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GE LOGIQ e user guide

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1. i 2 Certifications i 3 Original Documentation i 3 Country Specific Approval i 4 Table of Contents Chapter 1 Getting Started Console Overview Application Specific Systems 1 2 Indications for Use 1 3 Contraindication 1 3 Prescription Device 1 3 Important Notices 1 4 Console graphics 1 6 Moving the System Before moving the system 1 17 When moving the system 1 17 System Start Up Power On AEE eee 1 18 Power Off 1 19 Probes Connecting the Probe 1 20 Cable Handling 4 22 Disconnecting the Probe 4 22 Applications 1 23 Features 1 24 Beginning an Exam Scanning a New Patient 1 25 Patient Screen 1 27 Chapter 2
2. 3 20 Connectivity Functions 3 21 Electronic Documentation Accessing Documentation Via a PC 3 22 Using Online Help Via F1 3 23 Contact Information Contacting GE Healthcare Ultrasound 3 24 Manufacturer 3 28 Factory Sites 3 28 System Care and Maintenance Inspecting the System 3 29 Weekly Maintenance 3 30 Other Maintenance 3 33 Supplies Accessories 3 33 Chapter 4 Safety Safety Precautions Precaution Levels 4 2 Hazard Symbols 4 3 Patient Safety 4 5 Equipment and Personnel Safety 4 8 Device Labels 4 14 EMC Electromagnetic Compatibility 4 19 Patient Environmental Devices 4 28 Acoustic Output lt s949es62 seosececeee sees asses 4 30 Warning Label Locations 4 33 Chapter 5 Emergency Department ED Beginning an Exam Introdu
3. 7 5 M Mode 7 7 Color Flow CF Mode 7 8 Power Doppler Imaging PDI Mode 7 9 Pulsed Wave PW Doppler Mode 7 10 Measurement Introduction 7 11 List of General Measurements 7 11 General Instructions 7 12 Comment General Instructions 7 13 Using CINE Introduction 7 15 Activate CINE 7 15 CINE mode monitor display 7 16 Index LOGIQ e User Guide i 7 Direction 5314626 100 Rev 3 LOGIQ e User Guide Direction 5314626 100 Rev 3 Chapter 1 Getting Started Console Overview Moving the System System Start up Probes and Beginning an Exam LOGIQ e User Guide 1 1 Direction 5314626 100 Rev 3 Getting Started Console Overview Application Specific Systems For information on using the LOGIQ e system optimized for Emergency Department use refer to Chapter 5 For information on using the LOGIQ e system optimized for Nerve Block Guidance refer to Chapter 6 1 2 LOGIQ e User Guide Direction 5314626 100 Rev 3 Indications for Use Console Overview The LOGIQ e is intended for u
4. Dynamic Range Compression No Dynamic Range controls how echo intensities are converted to shades of gray thereby increasing the adjustable range of contrast The Dynamic Range control name changes to Compression on frozen images Line Density Yes Optimizes B Mode frame rate or spatial resolution for the best possible image Map No The system supplies B M and Doppler Mode system maps Frame Average No Temporal filter that averages frames together thereby using more pixels to make up one image This has the effect of presenting a smoother softer image Colorize No Colorize is the colorization of a conventional B Mode image or Doppler Spectrum to enhance the user s ability to discern B M and Doppler Mode intensity valuations Colorize is NOT a Doppler Mode Colorizes the gray scale image to enhance the eye s discrimination capability Spectrum Colorize colorizes the spectrum as a function of power using the inverse of the Colorize map for the signal intensity in each Doppler line Colorize enhances the visibility of the spectrum s characteristics and enhances your ability to identify spectral broadening and the edge contours of the spectrum used to define the peak frequency velocity LOGIQ e User Guide Direction 5314626 100 Rev 3 2 3 Performing an Exam Table 2 1 B Mode Controls Continued Possible Control
5. Mode Frequency Angle Correct 3 Baseline i PRE 6 Book Figure 6 9 Doppler Mode Display LOGIQ e User Guide 6 11 Direction 5314626 100 Rev 3 Nerve Block PW Doppler Mode Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimization See Chapter 2 for more details on these controls Baseline IRI 5 Invert PW Mode Sweep Speed Dynamic Range 48 dB Display Format Vert1 2B Full Timeline Off Trace Method Off nsitivity 10 ce Direction Both Duplex Off Time Resolution 3 Colorize Gray Map Power Output 100 4 Auto Calcs Off Spectral Avg Med Cycles to Average 1 Figure 6 10 6 12 PW Doppler Mode Top Sub Menu LOGIQ e User Guide Direction 5314626 100 Rev 3 Chapter 7 Using Touch Screen Describes the use of the Touch Screen with the LOGIQ e system LOGIQ e User Guide 7 1 Direction 5314626 100 Rev 3 Using Touch Screen Introduction 7 2 NOTE NOTE NOTE NOTE Beginning an Exam Activate Deactivate Touch Screen mode by pressing F12 All the function keys except F12 Cursor Set B Pause Power Key and keyboard of LOGIQ e will be disabled if Touch Screen mode is activated Pressing the Power key automatically deactivates the Touch Screen Mode Always use fingers or gloved fingers to operate on the Touch Screen improper use may cause damage to the monitor It is recommended to close the LOGIQ e LCD after activa
6. If you press Mode Measure while frozen B and CF Doppler M Once Distance Velocity Tissue Depth Twice Time interval Three Times Time and velocity LOGIQ e User Guide Direction 5314626 100 Rev 3 General Instructions The general steps for perform a measurement is as follows 1 2 3 Select the Measure Touch Screen key Click to place the first caliper Click to place the second caliper The result displays in the Results Window A GE Healthcare MI0 5 Tis0 5 i12L RS 08 04 08 10 11 27 PM wales t Carotid E mam Gain 42 a e se Patient x E a Frea 10 0 MHz Zz 7 Preset Aoc Comment A v Depth 3 0 cm M End Exam 4 Focus Position A B Pause Y7 M ee L 1 38 cm 4 L 1 39 cm L 1 28 cm 9 Clear All Power Output 100 Mode gt Measure mode Cursor Select Figure 7 13 Measurement example Clear Cursor Select Figure 7 14 Measurement screen Top Menu See Chapter 7 for more details of the Top Menu LOGIQ e User Guide Direction 5314626 100 Rev 3 General Instructions Comments Neo Abd Menu Aorta Liver CBD IVC Bladder Duodenum Pylorus Bowel Pancreas Gallblad Spleen Caudate Adrenal Stomach Fluid Appendix Left Trans Clicking Comment initiates the comment mode Select the comment in the list place it by clicking the target position on the Touch Screen Click More to select
7. When closing the LCD cover use caution to avoid injuring hands or fingers as there is a closing mechanism which allows the LCD cover to automatically close Bottom Os Do not connect the DVD RW to the system while scanning The DVD RW can be used when connecting to the Docking Cart DVD RW ME20 GOST symbol Russia Regulatory Country Clearance Bottom LAMP CONTAINS MERCURY DISPOSE ACCORDING TO STATE LOCAL LAW This product consists of devices that may contain mercury which must be recycled or disposed of in accordance with local state or country laws Within this system the backlight lamps in the monitor display contain mercury Bottom LOGIQ e User Guide Direction 5314626 100 Rev 3 4 17 Safety Label Icon Description continued Classifications Type of protection against electric shock e Class Equipment e LOGIQ e Console with AC Adapter 1 e Docking Cart Console Degree of protection against electric shock e Type BF Applied part 2 for Probes marked with BF symbol Type CF Applied part 3 for ECG marked with CF symbol Continuous Operation System is Ordinary Equipment IPX0 Footswitch is IPX8 FSU 1000 MKF 2 MED GP26 1 Class Equipment EQUIPMENT in which protection against electric shock does not rely on BASIC INSULATION only but includes a protective earth ground This additional safety precaution prevents exposed metal parts from b
8. B Mode Controls Continued Control Possible Bioeffect Description Benefit CrossxBeam Yes CrossXBeam is the process of combining three or more frames from different steering angles into a single frame The combined single image has the benefits of reduced speckle noise reduced clutter and continuity of specular reflectors Therefore this technique can improve contrast resolution with increased conspicuity of low contrast lesions better detection of calcifications biopsy needle visualization and cystic boundary definition TGC No TGC amplifies returning signals to correct for the attenuation caused by tissues at increasing depths TGC slide pots are spaced proportionately to the depth The area each pot amplifies varies as well A TGC curve may appear on the display if preset matching the controls that you have set except during zoom You can choose to deactivate the TGC curve on the image Scan Area Yes You can widen or narrow the size of the sector angle to maximize the image s region of interest ROI Tilt Yes You can steer the sector angle to get more information without moving the probe while in B Mode M Mode Doppler Mode and Color Flow Mode Tilt is not available on Linear probes Angle Steer Yes You can steer the PW Doppler or Color Flow sector angle to get more information without moving the probe Reverse No Flips the image 180 degrees left right
9. Safety Precautions Related Hazards continued e Electrical a Hazard CAUTION Smoke amp k Fire Hazard Biological AD Hazard LOGIQ e User Guide To avoid injury Do not remove protective covers No user serviceable parts are inside Refer servicing to qualified service personnel To assure adequate grounding connect the attachment plug to a reliable hospital grade grounding outlet having equalization conductor v Never use any adaptor or converter of a three prong to two prong type to connect with a mains power plug The protective earth connection will loosen Do not place liquids on or above the console Spilled liquid may contact live parts and increase the risk of shock Do not use this equipment if a safety problem is known to exist Have the unit repaired and performance verified by qualified service personnel before returning to use The system must be supplied from an adequately rated electrical circuit The capacity of the supply circuit must be as specified For patient and personnel safety be aware of biological hazards while performing invasive procedures To avoid the risk of disease transmission Use protective barriers gloves and probe sheaths whenever possible Follow sterile procedures when appropriate Thoroughly clean probes and reusable accessories after each patient examination and disinfect or sterilize as needed Refer to Probes and Biopsy for probe use and care instructi
10. Direction 5314626 100 Rev 3 Safety EMC Performance continued 4 20 CAUTION Proper installation following the service manual is required in order to achieve the full EMC performance of the product The product must be installed as stipulated in 4 2 Notice upon Installation of Product In case of issues related to EMC please call your service personnel 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 Do not use devices which intentionally transmit RF signals cellular phones transceivers or radio controlled products other than those supplied by GE wireless microphone broadband over power lines for example unless intended for use with this system in the vicinity of this equipment as it may cause performance outside the published specifications Keep power to these devices turned off when near this equipment 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 regulation LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions EMC Performance continued Portable and mobile radio communications equipment e g two way radio cellular cordless telephones
11. F End Exam Dd Focus Position R B Pause V7 T Clear All Power Output 100 lt 4 gt Mode gt CF mode a Scan Area Figure 7 7 Color Flow Mode Display CF Mode Top Menu The following Top Menu controls are available for functionality adjustment and image optimization See Chapter 5 for more details on these controls Scan Area Steer Invert Move ROI Auto Figure 7 8 CF Mode Top Menu 7 8 LOGIQ e User Guide Direction 5314626 100 Rev 3 Power Doppler Imaging PDI Mode Intended Uses Power Doppler Imaging PDI is a color flow mapping technique used to map the strength of the Doppler signal coming from the flow rather than the frequency shift of the signal Using this technique the ultrasound system plots color flow based on the number of reflectors that are moving regardless of their velocity PDI does not map velocity therefore it is not subject to aliasing GE Healthcare MI 1 1 Tis0 6 8L RS 3 Jogi08 08 11 35 22 PM ADM 090808 113053 PM 1 Carotid GE m 5 Gain 8 4 Patient a 7 Yv f7 Preset Freq 4 4 MHz Abc Comment v F7 Measure Depth 4 0 cm a End Exam Vv Focus Position if B Pause T Clear All Power Output 100 lt gt Mode gt PDI mode a Scan Area Move ROI Figure 7 9 Power Doppler Imaging Display PDI Top Menu The following Top Menu controls are available for functionality adjustment and image optimization See Chapter 5 for more
12. Mechanical Index MI and a relative Acoustic Output AO value Although not part of the NEMA AIUM standard the AO value informs the user of where the system is operating within the range of available output The Tl and MI are displayed at all times The TI display starts at a value of 0 0 and increments in steps of 0 1 The MI display values between 0 and 0 4 increment in steps of 0 01 and for values greater than 0 4 increments in steps of 0 1 Depending on the examination and type of tissue involved the TI parameter will be one of three types e Soft Tissue Thermal Index TIS Used when imaging soft tissue only it provides an estimate of potential temperature increase in soft tissue e Bone Thermal Index TIB Used when bone is near the focus of the image as in the third trimester OB examination it provides an estimate of potential temperature increase in the bone or adjacent soft tissue e Cranial Bone Thermal Index TIC Used when bone is near the skin surface as in transcranial examination it provides an estimate of potential temperature increase in the bone or adjacent soft tissue LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions Acoustic Output Display Specifications continued Mechanical Index Changing the Thermal Index Type MI recognizes the importance of non thermal processes cavitation in particular and the Index is an attempt to indicate the probability that they might occur wit
13. NOTE You must apply the changes on each setup page before moving to the next page 1 In Utility gt System gt General set the Language as desired Save this setting 2 Press Regional Options select the Language tab press Details under Installed Services press Add to set the Keyboard layout IME to United States International press OK set the Default input language to English United States United States International press Apply Press OK eyboard LOGIQ e User Guide 3 11 Direction 5314626 100 Rev 3 After the Exam is Over Keyboard Setup for non Russian Greek Chinese Japanese Languages continued 3 12 3 Select the Advanced tab then select the language in the Language for non Unicode programs pull down menu Press Apply Answer Yes to use files already loaded on the hard disk then answer No to not reboot the system yet press OK Press Save and Exit the Utility screen E 10000 MAC Roman 10001 MAC Japanese Z 10002 MAC Traditional Chinese Big5 10003 MAC Korean 10004 MAC Arabic 10005 MAC Hebrew Figure 3 3 Set Language Reboot the system When your system restarts the system appears in the selected language To type foreign characters press Ctrl Shift to change the keyboard to the international keyboard LOGIQ e User Guide Direction 5314626 100 Rev 3 System Presets Keyboard Setup Procedure for Russian Greek Chinese Japanese 1 In Utility gt Syste
14. e Age automatically calculated when birthdate is input e Sex 7 Category Selection Select from 8 exam application categories Abdomen Obstetrics Gynecology Cardiology Vascular Urology Small Parts or Pediatrics When a category is selected the measurement and category presets are displayed 8 Exam Information Shows the Current Active Exam information Information pertinent to the selected exam category appears in the window All possible information needs to be entered e Images Displays the selected exam s images e Clear Clears existing data e Past Exam only for OB Input past exam data register the patient before using 1 29 Direction 5314626 100 Rev 3 Getting Started Patient Screen continued 9 Patient View Lists the patients in the database NOTE NOTE NOTE Search key select search item from Patient ID Last Name First Name Birthdate Sex Exam Date Exam Today Accesstion Number Exam Description Exam Date Before Exam Date Between Exam Date After If Exam Date Between is selected the Input Dialog displays and you can select the date from the displayed calendar String enter appropriate information In the Search String the From and To dates are separated by a dash if Exam Date Between is used for the Search key Clear Clears the entered string Show All Displays all patients in the database Show XX XX Displays the searched
15. 60878 02 06 ECG Module Consult accompanying documents is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided on the label Various Do not push the system Rear of Docking Cart lsolation Cart This symbol indicates that waste electrical and electronic equipment must not be disposed of 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 Bottom LOGIQ e User Guide Direction 5314626 100 Rev 3 4 15 Safety Table 4 2 Label Icons Continued Label Icon Purpose Meaning Location Pb Cd Hg The separate collection symbol is affixed to a battery or its packaging to advise you that the battery must be recycled or disposed of in accordance with local or country laws The letters below the separate collection symbol indicate whether certain elements Pb Lead Cd Cadmium Hg Mercury are contained in the battery To minimize potential effects on the environment and human health it is important that all marked batteries that you remove from the product are properly recycled or disposed For information on how the battery may be safely removed from the device please consult the service manual or equipment instructions Information on the potential effects on
16. Direction 5314626 100 Rev 3 Chapter 5 Emergency Department ED Describes the LOGIQ e system for use in the Emergency Department LOGIQ e User Guide 5 1 Direction 5314626 100 Rev 3 Emergency Department ED Beginning an Exam Introduction You optimize the image on the LOGIQ e Emergency Department system by adjusting the Depth with Auto Focus Zone and Frequency control Further optimization should not be required though manual adjustment is allowed ED appears on the lower right and corner of the display screen 5 2 LOGIQ e User Guide Direction 5314626 100 Rev 3 Beginning an Exam Starting a New Patient Press Patient Figure 5 1 ED Patient Screen Refer to Beginning an Exam in Chapter 2 LOGIQ e User Guide 5 3 Direction 5314626 100 Rev 3 B Mode Intended Uses B Mode is intended to provide two dimensional images and measurement capabilities concerning the anatomical structure of soft tissue GE Healthcare MI 0 30 Tis0 2 4C RS 09 28 07 9 58 50 AM 1 1 Abd B Frq 4 0 MHz Gn 64 EA 1 1 Map C 0 0 D 16 0 cm DR 72 FR 31 Hz AO 100 XBeam On 232 232 22 4 22 4 s _ Abdomen Rt Lt Z Aorta X Gallbladder Worksheet Figure 5 2 B Mode Display 5 4 LOGIQ e User Guide Direction 5314626 100 Rev 3 Optimizing the Image B Mode Top Sub Menu Adjust the image by using the Depth control If additional functionality is needed the following Top Sub Menu controls are
17. Direction 5314626 100 Rev 3 Performing an Exam Body Patterns 2 10 To activate body patterns press the Body Mark control Select the desired body pattern with the Top Sub Menu controls The selected body pattern is displayed on the monitor Press the Move Pattern control on the Top Sub Menu to reposition the body pattern with the Trackball and Set controls A probe mark is associated with the body patterns and illustrates the probe position on the body pattern This marker can be placed with the Trackball and rotated with the Rotate Pattern control The probe mark type is selectable by rotating the Probe Type control on the Top Sub Menu There are different choices available with one being a blank selection To select the active side in dual B Mode use the Active Side rotary control at the bottom of the Top Sub Menu Press Clear to erase the body pattern The pattern is erased and the system exits the body pattern mode LOGIQ e User Guide Direction 5314626 100 Rev 3 Optimizing the Image Annotating an Image LOGIQ e User Guide Pressing the Comment key or any keys on the alphanumeric keyboard initiates the comment mode This assigns the trackball function to controlling the cursor and displays the comment library on the Top Sub Menu menu In comment mode text can be added by using the comment library or by typing from the alphanumeric keyboard After activating the comment mode a vertical bar type cursor ap
