System Integration and Preliminary Clinical Evaluation of a Robotic System for MRI-Guided Transperineal Prostate Biopsy.

Journal of medical robotics research Pub Date : 2019-06-01 Epub Date: 2018-05-15 DOI:10.1142/S2424905X19500016
Niravkumar A Patel, Gang Li, Weijian Shang, Marek Wartenberg, Tamas Heffter, Everette C Burdette, Iulian Iordachita, Junichi Tokuda, Nobuhiko Hata, Clare M Tempany, Gregory S Fischer
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引用次数: 29

Abstract

This paper presents the development, preclinical evaluation, and preliminary clinical study of a robotic system for targeted transperineal prostate biopsy under direct interventional magnetic resonance imaging (MRI) guidance. The clinically integrated robotic system is developed based on a modular design approach, comprised of surgical navigation application, robot control software, MRI robot controller hardware, and robotic needle placement manipulator. The system provides enabling technologies for MRI-guided procedures. It can be easily transported and setup for supporting the clinical workflow of interventional procedures, and the system is readily extensible and reconfigurable to other clinical applications. Preclinical evaluation of the system is performed with phantom studies in a 3 Tesla MRI scanner, rehearsing the proposed clinical workflow, and demonstrating an in-plane targeting error of 1.5mm. The robotic system has been approved by the institutional review board (IRB) for clinical trials. A preliminary clinical study is conducted with the patient consent, demonstrating the targeting errors at two biopsy target sites to be 4.0mm and 3.7mm, which is sufficient to target a clinically significant tumor foci. First-in-human trials to evaluate the system's effectiveness and accuracy for MR image-guide prostate biopsy are underway.

MRI引导下经会阴前列腺活检机器人系统的系统集成和初步临床评估
本文介绍了在直接介入性磁共振成像(MRI)引导下进行经会阴前列腺活检的机器人系统的开发、临床前评估和初步临床研究。临床集成机器人系统采用模块化设计方法,由手术导航应用、机器人控制软件、MRI机器人控制器硬件和机器人置针机械手组成。该系统为mri引导的程序提供了使能技术。它可以很容易地运输和设置,以支持介入手术的临床工作流程,并且系统易于扩展和可重构到其他临床应用。该系统的临床前评估是在一台3特斯拉的MRI扫描仪上进行的,模拟了提出的临床工作流程,并展示了1.5mm的平面内瞄准误差。该机器人系统已被机构审查委员会(IRB)批准用于临床试验。在患者同意的情况下,我们进行了初步的临床研究,发现两个活检靶位的靶向误差分别为4.0mm和3.7mm,足以靶向一个具有临床意义的肿瘤病灶。评估该系统在磁共振成像引导前列腺活检中的有效性和准确性的首次人体试验正在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.10
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