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Volume 100, Issue 1, Pages 97-107 (March 2008)


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Evolution of neuroleptic-induced extrapyramidal syndromes under long-term neuroleptic treatment

Jiri ModestinCorresponding Author Informationemail address, Marianne Vogt Wehrli, Patrik Lukas Stephan, Puspa Agarwalla

Received 30 July 2007; received in revised form 17 October 2007; accepted 25 October 2007. published online 06 December 2007.

Abstract 

Background

The long-term evolution of neuroleptic-induced extrapyramidal syndromes (EPS) of Parkinsonism, akathisia and tardive dyskinesia (TD) is still a controversial issue worth exploring.

Method

A total of 200 inpatients on regular typical neuroleptics (NL) and/or clozapine were assessed in 1995 with regard to the prevalence of EPS. Altogether, 83 patients could be reassessed in 2003/04 (63 had died) using the same methods. Strict definitions of EPS were used. The complete account of NL therapy the patients were prescribed between 1995 and 2003/04 (including atypical NL other than clozapine) was considered.

Results

The prevalences found in 1995 and 2003/04 were 17% and 29% for Parkinsonism, 14% and 14% for akathisia, and 24% and 13% for TD. There were considerable intra-individual fluctuations in EPS occurrence even when the overall prevalence rate remained the same. In intra-individual comparisons of EPS ratings on both assessments, there was a tendency for worsening of Parkinsonism to be associated with a current (2003/04) therapy with typical NL; worsening of akathisia was associated with a current therapy with atypical NL other than clozapine, amelioration of akathisia with a current therapy with clozapne; and, basically, there were no significant associations found between the changes in TD ratings and the long-term therapy with typical NL, clozapine, and other atypical NL, considering cumulative doses of all these drugs. In a multivariate analysis, there was a tendency for the long-term evolution of TD to depend on illness duration as the only variable.

Conclusions

There are intra-individual fluctuations in all EPS over longer time periods. The choice of current NL therapy has an impact on Parkinsonism and akathisia. The long-term evolution of TD appears independent of NL prescriptions.

University of Zurich, Department of Psychiatry (Burghölzli Hospital), Lenggstrasse 31, CH-8032 Zurich, Switzerland

Corresponding Author InformationCorresponding author. Tel.: +41 44 384 26 70; fax: +41 44 384 27 19.

PII: S0920-9964(07)00495-1

doi:10.1016/j.schres.2007.10.018


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