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在继发于缺血性或特发性扩张型心肌病的心力衰竭患者中,在不应期施加电流对心脏收缩力的调节作用。

Cardiac contractility modulation by electric currents applied during the refractory period in patients with heart failure secondary to ischemic or idiopathic dilated cardiomyopathy.

作者信息

Pappone Carlo, Rosanio Salvatore, Burkhoff Daniel, Mika Yuval, Vicedomini Gabriele, Augello Giuseppe, Shemer Itzhak, Prutchi David, Haddad Walid, Aviv Ricardo, Snir Yehuda, Kronzon Itzhak, Alfieri Ottavio, Ben-Haim Shlomo A

机构信息

Department of Cardiology, San Raffaele University Hospital, Milan, Italy.

出版信息

Am J Cardiol. 2002 Dec 15;90(12):1307-13. doi: 10.1016/s0002-9149(02)02868-0.

Abstract

We assessed the feasibility of cardiac contractility modulation (CCM) by electric currents applied during the refractory period in patients with heart failure (HF). Extracellular electric currents modulating action potential and calcium transients have been shown to potentiate myocardial contractility in vitro and in animal models of chronic HF. CCM signals were biphasic square-wave pulses with adjustable amplitude, duration, and time delay from sensing of local electric activity. Signals were applied to the left ventricle through an epicardial vein (in 12 patients) or to the right ventricular (RV) aspect of the septum endocardially (in 6 patients). Simultaneous left ventricular (LV) and aortic pressure measurements were performed using a Millar catheter (Millar Instruments, Houston, Texas). Hemodynamics during RV temporary dual-chamber pacing was regarded as the control condition. Both LV and RV CCM stimulation increased dP/dt(max) to a similar degree (9.1 +/- 4.5% and 7.1 +/- 0.8%, respectively; p <0.01 vs controls), with associated aortic pulse pressure changes of 10.3 +/- 7.2% and 10.8 +/- 1.1% (p <0.01 vs controls). Regional systolic wall motion assessed quantitatively by color kinesis echocardiography was markedly enhanced near the CCM electrode, and the area of increased contractility involved 4.6 +/- 1.2 segments per patient. In 6 patients with HF with left bundle branch block, CCM signals delivered during biventricular pacing (BVP) produced an additional 16.1 +/- 3.7% increase in dP/dt(max) and a 17.0 +/- 7.5% increase in pulse pressure compared with BVP alone (p <0.01). CCM stimulation in patients with HF enhanced regional and global measures of LV systolic function, regardless of the varied delivery chamber or whether modulation was performed during RV pacing or BVP.

摘要

我们评估了在心力衰竭(HF)患者的不应期施加电流进行心脏收缩力调制(CCM)的可行性。在体外和慢性HF动物模型中,已证明调节动作电位和钙瞬变的细胞外电流可增强心肌收缩力。CCM信号为双相方波脉冲,其幅度、持续时间和从感知局部电活动起的时间延迟均可调节。信号通过心外膜静脉施加于左心室(12例患者)或经心内膜施加于室间隔的右心室(RV)面(6例患者)。使用Millar导管(Millar仪器公司,得克萨斯州休斯顿)同时进行左心室(LV)和主动脉压力测量。将RV临时双腔起搏期间的血流动力学视为对照条件。LV和RV CCM刺激均使dP/dt(max)增加到相似程度(分别为9.1±4.5%和7.1±0.8%;与对照组相比,p<0.01),同时主动脉脉压变化分别为10.3±7.2%和10.8±1.1%(与对照组相比,p<0.01)。通过彩色室壁运动超声心动图定量评估的局部收缩期壁运动在CCM电极附近明显增强,每名患者收缩力增加的区域涉及4.6±1.2个节段。在6例患有左束支传导阻滞的HF患者中,与单独双心室起搏(BVP)相比,双心室起搏(BVP)期间传递的CCM信号使dP/dt(max)额外增加16.1±3.7%,脉压增加17.0±7.5%(p<0.01)。HF患者的CCM刺激增强了LV收缩功能的局部和整体指标,无论信号施加的腔室如何,也无论调制是在RV起搏还是BVP期间进行。

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