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南部非洲年轻女性中预防用药(PrEP)的接受率、持续率、依从性,以及回顾性药物水平反馈对 PrEP 依从性的影响:来自 HPTN 082 的随机对照试验结果。

PrEP uptake, persistence, adherence, and effect of retrospective drug level feedback on PrEP adherence among young women in southern Africa: Results from HPTN 082, a randomized controlled trial.

机构信息

Departments of Global Health, Medicine, and Epidemiology, University of Washington, Seattle, Washington, United States of America.

Department of Psychiatry, Stroger Hospital of Cook County, Chicago, Illinois, United States of America.

出版信息

PLoS Med. 2021 Jun 18;18(6):e1003670. doi: 10.1371/journal.pmed.1003670. eCollection 2021 Jun.


DOI:10.1371/journal.pmed.1003670
PMID:34143779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8253429/
Abstract

BACKGROUND: Pre-exposure prophylaxis (PrEP) is highly effective and an important prevention tool for African adolescent girls and young women (AGYW), but adherence and persistence are challenging. PrEP adherence support strategies for African AGYW were studied in an implementation study. METHODS AND FINDINGS: HIV Prevention Trials Network (HPTN) 082 was conducted in Cape Town, Johannesburg (South Africa) and Harare (Zimbabwe) from October 2016 to October 2018 to evaluate PrEP uptake, persistence, and the effect of drug level feedback on adherence. Sexually active HIV-negative women ages 16-25 were offered PrEP and followed for 12 months; women who accepted PrEP were randomized to standard adherence support (counseling, 2-way SMS, and adherence clubs) or enhanced adherence support with adherence feedback from intracellular tenofovir-diphosphate (TFV-DP) levels in dried blood spots (DBS). PrEP uptake, persistence through 12 months (no PrEP hold or missed visits), and adherence were assessed. The primary outcome was high adherence (TFV-DP ≥700 fmol/punch) at 6 months, compared by study arm. Of 451 women enrolled, median age was 21 years, and 39% had curable sexually transmitted infections (STIs). Most (95%) started PrEP, of whom 55% had uninterrupted PrEP refills through 12 months. Of those with DBS, 84% had detectable TFV-DP levels at month 3, 57% at month 6, and 31% at month 12. At 6 months, 36/179 (21%) of AGYW in the enhanced arm had high adherence and 40/184 (22%) in the standard adherence support arm (adjusted odds ratio [OR] of 0.92; 95% confidence interval [CI] 0.55, 1.34; p = 0.76). Four women acquired HIV (incidence 1.0/100 person-years), with low or undetectable TFV-DP levels at or prior to seroconversion, and none of whom had tenofovir or emtricitabine resistance mutations. The study had limited power to detect a modest effect of drug level feedback on adherence, and there was limited awareness of PrEP at the time the study was conducted. CONCLUSIONS: In this study, PrEP initiation was high, over half of study participants persisted with PrEP through month 12, and the majority of young African women had detectable TFV-DP levels through month 6 with one-fifth having high adherence. Drug level feedback in the first 3 months of PrEP use did not increase the proportion with high adherence at month 6. HIV incidence was 1% in this cohort with 39% prevalence of curable STIs and moderate PrEP adherence. Strategies to support PrEP use and less adherence-dependent formulations are needed for this population. TRIAL REGISTRATION: ClinicalTrials.gov NCT02732730.

摘要

背景:暴露前预防(PrEP)对非洲青少年女孩和年轻女性(AGYW)非常有效,是一种重要的预防工具,但坚持和持久使用是具有挑战性的。在一项实施研究中,研究了针对非洲 AGYW 的 PrEP 依从性支持策略。

方法和发现:HIV 预防试验网络(HPTN)082 于 2016 年 10 月至 2018 年 10 月在开普敦、约翰内斯堡(南非)和哈拉雷(津巴布韦)进行,旨在评估 PrEP 的采用、持续使用情况,以及药物水平反馈对依从性的影响。年龄在 16-25 岁之间、有性行为的 HIV 阴性女性被提供 PrEP,并随访 12 个月;接受 PrEP 的女性被随机分配到标准依从性支持(咨询、双向短信和依从俱乐部)或增强的依从性支持,后者提供通过干血斑(DBS)中细胞内替诺福韦二磷酸(TFV-DP)水平提供的依从性反馈。评估 PrEP 的采用、12 个月内的持续使用情况(无 PrEP 暂停或错过就诊)和依从性。主要结局是在第 6 个月时,与研究臂相比,达到高依从性(TFV-DP≥700fmol/针刺)。在 451 名入组的女性中,中位年龄为 21 岁,39%患有可治愈的性传播感染(STI)。大多数(95%)开始使用 PrEP,其中 55%在 12 个月内无中断地接受 PrEP 续药。在有 DBS 的女性中,84%在第 3 个月时可检测到 TFV-DP 水平,57%在第 6 个月时可检测到,31%在第 12 个月时可检测到。在第 6 个月时,增强依从性支持臂中的 36/179(21%)AGYW 达到高依从性,标准依从性支持臂中的 40/184(22%)(调整后的优势比[OR]为 0.92;95%置信区间[CI]为 0.55,1.34;p=0.76)。有 4 名女性感染了 HIV(发病率为 1.0/100 人年),在血清转换时或之前,她们的 TFV-DP 水平低或无法检测到,而且都没有发现替诺福韦或恩曲他滨耐药突变。该研究检测药物水平反馈对依从性的适度影响的能力有限,并且在研究进行时对 PrEP 的认识有限。

结论:在这项研究中,PrEP 的起始率很高,超过一半的研究参与者在第 12 个月时持续使用 PrEP,大多数年轻的非洲女性在第 6 个月时可检测到 TFV-DP 水平,其中五分之一达到了高依从性。在 PrEP 使用的前 3 个月内提供药物水平反馈并没有增加第 6 个月时高依从性的比例。在这一队列中,HIV 发病率为 1%,可治愈的 STI 患病率为 39%,PrEP 的依从性中等。需要针对这一人群制定支持 PrEP 使用和减少依赖依从性的制剂的策略。

试验注册:ClinicalTrials.gov NCT02732730。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec3/8253429/26ccbeb4aab9/pmed.1003670.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec3/8253429/64e3ee60a241/pmed.1003670.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec3/8253429/da0ad4efdb75/pmed.1003670.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec3/8253429/26ccbeb4aab9/pmed.1003670.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec3/8253429/64e3ee60a241/pmed.1003670.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec3/8253429/da0ad4efdb75/pmed.1003670.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ec3/8253429/26ccbeb4aab9/pmed.1003670.g003.jpg

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