PLEX: the best first-line treatment in nmosd attacks experience at a single center in Colombia

Primary outcome was to evaluate complete improvement at six months after acute treatment in NMOSD relapses. Retrospective observational cohort study of patients with diagnosis of NMOSD admitted for acute attacks. We performed an explanatory analysis using the univariate, bivariate and multivariate l...

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Published inHeliyon Vol. 7; no. 4; p. e06811
Main Authors Restrepo-Aristizábal, C., Giraldo, L.M., Giraldo, Y.M., Pino-Pérez, A.M., Álvarez-Gómez, F., Franco, C.A., Tobón, J.V., Ascencio, J.L., Zuluaga, M.I.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.04.2021
Elsevier
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Summary:Primary outcome was to evaluate complete improvement at six months after acute treatment in NMOSD relapses. Retrospective observational cohort study of patients with diagnosis of NMOSD admitted for acute attacks. We performed an explanatory analysis using the univariate, bivariate and multivariate logistic regression approach. We compared survival curves using the Kaplan Meier analysis and estimated the median time for the main outcome. In the univariate analysis, basal EDSS score, AQP4-IgG positivity, PLEX as a first-line treatment (IVMP + PLEX), less systemic complications related to acute treatment and total attack history were independently associated with complete improvement at six months. After adjusting for confounding variables and using multivariate analysis by Cox Regression, positive AQ4-IgG (HR 0.04, 95% CI: 0.02–0.66) and IVMP + PLEX (HR 5.1, 95% CI: 3.9–66.4), were kept as independent factors associated to time to complete improvement. Time from admission to PLEX initiation and complete improvement at six months had a median of seven days (95% CI: 5.2–8.8). In secondary effects, there were no statistical differences between the groups. PLEX + IVMP is the treatment of choice for NMOSD relapses and should be initiated as early as possible. Devic's syndrome; Autoimmune diseases; Transverse myelitis; Optic neuritis; All Demyelinating disease (CNS).
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These authors contributed equally to the manuscript.
ISSN:2405-8440
2405-8440
DOI:10.1016/j.heliyon.2021.e06811