Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet): Case Definition in Surveillance for Childhood-Onset Duchenne/Becker Muscular Dystrophy

Author:

Mathews Katherine D.1,Cunniff Chris2,Kantamneni Jiji R.3,Ciafaloni Emma4,Miller Timothy5,Matthews Dennis6,Cwik Valerie7,Druschel Charlotte8,Miller Lisa9,Meaney F. John2,Sladky John10,Romitti Paul A.11

Affiliation:

1. Departments of Pediatrics and Neurology, Roy and Lucille Carver College of Medicine, University of Iowa, Iowa City, Iowa,

2. Department of Pediatrics and Steele Research Center, University of Arizona College of Medicine, Tucson, Arizona

3. Center for Health Effects of Environmental Contamination, University of Iowa, Iowa City, Iowa

4. Department of Neurology, University of Rochester College of Medicine and Dentistry, Rochester, New York

5. Department of Pediatrics and Steele Research Center, University of Arizona College of Medicine, Tucson, Arizona, Department of Neurology, University of Arizona College of Medicine, Tucson, Arizona

6. Department of Physical Medicine and Rehabilitation, University of Colorado College of Medicine, Denver, Colorado

7. Muscular Dystrophy Association, Tucson, Arizona

8. New York Department of Health, Troy, New York

9. Colorado Department of Public Health and Environment, Denver, Colorado

10. Departments of Pediatrics and Neurology, Emory University, Atlanta, Georgia

11. College of Public Health, University of Iowa, Iowa City, Iowa

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.

Publisher

SAGE Publications

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

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