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Journal of the American College of Cardiology Vol. 34, No. 2, 1999 1999 by the American College of Cardiology ISSN 0735-1097/99/$20.00 Published by Elsevier Science Inc. PII S0735-1097(99)00234-X CLINICAL STUDIES Beta-Blocker Use and Survival in Patients With Ventricular Fibrillation or Symptomatic Ventricular Tachycardia: The Antiarrhythmics Versus Implantable Defibrillators (AVID) Trial Arrhythmias Derek V. Exner, MD, MPH,* James A. Reiffel, MD, FACC, Andrew E. Epstein, MD, FACC, Robert Ledingham, MS, Michael J. Reiter, MD, PHD, FACC, Qing Yao, PHD, Henry J. Duff, MD, Dean Follmann, PHD,* Eleanor Schron, RN,* H. Leon Greene, MD, FACC, Mark D. Carlson, MD, FACC, Michael A. Brodsky, MD, FACC, Toshio Akiyama, MD, FACC, Christina Baessler, MSN, Jeffrey L. Anderson, MD, FACC, and the AVID Investigators Bethesda, Maryland and Seattle, Washington OBJECTIVES BACKGROUND METHODS RESULTS CONCLUSIONS To evaluate whether use of beta-adrenergic blocking agents, alone or in combination with specific antiarrhythmic therapy, is associated with improved survival in persons with ventricular fibrillation (VF) or symptomatic ventricular tachycardia (VT). The ability of beta-blockers to alter the mortality of patients with VF or VT receiving contemporary medical management is not well defined. Survival of 1,016 randomized and 2,101 eligible, nonrandomized patients with VF or symptomatic VT followed in the Antiarrhythmics Versus Implantable Defibrillators (AVID) trial through December 31, 1996 was assessed using Cox proportional hazards analysis. The 817 (28%) patients discharged from hospital receiving beta-blockers had less ventricular dysfunction, fewer symptoms of heart failure and a different pattern of medication use compared with patients not receiving beta-blockers. Before adjustment for important prognostic variables, beta-blockade was not significantly associated with survival in randomized or in eligible, nonrandomized patients treated with specific antiarrhythmic therapy. After adjustment, beta-blockade remained unrelated to survival in randomized or in eligible, nonrandomized patients treated with amiodarone alone (n 1142; adjusted relative risk [RR] 0.96; 95% confidence interval [CI] 0.64 1.45; p 0.85) or a defibrillator alone (n 1347; adjusted RR 0.88; 95% CI 0.55 to 1.40; p 0.58). In contrast, beta-blockade was independently associated with improved survival in eligible, nonrandomized patients who were not treated with specific antiarrhythmic therapy (n 412; adjusted RR 0.47; 95% CI 0.25 to 0.88; p 0.018). Beta-blocker use was independently associated with improved survival in patients with VF or symptomatic VT who were not treated with specific antiarrhythmic therapy, but a protective effect was not prominent in patients already receiving amiodarone or a defibrillator. (J Am Coll Cardiol 1999;34:325 33) 1999 by the American College of Cardiology Beta-adrenergic blocking agents have been shown to reduce the incidence of sudden death and total mortality in patients with a recent myocardial infarction (MI) (1,2) and in patients with symptomatic heart failure (3 5). Furthermore, From the *National Heart, Lung, and Blood Institute, Bethesda, Maryland; the University of Washington, Seattle, Washington; and the Antiarrythmics Versus Implantable Defribillators (AVID) clinical sites. This study was supported by a contract (N01 HC-25117) with the National Heart, Lung, and Blood Institute. Dr. Exner is a Clinician-Scientist (phase I) of the Medical Research Council of Canada and Research Fellow of the Alberta Heritage Foundation for Medical Research. See reference 15 for a listing of AVID investigators and sites. Manuscript received October 5, 1998; revised manuscript received February 23, 1999, accepted April 30, 1999. beta-blockers have been advocated for use in patients with ventricular fibrillation (VF) and ventricular tachycardia (VT), in whom these agents appear to reduce the incidence of recurrent ventricular tachyarrhythmias (6,7). Although beta-blockade has been associated with a reduced risk of death for patients with VF and VT (8,9), the ability of these agents to alter survival in patients receiving contemporary medical therapy is not known. Post hoc analyses from two high-risk, post-mi trials have indicated that patients receiving amiodarone and a betablocker are at a substantially (30% to 72%) lower risk of death compared with patients treated with amiodarone alone (10 14). Whether beta-blockers alter the survival of

