Prior studies indicated opioid substitution treatment (OST)
reduces mortality risk and improves the odds of accessing highly active
antiretroviral therapy (HAART); however, the relative effects of these
treatments for human immunodeficiency virus (HIV)-positive people who inject
drugs (PWID) are unclear. We determine the independent and joint effects of OST
and HAART on mortality, by cause, within a population of HIV-positive PWID
initiating HAART.
Using a linked population-level database for British
Columbia, Canada, we used time-to-event analytic methods, including competing
risks models, proportional hazards models with time-varying covariates, and
marginal structural models, to identify the independent and joint effects of
OST and HAART on all-cause as well as drug- and HIV-related mortality,
controlling for covariates.
Among 1727 HIV-positive PWID, 493 (28.5%) died during a
median 5.1 years of follow-up:
- 18.7% due to drug-related causes,
- 55.8% due to HIV-related causes,
- and 25.6% due to other causes.
Standardized mortality ratios were 12.2 during OST and 30.0 during periods out of OST. Both OST and HAART decreased the hazard of all-cause mortality; however, individuals were at
lowest risk of death when these medications were used jointly. Both OST and HAART independently protected against HIV-related death,
drug-related death and death due to other causes.
While both OST and HAART are life-saving treatments, joint
administration is urgently needed to protect against both drug- and HIV-related
mortality.
Via: http://ht.ly/SpmkD
- 1BC Centre for Excellence in HIV/AIDS, Vancouver Faculty of Health Sciences, Simon Fraser University, Burnaby, Canada.
- 2BC Centre for Excellence in HIV/AIDS, Vancouver.
- 3University of California-Los Angeles Integrated Substance Abuse Programs.
- 4Department of Preventative Medicine, Northwestern University, Chicago, Illinois.
- 5BC Centre for Excellence in HIV/AIDS, Vancouver Division of AIDS, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
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