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HemoCue Hb 201 Training Session

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Laboratory testing performed in the clinical setting by non-laboratory healthcare ... Store UNOPENED bottles in fridge and 'in use' bottles at room temperature ... – PowerPoint PPT presentation

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Title: HemoCue Hb 201 Training Session


1
HemoCue Hb 201 Training Session
Emma James POCT CoordinatorCentral Site
February 2007Last update Dec 2007
2
Point of Care Testing
  • POCT is
  • Laboratory testing performed in the clinical
    setting by non-laboratory healthcare
    professionals
  • Subject to the same level of professional and
    judicial scrutiny as conventional lab testing
  • Advantages of POCT
  • Fast turnaround time for results
  • Improved patient management
  • Disadvantages of POCT
  • Increased risk of adverse incidents and
    litigation
  • 10 significant incidents on Central in 2006 3
    reported to MHRA
  • Trust and Operator liable
  • Reports from POCTc elsewhere in UK
  • unregistered HemoCue in use - optics faulty and
    results 4mg/dL out

3
The MHRA
  • Only staff whose training and competence has
    been established and recorded should be permitted
    to carry out POCT
  • Training should include
  • Basic principles of testing
  • Demonstration of proper use of system
  • Consequences of improper use
  • Instruction in sample collection
  • Instruction in the importance of complete
    documentation of all results
  • Appropriate calibration and QC testing
  • Practical experience to satisfy instructor that
    trainee is competent
  • Student staff grades are not permitted to perform
    testing independently, whether in the laboratory
    or POCT setting

4
So what can go wrong? - and how the risk is
reduced
  • Something wrong with the equipment
  • Daily check and documentation
  • Operator technique
  • Training
  • Proficiency Testing
  • Sample unsuitable for testing on device
  • Poor sampling
  • Limitations of device
  • The POCT Operator takes responsibility for all of
    these.
  • Make sure you follow the Standard Operating
    Procedure it is there to protect the patient
    and you!

5
Test cuvettes
  • Very sensitive to moisture in atmosphere
  • Risk of erroneous results
  • Now using individually wrapped
  • NB these cuvettes are chemically different from
    the old ones
  • do not use any old stock
  • can distinguish between old and new - no longer
    have wings

6
Daily Start-up
  • Purpose
  • Checks the lamp and light path are working
  • When
  • Every day before the device is used for patient
    testing
  • Meter dropped etc
  • How
  • Switch meter on
  • All the LEDs on the display will light up
  • Then the number 101 will appear then Hb
  • Pull out cuvette holder
  • Data and time displayed at top of screen and hour
    glass symbol at right hand side as self-test
    proceeds
  • Once successfully completed Hb replaced by
    three flashing lines appear on the screen and
    cuvette icon appears at top left

7
Daily Quality Control Check
  • Purpose
  • To check and document the meter and cuvettes are
    giving accurate readings
  • When
  • 2 levels (low and normal) every day before the
    device is used for patient testing
  • New batch of cuvettes
  • Unexpected patient result
  • Meter dropped etc
  • Practical Notes
  • Quality Control expires 1 month after opening
  • Replace shelf life expiry date with new expiry
    date when opening
  • Store UNOPENED bottles in fridge and in use
    bottles at room temperature

8
Filling the Cuvette with QC
  • Drop of QC onto plastic surface (eg Record Book
    cover) and draw into cuvette by capillary action
  • Clean any excess from outside cuvette using swab
  • Inspect optical eye for smears and bubbles

9
Processing the QC test
  • If cuvette is underfilled do not refill
  • Wait 1 minute for QC to react with chemicals in
    cuvette
  • (no wait time with patient samples)
  • Load cuvette into meter and rotate the holder
    shut
  • Result displayed after approx 15s

10
Documenting QC Result
  • Quality Control and Patient Record Book
  • Required to provide evidence of
  • meter checks
  • QC results
  • Complete audit trail of patient results
  • legal document archived for 30 years
  • Meter displays result in g/L, record in book in
    g/dL
  • Cuvette lot no and expiry date printed on
    individual wrappers
  • yyyy-mm-dd format
  • Review result check it falls within the
    acceptable range printed on the side of the
    bottle. If not
  • repeat test
  • check date on QC
  • try cleaning optics
  • If these actions fail, do not attempt to use
    meter for patient testing, document problem in
    record book and contact 4891

11
The puncture site patients gt1year
  • Health care professional
  • Wash and dry hands and put on gloves
  • Patient
  • Ensure hands are socially clean
  • If hands are cold ask patient to rub hands
    together
  • Puncture site
  • One of three outer fingers
  • Avoid finger pad and nail bed
  • Wash with water gauze swab (not alcohol)
  • Wipe dry and ensure completely dry before
    proceeding

