• Anasthesiol Intensivmed Notfallmed Schmerzther · Apr 2001

    Randomized Controlled Trial Comparative Study Clinical Trial

    [Ropivacaine 0.2% versus bupivacaine 0.125% plus sufentanil for continuous peridural analgesia following extended abdominal operations].

    • M A Burmeister, A Gottschalk, S Wilhelm, F Schroeder, C Becker, and T Standl.
    • Klinik und Poliklinik für Anästhesiologie, Universitätsklinikum Hamburg-Eppendorf. burmeister@uke.uni-hamburg.de
    • Anasthesiol Intensivmed Notfallmed Schmerzther. 2001 Apr 1; 36 (4): 219-23.

    ObjectiveAn improved opioid-free analgesia concept using thoracic epidural anlgesia with a low concentrated local anaesthetic alone could be of practical interest for hospitals which are unable to guarantee continuous monitoring on the wards.MethodsWe have compared in a prospective, randomized, double-blind study, the analgesic effects and side effects of ropivacaine 0.2% (Group 1) with bupivacaine 0.125% plus 0.5 microgram ml-1 sufentanil (Group 2) via a thoracic epidural catheter during the first 24 hours after major abdominal surgery in 28 gynaecological tumour patients. Assessments were performed 8, 12, 16, 20 and 24 hours after surgery.ResultsNo differences were seen in duration of surgery, intraoperative opioid and supplemental analgesic requirements. As a main result VAS values for pain during mobilisation were higher in Group 1 when compared with Group 2 (p < 0.01) after 20 and 24 hours of continuous epidural infusion (10 ml h-1) whereas VAS values at rest were comparable (p < 0.1) at all measurepoints. Intensity of motor block and side effects did not differ between groups.ConclusionThe present study shows that continuous epidural infusion of 0.2% ropivacaine alone provides comparable analgesia at rest, but less profound pain relief during mobilisation within the first 24 hours after major abdominal surgery than bupivacaine 0.125% with sufentanil.

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