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Arrhythmia and COVID-19 in children

Arrhythmia and COVID-19 in children

Article information

Clin Exp Pediatr. 2023;66(5):190-200
Publication date (electronic) : 2023 April 18
doi : https://doi.org/10.3345/cep.2023.00024
1Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, Korea
2Brown University, Providence, RI, USA
Corresponding author: Mi Kyoung Song, MD, PhD. Department of Pediatrics, Division of Pediatric Cardiology, Seoul National University Children’s Hospital, Seoul National University College of Medicine, 101 Daehak-Ro, Jongno-gu, Seoul 03080, Korea Email: mksong00@snu.ac.kr
Received 2023 January 3; Revised 2023 February 4; Accepted 2023 February 6.


The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection caused worldwide health problems, and coronavirus disease 2019 (COVID-19) was declared a pandemic by the World Health Organization in March 2020. Cardiovascular complications of COVID-19 are not uncommon; among them, arrhythmia is considered a significant risk factor for poor health outcomes in adults. However, data are scarce on the arrhythmia of pediatric patients with SARS-CoV-2 infection, possibly due to their mild symptoms and low incidence of cardiovascular involvement. Multisystem inflammatory syndrome in children reportedly features increased cardiovascular involvement, but arrhythmic complications remain unidentified. Thus, here we review the epidemiology, manifestations, and outcomes of pediatric arrhythmia associated with COVID-19.

Key message

· Pediatric patients have a relatively low incidence of tachyarrhythmia both in acute coronavirus disease 2019 and multisystem inflammatory syndrome in children (MIS-C), but it was associated with an increased risk of poor outcomes.

· Conduction abnormalities were not uncommon, especially in those with MIS-C. Most patients recovered to normal sinus rhythm; however, some progressed to advanced atrioventricular block and rarely required permanent pacemaker implantation.

Graphical abstract. Arrhythmia associated with SARS-CoV-2 infection in pediatric patients. SARS-CoV-2, severe acute respiratory syndrome coronavirus-2; COVID-19, coronavirus disease 2019; MIS-C, multisystem inflammatory syndrome in children; AV, atrioventricular; ECG, electrocardiogram.


Coronavirus disease 2019 (COVID-19) is an infectious disease caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). The rapid spread of the disease resulted in a global pandemic with 634 million confirmed cases and 6.6 million deaths reported as of late November 2022 by World Health Organization (WHO) [1]. Its clinical presentation ranges from asymptomatic to mild to severe respiratory illness, while its systemic complications include cardiovascular involvement. Its cardiovascular complications include acute myocarditis, pericarditis, vasculitis, heart failure, venous thromboembolism, and arrhythmia, all of which are associated with increased mortality in adults [2-5]. Children generally have milder symptoms than adults, but severe pediatric cases have been described [6]. Furthermore, multisystem inflammatory syndrome in children (MIS-C) with the feature of Kawasaki disease and toxic shock syndrome is a severe postinflammatory complication of SARS-CoV-2 infection reported mainly in children and adolescents [7-9]. Arrhythmia is among the critical cardiovascular complications reported in 18%–44% of adult patients [4,5,10,11]. However, there have been only a few reports of arrhythmia in pediatric patients, possibly related to the lower complication rates and milder disease course in this population. Therefore, the characterization, clinical course, and outcome of arrhythmia in the pediatric population have not been entirely clarified. This review aims to present the current state of knowledge and summarize the literature on arrhythmia associated with COVID-19 in pediatric patients.

Mechanism of cardiovascular complications of COVID-19

Coronaviruses are large and enveloped viruses with singlestranded RNA. While human coronaviruses cause common cold-like respiratory illnesses, SARS-CoV from China during 2002–2003 and Middle East respiratory syndrome coronavirus from the Middle East in 2012 and 2015 made outbreaks with increased fatality rates of 9.6% and 36%, respectively [12,13]. These viruses manifest not only mild respiratory symptoms but also severe illnesses such as acute respiratory distress syndrome and end organ damage.

SARS-CoV-2 utilizes human angiotensin-converting enzyme 2 (ACE2) as a host surface cellular receptor for virus entry similar to SARS-CoV.5,10) SARS-CoV-2 has a surface-located spike glycoprotein that includes a receptor-binding domain that is responsible for membrane fusion followed by endocytosis into target cells [14]. ACE2 expression is tissue-specific with distribution in the heart, intestines, kidneys, testes, and respiratory system, suggesting a correlation with extrapulmonary involvement [15,16]. Once the virus infects cells in the respiratory tract, viral replication and circulation can occur, leading to cardiac uptake and replication of the virus [17]. ACE2, together with ACE, plays a vital role in blood flow and volume via the renin-angiotensin system. ACE2 mRNA expression is upregulated in patients with heart failure, making those individuals more susceptible to SARS-CoV-2 infection and possibly explaining their worse outcomes [18].

