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Background <p>Brugada syndrome is an autosomal dominant inherited disorder that is generally rare but can potentially cause life-threatening arrhythmia, sudden cardiac arrest, or death in young adults with structurally normal hearts. It is characterized by coved-type ST-segment elevation with T-wave inversion and with or without a right bundle branch block.</p> Case presentation <p>A 42-year-old Ethiopian man presented with two episodes of loss of consciousness followed by palpitations and experienced documented in-hospital cardiac arrest due to ventricular tachycardia, which was successfully resuscitated. A diagnosis of Brugada syndrome was made after a typical electrocardiogram finding was noted postresuscitation.</p> Conclusion <p>Although rare, Brugada syndrome is not nonexistent in the Black population, and it should be considered in young adults presenting with syncope, sudden cardiac arrest, or death in otherwise structurally normal hearts.</p>

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Resuscitated cardiac arrest due to Brugada syndrome in an Ethiopian man: a case report

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年8月28日

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  • Mehariw Wondim Netsere,
  • Zekarias Seifu Ayalew,
  • Wubalem Belay,
  • Henok Benti,
  • Seifu Bacha,
  • Anteneh Meselu,
  • Asteway Mulat Haile,
  • Kibret Enyew Belay

摘要

Background

Brugada syndrome is an autosomal dominant inherited disorder that is generally rare but can potentially cause life-threatening arrhythmia, sudden cardiac arrest, or death in young adults with structurally normal hearts. It is characterized by coved-type ST-segment elevation with T-wave inversion and with or without a right bundle branch block.

Case presentation

A 42-year-old Ethiopian man presented with two episodes of loss of consciousness followed by palpitations and experienced documented in-hospital cardiac arrest due to ventricular tachycardia, which was successfully resuscitated. A diagnosis of Brugada syndrome was made after a typical electrocardiogram finding was noted postresuscitation.

Conclusion

Although rare, Brugada syndrome is not nonexistent in the Black population, and it should be considered in young adults presenting with syncope, sudden cardiac arrest, or death in otherwise structurally normal hearts.