Literature DB >> 21486116

Physicians' and nurses' perceived usefulness and acceptability of a family information booklet about comfort care in advanced dementia.

Jenny T van der Steen1, Franco Toscani, Tjomme de Graas, Silvia Finetti, Miharu Nakanishi, Taeko Nakashima, Kevin Brazil, Cees M P M Hertogh, Marcel Arcand.   

Abstract

BACKGROUND: Families of patients with advanced dementia need to be informed about the course of the dementia and comfort care. Conditional for health care providers educating families is their knowledge and comfort in family education.
METHODS: Perceived usefulness and acceptability of a Canadian family booklet explaining possible complications and comfort care in dementia was assessed by physicians and nurses caring for dementia patients in 14 nursing homes in Lombardy, Italy and 21 in the Netherlands. The practitioners received a questionnaire and translated versions adapted to local practice where needed. In 10 of 21 Dutch homes, physicians evaluated only the original Canadian version in English. A 15-item scale assessed the booklet's acceptability, for example, to inform families, or for educational purposes. Perceived usefulness referred to proportion of families of dementia patients for whom the booklet would be useful. A total of 168 evaluations were available for multivariable regression analyses.
RESULTS: The practitioners anticipated that the booklet would be useful for most families. Evaluation of the Dutch translation of the booklet was similar to the English version. Country (Netherlands) and profession (nurses) were independently associated with better acceptability. Usefulness was perceived as better by Italian respondents and nurses, but only in analyses unadjusted for the higher educational needs of these respondents.
CONCLUSION: Overall, the concept of written information on comfort care was appreciated by practitioners of European countries differing in attitudes toward end-of-life care. A booklet may help practitioners, and in particular nurses, in providing comfort care for dementia patients and their families.

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Year:  2011        PMID: 21486116     DOI: 10.1089/jpm.2010.0484

Source DB:  PubMed          Journal:  J Palliat Med        ISSN: 1557-7740            Impact factor:   2.947


  4 in total

Review 1.  End-of-life issues in advanced dementia: Part 1: goals of care, decision-making process, and family education.

Authors:  Marcel Arcand
Journal:  Can Fam Physician       Date:  2015-04       Impact factor: 3.275

2.  Information use environments of African-American dementia caregivers over the course of cognitive-behavioral therapy for depression.

Authors:  Michelle M Kazmer; Robert L Glueckauf; Jinxuan Ma; Kathleen Burnett
Journal:  Libr Inf Sci Res       Date:  2013-07-01

3.  General practitioners perceptions on advance care planning for patients living with dementia.

Authors:  Kevin Brazil; Gillian Carter; Karen Galway; Max Watson; Jenny T van der Steen
Journal:  BMC Palliat Care       Date:  2015-04-23       Impact factor: 3.234

4.  Practitioners' perceptions of acceptability of a question prompt list about palliative care for advance care planning with people living with dementia and their family caregivers: a mixed-methods evaluation study.

Authors:  Jenny T van der Steen; Sten Heck; Carla Cm Juffermans; Mirjam Marjolein Garvelink; Wilco P Achterberg; Josephine Clayton; Genevieve Thompson; Raymond Tcm Koopmans; Yvette M van der Linden
Journal:  BMJ Open       Date:  2021-04-12       Impact factor: 2.692

  4 in total

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