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MRI条件性起搏器:当前观点

MRI-conditional pacemakers: current perspectives.

作者信息

Ferreira António M, Costa Francisco, Tralhão António, Marques Hugo, Cardim Nuno, Adragão Pedro

机构信息

Cardiology Department, Hospital da Luz, Lisbon, Portugal ; Cardiology Department, Hospital Santa Cruz-CHLO, Lisbon, Portugal.

Cardiology Department, Hospital Santa Cruz-CHLO, Lisbon, Portugal.

出版信息

Med Devices (Auckl). 2014 May 7;7:115-24. doi: 10.2147/MDER.S44063. eCollection 2014.

Abstract

Use of both magnetic resonance imaging (MRI) and pacing devices has undergone remarkable growth in recent years, and it is estimated that the majority of patients with pacemakers will need an MRI during their lifetime. These investigations will generally be denied due to the potentially dangerous interactions between cardiac devices and the magnetic fields and radio frequency energy used in MRI. Despite the increasing reports of uneventful scanning in selected patients with conventional pacemakers under close surveillance, MRI is still contraindicated in those circumstances and cannot be considered a routine procedure. These limitations prompted a series of modifications in generator and lead engineering, designed to minimize interactions that could compromise device function and patient safety. The resulting MRI-conditional pacemakers were first introduced in 2008 and the clinical experience gathered so far supports their safety in the MRI environment if certain conditions are fulfilled. With this technology, new questions and controversies arise regarding patient selection, clinical impact, and cost-effectiveness. In this review, we discuss the potential risks of MRI in patients with electronic cardiac devices and present updated information regarding the features of MRI-conditional pacemakers and the clinical experience with currently available models. Finally, we provide some guidance on how to scan patients who have these devices and discuss future directions in the field.

摘要

近年来,磁共振成像(MRI)和起搏设备的使用都有了显著增长,据估计,大多数起搏器患者在其一生中都需要进行MRI检查。由于心脏设备与MRI中使用的磁场和射频能量之间存在潜在的危险相互作用,这些检查通常会被拒绝。尽管越来越多的报告称,在密切监测下,部分使用传统起搏器的患者进行MRI扫描时平安无事,但在这些情况下,MRI检查仍被视为禁忌,不能被视为常规程序。这些限制促使人们对发生器和导线进行了一系列改进,旨在尽量减少可能影响设备功能和患者安全的相互作用。由此产生的MRI兼容起搏器于2008年首次推出,到目前为止积累的临床经验表明,如果满足某些条件,它们在MRI环境中是安全的。随着这项技术的出现,在患者选择、临床影响和成本效益方面出现了新的问题和争议。在这篇综述中,我们讨论了电子心脏设备患者进行MRI检查的潜在风险,并提供了有关MRI兼容起搏器特点和现有型号临床经验的最新信息。最后,我们就如何对装有这些设备的患者进行扫描提供一些指导,并讨论该领域的未来发展方向。

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