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dc.contributor.authorDegenhardt, L.
dc.contributor.authorLarney, S.
dc.contributor.authorKimber, J.
dc.contributor.authorGisev, N.
dc.contributor.authorFarrell, M.
dc.contributor.authorDobbins, T.
dc.contributor.authorWeatherburn, D.
dc.contributor.authorGibson, A.
dc.contributor.authorMattick, R.
dc.contributor.authorButler, Tony
dc.contributor.authorBurns, L.
dc.date.accessioned2017-01-30T12:03:19Z
dc.date.available2017-01-30T12:03:19Z
dc.date.created2015-10-29T04:08:38Z
dc.date.issued2014
dc.identifier.citationDegenhardt, L. and Larney, S. and Kimber, J. and Gisev, N. and Farrell, M. and Dobbins, T. and Weatherburn, D. et al. 2014. The impact of opioid substitution therapy on mortality post-release from prison: Retrospective data linkage study. Addiction. 109 (8): pp. 1306-1317.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/17661
dc.identifier.doi10.1111/add.12536
dc.description.abstract

Aims: Release from prison is a high-risk period for mortality. We examined the impact of opioid substitution therapy (OST), for opioid dependence during and after incarceration, upon mortality post-release. Design: A cohort was formed of all opioid-dependent people who entered OST between 1985 and 2010 and who, following first OST entry, were released from prison at least once between 2000 and 2012. We linked data on OST history, court and prison records and deaths. Setting: New South Wales (NSW), Australia. Participants: A total of 16453 people released from prison 60161 times. Measurements: Crude mortality rates (CMRs) were calculated according to OST retention; multivariable Cox regressions for post-release periods were undertaken to examine the association between OST exposure (a time-dependent variable) and mortality post-release, for which covariates were updated per-release. Findings: There were 100978 person-years (PY) post-release; 1050 deaths occurred. Most received OST while incarcerated (76.5%); individuals were receiving OST in 51% of releases. Lowest post-release mortality was among those continuously retained in OST post-release CMR 4 weeks post-release=6.4 per 1000 PY; 95% confidence interval (CI)=5.2, 7.8, highest among those with no OST (CMR=36.7 per 1000 PY; 95% CI=28.8, 45.9). Multi-factorial models showed OST exposure in the 4 weeks post-release reduced hazard of death by 75% (adjusted hazard ratio 0.25; 95% CI=0.12, 0.53); OST receipt in prison had a short-term protective effect that decayed quickly across time. Conclusion: In New South Wales, Australia, opioid substitution therapy in prison and post-release appears to reduce mortality risk in the immediate post-release period. © 2014 Society for the Study of Addiction.

dc.titleThe impact of opioid substitution therapy on mortality post-release from prison: Retrospective data linkage study
dc.typeJournal Article
dcterms.source.volume109
dcterms.source.number8
dcterms.source.startPage1306
dcterms.source.endPage1317
dcterms.source.issn0965-2140
dcterms.source.titleAddiction
curtin.departmentNational Drug Research Institute (NDRI)
curtin.accessStatusFulltext not available


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