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Institutes of Anesthesiology and Clinical Pharmacology, State University of Groningen, The Netherlands, the Department of Anesthesiology, C.H.U. Pitié Salpètrière, Paris, France, and the Department of Anesthesiology, University Hospital, Vienna, Austria.
Abstract
The effect and plasma concentrations of vecuronium bromide were measured in normal patients after an intravenous dose of 50, 100, or 150 µg/kg and in patients with renal failure after 50 or 100 µg/kg. Urinary excretion of vecuronium was studied in normal patients after the 150 µg/kg dose. Pharmacokinetic parameters of patients with or without renal failure were similar. No metabolites of vecuronium were found in the plasma. Twenty percent of vecuronium was excreted unchanged in the urine; 5% as the 3-hydroxy derivative. No other metabolites of vecuronium were found in the urine. Increasing doses of vecuronium shortened the onset, but prolonged the duration of action and the recovery rate, to a similar extent in Patients with or without renal failure. It was concluded that the disposition of vecuronium was best described by a three compartment model. Both the disposition and the effect of vecuronium are only marginally disturbed by renal failure.
Key Words: NEUROMUSCULAR RELAXANTS—vecuronium
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