Literature DB >> 11921148

What are patients and their families told about the diagnosis of dementia? Results of a family survey.

Suzanne Holroyd1, Quentin Turnbull, Andrew M Wolf.   

Abstract

BACKGROUND: Controversy exists as to whether dementia patients should be told their diagnosis and prognosis.
OBJECTIVE: This study examined the experience of patients and families when a diagnosis of dementia is given.
METHOD: Fifty-seven family members from community dementia support groups answered a questionnaire regarding the diagnosis of dementia in a family member.
RESULTS: Family members were significantly more likely to have been told the diagnosis and symptoms to expect in dementia than patients themselves. Half of the families felt they were not given enough information regarding dementia. Interestingly, the majority of family members believed patients should be told their diagnosis and prognosis yet about half had reported that informed patients had reacted poorly to being told their diagnosis and only about a third felt it was helpful to the patient.
CONCLUSION: The results suggest physicians should better involve patients and their families in disclosing diagnoses and information regarding dementia. The results also suggest the current AMA guidelines to inform patients their diagnosis of dementia are inadequate to address the clinical complexities of this issue. Copyright 2002 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Year:  2002        PMID: 11921148     DOI: 10.1002/gps.552

Source DB:  PubMed          Journal:  Int J Geriatr Psychiatry        ISSN: 0885-6230            Impact factor:   3.485


  15 in total

1.  Agreement on diagnosis among patients, companions, and professionals after a dementia evaluation.

Authors:  Alexandra K Zaleta; Brian D Carpenter; Emily K Porensky; Chengjie Xiong; John C Morris
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Review 2.  Reluctance to disclose difficult diagnoses: a narrative review comparing communication by psychiatrists and oncologists.

Authors:  Alex J Mitchell
Journal:  Support Care Cancer       Date:  2007-07       Impact factor: 3.603

Review 3.  Diagnostic labels, stigma, and participation in research related to dementia and mild cognitive impairment.

Authors:  Linda Garand; Jennifer H Lingler; Kyaien O Conner; Mary Amanda Dew
Journal:  Res Gerontol Nurs       Date:  2009-04       Impact factor: 1.571

4.  [Disclosure and informative consultation after diagnosis of dementia: retrospective perception from the point of view of relatives].

Authors:  H Hesemann; F Petermann; K Reif
Journal:  Z Gerontol Geriatr       Date:  2013-10       Impact factor: 1.281

5.  Measuring primary care patients' attitudes about dementia screening.

Authors:  Malaz Boustani; Anthony J Perkins; Patrick Monahan; Chris Fox; Lea Watson; John Hopkins; Bridget Fultz; Siu Hui; Frederick W Unverzagt; Christopher M Callahan; Hugh C Hendrie
Journal:  Int J Geriatr Psychiatry       Date:  2008-08       Impact factor: 3.485

6.  Difficulties in disclosing the diagnosis of dementia: a qualitative study in general practice.

Authors:  Jill Phillips; Constance Dimity Pond; Nerida Elizabeth Paterson; Cate Howell; Allan Shell; Nigel P Stocks; Susan M Goode; John E Marley
Journal:  Br J Gen Pract       Date:  2012-08       Impact factor: 5.386

Review 7.  Mild cognitive impairment: conceptual, assessment, ethical, and social issues.

Authors:  Perla Werner; Amos D Korczyn
Journal:  Clin Interv Aging       Date:  2008       Impact factor: 4.458

8.  Case-finding of dementia in general practice and effects of subsequent collaborative care; design of a cluster RCT.

Authors:  Pim van den Dungen; Eric P Moll van Charante; Harm W J van Marwijk; Henriëtte E van der Horst; Peter M van de Ven; Hein P J van Hout
Journal:  BMC Public Health       Date:  2012-08-04       Impact factor: 3.295

9.  General practitioner's clinical practices, difficulties and educational needs to manage Alzheimer's disease in France: analysis of national telephone-inquiry data.

Authors:  Dominique Somme; Arnaud Gautier; Stéphanie Pin; Aline Corvol
Journal:  BMC Fam Pract       Date:  2013-06-13       Impact factor: 2.497

10.  The evaluation of a healthcare passport to improve quality of care and communication for people living with dementia (EQuIP): a protocol paper for a qualitative, longitudinal study.

Authors:  Gerard Leavey; Aine Abbott; Max Watson; Stephen Todd; Vivien Coates; Sonja McIlfactrick; Brendan McCormack; Bethany Waterhouse-Bradley; Emma Curran
Journal:  BMC Health Serv Res       Date:  2016-08-09       Impact factor: 2.655

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