Clinical Characteristics and Outcomes in Patients With Coronavirus Disease 2019 and Multiple Sclerosis.


Journal

JAMA neurology
ISSN: 2168-6157
Titre abrégé: JAMA Neurol
Pays: United States
ID NLM: 101589536

Informations de publication

Date de publication:
01 09 2020
Historique:
pubmed: 27 6 2020
medline: 4 11 2020
entrez: 27 6 2020
Statut: ppublish

Résumé

Risk factors associated with the severity of coronavirus disease 2019 (COVID-19) in patients with multiple sclerosis (MS) are unknown. Disease-modifying therapies (DMTs) may modify the risk of developing a severe COVID-19 infection, beside identified risk factors such as age and comorbidities. To describe the clinical characteristics and outcomes in patients with MS and COVID-19 and identify factors associated with COVID-19 severity. The Covisep registry is a multicenter, retrospective, observational cohort study conducted in MS expert centers and general hospitals and with neurologists collaborating with MS expert centers and members of the Société Francophone de la Sclérose en Plaques. The study included patients with MS presenting with a confirmed or highly suspected diagnosis of COVID-19 between March 1, 2020, and May 21, 2020. COVID-19 diagnosed with a polymerase chain reaction test on a nasopharyngeal swab, thoracic computed tomography, or typical symptoms. The main outcome was COVID-19 severity assessed on a 7-point ordinal scale (ranging from 1 [not hospitalized with no limitations on activities] to 7 [death]) with a cutoff at 3 (hospitalized and not requiring supplemental oxygen). We collected demographics, neurological history, Expanded Disability Severity Scale score (EDSS; ranging from 0 to 10, with cutoffs at 3 and 6), comorbidities, COVID-19 characteristics, and outcomes. Univariate and multivariate logistic regression models were used to estimate the association of collected variables with COVID-19 outcomes. A total of 347 patients (mean [SD] age, 44.6 [12.8] years, 249 women; mean [SD] disease duration, 13.5 [10.0] years) were analyzed. Seventy-three patients (21.0%) had a COVID-19 severity score of 3 or more, and 12 patients (3.5%) died of COVID-19. The median EDSS was 2.0 (range, 0-9.5), and 284 patients (81.8%) were receiving DMT. There was a higher proportion of patients with a COVID-19 severity score of 3 or more among patients with no DMT relative to patients receiving DMTs (46.0% vs 15.5%; P < .001). Multivariate logistic regression models determined that age (odds ratio per 10 years: 1.9 [95% CI, 1.4-2.5]), EDSS (OR for EDSS ≥6, 6.3 [95% CI. 2.8-14.4]), and obesity (OR, 3.0 [95% CI, 1.0-8.7]) were independent risk factors for a COVID-19 severity score of 3 or more (indicating hospitalization or higher severity). The EDSS was associated with the highest variability of COVID-19 severe outcome (R2, 0.2), followed by age (R2, 0.06) and obesity (R2, 0.01). In this registry-based cohort study of patients with MS, age, EDSS, and obesity were independent risk factors for severe COVID-19; there was no association found between DMTs exposure and COVID-19 severity. The identification of these risk factors should provide the rationale for an individual strategy regarding clinical management of patients with MS during the COVID-19 pandemic.

Identifiants

pubmed: 32589189
pii: 2767776
doi: 10.1001/jamaneurol.2020.2581
pmc: PMC7320356
doi:

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1079-1088

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Auteurs

Céline Louapre (C)

Institut du Cerveau et de la Moelle Épinière, Assistance Publique des Hôpitaux de Paris, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Clinical Investigation Center Neuroscience, Paris, France.

Nicolas Collongues (N)

Service de Neurologie, Clinical Investigation Center Institut National de la Santé et de la Recherche Médicale 1434, Centre Hospitalier Universitaire de Strasbourg, Strasbourg, France.

Bruno Stankoff (B)

Institut du Cerveau et de la Moelle Épinière, Assistance Publique des Hôpitaux de Paris, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Clinical Investigation Center Neuroscience, Paris, France.
Hôpital St Antoine, Assistance Publique des Hôpitaux de Paris, Paris, France.

Claire Giannesini (C)

Hôpital St Antoine, Assistance Publique des Hôpitaux de Paris, Paris, France.

Caroline Papeix (C)

Institut du Cerveau et de la Moelle Épinière, Assistance Publique des Hôpitaux de Paris, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Clinical Investigation Center Neuroscience, Paris, France.

Caroline Bensa (C)

Département de Neurologie, Hôpital Fondation Adolphe de Rothschild, Paris, France.

Romain Deschamps (R)

Département de Neurologie, Hôpital Fondation Adolphe de Rothschild, Paris, France.

Alain Créange (A)

Service de Neurologie, Centre de Ressources et de Compétences-Sclérose en Plaques, Assistance Publique des Hôpitaux de Paris, Groupe Hospitalier Henri Mondor, Université Paris-Est Créteil, Créteil, France.

Abir Wahab (A)

Service de Neurologie, Centre de Ressources et de Compétences-Sclérose en Plaques, Assistance Publique des Hôpitaux de Paris, Groupe Hospitalier Henri Mondor, Université Paris-Est Créteil, Créteil, France.

Jean Pelletier (J)

Service de Neurologie, Pôle de Neurosciences Cliniques, Assistance Publique-Hôpitaux de Marseille, Hôpital de la Timone, Aix Marseille Université, Marseille, France.

Olivier Heinzlef (O)

Département de Neurologie, Centre Hospitalier de Poissy, St Germain, France.

Pierre Labauge (P)

Département de Neurologie, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.

Laurent Guilloton (L)

Association des Neurologues Libéraux de Langue Française, Bergerac, France.

Guido Ahle (G)

Département de Neurologie, Hôpitaux Civils de Colmar, Colmar, France.

Mathilde Goudot (M)

Service de Neurologie, Groupe Hospitalier de la Region de Mulhouse, Mulhouse, France.

Kevin Bigaut (K)

Service de Neurologie, Clinical Investigation Center Institut National de la Santé et de la Recherche Médicale 1434, Centre Hospitalier Universitaire de Strasbourg, Strasbourg, France.

David-Axel Laplaud (DA)

Centre de Recherche en Transplantation et Immunologie-Institut National de la Santé et de la Recherche Médicale U1064, Service Neurologie, Clinical Investigation Center 1413, Centre Hospitalier Universitaire Nantes, Nantes, France.

Sandra Vukusic (S)

Hôpital Neurologique Pierre Wertheimer, Hospices Civils de Lyon, Lyon/Bron, France.

Catherine Lubetzki (C)

Institut du Cerveau et de la Moelle Épinière, Assistance Publique des Hôpitaux de Paris, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Institut National de la Santé et de la Recherche Médicale, Centre National de la Recherche Scientifique, Clinical Investigation Center Neuroscience, Paris, France.

Jérôme De Sèze (J)

Service de Neurologie, Clinical Investigation Center Institut National de la Santé et de la Recherche Médicale 1434, Centre Hospitalier Universitaire de Strasbourg, Strasbourg, France.

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Classifications MeSH