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dc.contributorVall d'Hebron Barcelona Hospital Campus
dc.contributor.authorSimpson-Yap, Steve
dc.contributor.authorPirmani, Ashkan
dc.contributor.authorKalincik, Tomas
dc.contributor.authorDe Brouwer, Edward
dc.contributor.authorGeys, Lotte
dc.contributor.authorParciak, Tina
dc.contributor.authorZabalza de Torres, Ana
dc.contributor.authorArrambide, Georgina
dc.date.accessioned2022-11-10T07:19:16Z
dc.date.available2022-11-10T07:19:16Z
dc.date.issued2022-11
dc.identifier.citationSimpson-Yap S, Pirmani A, Kalincik T, De Brouwer E, Geys L, Parciak T, et al. Updated Results of the COVID-19 in MS Global Data Sharing Initiative. Neurol Neuroimmunol Neuroinflamm. 2022 Nov;9(6):e200021.
dc.identifier.issn2332-7812
dc.identifier.urihttps://hdl.handle.net/11351/8427
dc.descriptionCOVID-19; Severe acute respiratory syndrome; Data set
dc.description.abstractBackground and Objectives Certain demographic and clinical characteristics, including the use of some disease-modifying therapies (DMTs), are associated with severe acute respiratory syndrome coronavirus 2 infection severity in people with multiple sclerosis (MS). Comprehensive exploration of these relationships in large international samples is needed. Methods Clinician-reported demographic/clinical data from 27 countries were aggregated into a data set of 5,648 patients with suspected/confirmed coronavirus disease 2019 (COVID-19). COVID-19 severity outcomes (hospitalization, admission to intensive care unit [ICU], requiring artificial ventilation, and death) were assessed using multilevel mixed-effects ordered probit and logistic regression, adjusted for age, sex, disability, and MS phenotype. DMTs were individually compared with glatiramer acetate, and anti-CD20 DMTs with pooled other DMTs and with natalizumab. Results Of 5,648 patients, 922 (16.6%) with suspected and 4,646 (83.4%) with confirmed COVID-19 were included. Male sex, older age, progressive MS, and higher disability were associated with more severe COVID-19. Compared with glatiramer acetate, ocrelizumab and rituximab were associated with higher probabilities of hospitalization (4% [95% CI 1–7] and 7% [95% CI 4–11]), ICU/artificial ventilation (2% [95% CI 0–4] and 4% [95% CI 2–6]), and death (1% [95% CI 0–2] and 2% [95% CI 1–4]) (predicted marginal effects). Untreated patients had 5% (95% CI 2–8), 3% (95% CI 1–5), and 1% (95% CI 0–3) higher probabilities of the 3 respective levels of COVID-19 severity than glatiramer acetate. Compared with pooled other DMTs and with natalizumab, the associations of ocrelizumab and rituximab with COVID-19 severity were also more pronounced. All associations persisted/enhanced on restriction to confirmed COVID-19. Discussion Analyzing the largest international real-world data set of people with MS with suspected/confirmed COVID-19 confirms that the use of anti-CD20 medication (both ocrelizumab and rituximab), as well as male sex, older age, progressive MS, and higher disability are associated with more severe course of COVID-19.
dc.language.isoeng
dc.publisherLippincott, Williams & Wilkins
dc.relation.ispartofseriesNeurology, Neuroimmunology and Neuroinflammation;9(6)
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.sourceScientia
dc.subjectEsclerosi múltiple
dc.subjectCOVID-19 (Malaltia) - Factors de risc
dc.subject.meshMultiple Sclerosis
dc.subject.meshCoronavirus Infections
dc.subject.meshRisk Factors
dc.titleUpdated Results of the COVID-19 in MS Global Data Sharing Initiative: Anti-CD20 and Other Risk Factors Associated With COVID-19 Severity
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1212/NXI.0000000000200021
dc.subject.decsesclerosis múltiple
dc.subject.decsinfecciones por Coronavirus
dc.subject.decsfactores de riesgo
dc.relation.publishversionhttps://doi.org/10.1212/NXI.0000000000200021
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.contributor.organismesInstitut Català de la Salut
dc.contributor.authoraffiliation[Simpson-Yap S] CORe, Department of Medicine, and Neuroepidemiology Unit, Melbourne School of Population & Global Health, The University of Melbourne, Menzies Institute for Medical Research, University of Tasmania, Australia. [Pirmani A, Geys L, Parciak T] ESAT-STADIUS, KU Leuven, Biomedical Research Institute–Data Science Institute, Hasselt University, Belgium. [Kalincik T] CORe, Department of Medicine, The University of Melbourne, MS Centre, Department of Neurology, Royal Melbourne Hospital, Australia. [De Brouwer E] ESAT-STADIUS, KU Leuven, Belgium. [Zabalza de Torres A, Arrambide G] Servei de Neurologia-Neuroimmunologia, Centre d’Esclerosi Múltiple de Catalunya (CEMCAT), Barcelona, Spain. Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain
dc.identifier.pmid36038263
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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