12
Safe-T-Pro Plus in detail
13
Using the lancet Step 1 remove the sterility
cap
  • Hold the device and twist off the sterility cap
    by twisting it either in direction.
  • Throw the sterility cap away
  • Select the depth setting
  • Depth adjuster is preset to medium

14
Using the lancet Step 3 selecting the depth
  • Shallow setting 1.3mm
  • 1 on Softclix pen 1.1mm
  • Most patients for blood glucose
  • Medium setting 1.8mm
  • 2 on Softclix pen 1.8mm
  • Patients with thick skin
  • Deep setting 2.3mm
  • 3 on Softclix pen 2.3
  • Other POCT devices e.g. coag, Hb
  • Never use deep on children
  • lt 1year

15
Using the lancet Step 3 perform the
finger-stick
  • Hold the lancet firmly against the side of finger
  • Press the purple button to fire the needle
  • Wait a few seconds for the puncture site to open
  • wipe away the first 3 drops as this will
    contain tissue fluid
  • If necessary, milk the finger starting at the
    base working towards the top

16
Capillary sampling
  • Collect second drop of blood into cuvette
  • Discard the used lancet in a Sharps Bin

17
Arterial venous samples
  • Use solid form anticoagulants eg EDTA/heparin
    sample tubes
  • Ensure art lines etc have been flushed to avoid
    dilution effect or contaminants
  • Invert 10 times before dispensing sample onto
    plastic film
  • Fill cuvette using capillary action

18
Patient Testing
  • Inspect optical eye for smears and bubbles
  • If cuvette is underfilled do not refill
  • Analyse immediately
  • Result displayed after 15s in g/L
  • Document the result in g/dL (divide by 10)
  • Discard cuvette as clinical waste

19
Reviewing the result
  • Ensure patient has had a recent lab FBC to
    exclude non-Hb pathology e.g. thrombocytopaenia
  • Single drop sampling less accurate
  • Blood cannot be issued on basis of HemoCue result
    alone
  • inappropriate transfusion in EOU
  • Lab will start X-match send FBC to prevent delay
    in issuing
  • Active bleeding blood will issued as normal
    without FBCs
  • If unexpected review possible causes of
    inaccurate measurement
  • Repeat and send sample to lab
  • Common causes of erroneous results
  • eg cuvette storage, tissue fluid, delayed
    analysis, regional oedema
  • If in doubt send a sample to the lab!!

20
Daily Cleaning
  • Switch off
  • Rotate cuvette to load position
  • Release catch by pressing pen into recess
  • Pull holder all way round and then remove
    completely
  • Clean holder daily with detergent wipe, (and then
    alcohol wipe if blood stained)
  • Completely air dry (overnight)
  • Wipe exterior of meter with detergent wipe, (and
    then alcohol if blood stained)

21
Advanced cleaning
  • Excessive blood spill blocking light path
  • Erroneous QC/patient results
  • Spatulas from HemoCue
  • Repeat with new spatulas until no blood staining

22
Health Safety
  • Wear gloves
  • Dispose used lancets cuvettes in Sharps Bin
  • Cuvettes QC material contain toxins
  • Not a problem in normal working practice
  • Refer to CoSHH Assessment for inhalation, skin
    contact, eye contact or ingestion

23
Proficiency Testing (External Quality Assessment)
  • Clinical Governance
  • CMMC Policy that operators participate in the
    scheme
  • independently documents the ongoing proficiency
    of operator
  • Compares performance of meter with labs and
    clinical areas nationally
  • 1-3 samples distributed by the NEQAS monthly
  • Operators analyse 1 sample each so 1-3 people in
    month 1
  • Participation is rotated so different operators
    analyse in month 2
  • Each operator must participate at least 1-2
    results a year

24
Standard operating procedure
  • In line with MHRA guidelines on POCT there must
    be an SOP in place wherever POCT is performed
  • The SOP is the on-site reference manual which
    incorporates the manufacturers instructions and
    Trust Policies and procedures
  • Failure to adhere to the most current
    instructions could result in you as an individual
    being liable for any error in testing
  • All operators must be able to access SOP so they
    can refer to this info error codes are given in
    the Manufacturers Guide

25
Accessing the SOP
From homepage, scroll down to Browse and
select Departments
From Departments select Point of Care Testing
26
POCT Homepage
27
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28
Auditing
  • Meter reliability
  • Workload (record results)
  • Cleanliness
  • Documentation
  • Stock control
  • IQC results
  • EQA/PT results
  • Auditors Internal POC and CPA
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