Brugada Syndrome: Difference between revisions

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The clinical diagnosis of Brugada syndrome is confirmed in an individual with the following:
The clinical diagnosis of Brugada syndrome is confirmed in an individual with the following:


{| class="wikitable" border="0" cellpadding="0" cellspacing="0" width="800px"
{| class="wikitable"
|-
! colspan="2" align=left | '''Findings'''
|-
|-
|- align=left
| ECG || Type 1 ECG with coved type ST-elevation
!colspan="2"|'''Findings'''
|-  
|- align=left
! colspan="2" align=left | '''And at least one of the following'''
|'''ECG'''
|'Type 1 ECG with coved type ST-elevation'
|-
|-
!colspan="2"|'''And at least one of the following'''
| rowspan="8" | '''Clinical history'''  
|- align=left
|-
|'''Clinical history'''
| - Documented ventricular fibrillation
|- Documented ventricular fibrillation
|-
| - Self-terminating polymorphic ventricular tachycardia
|-
| - Syncope
|-
| - A family history of sudden cardiac death <45yrs
|-
| - Coved-type ECGs in family members
|-
| - Inducibility of VT/VF during programmed electrical stimulation
|-
| - Noctural agonal respiration
|}
|}


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