School of Health Sciences, Wuhan University, Wuhan, China.
Department of Preventive Medicine and Public Health, University of Granada, Granada, Spain.
Breastfeed Med. 2021 Jul;16(7):516-529. doi: 10.1089/bfm.2020.0360. Epub 2021 Mar 25.
To evaluate the efficacy and safety of domperidone and metoclopramide used by breastfeeding women. A systematic literature search retrieved citations from PubMed, Embase, The Cochrane Library, Medline, EBSCO, Web of Science, ClinicalTrials.gov (from inception to January, 2021) and bibliographies of known articles. Randomized controlled trials exploring the effects of domperidone and metoclopramide in breastfeeding women with term and preterm infants experiencing adequate or low milk supply were identified. Human milk volume and maternal side effects were presented as mean difference (MD) or relative risks (RR) with 95% confidence intervals (CI). Sixteen trials involving 729 women were included in the qualitative analysis and 14 trials involving 607 women were included in the meta-analysis. In mothers of preterm infants with low milk supply, domperidone demonstrated a significant increase in daily human milk volume (MD = 90.53 mL/day, 95% CI [65.42 to 115.64], = 9%). However, metoclopramide did not show significant difference in daily human milk volume in women with preterm infants (MD = -1.14 mL/day, 95% CI [-31.42 to 29.14], = 0%). No differences in maternal side effects were noted with domperidone (RR = 1.20, 95% CI [0.74 to 1.97], = 0%) or metoclopramide (RR = 1.05, 95% CI [0.52 to 2.11], = 27%) in women with preterm infants. Regarding the women with term infants, there were insufficient data in the current review. Domperidone can be used to treat low milk supply in women with preterm infants without significant side effects based on the current review. More evidence exploring the efficacy and safety of domperidone and metoclopramide are still needed for breastfeeding women in the future.
评估哺乳期妇女使用多潘立酮和甲氧氯普胺的疗效和安全性。系统检索了 PubMed、Embase、The Cochrane Library、Medline、EBSCO、Web of Science、ClinicalTrials.gov(从创建到 2021 年 1 月)和已知文章的参考文献中的引文。确定了探索多潘立酮和甲氧氯普胺对足月和早产儿、泌乳量充足或不足的哺乳期妇女影响的随机对照试验。人乳量和母亲的副作用以均数差(MD)或相对风险(RR)和 95%置信区间(CI)表示。纳入了 16 项涉及 729 名妇女的定性分析试验和 14 项涉及 607 名妇女的荟萃分析试验。在泌乳量低的早产儿母亲中,多潘立酮显著增加了每日人乳量(MD=90.53ml/天,95%CI[65.42 至 115.64], = 9%)。然而,甲氧氯普胺在早产儿母亲中并未显示出人乳量的显著差异(MD=-1.14ml/天,95%CI[-31.42 至 29.14], = 0%)。多潘立酮(RR=1.20,95%CI[0.74 至 1.97], = 0%)或甲氧氯普胺(RR=1.05,95%CI[0.52 至 2.11], = 27%)在治疗早产儿母亲时,副作用无差异。关于足月婴儿的母亲,目前的综述中数据不足。根据目前的综述,多潘立酮可用于治疗早产儿泌乳量不足,且无明显副作用。未来仍需要更多证据来探索多潘立酮和甲氧氯普胺对哺乳期妇女的疗效和安全性。