Department of Radiology, Mater Private Hospital, Eccles St, Dublin, 7, Ireland.
Department of Radiology, Mater Misericordiae University Hospital, Eccles St, Dublin, 7, Ireland.
Ir J Med Sci. 2019 Aug;188(3):999-1004. doi: 10.1007/s11845-018-1922-y. Epub 2018 Oct 27.
Patients with cardiac implantable electronic devices (CIEDs) were traditionally denied access to MR imaging due to safety concerns.
The aim of this study was to review a single-center experience of MR imaging at 1.5T of patients with CIEDs and survey national availability of this service.
Three hundred thirty-four patients with CIEDs were included in the review. Two hundred nine patients did not progress to MRI due to non MR-conditional CIEDs, retained pacing leads, recent implant insertion, and other patient factors. A record was made of CIED type, number of body parts imaged, numbers of repeat studies and complications. All devices were scanned with cardiology involvement.
One hundred twenty-five patients, 90 males, 35 females, aged 20-91 years progressed to MR imaging. Eighty-six patients had pacemakers, 15 had implantable cardioverter devices (ICDs), and 24 had implantable loop recorders (ILRs). Twenty-one patients had more than one body part scanned. Regions scanned included spine n = 82, joints n = 42, head n = 40, heart n = 8, and abdomen/pelvis n = 13. Twenty-six patients had multiple separate MR studies (range 2-6). Three complications included diaphragmatic stimulation when the device was switched to MR-conditional mode resulting in scan abandonment, device failure post-MRI requiring manufacturer reprogramming, and patient dizziness post reprogramming requiring cardiology review. One cardiac study was non-diagnostic due to artifact from a low left-sided ICD. Imaging of patients with pacemakers is available in 14 of 42 (38%) hospitals with MR units nationally.
MR-conditional CIEDs can be safely scanned with diagnostic quality at 1.5T using a protocol involving radiology and cardiology.
由于安全问题,传统上患有心脏植入式电子设备(CIED)的患者被拒绝进行磁共振成像(MRI)检查。
本研究旨在回顾单中心 1.5T 场强下 CIED 患者行 MRI 的经验,并调查全国范围内该服务的可用性。
共纳入 334 例 CIED 患者。209 例患者因非 MRI 条件下的 CIED、保留的起搏导线、近期植入以及其他患者因素而未进行 MRI。记录 CIED 类型、成像身体部位数量、重复研究次数和并发症。所有设备均在心脏病学参与下进行扫描。
125 例患者(90 例男性,35 例女性),年龄 20-91 岁,进展至 MRI 检查。86 例患者为起搏器,15 例为植入式心律转复除颤器(ICD),24 例为植入式环路记录器(ILR)。21 例患者有超过一个身体部位被扫描。扫描区域包括脊柱 n=82,关节 n=42,头部 n=40,心脏 n=8,腹部/骨盆 n=13。26 例患者进行了多次单独的 MRI 检查(范围 2-6 次)。3 例并发症包括设备切换至 MRI 条件模式时膈肌刺激导致扫描中止、MRI 后设备故障需要制造商重新编程以及重新编程后患者头晕需要心内科评估。1 例心脏研究因来自低位左侧 ICD 的伪影而无法诊断。全国 42 家拥有 MRI 设备的医院中有 14 家(38%)可以为起搏器患者进行 MRI 检查。
使用涉及放射科和心脏病学的方案,可在 1.5T 场强下安全地扫描具有诊断质量的 MRI 条件下的 CIED。