Abstract
The use of corticosteroids for treatment of Duchenne and Becker muscular dystrophy in clinical practice from 1991 through 2005 was reviewed in a large population-based cohort (MD STARnet) of boys in 4 regional sites and 6 clinics of the United States. Corticosteroid use increased from 20% (11 of 56 individuals) in 1991 to 44% (93 of 218 individuals) in 2005. Average use varied by site and ranged from 15% to 49%. The median age of corticosteroid initiation was 6.9 years (range, 3.7-17.4 years). Dosage and growth information was available for 102 participants and showed a median dose as 0.729 mg/kg for prednisone and 0.831 mg/kg for deflazacort. T. The most common reasons that corticosteroids were discontinued included weight gain, behavioral side effects, and loss of ambulation, resulting in full-time wheelchair use. Substantial variations in clinical practice were identified among study sites. © The Author(s) 2010.
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Matthews, D. J., James, K. A., Miller, L. A., Pandya, S., Campbell, K. A., Ciafaloni, E., … Fox, D. J. (2010). Use of corticosteroids in a population-based cohort of boys with duchenne and becker muscular dystrophy. Journal of Child Neurology, 25(11), 1319–1324. https://doi.org/10.1177/0883073810362762
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