Wei Anji, Zhao Zhennan, Kong Xiangmei, Shao Tingting
Department of Ophthalmology and Vision Science, Eye Ear Nose and Throat Hospital of Fudan University, Shanghai, China.
NHC Key Laboratory of Myopia (Fudan University), Laboratory of Myopia, Chinese Academy of Medical Sciences, Shanghai, China.
J Ophthalmol. 2022 Jul 20;2022:1085692. doi: 10.1155/2022/1085692. eCollection 2022.
To compare accelerated and standard corneal collagen cross-linking (CXL) treatments in experimental keratitis models.
Twenty-six New Zealand rabbits were divided into two groups: a 1% voriconazole combined with standard CXL group, and a 1% voriconazole combined with accelerated CXL group. The ulcer area, corneal opacity, and corneal neovascularization score were measured via slit-lamp imaging, and the corneal and corneal epithelial thickness and ulcer depth were measured via anterior segment optical coherence tomography (AS-OCT). The duration of the hyphae was observed via confocal microscopy (IVCM), and the cornea was taken for pathological examination after modeling and at the end of the study to determine the hyphae and corneal repair. The observation times were as follows: at successful modeling (day 0) and at 1, 4, 7, 14, 21, and 28 days after the intervention.
The area and depth of the ulcer decreased in both groups after CXL (all < 0.05). Interestingly, the ulcer area in the accelerated CXL group still tended to increase on the first day after CXL although the difference was not statistically significant (=0.6649). On the 21st and 28th days after CXL, the ulcer area and depth of the standard CXL group were larger and deeper than those of the accelerated CXL group (all < 0.05). The ulcer healing time in the accelerated CXL group was 18.67 ± 6.21 days, while that in the standard CXL group was 23.55 ± 4.72 days, and the difference was statistically significant (=0.0475).
Both accelerated and standard CXL can significantly inhibit the progression of keratitis corneal ulcers and promote ulcer healing. The accelerated CXL was superior to the standard CXL, which could control infection faster and promote ulcer healing. However, it is important to note that there may be a risk of early deterioration of the ulcer with accelerated CXL.
在实验性角膜炎模型中比较加速角膜胶原交联(CXL)与标准角膜胶原交联治疗。
26只新西兰兔分为两组:1%伏立康唑联合标准CXL组和1%伏立康唑联合加速CXL组。通过裂隙灯成像测量溃疡面积、角膜混浊度和角膜新生血管评分,通过眼前节光学相干断层扫描(AS-OCT)测量角膜及角膜上皮厚度和溃疡深度。通过共聚焦显微镜(IVCM)观察菌丝持续时间,建模后及研究结束时取角膜进行病理检查以确定菌丝及角膜修复情况。观察时间如下:成功建模时(第0天)以及干预后1、4、7、14、21和28天。
CXL后两组溃疡面积和深度均减小(均P<0.05)。有趣的是,加速CXL组在CXL后第1天溃疡面积仍有增加趋势,尽管差异无统计学意义(P=0.6649)。CXL后第21天和28天,标准CXL组溃疡面积和深度大于加速CXL组(均P<0.05)。加速CXL组溃疡愈合时间为18.67±6.21天,标准CXL组为23.55±4.72天,差异有统计学意义(P=0.0475)。
加速和标准CXL均可显著抑制角膜炎性角膜溃疡进展并促进溃疡愈合。加速CXL优于标准CXL,能更快控制感染并促进溃疡愈合。然而,需要注意的是,加速CXL可能存在溃疡早期恶化的风险。