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Pharmacokinetics of 0.2% ropivacaine and 0.2% bupivacaine following caudal blocks in children
Author(s) -
AlaKokko T. I.,
Partanen A.,
Karinen J.,
Kiviluoma K.,
Alahuhta S.
Publication year - 2000
Publication title -
acta anaesthesiologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.738
H-Index - 107
eISSN - 1399-6576
pISSN - 0001-5172
DOI - 10.1034/j.1399-6576.2000.440911.x
Subject(s) - ropivacaine , bupivacaine , medicine , anesthesia , pharmacokinetics , local anesthetic , plasma concentration , venous blood , blockade , pharmacology , receptor
Background: Ropivacaine is the first S‐enantiomer aminoamide local anaesthetic in clinical use, and has been found to be less toxic than bupivacaine. Caudal ropivacine has been shown to cause less motor blockade and longer duration of analgesia in the postoperative period than bupivacaine in children. Plasma levels of ropivacaine and bupivacaine have not been previously compared in children. This study was undertaken to compare the total venous plasma concentrations of similar doses of ropivacaine and bupivacaine following caudal administration. Methods: Blood samples were obtained to determine the total venous plasma levels of the used local anaesthetic in 30 children, aged 2.3–8.7 years, ASA I, given 1 ml · kg −1 of either 0.2% ropivacaine or 0.2% bupivacaine in a prospective, randomised manner. Results: There were no differences in the individual peak plasma concentrations achieved. Time to the measured peak plasma concentration was significantly shorter in the bupivacaine group. The plasma concentrations of bupivacaine were significantly lower than for ropivacaine at 60, 90 and 120 min after the block. Conclusion: Absorption and tissue distribution of ropivacaine is slower than for bupivacaine following caudal administration in children.