Abstract
Background
Early initiation of breastfeeding after birth and exclusive breastfeeding for the first six months improves child survival, nutrition and health outcomes. However, only 42% of newborns worldwide are breastfed within the first hour of life. Small and sick newborns are at greater risk of not receiving breastmilk and often require additional support for feeding. This study compares breastfeeding practices in Rwandan neonatal care units (NCUs) before and after the implementation of a package of interventions aimed to improve breastfeeding.
Methods
This pre-post intervention study was conducted at two district hospital NCUs in rural Rwanda from October–December 2017 (pre-intervention) and September 2018–March 2019 (post-intervention). Only newborns admitted before their second day of life (DOL) were included. Data were extracted from patient charts for clinical and demographic characteristics, feeding, and patient outcomes. Exclusive breastfeeding at discharge was based on last recorded infant feeding on the day of discharge. Logistic regression analysis was used to evaluate factors associated with exclusive breastfeeding at discharge.
Results
Pre-intervention, 255 newborns were admitted in the NCUs and 793 were admitted in post-intervention. Exclusive breastfeeding on the day of birth (DOL0) increased from 5.4% (12/255) to 35.9% (249/793). At discharge, exclusive breastfeeding increased from 69.6% (149/214) to 87.0% (618/710). The mortality rate decreased from 16.1% (41/255) to 10.5% (83/793). Factors associated with greater odds of exclusive breastfeeding at discharge included admission during the post-intervention period (aOR 4.91; 95% CI 1.99, 12.11), and admission for infection (aOR 2.99; 95% CI 1.13, 7.93). Home deliveries (aOR 0.15; 95% CI 0.05, 0.47), preterm delivery (aOR 0.36; 95% CI 0.15, 0.87) and delayed first breastmilk feed (aOR 0.04 for DOL3 vs. DOL0; 95% CI 0.01, 0.35) reduced odds of exclusive breastfeeding at discharge.
Conclusions
Expansion and adoption of evidenced-based guidelines, using innovative approaches, aimed at the unique needs of small and sick newborns may help to improve earlier initiation of breastfeeding, decrease mortality, and improve exclusive breastfeeding on discharge from hospital among small and sick newborns. These interventions should be replicated in similar settings to determine their effectiveness.
Keywords: Neonatal nutrition; Small and sick newborns; Rwanda,; Exclusive breastfeeding,; Nurturing care; Baby-friendly
Background
Breastfeeding plays a paramount role in child survival, development and maternal health [1]. Early initiation of breastfeeding within one hour after birth and exclusive breastfeeding for the first six months is recommended by the World Health Organization (WHO) [2]. Immediate and early initiation of breastfeeding after birth is associated with better neonatal outcomes, in low- and middle-income countries (LMICs), such as reduction of neonatal deaths, length of hospital stay for sick infants and neonatal infections [3, 4]. A meta-analysis of LMIC settings, showed that non-breastfed infants under six months of age have a 14 times higher risk of death, and partially breastfed infants have a 4.8-fold higher risk of death compared to predominantly breastfed infants [5].
Even though the majority of deliveries globally are attended by skilled healthcare providers, only 42% of newborns are breastfed within the first hour of life worldwide [6]. Small and sick newborns requiring inpatient care after birth face unique challenges since the neonatal care unit environment is not always conducive for initiation of early and exclusive breastfeeding, including in settings such as Denmark, when an infant requires mechanical ventilation or is separated from the mother [7]. In addition, small and sick newborns may experience difficulties breastfeeding, or are too immature or unstable to breastfeed immediately after birth, so mothers require specialized support to establish and maintain their milk supply [8, 9]. Despite the strong recommendation from WHO that maternity and newborn services have trained and competent staff who can provide successful breastfeeding support to lactating mothers [10], they have noted that early breastfeeding is compromised by inappropriate procedures, such as infant-mother separation, performed by healthcare providers and outdated policies [6].
Many interventions exist at community and facility levels worldwide to promote early and exclusive breastfeeding. UNICEF and WHO launched the Baby-Friendly Hospital Initiative (BFHI) in 2009 to integrate breastfeeding with maternal and newborn care in hospitals. Through this multi-level approach, hospitals must implement the “Ten Steps to Successful Breastfeeding” to attain BFHI status, including having a breastfeeding policy, allowing rooming-in, and providing adequate training to staff [10, 11]. Specific recommendations for expanding BFHI to include the unique needs of small and sick newborns have also been developed [9, 12]. Additionally, utilizing lactation consultants for breastfeeding support and lactation education has shown to increase rates of initiation, duration of any breastfeeding and exclusive breastfeeding compared to usual practices in a systematic review of high-income countries [13]. Peer counseling approaches have also demonstrated improved early and continuous exclusive breastfeeding in an urban United States hospital setting [14].
