Author: Sormani, Maria P.; De Rossi, Nicola; Schiavetti, Irene; Carmisciano, Luca; Cordioli, Cinzia; Moiola, Lucia; Radaelli, Marta; Immovilli, Paolo; Capobianco, Marco; Trojano, Maria; Zaratin, Paola; Tedeschi, Gioacchino; Comi, Giancarlo; Battaglia, Mario A.; Patti, Francesco; Salvetti, Marco
Title: Diseaseâ€Modifying Therapies and Coronavirus Disease 2019 Severity in Multiple Sclerosis Cord-id: w0fwdo33 Document date: 2021_2_9
ID: w0fwdo33
Snippet: OBJECTIVE: This study was undertaken to assess the impact of immunosuppressive and immunomodulatory therapies on the severity of coronavirus disease 2019 (COVIDâ€19) in people with multiple sclerosis (PwMS). METHODS: We retrospectively collected data of PwMS with suspected or confirmed COVIDâ€19. All the patients had complete followâ€up to death or recovery. Severe COVIDâ€19 was defined by a 3â€level variable: mild disease not requiring hospitalization versus pneumonia or hospitalization ve
Document: OBJECTIVE: This study was undertaken to assess the impact of immunosuppressive and immunomodulatory therapies on the severity of coronavirus disease 2019 (COVIDâ€19) in people with multiple sclerosis (PwMS). METHODS: We retrospectively collected data of PwMS with suspected or confirmed COVIDâ€19. All the patients had complete followâ€up to death or recovery. Severe COVIDâ€19 was defined by a 3â€level variable: mild disease not requiring hospitalization versus pneumonia or hospitalization versus intensive care unit (ICU) admission or death. We evaluated baseline characteristics and MS therapies associated with severe COVIDâ€19 by multivariate and propensity score (PS)â€weighted ordinal logistic models. Sensitivity analyses were run to confirm the results. RESULTS: Of 844 PwMS with suspected (n = 565) or confirmed (n = 279) COVIDâ€19, 13 (1.54%) died; 11 of them were in a progressive MS phase, and 8 were without any therapy. Thirtyâ€eight (4.5%) were admitted to an ICU; 99 (11.7%) had radiologically documented pneumonia; 96 (11.4%) were hospitalized. After adjusting for region, age, sex, progressive MS course, Expanded Disability Status Scale, disease duration, body mass index, comorbidities, and recent methylprednisolone use, therapy with an antiâ€CD20 agent (ocrelizumab or rituximab) was significantly associated (odds ratio [OR] = 2.37, 95% confidence interval [CI] = 1.18–4.74, p = 0.015) with increased risk of severe COVIDâ€19. Recent use (<1 month) of methylprednisolone was also associated with a worse outcome (OR = 5.24, 95% CI = 2.20–12.53, p = 0.001). Results were confirmed by the PSâ€weighted analysis and by all the sensitivity analyses. INTERPRETATION: This study showed an acceptable level of safety of therapies with a broad array of mechanisms of action. However, some specific elements of risk emerged. These will need to be considered while the COVIDâ€19 pandemic persists. ANN NEUROL 2021;89:780–789
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