Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Pharmacogenomics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Department of Obstetrics and Gynecology, Northwestern University Feinberg School of Medicine, 250 East Superior Street, Suite 3-2303, Chicago, IL 60611, USA.
Semin Perinatol. 2020 Apr;44(3):151221. doi: 10.1016/j.semperi.2020.151221. Epub 2020 Jan 25.
Pharmacologic interventions play a major role in obstetrical care throughout pregnancy, labor and delivery and the postpartum. Traditionally, obstetrical providers have utilized standard dosing regimens developed for non-obstetrical indications based on pharmacokinetic knowledge from studies in men or non-pregnant women. With the recognition of pregnancy as a special pharmacokinetic population in the late 1990s, investigators have begun to study drug disposition in this unique patient dyad. Many of the basic physiologic changes that occur during pregnancy have significant impact on drug absorption, distribution and clearance. Activity of Phase I and Phase II drug metabolizing enzymes are differentially altered by pregnancy, resulting in drug concentrations sufficiently different for some medications that efficacy or toxicity is affected. Placental transporters play a major dynamic role in determining fetal drug exposure. In the past two decades, we have begun to expand our understanding of obstetrical pharmacology; however, to truly optimize pharmacologic care of our pregnant patients and their developing fetus, additional research is critically needed.
药物干预在整个妊娠、分娩和产后期间在产科护理中起着重要作用。传统上,产科医生根据男性或非孕妇的研究中的药代动力学知识,利用为非产科适应症开发的标准剂量方案。自 20 世纪 90 年代后期认识到妊娠是一种特殊的药代动力学人群以来,研究人员已开始研究这一独特的患者对子中药物的处置情况。许多在妊娠期间发生的基本生理变化对药物的吸收、分布和清除有重大影响。I 期和 II 期药物代谢酶的活性因妊娠而发生不同程度的改变,导致一些药物的浓度差异很大,从而影响其疗效或毒性。胎盘转运蛋白在决定胎儿药物暴露方面起着重要的动态作用。在过去的二十年中,我们开始加深对产科药理学的理解;然而,为了真正优化我们的孕妇及其发育中胎儿的药物治疗,还迫切需要开展更多的研究。