Park C K, Kim J H
Department of Ophthalmology, Catholic University of Korea, Medical College, Seoul, Korea.
J Cataract Refract Surg. 1999 Jun;25(6):842-50. doi: 10.1016/s0886-3350(99)00047-4.
To evaluate and compare the corneal wound-healing process after photorefractive keratectomy (PRK) and laser in situ keratomileusis (LASIK).
Kangnam St. Mary's Hospital, Seoul, Korea.
Two surgical procedures, PRK with the VISX Star excimer laser and LASIK with a MicroTech microkeratome, were performed in 24 rabbit eyes. In the PRK group (n = 12 eyes), the rabbit cornea was treated with a 20 microns ablation. In the LASIK group (n = 12 eyes), a 20 microns laser ablation was performed after a 150 microns thick hinged corneal flap had been made. During both procedures, dichlorotriazinyl aminofluorescien (DTAF) dye was applied to the ablated stromal bed; in the LASIK group, the stromal side of the corneal flap was also stained with DTAF to differentiate regenerated collagen from normal stromal tissue. Corneal wound healing was evaluated postoperatively at 1, 4, 8, and 12 weeks using light, electron, and fluorescence microscopy. The amount of regenerated stromal tissue and the number of keratocytes were analyzed by an image-analysis system.
In the PRK group, epithelial migration and regeneration were observed in the ablated area without any stromal regeneration 1 week postoperatively. However, newly regenerated, irregularly arranged stromal collagen, with epithelial hyperplasia in the ablated area, was observed 4 to 12 weeks postoperatively by light and fluorescence microscopy. The number of keratocytes in the surgical area was also increased. In ultrastructural observation using an electron microscope, the shape of keratocytes in the ablated area was changed, and the number of rough and smooth endoplasmic reticuli, ribosomes, mitochondria, and electron-dense vesicles in the cytoplasm were increased, suggesting that the cells were activated. In the LASIK group, there was no observed regenerated collagen between the corneal flap and the ablated stromal bed except in the wound margin. Lamellated, parallel collagen fibers in the cornealstroma were not disturbed. However, in the wound margin, corneal epithelial ingrowth between the flap and the stromal bed was observed, as was some regenerated stromal tissue. The amount of regenerated stromal tissue and the number of keratocytes in the wound area were statistically smaller than those in the PRK group (P < .05). Observation by electron microscopy showed no activated keratocytes, unlike in the PRK group. The collagen fibers in the wound area were parallel.
Stromal wound healing in the LASIK group was minimal compared with that in the PRK group, except in the wound margin. These results may support the clinical findings of less corneal haze in the human cornea after LASIK.
评估并比较准分子激光角膜切削术(PRK)和准分子原位角膜磨镶术(LASIK)后的角膜伤口愈合过程。
韩国首尔江南圣母医院。
对24只兔眼进行两种手术,即使用VISX Star准分子激光的PRK和使用MicroTech微型角膜刀的LASIK。在PRK组(n = 12只眼),对兔角膜进行20微米的消融。在LASIK组(n = 12只眼),制作150微米厚的带蒂角膜瓣后进行20微米的激光消融。在两种手术过程中,将二氯三嗪基氨基荧光素(DTAF)染料应用于消融的基质床;在LASIK组,角膜瓣的基质面也用DTAF染色,以区分再生胶原与正常基质组织。术后1、4、8和12周使用光学显微镜、电子显微镜和荧光显微镜评估角膜伤口愈合情况。通过图像分析系统分析再生基质组织的量和角膜细胞的数量。
在PRK组,术后1周在消融区域观察到上皮迁移和再生,无任何基质再生。然而,术后4至12周,通过光学显微镜和荧光显微镜观察到消融区域有新再生的、排列不规则的基质胶原,伴有上皮增生。手术区域的角膜细胞数量也增加。在使用电子显微镜的超微结构观察中,消融区域角膜细胞的形态发生改变,细胞质中粗面和滑面内质网、核糖体、线粒体和电子致密小泡的数量增加,表明细胞被激活。在LASIK组,除伤口边缘外,在角膜瓣和消融的基质床之间未观察到再生胶原。角膜基质中的层状平行胶原纤维未受干扰。然而,在伤口边缘,观察到角膜上皮长入瓣和基质床之间,也有一些再生的基质组织。伤口区域再生基质组织的量和角膜细胞的数量在统计学上低于PRK组(P <.05)。电子显微镜观察显示,与PRK组不同,未观察到角膜细胞被激活。伤口区域的胶原纤维是平行的。
与PRK组相比,LASIK组除伤口边缘外,基质伤口愈合极少。这些结果可能支持LASIK术后人眼角膜 haze较少的临床发现。