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Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors

Multiple sclerosis (MS) is the most prevalent immune-mediated disease affecting the central nervous system. A treatment strategy with multiple therapies is a frequent clinical scenario. Unmonitored multi-drug use can lead to adverse outcomes, higher health care costs and medication non-adherence. Th...

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Autores principales: Frahm, Niklas, Hecker, Michael, Zettl, Uwe Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403326/
https://www.ncbi.nlm.nih.gov/pubmed/30842515
http://dx.doi.org/10.1038/s41598-019-40283-5
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author Frahm, Niklas
Hecker, Michael
Zettl, Uwe Klaus
author_facet Frahm, Niklas
Hecker, Michael
Zettl, Uwe Klaus
author_sort Frahm, Niklas
collection PubMed
description Multiple sclerosis (MS) is the most prevalent immune-mediated disease affecting the central nervous system. A treatment strategy with multiple therapies is a frequent clinical scenario. Unmonitored multi-drug use can lead to adverse outcomes, higher health care costs and medication non-adherence. The primary aim of this study was to evaluate the frequency of polypharmacy and related clinicodemographic factors in a single-center MS patient cohort. Furthermore, medication aspects of therapy management were examined. After the patients agreed to participate in the study, data were collected through patient interviews, patient records and clinical investigations. Subsequently, a statistical data analysis regarding various medication subgroups and polypharmacy (use of at least five drugs) was performed. Polypharmacy was observed in 56.5% of the patients (N = 306). High degrees of disability (odds ratio [OR] = 1.385), comorbidities (OR = 4.879) and inpatient treatment (OR = 5.146) were associated with a significantly higher risk of polypharmacy (p ≤ 0.001). Among patients with polypharmacy, disease-modifying drugs, antihypertensives, gastrointestinal drugs, thrombosis prophylactics, osteoporosis medications and sedatives were frequently used. In summary, polypharmacy plays a large role in MS patients, especially in those with higher degrees of disability, those with comorbidities and those treated in an inpatient setting.
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spelling pubmed-64033262019-03-08 Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors Frahm, Niklas Hecker, Michael Zettl, Uwe Klaus Sci Rep Article Multiple sclerosis (MS) is the most prevalent immune-mediated disease affecting the central nervous system. A treatment strategy with multiple therapies is a frequent clinical scenario. Unmonitored multi-drug use can lead to adverse outcomes, higher health care costs and medication non-adherence. The primary aim of this study was to evaluate the frequency of polypharmacy and related clinicodemographic factors in a single-center MS patient cohort. Furthermore, medication aspects of therapy management were examined. After the patients agreed to participate in the study, data were collected through patient interviews, patient records and clinical investigations. Subsequently, a statistical data analysis regarding various medication subgroups and polypharmacy (use of at least five drugs) was performed. Polypharmacy was observed in 56.5% of the patients (N = 306). High degrees of disability (odds ratio [OR] = 1.385), comorbidities (OR = 4.879) and inpatient treatment (OR = 5.146) were associated with a significantly higher risk of polypharmacy (p ≤ 0.001). Among patients with polypharmacy, disease-modifying drugs, antihypertensives, gastrointestinal drugs, thrombosis prophylactics, osteoporosis medications and sedatives were frequently used. In summary, polypharmacy plays a large role in MS patients, especially in those with higher degrees of disability, those with comorbidities and those treated in an inpatient setting. Nature Publishing Group UK 2019-03-06 /pmc/articles/PMC6403326/ /pubmed/30842515 http://dx.doi.org/10.1038/s41598-019-40283-5 Text en © The Author(s) 2019 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
Frahm, Niklas
Hecker, Michael
Zettl, Uwe Klaus
Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors
title Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors
title_full Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors
title_fullStr Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors
title_full_unstemmed Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors
title_short Multi-drug use among patients with multiple sclerosis: A cross-sectional study of associations to clinicodemographic factors
title_sort multi-drug use among patients with multiple sclerosis: a cross-sectional study of associations to clinicodemographic factors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403326/
https://www.ncbi.nlm.nih.gov/pubmed/30842515
http://dx.doi.org/10.1038/s41598-019-40283-5
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