Literature DB >> 31606891

Assisted standing for Duchenne muscular dystrophy.

Katy Pedlow1, Suzanne McDonough, Sheila Lennon, Claire Kerr, Ian Bradbury.   

Abstract

BACKGROUND: Duchenne muscular dystrophy (DMD) is the most common X-linked neuromuscular disorder. When boys with DMD reach the second decade of life, they lose their ability to walk and become wheelchair dependent. Standing devices and orthoses are considered to be an essential component in the therapy management of DMD. Clinical opinion and research from other neurological conditions highlight the proposed benefits of standing device use, however, its effect within this population is currently unknown. A review of the evidence for the use of standing devices and orthoses is necessary to inform all stakeholders, including people with DMD, clinicians, decision makers and funders, and to guide future research.
OBJECTIVES: To assess the effects of standing devices and orthoses on musculoskeletal impairments (such as pain, contracture, scoliosis development and bone density) in boys and men with DMD, and secondarily to determine their effect on quality of life, participation in activities, and patient experience (satisfaction). We also considered any adverse events associated with their use. SEARCH
METHODS: We searched the Cochrane Neuromuscular Specialised Register, CENTRAL, MEDLINE, Embase, AMED, PsycINFO, CINAHL Plus, PEDro, and ProQuest Dissertations & Theses Global up to 5 September 2019. We checked references in identified trials, handsearched journal abstracts, and searched trials registries. SELECTION CRITERIA: We planned to include randomised controlled trials (RCTs) and quasi-RCTs of any model of standing device for use in DMD. The control interventions would have been any other comparison group, including no standing device, a different model of standing device, usual care, or an alternative form of assistive weight bearing. DATA COLLECTION AND ANALYSIS: We used standard Cochrane methodological procedures. MAIN
RESULTS: Although we identified 13 potentially relevant studies, none met the inclusion criteria for this review. AUTHORS'
CONCLUSIONS: Since there were no RCTs or quasi-RCTs available to evaluate the effectiveness of standing devices in people with DMD, studies are needed to investigate the effectiveness of standing devices in this population.

Entities:  

Year:  2019        PMID: 31606891      PMCID: PMC6790222          DOI: 10.1002/14651858.CD011550.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  36 in total

1.  Comparison of Cobb angle measurement of scoliosis radiographs with preselected end vertebrae: traditional versus digital acquisition.

Authors:  Brian P D Wills; Joshua D Auerbach; Xiaowei Zhu; Michelle S Caird; B David Horn; John M Flynn; Denis S Drummond; John P Dormans; Malcolm L Ecker
Journal:  Spine (Phila Pa 1976)       Date:  2007-01-01       Impact factor: 3.468

Review 2.  Effectiveness of static weight-bearing exercises in children with cerebral palsy.

Authors:  Tamis Wai-mun Pin
Journal:  Pediatr Phys Ther       Date:  2007       Impact factor: 3.049

3.  Predictive factors for the development of scoliosis in Duchenne muscular dystrophy.

Authors:  M Kinali; M Main; J Eliahoo; S Messina; R K Knight; J Lehovsky; G Edge; E Mercuri; A Y Manzur; F Muntoni
Journal:  Eur J Paediatr Neurol       Date:  2007-01-25       Impact factor: 3.140

4.  Changes in spirometry over time as a prognostic marker in patients with Duchenne muscular dystrophy.

Authors:  M F Phillips; R C Quinlivan; R H Edwards; P M Calverley
Journal:  Am J Respir Crit Care Med       Date:  2001-12-15       Impact factor: 21.405

5.  Prevention of rapidly progressive scoliosis in Duchenne muscular dystrophy by prolongation of walking with orthoses.

Authors:  E B Rodillo; E Fernandez-Bermejo; J Z Heckmatt; V Dubowitz
Journal:  J Child Neurol       Date:  1988-10       Impact factor: 1.987

6.  Use of knee-ankle-foot orthoses for transfers of nonambulatory boys with Duchenne muscular dystrophy.

Authors:  A k Hunt
Journal:  Phys Ther       Date:  1981-01

Review 7.  Diagnosis and management of Duchenne muscular dystrophy, part 2: respiratory, cardiac, bone health, and orthopaedic management.

Authors:  David J Birnkrant; Katharine Bushby; Carla M Bann; Benjamin A Alman; Susan D Apkon; Angela Blackwell; Laura E Case; Linda Cripe; Stasia Hadjiyannakis; Aaron K Olson; Daniel W Sheehan; Julie Bolen; David R Weber; Leanne M Ward
Journal:  Lancet Neurol       Date:  2018-02-03       Impact factor: 44.182

8.  Factors affecting prescription and implementation of standing-frame programs by school-based physical therapists for children with impaired mobility.

Authors:  Kristin Taylor
Journal:  Pediatr Phys Ther       Date:  2009       Impact factor: 3.049

9.  Disability and survival in Duchenne muscular dystrophy.

Authors:  M Kohler; C F Clarenbach; C Bahler; T Brack; E W Russi; K E Bloch
Journal:  J Neurol Neurosurg Psychiatry       Date:  2008-08-19       Impact factor: 10.154

10.  Supported Standing in Boys With Duchenne Muscular Dystrophy.

Authors:  Elise L Townsend; Christine Bibeau; Tara M Holmes
Journal:  Pediatr Phys Ther       Date:  2016       Impact factor: 3.049

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