Worldwide opioid-related overdose has become a major public health crisis. People with opioid use disorder (OUD) are overrepresented in the criminal justice system and at higher risk for opioid-related mortality. However, correctional facilities frequently adopt an abstinence-only approach, seldom offering the gold standard opioid agonist treatment (OAT) to incarcerated persons with OUD. In an attempt to inform adequate management of OUD among incarcerated persons, we conducted a systematic review of opioid-related interventions delivered before, during, and after incarceration.
Methods and findings
We systematically reviewed 8 electronic databases for original, peer-reviewed literature published between January 2008 and October 2019. Our review included studies conducted among adult participants with OUD who were incarcerated or recently released into the community (≤90 days post-incarceration). The search identified 2,356 articles, 46 of which met the inclusion criteria based on assessments by 2 independent reviewers. Thirty studies were conducted in North America, 9 in Europe, and 7 in Asia/Oceania. The systematic review included 22 randomized control trials (RCTs), 3 non-randomized clinical trials, and 21 observational studies. Eight observational studies utilized administrative data and included large sample sizes (median of 10,419 [range 2273–131,472] participants), and 13 observational studies utilized primary data, with a median of 140 (range 27–960) participants. RCTs and non-randomized clinical trials included a median of 198 (range 15–1,557) and 44 (range 27–382) participants, respectively. Twelve studies included only men, 1 study included only women, and in the remaining 33 studies, the percentage of women was below 30%. The majority of study participants were middle-aged adults (36–55 years). Participants treated at a correctional facility with methadone maintenance treatment (MMT) or buprenorphine (BPN)/naloxone (NLX) had lower rates of illicit opioid use, had higher adherence to OUD treatment, were less likely to be re-incarcerated, and were more likely to be working 1 year post-incarceration. Participants who received MMT or BPN/NLX while incarcerated had fewer nonfatal overdoses and lower mortality. The main limitation of our systematic review is the high heterogeneity of studies (different designs, settings, populations, treatments, and outcomes), precluding a meta-analysis. Other study limitations include the insufficient data about incarcerated women with OUD, and the lack of information about incarcerated populations with OUD who are not included in published research.
In this carefully conducted systematic review, we found that correctional facilities should scale up OAT among incarcerated persons with OUD. The strategy is likely to decrease opioid-related overdose and mortality, reduce opioid use and other risky behaviors during and after incarceration, and improve retention in addiction treatment after prison release. Immediate OAT after prison release and additional preventive strategies such as the distribution of NLX kits to at-risk individuals upon release greatly decrease the occurrence of opioid-related overdose and mortality. In an effort to mitigate the impact of the opioid-related overdose crisis, it is crucial to scale up OAT and opioid-related overdose prevention strategies (e.g., NLX) within a continuum of treatment before, during, and after incarceration.
Why was this study done?
- Opioid use disorder has been rising at an alarming rate, and opioid-related overdose is now a major public health crisis.
- Persons with opioid use disorder are overrepresented in the criminal justice system and face higher risks for opioid-related mortality.
- However, opioid use treatment is severely limited in correctional facilities.
- To address the opioid-related overdose crisis, it is pivotal to improve access to opioid use treatment inside correctional facilities and to assure proper linkage into addiction care post-incarceration.
What did the researchers do and find?
- We conducted a systematic review of opioid-related interventions delivered before, during, and after incarceration.
- Our search identified 2,356 scientific articles, of which 46 studies were eligible for inclusion in our review.
- Participants treated at a correctional institution with the gold standard treatment for opioid use disorders, opioid agonist treatment, had higher adherence to addiction treatment, had lower rates of relapse into illicit opioid use, were less likely to be re-incarcerated, and were more likely to be working 1 year post-incarceration.
- Participants who received opioid agonist treatment while incarcerated and were adequately linked into care post-release experienced a significant decrease in nonfatal overdose rates and mortality.
Citation: Malta M, Varatharajan T, Russell C, Pang M, Bonato S, Fischer B (2019) Opioid-related treatment, interventions, and outcomes among incarcerated persons: A systematic review. PLoS Med 16(12): e1003002. https://doi.org/10.1371/journal.pmed.1003002
Academic Editor: Alexander C. Tsai, Massachusetts General Hospital, UNITED STATES
Received: June 18, 2019; Accepted: November 22, 2019; Published: December 31, 2019
Copyright: © 2019 Malta et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: BF acknowledges funding from the Canadian Institutes of Health Research (CIHR) for the Ontario CRISM Node Team (grant #SMN-139150); support from the Chair in Addiction, Department of Psychiatry at the University of Toronto for partial development of the article; and support from the Hugh Green Foundation Chair in Addiction Research, Faculty of Medical and Health Sciences at the University of Auckland. MM acknowledges funding from Correctional Service of Canada - CSC (MOU #15-070). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Abbreviations: AHR, adjusted hazard ratio; AOR, adjusted odds ratio; BMT, buprenorphine maintenance treatment; BPN, buprenorphine; HR, hazard ratio; IRR, incidence rate ratio; MMT, methadone maintenance treatment; MR, mortality rate; NLX, naloxone; NNP, National Naloxone Program; OAT, opioid agonist treatment; OUD, opioid use disorder; PY, person-years; RCT, randomized control trial; RIDOC, Rhode Island Department of Corrections; XR-NTX, injectable extended-release naltrexone
Globally the rate of opioid use disorder (OUD) has been rising at an alarming rate, and the opioid-related overdose crisis is now considered a major global challenge, associated with high rates of morbidity and mortality . Unprecedented levels of opioid use and misuse and related health harms (e.g., hospitalizations, treatment admissions, overdose fatalities) have been reported worldwide in recent years, but have been most extensively documented in North America [1–4].
The pervasive general population trends of OUD and the opioid-related overdose crisis disproportionately affect criminal-justice-involved populations [5,6]. It is estimated that more than one-fourth of people with OUD in the United States pass through prisons and jails every year . Worldwide, the United Nations Office on Drugs and Crime reports that 10% of incarcerated individuals have used heroin at some point during incarceration, with one-third reporting current (i.e., past month) use while incarcerated . Similarly, individuals who used opioids prior to their incarceration often report continued use during the course of their incarceration . A report from the US Department of Justice indicated that the percentage of US-state-incarcerated individuals with a diagnosis of drug dependence or abuse is 14 times higher than that of the general population (4%) . A meta-analysis conducted by Fazel et al.  estimated a pooled prevalence of 30% and 51% for substance use disorders among incarcerated males and females, respectively, and revealed an overall increasing trend in the prevalence of substance use disorders among incarcerated individuals during recent decades.
Problematic substance use is associated with a range of harmful effects, including the likelihood of continued involvement with the criminal justice system  related to the societal responses to substance use, often centered on punishment and mass incarceration  rather than public health interventions, including harm reduction strategies and opioid agonist treatment (OAT) . Adverse health effects are also exacerbated when individuals have little control over their environment, such as in a correctional institution . Opioid-related overdose is a leading cause of death among the correctional population, during or after incarceration [5,6,15]. In the first few weeks after release from incarceration, individuals are at an increased risk of opioid use relapse and opioid-related overdose, likely higher when riskier patterns of substance use are adopted and in the absence of proper OAT or with treatment discontinuation [5,6,16].
Furthermore, incarcerated individuals who use opioids may further engage in high-risk behaviors such as needle sharing and/or reutilization, thus increasing the risk of acquiring blood-borne infections (e.g., HIV, hepatitis C) [1,7,17,18]. These factors compound and contribute to incarcerated individuals’ disproportionately worse health status relative to the general population [10,12].
Among the general population with diagnosed OUD, OAT is highly effective . OAT decreases the rates of opioid use relapse and transmission of HIV and other blood-borne infections, reduces opioid-related and all-cause mortality , and is associated with a broad range of personal and social gains, such as improvements in employment rates and better family functioning .
In spite of the disproportional burden of OUD among incarcerated populations, and the well-known benefits of OAT, interventions to address OUD-related risks and harms among this population have been limited . Few criminal justice facilities routinely and adequately screen their populations for OUD, and a smaller percentage provide OAT for incarcerated individuals with diagnosed OUD [12,13]. Significant barriers to adopting and routinizing OAT in correctional institutions exist, and concerns range from medication diversion and safety to constraints related to organizational resources, prohibitive legislations, and continuity of care [22,23].
Several potential linkage points throughout the criminal justice continuum exist, providing opportunities to screen individuals for OUD and overdose risk, and to provide prevention and treatment interventions (e.g., during law enforcement interactions, court hearings, incarceration, community re-entry, and community supervision, such as parole and probation) . Interventions can also be adapted to each step of the continuum, reflecting the different capabilities and programming needs of different correctional institutions . As such, correctional institutions present a unique opportunity to provide prevention, treatment, and post-release support for incarcerated individuals with OUD, thereby encouraging positive health and community reintegration outcomes post-release [12,13,24,25].
