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在晶状体的生物测量中,睫状肌麻痹剂能否被雾化剂或矫正镜片替代?

Could a cycloplegic agent be replaced by a fogging or a corrective lens in the biometric measurement of the crystalline lens?

作者信息

Kee C S, Do T C, Lai R Y, Wong G, Lam A K

机构信息

Department of Optometry and Radiography, Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong.

出版信息

Ophthalmic Physiol Opt. 1998 Nov;18(6):521-6.

Abstract

This study investigated whether a fogging or a corrective lens could be used to replace a cycloplegic agent in the ultrasonic measurement of crystalline lens thickness in myopia. A group of 28 Hong Kong Chinese adults with myopia was recruited. The crystalline lens thickness of the examined eye was measured by A-scan ultrasonography while the fixating eye was in one of three conditions: fog (+2.00 D fogging lens), full corrective lens, or cycloplegia (50 minutes after instillation of 1% cyclopentolate HCl). We found that the mean lens thickness was significantly different between the three conditions in our myopic subjects. The mean crystalline lens thickness under fogging and corrective lens conditions was significantly greater than the cycloplegic condition by 0.09 mm and 0.11 mm, respectively. The 95% limits of agreement compared to cycloplegia (fogging: -0.32 to +0.14; corrective: -0.35 to +0.13) showed marked intersubject variability, indicating that there is a risk of overestimating the lens thickness when substituting cycloplegia with either a fogging or a corrective lens.

摘要

本研究调查了在近视患者晶状体厚度的超声测量中,雾化镜或矫正镜片是否可用于替代睫状肌麻痹剂。招募了一组28名患有近视的中国香港成年人。使用A超超声检查法测量受检眼的晶状体厚度,同时注视眼处于三种状态之一:雾化(+2.00 D雾化镜片)、完全矫正镜片或睫状肌麻痹(滴入1%盐酸环喷托酯50分钟后)。我们发现,在我们的近视受试者中,这三种状态下的平均晶状体厚度存在显著差异。雾化和矫正镜片状态下的平均晶状体厚度分别比睫状肌麻痹状态显著厚0.09 mm和0.11 mm。与睫状肌麻痹相比的95%一致性界限(雾化:-0.32至+0.14;矫正:-0.35至+0.13)显示个体间存在明显差异,表明用雾化镜或矫正镜片替代睫状肌麻痹剂时存在高估晶状体厚度的风险。

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