Perinatal pharmacology and safety profiles

Research output: Chapter/Conference proceedingChapterAcademic

2 Citations (Scopus)

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.

Original languageEnglish
Title of host publicationHandbook of Clinical Neurology
PublisherElsevier
Pages161-178
Number of pages18
DOIs
Publication statusPublished - 2020

Publication series

SeriesHandbook of Clinical Neurology
Volume171
ISSN0072-9752

Bibliographical note

Funding Information:
K.A. is involved as coinvestigator in the Innovative Medicines Initiative (IMI). ConcePTION and the Co-Opt project are two projects related to the topic discussed in this chapter.

Publisher Copyright:
© 2020 Elsevier B.V.

Fingerprint

Dive into the research topics of 'Perinatal pharmacology and safety profiles'. Together they form a unique fingerprint.

Cite this