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Anesth Analg 2006;102:504-508
© 2006 International Anesthesia Research Society
doi: 10.1213/01.ane.0000194448.37407.6a


PAIN MEDICINE

Perioperative Nimodipine and Postoperative Analgesia

Gerri Casey, SRN*, Sally-Ann Nortcliffe, FRCA*, Paul Sharpe, FRCA*, and D. J. Buggy, MD, MSc, DME, FRCPI, FCA(Irel), FRCA{dagger}

*Departments of Anaesthesia, Critical Care and Pain Management, University Hospitals of Leicester, Leicester General Hospital, Leicester LE5 4PW, UK and {dagger}Mater Misericordiae University Hospital, Dublin 7, Ireland and Outcomes ResearchTM Institute, Louisville, Kentucky

Address correspondence to Donal Buggy, MD, Department of Anaesthesia, Mater Misericordiae University Hospital, Dublin 7, Ireland. Address e-mail to donal.buggy{at}nbsp.ie. Reprints will not be available from the author.

There is experimental evidence that nimodipine, an L-type dihydropiridine calcium channel blocker with relatively high blood-brain barrier penetration, enhances the antinociceptive properties of morphine. We tested the hypothesis that oral nimodipine taken preoperatively and 6 hourly for 48 h postoperatively would reduce visual analog scale pain scores and morphine consumption in morphine-naive patients with acute postoperative pain. Forty patients undergoing total knee replacement surgery (age 70 ± 7 yr, 28 male) were randomized by computer-generated numbers to receive capsules containing either nimodipine 30 mg or placebo in a double-blind study design. All patients received 3 capsules (nimodipine 90 mg or placebo) 1–2 h before induction of anesthesia followed by oral nimodipine 30 mg or placebo 6 hourly for 48 hours postoperatively. Spinal anesthesia was induced with hyperbaric bupivacaine 0.5% (2.4–3.0 mL) and fluids and ephedrine were given at the discretion of the anesthesiologist. Morphine patient-controlled analgesia (PCA, bolus 1 mg, lockout 5 min) was given for postoperative analgesia. Primary outcome measures were visual analog pain scores at rest and on moving (sitting forward) and PCA morphine consumption. Morphine consumption was significantly larger in nimodipine patients at 12 h (39 ± 18 versus 29 ± 15; P = 0.04), 24 h (62 ± 23 versus 45 ± 24; P = 0.02), and 48 h (88 ± 34 versus 61 ± 27; P = 0.01). There were no significant differences in pain scores at rest or moving or in time to first use of morphine analgesia. This study has demonstrated increased morphine consumption after 12 h in postoperative patients receiving nimodipine, suggesting that, in patients undergoing knee replacement surgery, it has no adjunctive analgesic effect and may actually inhibit the analgesic effect of morphine.







Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins and Stanford University Libraries' HighWire Press®. Copyright 2006 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 2006 by the International Anesthesia Research Society.