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

BACKGROUND: Subjective 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...

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Autores principales: de Haan, Lieuwe, van Tricht, Mirjam, van Dijk, Floor, Arango, Celso, Díaz-Caneja, Covadonga M., Bobes, Julio, García-Álvarez, Leticia, Leucht, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520587/
https://www.ncbi.nlm.nih.gov/pubmed/36520136
http://dx.doi.org/10.1017/S0033291722003142
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author de Haan, Lieuwe
van Tricht, Mirjam
van Dijk, Floor
Arango, Celso
Díaz-Caneja, Covadonga M.
Bobes, Julio
García-Álvarez, Leticia
Leucht, Stefan
author_facet de Haan, Lieuwe
van Tricht, Mirjam
van Dijk, Floor
Arango, Celso
Díaz-Caneja, Covadonga M.
Bobes, Julio
García-Álvarez, Leticia
Leucht, Stefan
author_sort de Haan, Lieuwe
collection PubMed
description BACKGROUND: Subjective 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. METHODS: Open-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). CONCLUSIONS: We 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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spelling pubmed-105205872023-09-27 Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders de Haan, Lieuwe van Tricht, Mirjam van Dijk, Floor Arango, Celso Díaz-Caneja, Covadonga M. Bobes, Julio García-Álvarez, Leticia Leucht, Stefan Psychol Med Original Article BACKGROUND: Subjective 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. METHODS: Open-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). CONCLUSIONS: We 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. Cambridge University Press 2023-10 2022-12-15 /pmc/articles/PMC10520587/ /pubmed/36520136 http://dx.doi.org/10.1017/S0033291722003142 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
spellingShingle Original Article
de Haan, Lieuwe
van Tricht, Mirjam
van Dijk, Floor
Arango, Celso
Díaz-Caneja, Covadonga M.
Bobes, Julio
García-Álvarez, Leticia
Leucht, Stefan
Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders
title Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders
title_full Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders
title_fullStr Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders
title_full_unstemmed Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders
title_short Optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders
title_sort optimizing subjective wellbeing with amisulpride in first episode schizophrenia or related disorders
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10520587/
https://www.ncbi.nlm.nih.gov/pubmed/36520136
http://dx.doi.org/10.1017/S0033291722003142
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