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2010 International Pharmaceutical Federation PSWC and AAPS Annual 
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FOCUS ON HIV CARE     Betty J. Dong, Section Advisor

Maternal, infant antiretroviral therapy decreases mother-to-child transmission of HIV

Key point: According to two recently published studies in the New England Journal of Medicine, the administration of antiretroviral therapy to HIV-infected women who are pregnant or nursing and to infants significantly decreased mother-to-child transmission of HIV.

Finer points: A total of 2,369 HIV-positive, breast-feeding mothers (and their infants) from Malawi participated in the largest study to date examining methods of preventing mother-to-child transmission of HIV. In the study, mothers and infants were randomized to one of three groups. In the maternal treatment group, only the mother received various antiretroviral regimens. In the infant treatment group, infants received daily nevirapine. In the maternal, infant, and control groups, both mothers and infants received single-dose nevirapine and 1 week of therapy with zidovudine and lamivudine from onset of labor to 7 days after birth. Mothers were asked to stop breast-feeding by 28 weeks postpartum. The study results were calculated after the maternal and infant groups completed 28 weeks of antiretroviral therapy. At 2 weeks postpartum, 5% of infants were HIV positive. From 2 to 28 weeks postpartum, the estimated risk of mother-to-child transmission of HIV was highest in the control group (5.7%) versus either the maternal treatment group (2.9%; P = 0.009) or the infant treatment group (1.7%; P < 0.001); the estimated risk of infant HIV infection or death was 7% in the control group, 4.1% in the maternal treatment group (P = 0.02), and 2.6% in the infant treatment group (P < 0.001).

In the second study, 560 pregnant women from Botswana who had CD4+ counts of at least 200 cells/mm3 were randomized to treatment with either abacavir, zidovudine, and lamivudine (reverse transcriptase inhibitor [NRTI] group) or lopinavir–ritonavir plus zidovudine–lamivudine (protease inhibitor group) from 26 to 34 weeks gestation through 6 months postpartum. An observational group of pregnant women with CD4+ counts less than 200 cells/mm3 received nevirapine plus zidovudine–lamivudine. Rates of virological suppression less than 400 copies/mL did not significantly differ among the three treatment groups at delivery (96% for NRTI group, 93% for protease inhibitor group, and 94% for observational group) or during the breast-feeding period (92% for NRTI group, 93% for protease inhibitor group, and 95% for observational group). By 6 months postpartum, 1.1% of infants (n = 8) were infected with HIV (95% CI 0.5–2.2). Six infants were infected in utero—four from the NRTI group, one from the protease inhibitor group, and one from the observational group—and two infants from the NRTI group were infected during the breast-feeding period.

What you need to know: An editorialist commenting on the two studies noted that “the choice of prophylaxis involves several considerations, including relative costs, feasibility, and risks and benefits.” According to the editorialist, while infant prophylaxis combined with prenatal antiretroviral therapy may be more cost-effective than maternal triple-drug regimen, it may be more difficult to implement. Conversely, maternal triple-drug prophylaxis is associated with more adverse outcomes (e.g., toxicity to mothers and/or infants, adverse pregnancy outcomes). The editorialist went on to explain that an ongoing trial (NCT01061151 at www.clinicaltrials.gov) is investigating the comparative efficacy and safety of these two prophylaxis options, but results will not be available for several years.

What your patients need to know: Antiretroviral therapy given to pregnant and nursing women suffering from HIV and to their infants during the postpartum period decreases mother-to-child transmission of HIV. In resource-sufficient areas, HIV-positive mothers should still be counseled to avoid breastfeeding as the most effective means to prevent HIV transmission to their child.

Sources:

Related resource on www.pharmacist.com:

Posted by Alex Egervary (aegervary@aphanet.org)
July 28, 2010, 9:15 am