Division of Infectious Diseases, Department of Medicine, Duke University School of Medicine, P.O. Box 102359, Durham, NC, 27710, USA.
Department of Population Health Sciences, Duke University School of Medicine, Durham, NC, USA.
Harm Reduct J. 2024 Mar 26;21(1):69. doi: 10.1186/s12954-024-00983-2.
People who inject drugs (PWID) are at high risk for opioid overdose and infectious diseases including HIV. We piloted PARTNER UP, a telemedicine-based program to provide PWID with medication for opioid use disorder (MOUD) with buprenorphine/naloxone (bup/nx) and oral pre-exposure prophylaxis (PrEP) with tenofovir disoproxil fumarate/emtricitabine through two syringe services programs (SSP) in North Carolina. We present overall results from this project, including participant retention rates and self-reported medication adherence.
Study participants met with a provider for an initial in-person visit at the SSP, followed by weekly telemedicine visits in month 1 and then monthly until program end at month 6. Participants were asked to start both MOUD and PrEP at initiation but could choose to discontinue either at any point during the study. Demographics and health history including substance use, sexual behaviors, and prior use of MOUD/PrEP were collected at baseline. Follow-up surveys were conducted at 3- and 6-months to assess attitudes towards MOUD and PrEP, change in opioid use and sexual behaviors, and for self-reported medication adherence. Participant retention was measured by completion of visits; provider notes were used to assess whether the participant reported continuation of medication.
Overall, 17 persons were enrolled and started on both bup/nx and PrEP; the majority self-identified as white and male. At 3 months, 13 (76%) remained on study; 10 (77%) reported continuing with both MOUD and PrEP, 2 (15%) with bup/nx only, and 1 (8%) with PrEP only. At 6 months, 12 (71%) remained on study; 8 (67%) reported taking both bup/nx and PrEP, and 4 (33%) bup/nx only. Among survey participants, opioid use and HIV risk behaviors decreased. Nearly all reported taking bup/nx daily; however, self-reported daily adherence to PrEP was lower and declined over time. The most common reason for not continuing PrEP was feeling not at risk for acquiring HIV.
Our study results show that MOUD and PrEP can be successfully administered via telemedicine in SSPs. PrEP appears to be a lower priority for participants with decreased continuation and adherence. Low perception of HIV risk was a reason for not continuing PrEP, possibly mitigated by MOUD use. Future studies including helping identify PWID at highest need for PrEP are needed.
Providing Suboxone and PrEP Using Telemedicine, NCT04521920. Registered 18 August 2020. https://clinicaltrials.gov/study/NCT04521920?term=mehri%20mckellar&rank=2 .
注射毒品者(PWID)存在阿片类药物过量和包括艾滋病毒在内的传染病的高风险。我们试点了 PARTNER UP,这是一个基于远程医疗的项目,通过北卡罗来纳州的两个注射器服务项目(SSP)为 PWID 提供丁丙诺啡/纳洛酮(丁丙诺啡/纳洛酮)和替诺福韦二吡呋酯/恩曲他滨的口服暴露前预防(PrEP),以治疗阿片类药物使用障碍(MOUD)。我们目前正在介绍该项目的总体结果,包括参与者保留率和自我报告的药物依从性。
研究参与者在 SSP 与提供者进行了首次面对面就诊,然后在第 1 个月进行每周的远程医疗就诊,然后每月进行一次,直到第 6 个月项目结束。参与者在开始时被要求同时开始使用 MOUD 和 PrEP,但在研究期间的任何时候都可以选择停止使用任何一种药物。在基线时收集了人口统计学和健康史,包括药物使用、性行为和之前使用 MOUD/PrEP 的情况。在 3 个月和 6 个月时进行了后续调查,以评估对 MOUD 和 PrEP 的态度、阿片类药物使用和性行为的变化,以及自我报告的药物依从性。参与者保留率通过完成就诊来衡量;使用提供者的记录来评估参与者是否报告继续使用药物。
总体而言,有 17 人入组并开始同时使用丁丙诺啡/纳洛酮和 PrEP;大多数人自我认定为白人且为男性。在 3 个月时,有 13 人(76%)仍在研究中;10 人(77%)报告继续同时使用 MOUD 和 PrEP,2 人(15%)仅使用丁丙诺啡/纳洛酮,1 人(8%)仅使用 PrEP。在 6 个月时,有 12 人(71%)仍在研究中;8 人(67%)报告同时使用丁丙诺啡/纳洛酮和 PrEP,4 人(33%)仅使用丁丙诺啡/纳洛酮。在调查参与者中,阿片类药物使用和艾滋病毒风险行为减少。几乎所有人都报告每天服用丁丙诺啡/纳洛酮;然而,自我报告的 PrEP 每日依从性较低,且随时间下降。不继续使用 PrEP 的最常见原因是感觉不会感染艾滋病毒。
我们的研究结果表明,MOUD 和 PrEP 可以通过 SSP 中的远程医疗成功实施。PrEP 似乎是参与者的次要优先事项,因为参与者的持续使用和依从性降低。对艾滋病毒风险的低认识是不继续使用 PrEP 的一个原因,这可能通过 MOUD 的使用而得到缓解。未来的研究包括帮助确定最需要 PrEP 的 PWID 是必要的。
使用远程医疗提供丁丙诺啡和 PrEP,NCT04521920。2020 年 8 月 18 日注册。https://clinicaltrials.gov/study/NCT04521920?term=mehri%20mckellar&rank=2。