Evidence map›Paper›PMID 41773437›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2025

Fat embolism syndrome in Duchenne muscular dystrophy: an underdiagnosed complication.

Michele Tosi, Michela Catteruccia, Nicoletta Cantarutti, Daniela Perrotta, Adele D'Amico

Abstract readCase Reports
In one paragraph

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

5 authors.

Michele TosiUnit of Muscular and Neurodegenerative Disorders, IRCCS Bambino Gesù Children's Hospital.
Michela CatterucciaUnit of Muscular and Neurodegenerative Disorders, IRCCS Bambino Gesù Children's Hospital.
Nicoletta CantaruttiPediatric Cardiology and Cardiac Arrhythmia/Syncope Unit, IRCCS Bambino Gesù Children's Hospital.
Daniela PerrottaDepartment of Anesthesia and Critical Care, IRCCS Bambino Gesù Children's Hospital.
Adele D'AmicoUnit of Muscular and Neurodegenerative Disorders, IRCCS Bambino Gesù Children's Hospital.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Fat embolism syndrome (FES) is a rare but potentially life-threatening complication of long bone fractures, typically described in high-energy trauma. In patients with Duchenne Muscular Dystrophy (DMD), even minor trauma can result in FES, owing to long-standing osteoporosis and prolonged corticosteroid therapy, and the recognition can be challenging. Materials and methods: We report a case series of three non-ambulatory patients with DMD who developed fat embolism syndrome following traumatic events. Clinical presentation, diagnostic challenges, and management strategies were retrospectively analyzed. Results: All three patients presented with features consistent with FES, with diagnostic difficulties related to atypical mechanisms of injury and overlapping neuromuscular symptoms. Timely supportive management led to favorable clinical outcomes in all cases. Discussion: These cases illustrate the critical need to closely consider FES in DMD patients who experience unexplained respiratory or neurological decline following trauma. Conclusion: Prompt recognition and a multidisciplinary approach are critical to minimizing morbidity and supporting recovery.

Indexed as

Embolism, FatFemoral FracturesMuscular Dystrophy, DuchenneAdolescentChildHumansMaleRetrospective StudiesDuchenne muscular dystrophyfat embolism syndromefemoral fractures

Identifiers

PMID41773437
PMCPMC12958405

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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.