V entricular fibrillation (VF) can occur in patients without structural heart diseases; when it does, it is called idiopathic VF.1,2 Among primary electric diseases, Brugada syndrome (BS) is characterized by unique ECG patterns of J/ ST/T waves.3 This ECG pattern has been shown to be associated with an increased risk of sudden cardiac death compared with control subjects, 4 and an ECG diagnosis of BS is very important for risk stratification.
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Clinical Perspective on p 1054Recently, we observed a case in which the characteristic ECG phenotype of BS was unmasked by relief of complete right bundlebranch block (CRBBB); when CRBBB resolved spontaneously, the characteristic ECG pattern of BS was found to be underlying.
7A similar case was reported by others. [8][9][10] The goal of this study is to discuss patients with BS that were complicated by CRBBB and to present evidence for the presence of BS in CRBBB patients.
Methods PatientsThe study consisted of 11 patients who had CRBBB with the diagnosis of BS.5 Structural heart diseases were excluded by ECG, transthoracic echocardiography, and cardiac catheterization. Coronary spasm was excluded as the cause of VF by provocation tests using acetylcholine or ergonovine maleate at catheterization.
Definitions of CRBBB and BSCRBBB was defined as a late R (R′) wave presenting in V 1 or V 2 , with a slurred, wide S in leads I and V 5 /V 6 and with prolonged duration of QRS ≥120 milliseconds. 11,12 If CRBBB was seen on the baseline ECG, we divided the patients into 2 groups. One group consisted of the patients in whom ECG revealed BS and CRBBB occurred subsequently during the follow-up (n=7). The other group consisted of the patients who had CRBBB on the baseline ECG but in whom BS was diagnosed in the following situations (n=4). First, resolution of CRBBB resulted in normal ventricular conduction, in which the characteristic ECG pattern for BS could be seen. The resolution of Background-The characteristic ECG of Brugada syndrome (BS) can be masked by complete right bundle-branch block (CRBBB) and exposed by resolution of the block or pharmacological or pacing maneuvers. Methods and Results-The study consisted of 11 patients who had BS and CRBBB. BS was diagnosed before the development of CRBBB, on the resolution of CRBBB, or from new characteristic ST-segment changes that could be attributable to BS. Structural heart diseases were excluded, and coronary spasm was excluded on the basis of a provocation test at catheterization. In 7 patients, BS was diagnosed before the development of CRBBB. BS was diagnosed when CRBBB resolved spontaneously (n=1) or by right ventricular pacing (n=3). The precipitating cause for the spontaneous resolution of CRBBB, however, was not apparent. On repeated ECGs, new additional upward-convex ST-segment elevation was found in V 2 or V 3 in 3 patients. In 2 patients, new ST-segment elevation was induced by class I C drugs. The QRS duration was more prolonged in patients with BS and CRBBB compared with age-and sex-matched controls: 170±13 versus 14...