18. Double click on the gedocumentation html document 4 Select the item you want to view click on the blue underlined link in the File Name column To close the window click on the X in the upper right hand corner of the browser window NOTE If your PC does not have Adobe Reader a free download is available on the Adobe website at http www adobe com 3 22 LOGIQ e User Guide Direction 5314626 100 Rev 3 Electronic Documentation Using Online Help Via F1 Online Help is available via the F1 key After pressing F1 Help appears The Help screen is divided into three sections navigational tools on the top left portion of the screen Hide Back Forward help book navigational tools on the left portion of the screen Contents Index Search Favorites and the content portion on the right side of the screen where help topics are displayed NOTE If the cursor is lost while using Online Help press Alt F4 to exit or press F1 to activate the cursor Direction 5173182 300 Direction 5315496 300 Rev 2 CE one LOGIQ e Online Help Figure 3 8 Opening Help Screen Exiting Online Help To exit Online Help press the X in the upper right hand corner of the Online Help window LOGIQ e User Guide 3 23 Direction 5314626 100 Rev 3 After the Exam is Over Contact Information Contacting GE Healthcare Ultrasound INTERNET USA Clinical Questions Service Questions Accessor
19. Exclude Value To type a comment on a worksheet 1 Select Comments The Comments window opens 2 Type comments about the exam 3 To close the Comments window select Comments Some fields on the worksheet are view only and others you can change or select To easily see which fields you can change or select move the Trackball As the cursor moves over a field that you can change or select the field is highlighted LOGIQ e User Guide Direction 5314626 100 Rev 3 Chapter 3 After the Exam is Over Probe Overview System Presets DataBackup Configuring Connectivity Electronic Documentation and System Care and Maintenance LOGIQ e User Guide 3 1 Direction 5314626 100 Rev 3 After the Exam is Over Probe Overview Probe handling and infection control 3 2 CAUTION CAUTION This information is intended to increase user awareness of the risks of disease transmission associated with using this equipment and provide guidance in making decisions directly affecting the safety of the patient as well as the equipment user Diagnostic ultrasound systems utilize ultrasound energy that must be coupled to the patient by direct physical contact Depending on the type of examination this contact occurs with a variety of tissues ranging from intact skin in a routine exam to recirculating blood in a surgical procedure The level of risk of infection varies greatly with the type of contact One of the most effective ways to preve
20. Manufactured for GE Medical Systems China Co Ltd No 19 Changjiang Road Wuxi Jiangsu China 214028 AC Adapter for LOGIQ e LOGIQi LOGIQ Book GX Vivid e series LOGIQ e LOGH i LOGIQ Book GX Vivid e KAZNE S Model TWADP100 koutth A 100 240 S06GOHz 130VA Output 20V 725A Nodoad power oonsuroton PRIIP lt 20 7 Sw Average active oficercy FQ RR 3 Figure 4 12 AC Adapter Label LOGIQ e User Guide 4 39 Direction 5314626 100 Rev 3 Safety Warning Label Locations continued Manufactured for GE Medkal Systems China Co Ltd aiit No 19 Changilang Road Systems China Co Lid Wuxi National Hi Tech Development Zone Jlangsu P R China 214028 Rechargeable Smart Battery Pack WJ 4 tit X Model S S TWBP42 5 LHon 14 8V 5200mAh 77Wh LHon 14 8V 5200mAh 77Wh For LOGIQ e LOGIQILVIM e serdes use For LOGIQ e LOGIQ I Vivi e serles use ol TRE LOGIQ LOGIO LVA o KIH XA nly MH LOGIQ e LOGIQ LVMd e KAIA ZA O OT Made h China ell HRM Ril HRA Figure 4 13 Battery Label 1 Do not put the battery in fire 2 Do not disassemble or mistreat the battery CAUTION Do not disassemble or mistreat the battery Do not put the battery in fire Replace the battery with the same battery type only Failure to follow these instructions many present risk of explosion fire or high temperature See the battery user manual for additional safety instructions 4 40 LOGIQ e User Guide
21. Performing an Exam Optimizing the Image B Mode Controls 2 2 M Mode Controls 2 4 Color Flow Mode Controls 2 5 Doppler Mode Controls 2 7 Other Controls 2 9 Measurement and Analysis B Mode Measurements 2 12 Doppler Mode Measurements 2 18 M Mode Measurements 2 22 LOGIQ e User Guide i 5 Direction 5314626 100 Rev 3 Viewing and Editing Worksheets 2 24 Chapter 3 After the Exam is Over Probe Overview Probe handling and infection control 3 2 Endocavitary Probe Handling Precautions 3 3 Probe Cleaning Process 3 4 Coupling gels rrr crc rrr rrr rrr cere 3 10 System Presets Foreign Language Keyboard Setup 3 11 Backup and Restore Backup and restore strategy patient data 3 16 Restore procedure patient data 3 17 Backup procedure user defined configurations 3 18 Restore procedure user defined configurations 3 19 Configuring Connectivity Overview
22. accommodate higher velocity blood flow Minimizes aliasing by displaying a greater range of forward flow with respect to reverse flow or vice versa Baseline adjusts the alias point The default baseline is at the midpoint of the color display and at the midpoint of the color bar reference display Angle Steer Yes You can slant the ROI of the Color Flow linear image left or right to get more information without moving the probe The Angle Steer function only applies to linear probes Color Flow Line Yes Optimizes the Color Flow frame rate or spatial resolution for the best Density possible color image Map No Allows you to select a specific color map After you have made your selection the color bar displays the resultant map Threshold No Threshold assigns the gray scale level at which color information stops Frame Average No Averages color frames Transparency Map No Brings out the tissue behind the color map Spatial Filter No Smooths out the color makes it look less pixely LOGIQ e User Guide Direction 5314626 100 Rev 3 2 5 Performing an Exam Table 2 3 Color Flow Mode Controls Continued Possible Control Bioeffect Description Benefit Packet Size Yes Controls the number of samples gathered for a single color flow vector Power Doppler No Power Doppler Imaging PDI is a color flow mapping technique Imaging PDI used to map the strength of the Doppler signal coming from the tissue rathe
23. 2 20m A a CE EOIN STSTENS OPMCE L19 B NO WO OUNGAN ROAD DUCI RATIONAL HI TCOH CCVELOPRENT TOE JANGU LR CENA 214008 AMQNACAR Om ARAR PRUBGAROREARAAA SARE RAR Mm 2100 OS GB ENE CART OLE COOKING CART Cry foe use sius LOGIO eI a sertes RAFLI ail BARAA DPU RA IIG 5060 OOA ORNOS D II SOSO OA 2 TO GA Figure 4 6 Docking Cart Rating Plate 4 34 LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions Warning Label Locations continued Figure 4 7 Table 4 7 t GE MEDICAL SYSTEMS CHINA CO LTD NO 19 CHANGJIANG ROAD WUXI NATIONAL HI TECH DEV ZONE JIANGSU P R CHINA 214028 oAA Zs United States law restricts this device to sale or use by or on the order of a physician C 0197 x CISPR 11 EN 55011 CLASS A GROUP 1 CLASSE A GROUPE 1 2a Go DESC LOGIQ e INPUT 20V 5A For use with adapter mode TWADP100 MEZO MADE IN CHINA This machine should be used In compliance with law Some Jurisdictions restrict certaln uses such as gender determination SAAS ARR ESIN A SIAN SUG SAG NS ELEDE CEET EEEE Ep Sc AAU ANIERARE KEMRNARRERARMELENETE LOGIQ e R5 2 x TUV and Identification Rating Plate Label Location Rating Plate Explanations Date of manufacture The date could be a year year and month or year month and day as appropriate See ISO 8601 for date formats ENES Catalog or model number Ser
24. Bioeffect Description Benefit Edge Enhance No Edge Enhance brings out subtle tissue differences and boundaries by enhancing the gray scale differences corresponding to the edges of structures Adjustments to M Mode s edge enhancement affects the M Mode only Rotation No Flips the image 180 degrees up down CAUTION When reading an rotated image be careful to observe the probe orientation to avoid possible confusion over scan direction or left right image reversal Virtual Convex Yes On Linear probes Virtual Convex provides a larger field of view in the far field SRI HD No SRI HD Speckle Reduction Imaging High Definition is an adaptive algorithm to reduce the unwanted effects of speckle in the ultrasound image B Softener No Affects the amount of lateral smoothing It s similar to dynamic range by softening the appearance edges of the image Virtual Apex Yes On sector probes Virtual Apex provides a larger field of view in the far field Range Focus Yes Improves the near mid field image quality borders interfaces increases contrast and detail resolution across the image and allows for less filling in the vessels CenterLine No The centerline of the image for 12L RS only B Steer Yes Slants the B Mode or Color Flow linear image left right to get more information without moving the probe The anglesteer function only applies to linear probes Rejection No Selects a level below which echoes will not be amplified an echo must have
25. Direction 5314626 100 Rev 3 Safety Precautions Peripheral Update for EC countries continued Peripheral used in The LOGIQ e has also been verified for compatibility and the non patient compliance for connection to a local area network LAN via a environment wireless LAN provided the LAN components are IEC EN 60950 compliant The LOGIQ e has also been verified for compatibility and compliance for connection to a DVD RW via the system USB port provided the DVD RW is IEC EN 60950 compliant General precautions for installing an alternate off board remote device or a network would include 1 The added device s must have appropriate safety standard conformance and CE Marking 2 The added device s must be used for their intended purpose having a compatible interface LOGIQ e User Guide 4 25 Direction 5314626 100 Rev 3 Safety Declaration of Emissions This system is suitable for use in the following environment The user must assure that it is used only in the electromagnetic environment as specified Table 4 5 Declaration of Emissions Guidance and manufacturer s declaration electromagnetic emissions The system is intended for use in the electrmagnetic environment specified below The user of the system should assure that it is used in such an environment Emission Type Compliance Electromagnetic Environment RF Emissions Group 1 This system uses RF energy only for its in
26. FAX 86 510 85226688 GE Medical Systems Ultrasound amp Primary Care Diagnostics LLC Also DBA GE Healthcare 9900 Innovation Drive Wauwatosa WI 53226 U S A LOGIQ e User Guide Direction 5314626 100 Rev 3 System Care and Maintenance system Care and Maintenance Inspecting the System Examine the following on a monthly basis e Connectors on cables for any mechanical defects e Entire length of electrical and power cables for cuts or abrasions e Equipment for loose or missing hardware e Control panel and keyboard for defects e Casters for proper locking operation CAUTION To avoid electrical shock hazard do not remove panels or covers from console This servicing must be performed by qualified service personnel Failure to do so could cause serious injury Biological If any defects are observed or malfunctions occur do not Hazard operate the equipment but inform a qualified service person Contact a Service Representative for information iS LOGIQ e User Guide 3 29 Direction 5314626 100 Rev 3 After the Exam is Over Weekly Maintenance System Cabinet NOTE LCD Monitor 3 30 NOTE Failure to perform required maintenance may result in unnecessary service calls Prior to cleaning any part of the system 1 Turn off the system power If possible disconnect the power cord See Power Off on page 1 19 for more information To clean the system cabinet 1 Moisten a soft non abrasive
27. Start Menu Icon Battery Icon Card Icon Trackball Functionality Status Scroll M amp A Measurement and Analysis Position Size Scan Area Width and Tilt 1 15 Getting Started Brightness NOTE NOTE Adjusting the LCD monitor s brightness is one of the most important factors for proper image quality The proper setup displays a complete gray scale The lowest level of black should just disappear into the background and the highest white should be bright but not saturated To adjust the brightness volume 1 On the alphanumeric keyboard e adjust brightness with the Ctrl Up Down keys adjust volume with the Ctrl Left Right keys Figure 1 9 Brightness and Volume 1 Brightness 2 Volume After readjusting the LCD monitor s Brightness readjust all preset and peripheral settings The brightness of the LCD monitor should be set first as it affects the Gain and Dynamic Range settings of your image Once set this should not be changed unless the brightness of your scanning environment changes LOGIQ e User Guide Direction 5314626 100 Rev 3 Moving the System Moving the System Before moving the system 1 Shut down the system See Power Off on page 1 19 for more information Unplug the power cord if the system is plugged in Disconnect all cables from off board peripheral devices external printer etc from the console To prevent damage to the Power Cord DO NOT pull exces
28. The average value over a number of cycles from 1 5 Trace Direction No Specifies trace direction LOGIQ e User Guide Direction 5314626 100 Rev 3 2 7 Performing an Exam Table 2 4 Doppler Mode Controls Continued Possible Control Bioeffect Description Benefit Full Timeline No Expands display to full timeline display Display Format No Changes the horizontal vertical layout between B Mode and M Mode or timeline only Duplex Triplex No Duplex allows two modes to be active at the same time B PW or B CW or B CF Triplex allows three modes to be active at the same time C PW CF or B CW CF When Duplex Triplex is OFF either the image or timeline is active B Pause then switches the activce side between image and the timeline With Duplex Triplex active M D Cursor functions the same as the Duplex Triplex control by cycling Duplex Triplex on off B Pause pauses the image while keeping the CW PW timeline active Time Resolution No Adjusts image appearance so that if you select a lower setting the image appears smoother if you select a higher setting the image appears sharper Spectral Average No Averages the spectrum in a vertical direction and timeline direction Modify Auto Calcs No Activates the menu to select which calculations are automatically calculated Auto Calcs No Activates the calculation automatically which you select in the Modify Auto Calculation when the sys
29. You optimize the image on the LOGIQ e Nerve Block system adjust the image by adjusting the Depth with Auto Focus Zone and Frequency control Further optimization should not be required though manual adjustment is allowed NERVE appears on the lower right and corner of the display screen LOGIQ e User Guide Direction 5314626 100 Rev 3 Beginning an Exam Starting a New Patient Press Patient Figure 6 1 Nerve Block Patient Screen Refer to Beginning an Exam in Chapter 2 LOGIQ e User Guide 6 3 Direction 5314626 100 Rev 3 Nerve Block Selecting an Application Preset and a Probe 1 i 12L RS Application NERVE Presets Superficial Figure 6 2 Nerve Application Preset 6 4 LOGIQ e User Guide Direction 5314626 100 Rev 3 B Mode Intended Uses 9 GE Healthcare 04 26 10 7 57 04 AM ADM Z Stenosis X Volume C Angle AB Ratio Generic Worksheet Figure 6 3 B Mode Display LOGIQ e User Guide Direction 5314626 100 Rev 3 MI0 6 Tis0 3 E8C RS Superficial XBea m Off 6 5 Nerve Block B Mode Top Sub Menu Adjust the image by using the Depth control If additional functionality is needed the following Top Sub Menu controls are available See Chapter 2 for more details on these controls Frequency 6 Focus Position B Mode Biopsy Kit None Frame Average 3 Line Density 4 Focus Width Wide B Softener Med Power Output 100 Suppre
30. call the GE Ultrasound Clinical Answer Center at 1 800 682 5327 or 1 262 524 5698 LOGIQ e User Guide i 1 Direction 5314626 100 Rev 3 Regulatory Requirements Conformance Standards The following classifications are in accordance with the IEC EN 60601 1 6 8 1 According to 93 42 EEC Medical Device Directive this is Class Ila Medical Device According to IEC EN 60601 1 e Equipment is Class I Type B with BF or CF Applied Parts e Docking Cart console is Class I According to CISPR 11 e Equipment is Group 1 Class A ISM Equipment e Docking Cart is Group 1 Class A ISM Equipment According to IEC 60529 the footswitch rate is IPx1 FSU 2001 or IPx8 MKF 2 MED GP26 FSU 1000 This product complies with the regulatory requirement of the following Council Directive 93 42 EEC concerning medical devices the CE label affixed to the product testifies compliance to the Directive The location of the CE marking is shown in the Safety chapter of this manual Authorized EU Representative European registered place of business GE Medical Systems Information Technologies GmbH GEMS IT GmbH Munzinger Strasse 5 D 79111 Freiburg GERMANY Tel 49 761 45 43 0 Fax 49 761 45 43 233 LOGIQ e User Guide Direction 5314626 100 Rev 3 Conformance Standards continued Certifications International Electrotechnical Commission IEC e IEC EN 60601 1 Medical Electrical Equipment Part 1 General Requirements for
31. following figure Figure 4 1 Capacity load of the Docking Cart Direction 5314626 100 Rev 3 Safety General Caution continued of B W Printer 1 is 4kg Color Printer Shelf 2 is 7kg DVD RW Shelf 3 is 2kg and Bottom Shelf 4 is 6kg refer to the CAUTION Capacity load of the Isolation Cart The maximum capacity load following figure Figure 4 2 Capacity load of the Isolation Cart 4 12 LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions General Caution continued maximum capacity load of Basket 1 and Drawer 5 is 3kg ACDC Shelf 2 is 1 5kg DVD RW Shelf 3 is 1 5kg and B W CAUTION Capacity load of the Isolation Cart Enhanced Version The Printer Shelf 4 is 3kg refer to the following figure Figure 4 3 Capacity load of the Isolation Cart Enhanced Version LOGIQ e User Guide 4 13 Direction 5314626 100 Rev 3 Safety Device Labels Label Icon Description The following table describes the purpose and location of safety labels and other important information provided on the equipment Table 4 2 Label Icons Label icon Purpose Meaning Location Identification and Rating Plate ual e Manufacture s name and address e Date of manufacture Model and serial numbers Electrical ratings Volts Amps phase and frequency AC Adapter Label Type Class Label Used to indicate the degree of safety or protection IP Code IPX8 IPX8 MK
32. in other applications Click Edit to reset cursor position en GE Healthcare MI0 8 Tis0 4 8C RS Ss 08 01 08 10 50 31 PM 1 1 Neo Abd Gain 42 a s z Frequency 8 0 MHz a 4 Depth 8 0 cm 7 N 4 J Focus Position M Yy Power Output 100 Arnot made xit Grab word Word Delete Figure 7 15 Comment Screen Grab word Word Delete Undo Clear Figure 7 16 Comment screen Top Menu LOGIQ e User Guide 7 13 Direction 5314626 100 Rev 3 Using Touch Screen General Instructions continued To reposition a comment 1 Select Grab Word to select the comment 2 Select the target position on the Touch Screen to reposition See Chapter 6 for more details of the Top Menu 7 14 LOGIQ e User Guide Direction 5314626 100 Rev 3 Using CINE Using CINE Introduction CINE images are constantly being stored by the system and are available for playback or manual review via CINE Activate CINE Select Freeze to freeze the image LOGIQ e User Guide 7 15 Direction 5314626 100 Rev 3 CINE mode monitor display 9 GE Healthcare MI0 5 Tis0 5 i12L RS Nes 08 05 08 1 48 54 AM 1 1 Carotid Gain 42 A Patient A 4 a A f7 Preset Erea 10 0 MHz Abc Comment v 7 Measure Depth 3 0 cm a f End Exam v Position te Y B Pause a Clear All y Power Output 100 Mode gt Cine mode a Reverse Loop Forward Loop Run Stop 08 05 08 1 48 59AM start w a
33. page are specified to be suitable for use within the PATIENT ENVIRONMENT CAUTION DO NOT connect any probes or accessories without approval by GE within the PATIENT ENVIRONMENT See Peripheral Update for EC countries on page 4 24 for more information Unapproved Devices CAUTION DO NOT use unapproved devices If devices are connected without the approval of GE the warranty will be INVALID Any device connected to the LOGIQ e must conform to one or more of the requirements listed below 1 IEC standard or equivalent standards appropriate to devices 2 The devices shall be connected to PROTECTIVE EARTH GROUND Accessories Options Supplies CAUTION Unsafe operation or malfunction may result Use only the accessories options and supplies approved or recommended in these instructions for use LOGIQ e User Guide 4 29 Direction 5314626 100 Rev 3 Safety Acoustic Output Located on the upper right section of the system display monitor the acoustic output display provides the operator with real time indication of acoustic levels being generated by the system See the Acoustic Output chapter in the Advanced Reference Manual for more information This display is based on NEMA AIUM Standards for Real time Display of Thermal and Mechanic Acoustic Output Indices on Diagnostic Ultrasound Equipment Acoustic Output Display Specifications Thermal Index 4 30 The display consists of three parts Thermal Index TI
