Literature DB >> 19111853

Educating nursing home staff about the progression of dementia and the comfort care option: impact on family satisfaction with end-of-life care.

Marcel Arcand1, Johanne Monette, Michèle Monette, Nadia Sourial, Lynn Fournier, Brian Gore, Howard Bergman.   

Abstract

OBJECTIVE: There is a growing consensus on the relevance of a palliative care approach in end-stage dementia. The objective of this study was to assess the impact, in terms of family satisfaction with end-of-life care, of a nursing home (NH) pilot educational program for nursing staff and physicians on comfort care and advanced dementia.
METHODS: The intervention, implemented in one voluntary NH, consisted of an educational program that included providing an information booklet to all NH staff, and optionally to families. Satisfaction with care was compared using a validated instrument, the "After death bereaved family member interview" pre- and post-intervention. Pre and post groups were composed of close relatives of residents who died in the context of advanced dementia.
RESULTS: Twenty-seven contact persons were interviewed pre-intervention and 21 post-intervention (participation rate of 60% for both groups). Descriptive statistics showed better scores on satisfaction with pain control, emotional support, treating patient with respect, and information on what to expect while patient was dying, in the post-intervention group. Comparison of overall scale scores revealed no statistical differences between the 2 groups, although the post-intervention group expressed greater satisfaction in the area of communication with the health care team (8.0 versus 6.6, P = .109) and greater global satisfaction with care (8.3 versus 7.3, P = .087). DISCUSSION: Although not significant, results as to the effectiveness of such an intervention to improve family satisfaction with end-of-life care are encouraging.
CONCLUSION: The booklet, as support tool, and the educational program may have facilitated communication within the team, and between the team and family members. Replication of this intervention in a multicenter NH population is needed to adequately assess its effectiveness.

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Year:  2008        PMID: 19111853     DOI: 10.1016/j.jamda.2008.07.008

Source DB:  PubMed          Journal:  J Am Med Dir Assoc        ISSN: 1525-8610            Impact factor:   4.669


  21 in total

1.  Clinical practice in nursing homes as a key for progress.

Authors:  J E Morley
Journal:  J Nutr Health Aging       Date:  2010-08       Impact factor: 4.075

Review 2.  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

Review 3.  Measuring Experience With End-of-Life Care: A Systematic Literature Review.

Authors:  Jessica Penn Lendon; Sangeeta C Ahluwalia; Anne M Walling; Karl A Lorenz; Oluwatobi A Oluwatola; Rebecca Anhang Price; Denise Quigley; Joan M Teno
Journal:  J Pain Symptom Manage       Date:  2014-12-24       Impact factor: 3.612

4.  Selection bias in family reports on end of life with dementia in nursing homes.

Authors:  Jenny T van der Steen; Luc Deliens; Miel W Ribbe; Bregje D Onwuteaka-Philipsen
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5.  Measuring Patient-Centeredness of Care for Seriously Ill Individuals: Challenges and Opportunities for Accountability Initiatives.

Authors:  Rebecca Anhang Price; Marc N Elliott
Journal:  J Palliat Med       Date:  2017-11-01       Impact factor: 2.947

Review 6.  A review of interprofessional dissemination and education interventions for recognizing and managing dementia.

Authors:  Abraham A Brody; James E Galvin
Journal:  Gerontol Geriatr Educ       Date:  2013

Review 7.  A review of advance care planning programs in long-term care homes: are they dementia friendly?

Authors:  Abigail Wickson-Griffiths; Sharon Kaasalainen; Jenny Ploeg; Carrie McAiney
Journal:  Nurs Res Pract       Date:  2014-03-16

Review 8.  UK quality statements on end of life care in dementia: a systematic review of research evidence.

Authors:  Bridget Candy; Margaret Elliott; Kirsten Moore; Victoria Vickerstaff; Elizabeth Sampson; Louise Jones
Journal:  BMC Palliat Care       Date:  2015-10-19       Impact factor: 3.234

9.  Family members' perceptions of end-of-life care across diverse locations of care.

Authors:  Romayne Gallagher; Marian Krawczyk
Journal:  BMC Palliat Care       Date:  2013-07-20       Impact factor: 3.234

10.  Conceptual foundations of a palliative approach: a knowledge synthesis.

Authors:  Richard Sawatzky; Pat Porterfield; Joyce Lee; Duncan Dixon; Kathleen Lounsbury; Barbara Pesut; Della Roberts; Carolyn Tayler; James Voth; Kelli Stajduhar
Journal:  BMC Palliat Care       Date:  2016-01-15       Impact factor: 3.234

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