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Optic nerve head morphometry for glaucoma diagnosis, optimization of clinical measurement strategy

机译:视神经头形态计量学用于青光眼的诊断,临床测量策略的优化

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摘要

The present study aimed to develop a strategy for evaluation of instant PIMD-2π measurements as a basis for clinicalmonitoring of glaucoma. PIMD-2π is a morphometric measure of the waist of the nerve fiber layer at the optic nerve head(ONH). Clinical measurements of PIMD-2π in patients with early to moderate stage glaucoma demonstrated a highvariability among subjects. The high variability among subjects renders comparison of instant PIMD-2π measurements totolerance limits for normality derived from a normative database inefficient. It is suggested to instead compare sequentialmeasurements of PIMD-2π within a patient. Initially, the difference between an instant measurement and the average ofprevious measurements can be compared to tolerance limits for difference between measurements within subject. Once, apotential loss of PIMD-2π is detected, a sufficient number of measurements within a sufficiently wide time interval can beused to estimate the PIMD-2π loss rate with regression and the deviation of the estimated loss rate can be evaluated as a95 % confidence interval for the loss rate. If the upper confidence limit excludes 0, a significant loss rate has been detected.The currently proposed strategy has the potential to detect glaucoma earlier than the current gold standard, computerperimetry, with less inconvenience for the patient.
机译:本研究旨在开发一种评估即时PIMD-2π测量值的策略,作为临床\ r \ n监测青光眼的基础。 PIMD-2π是视神经头\ r \ n(ONH)处神经纤维层腰部的形态测量。 PIMD-2π在早期至中度青光眼患者中的临床测量结果显示,受试者之间存在较高的\ r \ n变异性。受试者之间的高变异性使得即时PIMD-2π测量值与标准数据库效率低下的正常性的公差范围比较。建议改为比较患者体内PIMD-2π的顺序测量。最初,可以将即时测量结果与先前测量结果的平均值之间的差异与受试者体内各测量值之间的差异的公差极限进行比较。一旦检测到PIMD-2π的潜在损失,就可以在足够宽的时间间隔内进行足够的测量,以估计PIMD-2π的损失率,并进行回归和估计损失率的偏差可以评估为丢失率的置信区间为95%。如果置信度上限不包括0,则表示已检测到显着的丢失率。\ r \ n当前提出的策略有可能比当前的金本位标准计算机\ r>尿量测定法更早地检测青光眼,给患者带来的不便较少。

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  • 来源
    《Ophthalmic Technologies XXIX》|2019年|108581C.1-108581C.7|共7页
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    Gullstrand lab, Ophthalmology, Dept. of Neuroscience, Uppsala University, University hospital,SE-751 UPPSALA, SWEDEN per.soderberg@neuro.uu.se phone +46 708 418447;

    Gullstrand lab, Ophthalmology, Dept. of Neuroscience, Uppsala University, University hospital,SE-751 UPPSALA, SWEDEN;

    Gullstrand lab, Ophthalmology, Dept. of Neuroscience, Uppsala University, University hospital,SE-751 UPPSALA, SWEDEN Gävle regional hospital, Sweden;

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