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New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study

AIMS: To provide public health‐related research evidence on types and usage patterns of new psychoactive substances (NPS), developmental pathways into NPS and decision‐making factors for, and associated harms of, NPS use. DESIGN: Three‐phase mixed‐methods design, including a latent class analysis (L...

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Autores principales: Higgins, Kathryn, O'Neill, Nina, O'Hara, Leeanne, Jordan, Julie‐Ann, McCann, Mark, O'Neill, Tara, Clarke, Mike, O'Neill, Tony, Kelly, Grace, Campbell, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638670/
https://www.ncbi.nlm.nih.gov/pubmed/33506985
http://dx.doi.org/10.1111/add.15422
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author Higgins, Kathryn
O'Neill, Nina
O'Hara, Leeanne
Jordan, Julie‐Ann
McCann, Mark
O'Neill, Tara
Clarke, Mike
O'Neill, Tony
Kelly, Grace
Campbell, Anne
author_facet Higgins, Kathryn
O'Neill, Nina
O'Hara, Leeanne
Jordan, Julie‐Ann
McCann, Mark
O'Neill, Tara
Clarke, Mike
O'Neill, Tony
Kelly, Grace
Campbell, Anne
author_sort Higgins, Kathryn
collection PubMed
description AIMS: To provide public health‐related research evidence on types and usage patterns of new psychoactive substances (NPS), developmental pathways into NPS and decision‐making factors for, and associated harms of, NPS use. DESIGN: Three‐phase mixed‐methods design, including a latent class analysis (LCA) of the longitudinal Belfast Youth Development Study (BYDS), a narrative analysis of interviews with NPS users and a three‐step approach manual method modelling using regressions to reveal classes of substance use and their associated predictors and outcomes. SETTING: Northern Ireland. PARTICIPANTS: A total of 2039 people who responded to the questions on ‘ever use’ of the drug variables included at wave 7 (aged 21 years) of the BYDS. Eighty‐four narrative interviews with NPS users. MEASUREMENTS: Categories of drug use identified by LCA. Predictors and outcomes included measures of family, partners, peers, substance use, school, delinquency and mental health. FINDINGS: A four‐class solution provided the best fit for the data: alcohol; alcohol and tobacco; alcohol, tobacco and cannabis; and polydrug (the latter including NPS). The qualitative analysis yielded a taxonomy that distinguished how NPS operate within a wider range of drug repertoires from experimental to problematic. CONCLUSIONS: In Northern Ireland, new psychoactive substances appear to be a feature of broader polydrug use rather than a standalone class of drug use.
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spelling pubmed-86386702021-12-09 New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study Higgins, Kathryn O'Neill, Nina O'Hara, Leeanne Jordan, Julie‐Ann McCann, Mark O'Neill, Tara Clarke, Mike O'Neill, Tony Kelly, Grace Campbell, Anne Addiction Research Reports (Alcohol‐Drugs‐Solvents‐Gambling‐Nicotine) AIMS: To provide public health‐related research evidence on types and usage patterns of new psychoactive substances (NPS), developmental pathways into NPS and decision‐making factors for, and associated harms of, NPS use. DESIGN: Three‐phase mixed‐methods design, including a latent class analysis (LCA) of the longitudinal Belfast Youth Development Study (BYDS), a narrative analysis of interviews with NPS users and a three‐step approach manual method modelling using regressions to reveal classes of substance use and their associated predictors and outcomes. SETTING: Northern Ireland. PARTICIPANTS: A total of 2039 people who responded to the questions on ‘ever use’ of the drug variables included at wave 7 (aged 21 years) of the BYDS. Eighty‐four narrative interviews with NPS users. MEASUREMENTS: Categories of drug use identified by LCA. Predictors and outcomes included measures of family, partners, peers, substance use, school, delinquency and mental health. FINDINGS: A four‐class solution provided the best fit for the data: alcohol; alcohol and tobacco; alcohol, tobacco and cannabis; and polydrug (the latter including NPS). The qualitative analysis yielded a taxonomy that distinguished how NPS operate within a wider range of drug repertoires from experimental to problematic. CONCLUSIONS: In Northern Ireland, new psychoactive substances appear to be a feature of broader polydrug use rather than a standalone class of drug use. John Wiley and Sons Inc. 2021-01-28 2021-09 /pmc/articles/PMC8638670/ /pubmed/33506985 http://dx.doi.org/10.1111/add.15422 Text en © 2021 The Authors. Addiction published by John Wiley & Sons Ltd on behalf of Society for the Study of Addiction. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Reports (Alcohol‐Drugs‐Solvents‐Gambling‐Nicotine)
Higgins, Kathryn
O'Neill, Nina
O'Hara, Leeanne
Jordan, Julie‐Ann
McCann, Mark
O'Neill, Tara
Clarke, Mike
O'Neill, Tony
Kelly, Grace
Campbell, Anne
New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study
title New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study
title_full New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study
title_fullStr New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study
title_full_unstemmed New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study
title_short New psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study
title_sort new psychoactives within polydrug use trajectories—evidence from a mixed‐method longitudinal study
topic Research Reports (Alcohol‐Drugs‐Solvents‐Gambling‐Nicotine)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638670/
https://www.ncbi.nlm.nih.gov/pubmed/33506985
http://dx.doi.org/10.1111/add.15422
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