As problematic opioid use and its related harms continue to inflict a major public health burden on many regions, especially North America —and disproportionately so among correctional populations —a comprehensive and timely examination of the extant international literature is warranted in order to inform effective program and policy measures that sufficiently address the complex needs of incarcerated opioid-involved individuals [12,13]. The objective of this systematic review was to assess opioid-related interventions delivered during and after incarceration among adult correctional populations. Previous reviews have assessed the effectiveness of various opioid-related intervention modalities among correctional populations [25,27,28]. However, the present systematic review is the first to our knowledge to systematically review the literature to assess the effects of both treatment-based (e.g., methadone, buprenorphine [BPN], naltrexone) and preventive (e.g., naloxone [NLX]) opioid-related interventions delivered during and after incarceration among adult correctional populations. The study addresses the impact of the opioid-related overdose crisis and highlights effective public health strategies developed and evaluated among a highly disenfranchised and frequently forgotten population: incarcerated persons with OUD.
We identified all peer-reviewed original research articles in which opioid use interventions delivered to adult correctional populations were evaluated. The search strategy was developed by an experienced health science librarian (SB), and included studies published between January 1, 2008, and December 31, 2018. After initial peer review, the search was updated to October 17, 2019. The search did not include studies published before 2008 to avoid replication of findings from previous systematic reviews with similar objectives [25,27–31].
This present systematic review adheres to the guidelines outlined by the Cochrane Collaboration . Results are reported according to the PRISMA 2009 checklist  (S1 PRISMA Checklist). The review was submitted to PROSPERO (S1 Prospero Registration), an international prospective registry of systematic reviews (registration #135900). The initial search strategy was developed in MEDLINE and combined relevant MeSH terms and keywords regarding opioid use interventions (e.g., opiate substitution treatment, buprenorphine, methadone, naltrexone, naloxone) among incarcerated and post-incarceration populations (i.e., jail, prison, offender, detention, imprison, post-incarceration) that use opioids (i.e., opioid-related disorders, opiate, opioid). The complete MEDLINE search strategy is described on S1 MEDLINE Search Strategy. Detailed search strategies were subsequently developed and revised for each individual database, based on the initial MEDLINE search strategy. Reference lists of all articles selected for inclusion in the review were also scanned for additional relevant studies. The search included the following scientific literature databases: Criminal Justice Abstracts, Embase, MEDLINE, National Criminal Justice Reference Service (NCJRS), PsycINFO, Scopus, and Web of Science. Bibliographic references were managed using the software EndNote X9.
The review included studies conducted among adult participants who (1) were opioid users at the time of the study and/or had been diagnosed with OUD prior to or during incarceration and (2) were incarcerated or recently released into the community (≤90 days post-incarceration). Studies were excluded if participants were (1) not opioid users, (2) using opioids for medical purposes (not including for OUD), (3) released from incarceration for more than 90 days, (4) on probation or parole at the time of the study, or (5) involved in drug treatment court or other diversion programs. Only studies involving opioid use interventions (i.e., addiction treatment, relapse, or overdose prevention) for adults provided during incarceration or within 90 days post-incarceration were included for final review. Exclusion criteria were developed to select studies directly addressing the impact of providing OAT or opioid-overdose prevention (e.g., NLX) to incarcerated or recently released persons. Studies reporting the following intervention outcomes were included: mortality (e.g., all cause, opioid related), outcomes related to opioid addiction treatment (e.g., relapse, retention, withdrawal), and recidivism (e.g., re-incarceration, arrest). Studies presenting only cost-effectiveness analyses, opioid treatment impact on blood-borne and/or sexually transmitted infections, or self-screening or individual’s subjective experiences/feelings/attitudes towards opioid treatment were excluded.
Data extraction and analysis
Two reviewers (CR and TV) independently screened all articles in a 2-step screening process—first screening the titles/abstracts followed by the full-text articles. When consensus could not be reached among reviewers, a third reviewer (MM) became involved to resolve standing conflicts.
Relevant information was extracted and inputted into a standardized form, which included the following information: year of publication, location and setting of study, sample size, population characteristics (age, sex, and ethnicity), study design, intervention description, and study outcomes. All eligible studies were assessed for quality using the Joanna Briggs Institute Critical Appraisal Tools .
From the initial search, 2,356 unique peer-reviewed articles were identified. Of these, there was perfect agreement between reviewers on the eligibility of 186 articles, and the ineligibility of 2,170 abstracts that failed to meet the study inclusion criteria. At second screening, a total of 140 articles (S1 List of Manuscripts Excluded) were excluded for the following reasons: (1) were reviews, editorials, comments, or study protocols; (2) studied non-incarcerated individuals with OUD; (3) did not evaluate an opioid use intervention delivered during incarceration or within 90 days post-incarceration; and/or (4) reported duplicate results. Agreement on full-text screening was close to perfect. Ultimately, 46 original articles were deemed eligible for data extraction (Fig 1).
Characteristics of the 46 identified studies are summarized in Table 1. While the search included articles published in any language, all identified studies were published in English, and nearly all were conducted in high-income countries. Thirty studies were conducted in North America (US, 27; Canada, 3), 9 were conducted in Europe (United Kingdom, 7; France, 1; Norway, 1), and 7 were conducted in Asia/Oceania (Australia, 4; Malaysia, 2; Taiwan, 1).
Eight studies utilized administrative data and included large sample sizes (median of 10,419 [range 2,273–131,472] participants) [35,36,53,54,68,69,74,75]. All other studies assessed primary data, including 22 randomized control trials (RCTs) (median of 198 [range 15–1,557] participants), 13 longitudinal/observational studies (median of 140 [range 27–960] participants), and 3 non-randomized clinical trials (median of 44 [range 27–382] participants) (Table 1).
Studies were grouped according to when the opioid use intervention was provided relative to the incarceration period (pre-incarceration, during incarceration, or post-incarceration). Twenty-one studies evaluated the impact of opioid use interventions provided during a continuum of treatment (before, during, and after incarceration), 14 studies reported the effect of opioid use interventions offered to individuals while incarcerated, and 11 studies evaluated the effects of opioid use interventions post-incarceration. The last group included 3 studies that addressed the impact of NLX, a preventive intervention to reduce opioid-related overdose harms and mortality (Table 1). Interventions included various forms of pharmacological treatment for OUD (including methadone, BPN, BPN/NLX, naltrexone) and the distribution of NLX kits to at-risk individuals before their released into the community, to decrease the occurrences of opioid-related overdose and mortality.
Thirty-two studies were conducted in prisons, 6 in jails, and 8 in both types of correctional facilities. Incarcerated persons sentenced to terms longer than 1 year are generally sent to prison, while jails are characterized by a rapid turnover of both sentenced and non-sentenced arrested persons. This specificity should be taken into account when evaluating the results of OAT delivered in long-term versus short-term incarceration facilities.
Opioid use interventions during a continuum of treatment (i.e., before, during, and after incarceration)
Twenty-one studies reported the impact of an opioid intervention provided during a continuum of treatment prior to, during, and after incarceration (Table 2). Fourteen of these studies were experimental [37–50], and 7 were observational [35,36,51–55]. Five studies evaluated the impact of receiving opioid substitution therapy—primarily methadone—while incarcerated compared to treatment post-incarceration [35,36,51,53,54]. Seven studies evaluated the impact of receiving methadone maintenance treatment (MMT) while incarcerated, with participants continuing or discontinuing MMT post-release [38,39,43–46,52]. Four studies evaluated the impact of receiving BPN maintenance treatment (BMT) while incarcerated, with participants continuing or discontinuing BMT post-release [37,40,42,47], and 5 studies evaluated the impact of receiving injectable extended-release naltrexone (XR-NTX) while incarcerated compared to post-release [41,48–50,55].
Non-specified opioid substitution treatment.
Several Australian studies evaluated the impact of OAT provision while incarcerated on post-release OAT retention and related outcomes [35,36,51,53]. A 2012 study conducted by Larney et al.  found that among 375 incarcerated, heroin-using men from New South Wales, those who received OAT while in prison and continued OAT post-release reduced their risk of re-incarceration by 20% (hazard ratio [HR] = 0.80, 95% CI 0.71–0.90, p = 0002), compared to those who discontinued OAT post-release. Larney et al. published another study in 2016  to evaluate administrative data from 8,577 incarcerated persons who were in prison between 2007 to 2013 and experienced changes in the clinical governance of the New South Wales OAT program in 2011. The authors identified statistically significant higher rates of OAT retention while incarcerated (82%), higher rates of OAT prescription prior to release (90%), and higher rates of presentation to a community OAT clinic within 48 hours post-release (94%) among incarcerated persons following changes to the OAT program.
