Diferencia entre revisiones de «Brugada syndrome»

(more generlized term)
Sin resumen de edición
Línea 31: Línea 31:
*[[ST elevation]]
*[[ST elevation]]


== Source ==
==References==
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[[Category:Cards]]
[[Category:Cards]]

Revisión del 00:16 23 feb 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.

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.