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Circulation. 2003;107:e122
doi: 10.1161/01.CIR.0000071207.67541.01
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(Circulation. 2003;107:e122.)
© 2003 American Heart Association, Inc.


Correspondence

The Brugada Numbers

Laszlo Littmann, MD; Michael H. Monroe, MD

Department of Internal Medicine, Carolinas Medical Center, Charlotte, NC

To the Editor:

In a Consensus Report on proposed diagnostic criteria for the Brugada syndrome, Wilde et al1 report an incidence "ranging between 5 and 66 per 10 000." With a world population of 6 157 000 000,2 that would mean between 3 000 000 and 40 000 000 have the Brugada syndrome, similar in scope to the estimated 36 100 000 infected with HIV.2 This cannot be. More likely, the quoted numbers reflect the prevalence of the Brugada electrocardiographic pattern (the "Brugada sign").3 Herein lies the dilemma. As the authors and others have clearly stated, the Brugada sign should not be equated with the Brugada syndrome.1,4 How then do we judiciously screen millions of individuals with the Brugada sign, most of whom are not at risk for sudden death, to find the small percentage with the Brugada syndrome who are at risk of sudden death and in need of a defibrillator? The report by the Arrhythmia Working Group1 as well as other recent publications5 are "works in progress" to help answer that question.

References

1. Wilde AAM, Antzelevitch C, Borggrefe M, et al. Proposed diagnostic criteria for the Brugada syndrome: consensus report. Circulation. 2002; 106: 2514–2519.[Free Full Text]

2. The World Almanac and Book of Facts. New York, NY: World Almanac Books; 2002: 867–870.

3. Miyasaka Y, Tsuji H, Yamada K, et al. Prevalence and mortality of the Brugada-type electrocardiogram in one city in Japan. J Am Coll Cardiol. 2001; 38: 771–774.[Abstract/Free Full Text]

4. Surawicz B. Brugada syndrome: manifest, concealed, "asymptomatic," suspected and simulated. J Am Coll Cardiol. 2001; 38: 775–777.[Free Full Text]

5. Littmann L, Monroe MH, Kerns WP, et al. Brugada syndrome and "Brugada sign": clinical spectrum with a guide for the clinician. Am Heart J. 2003; 145: 768–778.[CrossRef][Medline] [Order article via Infotrieve]


 

Reply

Arthur A.M. Wilde, MD, PhD

Experimental and Molecular Cardiology Group, Academic Medical Center, Amsterdam, The Netherlands

Charles Antzelevitch, PhD

Masonic Medical Research Laboratory, Utica, NY

Martin Borggrefe, MD, PhD

Fakultät Klinische Medizin Mannheim, Universität Heidelberg, Mannheim, Germany

Josep Brugada, MD

Cardiovascular Institute, Hospital Clínic, University of Barcelona, Spain

Pedro Brugada, MD, PhD

Cardiovascular Center, Onze Lieve Vrouwe Ziekenhuis, Aalst, Belgium

Ramón Brugada, MD; Jeffrey A. Towbin, MD

Baylor College of Medicine, Houston, Tex

Domenico Corrado, MD

Divisione di Cardiología, Università di Padova, Italy

Richard N.W. Hauer, MD, PhD

Heart-Lung Center Utrecht, University Medical Center, Utrecht, The Netherlands

Robert S. Kass, PhD

Department of Pharmacology, Columbia University, New York, NY

Koonlawee Nademanee, MD

Division of Cardiology, University of Southern California, Los Angeles, Calif

Silvia G. Priori, MD, PhD

Molecular Cardiology and Electrophysiology Laboratories, Fondazione Salvatore Maugeri, Pavia, Italy

, For the Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology

We thank Drs Littmann and Monroe for their letter to the editor. The numbers stemming from the calculations presented by Drs Littmann and Monroe are perhaps not as dramatic as suggested, in that the incidence of 5 per 10 000 is limited to those regions of the world where the Brugada syndrome is endemic—parts of Southeast Asia and Japan. The incidence of 66 per 10 000 quoted in our consensus report1 is limited to a small region in Japan. Moreover, it is important to recognize that the actual prevalence of the syndrome is a sensitive function of the criteria applied in the individual studies,2 which is one of the main reasons for the consensus conference and report. With less than a decade since the identification of the Brugada syndrome as a distinct clinical entity, it would be safe to conclude that data on its worldwide incidence remain out of reach. We take no issue with the other excellent points made in the letter and consider the question of how one might go about screening for those at risk for sudden death as rhetorical in that this is the subject of the consensus document.

References

1. Wilde AAM, Antzelevitch C, Borggrefe M, et al. Diagnostic criteria for the Brugada syndrome: a consensus report. Circulation. 2002; 106: 2514–2519.[Free Full Text]

2. Remme CA, Wever EFD, Wilde AAM, et al. Diagnosis and long-term follow-up of Brugada syndrome in patients with idiopathic ventricular fibrillation. Eur Heart J. 2001; 22: 400–409.[Abstract/Free Full Text]




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Right arrow Electrophysiology
Right arrow Clinical genetics
Right arrow Ion channels/membrane transport
Right arrow Ablation/ICD/surgery
Right arrow Arrhythmias, clinical electrophysiology, drugs