Larney et al. and Degenhardt et al. both examined the relationship between receipt of OAT and mortality risk, based on administrative data from a cohort of over 16,000 incarcerated persons in New South Wales, Australia [35,36]. In Larney et al.’s study , the majority of individuals received OAT while incarcerated (76.9%), and this intervention reduced the hazard of all-cause and unnatural death by 74% (adjusted hazard ratio [AHR] = 0.26, 95% CI 0.13–0.50) and 87% (AHR = 0.13, 95% CI 0.05–0.35), respectively, compared to those out of OAT. Moreover, the hazard of all-cause death and unnatural death during the first 4 weeks of incarceration was reduced by 94% (AHR = 0.06, 95% CI 0.01–0.48) and 93% (AHR = 0.07, 95% CI 0.01–0.53), respectively, during periods on OAT compared to those out of OAT. Degenhardt et al.  also found that the majority of individuals received OAT while incarcerated (76.5%), determining that OAT exposure by 4 weeks post-release reduced the hazard of death by 75% (AHR = 0.25, 95% CI 0.12–0.53). Post-release mortality rates (MRs) were lowest among those continuously engaged in OAT at 4 weeks post-release (8.8 per 1,000 person-years [PY], 95% CI 5.0–14.3) and highest among those not receiving OAT 4 weeks post-release (36.7 per 1,000 PY, 95% CI 28.8–45.9).
Bird et al.  evaluated a large administrative dataset (n = 131,427) of all incarcerated persons in Scottish prisons between 1996 and 2007 to determine the effects of receiving OAT on drug-related deaths post-release. The drug-related death rate within 12 weeks after prison release fell from 3.8 per 1,000 releases (95% CI 3.4–4.2) to 2.2 per 1,000 releases (95% CI 1.8–2.5) following the implementation of a universal prison-based OAT policy for incarcerated individuals with OUD between 2003 and 2007. Furthermore, the decrease in MR of 1.6 per 1,000 (95% CI 1.0–2.2) was found to be highly statistically significant (p < 0.001).
Methadone maintenance treatment.
Gordon et al. and Kinlock et al. [38,39,43–45] conducted an RCT comparing 3 groups of heroin-dependent incarcerated persons in a Baltimore prison (n = 211), with one group receiving only counseling while incarcerated, a second group receiving counseling and referral to MMT upon release, and a third group receiving both counseling and MMT while incarcerated and MMT referral post-release. Short-term results at 3 months post-release  and long-term results at 6 and 12 months post-release [39,44] found that participants who received both MMT and counseling while in prison displayed higher adherence and retention to opioid-related community-based treatment, lower rates of illicit opioid use, and lower re-incarceration rates, compared to those who received counseling only during incarceration, independent of whether they were referred or not to MMT upon prison release. Specifically, the results showed that participants who initiated MMT while in prison were more likely to engage in community-based treatment within 90 days post-release (p < 0.01), remained in addiction treatment for a greater number of days at 6 and 12 months post-release (p < 0.001), and were less likely to test positive for opioid use at 3, 6, and 12 months post-release (p = 0.014, p = 0.009, and p = 0.001, respectively) compared to the counseling only group [39,43,44]. Participants who received both MMT and counseling while in prison were also less likely to report engagement in criminal activities at 3 months (p = 0.005) and 6 months (p = 0.025) post-release, compared to the other groups [39,43]. Further secondary analyses conducted by Kinlock et al.  found that participants who completed 1 year of community-based MMT post-release worked twice as many days (122 days versus 56 days) relative to those who did not complete 1 year of MMT after prison release.
McKenzie et al.  reported findings from an RCT (n = 62) assessing 3 conditions: one group of incarcerated persons who received MMT while in prison and a 12-week financial subsidy to continue treatment upon release (arm 1), a second group referred to MMT after prison release and provided with a 12-week financial subsidy (arm 2), and a third group referred to MMT with no provision of a financial subsidy upon release. Participants who received MMT while in prison were more likely to initiate MMT within 30 days post-prison release (86%, 41%, and 22% for arm 1, 2, and 3, respectively, p < 0.001). Among those who entered MMT after prison release, those who received MMT in prison entered within fewer days (2, 9, and 5 days for arm 1, 2, and 3, respectively, p = 0.03). Those who received MMT pre-release reported, for the last 30 days, less heroin use (3, 18, and 4 days for arm 1, 2, and 3, respectively, p = 0.008), less use of other opiates (0, 6, and 1 day, p = 0.09), less crack/cocaine use (4, 13, and 6 days, p = 0.05), and less injection drug use (2, 12, and 3 days, p = 0.06). Farrell-MacDonald et al.  examined administrative data from a cohort of 137 incarcerated women with OUD at a Canadian federal facility, comparing 3 groups: group 1 initiated MMT while incarcerated and continued MMT post-release, group 2 initiated MMT while incarcerated but terminated treatment post-release, and group 3 were women with OUD who did not participate in MMT while incarcerated. Women with OUD who received MMT while incarcerated and continued MMT post-release had a 65% lower risk of returning to custody during the 6-year follow-up period (HR = 0.35, 95% CI 0.13–0.90) compared to the women who did not participate in MMT while incarcerated.
Buprenorphine maintenance treatment.
Gordon et al. [37,40,42] conducted an RCT (n = 211) comparing incarcerated persons with histories of heroin dependence. Participants were randomly assigned into 1 of 4 conditions: one group received in-prison BMT and continued treatment at an OAT program post-release, a second group received in-prison BMT and continued treatment at a community health center post-release, a third group received counseling only during their incarceration and treatment at an OAT program post-release, and a fourth group received counseling only during their incarceration and treatment at a community health center post-release. The authors determined that those who received BMT while incarcerated and continued at an OAT program post-release were more likely than the counseling only groups to enter prison treatment (adjusted odds ratio [AOR] = 2.8, 95% CI 1.3–5.7, p = 0.006) and to enter community treatment post-release (AOR = 1.5, 95% CI 1.1–2.1, p = 0.01) . Participants who received BPN while incarcerated had also higher rates of treatment retention at 12 months post-release compared to those who initiated BPN after release (p = 0.005) . However, the study did not discern any statistically significant effects of the receipt of BPN treatment during incarceration on days of heroin use, positive opioid and cocaine urine screening test results, and re-arrest rate at 12 months of follow-up [40,42].
Zaller et al.  conducted a clinical trial (n = 44) to evaluate the provision of BPN/NLX to incarcerated persons from the Rhode Island Department of Corrections (RIDOC) diagnosed with opioid dependence, specifically comparing those who initiated OAT during incarceration and post-release. Participants who received BPN/NLX while incarcerated started treatment earlier post-release (3.9 versus 8.8 days, p = 0.1) and had longer retention in OAT after release (24 versus 9 weeks, p = 0.007). The authors also determined that treatment retention was higher at 6 months post-release among those who started BPN/NLX treatment in prison relative to those who initiated BPN/NLX post-release (p = 0.005). Furthermore, rates of heroin use and re-incarceration were higher among those who started BPN treatment post-release, compared to participants who initiated BPN/NLX during their incarceration period.
Injectable extended-release naltrexone.
Six studies evaluated the impact of XR-NTX on relapse into illicit opioid use, treatment retention, re-incarceration, and healthcare utilization [41,48–50,55]. Gordon et al.  conducted a clinical trial (n = 27) to evaluate the relationship between XR-NTX adherence and re-incarceration among persons with OUD prior to incarceration. The authors found that participants who completed XR-NTX treatment (involving 1 injection prior to release and 6 monthly injections post-release) were less likely to use illicit opioids during the course of the study, compared to those who did not complete the treatment (i.e., received <6 injections, p = 0.003). In addition, participants who did not complete the treatment were more likely to be re-arrested (31.3% versus 0%) or re-incarcerated (18.8% versus 0%) relative to those who did complete the treatment; however, the differences in recidivism outcomes—including re-arrest and re-incarceration rates—were not statistically significant.
Lee et al.  conducted a 5-site RCT (n = 308) comparing previously incarcerated participants receiving XR-NTX (n = 153) with those receiving treatment as usual, including BPN or MMT (n = 155). After the 24-week treatment and follow-up period, the participants assigned to receive XR-NTX had a longer median time to opioid relapse (10.5 versus 5.0 weeks, p < 0.001; HR = 0.49, 95% CI 0.36–0.68), a lower rate of opioid relapse (43% versus 64%, p < 0.001; OR = 0.43, 95% CI 0.28–0.65), and a higher rate of opioid-negative urine samples (74% versus 56%, p < 0.001; OR = 2.30, 95% CI 1.48–3.54). However, at week 78 (approximately 1 year after the end of the treatment phase), the rates of opioid-negative urine samples were equal (46% in each group, p = 0.91). After 78 weeks of follow-up, there were no overdose events (fatal or nonfatal) among participants allocated to XR-NTX, and 7 among participants assigned to treatment as usual (p = 0.02).
Friedmann et al.  conducted an RCT study with 15 incarcerated persons from RIDOC comparing one group of participants who received 1 XR-NTX injection prior to release followed by 5 monthly treatments post-release and a second group where participants received 6 XR-NTX injections in the community exclusively. The authors found that participants, who received their first dose of XR-NTX treatment prior to release, exhibited greater abstinence rates as determined by a higher proportion of self-reported opioid-free days at 2 weeks and 1 month post-release, relative to participants who received 6 doses of XR-NTX post-release (OR = 5.6, 95% CI 0.8–37.9, p = 0.08).
