GE LOGIQ 200 Pro User manual
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LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
Regulatory Requirement
This product complies with regulatory requirements of the following European
Directive 93/42/EEC concerning medical devices
This manual is a reference for the LOGIQ200 PRO Series. It applies to all
version of the 3.1X software for the LOGIQ200 PRO Series.
GE Medical Systems
GE Medical Systems: Telex 3797371
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)
GE Ultrasound Europe: Tel: +49(0)212 2802 0
Kranzbühler GmbH & Co KG
Beethovenstraße 239, Postfach 110560, D–42655
Solingen
GERMANY
Revision History
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REV DATE REASON FOR CHANGE
0 August 1, 1999 Initial Release
1 January 15, 2000 Software Version 3.02 Release
2 June 15, 2000 Software Version 3.15 Release
3 November 21, 2000 Software Version 3.16 Release
#
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LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
1
Revision History
2
LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
Revision History
Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on GPC (GE Medical Systems Global
Product Configuration). If you need to know the latest revision, contact your
distributor, local GE Sales Representative or in the USA call the GE Ultrasound
Clinical Answer Center at 1-800-682–5327 or 414-524-5698.
LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
3
Regulatory Requirements
A
Regulatory Requirements
This product complies with the regulatory requirements of the
following:
S Council Directive 93/42/EEC concerning medical devices:
the label affixed to the product testifies compliance
to the Directive.
The location of the CE marking is shown on Safety chapter
of this manual.
European registered place of business:
GE Medical Systems Europe
Quality Assurance Manager
BP 34
F 78533 BUC CEDEX France
Tel: +33 (0)1 30 70 40 40
.
For US
Only
S Medical Device Good Manufacturing Practice Manual
issued by the FDA (Food and Drug Administration,
Department of Health, USA).
S Underwriters’ Laboratories, Inc. (UL), an independent
testing laboratory.
S Canadian Standards Association (CSA).
S International Electrotechnical Commission (IEC),
international standards organizations, when applicable.
Caution: United States law restricts this device to sale or use by
or on the order of a physician.
S
General Electric Medical Systems
EN 46001 certified.
S The original document was written in English.
is ISO 9001 and
LOGIQt200 PRO Series Basic Users Manual
2234813–100 Rev 1
1
Regulatory Requirements
NOTE: This equipment generates, uses and can radiate radio frequency energy. The
equipment may cause radio frequency interference to other medical and
non-medical devices and radio communications. To provide reasonable
protection against such interference, this product complies with emissions limits
for a Group 1, Class A Medical Devices Directive as stated in EN 60601–1–2.
However, there is no guarantee that interference will not occur in a particular
installation.
NOTE: If this equipment is found to cause interference (which may be determined by
turning the equipment on and off), the user (or qualified service personnel)
should attempt to correct the problem by one or more of the following
measure(s):
– reorient or relocate the affected device(s)
– increase the separation between the equipment and the affected device
– power the equipment from a source different from that of the affected device
– consult the point of purchase or service representative for further
suggestions
NOTE: The manufacturer is not responsible for any interference caused by using other
than recommended interconnect cables or by unauthorized changes or
modifications to this equipment. Unauthorized changes or modifications could
void the users’ authority to operate the equipment.
NOTE: To comply with the regulations on electromagnetic interference for a Class A
FCC Device, all interconnect cables to peripheral devices must be shielded and
properly grounded. Use of cables not properly shielded and grounded may
result in the equipment causing radio frequency interference in violation of the
FCC regulations.
NOTE: Do not use devices which intentionally transmit RF Signals (cellular phones,
transceivers, or radio controlled products) in the vicinity of the equipment as it
may cause performance outside the published specifications. Keep the power
to these type devices turned off when near this equipment.
The medical staff in charge of this equipment is required to instruct technicians,
patients, and other people who may be around this equipment to fully comply
with the above requirement.
2
LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
Table of Contents
Front Matter
Title Page
Revision History A. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Regulatory Requirements
Table of Contents Table of Contents 1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Chapter 1 – Introduction
System Overview 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Attention 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Prescription Device 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
System Components 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Documentation 1–3. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 1–4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
General Indications for Use 1–5. . . . . . . . . . . . . . . . . . . . . . . . .
