- Research
- Open access
- Published:
Breastfeeding in primiparous women with congenital heart disease − a register study
International Breastfeeding Journal volume 19, Article number: 19 (2024)
Abstract
Background
The number of pregnant women with congenital heart disease (CHD) is rising, and the disease poses increased risks of cardiovascular and obstetric complications during pregnancy, potentially impacting breastfeeding success. This study aimed to investigate breastfeeding in primiparous women with CHD compared to primiparous women without CHD, and to examine potential hindering factors for breastfeeding in women with CHD.
Methods
The data were gathered between 2014 and 2019 and obtained by merging the Swedish Congenital Heart Disease Register (SWEDCON) with the Swedish Pregnancy Register. Primiparous women ≥ 18 years of age with CHD (n = 578) were matched by age and municipality to 3049 women without CHD, giving birth after 22 gestational weeks. Multivariable logistic regression analysis was used to identify factors associated with non-breastfeeding in women with CHD.
Results
Fewer women with CHD breastfed than women without CHD two days (94% vs. 97%, p = 0.001) and four weeks after birth (84% vs. 89%, p = 0.006). When all women were analysed, having CHD was associated with non-breastfeeding at both two days and four weeks after birth. For women with CHD, body mass index (BMI) ≥ 30 (OR 3.1; 95% CI 1.4, 7.3), preterm birth (OR 6.4; 95% CI 2.1, 19.0), self-reported history of psychiatric illness (OR 2.4; 95% CI 1.2, 5.1), small for gestational age (OR 4.2; 95% CI 1.4, 12.2), and New York Heart Association Stages of Heart Failure class II − III (OR 6.0; 95% CI 1.4, 26.7) were associated with non-breastfeeding two days after birth. Four weeks after birth, factors associated with non-breastfeeding were BMI ≥ 30 (OR 4.3; 95% CI 2.1, 9.0), self-reported history of psychiatric illness (OR 2.2; 95% CI 1.2, 4.2), and preterm birth (OR 8.9; 95% CI 2.8, 27.9).
Conclusions
The study shows that most women with CHD breastfeed, however, at a slightly lower proportion compared to women without CHD. In addition, factors related to the heart disease were not associated with non-breastfeeding four weeks after birth. Since preterm birth, BMI ≥ 30, and psychiatric illness are associated with non-breastfeeding, healthcare professionals should provide greater support to women with CHD having these conditions.
Background
Breastfeeding is shown to be the most beneficial feeding method during the baby’s first six months of life, and has positive short and long-term health benefits for both mother and baby [1,2,3,4,5,6,7]. The World Health Organization (WHO) primarily recommends exclusive breastfeeding due to greater health effects than partial breastfeeding [1, 2]. However, there are advantages to both exclusive and partial breastfeeding when compared to not breastfeeding at all [8, 9]. In Sweden, > 90% of women breastfeed their newborn during the initial days after birth, and > 80% of all two-month-old babies are breastfed: a high level when compared to other European countries [10].
Congenital heart disease (CHD) is the most common birth malformation, seen in 1 / 100 newborns [11]. Thanks to advances in cardiac care, in high-income countries today > 90% of these children reach adulthood [12, 13], which in recent decades, has led to an increase in women with CHD becoming pregnant [14]. However, undergoing pregnancy is not without risks for women with CHD. Cardiovascular events such as heart failure, arrhythmia, and thromboembolism are more common in this group than among healthy women, and obstetric complications such as Caesarean section and preterm birth, known to be breastfeeding-reducing factors, also occur more often for women with CHD [15,16,17]. Among women in general, both emotional distress and impacts from the environment affect whether a woman continues to breastfeed [17, 18]. In the case of preterm birth, which is emotionally stressful for parents [19], length of stay in intensive neonatal care units has been linked to reduced breastfeeding rates six months after birth for both full-term and pre-term infants [20].
To our knowledge, only one study that previously has described breastfeeding in women with CHD, showed that cardiovascular events did not occur more often among breastfeeding women than among non-breastfeeding women [21]. However, no previous study has evaluated risk factors for non-breastfeeding in women with CHD compared to women without CHD. Data on breastfeeding rates, health, sociodemographic factors, obstetric complications, and factors related to heart disease, can provide healthcare professionals with new knowledge of how to support breastfeeding for women with CHD. This register study therefore, examined breastfeeding rates in women with CHD compared to women without CHD as well as factors that may hinder breastfeeding for women with CHD.
