High risk of adverse birth outcomes among adolescents living with HIV in Botswana compared to adult women living with HIV and adolescents without HIV
BMC Pregnancy and Childbirth volume 22, Article number: 372 (2022)
Adolescent girls are three times more likely to be living with HIV than boys of the same age. Prior studies have found associations between adolescent pregnancies and increased maternal morbidity and infant mortality, but few studies have assessed the impact of HIV infection on maternal and infant outcomes in adolescents.
The Tsepamo Study abstracts maternal and infant data from obstetric records in government maternity wards in Botswana. We assessed maternal complications and adverse birth outcomes for all singleton pregnancies from August 2014 to August 2020 at eighteen Tsepamo sites among adolescents (defined as 10–19 years of age) and adults (defined as 20–35 years of age), by HIV status. Univariate and multivariate logistic regression using a complete case analysis method were used to evaluate differences in outcomes.
This analysis included 142,258 singleton births, 21,133 (14.9%) to adolescents and 121,125 (85.1%) to adults. The proportion of adults living with HIV (N = 22,114, 22.5%) was higher than adolescents (N = 1593, 7.6%). The proportion of most adverse birth outcomes was higher in adolescents. Among adolescents, those with HIV had increased likelihoods of anemia (aOR = 1.89, 95%CI 1.66, 2.15) and cesarean sections (aOR = 1.49, 95%CI 1.3,1.72), and infants with preterm birth (aOR = 1.15, 95%CI 1.0, 1.32), very preterm birth (aOR = 1.35, 95%CI 1.0,1.8), small for gestational age (aOR = 1.37, 95%CI 1.20,1.58), and very small for gestational age (aOR = 1.46, 95%CI 1.20, 1.79).
Adolescent pregnancy and adolescent HIV infection remain high in Botswana. Adolescents have higher risk of adverse maternal and infant birth outcomes than adults, with the worst outcomes among adolescents living with HIV. Linking HIV prevention and family planning strategies for this age group may help minimize the number of infants with poor birth outcomes among this already vulnerable population.
In low-resourced countries, an estimated 2.5 million births occur in girls under age 16 each year, with the highest rates found in Sub-Saharan Africa . Adolescent pregnancy is associated with increased maternal morbidity from post-partum hemorrhage, puerperal endometritis, operative vaginal delivery, episiotomy, and pre-eclamptic/eclamptic events. There is also an increased risk of adverse birth outcomes including preterm delivery and small for gestational age infants with adolescent pregnancy [2,3,4,5,6,7,8,9,10,11,12]. Studies looking to better understand the reasons for these adverse outcomes are conflicting. Some suggest that social determinants of health such as early initiation of smoking, alcohol and substance abuse, low academic interest, single-parent families, poverty, and inadequate prenatal care put adolescents at increased risk [13,14,15,16]. Other studies hypothesize biological immaturity to be the underlying cause for this disparity [9, 13, 14, 16,17,18,19,20].
Poor outcomes in adolescent pregnancy may be exacerbated by the HIV epidemic. Studies have shown strong associations between maternal HIV infection in adults with infant mortality and adverse birth outcomes, particularly in low-resourced settings [21,22,23]. Although these studies have highlighted risks associated with vertical transmission and the potential immunologic impact on HIV-exposed uninfected children, few studies have looked at adverse birth outcomes in the adolescent age group . In Botswana, a country with a high HIV prevalence and high adolescent birth rate (52.3 per 1000), three in every ten new HIV infections occur among adolescents between 15 to 24 years of age. Adolescent girls between 10 to19 years of age are three times more likely to be infected than boys of the same age [25, 26]. Using data from a large birth surveillance study in Botswana (the Tsepamo Study), we compared birth outcomes between adolescent girls and adult women by HIV status to better understand the relationship between adolescent HIV infection and adverse pregnancy outcomes.
