The next phase of the COVID-19 pandemic is likely to see a surge in an associated chronic cardiopulmonary disease that will challenge health systems. Recovered patients are presenting with persistent dyspnea at the Duke Pulmonary Post-COVID clinic. Evidence is now mounting that recovered patients have significant residual pulmonary disease, while myocardial injury has also been increasingly reported. To optimally care for these patients, Duke Pulmonary study team must comprehensively assess and monitor the changes in cardiopulmonary function and relate the changes to physiologic and quality of life outcomes. The study team will deploy cutting-edge MRI to fully characterize cardiopulmonary function in enrolled 30 subjects (accrual 23 subjects) at time point 60-120 days post recovery and 6-9 months later. Cardiac MRI will assess the myocardial status and right ventricular function, while hyperpolarized 129Xe MRI will provide a 3D assessment of pulmonary ventilation, interstitial barrier integrity, and pulmonary vascular hemodynamics. The overall objective outlined in this study is to demonstrate the feasibility and value of comprehensive longitudinal imaging characterization of cardiopulmonary structure and function in patients recovered from Covid-19.
The proposed research builds on the established sensitivity of Hyperpolarized 129Xe MRI to obstructive and pulmonary vascular lung disease, features expected to represented in the Covid-19 cohort. It further incorporates a new understanding of the possible role of myocardial injury in these recovered patients by combining cutting-edge pulmonary and cardiac MRI. Although the initial presentation of patients with moderate to severe symptoms of COVID19 infections is dominated by respiratory symptoms, 10% go on to develop persistent post-infection symptoms which are thought to have an inflammatory etiology. Evidence suggests that pathologic activation of the inflammasome persists beyond the acute initial presentation that contributes to the persistent disabling symptoms characterized as "long-haul COVID". For this trial, subjects will be eligible for enrollment if subjects are outpatients with a history of a laboratory-confirmed diagnosis of COVID-19 infection, and after 60 days or longer. The study team will accrual 13 subjects who continue to have respiratory symptoms (i.e., cough, shortness of breath, dyspnea on exertion). An additional 10 subjects engaged in competitive sports and diagnosed with COVID-19 will also be enrolled. These subjects can be asymptomatic or mildly to moderately. Although rare, cardiac impairment has been documented in \<2% of these individuals. The study team knowledge, XeMRI has not yet been studied in this specific patient subset. Existing data highlight significant racial and ethnic disparities with historically underserved minority populations (i.e., Black, LatinX) suffering disproportionately higher infection rates and more severe illness compared to Whites. This is reflected by the population enrolled in the study team RedCAP database and biorepository. As such 30% of subjects enrolled will be required to be from underserved communities.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
18
Each xenon dose will be limited to a volume less than 25% of subject lung capacity (TLC),
Duke Asthma, Allergy, and Airway Center
Durham, North Carolina, United States
Red Blood Cell to Membrane (RBC:M) Ratio
To determine cardiopulmonary structure-function abnormalities that characterize early phase COVID-19 recovery.
Time frame: 1 year
Ventilation Defect Percent
To determine cardiopulmonary structure-function abnormalities that characterize early phase COVID-19 recovery.
Time frame: 1 year
High Membrane Percent
To determine cardiopulmonary structure-function abnormalities that characterize early phase COVID-19 recovery.
Time frame: 1 year
Red Blood Cell (RBC) Defect Percent
To determine cardiopulmonary structure-function abnormalities that characterize early phase COVID-19 recovery.
Time frame: 1 year
Red Blood Cell to Membrane (RBC:M) Ratio at 9 Months
To characterize the evolution of cardiopulmonary abnormalities over 9 months.
Time frame: 9 Months
Ventilation Defect Percent at 9 Months
To characterize the evolution of cardiopulmonary abnormalities over 9 months.
Time frame: 9 months
High Membrane Percent at 9 Months
To characterize the evolution of cardiopulmonary abnormalities over 9 months.
Time frame: 9 months
Red Blood Cell (RBC) Defect Percent at 9 Months
To characterize the evolution of cardiopulmonary abnormalities over 9 months.
Time frame: 9 months
Identify MRI Features That Predict Physiological Outcomes With DLCO (Diffusing Capacity of the Lungs for Carbon Monoxide)
DLCO is the extent to which oxygen passes from the air sacs of the lungs into the blood.
Time frame: Baseline
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