326 Exner et al. JACC Vol. 34, No. 2, 1999 Beta-blockers and Survival in AVID August 1999:325 33 Abbreviations and Acronyms ACE angiotensin-converting enzyme AVID Antiarrhythmics Versus Implantable Defibrillators CAMIAT Canadian Amiodarone Myocardial Infarction Arrhythmia Trial EMIAT European Myocardial Infarct Amiodarone Trial CI confidence interval ICD implantable cardioverter defibrillator LV left ventricular MI myocardial infarction NYHA New York Heart Association RR relative risk VF ventricular fibrillation VT ventricular tachycardia patients with VF or VT treated with amiodarone is uncertain. Likewise, the capacity of beta-blockers to alter the mortality of patients with these arrhythmias, who have already received an implantable cardioverter defibrillator (ICD), has not been fully investigated. The Antiarrhythmics Versus Implantable Defibrillators (AVID) trial evaluated the mortality difference of antiarrhythmic drugs versus ICD therapy in patients with VF or symptomatic VT. The AVID trial was terminated early due to improved survival in patients randomized to ICD therapy (15). Although these results are compelling, the more frequent use of beta-blockers in ICD-treated patients has led some authors to question the superiority of ICD therapy (16). This analysis evaluated the association of beta-blocker use, alone and in combination with amiodarone or an ICD, with survival in AVID patients with VF or symptomatic VT. METHODS Figure 1. The 2,901 persons in the present analysis included 970 randomized and 1,931 eligible, nonrandomized patients discharged from hospital with amiodarone alone, an ICD alone or neither of these therapies. Numbers of patients within each treatment strategy are shown in parentheses. Definitions. For the purpose of this analysis, symptomatic VT was defined as VT with syncope or VT with hemodynamic compromise and a left ventricular (LV) ejection fraction 0.40. Patients presenting with VF or symptomatic VT were eligible for randomization, whereas those already receiving amiodarone, with ventricular arrhythmias secondary to a correctable cause, a limited life expectancy, New York Heart Association (NYHA) class IV symptoms or contraindications to amiodarone or ICD therapy were not eligible for randomization (17 19). Study population (Fig. 1). The AVID registry included patients enrolled in the randomized trial (15) and patients screened, but not randomized (17 19). There were 3,117 registry patients with VF or symptomatic VT as their index arrhythmia, 2,901 (93%) of whom were discharged from hospital with aminodarone alone, an ICD alone or neither of these therapies. Survival of the 970 randomized and 1,931 eligible, nonrandomized patients with VF or symptomatic VT who received one of these three treatment strategies, and thus were included in the present analysis, was determined using the National Death Index, as of December 31, 1996. Beta-blocker use. Beta-blocker use was defined at the time of hospital discharge. Randomized patients had betablocker use reevaluated quarterly. Information on the specific agents and doses used were collected for all 284 randomized patients prescribed beta-blockers at any time during the course of the trial. Reasons for beta-blocker use were ascertained for all 220 randomized patients who were first prescribed beta-blockers after their index arrhythmia. Statistical analysis. Continuous baseline characteristics are presented as mean SD. Univariate comparisons were made using analysis of variance or the chi-square test. Pair-wise comparisons were made using a Student t test or chi-square test. All-cause mortality was the primary end point of this analysis. Deaths in randomized patients were further classified as cardiac or noncardiac (20), and cause-specific mortality rates were compared using the log-rank test statistic. The composite end point of death or recurrent arrhythmia (21,22) was also evaluated in randomized patients. Stratification by history of MI (23) and index arrhythmia (23) was performed in the combined groups of amiodarone-treated and ICD-treated patients. Amiodarone-treated patients were stratified by heart rate ( 70 vs. 70 beats/min) at the time of hospital discharge (12 14). Cox proportional hazards models were used to evaluate the univariate (unadjusted) and multivariate (adjusted) association of beta-blockers with survival. The prespecified multivariate model included beta-blocker use, age, gender, race, index arrhythmia, history of heart failure,

JACC Vol. 34, No. 2, 1999 August 1999:325 33 Exner et al. Beta-blockers and Survival in AVID 327 Table 1. Characteristics of Randomized Patients, by Use of Beta-blockers Characteristic Betablocker Amiodarone No Betablocker Betablocker Defibrillator No Betablocker Number 77 407 203 283 Age (yrs) 65 11 65 10 64 11 65 11 Male 88% 79% 82% 74% Non-white race 14% 15% 11% 14% Moderate-severe left 63% 73% 58% 76% ventricular dysfunction Heart rate (beats/min) 66 13 69 12 73 12 79 14 Systolic BP (mm Hg) 125 19 121 17 121 18 121 18 Ventricular fibrillation 44% 45% 45% 44% History of Myocardial infarction 73% 66% 70% 63% Hypertension 60% 55% 55% 56% Diabetes 27% 23% 23% 26% Heart failure 34%* 50% 36% 52% Medication use ACE inhibitor 60%* 71% 62% 73% Digoxin 32% 44% 37% 53% Calcium blocker 17% 12% 12% 22% Aspirin 62% 58% 68% 56% Warfarin 31% 34% 19% 19% Diuretic 37% 55% 36% 57% Sotalol 0% 0% 0% 1% Other antiarrhythmic 1% 2% 3% 7% Revascularization Before index arrhythmia 44% 34% 34% 36% After index arrhythmia 10% 12% 12% 9% *p 0.05; p 0.01 or p 0.001 for beta-blocker vs. no beta-blocker. ACE angiotensin-converting enzyme; BP blood pressure. ejection fraction, heart rate at hospital discharge and any relevant baseline differences between patients receiving, versus those not receiving, beta-blockers. The Cox models were used to determine relative risk (RR) estimates and 95% confidence intervals (CI). Analyses were performed using SIR (Scientific Information Retrieval Inc., New South