In Rwanda, 81% of newborns are breastfed within one hour of life and 87% are exclusively breastfed up to six months [15], however little is known about rates among small and sick newborns. Data from a neonatal care unit (NCU) in rural Rwanda found a large proportion of small and sick newborns had breastfeeding difficulties after discharge leading to use of infant formula and poor growth [16]. To address this, Partners In Health/Inshuti Mu Buzima (PIH/IMB) in collaboration with the Ministry of Health, implemented interventions for breastfeeding support for newborns and infants with feeding difficulties in NCUs. This included training of healthcare providers, breastfeeding counselling for mothers and health system strengthening to promote early and exclusive breastfeeding. This study aims to compare breastfeeding rates of newborns admitted to district hospital neonatal special care units before and after the implementation of a package of interventions aimed to improve breastfeeding practices.
Methods
Study setting
We conducted this study in the Rwinkwavu District Hospital (RDH) and Kirehe District Hospital (KDH) NCUs. RDH and KDH are Rwandan Ministry of Health public hospitals located in Kayonza and Kirehe Districts in the eastern province of Rwanda. Both RDH and KDH have been supported by PIH/IMB, an international non-governmental organization, since 2005 and 2007, respectively. RDH supervises eight health centers in its catchment area with a population of 215,555 and KDH supervises 16 health centers in its catchment area with a population of 384,776 [17], in addition to two health centers and over 60,000 people in a refugee camp in the catchment area [18]. The NCUs provide care for small and sick newborns and are equipped with incubators, radiant warmers, syringe pumps, phototherapy, oxygen and continuous positive airway pressure machines for the management of common neonatal conditions. They are staffed by nurses, with an average nurse to patient ratio of 1 to 8.5 [19], and general practitioners, with mentorship by a pediatrician and midwife. Typically, there is one general practitioner who conducts rounds on patients on the neonatal unit each day. The education level of the nurses vary, and include, either a general nurse with a two-year diploma (A1 level) or a general nurse with a Bachelor’s degree (A0 level).
Intervention
Several inputs were introduced into the hospital neonatal care units to promote exclusive breastfeeding, including porridge for mothers and water filters to provide a high calorie, high protein supplement and ensure adequate hydration; pillows for more comfortable breastfeeding positioning; screens for mothers to breastfeed or express breastmilk privately; refrigerator and materials for storage of expressed breastmilk, and educational posters promoting exclusive breastfeeding and Kangaroo Mother Care (KMC). In addition to these inputs, a training was conducted in February 2018 called Working with Infants with Feeding Difficulties delivered by two Speech and Language Therapists who are experts in infant feeding. A description of that training package and a case study from its implementation in Rwanda has been described elsewhere [20]. As a result of the training and in an effort to ensure sustainability of the skills learned during the training, each hospital hired two Expert Mothers to serve as peer counsellors to support mothers in assessing breastfeeding readiness, improve positioning and attachment, and create a breastfeeding-friendly, caring environment for mothers with a focus on one-to-one as well as group counselling. The Expert Mothers were chosen based on criteria including previously having an infant in the neonatal unit and commitment to sharing her experience with other mothers. The Expert Mothers are trained on the Working with Infants with Feeding Difficulties package, provided with a job aid and tablet loaded with Global Health Media videos for counselling of mothers.
Study design and population
We conducted a pre-post study. We included all newborns admitted to the RDH and KDH neonatology units in two periods including pre-intervention from October 2017 to December 2017 and post-intervention from September 2018 to March 2019 who were admitted before their second day of life. The manuscript was prepared following the Standards for Quality Improvement Reporting Excellence (SQUIRE 2.0) Guidelines [21].
Data collection
Data from nationally standardized neonatology patient charts is routinely collected by trained data collectors on a structured paper, two-page form and then entered in a Microsoft Access database. Data completeness and accuracy were checked through routine data quality assessment activities that are conducted by monitoring and evaluation staff. Types of data collected about the infant include the infant’s reason for admission, day of life on admission, relevant perinatal history, length of stay, and discharge outcomes. Data collected about the mother includes maternal history, such as age, gravida, and para, and type of delivery. A very detailed feeding and weight gain history is recorded on the paper form, including the nutrition method through which the infant was receiving nutritional support (via the breast, via a naso-gastric tube, via a cup, or nil per os [NPO, nothing by mouth].) and the nutrition type (breastmilk only, breastmilk and artificial milk, artificial milk only, or intravenous fluids).
Definition of variables
Our primary outcome was exclusive intake of breast milk at the time of discharge among infants discharged alive. Data on the infant’s feeding history which was last recorded in the patient chart on the day of discharge was used to assess exclusive breastfeeding at the time of discharge. Day of life 0 (DOL0) referred to the child’s day of birth. Newborns exclusively fed breastmilk were defined as the feeding type recorded in the patient’s chart as ‘only breast milk’, regardless of the method of feeding (i.e., via breast, via naso-gastric tube, etc.). Fed on breast was defined as the method of feeding recorded in the patient’s chart as ‘only on the mother’s breast’ (i.e., not via cup, not via naso-gastric tube, etc.). Low birthweight (LBW) was defined as any birth below 2,500 g and premature births are births before 37 weeks gestation. Home delivery was defined as a birth that takes place in the community outside of the care of a skilled healthcare provider, regardless of whether the home delivery was planned delivery or a precipitous delivery.
