Secondary Logo

Journal Logo

Epidemiology and Social

Weight gain of HIV-exposed, uninfected children born before and after introduction of the ‘Option B+’ programme in Malawi

Msukwa, Malango T.a,b; Estill, Jannea,c; Haas, Andreas D.d; van Oosterhout, Joep J.e,f; Tenthani, Lysond,g; Davies, Mary-Annh; Tal, Kalia,i; Phiri, Nozgechia,b; Spoerri, Adriand; Mthiko, Bryan C.a,b; Chimbwandira, Frankj; Keiser, Oliviaa

Author Information
doi: 10.1097/QAD.0000000000001942



Scaling up prevention of mother-to-child transmission (PMTCT) interventions has drastically lowered the number of HIV-infected children worldwide. Without intervention, the likelihood of mother-to-child transmission (MTCT) of HIV ranges from 15 to 45%, but effective PMTCT interventions can reduce this risk to under 5% [1]. In Malawi, PMTCT coverage remained sub-optimal until 2011, when the Ministry of Health (MoH) pioneered implementation of universal lifelong combination antiretroviral therapy (ART) for pregnant and breastfeeding women regardless of their CD4+ cell count or clinical stage [‘Option B+’ (OB+)] [2]. As a consequence of the scale-up of OB+, ART coverage in pregnant and breastfeeding women has increased and MTCT risk of HIV declined [3] resulting in a growing number of HIV-exposed, uninfected (HEU) children.

Although scaling up of PMTCT has greatly improved maternal health, there is concern that in-utero exposure to antiretrovirals may negatively affect birth outcomes, growth and development of infants born to HIV-infected mothers [4–6]. Some studies reported that in-utero antiretroviral exposure is associated with low birth weight [6–8]; others found no such association [9–12]. Some studies found differences in weight gain [13–17] between HEU infants and healthy controls. A systematic review published in 2014 was inconclusive about the effect of in-utero HIV and antiretroviral exposure on postnatal weight gain of HIV-exposed infants [4].

Although some studies have examined the association between in-utero ART exposure and adverse birth outcomes in the OB+ era [18,19], no study has investigated if OB+ affects the growth of HEU infants. We investigated the impact of OB+ on postnatal weight gain of Malawian HEU infants in the first 24 months of their lives under programmatic circumstances.


Study setting

Malawi's MoH provides integrated services for HIV-exposed infants in the national HIV care clinic (HCC) programme under Integrated HIV Management guidelines [20] as previously described [21]. Programme data suggest that most known HIV-exposed infants are enrolled and managed in this programme with regular clinic follow-up from 6 weeks after birth [20,22].

Study design and inclusion criteria

We included infants born to an HIV-infected woman, who enrolled in the HCC programme between January 2010 and December 2014 at any of the 21 large health facilities in central and southern Malawi that participated in our study to evaluate the implementation of OB+ ( (Fig. 1). The facilities included 13 district hospitals, two central hospitals, three faith based hospitals, and three large health centres. All infants who had a negative HIV test result were included. HIV-infected infants diagnosed positive at any point during follow-up and infants with unknown HIV status were excluded. We also excluded infants with missing birth date, birth weight or sex, and infants with no follow-up weight measurement. Infants were included in the analysis from enrolment until the last recorded follow-up visit.

Fig. 1
Fig. 1:
Study participants.

Data collection, preparation and management

Registration and follow-up data for HIV-exposed infants enrolled in the HCC programme are recorded on standardized paper-based treatment cards stored at health facilities. At each visit, trained healthcare workers measure infant's weight with a mechanical scale that is calibrated daily [23]. Routinely collected data were digitized from the treatment cards, followed by double data entry and cleaning. Records were de-duplicated using probabilistic linkage [21].

Definitions and outcomes

Programmatic outcomes at the end of follow-up were defined as under follow-up, died, discharged uninfected, transferred out to another health facility, or lost to follow-up (LTFU). LTFU was defined as missing a clinic appointment for more than 60 days and not returning to care. ART was defined as a combination of at least three antiretroviral drugs. Before OB+, women eligible for ART received a combination of stavudine, lamivudine and nevirapine. Women not eligible for ART received zidovudine monotherapy during pregnancy followed by zidovudine + lamivudine dual therapy or single-dose nevirapine during labour. During OB+, all women received a combination of tenofovir, lamivudine and efavirenz.

