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SYSTEMATIC REVIEW article

Front. Cardiovasc. Med., 25 October 2022
Sec. Cardiac Rhythmology
This article is part of the Research Topic Malignant Arrhythmias and Trigger Mechanisms View all 9 articles

Incidence, recurrence and management of electrical storm in Brugada syndrome

\nIbrahim El-Battrawy,,
Ibrahim El-Battrawy1,2,3*Gretje RoterbergGretje Roterberg1Jacqueline KowitzJacqueline Kowitz1Assem AweimerAssem Aweimer3Siegfried Lang,Siegfried Lang1,2Andreas MüggeAndreas Mügge3Xiaobo Zhou,Xiaobo Zhou1,2Ibrahim Akin,Ibrahim Akin1,2
  • 1First Department of Medicine, Faculty of Medicine, University Medical Centre Mannheim, University of Heidelberg, Heidelberg, Germany
  • 2DZHK (German Center for Cardiovascular Research), Mannheim, Germany
  • 3Bergmannsheil Bochum, Medical Clinic II, Department of Cardiology and Angiology, Ruhr University, Bochum, Germany

Background: Brugada syndrome (BrS) is associated with ventricular tachyarrhythmias. However, the presence of electrical strom (ES) and its management still debated.

Objectives: We present the outcome and management of 44 BrS patients suffering from ES.

Methods: A systematic literature review and pooled analysis Through database review including PubMed, Web of Science, Cochrane Libary and Cinahl studies were analyzed. Evidence from 7 reports of 808 BrS patients was identified.

Results: The mean age of patients suffering from ES was 34 ± 9.5 months (94.7% males, 65.8% spontaneous BrS type I). Using electrophysiological study ventricular tachycardia/ventricular fibrillation were inducible in 12/23 (52.2%). Recurrence of ES was documented in 6.1%. Death from ES was 8.2% after a follow-up of 83.5 ± 53.4. In up to 27 ES resolved without treatment. External shock was required in 35.6%, internal ICD shock in 13.3%, Overdrive pacing, left cardiac sympathetic block and atropin in 2.2%. Short-term antiarrhythmic management was as the following: Isopreterenol or Isopreterenol in combination with quinidine 35.5%, orciprenaline in 2.2%, quinidine 2.2%, disopyramide 2.2% or denopamide 2.2%. However, lidocaine, magensium sulfate, mexiletine and propanolol failed to control ES.

Conclusion: Although ES is rare in BrS, this entity challenges physicians. Despite its high mortality rate, spontaneous termination is possible. Short-term management using Isoproterenol and/or quinidine might be safe. Prospective studies on management of ES are warranted.

Introduction

Sudden cardiac death (SCD) could be caused by a non-structural heart disease. Brugada syndrome (BrS) belongs non-structural heart disease affecting the sodium channel current. It presents typical ECG findings such as coved ST-segment elevation in at least one precordial lead (≥2 mm). BrS patients are at high risk of malignant tachyarrhythmias (1, 2). In up to 30% of BrS mutations are found with a predominance of voltage-dependent sodium channels (SCN5A). Fever and sodium-channel blockers are known triggers of BrS (3, 4, 12). Therefore, consensus papers have recommended avoiding sodium-channel blocker or fever and by agressive and early treatment of fever (5).

Hydroquinidine (HQ) treatment and catheter ablation therapy might be effective in selected cases in patients with recurrent ventricular arrhythmias (6). Suffering from a prior SCD or syncopal events are predictors for recurrent ventricular tachyarrhythmias and therefore they should be prevented by ICD implantation (7). ICD implantation for primary prevention in BrS patients is controversial. A programmed ventricular stimulation (PVS) may be considered for risk stratification of BrS (79). Inducibility of a sustained ventricular tachyarrhythmias among BrS patients presenting type I is a further predictor for ventricular tachyarrhythmias (10). Of note, ICD is not adequate for every patient especially in cases of low risk of developing ventricular tachyarrhythmias over follow-up.