34. probe as needed using a soft sponge gauze or cloth to remove all visible residue from the probe surface Prolonged soaking or scrubbing with a soft bristle brush such as a toothbrush may be necessary if material has dried onto the probe surface Take extra care when handling the lens face of the Ultrasound transducer The lens face is especially sensitive and can easily be damaged by rough handling NEVER use excessive force when cleaning the lens face Rinse the probe with enough clean potable water to remove all visible soap residue Air dry or dry with a soft cloth LOGIQ e User Guide Direction 5314626 100 Rev 3 Probe Overview Cleaning probes continued E8C RS TO e NI 1 2 3 Figure 3 1 Probe Immersion Levels 1 Fluid Level 2 Aperature 3 Contact face within Patient Environment LOGIQ e User Guide 3 5 Direction 5314626 100 Rev 3 After the Exam is Over Disinfecting probes Perform After Ultrasound probes can be disinfected using liquid chemical Each Use germicides The level of disinfection is directly related to the duration of contact with the germicide Increased contact time produces a higher level of disinfection Table 3 1 Description of Pictogram on Care card Pictogram Description ATTENTION Consult accompanying documents is intended to alert the user to refer to the operator manual or other instructions when complete information cannot be provided
35. replacement as often You can expect one hour of battery life while scanning with a single fully charged battery The lithium ion technology used in your system s battery is significantly less hazardous to the environment than the lithium metal technology used in some other batteries such as watch batteries Used batteries should not be placed with common household waste products Contact local authorities for the location of a chemical waste collection program nearest you The battery is designed to work with LOGIQ e systems only Only use the batteries authorized by GE e The battery has a safety device Do not disassemble or alter the battery Charge the batteries only when the ambient temperature is between 0 and 40 degrees C 32 and 104 degrees F and discharge the batteries between 0 and 40 degrees C 32 and 104 degrees F e Do not short circuit the battery by directly connecting the negative terminals with metal objects e Do not heat the battery or discard it in a fire e Do not expose the battery to temperature over 50 degrees C 122 degrees F Keep it away from fire and other heat sources e Do not charge the battery near a heat source such as a fire or heater Do not leave the battery in direct sunlight e Do not pierce the battery with a sharp object hit it or step on it e Do not use a damaged battery Do not solder a battery e Do not connect the battery to an electrical power outlet LOGIQ
36. sure to verify the media after writing of data such as EZBackup SaveAs or Export Before deleting a patient or image from the patient screen make sure you have saved the data by EZBackup Backup or Export and verify that the media transfer of data was successful To perform backup and restore procedures you must login with administrator privileges LOGIQ e User Guide Direction 5314626 100 Rev 3 Backup and Restore Restore procedure patient data CAUTION NOTE LOGIQ e User Guide The restore procedure overwrites the existing database on the local hard drive Make sure to insert the correct media You cannot restore the data between systems with different software versions SON Insert the media into the media drive On the Control Panel press Utility Select System On the monitor display select Backup Restore The Backup Restore screen is displayed If you are not logged in with administrator privileges the Operator Login window is displayed Log on with administrator privileges In the Restore list select Patient Archive In the Media field select the Backup Restore media Select Restore The system performs the restore As it proceeds status information is displayed on the Backup Restore screen Direction 5314626 100 Rev 3 After the Exam is Over Backup procedure user defined configurations 3 18 CAUTION NOTE To avoid the risk of overwriting the local patient archives on the sy
37. the environment and human health of the substances used in batteries is available at this url http www gehealthcare com euen weee recycling index html Hg Battery Pack if contains Pb Cd No hazardous substance above the maximum concentration value is present Maximum concentration values for electronic information products as set by the People s Republic of China Electronic Industry Standard SJ T11364 2006 include the hazardous substances of lead mercury hexavalent chromium cadmium polybrominated biphenyl PBB and polybrominated diphenyl ether PBDE 4 16 LOGIQ e User Guide Direction 5314626 100 Rev 3 Table 4 2 Safety Precautions Label Icons Continued Label Icon Purpose Meaning Location Indicates the presence of hazardous substance s above the maximum concentration value Maximum concentration values for electronic information products as set by the People s Republic of China Electronic Industry Standard SJ T11364 2006 include the hazardous substances of lead mercury hexavalent chromium cadmium polybrominated biphenyl PBB and polybrominated diphenyl ether PBDE 10 indicates the number of years during which the hazardous substance s will not leak or mutate so that the use of this product will not result in any severe environmental pollution bodily injury or damage to any assets Probe and Rear Panel China Rating Plate
38. the vicinity of equipment marked with the symbol bad Image degradation or interference may occur due to conducted RF noise on the equipment mains power supply or other signal cable Such interference is easily recognized and distinguishable from patient anatomy and physiological waveforms Interference of this type may delay the examination without affecting diagnostic accuracy Additional mains signal RF isolation or filtering may be needed if this type interference occurs frequently NOTE These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people If noise generated from other electronic equipment is near the probe s center frequency noise may appear on the image Good power line isolation is required LOGIQ e User Guide Direction 5314626 100 Rev 3 4 27 Safety Patient Environmental Devices Figure 4 4 Patient Environmental Devices 1 Left side e 2 USB Ports Peripheral devices Printers Color and USB Memory Stick Footswitch Wireless LAN Adapter USB Hub ECG USB HDD 1 Earphone Port 2 Bottom side Lithium ion battery port Right side Probe port Security lock Rear panel e 1 VGA Port e 1 Network Port e 1 Docking Port Aw 4 28 LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions Acceptable Devices The Patient Environmental devices shown on the previous
39. these controls CrossXBeam Harmonics B Steer Virtual Convex Auto Figure 7 4 B Mode Top Menu LOGIQ e User Guide Direction 5314626 100 Rev 3 M Mode Intended Uses M Mode is intended to provide a display format and measurement capability that represents tissue displacement motion occurring over time along a single vector on GE Healthcare MIO 5 Tis0 5 8L RS 09 08 08 11 32 32 PM ADM 090808 113053 PM 1 1 Carotid Gain 48 ta 4 Patient a 4 m z 7 Preset Freq 10 0 MHz Abc Comment 7 Measure Depth 4 0 em a P End Exam v Focus Position B Pause w F Clear All Power Output 100 lt gt Mode gt M mode a Full Timeline Move ROI Figure 7 5 M Mode Display M Mode Top Menu The following Top Menu controls are available for functionality adjustment and image optimization See Chapter 5 for more details on these controls Full Timeline Move ROI Figure 7 6 M Mode Top Menu LOGIQ e User Guide 7 7 Direction 5314626 100 Rev 3 Color Flow CF Mode Intended Uses Color Flow Mode is a Doppler Mode intended to add color coded qualitative information concerning the relative velocity and direction of fluid motion within the B Mode image mn GE Healthcare MI 1 1 Tis0 56 8L RS 09 08 08 11 33 44 PM ADM 090808 113053 PM 1 1 Carotid GE zi ESE Gain 10 A Patient 7 Yv f7 Preset l Freq 4 4 MHz ADC Comment y a v F7 Measure Depth 4 0 cm a
40. 2 Figure 7 17 CINE mode monitor display Select Run to go through the image loop Select Reverse Loop to go backward frame by frame Select Forward Loop to go forward frame by frame 7 16 LOGIQ e User Guide Direction 5314626 100 Rev 3 A accessories ordering 3 24 requesting a catalog 3 24 acoustic output default levels 4 32 ALARA as low as reasonably achievable bioeffects 4 3 area measurements ellipse 2 14 spline 2 16 trace 2 15 2 16 B biological hazards 4 9 B Mode imaging intended uses 5 9 6 5 B Mode measurements general 2 12 B Mode measurements mode circumference and area ellipse 2 14 circumference and area spline trace 2 16 circumference and area trace 2 15 distance 2 13 Body Patterns 2 10 brightness video 1 16 Cc Care and maintenance cleaning the system monitor 3 30 operator controls 3 37 system cabinet 3 30 inspecting the system 3 29 maintenance schedule 3 30 Caution icon defined 4 2 CINE gauge display location 1 15 CINE mode activating 2 9 circumference measurements ellipse 2 14 spline 2 16 trace 2 15 2 16 cleaning probes 3 4 Color Flow imaging intended uses 5 7 LOGIQ e User Guide Direction 5314626 100 Rev 3 Index Connectivity configuring 3 20 overview of screens 3 20 presets 3 20 contacts clinical questions 3 24 Internet 3 24 service questions 3 24 contraindications 1 3 Contro
41. ENRRE REMMAAARLEARRH ETS This machine should be used In compliance with restrict certaln aap a SHO SUC BAG NS 44 Aes Sc AAU Figure 4 9 LOGIQe R6 x x TUV and Identification Rating Plate Label Location LOGIQ e User Guide Direction 5314626 100 Rev 3 4 37 Safety Warning Label Locations continued amp CISPR 11 EN 55011 c 1A GROUP 1 CLASSE A GROUPE 1 GAA FRAR BAEK PRBS LOGIQ e REWE FD MAO MMA 20V 5A STOPIO NARAR AEA a o s MAAM z Eek YB IR XX ames RBA OW 00000x od A RT RR PRD ARAR FMARBR RAPE LF BE KIMY 214028 7h Sih CE R This machine should be used In gales law Some Jurisdictions restrict certal such as gender SAAS AAR SCAN A SHAN SUG SAG NS AR AS CES a OPA Ab RC AAU RCTEARRE RENKHTARICARMEL ARES Figure 4 10 LOGIQ e R6 x x Rating Plate China only United States law restricts this device to sale or use by or on the order of a physician CISPR 11 EN 55011 CLASS A GROUP 1 CLASSE A GROUPE 1 Figure 4 11 4 38 LOGIQ e MADE IN USA C i x This machine should be used rorrpence wit law Some Jurisdictions restrict certa gender determinstion SAAS AAR ESHAAN Hae aS eS a ER APMAARRE REAMTTARLCARM ARTS SINI SUC sag NS wagas AIRAU LOGIQ e Rating Plate CKD version LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions Warning Label Locations continued
42. F 2 MED GP26 FSU 1000 Indicates the degree of protection provided by the enclosure per IEC60 529 IPX8 can be used in an operating room environment Bottom of Footswitch m B Authorized European Representative address RUS United States only Prescription Requirement label Type BF Applied Part man in the box symbol is in accordance with IEC 878 02 03 Beside the probe connector General Warning Various A A CAUTION Dangerous voltage the lightning flash with arrowhead is used to indicate electric shock hazards Various 4 14 LOGIQ e User Guide Direction 5314626 100 Rev 3 Table 4 2 Safety Precautions Label Icons Continued Label Icon Purpose Meaning Location ON indicates the power on position of the power switch CAUTION This Power Switch DOES NOT ISOLATE Mains Supply See the Console Overview section for location information Protective Earth indicates the protective earth grounding terminal Inside of AC adapter NRTL Listing and Certification Mark is used to designate conformance to nationally recognized product safety standards The Mark bears the name and or logo of the testing laboratory product category safety standard to which conformity is assessed and a control number Bottom Type CF Defib Proof Applied Part heart in the box with paddle symbol is in accordance with IEC
43. FLIHC Hadlock gt 19 71 13 67 16 81 HC AC Campbell 1 09 1 06 1 33 Figure 2 2 OB B Mode Worksheet To return to scanning do one of the following Select Worksheet e Press Esc 2 24 LOGIQ e User Guide Direction 5314626 100 Rev 3 Measurement and Analysis To view a worksheet continued To view worksheet data for a particular mode select the key for that mode To view a worksheet with data for more than one mode select Expand When Expand is selected it defaults to view all measurements noted by mode on the worksheet If a worksheet has more data on a second page to view the next page adjust the Page Change control LOGIQ e User Guide 2 25 Direction 5314626 100 Rev 3 Performing an Exam To edit a worksheet HINTS 2 26 To change data on a worksheet 1 To position the cursor at the field you want to change move the Trackball The field is highlighted 2 Press Set 3 Type the new data in the field The new data is displayed in blue to indicate that it was manually entered To delete or exclude data on a worksheet 1 To position the cursor at the field you want to delete or exclude move the Trackball The field is highlighted 2 Doone of the following e To delete the field select Delete Value e To exclude the field select Exclude Value The data in the field is not visible and is not included in worksheet calculations e To include a value that you previously excluded select
44. ISPR CAUTION The LOGIQ e conforms to 3 Do not use the following devices near this the CISPR11 Group 1 Class A of the equipment cellular phone radio receiver international standard for Electromagnetic mobile radio transmitter radio controlled toy disturbance characteristics etc Use of these devices near this equipment could cause this equipment to perform outside the published specifications Keep power to these devices turned off when near this equipment LOGIQ e User Guide 4 33 Direction 5314626 100 Rev 3 Safety Warning Label Locations continued a OF MEDICAL SYSTEMS CHINA CO LTO NO 19 CHANGJIANG ROAD SUKI NATIONAL HI TECH DEVELOPWENT ZONE JIANGSU PLR CHINA 214028 DESC MOBILE CART WODEL DOCKING CART Only for use with LOGIO e series INPUT 100 120 50 60Hz SOOVA OUTPUT 1 100 120 50 60ttz JOVA 2 20V GA GE MEDICAL SYSTEMS CHINA CO LTD NO 19 CHANGJIANG ROAD BUXI NATIONAL HI TECH DEVELOPMENT ZONE JIANGSU P R CHINA 214028 DESC MOBILE CART WOEL DOCKING CART Only for use wlth LOGIQ e Vivid e serles INPUT 100 120 50 60Hz SOOVA OUTPUT 1 100 120 50 60Hz 380VA 2 20V 6A ed SICAL srra iow ont C36 NO 19 OUNOMANE ROAD BIN KATINA HATO OOVELOPWENT IOE SNS P OUMA 21 ANANKE OM ARAR ONIBSANSRRAMEARNEI KLD I2 O56 A KONE CART WOE BG COOKING CART Oniy tor use slon LOCIO serios RAYN KARIE DA RA 220 20 0 OA AAS 12O S SO OA
45. L 1 800 472 3666 In other locations contact your local Applications Sales or Service Representative GE Healthcare TEL 1 800 668 0732 Ultrasound Service Engineering 9900 Innovation Drive Wauwatosa WI 53226 Customer Answer Center TEL 1 262 524 5698 GE Healthcare TEL 1 262 524 5300 Ultrasound Service Engineering 9900 Innovation Drive Wauwatosa WI 53226 Customer Answer Center TEL 1 262 524 5698 GE Ultraschall TEL 0130 81 6370 toll free Deutschland GmbH amp Co KG TEL 33 130 831 300 Beethovenstrasse 239 FAX 49 212 28 02 431 Postfach 11 05 60 D 42655 Solingen GE Ultrasound Asia Singapore TEL 65 291 8528 Service Department Ultrasound FAX 65 272 3997 298 Tiong Bahru Road 15 01 06 Central Plaza Singapore 169730 GE Healthcare Japan Corporation TEL 81 42 648 2910 Customer Service Center FAX 81 42 648 2905 3 25 Direction 5314626 100 Rev 3 After the Exam is Over Contacting GE Healthcare Ultrasound continued ARGENTINA GEME S A TEL 1 639 1619 Miranda 5237 FAX 1 567 2678 Buenos Aires 1407 AUSTRIA GE GesmbH Medical Systems Austria TEL 0660 8459 toll free Prinz Eugen Strasse 8 8 FAX 43 1 505 38 74 A 1040 WIEN TLX 136314 BELGIUM GE Healthcare BVBA TEL 32 0 2 719 72 04 Kouterveldstraat 20 FAX 3202 719 72 05 B 1831 Diegem BRAZIL GE Sistemas Medicos TEL 0800 122345 Av Nove de Julho 5229 FAX 011 3067 8298 01407 907 Sao Paulo SP CHINA GE Healthcare Asia
46. M Mode functions the same as distance measurement in B Mode It measures the vertical distance between calipers 1 Press Measure once an active caliper with a vertical and horizontal dotted line displays 2 To position the active caliper at the most anterior point you want to measure move the Trackball 3 To fix the start point press Set The system fixes the first caliper and displays a second active caliper 4 To position the second caliper at the most posterior point you want to measure move the Trackball 5 To complete the measurement press Set The system displays the vertical distance between the two points in the Results Window LOGIQ e User Guide Direction 5314626 100 Rev 3 Time interval Measurement and Analysis To measure a horizontal time interval and velocity 1 Press Measure twice an active caliper with a vertical dotted line displays To position the caliper at the start point move the Trackball To fix the first caliper press Set The system fixes the first caliper and displays a second active caliper To position the second caliper at the end point move the Trackball To complete the measurement press Set The system displays the time interval between the two calipers in the Results Window Time interval and Velocity To measure time and velocity between two points 1 LOGIQ e User Guide Press Measure three times an active caliper with a vertical and horizontal dotted l
47. Safety IEC EN 60601 1 1 Safety requirements for medical electrical systems e IEC EN 60601 1 2 Electromagnetic compatibility Requirements and tests e IEC EN 60601 1 4 Programmable electrical medical systems e IEC EN 60601 1 6 Usability EN 1041 Information supplied with medical devices e IEC 60601 2 37 Medical electrical equipment Particular requirements for the safety of ultrasonic medical diagnostic and monitoring equipment e IEC 61157 Declaration of acoustic output parameters International Organization of Standards ISO e ISO 10993 1 Biological evaluation of medical devices Underwriters Laboratories Inc UL an independent testing laboratory e UL 60601 1 Medical Electrical Equipment Part 1 General Requirements for Safety Canadian Standards Association CSA e CSA 22 2 601 1 Medical Electrical Equipment Part 1 General Requirements for Safety NEMA AIUM Acoustic Output Display Standard NEMA UD3 Medical Device Good Manufacturing Practice Manual issued by the FDA Food and Drug Administration Department of Health USA General Electric Medical Systems is ISO 9001 and ISO 13485 certified Original Documentation LOGIQ e User Guide The original document was written in English Direction 5314626 100 Rev 3 Country Specific Approval e JAPAN MHLW Certified Number 218ABBZX00060000 i 4 LOGIQ e User Guide Direction 5314626 100 Rev 3 Table of Contents Conformance Standards
48. T bend the power cable frequently 1 12 LOGIQ e User Guide Direction 5314626 100 Rev 3 Console Overview Control Panel Map Figure 1 6 Control Panel 1 Time Gain Compensation TGC 2 New Patient 3 Additional Feature Keys Steer Harmonics PDI 4 Mode Gain Auto keys M Mode Pulsed Wave Doppler PW Modes Color Flow CF Mode and B Mode 5 Imaging Measurement Keys Cursor Clear Bodymark Measure M D Cursor Scan Area Set B Pause Depth Zoom Ellipse Start Stop L R Programmable Print Keys Freeze 0 Keyboard en ae LOGIQ e User Guide 1 13 Direction 5314626 100 Rev 3 Getting Started Top Sub Menu NOTE Keyboard Esc Help F1 Key Arrow F2 Key Eject F3 Key Spooler F4 Key Reverse F5 Key User Defined Keys F6 through F11 Keys Touch Screen Mode On Off F12 Key Utility Preset Report The Top Sub Menu contains exam function and mode function specific controls Different menus are displayed depending on which Top Sub Menu is selected e 0 000000 Figure 1 7 Top Sub Menu Controls The Top Sub Menu contains adjustable knobs associated with it The adjustable knobs are used to toggle optional functions between up down selections the paddle switches are used to access and adjust the menu The functionality of these controls change depending upon the currently displayed menu The standard alpha numeric keyboard has some special functions E
