Gestational diabetes mellitus (GDM), which is a medical complication that develops during pregnancy, is associated with several long-term health problems. Despite several benefits of exclusive breastfeeding (EBF), including reduction in long-term health problems in mothers with GDM, few studies have investigated breastfeeding in women with GDM and information in the Thai population is lacking. The aim of the study was to determine the prevalence of breastfeeding and the factors associated with breastfeeding during the first six months postpartum in women with GDM.
A questionnaire-based prospective study was conducted during November 2014 to June 2017. Study participants were first interviewed on the second day post-delivery, and then by telephone at 6 weeks, 3 months and 6 months postpartum. Breastfeeding assessment based on infant feeding practice in the last 24-h period was classified according to World Health Organization definitions.
A total 229 women were enrolled in this study. Prevalence of any breastfeeding at 24 h, 6 weeks, 3 months, and 6 months postpartum was 28.8% (n = 66), 94.3% (n = 214), 71% (n = 154), and 49.8% (n = 104), respectively. Prevalence of EBF was 35.9% (n = 78) at 3 months, and 23% (n = 48) at 6 months after delivery. Maternal intention to breastfeed for 6 months was an independent predictor for both 6 months EBF (RR 16.38; 95% CI 2.29, 116.99) and any breastfeeding (RR 2.65; 95% CI 1.65, 4.25). Breastfeeding initiation within 24 h postpartum (RR 1.38; 95% CI 1.08, 1.76) and being a government officer or private business owner (RR 1.66; 95% CI 1.03, 2.68) were independent predictors of any breastfeeding and EBF for 6 months, respectively.
The prevalence of breastfeeding in Thai women with GDM was lower than the national and global target goal. Maternal intention to breastfeed for at least 6 months and breastfeeding initiation were important factors associated with 6 months’ breastfeeding. In order to improve the breastfeeding rate and duration, health care providers should support women’s feeding decision, emphasize the benefits of breastfeeding to enhance breastfeeding intention, seek to remove or minimize barriers to the initiation of breastfeeding and reduce mother-infant separation time.
Gestational diabetes mellitus (GDM) is a common medical complication that develops during pregnancy, with a pooled prevalence of 10.1% and substantial variations across nations . GDM is defined as new onset or first evidence of abnormal glucose tolerance that occurs during gestation . In addition to causing immediate adverse effects on pregnancy outcomes, GDM can also cause long-term health problems in both mother and child. Previous studies have reported increased risk of type 2 diabetes mellitus (T2DM), metabolic syndrome, and cardiovascular disease (CVD) later in life in women diagnosed with GDM [3,4,5,6]. An epidemiologic study reported increased risk of long-term adverse effects, such as T2DM, obesity, metabolic syndrome and other chronic non-communicable diseases in adulthood in children of mothers with GDM .
Several international strategies have been developed to strongly support and promote breastfeeding as an optimal infant feeding strategy to ensure that children receive appropriate nutrition for growth, development, and health. The World Health Organization (WHO) and the United Nations Children’s Fund (UNICEF) recommend exclusive breastfeeding (EBF) during the first six months of life, and the introduction of safe and nutritionally adequate complementary foods starting at 6 months, together with continued breastfeeding up to 2 years of age or beyond. In accordance with these recommendations, the Thai Ministry of Public Health implemented the National Breastfeeding Project in 1989 to promote EBF. The target compliance rates established by the 11th National Economic and Social Development Plan (NESDP) of Thailand 2012–2016 were 30% during 2012–2016, and 50% during 2017–2021. Despite the implementation of this initiative, the 6-month EBF rate from a national survey conducted in Thailand in 2015 was only 23.1% . This rate was lower than the 30% goal, and was lower than the global EBF rate of 34.8% reported by the WHO .
