Timing of Antiretroviral Therapy

Author:

Quinn M K1,Williams Paige L23,Muhihi Alfa4,Duggan Christopher P56,Ulenga Nzovu4,Alwy Al-Beity Fadhlun M7,Perumal Nandita8ORCID,Aboud Said9,Fawzi Wafaie W358,Manji Karim P10,Sudfeld Christopher R58

Affiliation:

1. Department of Pediatrics, Stanford University School of Medicine , Stanford, California , USA

2. Department of Biostatistics, Harvard T.H. Chan School of Public Health , Boston, Massachusetts , USA

3. Department of Epidemiology, Harvard T.H. Chan School of Public Health , Boston, Massachusetts , USA

4. Management and Development for Health , Dar es Salaam , Tanzania

5. Department of Nutrition, Harvard T.H. Chan School of Public Health , Boston, Massachusetts , USA

6. Division of Gastroenterology, Hepatology, and Nutrition, Boston Children’s Hospital and Harvard Medical School , Boston, Massachusetts , USA

7. Department of Obstetrics and Gynecology, Muhimbili University of Health and Allied Sciences , Dar es Salaam , Tanzania

8. Department of Global Health and Population, Harvard T.H. Chan School of Public Health , Boston, Massachusetts , USA

9. Department of Microbiology and Immunology, Muhimbili University of Health and Allied Sciences , Dar es Salaam , Tanzania

10. Department of Pediatrics and Child Health, Muhimbili University of Health and Allied Sciences , Dar es Salaam , Tanzania

Abstract

Abstract Background Combination antiretroviral therapy (cART) initiation during pregnancy reduces the risk of perinatal human immunodeficiency virus (HIV) transmission; however, studies have suggested that there may be unintended adverse consequences on birth outcomes for selected cART regimens. Methods We analyzed adverse birth outcomes among a prospective cohort of 1307 pregnant women with HIV in Dar es Salaam who initiated cART during the first or second trimester of a singleton pregnancy. Our primary analysis compared birth outcomes by gestational age at cART initiation among these women initiating cART in pregnancy. Results Among women who initiated cART in pregnancy, there was no relationship of gestational age at cART initiation with the risk of fetal death or stillbirth. However, women who initiated cART before 20 weeks of gestation compared with after 20 weeks had increased risk of preterm birth (risk ratio [RR], 1.30; 95% confidence interval [CI], 1.03–1.67) but decreased risk of small-for-gestational age birth (RR, 0.71; 95% CI, .55–.93). Conclusions With increasing use of cART preconception and early in pregnancy, clinicians should be aware of the benefits and potential risks of cART regimens to optimize birth outcomes.

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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