The novel SARS-CoV-2 virus has quickly spread worldwide, with substantial morbidity and mortality. There is very limited understanding of the short- and longer-term inflammatory/immunological and clinical course. However, the investigators expect survivors from severe COVID-19 to experience persistent functional impairments, as demonstrated in prior studies of patients with acute respiratory distress syndrome (ARDS) and other acute viral illnesses. Notably, however, few studies have ever investigated the biologic mechanisms underlying these functional impairments. Understanding these features of COVID-19 will improve the ability to design acute therapies and recovery-focused interventions. To address these knowledge gaps, the investigators propose a two-center, 225 patient longitudinal prospective cohort study of hospitalized COVID-19 patients with acute respiratory failure. Researchers will perform an in-depth evaluation of inflammatory/immunological biomarkers, and physical, pulmonary, and neuropsychological clinical outcomes during hospitalization, and over 3-, 6-, and 12-month follow-up.
The novel coronavirus (SARS-CoV-2) and associated COVID-19 illness has quickly spread
worldwide, with substantial morbidity and mortality. Early data suggest that most patients
with severe COVID-19 (i.e., experiencing acute respiratory failure (ARF) in an intensive care
unit) may have cytokine release syndrome and other major effects on the innate and adaptive
immune systems. However, there is limited understanding of both the
inflammatory/immunological and the clinical course of COVID-19, with no robust data published
beyond hospital discharge. Based on prior literature from acute viral illnesses, such as
Ebola and Severe Acute Respiratory Syndrome (SARS), persistent functional impairments in
COVID-19 survivors is expected. Despite the importance of these issues, very few studies have
ever investigated the biological mechanisms underlying persistent functional impairments
after ARF. Hence, understanding the short- and longer-term biological and clinical outcomes
of patients with COVID-19, and investigating associations between inflammation and clinical
outcomes is important to design acute therapies and recovery-focused interventions.
To address critical gaps in knowledge, the investigators propose a 2-center longitudinal
cohort study of hospitalized COVID-19 patients via an Administrative Supplement to our
existing grant (R01HL132887, MPIs Stapleton and Needham). Investigators will study COVID-19
patients with ARF who have either severe disease (requiring mechanical ventilation,
non-invasive ventilation, or high flow nasal cannula oxygen support) or non-severe disease
(new or increased supplemental oxygen requirement, without meeting severe criteria).
Researchers will perform an in-depth evaluation of inflammatory/immunological, physical,
pulmonary, and neuropsychological status during hospitalization, and over 3, 6, and 12-month
follow-up. Feasibility for accomplishing this prospective study is demonstrated by 1) a
successful existing collaboration between the University of Vermont (UVM) and Johns Hopkins
University (JHU), supported by multiple NIH grants, and 2) the current and projected COVID-19
census at both hospital systems. The investigators have the existing infrastructure,
expertise, and personnel to enroll 225 patients with COVID-19, and longitudinally follow
survivors for 12 months, to investigate short-term and longer-term inflammatory/immunologic
and clinical outcomes during this pandemic.
Other: COVID-19+ observational
This is observational -- there is no intervention
Inclusion Criteria:
1. Adult (≥18 years old) at the time of consent
2. Positive COVID-19 test result or highly suspicious for COVID-19 infection and have a
test pending
3. Acute Respiratory Failure (new requirement for supplemental oxygen or acute increase
in required supplemental oxygen)
Exclusion Criteria:
1. Expected death or withdrawal of life-sustaining treatments within 3 days
2. Unable to walk ≥150 feet prior to COVID-19 (due to 6-minute walk test being primary
outcome for in-person testing)
3. Hemoglobin ≤7.0 at the time of consent
4. Pre-existing cognitive/language impairment prohibiting clinical outcomes assessment
5. Prior lung resection (due to spirometry as part of in-person outcome assessment)
6. Unable to provide consent and no legally authorized representative (LAR) identified or
reached by phone
7. Pregnant
8. Incarcerated
9. Homelessness
10. Physician declines patient enrollment (attending physician or study physician)
11. Patient or LAR do not consent to participate in the study
University of Vermont College of Medicine
Burlington, Vermont, United States