Contraindications 1–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Table of Contents
Regulatory Req 1. . . . . . . . . . . . . . . . . . . . . .
Who to Contact 1–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Who To Contact 1–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
How This Book is Organized 1–9. . . . . . . . . . . . . . . . . .
Manual Content 1–9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Manual Format 1–11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Chapter 2 – Safety
Safety Precautions 2–2. . . . . . . . . . . . . . . . . . . . . . . . . . .
Icon Description 2–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Hazard Symbols 2–3. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Patient Safety 2–4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Equipment and Personnel Safety 2–6. . . . . . . . . . . . . . . . . . . .
Related Hazards 2–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Device Labels 2–8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Acoustic Output 2–16. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Controls Affecting Output 2–16. . . . . . . . . . . . . . . . . . . . . . . . . .
Warning Label Locations 2–18. . . . . . . . . . . . . . . . . . . . . . . . . . .
LOGIQ200 PRO Series Basic Users Manual
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Table of Contents
Chapter 3 – Preparing the System for Use
Site Requirements 3–2. . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 3–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Before the system arrives 3–3. . . . . . . . . . . . . . . . . . . . . . . . . .
Environmental Requirements 3–4. . . . . . . . . . . . . . . . . . . . . . .
Console Overview 3–5. . . . . . . . . . . . . . . . . . . . . . . . . . .
Console graphics 3–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Storage areas 3–7. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Peripheral/Accessory Connector Panel 3–8. . . . . . . . . . . . . .
Foot Switch (option) 3–10. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
System Positioning/Transporting 3–11. . . . . . . . . . . . .
Moving the System 3–11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Transporting the System 3–13. . . . . . . . . . . . . . . . . . . . . . . . . . .
Wheels 3–14. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Powering On the System 3–15. . . . . . . . . . . . . . . . . . . . .
Connecting and Using the System 3–15. . . . . . . . . . . . . . . . . . .
Power Up Sequence 3–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Adjusting the Display Monitor 3–18. . . . . . . . . . . . . . . .
Rotate, tilt, raise and lower the monitor 3–18. . . . . . . . . . . . . .
Brightness and Contrast 3–19. . . . . . . . . . . . . . . . . . . . . . . . . . .
Probes 3–21. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 3–21. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Connecting the Probe 3–21. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Activating the Probe 3–23. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Storing the Probe 3–23. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Deactivating the Probe 3–24. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Operator Controls 3–25. . . . . . . . . . . . . . . . . . . . . . . . . . .
Control Panel Map 3–25. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Preset Keys 3–26. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Measurement and Annotation 3–27. . . . . . . . . . . . . . . . . . . . . .
Mode, Display and Record 3–29. . . . . . . . . . . . . . . . . . . . . . . . .
Keyboard 3–31. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Special Key Function 3–32. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
2
LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
Chapter 4 – Preparing for an Exam
Beginning an Exam 4–2. . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 4–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Beginning a New Patient 4–2. . . . . . . . . . . . . . . . . . . . . . . . . . .
OB/GYN Exam Category 4–6. . . . . . . . . . . . . . . . . . . . . . . . . . .
ID/Name 4–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Chapter 5 – Modes
B–Mode 5–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 5–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Optimizing the Image 5–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
M-Mode 5–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 5–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
M-Mode Display 5–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Optimizing the Timeline 5–18. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Mixed Mode Display Formats 5–23. . . . . . . . . . . . . . . . .
Chapter 6 – Scanning/Display Functions
Zooming an Image 6–2. . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 6–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Zooming an Image 6–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Table of Contents
Freezing an Image 6–6. . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 6–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Foot Switch option 6–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Using Cine 6–7. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 6–7. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Accessing Cine 6–8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Cine Gauge 6–8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Exiting Cine 6–8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Annotating an Image 6–9. . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 6–9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Annotation Library 6–11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Adding Comments to an Image 6–12. . . . . . . . . . . . . . . . . . . . .
