The disease caused by a novel coronavirus identified as severe acute respiratory coronavirus 2 (SARS-CoV-2) was named Coronavirus Disease 2019 (COVID-19). The disease quickly spread to hundreds of countries within a few months, becoming a pandemic in March 2020. In childhood, COVID-19 mainly showed mild clinical course, and severe disease can be seen in 2–6% of cases. Reference Dong, Mo and Hu1,2 A hyperinflammatory syndrome characterised by fever longer than 24 hours, skin rashes, conjunctivitis, and multisystemic findings emerged from the United Kingdom and Italy in April 2020 and was named a multisystemic inflammatory syndrome in children. 2,Reference Verdoni, Mazza and Gervasoni3 Cardiac complications in children have been mainly reported among multisystemic inflammatory syndrome in children cases, such as coronary artery dilatation and aneurysms. However, several cardiac manifestations, including asymptomatic myocardial injury, myocarditis, and pericardial effusion, can be observed in COVID-19 patients. Reference Clerkin, Fried and Raikhelkar4 Arrhythmias such as ST/T wave abnormalities, QTc prolongation, and atrioventricular block due to these cardiac changes have been reported mostly in adult studies. Reference Mohammad, Emin, Bhutta, Gul, Voorhees and Afzal5 However, data on paediatric COVID-19 patients with cardiac manifestation and electrocardiographic abnormalities are still scarce. Reference Azevedo, Botelho and Hollanda6,Reference Sisko, Atik, Karadeniz, Guzeltas and Ergul7 Therefore, we aimed to determine the electrocardiographic abnormalities in hospitalised children with COVID-19 and multisystemic inflammatory syndrome in children.
Methods
The study was conducted at the Pediatric Infectious Diseases Division of the Faculty of Medicine, Ege University, Turkey, between March 2021 and December 2021. Patients aged 0–18 years with the diagnosis of COVID-19 and multisystemic inflammatory syndrome in children were included. Patients with a positive result of SARS-CoV-2 PCR and showing symptoms attributable to COVID-19 were hospitalised in the Pediatric Infectious Diseases Department. Multisystemic inflammatory syndrome in children was defined according to criteria declared by the Central Diseases Center of the United States. 8
The patients’ medical records were collected retrospectively, and demographic characteristics (age, gender, comorbidities), clinical features, and laboratory findings were recorded. A daily electrocardiography was performed for the patients who had electrocardiographic abnormalities on admission or developed electrocardiographic abnormality on the follow-up.
The patients with electrocardiographic abnormalities were also evaluated in terms of length of hospital stay, paediatric ICU admission, the medical treatments given (steroid, intravenous immunoglobulin, antiviral therapy, anticoagulant therapy), and the levels of inflammatory markers (C-reactive protein, ferritin) and cardiac markers (troponin T and pro-brain-natriuretic peptide).
Electrocardiography
Two different 12-lead standard electrocardiographic devices were used. Records were taken with the Philips ECG TC10 ECG device in the paediatric intensive care and emergency department and with the Cardiofax model 1250K ECG device in the paediatric infectious diseases department (Philips ECG TC10, Andover, MA, USA; Cardiofax GEM, Model 1250K; Nihon Kohden, Tokyo, Japan). Two different 12-lead standard electrocardiographic devices were performed with a speed of 25 mm/s and an amplitude of 10 mm/mV while the patients lay in supine. Electrocardiographics were read by a blind paediatric cardiologist. Paediatric cardiologists did not examine patients. Normal paediatric electrocardiographic parameters for age were used to determine heart rate and PR interval normal limits. Bradycardia was defined as a heart rate below the second percentile for age (Table 1). The first-degree Atrioventricular (AV) block on the electrocardiography was defined as PR interval >200 ms without associated disruption of atrial to ventricular conduction. ST-T segment normalised is the isoelectric line. In addition, elevation and depression of chest lead greater than 1 mV from the isoelectric line were considered as abnormal. Reference Park9–Reference Saarel, Granger and Kaltman11
Microbiological methods
In a viral transport medium containing VNat, combined nasopharyngeal and oropharyngeal swab specimens were obtained (Bioeksen, Turkey). All samples were evaluated at our Molecular Virology Laboratory using the Bio-speedy® SARS CoV-2 Double Gene RT-qPCR (Bioeksen, Turkey). The Rotor-Gene was used to reverse transcription-polymerase chain reaction (Qiagen, Luxemburg). This assay amplifies and detects two viral targets (ORF1ab and N), with a detection limit of 200 genomes per mL. The human gene target RNAse P (RP) was evaluated in each sample to employ an internal control. Results were considered positive if the signal was detected (Ct < 35) for RP, ORF1ab, and N genes.
