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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.
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页码:346 / 349
页数:4
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