Data for this analysis were collected from the ongoing Tsepamo Study, which has performed surveillance of pregnancy and birth outcomes at public hospital delivery sites in Botswana since 2014 . The current analysis includes eighteen study sites that have been operational throughout the entire study period, representing approximately 70% of all births in the country . These maternity wards are located in urban areas (the Princess Marina Hospital in Gaborone, Nyangabgwe Referral Hospital in Francistown) and rural areas (Letsholathebe II Memorial Hospital in Maun, Sekgoma Memorial Hospital in Serowe, the Selebi-Phikwe Hospital, the Mahalapye Hospital, Scottish Livingstone Hospital in Molepolole, and the Ghanzi Primary Hospital). This analysis includes all in-hospital deliveries between August 2014 and August 2020, to women aged 10 to 35 years with singleton births. The upper limit for this age cut off was intended to limit our comparison to younger adults at a standard risk for adverse birth outcomes. Adolescents and adults who delivered twins or triplets were excluded because of the known increased risk of birth complications with multiple gestations [29, 30]. Data were not collected on deliveries that occurred prior to arriving to the hospital, infants transferred from an outside hospital after delivery, or deliveries before 24 weeks gestational age (classified as miscarriage in Botswana).
Data were abstracted from the maternal obstetric records at the time of discharge as previously described [28, 31]. For this analysis, abstracted data included hemoglobin levels, initial pregnancy weights, blood pressure measurements, gestational age (GA) at time of delivery, mode of delivery, and infant outcomes. Additional data included demographics, maternal diagnoses during pregnancy, medications and antibiotics prescribed during pregnancy, self-reported alcohol use and smoking, outpatient antenatal care visit dates, and HIV status. For adolescents and women living with HIV, the date of HIV diagnosis and antiretroviral treatment (ART) history (including start date, regimen and any switch or discontinuation during pregnancy) were also recorded. Diagnoses were recorded as per documentation of the treating physician or midwife, except for maternal anemia which was defined as hemoglobin < 10 g/dL and maternal hypertension which was defined as systolic blood pressure ≥ 140 or diastolic blood pressure ≥ 90 in pregnancy. The diagnosis of underweight was defined as initial pregnancy weight < 50 kg . The estimated GA included in the obstetric record was used for analyses and if missing, gestational age was calculated using last menstrual period (LMP). Antenatal clinic nurses estimated GA by date of LMP in most cases but used fundal measurements or ultrasound if LMP was unknown. Infant data were abstracted from the medical record and included sex, birth weight, delivery complications, and admission to the neonatal unit [28, 31].
Exposures and outcomes
We defined participants 10 to 19 years of age as adolescents and 20 to 35 years of age as adults. The primary outcomes consisted of 1) maternal complications during pregnancy, labor and delivery and 2) adverse birth outcomes. Maternal complications included anemia, diagnosis of syphilis infection, hypertensive disease of pregnancy, and cesarean section. We defined hypertensive disease of pregnancy to include pregnancy induced hypertension and severe hypertension. We acknowledged that there may be unmeasured confounders in the relationships between adolescents and the particular outcomes of interest. Adverse birth outcomes included stillbirth, small for gestational age (SGA), very small for gestational age (VSGA), neonatal death, preterm delivery (PTD), and very preterm delivery (VPTD). Stillbirth was defined as a summed APGAR score of 0. Based on the Intergrowth-21 norms (defined for 24–42 weeks gestational age), infants were categorized as SGA if they weighed less than the tenth percentile birth weight by gestational age, and VSGA if they weighed less than the third percentile birth weight by gestational age . Neonatal death was defined as infant death prior to leaving the hospital within 28 days of delivery. Preterm delivery was defined as deliveries at less than 37 weeks gestational age. Very preterm delivery was defined as deliveries less than 32 weeks gestational age.
The proportions of all outcomes were individually assessed among adolescents and adults overall, then subsequently stratified by HIV status. Chi-square and Fischer exact tests were conducted to compare background information between groups and p-values were generated using two-sided tests with an α = 0.01 significance level. Univariate and multivariate logistic regression analyses were performed to evaluate differences in outcomes by age in the overall population and stratified by maternal HIV status. Variables were pre-selected for the logistic regression models based on prior Tsepamo analyses and existing literature and also included all univariate associations p < .05. These included Botswana citizenship (yes, no), education (lower education defined as primary school or no schooling, higher education defined as secondary or tertiary schooling), smoking and alcohol use during pregnancy (yes, no), location (urban, rural) to better understand if socioeconomic factors influenced maternal complications and adverse birth outcomes. Additional co-variates included initial pregnancy weight (< 50 kg, 50–80 kg, ≥80 kg, unknown) and HIV status (yes, no) [27, 28, 34,35,36,37]. For most of these analyses, adolescents living with HIV are the reference group, aside from the analyses comparing adolescents living without HIV and adults living without HIV. In this model, adolescents living without HIV are the reference group. Statistical analyses were performed using STATA/IC 16.1 software (STATACorp, College Station, TX).
