MIR spirolab III spirometer User Manual
広告
広告
spirolab
III
User Manual
User Manual Rev 2.0
Issued on
Approved on
04.04.2011
04.04.2011
spirolab
III – User Manual Code MIR 980067 REV 2.0 Page 1 / 74
Thank you for choosing a product from MIR
Medical International Research
WARNING
The paper mouthpiece, the nose clip and the disposable turbine with mouthpiece in the equipment should be considered disposable products.
WARNING
The oximetry function is not available for spirolab III with black and white display.
Before using your spirometer …
Please read this manual carefully, plus the labels and all of the information supplied together with the product.
WARNING
Note that this symbol means: read the instructions carefully before use.
Set up the device (date, time, language, predicted values, etc.) to your requirements as described under Configuration Menu in this Manual.
Keep the original packaging!
In the event that your spirometer has a problem, always use the original packaging to return it to your local distributor or to the manufacturer.
MIR has a policy of continuous product development and improvement, and the manufacturer therefore reserves the right to modify and to update the information contained in this User‟s Manual as required. Any suggestions and or comments regarding this product should be sent via email to: [email protected]. Thank you.
MIR accepts no responsibility for any loss or damage caused by the use of the device due to the use of this Manual and/or due to an incorrect use of the product.
Note that due to printing limitations the screenshots shown in this manual may differ from the display of the machine and/or from the keyboard graphics.
Copying this manual in whole or in part is strictly forbidden.
IMPORTANT NOTE
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If the instrument is returned for repair it must be accompanied by a clear and detailed explanation of the defect or problem found.
the unit must be returned in its original packaging;
transport costs must be prepaid.
Manufacturer‟s address:
MIR srl: Via Del Maggiolino, 125
00155 Roma, Italy
Tel ++ 39 0622754777
Fax ++ 39 0622754785 e-mail: [email protected]
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INDEX
Who can or must make the installation ........................................................... 7
Method of measurement and interpretation ...................................................... 46
Spot oximetry (MEMORIZED LIKE OXYTEST) ........................................ 53
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Data Transmission via Bluetooth to a cell phone .............................................. 57
Data Transmission through Bluetooth........................................................... 57
Data Transmission via Bluetooth for printing ................................................ 58
Connection to a PC through a USB port ....................................................... 59
Connection to PC through RS 232 port. ....................................................... 59
Cleaning and disinfection of the oximetry sensor .............................................. 62
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INTRODUCTION
The spirometers series MIR009 are sold with the spirolab III trademark.
spirolab
III is available with two different displays:
Colour LCD display
B/W LCD display
Unless otherwise specified, from this point onwards the term spirolab III is used to refer to both models.
1 GENERAL INFORMATION
1.1 I
NTENDED USE
Spirolab III spirometer and pulse oximeter is intended to be used by either a physician, respiratory therapist or technician.
The device is intended to test lung function and can make:
spirometry testing in people of all ages, excluding infants and neonates
oximetry testing in people of all ages.
It can be used in any setting.
1.1.1 User Category spirolab
III, spirometer + pulse oximeter calculates a series of parameters relating to human respiratory function.
1.1.2 Ability and experience required
The correct use of the device, the interpretation of the results and the maintenance of the device, with particular WARNING on cleaning operations (cross-contamination risk), all require qualified personnel.
WARNING
MIR cannot be held responsible for any damage caused by the user of the device failing to follow the instructions and warnings contained in this manual.
If the user of spirolab III is a person considered to be cognitively impaired, then the operation of the device must be made under the supervision and responsibility of whoever is legally charged with the supervision of this person.
The
spirolab
III
when used as a pulse oximeter is intended for spot-checking, overnight sleep screening and/or continuous monitoring when attended by a trained healthcare professional.
1.1.3 Operating environment
The device has been envisaged for use in a doctor‟s office or in a hospital setting.
The information necessary for the proper use of the device in surrounding electromagnetic environments (as required by EN 60601-1-2) is contained in the Annex.
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The device is not intended for use in an operating theatre nor in the presence of inflammable liquids or detergents, nor in the presence of inflammable anaesthetic gases
(oxygen or nitrogen).
The device is not designed to be used in direct air currents (e.g. wind), sources of heat or cold, direct sun rays or other sources of light or energy, dust, sand or any other chemical substances.
The user and/or the doctor are responsible for ensuring that the device is stored and used in appropriate environmental conditions; in this regard reference is made to the specifics described in paragraph 1.5 below.
WARNING
If the device is exposed to unsuitable environmental conditions, this could cause the device to malfunction and to give incorrect results.
1.1.4 Who can or must make the installation
The device requires installation by qualified personnel. The user shall normally configure the device accordingly.
1.1.5 Subject effect on the use of the device
A spirometry test should only be carried out when the subject is at rest and in good health, and thus in a suitable condition for the test. A spirometry test requires the collaboration of the subject, since the subject must make a complete forced expiration, in order to have a meaningful test result.
1.1.6 Limitations of use - Contraindications
An analysis of the results of a spirometry test is not by itself sufficient to make a correct diagnosis of the subject‟s clinical condition. Test comments, a test interpretation and suggested courses of treatment must be given by a doctor.
Any symptoms that the subject has at the time must be carefully considered before a spirometry test is made. The user is responsible to assess both the mental and the physical capacity of the subject to make a correct test and the user must also assess the degree of collaboration for each test carried out.
A correct spirometry test requires the complete collaboration of the subject. The results depend on the person‟s capability to inspire and to expire all air completely and as fast as possible. If these fundamental conditions are not respected then the results obtained during spirometry testing will not be accurate, and therefore the test results are "not acceptable".
The acceptability of a test is the responsibility of the user. Special WARNING should be given to testing elderly subjects, children and handicapped people.
The device should never be used when it is possible or probable that the validity of the results may be compromised due to any such external factors.
WARNING
The instrument must be used as described in the User‟s Manual with particular
WARNING to the paragraph on Intended Use utilizing only original spare parts and accessories as specified by the manufacturer may be used. Use of non original parts such as the turbine sensor or other accessories may cause errors in measurement and/or compromise the correct functioning of the device. Any
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use of the device which differs from the original is to be considered improper and therefore dangerous.
The
spirolab
III when used as a pulse oximeter has limited alarms, therefore the device requires frequent display observation of SpO2 and pulse rate.
1.2 I
MPORTANT SAFETY WARNINGS spirolab
III has been examined by an independent laboratory which has certified the conformity of the device to the European Safety Standards EN 601-1 and guarantees the
EMC Requirements within the limits laid down in the European Standard EN 60601-1-2
spirolab
III is constantly controlled during its production, therefore the product confirms to the established security levels and quality standards laid down by the Council Directive
93/42/CEE for medical devices.
After removing the device from its packaging, check that there is no visible damage. In case of damage do not use the device and return it to the manufacturer for repair.
WARNING
The safety and the correct performance of the device can only be assured if the user of the device respects all of the relevant safety rules and regulations.
The manufacturer cannot be held responsible for damage caused by the failure of the user to follow these instructions correctly.
In the event of any incident or accident of any kind resulting from the use of the device, the user is required to inform the manufacturer without delay, this procedure is laid down in article.9 of the European Regulations No. 46/1997, which confirmed the CE Directive No. 93/42
Safety and correct functioning of the device are guaranteed only if the safety standards in force are respected.
Keep the instructions for use together with the warranty conditions for any future reference or in case the device presents technical problems.
The manufacturer cannot be held responsible for damage caused by the failure of the user to follow these instructions correctly, misuse of the device whether that misuse is improper, incorrect and/or unreasonable, or when the device is connected to an electrical outlet which does not conform to the safety regulations in force.
The device and its accessories must be controlled before each and every use, so that any malfunction and/or damage caused during transport and/or storage may be detected.
Keep the device away from hot and/or cold sources.
The thermal paper used for printing is highly inflammable. Keep away from open flames.
High-frequency emissions that are outside the limits expressed by the EN60601-
1-2 may interfere with the correct functioning of the device. High frequency emissions coming from other electrical or electronic devices can interfere with the functioning of the device. For this reason certain minimum clearances (a few
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meters), should be observed when high-frequency appliances such as TV, radio, cellular phones, etc and other electronic units are operated in the same room.
When connecting the
spirolab
For the recycling of the
III to any other devices (PC, printer, modem etc.), the user must guarantee that the required security level for subjects and/or users in the same room are not in any way endangered by the connection.
If the PC and/or the printer connected to area containing patient data, ref. directive EN 60601-1-1, it is necessary that they conform to the directive EN 60601-1.
The instrument may give inaccurate readings if operated in the presence of strong electromagnetic sources, such as electrosurgical equipment, or in the presence of computed tomography (CT) equipment.
If the device is not functioning properly, switch it off and consult the instruction manual. After correctly following all the instructions, if the device does not function correctly, call the manufacturer or an authorized service centre for assistance.
For any repairs call only certified service centres that are authorized by the manufacturer, or directly call the manufacturer.
Do not open or tamper with the device.
Always use and demand only original spare parts.
spirolab
III
spirolab
III come into contact with the
, the accessories, plastic consumable materials (mouthpieces), and removable parts (for example the disposable turbine), use only the appropriate containers or return all such parts to the dealer or to a recycling centre. All applicable local regulations must be followed.
If any of these rules are not followed then MIR will decline all responsibility for any direct or indirect damages, however caused.
Use of non original parts such as the turbine flow sensor and other accessories may cause errors in measurement and/or compromise the correct functioning of the device and is therefore not permitted.
The installation must be carried out according to the manufacturer‟s instructions.
An incorrect installation may cause damage to people, animals or things, in which the manufacturer is not to be considered liable.
Modifications, adjustments, repairs, and reconfiguration must be carried out by the manufacturer or authorised persons.
In case problems arise do not attempt to personally repair the device.
The setting of configuration parameters must be carried out by qualified personnel. In any case the risks pertaining to incorrect settings do not constitute a danger for the patient.
Inadequate respect to any of the above-mentioned points may compromise the safety of the device.
Always respect the safety standards indicated for electrical devices, in particular:
use only original accessories and spare parts
do not immerse the device in any type of liquid
do not touch the device with wet or damp hands
do not leave the device exposed to atmospheric conditions
place the device on a stable and a level working surface for all maintenance operations
use of the device always requires full mental ability
when unplugging the device, never pull the cable of the power supply or of the device
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always place the device on a suitable rigid horizontal on a stable surface with at least 30 cm (6 in) of space all around the device. The ventilation slots must be free from any cover or obstruction of any kind. The ventilation slots are located both behind and underneath the plastic outer casing of the device.
Before plugging in the charging unit, make sure that the electrical information on the label of the charging unit corresponds to those of the electrical wiring of the mains supply.
In case the plug of the charging unit supplied with the device is not compatible with the electric socket of the mains supply, contact qualified personnel for the substitution of the plug with a suitable one. Generally, it is not advisable to use adapters and/or extension cables. If it is essential to use them, then only those conform to the safety standards must be used, paying WARNING that they tolerate the maximum limits which are indicated on adapters and extension cables.
Unplug the power supply cable when battery charging is not required.
Do not leave the device attached to the mains supply when not required.
In case of breakdown or damage of the charging unit, replace it only with the manufacturer‟s original spare parts.
Use of an unsuitable power supply may change the performance of the device and no longer guarantee the safety conditions.
In order to avoid dangerous overheating we recommend to totally unwind the power supply cable of the charging unit.
The maintenance operations detailed in this manual must be carried out precisely. If these instructions are not followed this can cause measurement errors and/or incorrect test interpretation.
Before doing any cleaning and/or maintenance operations always switch off the device and unplug the power supply.
Keep the device out of reach of children and of any person with mental handicap.
When deciding to no longer use the device, it is recommended to dispose of it according to the local regulations.
In order to avoid contamination of the environment provoked by disposing of the spirometer, of its accessories, of plastic consumable materials or parts, follow all local regulations.
Device lithium backup battery life is 10 years.
Do not use the device beyond the extimated life advised by the manufacturer.
The lithium battery is continuously monitored by the device; if the battery is discharged, a warning message indicates that it must be replaced. Contact an authorised service centre to change the battery.
If the LED of the lithium back-up battery flashes, the test data and spirometry parameters in the memory, plus the device configuration then all information stored may be cancelled automatically.
The batteries used for power supply and for data storage are both inside the device. It is not permitted to open the device in order to replace them. This procedure must be carried out only in an authorised service centre, authorized by the manufacturer.
The maintenance operations detailed in this manual must be carried out to the letter. If these instructions are not followed this can cause measurement errors and/or an incorrect test interpretation.
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1.2.1 Danger of cross-contamination
Two different types of turbine sensors can be used with the device, one is reusable and one is single-patient disposable. A mouthpiece is required in order to connect a subject to the spirometer. In order to avoid exposing the subject to the critical danger of crosscontamination, the reusable flow sensor must always be cleaned before each spirometry test, and always use a new disposable mouthpiece for each subject. The use of an anti bacterial filter is at the discretion of the doctor. If a single-patient disposable turbine is used, then a new one must be used for each patient.
