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本文引用的文献

1
Effect of N-Acetyltransferase 2 Genotype on the Pharmacokinetics of Hydralazine During Pregnancy.乙酰转移酶 2 基因型对妊娠期肼屈嗪药代动力学的影响。
J Clin Pharmacol. 2019 Dec;59(12):1678-1689. doi: 10.1002/jcph.1477. Epub 2019 Jun 30.
2
Use of Medication for Cardiovascular Disease During Pregnancy: JACC State-of-the-Art Review.妊娠期心血管疾病药物治疗:JACC 现状评论。
J Am Coll Cardiol. 2019 Feb 5;73(4):457-476. doi: 10.1016/j.jacc.2018.10.075.
3
Increasing the Participation of Pregnant Women in Clinical Trials.提高孕妇参与临床试验的比例。
JAMA. 2018 Nov 27;320(20):2077-2078. doi: 10.1001/jama.2018.17716.
4
Lamotrigine clearance increases by 5 weeks gestational age: Relationship to estradiol concentrations and gestational age.拉莫三嗪清除率随胎龄增加 5 周而增加:与雌二醇浓度和胎龄的关系。
Ann Neurol. 2018 Oct;84(4):556-563. doi: 10.1002/ana.25321. Epub 2018 Oct 11.
5
Organic Cation Transporter 3 Facilitates Fetal Exposure to Metformin during Pregnancy.有机阳离子转运体 3 促进孕期母体暴露于二甲双胍。
Mol Pharmacol. 2018 Oct;94(4):1125-1131. doi: 10.1124/mol.118.112482. Epub 2018 Jul 16.
6
Cytochrome P450 in Pharmacogenetics: An Update.药物遗传学中的细胞色素P450:最新进展
Adv Pharmacol. 2018;83:3-32. doi: 10.1016/bs.apha.2018.04.007.
7
Physiologically Based Pharmacokinetic Modeling in Pregnancy: A Systematic Review of Published Models.妊娠的生理药代动力学模型:已发表模型的系统评价。
Clin Pharmacol Ther. 2018 Dec;104(6):1110-1124. doi: 10.1002/cpt.1084. Epub 2018 May 6.
8
The Placental Barrier: the Gate and the Fate in Drug Distribution.胎盘屏障:药物分布的门户与命运。
Pharm Res. 2018 Feb 23;35(4):71. doi: 10.1007/s11095-017-2286-0.
9
Pregnancy- Associated Changes in Pharmacokinetics and their Clinical Implications.妊娠相关的药代动力学改变及其临床意义。
Pharm Res. 2018 Feb 12;35(3):61. doi: 10.1007/s11095-018-2352-2.
10
UGT polymorphisms and lamotrigine clearance during pregnancy.孕期UGT基因多态性与拉莫三嗪清除率
Epilepsy Res. 2018 Feb;140:199-208. doi: 10.1016/j.eplepsyres.2018.01.011. Epub 2018 Jan 31.

妊娠期用药:影响临床治疗的药物作用及生理变化。

Drugs in pregnancy: Pharmacologic and physiologic changes that affect clinical care.

机构信息

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.

出版信息

Semin Perinatol. 2020 Apr;44(3):151221. doi: 10.1016/j.semperi.2020.151221. Epub 2020 Jan 25.

DOI:10.1016/j.semperi.2020.151221
PMID:32115202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8195457/
Abstract

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.

摘要

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。