Institutional approval for this study was granted by the Health Research and Development Committee in Botswana and by the Office of Regulatory Affairs and Research Compliance at the Harvard T. H. Chan School of Public Health in Boston, Massachusetts.
Between August 2014 and August 2020, the Tsepamo Study recorded 165,457 births and we included 142,258 (86.0%) that met inclusion criteria in this analysis (Fig. 1). Of these, 21,133 (14.9%) were to adolescents (10 to 19 years), with a median age of 18 years, and 121,125 (85.1%) were to adult women (20 to 35 years), with a median age of 26 years. The characteristics of the study population are shown in Table 1. Adolescents were more likely to be unmarried (99.1% vs. 90.4%, p < .01), nulliparous (91.0% vs. 35.3%, p < .01) and weigh < 50 kg (21.7% vs 12.9%, p < .01), while adult women were more likely to have existing hypertension (2.3% vs 0.3%, p < .01). Among adolescents, 1593 (7.6%) were living with HIV, compared with 27,114 (22.6%) adult women (p < .01). Most adolescents were diagnosed during pregnancy in comparison to adult women (52.6% vs 27.8% p < .01). A majority of adolescents and adult women living with HIV were initiated on or continued on ARV therapy during their pregnancies. Adolescents living with HIV were more likely to have a lower education level (11.6% vs 7.3%, p < .01) and more likely to be multiparous (14.3% vs 8.5%, p < .01) than adolescents living without HIV (Table 1).
Adverse maternal and infant outcomes: adolescents vs. adults, by maternal HIV status
Table 2 shows the prevalence of maternal complications and adverse birth outcomes, stratified by age group and HIV status. Figures 2 and 3 show adjusted associations of age group and HIV status with maternal events (Fig. 2) and adverse birth outcomes (Fig. 3). Adjustment for covariates only modestly changed the odds ratios but did not affect the significance of any of the co-variates. Overall, adolescents were more likely than adults to have anemia during pregnancy, PTD, VPTD, SGA infants, and VSGA infants. Adolescents without HIV were more likely to have anemia during pregnancy (aOR = 1.48, 95%CI 1.41, 1.55), but were less likely than adult women living without HIV to be diagnosed with hypertension and severe hypertension (aOR = .92 95%CI .88, .96 and aOR = 0.77, 95%CI .69, .86 respectively). Additionally, these adolescents without HIV were more likely to have PTD (aOR = 1.47, 95%CI 1.41, 1.54), VPTD (aOR =1.15, 95%CI 1.02,1.28), SGA infants (aOR = 1.14, 95%CI 1.09,1.20), and VSGA infants (aOR = 1.12, 95%CI 1.04,1.20). Adolescents living without HIV were less likely to have cesarean sections at time of delivery (aOR = .58, 95%CI .55, .61) compared to adults without HIV. Among everyone living with HIV, adolescents were more likely to be anemic (aOR = 1.14, 95%CI 1.0,1.30) during pregnancy. Adolescents living with HIV were also more likely to have PTD (aOR = 1.02, 95%CI .76, 1.36), SGA infants (aOR = 1.12, 95%CI .98, 1.29), and VSGA infants (aOR = 1.12, 95% CI .91, 1.36). When controlled for ART use at time of conception, we found no difference in maternal complications and adverse birth outcomes between adolescents living with HIV and adults living with HIV.
Adverse maternal and infant outcomes: adolescents living with HIV vs adolescents without HIV
Adolescents living with HIV were more likely to be diagnosed with anemia (aOR = 1.89 CI 1.67, 2.14), more likely to have cesarean sections (aOR = 1.49 CI 1.30,1.72), and less likely to be diagnosed with hypertension during pregnancy (aOR = 0.78 CI 0.67, 0.91), than adolescents without HIV (Fig. 2). Additionally, adolescents living with HIV were more likely to have PTD (aOR = 1.15 CI 1.04,1.28), VPTD (aOR = 1.35 CI 1.0, 1.8), SGA infants (aOR = 1.37 CI 1.20,1.58), and VSGA infants (aOR = 1.46 CI 1.20,1.79).