1.2.2 Turbine
WARNING
Disposable
Turbine
If you are going to perform the spirometry test with a
“disposable” turbine it is of vital importance to use a new turbine for each patient. The characteristics, accuracy and the hygiene of the disposable turbine can only be guaranteed if it has been conserved beforehand in its original sealed packaging. The disposable turbine is made of plastic and its disposal after use must adhere to the local regulations and norms in force.
Reusable
Turbine
The correct functioning of the re-usable turbine can only be guaranteed if it has been cleaned in the correct manner and is free from foreign bodies, which could restrict its movement. If the turbine has not been cleaned sufficiently this could cause cross-contamination from one patient to another. Periodic cleaning should only be done when the instrument is for personal use and will only be used by one patient. The cleaning of the turbine should be performed according to the instructions contained in the User‟s Manual.
For cleaning operations see § MAINTENANCE AND CLEANING in this Manual.
The following information applies to both types of turbine:
The turbine must never be held under a jet of water or air and must never come into contact with high temperature fluids.
Do not allow dust or foreign bodies to enter the turbine sensor, in order to avoid incorrect functioning and possible damage. The presence of any impurities such as hair, sputum, threads etc. within the body of the turbine sensor may seriously compromise the accuracy of the measurements.
To avoid environmental contamination by cleaning waste products, the user must adhere to all relevant regulations.
1.2.3 Mouthpiece
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Any disposable mouthpieces included with the device are supplied only as a guide to the correct type and dimensions of the mouthpiece required for this device, they are clean but not sterile.
To purchase appropriate mouthpieces, generally either paper or plastic, but in any case mono-use/disposable, we suggest that you contact your local distributor who supplied the spirometer.
WARNING
Use a bio-compatible mouthpiece to avoid any problems to the patient; unsuitable materials could cause a bad functioning of the instrument, and therefore the test results could be incorrect.
The user is responsible for obtaining the correct type of mouthpieces for the device. Those required are a standard type with an outside diameter of 30 mm, they are commonly used and in general easily procured.
WARNING
To avoid environmental contamination caused by the disposal of used mouthpieces, the user must adhere to all relevant local regulations.
1.2.4 Oximetry sensor
The following oximetry sensors can be used with spirolab III
:
MANUFACTURER MANUFACTURER CODE
BCI
BCI
BCI
BCI
BCI
BCI
BCI
1300
3026
3043
3078
3178
3444
3044
DESCRIPTION
adult sensor (disposable) wrap-around sensor for infants universal Y sensor ear sensor pediatric finger sensor, reusable adult sensor reusable (Comfort Clip) adult sensor, reusable, for finger
These sensors require the use of an extension cable cod. 919100 to be correctly connected to the device.
The same sensors are also available with microconnector for the direct connection.
Prolonged use and/or the patient‟s condition may require changing of the sensor site periodically. Change sensor site and check skin integrity, circulatory status, and correct alignment at least every 4 hours.
WARNING
Incorrectly applied sensors or damaged cables may cause inaccurate readings.
Using a damaged sensor may cause inaccurate readings, possibly resulting in patient injury or death. Inspect each sensor before use.
If a sensor appears damaged then do not use it. Use another sensor or contact your authorized repair centre for assistance.
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Use only MIR sensors supplied with, or specifically intended for use with the spirolab
III. Use of other types of sensors may cause inaccurate readings.
Oximetry measurements may be inaccurate in the presence of high ambient light.
Shield the sensor area (with a surgical towel, for example) if necessary.
WARNING
Dyes introduced into the bloodstream, such as methylene blue, indocyanine green, indigo carmine, patent blue V (PBV), and fluorescein may adversely affect the accuracy of the oximetry reading.
Any condition that restricts blood flow, such as the use of a blood pressure cuff or a device for systemic vascular resistance, may cause an inability to determine accurate pulse rate and SpO2 readings.
Remove fingernail polish and/or false fingernails before applying SpO2 sensors.
Both may cause inaccurate oximetry measurement.
Significant levels of dysfunctional hemoglobins, such as carboxyhemoglobin or methemoglobin, may adversely affect the accuracy of the oximetry measurement.
Optical cross-talk can occur when two or more sensors are placed in close proximity. Optical cross-talk may adversely affect the accuracy of the oximetry readings. The danger can be eliminated by covering each site with opaque material.
Obstructions or dirt on the sensor‟s emitter and/or detector may cause a sensor failure or inaccurate readings. Make sure there are no obstructions and that the sensor is clean.
Autoclaving and/or ethylene oxide sterilizing may cause sensor damage. Do not attempt to sterilize the sensor.
Unplug the sensor from SpirolabIII before cleaning or disinfecting, to prevent damaging the sensor or the device and to prevent safety hazards for the user.
Do not use the instrument in the presence of magnetic resonance imaging (MRI) equipment. MRI equipment may cause an induced current to the oximetry sensor, resulting in patient injury.
1.3
PROBLEMS AND UNFORSEEN ERRORS
In case of a problem, one of a series of messages will appear on the screen together with an acoustic signal to indicate the nature of the problem.
Operation of the device beyond its declared life could provoke a loss of data in the memory of the device (SRAM memory).
Errors in measurement or in interpretation can also be caused by:
use by non-qualified or non-trained personnel, lacking ability or experience
user error
use of the instrument outside the guidelines described in this User's Manual
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use of the instrument even when some operational anomalies are encountered
non-authorised servicing of the instrument
improper, incorrect and/or unreasonable use of the product
If the archive is corrupted, the following message appears:
THE INTERNAL ARCHIVE STRUCTURE IS CORRUPTED
Press any key; the device requires the password (122333) to cancel all data in memory; if necessary download archive with winspiroPRO and then insert password to cancel the device memory.
WARNING
Following the European Directive:
93/42/EEC for MEDICAL DEVICES
In the event of any accident caused by the device, the user must inform the manufacturer without delay.
1.4 LABELS AND SYMBOLS
Identification label of the spirometer model SpirolabIII
For color display
For black and white
The identification label located on the underside of the casing shows the product name, plus the following:
Manufacturer‟s name and address
Mark of conformity with the directive 93/42 EEC
Serial number of the device
0476
EC mark for medical devices.
This product is certified to conform to the requirements of the 93/42/EEC medical devices directive.
Electrical safety symbol. In accordance with IEC 60601-1, this product and its component parts are of type BF and therefore protected against the dangers of direct and indirect contact with electricity
Warning symbol for the connection of the power supply.
To charge the internal battery use only and exclusively the original power supply ( 12 V - 1A DC) (MIR code
920665) guaranteed and certified to the EN 60601-1
Safety Standard.
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Warning symbol for the turbine connector.
Use only and exclusively the original turbine flow sensor.
Warning symbol for the serial port. To connect other devices such as PC or printer to the RS 232 serial port use only the serial cable supplied by the manufacturer and observe the safety regulations of EN 60601-1-1
Symbol laid down in the 2002/96/EEC requirements regarding the disposal of electrical and electronic devices, (WEEE). At the end of its useful life this device must not be thrown away with normal domestic waste, instead it must be delivered to a WEEE authorised collection centre.
An alternative is to return the device without charge to the dealer or distributor, when it is replaced by another equivalent device.
Due to the materials used in the manufacturing of the device, disposing it as a normal waste product could cause harm to the environment and/or to health.
Failure to observe these regulations can lead to prosecution.
For connection to other devices such as PC or printer. Use only the USB serial cable supplied by the manufacturer and observe the safety regulations of IEC 60601-1-1.
Warning symbol for the SpO2 port for oximetry.
SpO
2
FCC ID: TUK-MIR009
Warning symbol for the FCC
spirolab
III complies with Part 15 of the FCC Rules. The correct operation is subject to the following conditions:
(1) this device must not cause harmful interference
(2) this device must accept any interference received, including interference that may cause undesired operation.
Any modifications not expressly approved by this company could void the user's authority to operate the device.
NOTE: This device has been tested and found to comply with the limits for a
Class B digital device, pursuant to Part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates, uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications.
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1.5
However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures:
Re-orient or relocate the receiving antenna
Increase the distance between the equipment and receiver
Connect the equipment to a wall socket which is on a different circuit from that to which the receiver is connected.
Consult the dealer or an experienced radio/TV technician for assistance.
TECHICAL FEATURES OF THE SPIROMETER
Memory
Interface
Flow/volume measurement system
Measurement method
Temperature sensor
Power supply
Batteries charger
Communication port/interface
Wireless Communication
Dimensions
Weight
Volume range
Flow range
Volume accuracy
Flow accuracy
Dynamic resistance at 12 L/s
Type of electrical protection
Safety level for shock hazard
Protection against water ingress
Safety levels during use in presence of inflammable anaesthetic gases or oxygen or nitrogen
Conditions of use
Conditions of storage
Memory capacity for over 6000 spirometric tests. The precise number depends on the individual configuration, so it cannot be determined more closely
RS232, USB, Bluetooth
Bi-directional digital turbine
Infrared interruption
Semiconductor (0-45°C)
Rechargeable battery, Ni-MH, 6 elements
1.2V each, 4000 mAh
Output vonltage = 12 V, current = 1 A, compliant with EN 60601-1.
Use exclusively battery charger provided from manufacturer (MIR code 920665)
RS232, bidirectional and optoisolated to
4KV
Bluetooth
310x205x65mm
1.9 kg
10 L
16 L/s
± 3% or 50 mL
± 5% or 200 mL/s
<0.5 cm H
2
O/L/s
Class II device
Type BF Apparatus
IPX0
Apparatus not suitable
Apparatus for continuous use
Temperature: MIN -20 °C, MAX + 60 °C
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Operating Conditions
Applied norms
Humidity: MIN 10% RH; MAX 95%RH
Temperature: MIN + 10 °C, MAX + 40 °C
Humidity: MIN 10% RH, MAX 95%RH
Electrical Safety Standard EN 60601
Electro Magnetic Compatibility EN 60601
About 10 years.
Life expectancy
Storing of parameters, Flow/Volume and Volume/time curves. The number of tests cannot be precisely defined as it depends on the set up made by the individual user.
Display:
spirolab
III B/W: Graphic LCD passive type FSTN 320x240 Pixel
spirolab
III colour: Graphic LCD 16 colour passive type FSTN 320x240 Pixel
Keyboard:
Silicon rubber keyboard
07 Hardware function keys, with symbols
15 Software function keys, with symbols
05 Arrow keys with symbols (right, left, up, down, enter)
02 Gender identification with appropriate symbols
10 Number keys
29 International alphabet keys.
WARNING
This device is a Class IIa medical device, according to the European Directive
93/42/EEC, annez IX, rule 10.
1.6
TECHNICAL SPECIFICATIONS
1.6.1 Features of the spirometer
Measured parameters:
SYMBOL
*FVC
*FEV1
*PEF
Best FVC
Best FEV1
Best PEF
*FEV1/FVC Best FEV1/FVC
FVC
FEV1
FEV1/FVC
FEV1/VC
PEF
FEF2575
FEF25
FEF50
DESCRIPTION
Forced Vital Capacity
Volume expired in the 1 st
second of the test
FEV1/FVC x 100
FEV1 / best between EVC and IVC x 100
Peak expiratory flow
Average flow between 25% and 75% of the FVC
Forced Expiratory Flow at 25% of FVC
Forced Expiratory Flow at 50% of FVC
L
L
%
%
L
L
L/s
L/s
L/s
L/s
L/s
Units
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IVC
IC
ERV
TV
VE
RR t
I t
E
FIVC
FIV1
FIV1/FIVC
PIF
MVVcal
VC
ELA
EVC
TV/t
I t
I
/Ttot
MVV
SYMBOL
FEF75
FEV3
FEV3/FVC
DESCRIPTION
Forced Expiratory Flow at 75% of FVC
Volume expired in the initial 3 seconds of the test
FEV3/FVC x 100
FEV6 Volume expired in the initial 6 seconds of the test
FEV1/FEV6 FEV1/FEV6 x 100
FET
VEXT
Forced expiratory time
Extrapolated volume
Forced inspiratory volume
Volume inspired in the 1 st
second of the test
Inspiratory capacity (max between EVC and IVC) - ERV
Expiratory reserve volume
Current volume
Ventilation per minute, at rest
Respiratory frequency
Average time of inspiration, at rest
Average time of expiration, at rest
Average flow of inspiration, at rest t
E
/(t
I
+t
E
)
Maximum voluntary ventilation
L/s
L
%
L
% s mL
L
FIV1/FIVC x 100
Peak inspiratory flow
L
%
L/s
Maximum voluntary ventilation calculated from the FEV1 L/s
Slow vital capacity (expiratory)
Estimated lung age
Slow espiratory vital capacity
Slow inspiratory vital capacity
*= best values
Units
L years
L
L
L
L
L
L/min
Breath/min s s
L/min
/
L/min
1.6.2 Features of the oximeter
Measurement method:
Range of measurement %SpO
2
:
%SpO
2
accuracy:
Average number of heart beats for the %SpO
2 calculation:
Range of measurement of cardiac pulse:
Red and infrared absorption
0 – 99% (with 1% increments)
2% between 70-99% SpO2
8 beats
Accuracy of cardiac pulse:
Average interval for the calculation of cardiac pulse:
Signal quality indication:
Definitions:
Desaturation Event
30 – 254 BPM (with 1 BPM increments)
2 BPM or 2%
8 seconds
0 - 8 segments on display
Desaturation events SpO2 fall >= 4% in a limited period of 8-40 sec and successive rise > = 2% within a total period of 150 sec.
