ArticleKorean circulation journal2010
Magnetic resonance imaging assessment of arrhythmogenic right ventricular cardiomyopathy/dysplasia in children.
Article in Korean circulation journal, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 32 citations in OpenAlex.
- Inherited Arrhythmias in the Pediatric Population: An Updated Overview.Medicina (Kaunas, Lithuania) · 2024Review
- The Role of Multimodality Imaging in Pediatric Cardiomyopathies.Journal of clinical medicine · 2023Review
- Arrhythmogenic Cardiomyopathy: Diagnosis, Evolution, Risk Stratification and Pediatric Population-Where Are We?Journal of cardiovascular development and disease · 2022Review
- Electrocardiographic features of arrhythmogenic right ventricular cardiomyopathy in school-aged children.Heart and vessels · 2021Article
- Cardiac magnetic resonance in arrhythmogenic cardiomyopathies.La Radiologia medica · 2020Review
- Clinical features and arrhythmic complications of patients with pediatric-onset arrhythmogenic right ventricular dysplasia.Anatolian journal of cardiology · 2019Article
- Comparison of CMR Findings according to the Presence or Absence of Isolated Focal Right Ventricular Dyskinetic Segments in Patients with Clinical Suspicion of ARVC.Journal of cardiovascular imaging · 2019Article
- Diagnosing ARVC in Pediatric Patients Applying the Revised Task Force Criteria: Importance of Imaging, 12-Lead ECG, and Genetics.Pediatric cardiology · 2018Article
- Association betweenExperimental and therapeutic medicine · 2016Article
- Left-dominant arrhythmogenic cardiomyopathy in a Fila Brasileiro dog.Open veterinary journalArticle
Corrections and comments
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Authors and funding
3 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a genetically determined disease that progresses continuously from conception and throughout life. ARVC/D manifests predominantly in young adulthood. Early identification of the concealed cases in childhood is of utmost importance for the prevention of sudden cardiac death later in life. Magnetic resonance imaging (MRI) is routinely requested in patients with a confirmed or suspected diagnosis of ARVC/D and in family members of the patients with ARVC/D. Although the utility of MRI in the assessment of ARVC/D is well recognized in adults, MRI is a low-yield test in children as the anatomical, histological, and functional changes are frequently subtle or not present in the early phase of the disease. MRI findings of ARVC/D include morphologic changes such as right ventricular dilatation, wall thinning, and aneurismal outpouchings, as well as abnormal tissue characteristics such as myocardial fibrosis and fatty infiltration, and functional abnormalities such as global ventricular dysfunction and regional wall motion abnormalities. Among these findings, regional wall motion abnormalities are the most reliable MRI findings both in children and adults, while myocardial fibrosis and fat infiltration are rarely seen in children. Therefore, an MRI protocol should be tailored according to the patient's age and compliance, as well as the presence of other findings, instead of using the protocol that is used for adults. We propose that MRI in children with ARVC/D should focus on the detection of regional wall motion abnormalities and global ventricular function by using a cine imaging sequence and that the sequences for myocardial fat and late gadolinium enhancement of the myocardium are reserved for those who show abnormal findings at cine imaging. Importantly, MRI should be performed and interpreted by experienced examiners to reduce the number of false positive and false negative readings.
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Registered trials
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