Special Annotation Keys 6–13. . . . . . . . . . . . . . . . . . . . . . . . . . .
Editing Annotations 6–14. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Body Patterns 6–15. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
LOGIQ200 PRO Series Basic Users Manual
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Table of Contents
Chapter 7 – General Measurements and Calculations
Introduction 7–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Overview 7–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
General Instructions 7–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Erasing Measurements 7–3. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Locating measurement controls 7–4. . . . . . . . . . . . . . . . . . . . .
Measurement Key 7–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Cursors 7–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
B-Mode Measurements 7–6. . . . . . . . . . . . . . . . . . . . . . .
Distance Measurement 7–6. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Circumference/Area (Ellipse) Measurement 7–8. . . . . . . . . .
Circumference/Area (Trace) Measurement 7–10. . . . . . . . . . .
Echo Level Measurement 7–12. . . . . . . . . . . . . . . . . . . . . . . . . .
M-Mode Measurements 7–13. . . . . . . . . . . . . . . . . . . . . . .
Overview 7–13. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Tissue depth 7–14. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Time 7–15. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Slope 7–16. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Chapter 8 – Abdomen and Small Parts
General Calculations 8–2. . . . . . . . . . . . . . . . . . . . . . . . .
Overview 8–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Measuring Volume 8–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Measuring Angle 8–8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Measuring Stenosis Area Ratio (% stenosis) 8–9. . . . . . . . . .
Echo Level Histogram 8–15. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Measuring heart rate (HR) 8–17. . . . . . . . . . . . . . . . . . . . . . . . .
Helpful hints 8–19. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
General Calculation Formulas 8–19. . . . . . . . . . . . . . . . . . . . . .
4
LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
Chapter 9 – OB/GYN
Exam Preparation 9–3. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Overview 9–3. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
OB Measurements and Formulas 9–4. . . . . . . . . . . . .
Introduction 9–4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
OB Format Selection 9–4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
OB Measurement Menus and Formulas 9–4. . . . . . . . . . . . . .
OB Summary Reports 9–17. . . . . . . . . . . . . . . . . . . . . . . .
Overview 9–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Starting an Exam 9–19. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Formulas 9–20. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Editing the OB Summary Report 9–21. . . . . . . . . . . . . . . . . . . .
Gestational Age Error Markers 9–22. . . . . . . . . . . . . . . . . . . . . .
OB Report Layout 9–23. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Measurement Averaging Page Layout 9–27. . . . . . . . . . . . . . .
OB Anatomical Survey Page Layout 9–29. . . . . . . . . . . . . . . . .
OB Trend Graph Page Layout 9–30. . . . . . . . . . . . . . . . . . . . . .
OB Trend Graph Labeling 9–31. . . . . . . . . . . . . . . . . . . . . . . . . .
Changing OB Trend Graph Selection 9–33. . . . . . . . . . . . . . . .
Input Previous Data Page Layout 9–34. . . . . . . . . . . . . . . . . . .
Table of Contents
Fetal Trend Management 9–36. . . . . . . . . . . . . . . . . . . . .
Overview 9–36. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Storing Patient Information 9–36. . . . . . . . . . . . . . . . . . . . . . . . .
Growth Trending 9–41. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Patient List Management 9–42. . . . . . . . . . . . . . . . . . . . . . . . . . .
MGOB–Multigestational 9–47. . . . . . . . . . . . . . . . . . . . . .
Overview 9–47. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Patient Entry Menu 9–47. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Distinguishing Each Fetus 9–48. . . . . . . . . . . . . . . . . . . . . . . . . .
Measurements/Calculations 9–48. . . . . . . . . . . . . . . . . . . . . . . .
Change the Number of Fetuses 9–49. . . . . . . . . . . . . . . . . . . . .
Report Page Layout 9–50. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
OB Graph 9–52. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
GYN Measurements 9–54. . . . . . . . . . . . . . . . . . . . . . . . . .
B-Mode 9–54. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
GYN Summary Report 9–60. . . . . . . . . . . . . . . . . . . . . . . .
