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Fluorescein dye disappearance test in patients with different degrees of epiphora.

机译:荧光素染料消失试验对不同程度的泪溢患者。

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PURPOSE: To assess the diagnostic efficacy of a modification of the fluorescein dye disappearance test (DDT) in patients with different degrees of epiphora. METHODS: DDT was performed by instilling a drop of 2% fluorescein in the eye. Schirmer tear test strips were placed in the lower conjunctival fornix, after 3 and 10 minutes. The colour dilution on the strips was compared to a scale with known standards and the most closely comparable colour dilution was chosen and recorded as the visual scale test (VST) grade of the strip. The grey-scale value (GV) of each strip was calculated by computer image analysis. The control group comprised 44 patients, mean age 44.8 years (SD 7.5, range 30-60). There were 13 patients in group 1 with moderate epiphora; mean age was 44.2 years (SD 9.5, range 30-60). There were 17 patients in group 2 with severe epiphora; mean age was 48.3 years (SD 7.7, range 37- 60). RESULTS: VST and GV differed significantly between controls and group 1 patients at 3 minutes (p=0.002, p=0.001), and between controls and group 2 patients at 3 minutes (p<0.001, p<0.001). There was no difference between groups 1 and 2 patients in VST and GV at 3 minutes. The differences were highly significant between controls and group 1 at 10 minutes (p=0.001, p=0.007), and between controls and group 2 at 10 minutes (p<0.001, p<0.001). The differences in GV and VST between groups 1 and 2 were significant at 10 minutes (p=0.026, p=0.018). CONCLUSIONS: This modified DDT permits identification of different degrees of epiphora in a non-invasive manner, it can therefore be used to evaluate the outcome of different treatment strategies.
机译:目的:评估荧光素染料消失试验(DDT)的修改对不同程度的癫痫患者的诊断效力。方法:滴滴涕是通过在眼睛中滴入2%的荧光素进行的。在3和10分钟后,将Schirmer撕裂测试条放入结膜下穹for。将条带上的颜色稀释度与具有已知标准的刻度进行比较,选择最接近的颜色稀释度,并将其记录为条带的视觉刻度测试(VST)级。通过计算机图像分析计算每个条的灰度值(GV)。对照组包括44名患者,平均年龄为44.8岁(SD 7.5,范围30-60)。第1组中有13例中度癫痫发作。平均年龄为44.2岁(标准差9.5,范围30-60)。第2组17例有严重的泪溢。平均年龄为48.3岁(SD 7.7,范围37-60)。结果:对照组和第1组患者在3分钟时的VST和GV有显着差异(p = 0.002,p = 0.001),而对照组和第2组患者在3分钟时的VST和GV有显着差异(p <0.001,p <0.001)。在第3分钟时,VST和GV的第1组和第2组患者之间没有差异。对照组和第1组在10分钟时的差异非常显着(p = 0.001,p = 0.007),对照组和第2组在10分钟时的差异(p <0.001,p <0.001)。第1组和第2组之间的GV和VST差异在10分钟时显着(p = 0.026,p = 0.018)。结论:这种改良的滴滴涕可以非侵入性的方式鉴定出不同程度的癫痫病,因此可以用来评估不同治疗策略的结果。

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