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Randomized Controlled Trial
. 2010 Feb;26(1):88-100.
doi: 10.1016/j.midw.2008.03.001. Epub 2008 May 16.

Effect of an extended midwifery postnatal support programme on the duration of breast feeding: a randomised controlled trial

Affiliations
Randomized Controlled Trial

Effect of an extended midwifery postnatal support programme on the duration of breast feeding: a randomised controlled trial

Susan J McDonald et al. Midwifery. 2010 Feb.

Abstract

Objective: to evaluate the effects of an extended midwifery support (EMS) programme on the proportion of women who breast feed fully to six months.

Design: randomised controlled trial.

Setting: large public teaching hospital in Australia.

Participants: 849 women who had given birth to a healthy, term, singleton baby and who wished to breast feed.

Intervention: participants were allocated at random to EMS, in which they were offered a one-to-one postnatal educational session and weekly home visits with additional telephone contact by a midwife until their baby was six weeks old; or standard postnatal midwifery support (SMS). Participants were stratified for parity and tertiary education.

Measurements: the main outcome measures were prevalence of full and any breast feeding at six months postpartum.

Findings: there was no difference between the groups at six months postpartum for either full breast feeding [EMS 43.3% versus SMS 42.5%, relative risk (RR) 1.02, 95% confidence interval (CI) 0.87-1.19] or any breast feeding (EMS 63.9% versus SMS 67.9%, RR 0.94, 95%CI 0.85-1.04).

Conclusions: the EMS programme did not succeed in improving breast-feeding rates in a setting where there was high initiation of breast feeding. Breast-feeding rates were high but still fell short of national goals.

Implications for practice: continuing research of programmes designed to promote breast feeding is required in view of the advantages of breast feeding for all mothers and babies.

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