Anti-spike immunoglobulin G (IgG) and IgM antibodies were detected in serum samples using rapid lateral flow immunoassay (Colloidal Gold-Hotgen, Germany).
Statistical methods
Statistical analysis was performed with SPSS statistical package (version 25 for Windows). Data were expressed as either mean ± SD or percentages.
Ethics
This research was approved by Ege University Clinical Research Ethics Committee on 16.12.2021 (Number: 21-12.1T/22).
Results
A total of 216 paediatric patients hospitalised between March 2020 and December 2021 were included in the study. Of these, 168 (77.7%) were diagnosed with COVID-19 and 48 (22.2%) with multisystemic inflammatory syndrome in children, 98 (45%) were female and 118 (55%) were male. The mean age of the patients was 10.7 ± 4.69 years. There was an underlying disease in 84 (38.8%) of the hospitalised patients; neurometabolic disorders [n = 18, 8.2% (nine epilepsy and epileptic syndromes, three neurodegenerative disease, three organic acidemia, two glycogen storage disease, one mucopolysaccharidosis)], endocrinological pathologies [n = 14, 6.4% (11 obesity and 3 type 1 diabetes mellitus)], hemato-oncological malignancy [n = 11, 5% (five acute lymphoblastic laeukemia, three central nervous system tumour, one lymphoma, one neuroblastoma, one osteosarcoma)] were the most common comorbidities. It was remarkable that 5% of the patients were obese. Length of hospital stay-in median range was 6.1 days (1–22 days), and 51 (23.6%) patients had paediatric ICU admission. The variant analysis could not be performed in patients with positive SARS-CoV-2 PCR, but the delta variant was the most prevalent in Turkey from Marchto December of 2021. The demographic characteristics of the hospitalised patients are summarised in Table 2.
COVID-19 = coronavirus disease 2019; ECG = electrocardiography; MIS-C = multisystem inflammatory syndrome; PICU = paediatric ICU.
Electrocardiographic abnormality was detected in 12 (5.5%) hospitalised patients; 58.3% were male. Three (25%) were hospitalised for multisystemic inflammatory syndrome in children (with positive COVID-19 antibodies) and 9 (75%) for COVID-19 (with positive SARS-CoV-2 PCR). The mean age was 12.4 ± 3.4 years. Comorbidity was present in only 1 (obese) patient. While 5% (n = 11) of 216 patients in the study group were obese, sinus bradycardia developed as a result of severe COVID-19 pneumonia in only one of those with obesity. Length of hospital stay-in median range was 8.2 days (6–10 days). On admission, seven patients had respiratory symptoms such as cough, shortness of breath, and high-grade fever. Pneumonia findings were confirmed on thorax tomography imaging, favipiravir, antibiotherapy (ceftriaxone or ceftriaxone + vancomycin), low molecular weight heparin, and dexamethasone treatments were given. Intravenous immunoglobulin and high-dose methylprednisolone were given to three patients diagnosed with multisystemic inflammatory syndrome in children, and inotropic support was given to one patient. In addition, a patient diagnosed with myocarditis due to COVID-19 was given IVIG therapy. Eight (66.6%) patients had respiratory distress and seven (58.3%) patients had paediatric ICU admission. Bilevel positive airway pressure support was given to four patients following high-flow oxygen therapy. The length of stay-in median range at paediatric ICU was 2.6 days (2–7 days). The demographic characteristics and laboratory findings of the patients with electrocardiographic abnormality are summarised in Tables 3 and 4.
ALC = absolute lymphocyte count; ANC = absolute neutrophil count; CRP = C-reactive protein; ECG = electrocardiography; Hb = hemoglobin; NT-pro-BNP = N-terminal-pro-brain natriuretic peptide; PCT = procalcitonin; PLT = platelet count; WBC = white blood cell.
Electrocardiographic abnormalities were as follows: 2 (0.9%) patients developed first-degree AV block, 3 (1.4%) patients had transient ST elevation and concomitant T negativity, and the other 7 (3.2%) had sinus bradycardia. None of the patients received antiarrhythmic medications such as β-blockers and calcium channel blockers. Electrocardiographic abnormality was experienced in the second week of the disease in most patients (n = 10, 83.3%); the median time from the onset of disease symptoms to the detection of electrocardiographic abnormality was 9 days (range: 4–12 days). The median time to detection after admission and steroid therapy was 4 days (3–7 days). The patients did not undergo 24-hour Holter recording during the hospital stay, but daily electrocardiography was recorded for the patients who had electrocardiographic abnormality on admission or developed electrocardiographic abnormality on the follow-up. Patients who developed bradycardia were continuously monitored with bedside monitors. Although very low cardiac pulse values were recorded (even deeper while asleep), the patients did not suffer from haemodynamic deterioration. The electrocardiographic abnormality returned to normal without any medication or pacing on the third day after the initial abnormalities in all patients except one patient whose sinus bradycardia lasted 4 days. Most of the patients (n = 10) did not develop any symptoms due to the severe course of the disease, close monitoring of their vitals allowed these electrocardiographic changes to be noticed. Except for arrhythmias occurring during hospital follow-up, there were two patients with electrocardiographic abnormality and SARS-CoV2 PCR positivity at admission; one of them presented with syncope, first-degree AV block was detected, and the other presented with chest pain and fever, ST elevation was seen, and diagnosed as myocarditis due to COVID-19 (electrocardiographic findings are shown in Figs 1 and 2).
