Department of Ophthalmology, College of Medicine, The Catholic University of Korea, Seoul, Korea.
Department of Ophthalmology, Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Chuncheon, Korea.
Medicine (Baltimore). 2022 Sep 9;101(36):e30430. doi: 10.1097/MD.0000000000030430.
We aimed to quantitatively analyze the corneal endothelial cell damage by measuring the area stained with trypan blue dye, and to confirm the degree of corneal endothelial cell damage resulting from enucleation, corneal buttoning, and storage in donor corneas intended for use in human corneal transplantation. This study was a retrospective analysis of medical records and videos recorded during keratoplasty. Twenty-one corneal buttons of 21 donors that underwent endothelial cell staining using trypan blue for the donor preparation during DALK or DMEK were included in the study. The percentage of stained area in entire corneal endothelia and the percentage of the stained area in the 8-mm diameter circle were quantitatively analyzed using Adobe Photoshop. The mean percentage of the stained area in the entire corneal endothelia in 13 corneas was 8.1 ± 13.3% (range, 0.0-56.1%), and the mean percentage of the stained area in a circle with a diameter of 8 mm in 21 corneas was 3.4 ± 5.2% (range, 0.0-18.9%). The correlations between the death-to-preservation time, the training duration of the residents who performed donor corneal buttoning, and the percentage of the stained area in the 8-mm diameter circle were not significant(P = .441, P = .495, respectively). Cornea thickness and endothelial cell density did not differ between 10 eyes in the group with the percentage of the stained area in a circle with a diameter of 8 mm <5% and 5 eyes in the group with the percentage more than 5% damage (P = .854, P = .358). The corneal endothelial cell damage could be quantitatively analyzed using trypan blue staining before keratoplasty in donor cornea. The amount of corneal endothelial cell damage in the central 8-mm circle was mostly acceptable, but some cases showed significantly severe endothelial cell damage. The corneal thickness and endothelial cell density did not differ between 10 eyes in the group with the percentage of the stained area in a circle with a diameter of 8 mm <5% and 5 eyes in the group with the percentage more than 5% damage. Therefore, pachymetry and specular microscopy are not sufficient for evaluating donor corneas before keratoplasty.
我们旨在通过测量用台盼蓝染料染色的区域来定量分析角膜内皮细胞的损伤,并确认在用于人类角膜移植的供体角膜中进行眼摘、角膜环钻术和储存导致的角膜内皮细胞损伤程度。本研究是对穿透性角膜移植术中使用台盼蓝进行供体准备的病历和视频进行的回顾性分析。共纳入 21 名供体的 21 个角膜环钻术,这些供体在 DALK 或 DMEK 供体准备期间进行了内皮细胞台盼蓝染色。使用 Adobe Photoshop 对整个角膜内皮细胞染色区域的百分比和 8mm 直径圆内染色区域的百分比进行定量分析。13 个角膜的整个角膜内皮细胞染色区域的平均百分比为 8.1±13.3%(范围,0.0-56.1%),21 个角膜的 8mm 直径圆内染色区域的平均百分比为 3.4±5.2%(范围,0.0-18.9%)。死亡到保存时间、进行供体角膜环钻术的住院医师的培训时间与 8mm 直径圆内染色区域的百分比之间的相关性无统计学意义(P=0.441,P=0.495)。角膜厚度和内皮细胞密度在 8mm 直径圆内染色区域的百分比<5%的 10 只眼和百分比>5%损伤的 5 只眼之间无差异(P=0.854,P=0.358)。在供体角膜穿透性角膜移植术前使用台盼蓝染色可以定量分析角膜内皮细胞损伤。中央 8mm 圆内角膜内皮细胞损伤量大多可接受,但部分病例显示明显严重的内皮细胞损伤。角膜厚度和内皮细胞密度在 8mm 直径圆内染色区域的百分比<5%的 10 只眼和百分比>5%损伤的 5 只眼之间无差异。因此,在穿透性角膜移植术前,角膜测厚和共焦显微镜不足以评估供体角膜。