Covid-19 Respiratory Sequelae French Cohort (PNEUMOCOVID)

Centre Hospitalier Universitaire, Amiens

Status: Completed

Conditions: COVID-19; Sequelae; Spirometry DLCO; Follow-up; Cohort; Fibrosis

Study type: Observational

Funder types: Other

Identifiers

NCT05075785

PI2021_843_0135

Details and patient eligibility

About

As the investigators need data on long term outcome of Covid-19, especially respiratory sequelae, a national cohort is required. To better evaluate the potential respiratory sequelae after SARS-CoV-2 infection, it is fundamental to include patients with different management at the acute phase of the Covid-19: ambulatory management, hospitalization in non ICU and in ICU units. That is why the investigators will conduct a national cohort study with all components of french pneumology which will give the investigators the opportunity to include patients in general hospital, in university hospital and in private structure. As it is a "real life" study, the investigators will include all patients who will have a consultation with a pneumologist for an evaluation 5 to 7 months after a Covid-19 infection whatever their acute disease management. The investigators will collect all available data on Covid-19 acute phase, on patients characteristics and comorbidities, on persistent symptoms after Covid-19, on exams results during the outcome evaluation (CT-scan, 6 min walk test, spirometry and DLCO, blood gas, VO2 max if realized).

Enrollment: 2,933 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• adults, older than 18
• SARS-CoV-2 infection confirmed by polymerase chain reaction (PCR) in nasopharyngeal swab in patients who are evaluated by a pneumologist 5 to 7 months after their Covid-19 disease

Exclusion criteria

• patients for whom follow-up would be difficult owing to psychotic disorder
• dementia
• patients who have declined to participate.