Literature DB >> 8785138

Comparison of the pharmacodynamics and pharmacokinetics of an infusion of cis-atracurium (51W89) or atracurium in critically ill patients undergoing mechanical ventilation in an intensive therapy unit.

A H Boyd1, N B Eastwood, C J Parker, J M Hunter.   

Abstract

We have studied 12 critically ill, sedated patients who required a neuromuscular blocking drug to assist mechanical ventilation in an intensive care unit. Patients were randomized to receive an infusion of cis-atracurium 0.18 mg kg-1 h-1 (group 1, n = 6) or atracurium 0.6 mg kg-1 h-1 (group 2, n = 6) preceded, if necessary, by a bolus dose of 2 x ED95 of the same drug (cis-atracurium 0.1 mg kg-1 or atracurium 0.5 mg kg-1). Neuromuscular block was monitored using an accelerograph and the infusion rate adjusted regularly so that it was possible to detect the first response to train-of-four (TOF) stimulation of the ulnar nerve at the wrist. Blood samples were obtained for estimation of plasma cis-atracurium and laudanosine concentrations (group 1) or the three groups of atracurium isomers and laudanosine (group 2). There was no apparent haemodynamic or allergic response to either drug. The mean infusion time in group 1 was 37.6 h and in group 2, 27.5 h. On termination of the infusion, the time for the TOF ratio to reach 0.7 was similar in the two groups (group 1 = 60 min; group 2 = 62 min). The mean infusion rate of cis-atracurium was 0.19 mg kg-1 h-1 and of atracurium 0.47 mg kg-1 h-1 (expressed as mg of bis-cation): cis-atracurium was 2.5 times more potent than atracurium. Using the NONMEM program, a single compartment pharmacokinetic model was fitted to the plasma concentrations of cis-atracurium and the cis-cis, cis-trans and trans-trans isomers of atracurium. The mean population pharmacokinetic values for cis-atracurium were: volume of distribution (V) = 21,900 (SEM 416) ml; clearance (Cl) = 549 (79) ml min-1; half-life (T1/2) = 27.6 (3.6) min; and for the three groups of atracurium isomers were: cis-cis, V = 15,100 (720) ml, Cl = 449 (42) ml min-1, T1/2 = 23.4 (1.2) min; cis-trans, V = 18,000 (667) ml, Cl = 1070 (43) ml min-1, T1/2 = 11.7 (0.1); trans-trans, V = 13,100 (1280) ml, Cl = 1560 (55) ml min-1, T1/2 = 5.8 (0.4) min. Plasma laudanosine concentrations were lower in the cis-atracurium (peak value 1.3 micrograms ml-1) than in the atracurium (maximum 4.4 micrograms ml-1) group.

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Year:  1996        PMID: 8785138     DOI: 10.1093/bja/76.3.382

Source DB:  PubMed          Journal:  Br J Anaesth        ISSN: 0007-0912            Impact factor:   9.166


  11 in total

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Review 5.  Cisatracurium besilate. A review of its pharmacology and clinical potential in anaesthetic practice.

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Review 7.  Pharmacology, selection and complications associated with neuromuscular blocking drugs in ICU patients.

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8.  Clinical assessment and train-of-four measurements in critically ill patients treated with recommended doses of cisatracurium or atracurium for neuromuscular blockade: a prospective descriptive study.

Authors:  Pierre Bouju; Jean-Marc Tadié; Nicolas Barbarot; Julien Letheulle; Fabrice Uhel; Pierre Fillatre; Guillaume Grillet; Angélique Goepp; Yves Le Tulzo; Arnaud Gacouin
Journal:  Ann Intensive Care       Date:  2017-01-19       Impact factor: 6.925

9.  Compared efficacy and tolerance of the neuromuscular blockade induced by brand-name (Nimbex®) and generic (Cisatrex®) of cisatracurium in mechanically ventilated critically ill patients: a crossover double-blind randomized study.

Authors:  Nesrine Fraj; Khaoula Meddeb; Abdelbaki Azouzi; Sana Romdhani; Helmi Ben Saad; Mohamed Boussarsar
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10.  Pharmacodynamics of cisatracurium in the intensive care unit: an observational study.

Authors:  Eric Dieye; Vincent Minville; Karim Asehnoune; Claude Conil; Bernard Georges; Pierre Cougot; Olivier Fourcade; Jean-Marie Conil
Journal:  Ann Intensive Care       Date:  2014-02-11       Impact factor: 6.925

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