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User Manual AlgiScan

17

Measurement protocols

 

The different modes will allow the pupil to be measured over a variable period of 

time depending on the protocol chosen, with or without stimulation. In these different modes, 

the operator starts measuring by pressing the main button continuously (the button is held 

down  throughout  the  measurement)  after  selecting  the  desired  mode  (“Flash”,  “Tetanus”, 

“PRD”, “PPI”). While recording, the seconds are counted down and displayed on the AlgiScan 

screen. An audible beep indicates the start and finish of the recording (or measurement).

To ensure the quality of the results, the same precautions need to be respected as for an 

 

instantaneous measurement:

• The pupil must be fully visible throughout the recording

• The pupil must be centred on the AlgiScan screen

• The green zone covering the pupil must remain homogeneous and stable.

« Flash » mode:

  The  pupil  reactivity  is  tested  with  a  calibrated  flash  of  light  (photomotor 

 

reflex). Press the main button for 4 sec to start acquiring data. The stimulation is done with a 

flash of light. The objective is to measure the pupillary reactivity to light.

« Tetanus » mode: It is a test of the patient’s pupil reactivity to an adjustable continuous 

electrical stimulation (the reactivity of the patient’s pupil is recorded simultaneously to the 

electrical stimulation).

This mode is used to measure the pupil reactivity to a standardized electrical stimulation.  

Before starting the user selects the intensity of the electrical stimulation which will be applied 

and makes sure it is innocuous for the patient.

(see Section : Selecting the measurement protocol)

« PRD » mode:

 It is a protocol to record the pupil size variation (the pupil is filmed with no 

 

stimulation).

With this mode the variations of the pupil size are recorded during 60s in the course of medical 

or surgery acts.

« PPI » mode: Evaluation of the patient’s level of sensitivity to nociception.

With this mode the patient’s level of analgesia is measured with the PPI scale. Before use, the 

operator will check that the patient is in suitable conditions to withstand the different levels of 

PPI mode stimulation and ensure that they are safe for the patient.

Before launching a measurement protocol, check that the selected protocol corresponds to 

the desired one (“Flash”, “Tetanus”, “PRD” or “PPI”). If it is not the case, select the symbol of the 

desired test (see the section: Selecting the Measurement Protocol).

The default protocol is shown on the right side of the screen. Before starting recording the 

AlgiScan must be positioned on the patient and must detect the pupil correctly for at least 2 

seconds to leave time to the pupil to adapt its size with the darkness. 

Caution: before using the device, check the type of stimulation chosen, its intensity and 

its innocuousness regarding the patient. For more information on these operations refer 

to the following chapter. 

Summary of Contents for Algiscan

Page 1: ...User Manual AlgiScan 1 USER MANUAL AlgiScan Version 3 2 EN Last update 2021 04 19 Ref ALG IFU_EN USER MANUAL...

Page 2: ...User Manual AlgiScan 2...

Page 3: ...reen 12 General use 13 Fitting the positioning eyecup 13 Installation and positioning of the AlgiScan 13 Turning the device ON OFF 14 Patient Files Measurements identification 14 Settings 14 III Using...

Page 4: ...patient s file 29 IV Preventive maintenance cleaning and disinfection 30 Preventive maintenance 30 Battery and battery charging 30 Cleaning and Disinfection 31 V Appendix 1 32 Troubleshooting 32 VI A...

Page 5: ...also to the characteristics of its dynamic evolution minimum maximum latency and speed of evolution The size and reactivity of the pupil are considered as supplementary data which provide more precis...

Page 6: ...cessary to interpret with care values measured on patients suffering from neurological problems The AlgiScan conforms to the European directive covering medical devices and to the regulations in force...

Page 7: ...easurement Before and after the measurement the electric cable should be disconnected from the electrodes The AlgiScan must be connected to pacing electrodes or ECG electrodes supporting voltages up t...

Page 8: ...nt s face and head especially the eyes lips entire neck Do not position the electrodes on either side of the heart The use of the AlgiScan should not result in any significant pressure of its eyecup o...

Page 9: ...gesia and sedation of the patient as well as the site of stimulation We strongly advise against placing the electrodes on the patient s thorax because of the additional risks of cardiac fibrillation N...

Page 10: ...ds Not protected against liquids Refer to the user manual Type BF Applied Part Catalog reference Direct Current DC Prescription use only in the USA Curtis Straus Mark USA and Canada Manufacturing date...

Page 11: ...electrode symbol Correct electrode conduc tion level skin Yellow electrode symbol Moderate electrode conduc tion level skin Red electrode symbol Non functional electrical stimulation conduction probl...

Page 12: ...y screen in the Flash mode measurement mode used for measuring the pupillary light reflex Touch screen The AlgiScan is designed in such a way that all controls are accessible with a simple touch of a...