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Parameters measured during sleep oximetry:
SYMBOL
SpO2 Baseline
SpO2 Min
SpO2 Max
SpO2 Mean
BPM Baseline
BPM Min
BPM Max
BPM Mean
Recording time
Analysis Time
T90
T89
T88
T87
N SpO2. Events <89%
Index (12ses)
T< 40 BPM
T> 120 BPM
Bradycar. Events < 40
BPM
Tachycar. Events>120
BPM
Total Desat. Events
ODI
Mean Duration
Longest Duration
Desaturation Peak
Mean Desaturation
Mean Drop SpO2
Max Drop SpO2
N. Pulse Variations
Pulse Index
NOD 4%
NOD 89%
DESCRIPTION
SpO2 Average in first three minutes
SpO2 Minimum during analysis period
SpO2 Maximum during analysis period
%
%
%
% SpO2 Average during analysis period
Average pulse frequency in the first 3 minutes BPM
Minimum pulse frequency during the analysis period
BPM
Units
Maximum pulse frequency during the analysis period
Average pulse frequency during the analysis period
Total time measure of SpO2
Total time of analysis
Time passed with SpO2 < 90 %
Time passed with SpO2 < 89 %
Time passed with SpO2 < 88 %
Time passed with SpO2 < 87 %
Fall of SpO2 below 89% for at least 20 seconds
BPM
BPM hh:mm:ss hh:mm:ss
% hh:mm:ss
% hh:mm:ss
% hh:mm:ss
% hh:mm:ss
\
Index of SpO2 fluctuation calculated in intervals of 12 sec.
\
Time passed with pulse frequency < 40 BPM % hh:mm:ss
Time passed with pulse frequency > 120 BPM % hh:mm:ss
Bradycardia events during the entire analysis period
Tachycardia events during the entire analysis period
Desaturation events during the entire analysis period
Desaturation events per hour of analysis
Average duration of desaturation events
\
\
\
1/h s s
%
%
Longest duration of desaturation events
Minimum Sp02 during desaturation events
Average duration of desaturation events
Average SpO2 fall with respect to baseline, during the desaturation events
Maximum fall of SpO2 with respect of baseline, during the desaturation events
Variation of pulse frequency events during the entire analysis period
Variation of pulse frequency by hour of analysis
Time passed with SpO2 < 4 % with respect to
SpO2 base for continual periods above 5 minutes
Time passed with SpO2 < 89 % for continued periods above 5 minutes
%
%
\
1/h
\ hh:mm:ss
\ hh:mm:ss
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SYMBOL
NOD 90%
DESCRIPTION
Time passed with SpO2 < 90 % for continued periods above 5 minutes with minimum value
< 86 % (Nadir)
Units
\ hh:mm:ss
=
DELTA
Parameters measured during exercise test:
SYMBOL
SpO2 Baseline
SpO2 End
SpO2 Min
SpO2 Max
SpO2 Mean
BPM Baseline
BPM End
BPM Min
BPM Max
BPM Mean
T90
T89
T88
T87
T2 [
T4 [
SpO2≥ 2%]
SpO2 ≥ 4%]
T< 40 BPM
T> 120 BPM
Bradycar. Events < 40
BPM
Tachycar. Events>120
BPM
Recording Time
Analysis Time
Baseline Time
Exercise Time
Recovery Time
DESCRIPTION
SpO2 average before exercise
SpO2 after exercise
SpO2 minimum during exercise
SpO2 maximum during exercise
SpO2 average during exercise
Average pulse frequency before exercise
Pulse frequency after exercise
Pulse frequency minimum during exercise
Pulse frequency maximum during exercise
Pulse frequency average during exercise
Time passed with SpO2 < 90 %
Time passed with SpO2 < 89 %
Time passed with SpO2 < 88 %
Time passed with SpO2 < 87 %
Time passed during exercise test with SpO2 < 2
% with respect to SpO2 base
Time passed during SpO2 exercise test < 4 % with respect to SpO2 base
Time passed with pulse frequency < 40 BPM
Time passed with pulse frequency > 120 BPM
Bradycardia events during the entire period of analysis
Tachycardia events during the entire period of analysis
Total time measure of SpO2
Total time of analysis
Duration of baseline phase
Duration of exercise phase
Time for SpO2 value 99% of the average base value calculated during the initial phase of the test.
DYSPNEA Baseline Variation in grade of dyspnea during Baseline
DYSPNEA End
DYSPNEA CHG
FATIGUE Baseline
FATIGUE End
Fatigue CHG
Final grade of dyspnea
Variation in grade of dyspnea during exercise
Variation in grade of fatigue during Baseline
Final grade of fatigue
Variations in level of fatigue during exercise hh:mm:ss hh:mm:ss hh:mm:ss
\
\ hh:mm:ss hh:mm:ss hh:mm:ss hh:mm:ss hh:mm:ss
\
\
\
\
\
\
%
%
%
%
%
BPM
BPM
BPM
Units
BPM
BPM
% hh:mm:ss
% hh:mm:ss
% hh:mm:ss
% hh:mm:ss hh:mm:ss
=
DELTA
Parameters required for exercise test:
SYMBOL DESCRIPTION Units
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SYMBOL DESCRIPTION
Baseline DYSPNEA Grade of dyspnea before exercise
Final DYSPNEA
Baseline FATIGUE
Final FATIGUE
Grade of dyspnea after exercise
Level of fatigue before exercise
Level of fatigue after exercise
Parameters measured with SpO2 Analysis:
SYMBOL
SpO2 Baseline
SpO2 Min
SpO2 Max
SpO2 Mean
BPM Baseline
BPM Min
BPM Max
BPM Mean
Recording time
Analysis Time
T90
T89
T88
T87
N. SpO2 Events < 89%
Index (12sec)
T< 40 BPM
T> 120 BPM
Bradycar. Events < 40
BPM
Tachycar. Events>120
BPM
\
\
\
\
Units
DESCRIPTION
SpO2 Average in first three minutes
SpO2 Minimum during analysis period
SpO2 Maximum during analysis period
SpO2 Average during analysis period
%
%
%
%
Average pulse frequency in the first 3 minutes BPM
BPM
Units
Minimum pulse frequency during the analysis period
Maximum pulse frequency during the analysis period
Average pulse frequency during the analysis period
Total time measure of SpO2
Total time of analysis
Time passed with SpO2 < 90 %
Time passed with SpO2 < 89 %
Time passed with SpO2 < 88 %
Time passed with SpO2 < 87 %
Fall of SpO2 below 89 % for at least 20 seconds
Index of SpO2 fluctuation calculated in intervals of 12 seconds
BPM
BPM hh:mm:ss hh:mm:ss
% hh:mm:ss
% hh:mm:ss
% hh:mm:ss
% hh:mm:ss
\
\
Time passed with pulse frequency < 40 BPM % hh:mm:ss
Time passed with pulse frequency > 120 BPM % hh:mm:ss
Bradycardia events during the entire analysis period
\
Tachycardia events during the entire analysis period
\
=DELTA
Acoustic signals for oximetry:
Beep with frequency of the cardiac pulse
Continuous beep in the case of either %SpO
2
or cardiac pulse going outside of the programmed alarm levels
Continuous beep during oximetry measurement in the case of low battery level
If the patient‟s finger is not inserted correctly or the connecter is not properly attached there will be an intermittent beeping sound for 10 seconds
If the test has been interrupted due to low battery power an intermittent beeping will be heard for 10 seconds when the device is switched on again
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The specifications for both the oximetry and for the cardiac pulse are the same, regardless of which of the above mentioned oximetry sensors is used.
2 PRODUCT DESCRIPTION
Spirolab
III is a spirometer with an optional pulse oximetry module that facilitates the total valuation of lung function. It is a powerful and compact measurement device intended for use by a physician (respiratory specialist), and which is capable of calculating more than
30 spirometric parameters.
Spirolab
III is able to make FVC, VC, IVC, MVV and breathing profile tests, as well as the saturation of oxygen in the blood and the heart beat.
It can operate in stand alone mode, and it can be connected to a PC or to a printer using any one of several available methods: RS232, USB, Bluetooth.
It calculates an index of test acceptability (test quality control) and a measure of reproducibility; It also gives functional interpretation with 11 possible levels following the latest ATS (American Thoracic Society) classification; it has an internal memory sufficient for over 6000 spirometry tests or for 1000 hours (or 40 days) of oximetry monitoring.
The main spirometric parameters are measured and displayed and all data with
Flow/Volume and Volume/time curves can be printed out in seconds by the built-in thermal printer. The Flow/Volume curve is shown in real time on the display.
Each test can be repeated as required. The best parameters are always available for quick viewing or printing. The normal (predicted) values can be selected from five different authors. In general, within the European Union the ERS (European Respiratory Society) predicted values are used.
The device also calculates the response to drug administration, i.e., the percentage change between spirometry results obtained before and after the subject takes a drug) and the results of a bronchial challenge test or a bronchodilation test. A comparison of data is made between POST (after-drug) and PRE (before drug administration).
The flow and volume measurement sensor is a digital turbine, based on the infrared interruption principal. This principal ensures the accuracy and the reproducibility of the measurements without requiring a periodic calibration.
The main features of this kind of sensor are listed below:
Accurate measurement even at very low flow rates (end of expiration)
Not influenced by gas humidity nor density
Shockproof and unbreakable
Inexpensive to replace
The turbine flow measurement sensor is available both in reusable and in single-patient disposable versions.
REUSABLE TURBINE DISPOSABLE TURBINE
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The following precautions must be observed to ensure that the characteristics of the turbine remain unaltered over time:
For the disposable turbine: must always be substituted between patients.
For the reusable turbine: always clean the turbine between patients, to ensure the maximum level of hygiene and safety for the patient.
For a correct interpretation of a spirometry test, the measured values must be compared either with the so-called normal or predicted values which are calculated from the anthropometric details of the patient or, alternatively, with the personal best values from the clinical history of the subject.
The personal best values can vary considerably from the predicted values, which are taken from “healthy” subjects.
Spirolab
III is supplied with an RS-232 optoisolated serial communication port, which guarantees excellent electrical protection (> 4 KV) both for the health care worker and for the subject, in compliance with the most strict European safety standards (EN 60601-1).
The Bluetooth connection system can be used to connect the device directly to a printer
(the Bluetooth system must be installed and enabled on the printer as well).
Spirolab
III can also be connected to a PC (or to another computerised system) to configure the system. All spirometric test results plus the related subject details stored inside the device can be transferred from the device to the PC and then viewed within the winspiroPRO PC software (Flow/volume curves, spirometry parameters, plus optional oximetry parameters).
The connection to the PC can be made in the following ways:
through the RS232 port or
through the USB port
The internal software (or firmware) of the device can be upgraded quickly and simply from a PC.
For upgrading the system consult the manufacturer or an authorized representative.
spirolab
III gives an automatic interpretation of each spirometry test carried out, and assigns a “traffic light” feedback (green, yellow or red) to each test or series of tests. The set up of the traffic light settings is made by the doctor responsible for the system configuration.
Oximetry function
The oximetry sensor has two light emitting diodes (LEDs), one emits in the visible spectrum and one infrared. Both lights then pass through the finger and are “read” by the receiver. As these lights pass through the finger, a proportion of the light is absorbed by the blood and by the soft tissue, in function of the concentration of heamoglobin. The quantity of light absorbed, at each frequency, depends on the degree of oxygenation of the haemoglobin inside the soft tissue.
This measurement principal ensures accuracy and reproducibility, without requiring regular calibration.
The oximetry sensor can be disinfected with isopropilic alcohol for more information see paragraph 4.3.
The operating battery is a 3.6V lithium battery.
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2.1
ILLUSTRATION OF
S
PIROLAB
III
1. MiniFlowmeter sensor
2. Thermal paper container
3. Flow sensor compartment
4. Display
5. Keyboard
6. Oximeter sensor
2.2
KEYBOARD
SYMBOL
On/Off
Adjust contrast
Adjust brightness
DESCRIPTION
Advance the printer paper
Self-check key
Cancel the current operation
Select configuration menu
Correction key/cancel last data inserted
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SYMBOL DESCRIPTION
Information about options
View data in memory
Enter/modify patient data
View best test
View last test
View last oximetry test
Make POST test
Make oximetry test
Make FVC test
Make VC test
Make MVV test
...
