The causal effect of opioid substitution treatment on HAART medication refill adherence

被引:42
作者
Nosyk, Bohdan [1 ,2 ]
Min, Jeong E. [1 ]
Colley, Guillaume [1 ]
Lima, Viviane D. [1 ,3 ]
Yip, Benita [1 ]
Milloy, M. -J. S. [1 ]
Wood, Evan [1 ,3 ]
Montaner, Julio S. G. [1 ,3 ]
机构
[1] St Pauls Hosp, BC Ctr Excellence HIV AIDS, Vancouver, BC V6Z 1Y6, Canada
[2] Simon Fraser Univ, Fac Hlth Sci, Burnaby, BC V5A 1S6, Canada
[3] Univ British Columbia, Fac Med, Div Aids, Vancouver, BC V6Z 1Y6, Canada
基金
美国国家卫生研究院; 加拿大健康研究院; 比尔及梅琳达.盖茨基金会;
关键词
health administrative data; HAART; HIV/AIDS; marginal structural modelling; opioid dependence; opioid substitution treatment; ACTIVE ANTIRETROVIRAL THERAPY; COST-EFFECTIVENESS; HIV-INFECTION; INJECT DRUGS; METHADONE; EPIDEMIOLOGY; DEPENDENCE; IMPACT; RECOMMENDATIONS; TRANSMISSION;
D O I
10.1097/QAD.0000000000000642
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: People who inject drugs (PWID) account for roughly 13% of the prevalent HIV/AIDS population outside of sub-Saharan Africa, and access to opioid substitution treatment (OST) is limited in many settings globally. OST likely facilitates access to HAART, yet sparse evidence is available to support this hypothesis. Our objective was to determine the causal impact of OST exposure on HAART adherence among HIV-positive PWID in a Canadian setting. Methods: We executed a retrospective cohort study using linked population-level data for British Columbia, Canada (January 1996-March 2010). We considered HIV-positive PWID after meeting HAART initiation criteria. A marginal structural model was estimated on a monthly timescale using inverse probability of treatment weights. The primary outcome was 95% HAART adherence, according to pharmacy refill compliance. Exposure to OST was defined as 95% of OST receipt, and we controlled for a range of fixed and time-varying covariates. Results: Our study included 1852 (63.3%) HIV-positive PWID with a median follow-up of 5.5 years; 34% were female and 39% had previously accessed OST. The baseline covariate-adjusted odds of HAART adherence following OST exposure was 1.96 (95% confidence interval: 1.72-2.24), although the adjusted odds estimated within the marginal structural model was 1.68 (1.48-1.92). Findings were robust to sensitivity analyses on model specification. Conclusion: In a setting characterized by universal healthcare and widespread access to both office-based OST and HAART, OST substantially increased the odds of HAART adherence. This underlines the need to address barriers to OST globally to reduce the disease burden of both opioid dependence and HIV/AIDS. Copyright (c) 2015 Wolters Kluwer Health, Inc. All rights reserved.
引用
收藏
页码:965 / 973
页数:9
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