Department of Ophthalmology, University of Pécs, Medical School, Akác u. 1, Pécs, 7623, Hungary.
Doctoral School of Clinical Medicine, University of Debrecen, Debrecen, 4032, Hungary.
Graefes Arch Clin Exp Ophthalmol. 2021 Jul;259(7):1935-1943. doi: 10.1007/s00417-021-05162-8. Epub 2021 Mar 29.
The aim of our research was to investigate the reliability and clinical applicability of a modern tear film imaging tool by comparing the inter- and intragrader difference. The further goal was to compare the non-invasive tear break-up time (NIBUT) measured with the LacryDiag® device with traditional tear film break-up time (TBUT).
Comprehensive ophthalmological examination was performed, including LacryDiag® (Quantel Medical, France) (lower tear meniscus height measuring (LTMH), superior and inferior eyelid meibography (MeibS MeibI), interferometry (INT), NIBUT), slit lamp examination, and TBUT. Two independent, well-trained graders selected and analyzed the LTMH, MeibI, MeibS, and INT. The second grader reanalyzed the data 1 month later. Intra- and inter-examiner reliabilities were evaluated using intraclass correlation coefficients (ICC), while for categorical variable, Cohen's kappa statistics were provided. The Bland-Altman plot was used for visualization of the agreement between measurements.
Fifty healthy volunteers were examined. For LTMH both the inter- and intragrader variabilities were excellent. Between two graders, the ICC of MeibI was poor; however, between two graders, the ICC of MeibS was good, and the intragrader variability in MeibI and MeibS was excellent. For the INT, both intra- and intergrading were in fair and moderate agreement, although the intragrader agreement was higher. Comparing the NIBUT and TBUT, the agreement was slight.
Based on our results, examination of a patient during follow-up should be performed by the same examiner, because of the slight agreement. The LacryDiag® is a non-invasive, easy-to-use device, which can examine the tear film and save the recordings for easier follow-up.
我们的研究旨在通过比较观察者内和观察者间的差异来研究一种现代泪膜成像工具的可靠性和临床适用性。进一步的目标是比较 LacryDiag® 设备测量的非侵入性泪膜破裂时间 (NIBUT) 与传统泪膜破裂时间 (TBUT)。
进行全面的眼科检查,包括 LacryDiag®(法国 Quantel Medical)(下泪膜高度测量(LTMH)、上下眼睑睑板腺照相(MeibS、MeibI)、干涉测量(INT)、NIBUT)、裂隙灯检查和 TBUT。两名独立的、训练有素的评分员选择和分析 LTMH、MeibI、MeibS 和 INT。第二位评分员在 1 个月后重新分析数据。使用组内相关系数 (ICC) 评估组内和组间的可靠性,而对于分类变量,则提供 Cohen's kappa 统计量。Bland-Altman 图用于显示测量值之间的一致性。
对 50 名健康志愿者进行了检查。对于 LTMH,观察者内和观察者间的变异性均极好。两名评分员之间的 MeibI 相关性较差;然而,两名评分员之间的 MeibS 相关性较好,MeibI 和 MeibS 的观察者内变异性极好。对于 INT,组内和组间的分级均为中等至良好一致性,尽管组内分级的一致性更高。比较 NIBUT 和 TBUT,一致性稍差。
根据我们的结果,由于一致性稍差,在随访期间应由同一名检查者对患者进行检查。LacryDiag® 是一种非侵入性、易于使用的设备,它可以检查泪膜并保存记录,以便更轻松地进行随访。