revision F

neutral not available not applicable no connection nitrates near letter quality non-maskable interrupt N-channel metal-oxide semiconductor number normally open normal nanoseconds Normal Sinus Rhythm O

M m M

month millimeter per millivolt millimeter per second modulator/demodulator metal oxide semiconductor metallized polycarbonate expitaxial milliseconds Microsoft Disk Operating System mean time between failures mounting MOTOR multiplexer millivolt minus (inverted) aVR

meter megabyte, metric, vector electrode site, vector lead, male milliamperes Microcomputer Augmented Cardiograph voltage of a supply mains between 2 line conductors of a polyphase system or voltage between the line conductor and the neutral of a single-phase system maximum measurements medications memory metal film megahertz minutes, minimum miscellaneous millimeter minute

O OE OEM OH OneSec ORG Orig OUT oz

off, original other errors original equipment manufacturer off-hook relay one sector orange original output ounce P

P p-p PA Params Passwds PatData PatInfo PATN PC PCB pF


P wave (section of the ECG waveform) peak-to-peak P wave amplitude parameters passwords patient data patient information patient printed circuit, personal computer printed circuit board picofarad

A-5


Pgm PgmId Phenoth Phenytn PID PLCC PM pm, PM PM-2 PM-3 pn, PN PNH PPA PR Pro-Off Procain PROM Propran PSK PSU Psych PUP PVC PWM PWR PWR CRD

program program identification Phenothiazide Phenytoin patient identification digit plastic leadless chip carrier power module post meridiem, preventive maintenance Power Module-2 Power Module-3 part number pan head P wave amplitude ECG signal interval progressive offset Procainamide programmable read-only memory Propranolol phase shift keying power supply unit psychotropic pull-up signal polyvinyl chloride pulse-width modulation power power cord Q

Q QA QAD QAM QC QD QRS QT QTC QTY Quinid

transistor quality assurance, Q wave amplitude Quality Assurance Deviation quadrature amplitude modulation (phase and amplitude modulation) quality control Q wave duration QRS complex (portion of ECG waveform), interval of ventricular depolarization QRS interval QRS interval quantity Quinidine R

R RA RAM RC RD Ref REN Reserp REV RevdBy RevXmit

A-6

resistor, red, reset right angle, right arm or R wave amplitude random access memory resistor capacitor R wave duration reference, refresh Ringer Equivalence Number Reserpine revision reviewed by reverse transmission

rf RFI RGB RI RL RMR ROM RPA RPD rpt, Rpt RTC RTI RTN RVS R/W

radio frequency radio frequency interference red, green, blue ring indicate right leg Rhythm and Morphology Report read only memory R wave amplitude R wave duration report real time clock relative to patient input return reverse read/write S

12SL s, S SA SB SCL SD SE sec sec.s SEER SING SP SPA SPDT SRAM ST-T standrd, Standrd STD STE STJ STM stmts, Stmts supply mains SVT sw, SW SW

12 simultaneous leads second, select, switch s wave amplitude slow-blow safe current limits schematic diagram, S wave duration serial input/output errors second seconds Solid-state Electronic ECG Recorder Singapore Spanish S wave amplitude single-pole, double-throw static RAM ST-T wave (section of the ECG waveform) standard standard ST segment displacement at the end ST segment displacement at the J point ST segment displacement at the mid-point between STJ and STE statements permanently installed power source power cord type; 300 V switch, software Swedish, Sweden T

T Tone TA Tant TDML TE Tech Thiazid TM


touch tone T wave amplitude tantalum treadmill timeout errors technical Thiazide trademark

Revision F


Tot TP TPA TRAM Tricyli TTL TVS

total test point T’ wave amplitude Transport Remote Acquisition Monitor Tricylic antidepressant transistor-transistor logic, TTL levels transient voltage suppressor

undefined errors microfarad Underwriters’ Laboratory, Inc unconfirmed unit-under-test