Although it was observed that the detection of sinus bradycardia and firsst-degree AV block did not have a significant effect on patient management, it was important to detect ST changes, which can be considered as an indicator of myocardial injury, in 1.4% (3/216) patients, because in this way, the examinations and treatments (IVIG, steroid) of the patients were expanded and longer follow-up was planned. Also it has been shown in our data that COVID-19 can cause substantial myocarditis (1 of 216 cases; approximately 0.5%) in childhood and may present with significant electrocardiographic abnormalities.
In laboratory tests, there was a significant increase in cardiac markers troponin T and pro-BNP in multisystemic inflammatory syndrome in children patients and one patient with myocarditis. At the same time, no elevation was found in other COVID-19 patients.
In echocardiographic evaluation, pathology was detected only in patients with multisystemic inflammatory syndrome in children; one of the patients had mild mitral regurgitation, one had pericardial effusion, and the other one had low ejection fraction (35–40%), which completely regressed in follow-up. No pathology was detected in other patients. All patients recovered; no deaths from SARS-CoV-2 infection nor multisystemic inflammatory syndrome in children were recorded.
Discussion
In our single-centre experience, we detected an electrocardiographic change in 5.5% of the hospitalised paediatric patients with COVID-19. Sinus bradycardia accounted for more than half of the electrocardiographic abnormalities, followed by transient ST elevation-T negativity and first-degree AV block. Only three of the patients were multisystemic inflammatory syndrome in children patients from whom we expected cardiac involvement, but the others were COVID-19-related conditions. While multisystemic inflammatory syndrome in children data are found more frequently, and there are many adult studies of arrhythmias in COVID-19 patients in the literature, the number of studies examining electrocardiographic changes in paediatric patients with COVID-19 is very few.
Among cardiovascular manifestations associated with COVID-19, various articles have reported arrhythmias in adults, but there have been past arrhythmic history or significant comorbidities in most cases. Reference Guo, Fan and Chen12,Reference Ruan, Yang, Wang, Jiang and Song13 A study involving adult patients diagnosed with COVID-19 detected a new arrhythmia attack in 9% of hospitalised patients. Atrial fibrillation and atrial tachycardia were the most common arrhythmias. Reference Sala, Peretto and De Luca14 The patients were clinically stable, older and had longer in-hospital stays. Ventricular arrhythmias have also been reported as the first clinical manifestation of COVID-19. In the adult literature, AV block was noticed in the acute phase of the hospitalisation, and most were considered due to hypoxia or electrolyte imbalance. Reference Siripanthong, Nazarian and Muser15 However, the cause and mechanism of arrhythmia in children have not been fully elucidated. Reference Hundley and Bluemke16
The short- and long-term effects of new-onset bradyarrhythmias in patients with COVID-19 are unknown. A series of seven patients with COVID-19 and severe bradyarrhythmias requiring pacemakers was reported in adults. Reference Chinitz, Goyal and Harding17 Amir et al. reported a case series of six paediatric patients with symptomatic bradycardia in COVID-19. Reference Amir, Yoseph, Farisi, Phie and Adam18 As in our study, all of them were hospitalised for respiratory disease and needed oxygen support. The myocardial lesion was excluded with normal cardiac markers and echocardiogram. Half of the patients with persistent complete AV block or sinus bradycardia underwent permanent pacemaker implantation due to symptomatic (syncope, haemodynamic instability) clinical course. Our patients did not develop haemodynamic instability, and their self-limiting condition did not require additional medication or intervention during the follow-up.
Various theories have been proposed on the mechanism of cardiac involvement during COVID-19. During acute illness, bradycardia may develop due to invasion of myocardial tissue by SARS-CoV-2, hypotension, hypoxia due to pulmonary damage or inflammatory system activation, and collateral damage due to cytokine storm. Reference Kochi, Cagliari, Forelo, Fassini and Tondo19 ACE2 overexpression in sino-atrial node cells has also been associated with conduction abnormalities. Reference Ferreira, Moraes, Foureauz, Andrade, Santos and Almeida20,Reference Danilczyk and Penninger21 In our study, COVID-19-related myocarditis was the cause of transient ST elevation in one patient. It was thought that moderate pneumonia and hypoxia, which required severe respiratory support and oxygen, could be the causative factors in seven patients.
Arrhythmic manifestations are described in 7–60% of patients with multisystemic inflammatory syndrome in children with different presentation patterns. Reference Sperotto, Friedman, Son, VanderPluym, Newburger and Dionne22 The most frequently reported electrocardiographic anomalies were non-specific and included ventricular repolarization abnormality, QTc prolongation, and premature atrial or ventricular beats. In a study examining multisystemic inflammatory syndrome in children and cardiac conduction abnormalities, 32 patients were included, and first-degree AV block was detected in 6 (19%) patients. Cardiac enzymes, inflammatory markers, and cardiac function were not associated with AV block. The onset of first-degree AV block occurred at a median of 8 days after the initial onset of symptoms and resolved after 3 days in the follow-up. Reference Choi, Fremed and Starc23 The mechanism of myocardial dysfunction in multisystemic inflammatory syndrome in children has not been cleared, and probably several pathophysiological mechanisms may play a role. Possible causes include acute myocarditis, post-viral immunological reaction, and systemic inflammatory response syndrome. Reference Ciccarelli, Bruzzese and Aisle24 Choi et al. Reference Choi, Fremed and Starc23 emphasised that hyperinflammation and myocardial damage may be responsible for conduction defects in multisystemic inflammatory syndrome in children patients and that early immunosuppressive therapy (steroid and IVIG) also leads to conduction anomalies.
Some medications may also contribute to the development of arrhythmias. In COVID-19, paediatric cases with QT prolongation due to the combined use of hydroxychloroquine and azithromycin and paediatric cases with sinus bradycardia due to remdesivir use draw attention in the literature. Reference Chow, Maust, Kazmier and Stokes25,Reference Barkas, Style, Bechlioulis, Milionis and Liberopoulos26 Remdesivir was approved for severe COVID-19 in adults and patients 12 years of age and older as of October 2020 and was recently approved for all children beyond 28 days of age. 27,28 Besides the expected side effects of remdesivir, cardiovascular effects are also frequently mentioned due to increased use. Asymptomatic sinus bradycardia and QT interval prolongation, which develops during treatment and disappears when treatment is discontinued, are also reported in paediatric and adult cases. Reference Choi, Fremed and Starc23,Reference Gubitosa, Kakar and Gerula29 Remdesivir-associated mitochondrial dysfunction causing cardiotoxicity and the structural relationship of remdesvir with adenosine which can cause AV block is proposed to be potential mechanism. Reference Paw Cho Sing, Schechter, Ali, Sung and Dupuis30 None of our patients had a history of antiarrhythmic use, and none of them received azithromycin-hydroxychloroquine or remdesivir treatment. The literature reported bradycardia as a side effect of dexamethasone and other steroid therapies in some populations like oncological patients and Kawasaki disease. Reference Üsküdar Cansu, Bodakçi and Korkmaz31,Reference Nagakura, Morikawa, Sakakibara and Miura32 Steroid-induced decrease in the sensitivity of myocardial alpha-adrenergic and beta-adrenergic receptors, leading to a reduction in heart rate and mineralocorticoid activity causing hypertension and reflex bradycardia, are predicted as potential mechanisms. In our study, all of our patients who developed sinus bradycardia were treated with steroids, dexamethasone for those with COVID pneumonia, and low dose (2 mg/kg) or pulse-methylprednisolone for those with multisystemic inflammatory syndrome in children.
In conclusion, bradyarrhythmias and various electrocardiographic abnormalities may occur as a part of the clinical course in paediatric patients with COVID-19, not only in multisystemic inflammatory syndrome in children patients. Moderate to severe pneumonia-induced hypoxia, steroid therapy, and direct cardiac effects of SARS-CoV-2 may be potential causes of arrhythmias detected in our patients in the second week of the disease. Although these arrhythmias seem to have a benign course and most electrocardiographic abnormalities (sinus bradycardia, first-degree AV block) do not have a prominent effect on patient management, the reports of many patients requiring pacemakers and the scarce paediatric data raise doubts. It should also be kept in mind that significant electrocardiographic findings (ST-T abnormalities) may develop which changes the management of the patients considerably and electrocardiographic monitoring should be considered in these patients. Further prospective studies are needed to reveal the cardiac findings, arrhythmias, the underlying mechanism, and the short- and long-term effects of COVID-19 in the paediatric population.
Acknowledgements
None.
Financial support
This research received no specific grant from any funding agency, commercial, or not-for-profit sectors.
Conflicts of interest
None.