Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/28711
Title: Prolonged-release fampridine in multiple sclerosis: clinical data and real-world experience. Report of an expert meeting
Authors: Albrecht, Philipp
Bjorna, Ingrid Kristine
Brassat, David
Farrell, Rachel
FEYS, Peter 
Hobart, Jeremy
Hupperts, Raymond
Linnebank, Michael
Magdic, Jozef
Oreja-Guevara, Celia
Pozzilli, Carlo
Salgado, Antonio Vasco
Ziemssen, Tjalf
Issue Date: 2018
Publisher: SAGE PUBLICATIONS LTD
Source: Therapeutic Advances in Neurological Disorders, 11, p. 1-8
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 retreatment, and stopping criteria. This article summarizes the experts' opinions on how PRfampridine can be used in real-world clinical practice to optimize the benefits to people with MS with impaired walking ability.
Notes: [Albrecht, Philipp] Heinrich Heine Univ, Med Fac, Dept Neurol, Moorenstr 5, D-40225 Dusseldorf, Germany. [Bjorna, Ingrid Kristine] Vestre Viken, Drammen Sykehus, Neurol Dept, Drammen, Germany. [Brassat, David] Univ Toulouse III, CHU Toulouse, SEP, Ctr Resource & Competence, Toulouse, France. [Brassat, David] Univ Toulouse III, UMR1043, Toulouse, France. [Farrell, Rachel] UCL Inst Neurol, Dept Neuroinflammat, London, England. [Farrell, Rachel] UCLH NHS Fdn Trust, Natl Hosp Neurol & Neurosurg, London, England. [Feys, Peter] Hasselt Univ, Fac Rehabil Sci, BIOMED, REVAL, Hasselt, Belgium. [Hobart, Jeremy] Plymouth Univ Peninsula, Sch Med, Dept Clin Trials & Hlth Res Translat & Stratified, Plymouth, Devon, England. [Hobart, Jeremy] Plymouth Univ Peninsula, Sch Dent, Dept Clin Trials & Hlth Res Translat & Stratified, Plymouth, Devon, England. [Hupperts, Raymond] Zuyderland Med Ctr, Dept Neurol, Sittard Geleen, Netherlands. [Linnebank, Michael] Helios Clin Hagen Ambrock, Dept Neurol, Hagen, Germany. [Magdic, Jozef] Univ Med Ctr Maribor, Dept Neurol, Maribor, Slovenia. [Oreja-Guevara, Celia] Univ Complutense Madrid, Dept Med, Hosp Clin San Carlos, Neurol, Madrid, Spain. [Oreja-Guevara, Celia] Inst Invest Sanitaria Hosp Clin San Carlos IdISSC, Madrid, Spain. [Pozzilli, Carlo] Univ Roma La Sapienza, Dept Neurol, Rome, Italy. [Salgado, Antonio Vasco] Hosp Fernando Fonseca, Serv Neurol, Amadora, Portugal. [Ziemssen, Tjalf] Tech Univ Dresden, Univ Hosp Carl Gustav Carus, MS Ctr Dresden, Ctr Clin Neurosci,Dept Neurol, Dresden, Germany.
Keywords: multiple sclerosis; prolonged-release fampridine; real-world experience; treatment response; walking ability;multiple sclerosis; prolonged-release fampridine; real-world experience; treatment response; walking ability
Document URI: http://hdl.handle.net/1942/28711
ISSN: 1756-2856
e-ISSN: 1756-2864
DOI: 10.1177/1756286418803248
ISI #: 000455655900001
Rights: The Author(s), 2018. Article reuse guidelines: sagepub.com/journalspermissions Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License
Category: A1
Type: Journal Contribution
Validations: ecoom 2020
Appears in Collections:Research publications

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