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Gestational age, mode of birth and breastmilk feeding all influence acute early childhood gastroenteritis: a record-linkage cohort study

Abstract

Background

Acute gastroenteritis (AGE) is a leading cause of infectious morbidity in childhood. Clinical studies have implicated caesarean section, early birth and formula feeding in modifying normal gut microbiota development and immune system homeostasis in early life. Rates of early birth and cesarean delivery are also increasing worldwide. This study aimed to investigate the independent and combined associations of the mode and timing of birth and breastmilk feeding with AGE hospitalisations in early childhood.

Methods

Population-based record-linkage study of 893,360 singleton livebirths of at least 33 weeks gestation without major congenital conditions born in hospital, New South Wales, Australia, 2001–2011. Using age at first AGE hospital admission, Cox-regression was used to estimate the associations for gestational age, vaginal birth or caesarean delivery by labour onset and formula-only feeding while adjusting for confounders.

Results

There were 41,274 (4.6 %) children admitted to hospital at least once for AGE and the median age at first admission was 1.4 years. Risk of AGE admission increased with decreasing gestational age (37–38 weeks: 15 % increased risk, 33–36 weeks: 25 %), caesarean section (20 %), planned birth (17 %) and formula-only feeding (18 %). The rate of AGE admission was highest for children who were born preterm by modes of birth other than vaginal birth following the spontaneous onset of labour and who received formula-only at discharge from birth care (62–78 %).

Conclusions

Vaginal birth following spontaneous onset of labour at 39+ weeks gestation with any breastfeeding minimised the risk of gastroenteritis hospitalisation in early childhood. Given increasing trends in early planned birth and caesarean section worldwide, these results provide important information about the impact obstetric interventions may have on the development of the infant gut microbiota and immunity.

Peer Review reports

Background

Acute gastroenteritis is characterised by viral or bacterial infection causing diarrhea and vomiting and is a leading cause of infectious morbidity in infants and children worldwide even in developed countries including Australia, where the incidence is highest in the first two years of life [1, 2]. Many factors in early childhood are associated with an increased susceptibility to gastroenteritis, such as poor social conditions, diet and antibiotic use [3, 4]. Additionally, gut microbial composition and immunological immaturity in the newborn may also play an important role [58].

Bacterial exposures from the birth canal and perianal region during vaginal birth are important precursors for the colonisation of the gut in the first few days of life. To prepare for this, cells of the adaptive immune system are recruited to the fetal intestinal tissue with a transition to adult T-cells occurring in the third trimester [5]. Once born, a multitude of pathways activate to prepare the immune system and intestinal epithelial cells to manage the high density of bacteria in the gut, establishing a homeostasis between the immune system and gut microbiota [6]. The later the gestational age at birth, the better prepared the newborns immune system is for establishing homeostasis. Bacterial colonisation and the immune response in the gut are further supported by exposure to the nutritional, growth and immunological factors contained in breastmilk [7]. Clinical studies have shown gut colonisation is typically imbalanced towards bacterial species such as E. Coli. in infants delivered by caesarean section or fed formula rather than breastmilk [8].

This suggests potential common biological mechanisms by which shortened gestation, delivery by caesarean section and a lack of breastmilk exposure may increase susceptibility to gut infections by disturbing or modifying gut microbiota and immune system homeostasis in early life. Previous population-based studies have investigated the independent associations of vaginal birth and breastmilk feeding with childhood gastroenteritis [911]. Few have examined the association with gestational age, especially those born around term, either preterm or early term (37–38 weeks gestation) and there is evidence these infants and children are at an increased risk of morbidity generally [12]. The combined risk of gastroenteritis associated with these birth characteristics is currently unknown, but such information is important given worldwide increasing rates of early planned birth and delivery by caesarean section [1316], which are also associated with reduced rates of breastmilk feeding [17, 18]. Record linkage of large routinely collected population-based data with standardised clinical information provides a powerful approach to investigate the combined risk of gastroenteritis for multiple birth characteristics.

The aim of this study was to investigate the independent and combined associations of the mode and timing of birth and breastmilk feeding with gastroenteritis hospitalisations in early childhood.

Methods

Study population

The study population included all singleton live births of ≥33 weeks gestation from 2001 to 2011 in New South Wales (NSW), Australia. Stillbirths and births to non-NSW resident mothers were excluded as these births have no opportunity for follow-up through record linkage with hospital admissions in NSW. Infants with major congenital conditions, born before 33 weeks gestation, or twins and higher-order births were excluded as they have different risk profiles, outcomes and models of care [19]. Each child in the study population was followed from birth until the age of 6 years, death or the end of the study period (30 June 2012), whichever occurred first.

