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Child Mortality According to Maternal and Infant HIV Status in Zimbabwe

Marinda, Edmore MSc*; Humphrey, Jean H. ScD†; Iliff, Peter J. MRCPCH*; Mutasa, Kuda BSc*; Nathoo, Kusum J. MRCP‡; Piwoz, Ellen G. ScD§; Moulton, Lawrence H. PhD†; Salama, Peter MD, MPH∥; Ward, Brian J. MD¶; the ZVITAMBO Study Group

Pediatric Infectious Disease Journal:
doi: 10.1097/01.inf.0000264527.69954.4c
Original Studies
Abstract

Background: HIV causes substantial mortality among African children but there is limited data on how this is influenced by maternal or infant infection status and timing.

Methods: Children enrolled in the ZVITAMBO trial were divided into 5 groups: those born to HIV-negative mothers (NE, n = 9510), those born to HIV-positive mothers but noninfected (NI, n = 3135), those infected in utero (IU, n = 381), those infected intrapartum (IP, n = 508), and those infected postnatally (PN, n = 258). Their mortality was estimated.

Results: Two-year mortality was 2.9% (NE infants), 9.2% (NI), 67.5% (IU), 65.1% (IP), and 33.2% (PN). Between 8 weeks and 6 months, mortality in IU infants quintupled (from 309 to 1686/1000 c-y). The median time from infection to death was 208, 380, and >500 days for IU, IP, and PN infants, respectively. Among NI children, advanced maternal disease was predictive of mortality. Acute respiratory infection was the major cause of death.

Conclusions: Perinatally infected infants are at particular risk of death between 2 and 6 months: cotrimoxazole prophylaxis and early pediatric HAART should be scaled up. Uninfected infants of infected mothers have at least twice the mortality risk of infants born to uninfected mothers: all HIV-exposed infants should be targeted with child survival interventions. HIV-positive mothers with more advanced disease are not only more likely to infect their infants, but their infants are more likely to die, whether infected or not: provision of antiretroviral treatment to pregnant and lactating women is an urgent need for both mothers and their children.

Author Information

From the *ZVITAMBO Project, Harare, Zimbabwe; †Department of International Health, The Johns Hopkins Bloomberg School of Public Health, Baltimore, MD; ‡Department of Paediatrics and Child Health, The University of Zimbabwe College of Health Sciences, Harare, Zimbabwe; §Academy for Educational Development, Washington, DC; ∥UNICEF, New York City, NY; and ¶The Research Institute of the McGill University Health Centres, Montreal, Quebec, Canada.

Accepted for publication March 9, 2007.

Address for correspondence: J. H. Humphrey, ScD, ZVITAMBO project, No. 1 Borrowdale Rd., Borrowdale, Harare, Zimbabwe. E-mail: jhumphrey@zvitambo.co.zw.

© 2007 Lippincott Williams & Wilkins, Inc.