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围产期药理学和安全性特征。

Perinatal pharmacology and safety profiles.

机构信息

Department of Development and Regeneration, KU Leuven, Leuven, Belgium; Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium; Department of Clinical Pharmacy, Erasmus University Medical Center, Rotterdam, The Netherlands.

出版信息

Handb Clin Neurol. 2020;171:161-178. doi: 10.1016/B978-0-444-64239-4.00008-4.

Abstract

Most medications are not adequately evaluated for use during pregnancy, delivery, or the postpartum period, and package inserts fail to provide clear instructions for use in these contexts, despite major concerns among health-care providers and the community as to how to practice evidence-based pharmacotherapy. Valproate fetopathy hereby serves as one of the more recent illustrations of the scope of the problem. At its best, evidence-based pharmacotherapy is driven by a balanced decision between disease-related risks (natural course of the disease) and any risks related to exposure to medications for mother, fetus, or infant. This chapter aims to describe the general patterns of changes in pharmacokinetics (absorption, distribution, metabolism, elimination) in pregnant women and postpartum, with specific emphasis on placental drug transport and additional focus on lactation. The relevance of these changes is illustrated by discussing medications commonly prescribed to treat neurologic conditions.

摘要

大多数药物在妊娠、分娩或产后期间的使用都没有得到充分评估,尽管医疗保健提供者和社区非常关注如何在这些情况下进行循证药物治疗,但药物说明书也未能提供明确的使用说明。丙戊酸胎儿病就是一个最近的例子,说明了这个问题的范围。在最好的情况下,循证药物治疗是在疾病相关风险(疾病自然病程)与母亲、胎儿或婴儿暴露于药物相关的任何风险之间进行平衡决策的结果。本章旨在描述孕妇和产后期间药代动力学(吸收、分布、代谢、排泄)变化的一般模式,特别强调胎盘药物转运,并额外关注哺乳期。通过讨论常用于治疗神经系统疾病的药物,说明了这些变化的相关性。

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