The proposed mechanisms of myocardial injury include direct ACE2-mediated injury, hypoxia-induced injury from respiratory failure, microvascular thrombosis, and systemic inflammatory injury from an exaggerated immune response, including cytokine storm [19]. A reported 20%–30% of patients with COVID-19 showed elevated cardiac biomarkers such as troponin and B-type natriuretic peptide in the acute phase, suggesting that direct myocardial injury is not uncommon, especially in moderate to severely ill patients and non-survivors [3,20,21]. Elevated cardiac biomarkers are associated with COVID-19 severity and independent predictors of mortality. Cardiac magnetic resonance imaging has shown myocardial edema, impaired ventricular function, and myocardial fibrosis even after recovery from COVID-19 [19]. In cardiac autopsies, chamber dilatation, lymphocytic myocarditis, focal pericarditis, endocardial thrombosis, and small vessel thrombosis have been reported. Thus, SARS-CoV-2 may directly damage infected cardiac cells with inflammation, triggering severe cellular pathology and organ dysfunction [19].

Cardiovascular involvement of SARS-CoV-2 in children

Children infected with SARS-CoV-2 generally have mild symptoms, with reported mortality rates of <0.1% [6,22-25]. A significant number of children (15%–42%) are asymptomatic, whereas 18%–57% require hospitalization [25-29]. Typical symptoms and signs include fever (40%–64%), cough (33%–56%), fatigue, tachypnea, nasal congestion, feeding difficulty or intolerance, shortness of breath, sore throat, and headache [25-28]. However, severe cases requiring intensive care unit (ICU) admission have also been reported. In a European multicenter study of 582 individuals <18 years of age with polymerase chain reaction (PCR)-confirmed COVID-19, 8% of study participants required ICU admission, 4% required mechanical ventilation, 3% required inotropic support, and 1% required extracorporeal membrane oxygenation (ECMO) support [26]. A meta-analysis by Sumner et al. [6] demonstrated that, among 973 hospitalized school-aged patients, 10.1% required ICU admission, 4.2% had a severe outcome, and 1.1% (95% confidence interval, 0.2%–2.3%) died.

Cardiovascular involvement in children can occur in the setting of acute SARS-CoV-2 infection and post-infectious MIS-C [30]. During acute COVID-19 in children, cardiovascular complications are rare. Only a few case reports or case series have reported myocarditis, pericarditis, cardiogenic shock, and arrhythmia [31-33].

Cardiovascular involvement in children with MIS-C

MIS-C is characterized by hyperinflammatory shock syndrome with multiorgan involvement in previously asymptomatic children with SARS-CoV-2 infection and was first reported in case series in the United Kingdom in April 2020. It showed similar features of atypical Kawasaki disease, Kawasaki disease shock syndrome, or toxic shock syndrome [7]. Subsequently, similar cases began to be reported in series [34-36]. The United States Centers for Disease Control and the WHO termed this syndrome MIS-C [37,38]. It is also called pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 [39]. Among the pediatric patients with PCR-confirmed SARS-CoV-2 infection in an Australian multicenter study, 1.3% had MIS-C.

MIS-C reportedly occurs 2–6 weeks after COVID-19 symptom onset or contact with infected individuals [35,40-42]. Cardiac involvement in MIS-C occurs in up to 80% of patients [42]. Additionally, cardiogenic or vasodilatory shock is present in 37%–60% of MIS-C patients [9,43-46]. Half of one population of patients had reduced left ventricular (LV) ejection fraction on echocardiography, while 9%–17% developed coronary artery dilatation or aneurysm [9,35,44,46]. Myocarditis, valvular regurgitation, and pericardial effusion have also been identified. Arrhythmias or electrocardiographic abnormalities are common, reported in up to 60% of patients [35,47-49]. Outcomes are generally positive, with a resolution of inflammatory and cardiac abnormalities within 1–4 weeks. However, 0.3%–5% of patients received ECMO support, while 0%–2% of patients, most of whom were previously healthy individuals, died [9,35,43,46,48,50].

