British Journal of Anaesthesia, Vol 80, Issue 5 594-598, Copyright © 1998 by The Board of Management and Trustees of the British Journal of Anaesthesia
C. R. Cox, M. R. Checketts, N. Mackenzie, N. B. Scott and J. Bannister
Bupivacaine is used widely as a local anaesthetic but has potential for
severe cardiovascular and central nervous system (CNS) toxicity. It has an
asymmetric carbon atom giving it a chiral centre, and the commercial
preparation is a racemic mixture of its two enantiomers: dextro or R(+)-
bupivacaine and levo or S(-)-bupivacaine. Preclinical studies have
demonstrated reduced cardiotoxicity and CNS toxicity for S(-)- bupivacaine.
In this study we have compared the clinical efficacy of S(- )-bupivacaine
with racemic RS-bupivacaine for supraclavicular brachial plexus block in 75
patients undergoing elective hand surgery. Patients received 0.4 ml kg-1 of
either 0.25% or 0.5% S(-)-bupivacaine or 0.5% RS-bupivacaine in a
randomized, double-blind study. Clinical assessments of sensory and motor
block were performed at regular intervals. There were no significant
differences in onset time, dermatomal spread or duration of both sensory
and motor block between the three groups (the power of the study was 81% to
detect a 4-h difference in duration). Duration of sensory block was
prolonged with wide interpatient variation: 892 (SD 250) min, 1039 (317)
min and 896 (284) min for 0.25% S(-)-bupivacaine, 0.5% S(-)-bupivacaine and
0.5% RS- bupivacaine, respectively. There were no differences in the
overall success rate of the technique. We conclude that S(-)-bupivacaine
was suitable for local anaesthetic use in brachial plexus block
anaesthesia.
CLINICAL INVESTIGATIONS
Comparison of S(-)-bupivacaine with racemic (RS)-bupivacaine in supraclavicular brachial plexus block
Department of Anaesthesia, Ninewells Hospital and Medical School, Dundee DD1 9SY; Department of Anaesthesia, HCI International Medical Centre, Beardmore Street, Clydebank G81 4HX
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