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并非所有起搏器都一样:MRI 兼容起搏器和导线技术。

Not all pacemakers are created equal: MRI conditional pacemaker and lead technology.

机构信息

Manchester Heart Centre, Manchester Royal Infirmary, Manchester, UK; Cardiovascular Research Institute, University of Manchester, Manchester, UK.

出版信息

J Cardiovasc Electrophysiol. 2013 Sep;24(9):1059-65. doi: 10.1111/jce.12238.

Abstract

Due to expanding clinical indications and an aging society there has been an increase in the use of implantable pacemakers. At the same time, due to increased diagnostic yield over other imaging modalities and the absence of ionizing radiation, there has been a surge in demand for magnetic resonance imaging (MRI) assessment, of both cardiac and noncardiac conditions. Patients with an implantable device have a 50-75% chance of having a clinical indication for MRI during the lifetime of their device. The presence of an implantable cardiac device has been seen as a relative contraindication to MRI assessment, limiting the prognostic and diagnostic utility of MRI in many patients with these devices. The introduction of MRI conditional pacemakers will enable more patients to undergo routine MRI assessment without risk of morbidity or device malfunction. This review gives a general overview of the principles and current evidence for the use of MRI conditional implantable cardiac devices. Furthermore, we appraise the differences between those pacemakers currently released to market.

摘要

由于临床适应证的不断扩大和人口老龄化,植入式起搏器的使用也在不断增加。与此同时,由于其他成像方式的诊断效果提高,且没有放射性,因此对心脏和非心脏疾病的磁共振成像(MRI)评估的需求也出现了激增。在设备的使用寿命期间,有植入式设备的患者有 50-75%的机会出现 MRI 临床适应证。植入式心脏设备的存在被视为 MRI 评估的相对禁忌症,限制了许多带有这些设备的患者的 MRI 的预后和诊断效用。MRI 条件性起搏器的引入将使更多的患者能够接受常规 MRI 评估,而不会有发病或设备故障的风险。本综述概述了 MRI 条件性植入式心脏设备使用的原则和当前证据。此外,我们还评估了目前市场上已发布的起搏器之间的差异。

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