Fairlie Lee, Lavies Diane, Kalk Emma, Mhlongo Otty, Patel Faeezah, Technau Karl-Günter, Mahtab Sana, Moodley Dhayendre, Subedar Hasina, Mullick Saiqa, Sawry Shobna, Mehta Ushma
Wits RHI, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.
Centre for Infectious Disease Epidemiology and Research, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Front Reprod Health. 2023 Sep 29;5:1221101. doi: 10.3389/frph.2023.1221101. eCollection 2023.
The risk of HIV acquisition is higher during pregnancy and postpartum than other times. Newly acquired maternal HIV infection associated with high primary viraemia, substantially increases the risk of vertical HIV transmission. Pre-exposure prophylaxis (PrEP) reduces the risk of HIV acquisition. Currently available products include oral tenofovir/emtricitabine (TDF/FTC) and tenofovir alafenamide (TAF)/FTC), long-acting cabotegravir (CAB-LA) and the dapivirine ring (DVR). All except oral TDF/FTC have limited safety data available for use in pregnant and breastfeeding women. The safety of new PrEP agents for pregnant women and the fetus, infant and child, either exposed or during breastfeeding is an ongoing concern for health care workers and pregnant and breastfeeding women, particularly as the safety risk appetite for antiretroviral (ARV) agents used as PrEP is lower in pregnant and breastfeeding women who are HIV-uninfected, compared to women living with HIV taking ARVs as treatment. With the widespread rollout of TDF/FTC among pregnant women in South Africa and other low-middle income countries (LMIC) and the potential introduction of new PrEP agents for pregnant women, there is a need for safety surveillance systems to identify potential signals of risk to either the mother or fetus, measure the burden of such a risk, and where appropriate, provide specific reassurance to PrEP users. Safety data needs to be collected across the continuum of the product life cycle from pre-licensure into the post-marketing period, building a safety profile through both passive and active surveillance systems, recognising the strengths and limitations of each, and the potential for bias and confounding. Pharmacovigilance systems that aim to assess the risk of adverse birth outcomes in pregnant women exposed to PrEP and other agents need to consider the special requirements of pregnancy epidemiology to ensure that the data derived from surveillance are sufficiently robust to inform treatment policies. Here we review the known safety profiles of currently available PrEP candidates in women of child-bearing potential, pregnancy and breastfeeding and discuss pragmatic approaches for such surveillance in HIV-endemic LMICs.
孕期和产后感染艾滋病毒的风险高于其他时期。新获得的孕产妇艾滋病毒感染与高病毒血症相关,会大幅增加艾滋病毒垂直传播的风险。暴露前预防(PrEP)可降低感染艾滋病毒的风险。目前可用的产品包括口服替诺福韦/恩曲他滨(TDF/FTC)、替诺福韦艾拉酚胺(TAF)/FTC、长效卡博特韦(CAB-LA)和达匹韦林环(DVR)。除口服TDF/FTC外,其他产品在孕妇和哺乳期妇女中使用的安全性数据有限。新型PrEP药物对孕妇及其胎儿、婴儿和儿童(无论是否暴露或处于哺乳期)的安全性,一直是医护人员以及孕妇和哺乳期妇女关注的问题,特别是与感染艾滋病毒并服用抗逆转录病毒药物(ARV)进行治疗的妇女相比,未感染艾滋病毒的孕妇和哺乳期妇女对用作PrEP的抗逆转录病毒药物的安全风险接受度较低。随着TDF/FTC在南非和其他中低收入国家(LMIC)的孕妇中广泛推广,以及可能引入针对孕妇的新型PrEP药物,需要建立安全监测系统,以识别对母亲或胎儿的潜在风险信号,衡量此类风险的负担,并在适当情况下,向PrEP使用者提供具体的保证。需要在产品生命周期的连续过程中收集安全性数据,从上市前到上市后阶段,通过被动和主动监测系统建立安全概况,认识到每种系统的优势和局限性,以及偏差和混杂的可能性。旨在评估暴露于PrEP和其他药物的孕妇不良出生结局风险的药物警戒系统,需要考虑妊娠流行病学的特殊要求,以确保从监测中获得的数据足够可靠,为治疗政策提供依据。在此,我们回顾了目前可用的PrEP候选药物在有生育潜力的女性、孕期和哺乳期女性中的已知安全概况,并讨论了在艾滋病毒流行的中低收入国家进行此类监测的务实方法。