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通过患者模拟器模拟回路对SynCardia™ Freedom®驱动装置进行体外性能研究。

In vitro performance investigation of SynCardia™ Freedom® driver via patient simulator mock loop.

作者信息

Toninato Riccardo, Scuri Silvia, Tarzia Vincenzo, Gerosa Gino, Susin Francesca M

机构信息

Cardiovascular Fluid Dynamics Laboratory HER, Department of Civil, Environmental and Architectural Engineering - DICEA, University of Padua, Padua - Italy.

Padua Heart Project, Division of Cardiac Surgery, A.O. of Padua, Padua - Italy.

出版信息

Int J Artif Organs. 2016 Nov 29;39(10):502-508. doi: 10.5301/ijao.5000524. Epub 2016 Oct 15.

Abstract

PURPOSE

The gold standard therapy for patients with advanced heart failure is heart transplant. The gap between donors and patients in waiting lists promoted the development of circulatory support devices, such as the total artificial heart (TAH). Focusing on in vitro tests performed with CardioWest™ TAH (CW) driven by the SynCardia Freedom® portable driver (FD) the present study goals are: i) prove the reliability of a hydraulic circuit used as patient simulator to replicate a quasi-physiological scenario for various hydrodynamic conditions, ii) investigate the hydrodynamic performance of the CW FD, iii) help clinicians in possible interpretation of clinical cases outcomes.

METHODS

In vitro tests were performed using a mechanic-hydraulic patient simulator. Cardiac output (CO), CW ventricles filling, atrial, ventricles, aortic and pulmonary artery pressures were measured for different values of vascular resistance in both systemic (SVR) and pulmonary (PVR) physiological range.

RESULTS

After increasing the PVR, the left atrial pressure decreased according to the expected physiological trend, while aortic pressure remained almost stable, proving the ability of the simulator to mimic a physiological scenario. Unexpectedly, the mean pulmonary artery pressure (PPA) was found to increase above 30 mmHg in the range of physiological PVR (2.6 WU) and for constant CO.

CONCLUSIONS

The increase in PPA is probably associated with the pre-set driving setup of the FD. The finding suggests a possible explanation of the clinical course of a patient who experienced complications soon after being supported by the FD, with the occurrence of dyspnea and pulmonary edema despite a high cardiac index.

摘要

目的

晚期心力衰竭患者的金标准治疗方法是心脏移植。等待名单上供体与患者之间的差距推动了循环支持设备的发展,如全人工心脏(TAH)。本研究聚焦于使用由SynCardia Freedom®便携式驱动器(FD)驱动的CardioWest™ TAH(CW)进行的体外测试,其目标如下:i)证明用作患者模拟器的液压回路在各种流体动力学条件下复制准生理场景的可靠性,ii)研究CW FD的流体动力学性能,iii)帮助临床医生对临床病例结果进行可能的解释。

方法

使用机械液压患者模拟器进行体外测试。在体循环(SVR)和肺循环(PVR)生理范围内,针对不同血管阻力值测量心输出量(CO)、CW心室充盈、心房、心室、主动脉和肺动脉压力。

结果

增加PVR后,左心房压力按照预期的生理趋势下降,而主动脉压力几乎保持稳定,证明了模拟器模拟生理场景的能力。出乎意料的是,在生理PVR范围(2.6 WU)且CO恒定的情况下,发现平均肺动脉压力(PPA)升高至30 mmHg以上。

结论

PPA升高可能与FD的预设驱动设置有关。这一发现提示了对一名在接受FD支持后不久出现并发症、尽管心脏指数较高但仍出现呼吸困难和肺水肿的患者临床病程的一种可能解释。

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