Brugada syndrome: Difference between revisions

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== Disposition ==
== Disposition ==
*Pt requires admission for ICD placement.
*Pt requires admission for ICD placement
**Mortality around 10% per year without ICD placement
**Antidysrhythmics have no effect on prognosis


==See Also==
==See Also==

Revision as of 02:38, 8 March 2016

Background

  • Consider as cause of syncope in pts w/ family history of sudden death
  • Genetically-linked Na-channelopathy that increases the risk of sudden cardiac death (~10%/yr)[1]
  • Familial autosomal dominant
  • Much more common in men (up to 9x)
  • Particularly Southeast Asian males
  • ECG shows incomplete RBBB with ST elevation in V1-V3

Diagnosis

ECG Criteria

  • Note - ECG findings can be transient
  • Type 1-Elevated ST segment (>2mm) descends w/ 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

Differential Diagnosis

ST Elevation

Management

  • IV access
  • Cardiac monitor
  • Defibrillator at the bedside
  • Cardiology consultation

Disposition

  • Pt requires admission for ICD placement
    • Mortality around 10% per year without ICD placement
    • Antidysrhythmics have no effect on prognosis

See Also

References

  1. 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.