This study used linked birth, hospital and death records from the NSW Perinatal Data Collection (PDC), NSW Admitted Patient Data Collection (APDC) and Registry of Births, Deaths and Marriages Death Registrations (fact of death) respectively. The PDC is a population-based statutory collection covering all live births and stillbirths of at least 20 weeks gestation or, if gestational age is unknown, at least 400 grams birthweight. It contains information on maternal characteristics, pregnancy, labour and delivery factors, and infant outcomes. The APDC includes demographic and hospitalisation related data for every inpatient admitted to any public or private hospital in NSW. Diagnoses for each admission are coded according to the 10th revision of the International Classification of Disease, Australian Modification (ICD-10-AM) [20]. Probabilistic record linkage of these data was performed by the NSW Centre for Health Record Linkage using methods described previously and only de-identified information was provided to the researchers [21]. The data sources used for this study require ethical and data custodian approval to access, link (by an independent and approved authority) and release for research. Approval for the record linkage and use of the data for research was obtained from the NSW Population and Health Services Research Ethics Committee and the appropriate data custodians.

Mode of birth, timing of birth and infant feeding at discharge

The study factors of interest were mode of birth, gestational age (timing of birth) and infant feeding status at discharge from birth care. Mode of birth was defined using the combination of labour onset and type of birth (vaginal birth or caesarean section) and categorised as vaginal birth following spontaneous onset of labour, caesarean section following spontaneous onset of labour, vaginal birth following labour induction, caesarean section following labour induction, or pre-labour caesarean section. Gestational age is reported in completed weeks of gestation, as determined by the best clinical estimate including early ultrasound and last menstrual period. This was categorised as preterm (33–36 weeks), early-term (37–38 weeks) or term (39–42 weeks) birth. Infant feeding status at discharge from birth care is recorded using one or more of the following three categories: “breastfeeding”, “expressed breastmilk” or “infant formula”. These categories were used to create two independent groups: any breastmilk feeding (breastfeeding or expressed breastmilk feeding without infant formula) and formula-only feeding (infant formula without breastfeeding or expressed breastmilk feeding).

Study outcome

The study outcome was hospital admissions for gastroenteritis, which we refer to as acute gastroenteritis (AGE). Primary or additional diagnoses for gastroenteritis (ICD-10-AM: A00-A09 or K52) were used to identify admissions. Inter-hospital transfers were treated as a continuation of an admission and not a new admission. AGE admissions within 7 days of a previous AGE admission were also treated as a single event.

Statistical analysis

The proportion and number of children with none, one, or more than one AGE admission in the study period by maternal and perinatal characteristics were calculated. Cox proportional hazards regression was used to estimate the adjusted Hazard Ratios and 95 % confidence intervals for the independent and combined associations between the study exposures and first AGE hospitalisation with child age as the timescale and age at discharge from birth care as entry into observation. For censored individuals, age was recorded as the earliest of death, sixth birthday, or end of the study period (30 June 2012).

The covariates used in the study reflect known risk factors identified in the literature [4, 9, 12, 22]. Covariates included were: parity (primiparae or multiparae), maternal age (<20, 20–24, 25–29, 30–34, 35–39, 40+ years), country of birth (Australia-born or other), socio-economic status quintile (Australian Bureau of Statistics Socio-Economic Index For Areas – Index of Relative Socio-economic Advantage) [23], smoking during pregnancy, hypertensive disorders of pregnancy (gestational hypertension, preeclampsia or eclampsia), diabetes mellitus in pregnancy (gestational or pre-existing) [24, 25], baby’s sex, 5-minute Apgar score < 7, birthweight (standardised by gestational age and sex) [26], presence of AGE or other infection specific to the perinatal period (ICD-10-AM: P35-P39), admission to a Special Care Nursery (SCN) or Neonatal Intensive Care Unit (NICU) and infant birth admission length of stay (standardised by gestational age and type of birth using the study population). To account for the inclusion of rotavirus vaccination in the national immunisation program from 1 July 2007, year of birth was categorised as before July 2007 or July 2007 onwards. All covariates were adjusted for in the analysis except for admission to SCN or NICU and 5-minute Apgar score < 7 which were omitted from the model due to high co-linearity with birth at 33–36 weeks gestation. The assumption of proportional hazards was assessed using standard diagnostics and found to be reasonable.

