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A case of Commotio cordis in a young child caused by a fall
James Tibballs1, Timothy Thiruchelvam
1Intensive Care Unit, Royal Children's Hospital, Flemington Road, Parkville, Melbourne, Victoria 3052, Australia. james.tibballs@rch.org.au
Insights
Commotio cordis, a rare cause of cardiac arrest from chest impact, occurred in a child after a fall. Prompt defibrillation successfully treated the resulting ventricular fibrillation, with full recovery.
Area of Science:
- Pediatrics
- Cardiology
- Emergency Medicine
Background:
- Commotio cordis is a rare but life-threatening event.
- Sudden cardiac arrest in children typically has underlying cardiac pathology.
Observation:
- A young child experienced sudden cardiac arrest, including unconsciousness, apnea, and cyanosis, after falling chest-first.
- Ventricular fibrillation was diagnosed upon emergency services arrival.
- Extensive cardiac and systemic investigations ruled out pre-existing conditions or trauma.
Findings:
- The child's ventricular fibrillation responded successfully to biphasic defibrillation (3 J/kg).
- No evidence of chest trauma, brain injury, or underlying cardiac abnormalities (e.g., long QT, Brugada syndrome) was found.
- Neurological recovery was complete after therapeutic hypothermia and mechanical ventilation.
Implications:
- This case highlights commotio cordis as a critical differential diagnosis in pediatric sudden cardiac arrest, even without direct trauma.
- Highlights the importance of immediate cardiopulmonary resuscitation and defibrillation in suspected commotio cordis.
- Emphasizes the need for thorough investigation to exclude other causes of cardiac arrest in children.
Abstract:
Commotio cordis or ventricular fibrillation caused by a blow to the chest is a rare cause of cardiac arrest in a well child. We report a case of a young child falling from a low height landing chest first with rapid onset of unconsciousness, apnoea and cyanosis. Cardiopulmonary resuscitation was given by parents under telephone instruction from an ambulance dispatch centre. On arrival of officers, 7 min after the fall, ventricular fibrillation was present but responded to defibrillation (biphasic 3 J/kg). No clinical or CT evidence of chest or brain trauma was present and investigations (ECGs, cardiac MRI, echocardiography, viral tests, metabolic tests, drug tests, serum electrolytes) did not reveal any cardiac illness or abnormal cardiac anatomy. Specifically, a long QT was absent and a Flecainide challenge for Brugada syndrome was negative. There was no family history of sudden death. No further dysrrhythmia occurred and the child recovered neurologically well after 3 days of therapeutic hypothermia (for cerebral ischaemia) and 7 days of mechanical ventilation.
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