Background: Antiretroviral therapy is effective in reducing rates of mother-to child transmission of HIV to low levels in resource-limited contexts but the applicability and efficacy of these programs in the field are scarcely known. In order to explore such issues, we performed a descriptive study on retrospective data from hospital records of HIV-infected pregnant women who accessed in 2007-2010 the Luanda Municipal Hospital service for prevention of mother-to-child transmission (PMTCT). The main outcome measure was infant survival and HIV transmission. Our aim was to evaluate PMTCT programme in a local hospital setting in Africa. Results: Data for 104 pregnancies and 107 infants were analysed. Sixty-eight women (65.4%) had a first visit before or during pregnancy and received combination antiretroviral treatment (ART) in pregnancy. The remaining 36 women (34.6%) presented after delivery and received no ART during pregnancy. Across a median cohort follow-up time of 73 weeks, mortality among women with and without ART in pregnancy was 4.4% and 16.7%, respectively (death hazard ratio: 0.30, 95% CI 0.07-1.20, p = 0.089). The estimated rates of HIV transmission or death in the infants over a median follow up time of 74 weeks were 8.5% with maternal ART during pregnancy and 38.9% without maternal ART during pregnancy. Following adjustment for use of oral zidovudine in the newborn and exposure to maternal milk, no ART in pregnancy remained associated with a 5-fold higher infant risk of HIV transmission or death (adjusted odds ratio: 5.13, 95% CI: 1.31-20.15, p = 0.019). Conclusions: Among the women and infants adhering to the PMTCT programme, HIV transmission and mortality were low. However, many women presented too late for PMTCT, and about 20% of infants did not complete follow up. This suggests the need of targeted interventions that maintain the access of mothers and infants to prevention and care services for HIV. © 2012 Lussiana et al.
The study is a retrospective analysis of mother and infant data from the hospital records of the perinatal and HIV PMTCT service of the Municipal Hospital Divina Providencia, a general population hospital situated in the urban area of Luanda, Angola. Eligible subjects were HIV-infected pregnant women who accessed the service between March 2007 and August 2010 and delivered live newborns. For those women with repeated pregnancies during the study period, only the last occurred was considered. Cut-off date for follow up was June 2011. The Ethic Committee of our institution approved the study design. Written informed consent was obtained from all the participants in this study. Clinical HIV status was defined according to the WHO definition [6], and CD4 cell counts were measured by flow cytometry. Gestational age was determined on the basis of the last menstrual period, ultrasound biometry, or both. Start of treatment in pregnancy was referred to pregnancy week. Preterm delivery was defined as delivery before 37 completed weeks of gestation. Infant feeding was classified as replacement feeding, breastfeeding or mixed. Replacement feeding and breastfeeding were defined by exclusive assumption of either replacement feeding or breast milk, respectively, in the first six months. Mixed replacement/breastfeeding was defined by alternation of replacement feeding and breast milk in the first six months or by substitution of breastfeeding with formula before six completed months of life. In the newborns, diagnosis (positive tests after 18 months of life) or exclusion (negative tests before or after 18 months) of HIV infection required consistent results of two different rapid blood tests (Determine HIV 1/2, Unipath Limited, Inverness Medical, Bedford, UK; Uni-Gold HIV, Trinity Biotech, Bray, County Wicklow, Ireland), in two occasions at least three months apart. HIV testing for both mothers and infants was free of charge. The main outcomes evaluated were infant survival, HIV transmission rate and maternal survival after delivery. The main variables considered as possible determinants of HIV transmission were ART during pregnancy, oral zidovudine in the newborn, and mode of infant feeding. Women accessing the HIV PMTCT and perinatal care service at the Luanda Divina Providencia hospital are managed according to standardized procedures. Women who become pregnant while on treatment usually continue the ongoing regimen, unless the evaluation of treatment suggests a significant risk of toxicity or teratogenicity. In women with no previous antiretroviral treatment, a CD4 cell count is performed, and antiretroviral treatment is started soon if CD4 counts are below 350/mm3 or if the women has WHO clinical HIV stage III or IV. Otherwise, treatment is started at the beginning of third trimester. The standard regimen for pregnant women is zidovudine plus lamivudine plus nevirapine, administered twice a day. All antiretroviral drugs are given free of charge directly to the women in an amount sufficient to cover the interval between subsequent pregnancy visits (usually two weeks). Tolerability of treatment is assessed monitoring (free of charge) haemoglobin (Hb), blood urea nitrogen (BUN), aspartate aminotransferase (AST) and alanine aminotransferase (ALT), usually on a monthly basis. Women in clinical HIV stage II or higher according to the WHO definition also receive cotrimoxazole, and if tuberculosis (TB) treatment is needed, ART is suspended and specific TB treatment is given. At delivery, women receive intravenous zidovudine. If the woman presents before or at delivery, the newborn receives oral zidovudine within 2 hours from delivery, continued for the first four weeks of life. Cotrimoxazole is given to all infants. Replacement feeding is usually recommended as the preferred infant mode of feeding, but feeding options are evaluated on a single case basis, and a 6-month breastfeeding under antiretroviral treatment may be considered if formula feeding is not regarded as adequate according to AFASS criteria (acceptable, feasible, affordable, sustainable and safe). Replacement-feeding mothers receive free of charge 500 g of powder milk at every infant visit. After delivery, a CD4 count is performed in all women in order to evaluate the indication to antiretroviral treatment. Women already on ART with indication to treatment maintain ART, irrespective of mode of feeding. In women already on ART but with no personal indication to treatment, ART is discontinued if exclusive replacement feeding is the option selected, and otherwise continued until the end of breastfeeding (usually six months). In women with no previous ART presenting after delivery, treatment is started if needed, according to the above treatment recommendations criteria. Follow up of women and their infants takes place in the same health facility. HIV testing in the infants is performed at 9, 12 and 18 months, and infants are usually followed at regular intervals until 24 months of age (usually, with monthly visits). Demographic data were summarized with descriptive statistics. Quantitative data were compared by either Student’s t-test or Mann-Whitney U-test, according to the characteristics of data distribution (normal or skewed, respectively). Categorical data were compared using the chi-square test or the Fisher test, as appropriate. Odds ratios (OR) and 95% confidence intervals [CI] in univariate analyses were calculated by Mantel-Haenszel estimates. The variables with a potential association with the main outcome (HIV transmission or death) in univariate analysis (p<0.10) were included in a multivariable logistic regression model which used occurrence of the main outcome as the dependent variable, calculating an adjusted odds ratio [AOR] with 95% CI for HIV transmission or death. Survival analyses were based on Kaplan-Meyer analysis, log-rank test, and Cox regression. Significance levels were set at 0.05. All the analyses were performed using the SPSS software, version 17.0 (SPSS Inc., Chicago, IL, US).
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