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Remifentanil and fentanyl during anaesthesia for major abdominal and gynaecological surgery. An open, comparative study of safety and efficacy

Published online by Cambridge University Press:  16 August 2006

J. R. Sneyd
Affiliation:
Department of Anaesthesia, Derriford Hospital, Plymouth, PL6 8DH, Devon, UK
F. Camu
Affiliation:
Academisch Ziekenhuis, Vrije Universitiet Brussel, Laarbeeklaan 101, 1090 Brussels, Belgium
A. Doenicke
Affiliation:
Ludwig-Maximillian-Universitat Pettenkoferstrasse 8a, 80369 Munich, Germany
C. Mann
Affiliation:
Hˆpital de Bicetre, 78 Rue de General Leclerc, Le Kremlin-Bicetre, 94275 France
O. Holgersen
Affiliation:
Vest Agder Sentralsykehus, Kristiansand N-4604, Norway
J. H. J. H. Helmers
Affiliation:
Algemeen Christelijk Ziekenhuis Eemland, Utrechtsweg 160, Amersfoort, 3818ES, the Netherlands
L. Appelgren
Affiliation:
Anaesthetic Department, Sahlgrens Hospital, Goteborg S-413 45, Sweden
D. Noronha
Affiliation:
Medical Statistics, GlaxoWellcome Research & Development, Greenford Road, Greenford, Middlesex UB6 0HE, UK
B. K. Upadhyaya
Affiliation:
CV, CC and Anaesthesia Clinical Development, GlaxoWellcome Research & Development, Greenford Road, Greenford, Middlesex UB6 0HE, UK
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Abstract

Background and objective This open, multicentre study compared the efficacy and safety of remifentanil with fentanyl during balanced anaesthesia with 0.8% isoflurane (end-tidal concentration) for major abdominal and gynaecological surgery, and the efficacy and safety of remifentanil for pain management in the immediate postoperative period.

Methods Two-hundred and eighty-six patients were randomized to receive remifentanil 1 μg kg−1 followed by 0.2 μg kg−1 min−1 (n = 98), remifentanil 2 μg kg−1 followed by 0.4 μg kg−1 min−1 (n = 91) or fentanyl 3 μg kg−1 (n = 97) at induction. Thereafter, the study opioids and isoflurane were titrated to effect during the operation.

Results Compared with fentanyl, remifentanil 2 μg kg−1 followed by 0.4 μg kg −1 min−1 reduced the incidence of response to tracheal intubation (30% vs. 13%, P < 0.01), skin incision (33% vs. 4%, P < 0.001) and skin closure (11% vs. 3%, P< 0.05), respectively. Patients receiving remifentanil 1 μg kg−1 followed by 0.2 μg kg −1 min−1 had fewer responses to skin incision than the fentanyl group (12% vs. 33%, P< 0.001), but the incidences of response to tracheal intubation and skin closure were similar. Significantly fewer patients in both remifentanil groups had ≥ 1 responses to surgical stress intraoperatively compared with fentanyl (68% and 48% vs. 87%, P < 0.003). The mean isoflurane concentrations required were less in both remifentanil groups compared with the fentanyl group (0.1%, P = 0.05). In remifentanil-treated patients, continuation of the infusion at 0.1 μg kg−1 min−1 with titration increments of ± 0.025 μg kg−1 min−1 was effective for the management of immediate postoperative pain prior to transfer to morphine analgesia. However, a high proportion of patients experienced at least moderate pain whilst the titration took place.

Conclusions Anaesthesia combining isoflurane with a continuous infusion of remifentanil was significantly more effective than fentanyl at blunting responses to surgical stimuli. Significantly fewer patients responded to tracheal intubation with remifentanil at 0.4 μg kg−1min−1, supporting the use of a higher initial infusion rate before intubation. Both remifentanil and fentanyl were well-tolerated, with reported adverse events typical of μ-opioid agonists.

Type
Original Article
Copyright
2001 European Society of Anaesthesiology

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