Vent. VF VGA VIA VIO Volt VRAM vs

by (as in “8-1/2 x 11”) transceiver orthogonal leads Y year, yellow year years year Symbols

V v, V V1-V6 V123 V3R V456 V4R V ac V dc VA Var VDE

x XCV X,Y,Z

Y yr yrs YY

U UE uF UL Unconf UUT

X

volt, volts precordial leads V1, V2, V3 precordial lead V4, V5, V6 precordial lead volts, alternating current voltage, direct current volt-amperes variable Verband Deutscher Elektrotechniker (German regulatory agency) ventricular ventricular fibrillation video graphics array versatile interface adapter violet voltage video RAM versus

↑ µ µF µs, µsec 68K & # °C °F

Ω %

® > < ± *

12SL

SHIFTed or alternate function micro microfarad microsecond 68000 and number degrees Celsius degrees Fahrenheit Ohm, ohm percent registered greater than less than plus or minus An asterisk after a signal name indicates the signal is active at its relatively lower potential, or “active-low.” Signals without the asterisk suffix are active at their relatively higher potential, or “active-high.” 12 simultaneous leads

W w/ W Warfar WHT WI

Revision F

with watt Warfarin white Wisconsin


A-7


For your notes

A-8


Revision F

Appendix B Technical Description

Revision F


B-1

B-2


Revision F

Technical Description: Technical Specifications

Technical Specifications

Table 1. Performance Specifications - Signal Processing Item

Description

Instrument type

Unity-enhanced cardiac stress testing system with 14 channel acquisition and programmable lead configurations. Celeron-based, NT technology platform and hard drive storage delivers local and MUSE database access.

ECG analysis frequency

500 Hz

ST measurements

ST amplitudes, slope, integral, index, ST/HR slope, ST/HR loops, ST/HR index up to 15 leads

E, J, and post-J point

Manual or computer selected

Signal processing technique

Incremental updating to minimize artifact in all leads

Baseline correction

Cubic Spline or Finite Residual Filter algorithm

QRS detection and analysis

Based on automatic or manual lead selection

ECG output

Real-time ECG/QRS beep/TTL synchronization output

Heart rate

Automatic arrhythmia detection, documentation and annotation

Full disclosure ECG

Beat-to-beat ECG record and event review

Reanalysis

Post-test medians remeasurement from E, J, post-J point selections

ECG interpretation (optional)

12SL Adult and Pediatric ECG Analysis Program

Additional ECG function

Vectorcardiography

Table 2. Performance Specifications - Data Acquisi tion Item

Description

Technology

Active, “Type BF” floating isolated powered 14 channel acquisition module with built-in lead-fail detection and lead prep impedance measurement

Sampling rate

Over-sampling @ 4000 Hz, 12 leads

Dynamic range

320 mV, ±10 mV signal superimposed on ±150 mV DC offset

Resolution

4.88 µV/LSB @ 500 Hz

Noise

< 15 µV peak-to-peak noise over 0.01 to 150 Hz (-3 dB) bandwidth

Frequency response

-3dB, display and writer

High pass filter

0.01 Hz (or 0.05 Hz, special use) with DC offset control

Low pass filter

20, 40, 100 or 150 Hz (selectable)

Revision F


B-3


Table 2. Performance Specifications - Data Acquis ition (Continued) Item

Description

Line filter

50.0 or 60.0 Hz notch filter (selectable)

Baseline correction

Cubic spline algorithm

Artifact/baseline correction

Finite Residual Filter (FRF) algorithm

Common mode rejection

> 140 dB (123 dB with AC filter disabled)

Input impedance

> 10MΩ @ 10 Hz, defibrillator protected

Patient leakage

< 10 µA

Pace detect

Orthogonal LA, LL, and V6; 750 µV @ 50 µs

Communication/storage

 



   

