Literature DB >> 29241141

Plasma exchange in severe acute relapses of multiple sclerosis - Results from a Portuguese cohort.

Inês Correia1, Joana Jesus Ribeiro2, Luís Isidoro3, Sónia Batista2, Carla Nunes2, Carmo Macário2, Catarina Borges4, Jorge Tomaz4, Lívia Sousa2.   

Abstract

BACKGROUND: Relapses in Multiple Sclerosis (MS) are often associated with significant disability impairment which is resultant from poor response to corticosteroids. In such severe cases, plasma exchange (PLEX) may be used, although only a few studies with MS patients have been reported. Our objective was to evaluate the effectiveness of PLEX in severe relapses of MS.
METHODS: Retrospective study of MS patients treated with PLEX in acute relapses. Data regarding EDSS, annualized relapse rate (ARR), treatment with corticosteroids, number of PLEX sessions, adverse events, and gadolinium enhancement in brain MRI were analysed.
RESULTS: Included 46 patients, 76.09% female (n = 35) with mean age of 38.76 years and mean disease duration of 5.99 years, of which 84.78% had a Relapsing Remitting MS (n = 39), 15.22% Secondary Progressive MS (n = 7). The previous ARR was 1.1 and in 28.26% of the cases (n = 13) PLEX was used in the relapse that led to MS diagnosis. The majority of relapses had motor impairment (69.6%, n = 32), with a median EDSS increase of 1.5 points from baseline (maximum of 6.5) and higher than 1.5 points in 45.65% of cases (n = 21). Brain MRI was available in 69.57% of the cases (n = 32), and gadolinium enhancing lesions were present in 68.75% of cases (n = 22). Corticosteroids were used before PLEX in all patients for a mean of 6.09 days, without any immediate benefit in 41.30% of cases (n = 19), with the remaining cases showing only mild disability recovery. After a mean of 7.39 PLEX sessions, there was clinical benefit with complete EDSS recovery in 41.30% of patients (n = 19), and partial in 39.13% (n = 18). There were no adverse events related to PLEX in 89.13% of patients (n = 41) and in the remaining patients the reported adverse events included deep venous thrombosis (n = 1), anaemia (n = 1), fever (n = 1), hypoalbuminemia (n = 1) and arterial hypotension (n = 1).
CONCLUSION: Our results support the use of PLEX in severe relapses unresponsive to corticosteroids, since it was an effective and relatively safe treatment for most of our patients.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Multiple Sclerosis; Plasma exchange; Relapse; Treatment

Mesh:

Substances:

Year:  2017        PMID: 29241141     DOI: 10.1016/j.msard.2017.12.001

Source DB:  PubMed          Journal:  Mult Scler Relat Disord        ISSN: 2211-0348            Impact factor:   4.339


  5 in total

1.  Plasma exchange in acute attacks of demyelinating diseases of the central nervous system: clinical outcomes and predictors of response.

Authors:  Michael A Palacios-Mendoza; María L Martínez Ginés; Pedro J Melgarejo Otálora; Juan P Cuello; Antonio Sánchez-Soblechero; Alberto Lozano Ros; José A Aparcero-Suero; Sergio López Anguita; Fernando Anaya; José M García Domínguez
Journal:  Neurol Sci       Date:  2020-04-04       Impact factor: 3.307

Review 2.  Multiple Sclerosis: Therapeutic Strategies on the Horizon.

Authors:  Ramya Talanki Manjunatha; Salma Habib; Sai Lahari Sangaraju; Daniela Yepez; Xavier A Grandes
Journal:  Cureus       Date:  2022-05-10

3.  Therapeutic Plasma Exchange in Multiple Sclerosis and Autoimmune Encephalitis: a Comparative Study of Indication, Efficacy and Safety.

Authors:  Tobias Moser; Gayane Harutyunyan; Anush Karamyan; Ferdinand Otto; Carola Bacher; Vaclav Chroust; Markus Leitinger; Helmut F Novak; Eugen Trinka; Johann Sellner
Journal:  Brain Sci       Date:  2019-10-09

Review 4.  The Role of Plasma Exchange in the Treatment of Refractory Autoimmune Neurological Diseases: a Narrative Review.

Authors:  Saiju Jacob; Gordon Mazibrada; Sarosh R Irani; Anu Jacob; Anna Yudina
Journal:  J Neuroimmune Pharmacol       Date:  2021-10-02       Impact factor: 4.147

5.  Plasma Exchange or Immunoadsorption in Demyelinating Diseases: A Meta-Analysis.

Authors:  Mark Lipphardt; Manuel Wallbach; Michael J Koziolek
Journal:  J Clin Med       Date:  2020-05-25       Impact factor: 4.241

  5 in total

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