利辛普利向母乳转移的研究:定量分析

IF 2.6 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiovascular Pharmacology Pub Date : 2024-10-15 DOI:10.1097/FJC.0000000000001642
Julie Chugh, Jean Dai, Palika Datta, Kaytlin Krutsch
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引用次数: 0

摘要

利辛普利通常用于治疗高血压和心力衰竭等疾病。尽管对胎儿毒性的担忧传统上限制了利辛普利在育龄妇女中的使用,但最近的美国妇产科协会指南提倡积极治疗高血压,这可能需要在产后使用以前未考虑过的药物。我们的目的是估计婴儿通过母乳接触母体利辛普利的情况,并报告母乳喂养婴儿的耐受性。五名正在服用赖诺普利的志愿者通过婴儿风险中心母乳生物储存库提供了母乳样本及其相关健康信息供研究使用。使用液相色谱-质谱法测量了利辛普利在乳汁中的药代动力学。每10毫克每日剂量的利辛普利平均乳汁浓度为0.49纳克/毫升。赖诺普利的相对婴儿剂量(RID)为 0.06%,比 10%的标准安全阈值低 100 多倍。在这项研究中,赖诺普利向母乳中的转移极少,这表明该药物不太可能对健康的母乳喂养婴儿造成临床重大风险。
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Investigating the Transfer of Lisinopril into Human Milk: A Quantitative Analysis.

Lisinopril is commonly prescribed to manage conditions such as hypertension and heart failure. While concerns about fetal toxicity have traditionally limited the use of lisinopril in women of reproductive age, recent ACOG guidelines promote aggressive treatment of hypertension, which may require the use of pharmacologic agents not previously considered in the postpartum period. We aimed to estimate infant exposure to maternal lisinopril via breastmilk and report the tolerance of the breastfed infant. Five volunteers taking lisinopril provided samples of their human milk and their associated health information for research through the InfantRisk Center Human Milk Biorepository. The milk pharmacokinetics of lisinopril were measured using liquid chromatography-mass spectrometry. The mean milk concentration of lisinopril was 0.49 ng/mL per 10 mg daily dose. The Relative Infant Dose (RID) was 0.06% for lisinopril, more than 100 times lower than the standard 10% safety threshold. The minimal transfer of lisinopril into human milk in this study suggests the drug is unlikely to pose a clinically significant risk to healthy breastfed infants.

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来源期刊
CiteScore
5.10
自引率
3.30%
发文量
367
审稿时长
1 months
期刊介绍: Journal of Cardiovascular Pharmacology is a peer reviewed, multidisciplinary journal that publishes original articles and pertinent review articles on basic and clinical aspects of cardiovascular pharmacology. The Journal encourages submission in all aspects of cardiovascular pharmacology/medicine including, but not limited to: stroke, kidney disease, lipid disorders, diabetes, systemic and pulmonary hypertension, cancer angiogenesis, neural and hormonal control of the circulation, sepsis, neurodegenerative diseases with a vascular component, cardiac and vascular remodeling, heart failure, angina, anticoagulants/antiplatelet agents, drugs/agents that affect vascular smooth muscle, and arrhythmias. Appropriate subjects include new drug development and evaluation, physiological and pharmacological bases of drug action, metabolism, drug interactions and side effects, application of drugs to gain novel insights into physiology or pathological conditions, clinical results with new and established agents, and novel methods. The focus is on pharmacology in its broadest applications, incorporating not only traditional approaches, but new approaches to the development of pharmacological agents and the prevention and treatment of cardiovascular diseases. Please note that JCVP does not publish work based on biological extracts of mixed and uncertain chemical composition or unknown concentration.
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