Initiation and continued use of oral pre-exposure prophylaxis among pregnant and postpartum women in South Africa (PrEP-PP): a demonstration cohort study.

IF 12.8 1区 医学 Q1 IMMUNOLOGY
Dvora Leah Joseph Davey, Rufaro Mvududu, Nyiko Mashele, Kalisha Bheemraj, Nehaa Khadka, Leigh F Johnson, Sarah Schoetz Dean, Pamina Gorbach, Linda-Gail Bekker, Thomas J Coates, Landon Myer
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引用次数: 0

Abstract

Background: When used effectively, oral pre-exposure prophylaxis (PrEP; tenofovir disoproxil fumarate and emtricitabine) prevents maternal HIV acquisition and reduces the risk of vertical transmission. Our study aimed to better understand PrEP initiation, continued use, and adherence in pregnant and postpartum women.

Methods: The PrEP in Pregnancy and Postpartum (PrEP-PP) study is a demonstration cohort study that enrolled pregnant women aged 16 years and older without HIV attending their first antenatal care visit in Cape Town, South Africa, between Aug 29, 2019, and Oct 10, 2021. Eligible, consenting women were followed up quarterly up to 12 months postpartum with regular HIV testing and offer of PrEP with ongoing adherence counselling. The primary outcome was distribution of women across the PrEP cascade (ie, initiation and continuation up to 12 months postpartum) with crude and adjusted hazard ratios (HRs). We also report on HIV incidence by pregnancy and postpartum status.

Findings: Overall, 1195 pregnant women were recruited and followed up (median age 26 years, IQR 23-31; median gestational age 21 weeks, IQR 15-31); 1009 (84·4%) started PrEP at enrolment. Among women who initiated PrEP at enrolment, 668 (67·5%) of 990 continued PrEP at the 1-month follow-up, 485 (49·9%) of 972 continued at 3 months, 392 (39·4%) of 994 at 6 months, and 275 (27·4%) of 1005 at 12 months. Of 186 women who did not accept PrEP at enrolment, 70 (37·6%) of 186 subsequently initiated PrEP. Overall, 200 (18·6%) of 1076 women continued PrEP at 12 months postpartum. Of 186 women who did not initiate PrEP at baseline, 70 (37·6%) subsequently initiated PrEP during the study. Factors associated with PrEP discontinuation up to 12 months postpartum included being married or cohabiting (adjusted HR 1·32, 95% CI 1·16-1·50), condomless sex since last visit (1·43, 1·23-1·65), reporting intimate partner violence (2·03, 1·59-2·59), or depression in the past 12 months (1·53, 1·14-2·05). Overall, 16 women seroconverted over 1673·8 woman-years (HIV incidence rate 0·96 per 100 woman-years, 95% CI 0·49-1·42); 14 discontinued PrEP use and two never initiated PrEP. HIV incidence was 0·28 per 100 woman-years during pregnancy (95% CI 0·22-0·33), and the incidence rate ratio was 1·77 per 100 woman-years (0·53-5·90) 0-6 months postpartum and 2·19 per 100 woman-years (0·61-7·83) 6-12 months postpartum compared with pregnant women.

Interpretation: There is an urgent need for the integration of PrEP into antenatal and postnatal care and interventions that address barriers to continued use, including targeted counselling during pregnancy and postpartum to reduce PrEP discontinuation.

Funding: National Institute of Mental Health and Fogarty International, US National Institutes of Health.

Translation: For the French translation of the abstract see Supplementary Materials section.

