COVID-19 Infection Unmasking Brugada Syndrome.

Introduction

First described in the 1990s, the Brugada syndrome initially characterized unexplained sudden cardiac death in healthy Southeast Asian men. Mutations in the cardiac sodium channel were later identified in the SCN5A and SCN10A genes, accounting for nearly 50% of the cases., Brugada syndrome phenotype is associated with decrease in the sodium current owing to reduction in sodium channels and/or reduction of function of the sodium channels. Although the reduction in the sodium current manifests with characteristic electrocardiographic abnormalities, patients with the Brugada syndrome are often healthy and unaware of their genetic predisposition. As a result, the diagnosis of Brugada syndrome is often made after syncope or aborted sudden cardiac arrest.

Fever, alcohol, and medications causing sodium channel blockade are well-described provocative triggers that may incite arrhythmia in patients with Brugada syndrome. Here, we report a novel case of syncope due to Coronavirus Disease 2019 (COVID-19)-induced fever in a patient with previously unrecognized Brugada syndrome.

Case report

A 49-year-old Bangladeshi man without significant medical history presented after an episode of syncope. A colleague witnessed the patient suddenly lose consciousness while sitting in his chair at work. The patient regained consciousness after 1–2 minutes with no postictal symptoms. He reported a day of subjective fevers, which he attributed to hepatitis B vaccination received 48 hours prior to presentation. He had experienced a similar reaction after his first injection a month prior. He denied similar episodes in the past and also denied recent travel or sick contacts. Notably, the patient’s younger brother had a similar episode of syncope approximately a year ago; there was no family history of sudden cardiac death.

Upon presentation, the patient was afebrile with otherwise stable vital signs. An ST-elevation myocardial infarction was called following acquisition of his first electrocardiogram (ECG) (Figure 1) and the patient was taken for urgent coronary angiogram, which showed normal coronary arteries. Transthoracic echocardiogram was performed, which showed preserved cardiac function with no anatomic abnormalities. No pericardial or pleural effusions were noted. He was admitted for further evaluation. Overnight, the patient spiked a fever of 102°F with ECG changes, as shown in Figure 2. Given his persistent fevers overnight, the patient was placed on airborne isolation and tested for COVID-19 (UTM: Viral Transport; Copan, Murrieta, CA).

Figure 1

The patient’s initial 12-lead electrocardiogram in the emergency department.

Figure 2

The patient’s repeat 12-lead electrocardiogram with a fever of 102°F.

The patient’s fever improved with Tylenol and he remained asymptomatic with no respiratory symptoms, including cough and dyspnea. With defervescence, the patient’s ECG changes were noted, as shown in Figure 3. There were no significant arrhythmic events, including premature ventricular contractions and nonsustained ventricular tachycardia observed on telemetry. The respiratory viral panel and blood cultures were unremarkable. Approximately 24 hours after the viral swab was collected, the patient tested positive for COVID-19. He remained in airborne isolation for 7 days owing to persistent fevers but had no respiratory symptoms. The patient was discharged with a LifeVest (Zoll Medical, Pittsburgh, PA) with plan for outpatient cardiac magnetic resonance imaging and eventual implantation of a subcutaneous defibrillator when cleared from home quarantine. The medical staff in contact with the patient was screened and high-risk staff members were sent for the COVID-19 tests and quarantined.

Figure 3

The patient’s repeat 12-lead electrocardiogram with resolution of fever.

Discussion

Patients with the Brugada syndrome, a combination of the Brugada ECG pattern, clinical symptoms, and/or pertinent family history commonly present with an episode of syncope or aborted sudden cardiac arrest from ventricular arrhythmia. The 2 common Brugada ECG patterns are the type 1 Brugada ECG pattern “coved” with the ST-segment elevation that concaves down with inverted T waves in V1-V2 and the type 2 Brugada ECG pattern with the “saddle-back” ST-segment elevation and an upright or biphasic T waves in V1-V2. Of the 2 types, the type 1 Brugada ECG pattern has a higher risk for ventricular arrhythmias. Patients with a type 1 Brugada ECG pattern and pertinent clinical features such as a personal history of syncope, ventricular arrhythmia, or family history of sudden cardiac death meet the diagnosis for Brugada syndrome. Those with a type 2 Brugada ECG pattern and pertinent clinical features require a class I antiarrhythmic drug challenge to induce a type 1 Brugada ECG pattern in order to meet the diagnosis of Brugada syndrome.

Discerning the difference between Brugada syndrome and the Brugada pattern with no relevant clinical features is important for patient management. An implantable cardioverter-defibrillator implantation is a class 1 indication in patients with Brugada syndrome who survived a cardiac arrest and/or who have a history of spontaneous sustained ventricular tachycardia. On the other hand, asymptomatic patients with the Brugada ECG pattern but no clinical signs and family history suggestive of Brugada syndrome do not benefit from a defibrillator.

In patients without a clear indication for an implantable cardioverter-defibrillator but presenting with high clinical suspicion for Brugada syndrome, other clues may help guide treatment. Provocative triggers such as fever, alcohol, and medications may unmask a type 1 Brugada ECG pattern. For instance, a patient with a type 2 Brugada ECG pattern at rest presenting with a fever and a “coved” ST elevation resembling a type 1 Brugada ECG pattern may be diagnosed with Brugada syndrome without an antiarrhythmic drug challenge.

Fever is shown to precipitate arrhythmia in patients with Brugada syndrome, and 1 study showed that more than half of the study cohort experienced syncope or cardiac arrest in the setting of a fever., The biophysical properties of the cardiac sodium channel worsen at higher temperatures. Although the functional decline in mutated sodium channels in patients with Brugada syndrome from a physiological temperature to a higher temperature may be minimal, the loss of function of the intact sodium channels may clinically translate into a fever-induced arrhythmia. In addition, the shortening of the intraepicardial dispersion of action potential duration owing to elevated temperature may facilitate reentrant ventricular tachycardia.

COVID-19 was first identified in Wuhan, China, in early December 2019 as a case of pneumonia with unknown etiology. In January 2020, the novel viral pathogen was identified, and with rapid spread was declared an international pandemic in March 2020.12, 13, 14 The severe inflammatory response to COVID-19 results in a febrile illness in the vast majority of patients. As shown in our case, COVID-19-induced fever led to symptomatic Brugada syndrome.

Conclusion

Symptomatic COVID-19 infection is typified by high fever, a known precipitant of arrhythmia in patients with Brugada syndrome. In addition to standard isolation procedures for patients diagnosed with COVID-19, those with known or suspected Brugada ECG patterns may warrant more aggressive antipyretic therapy and serial screening ECGs. In addition, when managing a febrile patient with syncope, an ECG must be a part of the evaluation. Defibrillator implantation should be strongly considered in individuals with a provoked type 1 Brugada ECG pattern.

Fever is the most common clinical presentation in patients tested positive for COVID-19.

Uncontrolled fever in patients with Brugada syndrome portends higher risk for syncope and sudden cardiac arrest.

Health care providers encountering febrile patients with suspicious electrocardiogram findings must address all potential infectious etiologies and treat the fever.