Related Experiment Video
Updated: Oct 26, 2025

Lung CT Segmentation to Identify Consolidations and Ground Glass Areas for Quantitative Assesment of SARS-CoV Pneumonia
Published on: December 19, 2020
Spectrum of Suspected Cardiomyopathy Due to COVID-19: A Case Series
Austin Tutor1, Graham Unis2, Brent Ruiz1
1Department of Internal Medicine, Ochsner Health Foundation, New Orleans, LA.
Insights
COVID-19 can cause new cardiomyopathies in older adults, significantly impairing heart function. While some patients recover, the virus poses serious cardiovascular risks, necessitating further research into these COVID-19 related heart conditions.
Area of Science:
- Cardiology
- Infectious Diseases
- Critical Care Medicine
Background:
- Cardiovascular complications of COVID-19 are not fully understood.
- Limited baseline data exists for COVID-19 related cardiomyopathies.
- Previous studies lack pre-infection echocardiographic data.
Purpose of the Study:
- To examine de novo cardiomyopathies in patients post-COVID-19 infection.
- To analyze cardiac function changes following SARS-CoV-2 infection.
- To investigate outcomes in elderly patients with COVID-19 induced cardiomyopathies.
Main Methods:
- Retrospective analysis of four elderly patients (average age 80.5).
- Review of echocardiographic data before and after COVID-19 infection.
- Assessment of cardiac function, diagnosis (Takotsubo CM vs. myocarditis), and mortality.
Main Results:
- Four patients developed de novo cardiomyopathies after COVID-19.
- Left ventricular systolic function decreased to an average of 30%.
- 50% of patients died; 50% showed recovery of systolic function.
Conclusions:
- COVID-19 can lead to severe cardiovascular complications and poor prognosis.
- No correlation found between treatments, age, or inflammatory markers and functional recovery.
- Further research is crucial for understanding and treating COVID-19 induced cardiomyopathies, especially with potential endemicity.
Abstract:
The effects of COVID-19 on the cardiovascular system remains understudied given the early stage of the pandemic. Several case series and case reports have been published on COVID-19 related cardiomyopathies; however, there is often a lack of baseline echocardiographic data confirming a normal cardiac health prior to infection. Here we examine four patients with preserved left ventricular systolic function on prior echocardiogram who developed de novo cardiomyopathies which following COVID-19 infection. The study comprised of four individuals with an average age of 80.5 years, 75% of which were white males. 50% of cases were suspected to have Takotsubo CM vs. myocarditis while the remaining half were diagnosed as myocarditis. Left ventricular systolic function dropped from a normal range to an average of 30% during COVID-19 infection in these individuals. Moreover, half of the cases later died. In conclusion, the COVID-19 pandemic has demonstrated its ability to cause several serious cardiovascular complications with associated worsening of prognosis. Repeat TTE showed recovery of systolic function in 50% of the patients included. There does not appear to be any correlation between COVID-19 related treatments, age, or level of inflammatory markers in those who recovered systolic function versus those who remained depressed. Given the minimal literature on this topic, it is evident more information is needed to help advance treatment and understanding of COVID-19 induced cardiomyopathies; particularly if the vaccination fails to protect against novel strains of COVID-19 and the virus becomes endemic.
More Related Videos
03:45Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
18:11A Research Method For Detecting Transient Myocardial Ischemia In Patients With Suspected Acute Coronary Syndrome Using Continuous ST-segment Analysis
Published on: December 28, 2012
Related Concept Videos
Myocarditis II: Clinical Features and Diagnostic Tests
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Myocarditis I: Introduction