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首页> 外文期刊>Investigative ophthalmology & visual science >The effects of study design and spectrum bias on the evaluation of diagnostic accuracy of confocal scanning laser ophthalmoscopy in glaucoma.
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The effects of study design and spectrum bias on the evaluation of diagnostic accuracy of confocal scanning laser ophthalmoscopy in glaucoma.

机译:研究设计和光谱偏差对青光眼共聚焦扫描激光检眼镜的诊断准确性评估的影响。

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摘要

PURPOSE: To assess the effects of study design and spectrum bias on the evaluation of diagnostic accuracy of confocal scanning laser ophthalmoscopy (CSLO) in glaucoma. METHODS: Analysis 1 included 67 eyes with glaucomatous visual field loss and 56 eyes of normal volunteers. Estimates of diagnostic accuracy in this analysis were compared to those obtained from analysis 2, which included a cohort of patients with suspected glaucoma, but without visual field loss at the time of CSLO imaging. For analysis 2, 40 eyes with progressive glaucomatous optic disc change were included in the glaucoma group and 43 eyes without any evidence of progressive damage to the optic nerve that were observed untreated for an average time of 9.01 +/- 3.09 years were included in the normal group. Areas under the receiver operating characteristic (ROC) curves (AUC) were used to evaluate diagnostic accuracy of CSLO parameters. RESULTS: There was a statistically significant difference between the performance of the parameter withlargest AUC, discriminant function Bathija, in analysis 1 (AUC = 0.91) compared with its performance in analysis 2 (AUC = 0.71; P = 0.002). For the contour-line-independent parameter glaucoma probability score, a statistically significant difference was also observed in the performance obtained in analysis 1 (AUC = 0.89) compared with analysis 2 (AUC = 0.65; P < 0.001). CONCLUSIONS: Estimates of diagnostic accuracy of CSLO in glaucoma can be largely different depending on the population studied and the reference standard used to define disease. Diagnostic accuracy estimates obtained from case-control studies including well-defined groups of subjects with or without disease may not be applicable to the clinically relevant population.
机译:目的:评估研究设计和频谱偏差对青光眼共聚焦扫描激光检眼镜(CSLO)的诊断准确性评估的影响。方法:分析1包括67眼青光眼视野丧失和56眼正常志愿者。将本分析中诊断准确性的评估与从分析2中获得的评估进行了比较,分析2中包括了一批疑似青光眼但在CSLO成像时无视野损失的患者。为了进行分析2,青光眼组包括40眼具有渐进性青光眼视盘改变的眼,而43眼中没有任何证据表明对视神经的进行性损害,未经观察平均治疗时间为9.01 +/- 3.09年。正常组。接收器工作特性(ROC)曲线(AUC)下的区域用于评估CSLO参数的诊断准确性。结果:在分析1(AUC = 0.91)中,具有最大AUC判别函数Bathija的参数的性能与分析2(AUC = 0.71; P = 0.002)的性能之间在统计学上有显着差异。对于与轮廓线无关的参数性青光眼概率评分,与分析2(AUC = 0.65; P <0.001)相比,分析1(AUC = 0.89)获得的性能也有统计学差异。结论:根据所研究的人群和用于定义疾病的参考标准,对青光眼CSLO诊断准确性的估计可能会有很大差异。从病例对照研究中获得的诊断准确性估计值可能不适用于临床相关人群,包括病例组明确定义的有或没有疾病的受试者。

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