Studies in animals and several cellular models have suggested a voltage gradient in the early phase of repolarization as a part of the ECG phenotype in BrS. A notched phase 1 of the right ventricular outflow tract myocardial action potential may explain a part of the pathomechanism of J-wave in BrS (11). This is related to a loss of function sodium channel current (12). As a part of mode-of mechanism of recurrent ventricular fibrillation might be the previously described premature ventricular beat causing a short-QT-short sequence (13). and may be explained by a mechanism similar to that of the J waves observed in BrS. In addition, it seems that BrS patients, who are suffering from ES show more early repolarization pattern in the ECG.

We aimed to the prognosis and treatment approach of 44 BrS patients suffering from electrical storm (ES).

Methods

In this analysis, we include all patients diagnosed with BrS and suffering from ES from 2007 to 2018. Only 7 studies showed evidence focusing on ES in BrS (1318). A total of 7 studies were identified through a systematic database analysis (PubMed, Web of Science, Cochrane Libary, Cinahl) and their data was analyzed according to our model. We used the PICO strategy to identify significant literature by using controlled search items [(Brugada) AND (syndrome)] related to our clinical question (19). Three independent researchers did cross checks on the established database by comparing the collected data. The statistical analysis was performed using SPSS version 25 (IBM, Italy) and the PRISMA-IPD statement checklist was used as guideline to verify the systematic literature review (20).

A coved type 1 BrS pattern in precordial leads either at baseline or after the administration of a sodium channel blocking agent was relevant to confirm the diagnosis. The definition of type 1 ECG has been described and modified before (7, 21). If a non-type 1 BrS was shown administration of a sodium channel blockers was done.

Data collection of different studies

Several data were extracted from the published papers including age, gender, family history and symptoms. In case of drug testing results of drug testing, results of electrophysiological study and the genetic screening were extracted. The indication of ICD implantation including several predictors for SCD was evaluated.

Systematic literature review

PubMed, Web of Science, Cochrane Libary and Cinahl were screened for BrS and electrical storm (Figure 1). Published reports up to 2018, which were published in English language were taken into consideration. Case reports or studies not reporting on ES were excluded.

FIGURE 1
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Figure 1. Flowchart of recruitment criteria of the present study. Finally 44 patients were included from 7 studies.

Statistics

Data are presented as mean ± SD for continuous variables with a normal distribution, median (interquartile range) for continuous variables with a non-normal distribution, and as frequency (%) for categorical variables. The Kolmogorov–Smirnov test was used to assess normal distribution. Student's t-test and the Mann–Whitney U-test were used to compare continuous variables with normal and non-normal distributions, respectively. The Chi-squared-test or Fisher's exact test was used to compare categorical variables.

Results

Demographics

The mean age of patients suffering from ES was 34 ± 9.5 years with a predominance of males (94.7%). 65.8% of patients showed spontaneous BrS type I. Symptoms were documented as the following: prior VF was (42.1%), syncope (15.8%).

Inducibility of ventricular tachycardia/ventricular fibrillation was documented in 52.2% of cases. 67.3% of patients had an ICD being implanted before event, Table 1.

TABLE 1
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Table 1. Overview of baseline characteristics of BrS patients receiving ICD implantation and suffering from ES.

Short-term management of ES

Whereas, external shock was required in 35.6%, internal ICD shock was required in 13.3%. Interestingly in 26.7% of patients ES resolved without treatment. Furthermore, the use of different drugs was documented with a high presence of Isoproterenol 33.3%, Table 2. Other drugs such as lidocaine, mexiletine, propafol and magnesium sulfate were ineffective.

TABLE 2
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Table 2. Management of BrS suffering from ES.

Long-term management of ES

Catheter ablation of VT was documented in 13.3%. Following drugs were used bepridil (n = 6), quinidine (n = 11), amiodarone (n = 1), disopyramide (n = 1), denopamide (n = 1), denopamide + HQ + Isoproerenol (n = 1), denopamide + HQ (n = 1), quinidine + cilostazol + bepridil (n = 1). Interestingly one patient received heart transplantation. Overall recurrence of ES was 6.8% and overall death regarding ES was 9.1%.

Discussion

We describe the short- and long-term incidence and management of ES in BrS patients from 7 defined studies after a systematic literature review and found the following

(i) ES in BrS is resolving spontaneously in one third of cases.

