TY - JOUR
T1 - Muscular dystrophy surveillance tracking and research network (MD STARnet)
T2 - Case definition in surveillance for childhood-onset Duchenne/Becker muscular dystrophy
AU - Mathews, Katherine D.
AU - Cunniff, Chris
AU - Kantamneni, Jiji R.
AU - Ciafaloni, Emma
AU - Miller, Timothy
AU - Matthews, Dennis
AU - Cwik, Valerie
AU - Druschel, Charlotte
AU - Miller, Lisa
AU - Meaney, F. John
AU - Sladky, John
AU - Romitti, Paul A.
PY - 2010/9
Y1 - 2010/9
N2 - 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.
AB - 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.
KW - Becker muscular dystrophy
KW - Duchenne muscular dystrophy
KW - diagnostic testing
KW - dystrophin
UR - http://www.scopus.com/inward/record.url?scp=77956325548&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77956325548&partnerID=8YFLogxK
U2 - 10.1177/0883073810371001
DO - 10.1177/0883073810371001
M3 - Article
C2 - 20817884
AN - SCOPUS:77956325548
SN - 0883-0738
VL - 25
SP - 1098
EP - 1102
JO - Journal of Child Neurology
JF - Journal of Child Neurology
IS - 9
ER -