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An overview of the Cure SMA membership database: Highlights of key demographic and clinical characteristics of SMA members.
Belter, Lisa; Cook, Suzanne F; Crawford, Thomas O; Jarecki, Jill; Jones, Cynthia C; Kissel, John T; Schroth, Mary; Hobby, Kenneth.
Afiliação
  • Belter L; Cure SMA, Elk Grove Village, IL, USA.
  • Cook SF; Epidemiology Associates LLC, Chapel Hill, NC, USA.
  • Crawford TO; Johns Hopkins Hospital, Baltimore, MD, USA.
  • Jarecki J; Cure SMA, Elk Grove Village, IL, USA.
  • Jones CC; Biogen, Cambridge, MA, USA.
  • Kissel JT; The Ohio State University, Columbus, OH, USA.
  • Schroth M; Cure SMA, Elk Grove Village, IL, USA.
  • Hobby K; University of Wisconsin, Madison, WI, USA.
J Neuromuscul Dis ; 5(2): 167-176, 2018.
Article em En | MEDLINE | ID: mdl-29614694
BACKGROUND: The Cure SMA database is one of the largest patient reported databases for people affected with SMA. OBJECTIVE: The purpose of this study was to examine a subset of affected SMA persons with types I, II, and III from a patient reported database. METHODS: Individuals with SMA were selected from the database using a date of first contact to Cure SMA between 2010 and 2016. Data analyzed included age at diagnosis, number of weeks from SMA diagnosis to contacting Cure SMA, and geographic distribution of individuals. RESULTS: A total of 1,966 individuals with SMA were included in the analysis. Of these individuals, 51.9% had type I, 32.3% had type II, and 15.8% had type III. The average age of diagnosis for type I patients was 5.2 months, 22.1 months for type II, and 97.8 months for type III. From published incidence, about 59.0% of affected individuals in the US are registered in the Cure SMA database. CONCLUSIONS: The Cure SMA database is a unique and robust source of patient reported data that informs on the burden of illness and supports the development of new therapeutic modalities.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofias Musculares Espinais da Infância / Sistema de Registros Tipo de estudo: Incidence_studies / Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: J Neuromuscul Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Atrofias Musculares Espinais da Infância / Sistema de Registros Tipo de estudo: Incidence_studies / Prognostic_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged País/Região como assunto: America do norte Idioma: En Revista: J Neuromuscul Dis Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos