Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/14745
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Type: Journal article
Title: Epinephrine, norepinephrine and dopamine infusions decrease propofol concentrations during continuous propofol infusion in an ovine model
Author: Myburgh, J.
Upton, R.
Grant, C.
Martinez, A.
Citation: Intensive Care Medicine, 2001; 27(1):276-282
Publisher: Springer-Verlag
Issue Date: 2001
ISSN: 0342-4642
1432-1238
Abstract: Objective: To determine the effects of exogenous ramped infusions of epinephrine, norepinephrine and dopamine on arterial and effluent brain blood concentrations of propofol under steady state intra venous anesthesia. Design: Prospective, randomized animal study. Setting: University research laboratory. Subjects: Five adult female merino sheep. Interventions: Induction (5 mg/kg) and continuous infusion of propofol (15 mg/min) with controlled mechanical ventilation to maintain PaCO240 mmHg. After 1 h of continuous anesthesia, each animal randomly received ramped infusions of epinephrine, norepinephrine (10, 20 40 μg/min) and dopamine (10, 20, 40 μg.kg.min) in 3 x 5 min intervals followed by a 30-min washout period. Measurements: Arterial and sagittal sinus whole blood for determination of propofol concentrations using high-pressure liquid chromatography. Cardiac output using a thermodilution method. Level of consciousness using an observational scale. Main results: All three drugs significantly and transiently increased cardiac output in a dose-dependent fashion to a maximum of 146-169% of baseline. Baseline arterial and sagittal sinus propofol concentrations were not statistically different prior to catecholamine infusions. All three drugs significantly reduced mean arterial propofol concentrations (95 % CI, p < 0.05): epinephrine to 41.8 % of baseline (11.4-72), norepinephrine to 63 % (27-99) and dopamine to 52.9% (18.5-87.3). There were parallel reductions of concentrations in sagittal sinus blood leaving the brain. The lowest blood concentrations were associated with emergence from anesthesia. Arterial concentrations were inversely related to the simultaneously determined cardiac output (r2 = 0.74, p < 0.0001). Comparison of the data with the predictions of a previously developed recirculatory model of propofol disposition in sheep showed the data were consistent with a mechanism based on increased first pass dilution and clearance of propofol secondary to the increased cardiac output. Conclusions: Catecholamines produced circulatory changes that reversed propofol anesthesia. These observations have potential clinical implications for the use of propofol in hyperdynamic circulatory conditions, either induced by exogenous catecholamine infusions or pathological states.
Keywords: Animals; Sheep; Epinephrine; Norepinephrine; Dopamine; Propofol; Anesthetics, Intravenous; Cardiac Output; Metabolic Clearance Rate; Drug Therapy, Combination; Linear Models; Prospective Studies; Random Allocation; Consciousness; Drug Antagonism; Models, Biological; Female
RMID: 0020010729
DOI: 10.1007/s001340000793
Appears in Collections:Anaesthesia and Intensive Care publications

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