Korean Circ J.  2021 Oct;51(10):851-862. 10.4070/kcj.2021.0116.

Electrocardiographic Manifestations in Patients with COVID-19: Daegu in South Korea

Affiliations
  • 1Division of Cardiology, Daegu Catholic University College of Medicine, Daegu, Korea
  • 2Division of Cardiology, Daegu Fatima General Hospital, Daegu, Korea
  • 3Division of Cardiology, Yeungnam University College of Medicine, Daegu, Korea
  • 4Division of Cardiology, Kyungpook National University, Daegu, Korea
  • 5Division of Cardiology, Keimyung University Dongsan Medical Center, Daegu, Korea
  • 6Division of Cardiology, Daegu Veterans Hospital, Daegu, Korea
  • 7Division of Cardiology, Kyungpook National University Chilgok Hospital, Daegu, Korea

Abstract

Background and Objectives
As the coronavirus disease 2019 (COVID-19) spreads worldwide, cardiac injury in patients infected with COVID-19 becomes a significant concern. Thus, this study investigates the impact of several electrocardiogram (ECG) parameters and disease severity in COVID-19 patients.
Methods
Seven medical centers in Daegu admitted 822 patients with COVID-19 between February and April 2020. This study examined 267 patients among them who underwent an ECG test and evaluated their biochemical parameters like C-reactive protein (CRP), log N-terminal pro-B-type Natriuretic Peptide (NT-proBNP), cardiac enzyme, and ECG parameters (heart rate, PR interval, QRS interval, T inversion, QT interval, and Tpe [the interval between peak to end in a T wave]).
Results
Those patients were divided into 3 groups of mild (100 patients), moderate (89 patients), and severe (78 patients) according to clinical severity score. The level of CRP, log NT-proBNP, and creatinine kinase-myocardial band were significantly increased in severe patients. Meanwhile, severe patients exhibited prolonged QT intervals (QTc) and Tpe (Tpe-c) compared to mild or moderate patients. Moreover, deceased patients (58; 21.7%) showed increased dispersion of QTc and Tpe-c compared with surviving patients (78.2±41.1 vs. 40.8±24.6 ms and 60.2±37.3 vs. 40.8±24.5 ms, both p<0.05, respectively). The QTc dispersion of more than 56.1 ms could predict the mortality in multivariate analysis (odd ratio, 11.55; 95% confidence interval, 3.746–42.306).
Conclusions
COVID-19 infections could involve cardiac injuries, especially cardiac repolarization abnormalities. A prolonged QTc dispersion could be an independent predictable factor of mortality.

Keyword

Coronavirus; COVID-19; ECG

Figure

  • Figure 1 Dispersion of corrected QT and peak to end of T wave (Tpe) according to clinical severity score. (A) Dispersion of corrected QT (B) Dispersion of corrected Tpe. Red line is mean, and box lesion is quartile.QTc = corrected QT.

  • Figure 2 Dispersion of corrected QT and Tpe according to mortality. (A) Dispersion of corrected QT (B) Dispersion of corrected Tpe. Red line is mean, and box lesion is quartile.QTc = corrected QT.

  • Figure 3 QTc and T peak to end dispersion according to mortality by age group.QTc = corrected QT.


Cited by  1 articles

QTc Dispersion Predicts Prognosis in COVID-19 Disease
Sung-Won Jang
Korean Circ J. 2021;51(10):863-865.    doi: 10.4070/kcj.2021.0275.


