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[角膜移植术:最严重角膜疾病的最后希望]

[Keratoprostheses: Last Hope for the Most Severe Corneal Diseases].

作者信息

Bachmann Björn, Schaub Friederike, Cursiefen Claus

出版信息

Klin Monbl Augenheilkd. 2022 Sep;239(9):1165-1179. doi: 10.1055/a-1892-6142. Epub 2022 Aug 15.

Abstract

Corneal blindness affects over 8 million adults and 1.5 million children worldwide, making it one of the top 5 causes of blindness. Depending on the recipient's corneal condition corneal transplantation may not be a viable treatment option. In such seemingly no-alternative situations, keratoprosthesis implantation can be an option in some patients. In terms of numbers, two types of keratoprostheses are currently used: 1. Keratoprostheses with biological haptics made of tooth or tibia bone. 2. The Boston type I-keratoprosthesis. Both types have optics made of PMMA. The most common complication is the formation of an optically disturbing retroprosthetic membrane behind the optic, which can usually be removed with YAG laser. Causes of blindness after keratoprosthesis implantation are glaucoma, endophthalmitis and retinal detachment. The extrusion rate of the Boston type I-keratoprosthesis seems to be higher than after keratoprosthesis implantation with biological haptic. Autoimmunological corneal diseases have increased extrusion rates and higher rates of endophthalmitis when compared to non-autoimmunological diseases. Visual outcomes after keratoprosthesis implantation are potentially very good and usually limited by extracorneal concomitant diseases. Advances in glaucoma diagnostic (OCT, implantation of intraocular pressure sensors), standard glaucoma prophylaxis by medication or surgery, modern retinal surgery and better treatment options in case of extrusion improve the prognosis of keratoprosthesis surgery. Still, the ideal technique for permanent anchoring of artifical optics in biological tissue has yet to be developed.

摘要

全球有超过800万成年人和150万儿童患有角膜盲,这使其成为导致失明的五大主要原因之一。根据接受者的角膜状况,角膜移植可能并非可行的治疗选择。在这种看似没有其他选择的情况下,对于某些患者而言,植入角膜假体可能是一种选择。从数量上来说,目前使用两种类型的角膜假体:1. 带有由牙齿或胫骨制成的生物触觉装置的角膜假体。2. 波士顿I型角膜假体。这两种类型的角膜假体都有由聚甲基丙烯酸甲酯(PMMA)制成的光学部件。最常见的并发症是在光学部件后方形成干扰视力的人工晶状体后膜,通常可用钇铝石榴石(YAG)激光将其去除。角膜假体植入后导致失明的原因有青光眼、眼内炎和视网膜脱离。波士顿I型角膜假体的挤出率似乎高于带有生物触觉装置的角膜假体植入后的挤出率。与非自身免疫性疾病相比,自身免疫性角膜疾病的挤出率更高,眼内炎发生率也更高。角膜假体植入后的视觉效果可能非常好,通常受角膜外伴随疾病的限制。青光眼诊断(光学相干断层扫描、眼压传感器植入)方面的进展、通过药物或手术进行的标准青光眼预防、现代视网膜手术以及在发生挤出情况时更好的治疗选择,都改善了角膜假体手术的预后。尽管如此,将人工光学部件永久固定在生物组织中的理想技术仍有待开发。

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