The prevalence of patients with cardiomyopathies who referred to Rajaei Cardiovascular medical and research center is remarkable, and also the mission of this center is to achieve center of excellence in the field of cardiomyopathy. Rajaie Cardiomyopathy and myocarditis Registry study is an observational registry of consecutive patients with four cardiomyopathy subtypes: hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), arrhythmogenic right ventricular cardiomyopathy (ARVC), and restrictive cardiomyopathy (RCM) as well as myocarditis designed to determine clinical characteristics, natural history, current therapeutic approaches, response to treatment and long-term outcomes of patients with cardiomyopathy and myocarditis and to address limitations in extant evidence to improve prognostication in cardiomyopathies and myocarditis. Prediction of mortality and response to different treatments in these patients using artificial intelligence is another aim of this registry
Study Type
OBSERVATIONAL
Enrollment
6,000
Behshid Ghadrdoost
Tehran, Iran
RECRUITINGAdmissions to hospital
Number of hospitalizations for cardiovascular reasons
Time frame: 1 year
Development of chronic heart failure
significant decrease in left ventricular ejection fraction
Time frame: 1 year
Prevalence of Stroke/Transient ischemic attack
At least 80% CT/MRI verification of the diagnosis of ischemic stroke/Transient ischemic attack, within the first week of stroke onset
Time frame: 1 year
Incidence of sudden death
unexpected death from a cardiovascular cause in a person with or without preexisting heart disease
Time frame: 1 year
Incidence of heart trasplantation
Cardiac transplantation in patients with end-stage HF who remain symptomatic despite optimal medical therapy
Time frame: 1 year
response to current therapeutic approaches
Implantable cardioverter defibrillator implantation, Cardiac resynchronisation therapy, septal myectomy, ablation, cardiac transplantation and medications
Time frame: 1 year
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