Page 13: ...by the user by selecting one of the available modes of the AlgiScan This type of measurement will then give a series of results with figures and a curve representing the variation in the size of the p...

Page 14: ...es numbered 1 to 20 If there is no barcode scanning the user will either choose one of those files or create additional files numbered 21 and above to save the measurement results Settings Setting the...

Page 15: ...enu follow the steps below Select settings menu by pressing on Then select data transfer by pressing on Using the arrows select the transfer mode PC HL7 Connect your receiver module on PC ref NL WDT o...

Page 16: ...upil detection When the pupillometer is ready for a measure the following icon will appear at the bottom right of the video image Note when the pupil detection is not correct the red icon will appear...

Page 17: ...is used to measure the pupil reactivity to a standardized electrical stimulation Before starting the user selects the intensity of the electrical stimulation which will be applied and makes sure it i...

Page 18: ...s strength is fixed at 320 Lux The overall duration of the test is 4 seconds Selection of light stimulation To select light stimulation and adjust its power Press the symbol on the screen representing...

Page 19: ...red in green on the screen Start recording by pressing the main button Press and hold the main button for the duration of the recording Recording stops automatically at 60s or when the user releases t...

Page 20: ...by pressing the navigation arrows until the desired value is displayed Confirm your selection by pressing the following symbol Note To exit the pop up window or cancel the intensity selection press th...

Page 21: ...tion is more than 13 during the 30 mA stimulation stage 40 6 The pupil s variation is more than 13 during the 40 mA stimulation stage 50 5 The pupil s variation is more than 13 during the 50 mA stimul...

Page 22: ...the end of the electrical stimu lation Note that the AlgiScan emits a first beep when the electrical stimulation starts Dur ing the stimulation the device emits a beep at each new level the tone of wh...

Page 23: ...ring Patient Electrodes conduction level and skin resistance The level of conduction of the electrodes is checked by the AlgiScan as soon as an electrical stimulation with a non zero current is select...

Page 24: ...displayed depend on the protocol used It is important to control the quality of the displayed curve and to verify that measurement values are not artefacts Thus the blue and black horizontal lines ind...

Page 25: ...ualitative scale of the photomotor reflex 5 levels 3 colours to determine commentary on pupil reactivity level The quantitative and qualitative scale of the photomotor reflex and resulting commentary...

Page 26: ...time It also displays the evolution of the variations in pupil size for the same file over time Normal zone strong reactivity Diameter 10 01 12h00 12h00 2 mm 4 6 8 Variation 10 20 30 40 History scale...

Page 27: ...olours The value taken into account for the qualitative quantitative scale of the Pupillary Reflex Dilation and for the display of the comment is the amplitude of the reflex value as a percentage They...

Page 28: ...itude of the reflex value as a percentage They are only indicative and must be corroborated with other physiological indicators commonly used Amplitude of the PRD reflex in PRD 5 5 PRD 12 12 PRD 20 PR...

Page 29: ...ds Barcode reading Create new patient s file Home page Note If a data transfer mode is active the following icon is displayed on the screen It allows send all the patient s data to the configured rece...

Page 30: ...ed to carry out repairs or maintenance operations Battery and battery charging Battery The AlgiScan contains a rechargeable Lithium Ion battery It is fitted with thermal protection and protection agai...

Page 31: ...Note Only qualified technicians or IDMED personnel are authorised to carry out repairs or maintenance operations on the battery Cleaning and Disinfection Attention Do not autoclave the AlgiScan or any...

Page 32: ...be cleaned with a lint free cloth and wiped carefully to avoid any stains or reflections The electrode wire used with the AlgiScan should not come into direct contact be submerged sprayed or filled wi...

Page 33: ...isposed of or recycled according to the regulations in force Specification and warranty Environment Storage and expedition The AlgiScan and its accessories should be stored or transported within the l...

Page 34: ...icker IEC 61000 3 3 Compliant The AlgiScan can be connected to the public mains network EMC Immunity Phenomenon Basic EMC standard Professional healthcare facility environment Immunity Test Levels Com...

Page 35: ...ce keep minimum separa tion from RF communication equip ment of 30cm RATED power frequency magnetic fields IEC 61000 4 8 30 A m 50 Hz or 60 Hz 30 A m 50 Hz or 60 Hz Mains power quality should be that...

Page 36: ...IAB Please check with your authorized distributor or with the manufacturer which products are available and approved in your country Light Stimulation Duration 1 second Intensity fixed at 320 Lux prec...

Page 37: ...MED references Medical accessories of the AlgiScan Reference Description STA W2 Wireless charging station for AlgiScan CAB STIM3 Electric stimulation cable for AlgiScan Other accessories Reference Des...

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