We evaluated adverse maternal and birth outcomes among adolescents and adult women by HIV status in a large, nationally representative sample in Botswana. Adolescents had a greater likelihood than adults of anemia, and for infants with preterm birth, very preterm birth, small for gestational age, and very small for gestational age. Adolescents living with HIV were at the highest risk for these adverse outcomes. To our knowledge, this is the first study directly comparing maternal and birth outcomes of adolescents living with HIV to adults and adolescents living without HIV.
Consistent with findings from previous studies conducted in both low and high income countries, we found that adolescents have increased maternal complications during pregnancy and adverse birth outcomes when compared to adult women [16, 38, 39]. Multiple prior studies reported that socioeconomic factors are the main drivers for the increased susceptibility of adolescents to adverse outcomes [9, 16, 40, 41]. Our findings do not appear to be related to the socioeconomic factors that we could measure (education level, nationality, location, alcohol and tobacco use), but we cannot say this for certain. It is possible that our available socioeconomic indicators were insufficient to detect subtle differences in our study (or other sources of unmeasured confounding were present). It should be acknowledged that biological immaturity among adolescents may explain some of these differences.
We identified differences in birth outcomes by HIV status that were more pronounced among adolescents than adults. Prior studies have found that infants born to women living with HIV experience worse birth outcomes than those who are uninfected, even when they are on effective antiretroviral medication with viral suppression and high CD4 cell counts . We found that 52.6% of adolescents living with HIV were diagnosed during their pregnancy in comparison to 27.8% of adults. We also discovered that adolescents living with HIV were more likely to have several adverse outcomes when compared to adults living with HIV. While we cannot exclude socioeconomic differences, potential biological explanations include young gynecologic age (defined as conception within 2 years of menarche), altered prostaglandin production, immaturity of the uterine blood supply coupled with altered angiogenesis and low weight gain due to existing HIV infection [9, 42]. Additionally, ART adherence among adolescents may have differed from adults, and has been shown to be lower in prior studies, but we did not have adherence data available .
Our data reveal that adolescents living with HIV had even more adverse outcomes than adolescents without HIV, with both groups experiencing even worse outcomes than adults living with or without HIV. The increase of adverse maternal and infant outcomes among adolescents living with HIV, highlights the importance of accessible pregnancy family planning and contraceptive methods, routine HIV screening, and the accessibility of HIV prevention methods among this population. In 2004, Botswana began to perform routine HIV screening of women in the prenatal setting based on the joint recommendation by the United Nations and World Health Organizations . Although routine screening for HIV during antenatal visits is vitally important for the diagnosis and treatment of new HIV infections, a continued effort also needs to be placed on screening prior to pregnancy in places such as schools or at home using HIV self-testing kits. There is also the need to increase access to and promote the acceptability of HIV prevention methods, such as PrEP, to decrease the rate of new infections amongst this high-risk population.
Lower weight is highly associated with poor birth outcomes and it is more prevalent in adolescents. We found that 22.1% of our adolescents living with HIV and 21.6% of adolescents without HIV were underweight. While we adjusted for low weight upon the patient’s initial weight recorded during pregnancy in our analyses, we found that weight was not the only significant confounder in the overall model, so it is difficult to conclude how it impacts birth outcomes. In contrast to other outcomes, our study suggests that adolescents living with HIV were less likely to be diagnosed with hypertension during pregnancy than adolescents without HIV, even after adjusting for early pregnancy weight. Adolescents without HIV are thought to be at higher risk of experiencing pre-eclampsia and eclampsia during pregnancy in comparison to adult women, but we were unable to capture the necessary labs to identify preeclampsia in this study [12, 41].
