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Sharing the diagnosis of dementia

Sharing the diagnosis of dementia Alistair Burns Manchester Mental Health and Social Care Trust University of Manchester Manchester Academic Health Science Centre Declaration of interest. Sharing the diagnosis of dementia. Should we give the diagnosis? If yes, how should we?

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Sharing the diagnosis of dementia

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  1. Sharing the diagnosis of dementiaAlistair BurnsManchester Mental Health and Social Care TrustUniversity of ManchesterManchester Academic Health Science CentreDeclaration of interest

  2. Sharing the diagnosis of dementia Should we give the diagnosis? If yes, how should we? How should we support people afterwards? Mixture of opinion, experience and evidence

  3. Sharing the diagnosis of dementia Should we give the diagnosis? If yes, how should we? How should we support people afterwards?

  4. Sharing the diagnosis of dementia Against sharing the diagnosis A person will be viewed differently Malignant social psychology (Tom Kitwood) Confirms fears and removes hope They will forget Therapeutic nihilism (“nothing can be done”) Who helps afterwards “Do no harm”

  5. Sharing the diagnosis of dementia In favour of sharing the diagnosis The right to know They have asked First stage in adjustment Prevents conspiracy Encourages dialogue

  6. Disclosure of dementia diagnosis • Method • Survey of 21 National family associations in Europe in 2003 • Survey of 500 caregivers in 23 countries by Alzheimer Europe • Consultation with six leading experts from different European countries

  7. Should the patient be told of the diagnosis of dementia? • The following principle should be applied: • The diagnosis of dementia should be disclosed to the patient unless specific circumstances indicate that this would not contribute to the welfare of the patient nor improve the quality of care that they receive.

  8. Should the patient be told the diagnosis of dementia? • specific circumstances that limit the extent of disclosure of the diagnosis of dementia to the patient are: • the presence of severe impairment of cognition • the patients’ explicit wish not to know their diagnosis • the well founded opinion of the treating physician that the disclosure of the diagnosis might lead to a worsening of the patients’ state

  9. Evaluation and diagnosis of dementia associated with reductions in depression and anxiety (Carpenter et al, JAGS, 2008) Patients Carers

  10. Sharing the diagnosis of dementia Should we give the diagnosis? If yes, how should we? How should we support people afterwards?

  11. Sharing the diagnosis of dementiaFoy et al BMC Health Services Research 2007 7 207Lecouturier et al BMC Health Services Research 2008 8 95 Preparing for diagnosis Integrating family members Exploring the patient’s perspective Disclosing the diagnosis finding out what the patient knows using dementia and Alzheimer’s disease exploring what the diagnosis means Responding to patient’s reactions Focusing on quality of life and wellbeing Preparing for the future Communicating effectively

  12. Sharing the diagnosis of dementia Should we give the diagnosis? If yes, how should we? How should we support people afterwards?

  13. Psychotherapy in Alzheimer’s disease(Burns et al, British Journal of Psychiatry 2005 187 143-7) Description RCT of 40 patients with Alzheimer’s disease Six sessions of Interpersonal therapy Results Psychotherapy had no effect on primary outcomes Relatives reacted less to problem behaviours Conclusion No evidence to support routine use of psychotherapy in Alzheimer’s disease

  14. Brodaty et al, Journal of the American Geriatrics Society 2003 51 657-64

  15. The Three Country study(American Journal of Psychiatry 2008 16 893-904) Description 155 carer patient dyads across 3 centres RCT of caregiver intervention All patients had donepezil Results Harmonisation of intervention achieved Reduction in caregiver depression No significant effect on nursing home admission/mortality Some country differences: Americans reacted more strongly, less satisfied, English felt more supported, Australians more mastery Conclusion Caregiver interventions can be implemented across centres and have a positive effect in addition to anti-dementia medication

  16. Manchester Memory Clinic Brief description Two nurses, p/t psychologist, secretary, 3 consultant clinical sessions, plethora of trainees Modus operandi: all referrals from GPs usually seen at home by a nurse: standard assessment protocol discussed at management meeting discharged seen in outpatients psychological assessment seen again at home investigations (GPs do bloods and physical) Post diagnostic groups Research projects

  17. Manchester Memory Clinic What do we do (1)? Diagnosis often given at home by our nurse In the clinic: give the name reassure other things not present you are the same person who walked in follow up Time to reflect and answer questions: what is going to happen, can anything be done, is it genetic? Rarely a surprise Risk assessment

  18. Manchester Memory Clinic What do we do (2)? Post diagnostic counselling Confirming the diagnosis Practical information and advice eg driving, power of attorney, living will Treatment options Getting on with things Life history, reservoir of memories Memory retraining group Lifestyle intervention

  19. Sharing the diagnosis of dementia Conclusions 1. Disclosing/sharing the diagnosis of dementia is important2. It is possible to do it badly 3. Supporting people with dementia, and their families, after the diagnosis is essential

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