Impact of treatment duration on mortality among Veterans with opioid use disorder in the United States Veterans Health Administration

被引:10
作者
Ching, Jack H. [1 ,2 ,4 ]
Owens, Douglas K. [1 ,2 ,3 ]
Trafton, Jodie A. [4 ]
Goldhaber-Fiebert, Jeremy D. [1 ,2 ]
Salomon, Joshua A. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Ctr Hlth Policy, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Ctr Primary Care & Outcomes Res, Stanford, CA 94305 USA
[3] VA Palo Alto Hlth Care Syst, Palo Alto, CA USA
[4] VA Palo Alto Hlth Care Syst, Program Evaluat & Resource Ctr, Off Met Hlth & Suicide Prevent, Menlo Pk, CA USA
基金
美国医疗保健研究与质量局;
关键词
Buprenorphine; medications for addiction treatment; methadone; opioid use disorder; simulation modeling; Veterans; METHADONE-MAINTENANCE TREATMENT; BUPRENORPHINE; DEPENDENCE; RISK; SOCIETY;
D O I
10.1111/add.15574
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background and aims While long-term medication-assisted treatment (MAT) using methadone or buprenorphine is associated with significantly lower all-cause mortality for individuals with opioid use disorder (OUD), periods of initiating or discontinuing treatment are associated with higher mortality risks relative to stable treatment. This study aimed to identify the OUD treatment durations necessary for the elevated mortality risks during treatment transitions to be balanced by reductions in mortality while receiving treatment. Design Simulation model based on a compartmental model of OUD diagnosis, MAT receipt and all-cause mortality among Veterans with OUD in the United States Veterans Health Administration (VA) in 2017-2018. We simulated methadone and buprenorphine treatments of varying durations using parameters obtained through calibration and published meta-analyses of studies from North America, Europe and Australia. Setting United States. Participants Simulated cohorts of 10 000 individuals with OUD. Measurements All-cause mortality over 12 months. Findings Receiving methadone for 4 months or longer or buprenorphine for 2 months or longer resulted in 54 [95% confidence interval (CI) = 5-90] and 65 (95% CI = 21-89) fewer deaths relative to not receiving MAT for the same duration, using VA-specific mortality rates. We estimated shorter treatment durations necessary to achieve net mortality benefits of 2 months or longer for methadone and 1 month or longer for buprenorphine, using non-VA population literature estimates. Sensitivity analyses demonstrated that necessary treatment durations increased more with smaller mortality reductions on treatment than with larger relative risks during treatment transitions. Conclusions Short periods (< 6 months) of treatment with either methadone or buprenorphine are likely to yield net mortality benefits for people with opioid use disorder relative to receiving no medications, despite periods of elevated all-cause mortality risk during transitions into and out of treatment. Retaining people with opioid use disorder in treatment longer can increase these benefits.
引用
收藏
页码:3494 / 3503
页数:10
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