| Literature DB >> 32925088 |
V Hodgkinson1, J Lounsberry1, S M'Dahoma1, A Russell1, T Benstead2, B Brais3, C Campbell4, W Johnston5, H Lochmüller6,7, A McCormick6, C T Nguyen8, E O'Ferrall3,9, M Oskoui10, H Briemberg11,12, P Bourque13, S Botez14, N Cashman11,12, K Chapman12, N Chrestian15, M Crone16, P Dobrowolski4, S Dojeiji13, J J Dowling17, N Dupré18, A Genge9, H Gonorazky17, I Grant2, S Hasal16, A Izenberg19, S Kalra4, H Katzberg20, C Krieger11,12, E Leung21, G Linassi22, A Mackenzie5, J K Mah1,23, A Marrero24, R Massie8,9, G Matte14, L McAdam25, H McMillan5, M Melanson26, M M Mezei12, C O'Connell27,28, G Pfeffer1, C Phan4, S Plamondon1, C Poulin10, X Rodrigue18, K Schellenberg22, K Selby29, J Sheriko30, C Shoesmith31, G Smith32, M Taillon27,28, S Taylor2, S Venance31, J Warman-Chardon7, S Worley27,28, L Zinman19, L Korngut1.
Abstract
We report the recruitment activities and outcomes of a multi-disease neuromuscular patient registry in Canada. The Canadian Neuromuscular Disease Registry (CNDR) registers individuals across Canada with a confirmed diagnosis of a neuromuscular disease. Diagnosis and contact information are collected across all diseases and detailed prospective data is collected for 5 specific diseases: Amyotrophic Lateral Sclerosis (ALS), Duchenne Muscular Dystrophy (DMD), Myotonic Dystrophy (DM), Limb Girdle Muscular Dystrophy (LGMD), and Spinal Muscular Atrophy (SMA). Since 2010, the CNDR has registered 4306 patients (1154 pediatric and 3148 adult) with 91 different neuromuscular diagnoses and has facilitated 125 projects (73 academic, 3 not-for-profit, 3 government, and 46 commercial) using registry data. In conclusion, the CNDR is an effective and productive pan-neuromuscular registry that has successfully facilitated a substantial number of studies over the past 10 years.Entities:
Keywords: Registry; natural history; real-world evidence
Year: 2020 PMID： 32925088 DOI： 10.3233/JND-200538
Source DB: PubMed Journal: J Neuromuscul Dis