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Neostigmine and Edrophonium Antagonism of Varying Intensity Neuromuscular Blockade Induced by Atracurium, Pancuronium, or Vecuronium

 

作者: Stephen Rupp,   Jimmy McChristian,   Ronald Miller,   Jose Taboada,   Roy Cronnelly,  

 

期刊: Anesthesiology  (OVID Available online 1986)
卷期: Volume 64, issue 6  

页码: 711-717

 

ISSN:0003-3022

 

年代: 1986

 

出版商: OVID

 

关键词: Antagonists, neuromuscular relaxants: edrophonium;neostigmine;Neuromuscular relaxants: atracurium;pancuronium;vecuronium

 

数据来源: OVID

 

摘要:

To compare the time course of neostigmine and edrophonium antagonism of varying intensity neuromuscular blockade induced by atracurium, pancuronium, or vecuronium, the authors studied 98 patients anesthetized with nitrous oxide (60%) and halothane or enflurane. Neuromuscular blockade, as monitored by single stimulusinduced twitch tension (TT), was antagonized at varying degrees of spontaneous recovery (2–80% of control TT). Time to antagonism (time from injection of neostigmine or edrophonium to 90% recovery of control TT) was not different between edrophonium, 0.5 mg/kg, and neostigmine, 0.04 mg/kg, when spontaneous recovery had been allowed to occur to at least 11 % of control TT prior to antagonist administration (P> 0.05). For profound neuromuscular blockade (TT ≤ 10% of control) induced by pancuronium or vecuronium, time (mean ± SD) to antagonism with neostigmine, 0.04 mg/kg, was 7.0 ± 2.2 min and 5.6 ± 1.7 min, respectively, while the same for edrophonium, 0.5 mg/kg, was 20.0 ± 8.0 min and 15.0 ± 12.5 min, respectively (P< 0.05). Time to antagonism of profound atracuriuminduced neuromuscular blockade was 8.5 ± 3.3 min for neostigmine, 0.04 mg/kg, and 9.8 ± 7.0 min for edrophonium, 0.5 mg/kg, (P> 0.05). For profound vecuronium- and pancuronium-induced neuromuscular blockade, time to antagonism by edrophonium, 1.0 mg/ kg, was 4.6 ± 3.0 min and 3.9 ± 1.6 min respectively. The authors conclude that neostigmine, 0.04 mg/kg, antagonizes neuromuscular blockade within 12 min when TT is greater than 2% of control at time of reversal. When TT is greater than 10% of control, edrophonium, 0.5 mg/kg, produces similar time to antagonism. However, when TT is 2–10% of control, the dose of edrophonium dose should be at least 1.0 mg/kg to be as rapid as neostigmine, 0.04 mg/kg.

 

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