Cox-regression was used to estimate the associations for the study exposures under variations of the study population and design, to assess the robustness of the main findings and for comparability with other studies of associations between birth factors and childhood hospitalisations. The variations investigated were: a sub-population of low risk liveborn singleton pregnancies (infants born at ≥37 weeks gestation, cephalic presenting, and a birthweight between the 10th and 90th percentiles for gestational age and sex, to women aged 20–34 years without medical conditions), using children with no hospital admissions only as the controls, using only a primary diagnosis of gastroenteritis, restricting to AGE hospitalisations within the first year of life or within the first two years of life (rather than six), and restricting to births from July 2007 onwards (universal rotavirus vaccination).

The level of missing information was minimal for all variables (<0.01 to 0.10 %), with the exception of infant feeding at discharge. Collection of infant feeding status began in mid-2006 and was only available for 51.8 % of births, within which 0.95 % were missing. As the per cent missing across all variables except infant feeding affected only 0.23 % of records, these were excluded. However, as infant feeding was an exposure of interest, it was imputed using a logistic model following recommendations in the literature (see Additional file 1). All analyses were performed using Stata 13.0 (StataCorp LP, TX, USA).

Results

Of the 893,360 children included in the study, 28 % were delivered by caesarean section, 41 % were planned births (pre-labour caesarean or following labour induction), 27 % were born before 39 weeks gestation and 12 % were fed only formula in the birth admission (Table 1). There were 38,085 (4.3 %) children admitted to hospital for AGE once and 3,189 (0.4 %) more than once (7.7 % recurrence rate). The proportion of children admitted for AGE was higher for those delivered by caesarean section, born before 39 weeks gestation and fed only formula. Average follow-up per child was 4.37 years (standard deviation: 1.88), with a total follow-up time of 3,907,163 years. For the 41,274 children admitted, the median age at first AGE hospital admission was 1.43 years (Inter-quartile range 0.77 to 2.48 years).

Table 1 Maternal and perinatal characteristics for children admitted to hospital once and more than once for acute gastroenteritis, NSW 2001–2011

Compared to vaginal birth following spontaneous onset of labour, all other modes of birth were independently associated with a 12–23 % increased rate of AGE admission (Table 2). In general those modes of birth including delivery by caesarean section were similar with largely overlapping confidence intervals (19–23 % increased rate of admission), while vaginal birth following labour induction was intermediary to these modes of birth and vaginal birth following spontaneous onset of labour (12 % increased rate of admission). Adjusted associations for all variables are presented in the Additional file 2. The rate of AGE admission increased with decreasing gestational age. Birth at 37–38 weeks was associated with a 15 % increase in the rate of AGE admission (adjusted hazard ratio [aHR], 1.15; 95 % Confidence Interval [CI], 1.12–1.17), and for births at 33–36 weeks gestation was 23 % (aHR, 1.23; 95 % CI, 1.18–1.29). Infants fed only formula (aHR, 1.18; 95 % CI, 1.11–1.24) were also more likely to be admitted for AGE.

Table 2 Associations for age at first hospital admission for acute gastroenteritis by mode of birth, timing of birth and infant formula only at birth for the overall study and selected sub-populations, NSW 2001–2011a

Results for the combined associations are presented in Fig. 1. Compared with vaginal birth following spontaneous onset of labour at 39+ weeks gestation with any breastmilk feeding at discharge, early term births with formula-only feeding had an increased rate of AGE of 35 % and preterm birth a 45 % increased rate. Children born at early term with formula-only feeding had a higher rate of admission compared to preterm births that had some breastmilk feeding (35 % versus 23 %). For the other modes of birth with formula-only feeding, early term births had increased admission rates of 51–66 %, and preterm births had the highest rates ranging from 62–78 %. Within births 39+ weeks gestation, all modes of birth with formula-only feeding compared with vaginal birth following spontaneous onset of labour, had increased rates of admission by 31–45 %.

