User Guide
154 Pages
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AT-2 User Guide - English AT-2 Gebrauchsanweisung -Deutsch Guide de l’Utilisateur pour l’AT-2 - Français Article Number 2. 510199e Sept.95, March 96, June 2000, May 2001, August 2001
Associated Documents Guide to the SCHILLER Interpretation and Measurement Program E/ D/ F Article Number 2. 510 179
SCHILLER AG Altgasse 68 6341 Baar, Switzerland Phone: ++ 41 41 766 42 42 Fax: ++ 41 41 761 08 80 www.schiller.ch
AT-2 User Guide - English AT-2 Gebrauchsanweisung -Deutsch Guide de l’Utilisateur pour l’AT-2 - Français Article Number 2. 510199e Sept.95, March 96, June 2000, May 2001, August 2001
Associated Documents Guide to the SCHILLER Interpretation and Measurement Program E/ D/ F Article Number 2. 510 179
SCHILLER AG Altgasse 68 6341 Baar, Switzerland Phone: ++ 41 41 766 42 42 Fax: ++ 41 41 761 08 80 www.schiller.ch
Where to Obtain Service and Sales Advice Kundendienst und Verkaufs-/Beratungsstellen Coordonnées de nos services d’assistance technique et commerciale
WELCH ALLYN SCHILLER Inc., 7420 Carroll Road, San Diego, CA , US-92121-2334 USA USA / Canada
Tel.: +1 858 635 6023
Fax : +1 858 635 6611
Home Page : www.welchallyn.com Asia Pacific
Austria
France Germany
SCHILLER Asia Pacific, 10 Jalan SS 3/33, Taman Universiti, 47300 Petaling Jaya, Selangor, Malaysia Tel.: + 603 7877 5336
Fax : + 603 7877 5744
SCHILLER HmbH, Kampmüllerweg 24, A-4044 Linz, Austria Tel.: + 43 732 709 90
Fax : + 43 732 757 000
SCHILLER Medical S.A, BP 50, 19, Avenue de la Gare, F-67162 Wissembourg / Cedex, France Tel.: +33 3 88 63 36 00
Fax : +33 3 88 94 12 82
SCHILLER Medizintechnik GmbH, Rudolf-Diesel Strasse 14, D-85521 Ottobrunn, Germany
(EU authorized representative)
Tel.: + 4989 629 981 0
Fax : + 4989 609 509 0
India
Kondivitta Lane, Andheri - Kurla Road, Andheri (E, Mumbai - 400 059, India
SCHILLER Healthcare India Pvt. Ltd.,D.C.Silk Mills Compound, 'A' Wing, 1st floor, 5, Chunawala Estate,
Tel.: + 9122 826 3520 Italy
Switzerland
Fax : + 9122 826 3525
ESAOTE Spa (SCHILLER), Via di Caciolle 15, I-50127 Firenze, Italy Tel.: + 39055 4229 201
Fax : + 39055 4229 208
SCHILLER Reomed AG, Riedstrasse 14, CH-8953 Dietikon, Switzerland Tel.: +411 744 3000
Fax : + 411 740 3710
SCHILLER AG, Altgasse 68, CH-6341 Baar, Switzerland All other countries
Tel.: + 4141 766 4242
Fax : + 4141 761 0880
Home Page : www.schiller.ch
Where to Obtain Service and Sales Advice Kundendienst und Verkaufs-/Beratungsstellen Coordonnées de nos services d’assistance technique et commerciale
WELCH ALLYN SCHILLER Inc., 7420 Carroll Road, San Diego, CA , US-92121-2334 USA USA / Canada
Tel.: +1 858 635 6023
Fax : +1 858 635 6611
Home Page : www.welchallyn.com Asia Pacific
Austria
France Germany
SCHILLER Asia Pacific, 10 Jalan SS 3/33, Taman Universiti, 47300 Petaling Jaya, Selangor, Malaysia Tel.: + 603 7877 5336
Fax : + 603 7877 5744
SCHILLER HmbH, Kampmüllerweg 24, A-4044 Linz, Austria Tel.: + 43 732 709 90
Fax : + 43 732 757 000
SCHILLER Medical S.A, BP 50, 19, Avenue de la Gare, F-67162 Wissembourg / Cedex, France Tel.: +33 3 88 63 36 00
Fax : +33 3 88 94 12 82
SCHILLER Medizintechnik GmbH, Rudolf-Diesel Strasse 14, D-85521 Ottobrunn, Germany
(EU authorized representative)
Tel.: + 4989 629 981 0
Fax : + 4989 609 509 0
India
Kondivitta Lane, Andheri - Kurla Road, Andheri (E, Mumbai - 400 059, India
SCHILLER Healthcare India Pvt. Ltd.,D.C.Silk Mills Compound, 'A' Wing, 1st floor, 5, Chunawala Estate,
Tel.: + 9122 826 3520 Italy
Switzerland
Fax : + 9122 826 3525
ESAOTE Spa (SCHILLER), Via di Caciolle 15, I-50127 Firenze, Italy Tel.: + 39055 4229 201
Fax : + 39055 4229 208
SCHILLER Reomed AG, Riedstrasse 14, CH-8953 Dietikon, Switzerland Tel.: +411 744 3000
Fax : + 411 740 3710
SCHILLER AG, Altgasse 68, CH-6341 Baar, Switzerland All other countries
Tel.: + 4141 766 4242 Home Page : www.schiller.ch
Fax : + 4141 761 0880
This equipment has been tested and found to comply with the limits for a class A digital device, pursuant to both Part 15 of the FCC (Federal Communications Commission) Rules and the radio interference regulations of the Canadian Department of Communications. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with this instruction manual, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required to correct the interference at his own expense.
