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AIDS:
doi: 10.1097/QAD.0b013e328312c740
Epidemiology and Social

Infant feeding, HIV transmission and mortality at 18 months: the need for appropriate choices by mothers and prioritization within programmes

Rollins, Nigel Ca; Becquet, Renaudb,c,d; Bland, Ruth Mb,e; Coutsoudis, Annaa; Coovadia, Hoosen Mf; Newell, Marie-Louiseb,g

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Author Information

aDepartment of Paediatrics and Child Health, South Africa

bAfrica Centre for Health and Population Studies, University of KwaZulu-Natal, Congella, South Africa

cINSERM, Unité 897, Centre de Recherche ‘Epidémiologie et Biostatistique’

dInstitut de Santé Publique Epidémiologie Développement, Université Victor Segalen Bordeaux 2, Bordeaux, France

eDivision of Developmental Medicine, University of Glasgow, Glasgow, UK

fCentre for HIV/AIDS Networking, University of KwaZulu-Natal, Congella South Africa

gCentre for Paediatric Epidemiology and Biostatistics, Institute of Child Health, University College London, London, UK.

Received 31 March, 2008

Revised 25 July, 2008

Accepted 30 July, 2008

Correspondence to Nigel C. Rollins, Department of Paediatrics and Child Health, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Private Bag 7, Congella 4013, South Africa. Tel: +27 31 260 4352; fax: +27 31 260 4388; e-mail: rollins@ukzn.ac.za

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Abstract

Objectives: To determine the late HIV transmission and survival risks associated with early infant feeding practices.

Design: A nonrandomized intervention cohort.

Methods: HIV-infected pregnant women were supported in their infant feeding choices. Infant feeding data were obtained weekly; blood samples from infants were taken monthly to diagnose HIV infection. Eighteen-month mortality and HIV transmission risk were assessed according to infant feeding practices at 6 months.

Results: One thousand one hundred and ninety-three live-born infants were included. Overall 18-month probabilities of death (95% confidence interval) were 0.04 (0.03–0.06) and 0.53 (0.46–0.60) for HIV-uninfected and HIV-infected children, respectively. The eighteen-month probability of survival was not statistically significantly different for HIV-uninfected infants breastfed or replacement fed from birth. In univariate analysis of infant feeding practices, the probability of HIV-free survival beyond the first 6 months of life in children alive at 6 months was 0.98 (0.89–1.00) amongst infants replacement fed from birth, 0.96 (0.90–0.98; P = 0.25) and 0.91 (0.87–0.94; P = 0.03) in those breastfed for less or more than 6 months, respectively. In multivariable analyses, maternal unemployment and low antenatal CD4 cell count were independently associated with more than three-fold increased risk of infant HIV infection or death.

Conclusion: Breastfeeding and replacement feeding of HIV-uninfected infants were associated with similar mortality rates at 18 months. However, these findings were amongst mothers and infants who received excellent support to first make, and then practice, appropriate infant feeding choices. For programmes to achieve similar results, the quality of counselling and identification of mothers with low CD4 cell count need to be the targets of improvement strategies.

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Introduction

The dilemma of how best to feed infants and young children of HIV-infected mothers living in high HIV prevalence communities remains complex. Exclusive breastfeeding carries a lower risk of HIV transmission over the first 6 months of life [1] but is infrequently practiced by mothers or effectively supported by health systems [2,3]. Replacement feeding avoids all postnatal HIV transmission but carries the risk of death [4,5] when given in household circumstances that are not ideal. Early data suggest that highly active antiretroviral treatment (HAART) given to HIV-infected mothers during the period of breastfeeding can reduce transmission risks, even if she is already immunodeficient [6–9]. Yet, despite 15 years of effective therapeutic interventions being available to reduce peripartum transmission of HIV, more than 500 000 children become infected by this route each year, highlighting the gap between scientific evidence and feasibility or coverage of prevention of mother-to-child transmission of HIV (PMTCT) programmes.

Although not commonly measured in programmes, child survival without HIV infection, rather than avoidance of HIV infection alone, has emerged as the most important measure of PMTCT programme effectiveness [10]. This acknowledges not only the availability and effectiveness of therapeutic interventions but also the competing threats to child survival. The quality of counselling to guide women in their choice of infant feeding practice and the practical support to enable these choices is frequently deficient [11,12]. As a result, suboptimal feeding practices have resulted in high mortality of HIV-exposed infants [13].

