Table 2.
Points | |
---|---|
I. ECG (12-Lead/Ambulatory) | |
A. Spontaneous type 1 Brugada ECG pattern at nominal or high leads | 3.5 |
B. Fever-induced type 1 Brugada ECG pattern at nominal or high leads | 3 |
C. Type 2 or 3 Brugada ECG pattern that converts with provocative drug challenge | 2 |
*Only award points once for highest score within this category. One item from this category must apply. | |
II. Clinical History* | |
A. Unexplained cardiac arrest or documented VF/ polymorphic VT | 3 |
B. Nocturnal agonal respirations | 2 |
C. Suspected arrhythmic syncope | 2 |
D. Syncope of unclear mechanism/unclear etiology | 1 |
E. Atrial flutter/fibrillation in patients <30 years without alternative etiology | 0.5 |
*Only award points once for highest score within this category. | |
III. Family History | |
A. First- or second-degree relative with definite BrS | 2 |
B. Suspicious SCD (fever, nocturnal, Brugada aggravating drugs) in a first- or second-degree relative | 1 |
C. Unexplained SCD <45 years in first- or second- degree relative with negative autopsy | 0.5 |
*Only award points once for highest score within this category. | |
IV. Genetic Test Result | |
A. Probable pathogenic mutation in BrS susceptibility gene | 0.5 |
Score (requires at least 1 ECG finding) | |
≥3.5 points: Probable/definite BrS | |
2–3 points: Possible BrS | |
<2 points: Nondiagnostic |
BrS = Brugada syndrome; SCD = sudden cardiac death; VF = ventricular fibrillation; VT = ventricular tachycardia.