Brief Report: Subsequent Pregnancies in the IMPAACT 2010/VESTED Trial: High Rate of Adverse Outcomes in Women Living With HIV

Author:

Fairlie Lee1ORCID,Brummel Sean2,Ziemba Lauren2,Coletti Anne3,Chinula Lameck4,Shapiro Roger2,Stringer Jeffrey5,Malonga Grace2,Browning Renee6,Chakhtoura Nahida7,Mmbaga Blandina Theophil8,Mhembere Tsungai P.9,Omoz-Oarhe Ayotunde10,Nagaddya Beatrice11,Naidoo Megeshinee12,Hoffman Risa M.13,Lockman Shahin21014,

Affiliation:

1. Faculty of Health Sciences, Wits RHI, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa;

2. Harvard TH Chan School of Public Health, Boston, MA;

3. FHI 360, Durham, NC;

4. University of North Carolina Project–Malawi, Lilongwe, Malawi;

5. University of North Carolina at Chapel Hill, Chapel Hill, NC;

6. National Institute of Allergy and Infectious Diseases, Bethesda, MD;

7. National Institute of Child Health and Human Development, Bethesda, MD;

8. Kilimanjaro Christian Medical Centre and Kilimanjaro Christian Medical University College, Moshi, Tanzania;

9. University of Zimbabwe Clinical Trials Research Centre (UZ-CTRC), Harare, Zimbabwe;

10. Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana;

11. Baylor College of Medicine Children's Foundation-Uganda, Kampala, Uganda;

12. Centre for the Aids Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Durban, South Africa;

13. Division of Infectious Diseases, Department of Medicine, David Geffen School of Medicine at the University of California, Los Angeles, Los Angeles, California; and

14. Brigham and Women's Hospital, Boston, MA.

Abstract

Introduction: Women with HIV (WHIV) have higher risks of adverse pregnancy outcomes, particularly in the absence of antiretroviral treatment (ART), and timing of ART may impact risk. Methods: In the International Maternal Pediatric Adolescent AIDS Clinical Trials 2010/VESTED study, 643 pregnant WHIV in 9 countries were randomized in a 1:1:1 ratio to initiate ART: dolutegravir (DTG)+emtricitabine (FTC)/tenofovir alafenamide (TAF), DTG+FTC/tenofovir disoproxil fumarate (TDF), or efavirenz (EFV)/FTC/TDF. We describe adverse pregnancy outcomes in women with a subsequent pregnancy during 50 weeks of postpartum follow-up: spontaneous abortion (<20 weeks), stillbirth (≥20 weeks), preterm delivery (<37 weeks), and small for gestational age. Results: Of 643 women, 19 (3%) had 20 subsequent pregnancies while receiving ART at conception: DTG/FTC/TAF (3), DTG/FTC/TDF (2), EFV/FTC or lamivudine (3TC)/TDF (12), EFV/abacavir/3 TC (1), and no ART (1). Four spontaneous abortions, 3 stillbirths, and 1 induced abortion occurred. Three (25%) of 12 liveborn infants were preterm (24, 26, and 36 weeks of gestation). Only 12 subsequent pregnancies (60%) resulted in live birth, and at least 1 adverse pregnancy outcome occurred in 11 of 19 (58%) (induced abortion excluded). Of 7 women who experienced spontaneous abortion/stillbirth in the subsequent pregnancy, 4 experienced a stillbirth and 1 a neonatal death as outcomes of their earlier index pregnancy. No congenital anomalies were reported. Conclusions: Adverse pregnancy outcomes were common in this cohort of WHIV who conceived on ART shortly after an index pregnancy, 35% ended in stillbirth or spontaneous abortion. The majority of fetal losses occurred in women with recent prior pregnancy loss. Data from larger cohorts of WHIV conceiving on ART and surveillance are needed to elucidate rates and predictors of adverse pregnancy outcome.

Funder

NICHD, NIAID, NIMH

National Institute of Child Health and Human Development

NIH

Publisher

Ovid Technologies (Wolters Kluwer Health)

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