Battery Care and Disposal Instructions
Disposal Instructions and Battery Care
° ° °
DO NOT DISPOSE OF THE BATTERY BY FIRE OR INCINERATOR DANGER OF EXPLOSION DO NOT ATTEMPT TO RECHARGE THE BATTERY - DANGER OF EXPLOSION DO NOT OPEN THE BATTERY CASING - DANGER OF ACID BURN
Only dispose of the battery in official recycling centres or municipally approved areas. Alternatively, used batteries can be returned to Schiller AG for disposal.
Unit Disposal Instructions Units no longer required can be returned to Schiller AG for disposal. Alternatively dispose of the unit in municipally approved recycling centres.
This equipment has been tested and found to comply with the limits for a class A digital device, pursuant to both Part 15 of the FCC (Federal Communications Commission) Rules and the radio interference regulations of the Canadian Department of Communications. These limits are designed to provide reasonable protection against harmful interference when the equipment is operated in a commercial environment. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with this instruction manual, may cause harmful interference to radio communications. Operation of this equipment in a residential area is likely to cause harmful interference in which case the user will be required to correct the interference at his own expense.
Battery Care and Disposal Instructions
Disposal Instructions and Battery Care
° ° °
DO NOT DISPOSE OF THE BATTERY BY FIRE OR INCINERATOR DANGER OF EXPLOSION DO NOT ATTEMPT TO RECHARGE THE BATTERY - DANGER OF EXPLOSION DO NOT OPEN THE BATTERY CASING - DANGER OF ACID BURN
Only dispose of the battery in official recycling centres or municipally approved areas. Alternatively, used batteries can be returned to Schiller AG for disposal.
Unit Disposal Instructions Units no longer required can be returned to Schiller AG for disposal. Alternatively dispose of the unit in municipally approved recycling centres.
Power Supply The mains connection is on the rear of the unit. The power supply voltage is set by the factory for100-115V(nom. 110V) or 220-240V (nom. 230V) working. The setting is indicated by the indented metal strip on the fuse panel. Contact your dealer if the voltage needs to be changed. The mains indicator lamp on the keyboard is always lit when the unit is connected to the mains supply. The unit can either be operated from the mains supply or from the built-in rechargeable battery. Changing a Mains Fuse If it is necessary to change a fuse, always replace with the correct rating i.e 2x200mAT for 230V, or 2x315mAT for 110V . To change a fuse press the two retaining lugs on side of the fuse panel (situated below the mains connector on the back panel. Remove the fuse panel and replace the fuse(s). Click back the fuse panel.
Intended Use The CARDIOVIT AT-2 is a 6-channel ECG recorder with all (12) ECG signals simultaneously processed to provide instant ECG recordings. Two automatic recording modes can be individually preset to enable one button ECG recording of preferred print formats.
Power Supply The mains connection is on the rear of the unit. The power supply voltage is set by the factory for100-115V(nom. 110V) or 220-240V (nom. 230V) working. The setting is indicated by the indented metal strip on the fuse panel. Contact your dealer if the voltage needs to be changed. The mains indicator lamp on the keyboard is always lit when the unit is connected to the mains supply. The unit can either be operated from the mains supply or from the built-in rechargeable battery. Changing a Mains Fuse If it is necessary to change a fuse, always replace with the correct rating i.e 2x200mAT for 230V, or 2x315mAT for 110V . To change a fuse press the two retaining lugs on side of the fuse panel (situated below the mains connector on the back panel. Remove the fuse panel and replace the fuse(s). Click back the fuse panel.
Intended Use The CARDIOVIT AT-2 is a 6-channel ECG recorder with all (12) ECG signals simultaneously processed to provide instant ECG recordings. Two automatic recording modes can be individually preset to enable one button ECG recording of preferred print formats.
Terms of Warranty The SCHILLER AT-2 is warranted against defects in material and manufacture for the duration of one year (as from date of purchase). Excluded from this guarantee is damage caused by an accident or as a result of improper handling. The warranty entitles free replacement of the defective part. Any liability for subsequent damage is excluded. The warranty is void if unauthorized or unqualified persons attempt to make repairs. In case of a defect, contact your dealer or the manufacturer. The manufacturer can only be held responsible for the safety, reliability, and performance of the apparatus if:
•
assembly operations, extensions, readjustments, modifications, or repairs are carried out by persons authorized by him, and
•
the AT-2 and approved attached equipment are used in accordance with the manufacturers instructions.
THERE ARE NO EXPRESS OR IMPLIED WARRANTIES WHICH EXTEND BEYOND THE WARRANTIES HEREINABOVE SET FORTH. SCHILLER MAKES NO WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE WITH RESPECT TO THE PRODUCT OR PARTS THEREOF. About this Handbook The philosophy of SCHILLER is one of continuous improvement. Our aim is to provide the user with the most up-to-date information and the latest technological developments.
PHYSICIAN‘S RESPONSIBILITY THE AT-2 ELECTROCARDIOGRAPH IS PROVIDED FOR THE EXCLUSIVE USE OF QUALIFIED PHYSICIANS OR PERSONNEL UNDER THEIR DIRECT SUPERVISION. THE NUMERICAL AND GRAPHICAL RESULTS FROM A RECORDING MUST BE EXAMINED WITH RESPECT TO THE PATIENTS OVERALL CLINICAL CONDITION. THE RECORDING PREPARATION QUALITY AND THE GENERAL RECORDED DATA QUALITY, WHICH COULD EFFECT THE REPORT DATA ACCURACY, MUST ALSO BE TAKEN INTO ACCOUNT. IT IS THE PHYSICIANS RESPONSIBILITY TO MAKE THE DIAGNOSIS OR TO OBTAIN EXPERT OPINION ON THE RESULTS, AND TO INSTITUTE CORRECT TREATMENT IF INDICATED. FEDERAL LAW IN THE USA RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN
Your suggestions and comments are welcome on all SCHILLER documentation. Please contact the SCHILLER Technical Documentation Department.