49. TEL 8610 5806 9403 No 1 Yongchang North Road FAX 8610 6787 1162 Beijing Economic amp Technology Development Area Beijing 100176 China DENMARK GE Medical Systems TEL 45 4348 5400 Fabriksparken 20 FAX 45 4348 5399 DK 2600 GLOSTRUP FRANCE GE Medical Systems TEL 05 49 33 71 toll free 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 amp Co KG TEL 49 212 28 02 207 Beethovenstrasse 239 FAX 49 212 28 02 431 Postfach 11 05 60 D 42655 Solingen 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 1678 744 73 toll free Via Monte Albenza9 FAX 39 39 73 37 86 I 20052 MONZA TLX 3333 28 LUXEMBOURG _ TEL 0800 2603 toll free 3 26 LOGIQ e User Guide Direction 5314626 100 Rev 3 Contact Information Contacting GE Healthcare Ultrasound continued MEXICO NETHERLANDS POLAND PORTUGAL RUSSIA SPAIN SWEDEN SWITZERLAND TURKEY LOGIQ e User Guide GE Sistemas Medicos de Mexico S A de C V Rio Lerma 302 1 y 2 Pisos TEL 5 228 9600 Colonia Cuauhtemoc FAX 5 211 4631 06500 Mexico D F GE Medical Systems Nederland B V TEL 06 022 3797 toll free Atoomweg 512 FAX 31 304 11702 NL 3542 AB UTRECHT GE Medical Systems Polska TEL 48 2 625 59 62 Krzywickiego 34 FAX 48 2 615 59 66 P 02 078 WARSZA
50. Technical Publications Direction 5314626 100 Rev 3 CE ote LOGIQ e User Guide GE Healthcare R5 2 x R6 x x Operating Documentation Copyright 2008 2010 By General Electric Co Regulatory Requirement LOGIQ e complies with regulatory requirements of the following European Directive 93 42 EEC concerning medical devices CE ore This manual is a reference for the LOGIQ e It applies to all versions of the R5 2 x and R6 x x software for the LOGIQ e ultrasound system GE Healthcare GE Healthcare Telex 3797371 P O Box 414 Milwaukee Wisconsin 53201 U S A Asia Pacific Latin America North America GE Ultraschall TEL 49 212 28 02 208 Deutschland GmbH amp Co KG FAX 49 212 28 02 431 Beethovenstrasse 239 Postfach 11 05 60 D 42655 Solingen GERMANY Revision History Reason for Change DATE YYYY MM DD REASON FOR CHANGE 2008 09 17 Initial release 2010 04 08 Update for software update and adding probes 2010 11 29 Update to add Factory Site and CKD Rating Plate List of Effected Pages REVISION REVISION PAGE NUMBER NUMBER PAGE NUMBER NUMBER Title Page Rev 3 Chapter 3 Rev 3 Please verify that you are using the latest revision of this document Information pertaining to this document is maintained on MyWorkshop ePDM GE Healthcare electronic Product Data Management If you need to know the latest revision contact your distributor local GE Sales Representative or in the USA
51. To switch between the English and Russian or Greek or Japanese or Chinese keyboard press Ctrl Shift to change the keyboard to the Russian Greek or Chinese keyboard 7 Apply the changes by pressing Apply Press OK TWICE NOTE To have the settings take effect you MUST turn off the system and turn it back on 3 14 LOGIQ e User Guide Direction 5314626 100 Rev 3 System Presets Keyboard Setup Procedure for Russian Greek Chinese Japanese continued Here is an example of the Russian keyboard He he he HHH HH HY Jaaa saHa Hu He He He Me Me Hu Hu He He iHe i H j cHe Ha He Ha Ha He He Ha Ha He He HS J Le Ha He He Ha He He He He Ho H UES T Proset cut tReport Ena Comment an umy H cut i i frets estes e HHH ENEN Figure 3 7 Russian Keyboard LOGIQ e User Guide Direction 5314626 100 Rev 3 After the Exam is Over Backup and Restore Backup and restore strategy patient data CAUTION CAUTION NOTE 3 16 To minimize accidental loss of data perform backup of the patient archives stored on the local hard drive DAILY as described in this section Use a Backup Restore disk to back up patient archives from the hard drive using the backup procedure described in this section Data from the Backup Restore disk may be restored to the local hard drive using the restore procedure The restore procedure overwrites the existing database on the local hard drive Make
52. WA GE Medical Systems Portuguesa S A TEL 05 05 33 7313 toll free Rua Sa da Bandeira 585 FAX 351 2 2084494 Apartado 4094 TLX 22804 P 4002 PORTO CODEX GE VNIIEM TEL 7 495 739 6931 18C Krasnopresnenskaya nab FAX 7 495 739 6932 MOSCOW 123317 TLX 613020 GEMED SU GE Healthcare TEL 34 91 663 25 00 Edificio Gobelas FAX 34 91 663 25 01 C Gobelas 35 37 E 28023 Madrid GE Medical Systems TEL 020 795 433 toll free PO BOX 1243 FAX 46 87 51 30 90 S 16428 KISTA TLX 12228 CGRSWES GE Medical Systems Schweiz AG TEL 155 5306 toll free Sternmattweg 1 FAX 41 41 421859 CH 6010 KRIENS GE Healthcare Turkiye TEL 90 212 366 29 00 Sun Plaza FAX 90 212 366 29 99 Dereboyu Sok No 24 7 34398 Maslak ISTANBUL 3 27 Direction 5314626 100 Rev 3 After the Exam is Over Contacting GE Healthcare Ultrasound continued UNITED KINGDOM OTHER COUNTRIES Manufacturer Factory Sites 3 28 GE Medical Systems TEL 0800 89 7905 toll free Coolidge House FAX 44 753 696067 352 Buckingham Avenue SLOUGH Berkshire SL1 4ER NO TOLL FREE TEL international code 33 1 39 20 0007 GE Medical Systems China Co Ltd No 19 Changjiang Road WuXi National Hi Tech Development Zone Jiangsu P R China 214028 TEL 86 510 85225888 FAX 86 510 85226688 GE Medical Systems China Co Ltd No 19 Changjiang Road WuXi National Hi Tech Development Zone Jiangsu P R China 214028 TEL 86 510 85225888
53. X X Non Imaging x x x X CW CrossxBeam x X X X X X X X X ACO x x X x x x x X x x x Range Focus X X x x X X TDI x x X NOTE 16L RS is not available in China NOTE LOGIQ e R6 x x only 1 24 LOGIQ e User Guide Direction 5314626 100 Rev 3 Beginning an Exam Beginning an Exam Scanning a New Patient When starting a new patient s exam ensure you do the following 1 2 3 4 5 NOTE 6 NOTE 7 LOGIQ e User Guide Press Patient Press New Patient on the Patient menu If there are images on the clipboard a pop up menu appears Specify whether you want to store images permanently delete images or go to active images Choose the exam category Verify the dataflow DO NOT use the removable media Data Flows on the New Patient menu Fill in patient information You can also select a patient from the patient database at the bottom of the Patient menu if the patient has a patient ID Columns drive the ordering of the patients displayed The column that you select drives the order of the displayed patient database Select Register Enter Past OB Exam information if desired 1 25 Direction 5314626 100 Rev 3 Getting Started Scanning a New Patient continued 1 26 8 11 Select the probe to start scanning or select Exit Esc Scan or Freeze Perform the exam Store the raw data to the clipboard To store the still image press Freeze and run the cineloop using the Trackb
54. a certain minimum amplitude before it will be processed M Mode Controls Table 2 2 _M Mode Controls Possible Control Bioeffect Description Benefit Sweep Speed Yes Changes the speed at which the timeline is swept Available in M Mode Doppler Mode and M Color Flow Mode Anatomical M Mode Yes Anatomical M Mode gives you the ability to manipulate the cursor at different angles and positions The M Mode display changes according to the position of the cursor 2 4 LOGIQ e User Guide Direction 5314626 100 Rev 3 Optimizing the Image Color Flow Mode Controls Table 2 3 Color Flow Mode Controls Possible Control Bioeffect Description Benefit Gain No Gain amplifies the overall strength of echoes processed in the Color Flow window or spectral Doppler timeline PRF Pulse Yes Increases decreases the PRF on the color bar Repetition Frequency Wall Filter No Filters out low flow velocity signals It helps get rid of motion artifacts caused from breathing and other patient motion Color Scan Area Yes Scan Area sizes and positions the color window Invert Color Invert No Lets you view blood flow from a different perspective e g red away negative velocities and blue toward positive velocities You can invert a real time or frozen image NOTE Invert reverses the color map NOT the color PRF Baseline No Changes the Color Flow or Doppler spectrum baseline to
55. all Select the frame and press P1 or the assigned Printer key To store the cineloop press Freeze and run the cineloop using the Trackball Select the start end frame and run the selected loop Press P1 or the assigned Print key When you have completed the study press End Exam The image management screen displays Select the images still frame or cineloop you want to store or select Select All to store all images Select Permanent Store to store the images permanently LOGIQ e User Guide Direction 5314626 100 Rev 3 Patient Screen Beginning an Exam Figure 1 13 Patient Screen Example Category OB Enter Patient Data with the alphanumeric keyboard To navigate through the Patient Entry menu use the Tab key or Trackball and Set to move and fix the cursor The Patient Screen details are 1 Image Management LOGIQ e User Guide Direction 5314626 100 Rev 3 Patient Provides a search and creation of patient currently selected Image History Provides a list of images per exam for the currently selected patient Active Images Provides preview of the currently selected exam Data Transfer Provides an interface to handle patient data from a remote device 1 27 Getting Started Patient Screen continued 2 Function Selection e New Patient Used to clear patient entry screen in order to input a new patient s data into the database e Register Used to enter new patient information int
56. and similar equipment should be used no closer to any part of this system including cables than determined according to the following method LOGIQ e User Guide 4 21 Direction 5314626 100 Rev 3 Safety Notice upon Installation of Product Separation distance and effect from fixed radio communications equipment field strengths from fixed transmitters such as base stations for radio cellular cordless telephones and land mobile radios amateur radio AM and FM radio broadcast and TV broadcast transmitter 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 ultrasound system is used exceeds the applicable RF compliance level as stated in the immunity declaration the ultrasound system should be observed to verify normal operation If abnormal operation is observed additional measures may be necessary such as re orienting or relocating the ultrasound system or using an RF shielded examination room may be necessary 1 Use either power supply cords provided by GE Medical Systems or ones designated by GE Medical Systems Products equipped with a power source plug should be plugged into the fixed power socket which has the protective grounding conductor Never use any adaptor or converter to connect with a power source plug e g three prong to two prong conv
57. are moving regardless of their velocity PDI does not map velocity therefore it is not subject to aliasing 9 GE Healthcare MI 1 2 Tis 1 7 12L RS 07 24 07 2 46 17 PM 1 1 Superficial GE le 58 129 7 6 17 3 s Z Stenosis X Volume C Angle AB Ratio Generic Worksheet B g lt gt Menu 1 Frequency 2 x 4 PRF s B Mode Gain HERVE Figure 6 7 Power Doppler Imaging Display LOGIQ e User Guide 6 9 Direction 5314626 100 Rev 3 Nerve Block PDI Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimization See Chapter 2 for more details on these controls 1 Frequency 2 5 B Mode Gain NERVE PDI Mode Line Density 3 Flash Suppression 1 Transparency Map 0 Focus Position Power Output 100 Frame Average 2 Figure 6 8 PDI Top Sub Menu 6 10 LOGIQ e User Guide Direction 5314626 100 Rev 3 Pulsed Wave PW Doppler Mode Intended Use Doppler is intended to provide measurement data concerning the velocity of moving tissues and fluids PW Doppler lets you examine blood flow data selectively from a small region called the sample volume A GE Healthcare MI 0 18 Tis0 1 E8C RS 04 26 10 8 17 07 AM ADM ewftwrrrrrrrreyhrr Superficial B Frq 10 0 MHz Gn E A Map D 100 XBea m Off 2 Generic_ PI X RI C MaxPG V MeanPG B SY D M S D Ratio AB Ratio DiS Ratio HR Generic Worksheet
58. ation See Chapter 2 for more details on these controls 1 Frequency 2 3 1 R 6 BMode Gain PDI Mode Line Density 3 Flash Suppression 1 Transparency Map 0 Focus Position Power Output 100 Frame Average 3 Figure 5 9 PDI Top Sub Menu 5 10 LOGIQ e User Guide Direction 5314626 100 Rev 3 M Color Flow Mode Intended Uses M Color Flow is used for fetal cardiac applications Color Flow overlays color on the M Mode image using velocity and variance color maps The Color Flow wedge overlays the B Mode image and M Mode timeline GE Healthcare MIO 4 Tis0 4 12L RS 03 27 07 11 28 26 AM selectins Carotid amp B CHI Frq 13 0 MHz Gn 50 EA 5 1 Map Q 0 0 60 134 4 7 10 4 Carotid Rt Lt Z Stenosis M AB Ratio HR Worksheet cm 1 Frequency 2 Transparency 3 Axial Filter 4 Power Output 5 PRF Mode z M lt gt B Baseline 03 27 07 11 28 26AM_ start x QS Map Threshold Invert Wall Filter Figure 5 10 M Color Flow Display LOGIQ e User Guide 5 11 Direction 5314626 100 Rev 3 Emergency Department ED M Color Flow Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimization See Chapter 2 for more details on these controls Frequency 2 Transparency xia Power Output PRF Baseline Map weshok Invert Vall Fiter CM Mode Focus Position Flash Suppression 1 Figure 5 11 M Color Flow Top Sub Menu 5 12 LOGIQ e Us
59. ative humidity should be at least 30 IEC 61000 4 4 2 kV for mains 2 kV for mains Electrical fast transient burst 1 kV for SIP SOP 1 kV for SIP SOP IEC 61000 4 5 Surge Immunity 1 kV differential 2 kV common 1 kV differential 2 kV common IEC 61000 4 11 lt 507 gt 95 dip lt 507 gt 95 dip for Voltage dips for 0 5 cycle 0 5 cycle short 400 60 Oip for 5 400 60 Oip for 5 interruptions and cycles cycles voltage 7007 30 Oip for 7007 30 Oip for 25 variations a 25 cycles cycles MANSSHPPY lt 507 gt 95 dip lt 507 gt 95 dip for 5 for 5 sec sec IEC 61000 4 8 3 A m 3 A m Power frequency 50 60 Hz magnetic field IEC 61000 4 6 3 Vams 3 Vrms Conducted RF 150 kHz 80 MHz 150 kHz 80 MHz IEC 61000 4 3 3 V m 3 V m Radiated RF 80 MHz 2 5 GHz 80 MHz 2 5 GHz Mains power quality should be that of a typical commercial and or hospital environment If the user requires continued operation during power mains interruptions it is recommended that the system be powered from a UPS or a battery NOTE UT is the a c mains voltage prior to application of the test level Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial and or hospital environment Separation distance to radio communication equipment must be maintained according to the method below Interference may occur in
60. available See Chapter 2 for more details on these controls Frequency 2 3 CrosskBeam 4 5 Focus Position B Mode Biopsy Kit None Frame Average 3 Line Density 3 Focus Width Middle B Softener Med Power Output 100 Suppression 0 Range Focus Off SRI HD 3 Figure 5 3 B Mode Top Sub Menu LOGIQ e User Guide 5 5 Direction 5314626 100 Rev 3 M Mode Intended Use M Mode is intended to provide a display format and measurement capability that represents tissue displacement motion occurring over time along a single vector GE Healthcare MIO8 Tis0 56 8C RS 36 04 14 10 6 18 48 PM 1 i Ped Abd AO Yo XBea m Off Generic Stenosis AB Ratio HR Generic Worksheet Mode i Swoop Speed 2 Powor Output i Figure 5 4 M Mode Top Sub Menu M Mode Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimization See Chapter 2 for more details on these controls 1 Sweep Speed 2 Power Output 3 Full Timeline 4 Figure 5 5 M Mode Top Sub Menu 5 6 LOGIQ e User Guide Direction 5314626 100 Rev 3 Color Flow CF Mode Intended Use Color Flow Mode is a Doppler Mode intended to add color coded qualitative information concerning the relative velocity and direction of fluid motion within the B Mode image GE Healthcare MI0 6 Tis0 7 E8C RS 04 140 6 29 18 PM ADM Gyn B Frq 10 0 MHz Gn 44 EIA 2 1 Map AO XBea m O Gen
61. beam for a specific area A graphic caret corresponding to the focal zone position s appears on the right edge of the image Auto Optimize No Auto lets you optimize the image based upon the actual B Mode image data Auto Tissue Optimize ATO The preset levels Low Medium and High allow you to pick a preference for the contrast enhancement in the resulting image Low does the least amount of contrast enhancement high does the most Auto is available in single or multi image on live frozen or CINE images in B Mode only and while in zoom in Color Flow Mode and in Spectral Doppler Auto in Color Flow Mode automatically adjusts the overall color gain Auto in PW Doppler Mode optimizes the spectral data Auto adjusts the Velocity Scale PRF live image only baseline shift dynamic range and invert if preset Upon deactivation the spectrum is still optimized The benefit of Auto can be found in reduced optimization time and a more consistent and accurate optimization process M D Cursor No Displays the Doppler Mode cursor on the B Mode image Harmonics Yes Harmonics enhances near field resolution for improved small parts imaging as well as far field penetration Frequency Yes Multi Frequency mode lets you downshift to the probe s next lower frequency or shift up to a higher frequency 2 2 LOGIQ e User Guide Direction 5314626 100 Rev 3 Table 2 1 Optimizing the Image
62. box or a wall hanging unit LOGIQ e User Guide Direction 5314626 100 Rev 3 Probes Applications Table 1 2 Probe Indications for Use N n n o n aa a og N N N Sea cell tb E eg cca rt e ee EE E a D aj al dl N S g a 3 23 a S g bl Probe 2 Application S Abdomen X O X Small Parts X O X X X O Obstetrics X X Gynecology X X Pediatrics X O X O O O O X Neonatal O X O O O Urology x O Cardiac X X X Endocavity x Transcranial O X Intraoperative O O x O O O x x Vascular O X O X X X X O Biopsy O O O O O O Transesopha X geal Musculo x O x x x O skeletal Conventional Musculo X X skeletal Superficial Thoracic X X X Pleural X Main Application 0 Accessory Application NOTE 16L RS is not available in China NOTE LOGIQ e R6 x x only NOTE 6Tc RS probe can not be used with the Docking Cart LOGIQ e User Guide 1 23 Direction 5314626 100 Rev 3 Getting Started Features Table 1 3 Probe Features N w n vn ol alaj o N N N e NE E e E e E Cea E E E a a a dal dl A N S g 2 S 3 l amp g gli bj Probe 2 Application f LOGIQ View x X x x x x x X x x x x Virtual Convex X X X X X X Virtual Apex x x x Easy 3D X x x x x x x X x x M Color Flow x x X x x x x X x x x x Tru Access x X X X X x x X X X
63. ces This means that the user can configure a device with the DICOM service s that particular device supports 4 Dataflow allows you to adjust the settings of the selected dataflow and associated services Selecting a dataflow customizes the ultrasound system to work according to the services associated with the selected dataflow 5 Button allows you to assign a pre configured output service or a set of output services to the Print keys on the control panel 6 Removable Media enables formatting DICOM database or blank formatting and DICOM verification of removable media 7 Miscellaneous allows you to set up the patient exam menu options print and store options and the order of the columns in the examination list on the Patient menu Configure these screens from left to right starting with the Tcpip tab first NOTE The ultrasound system is pre configured for many services with default settings selected You can change these services and settings as needed CAUTION You must restart the LOGIQ e after making any changes to connectivity settings in the Utility menus This includes any changes on the TCPIP Device Properties or dataflow setup screens LOGIQ e User Guide 3 21 Direction 5314626 100 Rev 3 After the Exam is Over Electronic Documentation Accessing Documentation Via a PC To view user documentation on a PC 1 Insert the media into the media drive 2 Open the media drive on your desktop 3
64. ckball To fix the start point press Set To trace the maximum values of the desired portion of the spectrum move the Trackball NOTE To edit the trace line move the Trackball To complete the measurement press Set The system displays the measurement values in the Results Window Auto Trace The value measured depends upon the Vol Flow Method preset The selection available is the Peak TAMAX To auto trace TAMAX 1 NOTE LOGIQ e User Guide Press Measure twice an active caliper with a vertical dotted line displays To position the caliper at the trace start point in the Doppler spectrum move the Trackball To fix the start point press Set To position the vertical caliper at the end point move the Trackball To complete the measurement press Set The system automatically fixes both calipers and traces the maximum value between the two points The system displays this value in the Results Window When you set the Auto Trace for Both above and below the system picks up the maximum power of the signal NOT the maximum velocity If the maximum velocity is not the maximum power the system may not trace accurately If you want to use maximum velocity select either Above or Below 2 19 Direction 5314626 100 Rev 3 Performing an Exam 2 20 Edit Trace NOTE NOTE NOTE NOTE NOTE Auto Trace can be edited after taking an Auto Trace measurement 1 After taking an Auto Trac
