Dartmouth College, Thayer School of Engineering, Hanover, New Hampshire 03755, United States.
Dartmouth College, Thayer School of Engineering, Hanover, New Hampshire 03755, United StatesbFujian Normal University, MOE Key Laboratory of OptoElectronic Science and Technology for Medicine, Fujian Provincial Key Laboratory for Photonics Technology, Fuj.
J Biomed Opt. 2016 Aug 1;21(8):80901. doi: 10.1117/1.JBO.21.8.080901.
There is growing interest in using fluorescence imaging instruments to guide surgery, and the leading options for open-field imaging are reviewed here. While the clinical fluorescence-guided surgery (FGS) field has been focused predominantly on indocyanine green (ICG) imaging, there is accelerated development of more specific molecular tracers. These agents should help advance new indications for which FGS presents a paradigm shift in how molecular information is provided for resection decisions. There has been a steady growth in commercially marketed FGS systems, each with their own differentiated performance characteristics and specifications. A set of desirable criteria is presented to guide the evaluation of instruments, including: (i) real-time overlay of white-light and fluorescence images, (ii) operation within ambient room lighting, (iii) nanomolar-level sensitivity, (iv) quantitative capabilities, (v) simultaneous multiple fluorophore imaging, and (vi) ergonomic utility for open surgery. In this review, United States Food and Drug Administration 510(k) cleared commercial systems and some leading premarket FGS research systems were evaluated to illustrate the continual increase in this performance feature base. Generally, the systems designed for ICG-only imaging have sufficient sensitivity to ICG, but a fraction of the other desired features listed above, with both lower sensitivity and dynamic range. In comparison, the emerging research systems targeted for use with molecular agents have unique capabilities that will be essential for successful clinical imaging studies with low-concentration agents or where superior rejection of ambient light is needed. There is no perfect imaging system, but the feature differences among them are important differentiators in their utility, as outlined in the data and tables here.
人们对使用荧光成像仪器来指导手术越来越感兴趣,这里回顾了用于开放式成像的主要选项。虽然临床荧光引导手术(FGS)领域主要集中在吲哚菁绿(ICG)成像上,但更具特异性的分子示踪剂的开发也在加速。这些试剂应该有助于推进新的适应症,为这些适应症,FGS 在提供切除决策的分子信息方面带来了范式转变。商业化的 FGS 系统数量稳步增长,每个系统都具有自己独特的性能特点和规格。提出了一套理想的标准来指导仪器的评估,包括:(i)白光和荧光图像的实时叠加,(ii)在环境室内照明下操作,(iii)纳摩尔级灵敏度,(iv)定量能力,(v)同时进行多个荧光团成像,以及(vi)开放式手术的人体工程学实用性。在这篇综述中,评估了美国食品和药物管理局 510(k) 批准的商业系统和一些领先的上市前 FGS 研究系统,以说明这种性能特征基础的持续增长。一般来说,专为 ICG 成像设计的系统对 ICG 具有足够的灵敏度,但缺乏上述部分理想特性,包括灵敏度和动态范围较低。相比之下,新兴的研究系统针对分子试剂的使用进行了优化,具有独特的功能,对于使用低浓度试剂或需要更好地抑制环境光的成功临床成像研究至关重要。没有完美的成像系统,但它们之间的功能差异是其用途的重要区别因素,如这里的数据和表格所示。