Maternal benefits from breastfeeding include a reduction in the risk of developing hypertension, dyslipidemia, T2DM, CVD, breast cancer and ovarian cancer. Two studies reported that breastfeeding in mothers with GDM can decrease the risk of developing T2DM and metabolic syndrome later in life [10, 11]. Despite these advantages, some previous studies reported a lower rate and duration of breastfeeding in mothers with GDM compared to women without GDM [12,13,14]. Two previous studies reported the prevalence of any breastfeeding at 6 months postpartum among mothers with GDM, 83.9% in Vietnam  and 31.3% in the UK . However, those reports lacked data relating to either breastfeeding characteristics or prevalence of exclusive breastfeeding. Data specific to breastfeeding in Thai women with GDM are still lacking, with the few studies that did report breastfeeding rates in general Thai populations noting that these were lower than the 30% target [8, 16, 17]. Increased knowledge about the prevalence of and factors associated with breastfeeding in this Thai subpopulation will help us understand the negative and positive factors that influence breastfeeding behavior.
Accordingly, the aim of the present study was to determine the prevalence of breastfeeding and to identify factors associated with breastfeeding in mothers with GDM during the first six months postpartum.
This questionnaire-based prospective study was conducted at the Family Planning and Reproductive Health Unit, Department of Obstetrics and Gynecology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand during the November 2014 to June 2017.
Eligibility criteria were early postpartum women aged 20 years and over who delivered a singleton neonate, had attended antenatal care at Siriraj Hospital and had been diagnosed as having GDM during the antenatal period by Carpenter and Cousil criteria for 100-g oral glucose tolerance test (OGTT) or 1-h 50-g glucose challenge test (GCT) ≥ 200 mg/dL. Individuals with contraindications to breastfeed were excluded at recruitment. During the study period, woman with one or more of the following were additionally excluded: diagnosis of T2DM at 6 weeks postpartum, inability to follow up 75-g OGTT testing at 6 weeks postpartum, and/or death of infant prior to the age of 6 months.
Women diagnosed with GDM received standard antenatal care, including antenatal follow-up schedule as appropriate, dietary recommendation and monitoring of fasting and 2-h postprandial blood glucose. Women also received standard care during the intrapartum phase and the mode of delivery was determined by obstetric indications. After birth, all infants were admitted to the nursery ward to monitor blood glucose and to receive early infant formula feed to prevent hypoglycemia. Infant’s lingual frenulum and mother’s nipple anatomy were routinely assessed, as described elsewhere . The appointments for all women with GDM were scheduled at 6 weeks postpartum at the Family Planning and Reproductive Health Unit for routine postpartum checkup, family planning and contraceptive counseling, and for 75-g OGTT testing.
All enrolled participants were first interviewed on the second day post-delivery before hospital discharge to collect the following information: maternal baseline characteristics, obstetric history, intentions regarding breastfeeding, duration of maternity leave, breast-related problems, and infant-related problems. Subsequently, interviews were scheduled at 6 weeks, 3 months and 6 months postpartum. The follow-up interviews elicited information relative to breastfeeding type, duration of breastfeeding, and reason for breastfeeding discontinuation.
Breastfeeding was defined as an infant who received breast milk regardless of method of feeding. In terms of breastfeeding assessment, mothers were asked about infant feeding practices based on the last 24-h feeding period . Breastfeeding types were classified according to WHO definitions, as follows: EBF was defined as an infant who received only breast milk; predominant breastfeeding was defined as an infant who received breast milk as the predominant source of feeding which might also include water or fruit juice; complementary breastfeeding was defined as an infant who received breast milk and solid food, semisolid food and/or non-human milk; and no breastfeeding was defined as an infant who did not receive breast milk.
Sample size calculation and statistical analysis
The sample size was calculated using a 31.3% prevalence rate of any breastfeeding at 6 months postpartum in women with GDM from a previous study which compared breastfeeding rates in women with GDM and women with type 1 or type 2 diabetes in a UK population . Using a significance level of 0.05 (2-sided) and an absolute precision error of 7%, a total of 169 women was calculated.
Statistical analysis was performed using Stata statistical software (version 14) (StataCorp LLC, College Station, TX, USA). Demographic and clinical data were summarized using descriptive statistics. Data were presented as mean ± standard deviation (SD) or number (n) and percentage. Chi-square test or Fisher’s exact test was used for comparing categorical data, and t-test or Mann-Whitney U test was used for comparing continuous data as appropriated. Binary regression analysis was performed to identify factors significantly associated with breastfeeding for 6 months. A p-value less than 0.05 was considered to be statistically significant.