Arrhythmia in children with COVID-19 or MIS-C

Arrhythmia, reported in 18%–44% of adult patients with COVID-19, is associated with worse clinical health outcomes [4,5,10,11,51]. Among them, the majority (82%) developed atrial arrhythmias, 21% developed ventricular arrhythmias, and 23% had bradyarrhythmia [11]. Potential mechanisms of arrhythmia are hypoxia due to direct viral involvement in the lung, myocarditis, an abnormal host immune response, myocardial ischemia, myocardial strain due to pulmonary hypertension, electrolyte derangements, intravascular volume imbalances, and drugrelated side effects [52]. Arrhythmias are likely not only a direct effect of viral infection but also a complication of systemic illness [51].

The incidence of arrhythmia associated with SARS-CoV-2 in children is much lower, with only a few case series or case reports to date. Tachyarrhythmia in pediatric patients was reported at a rate of 0%–17%, albeit some studies did not specify the type of arrhythmia and included isolated premature ventricular/atrial complexes [35,44,47,48,53,54]. On the other hand, multicenter studies reported the incidence of tachyarrhythmia as 1.7%–1.8%4 [3,55]. Variations in the incidence of arrhythmia may exist among studies because measures depend on the included patient population, such as hospitalized patients, public surveillance, or PCR-confirmed SARS-CoV-2 patients. Moreover, monitoring methods, such as 12-lead electrocardiography and continuous telemetry, may influence the variations. Published articles on tachyarrhythmia in children are summarized in Table 1; these include only those that demonstrated specified types of arrhythmia as well as their management, clinical details, and outcomes. Data for the patients with isolated premature atrial or ventricular complex and studies lacking descriptions of specific types of arrhythmia were omitted.

Summary of studies of patients with tachyarrhythmia

Samuel et al. [54] reported that 6 patients (17%) among a sample of 36 hospitalized pediatric patients with acute COVID-19 had tachyarrhythmia on continuous telemetry; 5 had nonsustained monomorphic ventricular tachycardia (VT), and one had sustained atrial tachycardia. None had bradyarrhythmia. Among the 6 patients, 4 had underlying disease such as sickle cell anemia, hematologic malignancy, and Bloom syndrome. Two had mild to moderate LV dysfunction and 4 had normal LV systolic function. All arrhythmias were self-limiting, but amiodarone in one and beta-blockers in 2 patients were used for prophylactic purposes.

Most of the reported cases showed a benign disease course or complete recovery with timely and aggressive treatment. However, mortality in pediatric patients with tachyarrhythmia has been reported, and large multicenter studies demonstrated that tachyarrhythmia was associated with poor outcomes [56-58]. Using a public health surveillance registry of 63 hospitals in the United States, Dionne et al. [55] showed the characteristics and outcomes of tachyarrhythmia in patients aged <21 years and hospitalized with acute COVID-19 or MIS-C. Twenty-two of 1,257 patients (1.8%) with acute COVID-19 and 41 of 2,343 patients (1.7%) with MIS-C had tachyarrhythmia, including supra VT (44%), accelerated junctional rhythm (14%), and VT (60%). Among them, 8 (13%) required cardiopulmonary resuscitation, while 9 (14%) required ECMO support because of refractory tachyarrhythmia. Patients with tachyarrhythmia were older and more frequently required mechanical ventilation and ECMO support. They also had higher illness severity on hospital admission, a longer hospital length of stay, and higher mortality rates (14% vs. 2%, P<0.001). Among the patients with tachyarrhythmia, those with acute COVID-19 showed higher mortality rates than those with MIS-C (7 of 22 [32%] vs. 2 of 41 [5%], P=0.006). Although tachyarrhythmia rarely develops in pediatric patients based on the large population data, it may have a substantial clinical impact and require close monitoring and aggressive treatment. Arrhythmia can increase an individual’s risk of death by deteriorating their clinical condition, while tachyarrhythmia can reflect a severe underlying cardiac and respiratory condition.

Conduction abnormalities associated with SARS-CoV-2 (e.g., first-degree atrioventricular [AV] block, second-degree AV block, complete AV block, sinus bradycardia, and bundle branch block) are more common complications than tachyarrhythmia in children. Table 2 shows the clinical characteristics, management, and outcomes of the patients reported in the literature. Bradyarrhythmia was reported in 16%–20% of patients with MIS-C [56,59,60]. MIS-C usually presents several weeks after a viral infection, and a dysregulated inflammatory response is the presumed pathophysiology [41]. Therefore, inflammation of conduction tissue and edema adjacent to the AV nodal or His-Purkinje system can be assumed to contribute to the conduction abnormalities. Coronary insufficiency to the AV node and other conduction systems is also a possible mechanism. Conduction abnormalities such as sinus bradycardia and bundle branch block reportedly developed after the administration of anti-inflammatory drugs during admission in some patients, suggesting drug-related bradyarrhythmia as one etiology [59].

