4.3 Article

Effect of Postnatal HIV Treatment on Clinical Mastitis and Breast Inflammation in HIV-Infected Breast-feeding Women

Journal

PAEDIATRIC AND PERINATAL EPIDEMIOLOGY
Volume 31, Issue 2, Pages 134-143

Publisher

WILEY
DOI: 10.1111/ppe.12337

Keywords

Mastitis; breast-feeding; human immunodeficiency virus; prophylactic antiretroviral therapy; infant nevirapine

Funding

  1. Prevention Research Centers Special Interest Project of the Centers for Disease Control and Prevention [SIP 13-01 U48-CCU409660-09, SIP 26-04 U48-DP00005901, SIP 22-09 U48-DP001944-01]
  2. National Institute of Allergy and Infectious Diseases
  3. University of North Carolina Center for AIDS Research [P30-AI50410]
  4. NIH Fogarty AIDS International Training and Research Program [2-D43 TW01039-06, R24 TW007988]
  5. Fogarty Clayton-Dedonder Global Health Mentorship Program [R25TW009340-03S4]
  6. Abbott Laboratories
  7. GlaxoSmithKline
  8. Boehringer Ingelheim
  9. Roche Pharmaceuticals
  10. Bristol-Myers Squibb
  11. Elizabeth Glaser Pediatric AIDS Foundation
  12. United Nations Children's Fund
  13. World Food Program
  14. Malawi Ministry of Health and Population
  15. Johnson and Johnson
  16. US Agency for International Development

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Background: The relationship between mastitis and antiretroviral therapy among HIV-positive, breast-feeding women is unclear. Methods: In the Breastfeeding, Antiretrovirals, and Nutrition (BAN) study, conducted in Lilongwe, Malawi, 2369 mother-infant pairs were randomized to a nutritional supplement group and to one of three treatment groups: maternal antiretroviral therapy (ART), infant nevirapine (NVP) or standard of care for 24weeks of exclusive breast-feeding and 4weeks of weaning. Among 1472 HIV-infected women who delivered live infants between 2004 and 2007, we estimated cumulative incidence functions and sub-distribution hazard ratios (HR) of mastitis or breast inflammation comparing women in maternal ART (n = 487) or infant nevirapine (n = 492) groups to the standard of care (n = 493). Nutritional supplement groups (743 took, 729 did not) were also compared. Results: Through 28-weeks post-partum, 102 of 1472 women experienced at least one occurrence of mastitis or breast inflammation. The 28-week risk was higher for maternal ART (risk difference (RD) 4.5, 95% confidence interval (CI) 0.9, 8.1) and infant NVP (RD 3.6, 95% CI 0.3, 6.9) compared to standard of care. The hazard of late-appearing mastitis or breast inflammation (from week 5-28) was also higher for maternal ART (HR 6.7, 95% CI 2.0, 22.6) and infant NVP (HR 5.1, 95% CI 1.5, 17. 5) compared to the standard of care. Conclusions: Mastitis or breast inflammation while breast-feeding is a possible side effect for women taking prophylactic ART and women whose infants take NVP, warranting additional research in the context of postnatal HIV transmission.

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