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J. Cardiothorac. Vasc. Anesth. · Feb 1999
Randomized Controlled Trial Clinical TrialDoes sufentanil concentration influence isoflurane requirements during coronary artery bypass grafting?
- I R Thomson, M Moon, R J Hudson, and M Rosenbloom.
- Department of Anesthesia, University of Manitoba, St Boniface General Hospital, Winnipeg, Canada.
- J. Cardiothorac. Vasc. Anesth. 1999 Feb 1;13(1):9-14.
ObjectiveTo search for concentration-related suppression of hemodynamic responsiveness by sufentanil.DesignProspective, randomized, double-blind study.SettingUniversity hospital.ParticipantsPatients undergoing elective coronary artery bypass grafting (CABG).InterventionPatients were assigned to target effect-site sufentanil concentrations of 1.5 ng/mL (group L; n = 14), 3.0 ng/mL (group M; n = 13), or 4.5 ng/mL (group H; n = 12). Sufentanil was administered by computer-assisted continuous infusion. Isoflurane was used to maintain intraoperative hemodynamics near preoperative values.Measurements And Main ResultsHemodynamics, the electroencephalographic spectral edge (SE95), and end-tidal isoflurane concentration (ET-ISO) were measured every 10 to 30 seconds during the prebypass period. Serum sufentanil concentration was measured at intervals. Prebypass serum sufentanil concentrations were stable, averaging 3.0 +/- 0.7, 5.1 +/- 1.1, and 7.1 +/- 1.3 ng/mL in groups L, M, and H, respectively. The groups did not differ with respect to the speed of induction, intraoperative hemodynamics, incidence of isoflurane use, or isoflurane concentrations required. ET-ISO and serum sufentanil levels were not correlated. Among seven group L patients who did not require isoflurane, the average prebypass serum sufentanil concentration ranged from 1.7 to 3.3 ng/mL.ConclusionSufentanil does not induce concentration-related suppression of hemodynamic responsiveness over the range studied. A stable serum sufentanil concentration of 3.0 +/- 0.7 ng/mL induces the maximal opioid effect and need not be exceeded in patients undergoing CABG. A sufentanil concentration of 1.7 ng/mL provides clinically adequate anesthesia without supplementation in some premedicated patients undergoing CABG.
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