Wales, Australia), SPSS 6.1 (SPSS Inc., Chicago, Illinois) and Stata Release 5.0 (Stata Corporation, College Park, Texas) statistical software. RESULTS Characteristics and beta-blocker use, randomized patients. Patients discharged receiving beta-blockers had fewer symptoms of heart failure and were less likely to be prescribed a diuretic or angiotensin-converting enzyme (ACE) inhibitor compared with those not receiving betablockers (Table 1). Patients receiving an ICD and betablocker had less LV dysfunction, slower mean heart rates at hospital discharge and were less likely to be prescribed digoxin or a calcium channel blocker, but more likely to be prescribed aspirin compared with those receiving an ICD alone. Despite the encouraged use of beta-blockers in all patients in whom they were clinically indicated, amiodaronetreated patients were less likely to be discharged receiving a beta-blocker (16%) compared with ICD-treated patients (42%; p 0.001). Similarly, the use of beta-blockers at any time during follow-up was less frequent in amiodaronetreated patients (23% vs. 56% in ICD-treated patients; p 0.001). Information on beta-blocker use at one year was available for 62 amiodarone-treated and 186 ICD-treated patients. At one year, 65% of amiodarone-treated and 81% of ICD-treated patients discharged receiving a beta-blocker continued to take these agents. Reasons for use of beta-blockers, agents and doses, randomized patients. Beta-blockers were most commonly prescribed after the index arrhythmia for the ventricular arrhythmia itself or the presence of coronary artery disease. A greater proportion of ICD-treated patients received beta-blockers for supraventricular arrhythmias or sinus tachycardia, whereas a greater proportion of amiodaronetreated patients received beta-blockers for hypertension (Table 2). Most of the 284 randomized patients receiving betablockers during follow-up were prescribed metoprolol (n 180; 63%) or atenolol (n 74; 26%). Amiodarone and

328 Exner et al. JACC Vol. 34, No. 2, 1999 Beta-blockers and Survival in AVID August 1999:325 33 Table 2. Reasons for Beta-blocker Prescription, Randomized Patients After Their Index Arrhythmia (n 220) Reasons for Betablocker Use* Amiodarone (n 55) Defibrillator (n 165) Ventricular arrhythmia 47% 44% Coronary artery disease, 30% 29% prior myocardial infarction Coronary artery disease, 14% 16% angina Hypertension 22% 10% Supraventricular 2% 14% arrhythmia/sinus tachycardia Frequent defibrillator 0% 3% shocks Other reason 9% 4% *Multiple reasons were provided for 20% of amiodarone and 16% of defibrillator patients; p 0.05. ICD-treated patients received similar mean doses of metoprolol at the time of hospital discharge (68 mg vs. 71 mg per day, respectively; p 0.62), but amiodarone-treated patients tended to receive lower doses at one year of follow-up (61 mg vs. 80 mg per day for ICD-treated patients; p 0.07). Atenolol was prescribed at similar mean doses at the time of hospital discharge (40 mg vs. 48 mg daily, respectively; p 0.18) and at one year (34 mg vs. 47 mg daily, respectively; p 0.15). The remaining 30 (11%) patients received propranolol, another nonselective agent or acebutolol. Characteristics and beta-blocker use, eligible, nonrandomized patients. Among the three treatment groups, those receiving amiodarone were older and had slower mean heart rates at the time of hospital discharge (Table 3). Amiodarone-treated patients were also less likely to have had VF as their index arrhythmia, more likely to have a history of heart failure and more likely to be prescribed warfarin or a diuretic. The ICD-treated patients were more often white and less likely to have a history of hypertension, compared with the other two groups. Otherwise untreated patients had less LV dysfunction and were less likely to have a history of MI compared with those treated with amiodarone or an ICD. Untreated patients were also less likely to be prescribed an ACE inhibitor, but more likely to receive sotalol or another antiarrhythmic drug, and more likely to have undergone a coronary artery bypass or coronary artery angioplasty procedure after their index arrhythmia, compared with patients treated with amiodarone or an ICD. Amiodarone-treated patients were less likely to be prescribed beta-blockers at the time of hospital discharge (16%) Table 3. Characteristics of Eligible, Nonrandomized Patients Characteristic Amiodarone Defibrillator Neither Number 658 861 412 Age (yrs) 67 12* 62 13 63 12 Male 73% 75% 71% Non-white race 12% 6%* 10% Moderate-severe LV dysfunction 73% 65% 54%* Heart rate (bpm) 71 13 75 13 77 15 Systolic BP (mm Hg) 121 19 120 18 121 19 Ventricular fibrillation 41% 56% 51% History of Myocardial infarction 56% 57% 48%* Hypertension 54% 44% 53% Diabetes 24% 18% 20% Heart failure 51% 40% 33% Medication use Beta-blocker 16% 32% 40% ACE inhibitor 61% 57% 47% Digoxin 40% 43% 37% Calcium blocker 12% 14% 16% Aspirin 51% 56% 58% Warfarin 30% 23% 22% Diuretic 57% 45% 41% Sotalol 0% 6% 12% Other antiarrhythmic 5% 7% 17% Revascularization Before index arrhythmia 34% 38% 29% After index arrhythmia 9% 12% 33% *p 0.05; p 0.01 or p 0.001 for indicated group vs. the other groups. ACE angiotensin-converting enzyme; LV left ventricular; BP blood pressure.

