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Virtual Humans for Implantable Device Safety Assessment in MRI: Mitigating Magnetic Resonance Imaging Hazards for Implanted Medical Devices

机译:在MRI中用于植入式设备安全性评估的虚拟人:减轻植入式医疗设备的磁共振成像危害

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摘要

Magnetic resonance imaging (MRI) is the preferred modality for soft tissue imaging because of its nonionizing radiation and lack of contrast agent. Due to interactions between the MR system and active implantable medical devices (AIMDs), patients with implants such as pacemakers are generally denied access to MRI, which presents a detriment to that population. It has been estimated that 50-75% of patients with a cardiac device were denied access to MRI scanning and, moreover, that 17% of pacemaker patients need an MRI within 12 months of implantation [1]. In recent years, AIMD manufacturers, such as Biotronik, have assessed the conditional safety of devices in MRI.
机译:磁共振成像(MRI)是软组织成像的首选方式,因为它的非电离辐射和缺乏造影剂。由于MR系统与有源可植入医疗设备(AIMD)之间的相互作用,通常会禁止带有诸如起搏器之类的植入物的患者使用MRI,这不利于该人群。据估计,有50-75%的有心脏器械的患者无法进行MRI扫描,此外,有17%的起搏器患者在植入后12个月内需要MRI [1]。近年来,AIMD制造商(例如Biotronik)已经评估了MRI设备的条件安全性。

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