European Journal of Clinical Pharmacology 2008-12-01

Pharmacokinetics of lidocaine and its metabolite in peridural anesthesia administered to pregnant women with gestational diabetes mellitus.

Elaine Christine Dantas Moisés, Luciana de Barros Duarte, Ricardo de Carvalho Cavalli, Maria Paula Marques, Vera Lúcia Lanchote, Geraldo Duarte, Sérgio Pereira da Cunha

Index: Eur. J. Clin. Pharmacol. 64(12) , 1189-96, (2008)

Full Text: HTML

Abstract

Peridural blockade with lidocaine, bupivacaine, and fentanyl is an anesthetic procedure extensively used in obstetrics, justifying the pharmacokinetic study of these drugs during labor.To investigate the influence of the physiopathological changes of gestational diabetes mellitus (GDM) on the pharmacokinetics of lidocaine and its metabolite monoethylglycinexylidide (MEGX) in pregnant women subjected to peridural anesthesia.Ten normal pregnant women (group 1) and six pregnant women with GDM (group 2) were studied, all of them at term. The patients received 200 mg 2% lidocaine hydrochloride without a vasoconstrictor by the peridural locoregional route. Maternal blood samples were collected at predetermined times for the analysis of lidocaine and MEGX by chromatography and pharmacokinetic analysis.The median pharmacokinetic parameters of lidocaine for groups 1 and 2 (P

Related Compounds

Structure Name/CAS No. Articles
Monoethylglycinexylidide Structure Monoethylglycinexylidide
CAS:7728-40-7