Why the study?
Does split-dose atropine compared to single-dose glycopyrrolate (both with neostigmine) affect heart rate, salivation, arousal time, or arrhythmias during reversal of gallamine-induced neuromuscular blockade in patients undergoing gynaecological surgery?
Does split-dose atropine compared to single-dose glycopyrrolate (both with neostigmine) affect heart rate, salivation, arousal time, or arrhythmias during reversal of gallamine-induced neuromuscular blockade in patients undergoing gynaecological surgery?
Split-dose atropine provides similar chronotropic effects for reversal of neuromuscular blockade as glycopyrrolate but is associated with a higher risk of cardiac arrhythmias, suggesting it should be avoided in patients with cardiac disease.
Split-dose atropine increases arrhythmia risk versus glycopyrrolate during neostigmine reversal; supports preferring glycopyrrolate in cardiac patients.
The effects of a split-dose of atropine sulphate versus a single dose of glycopyrrolate given with neostigmine for the reversal of gallamine-induced neuromuscular blockade were studied in 55 patients undergoing gynaecological surgery. The patients were randomized to receive either a single dose of glycopyrrolate (7 micrograms.kg-1) or two doses of atropine (8 micrograms.kg-1 each), given with an interval of 1 min. There were no differences between the two methods with respect to percentage heart rate changes, salivation or arousal time. Four patients demonstrated cardiac arhythmias in the atropine group, whereas none occurred in the glycopyrrolate group (P less than 0.05). It is concluded that a split-dose of atropine has similar chronotropic effects to a single dose of glycopyrrolate for the reversal of gallamine-induced neuromuscular blockade. However, the finding of a higher incidence of cardiac arrhythmias in the atropine group suggests that this reversal regime should be reserved for patients without cardiac disease.
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Wetterslev et al. (1991) studied this question.
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