Antagonism of profound neuromuscular blockade induced by vecuronium or atracurium. Comparison of neostigmine with edrophonium.

The effectiveness of neostigmine 0.07 mg kg-1 and edrophonium 0.8 mg kg-1 as antagonists of profound neuromuscular blockade induced by vecuronium 0.1 mg kg-1 or atracurium 0.5 mg kg-1 was studied in 59 healthy patients. The antagonists were administered 5 min after total ablation of the twitch response and the end-point of recovery was a train-of-four ratio of 70%. In 30 patients given vecuronium the mean time to reach this point (duration TOF70) was 66.7 min in the control group (no antagonist), 43.5 min in the group given neostigmine and 59.8 min in the group given edrophonium. The duration TOF70 was shorter in the neostigmine group than in the control (P less than 0.01) and edrophonium (P less than 0.01) groups. The duration TOF70 did not differ from control in the edrophonium group. In 29 patients given atracurium, the durations TOF70 were 66.4, 44.1 and 54.9 min in the control, neostigmine and edrophonium groups, respectively. The durations TOF70 in the neostigmine (P less than 0.01) and edrophonium (P less than 0.01), groups were shorter than control. The duration TOF70 of the neostigmine group was shorter than in the edrophonium group (P less than 0.01). These results show that profound neuromuscular blockade cannot be rapidly antagonized by either of these two agents, but if reversal is required under these circumstances, neostigmine would be the more effective drug.

[1]  Bowman Wc The neuromuscular junction: recent developments. , 1985 .

[2]  Ronald D. Miller,et al.  NEOSTIGMINE ANTAGONIZES A PROFOUND NEUROMUSCULAR BLOCKADE MORE RAPIDLY THAN EDROPHONIUM , 1984 .

[3]  J. Williams,et al.  Recovery characteristics following antagonism of atracurium with neostigmine or edrophonium. , 1984, British journal of anaesthesia.

[4]  F. Donati,et al.  Twitch Depression and Train‐of–Four Ratio after Antagonism of Pancuronium with Edrophonium, Neostigmine, or Pyridostigmine , 1983, Anesthesia and analgesia.

[5]  R. Fragen,et al.  Clinical comparison of atracurium and vecuronium (Org NC 45). , 1983, British journal of anaesthesia.

[6]  Baird Wl,et al.  Reversal of atracurium with edrophonium. , 1983 .

[7]  S. Ágoston,et al.  Age-dependent dose-response relationship of ORG NC 45 in anaesthetized patients. , 1983, British journal of anaesthesia.

[8]  R. Miller,et al.  Edrophonium: Duration of Action and Atropine Requirement in Humans during Halothane Anesthesia , 1982, Anesthesiology.

[9]  P. Lilleaasen,et al.  Onset time and duration of action for atracurium, Org NC45 and pancuronium. , 1982, British journal of anaesthesia.

[10]  W. Kerr,et al.  Some actions of Org NC 45 and of edrophonium in the anaesthetized cat and in man. , 1982, British journal of anaesthesia.

[11]  D. Stanski,et al.  Pharmacokinetics of Edrophonium and Neostigmine When Antagonizing d‐Tubocurarine Neuromuscular Blockade in Man , 1981, Anesthesiology.

[12]  D. Bevan,et al.  Neostigmine, Pyridostigmine, and Edrophonium as Antagonists of Pancuronium , 1980, Anesthesiology.

[13]  D. Stanski,et al.  PHARMACOKINETICS OF EDROPHONIUM IN PATIENTS WITHOUT RENAL FUNCTION , 1980 .

[14]  Aaron F. Kopman Edrophonium Antagonism of Pancuronium‐induced Neuromuscular Blockade in Man: A Reappraisal , 1979, Anesthesiology.

[15]  D. Bevan Reversal of pancuronium with edrophonium , 1979, Anaesthesia.

[16]  E. Eger,et al.  Comparative Times to Peak Effect and Durations of Action of Neostigmine and Pyridostigmine , 1974, Anesthesiology.

[17]  L. Blaber,et al.  The mechanism of the facilitatory action of edrophonium in cat skeletal muscle , 1972, British journal of pharmacology.