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A comparison of clinical outcomes in PPMS in the INFORMS original trial data set
BACKGROUND: The expanded disability status scale (EDSS) is the standard clinical outcome measure in primary progressive multiple sclerosis (PPMS), even though the timed 25-foot walk (T25FW), nine-hole peg test (NHPT) or combinations of these measures may be more useful. The paced auditory serial add...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521359/ https://www.ncbi.nlm.nih.gov/pubmed/33464149 http://dx.doi.org/10.1177/1352458520987539 |
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author | Koch, Marcus W Mostert, Jop P Uitdehaag, Bernard Cutter, Gary |
author_facet | Koch, Marcus W Mostert, Jop P Uitdehaag, Bernard Cutter, Gary |
author_sort | Koch, Marcus W |
collection | PubMed |
description | BACKGROUND: The expanded disability status scale (EDSS) is the standard clinical outcome measure in primary progressive multiple sclerosis (PPMS), even though the timed 25-foot walk (T25FW), nine-hole peg test (NHPT) or combinations of these measures may be more useful. The paced auditory serial addition test (PASAT) is a widely used cognitive measure in MS, but little is known about change in PASAT scores over time in PPMS. OBJECTIVE: The objective of this study is to compare clinical outcome measures in a large PPMS trial data set. METHODS: We determined significant worsening events on the EDSS, T25FW and NHPT, and PASAT scores over the course of this 3-year trial. We compared unconfirmed, confirmed and sustained disability worsening and contrasted disability worsening with similarly defined improvement. We examined the association of baseline characteristics with the risk of disability worsening at 12, 24 and 36 months with logistic regression models. RESULTS: The EDSS and T25FW showed most worsening events, while only few patients worsened on the NHPT. Adding the NHPT to a combined outcome added only few further worsening events. PASAT scores slightly increased over time, possibly due to a practice effect. CONCLUSION: Both the EDSS and T25FW, but not NHPT or PASAT, appear to be useful outcome measures in PPMS. |
format | Online Article Text |
id | pubmed-8521359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-85213592021-10-19 A comparison of clinical outcomes in PPMS in the INFORMS original trial data set Koch, Marcus W Mostert, Jop P Uitdehaag, Bernard Cutter, Gary Mult Scler Original Research Papers BACKGROUND: The expanded disability status scale (EDSS) is the standard clinical outcome measure in primary progressive multiple sclerosis (PPMS), even though the timed 25-foot walk (T25FW), nine-hole peg test (NHPT) or combinations of these measures may be more useful. The paced auditory serial addition test (PASAT) is a widely used cognitive measure in MS, but little is known about change in PASAT scores over time in PPMS. OBJECTIVE: The objective of this study is to compare clinical outcome measures in a large PPMS trial data set. METHODS: We determined significant worsening events on the EDSS, T25FW and NHPT, and PASAT scores over the course of this 3-year trial. We compared unconfirmed, confirmed and sustained disability worsening and contrasted disability worsening with similarly defined improvement. We examined the association of baseline characteristics with the risk of disability worsening at 12, 24 and 36 months with logistic regression models. RESULTS: The EDSS and T25FW showed most worsening events, while only few patients worsened on the NHPT. Adding the NHPT to a combined outcome added only few further worsening events. PASAT scores slightly increased over time, possibly due to a practice effect. CONCLUSION: Both the EDSS and T25FW, but not NHPT or PASAT, appear to be useful outcome measures in PPMS. SAGE Publications 2021-01-19 2021-10 /pmc/articles/PMC8521359/ /pubmed/33464149 http://dx.doi.org/10.1177/1352458520987539 Text en © The Author(s), 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://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 page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Papers Koch, Marcus W Mostert, Jop P Uitdehaag, Bernard Cutter, Gary A comparison of clinical outcomes in PPMS in the INFORMS original trial data set |
title | A comparison of clinical outcomes in PPMS in the INFORMS original trial data set |
title_full | A comparison of clinical outcomes in PPMS in the INFORMS original trial data set |
title_fullStr | A comparison of clinical outcomes in PPMS in the INFORMS original trial data set |
title_full_unstemmed | A comparison of clinical outcomes in PPMS in the INFORMS original trial data set |
title_short | A comparison of clinical outcomes in PPMS in the INFORMS original trial data set |
title_sort | comparison of clinical outcomes in ppms in the informs original trial data set |
topic | Original Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8521359/ https://www.ncbi.nlm.nih.gov/pubmed/33464149 http://dx.doi.org/10.1177/1352458520987539 |
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