Emerging evidence from a systematic review of safety of pre‐exposure prophylaxis for pregnant and postpartum women: where are we now and where are we heading?

Abstract Introduction HIV incidence is high during pregnancy and breastfeeding with HIV acquisition risk more than doubling during pregnancy and the postpartum period compared to when women are not pregnant. The World Health Organization recommends offering pre‐exposure prophylaxis (PrEP) to pregnant and postpartum women at substantial risk of HIV infection. However, maternal PrEP national guidelines differ and most countries with high maternal HIV incidence are not offering PrEP. We conducted a systematic review of recent research on PrEP safety in pregnancy to inform national policy and rollout. Methods We used a standard Preferred Reporting Items for Systematic Reviews and Meta‐Analysis (PRISMA) approach to conduct a systematic review by searching for completed, ongoing, or planned PrEP in pregnancy projects or studies from http://www.clinicaltrials.gov, PubMed and NIH RePORTER from 2014 to March 2019. We performed a systematic review of studies that assess tenofovir disoproxil fumarate (TDF)‐based oral PrEP safety in pregnant and breastfeeding HIV‐uninfected women. Results and discussion We identified 14 completed (n = 5) and ongoing/planned (n = 9) studies that evaluate maternal and/or infant outcomes following PrEP exposure during pregnancy or breastfeeding. None of the completed studies found differences in pregnancy or perinatal outcomes associated with PrEP exposure. Nine ongoing studies, to be completed by 2022, will provide data on >6200 additional PrEP‐exposed pregnancies and assess perinatal, infant growth and bone health outcomes, expanding by sixfold the data on PrEP safety in pregnancy. Research gaps include limited data on (1) accurately measured PrEP exposure within maternal and infant populations including drug levels needed for maternal protection; (2) uncommon perinatal outcomes (e.g. congenital anomalies); (3) infant outcomes such as bone growth beyond one year following PrEP exposure; (4) outcomes in HIV‐uninfected women who use PrEP during pregnancy and/or lactation. Conclusions Expanding delivery of PrEP is an essential strategy to reduce HIV incidence in pregnancy and breastfeeding women. Early safety studies of PrEP among pregnant women without HIV infection are reassuring and ongoing/planned studies will contribute extensive new data to bolster the safety profile of PrEP use in pregnancy. However, addressing research gaps is essential to expanding PrEP delivery for women in the context of pregnancy.


| INTRODUCTION
HIV incidence is high during pregnancy and breastfeeding [1] with HIV acquisition risk more than doubling during pregnancy and the postpartum period compared to when women are not pregnant [2]. Risk of HIV acquisition during pregnancy and postpartum translates to a substantial cumulative period of risk over the course of women's lives in sub-Saharan African regions where both fertility and HIV prevalence are high [1]. Additionally, acute maternal HIV infection during pregnancy and breastfeeding threatens maternal health and increases the risk of vertical transmission accounting for an estimated 30% of new HIV infections in some settings [3][4][5]. Globally 160,000 infants and children were newly infected with HIV in 2018, mostly in low-and middle-income countries (LMICs) [6]. The World Health Organization (WHO) recommends offering tenofovir (TFV) disoproxil fumarate (TDF)-based oral pre-exposure prophylaxis (PrEP) to pregnant and postpartum women at substantial risk of HIV

| METHODS
This review focuses on research among HIV-uninfected women exposed to PrEP during pregnancy and/or the postpartum period, and complements previous reviews on TDF safety that predominantly included women living with HIV who were exposed to TDF within ART regimens [18,21]. We focused on studies that included maternal and infant outcomes following PrEP exposure during pregnancy and breastfeeding. We included studies that had been published, or were in progress, between January 2014 and March 2019. Maternal and infant outcomes included gestational age at birth, birth weight/length, pregnancy outcomes and complications, congenital anomalies, infant growth and bone health indicators, maternal adverse events and metabolic changes.

