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Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine

BACKGROUND: Gait impairment is common in multiple sclerosis (MS) and negatively impacts patients’ health-related quality of life (HRQoL). Prolonged-release fampridine (PR-fam) improves walking speed, but it is unclear which walking measures are the most suitable for identifying treatment response. O...

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Autores principales: Sola-Valls, Núria, Blanco, Yolanda, Sepúlveda, María, Llufriu, Sara, Martínez-Lapiscina, Elena H., Zubizarreta, Irati, Pulido-Valdeolivas, Irene, Montejo, Carmen, Villoslada, Pablo, Saiz, Albert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024337/
https://www.ncbi.nlm.nih.gov/pubmed/29977342
http://dx.doi.org/10.1177/1756286418780007
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author Sola-Valls, Núria
Blanco, Yolanda
Sepúlveda, María
Llufriu, Sara
Martínez-Lapiscina, Elena H.
Zubizarreta, Irati
Pulido-Valdeolivas, Irene
Montejo, Carmen
Villoslada, Pablo
Saiz, Albert
author_facet Sola-Valls, Núria
Blanco, Yolanda
Sepúlveda, María
Llufriu, Sara
Martínez-Lapiscina, Elena H.
Zubizarreta, Irati
Pulido-Valdeolivas, Irene
Montejo, Carmen
Villoslada, Pablo
Saiz, Albert
author_sort Sola-Valls, Núria
collection PubMed
description BACKGROUND: Gait impairment is common in multiple sclerosis (MS) and negatively impacts patients’ health-related quality of life (HRQoL). Prolonged-release fampridine (PR-fam) improves walking speed, but it is unclear which walking measures are the most suitable for identifying treatment response. Our aim was to assess the effect of PR-fam and the outcome measures that best identify short- and long-term clinically meaningful response. METHODS: We conducted a prospective study in 32 MS patients treated with PR-fam for a year. The assessments at 2 weeks, 3, 6 and 12 months included: timed 25-foot walk (T25FW), 6-minute walk test (6MWT), MS Walking Scale-12 (MSWS-12), a five-level version of the EuroQoL-5 dimensions, and accelerometry. PR-fam response was defined as an improvement in T25FW ⩾20%. RESULTS: Twenty-five (78%) patients were considered responders after 2 weeks of PR-fam and improved significantly in all measures. Responders to T25FW and MSWS-12 (n = 19) showed a significant improvement in HRQoL and accelerometer data compared with responders only to T25FW (n = 6). At 1 year, 15/20 (75%) patients remained responders, but only those with permanent response to T25FW and MSWS-12 (n = 8; 53%) showed a significant improvement in 6MWT and HRQoL. CONCLUSION: The combination of T25FW and MSWS-12 identify better those patients with a clinically significant benefit of PR-fam.
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spelling pubmed-60243372018-07-05 Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine Sola-Valls, Núria Blanco, Yolanda Sepúlveda, María Llufriu, Sara Martínez-Lapiscina, Elena H. Zubizarreta, Irati Pulido-Valdeolivas, Irene Montejo, Carmen Villoslada, Pablo Saiz, Albert Ther Adv Neurol Disord Original Research BACKGROUND: Gait impairment is common in multiple sclerosis (MS) and negatively impacts patients’ health-related quality of life (HRQoL). Prolonged-release fampridine (PR-fam) improves walking speed, but it is unclear which walking measures are the most suitable for identifying treatment response. Our aim was to assess the effect of PR-fam and the outcome measures that best identify short- and long-term clinically meaningful response. METHODS: We conducted a prospective study in 32 MS patients treated with PR-fam for a year. The assessments at 2 weeks, 3, 6 and 12 months included: timed 25-foot walk (T25FW), 6-minute walk test (6MWT), MS Walking Scale-12 (MSWS-12), a five-level version of the EuroQoL-5 dimensions, and accelerometry. PR-fam response was defined as an improvement in T25FW ⩾20%. RESULTS: Twenty-five (78%) patients were considered responders after 2 weeks of PR-fam and improved significantly in all measures. Responders to T25FW and MSWS-12 (n = 19) showed a significant improvement in HRQoL and accelerometer data compared with responders only to T25FW (n = 6). At 1 year, 15/20 (75%) patients remained responders, but only those with permanent response to T25FW and MSWS-12 (n = 8; 53%) showed a significant improvement in 6MWT and HRQoL. CONCLUSION: The combination of T25FW and MSWS-12 identify better those patients with a clinically significant benefit of PR-fam. SAGE Publications 2018-06-10 /pmc/articles/PMC6024337/ /pubmed/29977342 http://dx.doi.org/10.1177/1756286418780007 Text en © The Author(s), 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Sola-Valls, Núria
Blanco, Yolanda
Sepúlveda, María
Llufriu, Sara
Martínez-Lapiscina, Elena H.
Zubizarreta, Irati
Pulido-Valdeolivas, Irene
Montejo, Carmen
Villoslada, Pablo
Saiz, Albert
Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine
title Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine
title_full Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine
title_fullStr Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine
title_full_unstemmed Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine
title_short Combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine
title_sort combined walking outcome measures identify clinically meaningful response to prolonged-release fampridine
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6024337/
https://www.ncbi.nlm.nih.gov/pubmed/29977342
http://dx.doi.org/10.1177/1756286418780007
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