Medication for Opioid Use Disorder After Nonfatal Opioid Overdose and Association With Mortality A Cohort Study

被引:797
作者
Larochelle, Marc R. [1 ,2 ]
Bernson, Dana [3 ,8 ]
Land, Thomas [3 ,8 ]
Stopka, Thomas J. [4 ]
Wang, Na [5 ,9 ]
Xuan, Ziming [5 ,9 ]
Bagley, Sarah M. [1 ,2 ]
Liebschutz, Jane M. [1 ,2 ,6 ]
Walley, Alexander Y. [1 ,2 ,7 ]
机构
[1] Boston Univ, Clin Addict Res & Educ Unit, Sch Med, Boston, MA 02215 USA
[2] Boston Med Ctr, 801 Massachusetts Ave,2nd Floor, Boston, MA 02118 USA
[3] Massachusetts Dept Publ Hlth, Off Special Analyt Projects, Off Populat Hlth, Boston, MA USA
[4] Tufts Univ, Sch Med, 136 Harrison Ave,MV244, Boston, MA 02111 USA
[5] Boston Univ, Sch Publ Hlth, Biostat & Epidemiol Data Analyt Ctr, Boston, MA USA
[6] Univ Pittsburgh, Sch Med, Ctr Res Hlth Care, 200 Lothrop St,Suite 933W, Pittsburgh, PA 15213 USA
[7] Massachusetts Dept Publ Hlth, Bur Subst Addict Serv, Boston, MA USA
[8] Massachusetts Dept Publ Hlth, 250 Washington St,6th Floor, Boston, MA 02108 USA
[9] Boston Univ, Sch Publ Hlth, 801 Massachusetts Ave,3rd Floor, Boston, MA 02118 USA
基金
美国国家卫生研究院;
关键词
EXTENDED-RELEASE NALTREXONE; ORAL NALTREXONE; HEROIN OVERDOSE; FATAL OVERDOSE; DRUG-TREATMENT; UNITED-STATES; DEPENDENCE; BUPRENORPHINE; IMPLANT; RELAPSE;
D O I
10.7326/M17-3107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Opioid overdose survivors have an increased risk for death. Whether use of medications for opioid use disorder (MOUD) after overdose is associated with mortality is not known. Objective: To identify MOUD use after opioid overdose and its association with all-cause and opioid-related mortality. Design: Retrospective cohort study. Setting: 7 individually linked data sets from Massachusetts government agencies. Participants: 17 568 Massachusetts adults without cancer who survived an opioid overdose between 2012 and 2014. Measurements: Three types of MOUD were examined: methadone maintenance treatment (MMT), buprenorphine, and naltrexone. Exposure to MOUD was identified at monthly intervals, and persons were considered exposed through the month after last receipt. A multivariable Cox proportional hazards model was used to examine MOUD as a monthly time-varying exposure variable to predict time to all-cause and opioid-related mortality. Results: In the 12 months after a nonfatal overdose, 2040 persons (11%) enrolled in MMT for a median of 5 months (interquartile range, 2 to 9 months), 3022 persons (17%) received buprenorphine for a median of 4 months (interquartile range, 2 to 8 months), and 1099 persons (6%) received naltrexone for a me dian of 1 month (interquartile range, 1 to 2 months). Among the entire cohort, all-cause mortality was 4.7 deaths (95% CI, 4.4 to 5.0 deaths) per 100 person years and opioid related mortality was 2.1 deaths (CI, 1.9 to 2.4 deaths) per 100 person-years. Compared with no MOUD, MMT was associated with decreased all-cause mortality (adjusted hazard ratio [AHR], 0.47 [CI, 0.32 to 0.71]) and opioid-related mortality (AHR, 0.41 [CI, 0.24 to 0.70]). Buprenorphine was associated with decreased all-cause mortality (AHR, 0.63 [CI, 0.46 to 0.87]) and opioid-related mortality (AHR, 0.62 [CI, 0.41 to 0.92]). No associations between naltrexone and all-cause mortality (AHR, 1.44 [CI, 0.84 to 2.46]) or opioid-related mortality (AHR, 1.42 [CI, 0.73 to 2.79]) were identified. Limitation: Few events among naltrexone recipients preclude confident conclusions. Conclusion: A minority of opioid overdose survivors received MOUD. Buprenorphine and MMT were associated with reduced all-cause and opioid-related mortality. Primary Funding Source: National Center for Advancing Translational Sciences of the National Institutes of Health.
引用
收藏
页码:137 / +
页数:10
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