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Standard Operating Procedure Sop/Poct/49/8 Title: HEMOCUE HB 201+ Effective Date:15.05.2018
Standard Operating Procedure Sop/Poct/49/8 Title: HEMOCUE HB 201+ Effective Date:15.05.2018
COPY
Summary of Significant Changes at this Revision
CR6476 - Update locations
Competencies Required
Current Version of: FM/POCT/14
Risk Assessment:
Current Version of: RA/HA/57
Printed copies are uncontrolled unless there is an allocated Copy Number on page 1
Principle of test
The Hemocue 201 is used to determine the total amount of Haemoglobin in whole
blood. The system consists of the analyser and specially designed cuvettes containing
dried reagents. The cuvette serves as a pipette, reaction vessel and a measuring cuvette.
No dilution is required. The haemoglobin measurement takes place in the analyser and is
factory calibrated against the haemiglobincyanide (HiCN) method, the international
reference method.
Sodium deoxycholate haemolyses the erythrocytes and haemoglobin is released. Sodium
nitrite converts haemoglobin to methaemoglobin which, together with sodium azide gives
azidemethaemoglobin. The absorbance is measured at two wavelengths (570 and 880
nm) in order to compensate for turbidity in the sample.
Storage of reagents
HemoCue Hb 201 microcuvettes can be stored at room temperature(15-30 degrees
centigrade) They must not be stored in a refrigerator. Check expiry date before use.
Method
The Hemocue must only be used by competently trained staff, who have
successfully completed competence sheet FM/POCT/14.
Competency must be re-assessed every three years.
Start up procedure
• If mains power is available, connect the adapter to the socket in back of analyser.
• If no mains power is available insert 4 x AA batteries in the battery compartment
• Pull cuvette holder out to its loading position.
• Press and hold the left button until the display is activated (all symbols appear on
the display)
• Display shows the version number of the programme after which it shows an hour
glass timer and Hb symbols.
• After 10 seconds the display will show three flashing dashes and the HemoCue
symbol – it is now ready for use.
Set Up QC test
• Internal QC must be run daily or before use.
• Internal QC test – using HemoCue control
• Press both buttons on the HemoCue 201 together
• Display shows a flashing QC symbol
• Select QC test by pressing Left button
• Fill microcuvette with QC solution.
• Insert cuvette in the holder and await result.
• Record QC result on the iQC / maintenance log (FM/POCT/16). Check acceptance
limits, usually within 2SD of mean.
Printed copies are uncontrolled unless there is an allocated Copy Number on page 1
• If QC fails, fill in action on iQC / maintenance log, the analyser must be taken out of
use, until the problem has been resolved.. Samples should be taken for FBC and
sent to laboratory.
• If QC result is acceptable, no further action is required, the machine will
automatically return to patient mode after running QC.
Record Hb result on a Hemocue record label (FM/POCT/15) along with all other
essential information. Attach label to patient’s notes.
Maintenance
• If analyser has been contaminated with blood, maintenance must be performed.
• Turn analyser off.
• Pull cuvette holder out of the loading position – Use a pointed object to depress the
catch in the upper right corner of cuvette holder.
Printed copies are uncontrolled unless there is an allocated Copy Number on page 1
1. Gloves must be worn by all staff performing the finger prick technique.
2. Dispose of gloves in an appropriate clinical waste bin.
3. All sharps must be disposed of in a sharps bin.
4. If the machine is contaminated with blood, wipe with an alcohol base wipe.
5. After use, wipe machine down with an alcohol based wipe before storing
away.
Trouble Shooting
If battery symbol appears in display, the batteries are running low, replace as soon
as possible, the analyser will still give accurate results.
Report any problems to the senior nurse on duty, discontinue using until a Sister is
available.
If for any reason the result obtained is unexpected, (either too high or too low),
always send a venous EDTA sample to the laboratory for a Full blood count.
Printed copies are uncontrolled unless there is an allocated Copy Number on page 1