Methods
Study design and data source
This register study is based on data covering 2014 − 2019, collected from the Swedish Congenital Heart Disease Register (SWEDCON) and the Swedish Pregnancy Register. SWEDCON is a Swedish national register comprising information on individuals with CHD from diagnosis to end of life. It includes data on aspects such as sociodemographics, diagnoses, interventions, echocardiograms, medications, symptoms linked to heart disease, and New York Heart Association Stages of Heart Failure class (NYHA class) [22]. The Swedish Pregnancy Register is a national register collecting data on pregnancy, childbirth, the postpartum period, reproductive health, and sociodemographic characteristics from > 98% of pregnant women in 16 of the 20 healthcare regions in Sweden. Pregnant women on their first visit to antenatal care, are asked by the midwife about participation in the Swedish Pregnancy Register. Data on health history and diagnoses are downloaded directly from the healthcare region’s electronic medical record into the Swedish Pregnancy Register. Midwives at the maternity ward gather information on breastfeeding rates two days after birth. At the postpartum visit, which usually takes place between 6 − 18 weeks postpartum, the antenatal care midwife asks retrospectively whether the infant was breastfed at four weeks of age [23].
Participants and inclusion criteria
The two registers were merged, and women with CHD who matched the inclusion criteria were selected: (i) having been diagnosed with CHD with at least one visit to an adult CHD clinic after the age of 18 years, (ii) being primiparous women who had given birth after 22 + 0 gestational weeks, and (iii) having data on breastfeeding two days after birth. These were matched approximately 1:5 by residential area and year of birth to women without CHD. The final sample comprised 578 women with CHD (Table 1) and 3049 women without CHD (see Fig. 1).
Outcome measures and analysed factors
The register splits the variable breastfeeding into exclusive, partial, or non-breastfeeding. Exclusive breastfeeding is when the baby receives only the mother’s milk from the breast or bottle. Partial breastfeeding is when the child regularly receives donated breast milk or formula in combination with breastfeeding. Breastfeeding was dichotomised into breastfeeding (both exclusive and partial) and non-breastfeeding. The analysis included factors related to the heart disease (complexity of the heart disease, NYHA class, use of cardiovascular medication, and symptoms related to the heart disease) where the complexities of lesions were classified according to European Society of Cardiology guidelines [24], comorbidities, obstetric complications, and sociodemographic characteristics. Comorbidities among included women were BMI ≥ 30, hypertension prior to pregnancy, diabetes mellitus, hypothyroidism, and self-reported history of psychiatric illness, current or previously. Obstetric complications were defined as pre-eclampsia, preterm birth (represented in this study, children born between gestational weeks 31 and 36), induced labour, vacuum extraction / forceps, Caesarean section, major postpartum haemorrhage > 1000 ml [25], perineal trauma III − IV, and baby small for gestational age (SGA) based on Marsál’s curve [26]. Sociodemographics included age, civil status, level of education, and tobacco use.
Statistical analysis
Statistical analyses were conducted using version 28 of the IBM SPSS Statistics software package (IBM Corp., Armonk, NY, USA). All data were assessed for normality. Differences in means and ratios were tested using Student’s t-test, and Chi2 − test. Univariable logistic regression analyses were used to test whether non-breastfeeding at two days and four weeks after birth was associated with factors related to the heart disease, comorbidities, obstetric complications, and sociodemographic characteristics in all women and women with CHD separately. Independent factors that showed association with non-breastfeeding were further tested for collinearity using Spearman correlation. A correlation was seen between induced labour and Caesarean section, and between Caesarean section and premature birth. Due to this, Caesarean section was omitted from further analyses. Furthermore, missing data in the variables “NYHA” and “cardiovascular medication” resulted in a reduced total number in the multivariable analysis. Missing data was handled as an own category in these variables. In doing so, cases with missing data did not differ from the reference categories (i.e., “NYHA class I” and “no cardiovascular medication”) in the univariable regressions and were therefore merged with the reference category (NYHA 1 + missing data, no cardiovascular medication + missing data) in the following analyses. Finally, the remaining factors with a p-value < 0.1 in the univariable analyses were included in multivariable models and analysed in a stepwise backward elimination manner. The results from logistic regression are presented as odds ratios with 95% confidence intervals (95% CI), and the null hypothesis was rejected on p-values < 0.05.
