Brugada syndrome: a review of the literature

Key points

• Brugada syndrome, an autosomal dominant condition, is a disorder characterised by sudden death associated with one of several ECG patterns characterised by incomplete right bundle-branch block and ST-segment elevations in the anterior precordial leads.

• Patients with Brugada syndrome are prone to develop ventricular tachyarrhythmias that may lead to syncope, cardiac arrest, or sudden cardiac death.

• Diagnosis is based on clinical findings. Mutations in eight genes (SCN5A, GPD1L, CACNA1C, CACNB2, SCN1B, KCNE3, SCN3B, and HCN4) are known to cause Brugada syndrome.

• At present, implantation of an automatic implantable cardiac defibrillator (ICD) is the only treatment proven effective in treating ventricular tachycardia and fibrillation and preventing sudden death in patients with Brugada syndrome.

• No proven pharmacologic treatment for preventing SCD in BS have been found, although Isoproterenol has been proved to be useful for treatment of electrical storm in BS and Quinidine has also shown to be beneficial. Quinidine is currently being used in:

• –patients with ICD and multiple shocks;

• –cases in which ICD implantation is contraindicated; or

• –for the treatment of supraventricular arrhythmias.

Case 1

A 25-year-old man was admitted to the accident and emergency (A&E) department with a history of collapse. There was no significant previous history. His blood pressure was 129/65 mmHg and pulse was 160 beats per minute. Otherwise, examination was unremarkable.

An ECG showed atrial fibrillation (Fig 1a). Metoprolol 5 mg intravenous (IV) bolus had no effect. He was then given flecainide 150 mg over 30 minutes, but after 20 minutes of flecainide loading he became very pale and developed ventricular tachycardia leading to ventricular fibrillation (Fig 1b). One shock of 360 J resulted in return of spontaneous circulation (ROSC) and reversion to sinus rhythm. His repeat ECG showed RBBB with ST elevation in V1 to V2, suggesting Brugada syndrome Type 1 (Fig 1c). A repeat ECG after 3 hours proved to be normal without any feature of Brugada-type ECG pattern (Fig 1d).

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Fig 1.

(a) The 12-lead ECG on admission showing atrial fibrillation with fast ventricular rate. (b) The rhythm strip from the monitor showing ventricular fibrillation post flecainide loading. (c) The 12-lead ECG after the shock showing ST right bundle branch block with ST -elevation in V1–V2, suggestive of Brugada syndrome type 1. (d) Repeat 12-lead ECG 3 hours later showing no feature suggestive of Brugada syndrome. ECG = electrocardiography.

Case 2

A 57-year-old male collapsed and lost consciousness while sitting at home. His ECG showed RBBB with ST elevation in V1–V3 (Fig 2). His investigations showed a haemoglobin level of 13.7 g/dl, white cell count 12 × 10⁹/l, C-reactive protein 35 mg/l, sodium 137 mmol/l, potassium 4.3 mmol/l, creatinine 141 μg/l and urea 7.2 mmol/l. His chest X-ray (CXR) revealed consolidation of the right base and he was treated for chest infection with antibiotics. His transthoracic echocardiogram revealed good left ventricular systolic function with no evidence of structural heart disease. He was referred to an electrophysiologist for further management.

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Fig 2.

The 12-lead ECG showing Brugada ECG pattern. ECG = electrocardiography.

Diagnosis and types

Brugada syndrome is diagnosed in patients with typical ECG findings (coved ST elevation in leads V1–V3) plus at least one additional criterion from: a personal or family history of syncope, ventricular arrhythmias, or similar ECG findings in other family members.²⁴ The typical ECG changes alone are considered to represent an idiopathic Brugada ECG – ie the pattern is present, but BS is not.^2,24 Both ECG and clinical features are important in establishing the diagnosis.^2,24

Two different patterns of ST elevation have been described (Fig 3).²⁵

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Fig 3.

ECG patterns of -Brugada syndrome in leads V1–V2. Reproduced with permission from Bayés de Luna et al (2012).25 ECG = electrocardiography.

• In the classic Brugada Type 1 ECG, the elevated ST segment (≥2 mm) descends with an upward convexity to an inverted T wave. This is referred to as the ‘coved type’ Brugada pattern.

• In the Type 2 pattern (combined from the original designation of types 2 and 3 patterns, Table 1),²⁶ the ST segment is ≥2 mm elevated and has a ‘saddle back’ ST-T wave configuration, in which the elevated ST segment descends toward the baseline but remains at least 0.5 mm above the isoelectric baseline, and then rises again to an upright or biphasic T wave.

Diagnostic criteria

In view of the clinical variability in presentation and the different ECG manifestations which can be seen in patients with Brugada syndrome, diagnostic criteria have been proposed by professional societies from both Europe and North America.^2,24

Differential diagnosis

The differential diagnosis for Brugada pattern ECG changes includes other conditions that result in apparent conduction and ST segment abnormalities in leads V1 to V3 on the ECG. A list of such conditions are shown in Box 1.