| Search strategy and selection criteria
We used a standard Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) approach [22] to conduct a systematic review by searching for completed, ongoing, or planned PrEP in pregnancy projects or studies on clinicaltrials.gov, PubMed and NIH RePORTER using the following search terms: HIV pre-exposure prophylaxis; preexposure prophylaxis; PrEP; tenofovir disoproxil fumarate; pregnancy; postpartum; and breastfeeding. We limited the search terms to PrEP key words to only include studies among HIV-uninfected women, and not HIV-infected pregnant women on TFV, to intentionally capture the most up-to-date PrEP in pregnancy projects and complement prior reviews that sought to assess TDF safety more broadly in HIV-infected and HBV-infected women [18,21]. We included all studies that reported providing oral PrEP to pregnant and/or breastfeeding mothers in any year and in any geographic location. We excluded studies that: (1) did not evaluate maternal or infant outcomes (e.g. gestational age at birth, birth weight/length, pregnancy outcomes and complications, congenital anomalies, infant growth and bone health indicators, maternal adverse events and metabolic changes) following oral PrEP use (e.g. commentary/ review papers, formative or qualitative studies, evaluations of provider knowledge, etc.); (2) provided non-oral PrEP agents (e.g. vaginal microbicides, rings, etc.); and (3) excluded pregnant or breastfeeding women. Two reviewers (DJD and JP) independently assessed the papers, study descriptions and protocols to determine whether they should be included. The same two reviewers analysed the studies to determine if the study was ongoing or completed and what the study exposures and outcomes were. If there were any disagreements, they were resolved by a third party (GJS). DJD sent out the data to study investigators to ensure that the information was correct and to collect any additional information.

| RESULTS AND DISCUSSION
We identified 189 studies or publications that included HIV pre-exposure prophylaxis; preexposure prophylaxis; PrEP; pregnancy; postpartum; and breastfeeding in their search terms. After removal of duplicated studies (n = 36); or those that did not meet eligibility criteria (n = 139), we included a total of 14 studies (Figure 1). Of those studies, five were completed, while nine studies were ongoing or planned.

| Completed PrEP in pregnancy studies
These studies included a total of 1042 PrEP-exposed pregnancies. Four of the five completed studies found no differences in pregnancy or infant outcomes in the PrEP-exposed compared to unexposed arms. One study found that PrEP exposed infants had a lower z-score for length at 1-month; however, there was no difference at 1-year [25]. Most of the studies were sub-studies of PrEP randomized control trials among HIV-serodiscordant couples or young women in African settings, including the Partners PrEP Study [23], FEM-PrEP [24] and VOICE.
The original PrEP efficacy trials excluded pregnant women from enrolment and conducted monthly pregnancy testing, with discontinuation of study drug as soon as pregnancy was detected. Thus, they provide data based on early first trimester exposure, when teratogenic exposures can cause pregnancy loss and structural abnormalities such as neural tube defects (Figure 2a,b); no differences in perinatal outcomes were detected between exposure groups [24,25,29].
Maternal and/or infant exposure to TDF/FTC during pregnancy was not quantified using drug level testing in any PrEP in pregnancy safety study to date and TDF/FTC drug levels may vary by when PrEP use started in pregnancy, duration of PrEP use in pregnancy and breastfeeding and maternal adherence (Table 1). A recently completed evaluation of programmatic PrEP delivery via routine ante-/post-natal clinics in Kenya (the PrEP Implementation for Young Women and Adolescents [PrIYA] Programme) found no association between PrEP use during pregnancy and early infant outcomes including gestational age at birth, birth length/weight and growth indicators at six weeks [30]. Infants were evaluated at six weeks in n = 246 pregnant women. The Partners Demonstration Project enrolled 30 women in who elected to continue PrEP after becoming pregnant found that PrEP-exposed infants had a lower z-score for length at 1-month, but there was no difference at 1-year follow-up [25].

