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Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy

Purpose: This study evaluated the risk of opioid dose escalation as it relates to sex differences among patients receiving opioids for long-term therapy. Patients and methods: This retrospective cohort study was conducted in tertiary hospital settings in Malaysia using electronic prescription record...

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Autores principales: Zin, Che Suraya, Alias, Nor Elina, Taufek, Nor Hidayah, Ahmad, Mazlila Meor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499483/
https://www.ncbi.nlm.nih.gov/pubmed/31118748
http://dx.doi.org/10.2147/JPR.S199243
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author Zin, Che Suraya
Alias, Nor Elina
Taufek, Nor Hidayah
Ahmad, Mazlila Meor
author_facet Zin, Che Suraya
Alias, Nor Elina
Taufek, Nor Hidayah
Ahmad, Mazlila Meor
author_sort Zin, Che Suraya
collection PubMed
description Purpose: This study evaluated the risk of opioid dose escalation as it relates to sex differences among patients receiving opioids for long-term therapy. Patients and methods: This retrospective cohort study was conducted in tertiary hospital settings in Malaysia using electronic prescription records. Opioid naïve patients, aged ≥18 years, who were undergoing long-term opioid therapy of ≥90 days, with at least one opioid prescription (buprenorphine, morphine, oxycodone, fentanyl, dihydrocodeine or tramadol) between 1st January 2011 and 31st December 2016, were included in the study. They were followed until (i) the end of the study period, (ii) death from any cause or (iii) discontinuation of therapy from their first opioid prescription without any intervals of ≥120 days between successive prescriptions. The risk of high opioid dose escalation to ≥100 mg/day and ≥200 mg/day relative to men and women was measured. Results: A total of 4688 patients (58.8% women, 41.3% men) on long-term opioid therapy were identified. Among these patients, 248 (5.29%) were escalated to high opioid doses of ≥100 mg/day and 69 (1.47%) were escalated to ≥200 mg/day. The escalation to high-dose opioid therapy was more likely to occur in men than in women, even after adjustment for age (dose ≥100 mg/day [adjusted hazard ratio 2.32; 95% confidence interval (CI), 1.79 to 3.00; p<0.0001] and ≥200 mg/day [adjusted hazard ratio 6.10; 95% CI, 3.39 to 10.98; p<0.0001]). Conclusion: The risk of opioid dose escalation differed between men and women, as men were at higher risk than women for high opioid dose escalation.
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spelling pubmed-64994832019-05-22 Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy Zin, Che Suraya Alias, Nor Elina Taufek, Nor Hidayah Ahmad, Mazlila Meor J Pain Res Original Research Purpose: This study evaluated the risk of opioid dose escalation as it relates to sex differences among patients receiving opioids for long-term therapy. Patients and methods: This retrospective cohort study was conducted in tertiary hospital settings in Malaysia using electronic prescription records. Opioid naïve patients, aged ≥18 years, who were undergoing long-term opioid therapy of ≥90 days, with at least one opioid prescription (buprenorphine, morphine, oxycodone, fentanyl, dihydrocodeine or tramadol) between 1st January 2011 and 31st December 2016, were included in the study. They were followed until (i) the end of the study period, (ii) death from any cause or (iii) discontinuation of therapy from their first opioid prescription without any intervals of ≥120 days between successive prescriptions. The risk of high opioid dose escalation to ≥100 mg/day and ≥200 mg/day relative to men and women was measured. Results: A total of 4688 patients (58.8% women, 41.3% men) on long-term opioid therapy were identified. Among these patients, 248 (5.29%) were escalated to high opioid doses of ≥100 mg/day and 69 (1.47%) were escalated to ≥200 mg/day. The escalation to high-dose opioid therapy was more likely to occur in men than in women, even after adjustment for age (dose ≥100 mg/day [adjusted hazard ratio 2.32; 95% confidence interval (CI), 1.79 to 3.00; p<0.0001] and ≥200 mg/day [adjusted hazard ratio 6.10; 95% CI, 3.39 to 10.98; p<0.0001]). Conclusion: The risk of opioid dose escalation differed between men and women, as men were at higher risk than women for high opioid dose escalation. Dove 2019-04-24 /pmc/articles/PMC6499483/ /pubmed/31118748 http://dx.doi.org/10.2147/JPR.S199243 Text en © 2019 Zin et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Zin, Che Suraya
Alias, Nor Elina
Taufek, Nor Hidayah
Ahmad, Mazlila Meor
Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy
title Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy
title_full Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy
title_fullStr Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy
title_full_unstemmed Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy
title_short Sex differences in high opioid dose escalation among Malaysian patients with long term opioid therapy
title_sort sex differences in high opioid dose escalation among malaysian patients with long term opioid therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6499483/
https://www.ncbi.nlm.nih.gov/pubmed/31118748
http://dx.doi.org/10.2147/JPR.S199243
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