Overview 9–60. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
GYN Report Layout 9–62. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
GYN Calculation Formulas 9–63. . . . . . . . . . . . . . . . . . . . . . . . .
Measurement Averaging Page Layout 9–64. . . . . . . . . . . . . . .
IVF Report Page Layout 9–65. . . . . . . . . . . . . . . . . . . . . . . . . . .
LOGIQ200 PRO Series Basic Users Manual
2234813–100 Rev 1
5
Table of Contents
Chapter 10 – Cardiology
Introduction 10–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Overview 10–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Cardiology Calculations Measurement Menus 10–5. . . . . . . .
General Guidelines 10–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Auto Sequence Measurement 10–6. . . . . . . . . . . . . . . . . . . . . .
BSA Calculation Methods 10–7. . . . . . . . . . . . . . . . . . . . . . . . . .
LV Analysis Measurements 10–8. . . . . . . . . . . . . . . . . . .
Cubed, Teichholz, Gibson Methods 10–8. . . . . . . . . . . . . . . . . .
Cubed Method Formulas 10–9. . . . . . . . . . . . . . . . . . . . . . . . . . .
Teichholz Method Formulas 10–10. . . . . . . . . . . . . . . . . . . . . . . .
Gibson Method Formulas 10–11. . . . . . . . . . . . . . . . . . . . . . . . . .
Bullet and Modified Simpson’s Rule Methods 10–12. . . . . . . . .
Bullet Method Formulas 10–13. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Modified Simpson’s Rule Method Formulas 10–14. . . . . . . . . . .
Single Plane Ellipsoid Methods 10–15. . . . . . . . . . . . . . . . . . . . .
Bi Plane Ellipsoid Methods 10–15. . . . . . . . . . . . . . . . . . . . . . . . .
Single Plane Ellipsoid Method Formulas 10–16. . . . . . . . . . . . .
Bi Plane Ellipsoid Method Formulas 10–17. . . . . . . . . . . . . . . . .
M–Mode Analysis Measurement 10–18. . . . . . . . . . . . . .
Overview 10–18. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
M-Mode Analysis – Left/Right Ventricle (M-LV/RV) 10–19. . . . .
M-Mode Analysis – Left/Right Ventricle (M-LV/RV) Formulas 10–20. . . . . . . . . . .
M-Mode Analysis – Mitral Valve (M-MV) 10–22. . . . . . . . . . . . . .
M-Mode Analysis – Mitral Valve (M-MV) Formulas 10–23. . . . .
M-Mode Analysis – Aortic Valve (M-AV) 10–24. . . . . . . . . . . . . .
M-Mode Analysis – Aortic Valve (M-AV) Formulas 10–25. . . . .
M-Mode Analysis – Pulmonic Valve (M-PV) 10–26. . . . . . . . . . .
M-Mode Analysis – Pulmonic Valve (M-PV) Formulas 10–27. .
M-Mode Analysis – Tricuspid Valve (M-TV) 10–28. . . . . . . . . . .
M-Mode Analysis – Tricuspid Valve (M-TV) Formulas 10–29. .
Additional Cardiology Calculations 10–30. . . . . . . . . . .
ECG Option 10–31. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Overview 10–31. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ECG Lead Placement 10–32. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ECG Default Preset 10–33. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
ECG Controls 10–33. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
6
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Chapter 11 – Urology
Urology Calculations 11–2. . . . . . . . . . . . . . . . . . . . . . . . .
Overview 1 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Urology Summary Report Page 11–2. . . . . . . . . . . . . . . . . . . . .
Using the Transaxial Probe 11–8. . . . . . . . . . . . . . . . . . .
Transaxial Probe Preparation 11–8. . . . . . . . . . . . . . . . . . . . . . .
Use of Transaxial Probe with Volume Stepper Device 11–9. .
Stepper Volume Calculation 11–13. . . . . . . . . . . . . . . . . .
Stepper Volume Formula 11–13. . . . . . . . . . . . . . . . . . . . . . . . . . .
