Malignant Arrhythmias in Patients With COVID-19: Incidence, Mechanisms, and Outcomes
Mohit K Turagam1,2, Daniel Musikantow1,2, Martin E Goldman2
1Department of Cardiovascular Medicine, Helmsley Electrophysiology Center (M.K.T., D.M., E.C., P.S., I.K., M.B., W.W., M.A.M., S.C., J.S.K., N.L., A.S., S.R.D., V.Y.R.), Icahn School of Medicine at Mount Sinai, New York, NY.
Insights
Patients with COVID-19 experiencing cardiac injury face higher risks of malignant cardiac arrhythmias, particularly fatal tachyarrhythmias linked to metabolic issues. These arrhythmias are more common in those who die compared to survivors.
Area of Science:
- Cardiology
- Infectious Diseases
- Critical Care Medicine
Background:
- Patients with coronavirus disease 2019 (COVID-19) and cardiac injury show increased rates of malignant cardiac arrhythmias.
- Limited understanding exists regarding the frequency, mechanisms, and mortality impact of these arrhythmias in COVID-19 patients.
Purpose of the Study:
- To investigate the frequency, characteristics, and outcomes of malignant cardiac arrhythmias in hospitalized COVID-19 patients.
- To compare arrhythmia events between COVID-19 patients who died and those discharged.
Main Methods:
- Data extracted from a registry (NCT04358029) of consecutive COVID-19 inpatients with continuous telemetric ECG monitoring.
- Comparison of a composite endpoint (cardiac arrest from ventricular tachycardia/fibrillation or bradyarrhythmias) between deceased and discharged patients.
Main Results:
- Among 140 monitored COVID-19 patients (52 died, 88 discharged), 17% of those who died and 4% of discharged patients experienced primary endpoint events (P=0.01).
- Tachyarrhythmias drove the difference, occurring in the context of severe metabolic imbalance.
- Atrioventricular block was largely an independent event, unlike tachyarrhythmias.
Conclusions:
- Hospitalized COVID-19 patients who die have a higher incidence of malignant cardiac arrhythmias than survivors.
- Ventricular tachyarrhythmias in COVID-19 are primarily associated with severe metabolic derangement.
- These arrhythmia events constitute a minority of cardiovascular deaths in this cohort.
Background:
Patients with coronavirus disease 2019 (COVID-19) who develop cardiac injury are reported to experience higher rates of malignant cardiac arrhythmias. However, little is known about these arrhythmias-their frequency, the underlying mechanisms, and their impact on mortality.
Methods:
We extracted data from a registry (NCT04358029) regarding consecutive inpatients with confirmed COVID-19 who were receiving continuous telemetric ECG monitoring and had a definitive disposition of hospital discharge or death. Between patients who died versus discharged, we compared a primary composite end point of cardiac arrest from ventricular tachycardia/fibrillation or bradyarrhythmias such as atrioventricular block.
Results:
Among 800 patients with COVID-19 at Mount Sinai Hospital with definitive dispositions, 140 patients had telemetric monitoring, and either died (52) or were discharged (88). The median (interquartile range) age was 61 years (48-74); 73% men; and ethnicity was White in 34%. Comorbidities included hypertension in 61%, coronary artery disease in 25%, ventricular arrhythmia history in 1.4%, and no significant comorbidities in 16%. Compared with discharged patients, those who died had elevated peak troponin I levels (0.27 versus 0.02 ng/mL) and more primary end point events (17% versus 4%, P=0.01)-a difference driven by tachyarrhythmias. Fatal tachyarrhythmias invariably occurred in the presence of severe metabolic imbalance, while atrioventricular block was largely an independent primary event.
Conclusions:
Hospitalized patients with COVID-19 who die experience malignant cardiac arrhythmias more often than those surviving to discharge. However, these events represent a minority of cardiovascular deaths, and ventricular tachyarrhythmias are mainly associated with severe metabolic derangement. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT04358029.
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