We defined birth period as pre-Option B+ (pre-OB+) or Option B+ (OB+) using the date each facility switched to OB+. Infants born within a few months of the health facility's switch to OB+ were classified into the OB+ group, although they were not necessarily exposed to OB+ from the beginning of pregnancy. We converted birth weight and weight measurements into age and sex-adjusted z scores, based on the WHO 2006 standard [24].

The primary outcome was postnatal weight gain in the first 24 months of life, assessed with weight-for-age z scores (WAZ). We also assessed factors associated with birth weight (WAZ at birth).

Statistical analyses

Baseline characteristics by birth period were compared with Wilcoxon rank-sum tests for continuous variables and Chi-square tests for categorical variables. We used linear regression to investigate differences in WAZ at birth, and mixed effects models to examine changes in WAZ over time (with a random effect on the infant and fixed effects on the intercept and explanatory variables). We used a third order polynomial transformation for age (in months) because weight gain is not linear. We tested the effect of covariates on WAZ at birth and during follow-up, and for an interaction between the polynomial transformation of age and birth period, with a likelihood ratio test. We also did stratified analyses by birth period to identify predictors of postnatal weight gain in each birth period. All available weight measurements from enrolment up to the last follow-up visit (including infants who were LTFU, transferred out or who died) were included in the analysis. All mixed effects models were adjusted for the polynomial transformation of age. In multivariable models, we adjusted for infant's gender, birth weight (<2.5 kg, ≥2.5 kg), type of health facility (health centre, faith-based hospital, district hospital, central hospital), and infant antiretroviral exposure during pregnancy or labour (none, mono or dual-therapy, ART <4 weeks, or ART ≥4 weeks at any stage).

Results from models are presented as differences in WAZ with 95% confidence intervals. All analyses were performed in STATA version 14 (Stata Corporation, College Station, Texas, USA) and P values <0.05 were considered significant. The Malawi National Health Sciences Research Committee and the Cantonal Ethics Committee of Bern granted ethical approval.


Of the 16 200 infants enrolled in the HCC programme between February 2010 and May 2015, 9355 infants were excluded, of whom 1318 (14.1%) were born during the pre-OB+ and 8008 (85.6%) during the OB+ period. This resulted in a study population of 6845 HEU infants with a median follow-up of 11.3 months [interquartile range (IQR): 5.1–17.0 months] (Fig. 1). Baseline characteristics of included and excluded infants were significantly different except for birth weight and sex (Appendix, Table A1,

Baseline characteristics by birth period

A total of 784 (11.5%) HEU infants were born in the pre-OB+ period and 6061 (88.5%) in the OB+ period (Table 1). By the end of follow-up, 33.4% (n = 2285) of HEU infants were LTFU, 0.4% (n = 27) had died, and 1.9% (n = 127) had transferred to another facility. More HEU infants were LTFU in the pre-OB+ group (48.3%) than in the OB+ group (31.5%); rates of LTFU were 3.5 per 100 person-months (379/10756) in the pre-OB+ group and 2.7 per 100 person-months (1906/70298) in the OB+ group. Infants in the OB+ group were younger at enrolment, more likely exposed to ART in utero (85.1 vs. 64.1%) and ART exposure was longer (74.1 vs. 42.2% on ART for ≥4 weeks), than those in the pre-OB+ group.

Table 1
Table 1:
Characteristics of HIV-exposed, uninfected children by birth period.

Factors affecting birth weight

There were no statistically significant differences in WAZ at birth among infants born before and after introduction of OB+ (Table 2). Infants enrolled at a health centre or district hospital had significantly higher WAZ at birth than infants enrolled at a central hospital. Exposure to antiretrovirals during pregnancy or labour, irrespective of regimen or duration, had no significant effect on WAZ at birth.

Table 2
Table 2:
Linear regression analysis of weight-for-age z scores at birth, birth weight (n = 6845).

If the analysis was stratified by birth period, associations were similar (Appendix, Tables A2a and A2b, In the adjusted analysis the association between type of facility and WAZ at birth was however only present in the OB+ group.

Factors affecting postnatal weight gain

The interaction between polynomial transformation of age and birth period was not significant in univariable analysis (P = 0.287) and was therefore not included in the model. Postnatal WAZ was higher in the OB+ group (difference 0.211, 95% CI 0.117–0.306; P < 0.0001) irrespective of age after adjusting for gender, birth weight, facility type and maternal antiretroviral exposure (Table 3 and Fig. 2). Other predictors of WAZ over time included a birth weight of at least 2.5 kg and female gender. Infant's exposure to antiretrovirals during pregnancy or labour, regardless of type of regimen or length of exposure, had no significant impact on postnatal WAZ in the univariable analysis. Infants exposed to ART for at least 4 weeks during pregnancy had significantly lower WAZ in the first 24 months of life in adjusted analyses. However, when we stratified the analysis by birth period (Appendix, Tables 3a and 3b,, only infant gender and type of health facility had a significant effect on WAZ in the OB+ period, and there was no effect of type and duration of antiretroviral exposure on WAZ in either birth period.