Terms of Warranty The SCHILLER AT-2 is warranted against defects in material and manufacture for the duration of one year (as from date of purchase). Excluded from this guarantee is damage caused by an accident or as a result of improper handling. The warranty entitles free replacement of the defective part. Any liability for subsequent damage is excluded. The warranty is void if unauthorized or unqualified persons attempt to make repairs. In case of a defect, contact your dealer or the manufacturer. The manufacturer can only be held responsible for the safety, reliability, and performance of the apparatus if:
•
assembly operations, extensions, readjustments, modifications, or repairs are carried out by persons authorized by him, and
•
the AT-2 and approved attached equipment are used in accordance with the manufacturers instructions.
THERE ARE NO EXPRESS OR IMPLIED WARRANTIES WHICH EXTEND BEYOND THE WARRANTIES HEREINABOVE SET FORTH. SCHILLER MAKES NO WARRANTY OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE WITH RESPECT TO THE PRODUCT OR PARTS THEREOF. About this Handbook The philosophy of SCHILLER is one of continuous improvement. Our aim is to provide the user with the most up-to-date information and the latest technological developments. Your suggestions and comments are welcome on all SCHILLER documentation. Please contact the SCHILLER Technical Documentation Department.
PHYSICIAN‘S RESPONSIBILITY THE AT-2 ELECTROCARDIOGRAPH IS PROVIDED FOR THE EXCLUSIVE USE OF QUALIFIED PHYSICIANS OR PERSONNEL UNDER THEIR DIRECT SUPERVISION. THE NUMERICAL AND GRAPHICAL RESULTS FROM A RECORDING MUST BE EXAMINED WITH RESPECT TO THE PATIENTS OVERALL CLINICAL CONDITION. THE RECORDING PREPARATION QUALITY AND THE GENERAL RECORDED DATA QUALITY, WHICH COULD EFFECT THE REPORT DATA ACCURACY, MUST ALSO BE TAKEN INTO ACCOUNT. IT IS THE PHYSICIANS RESPONSIBILITY TO MAKE THE DIAGNOSIS OR TO OBTAIN EXPERT OPINION ON THE RESULTS, AND TO INSTITUTE CORRECT TREATMENT IF INDICATED. FEDERAL LAW IN THE USA RESTRICTS THIS DEVICE TO SALE BY OR ON THE ORDER OF A PHYSICIAN
Safety Notices TO PREVENT ELECTRIC SHOCK DO NOT DISASSEMBLE THE UNIT. NO SERVICEABLE PARTS INSIDE. REFER SERVICING TO QUALIFIED PERSONNEL ONLY. DO NOT USE THIS UNIT IN AREAS WHERE THERE IS ANY DANGER OF EXPLOSION OR THE PRESENCE OF FLAMMABLE GASES SUCH AS ANAESTHETIC AGENTS. IN THE EVENT OF ACCIDENTAL LCD BREAKAGE AND RESULTANT LEAKAGE OF FLUID, DO NOT INHALE, INGEST OR MAKE CONTACT WITH THE SKIN. IF CONTACT IS MADE RINSE IMMEDIATELY. THIS PRODUCT IS NOT DESIGNED FOR STERILE USE. THIS PRODUCT IS NOT DESIGNED FOR OUTDOOR USE. SWITCH THE UNIT OFF BEFORE CLEANING AND DISCONNECT FROM THE MAINS. DO NOT, UNDER ANY CIRCUMSTANCES, IMMERSE THE UNIT OR CABLE ASSEMBLIES IN LIQUID. THE DEVICE MUST ONLY BE OPERATED USING BATTERY POWER IF THE EARTH CONNECTION IS SUSPECT OR IF THE MAINS LEAD IS DAMAGED OR SUSPECTED OF BEING DAMAGED. DO NOT USE HIGH TEMPERATURE STERILISATION PROCESSES (SUCH AS AUTOCLAVING). DO NOT USE E-BEAM OR GAMMA RADIATION STERILISATION. DO NOT USE SOLVENT CLEANERS USE ONLY ACCESSORIES AND OTHER PARTS RECOMMENDED OR SUPPLIED BY SCHILLER AG. USE OF OTHER THAN RECOMMENDED OR SUPPLIED PARTS MAY RESULT IN INJURY INACCURATE INFORMATION AND/ OR DAMAGE TO THE UNIT. THE AT-2 COMPLIES WITH EMC REGULATIONS FOR MEDICAL PRODUCTS WHICH AFFORDS PROTECTION AGAINST EMISSIONS AND ELECTRICAL INTERFERENCE. HOWEVER SPECIAL CARE MUST BE EXERCISED WHEN THE UNIT IS USED WITH HIGH FREQUENCY EQUIPMENT. IT MUST BE ENSURED THAT NEITHER THE PATIENT NOR THE ELECTRODES (INCLUDING THE NEUTRAL ELECTRODE) COME INTO CONTACT WITH OTHER PERSONS OR CONDUCTING OBJECTS (EVEN IF THESE ARE EARTHED). THERE IS NO DANGER WHEN USING THE ECG UNIT FOR A PACEMAKER PATIENT OR WITH SIMULTANEOUS USE OF OTHER ELECTRICAL STIMULATION EQUIPMENT. HOWEVER, THE STIMULATION UNITS SHOULD ONLY BE USED AT A SUFFICIENT DISTANCE FROM THE ELECTRODES. IN CASE OF DOUBT, THE PATIENT SHOULD BE DISCONNECTED FROM THE RECORDER. THIS UNIT IS CF CLASSIFIED ACCORDING TO IEC 601-1. THIS MEANS THAT THE PATIENT CONNECTION IS FULLY ISOLATED AND DEFIBRILLATION PROTECTED. SCHILLER CAN ONLY GUARANTEE PROTECTION AGAINST DEFIBRILLATION VOLTAGE HOWEVER, WHEN THE ORIGINAL SCHILLER PATIENT CABLE IS USED. IF SEVERAL UNITS ARE COUPLED THERE IS A DANGER OF SUMMATION OF LEAKAGE CURRENT DO NOT TOUCH THE CASING DURING DEFIBRILLATION IF THE PATIENT CABLE SHOULD BECOME DEFECTIVE AFTER DEFIBRILLATION, LEAD OFF WILL BE DISPLAYED AND AN ACOUSTIC ALARM GIVEN
