Skip to main content
. 2022 Apr 4;24(8):1307–1367. doi: 10.1093/europace/euac030

Table 2.

Relevant clinical practice documents or guidelines

Title Publication year
Consensus documents/guidelines of scientific societies
 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families6 2021
 HRS/EHRA/APHRS/LAHRS Expert Consensus Statement on Catheter Ablation of Ventricular Arrhythmias7 2020
 Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association8 2020
 European Recommendations Integrating Genetic Testing into Multidisciplinary Management of Sudden Cardiac Death9 2019
 Pre-participation Cardiovascular Evaluation for Athletic Participants to Prevent Sudden Death: Position Paper from the EHRA and the EACPR, Branches of the ESC22 2019
 HRS Expert Consensus Statement on Evaluation, Risk Stratification, and Management of Arrhythmogenic Cardiomyopathy11 2019
 AHA/ACC/HRS Guideline for Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death12 2017
 ESC Guidelines for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death13 2015
 EHRA/HRS/APHRS Expert Consensus on Ventricular Arrhythmias14 2014
 HRS/EHRA/APHRS Expert Consensus Statement on the Diagnosis and Management of Patients with Inherited Primary Arrhythmia Syndromes15 2013
 HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies1 2011
 Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases16 2010
NIH-Clinical Genome Resource Consortium (ClinGen) documents
 A Multi-Centred, Evidence-Based Evaluation of Gene Validity in Sudden Arrhythmic Death Syndromes: CPVT and The Short QT Syndrome17 2022
 International Evidence Based Reappraisal of Genes Associated With Arrhythmogenic Right Ventricular Cardiomyopathy Using the Clinical Genome Resource Framework18 2021
 Evidence-Based Assessment of Genes in Dilated Cardiomyopathy19 2021
 An International, Multicentred Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome20 2020
 Reappraisal of Reported Genes for Sudden Arrhythmic Death: An Evidence-Based Evaluation of Gene Validity for Brugada Syndrome21 2018
 Evaluating the Clinical Validity of Hypertrophic Cardiomyopathy Genes10 2017