Description 11–14. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Prerequisite 1 1–14. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Area Measurement for Each Slice (Step Increment) 11–16. . .
Chapter 12 – Recording Images
Archiving Images 12–2. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Image Memory 12–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Recall 12–4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Helpful hints 12–4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Peripheral Devices 12–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Black /White Video Page Printer Operations 12–6. . . . . . . . . .
Multi-Image Camera (MIC) (IIE Model 460) 12–8. . . . . . . . . . .
Video cassette recorder (VCR) 12–9. . . . . . . . . . . . . . . . . . . . . .
MOD Image Archive (option) 12–10. . . . . . . . . . . . . . . . . . . . . . .
Table of Contents
Chapter 13 – Customizing Your System
Introduction 13–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Overview 13–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Setup Menu Command Lines 13–3. . . . . . . . . . . . . . . . . . . . . . .
Basic Operation 13–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Menu Structure 13–8. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
General System 1 Setup (page 1 of 11) 13–8. . . . . . . . . . . . . .
General System 2 Setup (page 2 of 11) 13–12. . . . . . . . . . . . . .
Probe Parameter 1 Setup (page 3 of 11) 13–19. . . . . . . . . . . . .
Probe Parameter 2 Setup (page 4 of 11) 13–22. . . . . . . . . . . . .
Image Display & Application Setup (page 5 of 11) 13–24. . . . .
Body Pattern Setup (page 6 of 11) 13–28. . . . . . . . . . . . . . . . . . .
Comment Setup (page 7 of 11) 13–31. . . . . . . . . . . . . . . . . . . . .
Measurement Setup (page 8 of 11) 13–32. . . . . . . . . . . . . . . . . .
Patient Entry Setup (page 9 of 11) 13–45. . . . . . . . . . . . . . . . . . .
User Define Category and Key Setup (page 10 of 11) 13–47. .
User Utility (page 11 of 11) 13–48. . . . . . . . . . . . . . . . . . . . . . . . .
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7
Table of Contents
Chapter 14 – Probes and Biopsy
Probe Overview 14–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Ergonomics 14–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Applications 14–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Specifications 14–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Connecting and Disconnecting a Probe 14–7. . . . . . . . . . . . . .
Care and Maintenance 14–8. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Probe Safety 14–9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Probe handling and infection control 14–11. . . . . . . . . . . . . . . . .
Coupling gels 14–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Planned Maintenance 14–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Probe Discussion 14–18. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 14–18. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Curved Array (Convex) Probes 14–19. . . . . . . . . . . . . . . . . . . . .
Linear Array Probes 14–22. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Sector Array Probes 14–24. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Biopsy Special Concerns 14–25. . . . . . . . . . . . . . . . . . . . .
Precautions Concerning the Use of Biopsy Procedures 14–25
Guidezones 14–27. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Biopsy Procedure 14–27. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Needle Guide Type Selection 14–28. . . . . . . . . . . . . . . . . . . . . . .
Biopsy Guide Attachment 14–30. . . . . . . . . . . . . . . . . . . . . . . . . .
MTZ Probe Biopsy Guide 14–33. . . . . . . . . . . . . . . . . . . . . . . . . .
Biopsy Probes 14–36. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
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Chapter 15 – User Maintenance
System Data 15–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Specifications 15–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
LOGIQ 200 PRO Series Clinical Measurement Accuracy 15–4
LOGIQ 200 PRO Series Clinical Calculation Accuracy 15–6.
Warranties 15–7. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Scope and Duration of Warranties 15–7. . . . . . . . . . . . . . . . . . .
Warranty Exclusions 15–9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Exclusive Warranty Remedies 15–10. . . . . . . . . . . . . . . . . . . . . .
System Care and Maintenance 15–11. . . . . . . . . . . . . . . .
Overview 15–11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Inspecting the System 15–11. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Weekly Maintenance 15–12. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Planned Maintenance 15–16. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Troubleshooting 15–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 15–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Loose cables 15–17. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Display Messages 15–18. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
System Error Message Description 15–19. . . . . . . . . . . . . . . . . .
Operation Error Message Description 15–20. . . . . . . . . . . . . . . .
