Lee Audrey, Baker Turner S, Bederson Joshua B, Rapoport Benjamin I
Department of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
Sinai BioDesign, Icahn School of Medicine at Mount Sinai, New York, New York, USA.
NPJ Digit Med. 2024 Apr 26;7(1):103. doi: 10.1038/s41746-024-01102-y.
The integration of robotics in surgery has increased over the past decade, and advances in the autonomous capabilities of surgical robots have paralleled that of assistive and industrial robots. However, classification and regulatory frameworks have not kept pace with the increasing autonomy of surgical robots. There is a need to modernize our classification to understand technological trends and prepare to regulate and streamline surgical practice around these robotic systems. We present a systematic review of all surgical robots cleared by the United States Food and Drug Administration (FDA) from 2015 to 2023, utilizing a classification system that we call Levels of Autonomy in Surgical Robotics (LASR) to categorize each robot's decision-making and action-taking abilities from Level 1 (Robot Assistance) to Level 5 (Full Autonomy). We searched the 510(k), De Novo, and AccessGUDID databases in December 2023 and included all medical devices fitting our definition of a surgical robot. 37,981 records were screened to identify 49 surgical robots. Most surgical robots were at Level 1 (86%) and some reached Level 3 (Conditional Autonomy) (6%). 2 surgical robots were recognized by the FDA to have machine learning-enabled capabilities, while more were reported to have these capabilities in their marketing materials. Most surgical robots were introduced via the 510(k) pathway, but a growing number via the De Novo pathway. This review highlights trends toward greater autonomy in surgical robotics. Implementing regulatory frameworks that acknowledge varying levels of autonomy in surgical robots may help ensure their safe and effective integration into surgical practice.
在过去十年中,机器人技术在手术中的应用日益广泛,手术机器人自主能力的进步与辅助机器人和工业机器人齐头并进。然而,分类和监管框架并未跟上手术机器人自主性不断提高的步伐。有必要对我们的分类进行现代化,以了解技术趋势,并准备围绕这些机器人系统规范和简化手术操作。我们对2015年至2023年期间美国食品药品监督管理局(FDA)批准的所有手术机器人进行了系统综述,使用一种我们称为手术机器人自主性水平(LASR)的分类系统,将每个机器人的决策和行动能力从1级(机器人辅助)到5级(完全自主)进行分类。我们于2023年12月搜索了510(k)、De Novo和AccessGUDID数据库,并纳入了所有符合我们对手术机器人定义的医疗设备。共筛选了37981条记录,以确定49台手术机器人。大多数手术机器人处于1级(86%),一些达到了3级(有条件自主)(6%)。有2台手术机器人被FDA认可具有机器学习能力,而更多的在其营销材料中声称具有这些能力。大多数手术机器人是通过510(k)途径引入的,但通过De Novo途径引入的数量在不断增加。本综述突出了手术机器人向更高自主性发展的趋势。实施承认手术机器人不同自主水平的监管框架可能有助于确保它们安全有效地融入手术实践。