2018
DOI: 10.1097/qai.0000000000001634
|View full text |Cite
|
Sign up to set email alerts
|

Extended-Release Naltrexone Improves Viral Suppression Among Incarcerated Persons Living With HIV With Opioid Use Disorders Transitioning to the Community: Results of a Double-Blind, Placebo-Controlled Randomized Trial

Abstract: XR-NTX improves or maintains VS after release to the community for incarcerated people living with HIV with OUD.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

3
68
0

Year Published

2019
2019
2023
2023

Publication Types

Select...
5
2

Relationship

3
4

Authors

Journals

citations
Cited by 70 publications
(71 citation statements)
references
References 52 publications
(69 reference statements)
3
68
0
Order By: Relevance
“…Those who received XR-NTX were more likely to maintain or improve to viral suppression at 6 months (31 to 56.7%, p = 0.001) as compared to those who received placebo (42 to 30.3%, p = 0.292). The 6-month between-group analysis also demonstrated that those who received XR-NTX had a greater proportion with viral suppression (56.7%) as compared to the placebo group (30.3%, p = 0.015), and receipt of XR-NTX was associated with viral suppression at 6 months in multivariate regression analysis (AOR 4.54 (95% CI, 1.43–14.43, p = 0.009) [12•]. The other double-blind, placebo-controlled trial of XR-NTX among PLH with OUD released from prison and jail had 98 participants also randomized in 2:1 fashion (XR-NTX: placebo) with the same design as the previously mentioned study.…”
Section: Naltrexonementioning
confidence: 98%
See 3 more Smart Citations
“…Those who received XR-NTX were more likely to maintain or improve to viral suppression at 6 months (31 to 56.7%, p = 0.001) as compared to those who received placebo (42 to 30.3%, p = 0.292). The 6-month between-group analysis also demonstrated that those who received XR-NTX had a greater proportion with viral suppression (56.7%) as compared to the placebo group (30.3%, p = 0.015), and receipt of XR-NTX was associated with viral suppression at 6 months in multivariate regression analysis (AOR 4.54 (95% CI, 1.43–14.43, p = 0.009) [12•]. The other double-blind, placebo-controlled trial of XR-NTX among PLH with OUD released from prison and jail had 98 participants also randomized in 2:1 fashion (XR-NTX: placebo) with the same design as the previously mentioned study.…”
Section: Naltrexonementioning
confidence: 98%
“…This study suggests the risk of hepatotoxicity is minimal in HIV-infected participants treated with naltrexone, and that there are no adverse immunologic or virologic effects of treatment. The safety of extended-released naltrexone (XR-NTX) is further demonstrated in PLH randomized to XR-NTX following release from prison, who experienced no change in hepatic enzymes compared to those receiving placebo in two double-blind, placebo-controlled randomized trials in PLH with alcohol use disorders and those with opioid use disorders [41], nor in the completed trials themselves [12, 42, 43]. HIV/HCV co-infection has no effect on XR-NTX hepatic safety [44].…”
Section: Naltrexonementioning
confidence: 99%
See 2 more Smart Citations
“…Evidence-based treatment of substance use disorders especially with medication-assisted treatments is seldom available, and in the absence of treatment, relapse is near-universal and undermine HIV care postrelease [25 ■■ ,62,67]. Unequivocal strategies that link relapse prevention using methadone [69,70], or buprenorphine [71,72] are recommended with newer emergent strategies using extended-release naltrexone that not only reduce opioid use in released prisoners [73], but also significantly improves HIV outcomes in released prisoners with HIV with alcohol [74] and opioid [75] dependence using placebo-controlled designs [76,77].…”
Section: Treatment Of Hiv and Hepatitis C Virus In Prisonmentioning
confidence: 99%