Literature DB >> 25178513

Thinking about the end of life: a common issue for patients with Huntington's disease.

Suzanne J Booij1, Aad Tibben, Dick P Engberts, Johan Marinus, Raymund A C Roos.   

Abstract

The aim of this study was to investigate the presence of thoughts or wishes for the end of life in patients with Huntington's disease (HD) or identified gene carriers (further mentioned together as patients). A custom-made questionnaire, based on previous qualitative research, was sent out to 242 patients with HD and identified gene carriers. Presence of wishes was investigated and correlated to demographic and clinical characteristics. A total of 134 patients (55 %) returned the questionnaire. 101 respondents (75 %) reported to have some kind of thoughts or wishes for the end of life. For 15 respondents (11 %) these thoughts concerned care; 86 respondents (64 %) reported to have also thoughts about euthanasia or physician-assisted suicide (PAS). The presence of any thoughts about the end of life was significantly related to being familiar with HD in the family, but not related to any other demographic or clinical variable. Participants with thoughts specifically about euthanasia or PAS were of higher education and in earlier stages of the disease than participants without such thoughts. Thoughts or wishes for the end of life are present amongst patients with HD. These thoughts include euthanasia or PAS in a majority of the respondents. It is suggested that prudential addressing of these issues may enhance the doctor-patient relationship.

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Year:  2014        PMID: 25178513     DOI: 10.1007/s00415-014-7479-4

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  24 in total

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Review 6.  Advance directives in dementia: issues of validity and effectiveness.

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7.  Promoting Excellence in End-of-Life Care: lessons learned from a cohort of nursing home residents with advanced Huntington disease.

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8.  Are religion and religiosity important to end-of-life decisions and patient autonomy in the ICU? The Ethicatt study.

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9.  Communication about euthanasia in general practice: opinions and experiences of patients and their general practitioners.

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10.  A plea for end-of-life discussions with patients suffering from Huntington's disease: the role of the physician.

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  7 in total

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Authors:  N E Carlozzi; N R Downing; M K McCormack; S G Schilling; J S Perlmutter; E A Hahn; J S Lai; S Frank; K A Quaid; J S Paulsen; D Cella; S M Goodnight; J A Miner; M A Nance
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2.  A new measure for end of life planning, preparation, and preferences in Huntington disease: HDQLIFE end of life planning.

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Journal:  J Neurol       Date:  2017-11-15       Impact factor: 4.849

3.  Factors Associated With End-of-Life Planning in Huntington Disease.

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Journal:  Am J Hosp Palliat Care       Date:  2017-06-28       Impact factor: 2.500

4.  End-of-life measures in Huntington disease: HDQLIFE Meaning and Purpose, Concern with Death and Dying, and End of Life Planning.

Authors:  Noelle E Carlozzi; Nicholas R Boileau; Jane S Paulsen; Joel S Perlmutter; Jin-Shei Lai; Elizabeth A Hahn; Michael K McCormack; Martha A Nance; David Cella; Stacey K Barton; Nancy R Downing
Journal:  J Neurol       Date:  2019-06-12       Impact factor: 4.849

5.  Gaining insight into the views of outpatients with Huntington's disease regarding their future and the way they deal with their poor prognosis: a qualitative study.

Authors:  Marina R Ekkel; Marja F I A Depla; Els M L Verschuur; Ruth B Veenhuizen; Cees M P M Hertogh; Bregje D Onwuteaka-Philipsen
Journal:  BMC Palliat Care       Date:  2021-01-12       Impact factor: 3.234

6.  Advance Directive Documentation in a Huntington's Disease Clinic: A Retrospective Chart Review.

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7.  Patient perspectives on advance euthanasia directives in Huntington's disease. A qualitative interview study.

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  7 in total

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