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      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?

      review-article
      1 , 2 , , 3 , 3 , 4 , 5 , 6 , 7 , 8 , 3 , 9 , 6 , 10 , 3 , 4 , 3 , 11 , 12 , 2 , 13 , 14 , 15 , 16 , 3 , 17 , 2 , 3 , 18 , 6 , 19 , 20 , 3 , 4 , for the PrEP in Pregnancy Working Group
      Journal of the International AIDS Society
      John Wiley and Sons Inc.
      preexposure prophylaxis, PrEP, pregnancy, breastfeeding, PMTCT, prevention of mother to child transmission, HIV

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          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.

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          Most cited references42

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          Physiologic and pharmacokinetic changes in pregnancy

          Physiologic changes in pregnancy induce profound alterations to the pharmacokinetic properties of many medications. These changes affect distribution, absorption, metabolism, and excretion of drugs, and thus may impact their pharmacodynamic properties during pregnancy. Pregnant women undergo several adaptations in many organ systems. Some adaptations are secondary to hormonal changes in pregnancy, while others occur to support the gravid woman and her developing fetus. Some of the changes in maternal physiology during pregnancy include, for example, increased maternal fat and total body water, decreased plasma protein concentrations, especially albumin, increased maternal blood volume, cardiac output, and blood flow to the kidneys and uteroplacental unit, and decreased blood pressure. The maternal blood volume expansion occurs at a larger proportion than the increase in red blood cell mass, which results in physiologic anemia and hemodilution. Other physiologic changes include increased tidal volume, partially compensated respiratory alkalosis, delayed gastric emptying and gastrointestinal motility, and altered activity of hepatic drug metabolizing enzymes. Understating these changes and their profound impact on the pharmacokinetic properties of drugs in pregnancy is essential to optimize maternal and fetal health.
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            Sexually transmitted infections in pregnancy: prevalence, impact on pregnancy outcomes, and approach to treatment in developing countries.

            Sexually transmitted infections (STIs) are common in the developing world. Management of STIs in pregnancy in many developing countries has, however, been complicated by the lack of simple and affordable diagnostic tests. This review examines the prevalence and impact on pregnancy outcome of STIs in developing countries and recommends approaches to management of STIs in pregnancy for resource poor settings.
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              The Contribution of Maternal HIV Seroconversion During Late Pregnancy and Breastfeeding to Mother-to-Child Transmission of HIV

              The prevention of mother-to-child transmission (PMTCT) of HIV has been focused mainly on women who are HIV positive at their first antenatal visit, but there is uncertainty regarding the contribution to overall transmission from mothers who seroconvert after their first antenatal visit and before weaning. A mathematical model was developed to simulate changes in mother-to-child transmission of HIV over time, in South Africa. The model allows for changes in infant feeding practices as infants age, temporal changes in the provision of antiretroviral prophylaxis and counseling on infant feeding, as well as temporal changes in maternal HIV prevalence and incidence. The proportion of mother-to-child transmission (MTCT) from mothers who seroconverted after their first antenatal visit was 26% [95% confidence interval (CI): 22% to 30%] in 2008, or 15,000 of 57,000 infections. It is estimated that by 2014, total MTCT will reduce to 39,000 per annum, and transmission from mothers seroconverting after their first antenatal visit will reduce to 13,000 per annum, accounting for 34% (95% CI: 29% to 39%) of MTCT. If maternal HIV incidence during late pregnancy and breastfeeding were reduced by 50% after 2010, and HIV screening were repeated in late pregnancy and at 6-week immunization visits after 2010, the average annual number of MTCT cases over the 2010-2015 period would reduce by 28% (95% CI: 25% to 31%), from 39,000 to 28,000 per annum. Maternal seroconversion during late pregnancy and breastfeeding contributes significantly to the pediatric HIV burden and needs greater attention in the planning of prevention of MTCT programs.
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                Author and article information

