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Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

Authors :
Bushby, Katharine
Finkel, Richard
Birnkrant, David J
Case, Laura E
Clemens, Paula R
Cripe, Linda
Kaul, Ajay
Kinnett, Kathi
McDonald, Craig
Pandya, Shree
Poysky, James
Shapiro, Frederic
Tomezsko, Jean
Constantin, Carolyn
DMD Care Considerations Working Group
Source :
Lancet Neurology. Jan2010, Vol. 9 Issue 1, p77-93. 17p.
Publication Year :
2010

Abstract

Summary: Duchenne muscular dystrophy (DMD) is a severe, progressive disease that affects 1 in 3600–6000 live male births. Although guidelines are available for various aspects of DMD, comprehensive clinical care recommendations do not exist. The US Centers for Disease Control and Prevention selected 84 clinicians to develop care recommendations using the RAND Corporation–University of California Los Angeles Appropriateness Method. The DMD Care Considerations Working Group evaluated assessments and interventions used in the management of diagnostics, gastroenterology and nutrition, rehabilitation, and neuromuscular, psychosocial, cardiovascular, respiratory, orthopaedic, and surgical aspects of DMD. These recommendations, presented in two parts, are intended for the wide range of practitioners who care for individuals with DMD. They provide a framework for recognising the multisystem primary manifestations and secondary complications of DMD and for providing coordinated multidisciplinary care. In part 1 of this Review, we describe the methods used to generate the recommendations, and the overall perspective on care, pharmacological treatment, and psychosocial management. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
14744422
Volume :
9
Issue :
1
Database :
Academic Search Index
Journal :
Lancet Neurology
Publication Type :
Academic Journal
Accession number :
47058716
Full Text :
https://doi.org/10.1016/s1474-4422(09)70355-2