• J. Cardiothorac. Vasc. Anesth. · Feb 2003

    Randomized Controlled Trial Comparative Study Clinical Trial

    Comparison of three remifentanil dose-finding regimens for coronary artery surgery.

    • Michael B Howie, Luis G Michelsen, Carl C Hug, David T Porembka, Michael W Jopling, Samuel M Warren, and Soraya Shaikh.
    • Department of Anesthesiology, The Ohio State University Hospitals, Columbus, OH 43210, USA.
    • J. Cardiothorac. Vasc. Anesth. 2003 Feb 1;17(1):51-9.

    ObjectivesTo identify the remifentanil dosing regimen providing safe and optimal anesthetic conditions during coronary artery bypass graft surgery and to evaluate postoperative recovery characteristics.DesignOpen-label, randomized, parallel group.SettingThree centers in the United States.ParticipantsSeventy-two patients with left ventricular stroke volumes >or=50 mL.InterventionsPatients were randomized to remifentanil doses of 1 microg/kg/min (group 1, n = 23); 2 microg/kg/min (group 2, n = 24), or 3 microg/kg/min (group 3, n = 25). Somatic, sympathetic, and hemodynamic responses indicating inadequate anesthesia were treated with bolus doses of remifentanil, 1 to 2 microg/kg, and infusion rate increases, and, if necessary, isoflurane 0.5% to 1.0% was added as a rescue anesthetic. In the intensive care unit, the remifentanil infusion was reset to 1 microg/kg/min, with midazolam administered for supplemental sedation and morphine for analgesia.Measurements And Main ResultsThe durations of anesthesia, surgery, and cardiopulmonary bypass were similar for the 3 study groups. In addition, dose of lorazepam premedication, time to loss of consciousness, preoperative left ventricular ejection fraction, age, weight, and sex were similar for the 3 study groups. Remifentanil alone (infusion and boluses) prevented and controlled all responses to stimulation in 44% of group 3, 37% of group 2 and 9% of group 1 patients intraoperatively. Isoflurane (0.5%-1% inspired) rescue was successful in the remaining patients in each group. Hypotension indicating discontinuation of isoflurane and reductions of remifentanil infusion rates occurred in 64% to 75% of all patients. The optimal range of remifentanil infusion was 2 to 4 microg/kg/min with isoflurane to supplement the opioid. Fifty-one patients (71%) met the criteria for extubation within 6 hours postoperatively; because of surgical practice differences, only 30 patients (59%) were actually extubated.ConclusionsAfter lorazepam premedication, remifentanil infusion (2-4 microg/kg/min) supplemented intermittently with low inspired concentrations of isoflurane provided an effective anesthetic regimen for coronary artery bypass graft surgery. Early extubation times were feasible after remifentanil continuous infusions (1-5 microg/kg/min) used as the primary anesthetic component intraoperatively and for analgesia (Copyright 2003, Elsevier Science (USA). All rights reserved.

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