Please use this identifier to cite or link to this item: http://hdl.handle.net/10400.10/2056
Title: Prolonged-release fampridine in multiple sclerosis: clinical data and real-world experience. Report of an expert meeting.
Author: Albrecht, P
Bjørnå, K
Brassat, D
Farrell, R
Feys, P
Hobart, J
Hupperts, R
Linnebank, M
Magdič, J
Oreja-Guevara, C
Pozzilli, C
Salgado, AV
Ziemssen, T
Keywords: Multiple sclerosis
Quality of life
Fampridine
Issue Date: 2018
Publisher: SAGE Publications
Citation: Ther Adv Neurol Disord. 2018 Oct 5;11:1756286418803248
Abstract: Prolonged-release (PR) fampridine is the only approved medication to improve walking in multiple sclerosis (MS), having been shown to produce a clinically meaningful improvement in walking ability in the subset of MS patients with Expanded Disability Status Scale 4-7. Recent responder subgroup analyses in the phase III ENHANCE study show a large effect size in terms of an increase of 20.58 points on the patient-reported 12-item MS Walking Scale in the 43% of patients classified as responders to PR-fampridine, corresponding to a standardized response mean of 1.68. Use of PR-fampridine in clinical practice varies across Europe, depending partly on whether it is reimbursed. A group of European MS experts met in June 2017 to discuss their experience with using PR-fampridine, including their views on the patient population for treatment, assessment of treatment response, re-testing and re-treatment, and stopping criteria. This article summarizes the experts' opinions on how PR-fampridine can be used in real-world clinical practice to optimize the benefits to people with MS with impaired walking ability.
Peer review: yes
URI: http://hdl.handle.net/10400.10/2056
DOI: 10.1177/1756286418803248.
ISSN: 1756-2864
Publisher Version: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6174649/pdf/10.1177_1756286418803248.pdf
Appears in Collections:NEU - Artigos publicados em revistas não indexadas

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