JACC Vol. 34, No. 2, 1999 August 1999:325 33 Exner et al. Beta-blockers and Survival in AVID 329 Table 4. Characteristics of Eligible, Nonrandomized Patients, by Use of Beta-blockers Characteristic Amiodarone Defibrillator Neither BB No BB BB No BB BB No BB Number 110 548 255 586 152 260 Age (yrs) 64 12* 67 12 62 12 62 13 62 12 63 12 Male 80% 73% 79% 74% 75% 69% Non-white race 8%* 17% 6% 9% 10% 14% Moderate-severe 61% 76% 55% 70% 39% 63% LV dysfunction Heart rate (beats/min) 68 13* 72 13 72 13 77 13 75 14 77 15 Systolic BP (mm Hg) 121 17 121 19 120 18 119 17 121 18 119 20 Ventricular fibrillation 53%* 39% 61% 54% 57% 47% History of Myocardial infarction 56% 57% 60% 55% 47% 49% Hypertension 61%* 52% 52% 41% 60% 47% Diabetes 17% 25% 18% 18% 18% 22% Heart failure 30% 55% 28% 45% 20% 42% Medication use ACE inhibitor 46% 61% 53% 58% 40%* 48% Digoxin 34% 42% 27% 50% 28% 40% Calcium blocker 12% 13% 16% 14% 16% 16% Aspirin 66%* 49% 65% 51% 65%* 50% Warfarin 27% 30% 16% 25% 19% 23% Diuretic 39% 61% 31% 51% 33% 47% Sotalol 0% 0% 2% 8% 1% 18% Other antiarrhythmic 3% 6% 6% 8% 16% 19% Revascularization Before index arrhythmia 33% 26% 35% 35% 22% 30% After index arrhythmia 14% 8% 16%* 11% 44% 23% *p 0.05; p 0.01 or p 0.001 for beta-blocker vs. no beta-blocker in that group. ACE angiotensin-converting enzyme; BB beta-blocker; BP blood pressure; LV left ventricular. than ICD-treated patients (32%), who, in turn, were less likely to receive these agents compared with otherwise untreated patients (37%) (Table 3). Information regarding the beta-blockers used and their doses was not available for eligible, nonrandomized patients. Eligible, nonrandomized patients receiving betablockers had less LV dysfunction, were less likely to have a history of heart failure and were less likely to be prescribed a diuretic, but more likely to be prescribed aspirin compared with those not receiving beta-blockers (Table 4). Patients receiving amiodarone and a betablocker were younger on average, and more often white compared with those receiving amiodarone alone. Patients receiving amiodarone and a beta-blocker had slower mean heart rates, were more likely to have VF or a history of hypertension but less likely to be prescribed an ACE inhibitor compared with those receiving amiodarone alone. Patients receiving an ICD and beta-blocker had slower mean heart rates and were more likely to have a history of hypertension, but were less likely to receive digoxin, warfarin or sotalol compared with those receiving an ICD alone. Patients receiving an ICD and beta-blocker were also more likely to have undergone a revascularization procedure after their index arrhythmia compared with those receiving an ICD alone. Untreated patients receiving beta-blockers were more likely to have VF, but less likely to be prescribed an ACE inhibitor, digoxin or sotalol compared with patients not receiving amiodarone, an ICD or beta-blocker. Untreated patients receiving beta-blockers were also more likely to have undergone a revascularization procedure after their index arrhythmia compared with patients not receiving betablockers (Table 4). Unadjusted (univariate) survival. Beta-blocker use at the time of hospital discharge was not associated with survival in randomized amiodarone-treated (RR 0.88; 95% CI 0.48 to 1.61; p 0.67) or ICD-treated patients (RR 0.69; 95% CI 0.39 to 1.24; p 0.22). Beta-blockade was similarly not associated with survival in eligible, nonrandomized patients treated with amiodarone alone (RR 0.67; 95% CI 0.42 to 1.05; p 0.08) or an ICD alone (RR 0.59; 95% CI 0.32 to 1.12; p 0.10). In contrast, beta-blockade was associated with significantly improved survival in patients not treated with amiodarone or an ICD (RR 0.36; 0.21 to 0.64; p 0.0004). Modes of death, randomized patients (Table 5). Most deaths in randomized patients were classified as cardiac.

