2002
DOI: 10.1177/0310057x0203000505
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Remifentanil Concentration during Target-controlled Infusion of Propofol

Abstract: After institutional approval and with written informed consent, eight surgical patients were infused intravenously with remifentanil at 250 ng.kg lean body mass (LBM)-1 .min-1 for 30 min. Cardiovascular and respiratory parameters were recorded and arterial blood samples were taken at regular intervals. In each patient, the same protocol was repeated 40 min later during propofol infused to a target concentration of 3.0 µg.ml-1. Blood concentrations of remifentanil and propofol were assayed using capillary gas c… Show more

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Cited by 14 publications
(4 citation statements)
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“…As a result, there is a possibility of opioid overdose during the induction period of MAC. Moreover, the presence of propofol in the body could result in a significantly greater remifentanil concentration compared with remifentanil infusion alone [7]. For these reasons, the target concentration must be carefully selected to avoid overdose of remifentanil.…”
Section: Discussionmentioning
confidence: 99%
“…As a result, there is a possibility of opioid overdose during the induction period of MAC. Moreover, the presence of propofol in the body could result in a significantly greater remifentanil concentration compared with remifentanil infusion alone [7]. For these reasons, the target concentration must be carefully selected to avoid overdose of remifentanil.…”
Section: Discussionmentioning
confidence: 99%
“…Remifentanil is rapidly metabolized to an inactive metabolite (remifentanil acid) by plasma and tissue esterases, and it is eliminated completely by tissue esterases in 9-10 minutes after administration. [28][29][30] Due to its rapid metabolism and elimination, it does not accumulate even after prolonged use.…”
Section: Mechanisms Of Action Metabolism and Pharmacokinetic Profilementioning
confidence: 99%
“…As a pure m-receptor agonist drug, it retains all of the pharmacodynamic properties of its class. The pharmacokinetics of remifentanil have been extensively studied because of its unique features, including rapid onset of effect (approximately 1 min), rapid degradation by plasma and tissue esterase to inactive metabolites, and a constant context-sensitive half-life of approximately 3 min with a T 1/2 Keo (the time required for the biophase concentration to reach 50% of the plasma concentration) of 1.3 min [25][26][27]. Therefore, it does not accumulate even after prolonged administration.…”
Section: Remifentanilmentioning
confidence: 99%