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Slide 1-

Practical Rate and Rhythm Management of Atrial Fibrillation New Paradigm in Managing Atrial Fibrillation: A Campaign to Promote Optimal Patient Care Slide set developed by: Michael C. Delaughter, MD, PHD: EP-Cardiology PA Michael Eifling, MD: Texas Heart Institute at St. Luke’s Episcopal Hospital and Baylor University Rohit Mehta, MD: Sanger Heart and Vascular Institute
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Management Principles of AF 2 Cornerstones of AF Management Control of symptoms Rate Control Anticoagulation Rhythm Control Therapeutic Goals Control of symptoms Treatment or prevention of Tachycardia Induced Cardiomyopathy (CMP) Reduction in Hospitalizations Reduction in Hospitalizations Prevention of thromboembolism Minimization of bleeding risk
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Rate versus Rhythm Control for AF The AFFIRM, RACE and AF-CHF trials have shown no mortality benefit from a rhythm control strategy compared to a rate control strategy. Therefore, a rate control strategy, without attempts at restoration or maintenance of sinus rhythm (SR), is reasonable in some patients with AF, especially those who are elderly and asymptomatic. If rate control offers inadequate symptomatic relief, restoration of SR may become a long-term goal. Restoration and maintenance of SR continues to be a reasonable treatment approach in many patients with AF. 3 Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed.
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Ventricular Rate Control Principles of a Rate Control Strategy: Adequate control of the ventricular response during AF can significantly improve symptoms and is critical to avoid tachycardia-mediated cardiomyopathy. Most patients managed using a rhythm control strategy also require medications for rate control. Rate control during atrial flutter tends to be more difficult than during AF. What is Adequate Rate Control? Control of the ventricular rate during AF is important both at rest and with exertion. No standard method for assessment of heart rate control has been established. Criteria for rate control vary with patient age but usually involve achieving ventricular rates between 60 and 80 bpm at rest and between 90 and 115 bpm during moderate exercise. For the AFFIRM trial, adequate control was defined as an average HR up to 80 bpm at rest and either an average rate up to 100 bpm during Holter monitoring with no rate above 100% of the maximum age-adjusted predicted exercise HR, or a maximum HR of 110 bpm during a 6-min walk test. In the RACE trial, rate control was defined as less than 100 bpm at rest. Only about 5%of patients from these trials required AV ablation to achieve HR control. 4 Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed.
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Ventricular Rate Control: Drugs to Control the Ventricular Response Beta blockers are the most effective drug class for rate control. Calcium channel antagonists (nondihydropyridine) are good choices for patients with asthma or COPD requiring beta agonist inhaler therapy. Digoxin provides relatively poor rate control during exertion and should be reserved for patients with systolic HF. Digoxin does not convert AF to SR and may perpetuate AF. Digoxin is marginally effective as a sole agent, but may prove useful in combination with beta blocker or calcium channel antagonists, particularly in hypotensive patients. 5 Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed. with modifications.
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Ventricular Rate Control: Drugs to Control the Ventricular Response A combination of a beta blocker and either a calcium channel antagonist or digoxin may be needed to control the HR. The choice of medication should be individualized and the dose modulated to avoid bradycardia. Beta blockers and calcium channel antagonists should be used cautiously in patients with HF. AV nodal blocking drugs at doses required to control the ventricular response can cause symptomatic bradycardia that requires pacemaker therapy. 6 Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed.
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Ventricular Rate Control: Drugs to Control the Ventricular Response Some antiarrhythmic drugs that are used to maintain sinus rhythm, such as sotalol, dronedarone, and amiodarone, also provide some control of the ventricular response when patients are in AF. Amiodarone should rarely be used for rate control because of its potential for toxicity. IV digoxin or nondihydropyridine calcium channel antagonists given to patients with AF and WPW may accelerate the ventricular response and are not recommended. 7 Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed.
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Ventricular Rate Control: AV Nodal Ablation Ablation of the AV conduction system and permanent pacing (the “ablate and pace” strategy) is an option for patients who have rapid ventricular rates despite maximum medical therapy and often yields remarkable symptomatic relief. There is growing concern about the negative effects of long-term RV pacing. Biventricular pacing, on the other hand, may overcome many of the adverse hemodynamic effects associated with RV pacing and is preferred when systolic dysfunction is present. Catheter ablation of the AV node should not be attempted without a prior trial of medication to control the rate. 8 Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed. with modifications.
