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Post-Myocardial Infarction Ventricular Tachycardia: should catheter ablation be performed before antiarrhythmic drug therapy? William G. Stevenson, M.D. Brigham and Women’s Hospital Boston, Ma Disclosures: patent for a needle ablation catheter – consigned to Brigham and Women’s Hospital Ventricular Tachycardia and Ventricular Fibrillation After Hospital Discharge from Myocardial Infarction – Patients with depressed ventricular function Sudden Death after Acute MI with ventricular dysfunction or heart failure: Valiant trial Solomon et al NEJM 2005; 352:2581. Sustained Ventricular arrhythmias in patients with LVEF < 0.40 followed for 2 yrs after myocardial infarction CARISMA Study Thomsen et al Circulation 2010; 122:1258 Sustained VT 3% VF 2.7% ICDs terminate VT or VF after it occurs: Shocks or Antitachycardia Pacing (ATP) ICD shock C Atrial lead VT LV lead RV lead VT Antitachycardia Pacing The Rationale for Preventing VT – an ICD is not enough ICD shocks reduce quality of life Spontaneous VT/VF is associated with increased risk of death and heart failure Moss et al. Circulation 2004;110:3760-3765 Poole JE et al. N Engl J Med 2008;359:1009-1017 SCD-HeFT: Spontaneous VT predicts Increased Risk of Death Poole JE et al. N Engl J Med 2008;359:1009-1017. Heart failure + ischemic heart disease + ICD shock 37% one year survival Episodes of VT/ VF predict increased mortality and heart failure despite ICD therapy – MADIT II Is VT a prognostic marker or directly contribute to mortality and heart failure? Moss et al. Circulation 2004;110:3760-3765 Need for Arrhythmia Management After ICD placement Secondary Prevention ICD Recurrent VT: 40 – 60% >3 shocks in 24 hrs: 20% Primary Prevention ICD Sustained VT - 5% year Symptomatic VT After ICD Antiarrhythmic Drugs Catheter Ablation SCD-HeFT Bardy, G. H. et al. N Engl J Med 2005;352:225-237 MADIT II N Engl J Med 202;346:877 AVID VT storm, Exner et al Circ 2001;103:201 AVID Quality of life, Schron Circ 2002;105:589 OPTIC Trial – Drug therapy to reduce recurrent VT in patients with ICDs 412 patients receiving ICD – spontaneous VT, or – LVEF ≤40% and cardiac arrest or inducible VT/VF Randomized to b-blocker - sotalol - b-blocker and amiodarone Baseline characteristics – 80% prior MI – 71% spontaneous VT or VF / 29% inducible VT or VF Connolly SJ. J Am Med Assoc. 2006;295:165-71 OPTIC Trial – Drug therapy to reduce recurrent VT in patients with ICDs Any VT (shock or ATP) at 1 Year p<0.001 50% p=NS P< 0.001 45.0% 39.0% 40% 30% 20% 13.0% 10% 0% b-blocker Sotalol b-Blocker w/ Amiodarone Connolly SJ. J Am Med Assoc. 2006;295:165-71 Optic TRIAL: Adverse Events of the 3 Treatment Assignments. Drug discontinuation at 1 yr 5.3% 18.2% 23.5% Connolly, S. J. et al. JAMA 2006;295:165-171 Amiodarone Toxicity meta-analysis of trials for sudden death prevention Piccini et al Eur H J 2009;30:1245 Drug withdrawal in VT trials: Serious toxicities – Lung – Liver – Thyroid – Bradyarrhythmia 29% 2.9% 1.9% 3.6% 2.8% ICD – Antiarrhythmic Drug Interactions Slower VT – Impairs discrimination between sinus tachycardia and VT – Slower incessant VT Sinus slowing – increased ventricular pacing Effect on antitachycardia pacing (ATP) / defibrillation efficacy Catheter Ablation for VT: Approach and efficacy depend on arrhythmia substrate Monomorphic VT s can be targeted for ablation – Scar – related reentry – Purkinje system – related VT Polymorphic VT – the initiating PVC can be targeted for ablation if identifiable – An option for rare patients with recurrent polymorphic VT not due to acute ischemia / other treatable cause if frequent PVCs are present Post – Myocardial Infarction Scars provide a stable substrate for recurrent monomorphic VT repeated VT episodes occur over years VT is inducible at EP study Drug