330 Exner et al. JACC Vol. 34, No. 2, 1999 Beta-blockers and Survival in AVID August 1999:325 33 Table 5. Modes of Death, Randomized Patients Cardiac Non-Cardiac Beta-blocker No Beta-blocker Beta-blocker No Beta-blocker Deaths Rate* Deaths Rate* Deaths Rate* Deaths Rate* Amiodarone 11.8% 9.1 17.2% 12.7 5.9% 4.6 3.7% 2.7 Defibrillator 5.3% 4.0 10.9% 7.1 3.2% 2.4 3.6% 2.4 *Incidence rate per 100 person-years over the initial 2 years of follow-up. All log rank p values were 0.1 for all beta-blocker vs. no beta-blocker comparisons. Cardiac death rates were somewhat lower in patients receiving beta-blockers, while noncardiac death rates were similar in patients receiving beta-blockers versus those not receiving beta-blockers. Adjusted survival, randomized patients. The use of betablockers at the time of hospital discharge was not independently associated with survival in randomized patients (Table 6). Furthermore, the survival of patients receiving beta-blockers at the time of their index arrhythmia who continued to receive these agents was similar to that of patients in whom beta-blockers were initiated after their index arrhythmia (RR 0.81; 95% CI 0.45 to 1.46; p 0.49). Patients receiving amiodarone and a beta-blocker, or an ICD and a beta-blocker, had a survival similar to patients receiving amiodarone alone, or an ICD alone. Age (RR 1.32 per decade increase), ejection fraction (RR 0.69 per 0.10 increase), history of heart failure (RR 3.06) and ACE inhibitor use (RR 0.44) were significantly associated with survival in the amiodaronetreatment multivariate model. For ICD-treated patients, age (RR 1.54 per decade), white race (RR 0.49), ACE inhibitor use (RR 0.47) and other antiarrhythmic drug use (RR 2.81) were significantly associated with survival in the multivariate model. Adjusted survival, eligible, nonrandomized patients. Overall, beta-blocker use was associated with improved survival in eligible, nonrandomized patients (Table 6). However, beta-blockade was not associated with an independent, survival benefit in patients treated with amiodarone alone or an ICD alone. In contrast, beta-blocker use remained associated with a significant, independent survival benefit in otherwise untreated patients. Furthermore, because 49 (12%) of these 412 otherwise untreated patients received sotalol (Table 3), the association of beta-blocker use with survival was evaluated in patients discharged without amiodarone, an ICD or sotalol. In these 363 patients, beta-blocker use remained independently associated with improved survival (RR 0.46; 95% CI 0.24 to 0.87; p 0.012), with a point estimate similar to that observed for the entire group of 412 patients (Table 6). For amiodarone-treated patients, age (RR 1.66 per decade increase), ejection fraction (RR 0.80 per 0.10 increase), discharge heart rate (RR 1.16 per 10 beats/min increase), history of heart failure (RR 1.56) and use of other antiarrhythmic drugs (RR 2.28) were significantly associated with survival in the multivariate model. For ICD-treated patients, age (RR 1.49 per decade increase), ejection fraction (RR 0.78 per 0.10 increase) and history of heart failure (RR 2.89) were significantly associated with survival in the multivariate model. In addition to Table 6. Adjusted Relative Risk Estimates, Association of Beta-blocker Use with Mortality Group Number Relative Risk (95% CI)* p Value Randomized patients 970 0.84 (0.53 1.28) 0.38 Amiodarone 484 1.00 (0.52 1.91) 0.99 Defibrillator 486 0.75 (0.39 1.46) 0.40 Nonrandomized patients 1,931 0.67 (0.47 0.94) 0.020 Amiodarone 658 0.98 (0.58 1.66) 0.94 Defibrillator 861 0.88 (0.43 1.78) 0.71 Neither 412 0.47 (0.25 0.88) 0.018 Randomized and nonrandomized Amiodarone 1,142 0.96 (0.64 1.45) 0.85 Defibrillator 1,347 0.88 (0.55 1.40) 0.58 *All Cox models included beta-blocker use at hospital discharge, age, gender, race, index arrhythmia, history of heart failure, ejection fraction, discharge heart rate and the baseline use of an angiotensin-converting enzyme inhibitor or diuretic. Specified models also included baseline: digoxin, calcium channel blocker or aspirin use; aspirin use; digoxin, aspirin, warfarin or sotalol use, history of hypertension and revascularization after the index event; digoxin, aspirin or sotalol use, and revascularization after the index event.