Although the transmission risks of infant feeding practices of HIV-infected mothers in the first 6 months of life has been substantially researched, the pattern of feeding beyond this period is equally important in determining child survival. The present study describes the outcomes of infants who were part of an intervention cohort study in which feeding practices were intensively supported. We report the 18-month HIV-free survival of HIV-exposed infants according to infant feeding practices implemented at birth and, secondly, by infant feeding practices between 0–6 months and subsequent feeding practices beyond 6 months of age.

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Methods

The study design and methods have been described previously [1]. In brief, HIV-infected pregnant women attending rural and semi-urban antenatal clinics in KwaZulu Natal (KZN) were enrolled into a nonrandomized intervention cohort study. All women were counselled antenatally regarding infant feeding options and supported in their choice [14]; those who chose to formula feed their infants were visited at home antenatally and shown how to safely prepare feeds [14]. All mothers were visited at home by infant feeding counsellors three or four times in the first 2 weeks of life and every 2 weeks thereafter until the infant was 6 months of age [1]. Mothers who chose to replacement feed and who encountered problems were principally supported by the infant feeding supervisor or study nurses when referred by infant feeding counsellors following a home visit or when they visited the study clinics. Mothers and infants were followed up at the study clinic when the infant was 6 weeks old, every month thereafter until the infant was 9 months of age and then every 3 months until 18 months of age. At each visit, a dried blood spot sample was collected for the determination of HIV status by quantitative HIV RNA assay (Nuclisens HIV-1 QT; Organon Teknika, Boxtel, The Netherlands and Nuclisens EasyQ HIV-1; Biomerieux, Boxtel, The Netherlands) [15,16]. HIV status was determined at 5 months to guide counselling on infant feeding practices after 6 months. An independent group of field monitors visited mothers at home every week from birth until the infant was 9 months of age and documented all feeds and morbidity episodes for each day of the preceding week.

When infants were 5 months of age, breastfeeding mothers were counselled to stop breastfeeding (at 6 months) of infants who were confirmed HIV uninfected; mothers were counselled to continue breastfeeding infants who were already HIV infected [17]. All mothers were counselled regarding the introduction of complementary feeds. Single-dose nevirapine was provided to all HIV-infected women and their infants for use during labour and delivery, and cotrimoxazole was provided to all HIV-exposed infants. Six-month supply of commercial infant formula was offered free through the KZN PMTCT programme from the end of 2002 [1,18]. CD4 cell counts were estimated on HIV-infected women antenatally but were not routinely considered in infant feeding counselling. At each clinic visit, all mothers were checked for symptoms and weight and referred to the local hospital for diagnostic services if indicated. At the time of the study, HAART was not available through the provincial health services. The study was approved by the Biomedical Research Ethics Committee of the University of KwaZulu-Natal (T050/01).

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Statistical methods

Analysis was based on a database created in April 2007 and included live-born children of HIV-infected mothers. Cumulative HIV-free survival probabilities in the first 18 months of life were assessed by Kaplan–Meier analysis [19]; associations with maternal and infant variables were quantified in Cox regression analysis [20]. The following variables were tested in univariable analysis to assess the determinants of HIV infection and death: multiple birth outcome, sex of the child, maternal education, water access, low birth weight (<2.5 kg), maternal employment, maternal antenatal CD4 cell count. Variables with a P value of less than 0.20 were included in multivariable analysis [20].

Feeding categories were determined from the analytical database by applying algorithms that first classified infants' feeding practices on each day of life and then determined the cumulative pattern from birth. WHO definitions for exclusive breastfeeding, mixed breastfeeding and replacement feeding were used to classify children from the time of introduction of these fluids or feeds [21–23]. A child who was only ever breastfed by his/her mother while having never received any other drink, food or nonhuman milk with the exception of drops or syrups consisting of vitamins, mineral supplements or medicines was defined as exclusively breastfed. A child who was breastfed at a given age while also having received water-based drinks, food-based fluid, solid food or nonhuman milk was mixed breastfed from the date of introduction of these fluids or foods. Replacement feeding was defined as giving any nonhuman milk and the exclusion of all breast milk, with or without other liquids or solids.

