Gichuhi Stephen, Macharia Ephantus, Kabiru Joy, Zindamoyen Alain M'bongo, Rono Hilary, Ollando Ernest, Wanyonyi Leonard, Wachira Joseph, Munene Rhoda, Onyuma Timothy, Jaoko Walter G, Sagoo Mandeep S, Weiss Helen A, Burton Matthew J
London School of Hygiene and Tropical Medicine, London, England2Department of Ophthalmology, University of Nairobi, Nairobi, Kenya.
PCEA Kikuyu Eye Unit, Kikuyu, Kenya.
JAMA Ophthalmol. 2015 Nov;133(11):1314-21. doi: 10.1001/jamaophthalmol.2015.3345.
Clinical features are unreliable for distinguishing ocular surface squamous neoplasia (OSSN) from benign conjunctival lesions.
To evaluate the adverse effects, accuracy, and interobserver variation of toluidine blue 0.05% vital staining in distinguishing OSSN, confirmed by histopathology, from other conjunctival lesions.
DESIGN, SETTING, AND PARTICIPANTS: Cross-sectional study in Kenya from July 2012 through July 2014 of 419 adults with suspicious conjunctival lesions. Pregnant and breastfeeding women were excluded.
Comprehensive ophthalmic slitlamp examination was conducted. Vital staining with toluidine blue 0.05% aqueous solution was performed before surgery. Initial safety testing was conducted on large tumors scheduled for exenteration looking for corneal toxicity on histology before testing smaller tumors. We asked about pain or discomfort after staining and evaluated the cornea at the slitlamp for epithelial defects. Lesions were photographed before and after staining.
Diagnosis was confirmed by histopathology. Six examiners assessed photographs from a subset of 100 consecutive participants for staining and made a diagnosis of OSSN vs non-OSSN. Staining was compared with histopathology to estimate sensitivity, specificity, and predictive values. Adverse effects were enumerated. Interobserver agreement was estimated using the κ statistic.
A total of 143 of 419 participants (34%) had OSSN by histopathology. The median age of all participants was 37 years (interquartile range, 32-45 years) and 278 (66%) were female. A total of 322 of the 419 participants had positive staining while 2 of 419 were equivocal. There was no histological evidence of corneal toxicity. Mild discomfort was reported by 88 (21%) and mild superficial punctate keratopathy seen in 7 (1.7%). For detecting OSSN, toluidine blue had a sensitivity of 92% (95% CI, 87%-96%), specificity of 31% (95% CI, 25%-36%), positive predictive value of 41% (95% CI, 35%-46%), and negative predictive value of 88% (95% CI, 80%-94%). Interobserver agreement was substantial for staining (κ = 0.76) and moderate for diagnosis (κ = 0.40).
With the high sensitivity and low specificity for OSSN compared with histopathology among patients with conjunctival lesions, toluidine blue 0.05% vital staining is a good screening tool. However, it is not a good diagnostic tool owing to a high frequency of false-positives. The high negative predictive value suggests that a negative staining result indicates that OSSN is relatively unlikely.
临床特征对于区分眼表鳞状上皮肿瘤(OSSN)与良性结膜病变并不可靠。
评估0.05%甲苯胺蓝活体染色在区分经组织病理学确诊的OSSN与其他结膜病变时的不良反应、准确性及观察者间差异。
设计、地点和参与者:2012年7月至2014年7月在肯尼亚对419例有可疑结膜病变的成年人进行的横断面研究。排除孕妇和哺乳期妇女。
进行全面的眼科裂隙灯检查。手术前用0.05%甲苯胺蓝水溶液进行活体染色。在对较小肿瘤进行检测之前,先对计划行眼球摘除术的大肿瘤进行初步安全性测试,观察组织学上的角膜毒性。我们询问染色后是否有疼痛或不适,并在裂隙灯下评估角膜有无上皮缺损。病变在染色前后拍照。
通过组织病理学确诊。6名检查者评估了100例连续参与者的子集中的照片的染色情况,并诊断为OSSN与非OSSN。将染色结果与组织病理学结果进行比较,以估计敏感性、特异性和预测值。列举不良反应。使用κ统计量估计观察者间的一致性。
419例参与者中,共有143例(34%)经组织病理学诊断为OSSN。所有参与者年龄中位数为37岁(四分位间距为32 - 45岁),278例(66%)为女性。419例参与者中共有322例染色阳性,419例中有2例结果不明确。没有角膜毒性的组织学证据。88例(21%)报告有轻度不适,7例(1.7%)在裂隙灯下可见轻度浅层点状角膜病变。对于检测OSSN,甲苯胺蓝的敏感性为92%(95%CI,87% - 96%),特异性为31%(95%CI,25% - 36%),阳性预测值为41%(95%CI,35% - 46%),阴性预测值为88%(95%CI,80% - 94%)。观察者间对染色的一致性较高(κ = 0.76),对诊断的一致性中等(κ = 0.40)。
与结膜病变患者的组织病理学相比,0.05%甲苯胺蓝活体染色对OSSN具有高敏感性和低特异性,是一种良好的筛查工具。然而,由于假阳性率高,它不是一种良好的诊断工具。高阴性预测值表明染色结果为阴性时,OSSN相对不太可能存在。