Department of Vision Sciences, Glasgow-Caledonian University, Cowcaddens Road, Glasgow G4 OBA, Scotland.
Graefes Arch Clin Exp Ophthalmol. 2012 Jan;250(1):111-21. doi: 10.1007/s00417-011-1812-8. Epub 2011 Sep 13.
The purpose of this work is to assess the reliability of endothelial cell-density (ECD) estimates in corneas with different severity pseudoguttata.
Specular microscopy was undertaken on grade 1, 2, or 3 pseudoguttata patients and age-matched controls aged 52-83 years. On high magnification prints of central cornea, areas of complete cells (all sides visible) and partial 'cells' (one or more sides obscured) were measured manually. Sets of 45 complete cells were selected, as well as 75 cells that were a mixture of complete and partial cells on guttate endothelia. ECD was calculated by a progressive averaging technique.
Each group comprised 12 patients with similar range of ECD values (1,230-4,587 cells/mm(2)). Based on 40 complete cells, ECD could be estimated to within ±3.1% for grade 3 pseudoguttata versus ±2.0% for controls. If a mixture of complete and partial cells were measured, ECD could be estimated to within ±2.8% for grade 3 pseudoguttata images (n = 70 cells) and ±1.1% for controls. The estimated variability increases to substantial levels of ±20% if only ten cells were measured. No statistical differences in ECD were noted between guttate and normal endothelia if only complete cells were measured, but could be different if partial 'cells' were included.
Providing adequate numbers of complete cells are measured and in the absence of obvious polymegathism, ECD estimates can be made to within around ±3% in the presence of typical but significant pseudoguttata.
本研究旨在评估不同严重程度假性大疱性角膜病变角膜内皮细胞密度(ECD)估计的可靠性。
对 1 级、2 级或 3 级假性大疱性角膜病变患者和年龄匹配的 52-83 岁对照组进行共焦显微镜检查。在中央角膜高倍打印件上,手动测量完整细胞(所有侧面可见)和部分“细胞”(一个或多个侧面被遮挡)的区域。选择 45 个完整细胞组和 75 个混合完整和部分细胞的细胞组,这些细胞位于大疱性角膜病变内皮。ECD 通过逐步平均技术计算。
每组包括 12 名患者,其 ECD 值范围相似(1,230-4,587 个细胞/mm²)。基于 40 个完整细胞,3 级假性大疱性角膜病变的 ECD 可以估计到±3.1%,而对照组为±2.0%。如果测量混合完整和部分细胞,则 3 级假性大疱性角膜病变图像(n=70 个细胞)的 ECD 可以估计到±2.8%,对照组为±1.1%。如果仅测量 10 个细胞,则估计的变异性增加到±20%的较大水平。如果仅测量完整细胞,在大疱性和正常内皮之间,ECD 无统计学差异,但如果包括部分“细胞”,则可能不同。
如果测量足够数量的完整细胞且不存在明显的多核性,在存在典型但显著假性大疱性角膜病变的情况下,ECD 估计可以在±3%左右。