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| Name | Class |
|---|---|
| Cabinet Medical valenciennes | UNKNOWN |
| CH Aix | UNKNOWN |
| hopital privé de bois bernard | UNKNOWN |
| Clinique La Croix du Sud |
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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).
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| Measure | Description | Time Frame |
|---|---|---|
| Variation of vital capacity at 5 months after Covid-19 episode | at 5 months | |
| Variation of vital capacity at 7 months after Covid-19 episode | at 7 months | |
| DLCO alteration at 5 months after Covid-19 episode | at 5 months | |
| DLCO alteration at 7 months after Covid-19 episode | at 7 months | |
| desaturation during the "6 min walk test" | at 5 months | |
| desaturation during the "6 min walk test" | at 7 months |
| Measure | Description | Time Frame |
|---|---|---|
| Variation of FEV1 spirometry parameters | at 5 months | |
| Variation of FEV1 spirometry parameters | at 7 months | |
| Variation of VC spirometry parameters |
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Inclusion Criteria:
Exclusion Criteria:
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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.
This is a cohort study with collection of different data. The proposed follow-up of these patients is the recommended follow-up of the french respiratory society. But, as it is a real life study, no exams are mandatory.
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| CHU Amiens Picardie | Amiens | Picardie | 80054 | France |
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| ID | Term |
|---|---|
| D000086382 | COVID-19 |
| D005355 | Fibrosis |
| ID | Term |
|---|---|
| D011024 | Pneumonia, Viral |
| D011014 | Pneumonia |
| D012141 | Respiratory Tract Infections |
| D007239 | Infections |
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| UNKNOWN |
| University Hospital, Bordeaux | OTHER |
| Hopital Forcilles | OTHER |
| Hopital d'instructions des armées | UNKNOWN |
| Hôpital Européen Marseille | OTHER |
| Rennes University Hospital | OTHER |
| Clinique Saint Augustin | UNKNOWN |
| Delafontaine Hospital | OTHER |
| Centre Hospitalier Universitaire de Saint Etienne | OTHER |
| Centre Hospitalier de Troyes | OTHER |
| Centre Hospitalier le Mans | OTHER |
| University Hospital, Clermont-Ferrand | OTHER |
| University Hospital, Tours | OTHER |
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| at 5 months |
| Variation of VC spirometry parameters | at 7 months |
| Variation of FVC spirometry parameters | at 5 months |
| Variation of FVC spirometry parameters | at 7 months |
| Variation of DLCO spirometry parameters | at 5 months |
| Variation of DLCO spirometry parameters | at 7 months |
| D014777 |
| Virus Diseases |
| D018352 | Coronavirus Infections |
| D003333 | Coronaviridae Infections |
| D030341 | Nidovirales Infections |
| D012327 | RNA Virus Infections |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |