Study design and setting
A cross-sectional survey was conducted from September to December 2021 in four Sri Lankan government hospitals. In Sri Lanka, 94% of births occur in government hospitals and they are the major maternity care service providers (DCS-Sri Lanka, 2017,2019). Stratified cluster random sampling was applied to select hospitals from which to draw the study sample. Government hospitals in Sri Lanka where women give birth (n= 385) were stratified into two groups. Stratum 1 were hospitals in the urban sector of Sri Lanka (n=54) and stratum 2 were hospitals in the rural sector (n=331). Hospitals with a minimum of 2200 births in 2018 (n=49) (DCS-Sri Lanka, 2019) were clustered from each stratum to increase sampling efficiency. This meant we could collect the most amount of data from women admitted to each hospital during the limited data collection period. Clusters of strata 1 and 2 included 41 and 8 hospitals respectively. Two hospitals were randomly selected from each cluster.
Participants
Women who (1) had live single or multiple births from 19th September to 20th December 2021 in selected hospitals, (2) did not have a neonatal death, (3) could understand and speak one of three languages (Sinhala/Tamil/English), and (4) were physically and mentally capable to consent to participate in this study, were approached and invited to participate at least 12 hours after birth. Women were eligible to participate until discharged from hospital.
Sample size
The required sample size for regression analysis was determined according to Green’s rule of thumb (Green, 2010) that N>50+8m is needed for multiple correlations and N> 104+m is needed for testing individual predictors, where ‘N’ is the required sample size, and ‘m’ is the number of independent variables (18 in our study). According to Green’s rule, the minimum number needed for testing multiple correlations and individual predictors were 195 [N>50+(8×18) =N>194] and 123 [N>104+18= N>122] respectively. Data collection feasibility was also considered. The principal researcher had 60 days available for data collection, approximately four hours permitted by the hospitals for data collection each day, and 30 to 40 planned with each participant. Approximately six women could be approached each day, with five women expected to participate based on a 90% estimated response rate (Wickramasinghe et al., 2019). Therefore, the research team aimed to approach a total of 360 women to achieve an expected sample of 300, providing sufficient power for planned statistical analyses.
Survey instrument
A structured electronic survey instrument including a questionnaire and data entry tool (Table S1) was used to collect self-reported data from postnatal women and clinical data from their medical records. Survey questions were selected from previously validated surveys (Table S1) and a review of previous research. Survey questions asked women’s socio-demographic details, and information about their pregnancy, labor and childbirth, and infant feeding practices.
Survey procedure
A health care worker who was either the nurse in-charge or one of the nursing officers of the postnatal wards of the selected hospitals assisted the principal researcher identify eligible women by providing their bed numbers. The health care worker also informed eligible women about the presence of the researcher in the postnatal ward, and that the researcher was independent from hospital staff. The researcher approached eligible women and invited to participate at their bedside. If women provided informed consent to participate, the researcher conducted a face-to-face interview and clinical data extraction. The researcher conducted the interview at each woman’s bedside and recorded participants’ responses on the survey. Clinical data regarding pregnancy, labor and childbirth were extracted from participants’ medical records and recorded in the survey. To assess sample representativeness, aggregate data for all women who had live babies in the selected hospitals from September to December 2021 were accessed from birth registers maintained in labor rooms of the selected hospitals.
Measures
Early initiation of breastfeeding was assessed as breastfeeding within one hour of birth. Participants were asked when they started feeding colostrum for the very first time after giving birth. Responses were recorded as: < 10 minutes after birth, 10-30 minutes after birth and 31-60 minutes after birth, later combined into “early initiation of breastfeeding”. More than 1 hour and not yet initiated were recoded as “no early initiation of breastfeeding”. Responses of “do not know/ do not remember” were excluded from analyses.
Independent variables were women’s socio-demographic and clinical characteristics. Socio-demographic factors collected via maternal self-report included age, area of residence, level of education, employment, annual household income, ethnicity, and relationship status. Maternal age and household income were collected continuously, and later categorised into six categories for age (“15-19 years”, “20-24 years”, “25-29 years”, “30-34 years”, and “35 years and older”) and four categories for income (“<100, 000”, “100, 000 – 500,000”, “501,000 – 1,000,000”, or “> 1,000,000” Sri Lankan Rupees). Clinical characteristics included pregnancy (antenatal clinic visits, parity, pregnancy complications) and childbirth (mode of birth, gestational age, baby’s birth weight, postpartum maternal complications, neonatal complications) factors. Self-reported data regarding antenatal clinic visits were transformed into dichotomous variables (“visited” / “not visited”). Dichotomous variables sourced from clinical data were derived for parity (“primipara” / “multiparous”), infant gestational age at birth (“<37 weeks”/ “≥37 weeks”), and infant birthweight (“< 2500 grams”/ “≥2500 grams”), consistent with standards commonly used to assess associations with early breastfeeding initiation. Standard Body Mass Index (BMI) categories for Asians were used to define pre-pregnancy BMI as “<18.5 kg/m2, “18.5-22.9 kg/m2”, “23-27.49 kg/m2”, and “≥27.5 kg/m2” (Senarath et al., 2012).
Dichotomous variables of “administered” / “not administered” were derived for assessing the administration of medications and “presented” / “not presented” were derived for pregnancy, birth and postpartum complications. Mode of birth was categorised into “unassisted vaginal birth”, “vaginal birth assisted with forceps”, vaginal birth assisted with vacuum”, “vaginal birth assisted with both forceps and vacuum”, “planned caesarean section” and “emergency caesarean section”.
Statistical Analysis
Data were analysed using SPSS for Windows version 28.0.1.0. Sample representativeness was determined by comparing participants’ characteristics with different populations for which comparable data was available: a) women who gave birth to a live baby in the selected hospitals from September to December 2021, b) live births that were registered in Sri Lanka in 2015, and c) live births reported in 2019. This approach enabled assessment of the generalisability of the study sample to birthing women of both the national population and our selected hospitals. Characteristics of participants were compared with populations using one-sample chi-square tests.
Multivariable logistic regression was used to identify independent significant predictors of early breastfeeding initiation. Socio-demographic characteristics and clinical measures related to pregnancy and childbirth were added to the model as independent variables. The association between early initiation of breastfeeding and every independent variable was assessed with univariate logistic regression, followed by multivariable modelling for all variables simultaneously using binary logistic regression with stepwise backward elimination to estimate odds ratios (OR) after adjustment for independent variables. Residuals and standard errors for multicollinearity were examined for independent variables. Variables that were significant at α < 0.05 were retained in the final model and results were expressed as crude and adjusted ORs of early initiation of breastfeeding, with 95% confidence intervals (CI).