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CHADS2 Risk Stratification Scheme Rockson et al. J Am Coll Cardiol. 2004;43:929-935.
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Maintenance of Sinus Rhythm: Principles of Antiarrhythmic Drug Therapy AF is a chronic disorder and is likely to recur in most patients without antiarrhythmic drugs (AADs). Pharmacological therapy is indicated in patients who can tolerate AADs and who have a reasonable chance to maintain sinus rhythm. Pharmacological therapy is indicated to suppress symptoms, improve exercise capacity, improve hemodynamic function, and prevent tachycardia-induced cardiomyopathy. The risk of stroke may not be reduced by suppression of AF. Before administering an antiarrhythmic drug, precipitants of AF such as hypertension, valve disease, CHF, hyperthyroidism, and OSA should be identified and corrected. Antiarrhythmic drug (AAD) choice is based on side-effect profiles and presence of structural heart disease, heart failure, or hypertension. Drug choice should be individualized and account for underlying renal and hepatic function. Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed.
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Maintenance of Sinus Rhythm: Principles of Antiarrhythmic Drug Therapy Drugs should be used to decrease the frequency and duration of episodes, and to improve symptoms. AF recurrence without symptoms is not indicative of treatment failure and does not necessitate a change in AAD therapy. An AAD should be abandoned when it does not result in symptomatic improvement or causes adverse events. Ensure normal electrolyte status and appropriate anticoagulation prior to starting antiarrhythmic drug therapy. Initiate AV nodal blockade prior to the use of antiarrhythmics such as flecainide that do not provide substantial AV node blockade. Initiate therapy at a low dose and titrate up as needed and after evaluating drug effects on ECG parameters. Knight, et al, Practical Rate and Rhythm Management of Atrial Fibrillation, January 2010 ed.
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ACC/AHA/ESC Guidelines Maintenance of Sinus Rhythm in Specific Patient Populations 12 Maintenance of Sinus Rhythm No (or minimal) Heart Disease Hypertension Coronary Artery Disease Heart Failure Flecainide PropafenoneSotalol Dofetilide Sotalol AmiodaroneDofetilide Substantial LVH No Yes AmiodaroneDofetilide CatheterAblation CatheterAblation Amiodarone CatheterAblation Amiodarone CatheterAblation AmiodaroneDofetilide Flecainide PropafenoneSotalol CatheterAblation Calkins et al. HeartRhythm 2007 HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation; 4: 1-46
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Maintenance of Sinus Rhythm in Specific Patient Populations Suggested Scheme Including Dronedarone 13 Maintenance of Sinus Rhythm No (or minimal) Heart Disease Hypertension Coronary Artery Disease Heart Failure Flecainide Propafenone Sotalol Dronedarone Dofetilide Sotalol Dronedarone AmiodaroneDofetilide Substantial LVH No Yes Amiodarone Dofetilide CatheterAblation CatheterAblation Amiodarone CatheterAblation AmiodaroneDronedarone CatheterAblation Amiodarone Dofetilide Flecainide Propafenone Sotalol Dronedarone Catheter Ablation Abbreviation: LVH, left ventricular hypertrophy. Modified from Fuster, V. et al. J. Am. Coll. Cardiol. 48, e149–e246 (2006).
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Rationale for Initial Trial of Medical Therapy The relative safety and efficacy of ablation vs. antiarrhythmic drugs has not been firmly established but large randomized trials are ongoing Ablation: Complication rate: 5.9% Single-procedure success rate without AADs: 57% Multiple-procedure success rate without AADs: 71% Multiple-procedure success rate with AADs: 77% AAD Therapy: Adverse event rate: 30% (common but less severe) Success rate: 52% Calkins et al. CircEP. 2009;2:349-361.
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Atrial Fibrillation Ablation Candidates Symptomatic Paroxysmal or Persistent Atrial Fibrillation Second-line Therapy Failure of Class IC or Class III agent Intolerance to Medical Therapy, Refusal of Medical Therapy Other Considerations: Young patients with paroxysmal atrial fibrillation, in whom decades-long drug therapy is undesirable Congestive Heart Failure due to tachycardia-induced cardiomyopathy, in whom drug choices are limited by the presence of CHF
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Atrial Fibrillation Ablation Candidates Limitations in Efficacy Longstanding Persistent Atrial Fibrillation (>1 year) Enlarged LA (>55 mm) Age > 70 years Left atrial or Left atrial appendage thrombus is an absolute contraindication to atrial fibrillation ablation. 16 Calkins et al. HeartRhythm 2007 HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation; 4: 1-46
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Atrial Fibrillation Ablation Outcomes Definition of success includes: Freedom from symptomatic atrial fibrillation Freedom from all atrial fibrillation Facilitation of antiarrhythmic therapy Eradication of anticoagulant therapy Duration of Success: Freedom from atrial fibrillation at one year Freedom from late atrial fibrillation Most common accepted success definition Freedom from atrial fibrillation off antiarrhythmic therapy at one year Late recurrences: greater than 12 months Calkins et al. HeartRhythm 2007; HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation; 4: 1-46
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Atrial Fibrillation Ablation Outcomes Blanking period of 2 months post ablation Early recurrence of AF events termed “early events” Minimum of symptomatic monitoring Suggested asymptomatic surveillance at 6 month intervals 30 day auto-triggered monitors Symptom triggered event monitors with weekly asymptomatic transmissions 24-72 hour Holter monitoring. Calkins et al. HeartRhythm 2007; HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation; 4: 1-46
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Atrial Fibrillation Ablation Outcomes Paroyxsmal 70-80% success at freedom from atrial fibrillation at one year off anti-arrhythmic therapy. 30% of patients required 2 procedures to achieve this result. Most utilized pure-pulmonary vein isolation approach Persistent Similar success rates in persistent patients with similar end-point and need for repeat procedure More commonly requires substrate modification (targeting of CFAE) and linear ablation Long-Standing Persistent Utilizing stepwise approach (PV isolation Linear ablation CFAE), some studies have demonstrated 70-80% freedom from atrial fibrillation at one year off anti-arrhythmic therapy Calkins et al. HeartRhythm 2007; HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation; 4: 1-46
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Atrial Fibrillation Ablation Outcomes Randomized Trials: Paroxysmal Atrial Fibrillation (Flecainide or Sotalol vs Ablation) One year freedom from atrial fibrillation (AF) 37% freedom from AF in anti-arrhythmic arm 87% freedom from AF in ablation arm Persistent Atrial Fibrillation (Ablation vs. Cardioversion) One year freedom from AF or atrial flutter 74% freedom from AF in ablation arm 58% freedom from AF in cardioversion arm Calkins et al. HeartRhythm 2007; HRS/EHRA/ECAS Expert Consensus Statement on Catheter and Surgical Ablation of Atrial Fibrillation; 4: 1-46
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Atrial Fibrillation Ablation Outcomes Randomized Trials: Paroxysmal or Persistent Atrial Fibrillation One year freedom from AF (ablation vs. anti-arrhythmic (AA) drug) 9% freedom from AF in the AA arm 56% freedom from AF in the ablation arm Paroxysmal Atrial Fibrillation One year freedom from AF (ablation vs anti-arrhythmic (AA) drug) 22% freedom from AF in AA arm 86% freedom from AF in ablation arm Stabile et al. European Heart Journal 2006; 27: 216-221
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Atrial Fibrillation Ablation Outcomes Paroxysmal Atrial Fibrillation One year freedom from AF (ablation vs anti-arrhythmic (AA) drug) 22% freedom from AF in AA arm 86% freedom from AF in ablation arm Paroxysmal and Persistent Atrial Fibrillation One year freedom from AF (ablation vs. anti-arrhythmic (AA) drug) 7% freedom from AF in AA arm 75% freedom from AF in ablation arm 63% of AA treated patients crossed over Stabile et al. European Heart Journal 2006; 27: 216-221
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Final Summary for AF Ablation Identifying appropriate ablation candidates Failing medical therapy Refusing medical therapy Need for symptoms Young patients Differences in approach for paroxysmal and persistent patients Lesion set Utility of isuprel post ablation Likelihood of recurrence / need for additional procedures (see Cappato, Circulation, AF registry outcomes paper) Definition of success / likelihood of success Managing atypical flutter / need for confirmation of block across lines Surgical based ablation Relative efficacy vs. catheter based Rationale / benefit of appendage ligation / resection Cox III – the “gold standard” Efficacy of other lesion sets, modalities (bipolar RF, cryo, HIFU) vs. Cox