Your browser doesn't support javascript.
loading
Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network.
LeBlanc, Kimberly; Kelley, Emily G; Nagy, Anna; Bater, Jorick; Berro, Tala; McGuinness, Molly A; Studwell, Courtney; Might, Matthew.
Afiliação
  • LeBlanc K; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. kimberly_leblanc@hms.harvard.edu.
  • Kelley EG; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
  • Nagy A; Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
  • Bater J; Department of Nutrition, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
  • Berro T; Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
  • McGuinness MA; Bass Center for Childhood Cancer and Blood Diseases, Stanford Children's Health, Palo Alto, CA, USA.
  • Studwell C; Department of Pathology, Brigham and Women's Hospital, Boston, MA, USA.
  • Might M; Hugh Kaul Precision Medicine Institute, University of Alabama at Birmingham, Birmingham, AL, USA.
Orphanet J Rare Dis ; 16(1): 210, 2021 05 10.
Article em En | MEDLINE | ID: mdl-33971915
BACKGROUND: Although clinician, researcher, and patient resources for matchmaking exist, finding similar patients remains an obstacle for rare disease diagnosis. The goals of this study were to develop and test the effectiveness of an Internet case-finding strategy and identify factors associated with increased matching within a rare disease population. METHODS: Public web pages were created for consented participants. Matches made, time to each inquiry and match, and outcomes were recorded and analyzed using descriptive statistics. A Poisson regression model was run to identify characteristics associated with matches. RESULTS: 385 participants were referred to the project and 158 had pages posted. 579 inquiries were received; 89.0% were from the general public and 24.7% resulted in a match. 81.6% of pages received at least one inquiry and 15.0% had at least one patient match. Primary symptom category of neurology, diagnosis, gene page, and photo were associated with increased matches (p ≤ 0.05). CONCLUSIONS: This Internet case-finding strategy was of interest to patients, families, and clinicians, and similar patients were identified using this approach. Extending matchmaking efforts to the general public resulted in matches and suggests including this population in matchmaking activities can improve identification of similar patients.
Assuntos
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Doenças Raras / Doenças não Diagnosticadas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Doenças Raras / Doenças não Diagnosticadas Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos