Official Title
Functional Recovery From Acute Respiratory Distress Syndrome (ARDS) Due to COVID-19: Influence of Socio-Economic Status
Brief Summary

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.

Unknown status
COVID19
ARDS
Functional Recovery

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

Eligibility Criteria

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)

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
France
Locations

Chu Dijon Bourgogne
Dijon, France

Investigator: Jean-Pierre QUENOT
Contact: 0380293685
jean-pierre.quenot@chu-dijon.fr

Contacts

Jean-Pierre QUENOT
0380293685 - +33
jean-pierre.quenot@chu-dijon.fr

Centre Hospitalier Universitaire Dijon
NCT Number
MeSH Terms
COVID-19
Respiratory Distress Syndrome
Respiratory Distress Syndrome, Newborn
Acute Lung Injury