(ii) Up to 6.1 and 8.2% of patients suffer from recurrence of ES and death; respectively.

(iii) Different drugs might be useful for short-term and long-term treatment of ES with highest presence of Isoproterenol and HQ; however catheter ablation could be another treatment strategy.

Although ES is a rare finding in BrS patients, this issue is important regarding its mortality nature. The mean age of sudden death in BrS is predominantly documented at the young with a mean age of 41 ± 15 years (22). Up to 18–30% of BrS account to mutations in the SCN5A. However, the majority of patients do not show any mutation (2225).

Recently published data showed 3-fold increased mortality risk of patients suffering from ES (26). Even more, it has been reported about 20% increased mortality rate per shock episode. Additionally multiple shock increase the risk of acute heart failure and consequently mortality rate (27).

The present study in BrS suffering from ES presents a mortality rate of 8.2% over mean follow-up of 83.5 months. This low mortality rate might be related to different factors such as spontaneous the termination of ES without treatment in up to 27% of patients. One important finding of our study is that the majority of patients suffering from ES are presenting spontaneously BrS type 1 ECG. Even more 42.1% of patients have had a prior VF and/or VT. Therefore, these data provide a further support for the requirement of ICD placement in Brugada patients with previous episodes of arrhythmic events.

Another important data point is the inducibility of VT and/or VF in BrS patients. Our data analysis shows that more than 52.2% of patients suffering from ES have inducible sustained ventricular tachyarrhythmias, which means that this cohort is a high risk cohort. Among patients with ES at least 42% of patients suffered from VT/VF in the past.

Sroubek et al. reported in a pooled analysis of 1,312 BrS patients, that in 527 patients arrhythmias were induced with programmed ventricular stimulation (8). Induction was associated with cardiac events during follow-up [hazard ratio, 2.66; 95% confidence interval (CI), 1.44–4.92, P < 0.001]. This risk was greatest with lowest extrastimuli (1–2 extrastimuli). Absence of syncope or presence of type 1 BrS ECG during sodium channel blocker use were associated with lowest risk of sudden cardiac death over follow-up. Therefore, when arrhythmias are induced within electrophysiology work-up other clinical factors should be taken into consideration before ICD implantation.

Different treatment strategies have been investigated in patients suffering from ES such as sympathetic blockade, different beta-blockers including propranolol, esmolol, and left stellate ganglionic blockade with combined therapy with Class I antiarrhythmic drugs (lidocaine, procainamide, and bretylium). Additionally, the combination of amiodarone and propranolol showed an improvement of survival rate (28, 29). However, BrS present a rare entity with different treatment strategy regarding triggering the risk of life-threatening arrhythmia with use of class I anti-arrhythmic drugs and beta-blockers. Whereas, reducing the sympathic activity is a sole treatment of patients suffering from ES, in BrS patients the use of sympatic triggers including isoproterenol are successfully for acute management of ES. Quinidine has been reported to reduced rate of ICD shock over follow-up among BrS patients (30).

Of note, the use of catheter ablation in the present cohort with 13% is low. This might be related to absence of arrhythmic events after acute and long-term use of anti-arrhythmic drugs. In addition, ablation in BrS might need a well-expertise, which may explain the low-rate use of this procedure in the past. Furthermore, the epicardial ablation procedure has been firstly well-described the last 7 years, whereas the included papers are in particular older. Of note, the reported guidelines by Priori et al. (7) classified the use of catheter ablation due to ES as class IIb. It is important to emphasize more robust cohorts of BrS undergoing epicardial ablation were reported the recent years. It was reported that these patients have unique abnormal low voltage, prolonged duration, and fractionated late potentials mainly in the anterior aspect of the right flow tract epicardium (31).

On the other hand isoproterenol use is recommend in BrS patients within ES (class IIa recommendation) (7). Regarding the mode of action of isoproterenol among BrS patients during ES published data 1999 suggested (32) that phase 2 re-entry is a part of mechanism of ventricular tachyarrhythmias among BrS patients. Either increased outward current or decreased inward current induces a change in the epicardial action potential, e.g., deepening of phase 1 notch and shortening of action potential duration, and excitation propagates as a difference in electrical voltage (phase 2 re-entry) (33). The stimulation of beta-adrenergic receptors, e.g., by use of isoproterenol causes increased inward calcium current and reduces the excess of outward current, consistent with changes in action potential characteristics.

