Evidence map›Paper›PMID 28395534›Full record

ArticleDisability and rehabilitation2018

Application of the International Classification of Functioning, Disability and Health system to symptoms of the Duchenne and Becker muscular dystrophies.

Kristin M Conway, Emma Ciafaloni, Dennis Matthews, Chris Westfield, Kathy James, Pangaja Paramsothy, Paul A Romitti

Abstract read
In one paragraph

Article in Disability and rehabilitation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.2field-weighted citation impact, top 45% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Management of motor rehabilitation in individuals with muscular dystrophies. 1Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2021
    Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 1 country.

Kristin M Conwaya Department of Epidemiology , The University of Iowa , Iowa City , IA , USA.
Emma Ciafalonib Departments of Neurology and Pediatrics , University of Rochester Medical Center , Rochester , NY , USA.
Dennis Matthewsc Department of Physical Medicine & Rehabilitation , University of Colorado School of Medicine and Children's Hospital Colorado , Aurora , CO , USA.
Chris Westfieldd New York State Department of Public Health , Congenital Malformations Registry (CMR) , Albany , NY , USA.
Kathy Jamese Department of Family Medicine , Colorado School of Public Health , Aurora , CO , USA.
Pangaja Paramsothyf National Center on Birth Defects and Developmental Disabilities , Centers for Disease Control and Prevention , Atlanta , GA , USA.
Paul A Romittia Department of Epidemiology , The University of Iowa , Iowa City , IA , USA.
University of Iowa · USChildren's Hospital Colorado · USColorado School of Public Health · USNational Center on Birth Defects and Developmental Disabilities · USNew York State Department of State · USUniversity of Rochester Medical Center · US

Funding

Surveillance and Epidemiologic Research of Duchenne and Becker Muscular DystrophyU01DD000189 · DD · UNIVERSITY OF IOWA · PI ROMITTI, PAUL A · 2006 to 2011
$4.1M
Arizona Muscular Dystrophy Surveillance and Research ProgramU01DD000187 · DD · UNIVERSITY OF ARIZONA · PI CUNNIFF, CHRISTOPHER MCCORD · 2006 to 2010
$2.9M
Surveillance and Epidemiologic Research of Duchenne and Becker Muscular DystrophyU01DD000190 · DD · NYSDOH/HEALTH RESEARCH, INC. · PI DRUSCHEL, CHARLOTTE MARIE · 2006 to 2010
$2.7M
Sureillance and Epidemiologic Research of Duchenne and Becker Muscular DystrophyU01DD000191 · DD · COLORADO STATE DEPT/PUB HLTH & ENVIRONMT · PI MILLER, LISA ANN · 2006 to 2010
$2.5M
Comp A-NY State Surveillance and Research of MD and Neuromuscular DisordersU01DD001123 · DD · CENTER OF ENVIRONMENTAL HEALTH · PI SOIM, AIDA · 2014 to 2018
$2.4M
Comp A-Surveillance and Research of Muscular Dystrophies and Neuromuscular DisordersU01DD001126 · DD · COLORADO STATE DEPT/PUB HLTH & ENVIRONMT · PI RUTTENBER, MARGARET · 2014 to 2018
$2.4M
Comp A-MD and Neuromuscular Disorder Surveillance and Research in IowaU01DD001119 · DD · UNIVERSITY OF IOWA · PI ROMITTI, PAUL A · 2014 to 2018
$2.4M
Hawaii MD STARnetU01DD000392 · DD · HAWAII STATE DEPARTMENT OF HEALTH · PI MANN, SYLVIA · 2008 to 2010
$823k
ACL HHS U01DD001119ACL HHS U01DD001123ACL HHS U01DD001126Intramural CDC HHS CC999999NCBDD CDC HHS U01 DD000187NCBDD CDC HHS U01 DD000189NCBDD CDC HHS U01 DD000190NCBDD CDC HHS U01 DD000191NCBDD CDC HHS U01 DD000392NCBDD CDC HHS U01 DD001119NCBDD CDC HHS U01 DD001123NCBDD CDC HHS U01 DD001126
6 · The paper itself

Abstract

purposeDuchenne and Becker muscular dystrophies, collectively referred to as dystrophinopathies, are X-linked recessive diseases that affect dystrophin production resulting in compromised muscle function across multiple systems. The International Classification of Functioning, Disability and Health provides a systematic classification scheme from which body functions affected by a dystrophinopathy can be identified and used to examine functional health. MATERIALS AND

methodsThe infrastructure of the Muscular Dystrophy Surveillance, Tracking, and Research Network was used to identify commonly affected body functions and link selected functions to clinical surveillance data collected through medical record abstraction.

resultsSeventy-one (24 second-, 41 third- and 7 fourth-level) body function categories were selected via clinician review and consensus. Of these, 15 of 24 retained second-level categories were linked to data elements from the Muscular Dystrophy Surveillance, Tracking, and Research Network surveillance database.

conclusionsOur findings support continued development of a core set of body functions from the International Classification of Functioning, Disability and Health system that are representative of disease progression in dystrophinopathies and the incorporation of these functions in standardized evaluations of functional health and implementation of individualized rehabilitation care plans. Implications for Rehabilitation Duchenne and Becker muscular dystrophies, collectively referred to as dystrophinopathies, are X-linked recessive disorders that affect the production of dystrophin resulting in compromised muscle function across multiple systems. The severity and progressive nature of dystrophinopathies can have considerable impact on a patient's participation in activities across multiple life domains. Our findings support continued development of an International Classification of Functioning, Disability and Health core set for childhood-onset dystrophinopathies. A standardized dystrophinopathy International Classification of Functioning, Disability and Health documentation form can be used as a screening tool by rehabilitation professionals and for patient goal setting when developing rehabilitation plans. Patient reports of perceived functional health should be incorporated into the rehabilitation plan and therapeutic progress monitored by a standardized form.

Indexed as

International Classification of Functioning, Disability and HealthHumansMuscular Dystrophy, DuchenneBecker’s muscular dystrophydisabilityDuchenne’s muscular dystrophydystrophinopathiesInternational classification of functioningsurveillance

Identifiers

PMID28395534
PMCPMC5636650
OpenAlexW2605449100

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.