12.07.2015 Views

What Works for Women and Girls

What Works for Women and Girls

What Works for Women and Girls

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

HIV acquisition was low birth weight, while infant feeding practice, gender, maternalARV regimen, CD4 count <strong>and</strong> age were not significant. (Tonwe-Gold et al., 2007). (GrayIII) (PMTCT-Plus, HAART, PMTCT, Côte d’Ivoire)A 2002 study in Nigeria found that among the 32 women who were given HAART,transmission of HIV to infants was 9.1%. Among the 22 women who had single dosenevirapine in labor there was a transmission rate of over 33%. The best outcome wasamong those that had HAART, an elective C-section <strong>and</strong> did not breastfeed; none of thebabies were HIV-positive at 18 months. “It is recommended that the single dose nevirapinebe ab<strong>and</strong>oned in favour of combination treatment… The single dose nevirapine….may lead to the spread of a nevirapine-resistant strain” (Chama et al., 2007: 134 <strong>and</strong>136). (Gray III) (HAART, PMTCT, treatment, Nigeria)A study in Mozambique from 2002 to 2005 of 985 HIV-positive pregnant women foundthat HAART was more widely accepted than single-dose nevirapine in earlier studies,with 80% completing a treatment protocol of HAART until six months postpartum<strong>and</strong> beyond. Maternal mortality was 0.8%, with vertical transmission rates of 1.4% atsix months, equivalent to those developed countries (Marazzi et al., 2007). (Gray III)(HAART, treatment, Mozambique)A study in Jamaica with over 69,995 pregnant women presenting <strong>for</strong> antenatal carebetween 2005 <strong>and</strong> 2007 found that the use of HAART decreased perinatal transmissionfrom 6% to 1.6% in 3 urban areas <strong>and</strong> to 4.75% isl<strong>and</strong>-wide (Christie et al., 2008).(Gray V) (antenatal care, HAART, PMTCT, Jamaica)2. For women who are pregnant <strong>and</strong> not eligible <strong>for</strong> HAART <strong>for</strong> their own health, shortcourseARV therapy used <strong>for</strong> prophylaxis can reduce nevirapine resistance.A 2009 study from Thail<strong>and</strong> found that one month of zidovudine (ZDV 300 mg twicedaily) <strong>and</strong> didanosine (ddI400 mg once daily) following a single dose of nevirapine(NVP) during labor prevented almost all NNRTI resistance. Two hundred <strong>and</strong> twentyARV-näive HIV-positive pregnant women with CD4 counts greater than 250 cells/mm 3receiving postpartum ZDV treatment during the third trimester, single dose NVP duringlabor, <strong>and</strong> 1 month of ZDV/ddI were matched with women (with similar CD4 counts)receiving ZDV treatment during the third trimester <strong>and</strong> single dose NVP during labor(but no postpartum treatment). Resistance mutations were found in 1.8% of womenwho received the 1 month postpartum ZDV/ddI <strong>and</strong> in 20.7% of the women who didnot receive postpartum treatment (Lallemant et al., 2009). (Gray III) (PMTCT, treatment,Thail<strong>and</strong>)A study from Thail<strong>and</strong> that enrolled 169 HIV-positive pregnant women (28 to 38 weeksgestation) from 2006 to 2008 found that postpartum antiretroviral treatment <strong>for</strong> atleast 7 days after a single dose of intrapartum nevirapine (NVP) significantly reducedthe development of NVP resistance. <strong>Women</strong> included in the study had CD4 counts ofgreater than 250 cells/mm 3 , may or may not have received zidovudine (ZDV) during240 CHAPTER 9 SAFE MOTHERHOOD AND PREVENTION OF VERTICAL TRANSMISSION

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!