Three hundred and ninety-eight postpartum Thai women with GDM were initially invited to participate in this study. Of those, 169 women were excluded from data analysis due to an abnormal result or no result of the 75-g OGTT testing at 6 weeks postpartum (n = 168) or early neonatal death (n = 1). The remaining 229 mothers with GDM were included. Baseline demographic and clinical characteristics of the 229 mothers with GDM and their infants are shown in Table 1. The mean age was 33.2 ± 5.1 years (range 20–47 years) and the mean body mass index was 24.5 ± 5.2 kg/m2 (range 15.56–44.08 kg/m2). The majority of participants were married (96.9%). Nearly half of women were primiparous (46.2%), graduated with a bachelor degree or higher (56.7%) and delivered by cesarean section (46.3%). The mean maternity leave length was 1.5 months and ranged from 0 to 3 months. Approximately 18% of participants had nipple inversion or retraction. Almost one-fifth (18.7%, 41/219) of infants had severe tongue tie and 38 of those (92.7%) underwent frenotomy. With regard to breastfeeding duration, 49 women breastfed a prior child for at least 6 months and 147 women expressed an intention to breastfeed their current babies for at least 6 months.
The prevalence of breastfeeding according to the WHO definition is shown in Fig. 1. Any breastfeeding rate at 24 h, 6 weeks, 3 months, and 6 months postpartum was 28.8, 94.3, 71.0, and 49.8%, respectively. Prevalence of EBF was 35.9% at 3 months and 23.0% at 6 months after delivery. The reasons cited for discontinuation of any breastfeeding before 6 months postpartum were self-perception of insufficient breast milk quantity (53.5%, 69/129), end of maternity leave (34.1%, 44/129), early infant feeding with semi-solid food (11.6%, 15/129) and a sick baby (0.8%, 1/129).
Factors associated with discontinuation of EBF and any breastfeeding prior to 6-months postpartum are shown in Table 2. Educational level, occupation, cesarean delivery, a reported intention to breastfeed for a full 6-months postpartum, and intended time to breastfeed in the index pregnancy were significantly associated with rates of 6-month EBF practice. Length of maternity leave, inverted/retracted nipple, a reported intention to breastfeed for a full 6-months postpartum, intention time to breastfeed in index pregnancy, initiation breastfeeding within 24 h after delivery, and contraceptive method were significantly associated with any breastfeeding for 6 months postpartum. Bachelor degree or higher educational level, working as a private business owner or government officer, vaginal delivery and an intention to breastfeed for 6-months postpartum in the index pregnancy were significantly associated with a higher rate of 6-month EBF practice. Reporting an intention to breastfeed for 6-months postpartum in the index pregnancy or initiation of breastfeeding within 24 h after delivery were significantly associated with a higher rate of any breastfeeding for 6 months postpartum. On the contrary, women with inverted/retracted nipple(s) were associated with a lower rate of any breastfeeding at 6 months postdelivery.
Univariate and multivariable analysis for factors that independently predicted 6 months postpartum of EBF or any breastfeeding are shown in Table 3. After adjustment for confounding factors, maternal intention to breastfeed until 6 months of infant age was an independent predictor of both 6 months of EBF and any breastfeeding practice. Initiation of breastfeeding within 24 h after delivery was an independent predictor of any breastfeeding for 6 months and having an occupation as a government officer or private business owner was an independent predictor of EBF for 6 months.
This is the first study focusing on EBF in women with GDM through to 6 months postpartum, and it is also the first study to investigate breastfeeding in Thai women with GDM. The prevalence of EBF in women with GDM in this study was approximately 23% at 6 months after delivery, which was comparable to the prevalence of EBF in the general Thai population from a national report (23.1%) . However, it was lower than the 2017–2021 national target of 50% and lower than the 34.8% prevalence from a global report published by the WHO . Despite the known importance of EBF, few studies had reported the prevalence of EBF at 6 months postpartum in the general Thai population [8, 16, 17, 20]. The prevalence rates reported from previous Thai studies were lower than our result. A previous study reported an EBF rate of 23.8% at 3 months in mothers with GDM , which was lower than our result (35.9% at 3 months). The rate of any breastfeeding in the present study was 49.8% at 6 months postpartum which was similar to the rate observed in the general Thai population . However, the rate of any breastfeeding in mothers with GDM differed among studies (31.3 to 65.7%), due to variations in breastfeeding definitions and assessment durations among studies [15, 22, 23].
