Zhao Jing, Shen Yang, Tian Mi, Sun Ling, Zhao Yu, Zhang Xiaoyu, Zhou Xingtao
Key Laboratory of Myopia, Ministry of Health, Department of Ophthalmology, Eye and ENT Hospital, Fudan University, Shanghai, China.
Cornea. 2017 Feb;36(2):222-228. doi: 10.1097/ICO.0000000000001076.
To investigate the feasibility of allotransplanting extracted lenticules after femtosecond laser-assisted small incision lenticule extraction (SMILE) in rabbits and the subsequent healing process.
Fourteen New Zealand white rabbits were divided evenly into 2 groups. The rabbits in group A received SMILE procedures with a -6.00 D correction. The lenticules from group A were immediately inserted into a femtosecond laser-created corneal stromal pocket in group B. After surgery, the anterior segment was assessed in vivo by slit-lamp microscopy, corneal topography, optical coherence tomography, and confocal microscopy. All eyes were enucleated for hematoxylin-eosin staining and transmission electron microscopy after the animals were killed.
At postoperative day 1, there was moderate corneal edema in the implanted lenticule stroma. At 6 months, the lenticules were integrated with the surrounding tissue, and the boundary could not be identified through slit-lamp microscopy; regenerated branches of the corneal nerves were thicker than at postoperative month 1 as observed through confocal microscopy. The central corneal thickness increased by 58.75 ± 21.58 μm. The lenticules were gradually integrated with the surrounding tissue, and their density was similar to the adjacent tissue according to optical coherence tomography; however, a clear boundary between the lenticule and surrounding tissue was detectable using light microscopy and transmission electron microscopy, revealing disordered fibers and decreased keratocytes in implanted lenticules.
In this model it is feasible and safe to allotransplant extracted corneal lenticules after SMILE. Healing of implanted lenticules after SMILE is stable at postoperative 6 months, but collagen fiber rearrangement requires further investigation.
探讨飞秒激光小切口基质透镜切除术(SMILE)后兔异体移植取出的透镜的可行性及后续愈合过程。
将14只新西兰白兔平均分为2组。A组兔接受-6.00 D矫正的SMILE手术。将A组的透镜立即植入B组经飞秒激光制作的角膜基质袋中。术后,通过裂隙灯显微镜检查、角膜地形图、光学相干断层扫描和共聚焦显微镜对眼前节进行活体评估。动物处死之后,所有眼睛均摘除用于苏木精-伊红染色和透射电子显微镜检查。
术后第1天,植入的透镜基质出现中度角膜水肿。6个月时,透镜与周围组织整合,裂隙灯显微镜检查无法识别边界;共聚焦显微镜观察发现,角膜神经再生分支比术后1个月时更粗。中央角膜厚度增加了58.75±21.58μm。根据光学相干断层扫描,透镜逐渐与周围组织整合,其密度与相邻组织相似;然而,使用光学显微镜和透射电子显微镜可检测到透镜与周围组织之间有清晰的边界,显示植入透镜中的纤维紊乱且角膜细胞减少。
在此模型中,SMILE术后异体移植取出的角膜透镜是可行且安全的。SMILE术后植入透镜在术后6个月愈合稳定,但胶原纤维重排情况有待进一步研究。