Number keys
Specifies female sex
Specifies male sex
Confirm last operation. This key is the ENTER key
Move cursor
2.3 C
HARGING THE BATTERY
WARNING spirolab
III is powered only by the internal batteries; the battery charger is used only to charge the internal batteries. In the charging phase the device can be used only after the internal batteries have recovered a minimum charge level.
WARNING
For charging internal battery of spirolab III use exclusively the battery charger provided with the device (MIR code 920665)
Make sure that the electrical information on the label of the charging unit corresponds to that of the power source.
Plug the power supply into an electrical outlet.
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Plug the power supply jack into the socket on the back of the device.
Do not use the power supply if it is wet or damp.
Green LED
POWER ON
Orange LED
Battery charging
Green LED
Battery charged
The charging process has several phrases which are indicated by two LEDs, green and orange (as shown above).
Immediately after connecting the power supply, the orange LED starts to flash.
After a few seconds the orange LED stops flashing and remains lit.
For about 10 minutes the charging is partial while device automatically checks the battery condition.
After about 10 minutes the charging starts and proceeds to a full charge.
When charging is completed, the orange LED turns off and the green LED lights up.
WARNING
It is possible that during battery charging there may be a slight increase of a few degrees in the temperature of the power supply. Always place the device on a suitable rigid horizontal on a stable surface with at least 30 cm (6 in) of space all around the device. The ventilation slots must be free from any cover or obstruction of any kind, they are located both behind and underneath the plastic outer casing of the device.
2.4 S
WITCHING ON THE SPIROMETER
First check that all the accessory items are in good condition.
Before using the device proceed with the cleaning operations, as described in the
MAINTENANCE AND CLEANING section.
Lift the LCD display, release the catch.
Press the red on/off key on the upper left corner of the keyboard. When the device is on, the green led on the right hand side of the on/off key will light up.
WARNING
When the device is connected to a PC via a USB cable then it will automatically power on, as the power supply is internal.
2.5 S
ETTINGS
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Backlight settings
The brightness of the display is a factory setting and cannot be adjusted.
2.5.1 Contrast settings
The contrast of the display can be adjusted by using the keys. The left arrow increases the contrast and the right arrow decreases it.
Keep the key pressed without using excessive force to adjust the contrast to your liking.
After adjusting the contrast of the display wait 5 seconds after releasing the key for the device to memorize the new contrast setting before turning off the Spirolab III.
2.5.2 Loading the thermal paper
Open the lid of the thermal paper compartment and remove it from the device; remove the paper roll holder.
Insert the new roll of paper onto the paper roll holder.
WARNING
The thermal paper must be inserted as shown in this picture, paying WARNING to the position of the paper holder roll pins inside the guides and to the direction of the roll, so that printing occurs on the correct side of the thermal paper. Note that the thermal paper cannot be printed on both sides but only on the one faceup of the paper roll.
Guide to the correct positioning of the paper roll holder
Push the paper into the slot located under the traction reel (black rubber reel).
A sensor (as indicated in the image) detects the paper and automatically advances it.
This image shows the position of the paper in relation to the traction reel. The paper must advance through the slot in the compartment when it is closed; close the lid of the compartment.
If necessary make the paper advance manually by pressing
WARNING
To avoid damage to the printer and/or defects in printing, it is recommended to use thermal paper with 112 mm width size. The sensibility of the thermal paper must be
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suitable for printers with a printing speed of 50 mm/s. This type of paper is easy to find at most medical device dealers.
2.5.3 Connecting the flow sensor
The flow sensor is made up of the elements shown in the following illustration.
Before carrying out a spirometry test, verify that there are no foreign bodies present inside the flow sensor.
Connect the connection cable to the Miniflowmeter until hearing the „click‟ which indicates that it has been correctly inserted.
Connect the other end to the
spirolab
III as shown in the image; again the „click‟ will indicate the correct insertion.
Make sure that a new disposable mouthpiece has been correctly inserted in the turbine
(mouthpiece holder).
Miniflowmeter Turbine Mouthpiece
WARNING
Follow carefully all of the instructions given in the various paragraphs of this manual, to ensure that all of the functions operate correctly.
Remove the used mouthpiece and dispose of it after finishing the spirometry testing.
When the flow sensor head is not in use, we recommend that it is kept in its compartment.
Press lightly on the connector to detach the flow sensor turbine from the socket on the left hand side of the device and proceed with the cleaning operations as outlined in the MAINTENANCE CLEANING
section of the manual.
2.5.4 Switching off the spirometer
The device has an auto power-off system for reducing battery consumption. This feature can be set up from the menu by selecting one of the following 3 options: 6, 60 or 240 minutes; the device will automatically switch off upon reaching the pre-set time, when no activity has been made for that time.
If instead the device remains switched on when all operations are complete, switch it off manually by pressing . When the device is switched off, the green (LED) indicator on the right hand side of the on/off
key should also be off.
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When the battery does not need charging then be sure to detach the power supply from the power supply socket on the back of the device and remove the charger from the mains supply.
2.5.5 Initial settings
WARNING
The sections of this Manual contained in a frame correspond to the wording shown on the screen of the device. spirolab
III allows for the personalised setting of certain parameters through the
Configuration Menu.
To access the configuration menu, with the device switched on, press contains the following list:
Delete data in memory
Print last calibration
Turbine calibration
Printout header text
Change Date/Time
Choose operating language
Choose predicted values
Setup parameters/printout
Bluetooth settings
Oximetry settings(*)
Incentive
Turbine type
Standard
Date format
Units format
Auto power-off
which
* function available only for spirolab III with colour display
Select the required option using alongside your selection; then press
or , until the symbol on the left of the screen is
to access the option.
Use this key to recall the Configuration Menu, to set-up and/or to change certain main functions of the device.
Delete data in memory
To delete all the data in memory.
The display will show:
DELETE DATA IN MEMORY
WARNING! ALL SPIROMETRY TESTS IN
MEMORY WILL BE DELETED.
Use test data.
to quit without deleting the
The password is
: 122333
TO PROCEED INSERT PASSWORD
( )
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After deleting the data in memory, the display shows:
If the password is entered incorrectly, the display shows:
Test data has been DELETED!
Available memory is: 100%
PRESS ANY KEY TO EXIT
PASSWORD INCORRECT
ENTER to Retry
ESC to Quit
Press to repeat the procedure.
Print last calibration
To print the turbine calibration coefficient currently in use plus the date of the last calibration made.
Turbine calibration
WARNING
The turbine flow sensor does not require calibration but needs only regular cleaning. If a calibration must be made then the following guidelines must be carefully noted.
Only the reusable turbine can be calibrated.
NOTE
Each time a calibration is made, the new correction factor is algebraically added to the previous correction factors. Therefore, before making a new calibration, make sure to delete the actual calibration in use as described above.
For an accurate and reliable calibration the syringe volume must be at least 3 L.
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To modify the calibration of the turbine based on the
FVC values (for the expiratory phase) and FIVC (for the inspiratory phase), measured during a test made with a calibration syringe.
From configuration menu choosing “turbine calibration”, on the display appears the following informations.
The values “FVC” and “FIVC” are retailed to the last calibration. The values under the “%COR” column indicate the actual correction. They are set on 0 for default.
WARNING
ATP stands for Ambient Temperature and Pressure which indicates that the measurement conditions are ambient temperature and pressure.
BTPS stands for Body Temperature and Pressure Saturated which represents a world standard reference condition for the measurement of spirometric parameters. All spirometric parameters are calculated at body temperature (37
°C) and pressure saturated.
In line with the publication "STANDARDISED LUNG FUNCTION TESTING" of the
European Respiratory Society (Vol 6, Supplement 16, March 1993), the air expired from the mouth is at a temperature of circa 33/34 °C.
The expired flow and volume, to be converted back to BTPS conditions (37 °C), must be increased by 2.6% - this is derived from the BTPS factor of 1.026 at a temperature of 33°C, which represents a correction of 2.6%. In practice the BTPS factor for the expired flow and volumes is therefore constant and equal to 1.026.
For the inspired volumes and flows, the BTPS factor depends instead upon the ambient temperature, as the inspired air is at ambient temperature.
For instance, at an ambient temperature of 20°C with relative humidity at 50%, the
BTPS factor is 1.102, a correction of +10.2%.
The correction of the inspired volumes and flows is made automatically, as the device has an internal temperature sensor; all parameters are thus reported at
BTPS.
To make the calibration:
1 - Insert the volume in cL of the calibration syringe in use (e.g. for a 3L syringe, insert 300 cL).
2 - Insert both the FVC and FIVC values, obtained by the measurement made with the calibration syringe, in the New FVC and New FIVC field. Use vertical scrolls to select the value to be modified (SIRIN, New FVC, New FIVC).
Use numeric keys to modify the parameter value selected.
If the calculated correction factors are acceptable (<20%), they are displayed beside the
New FVC and New FIVC parameters.
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Press ESC to return to the configuration Menu without entering the correction.
If the FVC and FIVC values produce a correction factor that is >20%, the FVC and FIVC values will not be accepted. This means that the system cannot correct for such a large calibration error. The following message appears:
WARNING ! ERROR too high
In this case:
- Check the correct functioning of the spirolab III with a new turbine and/or
- Clean the turbine.
To erase the calibration in use and reset to the factory calibration, input 0 in the New
FVC and New FIVC fields.
Then press to return to the Configuration Menu.
WARNING
With the new calibration, the correction factors are algebraically added to the previous correction factor(s).
Before to begin a new calibration set the two values FVC and FIVC at 0, then repeat the calibration procedure.
If a 3L syringe is used to make the calibration and if the spirometer is calibrated correctly then the FVC (syringe) value will be:
3.00 (FVC) x 1.026 (BTPS) = 3.08 L (FVC at BTPS).
If the ambient temperature is 20°C, the FIVC (syringe) value will be:
3.00 (FIVC) x 1.102 (BTPS) = 3.31 L (FIVC at BTPS).
The user must be aware that the volume of the syringe shown by the machine is converted to BTPS conditions, so that the "increase" of the results with respect to the expected values does not constitute an error.
For instance, if the calibration procedure is carried out with measured data:
20 ° C, FVC = 3.08, FIVC = 3.30 the spirometer is perfectly calibrated and the relative correction factors are null.
No calibration is required!
This does not represent an error, but is a logical consequence of the above detailed explanation.
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Printer header text
To insert a header that will be printed at the beginning of each spirometry report (see image).
Change DATE/TIME
To change the date and time.
The time is shown in the 24 hour format.
Select language
To change the language used for displaying messages on the screen and the printouts
.
Select predicted values
To select one of the standards available for the calculation of the predicted values. The parameters are organized in the following way:
REFERENCE
1
2
3
ADULTS
ERS
Knudson
Morris/Bass
4
5
ERS
MC-Barcelona
Zapletal
Zapletal
Select with the numeric keys the reference number, automatically the chosen values will set and the display shows the configuration menu.
CHILDREN
Knudson
Knudson
Knudson
Select printout
To enable or disable the printout of: spirometry parameters best values of: FVC, FEV1, FEV1/FVC, PEF, FEF2575 (the last one is always relative to the best test) spirometry interpretation
F/V and V/t curves.
Bluetooth settings
Select this function and the following menu is shown:
Search Device
Options PRINTER
Options PHONE
Remote line Number
Search Device
Select the required option with and confirm with ; spirolab III begins to search for
Bluetooth active devices; when one or more active devices are found then a list is shown, select a device and push to define the device (with vertical scroll) as a printer or as a phone (use PRINTER or PHONE); select one of the two options and push , otherwise
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push to return to the Bluetooth options. If the device is already present in the chosen list a warning message will be shown on the display; push a key to turn to the devices list.
Options PRINTER
To control the devices memorized within the “printers list”. Enter the list with having selected a device it is possible:
and
to set the device as default, identified with a yellow point near the device name (so
spirolab
III will automatically connect to this)
to delete the device from the list (spirolab III asks for a confirmation by pressing , otherwise press the list).
to return to the Bluetooth options and not delete the device from
If no devices are shown then a message advises the user to search for active devices; press to start the search or to return to the Bluetooth settings.
Options PHONE
To control the devices memorized in the “printers list”. Enter the list with selected a device it is possible:
and having
to set the device as default, identified with a yellow point near the device name (and
spirolab
III will automatically connect to this)
to delete the device from the list (spirolab III asks for a confirmation by pressing , otherwise press the list).
to return to the Bluetooth options and not delete the device from
Even if the list is empty, a search can be made for active devices as previously described.
Remote line Number
Enter the menu with then it is possible to insert the telephone number that spirolab III will use to connect to a Bluetooth telephone. Insert the required number using the numeric keyboard and then press .
