Jansson Lauren M, Spencer Nancy, McConnell Krystle, Velez Martha, Tuten Michelle, Harrow Cheryl A, Jones Hendrée E, Swortwood Madeleine J, Barnes Allan J, Scheidweiler Karl B, Huestis Marilyn A
1 Johns Hopkins University School of Medicine, Baltimore, MD, USA.
2 Johns Hopkins Bayview Medical Center, Baltimore, MD, USA.
J Hum Lact. 2016 Nov;32(4):675-681. doi: 10.1177/0890334416663198. Epub 2016 Sep 26.
In addition to the well-known benefits of human milk and breastfeeding for the mother and infant, breastfeeding may mitigate neonatal abstinence syndrome severity in prenatally opioid-exposed infants. However, lack of conclusive data regarding the extent of the presence of buprenorphine and active metabolites in human milk makes the recommendation of breastfeeding for buprenorphine-maintained women difficult for many providers.
This study seeks to determine the concentrations of buprenorphine and its active metabolites (norbuprenorphine, buprenorphine-glucuronide, and norbuprenorphine-glucuronide) in human milk, maternal plasma, and infant plasma of buprenorphine-maintained women and their infants.
Up to 10 buprenorphine-maintained women provided paired breast milk and plasma samples at 2, 3, 4, 14, and 30 days postdelivery, and 9 infants provided plasma samples on day 14 of life. All samples were analyzed via liquid chromatography tandem mass spectrometry to determine concentrations of buprenorphine, norbuprenorphine, buprenorphine-glucuronide, and norbuprenorphine-glucuronide by a fully validated method.
Concentrations of buprenorphine and metabolites are low in human milk and maternal plasma. Breastfed infant plasma concentrations of buprenorphine were low or undetectable and metabolite concentrations undetectable at 14 days of infant age. There were significant correlations between maternal buprenorphine dose and maternal plasma and human milk buprenorphine concentrations.
These data find low concentrations of buprenorphine and metabolites in human milk and lend support to the recommendation for lactation among stable buprenorphine-maintained women. However, the correlation between maternal dose and maternal plasma and human milk buprenorphine concentrations bears further study.
除了人乳和母乳喂养对母亲和婴儿具有众所周知的益处外,母乳喂养可能会减轻产前暴露于阿片类药物的婴儿的新生儿戒断综合征的严重程度。然而,关于人乳中丁丙诺啡及其活性代谢物存在程度的确定性数据不足,这使得许多医疗服务提供者难以建议接受丁丙诺啡维持治疗的女性进行母乳喂养。
本研究旨在确定接受丁丙诺啡维持治疗的女性及其婴儿的人乳、母体血浆和婴儿血浆中丁丙诺啡及其活性代谢物(去甲丁丙诺啡、丁丙诺啡 - 葡萄糖醛酸苷和去甲丁丙诺啡 - 葡萄糖醛酸苷)的浓度。
多达10名接受丁丙诺啡维持治疗的女性在产后第2、3、4、14和30天提供配对的母乳和血浆样本,9名婴儿在出生后第14天提供血浆样本。所有样本均通过液相色谱串联质谱法进行分析,以采用经过充分验证的方法测定丁丙诺啡、去甲丁丙诺啡、丁丙诺啡 - 葡萄糖醛酸苷和去甲丁丙诺啡 - 葡萄糖醛酸苷的浓度。
人乳和母体血浆中丁丙诺啡及其代谢物的浓度较低。母乳喂养婴儿在14日龄时血浆中丁丙诺啡浓度较低或无法检测到,代谢物浓度无法检测到。母体丁丙诺啡剂量与母体血浆和人乳中丁丙诺啡浓度之间存在显著相关性。
这些数据表明人乳中丁丙诺啡及其代谢物浓度较低,并支持对接受稳定丁丙诺啡维持治疗的女性进行母乳喂养的建议。然而,母体剂量与母体血浆和人乳中丁丙诺啡浓度之间的相关性值得进一步研究。