Summary of studies of patients with bradyarrhythmia

First-degree AV block was the most common bradyarrhythmia [56,60,61]. It presented at a median 6–8 days after symptom onset, and most patients returned to a normal sinus rhythm spontaneously. A transient complete AV block or second-degree AV block (type I or type II) has been also reported, and some patients required temporary pacemaker insertion [44,56,62]. The incidence of a complete AV block was as low as 2.1%–5%, and most cases recovered a normal sinus rhythm [44,56]. However, some patients who developed a first-degree AV block progressed to a second- or third-degree AV block [56,59,63]. In rare instances, some children required permanent pacemaker implantation, and the first-degree AV block persisted at the time of discharge in some, suggesting the possibility of irreversible damage to the conduction tissue [59,64]. Therefore, patients with conduction abnormalities require intensive electrocardiogram monitoring during hospitalization and long-term follow-up after discharge [56,60,61]. The therapeutic effect of anti-inflammatory drugs on AV block or the preventive effect on the progression to a complete AV block remains unknown because all related studies were retrospective.

Electrocardiographic changes such as nonspecific T wave changes, low QRS amplitudes, an abnormal QRS axis, ventricular hypertrophy, and significant ST-segment changes were findings in 26%–35% of patients with acute COVID-19 and 35%–60% of those with MIS-C [43,44,49,54,58,65].

Repolarization abnormality

There have been reports of QT prolongation or repolarization abnormalities in patients with COVID-19 and MIS-C irrespective of QT-prolonging drug use [44,59,61,65-68]. Repolarization abnormalities, with myocardial injury from acute myocarditis in COVID-19 and a hyperinflammatory state in MIS-C, can increase the risk of malignant arrhythmia in patients with inherited arrhythmia despite no reports to date. Pawar et al. [69] reported neonates with multiple inflammatory syndromes presenting with QTc prolongation with a 2:1 AV block who were born to mothers with a history of COVID-19. An AV block with 2:1 conduction was a functional block due to QT prolongation and disappeared with intravenous immunoglobulin and methylprednisolone, followed by normalization of the QTc interval in all patients.

Furthermore, some drugs used in patients with COVID-19, such as remdesivir, azithromycin, and hydroxychloroquine, can prolong the QTc interval even in patients without underlying disease (www.crediblemeds.org) [38]. An electrolyte imbalance (hypokalemia, hypocalcemia, and hypomagnesemia) and dehydration from a poor oral intake, diarrhea, or vomiting may further increase the QTc interval [52]. So, patients with COVID-19 and an increased risk of QT prolongation require electrocardiography and QTc change monitoring during the illness. As patients with congenital long QT syndrome have an extended QT interval with the increased risk of torsades de pointes, they require electrocardiography monitoring during acute COVID-19 or MIS-C and must avoid QT-prolonging drugs and hypokalemia with COVID-19-associated diarrhea.

Autonomic dysfunction

Palpitations, dizziness, and orthostatic intolerance have been noted in some patients for weeks to months after the initial SARS-CoV-2 infection [70-72]. Postural orthostatic tachycardia syndrome and autonomic dysfunction are among the causes of such symptoms. The proposed mechanisms are dehydration, increased cardiac sympathetic outflow from damaged or altered autonomic nervous system function, and autoimmunity [71]. Although the mechanism is not yet clarified, the symptoms usually significantly improved with lifestyle modifications and medications such as fludrocortisone, midodrine, or beta-blockers [70].

