Atrial overdrive pacing and incidence of heart failure-related adverse events in permanently paced patients

被引:4
|
作者
Schuchert, Andreas
Carlson, Mark
Ip, John
Messenger, John
Beau, Scott
Kalbfleisch, Steven
Gervais, Pierre
Cameron, Douglas A.
Duran, Aurelio
Val-Mejias, Jesus
Mackall, Judith
Gold, Michael
机构
[1] Friedrich Ebert Hosp, Med Clin, D-24531 Neumunster, Germany
[2] Case Western Reserve Univ, Sch Med, Dept Med, Cleveland, OH 44106 USA
[3] Univ Hosp Cleveland, Cleveland, OH 44106 USA
[4] Thorac Cardiovasc Inst, Lansing, MI USA
[5] Long Beach Mem Med Ctr, Long Beach, CA USA
[6] Arkansas Heart Hosp, Little Rock, AR USA
[7] Mid Ohio Cardiol, Columbus, OH USA
[8] St Joseph Hosp, Trois Rivieres, PQ, Canada
[9] Toronto Gen Hosp, Toronto, ON, Canada
[10] Orlando Heart Ctr, Orlando, FL USA
[11] St Francis Hosp, Wichita, KS USA
[12] Med Univ S Carolina, Charleston, SC 29425 USA
关键词
atrial pacing; overdrive pacing; overdrive pacing algorithm; atrial fibrillation; heart failure;
D O I
10.1007/s10840-007-9130-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Atrial overdrive pacing algorithms may be effective in preventing or suppressing atrial fibrillation (AF). However, the maintenance of a heart rate incessantly faster than spontaneous could induce left ventricular (LV) dysfunction and promote heart failure (HF) on the long term. Objective This post hoc analysis examined the effects of a new overdrive algorithm on the incidence of HF-related adverse events in 411 patients enrolled in the ADOPT-A trial. Materials and methods The AF Suppression (TM) algorithm was randomly programmed ON in 209 patients (treatment group) versus OFF in 202 patients (control group). The incidence of HF-related adverse events and HF-related deaths over a 6-month follow-up was compared between the two groups. Patients with versus without HF-related clinical events were also compared to each other within each group. Results There were eight HF-related adverse clinical events (3.8%) in the treatment group and 11 (5.4%) in the control group, including four HF-related deaths (1.9 vs. 2.0%) in each group during follow-up. Baseline NYHA functional class in patients with versus without HF-related adverse events was 1.4 +/- 0.5 versus 1.5 +/- 0.7 in the control, and 1.5 +/- 0.8 versus 1.5 +/- 0.6 in the treatment group. LV ejection fraction (EF) was 49 +/- 7% in patients with, versus 57 +/- 12% in patients without HF-related adverse events, in the control group, and 43 +/- 14% in patients with, versus 56 +/- 13% in patients without HF-related adverse events, in the treatment group. LVEF was lowest and similar in both groups among patients who died from HF (35 +/- 10% in the control and 38 +/- 27% in the treatment group). Conclusions In ADOPT-A, HF-related clinical events and deaths were related to LV dysfunction and not to atrial pacing overdriven by the AF suppression algorithm.
引用
收藏
页码:55 / 60
页数:6
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