Study limitation

This study provides registry data dominated by retrospective studies and, although the authors clinically evaluated all patients, clinical assessment and treatment algorithm was not uniform and consecutively ICD indications were heterogeneous throughout the study, some patients had an ICD implanted for reasons other than symptoms or ventricular fibrillation inducibility. The treatment of ES was not related to similar protocol.

Moreover, despite advantages of recruited ablation studies as a novel therapeutic approaches, this issue was not deeply analyzed in this study.

Finally, we present in this paper a pooled analysis of different study groups, therefore bias are not excluded.

Conclusions

Although ES is rare in BrS, this entity challenges physicians. Using of sympathicus triggers and the off-lable use of HQ might be successful in short- and long-management of in BrS.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author/s.

Ethics statement

The requirement of ethical review and approval was waived. The requirement of written informed consent from the patients/participants was waived.

Author contributions

IE-B: writing the first draft. GR and IE-B: data analysis. SL and XZ: supervision. SL and GR: statistical review. IA, AM, and AA: critical revision. All authors contributed to the article and approved the submitted version.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Amin AS, Verkerk AO, Bhuiyan ZA, Wilde AA, Tan HL. Novel Brugada syndrome-causing mutation in ion-conducting pore of cardiac Na+ channel does not affect ion selectivity properties. Acta Physiol Scand. (2005) 185:291–301. doi: 10.1111/j.1365-201X.2005.01496.x

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Morita H, Nagase S, Kusano K, Ohe T. Spontaneous T wave alternans and premature ventricular contractions during febrile illness in a patient with Brugada syndrome. J Cardiovasc Electrophysiol. (2002) 13:816–8.

PubMed Abstract | Google Scholar

3. Roterberg G, El-Battrawy I, Veith M, Liebe V, Ansari U, Lang S, et al. Arrhythmic events in Brugada syndrome patients induced by fever. Ann Noninvasive Electrocardiol. (2020) 25:e12723. doi: 10.1111/anec.12723

PubMed Abstract | CrossRef Full Text | Google Scholar

4. El-Battrawy I, Müller J, Zhao Z, Cyganek L, Zhong R, Zhang F, et al. Studying brugada syndrome with an SCN1B variants in human-induced pluripotent stem cell-derived cardiomyocytes. Front Cell Dev Biol. (2019) 7:261. doi: 10.3389/fcell.2019.00261

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Casado-Arroyo R, Berne P, Rao JY, Rodriguez-Manero M, Levinstein M, Conte G, et al. Long-term trends in newly diagnosed brugada syndrome: implications for risk stratification. J Am Coll Cardiol. (2016) 68:614–23. doi: 10.1016/j.jacc.2016.05.073

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Pappone C, Brugada J, Vicedomini G, Ciconte G, Manguso F, Saviano M, et al. Electrical substrate elimination in 135 consecutive patients with brugada syndrome. Circ Arrhythm Electrophysiol. (2017) 10:e005053. doi: 10.1161/CIRCEP.117.005053

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Priori SG, Blomstrom-Lundqvist C, Mazzanti A, Blom N, Borggrefe M, Camm J, et al. 2015 ESC guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: the task force for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death of the European society of cardiology (ESC). Eur Heart J. (2015) 36:2793–867. doi: 10.1093/eurheartj/ehv316

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Sroubek J, Probst V, Mazzanti A, Delise P, Hevia JC, Ohkubo K, et al. Programmed ventricular stimulation for risk stratification in the brugada syndrome: a pooled analysis. Circulation. (2016) 133:622–30. doi: 10.1161/CIRCULATIONAHA.115.017885

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Zeppenfeld K, Tfelt-Hansen J, de Riva M, Winkel BG, Behr ER, Blom NA, et al. 2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death. Eur Heart J. (2022) ehac262. doi: 10.1093/eurheartj/ehac262 [Epub ahead of print].