| Ongoing or planned PrEP in pregnancy studies
We identified nine ongoing or planned studies that evaluate pregnancy and infant outcomes following PrEP exposure during pregnancy and/or breastfeeding. These studies are being conducted at single-or multi-country sites across Kenya (n = 2), Malawi (n = 1), South Africa (n = 5), Uganda (n = 2), United States (n = 1), Zimbabwe (n = 1) and one International Registry. The cumulative number of anticipated PrEP-exposed pregnancies is approximately 6194 women, with planned enrolment in individual studies ranging from 40 to 4500 pregnant women. In South Africa, an ongoing open-label randomized controlled trial of pregnant women is comparing pregnancy and infant outcomes, maternal and infant bone health and infant growth over an 18-month period between women assigned to initiate PrEP in the second trimester of pregnancy versus delayed PrEP initiation at cessation of breastfeeding (CAP016; NCT#03227731). One ongoing cluster-randomized trial in Kenya, the PrEP Implementation for Mothers in Antenatal Care (PrIMA) Study (NCT#03070600), compares two approaches for programmatically delivering PrEP within routine antenatal care clinics (universal PrEP-offer versus targeted-offer based on an empiric HIV risk score). Another planned randomized trial (PrEP-P) is a US-based pharmacologic trial of TDF/FTC dosing which will compare 1 tablet of 300 mg TDF/200 mg FTC per day versus a pregnancy-adjusted 2 tablets of 300 mg TDF/200 mg FTC per day that will assess birth outcomes between arms (NCT#03834909).
The remaining six studies are non-randomized observational studies (Table 2). IMPAACT 2009 (NCT#03386578) is a parallel observational cohort study that is enrolling 350 women in South Africa, Malawi, Zimbabwe and Uganda to evaluate enhanced adherence support messaging and feedback from

Excluded projects/studies (n = 175)
-Excluded pregnant women (n = 30) -Evaluated non-oral PrEP (e.g. microbicides, rings) (n = 28) -Formative research without PrEP provision (n = 56) -Did not assess maternal or infant outcomes (n = 14) -Workshop/meeting/advocacy or position paper (n = 25) -Duplicated study (n = 36) Included projects/studies that provide PrEP to pregnant women and assess maternal and/or infant outcomes (n = 14) -Completed (n = 5) -Ongoing or planned (n = 9) counsellors on PrEP adherence. The PrEP in pregnancy and postpartum (PrEP-PP) study (NCT#03902418) in Cape Town is enrolling 1200 pregnant women at first antenatal care visit in an open cohort and follow them up over time to evaluate PrEP uptake, adherence (via dried blood spot [DBS] analysis of TFV) and contributing factors to PrEP uptake and adherence. The Monitoring PrEP in Young Adult women (MPYA) study is evaluating patterns of PrEP use and adherence among 350 women in Kenya using a real-time electronic monitor, as well as DBS in a subset of participants. The ZINK study in Durban, South Africa is assessing PrEP use as part of a safer conception package in 350 HIV-uninfected women who are planning to become pregnant with an HIV-seropositive or unknown-serostatus partner [31]. These studies are evaluating adverse events in women who take PrEP versus those who do not take PrEP during pregnancy and the lactation period and will compare adverse pregnancy and infant health outcomes (e.g. spontaneous abortion, stillbirth, preterm delivery or small for gestational age and frequency of infant death). Finally, the Evaluation of Maternal and Baby Outcome Registry After Chemoprophylactic Exposure study (EMBRACE) is evaluating maternal and infant outcomes in 550 women who participated in a PrEP or microbicide trial and became pregnant (NCT#01209754). The international Antiretroviral Pregnancy Registry (APR) is an international monitoring registry that prospectively monitors antiretroviral-exposed pregnancies that are reported to the APR for birth outcomes, including infants born to women receiving TFV-containing ART regimens and those receiving TDF/FTC for PrEP (NCT#01865786) [32].

