British Journal of Anaesthesia, Vol 80, Issue 3 299-301, Copyright © 1998 by The Board of Management and Trustees of the British Journal of Anaesthesia
P. S. Weir and JPH. Fee
We have compared 0.5% bupivacaine 75 mg (group A; n = 15) with three 0.5%
bupivacaine 75 mg-ketamine mixtures for extradural block in 59 ASA I-III
patients undergoing total knee replacement in a randomized, double-blind
study. The following doses of preservative-free 1% ketamine were used: 0.3
mg kg-1 (group B: n = 14); 0.5 mg kg-1 (group C: n = 5); and 0.67 mg kg-1
(group D: n = 15). Level of sensory block, degree of motor weakness and
sedation scores were recorded before and after operation. Duration of
postoperative analgesia was also noted. There was no difference between
groups in median maximum level of sensory block (group A: T4 (range
T10-T2); group B: T4 (T10-T2); group C: T4 (T8-T2); and group D: T3
(T8-C3)) or in the degree of motor block. Thirty-three of the 44 patients
who received ketamine showed signs of systemic absorption (blurred vision,
sedation) within 10 min of injection. There was no significant difference
between groups in median duration of analgesia (group A: 240 (range
115-340) min; group B: 198 (97-460) min; group C: 150 (122-448) min; and
group D: 210 (130- 390) min). No patient suffered any adverse psychomimetic
effects. We conclude that at the doses used, addition of ketamine to
extradural bupivacaine did not improve extradural block in adult patients
undergoing total knee replacement.
CLINICAL INVESTIGATIONS
Double-blind comparison of extradural block with three bupivacaine- ketamine mixtures in knee arthroplasty
Department of Anaesthetics, The Queen's University of Belfast, Whitla Medical Building, 97 Lisburn Road, Belfast BT9 7BL, and Musgrave Park Hospital, Stockman's Lane, Belfast BT9 7JB
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