ReviewJournal of arrhythmia2018
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.
Review in Journal of arrhythmia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.
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.
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Who cites it
17 citing papers in PubMed, 34 citations in OpenAlex.
- The Role of Ventricular Arrhythmias Inducibility in Arrhythmic Risk Stratification in Arrhythmogenic Right Ventricular Cardiomyopathy: A Meta-Analysis of Observational Studies.Journal of arrhythmia · 2025Article
- Consequences of Right Heart Disease for Cardiac Electrophysiology and Arrhythmias: Cellular and Structural Mechanisms.CJC open · 2025Review
- Atrial Tachyarrhythmia in Arrhythmogenic Right Ventricular Cardiomyopathy: A Case Report.Clinical case reports · 2025Article
- Toward the latest advancements in cardiac regeneration using induced pluripotent stem cells (iPSCs) technology: approaches and challenges.Journal of translational medicine · 2024Review
- Ventricular Tachycardia Due to Arrhythmogenic Right Ventricular Cardiomyopathy in the Setting of Acute Coronary Syndrome.JACC. Case reports · 2023Article
- Sudden cardiac death in the adolescent population: a narrative review.The Egyptian journal of internal medicine · 2023Review
- A Territory-Wide Study of Arrhythmogenic Right Ventricular Cardiomyopathy Patients from Hong Kong.Reviews in cardiovascular medicine · 2022Article
- A 3D high resolution MRI method for the visualization of cardiac fibro-fatty infiltrations.Scientific reports · 2021Article
- The Role of Cardiac Magnetic Resonance in Evaluation of Idiopathic Ventricular Arrhythmia in Children.Journal of clinical medicine · 2021Article
- Usefulness of three-dimensional echocardiography for the assessment of ventricular function in children: Comparison with cardiac magnetic resonance, with a focus on patients with arrhythmia.Cardiology journal · 2021Article
- Emergency department extracorporeal membrane oxygenation as a rescue therapy for ventricular tachycardia electrical storm: a case report.Journal of the American College of Emergency Physicians open · 2020Article
- Monozygotic twins with myocarditis and a novel likely pathogenic desmoplakin gene variant.ESC heart failure · 2020Article
- Right Ventricular Strain Predicts Structural Disease Progression in Patients With Arrhythmogenic Right Ventricular Cardiomyopathy.Journal of the American Heart Association · 2020Article
- Clinical Presentation, Cardiac Magnetic Resonance Findings, and Prognosis of Patients with Arrhythmogenic Right Ventricular Cardiomyopathy - An Experience from Pakistan.Journal of clinical imaging science · 2020Article
- A novel desmin mutation causing severe left ventricular arrhythmogenic cardiomyopathy/dysplasia.Journal of thoracic disease · 2018Article
- Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) in clinical practice.Journal of arrhythmia · 2018Review
- [Clinical profile and therapeutic strategies in patients with arrhythmogenic cardiomyopathy treated in a national reference institute].Archivos peruanos de cardiologia y cirugia cardiovascularArticle
Corrections and comments
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Authors and funding
12 authors at 6 institutions in 5 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is an inherited myocardial disease characterized by fibro-fatty replacement of the right ventricular myocardium, and associated with paroxysmal ventricular arrhythmias and sudden cardiac death (SCD). It is currently the second most common cause of SCD after hypertrophic cardiomyopathy in young people <35 years of age, causing up to 20% of deaths in this patient population. This condition has a male preponderance and is more commonly found in individuals of Italian and Greek descent. To date, there is no single diagnostic test for ARVC/D and the diagnosis is made based on clinical, electrocardiographic, and radiological findings according to the Revised 2010 Task Force Criteria. In this review, we will discuss the mainstay treatment which includes pharmacotherapy, implantable cardioverter-defibrillator insertion for abortion of sudden cardiac death, and in the advanced stages of the disease cardiac transplantation.
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Registered trials
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.