| Research gaps and opportunities
Despite the number of ongoing and planned studies, some gaps remain, including limited data on (1) accurately measured PrEP exposure within maternal and infant populations including drug levels needed for optimal protection; (2) uncommon perinatal outcomes such as congenital anomalies; (3) outcomes such as bone growth beyond one year in infants exposed to PrEP during pregnancy and/or lactation; (4) outcomes in HIVuninfected women who use PrEP during pregnancy and/or lactation. Below we describe these identified gaps and opportunities for potential research (Table 3).

| PrEP exposure within maternal and infant populations
Pregnancy can affect drug pharmacokinetics. Only one small study previously examined PrEP pharmacokinetics during pregnancy and found that plasma TFV and intracellular TFV-DP in DBS were 45-58% lower during pregnancy compared with non-pregnant periods after adjusting for adherence as measured by Medication Event Monitoring System (MEMS) openings [33]. Differences in drug concentrations were generally greater in the second and third trimester than in early pregnancy, consistent with known physiologic changes that occur during pregnancy that have the potential to affect drug pharmacokinetics, including changes in gastrointestinal absorption, renal excretion, hepatic metabolic enzymes and overall body water distribution [34,35]. Prevention-effective thresholds of PrEP exposure among African women have not been determined to date, and physiological changes during Presence of congenital malformations pregnancy may further obfuscate protective thresholds for pregnant women. It is uncertain whether lower drug levels during pregnancy have implications for protection against HIV among pregnant women receiving PrEP. All ongoing/planned studies we identified will measure HIV incidence among PrEPusing pregnant and postpartum women, though none are powered to detect significant differences in this important outcome. Two studies identified in our review will investigate pharmacokinetics of PrEP in pregnancy to establish reference thresholds for prevention-effective adherence for pregnant women using DBS, plasma and peripheral blood mononuclear cells (PBMCs) (IMPAACT 2009 and PrEP Dosing in Pregnancy to Optimize HIV Prevention studies). Additional studies among larger populations are needed to understand how pregnancy may affect prevention-effective PrEP exposure in this population. As more options beyond oral TDF-based PrEP become available, future studies are critical to examine bioavailability and metabolism of new PrEP agents among pregnant women to fully understand implications of pregnancy on preventioneffective PrEP exposure. Currently oral TDF/FTC is the only medication with a label indication as PrEP. Tenofovir alafenamide (TAF), a novel lower dose prodrug for TFV, delivers 90% lower plasma TFV concentrations with higher intracellular TFV-DP levels; the lower plasma levels are expected to result in less bone demineralization and renal toxicity. TAF recently received US FDA approval for HIV treatment and results of the DISCOVER trials which demonstrated non-inferiority of F-TAF and FTC-TDF TAF for PrEP among men who have sex with men has been submitted to the FDA (clinicaltrials.gov #NCT02842086) [36]. TAF has not been studied for PrEP in young women although PK and PD studies are underway. Therefore, safety data on prenatal TAF use will likely accumulate over time as TAF use as part of HIV treatment regimens expands among Women living with HIV of reproductive age. Unlike TDF, which had a long history of being used for HIV treatment among pregnant women prior to PrEP. TAF as PrEP and newer agents will take considerable time to accrue meaningful data on prenatal use. Given the trajectory to establish efficacy and obtain regulatory approvals, TAF as PrEP may take years to reach African populations and pregnant women. Thus, advancing safety evidence for TDF-based PrEP use in pregnancy will be immediately informative as TDF is available now and data on TAF as PrEP are unavailable in women, including pregnant women.
Although the clinical significance of the observed differences in DBS TFV-DP levels during pregnancy is unclear, this needs to be considered in interpretation of results from PrEP safety studies which will quantify maternal PrEP adherence using DBS TFV-DP levels and/or plasma TFV levels. Of the ongoing or planned PrEP in pregnancy studies, four studies include an objective measurement of maternal PrEP exposure during pregnancy and/or breastfeeding either in the entire cohort or among a subset. TFV-DP levels in DBS will be evaluated to determine maternal PrEP adherence and quantify TFV-DP concentrations in the pharmacokinetic phase of IMPAACT 2009 (under directly observed treatment conditions), PrIMA, the HPP study, PrEP-PP and ZINK; MPYA will report electronic adherence data, as well as DBS in a subset of participants. IMPAACT 2009 will also evaluate cord blood plasma TFV-DP concentrations (up to 14 days post-delivery).
Ongoing and future studies need to account for lower DBS TFV-DP levels during pregnancy when quantifying and defining PrEP exposure and adherence in maternal populations. When IMPAACT 2009 results are available, they could potentially serve as standardized DBS TFV-DP thresholds for PrEP exposure in pregnancy to understand optimal adherence levels, but will be underpowered to detect protection thresholds. Future studies could incorporate evaluation of PrEP exposure using other non-invasive biomarkers that may be less affected by pregnancy, such as TFV hair or urine levels, in parallel with other matrices. Hair ARV levels in women living with HIV strongly predict virologic outcomes during pregnancy, suggesting hair is an accurate biomarker for ARV exposure in pregnancy [37]. None of the completed, ongoing or planned studies identified to date will quantify direct infant exposure using infant biomarkers. Infant biomarkers provide precise measurement of infant exposure and are useful for interpreting safety data. Infant exposure to maternal drugs is commonly estimated as a percentage of the maternal dose. However, it is difficult to accurately determine foetal and infant ARV drug exposure based on maternal drug dosage due to variations in maternal adherence, pharmacokinetics, placental transfer, and foetal/infant metabolism. ARV concentrations in cord blood reflect maternal exposure over a short time period just prior to delivery and do not accurately represent exposure in a newborn already capable of drug metabolism [38][39][40][41]. Similarly, ARV levels in meconium measure short-term exposure and collection can be logistically challenging [42,43] While there is minimal penetration of TFV (the metabolite of TDF) into breastmilk, there is significant penetration of FTC, though breastmilk concentrations do not incorporate the effects of infant absorption and maturing pathways of infant metabolism in terms of drug exposure to the infant [44][45][46][47]. Given these limitations, few studies to date have been able to accurately quantify cumulative exposure to ARVs in the infant during pregnancy and breastfeeding, and only one has evaluated infant exposure to TDF/FTC used for PrEP in breastfeeding mothers [47]. One prior study evaluated hair levels of mother and infant ARVs as a metric of drug transfer in the perinatal and breastfeeding periods, though TFV was not assessed [48]. Future studies may consider similar approaches for quantifying PrEP exposure in utero through breastfeeding cessation to gain a more accurate measurement of infant PrEP exposure following maternal PrEP use in pregnancy and breastfeeding.