MUSE CV system compatible via diskette, network (optional) MUSE CV Web compatible for retrieval, view, printing of MUSE CV system data Local storage: minimum 10 GB hard drive storage of complete ECG record and test results CD-RW removable archive (optional) Adobe PDF export of final reports Microsoft Word export of configured reports XML or XL export of special data

Table 3. Display Item

Description

Type

LCD

Resolution

1280 x 1024

Size

19” diagonal DVI

Monitored leads

3, 6, or 15

Displayed leads

Number on screen 3 or 6 (12 lead check)

Format

3 rhythm, 3 rhythm + medians, 3 rhythm + trends, 6 rhythm, 4 x 2.5 + 1 rhythm, 2 x 6

Speeds

25, 50 mm/s

Sensitivity/Gain

2.5, 5, 10, 20 mm/mV

Displayed vital signs data (configurable)

Heart rate, target heart rate, blood pressure, exercise clock, stage clock, phase clock, protocol, speed, grade, Watts, METS, RPP, and SpO 2

Other displayed data

ST scan/median complexes, arrhythmias, ventricular ectopic/min. counter, 3 to 15 waveforms, lead check torso and 12 l eads, waterfall displays, trends, tabular summary, stored ECG strips, interpretation, time-of-day clock, patient name, warning messages and prompts

B-4


Revision F


Table 4. Writer Item

Description

Technology

“Instant” load thermal dot array

Leads

3, 6, 12, or 15 (standard, NEHB, Cabrera, configurable)

Speeds

5, 12.5, 25, and 50 mm/s (± 2%)

Sensitivity/Gain

2.5, 5, 10, or 20 mm/mV (± 5%)

Resolution

Horizontal 1000 lines/s x 200 dpi dedicated local printing, 200 x 200 dpi generic printing

Paper type

Thermal, perforated, fanfold, 300 sheets per pack

Paper size

A size 214.63 mm x 280 mm (8.45 in. x 11.7 in.)

Table 5. Environmental - Power Requirements Item

Description

Power supply

AC operation only

Operating voltage range

100-135 VAC, 45-63 Hz, 2.8 A 180-240 VAC, 45-63 Hz, 1.4 A

Power consumption

350 Watts maximum <250 Watts normal <30 Watts standby

1200 BTU/Hr 850 BTU/Hr 100 BTU/Hr

Operating conditions Temperature Humidity Pressure

+10 to + 40° C (+50 to 104 ° F) 20 to 95% RH non-condensing 700 to 1060 hPa

Storage/Transport conditions Temperature Humidity Pressure

-40 to +70° C (-40 to 158 ° F)* 15 to 95% RH non-condensing 500 to 1060 hPa

*. Paper discoloration may occur at higher temperatures.

Revision F


B-5


Table 6. Physi cal Item

Description

Height

125 cm (49 in.) floor to display shelf.

Width

62 cm (24 in.) with paper tray removed

Depth

75 cm (29 in.)

Weight

66.6 kg (147.5 lbs.) without monitor and KISS pump

Interfaces included

    



   

Acquisition module Keyboard (PS/2) and dedicated stress keypad (USB) Mouse (PS/2) Built-in thermal printer (USB) Parallel printer port (LPT1) Only printers modified by GE Medical Systems Information Technologies are allowed to be installed. Full Duplex IEEE 802.3 10 Base-T and 100 BaseTX compatible through RJ45, MUSE compatible 6 Serial ports (COM 1-2, COM A-D); treadmill, BP, ergometer, SpO2 4 Analog and 1 TTL (trigger) output; analog ergometer, camera synch., etc. Diskette drive; 3 ½ in., 1.44 MB PC-compatible for data storage CD-R/W drive; for software updates and optional patient data archival

Table 7. Safety Item

Certification

Description     

UL 2601-1 classified UL classified for CAN/CSA C22.2 No. 601.1 CB certified for IEC 601-1CSA certification CE marking for Council Directive 93/42/EEC concerning Medical Devices Meets applicable AAMI EC-11 requirements

Type of protection against electrical shock

Class 1

Degree of protection against ingress of liquids

Ordinary

Handling of disposable supplies and other consumables

 



Use only parts and accessories manufactured or recommended by GE. Follow manufacturer’s instructions for use for disposable/consumable product. Follow local environmental guidelines concerning the disposal of hazardous materials.

