Evidence map›Paper›PMID 40364815›Full record

ArticleFrontiers in pediatrics2025

Case Report: Complex cardiac arrhythmia management in the ICU for an adolescent with Friedreich ataxia.

Oluwatomini A Fashina, Stephen J Gleich, Derek N Opp, Yves Ouellette, Yu Kawai

Abstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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.

Oluwatomini A Fashina *Department of Pediatrics Medicine, Mayo Clinic Children's, Rochester, MN, United States.
Stephen J Gleich *Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, Rochester, MN, United States.
Derek N Opp *Division of Pediatric Cardiology, Mayo Clinic Children's, Rochester, MN, United States.
Yves Ouellette *Division of Pediatric Critical Care, Mayo Clinic Children's, Rochester, MN, United States.
Yu Kawai *Division of Pediatric Critical Care, Mayo Clinic Children's, Rochester, MN, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Friedreich ataxia (FRDA) is a progressive neurodegenerative disorder with specific clinical manifestations, such as scoliosis, which may impact the management of cardiac arrhythmias and heart failure. Case description: A 17-year-old male with FRDA and hypertrophic cardiomyopathy presented with atrial flutter and resultant acute-on-chronic systolic and diastolic heart failure with reduced ejection fraction. The arrhythmias were refractory to medical management with adenosine and amiodarone. An attempted cavotricuspid isthmus ablation was unsuccessful due to abnormal cardiac positioning caused by severe scoliosis. Despite optimization with dofetilide and metoprolol, he was readmitted with recurrent atrial arrhythmias and cardiogenic shock, secondary to probable amiodarone-induced thyrotoxicosis, requiring extracorporeal membrane oxygenation. His clinical course involved multisystem complications, prolonged hospitalization, and disease progression, with no recovery in systolic function despite control of his arrhythmia burden. Conclusion: Intensivists should be cognizant of multisystem complications that can arise when treating refractory cardiac arrhythmias, especially in those with concomitant genetic conditions.

Indexed as

arrhythmiaataxiaECMOFriedreichICUpediatric

Identifiers

PMID40364815
PMCPMC12069360

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