Clinical correlates of early onset antipsychotic treatment resistance

<strong>Background:<br></strong> 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 m...

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Main Authors: Fonseca de Freitas, D, Agbedjro, D, Kadra-Scalzo, G, Francis, E, Ridler, I, Pritchard, M, Shetty, H, Segev, A, Casetta, C, Smart, S, Morris, A, Downs, J, Christensen, S, Bak, N, Kinon, B, Stahl, D, Hayes, R, MacCabe, J
Format: Journal article
Language:English
Published: SAGE Publications 2022
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author Fonseca de Freitas, D
Agbedjro, D
Kadra-Scalzo, G
Francis, E
Ridler, I
Pritchard, M
Shetty, H
Segev, A
Casetta, C
Smart, S
Morris, A
Downs, J
Christensen, S
Bak, N
Kinon, B
Stahl, D
Hayes, R
MacCabe, J
author_facet Fonseca de Freitas, D
Agbedjro, D
Kadra-Scalzo, G
Francis, E
Ridler, I
Pritchard, M
Shetty, H
Segev, A
Casetta, C
Smart, S
Morris, A
Downs, J
Christensen, S
Bak, N
Kinon, B
Stahl, D
Hayes, R
MacCabe, J
author_sort Fonseca de Freitas, D
collection OXFORD
description <strong>Background:<br></strong> 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. <br><strong>Aim:<br></strong> This study investigates sociodemographic and clinical correlates of early onset of TRS. <br><strong>Method:<br></strong> 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. <br><strong>Results:<br></strong> 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). <br><strong>Conclusion:<br></strong> 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.
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spelling oxford-uuid:8a12825f-b708-47eb-8978-32288978c0dc2022-11-29T09:38:02ZClinical correlates of early onset antipsychotic treatment resistanceJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:8a12825f-b708-47eb-8978-32288978c0dcEnglishSymplectic ElementsSAGE Publications2022Fonseca de Freitas, DAgbedjro, DKadra-Scalzo, GFrancis, ERidler, IPritchard, MShetty, HSegev, ACasetta, CSmart, SMorris, ADowns, JChristensen, SBak, NKinon, BStahl, DHayes, RMacCabe, J<strong>Background:<br></strong> 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. <br><strong>Aim:<br></strong> This study investigates sociodemographic and clinical correlates of early onset of TRS. <br><strong>Method:<br></strong> 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. <br><strong>Results:<br></strong> 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). <br><strong>Conclusion:<br></strong> 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.
spellingShingle Fonseca de Freitas, D
Agbedjro, D
Kadra-Scalzo, G
Francis, E
Ridler, I
Pritchard, M
Shetty, H
Segev, A
Casetta, C
Smart, S
Morris, A
Downs, J
Christensen, S
Bak, N
Kinon, B
Stahl, D
Hayes, R
MacCabe, J
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
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