Safe use of human milk for preterms in the context of maternal polypharmacy: a framework to improve practices.

IF 3.1 3区 医学 Q1 PEDIATRICS
Dotan Shaniv, Anne Smits, Karel Allegaert
{"title":"Safe use of human milk for preterms in the context of maternal polypharmacy: a framework to improve practices.","authors":"Dotan Shaniv, Anne Smits, Karel Allegaert","doi":"10.1038/s41390-025-04416-z","DOIUrl":null,"url":null,"abstract":"<p><p>Maternal pharmacotherapy during lactation is an ongoing research field, which relies on scientific evidence, pharmacological reasoning and extrapolation to support risk-to-benefit assessment. Typically, drugs are studied individually for potential effects on a nursing infant, with limited information on the preterm infant. Polypharmacy during lactation is still poorly studied, leaving healthcare professionals without any scientific guidance when consulting on human milk safety in this scenario. When focusing on a dyad of a postpartum mother on polypharmacy and a preterm infant, the benefits of mother's own milk (MOM) should be weighed against the unknown potential risks of polypharmacy during lactation. Within this setting of limited evidence, a framework to improve clinical and research practices is provided. Possible measures to minimize the risk of maternal (poly)pharmacy to the newborn include: multi-disciplinary prenatal counseling; preferring medications with low passage rate into human milk; relative rating of medications according to safety profile; and 'mixed feeding' (alternating between MOM and other types of feed, preferably donor human milk). These measures can be used to support shared informed decisions on the risk-to-benefit assessment. As the topic of polypharmacy during lactation is still poorly explored, a research agenda is suggested. IMPACT: Polypharmacy during lactation is poorly studied, and practical, evidence-based guidelines for healthcare professionals are lacking. Various methods can be employed to reduce exposure to medications through human milk, even more so when applied concomitantly: preference of medications with low passage into human milk, relative rating of medications according to known safety profile, or 'mixed feeding' where mother's own milk is alternated with other types of feed, preferably donor human milk. A framework to improve clinical and research practices on provision of human milk in the setting of maternal polypharmacy and prematurity as an added challenge is provided.</p>","PeriodicalId":19829,"journal":{"name":"Pediatric Research","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Research","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1038/s41390-025-04416-z","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

Abstract

Maternal pharmacotherapy during lactation is an ongoing research field, which relies on scientific evidence, pharmacological reasoning and extrapolation to support risk-to-benefit assessment. Typically, drugs are studied individually for potential effects on a nursing infant, with limited information on the preterm infant. Polypharmacy during lactation is still poorly studied, leaving healthcare professionals without any scientific guidance when consulting on human milk safety in this scenario. When focusing on a dyad of a postpartum mother on polypharmacy and a preterm infant, the benefits of mother's own milk (MOM) should be weighed against the unknown potential risks of polypharmacy during lactation. Within this setting of limited evidence, a framework to improve clinical and research practices is provided. Possible measures to minimize the risk of maternal (poly)pharmacy to the newborn include: multi-disciplinary prenatal counseling; preferring medications with low passage rate into human milk; relative rating of medications according to safety profile; and 'mixed feeding' (alternating between MOM and other types of feed, preferably donor human milk). These measures can be used to support shared informed decisions on the risk-to-benefit assessment. As the topic of polypharmacy during lactation is still poorly explored, a research agenda is suggested. IMPACT: Polypharmacy during lactation is poorly studied, and practical, evidence-based guidelines for healthcare professionals are lacking. Various methods can be employed to reduce exposure to medications through human milk, even more so when applied concomitantly: preference of medications with low passage into human milk, relative rating of medications according to known safety profile, or 'mixed feeding' where mother's own milk is alternated with other types of feed, preferably donor human milk. A framework to improve clinical and research practices on provision of human milk in the setting of maternal polypharmacy and prematurity as an added challenge is provided.

在产妇多重用药的背景下,早产儿母乳的安全使用:改进做法的框架。
哺乳期间的母亲药物治疗是一个正在进行的研究领域,它依赖于科学证据,药理学推理和外推来支持风险-收益评估。一般来说,药物是单独研究对哺乳婴儿的潜在影响的,对早产儿的信息有限。哺乳期间的多重用药研究仍然很少,使得医疗保健专业人员在咨询这种情况下的母乳安全时没有任何科学指导。当关注产后母亲的多重用药和早产儿时,应权衡母乳(MOM)的益处与哺乳期多重用药的未知潜在风险。在这种有限证据的背景下,提供了一个改进临床和研究实践的框架。尽量减少产妇(多)药房对新生儿的风险的可能措施包括:多学科产前咨询;偏爱进入人乳通过率低的药物;根据安全性对药物进行相对评级;以及“混合喂养”(在母乳和其他类型的饲料之间交替喂养,最好是母乳供体)。这些措施可用于支持就风险-效益评估作出共同的知情决定。由于哺乳期间多药的主题仍然很少探索,建议一个研究议程。影响:哺乳期间的多种用药研究很少,缺乏实用的、基于证据的卫生保健专业人员指南。可以采用各种方法来减少通过母乳接触药物,同时使用时更是如此:优先选择进入母乳较少的药物,根据已知的安全性对药物进行相对评级,或“混合喂养”,即母亲的母乳与其他类型的饲料交替使用,最好是供体的母乳。提供了一个框架,以改善在产妇多药和早产的情况下提供母乳的临床和研究实践,作为一个额外的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Pediatric Research
Pediatric Research 医学-小儿科
CiteScore
6.80
自引率
5.60%
发文量
473
审稿时长
3-8 weeks
期刊介绍: Pediatric Research publishes original papers, invited reviews, and commentaries on the etiologies of children''s diseases and disorders of development, extending from molecular biology to epidemiology. Use of model organisms and in vitro techniques relevant to developmental biology and medicine are acceptable, as are translational human studies
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信