| Perinatal outcomes that occur uncommonly
Most of the studies we identified are insufficiently powered to detect differences in uncommon maternal and infant outcomes such as congenital anomalies. Combining data across studies may provide more statistical power to evaluate the association of PrEP exposure and uncommon pregnancy and infant outcomes. Additionally, most ongoing and planned studies are limited to women who initiate PrEP during pregnancy (Figure 2b), which will provide limited data on periconception or very early gestation PrEP exposure. Only in the MPYA and ZINK studies will women be on PrEP at the time of conception. The available data on women enrolled in PrEP efficacy trials who became pregnant provide some reassuring information on PrEP exposure during the early first trimester, when major organ development occurs [23]. During the second trimester, drug exposures could affect foetal growth and brain development, yet no ongoing or planned studies will comprehensively evaluate neurocognitive outcomes in exposed infants. As PrEP becomes more available in HIV high-burden settings and women receiving PrEP become pregnant or initiate PrEP at various times during pregnancy, it will be critical to monitor the timing of PrEP exposure and adverse pregnancy outcomes with sufficient sample sizes. Surveillance or contribution to birth registries such as the Antiretroviral Pregnancy Registry in settings with expanded PrEP use in young women may provide mechanisms to estimate risk of congenital abnormalities.
All ongoing or planned PrEP in pregnancy studies will evaluate pregnancy outcomes including gestational age at birth, birth length, birth weight, pregnancy loss and congenital abnormalities. None of study descriptions included power calculations for detecting differences in pregnancy outcomes. The field would benefit from well-powered observational PrEP safety studies reporting perinatal outcomes that are based on calculations of the minimum detectable difference between exposure groups, including low, medium and high levels of TDF, to strengthen the interpretation of findings. IMPAACT 2009 is the only study that requires ultrasound prior to enrolment. Other studies rely on last menstrual period and clinician assessment of fundal height to determine gestational age at enrolment and subsequently gestational age at birth. Across studies, birth outcomes will be abstracted from clinical records, self-reported by women at follow-up visits, or recorded by clinical staff if births take place at study sites. When possible, gold standard measurementssuch as first or early second trimester antenatal ultrasoundshould be used for key outcomes to produce the highest quality safety data. This may be more difficult, however, when conducting studies in high HIV burden low-resource settings with limited availability of technologies such as ultrasound and trained technicians.

