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Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysis
- Source :
- Heart rhythm, 15(7), 1097-1107. Elsevier, Heart Rhythm, 15(7), 1097. Elsevier
- Publication Year :
- 2017
-
Abstract
- While many studies evaluate predictors of ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy (ARVC), a systematic review consolidating this evidence is currently lacking. Therefore, we searched MEDLINE and Embase for studies analyzing predictors of ventricular arrhythmias (sustained ventricular tachycardia/fibrillation (VT/VF), appropriate implantable cardioverter-defibrillator therapy, or sudden cardiac death) in patients with definite ARVC, patients with borderline ARVC, and ARVC-associated mutation carriers. In the case of multiple publications on the same cohort, the study with the largest population was included. This yielded 45 studies with a median cohort size of 70 patients (interquartile range 60 patients) and a median follow-up of 5.0 years (interquartile range 3.3 - 6.7 years). The average proportion of arrhythmic events observed was 10.6%/y in patients with definite ARVC, 10.0%/y in patients with borderline ARVC, and 3.7%/y with mutation carriers. Predictors of ventricular arrhythmias were population dependent: consistently predictive risk factors in patients with definite ARVC were male sex, syncope, T-wave inversion in lead >V3, right ventricular dysfunction, and prior (non)sustained VT/VF; in patients with borderline ARVC, 2 additional predictors—inducibility during electrophysiology study and strenuous exercise—were identified; and with mutation carriers, all aforementioned predictors as well as ventricular ectopy, multiple ARVC-related pathogenic mutations, left ventricular dysfunction, and palpitations/presyncope determined arrhythmic risk. Most evidence originated from small observational cohort studies, with a moderate quality of evidence. In conclusion, the average risk of ventricular arrhythmia ranged from 3.7 to 10.6%/y depending on the population with ARVC. Male sex, syncope, T-wave inversion in lead >V3, right ventricular dysfunction, and prior (non)sustained VT/VF consistently predict ventricular arrhythmias in all populations with ARVC.
- Subjects :
- medicine.medical_specialty
Population
030204 cardiovascular system & hematology
Risk Assessment
Right ventricular cardiomyopathy
Sudden cardiac death
03 medical and health sciences
Electrophysiology study
Electrocardiography
0302 clinical medicine
Ventricular arrhythmias
Risk Factors
Internal medicine
Physiology (medical)
medicine
Humans
030212 general & internal medicine
cardiovascular diseases
Cardiac Resynchronization Therapy Devices
education
Risk stratification
Arrhythmogenic Right Ventricular Dysplasia
Fibrillation
education.field_of_study
Presyncope
medicine.diagnostic_test
business.industry
Arrhythmogenic right ventricular dysplasia/cardiomyopathy
medicine.disease
Prognosis
Arrhythmogenic right ventricular dysplasia
Meta-analysis
Cardiology
cardiovascular system
Systematic review
medicine.symptom
business
Arrhythmogenic right ventricular cardiomyopathy
Cardiology and Cardiovascular Medicine
Subjects
Details
- ISSN :
- 15563871 and 15475271
- Volume :
- 15
- Issue :
- 7
- Database :
- OpenAIRE
- Journal :
- Heart rhythm
- Accession number :
- edsair.doi.dedup.....193f4808c8f13515ab2b48d8d4add634