Patient mode of operation

Continuous

Patient leakage current

<10 µA

Degree of protection against electrical shock

Type BF defibrillation protection for the patient cable (acquisition module)

Maintenance frequency

 

B-6

Recommended user daily visual inspection and cleaning. Recommended six-month routine maintenance checks and test procedures performed by qualified technical personnel.


Revision F

Appendix C Electromagnetic Compatibility

Revision F


C-1

For your notes

C-2


Revision F

Electromagnetic Compatibility: Electromagnetic Compatibility (EMC)

Electromagnetic Compatibility (EMC) Changes or modification to this system not expressly approved by GE Medical System could cause EMC issues with this or other equipment. This system is designed and tested to comply with applicable regulation regarding EMC and needs to be installed and put into service according to the EMC information stated as follows.

Use of portable phones or other radio frequency (RF) emitting equipment near

the system may cause unexpected or adverse operation. The equipment or system should not be used adjacent to, or stacked with, other equipment. If adjacent or stacked use is necessary, the equipment or system should be tested to verify normal operation in the configuration in which it is being used.

Guidance and Manufacturer’s Declaratio n – Electromagnetic Emissions The CASE is intended for use in the electromagnetic environment specified below. It is the responsibility of the Em is si on s Tes t

Revision F

Co mp li an ce

RF emissions CISPR11

Group 1

RF emissions CISPR11

Class A

Harmonic Emissions EN 61000-3-2

Class A

Voltage fluctuations/ Flicker emissions EN 61000-3-3

Complies

customer or user to ensure that the CASE is used in such an environment. El ec tr om ag net ic En vi ro nm en t - Gu id an ce The equipment uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

The equipment is suitable for use in all establishments other than domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.


C-3


Guidance and Manufacturer’s Declaratio n – Electromagnetic Immunity The CASE is intended for use in the electromagnetic environment specified below. It is the responsibility of the

Immunity Test

EN 60601 Test Level

customer or user to ensure that the CASE is used in such an environment.

Compliance Level

Electromagnetic Environment Guidance

Electrostatic discharge (ESD) EN 61000-4-2

± 6 kV contact ± 8 kV air

± 6 kV contact ± 8 kV air

Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

Electrical fast transient/burst EN 61000-4-4

± 2 kV for power supply lines ±1 kV for input/output lines

± 2 kV for power supply lines ±1 kV for input/output lines

Mains power should be that of a typical commercial or hospital environment.

Surge EN 61000-4-5

± 1 kV differential mode ± 2 kV common mode

± 1 kV differential mode ± 2 kV common mode

Mains power should be that of a typical commercial or hospital environment.

Voltage dips, short interruptions and voltage variations on power supply input lines EN 61000-4-11

<5% Ut (>95% dip in Ut) for 0.5 cycles 40% Ut (60% dip in Ut) for 5 cycles 70% Ut (30% dip in Ut) for 25 cycles <5% Ut (>95% dip in Ut) for 5 sec

<5% Ut (>95% dip in Ut) for 0.5 cycles 40% Ut (60% dip in Ut) for 5 cycles 70% Ut (30% dip in Ut) for 25 cycles <5% Ut (>95% dip in Ut) for 5 sec

Mains power should be that of a typical commercial or hospital environment. If the user of the CASE requires continued operation during power mains interruptions, it is recommended that the CASE be powered from an uninterruptible power supply or a battery.

Power frequency (50/60 Hz) magnetic field EN 61000-4-8

3 A/m

3 A/m

Power frequency magnetic fields should be at levels characteristics of a typical location in a typical commercial or hospital environment.

