Frontotemporal Dementia: Change of Familial Caregiver Burden and Partner Relation in a Dutch Cohort of 63 Patients

Sam Riedijk, Hugo Duivenvoorden, Sonia Rosso, J.C. van Swieten, Martinus Niermeijer, Aad Tibben

Research output: Contribution to journalArticleAcademicpeer-review

33 Citations (Scopus)
49 Downloads (Pure)

Abstract

Background/Aims: The current study examined the change of caregiver burden and the development of the quality of the partner relation in frontotemporal dementia (FTD). Methods: During a 2-year period, deterioration, behavioural problems, caregiver burden, general psychopathology, quality of life, social support, coping strategies and relationship quality were inspected in 63 FTD caregiver-care recipient dyads. Results: After 2 years patients reached maximum dementia severity with stable Neuropsychiatric Inventory levels. Contrary to expectations, caregiver burden decreased and psychological well-being remained stable. Coping style and social support changed unfavourably. Relationship closeness and getting along were preserved, whereas communication and sharing viewpoint on life were dramatically reduced. Conclusions: FTD caregivers need support in coping with the increasingly hopeless situation of their patients. Future research methods into caregiver burden should address response shift as a means for psychological adjustment. Copyright (C) 2008 S. Karger AG, Basel
Original languageUndefined/Unknown
Pages (from-to)398-406
Number of pages9
JournalDementia and Geriatric Cognitive Disorders
Volume26
Issue number5
DOIs
Publication statusPublished - 2008

Research programs

  • EMC MGC-02-96-01
  • EMC MM-04-44-02

Cite this