Masiwa Lynett Erita, Moodley Vanessa
Department of Ophthalmology, University of Zimbabwe, College of Health Sciences, P. O. Box A178, Avondale, Harare, Zimbabwe.
School of Health Sciences, Department of Optometry, University of Kwazulu Natal, Durban, South Africa.
J Optom. 2020 Oct-Dec;13(4):269-275. doi: 10.1016/j.optom.2019.11.001. Epub 2020 Jan 6.
Keratoconus (KC) is a corneal ectasia characterised by steepening corneal curvature, changes in refractive error and corneal thickness that result in visual impairment. Early signs of KC include displacement of the thinnest part of the cornea from the central position, changes in the corneal epithelial layer cell distribution, variations in the anterior corneal astigmatism/posterior corneal astigmatism relationship and a variation in corneal thickness. It is important that we review the corneal imaging methods for the diagnosis of preclinical KC.
An online literature search was carried out on PubMed. Only publications detailing corneal assessment procedures were considered for this review and any publication on instruments that did not generate KC predictability indices were also excluded from the review. The 308 publications were reviewed.
Corneal assessment techniques, with the ability to characterise both the anterior and posterior corneal surfaces, are invaluable in the diagnosis of pre-clinical KC. Reflection based and elevation based corneal imaging systems should be used in conjunction with other assessments such as higher order aberration measuring systems to improve sensitivity and reliability in the diagnosis of pre-clinical KC. Ultra high resolution ultrasound can detect pre-clinical KC. The ability to asses both the epithelium and endothelium makes anterior surface optical coherence tomography a superior technique for pre-clinical KC diagnosis. There is a positive correlation between central corneal thickness and corneal hysteresis. Corneal biomechanics should be considered in conjunction with other corneal assessments in the diagnosis of pre-clinical KC.
圆锥角膜(KC)是一种角膜扩张性疾病,其特征为角膜曲率变陡、屈光不正改变以及角膜厚度变化,进而导致视力损害。KC的早期体征包括角膜最薄部位从中心位置移位、角膜上皮层细胞分布改变、角膜前散光/角膜后散光关系变化以及角膜厚度变化。对用于诊断临床前期KC的角膜成像方法进行综述很重要。
在PubMed上进行了在线文献检索。本综述仅考虑详细描述角膜评估程序的出版物,任何关于未生成KC预测指标的仪器的出版物也被排除在综述之外。共检索了308篇出版物。
能够对角膜前表面和后表面进行特征描述的角膜评估技术,在临床前期KC的诊断中具有重要价值。基于反射和基于高度的角膜成像系统应与其他评估方法(如高阶像差测量系统)结合使用,以提高临床前期KC诊断的敏感性和可靠性。超高分辨率超声可检测临床前期KC。能够同时评估上皮和内皮,使得前表面光学相干断层扫描成为临床前期KC诊断的一种优越技术。中央角膜厚度与角膜滞后之间存在正相关。在临床前期KC的诊断中,应将角膜生物力学与其他角膜评估结合起来考虑。