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Brugada J, Brugada R, Brugada P. Determinants of sudden cardiac death in individuals with the electrocardiographic pattern of Brugada syndrome and no previous cardiac arrest. Circulation. (2003) 108:3092–6. doi: 10.1161/01.CIR.0000104568.13957.4F

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Li Y, Lang S, Akin I, Zhou X, El-Battrawy I. Brugada syndrome: different experimental models and the role of human cardiomyocytes from induced pluripotent stem cells. J Am Heart Assoc. (2022) 11:e024410. doi: 10.1161/JAHA.121.024410

PubMed Abstract | CrossRef Full Text | Google Scholar

12. El-Battrawy I, Albers S, Cyganek L, Zhao Z, Lan H, Li X, et al. A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes. Europace. (2019) 21:1410–21. doi: 10.1093/europace/euz122

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Kaneko Y, Horie M, Niwano S, Kusano KF, Takatsuki S, Kurita T, et al. Electrical storm in patients with brugada syndrome is associated with early repolarization. Circ Arrhythm Electrophysiol. (2014) 7:1122–8. doi: 10.1161/CIRCEP.114.001806

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Gonzalez Corcia MC, Sieira J, Pappaert G, de Asmundis C, Chierchia GB, La Meir M, et al. Implantable cardioverter-defibrillators in children and adolescents with brugada syndrome. J Am Coll Cardiol. (2018) 71:148–57. doi: 10.1016/j.jacc.2017.10.082

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Hernandez-Ojeda J, Arbelo E, Borras R, Berne P, Tolosana JM, Gomez-Juanatey A, et al. Patients with brugada syndrome and implanted cardioverter-defibrillators: long-term follow-up. J Am Coll Cardiol. (2017) 70:1991–2002. doi: 10.1016/j.jacc.2017.08.029

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Ohgo T, Okamura H, Noda T, Satomi K, Suyama K, Kurita T, et al. Acute and chronic management in patients with Brugada syndrome associated with electrical storm of ventricular fibrillation. Heart Rhythm. (2007) 4:695–700. doi: 10.1016/j.hrthm.2007.02.014

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Sacher F, Probst V, Maury P, Babuty D, Mansourati J, Komatsu Y, et al. Outcome after implantation of a cardioverter-defibrillator in patients with Brugada syndrome: a multicenter study-part 2. Circulation. (2013) 128:1739–47. doi: 10.1161/CIRCULATIONAHA.113.001941

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Schukro C, Berger T, Stix G, Pezawas T, Kastner J, Hintringer F, et al. Regional prevalence and clinical benefit of implantable cardioverter defibrillators in Brugada syndrome. Int J Cardiol. (2010) 144:191–4. doi: 10.1016/j.ijcard.2009.03.136

PubMed Abstract | CrossRef Full Text | Google Scholar

19. da Costa Santos CM, de Mattos Pimenta CA, Nobre MR. The PICO strategy for the research question construction and evidence search. Rev Lat Am Enfermagem. (2007) 15:508–11. doi: 10.1590/s0104-11692007000300023

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. J Clin Epidemiol. (2009) 62:e1–34. doi: 10.1016/j.jclinepi.2009.06.006

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Antzelevitch C, Yan GX, Ackerman MJ, Borggrefe M, Corrado D, Guo J, et al. J-Wave syndromes expert consensus conference report: emerging concepts and gaps in knowledge. J Arrhythm. (2016) 32:315–39. doi: 10.1016/j.joa.2016.07.002

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Antzelevitch C, Brugada P, Borggrefe M, Brugada J, Brugada R, Corrado D, et al. Brugada syndrome: report of the second consensus conference: endorsed by the Heart rhythm society and the European heart rhythm association. Circulation. (2005) 111:659–70. doi: 10.1161/01.CIR.0000152479.54298.51

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Brugada J, Brugada R, Antzelevitch C, Towbin J, Nademanee K, Brugada P. Long-term follow-up of individuals with the electrocardiographic pattern of right bundle-branch block and ST-segment elevation in precordial leads V1 to V3. Circulation. (2002) 105:73–8.

