- Lanspa, Michael;
- Dugar, Siddharth;
- Prigmore, Heather;
- Boyd, Jeremy;
- Rupp, Jordan;
- Lindsell, Chris;
- Rice, Todd;
- Qadir, Nida;
- Lim, George;
- Shiloh, Ariel;
- Dieiev, Vladyslav;
- Gong, Michelle;
- Fox, Steven;
- Hirshberg, Eliotte;
- Khan, Akram;
- Kornfield, James;
- Schoeneck, Jacob;
- Macklin, Nicholas;
- Files, D;
- Gibbs, Kevin;
- Prekker, Matthew;
- Parsons-Moss, Daniel;
- Bown, Mikaele;
- Olsen, Troy;
- Knox, Daniel;
- Cirulis, Meghan;
- Mehkri, Omar;
- Duggal, Abhijit;
- Tenforde, Mark;
- Patel, Manish;
- Self, Wesley;
- Brown, Samuel
BACKGROUND: Cardiac function of critically ill patients with COVID-19 generally has been reported from clinically obtained data. Echocardiographic deformation imaging can identify ventricular dysfunction missed by traditional echocardiographic assessment. RESEARCH QUESTION: What is the prevalence of ventricular dysfunction and what are its implications for the natural history of critical COVID-19? STUDY DESIGN AND METHODS: This is a multicenter prospective cohort of critically ill patients with COVID-19. We performed serial echocardiography and lower extremity vascular ultrasound on hospitalization days 1, 3, and 8. We defined left ventricular (LV) dysfunction as the absolute value of longitudinal strain of < 17% or left ventricle ejection fraction (LVEF) of < 50%. Primary clinical outcome was inpatient survival. RESULTS: We enrolled 110 patients. Thirty-nine (35.5%) died before hospital discharge. LV dysfunction was present at admission in 38 patients (34.5%) and in 21 patients (36.2%) on day 8 (P = .59). Median baseline LVEF was 62% (interquartile range [IQR], 52%-69%), whereas median absolute value of baseline LV strain was 16% (IQR, 14%-19%). Survivors and nonsurvivors did not differ statistically significantly with respect to day 1 LV strain (17.9% vs 14.4%; P = .12) or day 1 LVEF (60.5% vs 65%; P = .06). Nonsurvivors showed worse day 1 right ventricle (RV) strain than survivors (16.3% vs 21.2%; P = .04). INTERPRETATION: Among patients with critical COVID-19, LV and RV dysfunction is common, frequently identified only through deformation imaging, and early (day 1) RV dysfunction may be associated with clinical outcome.