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Getting to the Heart of Genetics Arrhythmias and Cardiomyopathies PDF
Preview Getting to the Heart of Genetics Arrhythmias and Cardiomyopathies
Getting to the Heart of Genetics Arrhythmias and Cardiomyopathies Susan Conacher, MSc, CCGC Genetic Counsellor October 22, 2014 Getting to the Heart of Genetics Arrhythmias and Cardiomyopathies Presenter Disclosure: Susan Conacher has no potential for conflict of interest with this presentation Inherited Heart Rhythm Disorders • Long QT (Short QT) • CPVT ‐ Catecholamenergic Polymorphic Ventricular Tachycardia • Brugada Syndrome Cardiomyopathies • ARVC‐ Arrhythmogenic right ventricular cardiomyopathy • HCM ‐ Hypertrophic Cardiomyopathy • DCM ‐ Dilated Cardiomyopathy • LVNC ‐ Left ventricular Non‐compaction Familial Aneurysms • Familial TAAD (Familial thoracic aortic aneurysm and dissection ) • Marfan Syndrome • Loeys‐Dietz Syndrome • Ehlers‐Danlos Syndrome (vascular type) Long QT Syndrome • optimal cut‐off value to distinguish affected (≥420 for men and ≥440 QTc for women) • >499ms significant risk of events • History of syncope is most powerful indicator of SCD risk Syncope <18 years 18 fold increase in SCD Syncope >18 years 5 fold increase in SCD STRESS TEST – most useful test for diagnosing LQT LQT treatment /counselling • Beta blockers • ICD (only if cardiac arrest or beta blocker resistant) • Exercise avoidance (Competitive training) • Avoidance of LQT prolonging drugs • Family screening Brugada Approach London symptoms GGeenneettiiccss oorr UUrrggeenntt CClliinniicc BBrruuggaaddaa EECCGG** GGeenneettiicc TTeessttiinngg CCoonnssiiddeerr IICCDD TTyyppee 11 TTyyppee 22 oorr 33 ECG Guide PPrrooccaaiinnaammiiddee IInnffuussiioonn HHiigghh LLeeaaddss aanndd SSAAEECCGG Type 1 GGeenneettiiccss CClliinniicc Type 2 TTyyppee 22 oorr 33 TTyyppee 11 Type 3 RReeaassssuurraannccee RRiisskk DDiissccuussssiioonn ±± EEPP SSttuuddyy§§ ±± GGeenneettiicc TTeessttiinngg¶¶ * ECG should include high lead placement, and baseline signal averaged ECG §Discretionary EP testing, generally discouraged ¶ CCS Guidelines recommend genetic testing when there is a positive family history or phenotypicallyaffected first degree relative Standard type 1 Brugada pattern advice 1. Treat fever 2. Avoid specific drugs (www.brugadadrugs.org) 3. Report syncope, seizures, sleep disturbance 4. Family screening