Lincoln et al.  evaluated data from 67 incarcerated persons released from a Massachusetts county jail, comparing those who initiated XR-NTX treatment prior to release (n = 47) with those who initiated XR-NTX treatment post-release (n = 20). The authors found that receipt of XR-NTX injection prior to release was associated with increased XR-NTX treatment retention rates at 4, 8, and 24 weeks post-release (55% versus 25%, 36% versus 25%, and 21% versus 15%, respectively), compared to incarcerated persons who commenced the treatment post-release.
Soares et al.  conducted additional analysis of the study described by Lee and colleagues , evaluating the impact of XR-NTX treatment, compared to treatment as usual, on healthcare utilization among adults with a history of OUD involved in the criminal justice system. Although the authors did not identify any statistically significant differences in re-incarceration between those who received XR-NTX compared to those who received standard OAT, individuals who received XR-NTX experienced fewer medical and/or surgical hospital admissions during the 6-month treatment phase (incidence rate ratio [IRR] = 0.37, 95% CI 0.16–0.88, p = 0.02) and at 12 months post-treatment (IRR = 0.55, 95% CI 0.30–1.00, p = 0.05) relative to the treatment as usual group.
Opioid use interventions during incarceration
Fourteen studies assessed the impact of OAT provision while incarcerated (Table 3). Seven of these studies were experimental [56–62], and 7 were observational [26,63–68]. Eight studies evaluated the impact of receiving OAT—primarily methadone—while incarcerated compared to opioid detoxification [26,60–64,67,68], and 2 studies evaluated the impact of methadone dose at the time of release [65,66]. Three RCTs compared the efficacy of BPN and methadone [57–59], and 1 RCT compared BPN and dihydrocodeine for opiate detoxification within a UK prison setting .
Non-specified opioid substitution treatment.
Two studies assessed the impact of receiving OAT while incarcerated on opioid-related overdose mortality outcomes post-release, with both identifying large and significant reductions among incarcerated individuals with OUD who received OAT in prison/jail, compared to those who did not receive OAT during their incarceration period [26,68]. Green et al.  assessed the impact of a new model of screening and treatment for OUD started at RIDOC in 2016, involving the initiation and continuation of OAT in incarcerated individuals. Between 2016 and 2017, the authors identified a 60.5% reduction in opioid-related overdose deaths post-incarceration (26 deaths versus 9 deaths; risk ratio = 0.4, 95% CI 0.18–0.81, p = 0.01).
Marsden et al.  evaluated data from a large national cohort of 12,260 incarcerated persons diagnosed with OUD from 39 adult prisons in England, 6,662 of whom received OAT while incarcerated. The study found substantial reductions in all-cause mortality (AHR = 0.25, 95% CI 0.09–0.64) and drug-related mortality (85%; AHR = 0.15, 95% CI 0.04–0.52) within the first month of release associated with OAT exposure at the time of release. Receipt of prison-based OAT during incarceration was also associated with an increased likelihood of entering community drug treatment within 4 weeks post-release (OR = 2.47, 95% CI 2.31–2.65).
Methadone maintenance treatment.
Multiple studies showed that individuals with OUD who engage with MMT while incarcerated exhibit better opioid-use-related health outcomes, both during their incarceration period and post-release. Brinkley-Rubinstein et al.  reported 12-month findings from an RCT involving 179 incarcerated persons from Rhode Island (RIDOC) who had been engaged in MMT prior to their incarceration. Participants were randomly assigned into 1 of 2 groups, with the first group receiving continued access to MMT during their incarceration period (n = 128) and the second group undergoing tapered withdrawal from MMT within 1 week of their incarceration (n = 51). At 12 months post-release, participants who were assigned to tapered withdrawal from methadone after the first week of incarceration were more likely to use heroin (OR = 2.02, 95% CI 1.01–4.04, p < 0.05) and injection drugs (OR = 2.95, 95% CI 1.43–6.06, p < 0.05) compared to those who continued MMT while incarcerated.
Multiple studies have found that individuals with OUD who receive MMT during their incarceration period are more likely to access, initiate, and adhere to addiction treatment post-release, compared with individuals who do not receive MMT during their incarceration [60–62]. Findings from the RCT conducted by Brinkley-Rubinstein et al.  also indicated that those who were assigned to tapered withdrawal from methadone after the first week of incarceration were significantly more likely to experience a nonfatal overdose during the 12-month follow-up period, compared to those who received MMT while incarcerated (OR = 2.83, 95% CI 1.05–7.61, p < 0.05). Rich et al.  also conducted an RCT with 223 incarcerated persons from Rhode Island who had been engaged in MMT at the time of their arrest, comparing a group of participants who were maintained on MMT while incarcerated (n = 114) with a second group who underwent forced tapered withdrawal from MMT within 1 week of incarceration (n = 109). Participants who were maintained on MMT while incarcerated were 2 times more likely to return to a community methadone clinic within 1 month of release compared to incarcerated persons who underwent forced tapered withdrawal (HR = 2.04, 95% CI 1.48–2.80, p < 0.001).
A trial conducted by Moore et al.  compared incarcerated persons who continued engagement in MMT (n = 184) with a control group who underwent forced tapered withdrawal from MMT while in jail (n = 198). The authors found that participants who were maintained on MMT during incarceration were more likely to engage in community-based MMT within 1 day (OR = 32.04, 95% CI 7.55–136.01, p < 0.001) and 30 days post-release (OR = 6.08, 95% CI 3.42–10.79, p < 0.001), compared to incarcerated persons with OUD who underwent forced tapered withdrawal from MMT.
Wickersham et al. [65,66] conducted a longitudinal study among 72 HIV-positive incarcerated persons with OUD opioid dependence in Malaysia. Findings indicated that receiving MMT during incarceration and receiving a dose of ≥80 mg/day at the time of release was significantly associated with retention in addiction treatment at 12 months post-release compared to receiving a dose of <80 mg/day at the time of release (73.1% versus 29.0%, p < 0.001).
Westerberg et al.  examined re-incarceration outcomes among 960 incarcerated persons from a large US metropolitan detention center. The study compared individuals with OUD who were enrolled in community MMT prior to incarceration and continued MMT during their incarceration period (n = 118) with 3 groups: incarcerated individuals with no known substance use disorders (n = 385), incarcerated individuals receiving alcohol detoxification (n = 220), and incarcerated individuals receiving opioid detoxification (n = 237). The authors found that those enrolled in MMT while incarcerated were less likely to be re-incarcerated within 1 year post-release, compared to those who received opioid detoxification while incarcerated (53.4% versus 72.2%, p < 0.001). Among individuals who were re-incarcerated within 1 year, the number of days to rebooking into the detention center was higher for participants who received MMT during incarceration compared to the opioid detoxification group (275.6 days versus 236.3 days, p = 0.035). Furthermore, among individuals who received MMT while incarcerated, 97.8% continued to be enrolled in MMT at community clinics post-release.
Buprenorphine maintenance treatment.
Four studies compared the effects of providing BMT relative to other—primarily pharmacological—forms of treatment for OUD during incarceration [56–59]. Sheard et al.  conducted an RCT with 90 incarcerated persons from a large prison in England, comparing 1 group of participants who received daily sublingual BPN over 20 days (n = 42) with a second group receiving daily oral dihydrocodeine over 20 days (n = 48) on abstinence from illicit opiates. At 5 days post-detoxification, participants receiving BPN were more likely to present a negative urine test for opiates compared to those who received dihydrocodeine (57% versus 35%, relative risk = 1.61, 95% CI 1.02–2.56).
Magura et al.  conducted a study in 2009 among heroin-dependent incarcerated persons at Rikers Island in New York City (n = 116) to compare the effects of in-jail BMT and MMT. Participants were randomly assigned to receive BMT (n = 60) or MMT (n = 56). The authors found that incarcerated persons receiving BMT were less likely to withdraw from medication while in jail (3% versus 16%, p < 0.05) and more likely to report to assigned addiction treatment post-release (48% versus 14%, p < 0.001), compared to those receiving MMT while incarcerated. However, they observed no differences in self-reported rates of relapse into illicit opioid use post-release or in rates of re-incarceration between the 2 groups. Awgu et al. later  conducted a clinical trial in 2010 to compare in-jail BMT and MMT among 133 incarcerated persons with OUD at Rikers Island, with 77 participants enrolled in the BMT group and 56 participants enrolled in the MMT group. The authors found that participants who received in-jail MMT reported higher levels of opioid withdrawal symptoms (85% versus 53%, p < 0.001) and more side effects, including depression (p < 0.01), constipation (p < 0.01), confusion (p < 0.01), and fatigue/weakness (p < 0.05).
Wright et al.  compared the effects of receiving either a methadone or BPN detoxification during a reduced regimen of not more than 20 days among 306 UK incarcerated persons with OUD. Participants were randomly assigned to receive daily sublingual BPN (n = 141) or to receive oral methadone treatment (n = 148). Eight days after the detoxification, 73.7% of participants achieved abstinence—with no statistically significant difference between the BPN and MMT groups (OR = 1.69, 95% CI 0.81–3.51, p = 0.163). Incarceration was the major predictor of abstinence, compared to prison release (Table 3).
