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    							Patient Side Module, E-PSM, E-PSMP (Rev. 01)
    Technical Reference Manual Slot
    Conformity according to the Council Directive 93/42/EEC concerning Medical Devices amended by 2007/47/EC
    CAUTION: U.S. Federal law restricts this device to sale by or on the order of a li censed medical practitioner.
    Outside the USA, check local laws  for any restriction that may apply.
    All specifications subject to change without notice.
    Document number M1215098-002
    12 August, 2011
    GE Healthcare Finland Oy
    Kuortaneenkatu 2
    FI-00510 Helsinki, Finland
    Tel: +358 10 39411
    Fax: +358 9 1463310
     www.gehealthcare.com
    Copyright  © 2011 General Electric Com pany. All rights reserved. 
    						
    							Table of contentsi
    Document no. M1215098-002
    Table of contents
    Table of contents i
    Table of figures iii
    List of tables iv
    Introduction1
    1 Specif ications 3
    1.1 General specif ications  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  3
    1.2 Typical performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . .  3
    1.2.1 NIBP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . .  3
    1.2.2 ECG  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . .  4
    1.2.3 Pulse oximetry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . .  4
    1.2.4 Temperature. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . .  5
    1.2.5 Invasive blood pressure  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . .  5
    1.2.6 Respiration  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . .  5
    1.3 Technical specif ications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . .  6
    1.3.1 NIBP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . .  6
    1.3.2 ECG  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . .  6
    1.3.3 Pulse oximetry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . .  6
    1.3.4 Temperature. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . .  6
    1.3.5 Invasive blood pressure  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . .  7
    1.3.6 Respiration  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . .  7
    2 Functional description 8
    2.1 Measurement principle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  8
    2.1.1 NIBP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . .  8
    2.1.2 ECG  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . .  8
    2.1.3 Pulse oximetry . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . .  8
    2.1.4 Temperature. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . 10
    2.1.5 Invasive blood pressure  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . 10
    2.1.6 Respiration  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . 11
    2.2 Main components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . 11
    2.2.1 E-PSMP/E-PSM . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . 11
    2.2.2 NIBP board  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . 12
    2.2.3 ECG board in 12-lead measurement  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 5
    2.2.4 ECG f iltering . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . 16
    2.2.5 STP board  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . 17
    2.3 Connectors and signals  . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
    2.3.1 Module bus connector  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . 22
    2.3.2 Front panel connectors  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . 22 
    						
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    3 Service procedures25
    3.1 General service information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . 25
    3.2 Service check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . 25
    3.2.1 Recommended tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . 25
    3.2.2 Recommended parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . 26
    3.2.3 Visual inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . 26
    3.2.4 Functional inspection  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . 27
    3.3 Disassembly and reassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . 35
    3.3.1 Before disassembly  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . 35
    3.3.2 Tools needed  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . 35
    3.3.3 To disassemble the module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . 35
    3.3.4 To remove the manifold unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . 39
    3.3.5 To remove the module bus connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 41
    3.3.6 To replace the NIBP f ilter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . 42
    3.4 Adjustments and calibrations. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . 43
    3.4.1 NIBP calibrations  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . 43
    3.4.2 Temperature calibration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . 45
    3.4.3 Invasive pressure calibration  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . 45
    4Troubleshooting 46
    4.1 Troubleshooting charts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 46
    4.1.1 NIBP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . . . . . . . . . 46
    4.1.2 NIBP error code explanation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . 49
    4.1.3 Pulse oximetry (SpO2) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . . 50
    4.1.4 Invasive blood pressure  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  . . . . . . . 51
    4.2 Troubleshooting flowcharts  . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 52 4.2.1 Troubleshooting for NIBP parameter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  52
    4.2.2 Troubleshooting for ESP parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .  53
    5 Earlier revisions54
    Appendix A: Service check  form, Patient Side Module,
    E-PSM, E-PSMP (Rev. 01)  A-1 
    						
