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首页> 外文期刊>Current Eye Research >Histopathological evaluation of anterior lamellar corneal tissue-on/-off storage conditions on DSAEK donor tissue after storage in organ culture
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Histopathological evaluation of anterior lamellar corneal tissue-on/-off storage conditions on DSAEK donor tissue after storage in organ culture

机译:DSAEK供体组织在器官培养物中保存后,前片状角膜组织开/关存储条件的组织病理学评估

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Purpose: To compare the quality of corneal endothelium of precut Descemet-stripping automated endothelial keratoplasty (DSAEK) tissue when transported with and without the anterior lamellar corneal tissue (ALCT) when organ-culture corneal storage methods are used. Methods: After microkeratome-assisted excision of anterior corneal lamella, five pairs of corneas (10 eyes) were stored either with the ALCT on the stroma (five eyes) or with ALCT off the stroma (five eyes) in organ-culture medium. Three pairs (six matched corneas) were left in the transport medium for 24h prior to the microkeratome cut. Two pairs (four matched corneas) were left in the transport medium for 48h prior to the microkeratome cut. All cuts were performed using a 300 (four eyes) or 350 (six eyes) microns head. A vital dye assay (alizarin red S and trypan blue) was used to identify devitalized and necrotic endothelial cells. Results: In all matched cases, there was no difference between the endothelial cell appearance with or without the anterior corneal lamella. In all cases, there was no evidence for trypan blue stained cells beyond that normally seen on acceptable transplantable corneas and there was no evidence of loss of cells or any lifting of Descemet's membrane. Conclusions: There is no difference between the quality of the donor endothelial cell appearance with ALCT-on or -off when the donor cornea is stored using the organ-culture system of corneal storage. Organ-culture storage system is a safe and effective system in regard to preparation and transport of donor lenticules for DSAEK.
机译:目的:比较使用器官培养的角膜存储方法时,在有无前板层角膜组织(ALCT)的情况下运输时,预先切割的经Desmet剥离的自动内皮细胞角膜成形术(DSAEK)组织的角膜内皮质量。方法:在微型角膜刀辅助下切除角膜前薄片后,将五对角膜(10只眼)与ALCT一起储存在基质上(五只眼),或者将ALCT脱离基质(五只眼睛)储存在器官培养基中。在切开微型角膜刀之前,将三对(六对匹配的角膜)放在运输介质中24小时。在切开微型角膜刀之前,将两对(四个匹配的角膜)留在运输介质中48小时。所有切割均使用300(四眼)或350(六眼)微米的头进行。活体染料分析(茜素红S和锥虫蓝)用于鉴定失活和坏死的内皮细胞。结果:在所有匹配的病例中,有无前角膜薄层的内皮细胞外观无差异。在所有情况下,没有证据表明锥虫蓝染色的细胞超出了可接受的可移植角膜上的正常水平,也没有证据表明细胞丢失或Descemet膜升高。结论:使用角膜存储器官培养系统存储供体角膜时,ALCT开或关时供体内皮细胞外观的质量没有差异。器官培养物存储系统是用于DSAEK的供体微孔的准备和运输的安全有效的系统。

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