Oximetry settings
This function permits the following kinds of setting up :
reference values for Sp02 and BPM; if, during a test, these values go below the minimum or above the maximum values in the set up an acoustic alarm will ring to alert the user
activation/disactivation of the acoustic alarm
set the sampling time (2 or 4 seconds) of oximetry values during a test
The cursor at the beginning will rest on the minimum Sp02 value, use the numeric keys to select the desired value, then the cursor automatically pass to the next value; if a value
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must not be modified press ; once the four values have been set up you can then, if required, activate or disactivate the acoustic alarm by pressing key 1 for OFF and key 2 for
ON. To confirm the selection press . Then is possible to set the sampling time: press key
2 to set 2 sec or press key 4 to set 4 sec. Pressing the configuration menu is displayed.
Incentive
spirolab
III has a pediatric incentive program which can be useful to help a child (or an older person) make a correct spirometry test. The incentive is a hidden image, directly connected to the signal coming from the MiniFlowmeter so the harder the expiration then the further the “curtain” moves away, revealing the image and thus helping the patient to obtain the best possible result.
When the pediatric incentive is selected, a warning message is shown asking for the age of the patient. Set the correct value, the configuration menu is then shown.
Given that the FVC test requires collaboration that is difficult to obtain in children under the age of 4, then if an age of 4 or below is selected then spirolab III automatically shows the incentive during the FVC test.
Turbine setup
Select the type of turbine to be used for testing, either single-patient disposable or reusable. To select the correct option, follow the steps as described previously selecting the required item and press v to change the option.
Standard
To select one of the available standards: ATS/ERS or NANHES III, press .
WARNING
With the standard NAHNES III is not possible to select or to modify the predicted values.
DATE format: dd/mm/yy
To select the required format, toggles between dd/mm/yy or mm/dd/yy or yy/mm/dd or vice versa.
Press to toggle.
UNITS format: cm, kg
To change the units format from cm, kg to in, lb (inches and pounds) or vice versa.
Press to toggle.
Auto power-off: 6 min
To change the wait-time for auto power off to 6 min, 60 min or after 240 min.
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Press to toggle.
2.5.6 Functioning of the spirometer spirolab
III performs the following measurements:
The valuation and interpretation of test results are given by comparing the measured parameters with specific
„normal‟ spirometry values (known as
Forced Vital Capacity
Slow Vital Capacity
Maximum Voluntary Ventilation predicted values) which are calculated
SpO2/BPM* from subject data: age, height, weight, sex and ethnic group.
* only for spirolab III with colour display
For the calculation of the predicted values, there are several different sets available both for adults and for children.
For adults
“
“
“
For children
“
ERS (European Respiratory Society)
Knudson
Morris/Bass
Multicentrico Barcellona
Knudson
Zapletal
After each test session the results are compared to the selected predicted values and the percentage ratio between measured and predicted is shown for each parameter.
The test can be repeated more than once and the best result is memorized in order to be recalled from the spirolab III’s memory.
The best test result is determined following the ATS/ERS standards.
In practice, the best test is the one having the highest sum of FVC+FEV1.
All tests are analyzed by applying the quality criteria (quality control), following the ATS standards. In addition, the reproducibility of the FEV1, FVC and PEF parameters are also calculated.
It is possible to perform POST drug testing, in this case the test results are compared to a test made prior to the administration of drugs (PRE-test).
spirolab
III displays and prints the Flow/Volume and the Volume/time curves superimposed, with PRE and POST parameter comparison and percentage of change:
% PRE =
Value POST
Value PRE
x 100 spirolab
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After switching on the device, the main screen will show a summary of the current patient data.
Some values shown are as follows:
v. x.y
Indicates the version of the software
(firmware) inside the spirometer. In case of technical problems always note this version number.
DATE AND TIME
The current date and time, which can be modified from the Configuration Menu.
PRE
The first test for each new subject is a PRE type, i.e. without drug administration.
For the POST test i.e. after the administration of drugs, see Paragraph 2.6.2 POST in this
Manual.
FILE
spirolab
III assigns a progressive number to each new PRE, POST or SpO2/BPM oximetry test.
LAST NAME AND NAME
Are displayed data of the last patient inserted
#ID
Indicates the subject number or identification code which is inserted by the user.
TYPE OF TURBINE
STANDARD IN USE
BTPS (
Body Temperature Pressure Saturated
)
2.5.7 New subject data entry
Press .
The lower part of the screen will show the following message:
CHANGE
NEW
Use
or to modify patient data of patient displayed, otherwise insert new details.
SUBJECT NAME AND SURNAME spirolab
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Use or to modify data of a patient already inserted, or to enter the details of a new patient.
Enter the required information using the cursor positioned on the subject‟s surname. Use
to go to the next entry.
All data entered must be confirmed with after it has been entered use
or cancelled with correct numerical value and go to the next entry press .
. To modify a number
; to return the cursor to the area required, to enter the
#ID
Insert the patient ID code: this code is alphanumerical and can be a maximum combination of 16 characters; this code enables the quick recall of any patient data when required.
Recall a subject from memory and press the #ID key to create a new test session with the anthropometric details of the same subject. This avoids having to reinsert all of the data of that patient.
If the ID code inserted already exists in memory then the following message appears:
WARNING! #ID ALREADY ASSIGNED
CONFIRM ID CODE OR MODIFY
The user may either exit, enter a new ID code, or continue by using the patient file in memory.
Press
to confirm the code; press one of the arrow key to modify.
DATE OF BIRTH
Insert patient data with the numeric keys; spirolab III automatically calculates the patient age which is then shown in the space “AGE”. Insert the other data using
.
HEIGHT
Enter the subject‟s height (in cm or in inches, according to the current configuration), using the numeric keyboard. Go to next entry using .
WEIGHT
Enter the subject‟s weight (in Kg or Pounds, according to the current configuration), using the numeric keyboard. Go to next entry using .
SEX
Select gender using the keyboard, for male and for female.
ETHNIC GROUP
Select one type of ethnic group, enter the number corresponding to the required ethnical group. Press 0 for no conversion factor. This function allows the correction of the predicted values for a subject with the ethnic group to which he or she belongs.
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ATS/ERS Standard
Group
Without correction
Caucasian
Oriental
Hong Kong Chinese
% correc.
100%
100%
100%
100%
NAHNES III Standard
Caucasian
African-American
Mexican-American
Others
Japanese
Polynesian
North Indian
89%
90%
90%
South ndian
Pakistan
87%
African Descent
For ATS/ERS standards, the correction is applied to the predicted values of the following parameters:
90%
87%
FVC, FEV1, FEV3, FEV6, VC
For NAHNES III standards, the correction is based on several theoretical formulas (as described in the publication).
WARNING
By entering the number 0 (zero), no ethnic correction will be made to the calculation of the predicted values. It is possible to enter ethnic group no. 10, and to define a correction percentage of the predicted values between 50% and
200% of the predicted values in use.
WARNING
Note the settings pre-defined within the configuration menu when inserting patient data, in particular re date format, weight and height.
2.5.8 Modify subject data
To modify subject data press and then .
AIl data not to be modified must be confirmed by pressing
2.6 S
PIROMETRY
:
FVC
,
VC
/
IVC
,
MVV
WARNING
.
When connecting the spirometry sensor to the device, ensure that the connector has the arrow side UP towards you. When correctly inserted the connector will
“click” into place. See the following image.
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All subject data must be entered before carrying out a spirometry test.
The test can be made from the main screen or from any display that shows a previous test result (last test, best test or test in memory).
Select the spirometry test:
To make the FVC test tests
To make the VC/IVC and ventilatory profile
To make the MVV test.
WARNING
With standard NAHNES III it is not possible to make VC or MVV tests
When a test is being performed the display will show the real time Flow/Volume curve or the Volume/time curve (if the pediatric incentive is set, then the volume/time curve is displayed.).
The test must begin within 30 seconds of pressing the start key, otherwise the test is interrupted and the device returns to the main screen.
2.6.1 Spirometry testing
Insert a new mouthpiece into the MiniFlowMeter mouthpiece holder.
Fit the nose clip onto the nose of the subject, to ensure that air cannot escape through the nostrils.
The subject must insert the mouthpiece well into the mouth, it should be inserted at least 2 cm beyond the front teeth and held between the teeth, closing the lips to ensure that air cannot escape from the sides of the mouth.
Breathe as directed according to the test to be undertaken, details follow.
Make the test in either a standing or a sitting position. During total expiration (slowly or forced) lean forward to help the expiratory action with a compression of the abdomen.
FVC
If required (this part is optional), before the test make several breaths at rest. When ready, inspire slowly as much air as possible (opening the arms helps) and then expire all of the air as fast as possible. Then, without removing the mouthpiece from the mouth, finish the test by inspiring again as fast and as completely as possible.
This final inspiration is not necessary in the case that the inspiratory parameters (FIVC,
FIV1, FIV1%, PIF) are not required.
The cycle can be repeated several times, without removing the mouthpiece, in which case
Spirolab
III will automatically select and show the best test and measured parameters. To end test press or just wait for 10 seconds after the last volume cycle, the test terminates automatically.
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WARNING
In the case of an FVC test, after making at least two valid tests, the reproducibility of the parameters FVC, FEV1, and PEF is also shown.
VC/IVC and Ventilatory Profile tests
It is possible (optional) to begin the test by making several complete breaths at rest. After three or four similar breaths, a message (VC/IVC) on the display will indicate that the ventilatory profile has been measured and you can now proceed to carry out the VC or IVC test.
VC test: When the message VC/IVC appears, inspire slowly as much air as possible into the lungs and then expire slowly as much air as possible.
IVC test: When the message VC/IVC appears, expire slowly as much air as possible and then inspire slowly as much air as possible.
To end the test press or wait 3 seconds after the last volume cycle.
If you make the test without the ventilatory profile (respiratory function at rest) then the measured parameter will be only VC or IVC. Instead, by carrying out several complete breaths at rest, then in addition all measured parameters of the ventilatory profile will be given.
During the test the volume/time curve is displayed.
MVV
Start the test by carrying out a series of forced inspirations and expirations with the maximum possible amplitude. The suggested frequency is 30 breaths/min. The test will terminate automatically after 12 seconds.
To end test press or wait 3 seconds after the last volume cycle.
At the end of any test, the related curves and the main measured parameters are shown.
After viewing the curves, press to view the remaining test parameters, plus the predicted values and the percentage ratio between the measured value and the predicted value.
During the test the volume/time curve is displayed.
2.6.2 Spirometry post - drug
WARNING
To carry out a POST test it is necessary to have carried out at least one PRE FVC type test on the patient on the same day; it is not possible to do a POST test on the PRE VC or MVV tests; it is however possible to do a POST VC or MVV test if the archive already contains at least one PRE test carried out on the same day.
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1
st
case: current patient data
To perform a POST test on the current subject after completing e PRE test, follow these instructions:
Press to activate the POST phase. On the bottom of display it is shown the following message:
ENTER to make POST test
It is possible to carry out the POST test using one of the three tests available. Selected the test, in the lower part of display it is possible to define the dose administer to the patient before the test; the value can be inserted with numeric keys.
2 nd
case: subject file
To perform a POST test on a patient already in memory, firstly “recall from memory” the relavant PRE test spirometry parameters from the same subject file.
Press ; select using one of the research metods the PRE file. Confirm with .
Press phase. to set a new test with the same patient
.
Press to activate the POST
When the POST phase is activated, the patient data are shown and “POST” appears under file number.
WARNING
In the POST phase the FVC, VC and MVV tests can be performed.
In the POST phase, having selected one of these three tests administered drug dose must be entered.
or , the
Whenever the test is repeated using the same dose, the best test related to the dose used is saved.
When the dose is changed, then a new record is made with a progressive FILE number.
For example, if three tests are made on a subject at different doses, then three different records (POST tests) are saved for that subject.
Afterwards the separate best POST tests can be viewed.
The subject code in the POST test is the same as for the related PRE test.
The results allow the confrontation of the spirometry parameters calculated in the POST test against the best results obtained in the PRE test already present in the patient archive for that session* (*session refers to tests carried out on that day). It is not possible therefore to carryout a POST test on a patient if the patient archive only contains PRE tests carried out only on previous days.
When the results are displayed it is possible to see the variation between the PRE and
POST values (shown in column headed CHG)
In the POST phase, the measured result is compared to the values of the related PRE test.
The Flow/Volume curves of the PRE test and related POST test are shown superimposed.
After the two curves, the measured parameters (POST), the related PRE values and the percentage variations between POST and PRE are also shown.
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To make the results shown easier to understand a traffic light system has been used with the following icons and/or as per the criteria below:
significant broncodilatation with FEV1 POST ≥ 80% of predicted
significant broncodilatation with FEV1 POST < 80% of predicted
no significant broncodilatation
WARNING
In the POST phase no test interpretation is given, the test quality control messages are shown.
The POST test is available both in main display with the characteristics of the patient and in visualization of previous test (
or
) in this manner is easy to set post phase. Visualizing the data stored the active keys are:
;
#ID (for a new spirometric test with patient selected)
(for a POST test)
(print out of the selected test)
and for display
to go to the archivi menu.
(key for generic stop)
1, 2, 3 (if there are made more than one test).
