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The MSIS-29 and SF-36 as outcomes in secondary progressive MS trials
BACKGROUND: Patient-reported outcome measures (PROMs) are often used in clinical research, but little is known about their performance as longitudinal outcomes. METHODS: We used data from ASCEND, a large SPMS trial (n = 889), to investigate changes on the Short Form Health Survey 36 (SF-36 v2) and t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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SAGE Publications
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315187/ https://www.ncbi.nlm.nih.gov/pubmed/35876467 http://dx.doi.org/10.1177/13524585221105465 |
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author | Strijbis, Eva MM Repovic, Pavle Mostert, Jop Bowen, James D Uitdehaag, Bernard MJ Cutter, Gary Koch, Marcus W |
author_facet | Strijbis, Eva MM Repovic, Pavle Mostert, Jop Bowen, James D Uitdehaag, Bernard MJ Cutter, Gary Koch, Marcus W |
author_sort | Strijbis, Eva MM |
collection | PubMed |
description | BACKGROUND: Patient-reported outcome measures (PROMs) are often used in clinical research, but little is known about their performance as longitudinal outcomes. METHODS: We used data from ASCEND, a large SPMS trial (n = 889), to investigate changes on the Short Form Health Survey 36 (SF-36 v2) and the Multiple Sclerosis Impact Scale (MSIS-29) over 2 years of follow-up. RESULTS: PROM scores changed little over the 2 years of follow-up. In contrast to physical disability measures, there was no consistent trend in PROM change: significant worsening occurred about as often as improvement. Using a 6-month confirmation reduced the number of both worsening and improvement events without altering their relative balance. There was no clear difference in worsening events in groups based on population characteristics, nor was there a noticeable effect using different thresholds for clinically significant change. CONCLUSION: We found little consistent change in MSIS-29 and SF-36 over 2 years of follow-up in people with SPMS. Our findings show a disconnect between disability worsening and PROM change in this population. Our findings raise caution about the use of these PROMs as primary outcome measures in SPMS trials and call for a critical reappraisal of the longitudinal use of these measures in SPMS trials. |
format | Online Article Text |
id | pubmed-9315187 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-93151872022-07-27 The MSIS-29 and SF-36 as outcomes in secondary progressive MS trials Strijbis, Eva MM Repovic, Pavle Mostert, Jop Bowen, James D Uitdehaag, Bernard MJ Cutter, Gary Koch, Marcus W Mult Scler Original Research Papers BACKGROUND: Patient-reported outcome measures (PROMs) are often used in clinical research, but little is known about their performance as longitudinal outcomes. METHODS: We used data from ASCEND, a large SPMS trial (n = 889), to investigate changes on the Short Form Health Survey 36 (SF-36 v2) and the Multiple Sclerosis Impact Scale (MSIS-29) over 2 years of follow-up. RESULTS: PROM scores changed little over the 2 years of follow-up. In contrast to physical disability measures, there was no consistent trend in PROM change: significant worsening occurred about as often as improvement. Using a 6-month confirmation reduced the number of both worsening and improvement events without altering their relative balance. There was no clear difference in worsening events in groups based on population characteristics, nor was there a noticeable effect using different thresholds for clinically significant change. CONCLUSION: We found little consistent change in MSIS-29 and SF-36 over 2 years of follow-up in people with SPMS. Our findings show a disconnect between disability worsening and PROM change in this population. Our findings raise caution about the use of these PROMs as primary outcome measures in SPMS trials and call for a critical reappraisal of the longitudinal use of these measures in SPMS trials. SAGE Publications 2022-07-25 2022-09 /pmc/articles/PMC9315187/ /pubmed/35876467 http://dx.doi.org/10.1177/13524585221105465 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any 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 Papers Strijbis, Eva MM Repovic, Pavle Mostert, Jop Bowen, James D Uitdehaag, Bernard MJ Cutter, Gary Koch, Marcus W The MSIS-29 and SF-36 as outcomes in secondary progressive MS trials |
title | The MSIS-29 and SF-36 as outcomes in secondary progressive MS
trials |
title_full | The MSIS-29 and SF-36 as outcomes in secondary progressive MS
trials |
title_fullStr | The MSIS-29 and SF-36 as outcomes in secondary progressive MS
trials |
title_full_unstemmed | The MSIS-29 and SF-36 as outcomes in secondary progressive MS
trials |
title_short | The MSIS-29 and SF-36 as outcomes in secondary progressive MS
trials |
title_sort | msis-29 and sf-36 as outcomes in secondary progressive ms
trials |
topic | Original Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315187/ https://www.ncbi.nlm.nih.gov/pubmed/35876467 http://dx.doi.org/10.1177/13524585221105465 |
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