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评估一款用于植入式设备患者的紧凑型 3T MRI 扫描仪。

Evaluation of a compact 3 T MRI scanner for patients with implanted devices.

机构信息

Department of Radiology, Mayo Clinic, Rochester, MN, United States; Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic, Rochester, MN, United States.

Department of Radiology, Mayo Clinic, Rochester, MN, United States.

出版信息

Magn Reson Imaging. 2023 Nov;103:109-118. doi: 10.1016/j.mri.2023.07.009. Epub 2023 Jul 17.

Abstract

Access to high-quality MR exams is severely limited for patients with some implanted devices due to labeled MR safety conditions, but small-bore systems can overcome this limitation. For example, a compact 3 T MR scanner (C3T) with high-performance gradients can acquire exams of the head, extremities, and infants. Because of its reduced bore size and the patient being advanced only partially into the bore, the associated electromagnetic (EM) fields drop off rapidly caudal to the head, compared to whole-body systems. Therefore, some patients with MR conditional implanted devices can safely receive 3 T brain exams on the C3T using its strong gradients and a multiple-channel receive coil, while a corresponding exam on whole-body MR is precluded. The purpose of this study is to evaluate the performance of a small-bore scanner for subjects with MR conditional spinal or sacral nerve stimulators, or abandoned cardiac implantable electronic device (CIED) leads. The spatial dependence of specific absorption rate (SAR) on the C3T was compared to whole-body scanners. A device assessment tool was developed and applied to evaluate MR safety individually on the C3T for 12 subjects with implanted devices or abandoned CIED leads. Once MR safety was established, the subjects received a C3T brain exam along with their clinical, 1.5 T exam. The resulting images were graded by three board-certified neuroradiologists. The C3T exams were well-tolerated with no adverse events, and significantly outperformed the whole-body 1.5 T exams in terms of overall image quality.

摘要

由于标记的磁共振安全条件,一些植入设备的患者获得高质量的磁共振检查的机会受到严重限制,但小口径系统可以克服这一限制。例如,具有高性能梯度的紧凑型 3T 磁共振扫描仪(C3T)可以采集头部、四肢和婴儿的检查。由于其孔径较小,并且患者仅部分进入孔径,与全身系统相比,头端以外的电磁(EM)场迅速下降。因此,一些具有磁共振条件植入设备的患者可以在 C3T 上使用其强大的梯度和多通道接收线圈安全地进行 3T 脑部检查,而全身磁共振检查则被排除在外。本研究的目的是评估小口径扫描仪在具有磁共振条件的脊柱或骶神经刺激器或废弃的心脏植入式电子设备(CIED)导线的患者中的性能。比较了 C3T 上特定吸收率(SAR)的空间依赖性与全身扫描仪。开发了一种设备评估工具,并应用于 12 名植入设备或废弃 CIED 导线的患者,在 C3T 上单独评估磁共振安全性。一旦确定磁共振安全性,患者将在 C3T 上进行脑部检查,并进行其临床 1.5T 检查。由三位经过董事会认证的神经放射科医生对所得图像进行分级。C3T 检查耐受良好,无不良事件发生,并且在整体图像质量方面明显优于全身 1.5T 检查。

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