In this study, the investigators are attempting to evaluate the influence of socio-economic factors on the functional recovery (physical and psychological) of patients who developed ARDS after a COVID-19 infection, with the aim of offering personalized medical and social follow-up and support measures in order to avoid medium- and long-term complications, which can result in handicaps, reduced quality of life, and a higher risk of death.
Other: Paraclinical examination
Respiratory functional tests
Other: Clinical Examination
Clinical Examination
Other: Semi-directive interview
By phone
Other: quality of life questionnaires
SF36, VSRQ, IESR, HADS
Inclusion Criteria:
- Inpatient in ICU for PCR-proven SARS-VOC-2 infection regardless of specimen type
- Patient who received a chest CT scan in the initial phase of management (either just
before or during hospitalization in the intensive care unit)
- Patient who has received invasive or non-invasive ventilatory support, or humidified
and heated high-flow oxygen (HFO).
- ARDS meeting the criteria of the 2012 Berlin definition. For patients who have
received only HFO, a flow rate at least equal to 50L/minute with a FiO2 strictly
greater than 50% with a PaO2/FiO2 ratio less than or equal to 200 will be required for
inclusion.
- Patient who gave oral consent after being informed about the conduct of this study.
Exclusion Criteria:
- Patient with limited autonomy prior to hospitalization in limited intensive care unit:
walking distance of less than 50 meters, WHO classification status 3 and 4.
- Patient with a history of chronic respiratory failure as defined by the use of
long-term oxygen therapy or non-invasive home ventilation, excluding patients with SAS
and/or hypoventilation obesity syndrome.
- Patient with a history of central or peripheral neurological conditions limiting the
patient's motor autonomy and the performance on gait tests or Pulmonary function Tests
- Patient refusing to participate
- Patient < 18 years of age
- Patient not affiliated or not benefiting from national health insurance
- Patient under guardianship, curatorship or protected adult
- Patient unable to understand and consent to the research protocol
SECONDARY EXCLUSION CRITERIA
- Patient not showing up for visit at M6
- Patients who have not had all the examinations necessary to evaluate the main endpoint
(Spirometry, DLCO, TM6 and CT)
Chu Dijon Bourgogne
Dijon, France
Investigator: Jean-Pierre QUENOT
Contact: 0380293685
jean-pierre.quenot@chu-dijon.fr
Jean-Pierre QUENOT
0380293685 - +33
jean-pierre.quenot@chu-dijon.fr