Importantly, maternal intention to breastfeed until 6 months of infant age was an independent predictor of 6 months EBF and any breastfeeding practice. Other studies also reported a woman’s intention to breastfeed as being an important factor for optimizing breastfeeding practice in mothers with and without GDM [20, 24,25,26]. This finding suggests that a mother’s determination and willingness to breastfeed significantly influences breastfeeding duration. At the individual level, maternal intention to breastfeed was one of the important determinants of breastfeeding and the most commonly cited reasons for this intention was either personal norms or benefit of breastfeeding . Therefore, health-care providers should support feeding decision and emphasize the benefits of breastfeeding at key moments during the antenatal and early postpartum period in order to enhance maternal motivation to maintain EBF for a minimum of 6 months after delivery and continued breastfeeding thereafter .
Maternal occupation was another factor that showed significant association with EBF for 6 months postpartum in this study. Some previous studies found a negative effect of working outside the home on EBF rate among working mothers [28, 29]. The effect of work on breastfeeding cessation may be due to either work that disallows or makes EBF difficult or work that has a lack of privacy or that limits the time needed to express breast milk. Availability or sufficiency of time to breastfeed or to pump breast milk may be a potential contributing factor that influences the ability to continue breastfeeding after the end of maternity leave. In the present study, we found being a government officer or a private business owner to be an independent predictor of 6 months EBF. This may be explained by the flexibility that a private business owner often has compared to one who works for others. In Thailand, mothers working in the government sector receive support from the government such as paid maternity leave and various supporting system for nursing mothers at work as well as breastfeeding breaking time and space for breast pumping. In addition, we found breastfeeding initiation within the first 24 h after delivery to be significantly associated with any breastfeeding for 6 months postpartum. The infants of mothers with GDM may have higher rates of complications, such as hypoglycemia and prematurity, and these conditions can result in prolonged separation of the mother and infant after delivery, delayed bonding, and increased likelihood of a need for supplementation with infant formula during the hospital stay. All of the aforementioned factors can have a negative effect on the initiation and continuation of breastfeeding. Moreover, based on our hospital policy, all infants of mothers with GDM were admitted to the nursery ward immediately after birth to monitor blood glucose level and to receive infant formula in order to prevent hypoglycemia, which can lead to delayed breastfeeding initiation. This practice may need to be reconsidered because mother-infant separation and prelacteal feeds are important barriers to timely breastfeeding initiation and ongoing breastfeeding in women with GDM who deliver at our hospital. The other possible explanation for the impact of delayed initiation on ongoing breastfeeding could be that women with GDM have a higher probability of developing delayed stage II lactogenesis . Maternal overweight or obesity are also reported to be risk factors for delayed stage II lactogenesis [9, 31] due to a decreased prolactin response to infant suckling , which may cause breastfeeding difficulty and a lower rate of breastfeeding continuation. Thus, improved support from healthcare providers to enhance early initiation of breastfeeding, decrease mother and infant separation time, promote early skin-to-skin contact, and allow rooming-in after resolution of hypoglycemia may improve the breastfeeding initiation and continuation rate.
The strength of this study is that it is one of the few studies that provide information concerning the prevalence of breastfeeding and the factors associated with breastfeeding in women with GDM. Furthermore, we followed the breastfeeding behavior of mothers with GDM up to 6 months postpartum, which is the recommended duration of EBF. Another notable strength is the use of WHO definitions to define breastfeeding types. This study also has some mentionable limitations. First, there was no non-GDM control group to compare with mothers with GDM and there were a number of excluded women in our study. However, the size of our study population assured adequate statistic power to interpret the outcomes. Second, no data were collected from women with GDM relative to their attitudes toward or their knowledge about breastfeeding. We acknowledge that both of these factors could influence breastfeeding behavior. Third, we collected data concerning the amount of breastfeeding relative to the definitions of the different breastfeeding types, but data relating to the modes of feeding were not collected.
