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The burden, epidemiology, costs and treatment for Duchenne muscular dystrophy: an evidence review.

Steve RyderR M LeadleyN ArmstrongM WestwoodS de KockT ButtM JainJ Kleijnen
Published in: Orphanet journal of rare diseases (2017)
This is the first systematic review of treatment, progression, severity and quality of life in DMD. It also provides the most recent description of the burden, epidemiology, illness costs and treatment patterns in DMD. There are evidence gaps, particularly in prevalence and mortality. People with DMD seem to be living longer, possibly due to corticosteroid use, cardiac medical management and ventilation. Future research should incorporate registry data to improve comparability across time and between countries and to investigate the quality of life impact as the condition progresses.
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