Pharmacokinetics of levobupivacaine after caudal epidural administration in infants less than 3 months of age

被引:27
作者
Chalkiadis, GA
Anderson, BJ
Tay, M
Bjorksten, A
Kelly, JJ
机构
[1] Royal Childrens Hosp, Dept Anaesthesia & Pain Management, Parkville, Vic 3052, Australia
[2] Univ Auckland, Dept Anaesthesiol, Auckland, New Zealand
关键词
anaesthetic techniques; regional; caudal; anaesthetics local; levobupivacine; infants; neonates; pharmacokinetics; levobupivacaine;
D O I
10.1093/bja/aei218
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background. There are few data describing levobupivacaine pharmacokinetics in infants (< 3 months) after caudal administration. Methods. An open-label study was undertaken to examine the pharmacokinetics of levobupivacaine 2.5 mg ml(-1), 2 mg kg(-1) in children aged less than 3 months after single-shot caudal epidural administration. Plasma concentrations were determined at intervals from 0.5 to 4 h after injection. A population pharmacokinetic analysis of levobupivacaine time-concentration profiles (84 observations) from 22 infants with mean postnatal age (PNA) 2.0 (range 0.6-2.9) months was undertaken using non-linear mixed effects models (NONMEM). Time-concentration profiles were analysed using a one-compartment model with first-order input and first-order elimination. Estimates were standardized to a 70 kg adult using allometric size models. Results. Population parameter estimates (between-subject variability) for total levobupivacaine were clearance (CLt) 12.8 [ coefficient of variation (CV) 50.6%] litre h(-1) 70 kg(-1), volume of distribution (Vt) 202 (CV 31.6%) litre 70 kg(-1), absorption half-life (Tabs) 0.323 (CV 18.6%) h 70 kg(-1). Estimates for the unbound drug were clearance (CLfree) 104 (CV 43.5%) litre h(-1) 70 kg(-1), volume of distribution (Vfree) 1700 (CV 44.9%) litre 70 kg(-1), absorption half-life (Tabsfree) 0.175 (CV 83.7%) h 70 kg(-1). There was no effect attributable to PNA on CL or V. Time to peak plasma concentration (Tmax) was 0.82 (CV 18%) h. Peak plasma concentration (Cmax) was 0.69 (CV 25%) mg ml(-1) for total levobupivacaine and 0.09 (CV 37%) mg ml(-1) for unbound levobupivacaine. Conclusions. Clearance in infants is approximately half that described in adults, suggesting immaturity of P450 CYP3A4 and CYP1A2 enzyme isoforms that metabolize levobupivacaine in infants. This lower clearance delays Tmax, which was noted to occur approximately 50 min after administration of caudal epidural levobupivacaine.
引用
收藏
页码:524 / 529
页数:6
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