Opioid use interventions post-incarceration
Eleven studies evaluated opioid interventions delivered after incarceration, with follow-up periods ranging from 1 month to 7 years post-release (Table 4). Seven of these studies were observational [69–75], and 4 were experimental [76–79]. Two studies evaluated the impact of post-release MMT continuation on all-cause and overdose mortality  and on criminal recidivism . Five studies evaluated the impact of BPN-based opioid pharmacotherapy post-release on access to and/or retention in addiction treatment, levels of illicit opioid use, and criminal recidivism [70,72,73,76,77]. One RCT compared the efficacy of MMT and naltrexone implants post-release in reducing illicit drug use and criminal recidivism , and 3 studies evaluated the impact of NLX kit provision in preventing overdose-related deaths post-release [74,75,79].
Methadone maintenance treatment.
Two cohort studies evaluated the impact of providing MMT to incarcerated individuals post-release [69,71]. Huang et al.  analyzed administrative data from a cohort of 4,357 incarcerated persons with a history of opiate injection. The study found that 46% of individuals (n = 1,982) had enrolled in MMT by 18 months after their release from prison; however, the majority (n = 1,282, 65%) discontinued MMT shortly after enrolling. MRs were lowest among individuals who remained in MMT during the follow-up period (MR = 0.24/100 PY), followed by those who did not enroll in MMT post-release (MR = 2.6/100 PY). The highest mortality rate was observed among MMT enrollees who dropped out of treatment (MR = 7.0/100 person-years). Post-release MMT attendance had a significant protective effect on both overdose mortality (HR = 0.09, p = 0.02) and all-cause mortality (HR = 0.07, p < 0.001). Moreover, risk of re-incarceration was found to be the lowest among those who continued MMT post-release (3.4%), compared to those who had never enrolled in MMT (40.0%) or dropped out of MMT during the follow-up period (61.1%, p < 0.001).
Macswain et al.  examined data from a cohort of 856 incarcerated persons with OUD at a Canadian federal correctional facility, to determine the impact of MMT on re-incarceration. The study compared 3 groups: individuals who received MMT while incarcerated and continued treatment in the community post-release (n = 161), individuals who terminated MMT involvement upon release (n = 481), and individuals who did not participate in MMT during their incarceration (n = 214). The authors found that individuals who continued engagement in MMT post-release had a 36% lower risk of criminal recidivism, compared to those who did not engage in MMT during their incarceration (AHR = 0.64, 95% CI 0.47–0.88, p < 0.01). No significant difference in recidivism risk was found between those who terminated MMT involvement upon release and those who did not engage in MMT during their incarceration.
Buprenorphine maintenance treatment.
Five studies evaluated the impact of post-release BPN-based treatments on treatment retention, illicit opioid use, and criminal recidivism [70,72,73,76,77]. Springer et al. [76,77] examined data from a group of HIV-positive incarcerated persons with OUD who received BPN/NLX treatment post-release. The authors found high levels of treatment retention, with 91% of participants completing BPN/NLX induction and 74% remaining on treatment after 12 weeks. Participants further reported reduced opioid cravings and consistently high levels of treatment satisfaction at 12 weeks follow-up, and adverse events were found to be mild and few.
A study conducted by Lee et al.  compared treatment retention and opioid misuse among opioid-dependent adults seeking BPN/NLX treatment in the community, including one group of incarcerated persons recently released (n = 32, 22 of whom initiated BPN/NLX while incarcerated) and a second group of patients with no recent incarceration history (n = 110). At 48 weeks, the authors found similar BPN/NLX retention rates among previously incarcerated persons (37%) and general patients (30%). Positive urine test results for opiates, as well as rates of self-reported opioid misuse, were also similar between the 2 groups.
Fox et al.  examined electronic medical record data to determine health outcomes and healthcare utilization among a group of opioid-dependent patients (n = 27) released from the New York State Department of Corrections between 2009 and 2013. At 1-month follow-up, 82% of individuals were retained in BPN/NLX treatment and 44% had reduced opioid use (defined as ≥50% of urine drug test results without opioids). After 6 months of follow-up, 33% of participants were retained on BPN/NLX treatment, and 19% had reduced their opioid use.
Riggins et al.  analyzed data from a cohort of HIV-positive patients diagnosed with opioid dependence who were receiving BMT. Among patients incarcerated in the previous 30 days, those who were retained in BMT had lower rates of subsequent incarceration at 6 months (8.4% versus 27.9%, p < 0.01), 9 months (4.9% versus 20.4%, p < 0.01), and 12 months of follow-up (6.2% versus 24.8%, p < 0.01), compared to those who were not retained in BMT.
Lobmaier et al.  conducted an RCT with 44 incarcerated persons with OUD in Norway comparing treatment outcomes and retention among 2 groups: individuals who received naltrexone implants 1 month prior to release (n = 23) and individuals who received MMT 1 month prior to release (n = 21). After 6 months of follow-up, relapse to heroin use was less likely among the naltrexone group relative to the MMT group (p = 0.012). Moreover, at 6 months follow-up post-release, 69.6% of the participants in the naltrexone implant group remained engaged in the naltrexone treatment, compared to 23.8% in the MMT group (p = 0.003). Rates of re-incarceration during the 6-month follow-up period were comparable across both groups, at 21.7% in the naltrexone group and 23.8% in the MMT group.
Naloxone kit provision.
Three studies evaluated the impact of providing NLX kits to incarcerated persons upon release from a correctional institution, as a strategy to prevent opioid-related overdose deaths [74,75,79]. Parmar et al.  conducted a large-scale RCT among UK incarcerated persons with history of heroin injection (n = 1,557) in order to evaluate the feasibility of providing NLX kits upon prison release to prevent opioid-related overdose. Participants were randomly assigned to either the experimental group, where they received a pack containing a single “rescue” injection of NLX (n = 842), or the control group, where they received a pack containing a placebo injection (n = 843). Randomization was prematurely discontinued as it was found that only one-third of NLX administrations were delivered to former incarcerated persons. The study ultimately included results from 205 former incarcerated persons, with 112 in the experimental group and 93 in the control group. Twenty-one percent of experimental group participants reported administration of NLX to themselves or to someone else before the arrival of a doctor or ambulance, compared to 9% for the control group (p = 0.02).
Bird et al. conducted 2 studies [74,75] to evaluate the impact of Scotland’s implementation of the National Naloxone Program (NNP) for reducing opioid-related deaths, which involved training about NLX administration and distribution of NLX kits to at-risk incarcerated persons upon prison release. The first study assessed data from 2,273 formerly incarcerated persons, and found that post-release opioid-related deaths decreased significantly following the implementation of the program . Between 2006 and 2010—prior to the introduction of the NNP—9.8% of opioid-related deaths were among formerly incarcerated persons within 4 weeks of release (p < 0.001). Between 2011 and 2013—after NNP implementation—6.3% of opioid-related deaths were among formerly incarcerated persons within 4 weeks of release (p < 0.001). Bird et al. conducted a subsequent analysis arriving at similar results: specifically, the authors reported a 60% reduction in the proportion of opioid-related deaths within 4 weeks of prison release from 2006–2010 (i.e., prior to program implementation) to 2014–2015 . Rates of opioid-related deaths within 4 weeks of prison release were 19.8% in 2006–2010, 6.3% in 2011–2013, and 3.9% in 2014–2015, illustrating a continuous decrease in overdose-related deaths among former Scottish incarcerated persons, largely attributed to the introduction of the NNP.
The objective of this systematic review was to describe the impact of opioid-related interventions delivered during and after incarceration among adult correctional populations. A strong evidence base exists emphasizing the positive impact of providing opioid-related interventions to incarcerated persons with OUD, particularly during a continuum of treatment prior to, during, and after incarceration. A key finding in this review is that pharmacological interventions including MMT, BPN/NLX, and NLX have positive impacts on post-release mortality, substance use, treatment adherence, and criminogenic outcomes if treatment is administered during incarceration and continued upon release [35,41,48,52,53,71]. Evidence from this review also suggests that incarcerated individuals who are exposed to OAT in correctional institutions are more likely to be engaged and retained in community-based treatments upon release.
Studies identified the effectiveness of providing opioid-related interventions during a continuum of treatment (before, during, and/or after incarceration), in support of the highly important concept of the “criminal justice continuum of care” for opioid users at risk of overdose, as introduced by Dr. Lauren Brinkley-Rubinstein and colleagues . Our systematic review identified that receiving OAT during incarceration [35,36,51,53,54] was associated with reduced risk of re-incarceration , higher treatment adherence , and reduced mortality risk, both during and after incarceration [35,36,54]. Similarly, receiving MMT was, in general, associated with higher community-based treatment adherence and retention, reduced illicit opioid use, and reduced re-incarceration [38,39,43–45,52]. Receiving BPN while incarcerated [37,40,47] was also associated with higher treatment adherence post-release and lower rates of substance use and re-incarceration, compared with starting BPN treatment post-release . In the same regard, XR-NTX treatment during incarceration [41,48–50,55] was associated with reduced relapse into illicit opioid use [41,48,49], reduced re-arrest likelihood , and fewer hospital admissions , along with higher treatment retention  and reduced overdose events, compared to receiving other treatments, including BPN or MMT . However, the impact of XR-NTX treatment on re-incarceration rates remains unclear and warrants further research and evaluation.
