Auckland Bioengineering Institute, University of Auckland, Auckland, New Zealand.
Faculty of Medical and Health Sciences, University of Auckland, Auckland, New Zealand.
Artif Organs. 2020 Sep;44(9):955-967. doi: 10.1111/aor.13679. Epub 2020 Apr 8.
Current generation left ventricular assist devices (LVADs) are powered by a percutaneous driveline. The high prevalence of driveline infections has motivated the development of transcutaneous energy transfer (TET) systems which eliminate driveline associated complications by wirelessly delivering power across the skin. Destination therapy (DT) requires long-term reliable operation of the TET electronics suggesting the use of hermetic packaging techniques as used in all other chronically implanted devices. TET coils dissipate heat during operation and in order for the technology to be suitable for patient use, sufficient power must be delivered while maintaining temperatures at levels deemed safe. The heating of a TET system designed for DT which uses hermetic packaging technology was evaluated in silico and in vivo. A numerical model was used to evaluate the temperature of the TET coils. The TET system was fabricated and assessed in vivo using an ovine model. The receiving coil was implanted subcutaneously in a sheep and the transmission coil placed in contact with the skin and concentric to the implanted coil. Temperatures of the system were measured using sensors fixed to the surface of the coils. Numerical modeling indicated that the maximum temperatures of the primary and secondary coil surfaces were 38.13°C and 38.41°C, respectively, when delivering 10 W continuously. Stable temperatures were observed in vivo after 70 minutes and the maximum skin and implant surface temperatures were 37.73°C and 38.31°C, respectively. This study showed that a hermetic, chronically implantable TET system is thermally safe when continuously delivering 10 W of power, sufficient to power modern LVADs.
当前一代左心室辅助装置 (LVAD) 通过经皮动力轴驱动。由于动力轴感染的高发率,促使人们开发了经皮能量传输 (TET) 系统,该系统通过无线传输电能,消除了与动力轴相关的并发症。目标治疗 (DT) 需要 TET 电子设备长期可靠运行,这表明需要使用所有其他慢性植入设备中使用的密封包装技术。TET 线圈在运行过程中会散热,为了使该技术适合患者使用,在保持认为安全的温度水平的同时,必须输送足够的功率。使用密封包装技术的用于 DT 的 TET 系统的加热情况在计算机模拟和体内进行了评估。使用数值模型评估 TET 线圈的温度。该 TET 系统已制造并在绵羊模型中进行了体内评估。接收线圈被植入皮下,传输线圈与皮肤接触并与植入线圈同心。使用固定在线圈表面的传感器测量系统温度。数值模型表明,当连续输送 10 W 功率时,初级和次级线圈表面的最高温度分别为 38.13°C 和 38.41°C。70 分钟后在体内观察到稳定的温度,最大皮肤和植入表面温度分别为 37.73°C 和 38.31°C。这项研究表明,当连续输送 10 W 的功率时,密封的、慢性可植入的 TET 系统在热学上是安全的,足以为现代 LVAD 供电。