Evidence map›Paper›PMID 41880031›Full record

ArticleEuropean journal of pediatrics2026

Association between thoracic ultrasound findings and respiratory function in children with Duchenne muscular dystrophy.

Meltem Kürtül Çakar, Avni Merter Keçeli, Satı Özkan Tabakçı, Işıl Bilgiç, Gamze Akca Dinç, Ayyüce Aktemur Ünlü, Hande Yetişgin, Çelebi Yıldırım, Merve Kaşıkçı, Gökçen Dilşa Tuğcu and 4 more

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Article in European journal of pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Meltem Kürtül ÇakarDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye. krtlmeltem@gmail.com.ORCID http://orcid.org/0000-0002-1466-2369
Avni Merter KeçeliDepartment of Pediatric Radiology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Satı Özkan TabakçıDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Işıl BilgiçDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Gamze Akca DinçDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Ayyüce Aktemur ÜnlüDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Hande YetişginDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Çelebi YıldırımDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Merve KaşıkçıDepartment of Statistics, Hacettepe University, Ankara, Türkiye.
Gökçen Dilşa TuğcuDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Dilber Ademhan TuralDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Sanem Eryılmaz PolatDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.
Didem ArdıçlıDepartment of Pediatric Neurology, Ministry of Health Ankara Bilkent City Hospital, Ankara, Türkiye.
Güzin CinelDepartment of Pediatric Pulmonology, Ministry of Health, Ankara Bilkent City Hospital, Ankara, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Duchenne muscular dystrophy (DMD) is characterized by progressive muscle weakness, atrophy, and respiratory failure. As the primary inspiratory muscle, the diaphragm plays a crucial role in the respiratory progression of DMD. Therefore, this study aimed to evaluate diaphragmatic function and structure in children with DMD. This study included 60 children with DMD who underwent diaphragmatic evaluation with B-mode thoracic ultrasonography (USG) and pulmonary functional testing. The same pediatric pulmonologist (P1) and pediatric radiologist (P2) performed all USG scans. The participants were divided into ambulant (n = 39) and non-ambulant (n = 21) groups. The Pediatric Sleep Questionnaire (PSQ) was used to assess the risk of sleep-related breathing disorders. The participants' mean age was 10.2 ± 2.8 years. The forced vital capacity (FVC) and forced expiratory volume in one second (FEV

conclusionThoracic USG, alongside spirometry and MIP/MEP measurements, provides a simple and noninvasive means to evaluate respiratory function in children with DMD, revealing diaphragmatic changes associated with functional decline and the risk of sleep-related breathing disorders. WHAT IS KNOWN: • DMD causes progressive respiratory muscle weakness due to diaphragmatic involvement. • Spirometry and maximal inspiratory and expiratory pressures (MIP/MEP) are commonly used to monitor respiratory function but may be difficult to perform in some children. • Noninvasive assessment of diaphragmatic function in children with DMD is still limited. WHAT IS NEW: • Thoracic USG provides a simple, reproducible, and noninvasive method to evaluate diaphragmatic morphology and motion in children with DMD. • The study demonstrated that non-ambulant children have increased DT but reduced functional indices, reflecting structural adaptation to disease progression. • Significant correlations between USG measurements, spirometric parameters, and PSQ scores highlight the potential of USG as a valuable adjunct tool in respiratory monitoring and early detection of sleep-related breathing disorders in children with DMD.

Indexed as

DiaphragmMuscular Dystrophy, DuchenneAdolescentChildFemaleForced Expiratory VolumeHumansMaleRespiratory Function TestsUltrasonographyVital CapacityDiaphragmDuchenne muscular dystrophyPulmonary function testsThoracic ultrasound

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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.