Suppr超能文献

硫酸镁用于子痫和子痫前期:药代动力学原理

Magnesium sulfate in eclampsia and pre-eclampsia: pharmacokinetic principles.

作者信息

Lu J F, Nightingale C H

机构信息

Department of Clinical Pharmacology, Jingling Hospital, Nanjing, PR China.

出版信息

Clin Pharmacokinet. 2000 Apr;38(4):305-14. doi: 10.2165/00003088-200038040-00002.

Abstract

Magnesium sulfate (MgSO4) is the agent most commonly used for treatment of eclampsia and prophylaxis of eclampsia in patients with severe pre-eclampsia. It is usually given by either the intramuscular or intravenous routes. The intramuscular regimen is most commonly a 4 g intravenous loading dose, immediately followed by 10 g intramuscularly and then by 5 g intramuscularly every 4 hours in alternating buttocks. The intravenous regimen is given as a 4 g dose, followed by a maintenance infusion of 1 to 2 g/h by controlled infusion pump. After administration, about 40% of plasma magnesium is protein bound. The unbound magnesium ion diffuses into the extravascular-extracellular space, into bone, and across the placenta and fetal membranes and into the fetus and amniotic fluid. In pregnant women, apparent volumes of distribution usually reach constant values between the third and fourth hours after administration, and range from 0.250 to 0.442 L/kg. Magnesium is almost exclusively excreted in the urine, with 90% of the dose excreted during the first 24 hours after an intravenous infusion of MgSO4. The pharmacokinetic profile of MgSO4 after intravenous administration can be described by a 2-compartment model with a rapid distribution (a) phase, followed by a relative slow beta phase of elimination. The clinical effect and toxicity of MgSO4 can be linked to its concentration in plasma. A concentration of 1.8 to 3.0 mmol/L has been suggested for treatment of eclamptic convulsions. The actual magnesium dose and concentration needed for prophylaxis has never been estimated. Maternal toxicity is rare when MgSO4 is carefully administered and monitored. The first warning of impending toxicity in the mother is loss of the patellar reflex at plasma concentrations between 3.5 and 5 mmol/L. Respiratory paralysis occurs at 5 to 6.5 mmol/L. Cardiac conduction is altered at greater than 7.5 mmol/L, and cardiac arrest can be expected when concentrations of magnesium exceed 12.5 mmol/L. Careful attention to the monitoring guidelines can prevent toxicity. Deep tendon reflexes, respiratory rate, urine output and serum concentrations are the most commonly followed variables. In this review, we will outline the currently available knowledge of the pharmacokinetics of MgSO4 and its clinical usage for women with pre-eclampsia and eclampsia.

摘要

硫酸镁(MgSO4)是治疗子痫以及预防重度子痫前期患者发生子痫最常用的药物。通常通过肌肉注射或静脉注射给药。肌肉注射方案最常用的是静脉推注4 g负荷剂量,随后立即肌肉注射10 g,然后每4小时在双侧臀部交替肌肉注射5 g。静脉注射方案是给予4 g剂量,然后通过控制输液泵以1至2 g/小时的速度持续输注维持剂量。给药后,约40%的血浆镁与蛋白质结合。未结合的镁离子扩散到血管外-细胞外间隙、骨骼中,穿过胎盘和胎膜进入胎儿和羊水。在孕妇中,给药后3至4小时分布容积通常达到恒定值,范围为0.250至0.442 L/kg。镁几乎完全经尿液排出,静脉输注MgSO4后,90%的剂量在最初24小时内排出。静脉给药后MgSO4的药代动力学特征可用二室模型描述,即快速分布(α)相,随后是相对缓慢的消除β相。MgSO4的临床疗效和毒性与其血浆浓度有关。治疗子痫抽搐建议血浆浓度为1.8至3.0 mmol/L。预防所需的实际镁剂量和浓度从未得到过评估。当硫酸镁给药和监测仔细时,母体毒性很少见。母亲即将发生毒性的第一个警示信号是血浆浓度在3.5至5 mmol/L之间时髌反射消失。呼吸麻痹发生在5至6.5 mmol/L。血浆浓度大于7.5 mmol/L时心脏传导改变,当镁浓度超过12.5 mmol/L时可预期发生心脏骤停。仔细遵循监测指南可预防毒性。最常监测的变量是深腱反射、呼吸频率、尿量和血清浓度。在本综述中,我们将概述目前关于MgSO4药代动力学及其在子痫前期和子痫患者中的临床应用的现有知识。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验