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一种新型去氧肾上腺素-托吡卡胺复方药物引起的睫状肌麻痹的时间进程。

Time course of cycloplegia induced by a new phenylephrine-tropicamide combination drug.

作者信息

Lovasik J V, Kergoat H

机构信息

Université de Montréal, Ecole d'Optométrie, Montréal, Québec, Canada.

出版信息

Optom Vis Sci. 1990 May;67(5):352-8. doi: 10.1097/00006324-199005000-00009.

Abstract

A motorized and computer-interfaced phoropter was used to track the development of cycloplegia and recovery of accommodation over a 60-min period, after the topical application of a phenylephrine 5%-tropicamide 0.8% drug combination (Phenyltrope). Phenyltrope was introduced into the Canadian market about 2 years ago (Compendium of Pharmaceuticals and Specialties, 1987), and advertised as a fast acting cycloplegic and mydriatic drug. Here we report the results of our investigation of the depth of action and the temporal aspects of cycloplegia for this drug combination as a function of iris color. We also compare the action spectrum of Phenyltrope to that of tropicamide 1% under similar test conditions. Our results indicate that the latency for cycloplegia was shorter for tropicamide, the maximum rate of accommodative loss similar for both drugs, and the resultant cycloplegia at 20 min deeper for Phenyltrope. Recovery from induced cycloplegia was greater for tropicamide 60 min after drug administration. For both Phenyltrope and tropicamide, no significant differences in any of the parameters investigated were observed as a function of iris color. We conclude that even though Phenyltrope induced a measurably deeper cycloplegia than did tropicamide, the amount of residual accommodation present at 20 min (about 38%) is insufficient for most refractive purposes.

摘要

在局部应用5%去氧肾上腺素-0.8%托吡卡胺药物组合(苯托品)后,使用电动且与计算机接口的综合验光仪在60分钟内追踪睫状肌麻痹的发展和调节功能的恢复情况。苯托品大约在两年前进入加拿大市场(《药品和特殊产品手册》,1987年),并被宣传为一种速效睫状肌麻痹剂和散瞳剂。在此,我们报告了关于该药物组合睫状肌麻痹的作用深度和时间方面随虹膜颜色变化的研究结果。我们还在相似的测试条件下,将苯托品的作用光谱与1%托吡卡胺的作用光谱进行了比较。我们的结果表明,托吡卡胺引起睫状肌麻痹的潜伏期较短,两种药物的最大调节力丧失速率相似,且苯托品在20分钟时导致的睫状肌麻痹程度更深。用药60分钟后,托吡卡胺引起的睫状肌麻痹恢复程度更大。对于苯托品和托吡卡胺,在所研究的任何参数中,均未观察到随虹膜颜色变化的显著差异。我们得出结论,尽管苯托品引起的睫状肌麻痹程度比托吡卡胺更深,但20分钟时存在的残余调节量(约38%)对于大多数屈光目的而言是不足的。

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