Safety Notices TO PREVENT ELECTRIC SHOCK DO NOT DISASSEMBLE THE UNIT. NO SERVICEABLE PARTS INSIDE. REFER SERVICING TO QUALIFIED PERSONNEL ONLY. DO NOT USE THIS UNIT IN AREAS WHERE THERE IS ANY DANGER OF EXPLOSION OR THE PRESENCE OF FLAMMABLE GASES SUCH AS ANAESTHETIC AGENTS. IN THE EVENT OF ACCIDENTAL LCD BREAKAGE AND RESULTANT LEAKAGE OF FLUID, DO NOT INHALE, INGEST OR MAKE CONTACT WITH THE SKIN. IF CONTACT IS MADE RINSE IMMEDIATELY. THIS PRODUCT IS NOT DESIGNED FOR STERILE USE. THIS PRODUCT IS NOT DESIGNED FOR OUTDOOR USE. SWITCH THE UNIT OFF BEFORE CLEANING AND DISCONNECT FROM THE MAINS. DO NOT, UNDER ANY CIRCUMSTANCES, IMMERSE THE UNIT OR CABLE ASSEMBLIES IN LIQUID. THE DEVICE MUST ONLY BE OPERATED USING BATTERY POWER IF THE EARTH CONNECTION IS SUSPECT OR IF THE MAINS LEAD IS DAMAGED OR SUSPECTED OF BEING DAMAGED. DO NOT USE HIGH TEMPERATURE STERILISATION PROCESSES (SUCH AS AUTOCLAVING). DO NOT USE E-BEAM OR GAMMA RADIATION STERILISATION. DO NOT USE SOLVENT CLEANERS USE ONLY ACCESSORIES AND OTHER PARTS RECOMMENDED OR SUPPLIED BY SCHILLER AG. USE OF OTHER THAN RECOMMENDED OR SUPPLIED PARTS MAY RESULT IN INJURY INACCURATE INFORMATION AND/ OR DAMAGE TO THE UNIT. THE AT-2 COMPLIES WITH EMC REGULATIONS FOR MEDICAL PRODUCTS WHICH AFFORDS PROTECTION AGAINST EMISSIONS AND ELECTRICAL INTERFERENCE. HOWEVER SPECIAL CARE MUST BE EXERCISED WHEN THE UNIT IS USED WITH HIGH FREQUENCY EQUIPMENT. IT MUST BE ENSURED THAT NEITHER THE PATIENT NOR THE ELECTRODES (INCLUDING THE NEUTRAL ELECTRODE) COME INTO CONTACT WITH OTHER PERSONS OR CONDUCTING OBJECTS (EVEN IF THESE ARE EARTHED). THERE IS NO DANGER WHEN USING THE ECG UNIT FOR A PACEMAKER PATIENT OR WITH SIMULTANEOUS USE OF OTHER ELECTRICAL STIMULATION EQUIPMENT. HOWEVER, THE STIMULATION UNITS SHOULD ONLY BE USED AT A SUFFICIENT DISTANCE FROM THE ELECTRODES. IN CASE OF DOUBT, THE PATIENT SHOULD BE DISCONNECTED FROM THE RECORDER. THIS UNIT IS CF CLASSIFIED ACCORDING TO IEC 601-1. THIS MEANS THAT THE PATIENT CONNECTION IS FULLY ISOLATED AND DEFIBRILLATION PROTECTED. SCHILLER CAN ONLY GUARANTEE PROTECTION AGAINST DEFIBRILLATION VOLTAGE HOWEVER, WHEN THE ORIGINAL SCHILLER PATIENT CABLE IS USED. IF SEVERAL UNITS ARE COUPLED THERE IS A DANGER OF SUMMATION OF LEAKAGE CURRENT DO NOT TOUCH THE CASING DURING DEFIBRILLATION IF THE PATIENT CABLE SHOULD BECOME DEFECTIVE AFTER DEFIBRILLATION, LEAD OFF WILL BE DISPLAYED AND AN ACOUSTIC ALARM GIVEN
INTRODUCTION ... 2 OPERATION MODES ... 4 Automatic Mode ... 4 Manual Mode ... 5 LOCATION & POWER ... 6 Location ... 6 Power Supply ... 6
SETTINGS FOR AUTOMATIC MODE ... 22 Average Cycles ... 23 Measurements and Markings ... 24 Interpretation ... 25 Interpretation Settings ... 26 Selecting Rhythm Leads ... 27 PATIENT CABLE CONNECTIONS ... 28 Standard Leads ... 30
BASIC INFORMATION ... 7 Switching On and Off ... 7 Potential Equalisation ... 7
RECORDING AN ECG IN AUTOMATIC MODE ... 31
KEYBOARD ... 8
CARE & MAINTENANCE ... 35 Care of your CARDIOVIT AT-2 ... 35 Self-test ... 35 12 Monthly Check ... 36 Cleaning the Print Head ... 36
INDICATORS ... 10 GENERAL SETTINGS ... 11 Defaults ... 12 Language ... 15 Baseline Filter ... 16 Mains Filter ... 17 Myogram Filter ... 18 Defining Lead Sequence & Printout ... 19 Acoustic QRS Indication ... 20 Time / Date ... 21
CARDIOVIT AT-2 8.2001
ENGLISH
Contents - User Guide AT-2
RECORDING AN ECG IN MANUAL MODE ... 33
REPLACING THE RECORDING PAPER ... 38 TROUBLE SHOOTING ... 39 ORDERING INFORMATION ... 40 TECHNICAL DATA ... 41
Page 1
INTRODUCTION ... 2 OPERATION MODES ... 4 Automatic Mode ... 4 Manual Mode ... 5 LOCATION & POWER ... 6 Location ... 6 Power Supply ... 6
SETTINGS FOR AUTOMATIC MODE ... 22 Average Cycles ... 23 Measurements and Markings ... 24 Interpretation ... 25 Interpretation Settings ... 26 Selecting Rhythm Leads ... 27 PATIENT CABLE CONNECTIONS ... 28 Standard Leads ... 30
BASIC INFORMATION ... 7 Switching On and Off ... 7 Potential Equalisation ... 7
