Pharmacokinetics and pharmacodynamics of propofol infusions during general anesthesia
The pharmacokinetic and pharmacodynamic properties of propofol were studied in 50 surgical patients. Propofol was administered as a bolus dose, 2 mg/kg iv, followed by a variable-rate infusion, 0-20 mg/min, and intermittent supplemental boluses, 10-20 mg iv, as part of a general anesthetic technique...
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Veröffentlicht in: | Anesthesiology (Philadelphia) 1988-09, Vol.69 (3), p.348-356 |
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description | The pharmacokinetic and pharmacodynamic properties of propofol were studied in 50 surgical patients. Propofol was administered as a bolus dose, 2 mg/kg iv, followed by a variable-rate infusion, 0-20 mg/min, and intermittent supplemental boluses, 10-20 mg iv, as part of a general anesthetic technique that included nitrous oxide, meperidine, and muscle relaxants. For a majority of the patients (n = 30), the pharmacokinetics of propofol were best described by a two-compartment model. The propofol mean total body clearance rate was 2.09 +/- 0.65 1/min (mean +/- SD), the volume of distribution at steady state was 159 +/- 57 l, and the elimination half-life was 116 +/- 34 min. Elderly patients (patients older than 60 yr vs. those younger than 60 yr) had significantly decreased clearance rates (1.58 +/- 0.42 vs. 2.19 +/- 0.64 l/min), whereas women (vs. men) had greater clearance rates (33 +/- 8 vs. 26 +/- 7 l.kg-1.min-1) and volumes of distribution (2.50 +/- 0.81 vs. 2.05 +/- 0.65 l/kg). Patients undergoing major (intraabdominal) surgery had longer elimination half-life values (136 +/- 40 vs. 108 +/- 29 min). Patients required an average blood propofol concentration of 4.05 +/- 1.01 micrograms/ml for major surgery and 2.97 +/- 1.07 micrograms/ml for nonmajor surgery. Blood propofol concentrations at which 50% of patients (EC50) were awake and oriented after surgery were 1.07 and 0.95 microgram/ml, respectively. Psychomotor performance returned to baseline at blood propofol concentrations of 0.38-0.43 microgram/ml (EC50). This clinical study demonstrates the feasibility of performing pharmacokinetic and pharmacodynamic analyses when complex infusion and bolus regimens are used for administering iv anesthetics. |
doi_str_mv | 10.1097/00000542-198809000-00011 |
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A ; SHAFER, S. L ; WHITE, P. F</creator><creatorcontrib>SHAFER, A ; DOZE, V. A ; SHAFER, S. L ; WHITE, P. F</creatorcontrib><description>The pharmacokinetic and pharmacodynamic properties of propofol were studied in 50 surgical patients. Propofol was administered as a bolus dose, 2 mg/kg iv, followed by a variable-rate infusion, 0-20 mg/min, and intermittent supplemental boluses, 10-20 mg iv, as part of a general anesthetic technique that included nitrous oxide, meperidine, and muscle relaxants. For a majority of the patients (n = 30), the pharmacokinetics of propofol were best described by a two-compartment model. The propofol mean total body clearance rate was 2.09 +/- 0.65 1/min (mean +/- SD), the volume of distribution at steady state was 159 +/- 57 l, and the elimination half-life was 116 +/- 34 min. Elderly patients (patients older than 60 yr vs. those younger than 60 yr) had significantly decreased clearance rates (1.58 +/- 0.42 vs. 2.19 +/- 0.64 l/min), whereas women (vs. men) had greater clearance rates (33 +/- 8 vs. 26 +/- 7 l.kg-1.min-1) and volumes of distribution (2.50 +/- 0.81 vs. 2.05 +/- 0.65 l/kg). Patients undergoing major (intraabdominal) surgery had longer elimination half-life values (136 +/- 40 vs. 108 +/- 29 min). Patients required an average blood propofol concentration of 4.05 +/- 1.01 micrograms/ml for major surgery and 2.97 +/- 1.07 micrograms/ml for nonmajor surgery. Blood propofol concentrations at which 50% of patients (EC50) were awake and oriented after surgery were 1.07 and 0.95 microgram/ml, respectively. Psychomotor performance returned to baseline at blood propofol concentrations of 0.38-0.43 microgram/ml (EC50). 