Surgical treatment of a patient with the diagnosis of arrhythmogenic right ventricular dysplasia
[ X ]
Tarih
2020
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Edizioni Minerva Medica
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
Arrhythmogenic right ventricular dysplasia (ARVD) is a genetic heart disease that causes sudden deaths. especially in young people. Generally. right ventricle and left ventricular myocardial tissue are replaced with fat and fibrosis. Sudden death, rhythm disorders and heart failure in young ages are the most important symptoms of the disease. It is responsible for approximately 20% of sudden deaths in young people and the annual sudden death rate is 1-2%. Early diagnosis and treatment in people with a family history increases the quality of life. The diagnostic criteria for the diagnosis of the disease are divided into two groups as major and minor.2 major or 1 major + 2 minor criteria is sufficient for diagnosis. The diagnosis of the disease is made by the use of history, physical examination, electrocardiogram, echocardiography, 24-hour rhythm holter monitoring. right ventricular angiography, cardiac MRI, endomyocardial biopsy methods. According to the clinical course of the disease, antiarrhythmic drug, implanted cardioverter defibrillator (ICD), radiofrequency ablation and surgery are recommended. In this study, we present the both surgical treatment method and ICD implantation to a male patient with a family history' of ARVD.
Açıklama
Anahtar Kelimeler
Arrhythmogenic Right Ventricular Dysplasia, Tachycardia, Ventricular, Surgery
Kaynak
Chirurgia-Italy
WoS Q Değeri
N/A
Scopus Q Değeri
Q4
Cilt
33
Sayı
5
