No benefit from defibrillation threshold testing in the SCD-HeFT (Sudden Cardiac Death in Heart Failure Trial)

被引:113
作者
Blatt, Joseph A. [1 ]
Poole, Jeanne E.
Johnson, George W. [2 ]
Callans, David J. [3 ]
Raitt, Merritt H. [4 ]
Reddy, Ramakota K. [12 ]
Marchlinski, Francis E. [3 ]
Yee, Raymond [5 ]
Guarnieri, Thomas [6 ]
Talajic, Mario [7 ]
Wilber, David J. [8 ]
Anderson, Jill [2 ]
Chung, Kiyon [9 ]
Wong, Wai Shun [11 ]
Mark, Daniel B. [10 ]
Lee, Kerry L. [10 ]
Bardy, Gust H. [2 ]
机构
[1] Univ Washington, Dept Cardiol, Seattle, WA 98195 USA
[2] Seattle Inst Cardiac Res, Seattle, WA USA
[3] Univ Penn, Philadelphia, PA 19104 USA
[4] Portland VA Med Ctr, Portland, OR USA
[5] Univ Western Ontario, London, ON, Canada
[6] Johns Hopkins Univ, Baltimore, MD USA
[7] Montreal Heart Inst, Montreal, PQ H1T 1C8, Canada
[8] Loyola Univ Hlth Syst, Maywood, IL USA
[9] Everett Clin, Everett, WA USA
[10] Duke Univ, Sch Med, Durham, NC USA
[11] Univ Michigan, Ann Arbor, MI 48109 USA
[12] Oregon Cardiol PC, Eugene, OR USA
关键词
sudden cardiac death; implantable cardioverter-defibrillator; defibrillation threshold testing; DFT testing;
D O I
10.1016/j.jacc.2008.04.051
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study investigated whether defibrillation threshold (DFT) testing during implantable cardioverter-defibrillator (ICD) implantation predicts clinical outcomes. Background Defibrillation testing is often performed during insertion of ICDs to confirm shock efficacy. There are no prospective data to suggest that this procedure improves outcomes when modern ICDs are implanted for primary prevention of sudden death. Methods The analysis included the 811 patients who were randomized to the ICD arm of the SCD-HeFT (Sudden Cardiac Death in Heart Failure Trial) and had the device implanted. The DFT testing protocol in SCD-HeFT was designed to limit shock testing in a primary prevention heart failure population. Results Baseline DFT data were available for 717 patients (88.4%). All 717 patients had a DFT of <= 30 J, the maximum output of the device in this study. The DFT was <= 20 J in 97.8% of patients. There was no survival difference between patients with a lower DFT (<= 10 J, n = 547) and a higher DFT (> 10 J, n = 170) (p = 0.41). First shock efficacy was 83.0% for the first clinical ventricular tachyarrhythmia event; there were no differences in shock efficacies when the cohort was subdivided by baseline DFT. Conclusions Low baseline DFTs were obtained in patients with stable, optimally treated heart failure during ICD implantation for primary prevention of sudden death. First shock efficacy for ventricular tachyarrhythmias was high regardless of baseline DFT testing results. Baseline DFT testing did not predict long-term mortality or shock efficacy in this study.
引用
收藏
页码:551 / 556
页数:6
相关论文
共 27 条
[1]  
Bardy G., 2000, ARRHYTHMIA TREATMENT, P323
[2]   A SIMPLIFIED, SINGLE-LEAD UNIPOLAR TRANSVENOUS CARDIOVERSION-DEFIBRILLATION SYSTEM [J].
BARDY, GH ;
JOHNSON, G ;
POOLE, JE ;
DOLACK, GL ;
KUDENCHUK, PJ ;
KELSO, D ;
MITCHELL, R ;
MEHRA, R ;
HOFER, B .
CIRCULATION, 1993, 88 (02) :543-547
[3]   Amiodarone or an implantable cardioverter-defibrillator for congestive heart failure [J].
Bardy, GH ;
Lee, KL ;
Mark, DB ;
Poole, JE ;
Packer, DL ;
Boineau, R ;
Domanski, M ;
Troutman, C ;
Anderson, J ;
Johnson, G ;
McNulty, SE ;
Clapp-Channing, N ;
Davidson-Ray, LD ;
Fraulo, ES ;
Fishbein, DP ;
Luceri, RM ;
Ip, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (03) :225-237
[4]   A PROSPECTIVE RANDOMIZED EVALUATION OF BIPHASIC VERSUS MONOPHASIC WAVEFORM PULSES ON DEFIBRILLATION EFFICACY IN HUMANS [J].
BARDY, GH ;
IVEY, TD ;
ALLEN, MD ;
JOHNSON, G ;
MEHRA, R ;
GREENE, HL .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1989, 14 (03) :728-733
[5]   A PROSPECTIVE RANDOMIZED COMPARISON IN HUMANS OF BIPHASIC WAVE-FORM 60-MU-F AND 120-MU-F CAPACITANCE PULSES USING A UNIPOLAR DEFIBRILLATION SYSTEM [J].
BARDY, GH ;
POOLE, JE ;
KUDENCHUK, PJ ;
DOLACK, GL ;
MEHRA, R ;
DEGROOT, P ;
RAITT, MH ;
JONES, GK ;
JOHNSON, G .
CIRCULATION, 1995, 91 (01) :91-95
[6]  
BARDY GH, 1992, PACE, V15, P217
[7]  
Centers for Medicare and Medicaid Services, 2005, CAG00157R3 CTR MED M
[8]  
COX DR, 1972, J R STAT SOC B, V34, P187
[9]   Inductionless or limited shock testing is possible in most patients with implantable cardioverter-defibrillators/cardiac resynchronization therapy defibrillators - Results of the multicenter ASSURE Study (Arrhythmia Single Shock Defibrillation Threshold Testing Versus Upper Limit of Vulnerability: Risk Reduction Evaluation with Implantable Cardioverter-Defibrillator Implantations) [J].
Day, John D. ;
Doshi, Rahul N. ;
Belott, Peter ;
Birgersdotter-Green, Ulrika ;
Behboodikhah, Mahnaz ;
Ott, Peter ;
Glatter, Kathryn A. ;
Tobias, Serge ;
Frumin, Howard ;
Lee, Byron K. ;
Merillat, John ;
Wiener, Isaac ;
Wang, Samuel ;
Grogin, Harlan ;
Chun, Sung ;
Patrawalla, Rob ;
Crandall, Brian ;
Osborn, Jeffrey S. ;
Weiss, J. Peter ;
Lappe, Donald L. ;
Neuman, Stacey .
CIRCULATION, 2007, 115 (18) :2382-2389
[10]  
Ellenbogen K, 2007, Clinical Cardiac Pacing, Defibrillation, and Resynchronization Therapy, V3rd