Results
Women with CHD were more likely to suffer from obstetric complications during pregnancy and childbirth, and self-reported history of psychiatric illness was reported more frequently. The level of education was slightly higher in women with CHD compared to women without CHD. An overview of the women’s characteristics is presented in (Table 2). Women with CHD had a lower breastfeeding rate two days after birth compared to women without CHD (94% vs. 97%, p = 0.001). Four weeks after birth, the breastfeeding rate in women with CHD was still lower compared to women without CHD (84% vs. 89% p = 0.006) (Table 3). Analyses on breastfeeding were performed on women who gave birth at full-term. The differences in breastfeeding were lower among women with CHD compared to women without CHD two days (95% vs. 97%, p = 0.028) and four weeks after birth (86% vs. 89%, p = 0.04). Univariable and multivariable analyses, including all women, women with and without CHD, were carried out to explore whether being diagnosed with CHD was associated with non-breastfeeding. The models showed that being diagnosed with CHD was associated with non-breastfeeding both two days (OR 1.8; 95% CI 1.2, 2.7) and four weeks after birth (OR 1.5; 95% CI 1.1, 2.0).
Factors associated with non-breastfeeding in women with CHD
Univariable logistic regression analyses showed that among women with CHD, non-breastfeeding two days after birth was associated with BMI ≥ 30 (OR 4.0; 95% CI 1.8, 8.7), self-reported history of psychiatric illness (OR 2.8; 95% CI 1.4, 5.6), preterm birth (OR 7.5; 95% CI 2.9, 19.4), SGA (OR 4.5; 95% CI 1.7, 11.9), and NYHA class II − III (with NYHA class I as reference) (OR 5.3; 95% CI 1.3, 18.4). The multivariable model showed that BMI ≥ 30 (OR 3.1; 95% CI 1.4, 7,3), self-reported history of psychiatric illness (OR 2.4; 95% CI 1.2, 5.1), and preterm birth (OR 6.4; 95% CI 2.1, 19.0), SGA (OR 4.2; 95% CI 1.4, 12.2), and NYHA class II-III (OR 6.0; 95% CI 1.4, 26.7) were associated with non-breastfeeding two days after birth (Table 4).
Four weeks after birth, the univariable logistic regression analyses showed that non-breastfeeding for women with CHD was associated with ≤ 12 years of education (OR 1.9; 95% CI 1.1, 3.3), BMI ≥ 30 (OR 4.4; 95% CI 2.2, 8.8), self-reported history of psychiatric illness (OR 2.2; 95% CI 1.2, 3.9), induced labour (OR 1.8; 95% CI 1.0, 3.2), Caesarean section (OR 2.7; 95% CI 1.5, 4.7), preterm birth (OR 6.8; 95% CI 2.4, 19.5), and treatment with cardiovascular medication (OR 2.8; 95% CI 1.1, 7.4). In the multivariable model, BMI ≥ 30 (OR 4.3; 95% CI 2.1, 9.0), self-reported history of psychiatric illness (OR 2.2; 95% CI 1.2, 4.2), and preterm birth (OR 8.9; 95% CI 2.8, 27.9) were associated with non-breastfeeding four weeks after birth (Table 5).
Analyses were conducted on cases without breastfeeding data showing this group to be more affected by the heart disease, with more women having symptoms from the heart disease (11.4% vs. 25.9%, p = < 0.001), more women having an NYHA class II-III (5.7% vs. 13.8%, p = 0.007), and more women having moderate and severe complexity (22.5% vs. 30.2%, p = 0.019). They were also more often affected by obstetric complications such as Caesarean Sect. (23% vs. 32.1%, p = 0.006) and preterm birth (4.2% vs. 27.7%, p = 0.001).
Discussion
This register study examined breastfeeding rates two days and four weeks after birth in 578 women with CHD compared to 3049 women without CHD, as well as hindering factors for non-breastfeeding in women with CHD. The results show that women with CHD had slightly lower breastfeeding rates than women without CHD (two days after birth: 94% vs. 97%; and four weeks after birth: 84% vs. 89%), although both groups showed a relatively high level of breastfeeding compared to the general population of women in other European countries [10]. One explanation for the high level of breastfeeding in the present study might be the long paid parental leave in Sweden [10]; another might be the society’s high level of breastfeeding acceptance, which significantly affects women’s breastfeeding success [18].
