Vulnerability to neuroleptic side effects in frontotemporal lobar degeneration

Background Frontotemporal lobar degeneration (FTLD) is commonly associated with behavioural disturbances such as disinhibition and aggression; these often result in the use of neuroleptic medication. Methods All available case notes of patients attending a specialist cognitive disorders clinic with...

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Published inInternational journal of geriatric psychiatry Vol. 18; no. 1; pp. 67 - 72
Main Authors Pijnenburg, Y. A. L., Sampson, E. L., Harvey, R. J., Fox, N. C., Rossor, M. N.
Format Journal Article
LanguageEnglish
Published Chichester, UK John Wiley & Sons, Ltd 01.01.2003
Wiley
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Summary:Background Frontotemporal lobar degeneration (FTLD) is commonly associated with behavioural disturbances such as disinhibition and aggression; these often result in the use of neuroleptic medication. Methods All available case notes of patients attending a specialist cognitive disorders clinic with a diagnosis of FTLD were selected. This gave 100 subjects (62 male, 38 female). Results In 61 patients significant behavioural disturbances were present. Of these patients, 24 had been prescribed neuroleptics. Significant extrapyramidal side effects were reported in eight patients (33%); in five patients these were severe enough to cause severe mobility problems and in one patient resulted in impaired consciousness. In some instances the extrapyramidal side effects took weeks to wear off. Conclusion These results suggest that patients with FTLD may, as in Lewy body dementia, be particularly sensitive to the extrapyramidal side effects of neuroleptics. We suggest that neuroleptics should be used cautiously in FTLD and treatment should be started at low doses avoiding depot preparations until further prospective studies have been performed. Copyright © 2002 John Wiley & Sons, Ltd.
Bibliography:ark:/67375/WNG-QMZ3GXJW-T
istex:E29FB423556C0AAF074B36CD0A8091F53AFDCC70
Alzheimers Society, UK
ArticleID:GPS774
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0885-6230
1099-1166
DOI:10.1002/gps.774