    							 Table of figuresiii
    Document no. M1215098-002
    Table of f igures
    Figure 1 Patient Side Module, E-PSMP ............................................................................................ ...................................................... 1
    Figure 2 Absorption of infrared light in  the finger ............................................................................. .............................................. 9
    Figure 3 Pulse oximetry probe parts layout and sc hematic diagram .................................................................................10
    Figure 4 Front panel of E-PSMP .................................................................................................. ...........................................................11
    Figure 5 NIBP board functional block diag ram ..............................................................................................................................12
    Figure 6 NIBP pneumatics diagram ................................................................................................ .....................................................14
    Figure 7 12-lead ECG measurement block di agram....................................................................................................................15
    Figure 8 STP board block diagram ................................................................................................ .......................................................17
    Figure 9 Temperature measurement principle ...................................................................................... ........................................18
    Figure 10 Pressure measurement principle........................................................................................ ................................................19
    Figure 11 Pulse oximetry measurement block  diagram...............................................................................................................20
    Figure 12 Serial communication of E-PSM(P)  module ....................................................................................................................21
    Figure 13 Troubleshooting flowchart for NIBP  parameter ..........................................................................................................52
    Figure 14 Troubleshooting flowchart for ESP Parameters...........................................................................................................53 
    						
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    Document no. M1215098-002
    List of tables
    Table 1 Patient Side Module options................................................................................................................................. 1
    Table 2 Module bus connector description ........................................................................................ ........................ 22
    Table 3 ECG connector ........................................................................................................... .............................................. 22
    Table 4 SpO
    2 connector ..................................................................................................................... .................................. 23
    Table 5 Invasive blood pressure connectors (P1, P2) ............................................................................. ................ 23
    Table 6 Temp connector (T1, T2) ................................................................................................. ..................................... 24
    Table 7 Recommended tools ....................................................................................................... ...................................... 25
    Table 8 Recommended parts ....................................................................................................... ..................................... 26
    Table 9 NIBP calibration check pressures ........................................................................................ ........................... 44 
    						
    							Patient Side Module, E-PSM, E-PSMP (Rev. 01) 1
    Document no. M1215098-002
    Introduction
    This Technical Reference Manual Slot provides  information for the maintenance and service of 
    the Patient Side Modules E-PSMP and E-PSM. 
    Please also refer to “Technical Reference Ma nual” of the monitor for system specific 
    information e.g. related documentation, conv entions used, symbols on equipment, safety 
    precautions, system description, system installation, interfacing, functional check and planned 
    maintenance. 
    The E-PSMP and E-PSM modules provide general hemodynamic parameters.
    Figure 1 Patient Side Module, E-PSMP
    Table 1 Patient Side Module options
    Intended purpose (I ndications for use)
    The Patient Side Module (model family E-PS M(P)) and accessories are indicated for the 
    monitoring of hemodynamic parameters of all hospital patients. The hemodynamic 
    parameters of the module comprise ECG including ST-segment and arrhythmia, Impedance 
    respiration, NIBP, Temperature, SpO
    2 (including monitoring during  conditions of clinical patient 
    motion), and invasive blood pressure. Parameter E-PSMP E-PSM
    Two invasive blood pressures
    x
    Impedance respirationxx
    ECGxx
    Pulse oximetryxx
    Two temperaturesxx
    NIBPxx 
    						
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    Document no. M1215098-002
    Impedance respiration measurement is indicated for patients aged 3 and up. The NIBP 
    measurement is indicated for patients who weigh 5 kg (11 lb.) and up. This device is indicated 
    for use by qualified medical personnel only. 
    Monitor software compatibility
    Patient Side Module, E-PSM(P) Rev. 00 and 01 are designed for use with Datex-Ohmeda 
    monitors as follows: 
    −S/5 FM monitors using software L-FICU04(A) or later.
    − S/5 Anesthesia Monitors using software L- ANE04(A) or later equipped with 5-Module 
    Frame, F-CU5(P) or with S/5 8-Module Fram e, F-CU8. With the F-CU8, the E-INTPSM 
    interface module is needed. 
    − S/5 Critical Care Monitors using software L-ICU04(A) or later equipped with 5-Module 
    Frame, F-CU5(P) or with S/5 8-Module Fram e, F-CU8. With the F-CU8, the E-INTPSM 
    interface module is needed. 
    Equipment safety symbols
    When displayed on the E-PSM, E-PSMP module, indicates that protection 
    against cardiac defibrillator di scharge is due in part to the accessories for pulse 
    oximetry (SpO
    2), temperature (T) and invasive pressure (P) measurement. 
    						