JACC Vol. 34, No. 2, 1999 August 1999:325 33 Exner et al. Beta-blockers and Survival in AVID 331 beta-blockade, age (RR 1.48 per decade increase) was significantly associated with survival in the otherwise untreated patient multivariate model. Death or recurrent arrhythmia, randomized patients. Beta-blockade was not associated with a reduction in the composite end point of death or recurrent arrhythmia in amiodarone and ICD-treated patients separately, or combined (adjusted RR 0.97, 95% CI 0.73 to 1.30, p 0.86). Discharge heart rate, amiodarone-treated patients. In the combined group of 1,142 amiodarone-treated patients, a heart rate 70 beats/min at the time of hospital discharge was associated with an increased risk of death compared with a heart rate of 70 beats/min (adjusted RR 1.30; 95% CI 1.00 to 1.69; p 0.047). However, no significant association between survival and beta-blockade was observed in patients within either heart rate strata (p 0.4 for each). Influence of index arrhythmia and MI history. In the combined group of 1,142 amiodarone-treated patients, beta-blockade was not associated with survival in the 655 (57%) patients with symptomatic VT (RR 0.81; 95% CI 0.47 to 1.41; p 0.45) or the 487 (43%) patients with VF (RR 1.14; 95% CI 0.61 2.16; p 0.67). Similarly, in the combined group of 1,347 ICD-treated patients, betablockade was not associated with survival in the 649 (48%) patients with symptomatic VT (RR 0.69; 95% CI 0.33 to 1.43; p 0.30) or the 698 (52%) with VF (RR 1.03; 95% CI 0.54 to 2.00; p 0.91). In the combined group of amiodarone-treated patients, beta-blocker use was not associated with improved survival in the 450 (39%) patients with no history of MI (RR 0.80; 95% CI 0.41 to 1.59; p 0.52) or the 692 (61%) with a history of prior MI (RR 1.07; 95% CI 0.64 to 1.82; p 0.78). However, in the combined group of ICD-treated patients, beta-blocker use was associated with a trend toward improved survival in the 529 (39%) patients without a history of MI (RR 0.43; 95% CI 0.16 to 1.17; p 0.08). Beta-blocker use was not significantly associated with survival in the combined group of 818 (61%) ICD-treated patients with a history of MI (RR 0.99; 95% CI 0.55 to 1.76; p 0.97). DISCUSSION The present analysis demonstrates that beta-blocker use at the time of hospital discharge was not associated with improved survival in patients with VF or symptomatic VT treated with amiodarone alone or an ICD alone. However, beta-blocker use was associated with an independent mortality reduction in eligible, nonrandomized patients who were not treated with amiodarone or ICD therapy. Amiodarone-treated patients. Amiodarone has a variety of electrophysiologic effects, including a weak nonselective, noncompetitive beta-blocking property (24). Because amiodarone and beta-blockers may exert their antiarrhythmic effects by reducing sympathetic tone (25,26), their combination might be expected to be superior to the effect of either alone. Whereas combining these agents is often avoided because of concern over side effects, excess rates of adverse cardiovascular and noncardiovascular effects have not been observed compared with therapy with a betablocker alone (27) or amiodarone alone (10,11). The European Myocardial Infarct Amiodarone Trial (EMIAT) and Canadian Amiodarone Myocardial Infarction Arrhythmia Trial (CAMIAT) were randomized, placebo-controlled studies that evaluated the capacity of amiodarone to reduce overall mortality and arrhythmic death in high-risk post-mi patients, respectively (10,11). Whereas neither study found a significant reduction in overall mortality, post hoc analyses from both trials indicated that patients receiving amiodarone and a beta-blocker had a lower risk of death compared with patients receiving amiodarone alone (12 14). In EMIAT and CAMIAT, unadjusted all-cause mortality reductions of 30% (12) and 60% to 72% (14), respectively, were observed. Furthermore, in both analyses, the beneficial effect of combining amiodarone with a beta-blocker was most prominent in patients with more rapid baseline heart rates. In contrast with EMIAT and CAMIAT, the combination of amiodarone and a beta-blocker in AVID patients was not associated with improved survival. This result may reflect differences between the amiodarone-treated patients in AVID versus those in EMIAT and CAMIAT. Although the age and gender distribution of patients in the three trials was similar, patients in AVID had life-threatening ventricular arrhythmias, more advanced LV dysfunction and a greater use of heart failure medications. Finally, although the analyses from EMIAT and CAMIAT demonstrated that patients with more rapid heart rates had the greatest benefit from the combination of amiodarone and a beta-blocker (12 14), the present analysis did not corroborate this. However, amiodarone-treated patients in AVID with heart rates 70 beats/min were at a higher risk of death. This result may reflect differences in the timing of the baseline heart rate measurements in AVID (at hospital discharge) versus EMIAT and CAMIAT (before initiation of amiodarone) or differences in the study populations. Patients treated with an implantable cardioverter defibrillator. Because beta-blockers reduce mortality in persons with heart failure (3 5), they would be expected to be beneficial in ICD-treated patients, most of whom have LV dysfunction. Furthermore, although beta-blockers may be used in conjunction with ICD therapy to reduce the incidence of recurrent arrhythmias (21,22), this was not a common reason cited for the use of beta-blockers in randomized AVID patients. Furthermore, beta-blockade was not associated with a significant reduction in the composite end point of death or recurrent arrhythmia in randomized AVID patients.

