British Journal of Anaesthesia, Vol 77, Issue 4 544-545, Copyright © 1996 by The Board of Management and Trustees of the British Journal of Anaesthesia
L. Niemi, M. Pitkanen, P. Dunkel, E. Laakso and P. H. Rosenberg
Spinal anaesthesia in 47 ASA I-III patients was induced with 0.5%
bupivacaine 2 ml via a 28-gauge spinal catheter (L3-4 interspace) and
0.5-ml increments were given if needed before or during hip or knee
arthroplasty. Intrathecal 24-h infusions consisted of 0.5% bupivacaine 0.4
ml h-1 (2 mg h-1) (n = 12), 0.5% bupivacaine 0.2 ml h-1 (1 mg h-1) (n = 12)
or saline (n = 11) (12 exclusions). Patients received oxycodone 0.1-0.14 mg
kg-1 i.m. for rescue analgesia. Infusion of bupivacaine 2 mg h-1 provided
significantly better postoperative analgesia (19 oxycodone doses per group
in 24 h) compared with bupivacaine 1 mg h-1 (36 doses of oxycodone per
group) and saline (52 doses per group) (P < 0.05). Five patients in the
bupivacaine 2-mg h-1 group and none in the other groups had measurable
sensory block 24 h after the infusion was started. Three patients in the
bupivacaine 2-mg h-1 group, two with concomitant arterial hypotension, and
one patient in the bupivacaine 1-mg h-1 group experienced an increase in
block on the ward. The incidence of nausea and vomiting was similar in all
groups. Although an effective analgesic, intrathecal infusion of
bupivacaine 2 mg h-1 cannot be recommended for routine pain relief because
of the risk of increasing spinal block. Technical problems (19%) also
reduced the overall efficacy of the continuous intrathecal analgesic
regimen.
SHORT COMMUNICATION
Evaluation of the usefulness of intrathecal bupivacaine infusion for analgesia after hip and knee arthroplasty
Department of Anaesthesiology, Toolo Hospital, Helsinki University Central Hospital, FIN00260 Helsinki, Finland
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