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Low-dose ketamine failed to spare morphine after a remifentanil-based anaesthesia for ear, nose and throat surgery

Published online by Cambridge University Press:  02 June 2005

O. Ganne
Affiliation:
Hôpital de Villefranche-sur-Saône, Department of Anaesthesiology, Villefranche-sur-Saône, Lyon, France
M. Abisseror
Affiliation:
Hôpital de la Croix-Rousse, Department of Anaesthesiology and Intensive Care, Lyon, France
P. Menault
Affiliation:
Hôpital de la Croix-Rousse, Department of Anaesthesiology and Intensive Care, Lyon, France
S. Malhière
Affiliation:
Hôpital de la Croix-Rousse, Department of Anaesthesiology and Intensive Care, Lyon, France
V. Chambost
Affiliation:
Hôpital de la Croix-Rousse, Department of Pharmacy, Lyon, France
B. Charpiat
Affiliation:
Hôpital de la Croix-Rousse, Department of Pharmacy, Lyon, France
C. Ganne
Affiliation:
Hôpital de Villefranche-sur-Saône, Department of Anaesthesiology, Villefranche-sur-Saône, Lyon, France
J. P. Viale
Affiliation:
Hôpital de la Croix-Rousse, Department of Anaesthesiology and Intensive Care, Lyon, France
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Extract

Summary

Background: Ketamine has been claimed to prevent acute opioid tolerance and hyperalgesia following acute exposure to opioids and its use has been proposed to decrease postoperative morphine consumption.

Methods: We conducted a randomized, double-blind, controlled study to evaluate the effect of intravenous (i.v.) ketamine on postoperative pain for 48 h after major ear, nose and throat (ENT) surgery. Thirty-one patients received i.v. ketamine 0.15 mg kg−1 before induction and 2 μg kg−1 min−1 during anaesthesia, and 31 patients were administered placebo in a similar manner. Anaesthesia was standardized with remifentanil and propofol, but without nitrous oxide. Standardized postoperative analgesia included paracetamol, methylprednisolone and morphine administered via a patient controlled analgesia (PCA) device.

Results: Intra-operative remifentanil consumption was not different between the ketamine group (0.25 ± 0.07 μg kg−1 min−1) and the control group (0.22 ± 0.07 μg kg−1 min−1). In the postoperative period, both groups experienced an identical pain course evolution. Cumulative morphine consumption was not significantly different between groups: at 24 h it was 33.3 ± 14.9 with ketamine and 31.9 ± 15.3 mg in controls, at 48 h it was 40.4 ± 20.6 mg with ketamine and 42.5 ± 25.9 mg in controls.

Conclusion: Low-dose ketamine added to a remifentanil-based propofol anaesthesia did not reduce morphine consumption after major ENT surgery.

Type
Original Article
Copyright
© 2005 European Society of Anaesthesiology

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