Fig. 1
figure 1

Combined associations for age at first hospital admission for acute gastroenteritis by mode of birth, timing of birth and infant formula only at birth, NSW 2001–2011. The reference category is vaginal, birth following spontaneous onset of labour at 39+ weeks gestation with breastmilk feeding at discharge. Associations adjusted for maternal country of birth, maternal smoking during pregnancy, socio-economic advantage, parity, diabetes, hypertension, baby’s sex, year of birth, birthweight, and length of stay and infections in the birth admission (AGE or ICD-10-AM: P35-P39)

The results were mostly robust to changes in study population or design. Restriction to the first two years of life, low risk pregnancies, the period of rotavirus vaccination or a primary diagnosis of AGE provided generally similar adjusted hazard ratios to those for the selected study population (Table 2). The impact of formula-only feeding was stronger (34 % versus 18 %) when restricting to the first year of life. Restricting the control group to children with no hospital admissions provided a stronger association for gestational age (33–36 weeks, 44 % versus 23 %; 37–38 weeks, 21 % versus 15 %). For the adjusted final models and combined associations for the investigated changes in study population or design see Additional files 2 and 3.

Discussion

This is the first population-based study to specifically investigate the combined effects of mode and timing of birth and breastmilk feeding at discharge from birth care on early childhood gastroenteritis hospital admissions. The results show an increased rate of admission in early childhood for being born before 39 weeks gestation, by modes of birth other than vaginal birth following spontaneous onset of labour and formula-only feeding at discharge from birth care. The combined effects highlight the benefit of normal birth and early breastmilk exposure, and are also suggestive of their impact on subsequent gastrointestinal health by possibly modifying or disturbing gut microbiota and immune system homeostasis. These findings are also pertinent in the context of increasing rates of caesarean section and early planned birth.

To our knowledge this is the first study to identify that children born preterm and early term, compared with children born at full term (39+ weeks gestation), had a 38–52 % and 28–41 % increased rate of AGE admission respectively, regardless of the mode of birth. Previous studies have demonstrated an increased rate of overall pediatric or respiratory hospitalisations for preterm and early term births [12, 2729]. We also found for preterm and early term births, those with modes of birth other than vaginal birth following spontaneous onset of labour and formula-only feeding at discharge had even higher rates of AGE admission, 51–66 % and 62–78 % respectively. Interestingly, children born at early term had higher AGE admission rates than those born preterm who received any breastmilk feeding in the birth admission. Nevertheless, the most vulnerable group of children identified were those born preterm by modes of birth other than vaginal birth following the spontaneous onset of labour and who received formula-only at discharge from birth care.

The increased rate of AGE admission with decreasing gestational age may be explained in part by the under-preparedness of the newborns immune system, particularly in the gut epithelium, to respond to the initial microbial colonisation at birth. Differences in markers of immune function between infants born before and after 37 weeks gestation have been reported previously [30]. This may explain why vaginal births following labour induction had an increased rate of admission compared to those following the spontaneous onset of labour, as a decision has been made to deliver. Relative to the developmental trajectory of the infant, it may be that the necessary time required for the infant’s innate immune response to sufficiently mature has been circumvented.

Variation in gut microbial composition in infants by mode of birth (vaginal birth or caesarean section) and feeding status (breastmilk or formula) is well supported by clinical evidence [8, 31, 32]. These studies highlight that infants delivered by caesarean section or not exposed to breastmilk have less diverse gut microbiota dominated by “bad” bacteria [8, 31, 32]. The similarity of the adjusted associations for caesarean section regardless of the onset of labour is consistent with the theory of beneficial exposure to bacteria at the time of vaginal birth [9, 33]. The higher rate of admission for infants fed only formula is consistent with the idea that with minimal or no breastmilk exposure, there is a loss of the associated microbial and immunological benefits in early childhood. While our estimate (aHR, 1.18) was lower than other studies that have examined breastmilk feeding and AGE, these generally followed infants for the first 6–12 months of life, where a significant proportion of AGE admissions occur [34, 35]. The aHR of 1.34 from our analysis restricted to AGE admissions in the first year of life is similar to these studies, suggesting a potentially stronger association earlier in life.

Previous population-based record-linkage studies of term births and without breastmilk feeding information found, as we did, an increased risk of AGE for children delivered by caesarean section [9, 10]. However, with the known association between caesarean section and difficulty initiating breastfeeding [18], the combined association for both factors is of particular interest. We found that despite term birth, children delivered by caesarean section and formula-only feeding at discharge from birth care had a 40–45 % increased rate of admission. Even for infants with breastmilk exposure, caesarean section was still associated with increased rates of AGE admission (19–23 %). This suggests that for infants delivered by caesarean section, breastfeeding initiation and duration are important factors for reducing the risk of AGE in early childhood and alternative methods of exposure to beneficial bacteria at the time of birth are required.

