Rhythm control in atrial fibrillation: Endpoints for device-based trials

被引:7
作者
Gillis, AM
机构
[1] Univ Calgary, Fac Med, Cardiovasc Res Grp, Calgary, AB T2N 4N1, Canada
[2] Calgary Hlth Reg, Div Cardiol, Calgary, AB, Canada
基金
加拿大健康研究院;
关键词
atrial fibrillation; clinical outcomes; pacemaker diagnostics;
D O I
10.1016/j.hrthm.2004.03.075
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Newer generations of pacemakers and implantable cardioverter defibrillators have enhanced diagnostic features that permit detection and storage of information about the frequency, duration, time of onset, and rate characteristics of multiple consecutive episodes of atrial tachycardia and atrial fibrillation (AF). Parameters available in implantable devices that might serve as outcome measures to assess the impact of pharmacologic and nonpharmacologic therapies for prevention of AF include time to first recurrence of AF, intervals between successive episodes of AF, AF frequency, AF duration, AF burden (amount/ unit time), and episodes of symptomatic AF. Each parameter has advantages and limitations. The characteristics/temporal patterns of AF may determine the ideal study outcome measure to address a specific hypothesis. Clinical studies of therapies for prevention of AF need to be directed to populations with the arrhythmia substrate that will be targeted by the therapy. Device-based metrics are suitable to assess the impact of pacing or pharmacologic therapies for prevention of AF. However, it is important to establish that suppression of AF is associated with an improvement in some clinical outcome. Relevant outcomes might include improvement in symptoms, quality of life, or functional capacity; reduction in hospitalization for cardiovascular causes, stroke death, or overall mortality; or a composite of some of these parameters. (C) 2004 Heart Rhythm Society. All rights reserved.
引用
收藏
页码:B52 / B57
页数:6
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