Four-Month Clinical Status of a Cohort of Patients After Hospitalization for COVID-19

Writing Committee for the COMEBAC Study Group, Luc Morin, Laurent Savale, Tài Pham, Romain Colle, Samy Figueiredo, Anatole Harrois, Matthieu Gasnier, Anne-Lise Lecoq, Olivier Meyrignac, Nicolas Noel, Elodie Baudry, Marie-France Bellin, Antoine Beurnier, Walid Choucha, Emmanuelle Corruble, Laurent Dortet, Isabelle Hardy-Leger, François Radiguer, Sabine Sportouch, Christiane Verny, Benjamin Wyplosz, Mohamad Zaidan, Laurent Becquemont, David Montani, Xavier Monnet, Writing Committee for the COMEBAC Study Group, Luc Morin, Laurent Savale, Tài Pham, Romain Colle, Samy Figueiredo, Anatole Harrois, Matthieu Gasnier, Anne-Lise Lecoq, Olivier Meyrignac, Nicolas Noel, Elodie Baudry, Marie-France Bellin, Antoine Beurnier, Walid Choucha, Emmanuelle Corruble, Laurent Dortet, Isabelle Hardy-Leger, François Radiguer, Sabine Sportouch, Christiane Verny, Benjamin Wyplosz, Mohamad Zaidan, Laurent Becquemont, David Montani, Xavier Monnet

Abstract

Importance: Little is known about long-term sequelae of COVID-19.

Objective: To describe the consequences at 4 months in patients hospitalized for COVID-19.

Design, setting, and participants: In a prospective uncontrolled cohort study, survivors of COVID-19 who had been hospitalized in a university hospital in France between March 1 and May 29, 2020, underwent a telephone assessment 4 months after discharge, between July 15 and September 18, 2020. Patients with relevant symptoms and all patients hospitalized in an intensive care unit (ICU) were invited for further assessment at an ambulatory care visit.

Exposures: Survival of hospitalization for COVID-19.

Main outcomes and measures: Respiratory, cognitive, and functional symptoms were assessed by telephone with the Q3PC cognitive screening questionnaire and a checklist of symptoms. At the ambulatory care visit, patients underwent pulmonary function tests, lung computed tomographic scan, psychometric and cognitive tests (including the 36-Item Short-Form Health Survey and 20-item Multidimensional Fatigue Inventory), and, for patients who had been hospitalized in the ICU or reported ongoing symptoms, echocardiography.

Results: Among 834 eligible patients, 478 were evaluated by telephone (mean age, 61 years [SD, 16 years]; 201 men, 277 women). During the telephone interview, 244 patients (51%) declared at least 1 symptom that did not exist before COVID-19: fatigue in 31%, cognitive symptoms in 21%, and new-onset dyspnea in 16%. There was further evaluation in 177 patients (37%), including 97 of 142 former ICU patients. The median 20-item Multidimensional Fatigue Inventory score (n = 130) was 4.5 (interquartile range, 3.0-5.0) for reduced motivation and 3.7 (interquartile range, 3.0-4.5) for mental fatigue (possible range, 1 [best] to 5 [worst]). The median 36-Item Short-Form Health Survey score (n = 145) was 25 (interquartile range, 25.0-75.0) for the subscale "role limited owing to physical problems" (possible range, 0 [best] to 100 [worst]). Computed tomographic lung-scan abnormalities were found in 108 of 171 patients (63%), mainly subtle ground-glass opacities. Fibrotic lesions were observed in 33 of 171 patients (19%), involving less than 25% of parenchyma in all but 1 patient. Fibrotic lesions were observed in 19 of 49 survivors (39%) with acute respiratory distress syndrome. Among 94 former ICU patients, anxiety, depression, and posttraumatic symptoms were observed in 23%, 18%, and 7%, respectively. The left ventricular ejection fraction was less than 50% in 8 of 83 ICU patients (10%). New-onset chronic kidney disease was observed in 2 ICU patients. Serology was positive in 172 of 177 outpatients (97%).

Conclusions and relevance: Four months after hospitalization for COVID-19, a cohort of patients frequently reported symptoms not previously present, and lung-scan abnormalities were common among those who were tested. These findings are limited by the absence of a control group and of pre-COVID assessments in this cohort. Further research is needed to understand longer-term outcomes and whether these findings reflect associations with the disease.

Conflict of interest statement

Conflict of Interest Disclosures: Dr Harrois reported personal fees from LFB Laboratory and Edwards, and fees from Mindray Fees to his institution, outside the submitted work. Dr Lecoq reported nonfinancial support from Pfizer SAS and from Sanofi Aventis France outside the submitted work. Dr Noel reported personal fees from MSD and from Biogen outside the submitted work. Dr Beurnier reported personal fees from Sanofi outside the submitted work. Dr Becquemont reported grants from Sanofi Genzyme for a presentation concerning Gaucher disease, and pharmacogenetics and drug interactions with Eliglustat outside the submitted work. Dr Montani reported personal fees from Actelion, GSK, Pfizer, MSD, Chiesi, Boehringer, and Incyte Biosciences France; grants from Bayer and MSD; and nonfinancial support from Acceleron, outside the submitted work. Dr Monnet reported personal fees from Getinge Pulsion Medical and Baxter outside the submitted work. No other disclosures were reported.

Figures

Figure 1.. Flow of Patient Screening and…
Figure 1.. Flow of Patient Screening and Enrollment
aIncluding 51 of 97 patients (53%) with invasive mechanical ventilation, 51 (53%) receiving vasopressors, and 8 (8%) with extracorporeal membrane oxygenation. bIncluding 44 of 80 patients (55%) with persistent neurologic symptoms, 27 (34%) with persistent respiratory symptoms, 5 (6%) with abnormal computed tomographic scan results, and 2 (3%) with persistent kidney failure.
Figure 2.. Visualization of Symptoms and Findings…
Figure 2.. Visualization of Symptoms and Findings That Did Not Exist Before COVID-19 Infection in 177 Patients at the Outpatient Clinic, 4 Months After COVID-19 Hospitalization
Numbers represent patients with the symptoms/findings or association of symptoms; 60 patients did not report these symptoms or have these findings. Patients could have more than 1; hence, the sum of the groups exceeds 177.

Source: PubMed

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