Cardiovascular complications including arrhythmia in patients with congenital heart disease

Patients with underlying cardiac diseases, such as congenital heart disease (CHD) and cardiomyopathy, were initially considered at high risk for mortality and poor outcomes [57,73,74]. Strah et al. [75] demonstrated that pediatric patients with COVID-19 and moderate to severe CHD were younger at admission (1 vs. 11 years), had a longer length of stay, and had higher morbidity and mortality rates than those without CHD. However, other studies exhibited that worse New York Heart Association Functional class ≥III, genetic syndrome, and adults with CHD were significantly associated with the need for hospitalization/respiratory support as well as higher morbidity and mortality rates rather than CHD presence or severity [76,77]. A multicenter study from 58 adult CHD centers that included 1,044 infected patients also demonstrated that the COVID-19 case/fatality rate of 2.3% was similar to that (2.2%) of the general population. Cyanosis, previous heart failure admission, a worse physiological stage, pulmonary arterial hypertension, male sex, renal insufficiency, and diabetes were associated with death, while anatomic complexity was not predictive [78].

Patients with CHD are at increased risk for arrhythmia, but only one case series of arrhythmic events was published during the COVID-19 pandemic [57]. Simpson et al. presented 6 patients with CHD and one patient with hypertrophic cardiomyopathy for acute COVID-19, of whom 2 had newly developed VT requiring cardiopulmonary resuscitation or defibrillation. Both had respiratory failure and decompensated heart failure before the development of VT, and one eventually died of VT recurrence. Although the association between arrhythmia development in CHD patients and COVID-19 has not been identified, a proarrhythmic substrate in repaired or unrepaired CHD in a patient with diastolic and/or systolic dysfunction combined with right ventricular failure from respiratory failure may result in poor outcomes.


Cardiovascular complications are uncommon in children with SARS-CoV-2 infection, whereas those with MIS-C had increased cardiovascular involvement. Tachyarrhythmia was associated with poor clinical outcomes in a large multicenter study. Many patients improved with/without medical treatment, but some required ECMO support. Bradyarrhythmia was relatively common, reported in up to 20% of patients, and more frequently occurred in patients with MIS-C than acute COVID-19. Most patients with conduction abnormalities recovered a normal sinus rhythm, and permanent pacemaker implantation was rarely required.

Pediatric patients have a relatively low incidence of arrhythmic complications, but those with arrhythmia require a timely diagnosis with immediate aggressive treatment. Electrocardiography abnormalities and QT prolongation were not uncommon. Thus, among pediatric patients with acute COVID-19 or MIS-C, especially those who are critically ill, close monitoring for arrhythmia and QT prolongation is required as appropriate management. There are limited data for cardiovascular involvement in pediatric patients, and the effects of SARS-CoV-2 infection are still emerging. Therefore, continuous research with long-term follow-up is required.


Conflicts of interest

No potential conflict of interest relevant to this article was reported.


This study received no specific grant from any funding agency in the public, commercial, or not-for-profit sectors.


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Table 1.

