Oral pre-exposure prophylaxis initiation, continuation and adherence among pregnant and postpartum women receiving antenatal and postnatal care: a systematic review

IF 4.9 1区 医学 Q2 IMMUNOLOGY
Anke Rotsaert, Zaynab Essack, Shannon Bosman, Dvora Joseph Davey, Bernadette Hensen
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引用次数: 0

Abstract

Introduction

In 2023, one-fourth of new HIV acquisitions in children globally resulted from vertical transmission following incident HIV during pregnancy or breastfeeding. Oral pre-exposure prophylaxis (PrEP) with tenofovir disoproxil and emtricitabine is safe and effective in pregnancy and postpartum, with long-acting options emerging. Integrating PrEP into antenatal and postnatal care (ANC/PNC) is a crucial person-centred approach to prevent maternal HIV acquisition and vertical transmission. This review summarizes oral PrEP initiation, continuation and adherence among pregnant and postpartum women receiving ANC/PNC.

Methods

We systematically searched three databases for English-language quantitative studies published between 1 January 2015 and 28 March 2024. Eligible studies focused on pregnant and/or postpartum women accessing PrEP through ANC/PNC, and reported on initiation (receipt of prescription or self-reported use), continuation (persistent use over time) and/or adherence (self-reported and/or objective).

Results

We identified 481 articles; 12 studies from Kenya, Lesotho, Malawi and South Africa met our inclusion criteria. Study heterogeneity (e.g. definitions used, population included, follow-up time) precluded meta-analysis. All studies enrolled pregnant women; three also enrolled postpartum women. Median gestational age at enrolment ranged from 20 to 26 weeks, and follow-up periods from 1 month post-enrolment to 12 months postpartum. Oral PrEP initiation ranged from 14% to 84%. Continuation at 3 months ranged from 22% to 90% and declined postpartum in all studies. Self-reported adherence (daily use) ranged from 11% to 81% in the past 7 or 30 days at 1 month (four studies) and from 54% to 81% at 3 months (two studies). Objectively measured adherence ranged from 34% to 62% for detectable tenofovir or tenofovir diphosphate levels at 1 month (three studies). One Kenyan trial demonstrated that universal versus risk-based offers of oral PrEP resulted in similar PrEP use and HIV incidence. Two-way SMS communication (Kenya) and real-time adherence biofeedback counselling using urine tenofovir testing (South Africa) enhanced PrEP continuation/adherence compared to standard-of-care.

Discussion

Integrating oral PrEP into ANC/PNC showed high initiation among pregnant/postpartum women; however, continuation and adherence were suboptimal.

Conclusions

Oral PrEP integration into ANC/PNC can reach pregnant/postpartum women. Maximizing its impact will require offering long-acting PrEP, person-centred interventions to support adherence/continued use and differentiated delivery responsive to women's needs.

PROSPERO Number

CRD42024513442

Abstract Image

接受产前和产后护理的孕妇和产后妇女口服暴露前预防的开始、继续和坚持:一项系统综述
2023年,全球儿童艾滋病毒新感染病例中有四分之一是由于怀孕或哺乳期间艾滋病毒事件后的垂直传播造成的。口服暴露前预防(PrEP)与替诺福韦二oproxil和恩曲他滨在妊娠和产后是安全有效的,长期的选择正在出现。将预防措施纳入产前和产后护理(ANC/PNC)是预防孕产妇感染艾滋病毒和垂直传播的一项关键的以人为本的方法。本文综述了接受ANC/PNC的孕妇和产后妇女口服PrEP的开始、继续和依从性。方法系统检索三个数据库,检索2015年1月1日至2024年3月28日发表的英语定量研究。符合条件的研究侧重于通过ANC/PNC获得PrEP的孕妇和/或产后妇女,并报告起始(收到处方或自我报告使用)、持续(一段时间内持续使用)和/或依从性(自我报告和/或目标)。结果共鉴定出481篇;来自肯尼亚、莱索托、马拉维和南非的12项研究符合我们的纳入标准。研究异质性(如使用的定义、纳入的人群、随访时间)排除了meta分析。所有的研究都招募了孕妇;其中三名还招募了产后妇女。入组时的中位胎龄为20至26周,随访时间为入组后1个月至产后12个月。口服PrEP起始率从14%到84%不等。在所有的研究中,3个月时的持续时间从22%到90%不等,产后持续时间下降。自我报告的依从性(每日使用)在过去7天或30天内在1个月内从11%到81%(4项研究),在3个月时从54%到81%(2项研究)。对于1个月时可检测到的替诺福韦或替诺福韦二磷酸水平,客观测量的依从性范围为34%至62%(3项研究)。肯尼亚的一项试验表明,普遍提供口服PrEP与基于风险提供口服PrEP导致相似的PrEP使用和艾滋病毒发病率。与标准护理相比,双向短信通信(肯尼亚)和使用尿替诺福韦检测的实时依从性生物反馈咨询(南非)增强了PrEP的延续/依从性。将口服PrEP纳入ANC/PNC的孕妇/产后妇女的启动率较高;然而,持续性和依从性是次优的。结论口服PrEP整合ANC/PNC可覆盖孕妇/产后。最大限度地发挥其影响将需要提供长效PrEP和以人为本的干预措施,以支持坚持/继续使用,并根据妇女的需求提供差异化的服务。普洛斯彼罗号码CRD42024513442
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
Journal of the International AIDS Society
Journal of the International AIDS Society IMMUNOLOGY-INFECTIOUS DISEASES
CiteScore
8.60
自引率
10.00%
发文量
186
审稿时长
>12 weeks
期刊介绍: The Journal of the International AIDS Society (JIAS) is a peer-reviewed and Open Access journal for the generation and dissemination of evidence from a wide range of disciplines: basic and biomedical sciences; behavioural sciences; epidemiology; clinical sciences; health economics and health policy; operations research and implementation sciences; and social sciences and humanities. Submission of HIV research carried out in low- and middle-income countries is strongly encouraged.
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