Physiological test (placebo)
It is common practise prior to a POST test to carry out a test using physiological solution in place of a drug, to examine the subject‟s response to such a stimulus.
If the subject is healthy then the reaction to a placebo is almost zero, but in the case of hypersensitivity even this stimulus can have some effect.
In the physiological test the amount of the dose to enter is zero and it is still possible to compare the POST results with those of the PRE test.
The POST phase will show a coloured string highlighting the words POST FILE No. and
DOSE.
WARNING
The POST test can be based only on a PRE test made in the same day; it is not possible make a POST test referred to a PRE test made in the previous days.
WARNING
To end the POST phase and make new PRE tests, press
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Page 43 / 74
WARNING
If a new dose is set after a POST test then the device creates a new test session, still POST. A new test code ID is allocated. The interpretation is not based on the previous sessions with different drug doses; only the new test is utilized for the interpretation.
2.7 V
ISUALISATION OF SPIROMETRY DATA
The image below describes the information which appears inside the spirometry test results screen.
In particular, in this screen it is possible to visualise the data relative to a single curve by pressing respectively key 1, 2 or 3 starting from the best test onwards.
WARNING
For standard NAHNES III the parameters shown are:
FEV6, FEV1, FEV1/FEV6%, FEF2575, FVC, FEV1/FVC
By visualising the single curve it is then possible to directly carry out a new spirometry PRE or POST test or oximetry test
On the current patient by pressing respectively one of the following keys
, ,
, ,
. You can also do this if you recall a best test by selecting key
or the last test by selecting key (for spirometry) or key the test selected will be carried out on the current patient.
(for oximetry);
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WARNING
If the last spirometry test carried out was a POST test, the POST session should be maintained until a new patient is recalled from the archivi or a new patient created.
2.8 T
EST QUALITY CONTROL
-
SPIROMETRY
Through a mathematical analysis (quality control) which is applied to certain calculated indices and parameters, the spirolab III produces a series of comments, helpful for understanding the reliability of the test made.
This control quality check assigns a letter for the current session as described below:
PRE Test
A = At least two acceptable manoeuvres, with the highest two FEV1 values matching to within 100 mL and the largest two FEV6 values within 100 mL.
B= At least two acceptable manoeuvres, with the FEV1 values matching to within 101 to 150 mL
C= At least two acceptable manoeuvres, with FEV1 values matching to within 151 to
200 mL
D= only one acceptable manoeuvres, or more than one, but the FEV1 values not matching to within 200 mL (with no interpretation).
F= No acceptable manoeuvres (with no interpretation).
POST Test
A = two acceptable (1) FEV1 values matching within 100 mL
B= two acceptable (1) FEV1 values matching within 200 mL
C= two acceptable (1) FEV1 values that do not match within 200 mL
D= only one acceptable (1) FEV1 manoeuvre
F= No acceptable (1) FEV1 manoeuvres
Acceptable manoeuvre means: good start and satisfactory exhalation (duration and flow)
Where several comments related to the single test are calculated, spirolab III will only show the most important to facilitate the test interpretation.
ERROR IN Vext and PEFT
If the extrapolated volume Vext is greater than 500 mL or more than 5% of the FVC, or if the PEFT (time to peak flow) is greater than 200 ms, this message is shown:
Repeat test and blow faster
FET ERROR
If the FET is less than the minimum (3 seconds), this message is shown:
Expiry time insufficient
FLOW ERROR
If the last point of the F/V curve is greater than 200 mL/s, this indicates that the expiration was not complete and thus this message is shown:
Blow out all air in lungs
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2.9 R
EPEATABILITY OF THE FVC TEST
Following the international ATS and ERS standards, it is recommended to repeat each
FVC test at least 3 times to ensure the reliability of the spirometry test results. The device helps the user through the reproducibility control check.
Between tests, the repeatability of the following parameters is calculated:
PEF
VC repeatable when the difference between the two largest PEF is ≤ 0.67 L/s; repeatable when the difference between the two largest VC is ≤ 150 mL;
If FVC is > 1.0 L then:
FEV1
FVC repeatable when the difference between the two largest FEV1 is ≤ 150 mL; repeatable when the difference between the two largest FVC is ≤ 150 mL; if FVC is ≤ 1.0 L then:
FEV1
FVC repeatable when the difference between the two largest FEV1 is ≤ 100 mL; repeatable when the difference between the two largest FVC is ≤ 100 mL;
2.10 M
ETHOD OF MEASUREMENT AND INTERPRETATION
Spirometry test interpretation is based on the Forced Vital Capacity (FVC) test and is based on the ATS standard. For a faster comprehension this interpretation is illustrated by a traffic light code (green, yellow, red). For each test made, an arrow on the right of the screen indicates the worst level of interpretation of the test session.
The device uses the infrared interruption principle of measurement, with two sets of optoelectronic transmitters and receivers. A pair of deflectors positioned at the entry and at the exit of the turbine tube generates a vortex in the passing air, around the axis of the sensor. A rotor with a speed of rotation directly proportional to the air flow then interrupts the infrared beams and generates a digital signal. The measurement of the air volume that passes through the tube is proportional to the interruption of the infrared rays.
This measurement principle guarantees stability, reproducibility and reliability over a long period of time, and the measurement is not affected by gas density, humidity or pressure.
WARNING
The measurement of the air volume that passes through the tube is proportional to the interruption of the infrared rays.
The cleaning of the turbine flow sensor is very simple, and is essential for the protection of the subject from possible infections. For cleaning operations see Chapter 4 of this Manual.
No calibration of the turbine is required, but it is good practice to make a calibration check by following the simple instructions contained in the relevant paragraph in the maintenance section of this manual.
Method of test interpretation
Following each FVC test, the device carries out a quality control check to verify the acceptability of the test made and, if possible, compares the main measured parameters
FEV1, FEV1% and FVC with the respective predicted values. It also calculates a series of indices, based on the following criteria:
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The interpretation of these indices %, according to the ATS standards, generates a series of messages which correspond to possible levels of obstruction or restriction plus one level of normal spirometry, as shown in the following table:
normal mild
green
green-yellow
yellow
yellow-red moderate moderately severe severe very severe
red violet
If it is not possible to make the calculations for lack of data, the interpretation is not valid and this message appears:
NOT VALID
WARNING
The interpretation during a test session for each subject always refers to the best test results made by that subject.
2.11 O
XIMETRY TESTING spirolab
III can carry out different types of oximetry tests, which are described in the following paragraphs.
WARNING
If spirolab
III
has been purchased without the oximetry option, then only spirometry tests can be made. If the oximetry option is purchased afterwards, then contact the service centre or the manufacturer to enable the function.
If during the oximetry testing the SpO2 blood pulse rate goes below the lower threshold or goes over the upper threshold, spirolab
The values shown are the default settings.
III
will „beep‟ while this situation persists. This option can be switched off during sleep tests.
WARNING
Note: the sensor described below is for illustration purposes only. spirolab enabled for the use of any of the sensors described in the previous Paragraph
1.2.4. MIR does not recommend the use of a specific type of senor; this decision is made by the doctor.
During the oximetry test spirolab
III
III
is
cannot be switched off, to switch off the device it is necessary to interrupt the test in progress, this avoids unwanted interruptions which could compromise the accuracy of the data obtained.
For the non-invasive measurement of the SpO
Kg with limited activity.
2
oxygen saturation and blood pulse rate utilize the re-usable finger sensor. This sensor is recommended for patients weighing > 20
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spirolab
III memorises the two oximetry values every 2 or 4 seconds.
Carry out an oximetry test as follows:
Connect the sensor to the instrument: insert the connector with the arrow
(printed on the connector) face-up, as shown:
Choose a high perfusion site, which is easily adaptable to the sensor.
Insert finger into the sensor until the finger touches the end of the probe.
Ensure that the bottom part of the finger completely covers the detector. If the finger is not able to be correctly positioned, use another finger.
Position the sensor so that the cable is underneath the palm of the hand. This enables the light source to remain on the fingernail and the detector on the bottom part of the finger. From the main screen press to access the test menu.
Select required test using the vertical scroll arrow.
If this message appears:
OXIMETRY NOT DETECTED
then your instrument does not include an oximeter.
If this message appears:
OXIMETRY DISABLED
the function has not been enabled. In this case contact a service centre or the manufacturer.
WARNING
Before starting the test check to see that the battery is fully charged, if it is low the following message will be shown:
Batteries are low and may not be sufficient for an oximetry test.
In this case select ESC to exit the test, by pressing any key you can continue with the test already set up.
If the test is interrupted, due to low battery charge, the following message will appear on the display when the device is switched on again:
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The last oximetry test was interrupted before being properly completed
A beeping sound will be simultaneously heard for 10 seconds.
Afterwhich the spirolab III main screen will appear.
The oximetry tests that can be performed by Spirolab III are:
1. SPOT OXIMETRY
2. SLEEP OXIMETRY
3. EXSERCISE OXIMETRY
4. SPOT OXIMETRY (MEMORIZED LIKE OXYTEST)
Choose required test pushing corresponding number on numeric key board.
During the test the display shows the informations like in the following image
The number of blocks shown next to the SpO2 value are proportional to the signal quality
(maximum 8 blocks). Position the finger within the sensor in order to maximise the signal strength.
WARNING
In order not to compromise the reproducibility of the measurements and the integrity of the sensor, avoid twisting the sensor cable and handle with due care when using, connecting, disconnecting and when placing the finger into it.
During the first few seconds of the test the device searches for the best signal, after which the timer re-sets to zero and spirolab III starts to memorise the data.
For each type of test, if the sensor has not been correctly inserted, after a few seconds the following message will appear:
Connect sensor
Contemporaneously spirolab III emits a beep for 10 seconds.
If the sensor has been inserted but the finger is not inserted correctly, the following message will appear:
Insert fingher
Contemporaneously spirolab III emits a beep for 10 seconds.
If the sensor correctly receives the signal, after a few seconds the device starts to „beep‟ and the values will be displayed on the screen.
For all oximtery tests alarms can be set up in the case that the critical values are exceeded as described in paragraph 2.5.5. In the case that the alarm is activated during the test, the
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symbol on the display will be seen and this can be activated/disactivated by pressing to disactivate, and to activate.
For further information on the correct set up for this function please refer to paragraph
2.5.5.
2.11.1 Spot oximetry
WARNING
The sensor described below is for illustration purposes only spirolab III is enabled for the use of any of the sensors described in §1.2.4. MIR does not recommend the use of a specific type of senor; any decision in made by the individual doctor.
To perform a non-invasive continuous monitoring of arterial oxygen saturation, it is recommended to use the reusable "wrap" sensor. The use of this sensor is indicated for patients weighing more than 30 Kg and contraindicated for patients with allergy to adhesive tape.
WARNING
The materials used for manufacturing the sensor are NATURAL LATEX PROTEIN free. The materials used for the sensor are subject to biocompatibility tests.
Adult Single Patient Sensor – Instructions for Use
WARNING
This sensor is contraindicated for use on patients who exhibit allergic reactions to the adhesive tape. Do not reuse. One use on one patient.
Choose an application site on the patient‟s finger or toe where the light source will be directly over and in-line with the detector. The preferred sites are the forefinger or smaller thumb.
Remove nail polish or artificial fingernails
Place the patient‟s digit in the sensor nail-side up, lining up the digit‟s pad over the detector. The sensor‟s positioning line runs across the mid axis of the fingertip
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Wrap the bottom adhesive around the digit, being careful not to cover the nail.
Fold the sensor‟s top over the digit, making sure the light source is directly over and in-line with the detector. Wrap the adhesive around the finger or toe to secure the sensor. Route the cable along the palm or the bottom of the foot, and secure with adhesive tape if necessary.
Connect the sensor to the instrument: insert the connector with the arrow on the connector face-up and control the correct functioning according to the previous instructions.
WARNING
Do not twist unnecessarily or use excessive force when using, connecting, disconnecting, or storing the sensor.
An over-tight sensor can produce inaccurate saturation measurements.
Therefore avoid over tightening the adhesive tape.
It is recommended to fasten the cable to the wrist with a bandage.
Making a Test
Select “Oximetry (SpO2/BPM)” from the oximetry tests list pressing 1 on the numeric key.
The display shows: “Oximetry (SpO2/BPM)”. The test duration is unlimited and the aim is to record variations of the oximetry values during a period as decided by the doctor.
If the finger is removed from the sensor during the test, the following message will appear:
Please, wait for signal
The data shown during the test are:
Spo2
Quality of signal received
BPM
Test time extension
Time curve of the two parameters (SpO2 and BPM)
Test type in esecution
Possible warning message
To end test, press
To print data see Paragraph 3.1.2; see example of the test printout report attached to this
Manual.
2.11.2 Sleep Oximetry
To chose this test press 2 on numeric key.
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This test records the variations in the patient‟s parameters overnight.
After approximately 5 minutes spirolab III will go to standby i.e., it stops beeping and the display turns off. The led signal remains on. To control the correct functioning while on standby, press , after 5 minutes spirolab III will automatically return to standby. If there is no signal while on standby the device will automatically exit this phase and a warning message will appear (sensor unplugged or finger not detected correctly).
