Risk stratification in patients with Brugada syndrome

Česká verzia

Authors: M. Bébarová ¹; P. Lokaj ^1,2
Authors place of work: Fyziologický ústav Lékařské fakulty MU Brno, přednostka prof. MUDr. Nataša Honzíková, CSc. ¹; Interní kardiologická klinika Lékařské fakulty MU a FN Brno, pracoviště Bohunice, přednosta prof. MUDr. Jindřich Špinar, CSc., FESC ²
Published in the journal: Vnitř Lék 2012; 58(4): 280-285
Category: Reviews

Summary

Brugada syndrome (BrS), one of the most frequently diagnosed inherited arrhythmogenic syndromes, is responsible for more than 4% of all sudden deaths and at least 20% of sudden deaths in patients with structurally normal hearts. The sudden death is often the first symptom of BrS and appears most often already during the fourth decade of life of BrS patients. Implantation of cardioverter--defibrillator was proved to be the only effective treatment, i.e. prevention of the sudden death, in BrS. Thus, it is uniquely determined to be used in case of symptomatic BrS patients. On the contrary, the individual risk of life-threathening arrhythmias has to be thoroughly considered in case of asymptomatic BrS patients due to substantial side effects of implantation of cardioverter-defibrillator. This review first provides a summary of factors recommended for the risk stratification in BrS patients in 2005 including their support or rejection in the following studies. Subsequently, we focused on the most important risk factors newly suggested after 2005.

Key words:
Brugada syndrome – sudden death – risk stratification – risk factors – prognosis

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