Ut is the AC mains voltage prior to application of the

test level.

C-4


Revision F


Guidance and Manufacturer’s Declaratio n – Electromagnetic Immunity The CASE is intended for use in the electromagnetic environment specified below. It is the responsibility of the Immunity Test

EN 60601 Test Level

Compliance Level

customer or user to assure that the CASE is used in such an environment. Electromagnetic Environment – Guidance Portable and mobile RF communications equipment should not be used closer to any part of the equipment, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation d istance

Conducted RF EN 61000-4-6

3 Vrms 150 KHz to 80 MHz

2.6 V rms

Radiated RF EN 61000-4-3

3 V/m 80 MHz to 2.5 GHz

1.8 V/m

d = 1.2 P d = 1.2 P 80 MHz to 800 MHz d = 2.3 P 800 MHz to 2.5 GHz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer, and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya, should be less than the compliance level in each frequency rangeb. Interference may occur in the vicinity of equipment marked with the following symbol:

NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by reflection from structures, objects, and people. a

Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the equipment is used exceeds the applicable RF compliance level above, the equipment should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the equipment.

b

Over the frequency range 150 KHz to 80 MHz, field strengths should be less than 3 V/m.

Revision F


C-5


Recommended Separation Distances The table below provides the recommended separation distances (in meters) between portable and mobile RF communication equipment and the CASE.

controlled. The customer or the user of the CASE can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the CASE as recommended below, according to the maximum output power of the communications equipment.

The CASE is intended for use in the electromagnetic environment on which radiated RF disturbances are

Separation Distance in Meters (m) Accordin g to Frequency of Transmitter

Rated Maximum Output Power of Transmitter in Watts

150 kHz to 80 MHz outside ISM bands

150 kHz to 80 MHz in ISM bands

0.01

0.12

0.12

0.12

0.23

0.1

0.38

0.38

0.38

0.73

1

1.2

1.2

1.2

2.3

10

3.8

3.8

3.8

7.3

100

12

12

12

23

d = 1.2 P

80 MHz to 800 MHz

d = 1.2 P

d = 1.2

P

800 MHz to 2.5 GHz d = 2.3 P

NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.

For transmitters rated at a maximum output power not listed above, the recommended separation distance [d] in meters (m) can estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (w) according to the transmitter manufacturer.

These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

C-6


Revision F


Compliant Cables and Acc essor ies The table below lists cables, transducers, and other applicable accessories with which GE Medical Systems claims EMC compliance.

The use of accessories, transducers and cables other than those specified may result in increased emissions or decreased immunity performance of the equipment or system.

Part No

Revision F

Any supplied accessories that do not affect EMC compliance are not included. Description

