Department of Bioengineering, University of Pittsburgh McGowan Institute for Regenerative Medicine, University of Pittsburgh Cardiothoracic Surgery, Children's Hospital of Pittsburgh Department of Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Artif Organs. 2011 Jun;35(6):602-13. doi: 10.1111/j.1525-1594.2010.01124.x. Epub 2011 Apr 5.
The PediaFlow pediatric ventricular assist device (VAD) is a magnetically levitated turbodynamic pump under development for circulatory support of small children with a targeted flow rate range of 0.3-1.5 L/min. As the design of this device is refined, ensuring high levels of blood biocompatibility is essential. In this study, we characterized platelet activation during the implantation and operation of a second generation prototype of the PediaFlow VAD (PF2) and also performed a series of surgical sham studies to examine purely surgical effects on platelet activation. In addition, a newly available monoclonal antibody was characterized and shown to be capable of quantifying ovine platelet activation. The PF2 was implanted in three chronic ovine experiments of 17, 30, and 70 days, while surgical sham procedures were performed in five ovines with 30-day monitoring. Blood biocompatibility in terms of circulating activated platelets was measured by flow cytometric assays with and without exogenous agonist stimulation. Platelet activation following sham surgery returned to baseline in approximately 2 weeks. Platelets in PF2-implanted ovines returned to baseline activation levels in all three animals and showed an ability to respond to agonist stimulation. Late-term platelet activation was observed in one animal corresponding with unexpected pump stoppages related to a manufacturing defect in the percutaneous cable. The results demonstrated encouraging platelet biocompatibility for the PF2 in that basal platelet activation was achieved early in the pump implant period. Furthermore, this first characterization of the effect of a major cardiothoracic procedure on temporal ovine platelet activation provides comparative data for future cardiovascular device evaluation in the ovine model.
佩迪亚流儿科心室辅助装置(VAD)是一种磁悬浮涡轮动力泵,正在开发中,用于为小儿提供循环支持,目标流量范围为 0.3-1.5 L/min。随着该设备设计的不断完善,确保高水平的血液生物相容性至关重要。在这项研究中,我们对第二代佩迪亚流 VAD(PF2)的植入和运行过程中的血小板激活情况进行了表征,并进行了一系列手术假手术研究,以检查纯粹的手术对血小板激活的影响。此外,还对一种新的可用单克隆抗体进行了表征,并证明其能够定量检测绵羊血小板的激活情况。PF2 在 3 项为期 17、30 和 70 天的慢性绵羊实验中植入,而手术假手术在 5 只绵羊中进行了 30 天的监测。通过流式细胞术检测和无外源性激动剂刺激的方法,检测循环激活血小板的血液生物相容性。假手术后血小板激活在大约 2 周内恢复到基线水平。在所有 3 只动物中,植入 PF2 的绵羊血小板均恢复到基线激活水平,并表现出对激动剂刺激的反应能力。一只动物在晚期出现血小板激活,这与与经皮电缆制造缺陷相关的泵停止运行有关。结果表明,PF2 的血小板生物相容性令人鼓舞,即在泵植入早期就实现了基础血小板激活。此外,这是首次对重大心胸外科手术对绵羊血小板激活的时间影响进行的特征描述,为未来在绵羊模型中对心血管设备进行评估提供了比较数据。