Changes in clinical obstetric practice have seen an increase in rates of planned birth before 39 weeks gestation and caesarean section worldwide [1316], and the adverse impact of caesarean section on breastfeeding is well-established [18]. As these trends relate to factors hypothesised to have a common biological basis for affecting the risk of acute gastroenteritis, the impact of a continuation of these patterns on AGE should not be underestimated. Although, the increasing recognition of the potential harms of early elective births and subsequent introduction of clinical guidelines, policies and interventions to reduce labour induction or pre-labour caesarean section for non-medical reasons before 39–40 weeks gestation may counter these trends [3640].

As planned birth before 39 weeks increases the perceptions of women about what constitutes normal birth is also likely to be altered. Recent studies have demonstrated that almost one in four women believed that a baby was full-term at 34–36 weeks gestation, that one in two believed full term was 37–38 weeks and more than 90 % believed it was safe to deliver before 39 weeks [41, 42]. Another study demonstrated that many women had little knowledge of the benefits or risks of a caesarean section, yet almost half indicated that a caesarean section without medical indication should be given on request [43]. Given the multi-faceted changes in practice and attitudes towards earlier births and interventions, similar studies to ours are vital to assess the impact on long term outcomes to inform clinicians, and women and their families.

The strengths of this study are that it is a large population-based cohort, using data and variables with demonstrated accuracy and validity [44, 45]. Using a large population-based cohort also reduces the impact of genetic diversity and enables complete ascertainment of hospital admissions. The mode and timing of birth and infant feeding at discharge were all statistically significant and consistently so for all analyses (coefficient p-values were typically < 0.001), so it is unlikely our findings are due to chance. However, some caution is warranted as some of the associations for the study factors are small and by chance a statistically significant association may be found when performing many comparisons. Using available administrative data has some limitations, as not all potentially relevant characteristics such as diet, environment or antibiotic use during pregnancy and early childhood could be investigated. Despite the lack of information on long term breastfeeding outcomes such as the duration of exclusive breastfeeding, previous studies have found in-hospital formula supplementation is associated with early cessation of exclusive or any breastmilk feeding post-discharge [4648]. Identified cases of acute gastroenteritis were based on hospital admissions only which represent the severe end of the clinical spectrum and do not include mild cases that may be treated through out-patient facilities or primary care services.

Conclusions

We have shown using a large population-based record-linkage study that the rate of acute gastroenteritis hospitalisations in early childhood are increased for births by caesarean section or induction of labour, before 39 weeks gestation and for infants fed only formula at discharge from birth care. The combined effects of these factors highlight the benefit of normal birth and early breastmilk exposure, for reducing the risk of gastroenteritis hospitalisation in early childhood. These previously unknown combined effects represent useful information against a backdrop of increasing rates of caesarean section and early planned birth, and their potential impact on gut microbiota and immune system homeostasis.

Availability of data and materials

The data used in this study cannot be shared by the Authors due to the use and release of the data being subject to data custodian and ethics approval and conditions that require the data only be used for approved research, by approved persons directly involved in the project and following the completion of a confidentiality undertaking prior to the information being released.

Abbreviations

AGE:

acute gastroenteritis

aHR:

adjusted Hazard Ratio

APDC:

admitted patient data collection

CI:

confidence interval

ICD-10-AM:

International Classification of Disease, 10th revision, Australian Modification

NICU:

Neonatal Intensive Care Unit

NSW:

New South Wales

PDC:

perinatal data collection

SCN:

special care nursery

References

  1. Parashar UD, Gibson CJ, Bresee JS, Glass RI. Rotavirus and severe childhood diarrhea. Emerg Infect Dis. 2006;12(2):304–6.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Dey A, Wang H, Menzies R, Macartney K. Changes in hospitalisations for acute gastroenteritis in Australia after the national rotavirus vaccination program. Med J Aust. 2012;197(8):453–7.

    Article  PubMed  Google Scholar 

  3. Wilking H, Hohle M, Velasco E, Suckau M, Eckmanns T. Ecological analysis of social risk factors for Rotavirus infections in Berlin, Germany, 2007–2009. Int J Health Geogr. 2012;11(1):37.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Dennehy PH, Cortese MM, Bégué RE, Jaeger JL, Roberts NE, Zhang R, Rhodes P, Gentsch J, Ward R, Bernstein DI, et al. A case-control study to determine risk factors for hospitalization for rotavirus gastroenteritis in U.S. children. Pediatr Infect Dis J. 2006;25(12):1123–31.

