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Automated placement of retinal laser lesions in vivo

机译:体内视网膜激光病变的自动放置

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Abstract: Researchers at the University of Texas at Austin's Biomedical Engineering Laser Laboratory investigating the medical applications of lasers have worked toward the development of a retinal robotic laser system. The overall goal of the ongoing project is to precisely place and control the depth of laser lesions for the treatment of various retinal diseases such as diabetic retinopathy and retinal tears. Researchers at the USAF Academy's Department of Electrical Engineering and the Optical Radiation Division of Armstrong Laboratory have also become involved with this research due to similar related interests. Separate low speed prototype subsystems have been developed to control lesion depth using lesion reflectance feedback parameters and lesion placement using retinal vessels as tracking landmarks. Both subsystems have been successfully demonstrated in vivo on pigmented rabbits using an argon continuous wave laser. Work is ongoing to build a prototype system to simultaneously control lesion depth and placement. Following the dual-use concept, this system is being adapted for clinical use as a retinal treatment system as well as a research tool for military laser-tissue interaction studies. Specifically, the system is being adapted for use with an ultra-short pulse laser system at Armstrong Laboratory and Frank J. Seiler Research Laboratory to study the effects of ultra-short laser pulses on the human retina. The instrumentation aspects of the prototype subsystems were presented at SPIE Conference 1877 in January 1993. Since then our efforts have concentrated on combining the lesion depth control subsystem and the lesion placement subsystem into a single prototype capable of simultaneously controlling both parameters. We have designated this combined system CALOSOS for Computer Aided Laser Optics System for Ophthalmic Surgery. We have also investigated methods to improve system response time. Use of high speed nonstandard frame rate CCD cameras and high speed frame grabbers hosted on personal computers featuring the 32 bit, 33 MHz PCI bus have been investigated. Design details of an initial CALOSOS prototype design is provided in SPIE Conference proceedings 2396B-32 (Biomedical Optics Conference, Clinical Laser Delivery and Robotics Session). This paper will review in vivo testing to date and detail planned system upgrades.!36
机译:摘要:德克萨斯大学奥斯汀分校生物医学工程激光实验室的研究人员对激光的医学应用进行了研究,致力于开发视网膜机器人激光系统。正在进行的项目的总体目标是精确定位和控制激光损伤的深度,以治疗各种视网膜疾病,例如糖尿病性视网膜病和视网膜泪液。由于类似的相关兴趣,美国空军学院电气工程系和阿姆斯特朗实验室的光辐射分部的研究人员也参与了这项研究。已经开发了单独的低速原型子系统,以使用病变反射率反馈参数控制病变深度,并使用视网膜血管作为跟踪界标来控制病变位置。这两个子系统已使用氩连续波激光在色素兔身上成功地进行了体内证明。正在进行构建可同时控制病变深度和位置的原型系统的工作。遵循双重用途的概念,该系统适用于临床,作为视网膜治疗系统以及军事激光与组织相互作用研究的研究工具。具体而言,该系统适用于Armstrong实验室和Frank J. Seiler研究实验室的超短脉冲激光系统,以研究超短激光脉冲对人体视网膜的影响。在1993年1月的SPIE Con​​ference 1877上介绍了原型子系统的仪器方面。此后,我们的工作集中在将病灶深度控制子系统和病灶放置子系统组合为一个能够同时控制两个参数的原型中。我们已将此组合系统CALOSOS指定为眼科手术的计算机辅助激光光学系统。我们还研究了改善系统响应时间的方法。已经研究了使用具有32位,33 MHz PCI总线的个人计算机上托管的高速非标准帧速率CCD相机和高速帧采集器的使用。 SPIE会议记录2396B-32(生物医学光学会议,临床激光传输和机器人学会议)提供了初始CALOSOS原型设计的设计细节。本文将回顾迄今为止的体内测试,并详细说明计划的系统升级。!36

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