65. ction 5 2 Starting a New Patient 5 3 Optimizing the Image B Mode 5 4 M Mode ee rere eee eee ee eee 5 6 i 6 LOGIQ e User Guide Direction 5314626 100 Rev 3 Color Flow CF Mode 5 7 Power Doppler Imaging PDI Mode 5 9 M Color Flow Mode 5 11 Pulsed Wave PW Doppler Mode 5 13 Chapter 6 Nerve Block Beginning an Exam Introduction 6 2 Starting a New Patient 6 3 Selecting an Application Preset and a Probe 6 4 Optimizing the Image B Mode 6 5 Color Flow CF Mode 6 7 Power Doppler Imaging PDI Mode 6 9 Pulsed Wave PW Doppler Mode 6 11 Chapter 7 Using Touch Screen Beginning an Exam Introduction 7 2 Touch Screen Display 7 3 Starting a New Patient 7 4 Selecting an Application Preset and a Probe 7 4 Optimizing the Image B Mode
66. ctive calipers press Measure To erase the second caliper and the current data measured and start the measurement again press Clear once After you complete the measurement To rotate through and activate previously fixed calipers adjust Cursor Select e To erase all data that has been measured to this point but not data entered onto worksheets press Clear 2 13 Direction 5314626 100 Rev 3 Performing an Exam Circumference and area ellipse measurement 2 14 HINTS You can use an ellipse to measure circumference and area To measure with an ellipse 1 2 3 Press Measure once an active caliper displays To position the active caliper move the Trackball To fix the start point press Set The system fixes the first caliper and displays a second active caliper To position the second caliper move the Trackball Adjust the Ellipse control an ellipse with an initial circle shape displays To position the ellipse and to size the measured axes move the calipers move the Trackball To increase the size adjust the Ellipse control ina clockwise direction To decrease the size adjust the Ellipse control in a counterclockwise direction To toggle between active calipers press Measure To complete the measurement press Set The system displays the circumference and area in the Results Window Before you complete the ellipse measurement To erase the ellipse and the current data measured pres
67. d 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 e increase the separation between the equipment and the affected device power the equipment from a source different from that of the affected device e consult the point of purchase or service representative for further suggestions 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 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 All types of electronic equipment may characteristically cause electromagnetic interference with other equipment either transmitted through air or connecting cables The term EMC Electromagnetic Compatibility indicates the capability of equipment to curb electromagnetic influence from other equipment and at the same time not affect other equipment with similar electromagnetic radiation from itself 4 19
68. details on these controls Scan Area Steer Move ROI Auto Figure 7 10 PDI Top Menu LOGIQ e User Guide 7 9 Direction 5314626 100 Rev 3 Pulsed Wave PW Doppler Mode Intended Uses Doppler is intended to provide measurement data concerning the velocity of moving tissues and fluids PW Doppler lets you examine blood flow data selectively from a small region called the sample volume on GE Healthcare MIO 5 Tis0 2 8L RS 09 08 08 11 34 42 PM ADM 090808 113053 PM 1 1 Carotid c EE Gain 17 Oa Patient A a v Freq 4 4 MHz f 4 Preset Abc Comment Vv 7 Measure Depth 4 0 cm y N End Exam 4 Focus Position 5 Pause TS Clear All Power Output 100 Sn Mode gt PW mode A Invert Quick Angle Move ROI Figure 7 11 PW Doppler Mode Display PW Doppler Mode Top Menu The following Top Menu controls are available for functionality adjustment and image optimization See Chapter 5 for more details on these controls Invert Steer Quick Angle Move ROI Auto Figure 7 12 PW Doppler Mode Top Menu 7 10 LOGIQ e User Guide Direction 5314626 100 Rev 3 Measurement Measurement Introduction Measurement supports 2D caliper only when operating in Touch Screen mode List of General Measurements The following table shows the types of general measurements available when you select Measure Table 7 1 General Measurements by Mode
69. e User Guide Direction 5314626 100 Rev 3 Console Overview Battery continued WARNING If the LOGIQ e is not being used on a monthly basis the battery needs to be removed during the lengthy non use period CAUTION To avoid the battery bursting igniting or fumes from the battery causing equipment damage observe the following precautions LOGIQ e User Guide Do not immerse the battery in water or allow it to get wet Do not put the battery into a microwave oven or pressurized container If the battery leaks or emits an odor remove it from all possible flammable sources If the battery emits an odor or heat is deformed or discolored or in a way appears abnormal during use recharging or storage immediately remove it and stop using it If you have any questions about the battery consult GE or your local representative Short term less than one month storage of battery pack e Store the battery in a temperature range between 0 degrees C 32 degrees F and 50 degrees C 122 degrees F 1 9 Direction 5314626 100 Rev 3 Getting Started Battery continued CAUTION Long term 3 months or more storage of battery pack Store the battery in a temperature range between 20 degrees C 4 degrees F and 45 degrees C 113 degrees F Upon receipt of the LOGIQ e and before first time usage it is highly recommended that the customer performs one full discharge charge cycle NOTE A full discharge charge cycle m
70. e measurement select the measurement result on the result window The Edit Trace Edit Peak or Edit Mean menu window appears If the system cannot take the trace data correctly from the image Edit Trace does not work Select Edit Trace The first caliper manual trace caliper appears on the center of the image Use the Trackball to move the caliper on the trace line to the start point To cancel Edit Trace at this time press Clear or Freeze Press Set to fix the first caliper The second caliper appears Edit the trace manually using the second caliper The Ellipse control is used to edit the trace When pressing the Clear key once at this time the second caliper disappears and the first caliper appears in the center of the image If you press Freeze at this time the caliper is automatically fixed and the result window updates Press Set to fix the second caliper The trace and the result window update The trace data TAMAX and TAMEAN are updated though the other points e g PS ED are not updated by trace The points can be edited with Cursor Select While in Edit Trace Cursor Select is disabled Repeat Edit Trace as needed LOGIQ e User Guide Direction 5314626 100 Rev 3 Measurement and Analysis Velocity Time Interval and Acceleration To measure two velocity values the time interval ms and acceleration m s 1 Time interval Press Measure three times an active caliper with vertical and h
71. eans the system is turned on using battery power until the battery loses its charge completely and the system shuts down Plug the LOGIQ e in until the battery is fully charged as indicated by a green LCD light If the battery has not been used for gt 2 months the customer is recommended to perform one full discharge charge cycle It is also recommended to store the battery in a shady and cool area with FCC full current capacity One Full Discharge Charge Cycle Process 1 Full discharge of battery to let the LOGIQ e automatically shut down 2 Charge the LOGIQ e to 100 FCC full current capacity 3 Discharge of LOGIQ e for complete shut down takes one hour for discharge When storing packs for more than 6 months charge the pack at least once during the 6 month timeframe to prevent leakage and deterioration in performance e Use only GE recognized batteries LOGIQ e User Guide Direction 5314626 100 Rev 3 Console Overview Battery continued View current When the system is running there is a battery icon in the system battery status status bar 05 20 05 3 16 41PM Start Figure 1 3 Battery icon When you select this icon the following appears Battery Information Batt Figure 1 4 Battery Status Message Current power source displays the current power source AC power or Battery Total battery power remaining displays the current power remaining capacity When there is no battery Bat
72. ecoming LIVE in the event of an insulation failure 2 Type BF Applied Part TYPE BF APPLIED PART providing a specified degree of protection against electric shock with particular regard to allowable LEAKAGE CURRENT Table 4 3 Type BF Equipment Normal Mode Single fault condition Patient leakage current Less than 100 microA Less than 500 microA 3 Type CF Applied Part TYPE CF APPLIED PART providing a degree of protection higher than that for Type BF Applied Part against electric shock particularly regarding allowable LEAKAGE CURRENTS Table 4 4 Type CF Equipment Normal Mode Single fault condition Patient leakage current Less than 10 microA Less than 50 microA 4 18 LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions EMC Electromagnetic Compatibility NOTE NOTE NOTE NOTE EMC Performance LOGIQ e User Guide 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 If this equipment is found to cause interference which may be determine
73. ed for the E8C RS 8C RS 12L RS 3S RS and 8L RS probes T Spray II has been approved for all the probes available on the LOGIQ e except 6Tc RS 3 7 Direction 5314626 100 Rev 3 After the Exam is Over Disinfecting probes continued CAUTION CAUTION 3 8 In order for liquid chemical germicides to be effective all visible residue must be removed during the cleaning process Thoroughly clean the probe as described earlier before attempting disinfection You MUST disconnect the probe from the LOGIQ e prior to cleaning disinfecting the probe Failure to do so could damage the system DO NOT soak probes in liquid chemical germicide for longer than is stated by the germicide instructions for use Extended soaking may cause probe damage and early failure of the enclosure resulting in possible electric shock hazard 1 Prepare the germicide solution according to the manufacturer s instructions Be sure to follow all precautions for storage use and disposal 2 Place the cleaned and dried probe in contact with the germicide for the time specified by the germicide manufacturer High level disinfection is recommended for surface probes and is required for endocavitary and intraoperative probes follow the germicide manufacturer s recommended time Probes for neuro surgical intra operative use must NOT be sterilized with liquid chemical sterilants because of the possibility of neuro toxic residues remaining on the probe Ne
74. ended that all users receive proper training in applications before performing them in a clinical setting Please contact the local GE representative for training assistance ALARA training is provided by GE Application Specialists The ALARA education program for the clinical end user covers basic ultrasound principles possible biological effects the derivation and meaning of the indices ALARA principles and examples of specific applications of the ALARA principle LOGIQ e User Guide 4 7 Direction 5314626 100 Rev 3 Safety Equipment and Personnel Safety Related Hazards i A DANGER Explosion a Hazard 4 8 This equipment contains dangerous voltages that are capable of serious injury or death If any defects are observed or malfunctions occur stop operating the equipment and perform the proper action for the patient Inform a qualified service person and contact a Service Representative for information There are no user serviceable components inside the console Refer all servicing to qualified service personnel only Only approved and recommended peripherals and accessories should be used All peripherals and accessories must be securely mounted to the LOGIQ e The concerns listed below can seriously affect the safety of equipment and personnel during a diagnostic ultrasound examination Risk of explosion if used in the presence of flammable anesthetics LOGIQ e User Guide Direction 5314626 100 Rev 3
75. er Guide Direction 5314626 100 Rev 3 Pulsed Wave PW Doppler Mode Intended Use C MaxPG V MeanPG B SY D M S D Ratio AB Ratio DiS Ratio HR Generic Worksheet LOGIQ e User Guide Doppler is intended to provide measurement data concerning the velocity of moving tissues and fluids PW Doppler lets you examine blood flow data selectively from a small region called the sample volume GE Healthcare MI 0 30 Tis0 1 E8C RS 04 25 10 7 32 42 AM ADM online Gyn B Frq 10 0 MHz Gn 44 E A Map B DR FR AO o XBeam On 2 Angle Correct Figure 5 12 Doppler Mode Display 5 13 Direction 5314626 100 Rev 3 Emergency Department ED PW Doppler Mode Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimization See Chapter 2 for more details on these controls Frequency 2 Angle Correct 3 RF 5 invert PW Mode Display Format Full Timeline Off vity 10 stion Both Modify Auto Calcs Duplex Off Time Resolution 1 Colorize Gray Map Power Output 100 4 Auto Calcs Off Spectral Avg VeryHigh Cycles to Average 1 Figure 5 13 PW Doppler Mode Top Sub Menu 5 14 LOGIQ e User Guide Direction 5314626 100 Rev 3 Chapter 6 Nerve Block Describes the LOGIQ e system for use in regional anesthesia guidance LOGIQ e User Guide 6 1 Direction 5314626 100 Rev 3 Nerve Block Introduction 6 2 Beginning an Exam
76. er Output following the as low as reasonably achievable m principle Risk of explosion if used in the e Flammable anesthetic presence of flammable anesthetics e Patient user injury or adverse reaction e Replacing fuses from fire or smoke e Outlet guidelines e Patient user injury from explosion and fire LOGIQ e User Guide 4 3 Direction 5314626 100 Rev 3 Safety Important Safety Considerations CAUTION The following topic headings Patient Safety and Equipment and Personnel Safety are intended to make the equipment user aware of particular hazards associated with the use of this equipment and the extent to which injury can occur if precautions are not observed Additional precautions may be provided throughout the manual Improper use can result in serious injury The user must be thoroughly familiar with the instructions and potential hazards involving ultrasound examination before attempting to use the device Training assistance is available from GE Medical Systems if needed The equipment user is obligated to be familiar with these concerns and avoid conditions that could result in injury LOGIQ e User Guide Direction 5314626 100 Rev 3 Patient Safety Related Hazards WARNING Patient identification Diagnostic information LOGIQ e User Guide Safety Precautions The concerns listed can seriously affect the safety of patients undergoing a diagnostic ultrasound examination Always include pr
77. eric CF Right Ovary Fra x Gn X Left Ovary LIA AO PR WF S P Generic Worksheet Figure 5 6 Color Flow Mode Display LOGIQ e User Guide 5 7 Direction 5314626 100 Rev 3 Emergency Department ED CF Mode Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimization See Chapter 2 for more details on these controls B Mode Gain CF Mode Baseline Frame Average Power Output 100 Figure 5 7 CF Mode Top Sub Menu 5 8 LOGIQ e User Guide Direction 5314626 100 Rev 3 Power Doppler Imaging PDI Mode Intended Uses Power Doppler Imaging PDI is a color flow mapping technique used to map the strength of the Doppler signal coming from the flow rather than the frequency shift of the signal Using this technique the ultrasound system plots color flow based on the number of reflectors that are moving regardless of their velocity PDI does not map velocity therefore it is not subject to aliasing en GE Healthcare Mi05 Tis0 8 E8C RS 04 14 10 6 48 29 PM ADM ewgwegg Sete Gyn B Frq 10 0 MHz G 44 Gn 100 XBeam On Generic CF Right Ovary X Left Ovary Generic Worksheet 2 3 Invert 4 PRE 6 Figure 5 8 Power Doppler Imaging Display LOGIQ e User Guide 5 9 Direction 5314626 100 Rev 3 Emergency Department ED PDI Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimiz
78. erter 2 Locate the equipment as far away as possible from other electronic equipment 3 Be sure to use only the cables provided by or designated by GE Medical Systems Connect these cables following the installation procedures e g wire power cables separately from signal cables 4 Lay out the main equipment and other peripherals following the installation procedures described in the Option Installation manuals 4 22 LOGIQ e User Guide Direction 5314626 100 Rev 3 General Notice LOGIQ e User Guide Safety Precautions Designation of Peripheral Equipment Connectable to This Product The equipment indicated in Chapter 18 can be hooked up to the product without compromising its EMC performance Avoid using equipment not designated in the list Failure to comply with this instruction may result in poor EMC performance of the product Notice against User Modification The user should never modify this product User modifications may cause degradation in EMC performance Modification of the product includes changes in a Cables length material wiring etc b System installation layout c System configuration components d Securing system parts cover open close cover screwing 4 23 Direction 5314626 100 Rev 3 Safety Peripheral Update for EC countries The following is intended to provide the users in EC countries with updated information concerning the connection of the LOGIQ e to image recordi
79. folded cloth 2 Wipe down the top front back and both sides of the system cabinet Do not spray any liquid directly into the unit To clean the monitor face Use a soft folded cloth Gently wipe the monitor face Do NOT use a glass cleaner that has a hydrocarbon base such as Benzene Methyl Alcohol or Methyl Ethyl Ketone on monitors with the filter anti glare shield Hard rubbing will also damage the filter When cleaning the screen make sure not to scratch the LCD LOGIQ e User Guide Direction 5314626 100 Rev 3 System Care and Maintenance Operator Controls To clean the operator control panel 1 Moisten a soft non abrasive folded cloth with a mild general purpose non abrasive soap and water solution 2 Wipe down operator control panel 3 Useacotton swab to clean around keys or controls Use a toothpick to remove solids from between keys and controls NOTE When cleaning the operator control panel make sure not to spill or spray any liquid on the controls into the system cabinet or in the probe connection receptacle NOTE In case of SARS use bleach alcohol or Cidex in a normal diluted form for cleaning disinfecting the operator panel NOTE DO NOT use T spray or Sani Wipes on the control panel LOGIQ e User Guide 3 31 Direction 5314626 100 Rev 3 After the Exam is Over Touch Screen To clean the Touch Screen moisten a soft non abrasive folded cloth with lukewarm water and wipe the exter
80. front of the system once The System Exit window is displayed DO NOT press and hold down the Power On Off switch to shutdown the system Instead lightly press the Power On Off switch and select Shutdown Using the Trackball select Shutdown The shutdown process takes a few seconds and is completed when the second LED turns from green to off If the system has not fully shut down in 60 seconds press and hold down the On Off switch until the system shuts down Disconnect the probes Clean or disinfect all probes as necessary Store them in their shipping cases to avoid damage Disconnect AC adapter mains plug from the power outlet Disconnect the AC adapter mains plug from the outlet to ensure the system is disconnected from the power source Direction 5314626 100 Rev 3 Getting Started Connecting the Probe Probes Probes can be connected at any time regardless of whether the console is powered on or off To ensure that the ports are not active place the system in the image freeze condition To connect a probe 1 1 20 Place the probe s carrying case on a stable surface and open the case Carefully remove the probe and unwrap the probe cord DO NOT allow the probe head to hang free Impact to the probe head could result in irreparable damage Use the integrated cable management hook to wrap the cord Inspect the probe before and after each use for damage or degradation to the housing strain relief le
81. gh surface damage that could cause injury or tear protective barriers Become familiar with all instructions and precautions provided with special purpose probes A damaged probe can also increase the risk of electric shock if conductive solutions come in contact with internal live parts Inspect probes often for cracks or openings in the housing and holes in and around the acoustic lens or other damage that could allow liquid entry Become familiar with the probe s use and care precautions outlined in Probes and Biopsy Ultrasound transducers are sensitive instruments which can easily be damaged by rough handling Take extra care not to drop transducers and avoid contact with sharp or abrasive surfaces A damaged housing lens or cable can result in patient injury or serious impairment or operation Ultrasound can produce harmful effects in tissue and potentially result in patient injury Always minimize exposure time and keep ultrasound levels low when there is no medical benefit Use the principle of ALARA As Low As Reasonably Achievable increasing output only when needed to obtain diagnostic image quality Observe the acoustic output display and be familiar with all controls affecting the output level See the Bioeffects section of the Acoustic Output chapter in the Advanced Reference Manual for more information LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions Related Hazards continued Training It is recomm
