Department of Internal Medicine II, Division of Cardiology, Medical University of Vienna, Vienna, Austria.
Department of Biomedical Imaging and Image-guided Therapy, Medical University of Vienna, Vienna, Austria.
Eur J Radiol. 2019 Sep;118:96-100. doi: 10.1016/j.ejrad.2019.07.005. Epub 2019 Jul 9.
Low-field magnetic resonance imaging (MRI), i.e. MRI with a static magnetic field strength <0.5 T, has been reported to be safe in patients with pacemakers, however there are no data about the safety of low-field MRI in patients with implantable cardioverter defibrillators (ICD) and/or cardiac resynchronization therapy (CRT). We aimed to investigate the safety and diagnostic efficiency of routine low-field MRI in patients with different devices for cardiac rhythm management (i.e. pacemakers and ICD, including devices with CRT).
MRI scans of 446 regions of interest were evaluated with field strength of 0.2 T in 338 patients (62% male; age at MRI scan 76.1 ± 9.2 years; time since device implantation 4.1 ± 3.2 years) with cardiac rhythm management devices (298 pacemakers, 25 ICD, 8 CRT-ICD, and 7 CRT pacemakers). This analysis included 62 pacemaker-dependent patients (18.3%), 52 patients with 1.5-Tesla-MR conditional pacemakers (15.4%) and 13 patients with abandoned leads (3.9%).
Except for one examination, which was interrupted because of recurrent severe nausea, all MRI scans could be analyzed efficiently. No induction of arrhythmia or inhibition of pacemaker function occurred. Compared to the device interrogation before MRI, there were no significant changes in battery voltage, pacing capture threshold, sensing of intrinsic ECG, lead impedance, as well as shock impedance in ICD devices after completed examination.
Low-field MRI examinations (0.2 T) were efficient and safe regarding clinical and technical complications in patients with devices for cardiac rhythm management, even in case of pacemaker-dependency or the presence of abandoned leads.
低磁场磁共振成像(MRI),即磁场强度<0.5T 的 MRI,据报道在植入起搏器的患者中是安全的,然而,关于植入式心脏复律除颤器(ICD)和/或心脏再同步治疗(CRT)患者进行低磁场 MRI 的安全性尚无数据。我们旨在研究不同心脏节律管理设备(即起搏器和 ICD,包括具有 CRT 的设备)的患者进行常规低磁场 MRI 的安全性和诊断效率。
在 338 名患者(62%为男性;MRI 扫描时年龄 76.1±9.2 岁;植入设备后时间 4.1±3.2 年)中评估了 446 个感兴趣区域的 MRI 扫描,这些患者均具有心脏节律管理设备(298 个起搏器、25 个 ICD、8 个 CRT-ICD 和 7 个 CRT 起搏器)。该分析包括 62 名起搏器依赖患者(18.3%)、52 名 1.5-Tesla-MR 条件性起搏器患者(15.4%)和 13 名废弃导线患者(3.9%)。
除了一次因反复严重恶心而中断的检查外,所有 MRI 扫描都可以高效地进行分析。未发生心律失常的诱发或起搏器功能的抑制。与 MRI 检查前的设备检测相比,在完成检查后,ICD 设备中的电池电压、起搏捕获阈值、自身心电图感知、导线阻抗以及电击阻抗均无明显变化。
即使存在起搏器依赖或废弃导线的情况,低磁场 MRI 检查(0.2T)在具有心脏节律管理设备的患者中,在临床和技术并发症方面是高效且安全的。