首页> 美国卫生研究院文献>Journal of Applied Clinical Medical Physics >A technical evaluation of the Nucletron FIRST system: Conformance of a remote afterloading brachytherapy seed implantation system to manufacturer specifications and AAPM Task Group report recommendations
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A technical evaluation of the Nucletron FIRST system: Conformance of a remote afterloading brachytherapy seed implantation system to manufacturer specifications and AAPM Task Group report recommendations

机译:Nucletron FIRST系统的技术评估:远程后载近距离放射治疗植入系统符合制造商规范和AAPM任务组报告的建议

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摘要

The Fully Integrated Real‐time Seed Treatment (FIRST™) system by Nucletron has been available in Europe since November 2001 and is being used more and more in Canada and the United States. Like the conventional transrectal ultrasound implant procedure, the FIRST system utilizes an ultrasound probe, needles, and brachytherapy seeds. However, this system is unique in that it (1) utilizes a low‐dose‐rate brachytherapy seed remote afterloader (the seedSelectron), (2) utilizes 3D image reconstruction acquired from electromechanically controlled, nonstepping rotation of the ultrasound probe, (3) integrates the control of a remote afterloader with electromechanical control of the ultrasound probe for integrating the clinical procedure into a single system, and (4) automates the transfer of planning information and seed delivery to improve quality assurance and radiation safety. This automated delivery system is specifically intended to address reproducibility and accuracy of seed positioning during implantation. The FIRST computer system includes two software environments: SPOT PRO™ and seedSelectron™; both are used to facilitate treatment planning and brachytherapy seed implantation from beginning to completion of the entire procedure. In addition to these features, the system is reported to meet certain product specifications for seed delivery positioning accuracy and reproducibility, seed calibration accuracy and reliability, and brachytherapy dosimetry calculations. Consequently, a technical evaluation of the FIRST system was performed to determine adherence to manufacturer specifications and to the American Association of Physicists in Medicine (AAPM) Task Group Reports 43, 53, 56, 59, and 64 and recommendations of the American Brachytherapy Society (ABS). The United States Nuclear Regulatory Commission (NRC) has recently added Licensing Guidance for the seedSelectron system under 10 CFR 35.1000. Adherence to licensing guidance is made by referencing applicable AAPM Task Group recommendations. In general, results of this evaluation indicated that the system met its claimed specifications as well as the applicable recommendations outlined in the AAPM and ABS reports.PACS number(s): 87.53.Xd, 87.53.Jw
机译:Nucletron的完全集成实时种子处理(FIRST™)系统自2001年11月起在欧洲上市,并在加拿大和美国越来越多地使用。像常规的经直肠超声植入程序一样,FIRST系统使用超声探头,针头和近距离放射治疗种子。但是,该系统的独特之处在于:(1)利用低剂量率近距离放射治疗的远程种子加载器(seedSelectron),(2)利用从超声探头的机电控制,非步进旋转获得的3D图像重建,(3)将远程后装载器的控制与超声探头的机电控制集成在一起,以将临床程序集成到单个系统中;(4)使计划信息的传输和种子输送自动化,以提高质量保证和辐射安全性。该自动输送系统专门用于解决植入过程中种子定位的可重复性和准确性。 FIRST计算机系统包括两个软件环境:SPOT PRO™和seedSelectron™。从整个过程的开始到完成,这两种方法都可用于促进治疗计划和近距离放射治疗植入。除这些功能外,据报道该系统还满足某些产品规格的要求,如种子输送定位精度和可重复性,种子校准精度和可靠性以及近距离放射剂量学计算。因此,对FIRST系统进行了技术评估,以确定其是否符合制造商的规范以及对美国医学物理学家协会(AAPM)任务组报告43、53、56、59和64的建议以及美国近距离放射治疗协会的建议( ABS)。美国核管理委员会(NRC)最近添加了10 CFR 35.1000下的seedSelectron系统许可指南。通过参考适用的AAPM任务组建议来遵守许可指南。总体而言,该评估结果表明系统符合要求的规格以及AAPM和ABS报告中概述的适用建议.PACS编号:87.53.Xd,87.53.Jw

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