Summary of studies of patients with tachyarrhythmia

Study Age (yr) No. Arrhythmia Condition related to SARS-CoV-2 Underlying disease Clinical detail Management (for antiarrhythmiaa)+COVID-19 treatment) Outcome Study type Country
Samuel et al. [54] 2020 November Median age, 14.5 yr (range, 12-20 yr) 6/36 (17%) Nonsustained monomorphic VT (n=5), sus- tained AT (n= 1) Acute COVID-19 (6), acute myocarditis (2) No previous heart disease LV dysfunction (2), large pericardial effusion (1), normal LV function (4) All hemodynamically tolerated and sefl-lmit- ed arrhythmia.prophy- lactic antiarrhythmic drug; amiodarone (1), beta-blocker (2). Hy- droxychloroquine±azi- thromycin Self-resolving, no mortality Observation study New York, USA
Cantarutti et al. [65] 2021 August Total cohort mean, 9±5.9 3/294 (1%) Nonsustained VT (2), AF (1) Acute COVID-19 (248), MIS-C (46) NA NA Not requiring emer- gency treatment for arrhythmia. IVIG, cor- ticosteriod, anakinra in most severe pa- teints. All patients recovered. Multicenter observation study Rome, Italy
Dionne et al. [55] 2022 Median, 15.4 yr (range, 10.4–17.4 yr) 63/3,600 (1.8%) SVT (28, 44%): reentrant SVT (2), ectopic AT (10), AFL (8), AF (9), accelerated junctional rhy- thm (9, 14%), VT (38, 60%) Acute COVID-19 (22/1257,1,8%), MIS-C (41/ 2343, 1.7%) More patients with underlying heart disease in acute COVID-19 Severe LV dysfunction (31%), more respiratory support (81%), more vaso- pressor requirement and ECMO No intervention (41%), Antiarrhythmic medi- cation (49%), electri- cal cardioversion (17 %), CPR (13%), ECMO (14%) 9/63 (14%) died. 22% were discarged with medication. Multicenter USA, multicenter
Tseng et al. [79] 2021 March 5 1 Monomorphic VT Acute COVID-19, fulminant myocarditis Previously healthy Cardiogenic shock, biventricular dysfunction Cardioversion, lidoca- ine, amiodarone → no effect, VA ECMO on HD 4 Complete reco- very and discharged Case report Michgan, USA
Kohli et al. [80] 2022 15 1 AF Acute COVID-19, fulminant myocarditis Previously healthy Severe LV dysfunction, cardiogenic shock → milrinone, epinephrine, AF on HD2 Initropics, IVIG, steriod, anakinra, cardiover- sion followed by amio- darone for AF → no recur NSR, normaliz- ed LV function, no recur, discharged Case report Chicago, USA
Hopkins and Webster [81] 2021 April 9 Days, newborn 1 SVT Acute COVID-19 Normal heart. mother had acute COVID-19 Orthodromic SVT with aberrancy. Normal LV function Transesophageal over- drive pacing, oral pro- pranolol 2 mg/kg/day No recur of SVT, discharged Case report Chicago, USA
Whittaker et al. [9] 2020 June NA 4/58 (6.9%) Broad complex tachycardia (n=1), AF (n=1), second-degree AVB (n= 1), and first-degree AVB (n=1) MIS-C Most were previously healthy (88%) (1) A patient with wide complex ta- chycardia → low cardiac output- → ECMO, (2) a patient with AF → amiodarone, (3) a patient with 2nd degree AVB NSR For the total cohort: inotropics in 47%, IVIG in 71%, steroid in 64 %, Anakinra in 5%, and infliximab in 14%, supportive care alone in 22% NA Multicenter observation study England
Riollano‐Cruz et al. [82] 2020 June 14 1/15 (6.7%) VT, QT prolongation MIS-C NA Mild LV dysfunction 48% Inotropics, amiodarone (not specified for the management of arrhythmia), lidocaine, anakinra, tocilizumab, remdesivir Recovered LV function, discharged on HD 13 Obsrvasion study New York, USA
Clark et al. [44] 2020 September Total cohort mean 7±5.2 6/55 (11%) cAVB (n=3), transient 2nd AVB, sinus pause, 1 st degree AVB, and VT (1) MIS-C Previously healthy All had decreased LV EF (27%–55%) IVIG, steroid. Not specified for the antiarrhythmic therapy cAVB normalized within 2 weeks. Other arrhtyhmia out come is not described Multicenter observation study International (USA, UK, spain, pakistan)
Santi et al. [83] 2020 October 17 1 AF, nonsustained VT MIS-C Previously healthy Hypotensive → normal saline and epinephrine. Normal heart function, no pulmonary hypertension AF on HD 3 → DC cardioversion, recurrence of AF → cardioversion and amiodarone, anakinra, IVIG, methylPd Recovery, discharged home on HD 16 Case report Califonia, USA
Regan et al. [58] 2021 6 2/63 (3.2%) Nonsustained ectopic AT MIS-C NA Asymptomatic No treatment Live Observation study London, UK
14 Ectopic AT with RBBB MIS-C NA Cardiogenic shock → ECMO ECMO support and rate control with amiodarone → died following complications from the ECMO support Died following complications from the ECMO support
Tomlinson et al. [84] 2021 March 13 1 Accelerated idioventricular rhythm, sinus node dysfunction MIS-C Previously healthy Normal LV EF, hypotension → epinephrine. Sinus node dysfunction, idioventricular rhythym → HD2, sinus ta- chycardia with left axis deviation No antiarrhythmic drug. IVIG Normal sinus rhythm on discharge, HD 9 Case report Virginia, USA
Schneider et al. [85] 2022 6 1 VT MIS-C Previously healthy LV dysfunction, cardiogenic shock, brief cardiac arrest VT → VA ECMO VA ECMO, IVIG, steroid, tosilizumab, and remdesivir Complete recovery and discharged Case series Michgan, USA
15 1 VT MIS-C TIDM Severe both ventricular dysfunction → cardiogenic shock and development of VT VA ECMO, IVIG, steroid, infliximab, and remdesivir Decanulated after 4 days of ECMO. Discharged
Simpson et al. [57] 2020 July 18 Years 1 VT Acute COVID-19 HCM, obesity, TIIDM, HTN Preserved biventricular function→ VVECMO d/t respiratory failure→ escalated to VA ECMO d/t acute decompensated→ HF→VT→ stabilizaed after management Defibrillation, infusion of amiodarone and lidocaine. Hydroxychloroquine, azithromycin, tocilizumab, convalescent plasma, IVIG, methylPd Death d/t recurrence of VT on HD 31 Case series Multicenter, USA
6 Months 1 VT Acute COVID-19 Repaired ALCAPA with severe ven- tricular dysfunction New severe PHT with RV dysfunction, LV EF 20%. During intubation, bradycardia and VT → epinephrine, CPR Not specified. epinephrine, milrinone, iNO for PHT, tocilizumab, remdesivir Dischargedhome on HD 35 Case series Multicenter, USA

SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; COVID-19, coronavirus disease 2019; LV, left ventricular; VT, ventricular tachycardia; AF, atrial fibrillation; MIS-C, multisystem inflammatory syndrome in children; NA, not available; IVIG, intravenous immunoglobulin; SVT, supraventricular tachycardia; AT, atrial tachycardia; AFL, atrial flutter; CPR, cardiopulmonary resuscitation; ECMO, extracorporeal membrane oxygenation; VA, venoarterial; HD, hospital day; NSR, normal sinus rhythm; AVB, atrioventricular block; cAVB, complete atrioventricular block; RBBB, right bundle branch block; EF, ejection fraction; VV, venovenous; HCM, hypertrophic cardiomyopathy; TIDM, type I diabetes mellitus; TIIDM, type II diabetes mellitus; HF, heart failure; d/t, due to; HTN, hypertension; ALCAPA, anomalous left coronary artery from the pulmonary artery; PHT, pulmonary hypertension; RV, right ventricular; iNO, inhaled nitric oxide.


Arrhythmia management is underlined.


Four patients had underlying extracardiac disease: sickle cell disease (n=1), hematologic malignancy (n=2), Bloom syndrome (n=1)

Table 2.

Summary of studies of patients with bradyarrhythmia

Study Age (yr) No. of patients Arrhythmia Condition related to SARS-CoV-2 Past medical history Clinical detail Laboratory findings Management Outcome Study type Country
Lara et al. [62] 2020 12 1 Complete AVB Acute COVID-19, fulminant myocarditis Previously healthy Cardiac arrest following severe bradycardia with complete heart block, and hypotension. De- creased LV EF 27% Elevated BNP, and troponin I Epinephrine, IVIG NSR on HD 4, and improved LV function to normal Case report Louisiana, USA
El-Assaad et al. [86] 2020 May 10 1 First-degree AVB → complete AVB Acute COVID-19, myocarditis Pityriasis lichenoides chronica Sinus tachy, severe LV dysfunction EF 32% → 1st degree AVB on HD 2. complete degree AVB and 2nd degree AVB on HD 3. Elevated CRP, D- dimer, BNP, and high-sensitive troponin. IVIG, anakinra, methylPd, remdesivir. no intervention for bradyarrhythmia Spontaneously resolved Case report Boston, USA
Dionne et al. [56] 2020 August Median 12.1 5/25 (20%) First-degree AV block (n=5) → progressed to second- (n=3) or third- AVB (n=1) MIS-C NA All had ventricular dys- function (LV EF 40%– 55% in 4, <40% in 1). Inotropics support d/t hypotension or shock in 4 patients Elevated BNP (4/5), normal troponin (5) No treatment required for the AVB. Inotropics for shock NSR in all patients Single center observational study Boston, USA
Carmona et al. [59] 2021 October 19 3 1st AVB with RBBB on admission → complete AVB → type 2nd-degree AVB type I 2nddegree AVB → first-degree AVB MIS-C Previously healthy LV EF 40% improved to 50%. Cardiac MRI: sub- epicardial enhancement along the basal inferior wall Hypotensive, elevated CRP, ESR, and BNP. Mildly elevated troponin Isoproterenol for cAVB, IVIG, methylPd, azithromycin, Anakinra, tocilizumab Discharge, normal LV function, persistent firstdegree AVB Case report Florida, USA
9 Sinus bradycardia on HD 8 with prolonged QTc 545 msec MIS-C Previously healthy LV EF 35%–40%, hypotension Mildly elevated troponin, elevated BNP, CRP IVIG, methylPd, anakinra, inotropics Discharged with normal QTc and normal LV EF
9 RBBB on HD 4 (initially NSR → sinus bradycardia) MIS-C Obese Inicial ormal LV function On HD 3, mild LV dysfunction with RBBB → junctional rhythm, sinus brady 38–48 bpm Elevated BNP, IL- 6, lactic acid, and CRP. Normal troponin IVIG, methylPd, anakinra Discharged with NSR and normal LV function
