Brugada syndrome: Difference between revisions

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[[Category:Cardiology]]

Revision as of 13:53, 22 March 2016

Background

  • Consider as cause of syncope in pts w/ family history of sudden death
  • Autosomal dominant Na-channelopathy which increases the risk of sudden cardiac death (~10%/yr)[1]
  • Much more common in men (up to 9x), particularly Southeast Asian males
  • ECG shows incomplete RBBB with ST elevation in V1-V3
    • In uncomplciated RBBB, usually there no ST change to slight ST depression[2]
    • 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

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

Management

  • Cardiology consultation

Disposition

  • Needs electrophysiology c/s and EP lab
  • Inpatient vs outpatient ICD placement
    • Mortality around 10% per year without ICD placement[citation needed]
    • 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.
  2. Amal Mattu. Mattu ECG Case: March 4 2012. umemergencymed. Published Apr 9, 2012. https://www.youtube.com/watch?v=NJL8An6uO1Y.