efficacy is disappointing – decreasing membrane currents is usually insufficient to block conduction and prevent reentry Catheter ablation to interrupt reentry pathways in areas of scar Challenges: Areas of scar are often large Reentry circuits can be large Multiple potential reentry circuits Multiple VTs Hemodynamically unstable VT Substrate guided ablation: mapping and ablation during stable sinus rhythm for VTs that are hemodynamically unstable Define Low Voltage Ventricular Scar Identify potential reentry circuit channels based on pace-mapping and electrogram characteristics Ablation of reentry circuit exits and channels in the scar RF Catheter Ablation Guided by Electroanatomic Mapping for Recurrent VT After Myocardial Infarction Stevenson et al Circulation 2008; 118: 2773 CAD - median LVEF 0.25 Frequent VT failing therapy - 11 episodes in prior 6 months Characteristics of induced VTs in 231 patients: median of 3 VTs/patient Both Mappable and Unmappable* 38% Mappable Only 31% Unmappable* Only 31% 53% achieved primary endpoint: at 6 months no VT, or absence of recurrence of incessant VT Catheter Ablation Reduces VT Recurrences 6 months pre - ablation 6 months post - ablation N = 142 Median 11.5 VT episodes Median 0 P < 0.0001 >100 80 60 40 20 0 20 40 60 80 >100 Number of VT Events Stevenson et al Circulation 2008 Procedure Complications Thermocool Investigators, Circulation. 2008;118:2773. Death 7 Perforation / MI 1 Uncontrollable VT 6 Non-fatal serious complications 27 in 24 pts Stroke / peripheral embolism 0 Heart Failure 6 Increase in mitral regurgitation 1 Femoral bleeding / pseudoaneurysm Others (hematuria, HIT, sepsis, pericarditis, anemia, incessant VT) 7/4 9 3% 7.3% Ablation for VT late after Myocardial Infarction Reduces ICD therapies in > 70% of patients – Mortality 3% • Most due to uncontrollable VT when the procedure fails – Stroke 0 - 2.7% – Vascular complications: 10% • Femoral hematomas, pseudoaneurysms Catheter ablation has been largely used only after failure of antiarrhythmic drugs to control recurrent VT Does early use of ablation improve outcomes? – Lower risk of complications in less sick patients? – Improve quality of life? – Reduce heart failure hospitalizations? – Extend surviva? VTACH study – Kuck et al Lancet 2010 Randomized trial of ablation after first hemodynamically tolerated VT post MI Primary endpoint – time to recurrent VT Survival free from cardiac hospitalization Ablation reduced recurrent VT Ablation reduced hospitalizations Median time to recurrent VT: Ablation - 18.6 months Control - 5.9 months VTACH study Kuck et al Lancet 2010 Ablation Control p SMASH VT: Is there benefit to prophylactic VT ablation after one episode for ICD recipients with prior MI? Reddy et al NEJM 2007 133 patients having ICD placed for VT Randomized to substrate - guided ablation vs no ablation Survival Primary End Point: Survival Free from ICD Therapy Substrate guided ablation: - Reduced VT - No impact on mortality - No negative impact on LV function on serial echocardiograms Procedure Complications in Early Use of VT Ablation Procedure Death Major Complication Vtach Trial N = 52 Smash VT N=64 0 0 2 /52 3/64 1- Myocardial Ischemia 1 Pericardial effusion 1 - TIA 1 – deep venous thrombosus 1 – Heart Failure exacerbation SMASH VT - no impact of VT ablation on LV function Reddy et al NEJM 2007 Effect of Substrate Ablation on Ventricular Function Reddy V et al. N Engl J Med 2007;357:2657-2665 Disclosures: None Indications for Catheter Ablation of VT: Patients with structural heart disease (including prior MI, dilated cardiomyopathy, ARVC/D) Recommended: 1. for symptomatic sustained monomorphic VT (SMVT), including VT terminated by an ICD, that recurs despite drug therapy or when drugs are not tolerated or not desired; 2. for control of incessant SMVT or VT