Safety of Magnetic Resonance Imaging in Patients with Cardiac Implantable Electronic Devices.

IF 2.4 4区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS Journal of Cardiovascular Development and Disease Pub Date : 2024-10-08 DOI:10.3390/jcdd11100313
Hugo Lanz, Katharina Strauß, Julia Höpler, Marie Kraft, Sabine Hoffmann, Leonhard Binzenhöfer, Nils Gade, Daniel Roden, Inas Saleh, Stefan Kääb, Korbinian Lackermair, Sebastian Sadoni, Christian Hagl, Steffen Massberg, Heidi Estner, Stephanie Fichtner, Enzo Lüsebrink
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Abstract

Background: MRI (magnetic resonance imaging) represents the diagnostic image modality of choice in several conditions. With an increasing number of patients requiring MRI for diagnostic purposes, the issue of safety in patients with cardiac implantable electronic devices (CIED) undergoing this imaging modality will play an ever more important role. The purpose of this study was to assess the safety and device function following MRI in an unrestricted real-world cohort of patients with a wide array of cardiac devices.

Methods: We conducted a retrospective single-center study including 1010 MRI studies conducted in adult patients (≥18 years) with an implanted CIED treated in the University Hospital of Munich (LMU) between July 2012 and March 2024. Patients with non-MR conditionally labeled leads, abandoned or epicardial leads, as well as lead fragments, were included for analysis.

Results: Across a total of 1010 MRIs (920 total MR-conditional device generators) performed in patients with an implanted CIED, there were no deaths, reports of discomfort, palpitations, heating, or ventricular arrythmias in the 24 h following MRI. Only 2/1010 MRIs were followed by a reported atrial arrhythmia within 24 h, both in patients with an MR-conditional pacemaker (PM) device without an abandoned lead. No significant changes in device function following MRI from baseline were observed across all included CIEDs. Lastly, no instances of severe malfunction, such as generator failure, loss of capture, electrical reset, or inappropriate inhibition of pacing, were found in post-MRI interrogation reports across all MRI studies.

Conclusions: Based on the analysis of 1010 MRIs undergone by patients with CIEDs, following standardized device interrogation, manufacturer-advised device programming, monitoring of vital function, and manufacturer-advised reprogramming, MRI can be performed safely and without adverse events or changes in device function.

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心脏植入式电子装置患者的磁共振成像安全性。
背景:磁共振成像(MRI)是多种疾病的首选诊断成像方式。随着越来越多的患者需要通过核磁共振成像进行诊断,心脏植入式电子装置(CIED)患者接受这种成像方式的安全性问题将扮演越来越重要的角色。本研究的目的是在不受限制的真实世界中,对使用各种心脏设备的患者进行核磁共振成像后的安全性和设备功能进行评估:我们进行了一项回顾性单中心研究,其中包括 2012 年 7 月至 2024 年 3 月期间在慕尼黑大学医院(LMU)接受治疗的植入式 CIED 的成年患者(≥18 岁)进行的 1010 次 MRI 检查。分析对象包括非磁共振条件标记导联、废弃导联或心外膜导联以及导联碎片的患者:植入 CIED 的患者共进行了 1010 次 MRI(共 920 个 MR 条件设备发生器),在 MRI 后的 24 小时内没有死亡、不适、心悸、发热或室性心律失常报告。只有 2/1010 例患者在磁共振成像后 24 小时内出现房性心律失常,这两例患者均安装了磁共振条件性起搏器 (PM) 装置,但没有废弃导联。在所有纳入的 CIED 中,均未观察到核磁共振成像后设备功能与基线相比有明显变化。最后,在所有磁共振成像研究的磁共振成像后检查报告中均未发现严重故障,如发生器故障、捕获丢失、电复位或起搏抑制不当等:根据对 1010 例 CIED 患者进行的 MRI 分析,在进行标准化设备检查、制造商建议的设备编程、生命功能监测和制造商建议的重新编程后,可以安全地进行 MRI,且不会发生不良事件或设备功能变化。
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来源期刊
Journal of Cardiovascular Development and Disease
Journal of Cardiovascular Development and Disease CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
2.60
自引率
12.50%
发文量
381
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