RECORDING AN ECG IN AUTOMATIC MODE ... 31
KEYBOARD ... 8
CARE & MAINTENANCE ... 35 Care of your CARDIOVIT AT-2 ... 35 Self-test ... 35 12 Monthly Check ... 36 Cleaning the Print Head ... 36
INDICATORS ... 10 GENERAL SETTINGS ... 11 Defaults ... 12 Language ... 15 Baseline Filter ... 16 Mains Filter ... 17 Myogram Filter ... 18 Defining Lead Sequence & Printout ... 19 Acoustic QRS Indication ... 20 Time / Date ... 21
CARDIOVIT AT-2 8.2001
RECORDING AN ECG IN MANUAL MODE ... 33
REPLACING THE RECORDING PAPER ... 38 TROUBLE SHOOTING ... 39 ORDERING INFORMATION ... 40 TECHNICAL DATA ... 41
Page 1
ENGLISH
Contents - User Guide AT-2
Introduction
MAINS AND POTENTIAL EQUALISATION CONNECTORS
PAPER RELEASE CATCH
PATIENT CABLE CONNECTOR
LEAD INDICATORS
POWER INDICATORS SYSTEM INDICATORS
Page 2
CARDIOVIT AT-2 8.2001
Introduction
MAINS AND POTENTIAL EQUALISATION CONNECTORS
PAPER RELEASE CATCH
PATIENT CABLE CONNECTOR
LEAD INDICATORS
POWER INDICATORS SYSTEM INDICATORS
Page 2
CARDIOVIT AT-2 8.2001
ENGLISH
Introduction The CARDIOVIT AT-2 is a 6-channel ECG recorder. All ECG signals are simultaneously processed to provide instant ECG recordings. Two automatic recording modes can be individually preset to enable one button ECG recording of preferred print formats . Individual lamps are provided to give power, paper error, filter, lead group and lead off indications. In addition, any detected disturbance (i.e. loose electrode or end of paper), gives an audible alarm and the corresponding indicator lamp flashes. The AT-2 includes the following features: •
Low weight and compact dimensions
•
Large A4 size printout from integrated quality thermal printer
•
Built-in rechargeable battery for mains-independent use
•
Simple one key operation
•
Automatic or manual recording modes
•
Selectable printing formats
•
ECG memory for easy copying
•
Interpretation program option (including measurements)
CARDIOVIT AT-2 8.2001
Page 3
ENGLISH
Introduction The CARDIOVIT AT-2 is a 6-channel ECG recorder. All ECG signals are simultaneously processed to provide instant ECG recordings. Two automatic recording modes can be individually preset to enable one button ECG recording of preferred print formats . Individual lamps are provided to give power, paper error, filter, lead group and lead off indications. In addition, any detected disturbance (i.e. loose electrode or end of paper), gives an audible alarm and the corresponding indicator lamp flashes. The AT-2 includes the following features: •
Low weight and compact dimensions
•
Large A4 size printout from integrated quality thermal printer
•
Built-in rechargeable battery for mains-independent use
•
Simple one key operation
•
Automatic or manual recording modes
•
Selectable printing formats
•
ECG memory for easy copying
•
Interpretation program option (including measurements)
CARDIOVIT AT-2 8.2001
Page 3
Operation Modes Automatic Mode
Auto Mode Recording
Automatic Mode provides a printout giving 10 seconds of ECG recording of all 12 leads in 2 different formats.
Connect Patient Pages 28 to30
The following can be programmed freely in each of the formats before recording: Switch Unit ON
•
Lead Format
•
Chart Speed
•
With the optional interpretation program installed it is also possible to select the measurement table, average cycles with optional markings and interpretation statements for the printout.
Settings Pages 11 to 27
ALT
AUTO START
AUTO START
Automatic Recording in Format 1
Automatic Recording in Format 2
Pages 31 to 32
Pages 31 to 32
For further information see paragraph "Settings for Automatic Mode".
12 lead printout
Page 4
CARDIOVIT AT-2 8.2001
Operation Modes Automatic Mode
Auto Mode Recording
Automatic Mode provides a printout giving 10 seconds of ECG recording of all 12 leads in 2 different formats.
Connect Patient Pages 28 to30
The following can be programmed freely in each of the formats before recording: •
Switch Unit ON
Lead Format
Settings Pages 11 to 27
•
Chart Speed
•
With the optional interpretation program installed it is also possible to select the measurement table, average cycles with optional markings and interpretation statements for the printout.
ALT
For further information see paragraph "Settings for Automatic Mode".
