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Microkeratome versus femtosecond laser predissection of corneal grafts for anterior and posterior lamellar keratoplasty.

机译:微角膜刀与飞秒激光对角膜移植物进行前,后板层角膜移植术的比较。

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PURPOSE: To compare 2 different techniques for predissection of human anterior and posterior lamellar corneal grafts for eye bank storage. METHODS: A mechanical microkeratome (group 1, N = 5) and a femtosecond laser (group 2, N = 5) were used to dissect intended 350-microm-deep lamellar planes in deepithelialized donor corneas mounted on an artificial anterior chamber. These corneas were replaced in Optisol GS at 4 degrees C postoperatively and examined 2 days later to simulate a clinical scenario. Ultrasonic pachymetry of corneal lamellar sections was measured before and after separation of the lamellar grafts. Group 1 sections were separated by the mechanical microkeratome, whereas group 2 sections were manually separated 2 days after laser dissection. Endothelial cell viability was evaluated in posterior grafts. RESULTS: Total corneal thicknesses immediately before dissection were 559 +/- 61 (group 1) and 578 +/- 79 microm (group 2; P = 0.46). Immediate postdissection anterior and posterior graft thicknesses were 361 +/- 68 and 203 +/- 74 microm (group 1), respectively. Achieved anterior and posterior graft thicknesses 2 days later were 282 +/- 44 and 413 +/- 35 microm (group 1) and 324 +/- 112 and 397 +/- 51 microm (group 2), respectively. Percentage of devitalized endothelial cells were 3.4% +/- 1.6% (group 1) and 1.6% +/- 1.2% (group 2; P = 0.35). CONCLUSIONS: Centralized predissection by both techniques, cold storage, and shipping by airmail results in viable grafts without significant endothelial cell loss 2 days later.
机译:目的:比较2种不同的人眼前,后板层角膜移植术的眼睑存储技术。方法:使用机械微型角膜刀(第1组,N = 5)和飞秒激光(第2组,N = 5)在安装于人工前房的上皮化供体角膜中解剖预定的350微米深的层状平面。术后4℃在Optisol GS中更换这些角膜,并在2天后检查以模拟临床情况。在分离层状移植物之前和之后,测量角膜层状切片的超声测厚法。激光解剖后2天,通过机械显微角膜刀将第1组切片分开,而将第2组切片手动分开。在后移植物中评估内皮细胞的生存力。结果:刚剥离前的角膜总厚度为559 +/- 61微米(第1组)和578 +/- 79微米(第2组; P = 0.46)。解剖后立即的前和后移植物厚度分别为361 +/- 68微米和203 +/- 74微米(第1组)。 2天后获得的前和后移植物厚度分别为282 +/- 44和413 +/- 35微米(第1组)和324 +/- 112和397 +/- 51微米(第2组)。失活的内皮细胞百分比为3.4%+/- 1.6%(第1组)和1.6%+/- 1.2%(第2组; P = 0.35)。结论:冷藏和空运这两种技术的集中剥离术导致存活的移植物在两天后没有明显的内皮细胞损失。

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