There is also strong evidence from studies analyzing the impact of opioid-related interventions during incarceration. Receiving OAT during incarceration was associated with reduced opioid-related overdose deaths post-incarceration [26,68] and increased community-based treatment entry . Similarly, receiving MMT was associated with better health outcomes , including reduced nonfatal overdoses  and increased treatment adherence and retention [60,62,65,66,67]. Compared to incarcerated individuals undergoing tapered withdrawal from MMT, those who continue receiving MMT while in correctional institutions have reduced illicit opioid use  and higher rates of return to community-based treatment upon release . Compared to incarcerated individuals who received opioid detoxification, individuals who received MMT were less likely to be re-incarcerated . Similar findings were identified among individuals receiving BPN in correctional institutions [56–59], including reduced opioid use , increased treatment adherence , and lower withdrawal symptoms/treatment side effects, compared to those receiving MMT .
Studies evaluating the impact of opioid-related interventions post-incarceration identified that continuation of MMT decreases the risk of both overdose mortality  and re-incarceration [69,71]. Post-incarceration interventions involving BPN treatment also increase addiction treatment adherence, decrease opioid craving, and consequently reduce opioid use [70,72,73,76]. Studies evaluating the impact of naltrexone implants post-incarceration should be conducted with larger sample sizes.
Overall, the review suggests positive effects of pharmacological interventions in mitigating harmful effects of problematic opioid use among the correctional population [35,41,43,48,52,71]. The results are also consistent with observations in evaluations of opioid-related interventions provided to the general population, especially regarding reduced opioid-related mortality. Nonetheless, comparisons of intervention outcomes between these different populations are limited, considering that accessibility to services is more restricted in the correctional population, along with other program delivery and implementation barriers.
In any stage of the criminal justice continuum in which OAT interventions were provided, they were associated to reduced mortality risks [26,35,36,54,68] and higher treatment adherence [53,68]. In the same regard, MMT was found to also increase treatment adherence and retention [38,39,43–45,52,60–62,65–67], reduce re-incarceration [52,60,67,69,71], and decrease overdose mortality when continued post-release . Receiving BPN was found to increase OUD treatment adherence and decrease opioid use [37,40,47,57,70,72,73,76].
Our systematic review, thus, reinforces the positive impact of providing OAT in correctional settings. OAT decreases mortality rates, reduces opioid use, and improves addiction treatment intake and retention post-incarceration. Moreover, interventions such as immediate linkage with OAT services and the provision of preventive interventions (e.g., NLX kits) upon release are effective in decreasing overdose mortality in the often precarious weeks following incarcerated individuals’ release. Findings from this review highlight the positive impact that re-entry programs may have on incarcerated individuals who are transitioning back to the community, especially since the post-release period is characterized by poor continuity of care, inadequate social support, and increased rates of opioid-related overdose and mortality [12,13].
Previous studies have shown that the period immediately following release from jail or prison is a critical time point, during which opioid-related overdose deaths are highly prevalent, often as the result of lowered opioid tolerance developed during the incarceration period [5,6,12]. Our review determined that providing NLX kits to incarcerated individuals upon release from a correctional institution may aid in reducing opioid-related deaths post-release [74,75,79].
There is, however, significant variation across countries related to the criminal justice system, legislation towards addiction, and the healthcare system. While some countries, such as Canada  and Australia , offer OAT to incarcerated persons with OUD, in the US, prisons and jails frequently adopt an abstinence-only approach . This is of great concern, since the US has the highest incarceration rate in the world, with over 2 million incarcerated persons in jails and prisons . Despite the strong evidence of improved health, behavioral, and social outcomes, in 2019 the majority of US jails and prisons did not offer OAT to individuals with diagnosed OUD. According to Dr. Joanne Csete , “Expanding access to treatment of opioid use disorder (OUD) is central to addressing the US overdose mortality crisis.”
Our study corroborates this statement, identifying that incarcerated persons with OUD benefit from OAT, reaching similar levels of treatment adherence, health and social improvements as persons with OUD without incarceration history. Many persons with OUD will continue to be involved in the criminal justice system  given the high rate of addiction relapse, recidivism, and re-incarceration . Legislators, policy makers, public health professionals, researchers, and criminal justice representatives need to work together to address the dual crisis of mass incarceration and opioid-related overdose. The lack of effective treatment and opioid overdose prevention strategies for incarcerated persons with OUD is referred to, by some experts, as an unacceptable human rights violation , representing a key medical and public health concern [12,13,82].
This review has several limitations. First, we did not assess for any risk of biases, as the included studies were heterogeneous in terms of study design and settings, participant characteristics (e.g., type of opioid used, history of opioid use, length of incarceration, time of release from correctional institution), methods of data analysis, and reporting of findings. Receiving or initiating OAT in short-term (jails) versus long-term (prisons) incarceration facilities might affect OAT effectiveness in ways that are beyond the scope of this systematic review, and the impact of OAT provided in these different settings should be further evaluated. Second, the international scope of the review limited the generalizability of results, considering the potential influence of country-specific contexts, such as varied criminal justice systems, drug laws, correctional policies, and healthcare access. Third, the determination of whether there was a meaningful effect for each study outcome was based on statistical significance, which does not necessarily represent clinical or population-level significance. Fourth, considering the differences in program delivery, we excluded any study that focused on individuals involved in other areas of the criminal justice system (e.g., probationers, parolees), which excluded a large number of studies that assessed the effects of treatment and prevention interventions for other criminal-justice-involved individuals with OUD. Moreover, this review does not contain any grey literature; thus, any relevant studies that may been conducted but are not published have been excluded from the results.
In spite of the above limitations, our review reinforces the key benefits of providing opioid-related interventions within correctional settings. Our study also highlights the need to implement and scale up evidence-based strategies to ensure incarcerated individuals with OUD are able to access adequate treatment and care during and post-incarceration. Inadequate linkage to and provision of care for problematic opioid use and OUD immediately post-incarceration continues to serve as a missed opportunity to address the high rates of overdose and mortality typically observed among incarcerated adults living with OUD within the first weeks following release. The delivery of opioid-related interventions in correctional institutions constitutes a unique opportunity to provide treatment for a high-risk sub-group of opioid users, thus contributing to reduced illicit opioid use and high-risk behaviors within correctional settings and in the community.
S1 List of Manuscripts Excluded. List of full-text papers evaluated and excluded.
- 1. Volkow ND, Icaza MEM, Poznyak V, Saxena S, Gerra G, UNODC-WHO Informal Scientific Network. Addressing the opioid crisis globally. World Psychiatry. 2019;18:231–32. pmid:31059614
- 2. Han B, Compton WM, Blanco C, Crane E, Lee J, Jones CM. Prescription opioid use, misuse, and use disorders in U.S. adults: 2015 National Survey on Drug Use and Health. Ann Intern Med. 2017;167:293–301. pmid:28761945
- 3. Government of Canada. Opioid-related harms and deaths in Canada. Ottawa: Government of Canada; 2019 [cited 2019 Jun 4]. https://www.canada.ca/en/health-canada/services/substance-abuse/prescription-drug-abuse/opioids/apparent-opioid-related-deaths.html.
- 4. Substance Abuse and Mental Health Services Administration. Treatment Episode Data Set (TEDS) 2017: admissions to and discharges from publicly-funded substance use treatment. Rockville (MD): Substance Abuse and Mental Health Services Administration; 2019 [cited 2019 Jun 4]. https://www.samhsa.gov/data/sites/default/files/cbhsq-reports/TEDS-2017.pdf.
- 5. Binswanger IA, Blatchford PJ, Mueller SR, Stern MF. Mortality after prison release: opioid overdose and other causes of death, risk factors, and time trends from 1999 to 2009. Ann Intern Med. 2013;159:592–600. pmid:24189594
- 6. Merrall EL, Kariminia A, Binswanger IA, Hobbs MS, Farrell M, Marsden J, et al. Meta-analysis of drug-related deaths soon after release from prison. Addiction. 2010;105:1545–54. pmid:20579009
- 7. Bureau of Justice Statistics. Drug use, dependence, and abuse among state prisoners and jail inmates, 2007–2009. Washington (DC): Bureau of Justice Statistics; 2017 [cited 2019 Jun 4]. https://www.bjs.gov/content/pub/pdf/dudaspji0709.pdf.
- 8. United Nations Office on Drugs and Crime. World drug report 2018. Vienna: United Nations Office on Drugs and Crime; 2018 [cited 2019 Jun 4]. https://www.unodc.org/wdr2018/index.html.
- 9. Simpler AH, Langhinrichsen-Rohling J. Substance use in prison: how much occurs and is it associated with psychopathology? Addict Res Theory. 2005;13(5):503–11.
