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使用多潘立酮提高早产儿母亲的母乳产量。

Enhancing Human Milk Production With Domperidone in Mothers of Preterm Infants.

作者信息

Asztalos Elizabeth V, Campbell-Yeo Marsha, da Silva Orlando P, Ito Shinya, Kiss Alex, Knoppert David

机构信息

Department of Newborn and Developmental Paediatrics, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, ON, Canada.

Izaak Walton Killam Health Centre, Dalhousie University, Halifax, NS, Canada.

出版信息

J Hum Lact. 2017 Feb;33(1):181-187. doi: 10.1177/0890334416680176. Epub 2017 Jan 20.

Abstract

BACKGROUND

Mothers of preterm infants often are at risk of expressing an inadequate amount of milk for their infants and the use of galactogogues is often considered. Domperidone is a widely used galactogogue with little information available to guide clinicians regarding initiation, timing, and duration of treatment. Research aim: The primary objective of this study was to determine whether administration of domperidone within the first 21 days after delivery would lead to a higher proportion of mothers achieving a 50% increase in the volume of milk at the end of 14 days of treatment compared with mothers receiving placebo.

METHODS

Eligible mothers were randomized to one of two treatment arms: Group A-domperidone 10 mg orally three times daily for 28 days; or Group B-placebo 10 mg orally three times daily for 14 days followed by domperidone 10 mg orally three times daily for 14 days.

RESULTS

A total of 90 mothers of infants ≤ 29 weeks gestation were randomized. Mean milk volumes at entry were similar for both groups. More mothers achieved a 50% increase in milk volume after 14 days in Group A (77.8%) compared with Group B (57.8%), odds ratio = 2.56, 95% confidence interval [1.02, 6.25], p = .04.

CONCLUSION

A greater number of mothers experienced a 50% or more increase in human milk volume, but the absolute increase in milk volume was modest.

摘要

背景

早产婴儿的母亲往往有乳汁分泌量不足的风险,因此常常考虑使用催乳剂。多潘立酮是一种广泛使用的催乳剂,但关于其起始用药、用药时间和疗程,可供临床医生参考的信息较少。研究目的:本研究的主要目的是确定产后21天内服用多潘立酮的母亲与服用安慰剂的母亲相比,在治疗14天后,乳汁量增加50%的母亲比例是否更高。

方法

符合条件的母亲被随机分为两个治疗组之一:A组——口服多潘立酮10毫克,每日三次,共28天;或B组——口服安慰剂10毫克,每日三次,共14天;之后口服多潘立酮10毫克,每日三次,共14天。

结果

共有90名孕周≤29周婴儿的母亲被随机分组。两组入组时的平均乳汁量相似。与B组(57.8%)相比,A组在14天后乳汁量增加50%的母亲更多(77.8%),优势比=2.56,95%置信区间[1.02, 6.25]),p = 0.04。

结论

更多母亲的母乳量增加了50%或更多,但乳汁量的绝对增加幅度不大。

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