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Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study

BACKGROUND: Opioid prescribing has more than doubled in the UK between 1998 and 2016. Potential adverse health implications include dependency, falls and increased health expenditure. AIM: To describe the predictors of long‐term opioid prescribing (LTOP) (≥3 opioid prescriptions in a 90‐day period)....

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Autores principales: Naughton, Michael, Redmond, Patrick, Durbaba, Stevo, Ashworth, Mark, Molokhia, Mariam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305420/
https://www.ncbi.nlm.nih.gov/pubmed/35018644
http://dx.doi.org/10.1111/bcp.15231
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author Naughton, Michael
Redmond, Patrick
Durbaba, Stevo
Ashworth, Mark
Molokhia, Mariam
author_facet Naughton, Michael
Redmond, Patrick
Durbaba, Stevo
Ashworth, Mark
Molokhia, Mariam
author_sort Naughton, Michael
collection PubMed
description BACKGROUND: Opioid prescribing has more than doubled in the UK between 1998 and 2016. Potential adverse health implications include dependency, falls and increased health expenditure. AIM: To describe the predictors of long‐term opioid prescribing (LTOP) (≥3 opioid prescriptions in a 90‐day period). DESIGN AND SETTING: A retrospective cross‐sectional study in 41 general practices in South London. METHOD: Multi‐level multivariable logistic regression to investigate the determinants of LTOP. RESULTS: Out of 320 639 registered patients ≥18 years, 2679 (0.8%) were identified as having LTOP. Patients were most likely to have LTOP if they had ≥5 long‐term conditions (LTCs) (adjusted odds ratio [AOR] 36.5, 95% confidence interval [CI] 30.4‐43.8) or 2‐4 LTCs (AOR 13.8, CI 11.9‐16.1) in comparison to no LTCs, were ≥75 years compared to 18‐24 years (AOR 12.31, CI 7.1‐21.5), were smokers compared to nonsmokers (AOR 2.2, CI 2.0‐2.5), were female rather than male (AOR 1.9, CI 1.7‐2.0) and in the most deprived deprivation quintile (AOR 1.6, CI 1.4‐1.8) compared to the least deprived. In a separate model examining individual LTCs, the strongest associations for LTOP were noted for sickle cell disease (SCD) (AOR 18.4, CI 12.8‐26.4), osteoarthritis (AOR 3.0, CI 2.8‐3.3), rheumatoid arthritis (AOR 2.8, CI 2.2‐3.4), depression (AOR 2.6, CI 2.3‐2.8) and multiple sclerosis (OR 2.5, CI 1.4‐4.4). CONCLUSION: LTOP was significantly higher in those aged ≥75 years, with multimorbidity or specific LTCs: SCD, osteoarthritis, rheumatoid arthritis, depression and multiple sclerosis. These characteristics may enable the design of targeted interventions to reduce LTOP.
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spelling pubmed-93054202022-07-28 Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study Naughton, Michael Redmond, Patrick Durbaba, Stevo Ashworth, Mark Molokhia, Mariam Br J Clin Pharmacol Original Articles BACKGROUND: Opioid prescribing has more than doubled in the UK between 1998 and 2016. Potential adverse health implications include dependency, falls and increased health expenditure. AIM: To describe the predictors of long‐term opioid prescribing (LTOP) (≥3 opioid prescriptions in a 90‐day period). DESIGN AND SETTING: A retrospective cross‐sectional study in 41 general practices in South London. METHOD: Multi‐level multivariable logistic regression to investigate the determinants of LTOP. RESULTS: Out of 320 639 registered patients ≥18 years, 2679 (0.8%) were identified as having LTOP. Patients were most likely to have LTOP if they had ≥5 long‐term conditions (LTCs) (adjusted odds ratio [AOR] 36.5, 95% confidence interval [CI] 30.4‐43.8) or 2‐4 LTCs (AOR 13.8, CI 11.9‐16.1) in comparison to no LTCs, were ≥75 years compared to 18‐24 years (AOR 12.31, CI 7.1‐21.5), were smokers compared to nonsmokers (AOR 2.2, CI 2.0‐2.5), were female rather than male (AOR 1.9, CI 1.7‐2.0) and in the most deprived deprivation quintile (AOR 1.6, CI 1.4‐1.8) compared to the least deprived. In a separate model examining individual LTCs, the strongest associations for LTOP were noted for sickle cell disease (SCD) (AOR 18.4, CI 12.8‐26.4), osteoarthritis (AOR 3.0, CI 2.8‐3.3), rheumatoid arthritis (AOR 2.8, CI 2.2‐3.4), depression (AOR 2.6, CI 2.3‐2.8) and multiple sclerosis (OR 2.5, CI 1.4‐4.4). CONCLUSION: LTOP was significantly higher in those aged ≥75 years, with multimorbidity or specific LTCs: SCD, osteoarthritis, rheumatoid arthritis, depression and multiple sclerosis. These characteristics may enable the design of targeted interventions to reduce LTOP. John Wiley and Sons Inc. 2022-02-07 2022-07 /pmc/articles/PMC9305420/ /pubmed/35018644 http://dx.doi.org/10.1111/bcp.15231 Text en © 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Naughton, Michael
Redmond, Patrick
Durbaba, Stevo
Ashworth, Mark
Molokhia, Mariam
Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study
title Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study
title_full Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study
title_fullStr Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study
title_full_unstemmed Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study
title_short Determinants of long‐term opioid prescribing in an urban population: A cross‐sectional study
title_sort determinants of long‐term opioid prescribing in an urban population: a cross‐sectional study
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305420/
https://www.ncbi.nlm.nih.gov/pubmed/35018644
http://dx.doi.org/10.1111/bcp.15231
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