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Clinical correlates of early onset antipsychotic treatment resistance
BACKGROUND: There is evidence of heterogeneity within treatment-resistant schizophrenia (TRS), with some people not responding to antipsychotic treatment from illness onset and others becoming treatment-resistant after an initial response period. These groups may have different aetiologies. AIM: Thi...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643817/ https://www.ncbi.nlm.nih.gov/pubmed/36268751 http://dx.doi.org/10.1177/02698811221132537 |
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author | Fonseca de Freitas, Daniela Agbedjro, Deborah Kadra-Scalzo, Giouliana Francis, Emma Ridler, Isobel Pritchard, Megan Shetty, Hitesh Segev, Aviv Casetta, Cecilia Smart, Sophie E. Morris, Anna Downs, Johnny Christensen, Søren Rahn Bak, Nikolaj Kinon, Bruce J. Stahl, Daniel Hayes, Richard D. MacCabe, James H. |
author_facet | Fonseca de Freitas, Daniela Agbedjro, Deborah Kadra-Scalzo, Giouliana Francis, Emma Ridler, Isobel Pritchard, Megan Shetty, Hitesh Segev, Aviv Casetta, Cecilia Smart, Sophie E. Morris, Anna Downs, Johnny Christensen, Søren Rahn Bak, Nikolaj Kinon, Bruce J. Stahl, Daniel Hayes, Richard D. MacCabe, James H. |
author_sort | Fonseca de Freitas, Daniela |
collection | PubMed |
description | BACKGROUND: There is evidence of heterogeneity within treatment-resistant schizophrenia (TRS), with some people not responding to antipsychotic treatment from illness onset and others becoming treatment-resistant after an initial response period. These groups may have different aetiologies. AIM: This study investigates sociodemographic and clinical correlates of early onset of TRS. METHOD: Employing a retrospective cohort design, we do a secondary analysis of data from a cohort of people with TRS attending the South London and Maudsley. Regression analyses were conducted to identify the correlates of the length of treatment to TRS. Predictors included the following: gender, age, ethnicity, problems with positive symptoms, problems with activities of daily living, psychiatric comorbidities, involuntary hospitalisation and treatment with long-acting injectable antipsychotics. RESULTS: In a cohort of 164 people with TRS (60% were men), the median length of treatment to TRS was 3 years and 8 months. We observed no cut-off on the length of treatment until TRS presentation differentiating between early and late TRS (i.e. no bimodal distribution). Having mild to very severe problems with hallucinations and delusions at the treatment start was associated with earlier TRS (~19 months earlier). In sensitivity analyses, including only complete cases (subject to selection bias), treatment with a long-acting injectable antipsychotic was additionally associated with later TRS (~15 months later). CONCLUSION: Our findings do not support a clear separation between early and late TRS but rather a continuum of the length of treatment before TRS onset. Having mild to very severe problems with positive symptoms at treatment start predicts earlier onset of TRS. |
format | Online Article Text |
id | pubmed-9643817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-96438172022-11-15 Clinical correlates of early onset antipsychotic treatment resistance Fonseca de Freitas, Daniela Agbedjro, Deborah Kadra-Scalzo, Giouliana Francis, Emma Ridler, Isobel Pritchard, Megan Shetty, Hitesh Segev, Aviv Casetta, Cecilia Smart, Sophie E. Morris, Anna Downs, Johnny Christensen, Søren Rahn Bak, Nikolaj Kinon, Bruce J. Stahl, Daniel Hayes, Richard D. MacCabe, James H. J Psychopharmacol Original Papers BACKGROUND: There is evidence of heterogeneity within treatment-resistant schizophrenia (TRS), with some people not responding to antipsychotic treatment from illness onset and others becoming treatment-resistant after an initial response period. These groups may have different aetiologies. AIM: This study investigates sociodemographic and clinical correlates of early onset of TRS. METHOD: Employing a retrospective cohort design, we do a secondary analysis of data from a cohort of people with TRS attending the South London and Maudsley. Regression analyses were conducted to identify the correlates of the length of treatment to TRS. Predictors included the following: gender, age, ethnicity, problems with positive symptoms, problems with activities of daily living, psychiatric comorbidities, involuntary hospitalisation and treatment with long-acting injectable antipsychotics. RESULTS: In a cohort of 164 people with TRS (60% were men), the median length of treatment to TRS was 3 years and 8 months. We observed no cut-off on the length of treatment until TRS presentation differentiating between early and late TRS (i.e. no bimodal distribution). Having mild to very severe problems with hallucinations and delusions at the treatment start was associated with earlier TRS (~19 months earlier). In sensitivity analyses, including only complete cases (subject to selection bias), treatment with a long-acting injectable antipsychotic was additionally associated with later TRS (~15 months later). CONCLUSION: Our findings do not support a clear separation between early and late TRS but rather a continuum of the length of treatment before TRS onset. Having mild to very severe problems with positive symptoms at treatment start predicts earlier onset of TRS. SAGE Publications 2022-10-21 2022-11 /pmc/articles/PMC9643817/ /pubmed/36268751 http://dx.doi.org/10.1177/02698811221132537 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Papers Fonseca de Freitas, Daniela Agbedjro, Deborah Kadra-Scalzo, Giouliana Francis, Emma Ridler, Isobel Pritchard, Megan Shetty, Hitesh Segev, Aviv Casetta, Cecilia Smart, Sophie E. Morris, Anna Downs, Johnny Christensen, Søren Rahn Bak, Nikolaj Kinon, Bruce J. Stahl, Daniel Hayes, Richard D. MacCabe, James H. Clinical correlates of early onset antipsychotic treatment resistance |
title | Clinical correlates of early onset antipsychotic treatment
resistance |
title_full | Clinical correlates of early onset antipsychotic treatment
resistance |
title_fullStr | Clinical correlates of early onset antipsychotic treatment
resistance |
title_full_unstemmed | Clinical correlates of early onset antipsychotic treatment
resistance |
title_short | Clinical correlates of early onset antipsychotic treatment
resistance |
title_sort | clinical correlates of early onset antipsychotic treatment
resistance |
topic | Original Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643817/ https://www.ncbi.nlm.nih.gov/pubmed/36268751 http://dx.doi.org/10.1177/02698811221132537 |
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