The strengths of this study include a large sample size, a well-defined population of adolescent and adult women who were pregnant, and the ability to assess multiple maternal complications and adverse birth outcomes. We acknowledge that our study is not without its limitations. Diagnostics were unavailable to distinguish pre-eclampsia from other forms of hypertensive disease of pregnancy, and we were unable to confirm the diagnoses of STDs and UTIs, which could contribute to adverse birth outcomes. Gestational dating was largely dependent on last menstrual period assessed by midwives, which may be less accurate than early ultrasound; however, we would not expect differential bias between exposure groups. Because almost all women living with HIV received antiretroviral treatment, we were unable to distinguish differences in outcomes by the presence or absence of antiretroviral exposure. Lastly, this was an observational study and prone to both measured and unmeasured confounding.
The combination of adolescent pregnancy and HIV infection in Botswana remains of great concern. The resulting adverse maternal and birth outcomes continue to negatively impact this age-group disproportionately, despite available ART. Our findings reinforce the importance of high-risk obstetrical and pediatric support for adolescents with HIV, and support public health measures aimed at decreasing adolescent pregnancy and incident HIV to improve health outcomes in Botswana.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Last menstrual period
Small for gestational age
Very preterm delivery
Very small for gestational age
Neal S, Matthews Z, Frost M, Fogstad H, Camacho AV, Laski L. Childbearing in adolescents aged 12-15 years in low resource countries: a neglected issue. New estimates from demographic and household surveys in 42 countries. Acta Obstet Gynecol Scand. 2012;91(9):1114–8.
Conde-Agudelo A, Belizán JM, Lammers C. Maternal-perinatal morbidity and mortality associated with adolescent pregnancy in Latin America: cross-sectional study. Am J Obstet Gynecol. 2005;192(2):342–9.
Orvos H, Nyirati I, Hajdú J, Pál A, Nyári T, Kovács L. Is adolescent pregnancy associated with adverse perinatal outcome? J Perinat Med. 1999;27(3):199–203.
Buitendijk SE, van Enk A, Oosterhout R, Ris M. Obstetrical outcome in teenage pregnancies in the Netherlands. Ned Tijdschr Geneeskd. 1993;137(49):2536–40.
Kumar A, Singh T, Basu S, Pandey S, Bhargava V. Outcome of teenage pregnancy. Indian J Pediatr. 2007;74(10):927–31.
Sagili H, Pramya N, Prabhu K, Mascarenhas M, Reddi RP. Are teenage pregnancies at high risk? A comparison study in a developing country. Arch Gynecol Obstet. 2012;285(3):573–7.
Ogelle OM, Eke AC, Okafor CI, Mbamara SU, Obiechina NJ. Teenage pregnancies: a lingering obstetric problem in Nigeria. Niger J Med. 2011;20(4):414–20.
Azevedo WF, Diniz MB, Fonseca ES, Azevedo LM, Evangelista CB. Complications in adolescent pregnancy: systematic review of the literature. Einstein (Sao Paulo). 2015;13(4):618–26.
Fraser AM, Brockert JE, Ward RH. Association of young maternal age with adverse reproductive outcomes. N Engl J Med. 1995;332(17):1113–8.
Torvie AJ, Callegari LS, Schiff MA, Debiec KE. Labor and delivery outcomes among young adolescents. Am J Obstet Gynecol. 2015;213(1):95.e1–8.
Kirbas A, Gulerman HC, Daglar K. Pregnancy in adolescence: is it an obstetrical risk? J Pediatr Adolesc Gynecol. 2016;29(4):367–71.
de Vienne CM, Creveuil C, Dreyfus M. Does young maternal age increase the risk of adverse obstetric, fetal and neonatal outcomes: a cohort study. Eur J Obstet Gynecol Reprod Biol. 2009;147(2):151–6.
Malamitsi-Puchner A, Boutsikou T. Adolescent pregnancy and perinatal outcome. Pediatr Endocrinol Rev. 2006;3(Suppl 1):170–1.
McAnarney ER. Young maternal age and adverse neonatal outcome. Am J Dis Child. 1987;141(10):1053–9.
Amjad S, MacDonald I, Chambers T, Osornio-Vargas A, Chandra S, Voaklander D, et al. Social determinants of health and adverse maternal and birth outcomes in adolescent pregnancies: a systematic review and meta-analysis. Paediatr Perinat Epidemiol. 2019;33(1):88–99.