  5. Burt TD. Fetal regulatory T cells and peripheral immune tolerance in utero: implications for development and disease. Am J Reprod Immunol. 2013;69(4):346–58.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Maynard CL, Elson CO, Hatton RD, Weaver CT. Reciprocal interactions of the intestinal microbiota and immune system. Nature. 2012;489(7415):231–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Ballard O, Morrow AL. Human milk composition: nutrients and bioactive factors. Pediatr Clin North Am. 2013;60(1):49–74.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Azad MB, Konya T, Maughan H, Guttman DS, Field CJ, Chari RS, Sears MR, Becker AB, Scott JA, Kozyrskyj AL. Gut microbiota of healthy Canadian infants: profiles by mode of delivery and infant diet at 4 months. CMAJ. 2013;185(5):385–94.

  9. Roberts CL, Algert CS, Ford JB, Nassar N. Mode of delivery may be the risk factor for infant infectious morbidity. Arch Dis Child. 2012;97(8):759.

    Article  PubMed  Google Scholar 

  10. Håkansson S, Källén K. Caesarean section increases the risk of hospital care in childhood for asthma and gastroenteritis. Clin Exp Allergy. 2003;33(6):757–64.

    Article  PubMed  Google Scholar 

  11. Bager P, Simonsen J, Ethelberg S, Frisch M. Cesarean delivery and risk of intestinal bacterial infection. J Infect Dis. 2010;201(6):898–902.

    Article  PubMed  Google Scholar 

  12. Lain SJ, Nassar N, Bowen JR, Roberts CL. Risk factors and costs of hospital admissions in first year of life: a population-based study. J Pediatr. 2013;163(4):1014–9.

    Article  PubMed  Google Scholar 

  13. Morris JM, Algert CS, Falster MO, Ford JB, Kinnear A, Nicholl MC, Roberts CL. Trends in planned early birth: a population-based study. Am J Obstet Gynecol. 2012;207(3):186.e181–e188.

  14. Menacker F, Hamilton BE. Recent trends in cesarean delivery in the United States. NCHS Data Brief. 2010;35:1–8.

    Google Scholar 

  15. Betrán AP, Merialdi M, Lauer JA, Bing-Shun W, Thomas J, Van Look P, Wagner M. Rates of caesarean section: analysis of global, regional and national estimates. Paediatr Perinat Epidemiol. 2007;21(2):98–113.

  16. Nassar N, Schiff M, Roberts CL. Trends in the distribution of gestational age and contribution of planned births in New South Wales, Australia. PLoS ONE. 2013;8(2), e56238.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Lutsiv O, Giglia L, Pullenayegum E, Foster G, Vera C, Chapman B, Fusch C, McDonald SD. A population-based cohort study of breastfeeding according to gestational age at term delivery. J Pediatr. 2013;163(5):1283–8.

  18. Prior E, Santhakumaran S, Gale C, Philipps LH, Modi N, Hyde MJ. Breastfeeding after cesarean delivery: a systematic review and meta-analysis of world literature. Am J Clin Nutr. 2012;95(5):1113–35.

    Article  CAS  PubMed  Google Scholar 

  19. NSW Department of Health. In: Statewide Services Development Branch, editor. Guide to the Role Delineation of Health Services (3rd edition). Sydney: NSW Health Department; 2002.

  20. The International Statistical Classification of Diseases and Related Health Problems, Australian Modification – Tabular List of Diseases and Alphabetic Index of Diseases. http://nccc.uow.edu.au/CasemixTools/icd10am/index.html Accessed 6 Nov 2014.

  21. Bentley JP, Ford JB, Taylor LK, Irvine KA, Roberts CL. Investigating linkage rates among probabilistically linked birth and hospitalization records. BMC Med Res Methodol. 2012;12:149.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Newman RD, Grupp-Phelan J, Shay DK, Davis RL. Perinatal risk factors for infant hospitalization with viral gastroenteritis. Pediatrics. 1999;103(1), e3.

    Article  CAS  PubMed  Google Scholar 

  23. Australian Bureau of Statistics. Socio-economic Indexes for Areas (SEIFA), Data only, 2006. Catalogue 2033.0.55.001 http://www.abs.gov.au/AUSSTATS/abs@.nsf/DetailsPage/2033.0.55.0012006?OpenDocument Accessed 15 Jul 2014.

