Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Observational Study
. 2013 Jul;14(6):e289-97.
doi: 10.1097/PCC.0b013e31828a8624.

The effect of atropine on rhythm and conduction disturbances during 322 critical care intubations

Affiliations
Observational Study

The effect of atropine on rhythm and conduction disturbances during 322 critical care intubations

Peter Jones et al. Pediatr Crit Care Med. 2013 Jul.

Abstract

Objectives: Our objectives were to describe the prevalence of arrhythmia and conduction abnormalities before critical care intubation and to test the hypothesis that atropine had no effect on their prevalence during intubation.

Design: Prospective, observational study.

Setting: PICU and pediatric/neonatal intensive care transport.

Subjects: All children of age less than 8 years intubated September 2007-2009. Subgroups of intubations with and without atropine were analyzed.

Intervention: None.

Measurement and main results: A total of 414 intubations were performed in the study period of which 327 were available for analysis (79%). Five children (1.5%) had arrhythmias prior to intubation and were excluded from the atropine analysis. Atropine was used in 47% (152/322) of intubations and resulted in significant acceleration of heart rate without provoking ventricular arrhythmias. New arrhythmias during intubation were related to bradycardia and were less common with atropine use (odds ratio, 0.14 [95% CI, 0.06-0.35], p < 0.001). The most common new arrhythmia was junctional rhythm. Acute bundle branch block was observed during three intubations; one Mobitz type 2 rhythm and five ventricular escape rhythms occurred in the no-atropine group (n = 170). Only one ventricular escape rhythm occurred in the atropine group (n = 152) in a child with an abnormal heart. One child died during intubation who had not received atropine.

Conclusions: Atropine significantly reduced the prevalence of new arrhythmias during intubation particularly for children over 1 month of age, did not convert sinus tachycardia to ventricular tachycardia or fibrillation, and may contribute to the safety of intubation.

PubMed Disclaimer

Comment in

Publication types

MeSH terms