The data shown are the same as described in the preceding test, except for information on this present phase, which is not envisaged for this test.
The data shown are the same described previously.
After the required time the test can be interrupted as previously described.
Results can be printed as described in Paragraphs 2.13 and 3.1.2; see example of the test printout report attached to this Manual.
2.11.3 Exsercise oximetry
This test is made up of 3 phases:
Baseline (initial rest)
Exercise
Recovery
Baseline (initial rest)
The data shown are the same described previously.
The duration of the test is minimum 2 minutes, then this message appears:
pass to EXERCISE phase
press 1 to pass to the following phase. If the phase lasts for more than 6 minutes then
spirolab
III will emit a „beep‟ as a reminder to pass to the exercise phase.
Exercise Phase
At the beginning of this phase the timer is reset to zero, to give an accurate control of the duration of each single phase. The data on the display is the same as shown before.
The duration of this phase is minimum 2 minutes, this message will appear:
pass to RECOVERY phase
press 2 for a few seconds to pass to the recovery phase. If this phase lasts for more than 6 minutes then spirolab III will emit a „beep‟ after which the device passes to the initial phase and the timer is re-set to zero.
Recovery Phase
The user can decide freely on the duration of this phase, the duration is not suggested (at the beginning of the phase the timer re-sets to zero).
To end test press .
At the end of the test the data required for the calculation of the parameters must be inserted; more specifically:
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Baseline DYSPNEA
Final DYSPNEA
Baseline FATIGUE
Final FATIGUE
These follow the Borg scale and can have the following values: 0,
0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10.
The Borg scale coefficients represent the following severity values:
SCALE
0
0.5
1
2
3
4
5
6
7
8
9
10
SEVERITY
None
Very Very Slight (Just Noticeable)
Very Slight
Slight
Moderate
Some What Severe
Severe
“
Very Severe
“
Very Very Severe (Almost Maximum)
Maximum
Use
and
to enter data; use
or to go back or pass to next data.
Exercise test data results are given in the following screen, and can be printed as described in Paragraphs 2.13 and 3.1.2. if the test results are printed, the test printout will only show the exercise test results; an example of a test printout report is attached.
Press to end the test at any moment.
At the end of the test are shown calculated and inserted data with more than one display.
Use
or to read the various data.
WARNING
One of the parameters calculated by the Spirolab III during an oximetry test is the so-called Recovery Time. The Recovery Time is defined as the time taken for the
SpO2 value to return to at least 99% of the average base value calculated during the initial phase of the test.
2.11.4 Spot oximetry (MEMORIZED LIKE OXYTEST)
This test is the same described in 2.10.1; the only difference is that the test is without subject data; in the archive the test is memorized with the name: “OXYTEST”. The parameters calculated are like in spot oximetry (see 2.10.1).
2.12 F
ILE ORGANIZATION
The memory of the spirometer is a „string‟ of memory areas called records, each of which contain information regarding a single test session.
More specifically, each record is made up as follows:
Demographic details of the subject
Date, time and ambient temperature at the time of the
FVC test
repeatability and quality control test information
Parameters stored with the FVC test:
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FVC, FEV1, FEV1/FVC, FEV1/VC, PEF, FEF2575, FEF25, FEF50, FEF75, FEV3,
FEV3/FVC, FEV6, FEV6%, FET, EVol, FIVC, FIV1, FIV1/FIVC, PIF, MVVcal, VC, EVC,
IVC, IC, ERV, TV, VE, RR, t
I
, t
E
, TV/t
I
, t
I
/Ttot, MVV, ELA.
Parameters stored with the VC test: o
VC, IVC, EVC,* (EVC or IVC), ERV, IC, TV, VE, fr, ti, te, TV/ti, te/tt
Parameters stored with the MVV test: o
MVV
Points of the expiratory part and (if present) the inspiratory part of the Flow/Volume curves, plus the points of the Volume/time curve.
Parameters stored with the SpO2 test (in relation with the test recorded, see also paragraph 1.6.2):
WARNING
All of the parameters are always stored even if not all of the tests were performed
(in this case the results of those parameters are stored as zero). The symbol * indicates the best result of that subject.
Spirometry results can be recalled from the memory.
To access the database, press . The results of the selected test can be printed by pressing after visualization on display.
2.13 S
EARCH AND READ TESTS IN MEMORY
Press to access menu, from where to view all test data stored in the memory of the device.
The research can be made in three different manners:
Subject list by last name
Subject list by ID code
List by date
Memory list
Using and , select the method
with
, then press .
From this display it is also possible make the archive transmission with Bluetooth connection, using a cell phone (please see paragraph 3.1).
2.13.1 Subject List by last name:
This message appears:
INSERT LAST NAME OR THE FIRST
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LETTERS OF LAST NAME TO FIND
ALL MATCHING FILES IN MEMORY
Use keyboard to enter subject surname or first letters. All corresponding surnames found in memory will then be listed.
The first column on the right will show the file numbers corresponding to the tests made, use numeric keyboard to enter required test, press to view related values.
Print selected test results, using the internal printer, by pressing , pressing twice
the data are print on the external printer via Bluetooth system.
2.13.2 Subject List by ID code
The following message appears:
ENTER ID# CODE,
OR PARTIAL TO SEARCH
MATCHING FILES
Enter subject ID# and press to view the list containing all file linked with the patient.
The data can be printed like described previously.
2.13.3 Memory List
The screen will show the complete test memory list.
Indicate FILE No. to view corresponding spirometry test results and press .
The data can be printed like described previously.
The data shown can be printed individually or in group; it is possible to print a sequence of tests
(pressing the keys of the first and the last) otherwise a single test pressing the number on numeric keys, then press .
2.14 V
IEW AND PRINT RESULTS
WARNING
During a test session the device will automatically memorize up to 8 FVC tests.
Press to view the results arranged in 8 sections on the screen. Each of the
8 tests can be viewed and printed. These tests are numbered from 1 to 8, where test 1 represents the best test and 8 represents the worst test. The last test made is always highlighted in green.
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During the test session press (which recalls the best test), the device will always show the graphs and results of the 3 best tests. Each of the 3 tests can be viewed and printed.
At the end of the test session, when either a new subject is inserted or you pass to the POST phase, the 3 best tests corresponding to the previous session are automatically saved on file. These can be successively recalled from memory and viewed or printed either together or separately.
From the main screen it is possible to re-examine and to print all the spirometry parameters.
Generates the Flow/Volume curves of the best test.
Generates the Flow/Volume curves of the last test.
WARNING
All tests results saved on file can be recalled, viewed and printed.
The data stored in the memory are those of the best tests. The current test can be printed by pressing . To print a test saved on file after recalling it press . To interrupt printing press .
The printout report includes a header line with the date, time, the BTPS value at the time of the test, patient details, the FILE No., any pre-set ethnic correction factor and the predicted value set used.
There follow the Flow/Volume and Volume/time curves, which relate to either the last or best test performed.
Press from the main screen to print the best test results of the day relative to the displayed patient.
To print the last test press while viewing the last test.
Lastly, the measured parameters and spirometry test interpretation are shown.
In the case of a PRE test, the following are shown:
Predicted
PRE
%Predicted values calculated predicted values measured value before drug administration percentage value against predicted values
In the case of a POST test then the graph will show the two curves superimposed and in addition to the above-mentioned parameters, the following values:
POST
%CHG measured value after drug administration
% variation (+/-) between POST and PRE.
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From the measured parameter‟s screen ( or key, or recalled from memory) the subject‟s name, date and time of test is shown on the bottom of the screen.
3 DATA TRANSMISSION
spirolab
III includes a “Bluetooth” wireless data transmission system. This connection is via radio and allows the transferring of all the data in memory for two different operations:
transfer to a cell phone, which then transmits the data to a PC by modem;
transfer to a Bluetooth-enabled printer.
The following paragraphs contain in-depth information on these two procedures.
3.1 D
ATA
T
RANSMISSION VIA
B
LUETOOTH TO A CELL PHONE
WARNING
The transmission via mobile phone is possible only if the SIM is enabled for data transmission. Check with the network administrator to have this service. spirolab
III can be connected to a cell phone with this system installed. The transmission of data with this technology allows the transfer of all data in memory of the spirolab III .
The sequence of operations to follow is described below.
3.1.1 Preliminary operations
WARNING
The transmission of data through a Bluetooth connection requires the phone number of the unit where the data shall be transferred (the doctor‟s office, telemedicine service, etc.). The phone number is set up from the Configuration
Menu (see Paragraph 2.5.5). A device must also be setup for the connection; ; refer to Paragraph 2.5.5 for further details.
3.1.2 Setting the Phone Number
With spirolab III switched on, press
.
Use vertical scroll key to select “Bluetooth settings” then press
Use vertical scroll key to select “insert telephon number” then press
.
Enter the number with the numerical keyboard, and again press
Menu will appear.
Use to return to the main screen.
3.1.3 Data Transmission through Bluetooth
.
; the Bluetooth
From the main screen press
Use vertical scroll keys to select “Bluetooth transmission” and press
it is described the transmission way and, if correct, it is required to confirm it with “OK” to activate the connection to the device choosen as default in the configuration menu.
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when the request is from mobile phone, type the code shown on the screen (relative to the device‟s Serial Number reported on the back label of spirolab III)
are executed all the next connection steps.
When the connection is active, data are transmitted from the selected modem
At the end of the transfer data process the following message “Connection Completed” is shown.
The screen will show the following information:
The device used for the connection;
The pre-set phone number.
The preset PIN (corresponding to the serial number of the device).
To interrupt data transmission during the Bluetooth connection press connection and to return to the main screen.
to end the
Where no device has been setup for data transmission, a message will appear on the display to start searching for enabled devices. After setting the device the connection will start up automatically.
3.1.4 Data Transmission via Bluetooth for printing
WARNING
Printing of data from the patient management function is enabled only if the printer has a Bluetooth connection; alternatively a USB adapter can be installed on the printer in order to enable a Bluetooth connection.
The printer used must be in the list of printers accepted by the device. To have a copy of the updated list please contact the manufacturer or send an email to the following address: [email protected]
The Bluetooth system enables spirolab III to transfer test data directly to a printer with
Bluetooth. The sequence of activities to be followed is:
When the test is finished or searched in the archive press twice
spirolab III will carry out the phases of connection.
At the end of the transmission spirolab III will show the message “CONNECTION
COMPLETED”, returning automatically to the main screen
Previous tests stored on file can also be printed. Use the procedure described in
Paragraph 2.11 to print required tests. When the required test is shown on the display, press twice
To interrupt data transmission during Bluetooth connection press connection and to return to the main screen.
to end the
Where no printer has been set up, a message will appear to search for devices. After the device has been set up it will automatically be enabled for printing.
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When searching for Bluetooth enabled devices, spirolab III will check the address of that device and where a previously registered device has changed name, it will be automatically updated.
3.2 C
ONNECTION TO A PC spirolab
III can be connected to a PC and perform tests online. Two connection types are used: USB port or RS 232 port.
WARNING
Note that when using the device in online mode, if a turbine (disposable or reusable) is setup then the same turbine will remain by default the next time the device is used in stand-alone mode. Thus pay attention to the setting of the turbine.
3.2.1 Connection to a PC through a USB port
WARNING
Before connecting spirolab III to a PC via the USB port, the winspiroPRO software must be installed to interface with the device.
Prior to initiating the following procedure it is important to know the version of the operating system on the PC (from Control Panel click on “System”, and here the operating system installed on the PC can be checked).
To make the connection insert the mini USB connector supplied with spirolab III as shown in the picture and attach the other connector to the
USB port of the PC.
When initally making a connection, the PC will, depending on the version of the operating system, either make an automatic driver installation or request some information. To avoid errors in this phase please read the winspiroPRO User Manual very carefully.
3.2.2 Connection to PC through RS 232 port. spirolab
III can be connected to a PC through a
RS 232 serial port. This leaves the USB port free. The picture shows the RS 232 connector attached to spirolab III.
For the correct management of the device see the software manual.
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3.3 U
PGRADE INTERNAL SOFTWARE spirolab
III can be upgraded when connected to a PC (via USB or RS232). Upgrades can be downloaded by registering on www.spirometry.com. For further information on upgrading software see the “winspiroPRO” software manual.
4 MAINTENANCE AND CLEANING
spirolab
III is an instrument that requires very limited maintenance. The operations to perform periodically are:
Cleaning and controlling of the reusable turbine.
Changing the disposable turbine at each test.
Cleaning of the oximetry sensor (for reusable sensors).
Changing the adhesive tape of the oximetry wrap sensor.
Changing the battery.
The maintenance operations described in the User‟s Manual must be carried out carefully.
Failing to observe the instructions may cause errors in measurement or in the interpretation of measured values.
Modifications, adjustments, repairs, and reconfiguration must be carried out by the manufacturer or by authorised persons.
