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用于立体定向放射治疗的自适应磁共振成像

Synaptive Magnetic Resonance Imaging for Stereotactic Radiosurgery.

作者信息

Chaga Michael, Chen Timothy, Feng Wenzheng, Conti Darra, Feng Jing, Wang Tingyu, Rodrigo Ma Rhudelyn, Luick Elizabeth, Thompson Daniel, Baldwin Joy, Latif Brielle, Hanley Joseph, Danish Shabbar

机构信息

Radiation Oncology, Jersey Shore University Medical Center, Neptune, USA.

Neurological Surgery, Jersey Shore Medical Center, Neptune, USA.

出版信息

Cureus. 2024 Dec 12;16(12):e75600. doi: 10.7759/cureus.75600. eCollection 2024 Dec.

DOI:10.7759/cureus.75600
PMID:39803092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11724700/
Abstract

Introduction The Synaptive magnetic resonance imaging (MRI) system (Synaptive Medical, Toronto, Canada) is a midfield 0.5 T head-only scanner for imaging the head and neck in adults and pediatrics. The system received US FDA and Health Canada clearance for clinical use in 2020. Initial installations occurred at sites throughout Canada with the first international installation occurring in the USA at Hackensack Meridian's Jersey Shore University Medical Center (JSUMC) in October 2023. The design of the Synaptive MRI allows the system to be installed and operated outside the context of standard Radiology facilities. In this study, we describe the implementation and adaptation of the Synaptive MRI into the cranial stereotactic radiosurgery (SRS) workflow, with the intention of reducing the time between consultation, MRI, and treatment. Methods The Synaptive MRI was installed next to the cranial SRS suite in the Radiation Oncology (RO) department, dedicated solely to SRS planning image acquisition. Geometric distortion was evaluated using the Magphan 128 Distortion Phantom (Phantom Laboratory, Greenwich, NY). The simplicity of the Synaptive interface allows Radiation Therapist operation, in the State of New Jersey, without the need for the physical presence of an MRI technologist. During imaging acquisition, the Physician verifies image quality and can rescan or make adjustments as needed, allowing for instantaneous confirmation of image quality. The Synaptive comes with a full set of neuro pulse sequences and protocols ranging from T1 3D spoiled gradient recalled echo to time-of-flight magnetic resonance angiography. Patient MRI comfort was evaluated after treatment by questionnaire for 51 patients using a Likert scale from 1 to 5 (1 = "very poor", 5 = "very good"). The total Synaptive MRI time for 38 patients was tracked from arrival at the MRI suite to completion of imaging. Times from consult, imaging, and treatment for 58 ZAP-X (ZAP Surgical Systems, Inc., San Carlos, CA) SRS patients at JSUMC RO in 2024 who received Synaptive MRI were obtained from Aria (Varian Medical Systems, Palo Alto, CA) electronic medical records. JSUMC RO Departmental data was obtained on times from consult, imaging, and treatment for 58 randomly sampled patients from 2018 to 2023 whose treatment planning imaging was performed on out-of-department MRI units for comparison. Results The distortions on this system are less than 0.52 mm, for distances up to 90 mm from the isocenter. The average MRI comfort was 4.7 ± 0.5. The average total MRI time for 38 patients was 36 ± 3 minutes. The median time for 58 ZAP-X SRS patients from MRI to treatment was seven days (interquartile range: p25 = six days, p75 = 10 days), consult to MRI 1.5 days (p25 = 0 days, p75 = nine days), and consult to treatment 12 days (p25 = seven days, p75 = 19 days). The median time for 34 malignant ZAP-X SRS patients from MRI to treatment was six days (p25 = five days, p75 = eight days) and from consult to treatment nine days (p25 = six days, p75 = 18 days). Significant decreases in MRI to treatment times (P < 0.001) and benign consult to MRI times (P = 0.0039) were demonstrated for 2024 Synaptive patients compared to 2018-2023 patients. Conclusion Dedicated Synaptive MRI installation for SRS in RO departments can improve the SRS workflow, potentially providing a more streamlined experience and reducing the time from diagnosis and imaging to treatment for cranial pathologies.