Data analysis
We described sociodemographic characteristics of infants and their mothers, and clinical and feeding characteristics of infants using frequencies and percentages for categorical data and median and interquartile ranges for continuous data. We conducted bivariate analysis using Chi-square test to compare the pre- and post-intervention periods for all categorical sociodemographic, clinical and feeding characteristics described for infants with data recorded unless a cell contained a value of less than five, in which case Fisher’s exact test was used. Wilcoxon Ranksum test was used for bivariate analysis of continuous variables for infants with data recorded. We assessed change in mortality from pre- to post-intervention using multivariable logistic regression controlling for the child’s condition, birthweight in grams, and child’s sex. Then, we used multivariable logistic regression models to identify predictors associated with the outcome ‘exclusive breastfeeding on discharge’, built using backward stepwise procedures for all variables significant at α = 0.20 in bivariate analyses. All factors significant at the α = 0.05 significance level were retained in the final model. The data were analyzed using Stata v.15.1 (Stata Corp, College Station, TX, USA).
Ethics
The study received ethical approval from the Rwanda National Ethics Committee (No. 105/RNEC/20). Data was captured through review of routine records and so additional informed consent specific to this study was not required.
Results
In total, 255 newborns were admitted in the neonatology care units during the pre-intervention and 793 were admitted in the post-intervention periods (Table 1). There were no significant differences in admissions for prematurity at pre-intervention compared to post-intervention (40.0% [n = 96/240] vs. 40.6% [n = 309/762], p = 0.88), maternal age (50.0% [n = 12/240] age 25–34 years vs. 43.7% [n = 332/759], p = 0.24) maternal gravidity (27.1% [n = 66/244] primigravida vs 31.5% [n = 238/755], p = 0.40), and age on admission (83.1% [n = 212/255] admitted on DOL0 vs. 85.4% [n = 677/793, p = 0.39). Compared to the pre-intervention period, infants were also more likely than in the post-intervention period to be delivered by caesarean section (31.5% [n = 79/251] vs. 41.1% [n = 315/767], p = 0.01) and weigh more than 1,500 grams (86.6% [n = 220/254] vs. 91.9% [n = 722/786], p = 0.02).
Table 1.
Variable | Pre-intervention (N = 255) | Post-intervention (N = 793) | Bivariate analysis* | ||||
---|---|---|---|---|---|---|---|
n | % | n | % | p-value | Degrees of freedom | Test statistic | |
Hospital of admission | 0.003 | 1 | 8.98 | ||||
Kirehe | 141 | 55.3 | 521 | 65.8 | |||
Rwinkwavu | 114 | 44.7 | 272 | 34.3 | |||
Place of child's birth | (n = 253) | (n = 779) | 0.02 | 3 | 9.56 | ||
Hospital | 165 | 65.2 | 531 | 68.2 | |||
Health Center | 70 | 27.7 | 158 | 20.3 | |||
Home | 16 | 6.3 | 69 | 8.9 | |||
Other | 2 | 0.8 | 21 | 2.7 | |||
Type of delivery | (n = 251) | (n = 767) | 0.01 | 1 | 7.34 | ||
Vaginal | 172 | 68.5 | 452 | 58.9 | |||
Caesarean section | 79 | 31.5 | 315 | 41.1 | |||
