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Bradycardia in minor trauma: don't be slow on the uptake!
Pratik Shah1, Marcus Likeman, Lisa Munro-Davies
1Children's Emergency Department, Bristol Royal Hospital for Children, Bristol, UK. shahpratikh@rediffmail.com
Insights
A 13-year-old boy experienced profound bradycardia after minor neck trauma due to an odontoid peg anomaly. This rare craniocervical instability highlights potential autonomic risks from seemingly minor injuries.
Area of Science:
- Neurology
- Cardiology
- Pediatrics
Background:
- A 13-year-old male with a history of gastroschisis and learning difficulties presented after minor trauma.
- The patient sustained a cervical hyperextension injury while playing, leading to immediate tetraplegia and hyposensibility.
Observation:
- Ambulance personnel noted profound bradycardia with normotension.
- Neurological deficits resolved within 2 hours, but persistent bradycardia (30-60 bpm) was observed.
- Electrocardiogram (ECG) revealed sinus bradycardia with atrial ectopics; the patient remained hemodynamically stable.
Findings:
- Neuroimaging identified hypoplasia of the odontoid peg and relative spinal canal narrowing at the craniocervical junction.
- No evidence of spinal cord contusion or compression was found.
- The bradycardia resolved spontaneously over 36 hours without intervention.
Implications:
- This case highlights a previously undescribed association between craniocervical abnormality, learning difficulties, and gastroschisis.
- Odontoid peg instability can precipitate severe autonomic dysfunction, such as bradycardia, following minor trauma.
- The findings underscore the importance of considering underlying structural abnormalities in cases of unexplained autonomic symptoms after trauma.
Abstract:
We report the case of a 13-year-old boy presenting with profound bradycardia following minor trauma. Our patient had gastroschisis at birth and has moderate learning difficulties but is otherwise fit and well. Whilst playing at home he fell sustaining a minor cervical hyperextension injury. He immediately complained of tetraplegia and hyposensibility. The ambulance crew noted profound bradycardia with normotension and he was transported to hospital with full spinal immobilisation precautions. Over the subsequent 2 hours he made a full neurological recovery. Bradycardia persisted with a beat-to-beat variation of 30-60 bpm. ECG showed sinus bradycardia with atrial ectopics and he remained haemodynamically normal. Neuroimaging studies revealed hypoplasia of the odontoid peg with a relative narrowing of the spinal canal at this level. There was no evidence of spinal cord contusion or compression. His bradycardia resolved over 36 hours without further intervention. On discharge the patient was advised to wear a cervical hard collar when mobilising. This association of a craniocervical abnormality with learning difficulties, and gastroschisis has not been previously described. We discuss several other causes of odontoid peg instability, which may lead to severe autonomic effects with relatively insignificant trauma.
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