Operation Guide Message Description 15–21. . . . . . . . . . . . . . .
Table of Contents
Assistance 15–22. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Clinical Questions 15–22. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Service Questions 15–22. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Literature 15–22. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Accessories 15–22. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Supplies/Accessories 15–23. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
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9
Table of Contents
Chapter 16 – Acoustic Output
Bioeffects 16–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Concerns Surrounding the Use of Diagnostic Ultrasound 16–2
Operator Awareness and Actions to Minimize Bioeffect 16–5
Implementing ALARA Methods 16–8. . . . . . . . . . . . . . . . . . . . .
Training and User Assistance 16–9. . . . . . . . . . . . . . . . . . . . . . .
IEC Acoustic Output Tables 16–10. . . . . . . . . . . . . . . . . .
IEC Acoustic Output Tables 16–10. . . . . . . . . . . . . . . . . . . . . . . .
Index
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Introduction
System Overview 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . .
Attention 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Prescription Device 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
System Components 1–2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Documentation 1–3. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction 1–4. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
General Indications for Use 1–5. . . . . . . . . . . . . . . . . . . . . . . . .
Contraindications 1–5. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Who to Contact 1–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Who To Contact 1–6. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
How This Book is Organized 1–9. . . . . . . . . . . . . . . . . .
Manual Content 1–9. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Manual Format 1–11. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Introduction
Introduction
LOGIQ200 PRO Series Basic Users Manual
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1
System Overview
A
Attention
Prescription Device
System Overview
This manual contains enough information to operate the system
safely. Advanced equipment training will be provided by a
factory trained Applications Specialist for the agreed upon time
period.
Read and understand all instructions in this manual before
attempting to use the LOGIQt200 PRO Series system.
Keep this User’s Manual with the equipment at all times.
Periodically review the procedures for operation and safety
precautions.
.
System Components
For US
Only
.
Caution: United States law restricts this device to sale or use by
or on the order of a physician.
Refer to the Service Manual (2235374) for the LOGIQt200 PRO
Series sys te m c o m ponents.
2
LOGIQt200 PRO Series Basic Users Manual
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Documentation
System Overview
LOGIQt200 PRO Series Documentation consists of three
manuals:
S The Quick Start Guide (TRANSLATED) provides a
step-by-step description of the basic features and operation
of the LOGIQt200 PRO Series. It is intended to be used
in conjunction with the Basic User Manual in order to
provide the information necessary to operate the system
safely.
S The Basic User Manual (TRANSLATED) provides
information needed by the user to operate the system
safely. It describes basic functions of the system, safety
features, operating modes, basic
measurements/calculations, probes, user care and
maintenance.
S The Advanced Reference Manual (ENGLISH ONLY) is
intended for the trained, professional user. It contains all
the information found in the Quick Start Guide and Basic
User Manual, as well as information on options, advanced
customization techniques and data tables.
The LOGIQt200 PRO Series manuals are written for users
who are familiar with basic ultrasound principals and
techniques. They do not include sonography training or clinical
procedures.
LOGIQt200 PRO Series Basic Users Manual
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3
System Overview
Introduction
The LOGIQ200 PRO Series Ultrasound System is a high
performance and compact size ultrasound imaging system,
intended for general purpose applications.
The system provides image generation in B-Mode, M-Mode and
B/M-Mode with all transducer types. Digital architecture allows
maximum flexibility of all scanning modes and transducer types,
throughout the full spectrum of operating frequencies.
All transducers are precise solid state array devices, allowing
electronically controlled imaging with Convex, Micro-convex,
Sector and Linear probes. Use of solid state designs allows a
wide variety of scan parameters to be optimized including
focusing, scan control, spatial resolution, temporal resolution
and contrast resolution. The result is consistent generation of
finely detailed anatomical resolution with excellent dynamic
contrast tissue range and penetration.
The system display processor is highly versatile to produce the
optimal set of imaging parameters and display formats without
compromising important diagnostic information.