| Outcomes beyond infancy among PrEPexposed children
Current ongoing studies will contribute perinatal outcome data from >6000 PrEP-exposed pregnancies by 2022. However, we identified few studies evaluating prenatal PrEP exposure and longer-term infant outcomes. In the SMARTT cohort, TDF use in pregnancy among HIV-infected mothers was associated with reduced bone mineral content in neonates compared to exposure to other ARVs, though TFV concentrations in meconium were not associated with infant weight, length or bone mineral content [49,50]. A recent study using DXA suggests that prenatal TDF exposure in HIV-exposed infants may lead to decrement in neonatal bone mineral density [51]. One study of BMD among infants exposed to TDF-containing ART found no association between duration of TDF exposure in utero and infant growth or BMD, though sample sizes in each exposure group were relatively small (<120 infants) and BMD was only measured very early in life (<21 days and 26 weeks). Evaluating BMD beyond infancy among larger samples of children prenatally exposed to TDF for PrEP could help bolster the safety evidence base given the BMD-related concerns of TDF use [52]. Further study is needed to confirm if these bone and growth differences persist beyond the neonatal period and if they are clinically relevant. Few studies identified in our review will evaluate infant outcomes beyond one year of life. Only two studies, CAP016 and IMPAACT 2009, will evaluate BMD among women who used PrEP while pregnant or breastfeeding. Other infant outcomes such as growth indicators will be measured in eight studies with follow-up time ranging from six months to 1.4 years (Figure 2b). This highlights a need for studies on longer-term outcomes beyond infancy and into early childhood following prenatal PrEP exposure.

| Outcomes among HIV-uninfected women who use PrEP during pregnancy and/or lactation
The studies we identified included few maternal-specific outcomes except for monitoring renal and liver function post-PrEP initiation via routine laboratory tests. PrEP in pregnancy studies should include robust evaluation of mother-focused safety outcomes beyond just pregnancy/infant outcomes. For example, three sub-studies within PrEP efficacy trials found that unintended consequences of TDF-based PrEP use include decline in maternal bone mineral density (BMD), which may be exacerbated during pregnancy or breastfeeding [53][54][55]. Exposure to these agents during adolescence or early adulthood, critical periods for skeletal growth and when pregnancy frequently occurs in LMICs, could prevent the attainment of peak bone mass, a major determinant of increased fracture risk in later life [56]. Additionally, bone metabolism alterations that occur during normal pregnancy and lactation lower BMD, which could result in greater decreased BMD when PrEP is used among pregnant and breastfeeding mothers. Only one study, IMPAACT 2009, will evaluate BMD among women who used PrEP while pregnant or breastfeeding. Future safety evaluations would be strengthened by including maternal bone health outcomes.
PrEP demonstration projects among young women from ongoing studies have found high rates of laboratory-confirmed sexually transmitted infections (STIs) among young African women using PrEP [57]. Complications of STIs in pregnancy include spontaneous abortion, stillbirth, preterm birth, and low birth weight [58]. In PrIYA, researchers found that only 1% of pregnant women screened for PrEP recently had an STI diagnosed with syndromic algorithms, which have poor sensitivity and specificity for detection of STIs [59]. This contrasts to the >30% prevalence of laboratory-confirmed STIs (35% CT, 15% NG) detected among women screened for PrEP in PrEP demonstration projects among young women from the same region [57] These data suggest that an appreciable proportion of women who initiate PrEP in programmatic settings may have undiagnosed STIs. Prevalent STIs could confound the risk of adverse birth outcomes in PrEP studies, which could be more likely related to STIs and not PrEP. Evaluating STIs among maternal PrEP users is needed and only IMPAACT 2009 and the PrEP-PP study (NCT#03902418) will include laboratory STI testing within the context of PrEP in pregnancy.
Our review did not include summarization of social science and qualitative studies related to PrEP use among pregnant and breastfeeding women. This is an important dimension that complements clinical trial evidence [60].