In case problems arise, never attempt to repair the unit.
The setting of the configuration parameters must be carried out by qualified personnel. In any case, the risks from an incorrect setting do not constitute a danger for the patient.
The device is supplied with an internal lithium battery used to back-up the RAM; the average battery life is approximately 10 years. If this message appears:
WARNING ! Replace the internal lithium battery
Contact a service centre or the manufacturer for battery replacement.
4.1 C
LEANING THE DEVICE
Clean the device with a damp cloth. Make sure to dry it afterwards.
WARNING
Do not wet or immerse the device or power supply in any liquids.
Do not use any abrasive materials to clean the device.
4.2 C
LEANING THE REUSABLE TURBINE
The turbine utilized with spirolab III is of one of two categories: disposable or reusable.
These guarantee precise measurements and have the advantage of requiring no periodic calibration. In order to maintain these characteristics, a simple cleaning is required prior to each use ( only for the reusable turbine).
Cleaning of the disposable turbine is not required as it is supplied already clean in a sealed plastic bag. It must be disposed of after use.
The maintenance operations to perform are cleaning and controlling of the turbine.
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WARNING
It is good practice to control from time to time that dirt or foreign bodies such as threads or hair are not deposited inside the turbine. Any such deposit could brake or block the blade of the turbine and thus compromise the measurement accuracy.
To clean the reusable turbine, remove it from its compartment in the MiniFlowmeter by turning it anti-clockwise and pressing lightly. It can be helpful to push it gently from underneath with one finger.
Immerse the turbine in a cold detergent solution and move it within the liquid to remove any impurities which may be deposited inside. Leave the turbine immersed for the time specified in the instructions of the solution.
WARNING
Miniflowmeter Turbine Mouthpiece
To avoid any kind of damage to the reusable turbine please do not use any alcoholic or oily substances, do not immerge the turbine in hot water or hot solution.
Do not put the turbine under a direct jet of water or other liquid. If no detergent solution is available, clean the turbine in clean water.
MIR suggest the use of Perasafe, manufactured by Dupont, which has been tested with positive results on all MIR sensors.
Rinse the turbine by immerging it in clean water ( not hot).
Shake off the excess water from the turbine and leave it to dry, standing it vertically on a dry surface.
To ensure that the turbine is functioning correctly before replacing it inside the instrument it is good practice to make a visual check of the rotation blade. Placing the turbine tube horizontally and moving it gently from left to right and vice versa, the rotation blade (rotor) must rotate freely. Otherwise, accurate measurement is no longer guaranteed, so the turbine must be replaced.
Once the turbine has been cleaned, insert the turbine tube in its place following the instructions indicated by the “lock “ symbol printed on the MiniFlowmeter.
To insert the turbine correctly, push it and then turn it clockwise until reaching the stop, which ensures that the tube has been blocked inside the casing.
Verify the free movement of the turbine:
Switch on spirolab III as if to make a spirometry test (for example FVC).
Hold the MiniFlowmeter in one hand and move it gently from side to side, so that air passes through the turbine.
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If the rotor within the turbine is turning correctly, then you will hear a beep that indicates that the turbine is moving within the specific low flow range.
If moving the turbine from side to side at a constant velocity, regular beeps or no beeps at all are heard, then proceed with the cleaning of the turbine.
WARNING
If the disposable turbine is used, do not clean it but replace it after each test.
To avoid environmental contamination caused by the disposal of the cleaning solutions, the user must follow all local regulations.
4.3 C
LEANING AND DISINFECTION OF THE OXIMETRY SENSOR
WARNING
Do not sterilize by irradiation, steam, or, ethylene oxide. Do not immerse in liquids.
Before cleaning or disinfecting the sensor, unplug it from the device.
Clean the sensor with a soft cloth moistened with water or a mild soap solution. To disinfect the sensor, rub with isopropylic alcohol. Allow the sensor to dry completely after cleaning.
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5 PROBLEMS/CAUSES AND SOLUTIONS
The device does not switch on
Press firmly on the on key.
The internal battery may be discharged.
Make sure that the power supply cable of the charging unit is connected to the spirometer and that the plug is inserted correctly into the mains outlet, then proceed with charging.
The LCD does not display
Using the two keys which regulate the brightness and the contrast of the display.
The battery charging is not working correctly
The device is protected thermically. In case the power supply of the battery reaching a high temperature then a thermal protection intervenes and prevents the charging.
This thermo protector can intervene if:
the device has operated beyond the functioning limits indicated in this manual;
the device is operated near a heat source, or in ambients with a temperature either too high or too low.
Disconnect the power supply and let it cool down before continuing with charging.
The lithium battery for the data memory indicates discharged
If the internal lithium battery is discharged, the spirometry parameters in the memory and other configuration data may be cancelled automatically.
Contact an authorized service centre to replace it.
The printer does not print
The thermal paper may have run out, otherwise may be inserted in the wrong way.
Check the correct position of the thermal paper, if necessary insert a new roll of thermal paper.
The printer is in thermal protection
The printer is also protected thermically. In case the printer reaches elevated temperatures then a thermal protection intervenes and blocks the functioning of the printer.
A message on the display appears to signal the protection.
Let the printer cool down before turning on the device again.
The printer makes noises
Make sure there is a sufficient quantity of thermal paper.
Make sure that the thermal paper and the thermal paper holder are positioned correctly.
Make sure that the thermal paper container lid is in the correct position.
The device does not measure
Make sure that the turbine‟s cable is connected to the spirometer and that the plug is inserted properly in the appropriate connector.
Make sure that the turbine is inserted correctly into the MiniFlowmeter.
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The device does not measure correctly
Make sure the turbine is inserted correctly in the MiniFlowmeter. Verify the free movement of the turbine as illustrated in Paragraph 4.2.
WARNING
In case the device does not resume correct functioning in spite of the controls made, contact the manufacturer or an authorized service centre
.
WARNING
Before contacting the centre for technical assistance, please download the archive from the device on to the PC using the Winspiro PRO software. This procedure is necessary as the data could be lost whilst repairing the device and could also be of a confidential nature and therefore subject to laws on data privacy.
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5 LIMITED WARRANTY CONDITIONS
This MIR product together with its standard accessories is guaranteed for a period of ONE
YEAR from the date of purchase. In the case of any warranty claims the relevant sales invoice (or another proof of purchase document) must be submitted to MIR.
The instrument must be checked at the time of purchase, or upon delivery, and any claims must be made within 8 days in writing to the manufacturer.
This warranty covers the repair or the replacement (at the discretion of the manufacturer) of the product or of the defective parts without charge for the parts or for the labour.
All batteries and other consumable parts are specifically excluded from the terms of this guarantee.
The instrument must be returned to the authorized service centre for repair within 8 days from when the defect is detected.
This warranty is not valid, at the discretion of the manufacturer, in the following cases:
If the fault is due to an improper installation or operation of the machine, or if the installation does not conform to the current safety norms in the country of installation.
If the product is utilized differently from the use described in the User‟s Manual
(improper, incorrect and/or unreasonable use, etc.).
If any alteration, adjustment, modification or repair has been carried by the user or by personnel not authorised by MIR.
If the fault is caused by lack of or incorrect routine maintenance of the machine.
If the machine has been dropped, damaged or subjected to physical or electrical stress.
If the fault is caused by the mains or by another product to which the instrument has been connected.
If the serial number of the instrument is missing, tampered with and/or not clearly legible.
This warranty does not cover any liability for damage, caused directly or indirectly, of any kind whatsoever for persons or things for the period in which the device is not in use.
The repair or replacement described in this warranty is supplied for goods returned at the customers‟ expense to our certified service centres. For details of these centres please contact your local supplier of the spirometer or contact the manufacturer directly.
The customer is liable for all repairs not included under the terms of this guarantee.
The customer is responsible for all transportation charges.
Any instrument or accessory returned must be accompanied by a clear and detailed explanation of the defect or problem found. If units are to be returned to the manufacturer then written or verbal permission must be received before any instruments are returned to
MIR.
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MIR - Medical International Research reserves the right to modify the instrument if required, and a description of any modification made will be sent along with the returned goods.
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ANNEXES
MEDICAL INTERNATIONAL RESEARCH
Via del Maggiolino, 125 00155 - Roma - ITALY
DECLARATION OF CONFORMITY CE
(annex II excluding par.4)
We hereby declare that the following device:
Type
Spirometer
Brandname
Device name
MIR Medical International Research
spirolab III
Class
IIa
Complies with the Essential Requirements of directive 93/42/EC concerning
Medical Devices, and its amendments, and its transposition in the Member
States.
This statement is made on the basis of the CE Certificate n. MED 9826 issued by Cermet, Notified Body n. 0476.
Rome 01/01/2011
Paolo Sacco Boschetti
The Chairman
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E
XAMPLE OF TEST REPORT
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I
NFORMATION FOR CORRECT USE IN AN ELECTROMAGNETIC ENVIRONMENT
Guidance and manufacturer‟s declaration – electromagnetic emissions
The spirolab III is intended for use in the electromagnetic environment specified below.
The customer or the user of the
spirolab III should assure that it is used in such an environment.
Emissions test Compliance
RF emissions
CISPR 11
RF emissions
CISPR 11
Group 2
Class B
Electromagnetic
environment – guidance
The spirolab III must emit electromagnetic energy to perform its indended function. Nearby electronic equipment can be affected.
The spirolab III is suitable
Class D for use in all establishments, including domestic establishments and those directly connected to the public lowvoltage power supply network that supplies buildings used for domestic purposes.
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations/ flicker emissions
IEC 61000-3-3
Complies
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Guidance and manufacturer‟s declaration – electromagnetic immunity
The spirolab III is intended for use in the electromagnetic environment specified below.
The customer or the user of the spirolab III should assure that it is used in such an environment.
Immunity test
Electrostatic discharge (ESD)
IEC 61000-4-2
IEC 60601
test level
± 6 kV contact
± 8 kV air
Compliance level Electromagnetic
environment –
± 6 kV contact
± 8 kV air
guidance
Floors should be wood,
Electrical fast transient/burst
IEC 61000-4-4
±1 kV for input/output lines
±1 kV for input/output lines concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30 %.
Mains power quality should be that of a typical commercial or hospital environment.
Mains power quality should be that of a typical commercial or hospital environment.
Surge
IEC 61000-4-5
Voltage dips, short interruptions and voltage variations on power supply input lines
IEC 61000-4-11
± 1 kV differential mode
± 2 kV common mode
<5 % UT
(>95 % dip in
UT) for 0,5 cycle
40 % UT
(60 % dip in UT) for 5 cycles
70 % UT
(30 % dip in UT) for 25 cycles
<5 % UT
(>95 % dip in
UT) for 5 sec
3 A/m
±1 kV differential mode
± 2 kV common mode
<5 % UT
(>95 % dip in UT) for 0,5 cycle
40 % UT
(60 % dip in UT) for 5 cycles
70 % UT
(30 % dip in UT) for 25 cycles
<5 % UT
(>95 % dip in UT) for 5 sec
Power frequency
(50/60 Hz) magnetic field
IEC 61000-4-8
3 A/m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical
NOTE UT is the a.c. mains voltage prior to application of the test level. commercial or hospital environment.
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Guidance and manufacturer‟s declaration – electromagnetic immunity
The spirolab III is intended for use in the electromagnetic environment specified below. The customer or the user of the spirolab III should assure that it is used in such an environment.
Immunity test
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
IEC 60601 test
level
3 Vrms
150 kHz to 80
MHz
3 V/m
80 MHz to 2,5
GHz
Compliance level
[3 ] V
[3 ] V/m
Electromagnetic environment
– guidance
Portable and mobile RF communications should be used no closer to any part of the including cables, than the recommended distance calculated from the equation applicable to the frequency of the transmitter.
Recommended distance
d=[ 3.5 ] √P
3 equipment
spirolab III, separation
separation
d=[ 3.5 ] √P 80 MHz to 800
GHz
3
d=[ 7 ] √P 800 MHz to 2,5
GHz
3 where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in metres (m).
Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey, should be less than the compliance level in each frequency range.b
Interference may occur in the vicinity of equipment marked with the following symbol:
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies.
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NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. a 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 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 spirolab III is used exceeds the applicable RF compliance level above, the
spirolab III should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the
spirolab III. b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than [3] V/m.
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Recommended separation distances between
portable and mobile RF communications equipment and the Spirloab III
The spirolab III is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the spirolab III can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the spirolab III as recommended below, according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
Rated maximum
output
power
transmitter
W
of
d=[ 3.5 ] √P
V
1
80 MHz to 800 MHz
d=[ 3.5 ] √P
E
1
800 MHz to 2,5 GHz
d=[ 7 ] √P
E
1
0.01
0.1
1
10
0.12
0.37
1.17
5.28
0.24
0.37
1.17
5.28
0.24
0.74
2.34
1.056
100 11.66 11.66 23.32
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.
spirolab
III – User Manual Code MIR 980067 REV 2.0 Page 74 / 74
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