Page 4
AUTO START
AUTO START
Automatic Recording in Format 1
Automatic Recording in Format 2
Pages 31 to 32
Pages 31 to 32
12 lead printout
CARDIOVIT AT-2 8.2001
ENGLISH
Operation Modes Manual Mode Manual Mode Recording
Manual Mode provides a real time printout of 6 leads that are selected and indicated on the keyboard.
Connect Patient Pages 28 to 30
The following can be freely selected before or during recording: •
Lead Group
•
Chart Speed
Switch Unit ON Settings Pages 11 to 21
Manual Recording
MAN START
Pages 33 and 34
•
Sensitivity
•
Myogram Filter
Leads, Speed, Sensitivity Myogram filter Pages 18 + 33
For further information see paragraph "ECG Recording in Manual Mode".
Continuous printout of 6 leads STOP
CARDIOVIT AT-2 8.2001
Page 5
ENGLISH
Operation Modes Manual Mode Manual Mode provides a real time printout of 6 leads that are selected and indicated on the keyboard.
Manual Mode Recording
Connect Patient Pages 28 to 30
The following can be freely selected before or during recording: •
Lead Group
Switch Unit ON Settings Pages 11 to 21
•
Chart Speed
Manual Recording Pages 33 and 34
• •
MAN START
Sensitivity Myogram Filter
Leads, Speed, Sensitivity Myogram filter Pages 18 + 33
For further information see paragraph "ECG Recording in Manual Mode".
Continuous printout of 6 leads STOP
CARDIOVIT AT-2 8.2001
Page 5
Location & Power Location Do not keep or operate the apparatus in a wet, moist, or dusty environment. Also, avoid exposure to direct sunlight or heat from other sources. Do not allow the unit to come into contact with acidic vapours or liquids, as such contact may cause irreparable damage. The unit should not be placed near X-ray or diathermy units, large transformers or motors. The unit must be placed on a flat surface. The unit should not be operated in areas where there is any danger of explosion. Power Supply The unit can either be operated from the built-in rechargeable battery, or from the mains. The mains connection is on the rear of the unit. The mains indicator lamp is always lit when the unit is connected to the mains supply. A battery indicator lamp confirms battery operation. When the battery capacity is limited, the indicator flashes. To recharge the battery, connect the apparatus to the mains supply by means of the supplied power cable. A totally discharged battery needs less than 15 hours to be fully recharged (60% in less than 3 hours, 90% in less than 7 hours). A fully charged battery lasts approximately 6 hours of normal use. The unit can remain connected to the mains supply without any danger of damage to either the battery or the unit.
Page 6
CARDIOVIT AT-2 8.2001
Location & Power Location Do not keep or operate the apparatus in a wet, moist, or dusty environment. Also, avoid exposure to direct sunlight or heat from other sources. Do not allow the unit to come into contact with acidic vapours or liquids, as such contact may cause irreparable damage. The unit should not be placed near X-ray or diathermy units, large transformers or motors. The unit must be placed on a flat surface. The unit should not be operated in areas where there is any danger of explosion. Power Supply The unit can either be operated from the built-in rechargeable battery, or from the mains. The mains connection is on the rear of the unit. The mains indicator lamp is always lit when the unit is connected to the mains supply. A battery indicator lamp confirms battery operation. When the battery capacity is limited, the indicator flashes. To recharge the battery, connect the apparatus to the mains supply by means of the supplied power cable. A totally discharged battery needs less than 15 hours to be fully recharged (60% in less than 3 hours, 90% in less than 7 hours). A fully charged battery lasts approximately 6 hours of normal use. The unit can remain connected to the mains supply without any danger of damage to either the battery or the unit.
Page 6
CARDIOVIT AT-2 8.2001
ENGLISH
Basic Information Switching On and Off
The CARDIOVIT AT-2 is switched on by means of the green
of the red
key and off by means
key.
The unit is switched off after 5 minutes (30 seconds if battery capacity is limited) if no key is pressed and the patient cable is not connected. Potential Equalisation If the AT-2 is used in conjunction with other patient connected equipment, we recommend that the potential equalisation stud (
) on the rear of the unit is connected to the hospital/
building common ground with the yellow/green ground cable (Part-no. 2.310005). When working from an emergency vehicle, the vehicle common ground can be used.
CARDIOVIT AT-2 8.2001
Page 7
ENGLISH
Basic Information Switching On and Off
The CARDIOVIT AT-2 is switched on by means of the green
of the red
key and off by means
key.
The unit is switched off after 5 minutes (30 seconds if battery capacity is limited) if no key is pressed and the patient cable is not connected. Potential Equalisation If the AT-2 is used in conjunction with other patient connected equipment, we recommend that the potential equalisation stud (
) on the rear of the unit is connected to the hospital/
building common ground with the yellow/green ground cable (Part-no. 2.310005). When working from an emergency vehicle, the vehicle common ground can be used.