Versatile, yet easy to use, the LOGIQ200 PRO Series system
combines a wide variety of state-of-the-art operator features
without complicating operation. The operator can customize all
set-up parameters for a given mode, probe or clinical
application. Operator controls have been placed in a logical
clinical format. Two simultaneous probe connections allow
rapid switching electronically between probes without delaying
the examination.
The LOGIQ200 PRO Series System provides a total imaging
solution for today’s diverse ultrasound department needs, with
investment security through reliable upgrades, application
enhancements, and complete product support from GE.
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LOGIQ200 PRO Series Basic Users Manual
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General Indications for Use
The LOGIQt200 PRO Series diagnostic ultrasound system is
intended for use in diagnostic ultrasound imaging using B, M,
B/M combination modes in the following areas:
S Fetal
S Abdomen
S Intraoperative
S Pediatric
S Small organs including breast, neck, chest, male and
female reproductive organs, limbs, and extremities
S Adult cephalic
S Neonatal cephalic
S Adult cardiac
S Pediatric cardiac
S Trans-vaginal
S Trans-rectal
System Overview
Contraindications
S Urology
The System is NOT intended for use in the following areas:
Ophthalmic use (or any use causing the acoustic beam to pass
through the eye).
LOGIQt200 PRO Series Basic Users Manual
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5
Who to Contact
Who To Contact
Who to Contact
For additional information or assistance, please contact your
local distributor or the appropriate support resource listed
below:
USA
GE Medical Systems TEL: (1) 800–437–1171
Ultrasound Service Engineering FAX: (1) 414–647–4090
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center TEL: (1) 800–682–5327 or
(1) 414–524–5698
CANADA
GE Medical Systems TEL: (1) 800–664–0732
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center TEL: (1) 800–682–5327 or
(1) 414–524–5698
LATIN & SOUTH AMERICA
GE Medical Systems TEL: (1) 305–735–2304
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center TEL: (1) 800–682–5327 or
(1) 414–524–5255
EUROPE
GE Ultraschall TEL: 0130 81 6370 toll free
Deutschland GmbH & Co. KG TEL: (49)(0) 212.28.02.208
Beethovenstrae 239 FAX: (49)(0) 212.28.02.28
Postfach 1 1 05 60
D–42655 Solingen
ASIA
GE Medical Systems Asia TEL: (81) 426–56–0033
Asia Support Center FAX: (81) 426–56–0053
67–4 Takakura cho, Hachiouji–shi
Tokyo, 192 JAPAN
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Who To Contact (cont’d)
AUSTRIA
GE GesmbH Medical Systems Austria TEL: 0660 8651 toll free
Prinz Eugen Strasse 8/8 FAX: +43 1 505 38 74
A–1040 WIEN TLX: 136314
BELGIUM
GE Medical Systems Benelux TEL: +32 0 3 320 12 11
Gulkenrodestraat 3 FAX: +32 0 3 320 12 59
B–2160 WOMMELGEM TLX: 72722
DENMARK
GE Medical Systems Danmark TEL: +45 45 51 00 55
Skovlytoften 4 FAX: +45 42 42 59 89
DK–2840 HOL TE
FRANCE
GE Medical Systems TEL: +33 1 46 10 01 30
738 rue Yves Carmen FAX: +33 1 46 10 01 20
F–92658 BOULOGNE CEDEX
GERMANY
GE Ultraschall TEL: 0130 81 6370 toll free
Deutschland GmbH & Co. KG TEL: (49)(0) 212.28.02.208
Beethovenstrae 239 FAX: (49)(0) 212.28.02.28
Postfach 1 1 05 60
D–42655 Solingen
Who to Contact
GREECE
GE Medical Systems Hellas TEL: +30 1 93 24 582
41, Nikolaou Plastira Street FAX: +30 1 93 58 414
G–171 21 NEA SMYRNI
ITALY
GE Medical Systems Italia TEL: +39 39 20 881
Via Monte Albenza 9 FAX: +39 39 73 37 86
I–20052 MONZA TLX: 3333 28
NETHERLANDS
GE Medical Systems Nederland B.V. TEL: +31 304 7971 1
