Use of an intracardiac electrogram eliminates the need for a surface ECG during implantable cardioverter-defibrillator follow-up

被引:4
作者
Michael, Kevin A.
Peterson, Brett J.
Yue, Arthur M.
Wilson, Ryan D.
Wang, Li
Ousdigian, Kevin
Wilkoff, Bruce
Sterns, Laurence
Morgan, John M.
机构
[1] Southampton Gen Hosp, Wessex Cardiothorac Ctr, Southampton SO16 6YD, Hants, England
[2] Medtronic Inc, Minneapolis, MN USA
[3] Cleveland Clin Fdn, Cleveland, OH USA
[4] Royal Jubilee Hosp, Victoria, BC, Canada
来源
PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY | 2007年 / 30卷 / 12期
关键词
defibrillation-ICD; electrocardiogram; new technology; pacing;
D O I
10.1111/j.1540-8159.2007.00888.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: A surface electrocardiogram (SECG) for pacing threshold measurements during routine implantable cardioverter-defibrillator (ICD) follow-up can be cumbersome. This study evaluated the use of an intrathoracic far-field electrogram (EGM) derived between the Can and superior vena cava (SVC) electrode-the Leadless electrocardiogram (LLECG), in dual chamber ICDs in performing pacing threshold tests. Methods: The LLECG was evaluated prospectively during atrial and ventricular pacing threshold testing as a substudy of the Comparison of Empiric to Physician-Tailored Programming of Implantable Cardioverter-Defibrillators trial (EMPIRIC) in which dual chamber ICDs were implanted in 888 patients. Threshold tests were conducted at 1 volt by decrementing the pulse width. Follow-up at three months compared pacing thresholds measured using LLECG with those using Lead I of the surface ECG (SECG). The timesaving afforded by LLECG was assessed by a questionnaire. Results: The median threshold difference between LLECG and SECG measurements for both atrial (0.00 ms, P = 0.90) and ventricular (0.00 ms, P = 0.34) threshold tests were not significant. Ninety percent of atrial and ventricular threshold differences were bounded by +/- 0.10 ms and -0.10 to +0.04 ms, respectively. We found that 99% of atrial and ventricular thresholds tests at six and 12 months attempted using LLECG were successfully completed. The questionnaire indicated that 65% of healthcare professionals found LLECG to afford at least some timesaving during device follow-ups. Conclusion: Routine follow-up can be performed reliably and expeditiously in dual chamber Medtronic (Minneapolis, MN, USA) ICDs using LLECG alone, resulting in overall timesaving.
引用
收藏
页码:1432 / 1437
页数:6
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