The eighteen-month HIV-free survival was assessed according to first, infant feeding practices implemented at birth, and second, on cumulative feeding recall histories. If exclusively breastfed infants were given additional fluid or milk even on one occasion, they were immediately reclassified as mixed feeding, irrespective of subsequent feeding practices. Infants with no feeding or test data were excluded from the analyses. In case of missing data, information was censored at the time the infant was last seen. To assess HIV-free survival in children breastfed for less and more than 6 months, we had to take into account survival bias, as children needed to be alive at 6 months of age to be breastfed beyond that age. We thus calculated the probability of HIV-free survival between 7 and 18 months of age according to infant feeding practices from birth until 6 months of age among children who were still alive, HIV uninfected at 6 weeks and still being followed up in the cohort at 6 months of age. All statistical analyses were carried out using SAS software (version 9.1; SAS Institute, http://www.sas.com).

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Role of the funding source

Wellcome Trust and Sidaction did not contribute to, or influence the study design, implementation, analysis or drafting of the manuscript.

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Results

Overall 18-month HIV-free survival

Details of the cohort are shown in Table 1. One thousand one hundred and ninety-three live-born infants from HIV-infected mothers born between end October 2001 and mid-April 2005 were included. By 18 months of age, 147 had children died and 237 were diagnosed as HIV infected; 113 deaths (77%) occurred among HIV-infected children. The overall estimated 18-month probability of death [95% confidence interval (CI)] was 0.04 (0.03–0.06) for HIV-uninfected and 0.53 (0.46–0.60) for HIV-infected children. Infected children were 17 times more likely to die than uninfected children [unadjusted hazard ratio, 16.9 (11.5–24.8)]. By 18 months, an estimated 21% (19–23%) of children born to HIV-infected mothers would have acquired HIV infection. Combined, the overall probability of remaining free from HIV infection and death by 18 months was 0.76 (0.73–0.78). The overall estimated HIV transmission risk exposure for breastfeeding over the 18-month period was 9.1 cases per 100 child-years of breastfeeding (95% CI, 5.8–12.5).

Table 1
Table 1
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In univariate analyses, low birth weight (<2.5 kg), maternal unemployment and low maternal antenatal CD4 cell count were associated (P < 0.20) with increased child death or HIV infection and were therefore included in a multivariate analysis. Overall adjusted hazard ratio (AHR) of HIV infection/death was 1.5 (1.1–2.2, P = 0.03) for low-birth-weight children, 1.9 (1.3–2.9, P = 0.004) for children of unemployed mothers and 2.4 (1.7–3.2, P < 0.001) for children of mothers with an antenatal CD4 cell count below 200 cells/μl.

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Eighteen-month HIV-free survival according to infant feeding practices implemented at birth

Among the 1193 infants, infant feeding practices implemented at birth were: 937 (78%) exclusively breastfed, 105 (8.8%) mixed fed of whom 75 (71.4%) received breast milk and water-based drinks or solids and 30 (28.6%) breast milk and formula milk, and 118 (10%) had received replacement milk only. Thirty-three infants were excluded as they had received only water or were fed intravenously from birth [13] or were missing infant feeding data [20].

Table 2 shows the probability of remaining free from HIV infection and death as well as the probability of survival according to infant feeding practices implemented at birth. By 18 months of age, an estimated 25% of infants ever exclusively breastfed and born to HIV-infected mothers would have acquired HIV infection or have died as compared with 20% of infants never breastfed (P = 0.05). This difference is mostly due to acquisition of infection through breastfeeding. The 18-month probability of survival among HIV-uninfected children was 96% (94–97%) regardless of whether they were breastfed or replacement fed from birth.

Table 2
Table 2
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HIV-free survival according to infant feeding practices from birth until 6 months of age

Of the 893 children included (not HIV-infected peripartum and still alive at 6 months, Table 1), 69 (8%) were never breastfed, 136 (15%) were breastfed for less than 6 months and 688 (76%) were breastfed beyond 6 months of age. Cumulative feeding practices at 3 and 6 months of age are shown in Table 3.