    							Patient Side Module, E-PSM, E-PSMP (Rev. 01) 3
    Document no. M1215098-002
    1Specifications
    1.1 General specifications
    Module size51 x 132 (171 w/ tab) x 140 mm
    W x D x H 2 x 5.2 (67 w/ tab) x 5.5 in
    Module weight 0.6 kg /1.4 lb.
    Power consumption 2.3 W typical (NIBP pump off)
    7.5 W typical (NIBP pump on)
    Operation temperature 10 to 40°C / 50 to 104 °F
    1.2 Typical performance
    1.2.1 NIBP
    WARNING Non-invasive blood pres sure measurement is intended for patients 
    weighing over 5 kg (11 lb.) 
    Oscillometric measurement principle.
    Measurement range adult25 to 260 mmHg
    child 25 to 195 mmHg
    infant 15 to 140 mmHg
    Pulse rate range accepted 30 to 250 bpm
    Measurement interval from 1 min. to 4h 
    Typical measuring time adult23 s
    infant 20 s
    Initial inflation pressure adult170 ±10 mmHg
    child 150 ±10 mmHg
    infant 120 ±10 mmHg
    Venous stasis adult80 ±5 mmHg / 2 min.
    child 60 ±5 mmHg / 2 min. 
    infant 40 ±5 mmHg / 1 min.
    Cuff widths see User’s Guide
    Venous stasis pressure may be lower than the values above if the patient has low blood 
    pressure. The venous stasis pressure adapts to the measured mean pressure being the same 
    as mean pressure but always at least the following:
    Infant 20 ± 5 mmHg
    Child 30 ± 5 mmHg
    Adult 40 ± 5 mmHg 
    Overall system accuracy:  Meets  or exceeds SP10-2002 AAMI standards
    1 
    1 (According to SP10-2002 AAMI 4.4.5.2.B, Intra-arterial method as the reference standard, mean difference of the test 
    system and the comparison system shall be ± 5 mmHg or less with standard deviation of 8 mmHg or less). 
    						
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    1.2.2 ECG
    Lead selectionI, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6
    Sweep speeds  12.5, 25, 50 mm/sec.
    Display filter
    Diagnostic0.05 to 150 Hz
    Monitoring 0.5 to 30 Hz (-3 dB, with 50 Hz reject filter)
    0.5 to 40 Hz (-3 dB, with 60 Hz reject filter)
    ST filter 0.05 to 30 Hz (-3 dB, with 50 Hz reject filter)
    0.05 to 40 Hz (-3 dB, with 60 Hz reject filter)
    Heart rate from ECG
    Range 30 to 250 bpm
    Accuracy ±5 bpm or ±5%, whichever is greater
    Resolution 1 bpm
    Update interval 5 s
    Averaging time 5 s
    ST levels (in main software)
    ST level range-9 to +9 mm (-0.9 to +0.9 mV)
    Resolution 0.1 mm (0.01 mV)
    Averaging calculated from 8 QRS complexes
    Pacemaker pulse detection
    Detection level2 to 700 mV
    Pulse duration 0.5 to 2 ms
    The monitor is specified for both of the methods A and B in ANSI/AAMI EC13 4.1.4.2.
    Direct ECG and Synchronization
    for specifications see section “Specifications” in the “Frame for FM  Technical Reference Manual Slot” 
    1.2.3 Pulse oximetry
    Measurement range0 to 100%
    Calibration range 70 to 100%
    Accuracy
    1100 to 70%, ±2 digits
    ±3 digits during cl inical patient motion
    69 to 0%, unspecified
    Display resolu tion 1 digit = 1% of SpO
    2
    Display averaging time Slow, Normal, beat-to-beat
    Pulse beep pitch varies with SpO
    2 level
    The monitor is calibrated against  functional oxygen saturation SpO
    2 func.
    Pulse rate from Pleth
    Measurement range  30 to 250 bpm
    Accuracy 30 to 100, ±5 bpm,
    100 to 250, ±5%
    Resolution 1 bpm
    Display averaging 10 s
    Adjustable pulse beep volume.
    Pleth waveform
    Scales 2, 5, 10, 20, 50 mod%, Auto
    Start up scale is 20 mod% if AUTO is not selected to be the default setting.
    1 Accuracy is based on deep hypoxia stud ies with volunteered subjects during motion and non-motion conditions over a 
    wide range of arterial blood oxygen saturation as compared  to arterial blood CO-Oximetry. Accuracy may depend on the 
    sensor used, please refer to the instru ctions for use in the accessory package. 
    						
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