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UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model
OBJECTIVES: In 2002, the UK's National Institute for Health and Care Excellence concluded that the multiple sclerosis (MS) disease modifying therapies; interferon-β and glatiramer acetate, were not cost effective over the short term but recognised that reducing disability over the longer term m...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902459/ https://www.ncbi.nlm.nih.gov/pubmed/24441054 http://dx.doi.org/10.1136/bmjopen-2013-004073 |
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author | Palace, Jacqueline Bregenzer, Thomas Tremlett, Helen Oger, Joel Zhu, Fheng Boggild, Mike Duddy, Martin Dobson, Charles |
author_facet | Palace, Jacqueline Bregenzer, Thomas Tremlett, Helen Oger, Joel Zhu, Fheng Boggild, Mike Duddy, Martin Dobson, Charles |
author_sort | Palace, Jacqueline |
collection | PubMed |
description | OBJECTIVES: In 2002, the UK's National Institute for Health and Care Excellence concluded that the multiple sclerosis (MS) disease modifying therapies; interferon-β and glatiramer acetate, were not cost effective over the short term but recognised that reducing disability over the longer term might dramatically improve the cost effectiveness. The UK Risk-sharing Scheme (RSS) was established to ensure cost-effective provision by prospectively collecting disability-related data from UK-treated patients with MS and comparing findings to a natural history (untreated) cohort. However, deficiencies were found in the originally selected untreated cohort and the resulting analytical approach. This study aims to identify a more suitable natural history cohort and to develop a robust analytical approach using the new cohort. DESIGN: The Scientific Advisory Group, recommended the British Columbia Multiple Sclerosis (BCMS) database, Canada, as providing a more suitable natural history comparator cohort. Transition probabilities were derived and different Markov models (discrete and continuous) with and without baseline covariates were applied. SETTING: MS clinics in Canada and the UK. PARTICIPANTS: From the BCMS database, 898 ‘untreated’ patients with MS considered eligible for drug treatment based on the UK's Association of British Neurologists criteria. OUTCOME MEASURE: The predicted Expanded Disability Status Scale (EDSS) score was collected and assessed for goodness of fit when compared with actual outcome. RESULTS: The BCMS untreated cohort contributed 7335 EDSS scores over a median 6.4 years (6357 EDSS ‘transitions’ recorded at consecutive visits) during the period 1980–1995. A continuous Markov model with ‘onset age’ as a binary covariate was deemed the most suitable model for future RSS analysis. CONCLUSIONS: A new untreated MS cohort from British Columbia has been selected and will be modelled using a continuous Markov model with onset age as a baseline covariate. This approach will now be applied to the treated UK RSS MS cohort for future price adjustment calculations. |
format | Online Article Text |
id | pubmed-3902459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-39024592014-01-27 UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model Palace, Jacqueline Bregenzer, Thomas Tremlett, Helen Oger, Joel Zhu, Fheng Boggild, Mike Duddy, Martin Dobson, Charles BMJ Open Neurology OBJECTIVES: In 2002, the UK's National Institute for Health and Care Excellence concluded that the multiple sclerosis (MS) disease modifying therapies; interferon-β and glatiramer acetate, were not cost effective over the short term but recognised that reducing disability over the longer term might dramatically improve the cost effectiveness. The UK Risk-sharing Scheme (RSS) was established to ensure cost-effective provision by prospectively collecting disability-related data from UK-treated patients with MS and comparing findings to a natural history (untreated) cohort. However, deficiencies were found in the originally selected untreated cohort and the resulting analytical approach. This study aims to identify a more suitable natural history cohort and to develop a robust analytical approach using the new cohort. DESIGN: The Scientific Advisory Group, recommended the British Columbia Multiple Sclerosis (BCMS) database, Canada, as providing a more suitable natural history comparator cohort. Transition probabilities were derived and different Markov models (discrete and continuous) with and without baseline covariates were applied. SETTING: MS clinics in Canada and the UK. PARTICIPANTS: From the BCMS database, 898 ‘untreated’ patients with MS considered eligible for drug treatment based on the UK's Association of British Neurologists criteria. OUTCOME MEASURE: The predicted Expanded Disability Status Scale (EDSS) score was collected and assessed for goodness of fit when compared with actual outcome. RESULTS: The BCMS untreated cohort contributed 7335 EDSS scores over a median 6.4 years (6357 EDSS ‘transitions’ recorded at consecutive visits) during the period 1980–1995. A continuous Markov model with ‘onset age’ as a binary covariate was deemed the most suitable model for future RSS analysis. CONCLUSIONS: A new untreated MS cohort from British Columbia has been selected and will be modelled using a continuous Markov model with onset age as a baseline covariate. This approach will now be applied to the treated UK RSS MS cohort for future price adjustment calculations. BMJ Publishing Group 2014-01-17 /pmc/articles/PMC3902459/ /pubmed/24441054 http://dx.doi.org/10.1136/bmjopen-2013-004073 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 3.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Neurology Palace, Jacqueline Bregenzer, Thomas Tremlett, Helen Oger, Joel Zhu, Fheng Boggild, Mike Duddy, Martin Dobson, Charles UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model |
title | UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model |
title_full | UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model |
title_fullStr | UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model |
title_full_unstemmed | UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model |
title_short | UK multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved Markov model |
title_sort | uk multiple sclerosis risk-sharing scheme: a new natural history dataset and an improved markov model |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3902459/ https://www.ncbi.nlm.nih.gov/pubmed/24441054 http://dx.doi.org/10.1136/bmjopen-2013-004073 |
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