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Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health

BACKGROUND: Over the past decade, antidepressant prescriptions have increased in European countries and the United States, partly due to an increase in the number of new cases of mental illness. This paper demonstrates an innovative approach to the classification of population level change in mental...

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Autores principales: Cherrie, Mark, Curtis, Sarah, Baranyi, Gergő, McTaggart, Stuart, Cunningham, Niall, Licence, Kirsty, Dibben, Chris, Bambra, Clare, Pearce, Jamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684902/
https://www.ncbi.nlm.nih.gov/pubmed/33228576
http://dx.doi.org/10.1186/s12888-020-02952-y
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author Cherrie, Mark
Curtis, Sarah
Baranyi, Gergő
McTaggart, Stuart
Cunningham, Niall
Licence, Kirsty
Dibben, Chris
Bambra, Clare
Pearce, Jamie
author_facet Cherrie, Mark
Curtis, Sarah
Baranyi, Gergő
McTaggart, Stuart
Cunningham, Niall
Licence, Kirsty
Dibben, Chris
Bambra, Clare
Pearce, Jamie
author_sort Cherrie, Mark
collection PubMed
description BACKGROUND: Over the past decade, antidepressant prescriptions have increased in European countries and the United States, partly due to an increase in the number of new cases of mental illness. This paper demonstrates an innovative approach to the classification of population level change in mental health status, using administrative data for a large sample of the Scottish population. We aimed to identify groups of individuals with similar patterns of change in pattern of prescribing, validate these groups by comparison with other indicators of mental illness, and characterise the population most at risk of increasing mental ill health. METHODS: National Health Service (NHS) prescription data were linked to the Scottish Longitudinal Study (SLS), a 5.3% sample of the Scottish population (N = 151,418). Antidepressant prescription status over the previous 6 months was recorded for every month for which data were available (January 2009–December 2014), and sequence dissimilarity was computed by optimal matching. Hierarchical clustering was used to create groups of participants who had similar patterns of change, with multi-level logistic regression used to understand group membership. RESULTS: Five distinct prescription pattern groups were observed, indicating: no prescriptions (76%), occasional prescriptions (10%), continuation of prior use of prescriptions (8%), a new course of prescriptions started (4%) or ceased taking prescriptions (3%). Young, white, female participants, of low social grade, residing in socially deprived neighbourhoods, living alone, being separated/divorced or out of the labour force, were more likely to be in the group that started a new course of antidepressant prescriptions. CONCLUSIONS: The use of sequence analysis for classifying individual antidepressant trajectories offers a novel approach for capturing population-level changes in mental health risk. By classifying individuals into groups based on their anti-depressant medication use we can better identify how over time, mental health is associated with individual risk factors and contextual factors at the local level and the macro political and economic scale.
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spelling pubmed-76849022020-11-25 Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health Cherrie, Mark Curtis, Sarah Baranyi, Gergő McTaggart, Stuart Cunningham, Niall Licence, Kirsty Dibben, Chris Bambra, Clare Pearce, Jamie BMC Psychiatry Research Article BACKGROUND: Over the past decade, antidepressant prescriptions have increased in European countries and the United States, partly due to an increase in the number of new cases of mental illness. This paper demonstrates an innovative approach to the classification of population level change in mental health status, using administrative data for a large sample of the Scottish population. We aimed to identify groups of individuals with similar patterns of change in pattern of prescribing, validate these groups by comparison with other indicators of mental illness, and characterise the population most at risk of increasing mental ill health. METHODS: National Health Service (NHS) prescription data were linked to the Scottish Longitudinal Study (SLS), a 5.3% sample of the Scottish population (N = 151,418). Antidepressant prescription status over the previous 6 months was recorded for every month for which data were available (January 2009–December 2014), and sequence dissimilarity was computed by optimal matching. Hierarchical clustering was used to create groups of participants who had similar patterns of change, with multi-level logistic regression used to understand group membership. RESULTS: Five distinct prescription pattern groups were observed, indicating: no prescriptions (76%), occasional prescriptions (10%), continuation of prior use of prescriptions (8%), a new course of prescriptions started (4%) or ceased taking prescriptions (3%). Young, white, female participants, of low social grade, residing in socially deprived neighbourhoods, living alone, being separated/divorced or out of the labour force, were more likely to be in the group that started a new course of antidepressant prescriptions. CONCLUSIONS: The use of sequence analysis for classifying individual antidepressant trajectories offers a novel approach for capturing population-level changes in mental health risk. By classifying individuals into groups based on their anti-depressant medication use we can better identify how over time, mental health is associated with individual risk factors and contextual factors at the local level and the macro political and economic scale. BioMed Central 2020-11-23 /pmc/articles/PMC7684902/ /pubmed/33228576 http://dx.doi.org/10.1186/s12888-020-02952-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Cherrie, Mark
Curtis, Sarah
Baranyi, Gergő
McTaggart, Stuart
Cunningham, Niall
Licence, Kirsty
Dibben, Chris
Bambra, Clare
Pearce, Jamie
Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health
title Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health
title_full Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health
title_fullStr Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health
title_full_unstemmed Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health
title_short Use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health
title_sort use of sequence analysis for classifying individual antidepressant trajectories to monitor population mental health
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7684902/
https://www.ncbi.nlm.nih.gov/pubmed/33228576
http://dx.doi.org/10.1186/s12888-020-02952-y
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