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验证一种与三维超声心动图相比的除颤导联心室容量测量方法。

Validation of a defibrillation lead ventricular volume measurement compared to three-dimensional echocardiography.

机构信息

Beaumont Health, Royal Oak, Michigan.

Arkansas Heart Hospital, Little Rock, Arkansas.

出版信息

Heart Rhythm. 2017 Oct;14(10):1515-1522. doi: 10.1016/j.hrthm.2017.06.005. Epub 2017 Jun 9.

Abstract

BACKGROUND

There is increasing evidence that using frequent invasive measures of pressure in patients with heart failure results in improved outcomes compared to traditional measures. Admittance, a measure of volume derived from preexisting defibrillation leads, is proposed as a new technique to monitor cardiac hemodynamics in patients with an implantable defibrillator.

OBJECTIVE

The purpose of this study was to evaluate the accuracy of a new ventricular volume sensor (VVS, CardioVol) compared with 3-dimenssional echocardiography (echo) in patients with an implantable defibrillator.

METHODS

Twenty-two patients referred for generator replacement had their defibrillation lead attached to VVS to determine the level of agreement to a volume measurement standard (echo). Two opposite hemodynamic challenges were sequentially applied to the heart (overdrive pacing and dobutamine administration) to determine whether real changes in hemodynamics could be reliably and repeatedly assessed with VVS. Equivalence of end-diastolic volume (EDV) and stroke volume (SV) determined by both methods was also assessed.

RESULTS

EDV and SV were compared using VVS and echo. VVS tracked expected physiologic trends. EDV was modulated -10% by overdrive pacing (14 mL). SV was modulated -13.7% during overdrive pacing (-6 mL) and increased over baseline +14.6% (+8 mL) with dobutamine. VVS and echo mean EDVs were found statistically equivalent, with margin of equivalence 13.8 mL (P <.05). Likewise, mean SVs were found statistically equivalent with margin of equivalence 15.8 mL (P <.05).

CONCLUSION

VVS provides an accurate method for ventricular volume assessment using chronically implanted defibrillator leads and is statistically equivalent to echo determination of mean EDV and SV.

摘要

背景

越来越多的证据表明,与传统测量方法相比,频繁使用心力衰竭患者的有创压力测量方法可改善预后。心阻抗,一种从现有的除颤导联推导而来的容积测量方法,被提出作为一种监测植入式除颤器患者心血流动力学的新技术。

目的

本研究旨在评估一种新的心室容积传感器(VVS,CardioVol)与三维超声心动图(echo)在植入式除颤器患者中的准确性。

方法

22 名因发生器更换而就诊的患者将其除颤导联连接至 VVS,以确定与容积测量标准(echo)的一致性水平。心脏先后接受两种相反的血流动力学挑战(超速起搏和多巴酚丁胺给药),以确定 VVS 是否能可靠且重复地评估血流动力学的真实变化。还评估了两种方法确定的舒张末期容积(EDV)和每搏量(SV)的等效性。

结果

使用 VVS 和 echo 比较 EDV 和 SV。VVS 跟踪了预期的生理趋势。超速起搏(14 毫升)可使 EDV 降低 10%。SV 在超速起搏期间降低 13.7%(-6 毫升),多巴酚丁胺给药后基线增加 14.6%(+8 毫升)。发现 VVS 和 echo 的平均 EDV 具有统计学等效性,等效区间为 13.8 毫升(P <.05)。同样,平均 SV 也具有统计学等效性,等效区间为 15.8 毫升(P <.05)。

结论

VVS 使用慢性植入式除颤器导联提供了一种准确的心室容积评估方法,并且在统计学上与 echo 确定的平均 EDV 和 SV 等效。

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