The COVID-19 epidemic has now raged for more than a year with more than 100 million identified cases and nearly 2.5 million deaths worldwide. Since November 2020, we have been witnessing the emergence of viral variants in different regions of the world. This expected genetic drift of the virus, but somewhat abrupt since November, raises questions concerning the characteristics of transmissibility, pathogenicity, sensitivity to possible treatments, and escape from natural or vaccine immunity. The objective of this study is to find out whether the new variants of SARS-CoV-2 are associated with particular clinical forms. The results of this research will provide elements to determine whether the new variants of SARS-CoV-2 are associated with more severe clinical forms.
SEVASAR is a paired cohort study with retrospective data collection: * Presentation: patients hospitalized for COVID-19 with SARS-CoV-2 variant 20I / 501Y.V1 * Not exposed: patients hospitalized for COVID-19 with SARS-CoV-2 corresponding to wild variants type 20A. EU1 or 20A. EU2 The severity of illness will be compared between pairs. Disease severity will be assessed according to the following definition: defined by a composite criterion including, at 28 days after hospital admission: WHO scale \>5 /11 levels, (death OR need for invasive ventilation OR need for high flow ventilation (Optiflex or NIV or CPAP) or high concentration mask. This event will be taken into account regardless of its time of occurrence between the first day of the hospitalization studied and D29 after hospital admission.
Study Type
OBSERVATIONAL
Enrollment
2,200
Data collection
CHU Amiens Picardie Site Nord
Amiens, France
RECRUITINGCHU Angers
Angers, France
RECRUITINGCentre hospitalier de Béziers
Béziers, France
RECRUITINGhôpital Avicenne
Bobigny, France
To estimate the proportion of Severe disease form
Percentage of severe form. Severity was defined by a composite criterion including, at Day 28 days from hospital admission: WHO scale \>5 /11 levels, (death OR required invasive ventilation OR required high flow ventilation (Optiflex or NIV or CPAP) or high concentration mask.
Time frame: between the first day of hospitalization and Day 29
To estimate the proportion of Mortality
Percentage of mortality
Time frame: Day 29
To estimate the proportion of WHO score > 5
Percentage of WHO score \> 5
Time frame: between the first day of hospitalization and Day 29
To estimate the proportion of Patient who received critical care
Percentage of patients who received critical care
Time frame: between the first day of hospitalization and Day 29
To estimate the proportion of patients who had invasive ventilation
Percentage of patients who had invasive ventilation
Time frame: between the first day of hospitalization and Day 29
To estimate the proportion of patients who had high flow oxygen therapy
Percentage of patients who had high flow oxygen therapy
Time frame: between the first day of hospitalization and Day 29
Time between the first day of symptoms and the first day of hospitalization
Time between the first day of symptoms and the first day of hospitalization
Time frame: between first day of symptoms and the first day of hospitalization assessed up to one month
Delay between the first day of symptoms and the first day of hospitalization
Time between the first day of symptoms and the first day of hospitalization
Time frame: between first day of symptoms and the first day of hospitalization assessed up to one month
Time between the first day of symptoms and the severity of disease
Time between the first day of symptoms and the severity of disease
Time frame: between first day of symptoms and the severity assessed up to one month
Time between the first day of symptoms and mortality
Time between the first day of symptoms and mortality
Time frame: between first day of symptoms and mortality assessed up to two month
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RECRUITINGHôpital Ambroise Paré
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RECRUITINGCentre hospitalier métropole Savoie
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RECRUITING...and 43 more locations