Table 3
Table 3:
Mixed-effects model of weight-for-age z scores over time (age: 0–24 months).
Fig. 2
Fig. 2:
Predicted z scores from univariable mixed effects model for weight-for-age by birth period (i.e., pre Option B+ and Option B+) adjusted for the polynomial transformation of age (months).Dotted lines represent 95% confidence intervals.


The proportion of infants exposed to ART during pregnancy or labour increased significantly after OB+ was implemented, and infants were exposed to ART for a longer time. WAZ was similar at birth among HEU infants born before and after OB+, but postnatal weight gain was higher in HEU infants born in the OB+ period than infants born in the pre-OB+ period.

Prolonged exposure to ART, more common in the OB+ period, may increase adverse pregnancy outcomes like preterm delivery and low birth weight [25]. The European collaborative study found an association between prematurity and ART exposure, for all types of regimens [9]. Some studies from resource-limited settings found that lower birth weight was associated with in-utero ART exposure [8,26,27] but did not seem to impair postnatal growth [8,27,28].

We found that neither the type of antiretroviral regimen, nor length of in-utero ART exposure was associated with WAZ at birth in HEU infants consistent with other African studies [12,14,29]. Most infants in our study were exposed to ART in utero, so a potential negative effect of ART was probably counter balanced by the favourable immunological and virological response to ART in the pregnant woman, resulting in improved maternal health that benefits infants’ outcomes. However, we had no data on CD4+ cell counts and viral loads during pregnancy.

Disentangling the exact effect of the birth period, the type and length of ART exposure, and the CD4+ cell count on WAZ at birth and longitudinal weight gain was not possible. Since we compared the pre-OB+ period with the OB+ period, the number of drugs and the types of antiretroviral regimens depended on the birth period. During the pre-OB+ period, women who were on combination ART had low CD4+ cell counts or were in an advanced stage of the disease. The association of being on ART at least 4 weeks with slower weight gain may therefore be driven by observations in the pre-OB+ period. However, we could not confirm this hypothesis in stratified analyses, possibly because of the low sample size.

Since we did not capture the date of ART initiation, we also do not know whether the women had started ART preconception, in the first trimester, or in the last two trimesters. This is a relevant limitation because a study from Brazil showed that birth weight was lower in infants with exposure to ART in the first trimester than later exposure or no exposure to ART in utero[30]. Discrepant findings between studies may be related to differences in the populations studied, variations in antenatal and postnatal care and contrasting study designs (e.g. adjustment for different confounders and different selection criteria).

A number of additional factors were associated with postnatal WAZ. Contrary to other studies [31–35], we found no significant differences in WAZ at birth between boys and girls. However, girls had higher postnatal WAZ than boys, in agreement with a study done in South Africa [31]. HEU infants with normal weight at birth (≥2.5 kg) had higher postnatal WAZ than those with low birth weight (<2.5 kg) consistent with previous studies [17,36,37].

We faced several limitations. The first was our inability to determine if OB+ itself spurred improvement in postnatal weight gain, or if other factors were responsible. In developing countries, poverty, socio-economic conditions, malnutrition, and poor health affect the growth and development of children under the age of 5 [38]. Socioeconomic, environmental and immunological factors are also associated with undernutrition in children born to HIV-infected mothers [17,39,40]. We did not adjust for these factors because we had no data. Second, in routine clinical care LTFU is often high. Weight measurements are biased by LTFU, because children with impaired weight gain are more likely to be LTFU and to die. Therefore, we anticipate that weight gain was particularly overestimated in the pre OB+ group. Third, we only included large health facilities, so our findings may not be representative of infants from smaller rural health centres. Fourth, birth length was not recorded, and height was sporadically recorded during follow-up visits, so we could not compare length/height-for-age and weight-for-length/height z scores over time. Fifth, we determined birth period according to infant's date of birth. When a clinic implemented OB+, all women attending antenatal care, including those who were already on zidovudine prophylaxis, were instructed to switch to triple life-long ART at their next visit. In practice, however, the transition to OB+ may have taken some time, and infants born soon after the switch to OB+ were not exposed to the policy for the entire period. Therefore, inclusion of HEU infants born in the transition period in the OB+ group underestimates the positive effect of OB+ on weight gain. Finally, we excluded a large number of infants due to missing data whose characteristics were different from those included.

Our study has a number of strengths. We believe we are the first to assess weight gain in routine care during the first 24 months of life for HEU infants in the OB+ era. Our study had a large sample size, and followed HEU infants over a long period. Our study facilities were geographically diverse and included a variety of clinical settings.

Our finding of better postnatal weight gain among HEU infants born in the OB+ period is encouraging considering the widespread implementation of OB+. To confirm our findings, future studies should include small health centres and account for socioeconomic characteristics, infant feeding practices, and maternal disease progression. OB+ increased exposure to ART during pregnancy. The increase did not affect birth weight, and seems to have improved postnatal weight gain in HEU infants, possibly because OB+ also improved mothers’ health.


We would like to thank the health facility staff and the staff from the Ministry of Health and the Christian Health Association of Malawi (CHAM), who supported data collection at the sites. We thank the data entry team (Abigail Nkukumila, Alick Momba, Ashton Mwechumu, Bazaliel Chimosola (deceased), Chikondi Milanzi, Enock Chauwa, Florence Kamunga, Gomezgani Nyasulu, Imelda Banda (deceased), Jestina Mhango, Kondwani Nyirenda, Lloyd Mkomela, Memory Dzonzi, Monica Chimbaza, Olivia Kamanga, Racheal Gonani, Takondwa Zidana, Zelipher Ziyenda), who diligently entered our data into an electronic database. Finally, we thank Baobab Health Trust for the support provided during the course of this study.

Author contributions: O.K. and M.T.M. conceived the study. M.T.M. did the statistical analyses under the supervision of O.K. and J.E. B.C.M. contributed to the statistical analyses. M.T.M., O.K., J.E. and K.T. wrote the first draft of the paper, which was subsequently revised by all co-authors. M.T.M., A.D.H., A.S., N.P. and L.T. organized data entry and data management. M.A.D. and J.J.v.O. provided clinical and epidemiological input. M.A.D. is the co-principal investigator (PI) of the IeDEA grant; F.C. is the PI for the NIH PEER grant and O.K. is the PI of the grant from the Bill and Melinda Gates Foundation.

Declaration of interests: Research reported in this publication was supported by the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under award number U01AI069924. Additional support was provided by the Bill and Melinda Gates Foundation (Global Health Grant OPP1090200), The United States Agency for International Development-Partnerships for Enhanced Engagement in Research Health (PEER Health) grant AID OAA-A-11-0012. O.K. was supported by a professorship grant from the Swiss National Science Foundation (grant number 163878). The content is solely the responsibility of the authors and does not necessarily represent the official views of the sponsors.

Conflicts of interest

The authors declare no conflicts of interest.


