Priming with Atracurium

Priming with atracurium was evaluated by dividing 39 patients into 2 groups. All received 0.2 mg IV glycopyrrolate and fentanyl, 50 μg IV. Group 1 received saline, group 2 received 0.06 mg/kg atracurium and a stop watch was started. After 3.5 min the patients were asked to lift their heads and maximum negative inspiratory pressure (MIP) was measured. Anesthesia then commenced with thiorpental and a twitch monitor was applied to the ulnar nerve. At 5 min group 1 received 0.36 mg/kg atracurium and group 2 was given 0.30 mg/kg atracurium. At 6.5 min intubation was accomplished in all but one patient in group 1 and all but one in group 2. Mean T4/T1 ratios at 90 sec were 0.73 in group 1 and 0.51 in group 2. This difference was statistically significant (P < 0.001). Bucking on the endotracheal tube occurred in 72% of patients in group 1 and 62% of those in group 2 (not significant). Intubating conditions were “excellent” in 56% of those in group 1 and 75% in group 2 (not significant). “Good” conditions were seen in 33% of group 1 and 15% of group 2 patients (not significant). “Fair” conditions were noted in 6% of patients in group 1 and 5% of group 2 patients (not significant). The time to maximum twitch depression was 11.3 min and 11.5 min in groups 1 and 2 respectively (not significant). All patients in group 1 could sustain head lift whereas four patients in group 2 could not (not significant). A decrease in MIP was noted in 38% of patients in group 2, but MIP was not decreased in those in group 1. This difference was statistically significant (P < 0.005). We conclude that priming with atracurium, although providing a small improvement in T4/T1 ratio at intubation, does not significantly improve intubating conditions. It is complex, time consuming, is not well tolerated, and may put patients at risk for aspiration.

[1]  G. Weinberg,et al.  Single versus divided doses of atracurium: does 0.05 + 0.10 equal 0.15? , 1986, Anesthesiology.

[2]  G. Lavery,et al.  Atracurium in clinical anaesthesia: effect of dosage on onset, duration and conditions for tracheal intubation , 1985, Anaesthesia.

[3]  R. Miller,et al.  Clinical Pharmacology of Vecuronium and Atracurium , 1984, Anesthesiology.

[4]  H. Nagashima,et al.  FACILITATION OF RAPID ENDOTRACHEAL INTUBATION WITH ATRACURIUM , 1984 .

[5]  C. Lennmarken,et al.  Partial Curarization in the Postoperative Period , 1984, Acta anaesthesiologica Scandinavica.

[6]  F. Foldes Rapid tracheal intubation with non-depolarizing neuromuscular blocking drugs: the priming principle. , 1984, British journal of anaesthesia.

[7]  J. Viby-Mogensen,et al.  Precurarization ‐ a Hazard to the Patient? , 1984, Acta anaesthesiologica Scandinavica.

[8]  R. Katz,et al.  Atracurium for intubation in man. A clinical and electromyographic study. , 1984, Anaesthesia.

[9]  O. Kemmotsu,et al.  Intubation conditions after atracurium and suxamethonium. , 1983, British journal of anaesthesia.

[10]  R. Holle,et al.  RECOVERY OF AIRWAY PROTECTION IN HUMANS AFTER PARALYSIS WITH CURARE , 1982 .

[11]  R. Scott,et al.  Atracurium: its speed of onset. A comparison with suxamethonium. , 1982, British journal of anaesthesia.

[12]  H. H. Ali,et al.  Clinical Pharmacology of Atracurium Besylate (BW 33A): A New Non‐depolarizing Muscle Relaxant , 1982, Anesthesia and analgesia.

[13]  J. Bevan Suxamethonium , 1989 .

[14]  J. Viby-Mogensen,et al.  Residual curarization in the recovery room. , 1979, Anesthesiology.

[15]  H. H. Ali,et al.  Spontaneous Recovery From Nondepolarizing Neuromuscular Blockade: Correlation Between Clinical and Evoked Responses , 1977, Anesthesia and analgesia.

[16]  G. Gronert,et al.  Pathophysiology of hyperkalemia induced by succinylcholine. , 1975, Anesthesiology.

[17]  M Lippmann,et al.  An unusual sensitivity to d-tubocurarine. , 1974, Anesthesiology.

[18]  W. Paton,et al.  The margin of safety of neuromuscular transmission , 1967, The Journal of physiology.