The prevalence of EBF at 6-months postpartum was low among Thai mothers with GDM and was lower than the national and global target goal. Maternal intention to breastfeed for 6 months and breastfeeding initiation within 24-h postpartum were important factors associated with 6 months of breastfeeding. Health care providers should provide breastfeeding education, support feeding decision and help mothers to initiate breastfeeding in that might be improving breastfeeding rate. Hospital practice causing mother-infant separation is an important barrier to breastfeeding initiation and needs to be revised.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Nguyen CL, Pham NM, Binns CW, Duong DV, Lee AH. Prevalence of gestational diabetes mellitus in eastern and southeastern Asia: a systematic review and meta-analysis. J Diabetes Res. 2018;2018:6536974.
Agarwal MM. Gestational diabetes mellitus: an update on the current international diagnostic criteria. World J Diabetes. 2015;6:782–91.
Hakkarainen H, Huopio H, Cederberg H, Paakkonen M, Voutilainen R, Heinonen S. The risk of metabolic syndrome in women with previous GDM in a long-term follow-up. Gynecol Endocrinol. 2016;32:920–5.
Lao TT. The mother--the long-term implications on metabolic and cardiovascular complications. Best Pract Res Clin Obstet Gynaecol. 2015;29:244–55.
Li J, Song C, Li C, Liu P, Sun Z, Yang X. Increased risk of cardiovascular disease in women with prior gestational diabetes: a systematic review and meta-analysis. Diabetes Res Clin Pract. 2018;140:324–38.
Durnwald C. Gestational diabetes: linking epidemiology, excessive gestational weight gain, adverse pregnancy outcomes, and future metabolic syndrome. Semin Perinatol. 2015;39:254–8.
Mitanchez D, Yzydorczyk C, Siddeek B, Boubred F, Benahmed M, Simeoni U. The offspring of the diabetic mother--short- and long-term implications. Best Pract Res Clin Obstet Gynaecol. 2015;29:256–69.
National Statistical Office and. United Nations Children’s fund, Thailand 14 provinces multiple Indicator cluster survey 2015–2016, final report. Bangkok: NSO and UNICEF; 2017.
Trout KK, Averbuch T, Barowski M. Promoting breastfeeding among obese women and women with gestational diabetes mellitus. Curr Diab Rep. 2011;11:7–12.
Ziegler AG, Wallner M, Kaiser I, Rossbauer M, Harsunen MH, Lachmann L, et al. Long-term protective effect of lactation on the development of type 2 diabetes in women with recent gestational diabetes mellitus. Diabetes. 2012;61:3167–71.
Gunderson EP, Jacobs DR Jr, Chiang V, Lewis CE, Feng J, Quesenberry CP Jr, et al. Duration of lactation and incidence of the metabolic syndrome in women of reproductive age according to gestational diabetes mellitus status: a 20-year prospective study in CARDIA (coronary artery risk development in young adults). Diabetes. 2010;59:495–504.
Baerug A, Sletner L, Laake P, Fretheim A, Loland BF, Waage CW, et al. Recent gestational diabetes was associated with mothers stopping predominant breastfeeding earlier in a multi-ethnic population. Acta Paediatr. 2018;107:1028–35.
Haile ZT, Oza-Frank R, Azulay Chertok IR, Passen N. Association between history of gestational diabetes and exclusive breastfeeding at hospital discharge. J Hum Lact. 2016;32:NP36–43.
Nguyen PTH, Binns CW, Nguyen CL, Ha AVV, Chu TK, Duong DV, et al. Gestational diabetes mellitus reduces breastfeeding duration: a prospective cohort study. Breastfeed Med. 2019;14:39–45.
Soltani H, Arden M. Factors associated with breastfeeding up to 6 months postpartum in mothers with diabetes. J Obstet Gynecol Neonatal Nurs. 2009;38:586–94.
Plewma P. Prevalence and factors influencing exclusive breast-feeding in Rajavithi hospital. J Med Assoc Thail. 2013;96(Suppl 3):S94–9.
Barnes S, Perngparn U. Exclusive breastfeeding experiences among mothers in Bangkok, Thailand: findings from a mixed-methods study. J Health Res. 2013;27:19–25.
