Brugada syndrome

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Background

  • Consider as cause of syncope in patients with family history of sudden death
  • 80% of Brugada syndrome diagnosed only after a cardiac arrest[1]
  • Autosomal dominant Na-channelopathy which increases the risk of sudden cardiac death (~10%/yr)[2]
  • Much more common in men (up to 9x), particularly Southeast Asian males
  • ECG shows incomplete RBBB with ST elevation in V1-V3
    • In uncomplicated RBBB, usually there no ST change to slight ST depression
    • If presenting symptom is chest pain rather than syncope, consider strongly STEMI

Clinical Features

  • Typically asymptomatic
  • ECG findings can be more prominent during times of illness or fever
  • Patients may have Vfib arrest or sudden death

Differential Diagnosis

ST Elevation

Evaluation

ECG Criteria

Note - ECG findings can be transient

  • Type 1-Elevated ST segment (>2mm) descends with upward convexity to a TWI
  • Type 2-Elevated ST segment (>1mm) descends toward baseline then rises again (saddleback) to upright T wave
  • Type 3-Elevated ST segment (<1mm) descends toward baseline then rises again to upright T wave

Brugada.jpg

Management

  • Cardiology consultation

Disposition

  • Needs electrophysiology consult and EP lab
  • Inpatient vs outpatient ICD placement
    • Mortality around 10% per year without ICD placement[citation needed]
    • Antidysrhythmics have no effect on prognosis

External Links

See Also

References

  1. Paul M., Gerss J., Schulze-Bahr E.; Role of programmed ventricular stimulation in patients with Brugada syndrome: a meta-analysis of worldwide published data. Eur Heart J. 28 2007:2126-2133.
  2. Cerrato N, Giustetto C, et al. Prevalence of Type 1 Brugada Electrocardiographic Pattern Evaluated by Twelve-Lead Twenty-Four-Hour Holter Monitoring. The American Journal of Cardiology.115(1). 2015. 52-56.