Evidence map›Paper›PMID 42543477›Full record

ReviewEcho research and practice2026

Echocardiography in duchenne muscular dystrophy: a call for consistency and standardisation of reporting.

Lynne Williams, Sadie Bennett, Charlotte Atkinson, Daniel X Augustine, Maria Bland, Hatty Grant, Jade Hobday, Anna Johnson, Kadhim Kadhim, Lisa Kuhwald and 11 more

Abstract readReview
In one paragraph

Review in Echo research and practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Lynne Williams *Department of Cardiology, Royal Papworth Hospital, Cambridge, UK.
Sadie Bennett *Heart and Lung Clinic, University Hospitals of North Midlands, Stoke-on-Trent, UK.
Charlotte AtkinsonUniversity Hospital Southampton, Southampton, UK.
Daniel X AugustineDepartment of Cardiology, Royal United Hospitals, Bath, UK.
Maria BlandDepartment of Cardiology Freeman Hospital, NUTH Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Hatty GrantBritish Society of Echocardiography, London, UK.
Jade HobdayDepartment of Cardiology, Birmingham Children's Hospital, Birmingham, UK.
Anna JohnsonDepartment of Paediatric Cardiology, Freeman Hospital, NUTH Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Kadhim KadhimDepartment of Cardiology Freeman Hospital, NUTH Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Lisa KuhwaldDuchenne UK, London, UK.
Chiara Marini BettoloJohn Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle Upon Tyne, UK.
Adam KerrJohn Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle Upon Tyne, UK.
David OxboroughResearch Institute for Sports and Exercise Science, Liverpool John Moores University, Liverpool, UK.
Liam RingDepartment of Cardiology, West Suffolk Hospital NHS Trust, Bury St Edmonds, UK.
Shaun RobinsonDepartment of Cardiology, Imperial Healthcare NHS Trust, London, UK.
Jo SopalaBritish Society of Echocardiography, London, UK.
Cathy TurnerJohn Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle Upon Tyne, UK. catherine.turner@newcastle.ac.uk.
Chet VillaCincinnati Children's Hospital Medical Center, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA.
Michela GuglieriJohn Walton Muscular Dystrophy Research Centre, Newcastle University, Newcastle Upon Tyne, UK.
John BourkeDepartment of Cardiology Freeman Hospital, NUTH Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Caroline CoatsDepartment of Cardiology, Queen Elizabeth University Hospital, NHS Greater Glasgow and Clyde, Glasgow, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is a genetically determined, neuromuscular disorder occurring predominantly in males with a prevalence of 1:3,500 to 1:5,000 live male births. It is a life limiting condition with average life expectancy of only 28.1 years in the United Kingdom. A dilated cardiomyopathy occurs in all patients with DMD, and cardio-respiratory causes now account for about 80% of all deaths in adult patients. Transthoracic echocardiography (TTE) is a widely used non-invasive imaging modality to assess cardiac structure, chamber dimensions, and myocardial function, and so plays a central role in guiding the timely initiation and adjustment of 'heart failure' medications. However, obtaining high quality images in patients with DMD can be challenging, particularly after patients lose ambulation, become wheelchair reliant, and require non-invasive ventilatory support. We review the current literature and evidence pertaining to echocardiography and the assessment of cardiac function in this patient group. This article seeks to discuss the strengths and limitations of TTE in patients with DMD, recommends a standard set of the measures to be reported at all assessments, and offers consensus guidance, based on expert opinion, to allow valid comparisons of serial assessments even when performed by different TTE services.

Indexed as

Cardiac dystrophinopathyCardiac imagingEchocardiographyMuscular dystrophy

Identifiers

PMID42543477
PMCPMC13430808

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Registered trials

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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.