Since sociodemographic characteristics, health history, and obstetric complications were included, this study was able to show associations of non-breastfeeding with both social factors and obstetric complications, and a few heart-related factors in women with CHD. However, the heart-related factor NYHA class II-III was only associated with non-breastfeeding two days after birth and not four weeks after birth. One reason for this could be that included women were relatively young with a mean age at 29 years, and not yet exposed to comorbidities in their heart disease, such as cardiovascular medication, symptoms from their heart disease or a higher NYHA class. Furthermore, women with severe conditions may have been advised against pregnancy [15]. For women with CHD, preterm birth showed the highest OR for non-breastfeeding, both two days (OR 6.4) and four weeks after birth (OR 8.9), and this has also been shown as a breastfeeding reducing factor in the general population [27]. However, previous studies have reported preterm birth rates of up to 16% among women with CHD [16], and so from an international view, the preterm birth rate (4.2%) in the present sample can be considered low. This may be one reason why breastfeeding rates did not differ substantially in the current sample [27]. Other factors associated with non-breastfeeding were BMI ≥ 30, and self-reported history of psychiatric illness, which again are factors known to impact breastfeeding among women in general [17, 28, 29].
In line with our finding of lower breastfeeding rates among women with CHD than women without CHD, previous research describes women with chronic illness as more likely than healthy women to cease exclusive breastfeeding [30]. A possible explanation for the lower breastfeeding rates among women with CHD in the current study could be that there is less consideration of whether the infant should receive breast milk substitutes. The new mother, her family, and her healthcare professionals can all be influenced by breastfeeding expectations [18], and as the woman has a chronic disease people around her may think that they should not stress her about breastfeeding. However, the initiation of breastmilk substitutes (e.g., as a complement) is a known risk factor for breastfeeding cessation [29]. Moreover, studies have found that women who wish to breastfeed but fail to do so express dissatisfaction, personal stigma, and even a sense of failure [31, 32]. In addition to this, women with CHD have an increased risk of emotional distress during their postpartum period [33], and unsuccessful breastfeeding may be perceived as an additional stressor for these women.
These novel results highlight that CHD combined with preterm birth, BMI ≥ 30, or psychiatric illness history may add a further complex dimension to the situation. As preterm birth and a history of psychiatric illness are more common among women with CHD than among women without CHD [16], one could say CHD may affect breastfeeding indirectly through these factors. However, women experiencing preterm birth, BMI ≥ 30, or having a psychiatric illness history may be an extra-vulnerable group in terms of successful breastfeeding. Whether or not a woman intends to breastfeed exclusively, our results indicate that formula should be given solely on strict medical indication in order to avoid jeopardising lactation onset. Our data show that for a high proportion of women with CHD breastfeed, however, CHD is still a factor associated with non-breastfeeding. Therefore, healthcare personnel should pay attention to breastfeeding even if a high proportion of women with CHD breastfeed.
A strength of the study is the large sample, with comparable previous breastfeeding experience of participants, as only primiparous women were included. However, as in all register studies, the data were limited to those included in the register. In cases of non-significant results in some comparisons, the possibility of being underpowered cannot be excluded. As complete data on the exact method of cardiac intervention in all lesions were not available, we were unable to investigate whether a median sternotomy affected the breastfeeding rate. The results also showed a higher proportion of women without data on breastfeeding giving premature birth compared to those with data on breastfeeding. Since premature babies are cared for at a higher level of care, and in many cases with separate records, breastfeeding data are not automatically transferred into the Swedish Pregnancy Register. As premature birth is associated with non-breastfeeding, our data may underestimate the prevalence of non-breastfeeding.
Conclusion
The study shows that most women with CHD breastfeed, however, at a slightly lower proportion compared to women without CHD. In addition, factors related to the heart disease were not associated with non-breastfeeding four weeks after birth. Since preterm birth, BMI ≥ 30, and psychiatric illness are associated with non-breastfeeding, healthcare professionals should offer greater breastfeeding support to women with CHD having these conditions.
Data availability
No datasets were generated or analysed during the current study.
Abbreviations
- ACHD:
-
Adult congenital heart disease
- BMI:
-
Body mass index
- CHD:
-
Congenital heart disease
- CI:
-
Confidence interval
- NYHA:
-
New York Health Association
- OR:
-
Odds ratio
- SGA:
-
Small for gestational age
- SWEDCON:
-
Swedish Congenital Heart Disease Register
- WHO:
-
World Health Organization
References
World Health Organization. Health Topics, https://www.who.int/health-topics/breastfeeding#tab=tab_1 (2018). Accessed 6 Dec 2023.
