Key result
CPR and DC shocks restore sinus rhythm in refractory Brugada electrical storm complicated by hypoxic encephalopathy.
Why the study?
Brugada syndrome is a rare familial disorder causing sudden cardiac death, with rare presentations of incessant polymorphic ventricular tachycardia reported.
Case Report (n=1)
Brugada syndrome can rarely present with incessant polymorphic ventricular tachycardia leading to sudden cardiac arrest and severe neurological sequelae.
Raises awareness of encephalopathy risk after Brugada arrest; leaves open optimal resuscitation strategies in this rare presentation.
Brugada syndrome (BrS) is a familial disorder and an important though rare cause of sudden cardiac death (SCD). SCD occurs due to ventricular fibrillation (VF), though presentation with incessant polymorphic ventricular tachycardia has also been rarely reported in the literature. We report a case of BrS presenting with incessant polymorphic ventricular tachycardia that ultimately led to prolonged cerebral ischaemia and hypoxic ischaemic encephalopathy sequelae. A 34-year-old man, with no previous comorbidities, collapsed suddenly while attending to his morning routine work. He had a history suggestive of presyncopal episodes in the recent past. There was no family history of SCD. He was taken to a nearby hospital within 10–15 min of collapse, where cardiopulmonary resuscitation (CPR) was initiated. ECG monitor showed polymorphic ventricular tachycardia, so direct current (DC) shock and intravenous magnesium were given. After 20 min of CPR and five cycles of DC shock, the patient reverted to sinus rhythm. Simultaneously, he was intubated and put on ventilatory support. Intravenous amiodarone was …
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Ghosh et al. (2016) conducted a case report in Brugada syndrome presenting with incessant polymorphic ventricular tachycardia (n=1). Cardiopulmonary resuscitation, direct current shock, and intravenous magnesium was evaluated on Reversion to sinus rhythm and clinical outcome. A 34-year-old man with Brugada syndrome presenting with incessant polymorphic ventricular tachycardia reverted to sinus rhythm after CPR and DC shocks but developed hypoxic ischaemic encephalopathy.
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