Chen X-K, Wen SW, Fleming N, Demissie K, Rhoads GG, Walker M. Teenage pregnancy and adverse birth outcomes: a large population based retrospective cohort study. Int J Epidemiol. 2007;36(2):368–73.
Scholl TO, Hediger ML, Salmon RW, Belsky DH, Ances IG. Association between low gynaecological age and preterm birth. Paediatr Perinat Epidemiol. 1989;3(4):357–66.
Scholl T, Hediger M, Ances I, Cronk C. Growth during early teenage pregnancies. Lancet. 1988;331(8587):701–2.
Haiek L, Lederman SA. The relationship between maternal weight for height and term birth weight in teens and adult women. J Adolesc Health Care. 1989;10(1):16–22.
Hediger ML, Scholl TO, Belsky DH, Ances IG, Salmon RW. Patterns of weight gain in adolescent pregnancy: effects on birth weight and preterm delivery. Obstet Gynecol. 1989;74(1):6–12.
Brocklehurst P, French R. The association between maternal HIV infection and perinatal outcome: a systematic review of the literature and meta-analysis. Br J Obstet Gynaecol. 1998;105(8):836–48.
Wedi CO, Kirtley S, Hopewell S, Corrigan R, Kennedy SH, Hemelaar J. Perinatal outcomes associated with maternal HIV infection: a systematic review and meta-analysis. Lancet HIV. 2016;3(1):e33–48.
Macdonald EM, Ng R, Bayoumi AM, Raboud J, Brophy J, Masinde KI, et al. Adverse neonatal outcomes among women living with HIV: a population-based study. J Obstet Gynaecol Can. 2015;37(4):302–9.
Obare F, van der Kwaak A, Birungi H. Factors associated with unintended pregnancy, poor birth outcomes and post-partum contraceptive use among HIV-positive female adolescents in Kenya. BMC Womens Health. 2012;12:34.
World Health Organization. Adolescent birth rate data by WHO region 2020, Available from: https://apps.who.int/gho/data/view.main.1610A?lang=en.
Zash R, Jacobson DL, Diseko M, Mayondi G, Mmalane M, Essex M, et al. Comparative safety of antiretroviral treatment regimens in pregnancy. JAMA Pediatr. 2017;171(10):e172222.
Zash R, Jacobson DL, Diseko M, Mayondi G, Mmalane M, Essex M, et al. Comparative safety of dolutegravir-based or efavirenz-based antiretroviral treatment started during pregnancy in Botswana: an observational study. Lancet Glob Health. 2018;6(7):e804–e10.
Blondel B, Kogan MD, Alexander GR, Dattani N, Kramer MS, Macfarlane A, et al. The impact of the increasing number of multiple births on the rates of preterm birth and low birthweight: an international study. Am J Public Health. 2002;92(8):1323–30.
Robson D, Daniels S, Flatley C, Kumar S. Obstetric and perinatal outcomes for twin pregnancies in adolescent girls. Sci Rep. 2018;8(1):18072.
Zash R, Souda S, Chen JY, Binda K, Dryden-Peterson S, Lockman S, et al. Reassuring birth outcomes with Tenofovir/Emtricitabine/Efavirenz used for prevention of mother-to-child transmission of HIV in Botswana. J Acquir Immune Defic Syndr (1999). 2016;71(4):428–436.
Zash R, Caniglia EC, Diseko M, Mayondi G, Mabuta J, Luckett R, et al. Maternal weight and birth outcomes among women on antiretroviral treatment from conception in a birth surveillance study in Botswana. J Int AIDS Soc. 2021;24(6):e25763.
Lowenthal ED, Bakeera-Kitaka S, Marukutira T, Chapman J, Goldrath K, Ferrand RA. Perinatally acquired HIV infection in adolescents from sub-Saharan Africa: a review of emerging challenges. Lancet Infect Dis. 2014;14(7):627–39.
Caniglia EC, Shapiro R, Diseko M, Wylie BJ, Zera C, Davey S, et al. Weight gain during pregnancy among women initiating dolutegravir in Botswana. EClinicalMedicine. 2020;29-30:100615.
