Pharmacokinetics of tramadol in children after i.v. or caudal epidural administration

被引:76
|
作者
Murthy, BVS [1 ]
Pandya, KS [1 ]
Booker, PD [1 ]
Murray, A [1 ]
Lintz, W [1 ]
Terlinden, R [1 ]
机构
[1] Royal Liverpool Childrens NHS Trust, Liverpool L12 2AP, Merseyside, England
关键词
analgesics opioid; tramadol; pharmacokinetics; analgesia; paediatric; children; analgesic techniques; i.v; epidural;
D O I
10.1093/oxfordjournals.bja.a013437
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
We have studied the pharmacokinetics of a single bolus dose of tramadol 2 mg kg(-1) injected either i.v. or into the caudal epidural space in 14 healthy children, aged 1-12 yr, undergoing elective limb, urogenital or thoracic surgery. Serum concentrations of tramadol and its metabolite O-demethyl tramadol (MI) were measured in venous blood samples at various intervals up to 20 h by non-stereoselective gas chromatography with nitrogen-selective detection. All pharmacokinetic variables were evaluated using a non-compartmental model. After a single i.v. injection (n=9), the mean elimination half-life of tramadol was 6.4 (SD 2.7) h, with a volume of distribution of 3.1 (1.1) live kg(-1) and total plasma clearance of 6.1 (2.5) mi kg(-1) min(-1). All of these pharmacokinetic variables were similar to those reported previously in adults. After caudal epidural administration (n=5), mean elimination half-life was 3.7 (0.9) h, volume of distribution was 2.0 (0.4) litre kg(-1) and total clearance was 6.6 (1.9) ml kg(-1) min(-1) The caudal/i.v. quotient of the AUC was 0.83, which confirms that there is extensive systemic absorption of tramadol after caudal administration. Serum concentrations of MI showed a time course typical of a metabolite after both modes of administration. Serum concentrations of MI after caudal administration were lower than those after i.v. injection.
引用
收藏
页码:346 / 349
页数:4
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