CARDIOVIT AT-2 8.2001
Page 7
Keyboard
I II III aVR aVL aVF V1 V4
V2 V3 V5 V6
II V2
aVF III V4 V5
V4 V7
7
QRS 8 BEEP
9
AUTO START
COPY
ALT
MAN START
AUTO GAIN
4 5 mm/mV
10 5 20 6 mm/mV mm/mV
STOP
FILT
0
1 5 mm/s
25 2 mm/s
V5 V6 V8 V9
1mV
50 3 mm/s
Page 8
LEAD OFF PAPER FILTER
CARDIOVIT AT-2 8.2001
Keyboard
I II III aVR aVL aVF V1 V4
V2 V3 V5 V6
II V2
aVF III V4 V5
V4 V7
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V5 V6 V8 V9
7
QRS 8 BEEP
9
AUTO START
COPY
ALT
MAN START
AUTO GAIN
4 5 mm/mV
10 5 20 6 mm/mV mm/mV
STOP
FILT
0
1 5 mm/s
25 2 mm/s
1mV
50 3 mm/s
LEAD OFF PAPER FILTER
CARDIOVIT AT-2 8.2001
Switch unit on
Switch unit off
COPY
QRS BEEP
Cancel or enable QRS beeper
AUTO GAIN
Automatic ECG sensitivity adjustment from 10 to 5 mm/mV in order to avoid overlapping traces in automatic mode only
5 mm/mV
10 mm/mV
20 mm/mV
5 mm/s
25 mm/s
50 mm/s
1mV
Key for 1 mV indication mark on output during manual recording. Use this key also for baseline recentering
ALT
Key for initiation of setups and selection of second format for printout
Copy stored ECG
AUTO START
Start automatic recording
MAN START
Start manual recording
STOP
Stop recording/move paper to start position
FILT
ENGLISH
Keyboard
Switch myogram filter (muscle tremor filter) on or off
Lead group selector (forward)
ECG sensitivity selector (5, 10 or 20 mm/mV) manual recording only Chart speed selector (5, 25 or 50 mm/s) manual recording only
Lead group selector (backward)
CARDIOVIT AT-2 8.2001
Page 9
Switch unit on
Switch unit off
COPY
QRS BEEP
Cancel or enable QRS beeper
AUTO GAIN
Automatic ECG sensitivity adjustment from 10 to 5 mm/mV in order to avoid overlapping traces in automatic mode only
5 mm/mV
10 mm/mV
20 mm/mV
5 mm/s
25 mm/s
50 mm/s
1mV
Key for 1 mV indication mark on output during manual recording. Use this key also for baseline recentering
ALT
Key for initiation of setups and selection of second format for printout
Copy stored ECG
AUTO START
Start automatic recording
MAN START
Start manual recording
STOP
Stop recording/move paper to start position
FILT
ENGLISH
Keyboard
Switch myogram filter (muscle tremor filter) on or off
Lead group selector (forward)
ECG sensitivity selector (5, 10 or 20 mm/mV) manual recording only Chart speed selector (5, 25 or 50 mm/s) manual recording only
Lead group selector (backward)
CARDIOVIT AT-2 8.2001
Page 9
Indicators
Mains indicator (lit when mains connected) Battery lamp (lit when running on battery power - mains not connected) (blinking when battery capacity is limited)
LEAD OFF
Warning lamp for loose electrode connection or poor electrode contact
PAPER
Warning lamp for end of paper or paper jam
FILT
Myogram filter (lit when filter ON)
I II III aVR aVL aVF
Indicator lamp for selected lead group (Standard) (Cabrera: aVL, I, -aVR, II, aVF, III) in manual mode only
V1 V2 V3 V4 V5 V6
Indicator lamp for selected lead group (Standard) (in manual mode only
II aVF III V2 V4 V5
Indicator lamp for selected lead group in manual mode only
V4 V5 V6 V7 V8 V9
Indicator lamp for selected lead group in manual mode only
Page 10
CARDIOVIT AT-2 8.2001
Indicators
Mains indicator (lit when mains connected) Battery lamp (lit when running on battery power - mains not connected) (blinking when battery capacity is limited)
Page 10
LEAD OFF
Warning lamp for loose electrode connection or poor electrode contact
PAPER
Warning lamp for end of paper or paper jam
FILT
Myogram filter (lit when filter ON)
I II III aVR aVL aVF
Indicator lamp for selected lead group (Standard) (Cabrera: aVL, I, -aVR, II, aVF, III) in manual mode only
V1 V2 V3 V4 V5 V6
Indicator lamp for selected lead group (Standard) (in manual mode only
II aVF III V2 V4 V5
Indicator lamp for selected lead group in manual mode only
V4 V5 V6 V7 V8 V9
Indicator lamp for selected lead group in manual mode only
CARDIOVIT AT-2 8.2001
ENGLISH
General Settings Each parameter is set by means of a code. This code comprises a combination starting with the ALT key followed by a number of keys and is always confirmed with the STOP key. As soon as the ALT key is pressed, the keyboard is dedicated to the programming function. The setting is remembered and the keyboard is only released for other functions when the STOP key is pressed. Once the settings have been confirmed, they are stored in the memory even when the unit is switched off. As an example, if you want to set the language on your AT-2 to English, proceed as follows:
ALT
FILT
0
25 mm/s
Key 0
2
Key 2
25 mm/s
2
STOP
Key 2
Program sequence Start programming / Switch to numerical keyboard
CONFIRM SETTING
On the following pages the programmable parameters and the programming sequences are described in detail. NOTE THAT THE SETTINGS ARE ALWAYS CONFIRMED BY PRESSING THE
STOP
KEY.
CARDIOVIT AT-2 8.2001
Page 11
ENGLISH
General Settings Each parameter is set by means of a code. This code comprises a combination starting with the ALT key followed by a number of keys and is always confirmed with the STOP key. As soon as the ALT key is pressed, the keyboard is dedicated to the programming function. The setting is remembered and the keyboard is only released for other functions when the STOP key is pressed. Once the settings have been confirmed, they are stored in the memory even when the unit is switched off. As an example, if you want to set the language on your AT-2 to English, proceed as follows:
ALT
FILT
0
25 mm/s
Key 0
2
Key 2
25 mm/s
2
STOP
Key 2
Program sequence Start programming / Switch to numerical keyboard
CONFIRM SETTING
On the following pages the programmable parameters and the programming sequences are described in detail. NOTE THAT THE SETTINGS ARE ALWAYS CONFIRMED BY PRESSING THE
CARDIOVIT AT-2 8.2001
STOP
KEY.
