Suppr超能文献

在棕色虹膜儿童中滴入1%环喷托酯后最大睫状肌麻痹时间。

Time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises.

作者信息

Laojaroenwanit Sittikorn, Layanun Vimontip, Praneeprachachon Pokpong, Pukrushpan Parnchat

机构信息

Department of Ophthalmology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.

出版信息

Clin Ophthalmol. 2016 May 18;10:897-902. doi: 10.2147/OPTH.S102611. eCollection 2016.

Abstract

PURPOSE

We aimed to 1) determine the time of maximum cycloplegia after instillation of cyclopentolate 1% in children with brown irises, 2) evaluate the correlation between the pupillary reaction and time of maximum cycloplegia, and 3) identify any side effects of the medication.

PATIENTS AND METHODS

This was a prospective analytical study involving children aged 5 to 14 years who were attending refraction clinic. Cyclopentolate 1% was instilled three times at 10-minute intervals. The spherical equivalent, pupillary reaction, and pupillary diameter were recorded before the first drop and nine times after the last drop at 10-minute intervals. Side effects were assessed. Time of maximum cycloplegia was determined from the time point at which the 95% confidence interval of the differences between the mean spherical equivalent at each point and its final value at 110 minutes was reached and remained within the equivalence limit (±0.25 D).

RESULTS

Sixty children were enrolled in this study. Their mean age was 9.8 years (range: 5-4 years). Time of maximum cycloplegia was reached at 30 minutes after the first instillation of cyclopentolate. A poor correlation was observed between the pupillary reaction and the time of maximum cycloplegia (r=-0.07). The mean pupillary diameter at 30 minutes was 3.7±1.3 mm, and further dilation occurred thereafter. No side effects were observed.

CONCLUSION

In most children, maximum cycloplegia was reached 30 minutes after the first instillation of cyclopentolate. The absence of a pupillary reaction should not be used as an indicator of maximum cycloplegia.

摘要

目的

我们旨在1)确定在患有棕色虹膜的儿童中滴入1%环喷托酯后最大睫状肌麻痹的时间,2)评估瞳孔反应与最大睫状肌麻痹时间之间的相关性,以及3)确定该药物的任何副作用。

患者与方法

这是一项前瞻性分析研究,纳入了5至14岁在验光诊所就诊的儿童。每隔10分钟滴入1%环喷托酯3次。在第一滴药前以及最后一滴药后每隔10分钟记录9次等效球镜度、瞳孔反应和瞳孔直径。评估副作用。最大睫状肌麻痹时间是根据每个时间点的平均等效球镜度与其在110分钟时的最终值之间差异的95%置信区间达到并保持在等效限度(±0.25 D)内的时间点来确定的。

结果

本研究纳入了60名儿童。他们的平均年龄为9.8岁(范围:5 - 14岁)。在首次滴入环喷托酯后30分钟达到最大睫状肌麻痹时间。观察到瞳孔反应与最大睫状肌麻痹时间之间的相关性较差(r = -0.07)。30分钟时的平均瞳孔直径为3.7±1.3 mm,此后瞳孔进一步散大。未观察到副作用。

结论

在大多数儿童中,首次滴入环喷托酯后30分钟达到最大睫状肌麻痹。不应将瞳孔反应消失用作最大睫状肌麻痹的指标。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验