Victora CGP, Bahl RMD, Barros AJDP, França GVAP, Horton SP, Krasevec JM, et al. Breastfeeding in the 21st century: epidemiology, mechanisms, and lifelong effect. Lancet. 2016;387(10017):475–90.
Qiao J, Dai L-J, Zhang Q, Ouyang Y-Q. A meta-analysis of the association between breastfeeding and early childhood obesity. J Pediatr Nurs. 2020;53:57–66.
Nguyen P, Binns CW, Ha AVV, Chu TK, Nguyen LC, Duong DV, et al. Prelacteal and early formula feeding increase risk of infant hospitalisation: a prospective cohort study. Arch Dis Child. 2020;105(2):122–6.
Foster SF, Vazquez C, Cubbin C, Nichols AR, Rickman RR, Widen EM. Breastfeeding, socioeconomic status, and long-term postpartum weight retention. Int Breastfeed J. 2023;18:1.
Lambrinou C-P, Karaglani E, Manios Y. Breastfeeding and postpartum weight loss. Curr Opin Clin Nutr Metab Care. 2019;22(6):413–7.
Chen Y, Jiang P, Geng Y. The role of breastfeeding in breast cancer prevention: a literature review. Front Oncol. 2023;13:1257804.
Xia M, Luo J, Wang J, Liang Y. Association between breastfeeding and postpartum depression: a meta-analysis. J Affect Disord. 2022;308:512–9.
Park S-J, Lee H-J. Exclusive breastfeeding and partial breastfeeding reduce the risk of overweight in childhood: a nationwide longitudinal study in Korea. Obes Res Clin Pract. 2018;12(2):222–8.
Theurich MA, Davanzo R, Busck-Rasmussen M, Díaz-Gómez NM, Brennan C, Kylberg E, et al. Breastfeeding rates and programs in Europe– A survey of 11 national breastfeeding committees and representatives. J Pediatr Gastroenterol Nutr. 2019;68(3):400–7.
Liu Y, Chen S, Zühlke L, Black GC, Choy M-k, Li N, et al. Global birth prevalence of congenital heart defects 1970–2017: updated systematic review and meta-analysis of 260 studies. Int J Epidemiol. 2019;48(2):455–63.
Giang KW, Mandalenakis Z, Fedchenko M, Eriksson P, Rosengren A, Norman M, et al. Congenital heart disease: changes in recorded birth prevalence and cardiac interventions over the past half-century in Sweden. Eur J Prev Cardiol. 2023;30(2):169–76.
Mandalenakis Z, Giang KW, Eriksson P, Liden H, Synnergren M, Wåhlander H, et al. Survival in children with congenital heart disease: have we reached a peak at 97%? J Am Heart Association. 2020;9(22):017704.
Bottega N, Malhamé I, Guo L, Ionescu-Ittu R, Therrien J, Marelli A. Secular trends in pregnancy rates, delivery outcomes, and related health care utilization among women with congenital heart disease. Congenit Heart Dis. 2019;14(5):735–44.
Canobbio MM, Warnes CA, Aboulhosn J, Connolly HM, Khanna A, Koos BJ, et al. Management of pregnancy in patients with complex congenital heart disease: a scientific statement for healthcare professionals from the American Heart Association. Circulation. 2017;135(8):e50–87.
Haberer K, Silversides CK. Congenital heart disease and women’s health across the life span: focus on reproductive issues. Can J Cardiol. 2019;35(12):1652–63.
Asimaki E, Dagla M, Sarantaki A, Iliadou M. Main biopsychosocial factors influencing breastfeeding: a systematic review. Mædica. 2022;17(4):955–62.
Thomson G, Ingram J, Clarke J, Johnson D, Jolly K. Who gets to breastfeed? A narrative ecological analysis of women’s infant feeding experiences in the UK. Front Sociol. 2022;7:904773.
Ionio C, Lista G, Mascheroni E, Olivari MG, Confalonieri E, Mastrangelo M, et al. Premature birth: complexities and difficulties in building the mother-child relationship. J Reproductive Infant Psychol. 2017;35(5):509–23.
Ericson J, Eriksson M, Hoddinott P, Hellström-Westas L, Flacking R. Breastfeeding and risk for ceasing in mothers of preterm infants—long-term follow‐up. Maternal Child Nutr. 2018;14(4):e12618.
