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Muscular dystrophy surveillance tracking and research network (MD STARnet): Case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy

  • Katherine D. Mathews
  • , Chris Cunniff
  • , Jiji R. Kantamneni
  • , Emma Ciafaloni
  • , Timothy Miller
  • , Dennis Matthews
  • , Valerie Cwik
  • , Charlotte Druschel
  • , Lisa Miller
  • , F. John Meaney
  • , John Sladky
  • , Paul A. Romitti

Research output: Contribution to journalArticlepeer-review

Abstract

The Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet) is a multisite collaboration to determine the prevalence of childhood-onset Duchenne/Becker muscular dystrophy and to characterize health care and health outcomes in this population. MD STARnet uses medical record abstraction to identify patients with Duchenne/Becker muscular dystrophy born January 1, 1982 or later who resided in 1 of the participating sites. Critical diagnostic elements of each abstracted record are reviewed independently by >4 clinicians and assigned to 1 of 6 case definition categories (definite, probable, possible, asymptomatic, female, not Duchenne/Becker muscular dystrophy) by consensus. As of November 2009, 815 potential cases were reviewed. Of the cases included in analysis, 674 (82%) were either "definite" or "probable" Duchenne/Becker muscular dystrophy. These data reflect a change in diagnostic testing, as case assignment based on genetic testing increased from 67% in the oldest cohort (born 1982-1987) to 94% in the cohort born 2004 to 2009.

Original languageEnglish (US)
Pages (from-to)1098-1102
Number of pages5
JournalJournal of Child Neurology
Volume25
Issue number9
DOIs
StatePublished - Sep 2010

Keywords

  • Becker muscular dystrophy
  • Duchenne muscular dystrophy
  • diagnostic testing
  • dystrophin

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Clinical Neurology

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