Malignant Arrhythmias in Patients With COVID-19: Incidence, Mechanisms, and Outcomes.
Action Potentials
Adult
Aged
Aged, 80 and over
Arrhythmias, Cardiac
/ diagnosis
COVID-19
/ diagnosis
Female
Heart Conduction System
/ physiopathology
Heart Rate
Hospital Mortality
Hospitalization
Humans
Incidence
Male
Middle Aged
New York City
/ epidemiology
Prognosis
Registries
Risk Assessment
Risk Factors
Time Factors
Young Adult
arrhythmias, cardiac
atrioventricular block
coronavirus
myocardial infarction
ventricular fibrillation
Journal
Circulation. Arrhythmia and electrophysiology
ISSN: 1941-3084
Titre abrégé: Circ Arrhythm Electrophysiol
Pays: United States
ID NLM: 101474365
Informations de publication
Date de publication:
11 2020
11 2020
Historique:
pubmed:
8
10
2020
medline:
15
12
2020
entrez:
7
10
2020
Statut:
ppublish
Résumé
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. 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. 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%, 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.
Sections du résumé
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%,
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.
Identifiants
pubmed: 33026892
doi: 10.1161/CIRCEP.120.008920
pmc: PMC7668347
doi:
Banques de données
ClinicalTrials.gov
['NCT04358029']
Types de publication
Comparative Study
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
e008920Références
Lancet. 2020 Feb 22;395(10224):565-574
pubmed: 32007145
Lancet. 2020 Mar 28;395(10229):1054-1062
pubmed: 32171076
Circulation. 2020 Jul 7;142(1):7-9
pubmed: 32286863
Clin Infect Dis. 2020 Nov 19;71(16):2089-2098
pubmed: 32361738
JAMA Cardiol. 2020 Jul 1;5(7):802-810
pubmed: 32211816
Eur Heart J. 2020 Jun 7;41(22):2070-2079
pubmed: 32391877
Circulation. 2020 May 26;141(21):e823-e831
pubmed: 32228309
Eur Heart J. 2020 May 14;41(19):1798-1800
pubmed: 32186331
Heart Rhythm. 2020 Sep;17(9):1425-1433
pubmed: 32407884
JAMA. 2020 Apr 28;323(16):1574-1581
pubmed: 32250385
Euro Surveill. 2020 Jan;25(3):
pubmed: 31992387
N Engl J Med. 2020 Feb 20;382(8):727-733
pubmed: 31978945
Circulation. 2020 Jun 23;141(25):2113-2116
pubmed: 32352306
N Engl J Med. 2018 Jan 25;378(4):345-353
pubmed: 29365305
JAMA Cardiol. 2020 Jul 1;5(7):811-818
pubmed: 32219356
Circulation. 2018 Nov 13;138(20):e618-e651
pubmed: 30571511
N Engl J Med. 2020 Jun 18;382(25):2478-2480
pubmed: 32302081
JAMA. 2016 Feb 23;315(8):775-87
pubmed: 26903336
Circulation. 2020 Jun 2;141(22):1733-1735
pubmed: 32251612
N Engl J Med. 2020 Jun 25;382(26):2582
pubmed: 32501665
JAMA. 2012 Jun 20;307(23):2526-33
pubmed: 22797452