Table 3
Table 3
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Of the 688 children who received breast milk beyond 6 months of age, 278 (31%) had been exclusively breastfed throughout the first 6 months of life, 42 (5%) received liquids other than nonhuman milk at least once and 368 (40%) received food-based fluid, solid food or nonhuman milk in the first 6 months of life. Amongst these 688 children, the overall median duration of breastfeeding was 283 days (interquartile range, 206–491), and the Kaplan–Meier probabilities (95% CI) of still being breastfed at 7, 9, 12 and 18 months of age were 0.74 (0.71–0.78), 0.58 (0.54–0.61), 0.45 (0.41–0.49) and 0.22 (0.19–0.25), respectively.

Univariate and adjusted analyses of the risk of HIV infection or death between 7 and 18 months in 893 infants alive at 6 months showed a 2.7-fold increased risk for infants who continued to be breastfed beyond 6 months than the group who were either replacement fed, exclusively breastfed up to 6 months or ceased all breastfeeding any time before 6 months (Table 4). In a similar analysis but stratified on antenatal maternal CD4 cell count, the adjusted hazard ratio for infants breastfed beyond 6 months was 4.3 (0.9–18.0; P = 0.06) among women with CD4 cell count below 200 cells/μl and 2.5 (1.0–6.2; P = 0.05) among women with CD4 cell count over 200 cells/μl. Mothers who breastfed for less than 6 months (n = 136) were more often unemployed than the mothers who continued to breastfeed beyond 6 months (n = 688) (19.9 vs. 11.5%, P = 0.001); they also tended to more often have access to piped water inside their home (9.5 vs. 7.7%, P = 0.25). Mothers in both groups had similar levels of education and access to toilets. The mean antenatal CD4 cell count was slightly lower in mothers who breastfed for less than 6 months (487 vs. 514 cells/μl, P = 0.24), and the proportion of women with CD4 cell count below 200 cells/μl was also similar (breastfed <6 months 10.8% vs. breastfed >6 months 8.1%, P = 0.31). In multivariate analyses, maternal employment was associated with a three-fold increased likelihood of HIV-free survival between 7 and 18 months in children alive at 6 months (Table 4); antenatal maternal CD4 cell count below 200 cells/μl was associated with a 3.6-fold increased risk of HIV infection or death. Although low birth weight was associated with survival early in life, this was not the case for HIV-free survival between 7 and 18 months of age (P = 0.52).

Table 4
Table 4
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The probabilities of death and postnatal HIV acquisition between 7 and 18 months of age are shown separately in Fig. 1. Univariably, the probability of HIV-free survival (no corresponding figure) at 18 months (conditional on survival to 6 months and including postnatal transmissions) was 0.98 (0.89–1.00) in the 69 infants replacement fed from birth, 0.96 (0.90–0.98) in 136 children who were breastfed for any period up to 6 months (P = 0.25) and 0.91 (0.87–0.94) in 688 children who were breastfed for more than 6 months (P = 0.03). Overall, the probability of HIV-free survival was significantly lower in children who were breastfed for more than 6 months than in the combined group of children replacement fed or breastfed for less than 6 months [0.91 (0.88–0.93) vs. 0.96 (0.93–0.98), P = 0.001].

Fig. 1
Fig. 1
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Overall, breastfeeding beyond 6 months increased the risk of HIV acquisition (AHR 3.3; CI, 1.0–10.5, P = 0.05) compared with durations of breastfeeding less than 6 months. However, in multivariate analysis allowing for infant's HIV infection (data not shown), with replacement feeding only from birth as reference, the probability of survival beyond 6 months of age (excluding deaths in the first 6 months) did not differ by breastfeeding duration: infants breastfed for less than 6 months, AHR 1.2 (0.1–11.9, P = 0.86); breastfed for more than 6 months, AHR 0.9 (0.1–7.1, P = 0.92).

Among the infants breastfed beyond 6 months of age, although the differences in overall probability of death or HIV infection between 7 and 18 months in these three groups did not reach statistical significance, those who were exclusively breastfed in the first 6 months tended to do better than those mixed fed.

