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Patient and caregiver quality of life in Huntington's disease
Author(s) -
Ready Rebecca E.,
Mathews Melissa,
Leserman Anne,
Paulsen Jane S.
Publication year - 2008
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/mds.21920
Subject(s) - quality of life (healthcare) , disease , psychology , recall , huntington's disease , cognition , caregiver burden , clinical psychology , clinical trial , activities of daily living , psychiatry , medicine , dementia , psychotherapist , cognitive psychology
Little is known about subjective perceptions of quality of life (QOL) in Huntington's disease (HD). The current study determined correlates of patient and caregiver QOL and assessed change over time. Participants were 22 patient‐caregiver dyads, who rated QOL at baseline and 6 months later. Overall, patients' functional and cognitive impairment were significantly correlated with patient and caregiver QOL. Neuropsychiatric symptoms had differential impact on patient and caregiver QOL. Furthermore, when patients recalled their QOL about a previous time, their recall may have been negatively biased. Clinical implications of results are discussed. Future work is needed because subjective QOL is an important outcome measure in therapeutic trials. © 2008 Movement Disorder Society