Literature DB >> 23425394

How do family carers respond to behavioral and psychological symptoms of dementia?

Kirsten Moore1, Elizabeth Ozanne, David Ames, Briony Dow.   

Abstract

BACKGROUND: Behavioral and psychological symptoms of dementia (BPSD) have been associated with increased carer burden and early institutionalization. BPSD are more responsive to treatment than are cognitive and functional decline. Little is known about how family carers understand and try to reduce these symptoms. This study aimed to explore the strategies used by carers looking after someone with high levels of BPSD.
METHODS: Twenty-five carers were interviewed using a semi-structured interview with the Neuropsychiatric Inventory (NPI). They were all caring for someone eligible for an Extended Aged Care at Home Dementia Package, which targets people with BPSD.
RESULTS: Participants reported high levels of BPSD with a mean score of 8.2 for symptoms (range 2-12, SD = 2.38) and a mean NPI score of 51.4 (range 14-111, SD = 28.74). Distress scores were also high with a mean of 18.5 (range 2-42, SD = 11.33). Carers described on average, fewer than four strategies for managing BPSD. Encouraging activity, utilizing psychotropic medications, identifying triggers, restraining or treating in a paternalistic manner, and meeting physiological needs were the most commonly used strategies.
CONCLUSION: While family carers are often at the forefront of identifying triggers and addressing unmet needs, findings from this study suggest that some carers have a limited repertoire of strategies despite experiencing a large number of symptoms. There is a clear need for ensuring evidence-based programs to educate and support carers in identifying triggers, understanding symptoms and learning to cope with these symptoms.

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Mesh:

Year:  2013        PMID: 23425394     DOI: 10.1017/S1041610213000070

Source DB:  PubMed          Journal:  Int Psychogeriatr        ISSN: 1041-6102            Impact factor:   3.878


  6 in total

1.  "I've learned to just go with the flow": Family caregivers' strategies for managing behavioral and psychological symptoms of dementia.

Authors:  Courtney A Polenick; Laura M Struble; Barbara Stanislawski; Molly Turnwald; Brianna Broderick; Laura N Gitlin; Helen C Kales
Journal:  Dementia (London)       Date:  2018-06-09

2.  In the Information Age, do dementia caregivers get the information they need? Semi-structured interviews to determine informal caregivers' education needs, barriers, and preferences.

Authors:  Kendra Peterson; Howard Hahn; Amber J Lee; Catherine A Madison; Alireza Atri
Journal:  BMC Geriatr       Date:  2016-09-23       Impact factor: 3.921

3.  Validation Study of the Korean Version of the Brief Clinical Form of the Neuropsychiatric Inventory.

Authors:  Hee-Jin Kim; Kyoung Hue Choi; Seung H Kim; Jeffrey L Cummings; Dong-Won Yang
Journal:  Dement Geriatr Cogn Dis Extra       Date:  2016-06-03

4.  Self-management by family caregivers to manage changes in the behavior and mood of their relative with dementia: an online focus group study.

Authors:  Judith Huis In Het Veld; Renate Verkaik; Berno van Meijel; Paul-Jeroen Verkade; Wendy Werkman; Cees Hertogh; Anneke Francke
Journal:  BMC Geriatr       Date:  2016-05-03       Impact factor: 3.921

5.  Predicting the role of assistive technologies in the lives of people with dementia using objective care recipient factors.

Authors:  Stephen Czarnuch; Rose Ricciardelli; Alex Mihailidis
Journal:  BMC Geriatr       Date:  2016-07-20       Impact factor: 3.921

6.  Occupational therapy for people with dementia and their family carers provided at home: a systematic review and meta-analysis.

Authors:  Sally Bennett; Kate Laver; Sebastian Voigt-Radloff; Lori Letts; Lindy Clemson; Maud Graff; Jodie Wiseman; Laura Gitlin
Journal:  BMJ Open       Date:  2019-11-11       Impact factor: 2.692

  6 in total

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