Sex of child | (n = 210) | (n = 781) | < 0.001 | 1 | 15.73 | ||
Male | 83 | 39.5 | 429 | 54.9 | |||
Female | 127 | 60.5 | 352 | 45.1 | |||
Birthweight category | (n = 254) | (n = 786) | 0.02 | 3 | 9.89 | ||
Extremely low birthweight, < 1000 g | 13 | 5.1 | 16 | 2.0 | |||
Very low birthweight, < 1500 g | 21 | 8.3 | 48 | 6.1 | |||
Low birthweight, < 2500 g | 94 | 37.0 | 342 | 43.5 | |||
Normal birthweight, ≥ 2500 g | 126 | 49.6 | 380 | 48.4 | |||
Prematurity category recorded in hospital register | (n = 240) | (n = 762) | 0.88 | 1 | 0.02 | ||
Term | 144 | 60.0 | 453 | 59.5 | |||
Preterm | 96 | 40.0 | 309 | 40.6 | |||
Gestational age category (if gestational age in weeks reported) | (n = 225) | (n = 683) | 0.05 | 3 | 8.02 | ||
Extremely preterm < 28 weeks | 9 | 4.0 | 12 | 1.8 | |||
Very preterm 28–31 weeks | 21 | 9.3 | 39 | 5.7 | |||
Moderate/late 32–36 weeks | 51 | 22.7 | 179 | 26.2 | |||
Term 37 + weeks | 144 | 64.0 | 453 | 66.3 | |||
Mother's Age | (n = 240) | (n = 759) | 0.24 | 3 | 4.20 | ||
< 20 years | 19 | 7.9 | 79 | 10.4 | |||
20–24 years | 52 | 21.7 | 198 | 26.1 | |||
25–34 years | 120 | 50.0 | 332 | 43.7 | |||
35 + years | 49 | 20.4 | 150 | 19.8 | |||
Gravidity (# pregnancies) of mother | (n = 244) | (n = 755) | 0.40 | 2 | 1.85 | ||
1 pregnancy | 66 | 27.1 | 238 | 31.5 | |||
2–4 pregnancies | 121 | 49.6 | 358 | 47.4 | |||
5 + pregnancies (grand multigravida) | 57 | 23.4 | 159 | 21.1 | |||
Parity (# viable deliveries) of mother | (n = 244) | (n = 757) | 0.01 | 2 | 9.73 | ||
1 delivery | 79 | 32.4 | 330 | 43.6 | |||
2–4 deliveries | 127 | 52.1 | 323 | 42.7 | |||
5 + deliveries (grand multiparous) | 38 | 15.6 | 104 | 13.7 | |||
DOLa on admission | 0.39 | 1 | 0.75 | ||||
DOL 0 | 212 | 83.1 | 677 | 85.4 | |||
DOL 1 | 43 | 16.9 | 116 | 14.6 | |||
Diagnosis (not mutually exclusive) | |||||||
Preterm, or gestational age < 37 weeks | 102 | 40.0 | 308 | 38.8 | 0.74 | 1 | 0.11 |
LBWb, or birthweight < 2500 g | 123 | 48.2 | 406 | 51.2 | 0.41 | 1 | 0.68 |
Infection | 141 | 55.3 | 328 | 41.4 | < 0.001 | 1 | 15.15 |
HIEc/asphyxia | 29 | 11.4 | 70 | 8.8 | 0.23 | 1 | 1.46 |
Other | 23 | 9.0 | 145 | 18.3 | < 0.001 | 1 | 12.31 |
aDay of Life
bLow Birthweight
cHypoxic Ischemic Encephalopathy
The percentage of infants who were fed on the breast on DOL0 increased from 5.8% (n = 13/223) to 35.6% (n = 247/694), (p < 0.001) and exclusively breastfed on DOL0 increased from 5.4% (n = 12/255) to 35.9% (n = 249/793) (p < 0.001) (Table 2). On DOL1, feeding on the breast increased from 30.5% (n = 75/246) to 68.6% (n = 532/776) (p < 0.001) and exclusive feeding on breastmilk increased from 37.4% (n = 92/255) to 70.2% (n = 545/793) (p < 0.001). For newborns discharged alive, the proportion fed on the breast increased from 59.8% (n = 128/255) to 84.7% (n = 601/793) (p < 0.001) and the proportion exclusively feeding on breastmilk increased from 69.6% (n = 149/255) to 87.0% (n = 618/793) (p < 0.001). Introduction of first breast milk feeding on DOL0 increased from 7.1% (n = 18/255) pre-intervention to 31.9% (n = 253/793) in post-intervention (p < 0.001).
Table 2.
