Atracurium, pharmacokinetics and metabolites

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منابع مشابه

Pharmacokinetics of atracurium and its metabolites.

The pharmacokinetic profile of atracurium was studied in normal patients and in patients with renal failure, renal-hepatic failure, or hepatic disease. Its short elimination half-life was not significantly altered by renal failure, but in patients with severe liver disease elimination of its metabolites was prolonged, necessitating care during long-term i.v. infusions in patients with hepatic d...

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Pharmacokinetics of atracurium.

Sir,—We congratulate Drs Beetner, Bjorksten and Crankshaw on their description of the pharmacokinetics of atracurium [1]. As they observe correctly, the derivation of pharmacokinetic parameters after a single bolus dose is subject to difficulties because of the presumed degradation of atracurium in sites peripheral to the plasma. In our view, however, the crucial flaw in previous attempts to de...

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Pharmacokinetics of atracurium and laudanosine in patients with hepatic cirrhosis.

The pharmacokinetic profiles of atracurium and one of its derivatives, laudanosine were studied following an i.v. bolus of atracurium 0.6 mg kg-1 administered to eight patients with hepatic cirrhosis and to seven healthy controls. The central volume of distribution of atracurium was greater in the patients with cirrhosis (104.6 ml kg-1) compared with the controls (69.6 ml kg-1) (P less than 0.0...

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Pharmacokinetics and pharmacodynamics of pentoxifylline and metabolites

Pentoxifylline increases erythrocyte flexibility, reduces blood viscosity,and inhibits platelet aggregation and is thus used in the treatment of peripheral vasculardisease. It is transformed into at least seven phase I metabolites, of which two, M1 andM5, are active. The reduction of the keto group of pentoxifylline to a secondary alcoholin M1 takes place chiefly in erythrocytes...

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Pharmacokinetics and pharmacodynamics of atracurium with and without previous suxamethonium administration.

Suxamethonium increases neuromuscular block produced by non-depolarizing agents administered subsequently. To determine if this effect has a pharmacokinetic or pharmacodynamic origin, 18 ASA physical status I or II adults received atracurium 0.2 mg kg-1, with (n = 10) or without (n = 8) previous injection of suxamethonium 1 mg kg-1, during a thiopentone-nitrous oxide-isoflurane (0.5% end-tidal)...

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ژورنال

عنوان ژورنال: Canadian Journal of Anaesthesia

سال: 1989

ISSN: 0832-610X,1496-8975

DOI: 10.1007/bf03010761