storm that is not due to a transient reversible cause; Indications for Catheter Ablation of VT in Patients with structural heart disease (including prior MI, dilated cardiomyopathy, ARVC/D) Should be considered: 1. one or more episodes of SMVT despite therapy with one or more AADs 2. recurrent SMVT due to prior MI with LV ejection fraction >.0.30 and expectation for 1 year of survival; ablation is an acceptable alternative to amiodarone therapy 3. For haemodynamically tolerated SMVT due to prior MI with reasonably preserved LV ejection fraction (>.0.35) even if AADs have not failed There was consensus among the task force members that catheter ablation for VT should generally be considered early in the treatment of patients with recurrent VT. Heart Rhythm. 2009;6(6):886-933. Europace. 2009;11(6):771-817. Preventive Therapy for VT: An Individualized Approach to Selecting Therapy Catheter Ablation Drug Therapy Skilled operator required Easy to implement Procedure risks Amiodarone reduces VT Can reduce / prevent VT without ongoing toxicities but has toxicities requring monitoring - Sotalol less effective Potential ICD / drug interactions Catheter Ablation before Antiarrhythmic Drug An Individualized Approach Catheter Ablation Favored Drug Therapy Favored Monomorphic VT Polymorphic VT Experienced Center Experienced center Available Acceptable procedure risk Incessant or very frequent VT Increased risk for drug toxicities Not available Increased procedure risk Patient preference Thank You VT Ablation Should be Considered Early in the Course of Patients with Spontaneous VT Episodes of VT causing shocks decrease quality of life and may contribute to mortality Ablation risks are acceptable – No increase in mortality in SMASH VT Consensus of the EHRA/HRS Scientific Statement on Catheter Ablation of VT SMASH VT - depressed LV function with “first episode of VT/VF” Reddy et al NEJM 2007 Ablation Control 67 66 92% 81% VF 20% 16% VT 47% 52% Syncope + EPS 17% 25% Recent VT/VF with ICD 16% 8% LVEF 0.31 0.33 Beta-bl 94% 98% Age (yrs) Male Index arrhythmia SCD-HeFT: Spontaneous VT predicts Increased Risk of Death Shock Type Hazard Ratio 1 appropriate vs. none 5.68 (3.97-8.12) p <0.001 Risk of Death ≈ 6 times increase 1 inappropriate vs. none 1.98 (1.29-3.05) p =0.002 ≈ 2 times increase Both shock types vs. none 11.27 (6.70-18.94) p <0.001 ≈ 11 times increase Patients who receive a shock for VT or VF had a 1 year mortality > 20% with a median time to death of 6 – 7 months Poole J. N Eng J Med 2008;359:1009-1017 VT – an ICD is not enough? VT / VF are markers for increased mortality in patients with ICDs – After an ICD detects an episode of VT or VF 1 year mortality exceeds 20% with a median time to death of < 7 months SCD-HeFT Poole J et al. NEJM 2008;359:1009 Implications: – Ongoing ventricular remodeling? – Myocardial ischemia? – Hemodynamic deterioration Scars and VT – the future Anatomic characterization of scars to predict VT risk Modification of scars to treat arrhythmias – Pharmacologic therapies – Ablation – Biologic therapies Antiarrhythmic Proarrhythmic Mortality After VT Ablation Data are largely from a severely ill population – Prior MI – Depressed LV function, frequent heart failure Mortality after ablation is consistent with: – Severity of disease – Recurrent VT is a marker for increased mortality A focus on safety remains appropriate Clinical trials are needed to clarify the impact of ablation on mortality Ablation Efficacy and Outcomes Vary with heart disease – but there is limited data for comparison Prevents All VT Reduces VT recurrences Prospective multicenter data with > 50 pts Myocardial Infarct 49 – 84% >70% Yes Dilated Cardiomyopathy 32 – 64% Often No Sarcoidosis 38 – 56% In some pts No Tetralogy of Fallot >70% No ARVC 25% - 84% Often No HCM Reported Reported No