Comparison of Incidence of Left Ventricular Systolic Dysfunction Among Patients With Left Bundle Branch Block Versus Those With Normal QRS Duration

被引:31
|
作者
Sze, Edward [1 ]
Dunning, Allison [2 ]
Loring, Zak [1 ,2 ]
Atwater, Brett D. [1 ]
Chiswell, Karen [2 ]
Daubert, James P. [2 ]
Kisslo, Joseph A. [1 ]
Mark, Daniel B. [2 ]
Velazquez, Eric J. [2 ]
Samad, Zainab [1 ]
机构
[1] Duke Univ, Dept Med, Div Cardiol, Durham, NC 27708 USA
[2] Duke Univ, Duke Clin Res Inst, Durham, NC USA
来源
AMERICAN JOURNAL OF CARDIOLOGY | 2017年 / 120卷 / 11期
关键词
CARDIAC RESYNCHRONIZATION THERAPY; CORONARY-ARTERY-DISEASE; EJECTION FRACTION; HEART-FAILURE; EVOLUTION; TRIAL; RISK; ERA;
D O I
10.1016/j.amjcard.2017.08.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We compared the incidence of left ventricular systolic dysfunction (LVSD) among patients with left bundle branch block (LBBB) to a matched cohort of patients with a narrow QRS duration <120 ms (NQRS). We hypothesized patients with preserved ejection fraction (EF) >= 50% and LBBB would have higher incidence of LVSD compared with a matched population of NQRS patients. Patients with LBBB on electrocardiogram within 30 days of a baseline echocardiogram with >= 50%, who had at least 1 follow-up echocardiogram >= 6 months later, were matched 1:1 on risk factors for cardiomyopathy to patients with NQRS. Incident LVSD was defined as a decline in EF to <= 45% on follow-up echocardiogram, or heart transplant, receipt of a cardiac device for LVSD (defibrillator or biventricular pacemaker), or implantation of a left ventricular assist device >= 6 months post baseline echocardiogram. Relative risk was calculated using conditional Poisson regression techniques. The final study cohort consisted of 188 patients, 94 with LBBB and 94 with NQRS. On follow-up, progression to LVSD was noted in 36% of LBBB patients and 10% of NQRS patients. The relative risk for LVSD in patients with LBBB was 3.78 (95% confidence interval = 1.98 to 7.19). In conclusion, there is a strong association between LBBB and the subsequent development of LVSD independent of common risk factors for cardiomyopathy. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:1990 / 1997
页数:8
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