82. hin the tissue You can select the displayed TI type on Utility gt Imaging gt B Mode This preset is application dependent so each application could specify a different TI type Display precision is 0 1 and accuracy is 50 Accuracy of the power output displayed value on the Top Sub Menu is 2 in B and M Modes and 10 in all other modes Controls Affecting Acoustic Output LOGIQ e User Guide The potential for producing mechanical bioeffects MI or thermal bioeffects Tl can be influenced by certain controls Direct The Acoustic Output control has the most significant effect on Acoustic Output Indirect Indirect effects may occur when adjusting controls Controls that can influence MI and TI are detailed under the Bioeffects portion of each control in the Optimizing the Image chapter Always observe the Acoustic Output display for possible effects 4 31 Direction 5314626 100 Rev 3 Safety Best practices while scanning C NOTE n Acoustic Output Hazard Raise the Acoustic Output only after attempting image optimization with controls that have no effect on Acoustic Output such as Gain and TGC Refer to the sections in Chapter 5 for a complete discussion of each control Be sure to have read and understood control explanations for each mode used before attempting to adjust the Acoustic Output control or any control that can effect Acoustic Output Use the minimum necessary acoustic outp
83. hout approval by GE Not all features or products described in this document may be available or cleared for sale in all markets The following supplies accessories have been verified to be compatible with the system Peripherals Table 3 2 Peripherals and Accessories Accessory Units Sony B W Printer Each Sony Digital Color Printer Each HP470 Printer Each HP 8600 PC Printer Each DVD R W Each USB Wireless Card Each Measure Transfer Kit Each USB Memory Stick Each USB Hub Assy Each ECG USB Each USB HDD Each Docking Cart Each BarCode Reader Each Sandisk U3 USB Flash Drive Each Video Transfer Each 3 34 LOGIQ e User Guide Direction 5314626 100 Rev 3 System Care and Maintenance Console Table 3 3 Console Accessories Accessory Units Footswitch model FSU 1000 Each Footswitch model MKF 2 MED GP26 Each Battery Pack model Each Probes Table 3 4 Probes and Accessories Accessory Units 4C RS Each 8C RS Each E8C RS Each 8L RS Each 9L RS Each 12L RS Each 16L RS Each i12L RS Each 3S RS Each i739 RS t739 RS Each 6Tc RS Each 6S RS Each NOTE 16L RS is not available in China NOTE LOGIQ e R6 x x only LOGIQ e User Guide 3 35 Direction 5314626 100 Rev 3 After the Exam is Over Gel Table 3 5 Gel Accessory Units Thermasonic Gel Warmer Holds three p
84. ial number Direct Current For products to be powered from a DC supply Z U Cc pur Input LOGIQ e User Guide Direction 5314626 100 Rev 3 4 35 Safety Table 4 7 Rating Plate Explanations For use with adapter model TWADP100 For use with adapter model TWADP100 DESC Description 4 36 LOGIQ e User Guide Direction 5314626 100 Rev 3 Warning Label Locations continued Safety Precautions A A Cor X CISPR 11 EN 55011 CLASS A GROUP 1 CLASSE A GROUPE 1 ld PRE eee AMS LOGIQ 103 gaye r kanne r E GEED Fas PER a onzas EES Rae OW F ARER BRCM TRACOM AREA DMM EREKE WA RT AS 214028 This machine should be used In oe law Some Jurisdictions restrict certal such as gender SAAS AAR EAYN A SHON SUG SAO NS Je AS CESS Ad AN wag Abe Cl SAU RCTEARRE REUMHIARICARMEL ARES Figure 4 8 LOGIQ e R5 2 x Rating Plate China only United States law restricts this device to sale or use by or on the order of a physician C 0197 x CISPR 11 EN 55011 CLASS A GROUP 1 CLASSE A GROUPE 1 LOGIQ e REF SN INPUT 20V 5A For use with adapter model TWADP100 GE MEDICAL SYSTEMS CHINA CO LTO tad NO 19 CHANGJIANG ROAD WUXI NATIONAL HI TECH DEVELOPMENT ZONE JIANGSU P R CHINA 214028 MADE IN CHINA Some Jurisdictions gender determination SAAS ARR ESIN A Ae SS ad a RPR
85. ies Catalog Requests 3 24 For additional information or assistance please contact your local distributor or the appropriate support resource listed on the following pages http www gehealthcare com http Awww gehealthcare com usen ultrasound products probe_care html GE Healthcare TEL 1 800 437 1171 Ultrasound Service Engineering FAX 1 414 721 3865 9900 Innovation Drive Wauwatosa WI 53226 For information in the United States Canada Mexico and parts of the Caribbean call the Customer Answer Center TEL 1 800 682 5327 or 1 262 524 5698 In other locations contact your local Applications Sales or Service Representative For service in the United States call GE CARES TEL 1 800 437 1171 For service for compact products in the United States call TEL 1 877 800 6776 In other locations contact your local Service Representative To request the latest GE Accessories catalog or equipment brochures in the United States call the Response Center TEL 1 800 643 6439 In other locations contact your local Applications Sales or Service Representative LOGIQ e User Guide Direction 5314626 100 Rev 3 Contact Information Contacting GE Healthcare Ultrasound continued Placing an Order CANADA LATIN amp SOUTH AMERICA EUROPE ASIA JAPAN LOGIQ e User Guide To place an order order supplies or ask an accessory related question in the United States call the GE Access Center TE
86. ine displays To position the active caliper at the start point move the Trackball To fix the start point press Set The system fixes the first caliper and displays a second active caliper To position the second caliper at the end point move the Trackball To complete the measurement press Set The system displays time s and slope between the two points in the Results Window 2 23 Direction 5314626 100 Rev 3 Performing an Exam Viewing and Editing Worksheets NOTE Worksheets are not saved if the system crashes As you complete measurements the system puts measurement data in the appropriate worksheets To view a worksheet To view a worksheet select Worksheet on the Top Sub Menu The system displays the worksheet for the current study To view a different worksheet select the worksheet key for the desired worksheet 8 GE Healthcare TA 10 14 06 2 53 17 PM ADM Pt ID GA EDD 39w3d Origin EDD LMP BBT GA 39w3d EDD OPE 10 18 2006 Fetus AM CUA 16w2d i 1w0d EDD CUA 03 29 2007 FetusPos PLAC Ref Physician Page 1 B Mode Measurements BPD Hadlock 3 10 cm Avg 15w5d 14w4d 17w0d HC Hadlock 11 43 cm Avg 15w4d 14w3d 16w5d OFD HC 4 13 cm Avg AC Hadlock 10 49 cm Avg 16w3d 14w5d 18w1d FL Hadlock 2 25 cm Avg 16wSd 15w3d 18w1d g 2D Calculations EFW AC BPD FL HC 157 70g i 23 66g 60z EFW Hadlock GP lt 3 Cl Hadlock 75 01 70 00 86 00 FLIAC Hadlock AS FL BPD Hohler 7269
87. ith patients Wearing gloves protects the patient and operator CAUTION Sterilant Exposure to Patient e g Cidex Contact with a sterilant to the patient s skin or mucous membrane may cause an inflammation If this happens refer to the sterilant s instruction manual Sterilant Exposure from Probe Handle to Patient e g Cidex DO NOT allow the sterilant to contact the patient Only immerse the probe to its specified level Ensure that no solution has entered the probe s handle before scanning the patient If sterilant comes into contact with the patient refer the the sterilant s instruction manual Sterilant Exposure from Probe Connector to Patient e g Cidex DO NOT allow the sterilant to contact the patient Only immerse the probe to its specified level Ensure that no solution has entered the probe s connector before scanning the patient If sterilant comes into contact with the patient refer the the sterilant s instruction manual Endocavitary Probe Point of Contact Refer to the sterilant s instruction manual LOGIQ e User Guide 3 3 Direction 5314626 100 Rev 3 After the Exam is Over Probe Cleaning Process Cleaning probes Perform After Each Use CAUTION To clean the probe 1 Disconnect the probe from the ultrasound console and remove all coupling gel from the probe by wiping with a soft cloth and rinsing with flowing water Wash the probe with mild soap in lukewarm water Scrub the
88. l Panel description 1 13 Control panel replacing key caps 3 32 replacing key lamps 3 32 controls keyboard 1 14 operator 1 13 Touch Panel 1 14 D Danger icon defined 4 2 device labels 4 74 devices acceptable 4 29 unapproved 4 29 disinfecting probes 3 6 disinfecting solutions probes 3 6 distance measurement general 2 13 Doppler measurements mode TAMAX and TAMEAN 2 19 time interval 2 21 velocity 2 18 Doppler Mode general measurements 2 18 Doppler Mode PW intended uses 5 13 6 17 E electrical configurations 1 4 electrical hazard 4 9 electromagnetic compatiblity EMC 4 19 ellipse measurement general 2 14 EMC electromagnetic compatiblity 4 19 equipment safety 4 8 exam study display location 1 15 Index 1 explosion hazard 4 8 F Federal law USA requirements 1 3 focal zone display location 1 15 freezing an image 2 9 G Gels coupling 3 10 H hazards safety symbols 4 3 hazards types biological 4 9 electrical 4 6 4 9 explosion 4 8 mechanical 4 6 imaging parameters display location 1 15 Indications for Use 1 3 information requesting 3 24 K keyboard special keys 1 14 L LOGIQ system contraindications 1 3 Indications for Use 1 3 Measurement Summary window display location 1 15 measurements general 7 11 M Mode imaging intended uses 5 6 M Mode measurements mode time interval 2 23 time inte
89. lastic bottles 250ml or 8 oz Aquasonic 100 Scan Gel 5 liter jug 250 ml plastic bottles 12 case Scan Ultrasound Gel 8 oz plastic bottles 12 case 1 gallon plastic jug Four 1 gallon plastic jugs Disinfectant Table 3 6 Disinfectant Accessory Units Cidex Activated Dialdehyde 16 1 quart bottles 4 1 gallon bottles 2 2 5 gallon bottles 3 36 LOGIQ e User Guide Direction 5314626 100 Rev 3 System Care and Maintenance Ultrasound Probe and Cord Sheath Sets Table 3 7 Probe and Cord Sheath Sets Accessory Units Sterile Ultrasound Probe Sheath Set 20 Per Set Sterile Ultrasound Cord Sheath Set 20 Per Set Sanitary Rectal Vaginal Probe Cover 20 Per Set Sterile Combination Probe and Cord Cover Set 12 Per Set Sterile Ultrasound Probe Sheath Set for Wide 2 5 and 3 5 20 Per Set Aperture Sector Probes LOGIQ e User Guide 3 37 Direction 5314626 100 Rev 3 After the Exam is Over 3 38 LOGIQ e User Guide Direction 5314626 100 Rev 3 Chapter 4 Safety Describes the safety and regulatory information pertinent for operating this ultrasound system LOGIQ e User Guide 4 1 Direction 5314626 100 Rev 3 Safety Precaution Levels Icon description 4 2 DANGER WARNING CAUTION NOTE Safety Precautions Various levels of safety precautions may be found on the equipment and different levels of co
90. m gt General set the Language as Russian Greek Chinese Japanese Save this setting Location Figure 3 4 Changing the System Language to Russian Greek Chinese Japanese 2 Press Regional Options under Standards and Formats select Russian Greek Jpanese or Chinese PRC Under Location select Russia Greece Japan or China Press Apply Figure 3 5 Regional Options 3 Select the Language tab press Details under Installed Services select the Russian Greek Japanese or Chinese PRC keyboard under Default input language select Russian Russian Greek Greek Japanese Japanese or Chinese PRC Microsoft IME 3 0 Press Apply Press OK LOGIQ e User Guide 3 13 Direction 5314626 100 Rev 3 After the Exam is Over Keyboard Setup Procedure for Russian Greek Chinese Japanese continued 4 Select the Advanced tab then select Russian Greek Japanese or Chinese PRC in the Language for non Unicode programs pull down menu Press Apply Answer Yes to use files already loaded on the hard disk then answer No to not reboot the system yet press OK Press Save and Exit the Utility screen Regional and Language Options EZ 10000 MAC Roman C 10001 MAC Japanese C 10002 MAC Traditional Chinese Big5 C 10003 MAC Korean C 10004 MAC Arabic C 10005 MAC Hebrew Figure 3 6 Set Language 5 Reboot the system When your system restarts the system appears in the selected language 6
91. n to backup all data Go to the patient screen select the patients exams to delete so the remaining number is less than 1 000 Select Delete to delete the selected data Removing image data with the EZMove function does not reduce the patient number in the database For each media to do EZBackup or Move select a proper capacity for the Media capacity for estimate preset under Utility gt System gt Backup Restore For example you can select 700M for a CD or 4700M for a DVD 1 31 Direction 5314626 100 Rev 3 Getting Started 1 32 LOGIQ e User Guide Direction 5314626 100 Rev 3 Chapter 2 Performing an Exam Optimizing the Image and Measurement and Analysis LOGIQ e User Guide 2 1 Direction 5314626 100 Rev 3 Performing an Exam B Mode Controls Optimizing the Image Table 2 1 B Mode Controls Control Possible Bioeffect Description Benefit Depth Yes Depth controls the distance over which the B Mode images anatomy To visualize deeper structures increase the depth If there is a large part of the display which is unused at the bottom decrease the depth Gain No B Mode Gain increases or decreases the amount of echo information displayed in an image It may have the effect of brightening or darkening the image if sufficient echo information is generated Focus Yes Increases the number of focal zones or moves the focal zone s so that you can tighten up the
92. nal surface It can also be wiped by using the Sani cloth HB Replacing illuminated key caps lamps Contact a local Service Representative when a key cap or lamp needs to be replaced Other Peripheral Maintenance Refer to the peripheral manuals for more information 3 32 LOGIQ e User Guide Direction 5314626 100 Rev 3 Other Maintenance System Care and Maintenance Optimum Ultrasound system performance is your facility s responsibility Ensure that your facility establishes a regular maintenance program at the appropriate time intervals to perform the following tasks e inspect the system probes and peripherals e clean system parts e test leakage current e verify measurement accuracy e assure probe quality with phantom checks Your facility s Biomedical Department may perform this service or contact the GE Service Representative to verify contract for coverage Battery Replacement and Disposition NOTE NOTE LOGIQ e User Guide Battery replacement every three years is recommended Contact a local Service Representative for the replacement of the battery Used batteries will be discarded appropriately by GE Disposing of the battery should meet local law and regulatory requirements Dispose of the system according to local law and regulatory requirements 3 33 Direction 5314626 100 Rev 3 After the Exam is Over Supplies Accessories CAUTION DO NOT connect any probes or accessories wit
93. ncern are identified by one of the following flag words and icons which precede the precautionary statement Indicates that a specific hazard is known to exist which through inappropriate conditions or actions will cause e Severe or fatal personal injury e Substantial property damage Indicates that a specific hazard is known to exist which through inappropriate conditions or actions may cause e Severe personal injury e Substantial property damage Indicates that a potential hazard may exist which through inappropriate conditions or actions will or can cause e Minor injury e Property damage Indicates precautions or recommendations that should be used in the operation of the ultrasound system specifically Maintaining an optimum system environment e Using this Manual e Notes to emphasize or clarify a point LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions Hazard Symbols Icon Description Potential hazards are indicated by the following icons Table 4 1 Potential Hazards Icon Potential Hazard Usage Source e Patient user infection due to e Cleaning and care ISO 7000 contaminated equipment instructions No 0659 e Sheath and glove guidelines e Electrical micro shock to patient e g e Probes gt __ ventricular ECG if applicable Ys e Connections to back panel i Patient injury or tissue damage from e ALARA the use of ultrasound radiation Pow
94. ng and other devices or communication networks Peripheral used in The LOGIQ e has been verified for overall safety compatibility the patient and compliance with the following on board image recording environment devices Sony UP D897 B W Printer e Sony UP D25MD Color Printer The LOGIQ e may also be used safely while connected to devices other than those recommended above if the devices and their specifications installation and interconnection with the system conform to the requirements of IEC EN 60601 1 1 CAUTION The connection of equipment or transmission networks other than as specified in the user instructions can result in an electric shock hazard or equipment malfunction Substitute or alternate equipment and connections requires verification of compatibility and conformity to IEC EN 60601 1 1 by the installer Equipment modifications and possible resulting malfunctions and electromagnetic interference are the responsibility of the owner General precautions for installing an alternate off board remote device or a network would include 1 The added device s must have appropriate safety standard conformance and CE Marking 2 There must be adequate mechanical mounting of the device and stability of the combination 3 Risk and leakage current of the combination must comply with IEC EN 60601 1 1 4 Electromagnetic emissions and immunity of the combination must conform to IEC EN 60601 1 2 4 24 LOGIQ e User Guide
95. nistrator privileges the Operator Login window is displayed Log on with administrator privileges 5 Inthe Restore list select from the following depending on which configurations you want to restore e User Defined Configuration Select the parameters to be restored in the Detailed Restore section e Imaging Presets e Connectivity Configuration e Measurement Configuration e Comment Body Pattern Configuration e All Others 6 In the Media field select the media 7 Select Restore The system performs the restore As it proceeds status information is displayed on the System Backup Restore screen The system restarts Direction 5314626 100 Rev 3 After the Exam is Over Configuring Connectivity Overview You use Connectivity functionality to set up the connection and communication protocols for the ultrasound system This page gives an overview of each of the Connectivity functions Each function is described in detail in the following pages 3 20 LOGIQ e User Guide Direction 5314626 100 Rev 3 Configuring Connectivity Connectivity Functions To set up your institution s connectivity you must login with administrator privileges 1 TCPIP allows you to configure the Internet Protocol 2 Device allows you to set up devices 3 Service allows you to configure a service for example DICOM services such as printers worklist and other services such as video print and standard print from the list of supported servi
96. ns seal and connector DO NOT use a transducer which appears damaged until functional and safe performance is verified A thorough inspection should be conducted during the cleaning process Align the connector with the probe port and carefully push into place with the cable facing the front of the system Flip the connector locking lever up Carefully position the probe cord so it is free to move and is not resting on the floor When the probe is connected it is automatically activated LOGIQ e User Guide Direction 5314626 100 Rev 3 Probes Connecting the Probe continued when the probe is removed Do not touch the patient when CAUTION Fault conditions can result in electric shock hazard Do not touch the surface of probe connectors which are exposed connecting or disconnecting a probe LOGIQ e User Guide 1 21 Direction 5314626 100 Rev 3 Getting Started Cable Handling Disconnecting the 1 22 Take the following precautions with probe cables Do not bend the cable acutely Probe Probes can be disconnected at any time However the probe should not be active when disconnecting the probe Press the connector locking lever down Pull the probe and connector straight out of the probe port Carefully slide the probe and connector away from the probe port and around the right side of the keyboard Ensure the cable is free Be sure that the probe head is clean before placing the probe in its storage
