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用于磁共振成像的无导线经导管起搏器的安全性评估。

Safety evaluation of a leadless transcatheter pacemaker for magnetic resonance imaging use.

作者信息

Soejima Kyoko, Edmonson Jonathan, Ellingson Michael L, Herberg Ben, Wiklund Craig, Zhao Jing

机构信息

Department of Cardiology, Kyorin University Hospital, Tokyo, Japan.

Medtronic plc, Mounds View, Minnesota.

出版信息

Heart Rhythm. 2016 Oct;13(10):2056-63. doi: 10.1016/j.hrthm.2016.06.032. Epub 2016 Jun 29.

DOI:10.1016/j.hrthm.2016.06.032
PMID:27374239
Abstract

BACKGROUND

Increased magnetic resonance imaging (MRI) adoption and demand are driving the need for device patients to have safe access to MRI.

OBJECTIVE

The aim of this study was to address the interactions of MRI with the Micra transcatheter pacemaker system.

METHODS

A strategy was developed to evaluate potential MRI risks including device heating, unintended cardiac stimulation, force, torque, vibration, and device malfunction. Assessment of MRI-induced device heating was conducted using a phantom containing gelled saline, and Monte Carlo simulations incorporating these results were conducted to simulate numerous combinations of human body models, position locations in the MRI scanner bore, and a variety of coil designs. Lastly, a patient with a Micra pacemaker who underwent a clinically indicated MRI scan is presented.

RESULTS

Compared to traditional MRI conditional pacemakers, the overall risk with Micra was greatly reduced because of the small size of the device and the absence of a lead. The modeling results predicted that the nonperfused temperature rise of the device would be less than 0.4°C at 1.5 T and 0.5°C at 3 T and that the risk of device heating with multiple device implants was not increased as compared with a single device. The clinical case study revealed no MRI-related complications.

CONCLUSION

The MRI safety assessment tests conducted for the Micra pacemaker demonstrate that patients with a single device or multiple devices can safely undergo MRI scans in both 1.5- and 3-T MRI scanners. No MRI-related complications were observed in a patient implanted with a Micra pacemaker undergoing a clinically indicated scan.

摘要

背景

磁共振成像(MRI)的应用增加及需求增长促使需要让植入设备的患者能够安全地接受MRI检查。

目的

本研究旨在探讨MRI与Micra经导管起搏器系统之间的相互作用。

方法

制定了一项策略来评估潜在的MRI风险,包括设备发热、意外心脏刺激、力、扭矩、振动和设备故障。使用含有凝胶状盐水的体模对MRI诱导的设备发热进行评估,并结合这些结果进行蒙特卡洛模拟,以模拟多种人体模型、MRI扫描仪孔内的位置以及各种线圈设计的组合。最后,介绍了一名植入Micra起搏器并接受临床指征MRI扫描的患者。

结果

与传统的MRI兼容起搏器相比,由于Micra设备体积小且无导线,其总体风险大大降低。建模结果预测,在1.5 T时设备的非灌注温度升高将小于0.4°C,在3 T时小于0.5°C,并且与单个设备相比,多个设备植入时设备发热的风险并未增加。临床病例研究未发现与MRI相关的并发症。

结论

对Micra起搏器进行的MRI安全性评估测试表明,植入单个或多个设备的患者可以在1.5 T和3 T的MRI扫描仪中安全地接受MRI扫描。在接受临床指征扫描的植入Micra起搏器的患者中未观察到与MRI相关的并发症。

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