Beat-to-beat three-dimensional ECG variability predicts ventricular arrhythmia in ICD recipients.
Beat-to-beat three-dimensional ECG variability predicts ventricular arrhythmia in ICD recipients.
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DOI:
10.1016/j.hrthm.2010.08.022
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发表时间:
2010-11
期刊:
影响因子:
5.5
通讯作者:
Berger, Ronald D.
中科院分区:
文献类型:
--
作者:
Tereshchenko, Larisa G.;Han, Lichy;Cheng, Alan;Marine, Joseph E.;Spragg, David D.;Sinha, Sunil;Dalal, Darshan;Calkins, Hugh;Tomaselli, Gordon F.;Berger, Ronald D.
Methodological difficulties associated with QT measurements prompt search for new ECG markers of repolarization heterogeneity. We hypothesized that beat-to-beat 3-dimensional vectorcardiogram variability predicts ventricular arrhythmia (VA) in patients with structural heart disease left ventricular systolic dysfunction and implanted ICD. Baseline orthogonal ECGs were recorded in 414 patients with structural heart disease [mean age 59.4±12.0; 280 whites (68%) and 134 blacks (32%)] at rest before implantation of ICD for primary prevention of sudden cardiac death. R and T peaks of 30 consecutive sinus beats were plotted in 3-D to form an R peaks cloud and a T peaks cloud. The volume of the peaks cloud was calculated as the volume within the convex hull. Patients were followed at least 6 months; sustained VA with appropriate ICD therapies served as an endpoint. During a mean follow-up time of 18.4±12.5 months, 61 of the 414 patients (14.73% or 9.6% per person-year of follow-up) experienced sustained VA with appropriate ICD therapies: 41 of them were whites and 20 were blacks. In the multivariate Cox model that included inducibility of VA and use of beta-blockers, the highest tertile of T/R peaks cloud volume ratio significantly predicted VA (HR 1.68 95% CI 1.01–2.80;p=0.046) in all patients. T peaks cloud volume and T/R peaks cloud volume ratio were significantly smaller in blacks [0.09 (0.04–0.15) vs. 0.11 (0.06–0.22), p=0.002]. Relatively large T peaks cloud volume is associated with increased risk of VA in patients with structural heart disease and systolic dysfunction.
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DOI:
10.1056/nejmoa071098
发表时间:
2008-09-04
期刊:
The New England journal of medicine
影响因子:
--
作者:
Poole JE;Johnson GW;Hellkamp AS;Anderson J;Callans DJ;Raitt MH;Reddy RK;Marchlinski FE;Yee R;Guarnieri T;Talajic M;Wilber DJ;Fishbein DP;Packer DL;Mark DB;Lee KL;Bardy GH
通讯作者:
Bardy GH
影响因子:
24
作者:
Haigney, MC;Zareba, W;Moss, AJ
通讯作者:
Moss, AJ
影响因子:
37.8
作者:
Fuller, MS;Sándor, G;Lux, RL
通讯作者:
Lux, RL
影响因子:
37.8
作者:
Russo, AM;Hafley, GE;Buxton, AE
通讯作者:
Buxton, AE
DOI:
10.1152/ajpheart.00936.2009
发表时间:
2010-05-01
影响因子:
4.8
作者:
Pueyo, Esther;Husti, Zoltan;Rodriguez, Blanca
通讯作者:
Rodriguez, Blanca