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Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness

Plasma exchange (PE) and immunoadsorption (IA) are standard therapeutic options of immune-mediated neurological disorders. This study evaluates the relation of the relative quantity of applied dose of PE and/ or IA and its achieved therapeutic effectiveness within the treated underlying neurological...

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Autores principales: Klingele, Matthias, Allmendinger, Carina, Thieme, Solmaz, Baerens, Lea, Fliser, Danilo, Jan, Bürmann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220931/
https://www.ncbi.nlm.nih.gov/pubmed/32404917
http://dx.doi.org/10.1038/s41598-020-64744-4
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author Klingele, Matthias
Allmendinger, Carina
Thieme, Solmaz
Baerens, Lea
Fliser, Danilo
Jan, Bürmann
author_facet Klingele, Matthias
Allmendinger, Carina
Thieme, Solmaz
Baerens, Lea
Fliser, Danilo
Jan, Bürmann
author_sort Klingele, Matthias
collection PubMed
description Plasma exchange (PE) and immunoadsorption (IA) are standard therapeutic options of immune-mediated neurological disorders. This study evaluates the relation of the relative quantity of applied dose of PE and/ or IA and its achieved therapeutic effectiveness within the treated underlying neurological disorders. In a retrospective study, we evaluated data from PE and IA carried out 09/2009-06/2014 in neurological patients at the University-Hospital of Saarland, Germany. Apheresis dose was defined as the ratio of the extracorporeal treated plasma volume to the patient’s plasma volume. Effectiveness was assessed through disease-specific tests and scores by the attending neurologist(s); results were classified into response or no response. 1101 apheresis (PE:238, IA:863), in 153 hospital-stays were carried out, averaged, 7.0 treatments per patients, 82% responded, 18% not. Mean applied apheresis dose per treatment was 0.91 with mean doses of 1.16 for PE and 0.81 for IA. The totally applied mean dose per stay was 5.6 (PE:5.01, IA:5.81). No correlation was seen between apheresis dosing and treatment effectiveness (PE:R2 = 0.074, IA:R2 = 0.0023). PE and IA in therapy-refractory immune-mediated neurological disorders majorly achieved a measurable severity improvement – without correlation to the applied dose. Moreover, our data rather suggest, that effectiveness may be given with volumes below currently recommended volumes.
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spelling pubmed-72209312020-05-20 Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness Klingele, Matthias Allmendinger, Carina Thieme, Solmaz Baerens, Lea Fliser, Danilo Jan, Bürmann Sci Rep Article Plasma exchange (PE) and immunoadsorption (IA) are standard therapeutic options of immune-mediated neurological disorders. This study evaluates the relation of the relative quantity of applied dose of PE and/ or IA and its achieved therapeutic effectiveness within the treated underlying neurological disorders. In a retrospective study, we evaluated data from PE and IA carried out 09/2009-06/2014 in neurological patients at the University-Hospital of Saarland, Germany. Apheresis dose was defined as the ratio of the extracorporeal treated plasma volume to the patient’s plasma volume. Effectiveness was assessed through disease-specific tests and scores by the attending neurologist(s); results were classified into response or no response. 1101 apheresis (PE:238, IA:863), in 153 hospital-stays were carried out, averaged, 7.0 treatments per patients, 82% responded, 18% not. Mean applied apheresis dose per treatment was 0.91 with mean doses of 1.16 for PE and 0.81 for IA. The totally applied mean dose per stay was 5.6 (PE:5.01, IA:5.81). No correlation was seen between apheresis dosing and treatment effectiveness (PE:R2 = 0.074, IA:R2 = 0.0023). PE and IA in therapy-refractory immune-mediated neurological disorders majorly achieved a measurable severity improvement – without correlation to the applied dose. Moreover, our data rather suggest, that effectiveness may be given with volumes below currently recommended volumes. Nature Publishing Group UK 2020-05-13 /pmc/articles/PMC7220931/ /pubmed/32404917 http://dx.doi.org/10.1038/s41598-020-64744-4 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Klingele, Matthias
Allmendinger, Carina
Thieme, Solmaz
Baerens, Lea
Fliser, Danilo
Jan, Bürmann
Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness
title Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness
title_full Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness
title_fullStr Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness
title_full_unstemmed Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness
title_short Therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness
title_sort therapeutic apheresis within immune-mediated neurological disorders: dosing and its effectiveness
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220931/
https://www.ncbi.nlm.nih.gov/pubmed/32404917
http://dx.doi.org/10.1038/s41598-020-64744-4
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