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LenStar LS900在白内障人群中生物测量的可重复性

Repeatability of biometric measures from the LenStar LS900 in a cataractous population.

作者信息

Langenbucher Achim, Szentmáry Nóra, Wendelstein Jascha, Cayless Alan, Hoffmann Peter, Cooke David

机构信息

Department of Experimental Ophthalmology, Saarland University, Homburg, Germany.

Dr. Rolf M. Schwiete Center for Limbal Stem Cell and Aniridia Research, Saarland University, Homburg, Germany.

出版信息

PLoS One. 2025 May 5;20(5):e0321786. doi: 10.1371/journal.pone.0321786. eCollection 2025.

Abstract

PURPOSE

To investigate the repeatability of biometric measures and assess interactions between their uncertainties for use in an error propagation model, using patient data.

METHODS

Cross-sectional non-randomised study evaluating a dataset containing 969 LenStar 900 biometric measurements taken before cataract surgery. Only complete scans with at least 3 successful measurements for each eye performed on the same day were considered. For each sequence, the aggregated mean (AMEAN) and population standard deviations (ASD) were derived. The within-subject standard deviation Sw was extracted for: corneal thickness, CCT, anterior chamber depth ACD, lens thickness LT, axial length AL, corneal diameter WTW, and the keratometric power vector components equivalent power KEQ, and the projections of corneal astigmatism KC0 and KC45. Correlations between the uncertainties were assessed using Spearman rank correlations.

RESULTS

For the 266 eyes matching the inclusion criteria, Sw was 3.6/ 24.7/35.5/ 17.7/ 107.5 µm for CCT/ ACD/ LT/ AL WTW and 0.18/ 0.12/ 0.10 dioptres for KEQ/ KC0/ KC45. The keratometric axis ASD is inversely proportional to the keratometric astigmatism AMEAN. LT and ACD uncertainties are strongly negatively correlated, with KEQ and KC0 uncertainties moderately correlated.

CONCLUSIONS

The uncertainty and correlation data presented here could be used to define a Monte-Carlo based error propagation model mapping the biometric measures and uncertainties to variations in predicted refraction after cataract surgery. We recommend using power vector components for error propagation models since the large decay over keratometric astigmatism makes keratometric axis uncertainty unreliable.

摘要

目的

利用患者数据研究生物测量指标的可重复性,并评估其不确定性之间的相互作用,以用于误差传播模型。

方法

横断面非随机研究,评估一个包含969例白内障手术前LenStar 900生物测量数据的数据集。仅考虑在同一天对每只眼睛进行的至少3次成功测量的完整扫描。对于每个序列,得出汇总平均值(AMEAN)和总体标准差(ASD)。提取以下各项的受试者内标准差Sw:角膜厚度、中央角膜厚度(CCT)、前房深度(ACD)、晶状体厚度(LT)、眼轴长度(AL)、角膜直径(WTW),以及角膜曲率计屈光度矢量分量等效屈光度(KEQ),和角膜散光投影KC0和KC45。使用Spearman等级相关性评估不确定性之间的相关性。

结果

对于符合纳入标准的266只眼睛,CCT/ACD/LT/AL/WTW的Sw分别为3.6/24.7/35.5/17.7/107.5 µm,KEQ/KC0/KC45的Sw分别为0.18/0.12/0.10屈光度。角膜曲率计轴位ASD与角膜曲率散光AMEAN成反比。LT和ACD的不确定性呈强负相关,KEQ和KC0的不确定性呈中度相关。

结论

此处呈现的不确定性和相关性数据可用于定义基于蒙特卡洛的误差传播模型,该模型将生物测量指标和不确定性映射到白内障手术后预测屈光不正的变化。我们建议在误差传播模型中使用屈光度矢量分量,因为角膜曲率散光的大幅衰减使得角膜曲率计轴位不确定性不可靠。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c480/12052171/5513143faf47/pone.0321786.g001.jpg

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