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Prevalence of cognitive impairment in patients with substance use disorder

INTRODUCTION AND AIMS: Cognitive impairments in substance use disorder predict treatment outcome and are assumed to differ between substances. They often go undetected, thus the current study focuses on the prevalence of and differences in cognitive functioning across substances by means of a cognit...

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Autores principales: Bruijnen, Carolien J. W. H., Dijkstra, Boukje A. G., Walvoort, Serge J. W., Markus, Wiebren,  VanDerNagel, Joanne E. L., Kessels, Roy P. C., DE Jong, Cornelis A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593747/
https://www.ncbi.nlm.nih.gov/pubmed/30916448
http://dx.doi.org/10.1111/dar.12922
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author Bruijnen, Carolien J. W. H.
Dijkstra, Boukje A. G.
Walvoort, Serge J. W.
Markus, Wiebren
 VanDerNagel, Joanne E. L.
Kessels, Roy P. C.
DE Jong, Cornelis A. J.
author_facet Bruijnen, Carolien J. W. H.
Dijkstra, Boukje A. G.
Walvoort, Serge J. W.
Markus, Wiebren
 VanDerNagel, Joanne E. L.
Kessels, Roy P. C.
DE Jong, Cornelis A. J.
author_sort Bruijnen, Carolien J. W. H.
collection PubMed
description INTRODUCTION AND AIMS: Cognitive impairments in substance use disorder predict treatment outcome and are assumed to differ between substances. They often go undetected, thus the current study focuses on the prevalence of and differences in cognitive functioning across substances by means of a cognitive screen at the early stage of addiction treatment. DESIGN AND METHODS: The Montreal Cognitive Assessment was administered to outpatients seeking treatment for substance use disorder. Patient characteristics (age, years of regular use, polysubstance use, severity of dependence/abuse, depression, anxiety and stress) were also taken into account. RESULTS: A total of 656 patients were included (n = 391 used alcohol, n = 123 used cannabis, n = 100 used stimulants and n = 26 used opioids). The prevalence of cognitive impairments was 31%. Patients using alcohol had a lower total‐ and memory domain score than those using cannabis. Patients using opioids scored lower on visuospatial abilities than those using cannabis or stimulants. Younger patients scored higher than older patients. No effect was found for the other investigated characteristics. DISCUSSION AND CONCLUSIONS: Given the high prevalence of cognitive impairments, standard screening at an early stage of treatment is important to determine the course of treatment and maximise treatment outcome. Caution is needed in interpreting results about opioids due to an underrepresentation of this patient group, and more research is needed on the effect of age on Montreal Cognitive Assessment performance.
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spelling pubmed-65937472019-07-10 Prevalence of cognitive impairment in patients with substance use disorder Bruijnen, Carolien J. W. H. Dijkstra, Boukje A. G. Walvoort, Serge J. W. Markus, Wiebren  VanDerNagel, Joanne E. L. Kessels, Roy P. C. DE Jong, Cornelis A. J. Drug Alcohol Rev Original Papers INTRODUCTION AND AIMS: Cognitive impairments in substance use disorder predict treatment outcome and are assumed to differ between substances. They often go undetected, thus the current study focuses on the prevalence of and differences in cognitive functioning across substances by means of a cognitive screen at the early stage of addiction treatment. DESIGN AND METHODS: The Montreal Cognitive Assessment was administered to outpatients seeking treatment for substance use disorder. Patient characteristics (age, years of regular use, polysubstance use, severity of dependence/abuse, depression, anxiety and stress) were also taken into account. RESULTS: A total of 656 patients were included (n = 391 used alcohol, n = 123 used cannabis, n = 100 used stimulants and n = 26 used opioids). The prevalence of cognitive impairments was 31%. Patients using alcohol had a lower total‐ and memory domain score than those using cannabis. Patients using opioids scored lower on visuospatial abilities than those using cannabis or stimulants. Younger patients scored higher than older patients. No effect was found for the other investigated characteristics. DISCUSSION AND CONCLUSIONS: Given the high prevalence of cognitive impairments, standard screening at an early stage of treatment is important to determine the course of treatment and maximise treatment outcome. Caution is needed in interpreting results about opioids due to an underrepresentation of this patient group, and more research is needed on the effect of age on Montreal Cognitive Assessment performance. John Wiley & Sons Australia, Ltd 2019-03-27 2019-05 /pmc/articles/PMC6593747/ /pubmed/30916448 http://dx.doi.org/10.1111/dar.12922 Text en © 2019 The Authors Drug and Alcohol Review published by John Wiley & Sons Australia, Ltd on behalf of Australasian Professional Society on Alcohol and other Drugs This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Papers
Bruijnen, Carolien J. W. H.
Dijkstra, Boukje A. G.
Walvoort, Serge J. W.
Markus, Wiebren
 VanDerNagel, Joanne E. L.
Kessels, Roy P. C.
DE Jong, Cornelis A. J.
Prevalence of cognitive impairment in patients with substance use disorder
title Prevalence of cognitive impairment in patients with substance use disorder
title_full Prevalence of cognitive impairment in patients with substance use disorder
title_fullStr Prevalence of cognitive impairment in patients with substance use disorder
title_full_unstemmed Prevalence of cognitive impairment in patients with substance use disorder
title_short Prevalence of cognitive impairment in patients with substance use disorder
title_sort prevalence of cognitive impairment in patients with substance use disorder
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593747/
https://www.ncbi.nlm.nih.gov/pubmed/30916448
http://dx.doi.org/10.1111/dar.12922
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