The Brugada pattern on ECG can be seen as an early subclinical manifestation of arrhythmogenic right ventricular cardiomyopathy (ARVC).⁸ An association between ARVC and the Brugada pattern on ECG is suggested by a report of 96 victims of sudden cardiac death (SCD) who were aged ≤35 years and had a baseline ECG available.²⁰ Right precordial ST segment elevation with or without RBBB was present in 13 (14%) of these; at autopsy, all but one had ARVC.

In patients with clinical manifestations of ventricular tachyarrhythmias and no apparent cardiac structural abnormalities, a number of other conditions should be considered along with:

• congenital long QT syndrome (LQTS)

• acquired LQTS with polymorphic ventricular tachycardia (VT)

• catecholaminergic polymorphic VT

• idiopathic VT

• idiopathic ventricular fibrillation

• short QT syndrome

• commotio cordis.

Analysis of the ST-T waveform usually permits differential diagnosis between a Brugada ECG and right precordial early repolarisation seen in athlete's heart. Athletes exhibit an upsloping ST-segment with a mean ST_j :ST₈₀ ratio of ≤1, whereas Brugada patients show a downsloping ST-segment with a ST_j:ST₈₀ ratio of >1.³¹ The athlete with a suspected Brugada ECG should be referred to a cardiologist/electrophysiologist for further clinical work up, including a pharmacological test with sodium channel blocking, risk stratification and familial evaluation.

For most conditions in which VT or SCD occurs with no apparent cardiac structural abnormalities, the clinical scenario and the ECG findings can be used to exclude other conditions. For example:

• Patients with VT or SCD associated with prolongation of the QT interval are more likely to have LQTS than Brugada syndrome, particularly if the patient has been exposed to medications which may prolong the QT interval. Similarly, patients with VT or SCD whose QT interval is markedly shortened are more likely to have short QT syndrome.

• Patients who experience VT or SCD in the setting of exertion are more likely to have catecholaminergic polymorphic VT than Brugada syndrome, in which symptomatic tachyarrhythmias are more likely to occur at rest.

• Patients with VT or SCD following blunt chest trauma are more likely to have experienced commotio cord.

Among patients with the Brugada Type 2 ECG pattern, the Brugada Type 1 ECG pattern can occasionally be unmasked by sodium channel blockers (eg flecainide, procainamide, ajmaline and pilsicainide) (Table 2).^2,32 The reported sensitivity of pharmacologic challenge with these drugs range between 100%³² to as low as 15%.³³

Electrophysiology studies

The role of electrophysiology (EP) testing in patients with known or suspected BS depends largely upon the presence or absence of associated symptoms. Patients with a Brugada ECG pattern and certain high-risk clinical features (ie history of SCA and/or sustained ventricular arrhythmias) are known to have an increased risk of SCD.^3,8,19 In asymptomatic patients, EP testing remains debatable.³⁴

In the PRogrammed ELectrical stimUlation preDictive valuE (PRELUDE) trial, Priori and colleagues enrolled 308 patients with no history of cardiac arrest but with a spontaneous or drug-induced Type I Brugada ECG pattern.³⁵ Seventy-eight of these patients had an implantable cardiac defibrillator (ICD) implanted prophylactically. An EP study with a consistent stimulation protocol was performed. Over a mean follow up of 34 months no differences were found in the incidence of appropriate ICD shocks or cardiac arrest between patients who had or did not have inducible arrhythmias during the EP study.

Management

No proven pharmacologic treatment for preventing SCD in BS have been found, although isoproterenol has been proved to be useful for treatment of electrical storm in BS³⁶ and quinidine has also shown to be beneficial.³⁷

Among 25 patients (15 symptomatic and 10 asymptomatic) before and after treatment with quinidine bisulfate (mean dose 1483±240 mg/day),³⁷ ventricular fibrillation was inducible in all patients at baseline electrophysiology testing, but in only three after a few days of quinidine therapy. Quinidine treatment was continued in 19 patients for a mean of 56 months and none had arrhythmic events. Quinidine is currently being used in patients with ICD and multiple shocks, cases in which ICD implantation is contraindicated or for the treatment of supraventricular arrhythmias.³⁸ A list of potential antiarrhythmic drugs for the treatment of patients with BS are given in Table 3.

Some drugs have been reported to induce the Type 1 BS ECG pattern and/or (fatal) arrhythmias in BS patients. Patients with BS can prevent arrhythmias by avoiding these drugs (Table 4 and Table 5)³⁹ or by using them only in controlled conditions.¹⁰

The only treatment with proven efficacy in preventing SCD is an ICD. In a cohort of 63 patients, both amiodarone and β-blockers were found to be inferior to ICD.⁴⁰ Selecting patients for an ICD is challenging. The proposed recommendations of ICD in patients with BS are shown in Fig 4.²⁷

Box 1. Differential diagnosis of Brugada pattern ECG.

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Fig 4.

Consensus recommendations for implantable cardiac defibrillators (ICDs) in patients diagnosed with Brugada syndrome. Reproduced with permission from Priori et al (2013).27 ECG = electrocardiography; EP = electrophysiology; ICD = implantable cardiac defibrillator; SCD = sudden cardiac death; VT = ventricular tachycardia.

Asymptomatic BS patients do not qualify for an ICD as their risk for life-threatening events is very low.⁴¹ Patients in this group need to be assessed individually based on their gender, age, baseline ECG and inducibility.