Variable | Pre-intervention (n = 255) | Post-intervention (n = 793) | Bivariate analysis | ||||
---|---|---|---|---|---|---|---|
n | % | n | % | p-value* | Degrees of freedom | Test statistic | |
Newborn fed on breast day of life (DOLa) 0 | (n = 223) | (n = 694) | < 0.001 | 1 | 61.64 | ||
Yes | 13 | 5.8 | 247 | 35.6 | |||
No | 158 | 70.9 | 381 | 54.9 | |||
Not documented | 52 | 23.3 | 66 | 9.5 | |||
Newborn exclusively fed breastmilk on DOL 0 | < 0.001 | 1 | 65.07 | ||||
Yes | 12 | 5.4 | 249 | 35.9 | |||
No | 159 | 71.3 | 379 | 54.6 | |||
Not documented | 52 | 23.3 | 66 | 9.5 | |||
Newborn fed on breast on DOL 1 | (n = 246) | (n = 776) | < 0.001 | 1 | 118.63 | ||
Yes | 75 | 30.5 | 532 | 68.6 | |||
No | 156 | 63.4 | 205 | 26.4 | |||
Not documented | 15 | 6.1 | 39 | 5.0 | |||
Newborn exclusively fed breastmilk on DOL 1 | < 0.001 | 1 | 89.32 | ||||
Yes | 92 | 37.4 | 545 | 70.2 | |||
No | 137 | 55.7 | 191 | 24.6 | |||
Not documented | 17 | 6.9 | 40 | 5.2 | |||
Newborn fed on breast on DOL 2 | (n = 238) | (n = 736) | < 0.001 | 1 | 91.11 | ||
Yes | 107 | 45.0 | 568 | 77.2 | |||
No | 114 | 47.9 | 133 | 18.1 | |||
Not documented | 17 | 7.1 | 35 | 4.8 | |||
Newborn exclusively fed breastmilk on DOL 2 | < 0.001 | 1 | 64.65 | ||||
Yes | 135 | 56.7 | 600 | 81.5 | |||
No | 87 | 36.6 | 100 | 13.6 | |||
Not documented | 16 | 6.7 | 36 | 4.9 | |||
Newborn fed on breast DOL 7 | (n = 195) | (n = 441) | < 0.001 | 1 | 33.97 | ||
Yes | 106 | 54.4 | 331 | 75.1 | |||
No | 68 | 34.9 | 66 | 15.0 | |||
Not documented | 21 | 10.8 | 44 | 10.0 | |||
Newborn exclusively fed breastmilk on DOL 7 | < 0.001 | 1 | 25.62 | ||||
Yes | 124 | 63.6 | 351 | 79.6 | |||
No | 48 | 24.6 | 43 | 9.8 | |||
Not documented | 23 | 11.8 | 47 | 10.7 | |||
Newborn fed on breast on discharge day if discharged alive | < 0.001 | 1 | 50.81 | ||||
Yes | 128 | 59.8 | 601 | 84.7 | |||
No | 41 | 19.2 | 38 | 5.4 | |||
Not documented | 45 | 21.0 | 71 | 10.0 | |||
Newborn fed breastmilk on discharge day if discharged alive | < 0.001 | 1 | 31.42 | ||||
Yes | 149 | 69.6 | 618 | 87.0 | |||
No | 19 | 8.9 | 12 | 1.7 | |||
Not documented | 46 | 21.5 | 80 | 11.3 | |||
DOL of first documented breastmilk feed | < 0.001 | 3 | 91.01 | ||||
DOL0 | 18 | 7.1 | 253 | 31.9 | |||
DOL1 | 99 | 38.8 | 330 | 41.6 | |||
DOL2 | 66 | 25.9 | 105 | 13.2 | |||
DOL3 or later | 72 | 28.2 | 105 | 13.2 |
aDay of Life
*P-value compares only non-missing data values; "Not documented" is not included in the chi-square test
The median length of hospital stay among infants admitted to the neonatal unit was reduced from eight days in the pre- to seven days in the post-intervention periods (p < 0.001) (Tables 3 and 4). The overall mortality rate for all newborns admitted decreased from 16.1% (n = 41/255) in pre- to 10.5% (n = 83/793) in post-intervention periods (p = 0.02). Mortality rate for LBW newborns reduced from the pre-intervention to post-intervention period (23.6% [n = 29/255] vs. 15.0% [n = 61/793], p = 0.03), but remained similar among babies diagnosed with other conditions. Reduced odds of mortality post-intervention were significant when controlling for diagnosis, birthweight, and child’s sex (adjusted odds ratio [aOR] 0.57; 95% confidence interval [CI] 0.34, 0.96).
Table 3.
Variable |
Pre-intervention (n = 255) |
Post-intervention (n = 793) |
Bivariate analysis* | ||||
---|---|---|---|---|---|---|---|
n | % | n | % | p-value | Degrees of freedom | Test statistic | |
LOSa, median [IQRb] | 8 | [6, 8] | 7 | [3, 9] | < 0.001 | NA | z = 4.84 |
Mortality | |||||||
Yes | 41 | 16.1 | 83 | 10.5 | 0.02 | 1 | 5.83 |
No | 214 | 83.9 | 710 | 89.5 | |||
Mortality by condition | |||||||
Preterm | 0.13 | 1 | 2.31 | ||||
Died | 26 | 25.5 | 57 | 18.5 | |||
Discharged alive | 76 | 74.5 | 251 | 81.5 | |||
LBWc | 0.03 | 1 | 4.89 | ||||
Died | 29 | 23.6 | 61 | 15.0 | |||
Discharged alive | 94 | 76.4 | 345 | 85.0 | |||
Hypoxic ischemic encephalopathy (HIEd) | 0.65 | 1 | 0.20 | ||||
Died | 7 | 24.1 | 20 | 28.6 | |||
Discharged alive | 22 | 75.9 | 50 | 71.4 | |||
Neonatal infection | 0.28 | 1 | 1.15 | ||||
Died | 15 | 10.6 | 25 | 7.6 | |||
Discharged alive | 126 | 89.4 | 303 | 92.4 | |||
Mortality by birthweight | |||||||
Extremely low birthweight, < 1000 g | 0.12 | 1 | 2.43 | ||||
Died | 12 | 92.3 | 11 | 68.8 | |||
Discharged alive | 1 | 7.7 | 5 | 31.3 | |||
Very low birthweight, < 1500 g | 0.05 | 1 | 3.85 | ||||
Died | 6 | 28.6 | 26 | 54.2 | |||
Discharged alive | 15 | 71.4 | 22 | 45.8 | |||
LBW, < 2500 g | 0.11 | 1 | 2.54 | ||||
Died | 11 | 11.7 | 23 | 6.7 | |||
Discharged alive | 83 | 88.3 | 319 | 93.3 | |||
Normal birthweight ≥ 2500 g | 0.20 | 1 | 1.64 | ||||
Died | 11 | 8.7 | 21 | 5.5 | |||
Discharged alive | 115 | 91.3 | 359 | 94.5 |
aLength of Stay
bInterquartile Range
cLow Birthweightd Hypoxic Ischemic Encephalopathy
eExtremely Low Birthweight
fVery Low Birthweight
*A z value was reported for the Wilcoxon rank sum test, but no degree of freedom
NA, not applicable
Table 4.