- 10. Fazel S, Yoon IA, Hayes AJ. Substance use disorders in prisoners: an updated systematic review and meta-regression analysis in recently incarcerated men and women. Addiction. 2017;112:1725–39. pmid:28543749
- 11. Belenko S, Hiller M, Hamilton L. Treating substance use disorders in the criminal justice system. Curr Psychiatry Rep. 2013;15(11):414. pmid:24132733
- 12. Csete J. Criminal justice barriers to treatment of opioid use disorders in the United States: the need for public health advocacy. Am J Public Health. 2019;109:419–22. pmid:30676805
- 13. Brinkley-Rubinstein L, Zaller N, Martino S, Cloud DH, McCauley E, Heise A, et al. Criminal justice continuum for opioid users at risk of overdose. Addict Behav. 2018;86:104–10. pmid:29544869
- 14. Babor T, Caulkins J, Fischer B, Foxcroft D, Humphreys K, Medina-mora ME, et al. Drug policy and the public good. Oxford: Oxford University Press; 2018.
- 15. Binswanger IA, Stern MF, Deyo RA, Heagerty PJ, Cheadle A, Elmore JG, et al. Release from prison—a high risk of death for former inmates. N Engl J Med. 2007;356:157–65. pmid:17215533
- 16. Kinner SA, Milloy MJ, Wood E, Qi J, Zhang R, Kerr T. Incidence and risk factors for non-fatal overdose among a cohort of recently incarcerated illicit drug users. Addict Behav. 2012;37:691–6. pmid:22385733
- 17. Calzavara LM, Burchell AN, Schlossberg J, Myers T, Escobar M, Wallace E, et al. Prior opiate injection and incarceration history predict injection drug use among inmates. Addiction. 2003;98:1257–65. pmid:12930213
- 18. Werb D, Kerr T, Small W, Li K, Montaner J, Wood E. HIV risks associated with incarceration among injection drug users: implications for prison-based public health strategies. J Public Health (Oxf). 2008;30:126–32.
- 19. Sordo L, Barrio G, Bravo MJ, Indave BI, Degenhardt L, Wiessing L, et al. Mortality risk during and after opioid substitution treatment: systematic review and meta-analysis of cohort studies. BMJ. 2017;357:j1550. pmid:28446428
- 20. Ma J, Bao YP, Wang RJ, Su MF, Liu MX, Li JQ, et al. Effects of medication-assisted treatment on mortality among opioids users: a systematic review and meta-analysis. Mol Psychiatry. 2018 Jun 22. pmid:29934549
- 21. Sander G, Scandurra A, Kamenska A, MacNamara C, Kalpaki C, Bessa CF, et al. Overview of harm reduction in prisons in seven European countries. Harm Reduct J. 2016;13:28. pmid:27717368
- 22. Friedmann PD, Hoskinson R, Gordon M, Schwartz R, Kinlock T, Knight K, et al. Medication-assisted treatment in criminal justice agencies affiliated with the Criminal Justice–Drug Abuse Treatment Studies (CJ-DATS): availability, barriers, and intentions. Subst Abus. 2012;33:9–18. pmid:22263709
- 23. Kouyoumdjian FG, Patel A, To MJ, Kiefer L, Regenstreif L. Physician prescribing of opioid agonist treatments in provincial correctional facilities in Ontario, Canada: a survey. PLoS ONE. 2018;13(2):e0192431. pmid:29447177
- 24. McKenzie M, Nunn A, Zaller ND, Bazazi AR, Rich JD. Overcoming obstacles to implementing methadone maintenance therapy for prisoners: implications for policy and practice. J Opioid Manag. 2009;5:219–27. pmid:19736902
- 25. Hedrich D, Alves P, Farrell M, Stover H, Moller L, Mayet S. The effectiveness of opioid maintenance treatment in prison settings: a systematic review. Addiction. 2012;107:501–17. pmid:21955033
- 26. Green TC, Clarke J, Brinkley-Rubinstein L, Marshall BDL, Alexander-Scott N, Boss R, et al. Postincarceration fatal overdoses after implementing medications for addiction treatment in a statewide correctional system. JAMA Psychiatry. 2018;75:405–7. pmid:29450443
- 27. Moore KE, Roberts W, Reid HH, Smith KMZ, Oberleitner LMS, McKee SA. Effectiveness of medication assisted treatment for opioid use in prison and jail settings: a meta-analysis and systematic review. J Subst Abuse Treat. 2019;99:32–43. pmid:30797392
- 28. Kouyoumdjian FG, McIsaac KE, Liauw J, Green S, Karachiwalla F, Siu W, et al. A systematic review of randomized controlled trials of interventions to improve the health of persons during imprisonment and in the year after release. Am J Public Health. 2015;105(4):e13–33. pmid:25713970
- 29. Fazel S, Hayes AJ, Bartellas K, Clerici M, Trestman R. Mental health of prisoners: prevalence, adverse outcomes, and interventions. Lancet Psychiatry. 2016;3:871–81. pmid:27426440
- 30. Kouyoumdjian F, Schuler A, Matheson FI, Hwang SW. Health status of prisoners in Canada: narrative review. Can Fam Physician. 2016;62:215–22. pmid:27427562
- 31. Larney S, Dolan K. A literature review of international implementation of opioid substitution treatment in prisons: equivalence of care? Eur Addict Res. 2009;15:107–12. pmid:19182485
- 32. Higgins JPT, Thomas J, Chandler J, Cumpston M, Li T, Page MJ, et al., editors. Cochrane handbook for systematic reviews of interventions. Version 6.0, 2019. Cochrane Collaboration; 2019 [cited 2019 Nov 22]. https://www.training.cochrane.org/handbook.
- 33. Moher D, Liberati A, Tetzlaff J, Altman DG. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann Intern Med. 2009;151(4):264–9. pmid:19622511
- 34. Joanna Briggs Institute. Critical appraisal tools. Adelaide: Joanna Briggs Institute; 2019 [cited 2019 Jun 4]. https://joannabriggs.org/critical_appraisal_tools.
- 35. Degenhardt L, Larney S, Kimber J, Gisev N, Farrell M, Dobbins T, et al. The impact of opioid substitution therapy on mortality post-release from prison: retrospective data linkage study. Addiction. 2014;109(8):1306–17. pmid:24612249
- 36. Larney S, Gisev N, Farrell M, Dobbins T, Burns L, Gibson A, et al. Opioid substitution therapy as a strategy to reduce deaths in prison: retrospective cohort study. BMJ Open. 2014;4(4):e004666. pmid:24694626
- 37. Gordon MS, Kinlock TW, Schwartz RP, Fitzgerald TT, O’Grady KE, Vocci FJ. A randomized controlled trial of prison-initiated buprenorphine: prison outcomes and community treatment entry. Drug Alcohol Depend. 2014;142:33–40. pmid:24962326
- 38. Gordon MS, Kinlock TW, Couvillion KA, Schwartz RP, O’Grady K. A randomized clinical trial of methadone maintenance for prisoners: prediction of treatment entry and completion in prison. J Offender Rehabil. 2012;51(4):222–38. pmid:25392605
- 39. Gordon MS, Kinlock TW, Schwartz RP, O’Grady KE. A randomized clinical trial of methadone maintenance for prisoners: findings at 6 months post-release. Addiction. 2008;103(8):1333–42. pmid:18855822
- 40. Gordon MS, Kinlock TW, Schwartz RP, O’Grady KE, Fitzgerald TT, Vocci FJ. A randomized clinical trial of buprenorphine for prisoners: findings at 12-months post-release. Drug Alcohol Depend. 2017;172:34–42. pmid:28107680
- 41. Gordon MS, Kinlock TW, Vocci FJ, Fitzgerald TT, Memisoglu A, Silverman B. A phase 4, pilot, open-label study of VIVITROL(R) (extended-release naltrexone XR-NTX) for prisoners. J Subst Abuse Treat. 2015;59:52–8. pmid:26299956
- 42. Gordon MS, Blue TR, Couvillion K, Schwartz RP, O’Grady KE, Fitzgerald TT, et al. Initiating buprenorphine treatment prior to versus after release from prison: arrest outcomes. Drug Alcohol Depend. 2018;188:232–8. pmid:29783095
- 43. Kinlock TW, Gordon MS, Schwartz RP, O’Grady KE. A study of methadone maintenance for male prisoners: 3-month postrelease outcomes. Crim Justice Behav. 2008;35(1):34–47. pmid:18612373
- 44. Kinlock TW, Gordon MS, Schwartz RP, Fitzgerald TT, O’Grady KE. A randomized clinical trial of methadone maintenance for prisoners: results at 12 months postrelease. J Subst Abuse Treat. 2009;37(3):277–85. pmid:19339140
- 45. Kinlock TW, Gordon MS, Schwartz RP, O’Grady KE. Individual patient and program factors related to prison and community treatment completion in prison-initiated methadone maintenance treatment. J Offender Rehabil. 2013;52(8):509–28. pmid:25580067
- 46. McKenzie M, Zaller N, Dickman SL, Green TC, Parihk A, Friedmann PD, et al. A randomized trial of methadone initiation prior to release from incarceration. Subst Abus. 2012;33(1):19–29. pmid:22263710