Reference

1. World Health Organization. Coronavirus disease (COVID-19) outbreak [Internet]. Geneva: World Health Organization;2020. cited 2020 September 27. Available from: https://www.who.int/emergencies/diseases/novel-coronavirus-2019.
2. Inciardi RM, Lupi L, Zaccone G, et al. Cardiac involvement in a patient with coronavirus disease 2019 (COVID-19). JAMA Cardiol. 2020; 5:819–824. PMID: 32219357.
Article
3. Sinkeler FS, Berger FA, Muntinga HJ, Jansen MM. The risk of QTc-interval prolongation in COVID-19 patients treated with chloroquine. Neth Heart J. 2020; 28:418–423. PMID: 32648153.
Article
4. Magadum A, Kishore R. Cardiovascular manifestations of COVID-19 infection. Cells. 2020; 9:2508.
Article
5. Sandoval Y, Januzzi JL Jr, Jaffe AS. Cardiac troponin for assessment of myocardial injury in COVID-19: JACC review topic of the week. J Am Coll Cardiol. 2020; 76:1244–1258. PMID: 32652195.
6. Farré N, Mojón D, Llagostera M, et al. Prolonged QT interval in SARS-CoV-2 infection: prevalence and prognosis. J Clin Med. 2020; 9:2712.
Article
7. Kochi AN, Tagliari AP, Forleo GB, Fassini GM, Tondo C. Cardiac and arrhythmic complications in patients with COVID-19. J Cardiovasc Electrophysiol. 2020; 31:1003–1008. PMID: 32270559.
Article
8. Sahu P, Lim PO, Rana BS, Struthers AD. QT dispersion in medicine: electrophysiological holy grail or fool's gold? QJM. 2000; 93:425–431. PMID: 10874051.
Article
9. Rosenthal TM, Masvidal D, Abi Samra FM, et al. Optimal method of measuring the T-peak to T-end interval for risk stratification in primary prevention. Europace. 2018; 20:698–705. PMID: 28339886.
Article
10. Tschope C, Ammirati E, Bozkurt B, et al. Myocarditis and inflammatory cardiomyopathy: current evidence and future directions. Nat Rev Cardiol. 2021; 18:169–193. PMID: 33046850.
Article
11. Jakhmola S, Indari O, Kashyap D, et al. Recent updates on COVID-19: a holistic review. Heliyon (Lond). 2020; 6:e05706.
Article
12. Clerkin KJ, Fried JA, Raikhelkar J, et al. COVID-19 and cardiovascular disease. Circulation. 2020; 141:1648–1655. PMID: 32200663.
Article
13. Frangogiannis NG. The significance of COVID-19-associated myocardial injury: how overinterpretation of scientific findings can fuel media sensationalism and spread misinformation. Eur Heart J. 2020; 41:3836–3838. PMID: 33006608.
Article
14. Dou Q, Wei X, Zhou K, Yang S, Jia P. Cardiovascular manifestations and mechanisms in patients with COVID-19. Trends Endocrinol Metab. 2020; 31:893–904. PMID: 33172748.
Article
15. Zhang P, Zhu L, Cai J, et al. Association of inpatient use of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers with mortality among patients with hypertension hospitalized with COVID-19. Circ Res. 2020; 126:1671–1681. PMID: 32302265.
Article
16. Li J, Wang X, Chen J, Zhang H, Deng A. Association of renin-angiotensin system inhibitors with severity or risk of death in patients with hypertension hospitalized for coronavirus disease 2019 (COVID-19) infection in Wuhan, China. JAMA Cardiol. 2020; 5:825–830. PMID: 32324209.
Article
17. Lutz C, Maher L, Lee C, Kang W. COVID-19 preclinical models: human angiotensin-converting enzyme 2 transgenic mice. Hum Genomics. 2020; 14:20. PMID: 32498696.
Article
18. Oudit GY, Kassiri Z, Jiang C, et al. SARS-coronavirus modulation of myocardial ACE2 expression and inflammation in patients with SARS. Eur J Clin Invest. 2009; 39:618–625. PMID: 19453650.
Article
19. Johansen MD, Irving A, Montagutelli X, et al. Animal and translational models of SARS-CoV-2 infection and COVID-19. Mucosal Immunol. 2020; 13:877–891. PMID: 32820248.
Article
20. Viljoen C, Sliwa K, Chin A. Interpreting the need for implantable loop recorder monitoring in pregnant women at high risk of arrhythmias-reply. JAMA Cardiol. 2020; 5:1304–1305.
Article
21. Öztürk F, Karaduman M, Çoldur R, İncecik Ş, Güneş Y, Tuncer M. Interpretation of arrhythmogenic effects of COVID-19 disease through ECG. Aging Male. 2020; 23:1362–1365. PMID: 32449420.
Article
22. Jiménez-Jáimez J, Macías-Ruiz R, Bermúdez-Jiménez F, et al. Absence of relevant QT interval prolongation in not critically ill COVID-19 patients. Sci Rep. 2020; 10:21417. PMID: 33293554.
Article
23. Gittleman IW, Thorner MC, Griffith GC. The Q-T interval of the electrocardiogram in acute myocarditis in adults, with autopsy correlation. Am Heart J. 1951; 41:78–90. PMID: 14799440.
Article
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