Page 11
General Settings Defaults Default Settings Setting
AT-2
AT-2 with Interpretation Option
Language
English
English
Leads
Standard (S)
Standard (S) ECG: 25 mm/s, short (o) MECG: 2 x 6 (25 mm/s) + 2
Format 1
ECG: 25mm/s short (o)
Measurements: suppressed (-) Marks: enabled (+) Interpretation: enabled (+) ECG: 25 mm/s, long (ooo) MECG: none (-)
Format 2
ECG: 25 mm/s, long (ooo)
Measurements: disabled (-) Marks: enabled (+) Interpretation: disabled (-)
Rhythm Leads
V1 = ECG; V1, II = MECG
V1 = ECG; V1, II = MECG
Autom. Centering
Enabled (+)
Enabled (+)
Printout of Signals
Sequential
Sequential
Baseline Filter Setting
0.05 Hz
0.05 Hz
Mains Filter Setting
50 Hz (USA - 60Hz)
50 Hz (USA - 60Hz)
Myogram Filter Setting
35 Hz, OFF
35 Hz, OFF
Interpretation Settings
N/A: - U: +
A30: -
S: -
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CARDIOVIT AT-2 8.2001
General Settings Defaults Default Settings Setting
AT-2
AT-2 with Interpretation Option
Language
English
English
Leads
Standard (S)
Standard (S) ECG: 25 mm/s, short (o) MECG: 2 x 6 (25 mm/s) + 2
Format 1
ECG: 25mm/s short (o)
Measurements: suppressed (-) Marks: enabled (+) Interpretation: enabled (+) ECG: 25 mm/s, long (ooo) MECG: none (-)
Format 2
ECG: 25 mm/s, long (ooo)
Measurements: disabled (-) Marks: enabled (+) Interpretation: disabled (-)
Rhythm Leads
V1 = ECG; V1, II = MECG
V1 = ECG; V1, II = MECG
Autom. Centering
Enabled (+)
Enabled (+)
Printout of Signals
Sequential
Sequential
Baseline Filter Setting
0.05 Hz
0.05 Hz
Mains Filter Setting
50 Hz (USA - 60Hz)
50 Hz (USA - 60Hz)
Myogram Filter Setting
35 Hz, OFF
Interpretation Settings
Page 12
35 Hz, OFF N/A: - U: +
A30: -
S: -
CARDIOVIT AT-2 8.2001
ENGLISH
General Settings The defined formats and settings can be checked as follows: Setup Printout Entry Key Sequence ALT
0
1
Action 1
Printout of programmed settings
A printout of the defined settings will be produced and gives the following information, depending on the installed software: Unit designation (AT-2),
Software option installed (C = Interpretation) and Software version
Serial number Leads
Standard (S) or Cabrera (C)
ECG Format
Long (ooo), Short (o) or Suppressed (-)
MECG
Average cycles as defined in auto ECG recording setup (e.g. 4 * 3 (25 mm/s)+2)
Measurements
Enabled (+) or Suppressed (-)
Marks
Enabled (+) or Suppressed (-)
Interpretation
Enabled (+) or Suppressed (-)
Selected Rhythm leads
Leads selected for R1, R2 resp.
Automatic Centering
Enabled (+) or Suppressed (-)
Printout of signals
Sequential or Simultaneous
CARDIOVIT AT-2 8.2001
Page 13
ENGLISH
General Settings The defined formats and settings can be checked as follows: Setup Printout Entry Key Sequence ALT
0
1
Action 1
Printout of programmed settings
A printout of the defined settings will be produced and gives the following information, depending on the installed software: Unit designation (AT-2),
Software option installed (C = Interpretation) and Software version
Serial number Leads
Standard (S) or Cabrera (C)
ECG Format
Long (ooo), Short (o) or Suppressed (-)
MECG
Average cycles as defined in auto ECG recording setup (e.g. 4 * 3 (25 mm/s)+2)
Measurements
Enabled (+) or Suppressed (-)
Marks
Enabled (+) or Suppressed (-)
Interpretation
Enabled (+) or Suppressed (-)
Selected Rhythm leads
Leads selected for R1, R2 resp.
Automatic Centering
Enabled (+) or Suppressed (-)
Printout of signals
Sequential or Simultaneous
CARDIOVIT AT-2 8.2001
Page 13
General Settings Baseline Filter
0.05, 0.15 or 0.30 Hz
Mains Filter
50, 60 Hz or OFF (-)
Myogram Filter
25 or 35 Hz, ON (+) or OFF (-)
Interpretation settings:
N/A: +/- ('normal/abnormal' is written (+) or suppressed (-); U: +/- ('unconfirmed report' is written (+) or suppressed (-); A30: +/- (patient age is assumed to be < 30 (-) or >30 (+); S: +/- (low (-) or high (+) sensitivity)
To reset the unit to the basic default settings, proceed as follows: Reset Setup Entry Key Sequence ALT
0
6
Action 6
Reset to default base settings.
Page 14
CARDIOVIT AT-2 8.2001
General Settings Baseline Filter
0.05, 0.15 or 0.30 Hz
Mains Filter
50, 60 Hz or OFF (-)
Myogram Filter
25 or 35 Hz, ON (+) or OFF (-)
Interpretation settings:
N/A: +/- ('normal/abnormal' is written (+) or suppressed (-); U: +/- ('unconfirmed report' is written (+) or suppressed (-); A30: +/- (patient age is assumed to be < 30 (-) or >30 (+); S: +/- (low (-) or high (+) sensitivity)
To reset the unit to the basic default settings, proceed as follows: Reset Setup Entry Key Sequence ALT
Page 14
0
6
Action 6
Reset to default base settings.
CARDIOVIT AT-2 8.2001