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Intravenous administration of tenoxicam 40 mg for post-operative analgesia: A double-blind, placebo-controlled multicentre study

Published online by Cambridge University Press:  16 August 2006

E. P. Vandermeulen
Affiliation:
Department of Anaesthesiology, Universitaire Ziekenhuizen, Katholieke Universiteit Leuven, Herestraat 49, B-3000 Leuven, Belgium
H. Van Aken
Affiliation:
Klinik und Poliklinik für Anästhesiologie und Operative Intensivmedizin, Westfälische Wilhelms Universität, Albert-Schweitzer Straße 33, 48149 Müunster, Deutschland
J. L. Scholtes
Affiliation:
Department of Anaesthesiology, Cliniques Universitaires Saint Luc, Université Catholique de Louvain, Avenue Hippocrate 10-1821, B-1200 Bruxelles
F. Singelyn
Affiliation:
Department of Anaesthesiology, Cliniques Universitaires Saint Luc, Université Catholique de Louvain, Avenue Hippocrate 10-1821, B-1200 Bruxelles
A. Buelens
Affiliation:
BRI (Biometric Research Institute), International n.v., Ragheno Business Centre, Motstraat 54, B-2800 Mechelen
L. Haazen
Affiliation:
N. V. Roche S. A., Rue Dante 75, B-1070 Brussel, Belgium
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Abstract

The analgesic efficacy of tenoxicam, a newer injectable non-steroidal anti-inflammatory drug, for post-operative analgesia after abdominal or orthopaedic surgery in ASA Grade I/II patients is reported. Two hundred and fifty-six patients received a single dose of tenoxicam 40 mg intravenous (i.v.) at the end of surgery and this was repeated 24 h later. These patients were compared, with respect to pain or adverse events, with 258 patients that received placebo. All patients were monitored for the next 72 h. Overall, tenoxicam provided reliable analgesia with comparable pain scores at rest, moving and coughing. The cumulative rescue PCA-morphine consumption was always lower in the tenoxicam treated patients and was most marked at 4 and 24 h after the second injection of tenoxicam. This effect was more pronounced after abdominal surgery. The intravenous administration of tenoxicam was associated with a low incidence of adverse events and a high tolerability.

Type
Original Article
Copyright
1997 European Society of Anaesthesiology

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