| Literature DB >> 31022227 |
Chin Ang Ng1, Jacqueline J Ho2, Zcho Huey Lee1.
Abstract
BACKGROUND: The benefits of six months exclusive breastfeeding are well established for both mother and infant. One of the 10 steps of the Baby Friendly Hospital Initiative is rooming-in (mother and baby together in the same room throughout hospitalisation). A Cochrane review found only one randomised controlled trial (RCT) examining the effects of continuous rooming-in versus nursery care on breastfeeding duration, and concluded there was insufficient evidence to support or refute either practice. We aimed to examine the effect of continuous or intermittent rooming-in on breastfeeding duration. METHODS ANDEntities:
Mesh:
Year: 2019 PMID: 31022227 PMCID: PMC6483355 DOI: 10.1371/journal.pone.0215869
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 1PRISMA flow chart of the included the studies.
Characteristic of included studies.
| Author | Study design | Setting/ study period/ Sample size | Study population, inclusion criteria | Rooming-in intervention | Nursery care intervention | Breastfeeding outcomes/time point |
|---|---|---|---|---|---|---|
| Bystrova et al. [ | RCT | Maternity home in Russia; 1995–1998 | Healthy mothers of any parity; uncomplicated pregnancies; normal vaginal deliveries; full term babies | 1. Skin-to-skin on | Placed in a cot in delivery room followed by nursery care | 'Nearly exclusive breastfeeding’ (we defined it as full breastfeeding) at 3, 4, and 6 months, frequency of breastfeeding per day and duration of each feed (minutes) on day 4 |
| Elander et al. [ | Quasi-RCT | A hospital in Sweden; 1983–1984 | Maternal parity not stated | 24 hours per day, with 2 hours instruction on how to care for infants | Mothers had free access to babies. No additional instruction on how to care for infants | Breastfeeding not defined. Results extrapolated from survival curves. Time points: after discharge and at 3 months (12 weeks) |
| Greenberg et al. [ | Quasi random | Hospital in Sweden; unknown study date | Primiparous women; baby >37 weeks or 2500 g, born via vaginal delivery | 8 hours per day starting after 12–36 hours of life | Regular feeding schedule with 20 minutes interaction at each feeding | Breastfeeding problems reported by mothers in the first week after infant’s birth |
| Lind et al. | RCT | Hospital in Sweden; unknown study date | Primiparous women; uncomplicated pregnancies, deliveries, and puerperium; mothers with enough breastmilk for their babies upon leaving the hospital; | Day-time only | Maternal access not described | Exclusive breastfeeding at unknown timepoint (timepoint was described as first months) |
| Lindenberg et al. [ | Before-and-after study | Hospital in Nicaragua; 1982–1983 | Primiparous women; from poor urban areas of Managua; normal vaginal deliveries | 24 hours per day with breastfeeding promotion | Two control groups | Exclusive and partial breastfeeding at 1 week and 4 months |
| Perez-Escamilla et al. [ | Prospective cohort study | 2 hospitals in Mexico; 1989 | Healthy women who planned to breastfeed; mothers of all parity; normal vaginal deliveries; healthy term babies of >2.5kg; Apgar score at 1 and 5 min >7 | Two intervention groups | Maternal access not stated | Full (exclusive and almost exclusive), partial and any breastfeeding, plotted as a survival curve from 0 to 4 months |
| Sousa et al. (abstract only) [ | Two groups, method of allocation unclear | Maternity ward in Brazil; unknown study date | Maternal parity not stated; normal full-term babies | 24 hours per day | Mothers visit nursery for 30 minutes every 3 hours | Successful (Full) breastfeeding up to 2 months |
Assessment of risk of bias.
| Studies | Random sequence generation and allocation concealment (selection bias) | Blinding of participants and personnel | Incomplete outcome data (attrition bias) | Selective reporting (reporting bias) | Other bias |
|---|---|---|---|---|---|
| Bystrova et al. [ | Low | High | High | Low | Low |
| Table of allocation sequence | Not described | Attrition due to treatment refusal in the nursery care group was higher in nursery care than rooming-in (11% vs 4%) | Not detected | Not detected | |
| Elander et al. [ | High | Low | Low | Low | High |
| Alternating allocation but affected by bed availability | Participants and personnel were blinded to the purpose of the study | No attrition | Not detected | The rooming in group also received Infant care guidance which could independently affect outcome | |
| Greenberg et al. [ | High | High | Low | Low | Low |
| Randomised, but allocation was affected by bed availability | No blinding. Outcome self-reported | No attrition | Not detected | Not detected | |
| Lind et al. [ | Unclear | Unclear | Unclear | Unclear | Low |
| Randomised. Randomisation and allocation method not described | Not described | Details of attrition not provided | Insufficient information available for judgement | Not detected | |
| Lindenberg et al. [ | High | Unclear | Unclear | Low | High |
| Before (nursery care)-and-after (rooming-in) comparison. | “Both mothers and interviewers were blind to the purpose of the study.” Blinding of healthcare personnel to the purpose of the study was not described | Overall attrition rate was 27%. Details of attrition rate in individual groups was not reported | Not detected | The rooming in group also received ‘standardised breastfeeding promotion’ which could independently affect outcome | |
| Perez-Escamilla et al. [ | High | Low | High | Low | Low |
| Allocation was by participant preference | Participants were blinded to the study objectives and the existence of different groups. We judged that lack of blinding of the care takers did not influence the outcome because the rooming-in and nursery care groups were in different hospitals | Imbalance of attrition distribution across the groups (2% versus 14% versus 14%). Reasons for attrition not reported | Not detected | Not detected | |
| Sousa et al. [ | Unclear | Unclear | Unclear | Unclear | Low |
| Method of allocation not described | Not described | Not described | Not described | Not detected |
1. Using Cochrane risk of bias tool [14]
2 We judged that blinding of participants and personnel to the intervention was not impossible but that blinding of participants and personnel to the study objectives means low risk of performance bias.
3 No full text available. Risk of bias assessment based on the abstract.
4 We judged the outcome breastfeeding at 3, 4 and 6 months of age to be an objective outcome not likely to be affected by lack of blinding of the outcome assessor. Hence, six studies that measured these breastfeeding outcomes had low risk of detection bias, the other one studya that measured maternal self-reported breastfeeding problems had high risk of detection bias due to lack of blinding of outcome assessor.
Fig 2Full breastfeeding.
(A) at 3 months, (B) 4 months (C) 6 months of age.
Fig 3Partial breastfeeding at 3–4 months of age.
Mean breastfeeding frequency (SD) during intervention.
| Rooming-in mean (SD) | Nursery care mean (SD) | P value | |
|---|---|---|---|
| Bystrova et al. [ | 8.6 (2.0) n = 109 | 7 (0) n = 37 | Not estimable |
| Perez-Escamilla et al. [ | 3.7 (2.57) n = 107 | 0.9 (1.2) n = 58 | < .0.001 |