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Systematic review of prediction models in relapsing remitting multiple sclerosis

The natural history of relapsing remitting multiple sclerosis (RRMS) is variable and prediction of individual prognosis challenging. The inability to reliably predict prognosis at diagnosis has important implications for informed decision making especially in relation to disease modifying therapies....

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Autores principales: Brown, Fraser S., Glasmacher, Stella A., Kearns, Patrick K. A., MacDougall, Niall, Hunt, David, Connick, Peter, Chandran, Siddharthan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250448/
https://www.ncbi.nlm.nih.gov/pubmed/32453803
http://dx.doi.org/10.1371/journal.pone.0233575
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author Brown, Fraser S.
Glasmacher, Stella A.
Kearns, Patrick K. A.
MacDougall, Niall
Hunt, David
Connick, Peter
Chandran, Siddharthan
author_facet Brown, Fraser S.
Glasmacher, Stella A.
Kearns, Patrick K. A.
MacDougall, Niall
Hunt, David
Connick, Peter
Chandran, Siddharthan
author_sort Brown, Fraser S.
collection PubMed
description The natural history of relapsing remitting multiple sclerosis (RRMS) is variable and prediction of individual prognosis challenging. The inability to reliably predict prognosis at diagnosis has important implications for informed decision making especially in relation to disease modifying therapies. We conducted a systematic review in order to collate, describe and assess the methodological quality of published prediction models in RRMS. We searched Medline, Embase and Web of Science. Two reviewers independently screened abstracts and full text for eligibility and assessed risk of bias. Studies reporting development or validation of prediction models for RRMS in adults were included. Data collection was guided by the checklist for critical appraisal and data extraction for systematic reviews (CHARMS) and applicability and methodological quality assessment by the prediction model risk of bias assessment tool (PROBAST). 30 studies were included in the review. Applicability was assessed as high risk of concern in 27 studies. Risk of bias was assessed as high for all studies. The single most frequently included predictor was baseline EDSS (n = 11). T2 Lesion volume or number and brain atrophy were each retained in seven studies. Five studies included external validation and none included impact analysis. Although a number of prediction models for RRMS have been reported, most are at high risk of bias and lack external validation and impact analysis, restricting their application to routine clinical practice.
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spelling pubmed-72504482020-06-08 Systematic review of prediction models in relapsing remitting multiple sclerosis Brown, Fraser S. Glasmacher, Stella A. Kearns, Patrick K. A. MacDougall, Niall Hunt, David Connick, Peter Chandran, Siddharthan PLoS One Research Article The natural history of relapsing remitting multiple sclerosis (RRMS) is variable and prediction of individual prognosis challenging. The inability to reliably predict prognosis at diagnosis has important implications for informed decision making especially in relation to disease modifying therapies. We conducted a systematic review in order to collate, describe and assess the methodological quality of published prediction models in RRMS. We searched Medline, Embase and Web of Science. Two reviewers independently screened abstracts and full text for eligibility and assessed risk of bias. Studies reporting development or validation of prediction models for RRMS in adults were included. Data collection was guided by the checklist for critical appraisal and data extraction for systematic reviews (CHARMS) and applicability and methodological quality assessment by the prediction model risk of bias assessment tool (PROBAST). 30 studies were included in the review. Applicability was assessed as high risk of concern in 27 studies. Risk of bias was assessed as high for all studies. The single most frequently included predictor was baseline EDSS (n = 11). T2 Lesion volume or number and brain atrophy were each retained in seven studies. Five studies included external validation and none included impact analysis. Although a number of prediction models for RRMS have been reported, most are at high risk of bias and lack external validation and impact analysis, restricting their application to routine clinical practice. Public Library of Science 2020-05-26 /pmc/articles/PMC7250448/ /pubmed/32453803 http://dx.doi.org/10.1371/journal.pone.0233575 Text en © 2020 Brown et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Brown, Fraser S.
Glasmacher, Stella A.
Kearns, Patrick K. A.
MacDougall, Niall
Hunt, David
Connick, Peter
Chandran, Siddharthan
Systematic review of prediction models in relapsing remitting multiple sclerosis
title Systematic review of prediction models in relapsing remitting multiple sclerosis
title_full Systematic review of prediction models in relapsing remitting multiple sclerosis
title_fullStr Systematic review of prediction models in relapsing remitting multiple sclerosis
title_full_unstemmed Systematic review of prediction models in relapsing remitting multiple sclerosis
title_short Systematic review of prediction models in relapsing remitting multiple sclerosis
title_sort systematic review of prediction models in relapsing remitting multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250448/
https://www.ncbi.nlm.nih.gov/pubmed/32453803
http://dx.doi.org/10.1371/journal.pone.0233575
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