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Discussion

The most striking, though not new, message from these data is that HIV infection is the major driver of childhood mortality in these rural and urban communities. About 53% of infants who became infected would have died by 18 months compared with 4% of infants who were not. This again emphasizes the gains for child survival if effective PMTCT programming were achieved [24,25].

In this population, replacement feeding of HIV-uninfected infants between 7 and 18 months, or those who were switched earlier, did not increase the mortality as compared with infants who continued to receive breast milk. It is essential, however, to contextualize these findings, including the circumstances that guided the initial feeding choices of these mothers [14] and the support available to them, before simple generalizations are drawn. Mothers who had limited access to safe water, poor sanitation at home, as well as higher CD4 cell count tended to initiate breastfeeding; mothers with lower CD4 cell count and access to personal income tended to start replacement feeds [14]. Mothers also received on-going guidance and support in their feeding choice and had immediate access to study teams at clinics. The sum of these ‘interventions’ is likely to have optimized the environment in which these feeding choices were practiced and reduced potential morbidity and mortality. This is evidenced by results of an operational study describing the South African national PMTCT programme [3] in which infants of women who were given replacement feeds under inappropriate conditions experienced the highest risk of HIV transmission or death (AHR 3.63; 95% CI, 1.48–8.89) in comparison with those who received replacement feeds under appropriate circumstances.

We were unable to determine whether there had been changes in household circumstances from the antenatal period that might have influenced mothers' decisions to switch from breastfeeding to nonbreastfeeding in the postpartum period. Antenatal demographic and socio-economic characteristics were available, but although counsellors and nurses would have learned of changes in mothers' circumstances and this would have influenced subsequent counselling, this information was not systematically captured in the database. All HIV-infected mothers had been counselled, both antenatally and postpartum, to stop breastfeeding at around 6 months, as long as there was a safe and nutritionally adequate alternative. In spite of this, 688 (77%) mothers of infants uninfected at 6 months decided to continue breastfeeding. Amongst this group, 22% would have continued for at least 18 months. For these infants, although at continued risk of HIV infection, this strategy might still have been correct to promote their long-term overall survival. Given that this was not a randomized trial, we are unable to determine what might have happened if those same mothers had chosen to stop breastfeeding earlier and adopt a feeding practice that could not have been safely practiced in their homes.

Continued breastfeeding resulted in significantly more infections over the 18-month period. Children who were breastfed for more than 6 months were 2.7 times more likely to become infected than those who were breastfed for less than 6 months. The low risk of death, apart from HIV transmission, highlights the feasibility of supporting good infant feeding to promote child survival. HIV-free survival could be achieved, even in rural settings, if strategies to reduce the risk of postnatal infection such as HAART to breastfeeding mothers are demonstrated to be effective and feasible at scale.

In this study, amongst infants who never became infected, early feeding practices did not influence long-term survival. As in the previous analyses of this cohort [1], the number of infants in the mixed feeding categories in the first 6 months was too small to make statistical comparisons regarding transmission, including the risk of mixed feeding in the first 6 months compared with the risk of receiving breast milk and complementary feeds beyond 6 months. The overall estimated HIV transmission risk exposure for breastfeeding over the 18-month period (9.1 cases per 100 child-years of breastfeeding) was similar to previous estimates [26]. Among the infants breastfed beyond 6 months of age and allowing for maternal CD4 cell count, although the differences in overall probability of HIV-free survival between 7 and 18 months did not reach statistical significance, those who were exclusively breastfed in the first 6 months tended to do better than those mixed fed.

Maternal health remained a major determinant of HIV infections and mortality of exposed infants throughout the 18-month period. Overall, the probability of HIV infection or death was not only highest amongst infants born to mothers with low antenatal CD4 cell count but also significantly higher if the mother was unemployed antenatally. Unemployment could represent several independent influences including dependency and lack of autonomy to make choices about infant feeding practices, impaired nutrition and lack of resources, for example, taxi fares for access to health services. Low birth weight of exposed infants also increased the likelihood of adverse outcomes in early life and may similarly reflect poor maternal health and antenatal care. Perhaps surprisingly, infant outcomes between 7 and 18 months were more substantially determined by these maternal factors than by feeding practices.

