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Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study

BACKGROUND: Therapeutic plasma exchange (TPE) is frequently used in glucocorticosteroid (GCS)-refractory multiple sclerosis (MS) relapses. Data regarding predictors of treatment response are scarce. The objective of this study was to analyze predictive factors for response to TPE in GCS-refractory M...

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Autores principales: Blechinger, Stephan, Ehler, Johannes, Bsteh, Gabriel, Winkelmann, Alexander, Leutmezer, Fritz, Meister, Stefanie, Santer, Agnes, Hecker, Michael, Berger, Thomas, Rommer, Paulus, Zettl, Uwe Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844455/
https://www.ncbi.nlm.nih.gov/pubmed/33552236
http://dx.doi.org/10.1177/1756286420975642
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author Blechinger, Stephan
Ehler, Johannes
Bsteh, Gabriel
Winkelmann, Alexander
Leutmezer, Fritz
Meister, Stefanie
Santer, Agnes
Hecker, Michael
Berger, Thomas
Rommer, Paulus
Zettl, Uwe Klaus
author_facet Blechinger, Stephan
Ehler, Johannes
Bsteh, Gabriel
Winkelmann, Alexander
Leutmezer, Fritz
Meister, Stefanie
Santer, Agnes
Hecker, Michael
Berger, Thomas
Rommer, Paulus
Zettl, Uwe Klaus
author_sort Blechinger, Stephan
collection PubMed
description BACKGROUND: Therapeutic plasma exchange (TPE) is frequently used in glucocorticosteroid (GCS)-refractory multiple sclerosis (MS) relapses. Data regarding predictors of treatment response are scarce. The objective of this study was to analyze predictive factors for response to TPE in GCS-refractory MS patients. METHODS: A total of 118 MS patients in two tertiary MS centers were analyzed. Primary outcome was TPE response defined as marked, mild, or no improvement. Secondary outcome was change in expanded disability status scale (ΔEDSS). ΔEDSS and relapse activity within 6 months after TPE were studied. RESULTS: Marked or mild improvement was observed in 78.8% of patients. ΔEDSS correlated significantly inversely with time from relapse to start of TPE (τ = –0.239, p = 0.001), age (τ = 0.182, p = 0.009) and disease duration (τ = –0.167, p = 0.017). In multivariate analysis, TPE response was predicted by diagnosis of relapsing MS [odds ratio (OR): 3.1], gadolinum-enhancement on magnetic resonance imaging (OR 3.2), age (OR 0.5 per 5 years older) and time from relapse onset to TPE (OR 0.7 per 7 days longer). CONCLUSION: Patients with longer disease duration and higher EDSS pre and post-TPE were more likely to show further disability progression or relapses within 6 months after TPE. No sustained effects were observed during the follow-up period.
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spelling pubmed-78444552021-02-05 Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study Blechinger, Stephan Ehler, Johannes Bsteh, Gabriel Winkelmann, Alexander Leutmezer, Fritz Meister, Stefanie Santer, Agnes Hecker, Michael Berger, Thomas Rommer, Paulus Zettl, Uwe Klaus Ther Adv Neurol Disord Original Research BACKGROUND: Therapeutic plasma exchange (TPE) is frequently used in glucocorticosteroid (GCS)-refractory multiple sclerosis (MS) relapses. Data regarding predictors of treatment response are scarce. The objective of this study was to analyze predictive factors for response to TPE in GCS-refractory MS patients. METHODS: A total of 118 MS patients in two tertiary MS centers were analyzed. Primary outcome was TPE response defined as marked, mild, or no improvement. Secondary outcome was change in expanded disability status scale (ΔEDSS). ΔEDSS and relapse activity within 6 months after TPE were studied. RESULTS: Marked or mild improvement was observed in 78.8% of patients. ΔEDSS correlated significantly inversely with time from relapse to start of TPE (τ = –0.239, p = 0.001), age (τ = 0.182, p = 0.009) and disease duration (τ = –0.167, p = 0.017). In multivariate analysis, TPE response was predicted by diagnosis of relapsing MS [odds ratio (OR): 3.1], gadolinum-enhancement on magnetic resonance imaging (OR 3.2), age (OR 0.5 per 5 years older) and time from relapse onset to TPE (OR 0.7 per 7 days longer). CONCLUSION: Patients with longer disease duration and higher EDSS pre and post-TPE were more likely to show further disability progression or relapses within 6 months after TPE. No sustained effects were observed during the follow-up period. SAGE Publications 2021-01-27 /pmc/articles/PMC7844455/ /pubmed/33552236 http://dx.doi.org/10.1177/1756286420975642 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Blechinger, Stephan
Ehler, Johannes
Bsteh, Gabriel
Winkelmann, Alexander
Leutmezer, Fritz
Meister, Stefanie
Santer, Agnes
Hecker, Michael
Berger, Thomas
Rommer, Paulus
Zettl, Uwe Klaus
Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study
title Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study
title_full Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study
title_fullStr Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study
title_full_unstemmed Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study
title_short Therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. A retrospective two-center study
title_sort therapeutic plasma exchange in steroid-refractory multiple sclerosis relapses. a retrospective two-center study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7844455/
https://www.ncbi.nlm.nih.gov/pubmed/33552236
http://dx.doi.org/10.1177/1756286420975642
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