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vCJD in the UK The Patients Perspective

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Title: vCJD in the UK The Patients Perspective


1
vCJD in the UKThe Patients Perspective
  • Chris James
  • Haemophilia Society UK
  • October 2009

2
Issues
  • What are the expectations of patients in the UK?
  • Do they want to be tested and if so to know the
    results?
  • Who will do the tests?
  • What support will be available?
  • What would be the implications of a positive test
    in terms of health care?

3
The UK Risk
  • Everyone who ate beef in the UK between 1980 and
    2001 has a very low but continuing risk of
    developing vCJD
  • There is an additional slight increase in risk
    for people who recieved plasma products in the
    same period

4
What have patients been told?
  • Between 4,000 and 5,000 received a letter in 2004
    all those with haemophilia who were treated
    with UK plasma products between 1980 and 2001 are
    at risk for public health purposes
  • Also offered chance to find out if you were a
    recipient of an implicated batch
  • From a question to UK Parliament we know the
    implicated group is 802

5
Developments in 2009
  • Discovery of abnormal prions at autopsy of a man
    with haemophilia announced Feb 2009
  • UK Government updated its risk assessment
    probable cause plasma products
  • Further letter to patients caused considerable
    anxiety within the haemophilia community

6
Completion of Risk Assessment
  • In 2009 UK Government published full risk
    assessment
  • Main finding risk was greater from
    non-implicated batches than implicated batches of
    plasma
  • No change to risk status of patients but greater
    anxiety
  • UK Government sent letter to go to patients from
    Haemophilia Centres
  • UK Society intervened and produced our own
    guidance

7
Impact on Patients
  • Suffering discrimination due to being at risk
    for health purposes
  • Yet another infection following HIV and HCV
    ....will it never end?
  • Uncertainty over vCJD and the risks
  • Are haemophilia patients are being singled out as
    an easily identifiable group?

8
The Test
  • Department of Health
  • Mapping out the consequences of screening blood
    donations for PrPSC
  • Sets out the DOHs view testing, its
    implications, and how the health services would
    react
  • Trade-off creation of new at risk groups, risk
    reduction, legal, supply etc

9
The Test
  • Potential for testing those at risk
  • Clinical Governance Advisory Group recommended
    help in gaining access to test
  • Increase Positive Predictive Value of test
  • Access to a test with a specificity below that
    required
  • May test positive but balance of probability
    would be against being infected let alone go on
    to develop clinical symptoms
  • Raises problems with communication

10
The Test
  • Difficult to judge meaning of a positive
    screening test (Gigerenzer, 2002)
  • Possibilty of raised anxiety
  • Simple explanation can be effective in
    communicating meaning and avoiding high levels of
    anxiety (Wilkinson et al, 2007)

11
The Test
  • Testing may not be emotionally devastating
  • Best predictor of depression post-testing is
    pre-test depression, not test results (Broadstock
    et al, 2000)
  • N.B. These people had decided to undergo testing,
    and were treated in the context of intensive pre
    and post test counselling
  • Against the positive there is a reported case of
    a suicide on being told of a positive HIV test
    and one amongst those at risk of vCJD

12
The Test
  • Qualitative research is currently being completed
    in the UK
  • Exploring how individuals judged to be at risk
    of prion disease reacted to notification of
    status
  • Relatively few individuals
  • Provisional results suggest that most were able
    to deal with the unwelcome information and
    continue their lives
  • (Elam et al, 2009)

13
Care and Support- Informed choice
  • Ensure access to designated neurologist and
    National Prion Centre
  • Meeting demand for additional testing
  • Provision of normal medical care not
    compromised
  • Deal with problems raised by potential refusal of
    life insurance, employment etc
  • Helpline support provided by Society

14
UK Society Position
  • We call for any test for vCJD to be brought in as
    soon as available and with proven efficacy
  • Gold standard Pre and Post Test Counselling and
    funding for on-going helpline support

15
vCJD Meeting with Department of Health
  • Purpose
  • for people with haemophilia to
  • give their views and experiences as
  • people at risk of vCJD
  • to inform people with haemophilia, and those
    responsible for their care of current vCJD issues
  • describe opportunities for participation in
    research studies

16
Thank You
  • chris_at_haemophilia.org.uk
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