Study Project Comparing the Sequelae of COVID-19 Infection in Patients Who Have and Have Not Received Ventilatory Support in Critical Care

Assistance Publique - Hôpitaux de Paris478 enrolled

Overview

To assess the proportion of post-intensive care syndrome (PICS) of patients who received high flow humidified oxygen with FiO2 ≥50% for more than 48h and / or who received mechanical ventilation for more than 48h in a context of hospitalization in intensive care for COVID-19 pneumonia

Study Type

OBSERVATIONAL

Enrollment

478

Conditions

Covid19

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: \- Group 1: patients hospitalized in intensive care units for ARDS with SARS-CoV-2 * Major * Admitted between March 1 and May 10, 2020 in one of the sectors of the Bicêtre hospital approved for critical care * proven SARS-CoV-2 infection * Treated by invasive mechanical ventilation or high flow humidified oxygen with FiO2 ≥50% for more than 48 hours. Group 2: patients hospitalized outside intensive care units * Major * Admitted between March 1 and May 10, 2020 in an area of Bicêtre hospital having cared for patients infected with SARS-CoV-2 excluding critical care: pulmonology, internal medicine / orthopedics, infectious diseases, nephrology , acute geriatrics, neurology. Exclusion Criteria: * Patients having refused the post consultation at 3 month * Without social security coverage

Locations (1)

Bicêtre Hospital

Le Kremlin-Bicêtre, France

Outcomes

Primary Outcomes

post-intensive care syndrome (PICS)

Time frame: 3 month after hospitalisation

Secondary Outcomes

Evaluate the 3-month mortality of patients released alive from intensive care

Number of patient deceased

Time frame: 3 month after end of hospitalisation

Describe the overall state of health and the main organ sequelae of these patients

Description of the data collected

Time frame: 3 month after hospitalisation

functional respiratory sequelae

Compare the functional respiratory sequelae of these patients to those who were hospitalized outside of critical care for COVID-19 pneumonia requiring lower oxygen support.

Time frame: 3 month after hospitalisation

Data from ClinicalTrials.gov

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