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The Case for Rate Control: In the Management of Atrial Fibrillation Charles W. Clogston, M.D. Cardiologist CHI St. Vincent Heart Clinic Arkansas April 25, 2015 Atrial Fibrillation • Atrial Fibrillation is the most common sustained arrhythmia • Associated with increased mortality (1.5-1.9 by Framingham Study) • Associated with increased morbidity (both in stroke and limiting symptoms) Atrial Fibrillation Consequences • Deterioration in hemodynamics (due to increased HR and loss of AV synchrony) • Increased risk of stroke secondary to left atrial thrombi • Progressive dysfunction of the left atrium and left ventricle Goals of Therapy in Atrial Fibrillation • Symptom Control Improved by both rhythm and rate control • Prevention of thromboembolism Achieved with anticoagulation with warfarin or newer novel anticoagulants Management Strategies for Atrial Fibrillation • Rhythm Control -- uses antiarrhythmic drug therapy, radiofrequency catheter ablation and/or surgical (Maze) ablation therapy at time of open heart surgery. Still requires rate slowing drugs. • Rate Control – uses drugs that block or slow conduction thru the AV-node such as beta blockers, non-dihydropyridine calcium channel blockers or digoxin. AV-node ablation with ventricular pacing may be used when drugs are ineffective. • Both therapies require anticoagulation to prevent thromboembolism. Thromboembolic Risk with Atrial Fibrillation • Thromboembolism is the most important adverse outcome. • Maintaining NSR does not reduce the frequency despite cardioversion and antiarrhythmic drugs recurrence rate is 3560% at one year by intermittent monitoring and as much as 88% by continuous monitoring for more than 18 months. Thromboembolic Risk with Atrial Fibrillation • Up to 90% of recurrences are asymptomatic • 17% of asymptomatic events last >48 hours In a study of pacemakers for arrhythmia detection in patients with no history of AF, AF duration of >5 min. increased risk of thromboembolism >6 fold compared with patients with similar CHADS2 scores and no AF. Risk factor-based point-based scoring system - CHA2DS2-VASc Risk Factor Score Congestive Heart Failure/ LV Dysfunction 1 Hypertension 1 Age ≥ 75 years 2 Diabetes Mellitus 1 Stroke/ TIA/ Thrombo-embolism 2 Vascular Disease* 1 Age 65-74 1 Sex Category (i.e. female sex) 1 Maximum Score 9 Adjusted stroke rate according to CHA2DS2-VASc score Approach to Anticoagulation in AF Presumed Benefits of Maintaining NSR • Fewer symptoms/better exercise tolerance • Lower risk of stroke • Long-term anticoagulation may not be needed if sinus rhythm is successfully maintained • Better quality of life • Better survival Trials of Rate vs Rhythm Control AFFIRM Baseline Characteristics • Age = 69.7 ± 9 years • 39% female • >2 days of AF in 69% • CHF class > II in 9% • Symptomatic AF in 88% Studies Comparing Rate and Rhythm Control • AFFIRM • Randomized 4060 patients with recurrent AF • Goal for rate control of VR<80 bpm at rest and <110 bpm with 6 minute walk test • Both received anticoagulation but rhythm control could remove if patient maintained NSR. (82 and 63% of patients at 1 and 5 years) AFFIRM Cross Over Rates • Cross over to Rate Control arm occurred in 17 and 38% of patients in Rhythm Control arm at 1 and 5 years due to inability to maintain NSR or drug intolerance. • Cross over to Rhythm Control arm occurred in 8 and 15% in Rate Control arm due to failure to control symptoms or CHF. AFFIRM Findings • At 3.5 years there was almost a significant decrease in all cause mortality (primary endpoint) in rate control arm • There was no significant difference in the composite secondary endpoint of death, ischemic stroke, anoxic encephalopathy, major bleeding or cardiac arrest • There was no significant difference in global functional status or quality of life in the initial report • Number of patients requiring hospitalization was lower in the Rate Control arm (73 vs 80%) RACE Trial Rate Control versus Electrical Cardioversion for Persistent Atrial Fibrillation Study • Similar to AFFIRM but • Enrolled only patients with persistent atrial fibrillation who had been cardioverted at least once prior to enrollment and were in recurrent atrial fibrillation • Primary end point was a composite of cardiovascular death, heart failure, thromboembolism, bleeding, pacemaker insertion, or severe side effects of antiarrhythmic drugs Rate Control versus Electrical Cardioversion for Persistent Atrial Fibrillation (RACE) Trial (n=522) AF-CHF Results • No difference in primary endpoint of CV death between groups (Figure) • Cardioversion 39% vs 8% • Also no difference in total mortality (31.8% vs. 32.9%, p = 0.73), stroke (2.6% vs. 3.6%, p = 0.32), worsening heart failure (27.6% vs. 30.8%, p = 0.17), or composite (42.7% vs. 45.8%, p = 0.20) • Higher hospitalization rates (46% vs 39% p=.006) and cost with rhythm control • Bradyarrhythmias ↑ in rhythm control group Cost Effectiveness of Rate Control over Rhythm Control • AFFIRM Trial Cost Effectiveness Analysis • Patients in the rate-control group used fewer resources, such as hospital days, cardioversions, and emergency department visits • Estimated cost savings per patient treated with rate control ranged from $2189 to $5481 per person Conclusions Ventricular rate control is equally (or more) effective than rhythm control in terms of survival, quality of life and other end points Current antiarrhythmics have a relatively low efficacy while having significant cardiac and noncardiac side effects compared with rate control agents There are significant cost savings with rate control compared with rhythm control