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Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study

OBJECTIVE: To compare the risk of mortality among people with opioid use disorder on and off opioid agonist treatment (OAT) in a setting with a high prevalence of illicitly manufactured fentanyl and other potent synthetic opioids in the illicit drug supply. DESIGN: Population based retrospective coh...

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Autores principales: Pearce, Lindsay A, Min, Jeong Eun, Piske, Micah, Zhou, Haoxuan, Homayra, Fahmida, Slaunwhite, Amanda, Irvine, Mike, McGowan, Gina, Nosyk, Bohdan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190018/
https://www.ncbi.nlm.nih.gov/pubmed/32234712
http://dx.doi.org/10.1136/bmj.m772
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author Pearce, Lindsay A
Min, Jeong Eun
Piske, Micah
Zhou, Haoxuan
Homayra, Fahmida
Slaunwhite, Amanda
Irvine, Mike
McGowan, Gina
Nosyk, Bohdan
author_facet Pearce, Lindsay A
Min, Jeong Eun
Piske, Micah
Zhou, Haoxuan
Homayra, Fahmida
Slaunwhite, Amanda
Irvine, Mike
McGowan, Gina
Nosyk, Bohdan
author_sort Pearce, Lindsay A
collection PubMed
description OBJECTIVE: To compare the risk of mortality among people with opioid use disorder on and off opioid agonist treatment (OAT) in a setting with a high prevalence of illicitly manufactured fentanyl and other potent synthetic opioids in the illicit drug supply. DESIGN: Population based retrospective cohort study. SETTING: Individual level linkage of five health administrative datasets capturing drug dispensations, hospital admissions, physician billing records, ambulatory care reports, and deaths in British Columbia, Canada. PARTICIPANTS: 55 347 people with opioid use disorder who received OAT between 1 January 1996 and 30 September 2018. MAIN OUTCOME MEASURES: All cause and cause specific crude mortality rates (per 1000 person years) to determine absolute risk of mortality and all cause age and sex standardised mortality ratios to determine relative risk of mortality compared with the general population. Mortality risk was calculated according to treatment status (on OAT, off OAT), time since starting and stopping treatment (1, 2, 3-4, 5-12, >12 weeks), and medication type (methadone, buprenorphine/naloxone). Adjusted risk ratios compared the relative risk of mortality on and off OAT over time as fentanyl became more prevalent in the illicit drug supply. RESULTS: 7030 (12.7%) of 55 347 OAT recipients died during follow-up. The all cause standardised mortality ratio was substantially lower on OAT (4.6, 95% confidence interval 4.4 to 4.8) than off OAT (9.7, 9.5 to 10.0). In a period of increasing prevalence of fentanyl, the relative risk of mortality off OAT was 2.1 (95% confidence interval 1.8 to 2.4) times higher than on OAT before the introduction of fentanyl, increasing to 3.4 (2.8 to 4.3) at the end of the study period (65% increase in relative risk). CONCLUSIONS: Retention on OAT is associated with substantial reductions in the risk of mortality for people with opioid use disorder. The protective effect of OAT on mortality increased as fentanyl and other synthetic opioids became common in the illicit drug supply, whereas the risk of mortality remained high off OAT. As fentanyl becomes more widespread globally, these findings highlight the importance of interventions that improve retention on opioid agonist treatment and prevent recipients from stopping treatment.
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spelling pubmed-71900182020-05-01 Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study Pearce, Lindsay A Min, Jeong Eun Piske, Micah Zhou, Haoxuan Homayra, Fahmida Slaunwhite, Amanda Irvine, Mike McGowan, Gina Nosyk, Bohdan BMJ Research OBJECTIVE: To compare the risk of mortality among people with opioid use disorder on and off opioid agonist treatment (OAT) in a setting with a high prevalence of illicitly manufactured fentanyl and other potent synthetic opioids in the illicit drug supply. DESIGN: Population based retrospective cohort study. SETTING: Individual level linkage of five health administrative datasets capturing drug dispensations, hospital admissions, physician billing records, ambulatory care reports, and deaths in British Columbia, Canada. PARTICIPANTS: 55 347 people with opioid use disorder who received OAT between 1 January 1996 and 30 September 2018. MAIN OUTCOME MEASURES: All cause and cause specific crude mortality rates (per 1000 person years) to determine absolute risk of mortality and all cause age and sex standardised mortality ratios to determine relative risk of mortality compared with the general population. Mortality risk was calculated according to treatment status (on OAT, off OAT), time since starting and stopping treatment (1, 2, 3-4, 5-12, >12 weeks), and medication type (methadone, buprenorphine/naloxone). Adjusted risk ratios compared the relative risk of mortality on and off OAT over time as fentanyl became more prevalent in the illicit drug supply. RESULTS: 7030 (12.7%) of 55 347 OAT recipients died during follow-up. The all cause standardised mortality ratio was substantially lower on OAT (4.6, 95% confidence interval 4.4 to 4.8) than off OAT (9.7, 9.5 to 10.0). In a period of increasing prevalence of fentanyl, the relative risk of mortality off OAT was 2.1 (95% confidence interval 1.8 to 2.4) times higher than on OAT before the introduction of fentanyl, increasing to 3.4 (2.8 to 4.3) at the end of the study period (65% increase in relative risk). CONCLUSIONS: Retention on OAT is associated with substantial reductions in the risk of mortality for people with opioid use disorder. The protective effect of OAT on mortality increased as fentanyl and other synthetic opioids became common in the illicit drug supply, whereas the risk of mortality remained high off OAT. As fentanyl becomes more widespread globally, these findings highlight the importance of interventions that improve retention on opioid agonist treatment and prevent recipients from stopping treatment. BMJ Publishing Group Ltd. 2020-03-31 /pmc/articles/PMC7190018/ /pubmed/32234712 http://dx.doi.org/10.1136/bmj.m772 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Pearce, Lindsay A
Min, Jeong Eun
Piske, Micah
Zhou, Haoxuan
Homayra, Fahmida
Slaunwhite, Amanda
Irvine, Mike
McGowan, Gina
Nosyk, Bohdan
Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study
title Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study
title_full Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study
title_fullStr Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study
title_full_unstemmed Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study
title_short Opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study
title_sort opioid agonist treatment and risk of mortality during opioid overdose public health emergency: population based retrospective cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190018/
https://www.ncbi.nlm.nih.gov/pubmed/32234712
http://dx.doi.org/10.1136/bmj.m772
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