| CONCLUSIONS
Expanding delivery of PrEP to young women of reproductive age and pregnant women at high risk of HIV acquisition is an essential strategy to reduce HIV incidence in pregnancy and breastfeeding women. Prior studies demonstrate that exposure to TDF and FTC as ART in pregnancy among women living with HIV is safe and well-tolerated; limited studies of PrEP among pregnant women not living with HIV are also reassuring [18]. Given the significant implications of acquiring HIV in pregnancy for both the woman and her child and the available safety data, the benefits of using PrEP for prevention of HIV acquisition in pregnancy and breastfeeding clearly outweigh potential risks and could substantially reduce maternal and infant HIV acquisition globally [7,13,15,16,61].
However, as PrEP in pregnancy research and programmes expand, there will also be an increase in the frequency of fetal PrEP exposure, and it is critical to augment the current data on maternal and infant safety. Future studies should better elucidate PrEP exposure within maternal and infant populations and evaluate implications of TDF drug levels for HIV protective efficacy in the context of pregnancy or the postpartum period. Pooling data across studies will enable more robust analyses of uncommon outcomes, though standardized assessment approaches are needed. Studies should also evaluate outcomes beyond infancy among children exposed to PrEP and woman-focused safety outcomes following PrEP use during pregnancy and/or lactation. Planned studies will provide important new data on perinatal and infant outcomes following prenatal PrEP exposure, but research gaps remain that will be important to address as maternal PrEP programmes are implemented. Research and pharmacovigilance to provide more and longer-term safety data and better quantification of amount and duration of PrEP exposure during pregnancy and breastfeeding are relevant to policymakers, programme implementers, providers, and pregnant and lactating women. As PrEP use in pregnancy burgeons, it is paramount to maximize opportunities to evaluate PrEP safety and develop a more complete body of evidence. In parallel, expanding PrEP delivery to pregnant and breastfeeding women at high risk of HIV is an essential prevention strategy. 15 Centre for AIDS Research in South Africa, Durban, South Africa; 16 Elizabeth Glaser Pediatric AIDS Foundation, Washington, DC, USA; 17   DJD conceptualized the idea for the analysis, convened the initial meeting of the group, conducted the meta-analysis, reviewed the data in the tables, wrote the first drafts, conducted the edits for the drafts, reviewed and approved final draft. JP conceptualized the idea for the analysis, reviewed articles for the meta-analysis, reviewed the data in the tables, wrote components of the first draft, conducted the edits for the drafts, drafted the figures, reviewed and approved final draft. JB conceptualized the idea for the analysis, reviewed the data in the tables, revised first and second drafts, reviewed and approved final draft. RB, CC, BC, DM, LM, NM, RH, LTM, and LSC, reviewed data in tables/ manuscript, reviewed drafts and provided substantial edits and contributed towards final draft, reviewed and approved final draft. LGB, JEH, JM, TC, LM, JK, GA, SS, and AM reviewed drafts and provided substantial edits and contributed towards final draft, reviewed and approved final draft. GJS conceptualized the idea for the analysis, reviewed the data in the tables, revised first and second drafts, reviewed and approved final draft.

A C K N O W L E D G E M E N T S
None declared.