S. Ilkjaer et al., EFFECT OF IV KETAMINE IN COMBINATION WITH EPIDURAL BUPIVACAINE OR EPIDURAL MORPHINE ON POSTOPERATIVE PAIN AND WOUND TENDERNESS AFTER RENAL SURGERY, British Journal of Anaesthesia, 81(5), 1998, pp. 707-712
We studied 60 patients undergoing operation on the kidney with combine
d general and epidural anaesthesia, in a double-blind, randomized, con
trolled study. Patients were allocated to receive a preoperative bolus
dose of ketamine 10 mg i.v., followed by an i.v. infusion of ketamine
10 mg h(-1) for 48 h after operation, or placebo. During the first 24
h after surgery, all patients received 4 ml h(-1) of epidural bupivac
aine 2.5 mg ml(-1). From 24 to 48 h after operation, patients received
epidural morphine 0.2 mg h(-1) preceded by a bolus dose of 2 mg. In a
ddition, patient-controlled analgesia (PCA) with i.v. morphine (2.5 mg
, lockout time 15 min) was offered from 0 to 48 h after operation. Pat
ients who received keta mine felt significantly more sedated at 0-24 h
, but not at 24-48 h after operation, compared with patients who recei
ved placebo (P=0.002 and P=0.127, respectively). There were no signifi
cant differences in pain (VAS) at rest, during mobilization or cough,
PCA morphine consumption, sensory block to pinprick, pressure pain det
ection threshold assessed with an algometer, touch and pain detection
thresholds assessed with von Frey hairs, peak flow or side effects oth
er than sedation. The power of detecting a reduction in VAS scores of
20 mm in our study was 80% at the 5% significance level. We conclude t
hat we were unable to demonstrate an (additive) analgesic or opioid sp
aring effect of ketamine 10 mg h(-1) i.v. combined with epidural bupiv
acaine at 0-24 h, or epidural morphine at 24-48 h after renal surgery.