  24. Chen JS, Roberts CL, Simpson JM, Ford JB. Prevalence of pre-eclampsia, pregnancy hypertension and gestational diabetes in population-based data: impact of different ascertainment methods on outcomes. Aust N Z J Obstet Gynaecol. 2012;52(1):91–5.

    Article  PubMed  Google Scholar 

  25. Tran DT, Roberts CL, Havard A, Jorm LR. Linking birth records to hospital admission records enhances the identification of women who smoke during pregnancy. Aust N Z J Public Health. 2014;38(3):258–64.

    Article  PubMed  Google Scholar 

  26. Dobbins TA, Sullivan EA, Roberts CL, Simpson JM. Australian national birthweight percentiles by sex and gestational age, 1998–2007. Med J Aust. 2012;197(5):291–4.

    Article  PubMed  Google Scholar 

  27. Boyle EM, Poulsen G, Field DJ, Kurinczuk JJ, Wolke D, Alfirevic Z, Quigley MA. Effects of gestational age at birth on health outcomes at 3 and 5 years of age: population based cohort study. BMJ. 2012;344, e896.

  28. Brown HK, Speechley KN, Macnab J, Natale R, Campbell MK. Neonatal morbidity associated with late preterm and early term birth: the roles of gestational age and biological determinants of preterm birth. Int J Epidemiol. 2014;43(3):802–14.

    Article  PubMed  Google Scholar 

  29. Paranjothy S, Dunstan F, Watkins WJ, Hyatt M, Demmler JC, Lyons RA, Fone D. Gestational age, birth weight, and risk of respiratory hospital admission in childhood. Pediatrics. 2013;132(6):e1562–9.

  30. Skogstrand K, Hougaard DM, Schendel DE, Bent N-P, Sværke C, Thorsen P. Association of preterm birth with sustained postnatal inflammatory response. Obstet Gynecol. 2008;111(5):1118–28.

    Article  CAS  PubMed  Google Scholar 

  31. Biasucci G, Rubini M, Riboni S, Morelli L, Bessi E, Retetangos C. Mode of delivery affects the bacterial community in the newborn gut. Early Hum Dev. 2010;86 Suppl 1:13–5.

    Article  PubMed  Google Scholar 

  32. Penders J, Thijs C, Vink C, Stelma FF, Snijders B, Kummeling I, van den Brandt PA, Stobberingh EE. Factors influencing the composition of the intestinal microbiota in early infancy. Pediatrics. 2006;118(2):511–21.

  33. Romero R, Korzeniewski SJ. Are infants born by elective cesarean delivery without labor at risk for developing immune disorders later in life? Am J Obstet Gynecol. 2013;208(4):243–6.

    Article  PubMed  Google Scholar 

  34. Duijts L, Ramadhani MK, Moll HA. Breastfeeding protects against infectious diseases during infancy in industrialized countries. A systematic review. Matern Child Nutr. 2009;5(3):199–210.

    Article  PubMed  Google Scholar 

  35. Ladomenou F, Moschandreas J, Kafatos A, Tselentis Y, Galanakis E. Protective effect of exclusive breastfeeding against infections during infancy: a prospective study. Arch Dis Child. 2010;95(12):1004–8.

    Article  PubMed  Google Scholar 

  36. Clark SL, Frye DR, Meyers JA, Belfort MA, Dildy GA, Kofford S, Englebright J, Perlin JA. Reduction in elective delivery at <39 weeks of gestation: comparative effectiveness of 3 approaches to change and the impact on neonatal intensive care admission and stillbirth. Am J Obstet Gynecol. 2010;203(5):449.e441–6.

  37. MacDorman MF, Reddy UM, Silver RM. Trends in stillbirth by gestational age in the United States, 2006–2012. Obstet Gynecol. 2015;126(6):1146–50.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Little SE, Zera CA, Clapp MA, Wilkins-Haug L, Robinson JN. A Multi-State Analysis of Early-Term Delivery Trends and the Association With Term Stillbirth. Obstet Gynecol. 2015;126(6):1138–45.

    Article  PubMed  Google Scholar 

  39. March of Dimes. Prematurity Campaign 10-year anniversary report. 2013. Available at:www.marchofdimes.com/materials/prematurity-campaign-progress-report-2012.pdf. Accessed July 6, 2014.

