Treatment Switching and Discontinuation Over 20 Years in the Big Multiple Sclerosis Data Network

Although more than a dozen disease-modifying treatments (DMTs) are available for relapsing forms of multiple sclerosis (MS), treatment interruptions, switches, and discontinuations are common challenges. This study focuses on describing treatment interruptions and discontinuations within the Big Multiple Sclerosis Data Network. Under the leadership of Prof. Jan Hillert from Sweden's Karolinska Institutet, data from five clinical registries covering a 20-year period...

What data does the national registry of patients with multiple sclerosis ReMuS offer?

In a review article in the professional journal Neurologie pro praxi the professional guarantor of the ReMuS registry focused on presenting the ReMuS registry and, in particular, the range of data it contains. The article also provides insight into the representation of patients in individual MS centers across the Czech Republic, the development of the use of highly effective medicinal products, and the critically important area of...

Multiple sclerosis registries in Europe - Updated overview

In 2018, an updated mapping of multiple sclerosis (MS) registries in Europe was conducted, building on a previous survey from 2014. This survey includes 19 registries, mostly from Europe, and provides detailed information on the organization, data collection methods, quality control mechanisms, and funding of these registries...

A comparison of efficacy of subcutaneous interferon β-1a 44 μg, dimethyl fumarate and fingolimod in the real-life clinical practise – a multicenter observational study

Multiple sclerosis (MS) is a chronic inflammatory demyelinating and neurodegenerative disease affecting the central nervous system. Interferon (IFN) β-1a 44 μg, dimethyl fumarate (DMF), and fingolimod are established medications for the treatment of relapsing-remitting MS (RR MS). The aim of this project, which includes an analysis of data from the ReMuS registry, was...

ReMuS - The Czech Republic National Multiple Sclerosis Patient Registry

The article by Dr. Dana Horáková, published in Multiple Sclerosis News offers a detailed look at the creation and development of the Czech national registry of multiple sclerosis patients, ReMuS, since its establishment in 2013. Readers will find information on the structure of the registry, the data collection process, and...

Newsletter of the ReMuS registry

Occasionally, we will send you news from the field of multiple sclerosis research and the ReMuS registry in the form of a digital newsletter.