Study time period | ORa | Standard error | z | [95% CI] |
---|---|---|---|---|
Pre-intervention | ref | |||
Post-intervention | 0.57 | 0.15 | -2.10 | [0.34, 0.96] |
ref, reference category
aOdds ratio, adjusted for conditions (preterm, HIE, infections), birthweight, and child’s sex
In the final model (Table 5), there was a significant increase in exclusive feeding of breastmilk at discharge if admitted in the post-intervention period (aOR 4.91; 95% CI 1.99, 12.11). Factors associated with increased odds of exclusive breastfeeding at discharge included diagnosis of infection or infection risk (aOR 2.99; 95% CI 1.13, 7.93). Factors associated with reduced odds of exclusive breastfeeding at discharge included home birth (aOR 0.15; 95% CI 0.05, 0.47), prematurity (aOR 0.36; 95% CI 0.15, 0.87), and later timing of first breastmilk feed (DOL2 aOR 0.11; 95% CI 0.01, 0.995; DOL3 or later aOR 0.04; 95% CI 0.005, 0.35).
Table 5.
Variable | Model 1 (Full) | Model 2 (Reduced) | ||||||
---|---|---|---|---|---|---|---|---|
Adjusted odds ratio (aOR) | Standard error | z | 95% confidence interval (CI) | Adjusted odds ratio (aOR) | Standard error | z | 95% confidence interval (CI) | |
Study time period | ||||||||
Pre-intervention | ref | ref | ||||||
Post-intervention | 3.53 | 2.00 | 2.24 | 1.17, 10.72 | 4.91 | 2.26 | 3.46 | 1.99, 12.11 |
Hospital of admission | ||||||||
Kirehe | ref | |||||||
Rwinkwavu | 0.40 | 0.21 | -1.75 | 0.14, 1.12 | ||||
Place of child's birth | ||||||||
Hospital | ref | ref | ||||||
Health center | 0.40 | 0.30 | -1.23 | 0.09, 1.73 | 0.44 | 0.22 | -1.68 | 0.17, 1.15 |
Home | 0.22 | 0.19 | -1.79 | 0.04, 1.16 | 0.15 | 0.09 | -3.25 | 0.05, 0.47 |
Type of delivery | ||||||||
Vaginal | ref | |||||||
Caesarean-section | 0.83 | 0.64 | -0.23 | 0.19, 3.77 | ||||
Sex of child | ||||||||
Male | ref | |||||||
Female | 0.63 | 0.34 | -0.84 | 0.22, 1.83 | ||||
Birthweight category | ||||||||
Extremely low birthweight, < 1000 g | ref | |||||||
Very low birthweight, < 1500 g | 1.76 | 3.11 | 0.32 | 0.06, 56.25 | ||||
LBWa, < 2500 g | 3.46 | 5.61 | 0.76 | 0.14, 83.08 | ||||
Normal birthweight ≥ 2500 g | 1.60 | 2.85 | 0.26 | 0.05, 52.78 | ||||
Prematurity category recorded in hospital register | ||||||||
Term | ref | ref | ||||||
Preterm | 0.31 | 0.23 | -1.57 | 0.07, 1.34 | 0.36 | 0.17 | -2.22 | 0.15, 0.87 |
Mother's age | ||||||||
< 20 years | ref | |||||||
20–24 years | 0.89 | 1.15 | -0.09 | 0.07, 11.24 | ||||
25–34 years | 0.45 | 0.60 | -0.60 | 0.03, 6.06 | ||||
35 + years | 0.58 | 0.84 | -0.38 | 0.03, 9.87 | ||||
Parity (# viable deliveries) of mother | ||||||||
1 delivery | ref | |||||||
2–4 deliveries | 0.76 | 0.56 | -0.38 | 0.18, 3.21 | ||||
5 + deliveries (grand multiparous) | 0.59 | 0.55 | -0.56 | 0.09, 3.71 | ||||
Diagnosed with infection or infection risk | ||||||||
No | ref | ref | ||||||
Yes | 3.09 | 1.82 | 1.91 | 0.97, 9.83 | 2.99 | 1.49 | 2.21 | 1.13, 7.93 |
Diagnosed with HIEb/asphyxia | ||||||||
No | ref | |||||||
Yes | 0.79 | 0.75 | -0.25 | 0.12, 5.09 | ||||
Day of life (DOLc) of first breastmilk feed | ||||||||
DOL0 | ref | ref | ||||||
DOL1 | 0.24 | 0.26 | -1.32 | 0.03, 2.03 | 0.24 | 0.26 | -1.32 | 0.03, 2.00 |
DOL2 | 0.12 | 0.14 | -1.81 | 0.01, 1.19 | 0.11 | 0.13 | -1.96 | 0.01, 0.995 |
DOL3 or later | 0.05 | 0.06 | -2.55 | 0.01, 0.51 | 0.04 | 0.04 | -2.92 | 0.005, 0.35 |
The variance inflation factor (VIF) for collinearity diagnosis among predictor variables in Model 1, ranged between 1.09 and 1.84
VIF for Model 2, ranged between 1.01 and 1.12
ref reference category
a Low Birthweight
b Hypoxic Ischemic Encephalopathy
c Day of Life
Discussion
Our study showed that a multi-level intervention, aimed at improving rates of exclusive breastfeeding on a hospital neonatology unit in rural Rwanda, increased early and exclusive breastmilk feeding, and was also associated with a reduced length of stay and decreased mortality among small and sick newborns. These strategies have potential for expansion to other similar contexts, and may improve hospital neonatal outcomes and ensure small and sick newborns will benefit from the well-known long-term benefits of breastfeeding [1].
