Pharmacokinetics of Propofol in Elderly Coronary Artery Bypass Graft Patients under Total Intravenous Anesthesia
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概要
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The present paper investigates the pharmacokinetics of propofol in the plasma of two elderly patients operated on under total intravenous anesthesia using propofol. A 78-year-old (patient A) and a 76-year-old (patient B), both Japanese men with unstable angina pectoris, were operated on for coronary artery bypass grafts. For the induction of anesthesia, 1.5 mg/kg propofol was administered as a single bolus infusion, and anesthesia was maintained using the step-down infusion regimens of propofol. Propofol concentration in the plasma was measured by HPLC with a fluorescence detector. The simulation curves, following the two-compartment model, fitted well to the profiles of the individual data of propofol concentrations in the plasma. When 4mg/kg/h of propofol was administered to both patients while maintaining anesthesia, propofol concentrations in the plasma were maintained at over 1.0 μg/ml. In patient A, the propofol concentration in the plasma was 140 ng/ml at 6 h after the end of the infusion. In patient B, the propofol concentrations in the plasma were 73 ng/ml at 6 h and 35 ng/ml at 12 h after the end of the infusion. The apparent distribution volumes of patients A and B were 1.43 and 1.621/kg, respectively. The half-lives of propofol in the plasma of patients A and B were estimated to be 13.3 and 17.4 min as the a phase, and 10.1 and 10.5 h as the βphase, respectively. In elderly patients with cardiac surgery, the maintenance concentrations of propofol in the plasma were enough to maintain a concentration of 1.0 μg/ml, and the half-life may be longer than previously reported values in adult patients.
- 公益社団法人日本薬学会の論文
- 2002-06-01
著者
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TAKEYAMA MASAHARU
Department of Anesthesiology and Critical Care Medicine, Kagoshima University School of Medicine
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Takeyama Masaharu
Department Of Clinical Pharmacy Oita Medical University
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MORIKAWA Norifumi
Department of Clinical Pharmacotherapy, Division of Clinical Pharmacotherapeutics, Graduate School o
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NOGUCHI Takayuki
Department of Anesthesiology and Intensive Care Medicine, Oita University Faculty of Medicine
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Takeyama Masaharu
Department Of Anesthesiology And Critical Care Medicine Kagoshima University School Of Medicine
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Noguchi T
Sumitomo Pharmaceuticals Research Center
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Noguchi T
Research Center Sumitomo Pharmaceuticals Co. Ltd
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OISHI Kazushige
Department of Anesthesiology, Oita Medical University
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Noguchi Takayuki
Department Of Anesthesiology And Intensive Care Medicine Oita University Faculty Of Medicine
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Noguchi Takayuki
Department Of Anesthesiology Oita Medical University
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Morikawa Norifumi
Department Of Clinical Pharmacotherapy Graduate School Of Biomedical Sciences Hiroshima University
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Oishi Kazushige
Department Of Anesthesiology Oita Medical University
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