Domico et al. [63] 2020 11 1 Sinus bradycardia with 1st and 2nd degree on HD 4 type II 2nd-degree AVB, nonspecific intraventricular conduction delay, nonsustained VT MIS-C, giant aneurysm in coronary arterie Previously healthy Vasogenic shock, normal LV EF → intubation, inotropes → On HD 4, sinus brady with varying degree AV block (1st and 2nd degree) type II 2nd degree AVB Elevated CRP, ESR, IL-6, and lactate. Serial troponin during admission: within normal range Temporary transvenous pacing and methylPd, IVIG, infliximab NSR. Complete recovery before discharge Case report Califonia, USA
Choi et al. [61] 2020 December Median 11.5 (range 9–17) 6/32 (19%) First-degree AVB (n=6), RBBB (n=1) MIS-C NA Onset of AVB: median 8 days after the initial symptom. No advanced AVB Elevated CRP, IL- 6, NT pro-BNP, high-sensitive troponin T, LDH, D-dimer No management for first-degree AVB, IVIG, methylPd, anakinra (13%) NSR 3 days there after obs. Study New York, USA
Mehta et al. [64] 2021 6 1 Complete AVB with a HR of 32 bpm on admission MIS-C Previously healthy 4 Days after fever onset, Shock with HR 32 bpm with poor perfusion on admission. Mild LV dysfunction Elevated CRP, LDH, NT pro-BNP, and tropoin I Isoproterenol/adrenaline followed by temporary PM implantation. IVIG, methylPd, NSR after 5 days. NSR during fol- lo w-up at 2 months after the illness Case report West Bengal, India
7 1 Complete AVB with HR of 26/min on admission MIS-C NA 6 Days after fever onset, shock with HR 26 bpm on admission. mild LV dilatation and dysfunction Elevated CRP, LDH, NT pro-BNP, and tropoin I Isoproterenol/adrenaline followed by temporary PM implantation → no recovery for 12 days → permanent PM implantation Permanent PM. Remained pace- maker dependent at 1 month of follow-up
Giordano et al. [87] 2021 14 1 First-degree AVB MIS-C Previously healthy Hypotensive shock Elevated CRP, ESR, LDH, D-dimer, and troponin IVIG, methylPd Recovered to NSR Case report Italy
Di Filippo et al. [88] 2021 August 12 1 First-degree AVB MIS-C Previously healthy Improved clincial condition after IVIG and methylPd, but on day 8 after fever worsening EF 53% with increased BNP, moderate MR and first-degree AVB appeared Elevated CRP, Ddimer, IL-6, BNP, and troponin IVIG, methypPd 12 Days after fever, normal ECG and normal LV EF Case report Italy
Sisko et al. [89] 2021 October 8 1 Complete AVB with ventricular escaped beat 30 bpm Chronic phase of COVID-19 (COVID-19 infection 4 months ago) Previously healthy Severe RV dysfunction, severe TR, abdominal pain, marked bradycardia, hepatomegaly Normal CRP, ESR, and torponin I. Elevated BNP. Diffuse late gadolinium enhancement in RV free wall in MRI Dopamine, milrinone, IVIG, methylPd, favipiravir, temporary PM implantation on HD#7 Permanent PM implantation and TV repair on the 19th day on admission Case report Izmir, Turkey

SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; AVB, atrioventricular block; COVID-19, coronavirus disease 2019; LV, left ventricular; EF, ejection fraction; BNP, brain natriuretic peptide; bpm, beat for minute; IVIG, intravenous immunoglobulin; NSR, normal sinus rhythm; HD, hospital day; CRP, C-reactive protein; methylPd, methylprednisolone; NA, not available; MIS-C, multisystem inflammatory syndrome in children; MRI, magnetic resonance imaging; ESR, erythrocyte sedimentation rate; cAVB, complete atrioventricular block; RBBB, right bundle branch block; IL-6, interleukin-6; ECG, electrocardiogram; MIS-C, giant aneurysm in coronary arteries; NT pro-BNP, N-terminal-pro-hormone brain natriuretic peptide; HR, heart rate; PM, pacemaker; LDH, lactate dehydrogenase; MR, mitral regurgitation: TR, tricuspid regurgitation; RV, right ventricular.