1. World Health Organization. Mother-to-child transmission of HIV [Internet]. WHO. [Accessed 17 October 2017]
2. Schouten EJ, Jahn A, Midiani D, Makombe SD, Mnthambala A, Chirwa Z, et al. Prevention of mother-to-child transmission of HIV and the health-related Millennium Development Goals: time for a public health approach. Lancet 2011; 378:282–284.
3. Chimbwandira F, Mhango E, Makombe S, Midiani D, Mwansambo C, Njala J, et al. Impact of an innovative approach to prevent mother-to-child transmission of HIV-Malawi, July 2011-September 2012. Morb Mortal Wkly Rep 2013; 62:148–151.
4. Jao J, Abrams EJ. Metabolic Complications of in utero Maternal HIV and Antiretroviral Exposure in HIV-exposed Infants. Pediatr Infect Dis J 2014; 33:734–740.
5. Darak S, Darak T, Kulkarni S, Kulkarni V, Parchure R, Hutter I, et al. Effect of Highly Active Antiretroviral Treatment (HAART) during pregnancy on pregnancy outcomes: experiences from a PMTCT program in Western India. AIDS Patient Care STDs 2013; 27:163–170.
6. Ekouevi DK, Coffie PA, Becquet R, Tonwe-Gold B, Horo A, Thiebaut R, et al. Antiretroviral therapy in pregnant women with advanced HIV disease and pregnancy outcomes in Abidjan, Côte d’Ivoire. AIDS Lond Engl 2008; 22:1815–1820.
7. Briand N, Le Coeur S, Traisathit P, Karnchanamayul V, Hansudewechakul R, Ngampiyasakul C, et al. Growth of human immunodeficiency virus-uninfected children exposed to perinatal zidovudine for the prevention of mother-to-child human immunodeficiency virus transmission. Pediatr Infect Dis J 2006; 25:325–332.
8. Powis KM, Smeaton L, Ogwu A, Lockman S, Dryden-Peterson S, Widenfelt, van E, et al. Effects of in utero antiretroviral exposure on longitudinal growth of HIV-exposed uninfected infants in Botswana. J Acquir Immune Defic Syndr 19992011; 56:131.
9. European Collaborative Study. Exposure to antiretroviral therapy in utero or early life: the health of uninfected children born to HIV-infected women. J Acquir Immune Defic Syndr 1999 2003; 32:380–387.
10. Cotter AM, Garcia AG, Duthely ML, Luke B, O'Sullivan MJ. Is antiretroviral therapy during pregnancy associated with an increased risk of preterm delivery, low birth weight, or stillbirth?. J Infect Dis 2006; 193:1195–1201.
11. Tuomala RE, Shapiro DE, Mofenson LM, Bryson Y, Culnane M, Hughes MD, et al. Antiretroviral therapy during pregnancy and the risk of an adverse outcome. N Engl J Med 2002; 346:1863–1870.
12. Szyld EG, Warley EM, Freimanis L, Gonin R, Cahn PE, Calvet GA, et al. Maternal antiretroviral drugs during pregnancy and infant low birth weight and preterm birth. AIDS Lond Engl 2006; 20:2345–2353.
13. Rosala-Hallas A, Bartlett JW, Filteau S. Growth of HIV-exposed uninfected, compared with HIV-unexposed, Zambian children: a longitudinal analysis from infancy to school age. BMC Pediatr 2017; 17:80.
14. Siberry GK, Williams PL, Mendez H, Seage GR, Jacobson DL, Hazra R, et al. Safety of tenofovir use during pregnancy: early growth outcomes in HIV-exposed uninfected infants. AIDS Lond Engl 2012; 26:1151–1159.
15. Paul ME, Chantry CJ, Read JS, Frederick MM, Lu M, Pitt J, et al. Morbidity and mortality during the first two years of life among uninfected children born to human immunodeficiency virus type 1-infected women: the women and infants transmission study. Pediatr Infect Dis J 2005; 24:46–56.
16. Makasa M, Kasonka L, Chisenga M, Sinkala M, Chintu C, Tomkins A, et al. Early growth of infants of HIV-infected and uninfected Zambian women. Trop Med Int Health 2007; 12:594–602.
17. Muhangi L, Lule SA, Mpairwe H, Ndibazza J, Kizza M, Nampijja M, et al. Maternal HIV infection and other factors associated with growth outcomes of HIV-uninfected infants in Entebbe, Uganda. Public Health Nutr 2013; 16:1548–1557.
18. Rempis EM, Schnack A, Decker S, Braun V, Rubaihayo J, Tumwesigye NM, et al. Option B+ for prevention of vertical HIV transmission has no influence on adverse birth outcomes in a cross-sectional cohort in Western Uganda. BMC Pregnancy Childbirth 2017; 17:82.
19. Chagomerana MB, Miller WC, Pence BW, Hosseinipour MC, Hoffman IF, Tweya H, et al. PMTCT option B+ does not increase preterm birth risk and may prevent extreme prematurity: a retrospective cohort study in Malawi. J Acquir Immune Defic Syndr 2017; 74:367–374.
20. Ministry of Health Malawi. Clinical management of HIV in children and adults [Internet]. 2014 [Accessed 8 December 2017]