97. nt transmission between patients is with single use or disposable devices However ultrasound transducers are complex and expensive devices that must be reused between patients It is very important therefore to minimize the risk of disease transmission by using barriers and through proper processing between patients Risk of Infection ALWAYS clean and disinfect the probe between patients to the level appropriate for the type of examination and use FDA cleared probe sheaths where appropriate See Supplies Accessories on page 3 33 for ordering information Adequate cleaning and disinfection are necessary to prevent disease transmission It is the responsibility of the equipment user to verify and maintain the effectiveness of the infection control procedures in use Always use sterile legally marketed probe sheaths for intra cavitary and intra operative procedures For neurological intra operative procedures use of a legally marketed sterile pyrogen free probe sheath is REQUIRED Probes for neuro surgical use must not be sterilized with liquid chemical sterilants because of the possibility of neuro toxic residues remaining on the probe LOGIQ e User Guide Direction 5314626 100 Rev 3 Probe Overview Endocavitary Probe Handling Precautions If the sterilization solution comes out of the endocavitary probe please follow the cautions below CAUTION Sterile sanitary sheaths are to be used on the probe during its actual use w
98. o the database prior to the exam NOTE If you are using the auto generate Patient ID feature do not select Register e Details Select the Detail box to activate deactivate the exam details Exam details include Indications Comments Admission Number and Exam Description Figure 1 14 Detail Window 3 EZBackup One step method to backup patient images to an external media EZMove Move and delete patient images 1 28 LOGIQ e User Guide Direction 5314626 100 Rev 3 Beginning an Exam Patient Screen continued WARNING NOTE NOTE NOTE NOTE LOGIQ e User Guide 4 Dataflow Selection Select the appropriate dataflow If you place the cursor on the icon the pop up menu displays disk capacity Ensure you have selected a dataflow If No Archive is selected no patient data is saved A appears next to Dataflow if No Archive is selected 5 Exit Used to exit Patient Menu 6 Patient Information e Patient ID Number e Other ID Number The Other ID is used to add additional information of the patient such as Citizen ID The Other ID field is only available on LOGIQ e R6 x x To enable disable the Other ID field go to Utility gt Connectivity gt Miscellaneous To select Other ID format go to Utility gt Connectivity gt Miscellaneous The Other ID must be unique The Other ID must be accordant with the selected format e Patient Name Last First and Middle DOB Birthdate
99. on 220 240 VAC 2 5A China 220 240 VAC 2 5A Switzerland 220 240 VAC 2 5A India 220 240 VAC 2 54 U K 220 240 VAC 2 5A Argentina 100 120 VAC 2 5A USA 220 240 VAC 2 5A Europe 220 240 VAC 2 5A Israel 100 120 VAC 2 5A Japan 220 240 VAC 2 5A Australia LOGIQ e User Guide Direction 5314626 100 Rev 3 1 5 Getting Started Console graphics The following are illustrations of the console Figure 1 1 LOGIQ e System opened view 1 Handle 2 Soft Menu use same as menu key 3 LCD 4 Alphanumeric keys 5 Control Panel 1 6 LOGIQ e User Guide Direction 5314626 100 Rev 3 Console Overview Console graphics continued i ooo 0 Om Figure 1 2 LOGIQ e System side views CAUTION Do not push objects into air vents and openings of LOGIQ e Doing so can cause fire or electric shock by shorting out interior components CAUTION For compatibility reasons use only GE approved probes peripherals or accessories DO NOT connect any probes or accessories without approval by GE LOGIQ e User Guide 1 7 Direction 5314626 100 Rev 3 Getting Started Battery NOTE WARNING 1 8 The lithium ion battery provides power when an AC power source is not available A battery in the battery bay is standard with the LOGIQ e Lithium ion batteries last longer than conventional batteries and do not require
100. on the label CAUTION Dangerous voltage the lightning flash with arrowhead is used to indicate electric shock hazards Biohazard Patient user infection due to contaminated equipment Usage Cleaning and care instructions Sheath and glove guidelines ae gt gt Ultrasound probes are highly sensitive medical instruments that can easily be damaged by improper handling Use care when handling and protect from damage when not in use Do not immerse the probe into any liquid beyond the level specified for that probe Refer to the user manual of the ultrasound system Since there is a possibility of having negative effects on the probe observe the specified immersing time by the germicide manufacturer strictly Do not immerse the probe in liquid chemical germicides more than the time prescribed in the care card 3 6 LOGIQ e User Guide Direction 5314626 100 Rev 3 Probe Overview Disinfecting probes continued CAUTION LOGIQ e User Guide Review the probe care card that is packed with each probe The following website contains the most current and up to date recommendations http www gehealthcare com usen ultrasound products probe_care html Cidex Plus has been approved for all probes available on the LOGIQ e Pera Safe high level disinfectant has been approved for the E8C RS 8C RS and 12L RS probes T spray low level disinfectant has been approv
101. ons Follow all infection control policies established by your office department or institution as they apply to personnel and equipment 4 9 Direction 5314626 100 Rev 3 Safety Related Hazards continued 4 10 CAUTION CAUTION CAUTION Contact with natural rubber latex may cause a severe anaphylactic reaction in persons sensitive to the natural latex protein Sensitive users and patients must avoid contact with these items Refer to package labeling to determine latex content and FDA s March 29 1991 Medical Alert on latex products Archived data is managed at the individual sites Performing data backup to any device is recommended DO NOT use high frequency surgical equipment with the LOGIQ e LOGIQ e User Guide Direction 5314626 100 Rev 3 General Caution CAUTION CAUTION CAUTION LOGIQ e User Guide Safety Precautions Standard maintenance must be performed by authorized service personnel for the lifetime of the product 7 years Proceed cautiously when crossing door or elevator thresholds with the Docking Cart or Isolation Cart Use the handle to push pull the system e g do not use the Docking Cart external LCD Failure to do so may cause serious injury or system damage Capacity load of the Docking Cart The maximum capacity load of the Storage rack 1 is 2kg DVD RW Shelf 2 is 2kg B W Printer Shelf 3 is 4kg Color Printer Shelf 4 is 7kg and UPS Shelf 5 is 9kg refer to the
102. oper identification with all patient data and verify the accuracy of the patient s name and ID numbers when entering such data Make sure correct patient ID is provided on all recorded data and hard copy prints Identification errors could result in an incorrect diagnosis If the LOGIQ e needs to be sent for repair ensure that any patient information is backup and erased from the system before shipping In case that any patient information is still residing on the LOGIQ e GE will contact the customer and request for urgent collection of that patient information GE will keep this patient information in a secure environment for a maximum period of 1 month All patient information will be permanently deleted at that point Equipment malfunction or incorrect settings can result in measurement errors or failure to detect details within the image The equipment user must become thoroughly familiar with the equipment operation in order to optimize its performance and recognize possible malfunctions Applications training is available through the local GE representative Added confidence in the equipment operation can be gained by establishing a quality assurance program 4 5 Direction 5314626 100 Rev 3 Safety Related Hazards continued Mechanical hazards e Electrical a Hazard CAUTION CAUTION 4 6 The use of damaged probes can result in injury or increased risk of infection Inspect probes often for sharp pointed or rou
103. orizontal dotted lines displays To position the caliper at the start point move the Trackball To fix the start point press Set The system fixes the first caliper and displays a second active caliper To position the second caliper at the end point move the Trackball To complete the measurement press Set The system displays the two peak end point velocities the time interval and the acceleration in the Results Window To measure a horizontal time interval 1 LOGIQ e User Guide Press Measure four times an active caliper with a vertical dotted line displays To position the active caliper at the start point move the Trackball To fix the start point press Set The system fixes the first caliper and displays a second active caliper To position the second caliper at the end point move the Trackball To complete the measurement press Set The system displays the time interval between the two calipers in the Results Window 2 21 Direction 5314626 100 Rev 3 Performing an Exam M Mode Measurements NOTE Tissue depth 2 22 Basic measurements that can be taken in the M Mode portion of the display are e Tissue Depth Distance e Time Interval e Time Interval and Velocity The following instructions assume that you do the following 1 In the B Mode part of the display scan the anatomy you want to measure 2 Go to the M Mode part of the display 3 Press Freeze Tissue depth measurement in
104. pears on the screen Use the Trackball to move the cursor To delete all comments press the Clear key twice immediately after entering the comment mode Arrow pointers can be used by activating the F2 Arrow key on the keyboard When the pointer comes up it is a GREEN color indicating it is active and can be moved Direction 5314626 100 Rev 3 Performing an Exam Measurement and Analysis B Mode Measurements Two basic measurements can be made in B Mode e Distance e Circumference and Area e Ellipse Method e Trace Method Spline Method NOTE The following instructions assume that you first scan the patient and then press Freeze 2 12 LOGIQ e User Guide Direction 5314626 100 Rev 3 Distance measurement Measurement and Analysis To make a distance measurement 1 2 Press Measure once an active caliper displays To position the active caliper at the start point move the Trackball To fix the start point press Set The system fixes the first caliper and displays a second active caliper To position the second active caliper at the end point move the Trackball A dotted line connects the measurement points if preset accordingly To complete the measurement press Set The system displays the distance value in the Results Window The following hints can help you to perform distance measurements HINTS LOGIQ e User Guide Before you complete a measurement e To toggle between a
105. r than the frequency shift of the signal Using this technique the ultrasound system plots color flow based on the number of reflectors that are moving regardless of their velocity PDI does not map velocity therefore it is not subject to aliasing M Color Flow Mode Yes M Color Flow is used for fetal cardiac applications Color Flow overlays color on the M Mode image using velocity and variance color maps The Color Flow wedge overlays the B Mode image and M Mode timeline The Color Flow maps available in M Mode are the same as in Color Flow Mode The size and position of the Color Flow window in B Mode determines the size and position of the Color Flow window in M Mode All M Mode measurements are available with M Color Flow active depth distance along a straight line stenosis volume trace circumference enclosed area distance time slope and heart rate 2 6 LOGIQ e User Guide Direction 5314626 100 Rev 3 Doppler Mode Controls Optimizing the Image Table 2 4 Doppler Mode Controls Possible Control Bioeffect Description Benefit B Pause Yes Toggles between simultaneous and update presentation while viewing the timeline Doppler sample Yes Moves the sample volume gate on the B Mode s Doppler Mode volume gate position cursor The gate is positioned over a specific position within the Trackball vessel Doppler sample Yes Sizes the sample volume ga
106. re environmentally qualified The use of this equipment in an inappropriate environment may cause some electronic interference to radios and televisions around the equipment Ensure that the following is provided for the new system e A separate power outlet with a 6 amp circuit breaker for 220 240 VAC or a 10 amp circuit breaker for 100 120 VAC e Take precautions to ensure that the console is protected from electromagnetic interference Precautions include e Operate the console at least 15 feet away from motors typewriters elevators and other sources of strong electromagnetic radiation e Operation in an enclosed area wood plaster or concrete walls floors and ceilings helps prevent electromagnetic interference e Special shielding may be required if the console is to be operated in the vicinity of radio broadcast equipment To avoid risk of fire the system power must be supplied from a separate properly rated outlet Under no circumstances should the AC power plug be altered changed or adapted to a configuration rated less than specified Never use an extension cord or adapter plug To help assure grounding reliability connect to a hospital grade or hospital only grounded power outlet LOGIQ e User Guide Direction 5314626 100 Rev 3 Important Notices continued Table 1 1 Console Overview Example Plug and Outlet Configurations AC DC Type Specification AC DC Type Specificati
107. rval and velocity 2 23 tissue depth 2 22 M Mode general measurements 2 22 Monitor 3 30 moving the system 1 17 O Operator controls 3 31 P patient safety 4 5 Index 2 Power Cord 1 17 On Off Standby 1 18 switch location 1 78 power shut down 1 19 prescription device caution 1 3 presets changing Connectivity 3 20 Probe handling and infection control 3 2 probe identifier locating 1 15 probes cable handling 1 22 cleaning 3 4 connecting 1 20 coupling gels coupling gels probes 3 10 disconnecting 1 22 disinfecting 3 6 prudent use 4 2 R Results window display location 1 15 moving to new location 1 15 S safety electromagnetic compatiblity EMC 4 19 equipment 4 8 hazards 4 3 4 8 4 9 4 32 smoke and fire 4 9 labels 4 14 patient 4 5 acoustic output hazard hazard types acoustic output 4 6 electrical hazards 4 6 mechanical hazards 4 6 patient identification 4 5 patient training ALARA 4 7 personnel 4 8 precaution icons defined 4 2 precaution levels defined 4 2 probes handling precautions 3 2 service requesting 3 24 system electrical configurations 1 4 power down 1 19 System cabinet 3 30 T TAMAX and TAMEAN Doppler mode measurement auto trace 2 19 manual trace 2 19 LOGIQ e User Guide Direction 5314626 100 Rev 3 Time interval Doppler mode measurement 2 27 M Mode measurement 2 23
108. s Clear once The original caliper is displayed to restart the measurement To exit the measurement function without completing the measurement press Clear a second time LOGIQ e User Guide Direction 5314626 100 Rev 3 Measurement and Analysis Circumference and area trace measurement Trace To trace the circumference of a portion of the anatomy and calculate its area 1 2 Press Measure until a trace caliper displays To position the trace caliper at the start point move the Trackball To fix the trace start point press Set The trace caliper changes to an active caliper To trace the measurement area move the Trackball around the anatomy A dotted line shows the traced area To complete the measurement press Set The system displays the circumference and the area in the Results Window Open Trace To trace the circumference of a portion of the anatomy and calculate its length 1 Press Measure until a trace caliper displays NOTE For open trace Area A is not displayed in the result window 2 To position the trace caliper at the start point move the Trackball 3 To fix the trace start point press Set The trace caliper changes to an active caliper 4 To trace the measurement area move the Trackball around the anatomy A dotted line shows the traced area 5 To complete the measurement press Set The system displays the circumference and the length in the Results Window HINTS Before you comple
109. se by a qualified physician for ultrasound evaluation Specific clinical applications and exam types include Fetal Obstetrics Abdominal including GYN Pediatric Small Organ including breast testes thyroid Neonatal Cephalic Adult Cephalic Cardiac adult and pediatric Peripheral Vascular Intraoperative abdominal thoracic and peripheral Thoracic Pleural fluid motion detection Musculo skeletal Superficial Musculo skeletal Conventional Urology including prostate Transrectal Transvaginal Transesophageal CAUTION This machine should be used in compliance with law Some jurisdictions restrict certain uses such as gender determination Contraindication The LOGIQ e ultrasound system is not intended for ophthalmic use or any use causing the acoustic beam to pass through the eye Prescription Device ONLY CAUTION United States law restricts this device to sale or use R U S by or on the order of a physician e e LOGIQ e User Guide 1 3 Direction 5314626 100 Rev 3 Getting Started Important Notices NOTICE WARNING Do not attempt to install the system alone General Electric Affiliate or Distributor Field Engineers and Application Specialists will install and setup the system See Contact Information on page 3 24 for more information This medical equipment is approved in terms of the prevention of radio wave interference to be used in hospitals clinics and other institutions which a
110. selected patients number of patients currently displayed on the list number of patients in the database Review Select Patient Exam for review Resume Exam Continues the exam for that patient if you select the last exam of the day New Exam Creates a new exam on a current patient Delete Deletes Patient Exam Delete is only displayed when you login as Administrator Hide Hides the Patient List Section Lock Unlock Locks the exam patient Prevents move and delete functions Exam View Displays the Exam History of the selected patient CAUTION To avoid patient identification errors always verify the identification with the patient Make sure the correct patient identification appears on all screens and hard copy prints LOGIQ e User Guide Direction 5314626 100 Rev 3 Beginning an Exam Patient Screen continued CAUTION NOTE NOTE NOTE LOGIQ e User Guide To maintain optimum performance and to safeguard patient data keep the total number of patients in the database below 1 000 To reduce the total number of patients in the database perform the following procedure 1 Prepare the unformatted CD R DVD R or USB HDD before EZBackup Formatted CD R or DVD R cannot be used for EZBackup Backup all patient data by EZBackup Before beginning EZBackup set the Backup Files Older Than in Days to 0 on the Utility gt System gt Backup Restore gt EZBackup Move scree
111. sively on the cord or make sharp bends while wrapping Store all probes in their original cases or in soft cloth or foam to prevent damage Store sufficient gel and other essential accessories in the special storage case When moving the system 1 Always use the handle to move the system CAUTION The system weighs approximately 4 6 kg 10 1 Ibs To avoid possible injury and equipment damage LOGIQ e User Guide Do not let the system strike walls or door frame Limit movement to a slow careful walk Direction 5314626 100 Rev 3 Getting Started System Start Up Power On CAUTION Press the Power On Off switch to turn the power on The circuit breaker must also be in the on position Figure 1 10 LED Indicators 1 Indicates hard disk working status When the LED is flashing the system is writing or reading from the hard disk Color Green 2 Indicates power status After pressing the Power On Off switch the system power is on and this LED is lit Color Green 3 Indicates battery status When the battery is charged the LED is green When battery power is low the LED is orange Color Green and Orange 4 The fourth LED does not work on the LOGIQ e 1 18 LOGIQ e User Guide Direction 5314626 100 Rev 3 Power Off NOTE NOTE NOTE LOGIQ e User Guide System Start Up To power off the system 1 When you shutdown the system enter the scan screen and lightly press the Power On Off switch at the