摘要

引言

Synaptive磁共振成像(MRI)系统(加拿大多伦多的Synaptive Medical公司)是一款中场0.5T的仅用于头部的扫描仪,用于对成人和儿童的头部及颈部进行成像。该系统于2020年获得美国食品药品监督管理局(US FDA)和加拿大卫生部的临床使用许可。最初在加拿大各地的医疗机构安装,2023年10月在美国哈肯萨克子午线医疗集团(Hackensack Meridian)的泽西海岸大学医学中心(JSUMC)进行了首次国际安装。Synaptive MRI的设计使得该系统能够在标准放射科设施之外进行安装和操作。在本研究中,我们描述了将Synaptive MRI应用于立体定向放射外科(SRS)治疗流程的过程及调整,旨在缩短会诊、MRI检查和治疗之间的时间间隔。

方法

Synaptive MRI安装在放射肿瘤学(RO)部门的颅脑SRS治疗室旁边,专门用于SRS治疗计划图像采集工作。使用Magphan 128畸变模型(纽约格林威治的Phantom Laboratory公司)评估几何畸变情况。Synaptive的操作界面简单,在新泽西州,放射治疗师无需MRI技术人员在场即可操作。在图像采集过程中,医生可检查图像质量,并根据需要重新扫描或进行调整,以便即时确认图像质量。Synaptive配备了全套神经脉冲序列和协议,从T1 3D扰相梯度回波序列到时间飞跃磁共振血管造影序列。治疗后通过问卷调查评估了51例患者对MRI检查的舒适度,采用1至5分的李克特量表(1 = “非常差”,5 = “非常好”)。记录了38例患者从到达MRI检查室到完成成像的总Synaptive MRI检查时间。从Aria(加利福尼亚州帕洛阿尔托的Varian Medical Systems公司)电子病历中获取了2024年在JSUMC RO接受Synaptive MRI检查的58例ZAP-X(加利福尼亚州圣卡洛斯的ZAP Surgical Systems公司)SRS患者的会诊、成像和治疗时间。获取了JSUMC RO部门2018年至2023年58例随机抽样患者的会诊、成像和治疗时间数据,这些患者的治疗计划成像在科室外的MRI设备上进行,用于对比。

结果

该系统在距等中心90mm范围内的畸变小于0.52mm。MRI检查舒适度平均评分为4.7 ± 0.5。38例患者的平均总MRI检查时间为36 ± 3分钟。58例ZAP-X SRS患者从MRI检查到治疗的中位时间为7天(四分位间距:第25百分位数 = 6天,第75百分位数 = 10天),从会诊到MRI检查为1.5天(第25百分位数 = 0天,第75百分位数 = 9天),从会诊到治疗为12天(第25百分位数 = 7天,第75百分位数 = 19天)。34例恶性ZAP-X SRS患者从MRI检查到治疗的中位时间为6天(第25百分位数 = 5天,第75百分位数 = 8天),从会诊到治疗为9天(第25百分位数 = 6天,第75百分位数 = 18天)。与2018 - 2023年的患者相比,2024年接受Synaptive MRI检查的患者在MRI检查到治疗时间(P < 0.001)和良性疾病会诊到MRI检查时间(P = 0.0039)上显著缩短。

结论

在RO部门为SRS治疗专门安装Synaptive MRI可改善SRS治疗流程,有可能提供更简化的体验,并减少从颅部疾病诊断、成像到治疗的时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/5048f0115e81/cureus-0016-00000075600-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/44f3a9991405/cureus-0016-00000075600-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/d1057618d5c0/cureus-0016-00000075600-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/ec6145296b15/cureus-0016-00000075600-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/5048f0115e81/cureus-0016-00000075600-i04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/44f3a9991405/cureus-0016-00000075600-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/d1057618d5c0/cureus-0016-00000075600-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/ec6145296b15/cureus-0016-00000075600-i03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e476/11724700/5048f0115e81/cureus-0016-00000075600-i04.jpg

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