21. Haas AD, van Oosterhout JJ, Tenthani L, Jahn A, Zwahlen M, Msukwa MT, et al. HIV transmission and retention in care among HIV-exposed children enrolled in Malawi's prevention of mother-to-child transmission programme. J Int AIDS Soc 2017; 20:21947.
22. Ministry of Health Malawi. Integrated HIV program report: October -December 2014 [Internet]. 2014. [Accessed 8 December 2017]
23. Ministry of Health (MOH). Guidelines for community-based management of acute malnutrition. 2nd. ed. [Internet]. 2016. [Accessed 11 December 2017]
24. Leroy Jef L. zscore06: Stata command for the calculation of anthropometric z-scores using the 2006 WHO child growth standards. 2011. [Accessed 11 July 2018]
25. Chen JY, Ribaudo HJ, Souda S, Parekh N, Ogwu A, Lockman S, et al. Highly active antiretroviral therapy and adverse birth outcomes among HIV-infected women in Botswana. J Infect Dis 2012; 206:1695–1705.
26. Njom Nlend AE, Nga Motazé A, Moyo Tetang S, Zeudja C, Ngantcha M, Tejiokem M. Preterm birth and low birth weight after in utero exposure to antiretrovirals initiated during pregnancy in Yaoundé, Cameroon. PloS One 2016; 11:e0150565.
27. Gibb DM, Kizito H, Russell EC, Chidziva E, Zalwango E, Nalumenya R, et al. Pregnancy and infant outcomes among hiv-infected women taking long-term ART with and without tenofovir in the DART trial. PLOS Med 2012; 9:e1001217.
28. Viganò A, Mora S, Giacomet V, Stucchi S, Manfredini V, Gabiano C, et al. In utero exposure to tenofovir disoproxil fumarate does not impair growth and bone health in HIV-uninfected children born to HIV-infected mothers. Antivir Ther 2011; 16:1259–1266.
29. van der Merwe K, Hoffman R, Black V, Chersich M, Coovadia A, Rees H. Birth outcomes in South African women receiving highly active antiretroviral therapy: a retrospective observational study. J Int AIDS Soc 2011; 14:42.
30. Hofer CB, Keiser O, Zwahlen M, Lustosa CS, Frota ACC, de Oliveira RH, et al. In utero exposure to antiretroviral drugs: effect on birth weight and growth among HIV-exposed uninfected children in Brazil. Pediatr Infect Dis J 2016; 35:71–77.
31. Morden E, Technau KG, Giddy J, Maxwell N, Keiser O, Davies MA. Growth of HIV-exposed uninfected infants in the first 6 months of life in South Africa: the IeDEA-SA collaboration. PLOS One 2016; 11:e0151762.
32. Natchu UC, Liu E, Duggan C, Msamanga G, Peterson K, Aboud S, et al. Exclusive breastfeeding reduces risk of mortality in infants up to 6 mo of age born to HIV-positive Tanzanian women. Am J Clin Nutr 2012; 96:1071–1078.
33. Landes M, van Lettow M, Chan AK, Mayuni I, Schouten EJ, Bedell RA. Mortality and health outcomes of HIV-exposed and unexposed children in a PMTCT cohort in Malawi. PLoS One 2012; 7:e47337.
34. Taha TE, Dadabhai SS, Rahman MH, Sun J, Kumwenda J, Kumwenda NI. Trends in birth weight and gestational age for infants born to HIV-infected, antiretroviral treatment-naive women in Malawi. Pediatr Infect Dis J 2012; 31:481–486.
35. Homsy J, Moore D, Barasa A, Were W, Likicho C, Waiswa B, et al. Breastfeeding, mother-to-child HIV transmission, and mortality among infants born to HIV-Infected women on highly active antiretroviral therapy in rural Uganda. J Acquir Immune Defic Syndr 19992010; 53:28–35.
36. Arpadi S, Fawzy A, Aldrovandi GM, Kankasa C, Sinkala M, Mwiya M, et al. Growth faltering due to breastfeeding cessation in uninfected children born to HIV-infected mothers in Zambia. Am J Clin Nutr 2009; 90:344–353.
37. Patel D, Bland R, Coovadia H, Rollins N, Coutsoudis A, Newell M-L. Breastfeeding, HIV status and weights in South African children: a comparison of HIV-exposed and unexposed children. AIDS 2010; 24:437–445.
38. Grantham-McGregor S, Cheung YB, Cueto S, Glewwe P, Richter L, Strupp B, et al. Developmental potential in the first 5 years for children in developing countries. Lancet 2007; 369:60–70.
39. Ram M, Gupte N, Nayak U, Kinikar AA, Khandave M, Shankar AV, et al. Growth patterns among HIV-exposed infants receiving nevirapine prophylaxis in Pune, India. BMC Infect Dis 2012; 12:282.
40. Venkatesh KK, Lurie MN, Triche EW, De Bruyn G, Harwell JI, McGarvey ST, et al. Growth of infants born to HIV-infected women in South Africa according to maternal and infant characteristics. Trop Med Int Health 2010; 15:1364–1374.

HIV-exposed uninfected infant; Option B+; weight gain; weight-for-age z scores

Supplemental Digital Content

Copyright © 2018 Wolters Kluwer Health, Inc.