    Google Scholar 

  40. Chang HH, Larson J, Blencowe H, Spong CY, Howson CP, Cairns-Smith S, Lackritz EM, Lee SK, Mason E, Serazin AC, et al. Preventing preterm births: analysis of trends and potential reductions with interventions in 39 countries with very high human development index. Lancet. 2013;381(9862):223–34.

  41. Goldenberg RL, McClure EM, Bhattacharya A, Groat TD, Stahl PJ. Women’s perceptions regarding the safety of births at various gestational ages. Obstet Gynecol. 2009;114(6):1254–8.

    Article  PubMed  Google Scholar 

  42. Zhang LY, Todd AL, Khambalia A, Roberts CL. Women’s beliefs about the duration of pregnancy and the earliest gestational age to safely give birth. Aust N Z J Obstet Gynaecol. 2015;55(2):156–62.

    Article  PubMed  Google Scholar 

  43. Dursun P, Yanik FB, Zeyneloglu HB, Baser E, Kuscu E, Ayhan A. Why women request cesarean section without medical indication? J Matern Fetal Neonatal Med. 2011;24(9):1133–7.

    Article  PubMed  Google Scholar 

  44. Roberts CL, Bell JC, Ford JB, Morris JM. Monitoring the quality of maternity care: how well are labour and delivery events reported in population health data? Paediatr Perinat Epidemiol. 2009;23(2):144–52.

    Article  PubMed  Google Scholar 

  45. NSW Health Department: Validation Study: NSW Midwives Data Collection 1998. NSW Public Health Bull. 2000;9:97–9.

  46. Chantry CJ, Dewey KG, Peerson JM, Wagner EA, Nommsen-Rivers LA. In-hospital formula use increases early breastfeeding cessation among first-time mothers intending to exclusively breastfeed. J Pediatr. 2014;164(6):1339–45.

    Article  PubMed  PubMed Central  Google Scholar 

  47. Semenic S, Loiselle C, Gottlieb L. Predictors of the duration of exclusive breastfeeding among first-time mothers. Res Nurs Health. 2008;31(5):428–41.

    Article  PubMed  Google Scholar 

  48. Forster D, McLachlan H, Lumley J. Factors associated with breastfeeding at six months postpartum in a group of Australian women. Int Breastfeed J. 2006;1(1):18.

    Article  PubMed  PubMed Central  Google Scholar 

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Acknowledgements

We would like to acknowledge the NSW Ministry of Health for providing access to population health data and the NSW Centre for Health Record Linkage for linking the data sets. JPB was supported by an Australian Postgraduate Award Scholarship, Sydney University Merit Award and a Northern Clinical School Scholarship Award, CLR was supported by an Australian National Health and Medical Research Council Senior Research Fellowship (#APP1021025) and NN an Australian National Health and Medical Research Career Development Fellowship (#APP1067066).

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Correspondence to Jason P. Bentley.

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The author(s) declare that they have no competing interests.

Authors’ contributions

JPB and NN conceived the project and developed the idea in collaboration with JMS, JRB, JMM and CLR. All authors (JPB, JMS, JRB, JMM, CLR, NN) contributed to the study design, CLR and NN were responsible for data acquisition and JPB analysed the data with the support of JMS. All authors (JPB, JMS, JRB, JMM, CLR, NN) were involved in the interpretation of results. JPB and NN initially drafted the manuscript and all authors (JPB, JMS, JRB, JMM, CLR, NN) were involved in critical revision of the intellectual content. All authors (JPB, JMS, JRB, JMM, CLR, NN) approved the final version of the manuscript.

Additional files

Additional file 1:

“Imputation.pdf” summarises the imputation approach for formula-only feeding at discharge from birth care, and compares the associations for the study factors and all covariates between the imputation and complete case analysis. (DOC 92 kb)

Additional file 2:

“All adjusted associations.pdf” summarises the adjusted associations for the study factors and all covariates used in the adjustment for the main and additional study populations. (DOC 84 kb)

Additional file 3:

“Additional combined adjusted associations.pdf” summarises the combined associations for the study factors for all additionally investigated study populations. (DOC 443 kb)

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Bentley, J.P., Simpson, J.M., Bowen, J.R. et al. Gestational age, mode of birth and breastmilk feeding all influence acute early childhood gastroenteritis: a record-linkage cohort study. BMC Pediatr 16, 55 (2016). https://doi.org/10.1186/s12887-016-0591-0

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