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Initial In Vivo Evaluation of the DexAide Right Ventricular Assist Device

机译:DexAide右心室辅助装置的体内初步评估

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摘要

>Objectives: Despite the increasing use of left ventricular assist devices for patients with end-stage congestive heart failure, no implantable, centrifugal right ventricular assist devices (RVADs) are available for those patients with significant right ventricular failure. The DexAide RVAD was developed to provide an implantable RVAD option to surgeons. The aim of this study was to evaluate pump performance in an acute in vivo model.>Methods: The DexAide RVAD, developed as a modified CorAide™ left ventricular assist device, was implanted between the right ventricle and the pulmonary artery in four healthy calves. Pump speed was varied from 1,800 rpm to 3,600 rpm. RVAD performance was analyzed acutely at baseline and under conditions of low circulating volume, high contractility, high pulmonary arterial pressure, vasodilation, and low contractility.>Results: Pump flow was well maintained even under conditions of high pulmonary arterial pressure and vasodilation, with the exception of low circulating volume. Under all conditions, pulmonary arterial pressures were not affected by changing pump speed.>Conclusions: The DexAide RVAD demonstrated acceptable hemodynamic characteristics for use as an implantable RVAD in the initial acute studies. Further studies are ongoing to examine the biocompatibility of the pump under chronic conditions.
机译:>目标:尽管对于患有晚期充血性心力衰竭的患者,越来越多地使用左心室辅助设备,但对于那些患有严重右心室衰竭的患者,尚无可植入的离心右心室辅助设备(RVAD)。 DexAide RVAD的开发旨在为外科医生提供可植入的RVAD选项。这项研究的目的是评估急性体内模型中的泵性能。>方法:开发为改良的CorAide™左心室辅助装置的DexAide RVAD植入右心室和肺之间四个健康小牛的大动脉。泵速从1800 rpm更改为3600 rpm。在基线和低循环量,高收缩性,高肺动脉压,血管舒张和低收缩性的情况下,对RVAD性能进行了急性分析。>结果:即使在肺动脉高的情况下,泵的流量也能保持良好血压和血管舒张,低循环量除外。在所有情况下,肺动脉压均不受泵速度变化的影响。>结论:在最初的急性研究中,DexAide RVAD表现出可接受的血液动力学特性,可用作植入式RVAD。正在进行进一步的研究以检查泵在慢性条件下的生物相容性。

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