Sufentanil disposition during cardiopulmonary bypass

26Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

This article is free to access.

Abstract

In order to investigate the ability of a computer-assisted continuous infusion (CACI) system to maintain constant plasma levels of sufentanil during cardiopulmonary bypass (CPB) using pharmacokinetic data derived from healthy surgical patients to determine the infusion rate, ten patients were anaesthetized with diazepam, enfturane and oxygen until ten minutes prior to the expected time of initiation of CPB. At that point, an infusion of sufentanil, aimed to reach a central compartment concentration of 5 ng-ml-1, was started via CACI. Plasma concentrations of sufentanil, haematocrit, total protein and albumin concentrations, and nasopharyngeal and CPB inflow temperatures were obtained at predetermined intervals before and up to 90 min after the initiation of CPB. Plasma concentrations of sufentanil reached 3.8 ± 0.4 ng-ml-1 before CPB and approached the 5.0 ng-m-1 set point (4.7 ± 0.4 ng-m-1) over the 90 min of CPB. In conclusion, our results show that it is possible to obtain stable plasma levels of sufentanil on CPB using a pharmacokinetically driven infusion scheme; however, our data suggest that use of such a system may lead to accumulation of drug during CPB. © 1987 Canadian Anesthesiologists.

Cite

CITATION STYLE

APA

Flezzani, P., J.Alvis, M., Jacobs, J. R., Schilling, Bai, S., & Reves, J. G. (1987). Sufentanil disposition during cardiopulmonary bypass. Canadian Journal of Anaesthesia, 34(6), 566–569. https://doi.org/10.1007/BF03010512

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free