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A</creatorcontrib><creatorcontrib>SHAFER, S. L</creatorcontrib><creatorcontrib>WHITE, P. F</creatorcontrib><title>Pharmacokinetics and pharmacodynamics of propofol infusions during general anesthesia</title><title>Anesthesiology (Philadelphia)</title><addtitle>Anesthesiology</addtitle><description>The pharmacokinetic and pharmacodynamic properties of propofol were studied in 50 surgical patients. Propofol was administered as a bolus dose, 2 mg/kg iv, followed by a variable-rate infusion, 0-20 mg/min, and intermittent supplemental boluses, 10-20 mg iv, as part of a general anesthetic technique that included nitrous oxide, meperidine, and muscle relaxants. For a majority of the patients (n = 30), the pharmacokinetics of propofol were best described by a two-compartment model. The propofol mean total body clearance rate was 2.09 +/- 0.65 1/min (mean +/- SD), the volume of distribution at steady state was 159 +/- 57 l, and the elimination half-life was 116 +/- 34 min. Elderly patients (patients older than 60 yr vs. those younger than 60 yr) had significantly decreased clearance rates (1.58 +/- 0.42 vs. 2.19 +/- 0.64 l/min), whereas women (vs. men) had greater clearance rates (33 +/- 8 vs. 26 +/- 7 l.kg-1.min-1) and volumes of distribution (2.50 +/- 0.81 vs. 2.05 +/- 0.65 l/kg). Patients undergoing major (intraabdominal) surgery had longer elimination half-life values (136 +/- 40 vs. 108 +/- 29 min). Patients required an average blood propofol concentration of 4.05 +/- 1.01 micrograms/ml for major surgery and 2.97 +/- 1.07 micrograms/ml for nonmajor surgery. Blood propofol concentrations at which 50% of patients (EC50) were awake and oriented after surgery were 1.07 and 0.95 microgram/ml, respectively. Psychomotor performance returned to baseline at blood propofol concentrations of 0.38-0.43 microgram/ml (EC50). This clinical study demonstrates the feasibility of performing pharmacokinetic and pharmacodynamic analyses when complex infusion and bolus regimens are used for administering iv anesthetics.</description><subject>Adult</subject><subject>Anesthesia, General - methods</subject><subject>Anesthetics - administration & dosage</subject><subject>Anesthetics - pharmacokinetics</subject><subject>Anesthetics - pharmacology</subject><subject>Anesthetics. Neuromuscular blocking agents</subject><subject>Biological and medical sciences</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Drug Evaluation</subject><subject>Half-Life</subject><subject>Humans</subject><subject>Infusions, Intravenous</subject><subject>Medical sciences</subject><subject>Neuropharmacology</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenols - administration & dosage</subject><subject>Phenols - pharmacokinetics</subject><subject>Phenols - pharmacology</subject><subject>Propofol</subject><subject>Psychomotor Performance - drug effects</subject><subject>Time Factors</subject><issn>0003-3022</issn><issn>1528-1175</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UMtOwzAQtBColMInIOWAuAXsOI7tI6p4SZXgQM_Rxo_WkMTBbg78PS4NXcla7eyMd3cQygi-I1jye7wPVhY5kUJgmYo8PUJO0JywQuSEcHaK5gmjOcVFcY4uYvxMJWdUzNCMFhWRrJyj9fsWQgfKf7ne7JyKGfQ6GyZQ__TQ7UFvsyH4wVvfZq63Y3S-j5keg-s32cb0JkCblCbutiY6uERnFtporqa8QOunx4_lS756e35dPqxyVTK2y4EzWWmNlVXCNkUjoSEMk6aqpGC6rJQujCINxU1lKJRKMlxgobQmwMDihi7Q7eHftNz3mKbXnYvKtG1axY-x5qJMx_MyEcWBqIKPMRhbD8F1EH5qguu9o_W_o_XR0frP0SS9nmaMTWf0UThZmPo3Ux-igtYG6JWLRxrn6RYu6S8yc3_o</recordid><startdate>19880901</startdate><enddate>19880901</enddate><creator>SHAFER, A</creator><creator>DOZE, V. A</creator><creator>SHAFER, S. L</creator><creator>WHITE, P. F</creator><general>Lippincott</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19880901</creationdate><title>Pharmacokinetics and pharmacodynamics of propofol infusions during general anesthesia</title><author>SHAFER, A ; DOZE, V. A ; SHAFER, S. L ; WHITE, P. F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-a7596dd0cfc8fb2b9ab1501b66985d46cd2ec1b30b6e3a4c950208cdd1a5af0b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1988</creationdate><topic>Adult</topic><topic>Anesthesia, General - methods</topic><topic>Anesthetics - administration & dosage</topic><topic>Anesthetics - pharmacokinetics</topic><topic>Anesthetics - pharmacology</topic><topic>Anesthetics. Neuromuscular blocking agents</topic><topic>Biological and medical sciences</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Drug Evaluation</topic><topic>Half-Life</topic><topic>Humans</topic><topic>Infusions, Intravenous</topic><topic>Medical sciences</topic><topic>Neuropharmacology</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenols - administration & dosage</topic><topic>Phenols - pharmacokinetics</topic><topic>Phenols - pharmacology</topic><topic>Propofol</topic><topic>Psychomotor Performance - drug effects</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SHAFER, A</creatorcontrib><creatorcontrib>DOZE, V. A</creatorcontrib><creatorcontrib>SHAFER, S. L</creatorcontrib><creatorcontrib>WHITE, P. 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F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pharmacokinetics and pharmacodynamics of propofol infusions during general anesthesia</atitle><jtitle>Anesthesiology (Philadelphia)</jtitle><addtitle>Anesthesiology</addtitle><date>1988-09-01</date><risdate>1988</risdate><volume>69</volume><issue>3</issue><spage>348</spage><epage>356</epage><pages>348-356</pages><issn>0003-3022</issn><eissn>1528-1175</eissn><coden>ANESAV</coden><abstract>The pharmacokinetic and pharmacodynamic properties of propofol were studied in 50 surgical patients. Propofol was administered as a bolus dose, 2 mg/kg iv, followed by a variable-rate infusion, 0-20 mg/min, and intermittent supplemental boluses, 10-20 mg iv, as part of a general anesthetic technique that included nitrous oxide, meperidine, and muscle relaxants. For a majority of the patients (n = 30), the pharmacokinetics of propofol were best described by a two-compartment model. The propofol mean total body clearance rate was 2.09 +/- 0.65 1/min (mean +/- SD), the volume of distribution at steady state was 159 +/- 57 l, and the elimination half-life was 116 +/- 34 min. Elderly patients (patients older than 60 yr vs. those younger than 60 yr) had significantly decreased clearance rates (1.58 +/- 0.42 vs. 2.19 +/- 0.64 l/min), whereas women (vs. men) had greater clearance rates (33 +/- 8 vs. 26 +/- 7 l.kg-1.min-1) and volumes of distribution (2.50 +/- 0.81 vs. 2.05 +/- 0.65 l/kg). Patients undergoing major (intraabdominal) surgery had longer elimination half-life values (136 +/- 40 vs. 108 +/- 29 min). Patients required an average blood propofol concentration of 4.05 +/- 1.01 micrograms/ml for major surgery and 2.97 +/- 1.07 micrograms/ml for nonmajor surgery. Blood propofol concentrations at which 50% of patients (EC50) were awake and oriented after surgery were 1.07 and 0.95 microgram/ml, respectively. Psychomotor performance returned to baseline at blood propofol concentrations of 0.38-0.43 microgram/ml (EC50). This clinical study demonstrates the feasibility of performing pharmacokinetic and pharmacodynamic analyses when complex infusion and bolus regimens are used for administering iv anesthetics.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott</pub><pmid>3261954</pmid><doi>10.1097/00000542-198809000-00011</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Anesthesia, General - methods Anesthetics - administration & dosage Anesthetics - pharmacokinetics Anesthetics - pharmacology Anesthetics. Neuromuscular blocking agents Biological and medical sciences Chromatography, High Pressure Liquid Drug Evaluation Half-Life Humans Infusions, Intravenous Medical sciences Neuropharmacology Pharmacology. Drug treatments Phenols - administration & dosage Phenols - pharmacokinetics Phenols - pharmacology Propofol Psychomotor Performance - drug effects Time Factors |
title | Pharmacokinetics and pharmacodynamics of propofol infusions during general anesthesia |
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