- 47. Zaller N, McKenzie M, Friedmann PD, Green TC, McGowan S, Rich JD. Initiation of buprenorphine during incarceration and retention in treatment upon release. J Subst Abuse Treat. 2013;45(2):222–6. pmid:23541303
- 48. Lee JD, Friedmann PD, Kinlock TW, Nunes EV, Boney TY, Hoskinson RA Jr, et al. Extended-release naltrexone to prevent opioid relapse in criminal justice offenders. N Engl J Med. 2016;374:1232–42. pmid:27028913
- 49. Friedmann PD, Wilson D, Hoskinson R Jr, Poshkus M, Clarke JG. Initiation of extended release naltrexone (XR-NTX) for opioid use disorder prior to release from prison. J Subst Abuse Treat. 2018;85:45–8. pmid:28527855
- 50. Soares WE 3rd, Wilson D, Rathlev N, Lee JD, Gordon M, Nunes EV, et al. Healthcare utilization in adults with opioid dependence receiving extended release naltrexone compared to treatment as usual. J Subst Abuse Treat. 2018;85:66–9. pmid:28576389
- 51. Larney S, Toson B, Burns L, Dolan K. Effect of prison-based opioid substitution treatment and post-release retention in treatment on risk of re-incarceration. Addiction. 2012;107:372–80. pmid:21851442
- 52. Farrell-MacDonald S, MacSwain MA, Cheverie M, Tiesmaki M, Fischer B. Impact of methadone maintenance treatment on women offenders’ post-release recidivism. Eur Addict Res. 2014;20(4):192–9. pmid:24513717
- 53. Larney S, Lai W, Dolan K, Zador D. Monitoring a prison opioid treatment program over a period of change to clinical governance arrangements, 2007–2013. J Subst Abuse Treat. 2016;70:58–63. pmid:27692189
- 54. Bird SM, Fischbacher CM, Graham L, Fraser A. Impact of opioid substitution therapy for Scotland’s prisoners on drug-related deaths soon after prisoner release. Addiction. 2015;110:1617–24. pmid:25940815
- 55. Lincoln T, Johnson BD, McCarthy P, Alexander E. Extended-release naltrexone for opioid use disorder started during or following incarceration. J Subst Abuse Treat. 2018;85:97–100. pmid:28479011
- 56. Sheard L, Wright NM, El-Sayeh HG, Adams CE, Li R, Tompkins CN. The Leeds Evaluation of Efficacy of Detoxification Study (LEEDS) prisons project: a randomised controlled trial comparing dihydrocodeine and buprenorphine for opiate detoxification. Subst Abuse Treat Prev Policy. 2009;4:1. pmid:19196468
- 57. Magura S, Lee JD, Hershberger J, Joseph H, Marsch L, Shropshire C, et al. Buprenorphine and methadone maintenance in jail and post-release: a randomized clinical trial. Drug Alcohol Depend. 2009;99:222–30. pmid:18930603
- 58. Awgu E, Magura S, Rosenblum A. Heroin-dependent inmates’ experiences with buprenorphine or methadone maintenance. J Psychoactive Drugs. 2010;42(3):339–46. pmid:21053756
- 59. Wright NM, Sheard L, Adams CE, Rushforth BJ, Harrison W, Bound N, et al. Comparison of methadone and buprenorphine for opiate detoxification (LEEDS trial): a randomised controlled trial. Br J Gen Pract. 2011;61(593):e772–80. pmid:22137413
- 60. Rich JD, McKenzie M, Larney S, Wong JB, Tran L, Clarke J, et al. Methadone continuation versus forced withdrawal on incarceration in a combined US prison and jail: a randomised, open-label trial. Lancet. 2015;386:350–9. pmid:26028120
- 61. Brinkley-Rubinstein L, McKenzie M, Macmadu A, Larney S, Zaller N, Dauria E, et al. A randomized, open label trial of methadone continuation versus forced withdrawal in a combined US prison and jail: findings at 12 months post-release. Drug Alcohol Depend. 2018;184:57–63. pmid:29402680
- 62. Moore KE, Oberleitner L, Smith KMZ, Maurer K, McKee SA. Feasibility and effectiveness of continuing methadone maintenance treatment during incarceration compared with forced withdrawal. J Addict Med. 2018;12:156–62. pmid:29341974
- 63. McMillan GP, Lapham S, Lackey M. The effect of a jail methadone maintenance therapy (MMT) program on inmate recidivism. Addiction. 2008;103:2017–23. pmid:19469745
- 64. Marzo JN, Rotily M, Meroueh F, Varastet M, Hunault C, Obradovic I, et al. Maintenance therapy and 3-year outcome of opioid-dependent prisoners: a prospective study in France (2003–06). Addiction. 2009;104:1233–40. pmid:19426291
- 65. Wickersham JA, Zahari MM, Azar MM, Kamarulzaman A, Altice FL. Methadone dose at the time of release from prison significantly influences retention in treatment: implications from a pilot study of HIV-infected prisoners transitioning to the community in Malaysia. Drug Alcohol Depend. 2013;132:378–82. pmid:23414931
- 66. Wickersham JA, Marcus R, Kamarulzaman A, Zahari MM, Altice FL. Implementing methadone maintenance treatment in prisons in Malaysia. Bull World Health Organ. 2013;91:124–9. pmid:23554524
- 67. Westerberg VS, McCrady BS, Owens M, Guerin P. Community-based methadone maintenance in a large detention center is associated with decreases in inmate recidivism. J Subst Abuse Treat. 2016;70:1–6. pmid:27692182
- 68. Marsden J, Stillwell G, Jones H, Cooper A, Eastwood B, Farrell M, et al. Does exposure to opioid substitution treatment in prison reduce the risk of death after release? A national prospective observational study in England. Addiction. 2017;112:1408–18. pmid:28160345
- 69. Huang YF, Kuo HS, Lew-Ting CY, Tian F, Yang CH, Tsai TI, et al. Mortality among a cohort of drug users after their release from prison: an evaluation of the effectiveness of a harm reduction program in Taiwan. Addiction. 2011;106:1437–45. pmid:21438941
- 70. Lee JD, Grossman E, Truncali A, Rotrosen J, Rosenblum A, Magura S, et al. Buprenorphine-naloxone maintenance following release from jail. Subst Abus. 2012;33:40–7. pmid:22263712
- 71. Macswain M-A, Farrell-MacDonald S, Cheverie M, Fischer B. Assessing the impact of methadone maintenance treatment (MMT) on post-release recidivism among male federal correctional inmates in Canada. Crim Justice Behav. 2014;41:380–94.
- 72. Fox AD, Anderson MR, Bartlett G, Valverde J, Starrels JL, Cunningham CO. Health outcomes and retention in care following release from prison for patients of an urban post-incarceration transitions clinic. J Health Care Poor Underserved. 2014;25:1139–52. pmid:25130230
- 73. Riggins DP, Cunningham CO, Ning Y, Fox AD. Recent incarceration and buprenorphine maintenance treatment outcomes among human immunodeficiency virus-positive patients. Subst Abus. 2017;38:297–302. pmid:27715904
- 74. Bird SM, McAuley A, Perry S, Hunter C. Effectiveness of Scotland’s National Naloxone Programme for reducing opioid-related deaths: a before (2006–10) versus after (2011–13) comparison. Addiction. 2016;111:883–91. pmid:26642424
- 75. Bird SM, McAuley A, Munro A, Hutchinson SJ, Taylor A. Prison-based prescriptions aid Scotland’s National Naloxone Programme. Lancet. 2017;389:1005–6. pmid:28290986
- 76. Springer SA, Chen S, Altice FL. Improved HIV and substance abuse treatment outcomes for released HIV-infected prisoners: the impact of buprenorphine treatment. J Urban Health. 2010;87:592–602. pmid:20177974
- 77. Springer SA, Qiu J, Saber-Tehrani AS, Altice FL. Retention on buprenorphine is associated with high levels of maximal viral suppression among HIV-infected opioid dependent released prisoners. PLoS ONE. 2012;7(5):e38335. pmid:22719814
- 78. Lobmaier PP, Kunoe N, Gossop M, Katevoll T, Waal H. Naltrexone implants compared to methadone: outcomes six months after prison release. Eur Addict Res. 2010;16:139–45. pmid:20424458
- 79. Parmar MK, Strang J, Choo L, Meade AM, Bird SM. Randomized controlled pilot trial of naloxone-on-release to prevent post-prison opioid overdose deaths. Addiction. 2017;112(3):502–15. pmid:27776382
- 80. Wildeman C, Wang EA. Mass incarceration, public health, and widening inequality in the USA. Lancet. 2017;389:1464–147. pmid:28402828
- 81. Bone C, Eysenbach L, Bell K, Barry DT. Our Ethical obligation to treat opioid use disorder in prisons: a patient and physician’s perspective. J Law Med Ethics. 2018;46:268–71. pmid:30146992
- 82. Binswanger IA. Opioid use disorder and incarceration—hope for ensuring the continuity of treatment. N Engl J Med. 2019;380:1193–5. pmid:30811904