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What Works for Women and Girls

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chose elective cesarean section to further reduce the risk of MTCT. Of 770 mother-infantpairs included, 87 percent of women had viral loads below 1000 copies/mL, 99 percentof women received one or more antiretrovirals during pregnancy, <strong>and</strong> 41 percent deliveredthrough elective cesarean section. Less than one percent of infants were diagnosedas HIV-positive at the end of the study period (Read et al., 2007). (Gray III) (treatment,cesarean section, PMTCT, Latin America, Caribbean)A study from the United States from 1997 to 2004 with 759 HIV-positive women (139pregnant women <strong>and</strong> 620 non-pregnant women) receiving HIV care found that incomparison to non-pregnant women, pregnant women had a lower risk of HIV diseaseprogression (defined as an AIDS defining event or death). All pregnant women weretreated with either HAART (86%) or non-HAART ART (14%). In comparison, 68%of non-pregnant women were treated with HAART, 9% with non-HAART ART <strong>and</strong>23% received no treatment. At the end of the study period 5% of pregnant vs. 7% ofnon-pregnant women experienced an AIDS-defining event only, 1% of pregnant vs.11% of non-pregnant women died <strong>and</strong> 2% of pregnant vs. 7% of non-pregnant womenexperienced both an AIDS-defining event <strong>and</strong> death. Overall 8% of pregnant womenvs. 24% of non-pregnant women experienced an AIDS-defining event or death. Otherpredictors of disease progression included a baseline CD4 count of greater than 200cells/mm 3 , a baseline HIV-1 RNA level of greater than 10,000 copies/mL, maternal age,HAART duration, non-HAART ART duration <strong>and</strong> durable virologic suppression. Theeffect of pregnancy on slower disease progression was still significant after controlling<strong>for</strong> these previously listed clinical variables. Finally, women with more than one pregnancytended to have a lower risk of disease progression than women with only onepregnancy; however, this association was not statistically significant (Tai et al., 2007).(Gray III) (pregnancy, HAART, United States)A study from Côte d’Ivoire that enrolled HIV-positive pregnant women between 2003<strong>and</strong> 2005 in an MTCT-Plus program found that antiretroviral treatment <strong>for</strong> pregnantwomen, both indicated <strong>for</strong> the mother’s health as well as solely <strong>for</strong> PMTCT purposes,was effective <strong>and</strong> safe. <strong>Women</strong> with CD4 counts below 200 cells/mm 3 were consideredeligible <strong>for</strong> HAART <strong>for</strong> their own health <strong>and</strong> received a treatment combination ofmainly zidovudine (ZDV), lamivudine (3TC), <strong>and</strong> nevirapine (NVP). <strong>Women</strong> not eligible<strong>for</strong> HAART <strong>for</strong> their own health received a short course of ARVs, mainly ZDV <strong>and</strong> 3TCfrom 32 weeks of pregnancy until 3 days postpartum <strong>and</strong> a single dose of NVP duringlabor; ZDV from 28 weeks of pregnancy; single dose NVP; or ZDV <strong>and</strong> single dose NVP.All infants in the sample received ZDV syrup <strong>for</strong> 7 days after birth <strong>and</strong> a single dose ofNVP 3 days after birth regardless of mother’s ARV regimen. Of the 261 HIV-infectedwomen identified <strong>and</strong> enrolled in the study, 57% (143) received short-course ARVs <strong>and</strong>43% (107) received HAART. Overall, the HIV status of 97.4% (225) children was determinedwith 12 confirmed HIV infections. The probability of peripartum HIV infectionwas 2.2% <strong>for</strong> children born to mothers using HAART <strong>and</strong> 3.1% <strong>for</strong> children born tomothers using short-course ARVs. The only factor found to be significant in peripartumWHAT WORKS FOR WOMEN AND GIRLS239

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