| Literature DB >> 28966312 |
Junichi Ooka1, Hidekazu Tanaka1, Yutaka Hatani1, Keiko Hatazawa1, Hiroki Matsuzoe1, Hiroyuki Shimoura1, Hiroyuki Sano1, Takuma Sawa1, Yoshiki Motoji1, Yasuhide Mochizuki1, Keiko Ryo-Koriyama1, Kensuke Matsumoto1, Koji Fukuzawa1, Ken-Ichi Hirata1.
Abstract
Although right ventricular (RV) pacing is the only effective treatment for patients with symptomatic bradycardia, it creates left ventricular (LV) dyssynchrony, which can induce LV dysfunction and heart failure. The current criterion for consideration of cardiac resynchronization therapy (CRT) is LV ejection fraction (LVEF) ≤ 35%, but indication for CRT in patients required for RV pacing with LVEF > 35% remains unclear.We studied 40 patients, all LVEF ≥ 35%, who had undergone implantable cardioverter-defibrillator implantation with RV pacing < 5%. Echocardiography was performed at baseline and during RV pacing. LV dyssynchrony was defined as anteroseptal-to-posterior wall delay from the mid-LV short-axis view using two-dimensional speckle-tracking radial strain (significant: ≥ 130 ms). Patients were divided into two groups based on baseline LVEF: normal LVEF ( ≥ 50%; n = 20) and mildly reduced LVEF (35-50%; n = 20).LVEF and LV dyssynchrony in patients with mildly reduced LVEF deteriorated significantly during RV pacing compared to those in patients with normal LVEF. Moreover, changes in LV dyssynchrony during RV pacing significantly correlated with changes in LVEF (r = -0.44, P < 0.01). Multivariate logistic regression analysis showed that baseline LVEF was the only independent predictor and baseline LVEF < 48% predictive of significant LV dyssynchrony during RV pacing.The extent of RV pacing-induced LV dysfunction may be associated with baseline LV function. These adverse effects on patients with mildly reduced LVEF of 35-50% and indications for RV pacing due to bradycardia can thus be prevented by CRT.Entities:
Keywords: Dyssynchrony; Echocardiography; Heart failure; Left ventricular function; Right ventricular pacing
Mesh:
Year: 2017 PMID: 28966312 DOI: 10.1536/ihj.16-415
Source DB: PubMed Journal: Int Heart J ISSN: 1349-2365 Impact factor: 1.862