Your browser doesn't support javascript.
loading
Eligibility and implementation of disease-modifying therapy for primary progressive multiple sclerosis in a UK cohort.
Tallantyre, Emma C; Castle, Daniel; Karamura, Paul; Brice, Thomas A W; Joseph, Fady; Harding, Katharine E; Robertson, Neil P.
Afiliação
  • Tallantyre EC; Department of Psychological Medicine and Clinical Neurosciences, Cardiff University, UK; Helen Durham Neuro-inflammatory Centre, Cardiff and Vale University Health Board, UK. Electronic address: TallantyreEC@cardiff.ac.uk.
  • Castle D; Department of Psychological Medicine and Clinical Neurosciences, Cardiff University, UK.
  • Karamura P; Department of Psychological Medicine and Clinical Neurosciences, Cardiff University, UK.
  • Brice TAW; Department of Psychological Medicine and Clinical Neurosciences, Cardiff University, UK.
  • Joseph F; Royal Gwent Hopsital, Aneurin Bevan Health Board, Newport, UK.
  • Harding KE; Royal Gwent Hopsital, Aneurin Bevan Health Board, Newport, UK.
  • Robertson NP; Department of Psychological Medicine and Clinical Neurosciences, Cardiff University, UK; Helen Durham Neuro-inflammatory Centre, Cardiff and Vale University Health Board, UK.
Mult Scler Relat Disord ; 42: 102056, 2020 Jul.
Article em En | MEDLINE | ID: mdl-32353753
BACKGROUND: As disease-modifying therapies become approved for primary progressive multiple sclerosis (PPMS), services must be aligned in readiness. METHODS: In this paper we use population and clinic-based data to estimate eligibility rates for ocrelizumab, and the extent of additional service requirements necessary to ensure its widespread introduction in PPMS. RESULTS: Overall population estimates for the incidence and prevalence of people with PPMS who are eligible for ocrelizumab are 1.6 and 4.2 per 100,000 respectively. The majority (87%) of incident cases of PPMS satisfied clinical eligibility criteria for ocrelizumab but lacked radiological evidence of disease activity due to a historical tendency not to routinely monitor using MRI in this group. The majority of prevalent patients did not satisfy clinical eligibility criteria for ocrelizumab, mainly because of advanced disease duration or disability. CONCLUSIONS: These findings illustrate the fact that there has been a tendency for people with PPMS not to receive routine clinical and radiological monitoring. Additional planning or resources will be required to facilitate contemporary disease re-evaluation and surveillance at a population level.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema de Registros / Pessoas com Deficiência / Esclerose Múltipla Crônica Progressiva / Definição da Elegibilidade / Anticorpos Monoclonais Humanizados / Utilização de Instalações e Serviços / Fatores Imunológicos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Mult Scler Relat Disord Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema de Registros / Pessoas com Deficiência / Esclerose Múltipla Crônica Progressiva / Definição da Elegibilidade / Anticorpos Monoclonais Humanizados / Utilização de Instalações e Serviços / Fatores Imunológicos Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa Idioma: En Revista: Mult Scler Relat Disord Ano de publicação: 2020 Tipo de documento: Article