Atoomweg 512 FAX: +31 304 11702
NL–3542 AB UTRECHT
POLAND
GE Medical Systems Polska TEL: +48 2 625 59 62
Krzywickiego 34 FAX: +48 2 615 59 66
P–02–078 WARSZAWA
LOGIQ200 PRO Series Basic Users Manual
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7
Who to Contact
Who to Contact (cont’d)
PORTUGAL
GE Medical Systems Portuguesa S.A. TEL: +351 2 2007696/97
Rua Sa da Bandeira, 585 FAX: +351 2 2084494
Apartado 4094 TLX: 22804
P–4002 PORTO CODEX
RUSSIA
GE VNIIEM TEL: +7 095 956 7037
Mantulinskaya UI. 5A FAX: +7 502 220 32 59
123100 MOSCOW TLX: 613020
SPAIN
GE Medical Systems España TEL: +34 1 676 4012
Hierro 1 Arturo Gimeno +34 1 676 4047
Poligono Industrial I FAX: +34 1 675 3364
E–28850 TORREJON DE ARDOZ TLX: 22384 A/B GEMDE
SWEDEN
GE Medical Systems TEL: +46 87 50 57 00
PO–BOX 1243 FAX: +46 87 51 30 90
S–16428 KIST A TLX: 12228
SWITZERLAND
GE Medical Systems (Schweiz) AG TEL: +41 41 425577
Sternmattweg 1 FAX: +41 41 421859
CH–6010 KRIENS
GEMED SU
CGRSWES
Manufacturer
TURKEY
GE Medical Systems Turkiye A.S. TEL: +90 212 75 5552
Mevluk Pehliran Sodak FAX: +90 212 211 2571
Yilmaz Han, No 24 Kat 1
Gayretteppe
IST ANBUL
UNITED KINGDOM
IGE Medical Systems TEL: +44 753 874000
Coolidge House FAX: +44 753 696067
352 Buckingham Avenue
SLOUGH
Berkshire SL1 4ER
SAMSUNG GE MEDICAL SYSTEMS
65–1, Sangdaewon–Dong, Chungwon–Ku, TEL: (82) 342–740–6114
Sungnam–Si,Kyunggi–Do FAX: (82) 342–746–9634
KOREA
8
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Manual Content
How This Book Is Organized
How This Book is Organized
The LOGIQt200 PRO Series User Manual is organized to
provide the information needed to start scanning right away.
Detailed information is also provided for more time-intensive
studies.
S Getting started. These sections give an overview of the
system to help the operator start scanning as soon as
possible.
S
Introduction.
contraindications for use, who to contact and how this
documentation is organized.
S
Safety
operation of the LOGIQt200 PRO Series system.
Information concerning indications/
. Important information concerning the safe
S
Preparing the System for Use.
system for use and a map of the control layout.
S
Preparing for an Exam.
information, select an exam category.
S Image optimization. These sections detail how to improve
image, trace, or spectral information.
S
Modes
. How to adjust and optimize B-Mode and
M-Mode imaging.
S
Scanning and Display Functions.
concerning Zoom, Freeze, Cine and Annotation
functions.
How to enter patient
How to prepare the
Information
LOGIQt200 PRO Series Basic Users Manual
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9
How This Book Is Organized
Manual Content (cont’d)
S Measurements and Reports. Shows how to do general
and exam category specific measurements and
calculations.
S
General Measurements and Calculations
on basic measurements for each mode.
S
Exam Categories.
S Recording Images. Explains the use of image archive and
peripheral options.
S Customizing your system. Shows how to customize the
system for your particular institution, clinic, or exam type.
S Probes and Biopsy. Provides intended uses,
specifications, care and maintenance, and biopsy capability
instructions for each probe.
S
Abdomen and Small Parts.
S
OB/GYN
S
Cardiology.
S
Urology.
.
. Emphasis
S User Maintenance. Provides information concerning
system specifications, warranties, error messages, user
diagnostics, bioeffects, quality assurance, system care and
assistance.
S Data Tables. Provides necessary data for reference.
S
Acoustic Output.
10
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