We were surprised by the relatively large number of mothers who continued to breastfeed beyond 6 months, despite counselling, planning and access to replacement feeds. That so many mothers opted to continue breastfeeding likely reflects the socio-demographics of the study population and cultural issues within the communities. These mothers presumably weighed up the complexities and relative inconvenience of safe replacement feeding and decided that continued breastfeeding was still preferable. PMTCT programmes need to offer better counselling and support throughout this time if overall child health and survival are to improve.

Methodologically, we did not permit any lapses whatsoever when allocating infants to specific feeding practices. If an infant received water, nonhuman milk or solids even for 1 day, the infant was reclassified as mixed fed. In comparison with our analysis of HIV transmission in the first 6 months [1], in which we permitted up to 3 lapsed days before exclusion to another category, this approach significantly reduced the number of infants within the exclusive breastfeeding group. Also, because in this analysis we were interested in transmission and survival by initial feeding mode, or feeding mode up to a certain age, we did not censor when the child dropped out of the initial feeding mode.

The question remains how best to identify and support the optimal infant feeding strategy beyond 6 months for individual HIV-infected women. Any approach must consider a mother's prevailing or changing household circumstances as well as her own disease status to determine if, or when, she should stop breastfeeding. Health workers such as counsellors and nurses involved with PMTCT programmes need to remain in contact with mothers in order to assist with the process of stopping breastfeeding and offer advice on complementary feeding. Amidst the many difficult contextual issues remains the greatest opportunity, namely to identify the women with low CD4 cell count and start them on HAART for life. When HAART is not available for this group of women, the balance of evidence suggests that when possible and safe, stopping breastfeeding at 6 months or before will increase the child's long-term prospects of survival. The ability of international recommendations, national policies, individual programmes and community responses to promote and protect the equality and autonomy of women and mothers, to benefit from employment and access to health interventions, will be measured by the most tangible of child health outcomes, namely whether they live or die.

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Acknowledgements

Authors contributions: N.C.R.: design, implementation and project management of the study, analysis of data and drafting the manuscript. R.B.: analysis of data and drafting the manuscript. R.M.B.: design, implementation and project management of the study, analysis of data and reviewing the manuscript. A.C.: conceptualization, design and implementation of the study and drafting the manuscript. H.M.C.: conceptualization, design and implementation of the study and drafting the manuscript. M.-L.N.: design of study, analysis of data and drafting the manuscript.

We are grateful to all women and children enrolled in the study and the continued dedication of field, clinic and data management staff at the Africa Centre, in particular Thembi Blose, Zanele Fakude, Cookie Govender, Nqobile Mkhwanazi, Londiwe Mthethwa, Samukelisiwe Mtshali and Ntombizodumo Mkwanazi. We are also grateful to Jan van den Broeck and Colin Newell who assisted with data management during the study and analyses, Dave Perlman and Kobus Herbst for their assistance in the design of the database, Deven Patel for advice and analytical support, Geoff Solarsh, Shuaib Kauchali and Ameena Goga, Jane Lucas and Felicity Savage King for assistance in the initial formative pilot work and training. In particular, we wish to thank the Community Liaison Office of the Africa Centre and the Community Advisory Board for their guidance and feedback throughout the study.

We are also grateful to the independent members of the Study Steering Committee and the Data Monitoring and Safety Committees. Study Steering Committee: Janet Darbyshire (Chair), Nono Simelela (South Africa National Department of Health), Victoria Sithole (Community Advisory Board). Data Monitoring and Safety Committee: Cathy Wilfert (Chair, Elizabeth Glaser Pediatric AIDS foundation), Carl Lombard (Statistician, MRC, South Africa), Ames Dhai (Department of Obstetrics and Gynaecology and the Biomedical Ethics Unit, University of KwaZulu-Natal) and Francis Crawley (Good Clinical Practice Alliance).

The Africa Centre for Health and Population Studies was supported by a core centre grant from the Wellcome Trust (050524) and the Vertical Transmission Study by an additional grant (Wellcome Trust, UK 063009/Z/00/2). R.B. was funded by the French charity SIDACTION as a visiting scientist at the Africa Centre for Health and Population Studies (University of KwaZulu-Natal, South Africa).

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Keywords:

HIV infection; infant feeding; maternal health; mortality; transmission

© 2008 Lippincott Williams & Wilkins, Inc.

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