112. ssion 0 Range Focus Off SRI HD 3 Figure 6 4 6 6 B Mode Top Sub Menu LOGIQ e User Guide Direction 5314626 100 Rev 3 Color Flow CF Mode Intended Uses Color Flow Mode is a Doppler Mode intended to add color coded qualitative information concerning the relative velocity and direction of fluid motion within the B Mode image GE Healthcare MI0 8 Tis1 5 12L RS 07 24 07 2 43 40 PM 1 1 Superficial GE Le 205 205 15 1 15 1 s Carotid Rt Lt Z Stenosis AB Ratio 4 8 kHz 447 Hz HR SIP 3 4 Worksheet CF z ee hi Frequency 2 B Mode Gain OE BE Figure 6 5 Color Flow Mode Display LOGIQ e User Guide 6 7 Direction 5314626 100 Rev 3 Nerve Block CF Mode Top Sub Menu The following Top Sub Menu controls are available for functionality adjustment and image optimization See Chapter 2 for more details on these controls Frequency 2 3 Invert 5 B Mode Gain CF Mode Baseline Line Density 0 Flash Suppression 1 Transparency Map 0 Focus Position Frame Average 3 Figure 6 6 CF Mode Top Sub Menu 6 8 LOGIQ e User Guide Direction 5314626 100 Rev 3 Power Doppler Imaging PDI Mode Intended Uses Power Doppler Imaging PDI is a color flow mapping technique used to map the strength of the Doppler signal coming from the flow rather than the frequency shift of the signal Using this technique the ultrasound system plots color flow based on the number of reflectors that
113. stem to update DO NOT check Patient Archive when making a backup of configuration settings Insert media into the media drive On the Control Panel press Utility Select System On the monitor display select Backup Restore The Backup Restore screen is displayed If you are not logged in with administrator privileges the Operator Login window is displayed Log on with administrator privileges Os E 5 In the Backup list select User Defined Configuration 6 In the Media field select a media 7 Select Backup The system performs the backup As it proceeds status information is displayed on the Backup Restore screen 8 After the backup is complete press F3 to eject the media LOGIQ e User Guide Direction 5314626 100 Rev 3 Backup and Restore Restore procedure user defined configurations CAUTION CAUTION NOTE LOGIQ e User Guide The restore procedure overwrites the existing database on the local hard drive Make sure to insert the correct media DO NOT restore data between systems with different software versions To avoid the risk of overwriting the local patient archives DO NOT check Patient Archive when restoring user defined configurations 1 Insert the media with the user defined configurations into the drive 2 On the Control Panel press Utility 3 Select System 4 Onthe monitor display select Backup Restore The Backup Restore screen is displayed If you are not logged in with admi
114. te volume length PRF Yes Adjusts the velocity scale to accommodate faster slower blood flow velocities Velocity scale determines pulse repetition frequency If the sample volume gate range exceeds single gate PRF capability the system automatically switches to high PRF mode Multiple gates appear and HPRF is indicated on the display Angle Correct No Estimates the flow velocity in a direction at an angle to the Doppler vector by computing the angle between the Doppler vector and the flow to be measured NOTE When the Doppler Mode Cursor and angle correct indicator are aligned the angle is O you cannot see the angle correct indicator Quick Angle No Quickly adjusts the angle by 60 degrees Wall Filter No Insulates the Doppler signal from excessive noise caused from vessel movement Baseline No Adjusts the baseline to accommodate faster or slower blood flows to eliminate aliasing M D Cursor No Displays the Doppler Mode cursor on the B Mode image Audio Volume No Controls audio output Invert No Vertically inverts the spectral trace without affecting the baseline position Dynamic Range No Dynamic range controls how echo intensities are converted to shades of gray thereby increasing the range of contrast you can adjust Spectral Trace No Traces the average mean and peak velocities in realtime or frozen Trace Method images Trace Sensitivity No Adjust the trace to follow the waveform for signal strength Cycles to Average No
115. te the trace measurement LOGIQ e User Guide To erase the line bit by bit back from its current point move the Trackball or adjust the Ellipse control counterclockwise To erase the dotted line but not the trace caliper press Clear once To clear the trace caliper and the current data measured press Clear twice Direction 5314626 100 Rev 3 Performing an Exam Circumference and area spline trace measurement To trace the circumference of a portion of the anatomy and calculate its area 1 2 3 NOTE 4 NOTE 5 NOTE 2 16 Press Measure until a trace caliper displays To position the first caliper at the start point move the Trackball To fix the trace start point press Set The first caliper turns yellow The second caliper appears at the same position as the first caliper and is green When pressing the Clear key once the second caliper disappears and the first caliper is activated If Clear is pressed again the first caliper disappears and the Spline trace is cancelled To position the second caliper move the Trackball and press Set The third caliper appears at the same position The Clear key functionality is the same as noted in the previous step The spline trace requires at least three points to draw the trace Continue setting the points of the trace until the desired points are set Press Set twice to finish this measurement If Clear is pressed twice when more than 3 poin
116. tem is in a state of freeze or live Continuous Wave No Allows examination of blood flow data all along the Doppler Mode Doppler CWD cursor rather than from any specific depth Gather samples along the entire Doppler beam for rapid scanning of the heart Range gated CW allows information to be gathered at higher velocities 2 8 LOGIQ e User Guide Direction 5314626 100 Rev 3 Optimizing the Image Other Controls Zoom amp Acoustic Output Hazard Freezing an image NOTE Activating CINE LOGIQ e User Guide Zoom is used to magnify a zoom region of interest ROI The system adjusts all imaging parameters accordingly You can also zoom frozen images Observe the output display for possible effects To zoom an image adjust Zoom A reference image appears in the upper left hand section of the display To exit zoom adjust Zoom until the reference zoom image is removed or press B Mode To freeze an image 1 Press Freeze The key backlights If you are in a mixed mode both screen formats stop immediately Deactivating Freeze restarts both modes and places a black bar on the trace to indicate the time discontinuity To reactivate the image 1 Press Freeze again Deactivating Freeze erases all measurements and calculations from the display but not from the worksheet Use the Trackball to start CINE after pressing Freeze To activate CINE 1 Press Freeze 2 Move the Trackball 2 9
117. ternal function CISPR 11 Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF Emissions Class A This system is suitable for use in all establishments other than CISPR 11 domestic establishments and those directly connected to the public low voltage power supply network that supplies buildings Harmonic Class A used for domestic purposes provided the following warning is Emissions heeded IEC 61000 3 2 WARNING This system is intended for use by healthcare Vol c ji professionals only This system may cause radio interference or B tage ions Flick ompiies may disrupt the operation of nearby equipment It may be uctuations lex necessary to take mitigation measures such as re orienting or Emissions relocating the system or shielding the location IEC 61000 3 3 4 26 LOGIQ e User Guide Direction 5314626 100 Rev 3 Declaration of Immunity Safety Precautions This system is suitable for use in the following environment The user must assure that the system is used according to the specified guidance and only in the electromagnetic environment listed Table 4 6 Declaration of Immunity Immunity Equipment Regulatory EMC Environment and Type Capability Acceptable Level Guidance IEC 61000 4 2 6 kV contact 6 kV contact Floors should be wood concrete or Static discharge ceramic tile If floors are covered with ESD 8 KV air 8 kV air synthetic material the rel
118. tery not present appears When using a battery it s current capacity in percent appears current capacity unit percent If the battery is not in use it states current capacity charging Warning information displays warning information when battery power is low See Figure 1 5 LOGIQ e User Guide 1 11 Direction 5314626 100 Rev 3 Getting Started Battery continued Battery power low If the battery is in use and the battery power is low a warning warning message appears to warn the user that the battery power is low and that it needs to be charged Figure 1 5 Low battery power warning NOTE When the battery power is low and the user cannot charge the battery in time the system automatically shuts down in 2 minutes This protects the whole system You need to save all unsaved data before the system shuts down or you may lose useful information AC Adapter CAUTION Do not use an AC adapter without approval by GE Be sure that nothing rests on the AC adapter s power cable and that the cable is not located where it can be tripped over or stepped on Place the AC adapter in a ventilated area such as a desk when you use it to run LOGIQ e Do not cover the AC adapter with paper or other items that will reduce cooling do not use the AC adapter inside a carrying case To prevent damage to the power cable of the AC adapter DO NOT pull excessively on the cable DO NOT make any sharp bends DO NO
119. th solutions containing alcohol bleach ammonium chloride compounds or hydrogen peroxide e Avoid contact with solutions or coupling gels containing mineral oil or lanolin e Avoid temperatures above 60 C e Inspect the probe prior to use for damage or degeneration to the housing strain relief lens and seal Do not use a damaged or defective probe 3 9 Direction 5314626 100 Rev 3 After the Exam is Over Coupling gels WARNING Applying CAUTION Precautions 3 10 Do not use unrecommended gels lubricants They may damage the probe and void the warranty In order to assure optimal transmission of energy between the patient and probe a conductive gel or couplant must be applied liberally to the patient where scanning will be performed Do not apply gel to the eyes If there is gel contact to the eye flush eye thoroughly with water Coupling gels should not contain the following ingredients as they are known to cause probe damage Methanol ethanol isopropanol or any other alcohol based product Mineral oil lodine Lotions Lanolin Aloe Vera Olive Oil Methyl or Ethyl Parabens para hydroxybenzoic acid Dimethylsilicone Polyether glycol based LOGIQ e User Guide Direction 5314626 100 Rev 3 System Presets System Presets Foreign Language Keyboard Setup Keyboard Setup for non Russian Greek Chinese Japanese Languages To set up the keyboard for non Russian Greek Chinese Japanese languages
120. time interval and velocity M Mode measurements 2 23 Tissue depth M Mode measurement 2 22 Trace measurement general 2 15 2 16 Trackball functionality status display location 1 15 U Utility screens connectivity 3 20 V Velocity Doppler measurement 2 18 Ww Warning icon defined 4 2 Worksheet changing data 2 26 viewing 2 24 LOGIQ e User Guide Direction 5314626 100 Rev 3 Index 3 Index 4 LOGIQ e User Guide Direction 5314626 100 Rev 3
121. ting the Touch Screen mode to avoid keyboard contamination of blood chemicals etc LOGIQ e User Guide Direction 5314626 100 Rev 3 Touch Screen Display GE Healthcare 09 08 08 11 25 37 PM ADM 090808 112707 PM 1 1 GE le bi Patient 4 f7 Preset ADC Comment 7 Measure End Exam Clear All lt gt Mode gt Cine mode Reverse Loop Forward Loop Figure 7 1 Patient click to register patient Preset click to go into Preset Screen Comment click to add comments Measure click to start 2D measurement End Exam click to end current exam and system will auto store images permanently B Pause click to toggle between real time B Mode with Doppler Mode with audio 7 Clear All click to clear all the annotations an measurements 8 Mode Panel Bar click to select mode De ON D LOGIQ e User Guide Direction 5314626 100 Rev 3 9 10 11 12 13 14 15 16 17 MI 0 5 Tis0 3 8L RS Carotid E 48 a WW Freq 10 0 MHz Depth a0 em y v Focus Position Run Stop Touch Screen Display Tour Top Menu Freeze P1 P3 click to store images Power Output Focus Position Control Depth Control Frequency Control Gain Control click fast forward to increase or fast backward to decrease gain by larger steps Scroll Button click to go to previous next clipboard gallery 7 3 Starting a New Patient Press the Patient Touch Screen key a patient ID
122. ts exist on the trace all points are removed and the first caliper again displays Spline trace is not available through the factory default The system defaults to trace To enable spline trace modify the Measure Key Sequence preset found in Utility gt Measure gt Advanced preset menu LOGIQ e User Guide Direction 5314626 100 Rev 3 Measurement and Analysis Circumference and area spline trace measurement continued Edit the spline trace NOTE NOTE NOTE NOTE LOGIQ e User Guide 1 Select Cursor Select The spline trace changes to green and all points appear on the trace as yellow A pick caliper appears on the center of the image and the message Edit spline trace displays at the bottom of the screen The pick caliper is used to select and move the trace points p Figure 2 1 Edit spline trace Select Cursor Select again The trace is deactivated changes to yellow and all points including the pick caliper are removed If the previous next fixed caliper exists on the image it is activated Pressing Clear at this time removes all points and the trace graphic Move the pick caliper to the desired point and press Set The point is activated and turns green Move the point to the desired position and press Set The point is fixed and turns yellow The pick caliper appears on the center of the image The spline trace is updated at run time To remove a point press Clear while mo
123. urological procedures must be done with the use of legally marketed sterile pyrogen free probe sheaths 3 After removing from the germicide rinse the probe following the germicide manufacturer s rinsing instructions Flush all visible germicide residue from the probe and allow to air dry LOGIQ e User Guide Direction 5314626 100 Rev 3 Probe Overview Disinfecting probes continued WARNING Biological Hazard Ss WARNING LOGIQ e User Guide CREUTZFIELD JAKOB DISEASE Failure of the probe sheath or direct contact of the probe with dura or any intra cranial tissue of patients with Creutzfield Jakob disease requires that the probe be destroyed There is no effective means for decontamination of the probe For more information see the Center of Disease Control and Prevention http www cdc gov ncidod hip sterile cjd htm Ultrasound transducers can easily be damaged by improper handling and by contact with certain chemicals Failure to follow these precautions can result in serious injury and equipment damage Do not immerse the probe into any liquid beyond the level specified for that probe Never immerse the transducer connector or probe adapters into any liquid e Avoid mechanical shock or impact to the transducer and do not apply excessive bending or pulling force to the cable e Transducer damage can result from contact with inappropriate coupling or cleaning agents Do not soak or saturate transducers wi
124. ut to get the best diagnostic image or measurement during an examination Begin the exam with the probe that provides an optimum focal depth and penetration Acoustic Output Default Levels 4 32 In order to assure that an exam does not start at a high output level the LOGIQ e initiates scanning at a reduced default output level This reduced level is preset programmable and depends upon the exam category and probe selected It takes effect when the system is powered on or New Patient is selected To modify acoustic output adjust the Power Output level on the Top Sub Menu LOGIQ e User Guide Direction 5314626 100 Rev 3 Safety Precautions Warning Label Locations LOGIQ e warning labels are provided in English United States law restricts this device to sale or use by or on the order of a 5 physician To C Eio X CISPR 11 EN 55011 CLASS A GROUP 1 CLASSE A GROUPE 1 Figure 4 5 Label location Be careful of static Prescription Device For U S A Only 1 Consult accompanying document is intended to alert the user to refer to the operator manual Oso or other instructions when complete information WEEE Label cannot be provided on the label The CE Mark of Conformity indicates this 2 Possible shock hazard Do not remove covers equipment conforms with the Council Directive or panels No user serviceable parts are inside 93 42 EEC Refer servicing to qualified service personnel 8 C
125. ving the point The trace turns green and the remaining points continue to be shown as yellow If there are less than three points the spline trace is removed Press Set again All points are removed from the trace and the trace is shown as yellow Direction 5314626 100 Rev 3 Performing an Exam Doppler Mode Measurements Velocity 2 18 NOTE Four basic measurements can be made in Doppler Mode e Velocity TAMAX and TAMEAN Manual or Auto Trace e Two Velocities with the Time Interval and Acceleration between them e Time Interval The following instructions assume that you do the following 1 In the B Mode part of the display scan the anatomy you want to measure 2 Go to the Doppler Mode part of the display 3 Press Freeze To measure velocity 1 Press Measure an active caliper with a vertical dotted line displays 2 To position the caliper at the desired measurement point move the Trackball 3 To complete the measurement press Set The system displays the velocity measurement in the Results Window LOGIQ e User Guide Direction 5314626 100 Rev 3 TAMAX and TAMEAN Measurement and Analysis Manual Trace The value measured depends upon the Vol Flow Method preset The two selections available are Peak TAMAX and Mean TAMEAN To do a manual trace of TAMAX or TAMEAN 1 2 Press Measure twice a trace caliper displays To position the caliper at the trace start point move the Tra
126. will be auto generated and begins a new exam Selecting an Application Preset and a Probe Press the Preset Touch Screen key to display the Preset Screen on the monitor Select the probe or application by pressing it GE Healthcare MI0 5 Tis0 2 4C RS 96 07 08 08 11 33 11 PM 1 1 Abdomen Gain 86 Ea Patient re Vv z 7 Preset Frea 5 2 MHz Abc Comment 7 Measure Depth 20 0 cm a End Exam v E Focus Position R B Pause Clear All Power Output 100 Mode gt Cine mode Reverse Loop Forward Loop Run Stop Figure 7 2 Application Preset 7 4 LOGIQ e User Guide Direction 5314626 100 Rev 3 B Mode Intended Uses B Mode is intended to provide two dimensional images and measurement capabilities concerning the anatomical structure of soft tissue GE Healthcare MI0 8 Tis0 4 8C RS 96 08 01 08 10 36 08 PM 1 1 Neo Abd C Ea g Patient A f7 Preset Frequency 8 0 MHz Abc Comment A v f7 Measure Depth 8 0 cm N v Focus Position A Clear All v Power Output 100 Mode gt B mode CrossXBeam Harmonics B Steert Virtual Convex Figure 7 3 B Mode Display LOGIQ e User Guide 7 5 Direction 5314626 100 Rev 3 Using Touch Screen B Mode Top Menu 7 6 Adjust the image by using the controls on the right If additional functionality is needed the following Top Menu controls are available See Chapter 5 for more details on
127. xit current display screen Access Online help user manual Annotation arrow Eject media Activates DICOM Job Spooler screen Reverse The following functions are available for the F6 F11 keys TDI CWD 3D LOGIQ View CrossxBeam ECG On Off Set Home Text Overlay Grab Last Word Delete Protocol and Video DVR Activates deactivates Touch Screen Mode Enter the Utility function for system configuration and customization Access system Applications and presets Access the report page LOGIQ e User Guide Direction 5314626 100 Rev 3 Monitor Display ZN GE Healthcare amp Lastname Firstname 10 24 05 10 34 40 PM ADM 11 v 20 42 1 4 3 1 s 28 cm s Vascular 20 942249 Console Overview MI 1 4 Tis 2 5 8L RS mien Carotid SIP 4m4 Cursor Select 23 Figure 1 8 Monitor Display Tour 1 Institution Hospital Name Date Time Operator Identification 2 Patient Name Patient Identification 3 Power Output Readout 4 GE Symbol Probe Orientation Marker 5 Image Preview 6 Gray Color Bar 7 Cine Gauge 8 Measurement Summary Window 9 Image 10 Measurement Calipers 11 Measurement Results Window 12 Probe Identifier Exam Preset LOGIQ e User Guide Direction 5314626 100 Rev 3 13 14 15 16 17 18 19 20 21 22 23 Imaging Parameters by Mode Focal Zone Indicator TGC Body Pattern Depth Scale Top Sub Menu Caps Lock On or Off

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