332 Exner et al. JACC Vol. 34, No. 2, 1999 Beta-blockers and Survival in AVID August 1999:325 33 Beta-blockers have been shown to reduce mortality when initiated in the early phase of an acute MI, particularly in patients with LV dysfunction (1,2), yet the ability of beta-blockers to reduce mortality when administered beyond the immediate post-mi period appears less certain (28,29). However, recent randomized trials in patients with heart failure which have included persons with ischemic heart disease have demonstrated significant mortality reductions in patients treated with beta-blockers, mostly the result of a reduced risk of sudden death (4,5). Otherwise untreated patients. In the same clinical practice setting, patients with VF or symptomatic VT who receive amiodarone or ICD therapy are likely to differ from patients who are otherwise untreated. In the present analysis, these otherwise untreated patients had less LV dysfunction, fewer symptoms of heart failure and less frequent ACE inhibitor or diuretic use compared with eligible, nonrandomized patients treated with amiodarone or an ICD. Because beta-blockers appear to decrease mortality by reducing the incidence of sudden death in patients with ischemic heart disease (30) and heart failure (4,5), it is probable that the survival benefit observed with betablockade in the otherwise untreated AVID patients was due to a decline in sudden death. Because amiodarone and ICD therapy are primarily used to reduce sudden, arrhythmic death in patients with VF or VT, it is not surprising that beta-blocker use was not associated with a prominent, additive survival benefit in AVID. Finally, the rate of revascularization after the index arrhythmia was also greatest in the otherwise untreated patients. This discrepancy may also have been an important factor in the results observed (31). However, the results of the present analysis are consistent with previous work by Brodsky and colleagues, who reported that concomitant beta-blockade was most efficacious in VT/VF patients who were younger, had less LV dysfunction and no history of coronary artery disease (23). Study limitations. This analysis was not a randomized comparison of outcome in patients receiving, versus those not receiving, beta-blockers. Although adjustments were made for known relevant differences, it is possible that the groups differed in other important respects. In addition, the present analysis lacked sufficient power to detect a small, but perhaps clinically relevant, effect from beta-blockade. However, the present analysis had reasonable ( 80%) power to detect a prominent (35%) mortality reduction associated with beta-blocker use (12,14). Finally, although the doses of beta-blockers prescribed in randomized patients are lower than what have been used in post-mi (1,2,29) and heart failure trials (4,5), these doses are similar to what have been reported in studies of similar patients with VT and VF (6,32). Conclusions. Although eligible, nonrandomized patients who did not receive amiodarone or an ICD had a significant survival benefit associated with beta-blockade, the role of beta-blockers as monotherapy in patients with VT or VF is limited because the ICD is more efficacious (33). The AVID patients treated with amiodarone or an ICD had no significant additional mortality reduction associated with concurrent beta-blockade. However, because betablockers confer additional benefits in the management of patients with heart disease, it remains appropriate to prescribe beta-blockers to patients with VF and symptomatic VT in whom they are clinically indicated for other reasons. Moreover, differences in the use of beta-blockers in randomized AVID patients do not explain the increased survival observed with ICD therapy. Acknowledgments We thank Myron Waclawiw, PhD, Division of Biostatistics, and Jeffrey Cutler, MD, Division of Epidemiology and Clinical Applications, at the National Heart, Lung, and Blood Institute, for their expert advice and assistance. Reprint requests and correspondence: Dr. Derek V. Exner, National Heart, Lung, and Blood Institute, 6701 Rockledge Drive, Room 8146, Bethesda, Maryland 20892. E-mail: Derek_Exner@nih.gov. REFERENCES 1. The Beta-blocker Heart Attack (BHAT) Investigators. A randomized trial of propranolol in patients with acute myocardial infarction. I. Mortality results. JAMA 1982;247:1707 14. 2. The Norwegian Multicenter Study Group. Timolol-induced reduction in mortality and reinfarction in patients surviving acute myocardial infarction. N Engl J Med 1981;304:801 7. 3. Heidenreich PA, Lee TT, Massie BM. Effect of beta-blockade on mortality in patients with heart failure: a meta-analysis of randomized clinical trials. J Am Coll Cardiol 1997;30:27 34. 4. Packer M, Bristow MR, Cohn JN, et al. The effect of carvedilol on morbidity and mortality in patients with chronic heart failure. N Engl J Med 1996;334:1349 55. 5. The Cardiac Insufficiency Bisoprolol Investigators and Committees. Cardiac Insufficiency Bisoprolol Study (CIBIS II): a randomised trial. Lancet 1999;353:9 13. 6. Steinbeck G, Andresen D, Bach P, et al. A comparison of electrophysiologically guided antiarrhythmic drug therapy with beta-blocker therapy in patients with symptomatic, sustained ventricular tachyarrhythmias. N Engl J Med 1992;327:987 92. 7. Antz M, Cappato R, Kuck KH. Metoprolol versus sotalol in the treatment of sustained ventricular tachycardia. J Cardiovasc Pharmacol 1995;26:627 35. 8. Hallstrom AP, Cobb LA, Yu BH, Weaver WD, Fahrenbruch CE. An antiarrhythmic drug experience in 941 patients resuscitated from an initial cardiac arrest between 1970 and 1985. Am J Cardiol 1991;68: 1025 31. 9. Szabo BM, Crijns HJ, Wiesfeld AC, van Veldhuisen DJ, Hillege HL, Lie KI. Predictors of mortality in patients with sustained ventricular tachycardias or ventricular fibrillation and depressed left ventricular function: importance of beta-blockade. Am Heart J 1995;130:281 6. 10. Julian DG, Camm AJ, Frangin G, et al. Randomised trial of effect of amiodarone on mortality in patients with left-ventricular dysfunction after recent myocardial infarction: EMIAT. European Myocardial Infarct Amiodarone Trial Investigators. Lancet 1997;349:667 74. 11. Cairns JA, Connolly SJ, Roberts R, Gent M. Randomised trial of outcome after myocardial infarction in patients with frequent or