Maximum Lengths

2019792-001

Cable Assy DVI-D to DVI-D Video

1.8m

700609-001

Cable Treadmill to Stress Sys

6.096m

900995-001

Cam 14

NA

2026400-001

Display LCD 17” NEC 1770NX

N/A

2023603-001

Display LCD 19” NEC 19805XI

N/A

2032323-001

Display LCD CHILIN TECH MDC1900

N/A

2005125-0XX

Keyboard

NA

901142-001

Kit Cam 14 Resting W/AHA Adaptors

NA

901142-002

Kit Cam 14 Resting W/IEC Adaptors

NA

420403-001

Mouse Two Button Logitech

NA

401855-0XX

Power Supply Cord European 10A 250V

2.5m

405535-002

Power Supply Cord US 15A 125V

3.0m

2008712-001

Pump Internal KISS CASE

NA

400073-001

Serial Comm. Cable 8 Pin Mini DIN

6.1m

2031030-001

Set KISS Multilead for Ger, Eng, Fre

N/A

2031030-004

Set KISS Multilead for Hun, Cze, Sla

N/A

2031030-002

Set KISS Multilead for Ita, Spa, Dut

N/A

2031030-006

Set KISS Multilead for Jpn, Chs

N/A

2031030-005

Set KISS Multilead for Rus, Pol

N/A

2031030-003

Set KISS Multilead for Swe, Dan, Nor

N/A

2024040-001

Set Upgrade Electrodes A1-A4

N/A

2024038-001

Set Upgrade Electrodes FRANK

N/A

2024039-001

Set Upgrade Electrodes NEHB

N/A


C-7


For your notes

C-8


Revision F

Appendix D CASE Files

Revision F


D-1

For your notes

D-2


Revision F

CASE Files: Directory Structure and Notes on CASE Files

Directory Structure and Notes on CASE Files When installing CASE, a subdirectory (default: D:\CASE) is created into which the files required for execution are copied. When calling up CardioSoft for the first time, several subdirectories are then created in this directory for CARDIO

the examination data, speech entries and the configuration data. After calling up CASE, the directory structure is as follows:

DATABASE

Databases for Patient Examination Data

RESTECG

Resting ECG Reports

SPIR

Spirograms

SOUND

Sound Files from all Examinations.

ONLINE

Full Disclosure ECG from all Examinations.

SETUP

Configurations

TAPE

Dictated Data

AVER

Late Potential Reports

DOC

User manual and Help Files

CAS

Ergometry Reports

NARRATIV

Configured report templates

ONL500

not used

ONL2000

not used

RHK

Right-Heart-Catheterization

HOLTERBP

Long-Term Blood Pressure Reports

EXTPROG

Reports from all External Progs.

DIAGS

Diagnostic Software

HELP

Help files

WRITER

Thermal Writer Windows Driver

Files in Window s sys tem32 director y: CardioSoft requires the following files from the Windows system32 directory: Filename mfc42.dll msvcrt.dll

Visual C++ class library Functions

hel_grid.ttf

Special Font

msflxgrd.ocx

Revision F

Description

Flex Grid Tools for Stress Test Table


D-3

CASE Files: Directory Structure and Notes on CASE Files

File name nomenclature of t he examination pr ocedure The file name consists of the following components: 

the ID letter for the examination procedure A: late potential analysis         

U: ultrasound  X: external programs  Y: X-ray  Z: Right-Heart-Catheterization the identification letter for the compression  C: compressed 

B: ambulatory blood pressure measurement C: Ergometry H: Holter ECG K: cardiac catheterization



U: uncompressed the internal patient ID 



N: STAT (emergency) ECG R: Resting ECG S: spirometry T: stress echocardiography

 

6-digit with leading zeros

the internal examination ID, which gives additional file data  3-digit with leading zeros

File in th e Window s INF directory CardioSoft requires the following file in the Windows INF Filename

directory: Description

camusb.inf

Information file for the USB cam device

Files in th e Window s dir ectory Cardiosoft creates the following files in the Windows Filename

Description

cardio.ini

Initialization file that stores program settings. These settings

ca_sys.ini

Initialization file that stores system settings.

erg_prot_vsan.dat

The program settings in cardio.ini can be allocated with an identifier and stored in the help functions under Settings in the \SETUP directory, thus making them available to all users of a network (load help functions under Settings). Up to 10 settings can be stored with file names from SETUP0.INI to SETUP9.INI. Stress test driver settings are stored in file PA5V0.DAT to PA5V9.DAT.

D-4

directory:

Data file that stores the settings for the stress test driver (e.g., ergometer, treadmill).

If the profiles in erg_prot_vsan.dat are modified or recreated, the file should be saved. It has been known for this file to have been deleted during new installations. It can also prove useful to assign the file with the attribute READONLY. This prevents overwriting or deletion. However, this attribute must be removed again before making any new changes in the profile. It is more advisable, however, to make a backup of the file as it cannot then be lost, even in the event of a hard disk error.


Revision F

CASE - ServiceManual

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