将水渗透到可植入的微型望远镜中。

L. Werner, M. Kaşkaloğlu, D. Apple, S. Pandey, T. Macky, A. Izak, R. Trivedi, Martin L Heredia, S. E. Morse
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引用次数: 3

摘要

植入式微型望远镜(IMT)是第一个用于年龄相关性黄斑变性(ARMD)患者光学矫正的眼内放大系统。该光学元件被嵌入一个携带装置中,该装置被设计为白内障手术后植入的人工晶状体。在这项研究中,我们报告了由于水浸润到IMT的光学而被移出的结果,并描述了该装置的结构和其植入所需的手术技术。患者为75岁男性,患有双侧白内障和非渗出性ARMD,在右眼行超声乳化术并植入IMT。这种刚性装置在水中的重量为46.1毫克,总直径为13.5毫米,需要通过一个大的唇缘切口植入。它被固定在子午线6至12点钟方向。后续检查显示IMT光学内存在大量液滴。该装置被取出并送到我们中心进行评估。在搬运装置上发现了一个大裂缝。然而,它不太可能是水渗透的场所。在光学圆柱体的密封水平上的微缺陷似乎为形成液滴的水的流入提供了开口。根据这份报告的发现,制造商修改了密封技术以避免这种并发症。目前正在进行临床试验,以评估该装置在为ARMD患者提供视力康复方面的功效。
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Aqueous infiltration into an implantable miniaturized telescope.
The implantable miniaturized telescope (IMT) is the first intraocular magnifying system proposed for optical correction in patients with age-related macular degeneration (ARMD). The optical component is embedded in a carrying device designed as an intraocular lens that is implanted after cataract surgery. In this study, we report findings on an IMT that was explanted because of aqueous infiltration into its optic and describe the configuration of this device and the surgical technique required for its implantation. The patient, a 75-year-old male with bilateral cataract and nonexudative ARMD, underwent phacoemulsification with implantation of an IMT in the right eye. The rigid device, weighing 46.1 mg in aqueous, has an overall diameter of 13.5 mm and requires implantation through a large limbal incision. It is fixated at the 6 to 12 o'clock meridian. Follow-up examination revealed the presence of numerous droplets inside the IMT optic. The device was explanted and sent to our center for evaluation. A large fissure was found on the carrying device. However, it was unlikely the site for aqueous infiltration. Microdefects at the level of the sealing of the optical cylinder appeared to provide the opening for the inflow of aqueous that formed droplets. Based on the findings of this report the manufacturer has modified the sealing technique to avoid this complication. Current clinical trials are now ongoing to assess the efficacy of this device in providing visual rehabilitation for ARMD patients.
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