Aim: This study aimed to assess the effect of atropine premedication prior
to flexible bronchoscopy. The rationale for using atropine is that it will
dry secretions and allow a better view of the bronchial tree. There is also
the theoretical benefit of protection against vasovagal episodes and bronc
hospasm.
Methods: Twenty patients were randomised in a double-blind manner to receiv
e either 500 mcg of atropine intramuscularly or 1 mL of 0.9% saline intramu
scularly 30 minutes prior to bronchoscopy. Both groups received a standard
dose of intramuscular pethidine. Variables studied included a pre-procedure
electrocardiograph, a rhythm strip during the procedure, serial measuremen
ts of blood pressure, continuous pulse oximetry, and spirometry pre- and po
st-bronchoscopy. Subjective measures recorded were a secretion score, rated
0-3 by the bronchoscopist using a four point visual analogue scale. A pati
ent questionnaire was designed to establish the presence or absence of symp
toms, including those related to atropine.
Results: There were no significant differences recorded in the duration of
procedure, percentage fall in FEV1, secretion scores, or other physiologica
l measures. The only significant difference between the two groups was dry
mouth in the atropine group (p<0.001). There was a fall in forced vital cap
acity from baseline which was significant in the saline group (p<0.005), an
d not the atropine group, but it was not significant when compared between
groups. A beta(2) adrenergic agonist would, however, be more appropriate to
prevent such a fall in spirometry.
Conclusions: These results fail to demonstrate a benefit of intramuscular a
tropine as premedication for fibreoptic bronchoscopy.