We found that from the pre- to post-intervention period, significantly more infants were fed on the breast and were exclusively fed breastmilk. We also observed earlier initiation of breastfeeding in the post-intervention and this earlier initiation increased the odds that an infant was discharged exclusively feeding on breastmilk. This is consistent with other literature as it is well known that if milk removal does not occur either by infant suckling or expression by hand or pump, milk secretion will start to decline around day three postpartum [22, 23]. A study from the United States comparing milk expression within one hour after delivery to within 1–6 h after delivery showed that the earlier expression group had earlier lactogenesis stage II (transition from colostrum to copious breast milk production) and resulted in higher milk volume [24]. Another study from the United States showed that milk volume on postpartum day four is predictive of having an adequate milk supply at six weeks [25]. These studies demonstrate the critical need for early expression of breast milk after delivery, whether the infant is able to breastfeed on the breast or if the mother expresses breastmilk and the infant receives breastmilk through other enteral feeding routes (i.e., cup, nasogastric tube).
Mortality among newborns decreased from the pre- to post-intervention period, particularly among infants born with a low birthweight. The association between decreased mortality and exclusive breastfeeding among infants in all settings has been well established in the literature and is often promoted as strong support for initiation of early and exclusive breastfeeding [1, 3–6, 26].
Overall length of hospital stay showed a significant reduction from the pre- to post-intervention period. While hospital neonatology units are meant to be an environment for infants to improve from various illnesses or conditions, a study from a United States hospital has shown that long length of stay in hospitals also increases an infant’s chance of contracting hospital acquired infections [27]. Therefore, the ability to reduce the length of stay for newborns may have an impact on the overall morbidity of the infant. While we did not measure morbidity in this study, early initiation of breastfeeding has been shown to reduce morbidity in newborns in LMIC settings [3], which likely has a positive impact on the total length of hospitalization. Studies from the United States and New Zealand have shown that reducing the time families, particularly mothers, spend in hospitals can also have a significant impact on the mother’s stress, and the family’s economic situation [28, 29]. Reduced length of stay was likely a secondary outcome of improved breastfeeding rates in the post-intervention period. The overall larger number of admissions with a birthweight greater than 1,500 g and gestational age over 32 weeks in the post-intervention period may have also contributed to lower mortality and shorter length of stay.
We found that the location of where the infant is born was associated with whether they are discharged from the hospital with exclusive breastfeeding or not. Infants born at health centers or in the home (including both planned home deliveries and precipitous deliveries) were less likely to be discharged with exclusive breastfeeding, compared to those born in the hospital which has also been seen in other studies of sub-Saharan Africa and LMIC settings [30, 31]. There may be many reasons for this. Infants born at home need to first be transferred to the health center, and subsequently to the hospital which may delay the introduction of breastmilk for those infants, and subsequently impact whether the infant is discharged exclusively breastfeeding. The clinical staff at health centers may also be less experienced in caring for high-risk newborns, and may not follow essential newborn care practices and delay introduction of breastmilk since the infant needs to be clinically stabilized and then transferred to the hospital.
