Literature DB >> 10595867

Rapacuronium bromide: a review of its use in anaesthetic practice.

S V Onrust1, R H Foster.   

Abstract

UNLABELLED: Rapacuronium bromide (rapacuronium) is an aminosteroid, nondepolarising neuromuscular blocking agent (NMBA). At the recommended dose for endotracheal intubation (1.5 mg/kg), an intravenous bolus of rapacuronium has a rapid onset (approximately 1.2 to 1.8 minutes) and short duration of action (10.2 to 16.5 minutes) in adults undergoing elective surgery. Rapacuronium 1.5 mg/kg produced clinically acceptable intubating conditions in 68 to 89% of these patients at about 1 minute after administration. The onset, extent and duration of action and clinical efficacy of an intubating dose of rapacuronium appeared to be similar in the general adult population, adult patients with renal or hepatic dysfunction, patients undergoing Caesarean section, and elderly, paediatric or obese adult patients. Onset time with rapacuronium 1.3 to 2.5 mg/kg (0.9 to 1.8 minutes) was similar to or slower than that with a 1 mg/kg dose of the depolarising NMBA suxamethonium chloride (0.8 to 1.2 minutes). Intubating conditions were clinically acceptable about I minute after administration in 86 to 100% of patients with rapacuronium 1.3 to 2.5 mg/kg compared with in 88 to 97% of patients with suxamethonium chloride 1 or 1.5 mg/kg. Spontaneous recovery was slower with rapacuronium than with suxamethonium chloride, but neostigmine 0.04 or 0.05 mg/kg administered 2 or 5 minutes after rapacuronium 1.3 or 1.5 mg/kg accelerated recovery. In the few available comparative clinical trials, rapacuronium 1.5 mg/kg appeared to have a more rapid onset of action than the nondepolarising NMBAs mivacurium chloride 0.25 mg/kg, rocuronium bromide 0.45 or 0.6 mg/kg or vecuronium bromide 0.07 mg/kg, and a shorter duration of action than rocuronium bromide 0.45 or 0.6 mg/kg or vecuronium bromide 0.07 mg/kg. Additional boluses (< or =3) of rapacuronium 0.5 or 0.55 mg/kg after an intubating bolus of 1.5 mg/kg provided continued skeletal muscle relaxation during short surgical procedures in adult patients. However, these patients may recover more slowly than those who receive a single bolus of the drug. Bronchospasm was the most common treatment-related adverse event with rapacuronium 0.3 to 3 mg/kg (3.4% of adult patients). Tachycardia, injection site reaction and hypotension were also reported in small proportions of patients (1.6, 1.1 and 0.9%). The overall incidence of drug-related adverse events was similar with rapacuronium 1.5 or 2.5 mg/kg or suxamethonium chloride 1 mg/kg (8 vs. 6%) but bronchospasm, tachycardia and injection site reaction tended to occur more often with rapacuronium.
CONCLUSIONS: At the recommended dose of 1.5 mg/kg, the nondepolarising NMBA rapacuronium has a rapid onset and short duration of action. It may provide a nondepolarising alternative to suxamethonium chloride for endotracheal intubation. Rapacuronium may be preferred over rocuronium bromide, vecuronium bromide or mivacurium chloride in this indication.

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Year:  1999        PMID: 10595867     DOI: 10.2165/00003495-199958050-00011

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  44 in total

1.  Relationship between chemical structure and physicochemical properties of series of bulky organic cations and their hepatic uptake and biliary excretion rates.

Authors:  J H Proost; J Roggeveld; J M Wierda; D K Meijer
Journal:  J Pharmacol Exp Ther       Date:  1997-08       Impact factor: 4.030

2.  Effects on laryngeal muscles and intubating conditions with new generation muscle relaxants.

Authors:  C Meistelman
Journal:  Acta Anaesthesiol Belg       Date:  1997

3.  Factors affecting the pharmacokinetic characteristics of rapacuronium.

Authors:  D M Fisher; R Kahwaji; D Bevan; G Bikhazi; R J Fragen; M S Angst; E Ornstein; R S Matteo
Journal:  Anesthesiology       Date:  1999-04       Impact factor: 7.892

4.  Structure-pharmacodynamic-pharmacokinetic relationships of steroidal neuromuscular blocking agents.

Authors:  J M Wierda; J H Proost
Journal:  Eur J Anaesthesiol Suppl       Date:  1995-09

5.  The FDA protects the public by regulating the manufacture of anesthetic agents and the production devices used in anesthetic practice.

Authors:  R F Bedford
Journal:  Anesthesiology       Date:  1995-01       Impact factor: 7.892

Review 6.  Recent advances in neuromuscular blocking agents.

Authors:  R R Bartkowski
Journal:  Am J Health Syst Pharm       Date:  1999-06-01       Impact factor: 2.637

7.  Intramuscular rapacuronium in infants and children: dose-ranging and tracheal intubating conditions.

Authors:  L M Reynolds; A Infosino; R Brown; J Hsu; D M Fisher
Journal:  Anesthesiology       Date:  1999-11       Impact factor: 7.892

8.  Comparison of vecuronium with ORG 9487 and their interaction.

Authors:  S Schiere; L van den Broek; J H Proost; B Molenbuur; J M Wierda
Journal:  Can J Anaesth       Date:  1997-11       Impact factor: 5.063

9.  Pancuronium, gallamine, and d-tubocurarine compared: is speed of onset inversely related to drug potency?

Authors:  A F Kopman
Journal:  Anesthesiology       Date:  1989-06       Impact factor: 7.892

10.  Tracheal intubation without the use of muscle relaxants: a technique using propofol and varying doses of alfentanil.

Authors:  M S Scheller; M H Zornow; L J Saidman
Journal:  Anesth Analg       Date:  1992-11       Impact factor: 5.108

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  2 in total

Review 1.  Newer neuromuscular blocking agents: how do they compare with established agents?

Authors:  H J Sparr; T M Beaufort; T Fuchs-Buder
Journal:  Drugs       Date:  2001       Impact factor: 9.546

Review 2.  Pharmacokinetics and pharmacodynamics of rapacuronium bromide.

Authors:  William J Wight; Peter M C Wright
Journal:  Clin Pharmacokinet       Date:  2002       Impact factor: 6.447

  2 in total

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