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What Works for Women and Girls

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uption of therapy, the virus <strong>and</strong> risk <strong>for</strong> opportunistic infections increase, even in patientswhere the virus has been suppressed <strong>for</strong> long periods of time (SMART Study Group, 2006).A recent review found that gender-specific differences in recommendations concerninginitiation of therapy are not warranted (Floridia et al., 2008). An analysis of United States Food<strong>and</strong> Drug Administration (FDA) databases also found “no clinically or statistically significantgender differences” in 48-week efficacy of ART in r<strong>and</strong>omized controlled trials between 2000<strong>and</strong> 2008 (Stubbel et al., 2009).While there may not be a need <strong>for</strong> different recommendations <strong>for</strong> initiation of therapy bygender, there are indications that certain interventions can be highly beneficial to women specificallyin treatment provision <strong>and</strong> access, adherence <strong>and</strong> support, <strong>and</strong> reducing transmission.7A. Treatment: Provision <strong>and</strong> AccessEvidence has repeatedly demonstrated that antiretroviral therapy has been successfully accessedby both men <strong>and</strong> women with near perfect adherence, good patient retention, <strong>and</strong> good clinicaloutcomes in resource-poor settings common to many developing countries; results have beensimilar to those achieved in resource-rich countries. A systematic comparison of 4,810 treatment-naïveadult patients (51% female) from 18 HAART treatment programs in Africa, Asia<strong>and</strong> South America (low-income settings) with 22,217 treatment-naïveadults (25% female) in 12 HIV cohort studies“I am still on ARVs but myhusb<strong>and</strong> does not know...I hidemedicine. I don’t want to lose mymarriage <strong>and</strong> I do not want to losemy life. If I am divorced I cannotlook after the children.”—HIV-positive woman, Zambia(Human Rights Watch, 2007: 30)from Europe <strong>and</strong> North America (high-income settings)found that antiretroviral therapy is feasible <strong>and</strong> effective inlow-income settings. Mortality was higher in the first fewmonths of treatment <strong>for</strong> patients in low-income settings.Those in low-income settings started treatment withconsiderably more advanced immunodeficiency than thosefrom industrialized countries, but virological <strong>and</strong> immunologicalresponse to HAART were similar in both settings(ART-LINC & ART-CC, 2006). A review of nine articles<strong>and</strong> 18 abstracts until 2006 from sub-Saharan Africa, with12,116 patients found favorable levels of adherence, with 77% of patients achieving 95% adherenceaccording to patient self-reports. Adherence from studies in sub-Saharan Africa showedthat that more patients were adherent than patients in North America, based on 31 studies with17,537 patients (Mills et al., 2006).168 CHAPTER 7 TREATMENT

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