Matsuzaka Y, Aoki-Kamiya C, Yokouchi-Konishi T, Shionoiri T, Nakanishi A, Iwanaga N, et al. Breastfeeding and postpartum outcomes among women with congenital heart disease. Int J Cardiol Congenital Heart Disease. 2021;4:100167.
Bodell A, Björkhem G, Thilén U, Naumburg E. National quality register of congenital heart diseases– can we trust the data? J Congenital Cardiol. 2017;1:11.
Stephansson O, Petersson K, Björk C, Conner P, Wikström AK. The Swedish pregnancy Register– for quality of care improvement and research. Acta Obstet Gynecol Scand. 2018;97(4):466–76.
Baumgartner H, de Backer J, Babu-Narayan SV, Budts W, Chessa M, Diller G-P, et al. 2020 ESC guidelines for the management of adult congenital heart disease. Eur Heart J. 2021;42(6):563–645.
Mavrides EAS, Chandraharan E, Collins P, Green L, Hunt BJ, Riris S, Thomson AJ. Prevention and management of postpartum haemorrhage: green-top guideline 52. BJOG: Int J Obstet Gynecol. 2017;124(5):e106–49.
Maršál K, Persson PH, Larsen T, Lilja H, Selbing A, Sultan B. Intrauterine growth curves based on ultrasonically estimated foetal weights. Acta Paediatr. 1996;85(7):843–8.
Ericson J, Flacking R, Hellström-Westas L, Eriksson M. Changes in the prevalence of breast feeding in preterm infants discharged from neonatal units: a register study over 10 years. BMJ Open. 2016;6(12):e012900.
Wallenborn JT, Joseph A-C, Graves WC, Masho SW. Prepregnancy depression and breastfeeding duration: a look at maternal age. J Pregnancy. 2018;2018:4825727–7.
Hemmingway A, Fisher D, Berkery T, Dempsey E, Murray DM, Kiely ME. A detailed exploration of early infant milk feeding in a prospective birth cohort study in Ireland: combination feeding of breast milk and infant formula and early breast-feeding cessation. Br J Nutr. 2020;124(4):440–9.
Scime NV, Patten SB, Tough SC, Chaput KH. Maternal chronic disease and breastfeeding outcomes: a Canadian population-based study. J Maternal-Fetal Neonatal Med. 2022;35(6):1148–55.
Bresnahan M, Zhuang J, Goldbort J, Bogdan-Lovis E, Park S-Y, Hitt R. Made to feel like less of a woman: the experience of stigma for mothers who do not breastfeed. Breastfeed Med. 2020;15(1):35–40.
Ericson J, Palmér L. Cessation of breastfeeding in mothers of preterm infants—A mixed method study. PLoS ONE. 2020;15(5):e0233181.
Freiberg A, Beckmann J, Freilinger S, Kaemmerer H, Huber M, Nicole N, et al. Psychosocial well-being in postpartum women with congenital heart disease. Cardiovasc Diagnosis Therapy. 2022;12:4389–99.
World Medical Association Declaration. Of Helsinki: ethical principles for medical research involving human subjects. JAMA: J Am Med Association. 2013;310(20):2191–4.
Acknowledgements
Not applicable.
Funding
Open access funding provided by Umea University. This study was supported by Umeå University, the Swedish Children’s Heart Association, the Heart Foundation of Northern Sweden, the Swedish Heart–Lung Foundation, and the Swedish Heart and Lung Association.
Open access funding provided by Umea University.
Author information
Authors and Affiliations
Contributions
YH and AB led the study process with support from BJ, AW, and ML. ISP, CC, MD, ATK, PS, UT, and AKW participated in the manuscript’s progress and contributed their knowledge to complete the manuscript. All authors reviewed and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate
The study adhered to the principles for medical research as described in the Declaration of Helsinki [34], and was approved by the Swedish Ethical Review Authority (ref:2020 − 00701).
Consent for publication
Not applicable.
Competing interests
The authors declare no competing interests.
Additional information
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
About this article
Cite this article
Holstad, Y., Johansson, B., Lindqvist, M. et al. Breastfeeding in primiparous women with congenital heart disease − a register study. Int Breastfeed J 19, 19 (2024). https://doi.org/10.1186/s13006-024-00627-y
Received:
Accepted:
Published:
DOI: https://doi.org/10.1186/s13006-024-00627-y