Literature DB >> 18791893

Support to family carers of patients with frontotemporal dementia.

Tor Atle Rosness1, Per Kristian Haugen, Knut Engedal.   

Abstract

OBJECTIVES: To examine the provision of support to patients with frontotemporal dementia (FTD) and their family carers compared with patients with early onset Alzheimer's dementia (AD) and their carers, and the carers' satisfaction with the support.
METHOD: Data came from 60 dyads of patients with dementia and their principal family carers, 23 subjects with frontotemporal dementia and their 23 carers, and 37 subjects with early onset Alzheimer's disease and their 37 carers.
RESULTS: Patients with a frontotemporal dementia diagnosis were significantly more frequently offered stays in nursing homes (p = 0.04). Carers of patients with frontotemporal dementia were significantly less satisfied with the provision of information about the disease compared with carers of early onset Alzheimer's disease patients (p = 0.05) and were significantly less satisfied with counseling and follow-up advice (p = 0.05).
CONCLUSION: Changes of personality in patients with frontotemporal dementia may be the major reason why they were offered more stays in institutions. These family carers tend to be less satisfied with the provision of support they received from the specialist health service compared to carers of Alzheimer's disease patients, and are in need of more, and other forms of support.

Entities:  

Mesh:

Year:  2008        PMID: 18791893     DOI: 10.1080/13607860802224334

Source DB:  PubMed          Journal:  Aging Ment Health        ISSN: 1360-7863            Impact factor:   3.658


  11 in total

1.  Accessing community-based and long-term care services: challenges facing persons with frontotemporal dementia and their families.

Authors:  Darby Morhardt
Journal:  J Mol Neurosci       Date:  2011-08-09       Impact factor: 3.444

Review 2.  Update on frontotemporal dementia.

Authors:  Zoe Arvanitakis
Journal:  Neurologist       Date:  2010-01       Impact factor: 1.398

3.  Caring for loved ones with frontotemporal degeneration: the lived experiences of spouses.

Authors:  Lauren Massimo; Lois K Evans; Patricia Benner
Journal:  Geriatr Nurs       Date:  2013-05-30       Impact factor: 2.361

4.  A cross-sectional evaluation of the Dutch RHAPSODY program: online information and support for caregivers of persons with young-onset dementia.

Authors:  Maud Daemen; Jeroen Bruinsma; Christian Bakker; Rob Groot Zwaaftink; Raymond Koopmans; Andrea Oostijen; Bernard Loose; Frans Verhey; Marjolein de Vugt; Kirsten Peetoom
Journal:  Internet Interv       Date:  2022-03-26

Review 5.  Managing cognition in progressive supranuclear palsy.

Authors:  Timothy Rittman; Ian Ts Coyle-Gilchrist; James B Rowe
Journal:  Neurodegener Dis Manag       Date:  2016-11-23

6.  Dignity in people with frontotemporal dementia and similar disorders - a qualitative study of the perspective of family caregivers.

Authors:  Mette Sagbakken; Dagfinn Nåden; Ingun Ulstein; Kari Kvaal; Birgitta Langhammer; May-Karin Rognstad
Journal:  BMC Health Serv Res       Date:  2017-06-23       Impact factor: 2.655

7.  Gaining Longitudinal Accounts of Carers' Experiences Using IPA and Photograph Elicitation.

Authors:  Val Morrison; Karina Williams
Journal:  Front Psychol       Date:  2020-12-04

8.  Diagnostic experience reported by caregivers of patients with frontotemporal degeneration.

Authors:  Lilah M Besser; James E Galvin
Journal:  Neurol Clin Pract       Date:  2020-08

Review 9.  Family caregivers of people with dementia.

Authors:  Henry Brodaty; Marika Donkin
Journal:  Dialogues Clin Neurosci       Date:  2009       Impact factor: 5.986

Review 10.  Enhancement of carer skills and patient function in the non-pharmacological management of frontotemporal dementia (FTD): A call for randomised controlled studies.

Authors:  Claire M O'Connor; Lindy Clemson; Thaís Bento Lima da Silva; Olivier Piguet; John R Hodges; Eneida Mioshi
Journal:  Dement Neuropsychol       Date:  2013 Apr-Jun
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