Ngerncham S, Laohapensang M, Wongvisutdhi T, Ritjaroen Y, Painpichan N, Hakularb P, et al. Lingual frenulum and effect on breastfeeding in Thai newborn infants. Paediatr Int Child Health. 2013;33:86–90.
Noel-Weiss J, Boersma S, Kujawa-Myles S. Questioning current definitions for breastfeeding research. Int Breastfeed J. 2012;7:9.
Laisiriruangrai P, Wiriyasirivaj B, Phaloprakarn C, Manusirivithaya S. Prevalence of exclusive breastfeeding at 3, 4 and 6 months in Bangkok metropolitan administration medical college and Vajira hospital. J Med Assoc Thail. 2008;91:962–7.
Schaefer-Graf UM, Hartmann R, Pawliczak J, Passow D, Abou-Dakn M, Vetter K, et al. Association of breast-feeding and early childhood overweight in children from mothers with gestational diabetes mellitus. Diabetes Care. 2006;29:1105–7.
Fenger-Gron J, Fenger-Gron M, Blunck CH, Schonemann-Rigel H, Wielandt HB. Low breastfeeding rates and body mass index in Danish children of women with gestational diabetes mellitus. Int Breastfeed J. 2015;10:26.
Oza-Frank R, Chertok I, Bartley A. Differences in breast-feeding initiation and continuation by maternal diabetes status. Public Health Nutr. 2015;18:727–35.
Loewenberg Weisband Y, Rausch J, Kachoria R, Gunderson EP, Oza-Frank R. Hospital supplementation differentially impacts the association between breastfeeding intention and duration among women with and without gestational diabetes mellitus history. Breastfeed Med. 2017;12:338–44.
Forster DA, McLachlan HL, Lumley J. Factors associated with breastfeeding at six months postpartum in a group of Australian women. Int Breastfeed J. 2006;1:18.
de Jersey SJ, Mallan K, Forster J, Daniels LA. A prospective study of breastfeeding intentions of healthy weight and overweight women as predictors of breastfeeding outcomes. Midwifery. 2017;53:20–7.
Rollins NC, Bhandari N, Hajeebhoy N, Horton S, Lutter CK, Martines JC, et al. Why invest, and what it will take to improve breastfeeding practices? Lancet. 2016;387:491–504.
Al-Ruzaihan SA, Al-Ghanim AA, Bu-Haimed BM, Al-Rajeh HK, Al-Subaiee WR, Al-Rowished FH, et al. Effect of maternal occupation on breast feeding among females in Al-Hassa, southeastern region of KSA. J Taibah Univ Sci. 2017;12:235–40.
El-Gilany AH, Shady E, Helal R. Exclusive breastfeeding in Al-Hassa, Saudi Arabia. Breastfeed Med. 2011;6:209–13.
De Bortoli J, Amir LH. Is onset of lactation delayed in women with diabetes in pregnancy? A systematic review. Diabet Med. 2016;33:17–24.
Matias SL, Dewey KG, Quesenberry CP Jr, Gunderson EP. Maternal prepregnancy obesity and insulin treatment during pregnancy are independently associated with delayed lactogenesis in women with recent gestational diabetes mellitus. Am J Clin Nutr. 2014;99:115–21.
Rasmussen KM, Kjolhede CL. Prepregnant overweight and obesity diminish the prolactin response to suckling in the first week postpartum. Pediatrics. 2004;113:e465–71.
The study was financially supported by Siriraj Grant for Research Development, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand (Grant number R015832001).
Ethics approval and consent to participate
The protocol for this study was approved by the Siriraj Institutional Review Board (COA no. Si 386/2014). This study complied with the principles set forth in the Declaration of Helsinki (1964) and all of its subsequent amendments, and written informed consent was obtained from all participants.
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Jirakittidul, P., Panichyawat, N., Chotrungrote, B. et al. Prevalence and associated factors of breastfeeding in women with gestational diabetes in a University Hospital in Thailand. Int Breastfeed J 14, 34 (2019). https://doi.org/10.1186/s13006-019-0227-8
- Exclusive breastfeeding
- Gestational diabetes mellitus