Literature DB >> 27008581

Supported Standing in Boys With Duchenne Muscular Dystrophy.

Elise L Townsend1, Christine Bibeau, Tara M Holmes.   

Abstract

PURPOSE: To evaluate the safety, tolerability, and efficacy of supported standing in a small sample of boys with Duchenne muscular dystrophy (DMD).
METHODS: Four 12- to 15-year-old boys with DMD engaged in a home-based supported standing program for 6 to 12 months. A single-subject design was employed to examine muscle length. Bone mineral density was assessed at 4-month intervals using dual-energy x-ray absorptiometry.
RESULTS: Upright, sustained supported standing was tolerated in 3 of the 4 boys. Mean weekly stand times ranged from 1.3 to 3.3 hours. Improved hip or knee flexor muscle length was seen in 3 of the 4 boys. No boys showed improved plantar flexor muscle length or increased lumbar bone mineral density.
CONCLUSIONS: Findings offer preliminary empirical evidence addressing the safety, tolerability, and efficacy of standing in boys with DMD. Additional research with an emphasis on better program adherence is indicated.

Entities:  

Mesh:

Year:  2016        PMID: 27008581      PMCID: PMC5603175          DOI: 10.1097/PEP.0000000000000251

Source DB:  PubMed          Journal:  Pediatr Phys Ther        ISSN: 0898-5669            Impact factor:   3.049


  34 in total

1.  Bone health in Duchenne muscular dystrophy: a workshop report from the meeting in Cincinnati, Ohio, July 8, 2004.

Authors:  W D Biggar; L K Bachrach; R C Henderson; H Kalkwarf; H Plotkin; B L Wong
Journal:  Neuromuscul Disord       Date:  2005-01       Impact factor: 4.296

Review 2.  Measurement in Duchenne muscular dystrophy: considerations in the development of a neuromuscular assessment tool.

Authors:  Elaine Scott; Susan J Mawson
Journal:  Dev Med Child Neurol       Date:  2006-06       Impact factor: 5.449

3.  Dual energy X-ray absorptiometry interpretation and reporting in children and adolescents: the 2007 ISCD Pediatric Official Positions.

Authors:  Catherine M Gordon; Laura K Bachrach; Thomas O Carpenter; Nicola Crabtree; Ghada El-Hajj Fuleihan; Stepan Kutilek; Roman S Lorenc; Laura L Tosi; Katherine A Ward; Leanne M Ward; Heidi J Kalkwarf
Journal:  J Clin Densitom       Date:  2008 Jan-Mar       Impact factor: 2.617

Review 4.  Limb contractures in progressive neuromuscular disease and the role of stretching, orthotics, and surgery.

Authors:  C M McDonald
Journal:  Phys Med Rehabil Clin N Am       Date:  1998-02       Impact factor: 1.784

5.  Bone mineral density and fractures in boys with Duchenne muscular dystrophy.

Authors:  C M Larson; R C Henderson
Journal:  J Pediatr Orthop       Date:  2000 Jan-Feb       Impact factor: 2.324

Review 6.  Diagnosis and management of Duchenne muscular dystrophy, part 2: implementation of multidisciplinary care.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

7.  Prednisolone therapy in Duchenne muscular dystrophy prolongs ambulation and prevents scoliosis.

Authors:  O Yilmaz; A Karaduman; H Topaloğlu
Journal:  Eur J Neurol       Date:  2004-08       Impact factor: 6.089

8.  Orthopedic outcomes of long-term daily corticosteroid treatment in Duchenne muscular dystrophy.

Authors:  W M King; R Ruttencutter; H N Nagaraja; V Matkovic; J Landoll; C Hoyle; J R Mendell; J T Kissel
Journal:  Neurology       Date:  2007-05-08       Impact factor: 9.910

9.  Participation and quality of life in children with Duchenne muscular dystrophy using the International Classification of Functioning, Disability, and Health.

Authors:  Roxanna M Bendixen; Claudia Senesac; Donovan J Lott; Krista Vandenborne
Journal:  Health Qual Life Outcomes       Date:  2012-05-22       Impact factor: 3.186

Review 10.  The role of corticosteroids in muscular dystrophy: a critical appraisal.

Authors:  Corrado Angelini
Journal:  Muscle Nerve       Date:  2007-10       Impact factor: 3.217

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  3 in total

Review 1.  Assisted standing for Duchenne muscular dystrophy.

Authors:  Katy Pedlow; Suzanne McDonough; Sheila Lennon; Claire Kerr; Ian Bradbury
Journal:  Cochrane Database Syst Rev       Date:  2019-10-13

2.  Facilitators and Barriers to Wearing Hand Orthoses by Adults with Duchenne Muscular Dystrophy: A Mixed Methods Study Design.

Authors:  S L S Houwen-van Opstal; Y M E M van den Elzen; M Jansen; M A A P Willemsen; E H C Cup; I J M De Groot
Journal:  J Neuromuscul Dis       Date:  2020

3.  Policy analysis on power standing systems.

Authors:  Cara E Masselink; Nicole LaBerge; Ashley Detterbeck
Journal:  Prev Med Rep       Date:  2021-10-12
  3 in total

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