4.7 Article

Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders

Journal

PSYCHOLOGICAL MEDICINE
Volume 53, Issue 13, Pages 5986-5991

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291722003142

Keywords

schizophrenia; antipsychotic; subjective wellbeing; response; amisulpiride

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This study evaluated the variation in subjective response (SR) to a single antipsychotic medication in patients with a first episode of schizophrenia spectrum disorder. It found that there is substantial variation in individual proneness for an unfavorable SR, and the relationship between SR and symptomatic response is only modest. Factors such as baseline affective symptoms and lower start dosage of the medication were associated with subjective remission.
BackgroundSubjective response (SR) to antipsychotic medication is relevant for quality of life, adherence and recovery. Here, we evaluate (1) the extent of variation in SR in patients using a single antipsychotic; (2) the association between subjective and symptomatic response; and (3) predictors of SR. MethodsOpen-label, single treatment condition with amisulpride in 339 patients with a first episode of a schizophrenia spectrum disorder, at most minimally treated before inclusion. Patients were evaluated at baseline, before start with amisulpride and after four weeks of treatment with the Subjective Wellbeing under Neuroleptic scale, the Positive and Negative Syndrome Scale, and the Calgary Depression Scale for Schizophrenia. Results(1) 26.8% of the patients had a substantial favorable SR, and 12.4% of the patients experienced a substantial dysphoric SR during treatment with amisulpride. (2) Modest positive associations were found between SR and 4 weeks change on symptom subscales (r = 0.268-0.390, p values < 0.001). (3) Baseline affective symptoms contributed to the prediction of subjective remission, demographic characteristics did not. Lower start dosage of amisulpride was associated with a more favorable SR (r = -0.215, p < 0.001). ConclusionsWe conclude that variation in individual proneness for an unfavorable SR is substantial and only modestly associated with symptomatic response. We need earlier identification of those most at risk for unfavorable SR and research into interventions to improve SR to antipsychotic medication in those at risk.

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