                Contributors
                dvoradavey@ucla.edu
                Journal
                J Int AIDS Soc
                J Int AIDS Soc
                10.1002/(ISSN)1758-2652
                JIA2
                Journal of the International AIDS Society
                John Wiley and Sons Inc. (Hoboken )
                1758-2652
                08 January 2020
                January 2020
                : 23
                : 1 ( doiID: 10.1002/jia2.v23.1 )
                : e25426
                Affiliations
                [ 1 ] Department of Epidemiology Fielding School of Public Health University of California Los Angeles CA USA
                [ 2 ] Division of Epidemiology and Biostatistics School of Public Health and Family Medicine University of Cape Town Cape Town South Africa
                [ 3 ] Department of Global Health University of Washington Seattle WA USA
                [ 4 ] Department of Epidemiology University of Washington Seattle WA USA
                [ 5 ] Department of Medicine University of Washington Seattle WA USA
                [ 6 ] Geffen School of Medicine University of California Los Angeles CA USA
                [ 7 ] World Health Organization Geneva Switzerland
                [ 8 ] Faculty of Health Sciences Desmond Tutu HIV Centre Institute of Infectious Disease and Molecular Medicine University of Cape Town Cape Town NC South Africa
                [ 9 ] Department of Obstetrics and Gynecology University of North Carolina at Chapel Hill Chapel Hill NC USA
                [ 10 ] Center for Global Health Massachusetts General Hospital Boston MA USA
                [ 11 ] Department of Research and Programs Kenyatta National Hospital Nairobi Kenya
                [ 12 ] Department of Medicine University of Alabama Birmingham AL USA
                [ 13 ] ANOVA Johannesburg South Africa
                [ 14 ] Department of Obstetrics and Gynaecology University of KwaZulu‐Natal Durban South Africa
                [ 15 ] Centre for AIDS Research in South Africa Durban South Africa
                [ 16 ] Elizabeth Glaser Pediatric AIDS Foundation Washington DC USA
                [ 17 ] Center for Clinical Research Kenya Medical Research Institute (KEMRI) Nairobi Kenya
                [ 18 ] Infectious Diseases Institute Makerere University Kampala Uganda
                [ 19 ] Department of Family Medicine University of California Los Angeles CA USA
                [ 20 ] University of Zimbabwe College of Health Sciences Harare Zimbabwe
                Author notes
                [*] [* ] Corresponding author: Dvora L Joseph Davey, University of California Los Angeles, Fielding School of Public Health, Department of Epidemiology, 650 Charles E Young Dr S, Los Angeles, California 90095, USA. Tel: 310-701-1526. ( dvoradavey@ 123456ucla.edu )

                Author information
                https://orcid.org/0000-0001-6290-9293
                https://orcid.org/0000-0003-1255-7191
                https://orcid.org/0000-0001-8242-8438
                https://orcid.org/0000-0003-1604-9637
                https://orcid.org/0000-0001-6320-3444
                https://orcid.org/0000-0002-0755-4386
                https://orcid.org/0000-0002-8813-3419
                https://orcid.org/0000-0002-1435-8455
                https://orcid.org/0000-0002-2470-2096
                https://orcid.org/0000-0001-5845-3190
                https://orcid.org/0000-0001-6039-0352
                https://orcid.org/0000-0001-6571-8927
                https://orcid.org/0000-0001-6167-6328
                https://orcid.org/0000-0002-9150-1059
                https://orcid.org/0000-0003-1849-9631
                https://orcid.org/0000-0002-2818-9808
                https://orcid.org/0000-0002-2347-006X
                https://orcid.org/0000-0002-8106-7658
                https://orcid.org/0000-0001-6646-6733
                https://orcid.org/0000-0002-3583-0026
                https://orcid.org/0000-0003-3566-1688
                https://orcid.org/0000-0002-4301-1573
                Article
                JIA225426
                10.1002/jia2.25426
                6948023
                31912985
                4f5b680d-51f2-4174-8997-f5c855221f1b
                © 2020 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 06 July 2019
                : 20 November 2019
                Page count
                Figures: 2, Tables: 3, Pages: 13, Words: 9716
                Funding
                Funded by: NIH-NIAID , open-funder-registry 10.13039/100000060;
                Award ID: T32DA023356
                Funded by: NIH/FIC , open-funder-registry 10.13039/100000061;
                Award ID: R25TW009340
                Funded by: CHIPTS
                Award ID: P30 MH058107
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                January 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.4 mode:remove_FC converted:08.01.2020

                Infectious disease & Microbiology
                preexposure prophylaxis,prep,pregnancy,breastfeeding,pmtct,prevention of mother to child transmission,hiv

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