Discontinuing disease-modifying therapy in progressive multiple sclerosis: can we stop what we have started?
Authors
Lonergan, RoisinKinsella, Katie
Duggan, Marguerite
Jordan, Sinead
Hutchinson, Michael
Tubridy, Niall
Affiliation
St Vincent's University Hospital, Neurology, Dublin, Republic of Ireland., roisin.lonergan@st-vincents.ieIssue Date
2012-02-01T10:31:50ZMeSH
AdultCost Savings
Cost-Benefit Analysis
Disability Evaluation
Drug Administration Schedule
Drug Costs
Guideline Adherence
Humans
Immunosuppressive Agents/*administration & dosage/economics
Ireland/epidemiology
Medical Futility
Middle Aged
Multiple Sclerosis, Chronic Progressive/diagnosis/*drug
therapy/economics/epidemiology
*Neurology/economics
*Physician's Practice Patterns/economics
Practice Guidelines as Topic
Questionnaires
Rural Health Services
Severity of Illness Index
Treatment Failure
Urban Health Services
Metadata
Show full item recordCitation
Mult Scler. 2009 Dec;15(12):1528-31. Epub 2009 Dec 7.Journal
Multiple sclerosis (Houndmills, Basingstoke, England)DOI
10.1177/1352458509351730PubMed ID
19995848Abstract
Disease-modifying therapy is ineffective in disabled patients (Expanded Disability Status Scale [EDSS] > 6.5) with secondary progressive multiple sclerosis (MS) without relapses, or in primary progressive MS. Many patients with secondary progressive MS who initially had relapsing MS continue to use disease-modifying therapies. The enormous associated costs are a burden to health services. Regular assessment is recommended to guide discontinuation of disease-modifying therapies when no longer beneficial, but this is unavailable to many patients, particularly in rural areas. The objectives of this study are as follows: 1. To observe use of disease-modifying therapies in patients with progressive multiple sclerosis and EDSS > 6.5. 2. To examine approaches used by a group of international MS experts to stopping-disease modifying therapies in patients with secondary progressive MS without relapses. During an epidemiological study in three regions of Ireland (southeast Dublin city, and Wexford and Donegal Counties), we recorded details of disease-modifying therapies in patients with progressive MS and EDSS > 6.5. An e-questionnaire was sent to 26 neurologists with expert knowledge of MS, asking them to share their approach to stopping disease-modifying therapies in patients with secondary progressive MS. Three hundred and thirty-six patients were studied: 88 from southeast Dublin, 99 from Wexford and 149 from Donegal. Forty-four had EDSS > 6.5: 12 were still using disease-modifying therapies. Of the surveyed neurologists, 15 made efforts to stop disease-modifying therapies in progressive multiple sclerosis, but most did not insist. A significant proportion (12 of 44 patients with progressive MS and EDSS > 6.5) was considered to be receiving therapy without benefit. Eleven of the 12 were from rural counties, reflecting poorer access to neurology services. The costs of disease-modifying therapies in this group (>170,000 euro yearly) could be re-directed towards development of neurology services to optimize their management.Language
engISSN
1477-0970 (Electronic)1352-4585 (Linking)
ae974a485f413a2113503eed53cd6c53
10.1177/1352458509351730
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