Infants born preterm were less likely to be discharged exclusively breastfeeding compared to infants born at term. Infants born preterm have unique feeding needs that require specialized interventions and management, and a study from Australia has demonstrated similar findings of reduced exclusive breastfeeding rates even among moderate to late preterm newborns compared to term newborns [32]. Similarly, infants admitted for infection risk or neonatal infection in our study had much higher odds of exclusive breastfeeding. These findings are not surprising, as these infants are often term and feed easily. But notably, even when considering all of these factors in multivariate analysis the admission during the post-intervention period was the strongest predictor of exclusive breastfeeding at the time of discharge with nearly double the odds of exclusive breastfeeding compared to the pre-intervention period. Other factors in the neonatal care unit environment may also interfere with early and exclusive breastfeeding, including delayed initiation of KMC, or skin-to-skin contact, especially for sick newborns as seen in high- and middle-income country setting [33]. We were unable to measure timing or duration of KMC but this is an area that warrants further attention to reduce breastfeeding barriers.
Our study has some limitations. First, we used routinely collected data for the study, which results in some missing data and reliance on clinician skills in completion of medical files. In addition, precise measurement of gestational age is a challenge in Rwanda like in other low- and middle-income countries where availability of ultrasound dating is limited. Due to the use of routine data, it was not possible to reliably discriminate between newborns with infection or those with risk of infection and so we included all of these newborns in our sample. We also had a small sample size of patients born with HIE and those born with extremely low birthweight, which prevented measurement of the impact of interventions on these subsets. In addition, our pre-post design without a comparison group in only two hospitals does not allow us to determine effectiveness of the intervention as changes over time could be influenced by other factors and may not be generalizable to other hospitals. Another potential limitation of this study is that the two study periods, pre-intervention from October 2017 to December 2017 and post-intervention from September 2018 to March 2019, were not exactly aligned which may have led to differences in characteristics among the study populations, including the nutritional status of the mother in both the prenatal and postpartum periods. We also had a small proportion of cases of home births (6.3% in the pre-intervention and 8.9% in the post-intervention group). While most deliveries in Rwanda take place in a health facility (greater than 90%) [15], we do not know whether the home births in our study were planned deliveries or precipitous deliveries, which may also have implications for the prenatal care that was received, as well as other factors.
Conclusions
A multi-level breastfeeding intervention was feasible to implement in rural Rwandan hospitals and was associated with improvements in earlier initiation of breastmilk feeding, exclusive breastfeeding on discharge, reduced length of stay, and decreased mortality among infants admitted to the hospital neonatal care units. Adoption of evidenced-based guidelines such as the Baby Friendly Hospital Initiative aimed at the unique needs of small and sick newborns and innovative interventions should be expanded and adapted in similar settings to improve outcomes for these infants.
Acknowledgements
We would like to acknowledge the contributions of the neonatal unit nurses and the Expert Mothers for their commitment to the care of small and sick newborns. The manuscript was developed as part of a research-capacity building training in maternal and child health research at Partners In Health/Inshuti Mu Buzima led by Alphonse Nshimyiryo, Catherine M. Kirk, and Kathryn Beck and based on the Intermediate Operational Research Training developed by Bethany Hedt-Gauthier at Harvard Medical School
Abbreviations
- BFHI
Baby-Friendly Hospital Initiative
- DOL
Day of life
- HIE
Hypoxic ischemic encephalopathy
- LBW
Low birth weight
- LMIC
Low- and middle-income countries
- KMC
Kangaroo Mother Care
- KDH
Kirehe District Hospital
- NCU
Neonatal Care Unit
- PIH/IMB
Partners In Health/Inshuti Mu Buzima
- RDH
Rwinkwavu District Hospital
Authors' contributions
SG, AM, and FB led the study design, literature search, data cleaning and analysis, results interpretation, and writing manuscript. HH, CMK, and KB provided input in the study design, literature search, data cleaning and analysis, results interpretation, and critically reviewed the writing manuscript. CPDS, MA, HDS, AN, MLM, EK, and TA contributed to the interpretation of results and review of final manuscript. All authors reviewed and approved the final manuscript and had access to the data.
Funding
This study was funded by the Primates World Relief and Development Fund and Global Affairs Canada, who provided the funding for the interventions and evaluations. MAITS provided funding for the Infants with Feeding Difficulties trainers. Primates World Relief and Development Fund,Global Affairs Canada,MAITS
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Declarations
Ethics approval and consent to participate
This study was approved by the Rwanda National Ethics Committee (No. 105/RNEC/20). Data was captured through review of routine records and so informed consent was not required.
Consent for publication.
Not applicable.
Competing interests
The authors declare that they have no competing interests.
Footnotes
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.