Outcomes of coronavirus disease 2019 in patients with neuromyelitis optica and associated disorders.


Journal

European journal of neurology
ISSN: 1468-1331
Titre abrégé: Eur J Neurol
Pays: England
ID NLM: 9506311

Informations de publication

Date de publication:
Oct 2021
Historique:
revised: 05 09 2020
received: 08 07 2020
accepted: 18 10 2020
pubmed: 27 10 2020
medline: 22 9 2021
entrez: 26 10 2020
Statut: ppublish

Résumé

Outcomes of coronavirus disease 2019 (COVID-19) in patients with neuromyelitis optica spectrum disorders (NMOSD) or myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), often treated with immunosuppressive therapies, are still unknown. We conducted a multicenter, retrospective, observational cohort study among all French expert centers for neuromyelitis optica and related disorders. Patients with NMOSD or MOGAD included in the study received a confirmed or highly suspected diagnosis of COVID-19 between 1 March 2020 and 30 June 2020. Main outcome was COVID-19 severity score assessed on a seven-point ordinal scale ranging from 1 (not hospitalized with no limitations on activities) to 7 (death). Fifteen cases (mean [SD] age: 39.3 [14.3] years, 11 female) were included. Five patients (33.3%) were hospitalized, all receiving rituximab. A 24-year-old patient with positive aquaporine-4 antibody, with obesity as comorbidity, needed mechanical ventilation. Outpatients were receiving anti-CD20 (5), mycophenolate mofetil (3) or azathioprine (3). They were younger (mean [SD] age: 37.0 [13.4] years), with a longer disease duration (mean [SD]: 8.3 [6.3] years) and had a lower expanded disability severity score (EDSS) score (median [range] EDSS: 2.5 [0-4]) relative to patients requiring hospitalization (mean [SD] age: 44.0 [16.4] years, mean [SD] disease duration: 5.8 [5.5] years, median [range] EDSS: 4 [0-6.5]). COVID-19 outcome was overall favorable in this cohort. Larger international studies are needed to identify risk factors of severe COVID-19; however, we recommend personal protective measures to reduce risk of SARS-CoV-2 infection in this immunocompromised population.

Sections du résumé

BACKGROUND BACKGROUND
Outcomes of coronavirus disease 2019 (COVID-19) in patients with neuromyelitis optica spectrum disorders (NMOSD) or myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD), often treated with immunosuppressive therapies, are still unknown.
METHODS METHODS
We conducted a multicenter, retrospective, observational cohort study among all French expert centers for neuromyelitis optica and related disorders. Patients with NMOSD or MOGAD included in the study received a confirmed or highly suspected diagnosis of COVID-19 between 1 March 2020 and 30 June 2020. Main outcome was COVID-19 severity score assessed on a seven-point ordinal scale ranging from 1 (not hospitalized with no limitations on activities) to 7 (death).
RESULTS RESULTS
Fifteen cases (mean [SD] age: 39.3 [14.3] years, 11 female) were included. Five patients (33.3%) were hospitalized, all receiving rituximab. A 24-year-old patient with positive aquaporine-4 antibody, with obesity as comorbidity, needed mechanical ventilation. Outpatients were receiving anti-CD20 (5), mycophenolate mofetil (3) or azathioprine (3). They were younger (mean [SD] age: 37.0 [13.4] years), with a longer disease duration (mean [SD]: 8.3 [6.3] years) and had a lower expanded disability severity score (EDSS) score (median [range] EDSS: 2.5 [0-4]) relative to patients requiring hospitalization (mean [SD] age: 44.0 [16.4] years, mean [SD] disease duration: 5.8 [5.5] years, median [range] EDSS: 4 [0-6.5]).
CONCLUSIONS CONCLUSIONS
COVID-19 outcome was overall favorable in this cohort. Larger international studies are needed to identify risk factors of severe COVID-19; however, we recommend personal protective measures to reduce risk of SARS-CoV-2 infection in this immunocompromised population.