PubMed Abstract | Google Scholar

24. Eckardt L, Probst V, Smits JP, Bahr ES, Wolpert C, Schimpf R, et al. Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome. Circulation. (2005) 111:257–63. doi: 10.1161/01.CIR.0000153267.21278.8D

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Miyazaki T, Mitamura H, Miyoshi S, Soejima K, Aizawa Y, Ogawa S. Autonomic and antiarrhythmic drug modulation of ST segment elevation in patients with Brugada syndrome. J Am Coll Cardiol. (1996) 27:1061–70. doi: 10.1016/0735-1097(95)00613-3

PubMed Abstract | CrossRef Full Text | Google Scholar

26. Guerra F, Shkoza M, Scappini L, Flori M, Capucci A. Role of electrical storm as a mortality and morbidity risk factor and its clinical predictors: a meta-analysis. Europace. (2014) 16:347–53. doi: 10.1093/europace/eut304

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Sweeney MO, Sherfesee L, DeGroot PJ, Wathen MS, Wilkoff BL. Differences in effects of electrical therapy type for ventricular arrhythmias on mortality in implantable cardioverter-defibrillator patients. Heart Rhythm. (2010) 7:353–60. doi: 10.1016/j.hrthm.2009.11.027

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Chatzidou S, Kontogiannis C, Tsilimigras DI, Georgiopoulos G, Kosmopoulos M, Papadopoulou E, et al. Propranolol versus metoprolol for treatment of electrical storm in patients with implantable cardioverter-defibrillator. J Am Coll Cardiol. (2018) 71:1897–906. doi: 10.1016/j.jacc.2018.02.056

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Nademanee K, Taylor R, Bailey WE, Rieders DE, Kosar EM. Treating electrical storm : sympathetic blockade versus advanced cardiac life support-guided therapy. Circulation. (2000) 102:742–7.

PubMed Abstract | Google Scholar

30. Anguera I, Garcia-Alberola A, Dallaglio P, Toquero J, Perez L, Martinez JG, et al. Shock reduction with long-term quinidine in patients with brugada syndrome and malignant ventricular arrhythmia episodes. J Am Coll Cardiol. (2016) 67:1653–4. doi: 10.1016/j.jacc.2016.01.042

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Nademanee K, Veerakul G, Chandanamattha P, Chaothawee L, Ariyachaipanich A, Jirasirirojanakorn K, et al. Prevention of ventricular fibrillation episodes in Brugada syndrome by catheter ablation over the anterior right ventricular outflow tract epicardium. Circulation. (2011) 123:1270–9. doi: 10.1161/CIRCULATIONAHA.110.972612

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Yan GX, Antzelevitch C. Cellular basis for the Brugada syndrome and other mechanisms of arrhythmogenesis associated with ST-segment elevation. Circulation. (1999) 100:1660–6. doi: 10.1161/01.cir.100.15.1660

PubMed Abstract | CrossRef Full Text | Google Scholar

33. Antzelevitch C. The Brugada syndrome: diagnostic criteria and cellular mechanisms. Eur Heart J. (2001) 22:356–63. doi: 10.1053/euhj.2000.2461

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: Brugada, outcome, electrical storm, complications, cardiac death

Citation: El-Battrawy I, Roterberg G, Kowitz J, Aweimer A, Lang S, Mügge A, Zhou X and Akin I (2022) Incidence, recurrence and management of electrical storm in Brugada syndrome. Front. Cardiovasc. Med. 9:981715. doi: 10.3389/fcvm.2022.981715

Received: 29 June 2022; Accepted: 04 October 2022;
Published: 25 October 2022.

Edited by:

Dirk Bandorski, Semmelweis University, Hungary

Reviewed by:

Gabor Szeplaki, Mater Private Hospital, Ireland
Ivo Roca Luque, Hospital Clinic of Barcelona, Spain

Copyright © 2022 El-Battrawy, Roterberg, Kowitz, Aweimer, Lang, Mügge, Zhou and Akin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Ibrahim El-Battrawy, SWJyYWhpbS5lbGJhdHRyYXd5MjAwNiYjeDAwMDQwO2dtYWlsLmNvbQ==

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.