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测量软性隐形眼镜在佩戴时的折射率。

Measurement of the refractive index of soft contact lenses during wear.

机构信息

Centre for Contact Lens Research, School of Optometry, University of Waterloo, Waterloo, ON, Canada.

出版信息

Eye Contact Lens. 2010 Jan;36(1):2-5. doi: 10.1097/ICL.0b013e3181c8135f.

Abstract

PURPOSE

To determine whether the refractive index (RI) of a soft contact lens can be evaluated using refractometry while the lens remains on the eye and to compare this with more traditional ex vivo RI measurements.

METHODS

A slitlamp apparatus was modified to incorporate a customized Atago hand refractometer. With a double-masked study design, nine adapted symptomatic soft contact lens wearers wore a contact lens in each eye (lotrafilcon B and etafilcon A) in a randomized order. In vivo RI was determined from the relative Brix scale measurements immediately after lens insertion and after 1 and 10 hr of lens wear. Ex vivo refractometry was performed after 10 hr of lens wear for comparison. Means +/- standard errors of the means are reported.

RESULTS

In vivo RI values at baseline were 1.422 +/- 0.0004 (lotrafilcon B) and 1.405 +/- 0.0021 (etafilcon A); after 1 hr of lens wear, values were 1.423 +/- 0.0006 and 1.408 +/- 0.0007, respectively; and after 10 hr of lens wear, values were 1.424 +/- 0.0004 and 1.411 +/- 0.0010, respectively. Ex vivo RI values at the end of the 10 hr wearing period were 1.424 +/- 0.0003 (lotrafilcon B) and 1.412 +/- 0.0017 (etafilcon A). The change in in vivo RI across the day was statistically significant for the etafilcon A lens (repeated-measures analysis of variance, P<0.01) but not for the lotrafilcon B lens (P>0.05).

CONCLUSIONS

This novel adaptation of refractometry was able to measure the RI of soft contact lenses during wear (without lens removal). End of day RI measurements using in vivo and ex vivo refractometry were comparable with each other. Future work is required to determine whether this in vivo method can improve our understanding of the relationships between soft contact lens RI, hydration, on-eye lens performance, and symptomology.

摘要

目的

确定在软性隐形眼镜保留于眼睛上时是否可以使用折射仪评估其折射率(RI),并将其与更传统的离体 RI 测量进行比较。

方法

对裂隙灯设备进行改良,纳入定制的 Atago 手持折射仪。采用双盲研究设计,9 名适应症状的软性隐形眼镜佩戴者以随机顺序左右眼各佩戴一种隐形眼镜(Lotrafilcon B 和 Etafilcon A)。在隐形眼镜插入后即刻以及佩戴 1 小时和 10 小时后,根据相对 Brix 刻度测量值确定体内 RI。在佩戴 10 小时后进行离体折射仪测量以进行比较。报告均值±标准误差。

结果

基础时的体内 RI 值分别为 1.422±0.0004(Lotrafilcon B)和 1.405±0.0021(Etafilcon A);佩戴 1 小时后,值分别为 1.423±0.0006 和 1.408±0.0007;佩戴 10 小时后,值分别为 1.424±0.0004 和 1.411±0.0010。在佩戴 10 小时结束时的离体 RI 值分别为 1.424±0.0003(Lotrafilcon B)和 1.412±0.0017(Etafilcon A)。对于 Etafilcon A 隐形眼镜,体内 RI 的日间变化具有统计学意义(重复测量方差分析,P<0.01),但对于 Lotrafilcon B 隐形眼镜则没有(P>0.05)。

结论

这项折射仪的新应用能够在佩戴隐形眼镜期间(无需取下镜片)测量软性隐形眼镜的 RI。使用体内和离体折射仪测量的一天结束时 RI 值相互可比。需要进一步的研究来确定这种体内方法是否可以提高我们对软性隐形眼镜 RI、水合作用、眼内镜片性能和症状之间关系的理解。

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