Identifiants

pubmed: 33103295
doi: 10.1111/ene.14612
doi:

Substances chimiques

Aquaporin 4 0
Rituximab 4F4X42SYQ6

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

3461-3466

Informations de copyright

© 2020 European Academy of Neurology.

Références

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Auteurs

Céline Louapre (C)

Centre de Référence des Maladies Inflammatoires Rares du Cerveau et de la Moelle, Institut du Cerveau, CIC Neuroscience, ICM, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Paris, France.

Elisabeth Maillart (E)

Centre de Référence des Maladies Inflammatoires Rares du Cerveau et de la Moelle, Institut du Cerveau, CIC Neuroscience, ICM, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Paris, France.

Caroline Papeix (C)

Centre de Référence des Maladies Inflammatoires Rares du Cerveau et de la Moelle, Institut du Cerveau, CIC Neuroscience, ICM, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Paris, France.

Sinead Zeidan (S)

Centre de Référence des Maladies Inflammatoires Rares du Cerveau et de la Moelle, Institut du Cerveau, CIC Neuroscience, ICM, Hôpital de la Pitié Salpêtrière, Sorbonne Université, Paris, France.

Damien Biotti (D)

Pole des Neurosciences, B4 Neurology Unit, Centre de ressources et de compétences Sclérose en plaques, CHU Purpan, Toulouse, France.

Zoé Lepine (Z)

Pole des Neurosciences, B4 Neurology Unit, Centre de ressources et de compétences Sclérose en plaques, CHU Purpan, Toulouse, France.

Abir Wahab (A)

Service de Neurologie et CRC SEP, Groupe Hospitalier Henri Mondor, APHP, UPEC Université, Créteil, France.

Mickael Zedet (M)

Unité de neurologie inflammatoire, Département de Neurologie, Hôpital Roger Salengro, Chu de Lille, Lille, France.

Pierre Labauge (P)

Département de neurologie, CHU de Montpellier, Montpellier, France.

Caroline Tilikete (C)

Equipe impact, Service de Neurocognition et Neuro-ophtalmologie, Groupe Hospitalier Est, Centre de Recherche en Neurosciences de Lyon, Hospices Civils de Lyon, Université de Lyon, Lyon, France.

Julie Pique (J)

Centre de référence des maladies inflammatoires rares du cerveau et de la moelle (MIRCEM), Service de neurologie, sclérose en plaques, Pathologies de la myéline et neuro-inflammation, Hôpital Neurologique Pierre Wertheimer Hospices Civils de Lyon, Lyon, France.

Ayman Tourbah (A)

Service de Neurologie, Hôpital Raymond Poincaré, UFR Simone Veil UVSQ, Université Paris Saclay, Garches, France.

Guillaume Mathey (G)

Service de neurologie, Centre Régional Hospitalo-Universitaire de Nancy, Hôpital Central, Nancy, France.
Université de Lorraine, Vandoeuvre-lès-Nancy, France.

Dalia Dimitri Boulos (D)

Service de neurologie, CHU Bicêtre, Le Kremlin Bicêtre, France.

Pierre Branger (P)

Service de Neurologie, CHU de Caen Normandie, Caen, France.

Laurent Daniel Kremer (LD)

Service de Neurologie and CIC INSERM 1434, CHU de Strasbourg, Strasbourg, France.

Romain Marignier (R)

Centre de référence des maladies inflammatoires rares du cerveau et de la moelle (MIRCEM), Service de neurologie, sclérose en plaques, Pathologies de la myéline et neuro-inflammation, Hôpital Neurologique Pierre Wertheimer Hospices Civils de Lyon, Lyon, France.

Nicolas Collongues (N)

Service de Neurologie and CIC INSERM 1434, CHU de Strasbourg, Strasbourg, France.

Jérôme De Seze (J)

Service de Neurologie and CIC INSERM 1434, CHU de Strasbourg, Strasbourg, France.

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