南非孕妇和产后妇女开始和继续使用口服暴露前预防药物(PrEP-PP):一项示范性队列研究。
背景:如果有效使用口服暴露前预防药物(PrEP;富马酸替诺福韦二吡呋酯和恩曲他滨),可预防孕产妇感染艾滋病毒并降低垂直传播的风险。我们的研究旨在更好地了解孕妇和产后妇女开始、继续使用和坚持使用 PrEP 的情况:妊娠期和产后 PrEP(PrEP-PP)研究是一项示范性队列研究,该研究招募了 2019 年 8 月 29 日至 2021 年 10 月 10 日期间在南非开普敦接受首次产前检查的 16 岁及以上未感染艾滋病毒的孕妇。每季度对符合条件、征得同意的妇女进行随访,直至产后 12 个月,并定期进行 HIV 检测、提供 PrEP 和持续的依从性咨询。主要结果是妇女在 PrEP 级联中的分布情况(即启动和产后 12 个月内的持续情况)以及粗略和调整后的危险比 (HR)。我们还报告了按孕期和产后状况分列的艾滋病发病率:总共招募并随访了 1195 名孕妇(中位年龄 26 岁,IQR 23-31;中位孕龄 21 周,IQR 15-31);其中 1009 人(84-4%)在入组时开始 PrEP。在报名时开始 PrEP 的妇女中,990 人中有 668 人(67-5%)在随访 1 个月时继续 PrEP,972 人中有 485 人(49-9%)在随访 3 个月时继续 PrEP,994 人中有 392 人(39-4%)在随访 6 个月时继续 PrEP,1005 人中有 275 人(27-4%)在随访 12 个月时继续 PrEP。在 186 名在注册时未接受 PrEP 的女性中,有 70 人(37-6%)后来开始接受 PrEP。总体而言,1076 名妇女中有 200 名(18-6%)在产后 12 个月继续接受 PrEP。在基线时未开始 PrEP 的 186 名妇女中,有 70 人(37-6%)随后在研究期间开始了 PrEP。与产后 12 个月内停止 PrEP 相关的因素包括:已婚或同居(调整后 HR 1-32,95% CI 1-16-1-50)、自上次就诊以来无避孕套性行为(1-43,1-23-1-65)、报告亲密伴侣暴力(2-03,1-59-2-59)或过去 12 个月内抑郁(1-53,1-14-2-05)。总体而言,在 1673-8 个妇女年中,有 16 名妇女发生了血清转换(HIV 感染率为每 100 个妇女年 0-96 例,95% CI 为 0-49-1-42);14 名妇女停止使用 PrEP,2 名妇女从未开始使用 PrEP。与孕妇相比,孕期的艾滋病毒发病率为每 100 名妇女年 0-28 例(95% CI 0-22-0-33),产后 0-6 个月的发病率比率为每 100 名妇女年 1-77 例(0-53-5-90),产后 6-12 个月的发病率比率为每 100 名妇女年 2-19 例(0-61-7-83):迫切需要将 PrEP 纳入产前和产后护理,并采取干预措施解决继续使用的障碍,包括在孕期和产后提供有针对性的咨询,以减少 PrEP 的中断:资金来源:美国国立卫生研究院国家精神卫生研究所和 Fogarty 国际:摘要的法文译文请参见补充材料部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Lancet Hiv
Lancet Hiv IMMUNOLOGYINFECTIOUS DISEASES&-INFECTIOUS DISEASES
CiteScore
19.90
自引率
4.30%
发文量
368
期刊介绍: The Lancet HIV is an internationally trusted source of clinical, public health, and global health knowledge with an Impact Factor of 16.1. It is dedicated to publishing original research, evidence-based reviews, and insightful features that advocate for change in or illuminates HIV clinical practice. The journal aims to provide a holistic view of the pandemic, covering clinical, epidemiological, and operational disciplines. It publishes content on innovative treatments and the biological research behind them, novel methods of service delivery, and new approaches to confronting HIV/AIDS worldwide. The Lancet HIV publishes various types of content including articles, reviews, comments, correspondences, and viewpoints. It also publishes series that aim to shape and drive positive change in clinical practice and health policy in areas of need in HIV. The journal is indexed by several abstracting and indexing services, including Crossref, Embase, Essential Science Indicators, MEDLINE, PubMed, SCIE and Scopus.
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