Davey S, Ajibola G, Maswabi K, Sakoi M, Bennett K, Hughes MD, et al. Mother-to-child HIV transmission with in utero dolutegravir vs. efavirenz in Botswana. J Acquir Immune Defic Syndr. 2020;84(3):235–41.
Fennell C, Seage GR, Zash R, Phiri K, Diseko M, Mayondi G, et al. Adverse Birth Outcomes in Botswana Among Women With Vertically or Horizontally Acquired Human Immunodeficiency Virus. J Pediatric Infect Dis Soc. 2021;10(3):252–8.
Zash R, Souda S, Chen JY, Binda K, Dryden-Peterson S, Lockman S, et al. Reassuring birth outcomes with tenofovir/emtricitabine/efavirenz used for prevention of mother-to-child transmission of HIV in Botswana. J Acquir Immune Defic Syndr. 2016;71(4):428–36.
Kassa GM, Arowojolu AO, Odukogbe AA, Yalew AW. Adverse neonatal outcomes of adolescent pregnancy in Northwest Ethiopia. Plos One. 2019;14(6):e0218259.
Zhang T, Wang H, Wang X, Yang Y, Zhang Y, Tang Z, et al. The adverse maternal and perinatal outcomes of adolescent pregnancy: a cross sectional study in Hebei, China. BMC Pregnancy Childbirth. 2020;20(1):339.
Mahfouz AA, el-Said MM, al-Erian RA, Hamid AM. Teenage pregnancy: are teenagers a high risk group? Eur J Obstet Gynecol Reprod Biol. 1995;59(1):17–20.
Althabe F, Moore JL, Gibbons L, Berrueta M, Goudar SS, Chomba E, et al. Adverse maternal and perinatal outcomes in adolescent pregnancies: the Global Network’s Maternal Newborn Health Registry study. Reprod Health. 2015;12 Suppl 2(Suppl 2):S8.
Conroy AL, McDonald CR, Gamble JL, Olwoch P, Natureeba P, Cohan D, et al. Altered angiogenesis as a common mechanism underlying preterm birth, small for gestational age, and stillbirth in women living with HIV. Am J Obstet Gynecol. 2017;217(6):684.e1–e17.
MacCarthy S, Saya U, Samba C, Birungi J, Okoboi S, Linnemayr S. “How am I going to live?”: exploring barriers to ART adherence among adolescents and young adults living with HIV in Uganda. BMC Public Health. 2018;18(1):1158.
Centers for Disease Control and Prevention (CDC). Introduction of routine HIV testing in prenatal care--Botswana, 2004. MMWR Morb Mortal Wkly Rep. 2004;53(46):1083–6.
We would like to acknowledge all of the Botswana Ministry of Health and the staff at the Botswana-Harvard Partnership AIDS Institute for continued support throughout this project. Additionally, we would like to give special thanks to the dedicated research assistants working on the ongoing Tsepamo Birth Outcomes Surveillance Study whose efforts have allowed for quality data collection.
Research reported in this publication was supported by the Fogarty International Center and.
National Institute of Mental Health, of the National Institutes of Health under Award Number D43 TW010543, the National Institutes of Health (NIH)/the Eunice Kennedy Shriver National Institute of Child Health and Human Development (R01 HD080471, K23 HD088230-01A1, and K01 HD100222-01A1), and NIH/the National Institute of Allergy and Infectious Diseases (K24AI131924). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
Ethics approval and consent to participate
This study was performed in accordance with the Declaration of Helsinki and was approved by the ethics committees in Botswana and Boston (the Health Research and Development Committee in Botswana and the Office of Regulatory Affairs and Research Compliance at the Harvard T. H. Chan School of Public Health in Boston, Massachusetts). Informed consent was waived by the ethics committees in Botswana and Boston (the Health Research and Development Committee in Botswana and by the Office of Regulatory Affairs and Research Compliance at the Harvard T.H. Chan School of Public Health) as data were collected via chart abstraction.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Jackson-Gibson, M., Zash, R., Mussa, A. et al. High risk of adverse birth outcomes among adolescents living with HIV in Botswana compared to adult women living with HIV and adolescents without HIV. BMC Pregnancy Childbirth 22, 372 (2022). https://doi.org/10.1186/s12884-022-04687-y
- Adolescent pregnancy
- Adverse pregnancy outcomes