JACC Vol. 34, No. 2, 1999 August 1999:325 33 Exner et al. Beta-blockers and Survival in AVID 333 repetitive ventricular premature depolarisations: CAMIAT. Canadian Amiodarone Myocardial Infarction Arrhythmia Trial Investigators. Lancet 1997;349:675 82. 12. Malik M, Camm AJ, Julian DG, et al. Benefit of amiodarone vs. placebo in post-infarction patients with reduced heart rate variability is independent of concurrent beta-blocker treatment (Abstr). PACE 1997;20 Suppl:1144. 13. Janse MJ, Malik M, Camm AJ, Julian DG, Frangin GA, Schwartz PJ. Identification of post acute myocardial infarction patients with potential benefit from prophylactic treatment with amiodarone. A substudy of EMIAT (the European Myocardial Infarct Amiodarone Trial). Eur Heart J 1998;19:85 95. 14. Dorian P, Newman D, Connolly C, Roberts R, Gent M, Cairns J. Beta blockade may be necessary for amiodarone to exert its antiarrhythmic benefit Results from CAMIAT (Abstr). PACE 1997;20 Suppl:1144. 15. The Antiarrhythmics Versus Implantable Defibrillators (AVID) Investigators. A comparison of antiarrhythmic-drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias. N Engl J Med 1997;337:1576 83. 16. Myerburg RJ, Castellanos A. Clinical trials of implantable defibrillators. N Engl J Med 1997;337:1621 3. 17. The Antiarrhythmics versus Implantable Defibrillators (AVID) Investigators. Antiarrhythmics Versus Implantable Defibrillators (AVID): rationale, design, and methods. Am J Cardiol 1995;75:470 5. 18. Kim SG, Hallstrom A, Love JC, et al. Comparison of clinical characteristics and frequency of implantable defibrillator use between randomized patients in the Antiarrhythmics Versus Implantable Defibrillators (AVID) trial and nonrandomized registry patients. Am J Cardiol 1997;80:454 7. 19. Curtis AB, Hallstrom AP, Klein RC, et al. Influence of patient characteristics in the selection of patients for defibrillator implantation (the AVID Registry). Antiarrhythmics Versus Implantable Defibrillators. Am J Cardiol 1997;79:1185 9. 20. The Antiarrhythmics Versus Implantable Defibrillators (AVID) Investigators. Causes of death in the Antiarrhythmics Versus Implantable Defibrillators (AVID) Trial. J Am Coll Cardiol. Submitted. 21. Levine JH, Mellits ED, Baumgardner RA, et al. Predictors of first discharge and subsequent survival in patients with automatic implantable cardioverter-defibrillators. Circulation 1991;84:558 66. 22. Leclercq JF, Leenhardt A, Coumel P, Slama R. Efficacy of betablocking agents in reducing the number of shocks in patients implanted with first-generation automatic defibrillators. Eur Heart J 1992;13:1180 4. 23. Brodsky MA, Allen BJ, Luckett CR, Capparelli EV, Wolff LJ, Henry WL. Antiarrhythmic efficacy of solitary beta-adrenergic blockade for patients with sustained ventricular tachyarrhythmias. Am Heart J 1989;118:272 80. 24. Singh BN, Venkatesh N, Nademanee K, Josephson MA, Kannan R. The historical development, cellular electrophysiology and pharmacology of amiodarone. Prog Cardiovasc Dis 1989;31:249 80. 25. Crijns HJ, Wiesfeld AC, Posma JL, Lie KI. Favourable outcome in idiopathic ventricular fibrillation with treatment aimed at prevention of high sympathetic tone and suppression of inducible arrhythmias. Br Heart J 1995;74:408 12. 26. Billman GE, Castillo LC, Hensley J, Hohl CM, Altschuld RA. Beta2-adrenergic receptor antagonists protect against ventricular fibrillation: in vivo and in vitro evidence for enhanced sensitivity to beta2-adrenergic stimulation in animals susceptible to sudden death. Circulation 1997;96:1914 22. 27. Krum H, Shusterman N, MacMahon S, Sharpe N. Efficacy and safety of carvedilol in patients with chronic heart failure receiving concomitant amiodarone therapy. Australia/New Zealand Heart Failure Research Collaborative Group. J Card Fail 1998;4:281 8. 28. The TIMI Study Group. Comparison of invasive and conservative strategies after treatment with intravenous tissue plasminogen activator in acute myocardial infarction. Results of the thrombolysis in myocardial infarction (TIMI) phase II trial. N Engl J Med 1989;320:618 27. 29. Herlitz J, Hjalmarson A, Swedberg K, et al. The influence of early intervention in acute myocardial infarction on long-term mortality and morbidity as assessed in the Goteborg metoprolol trial. Int J Cardiol 1986;10:291 301. 30. Kendall MJ, Lynch KP, Hjalmarson A, Kjekshus J. Beta-blockers and sudden cardiac death. Ann Intern Med 1995;123:358 67. 31. O Rourke RA. Role of myocardial revascularization in sudden cardiac death. Circulation 1992;85:112 7. 32. Tonet J, Frank R, Fontaine G, Grosgogeat Y. Efficacy and safety of low doses of beta-blocker agents combined with amiodarone in refractory ventricular tachycardia. PACE 1988;11:1984 9. 33. Ferguson JJ. Meeting highlights: 47th Annual Scientific Sessions of the American College of Cardiology. Preliminary results of the Cardiac Arrest Survival Hamburg (CASH) trial. Circulation 1998;97: 2377 81.