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局部毛果芸香碱治疗的依从性。

Compliance with topical pilocarpine treatment.

作者信息

Kass M A, Meltzer D W, Gordon M, Cooper D, Goldberg J

出版信息

Am J Ophthalmol. 1986 May 15;101(5):515-23. doi: 10.1016/0002-9394(86)90939-6.

Abstract

Using an unobtrusive eyedrop medication monitor, we measured compliance with topical pilocarpine treatment in a sample of 184 patients. The eyedrop monitor recorded electronically the date and time of each pilocarpine administration over a four- to six-week period. The subjects administered a mean +/- S.D. of 76.0% +/- 24.3% of the prescribed pilocarpine doses. Eleven patients (6%) took less than one quarter and 28 patients (15.2%) took less than one half of the prescribed administrations. In contrast, when the subjects were interviewed they reported taking a mean +/- S.D. of 97.1% +/- 5.9% of the prescribed pilocarpine doses. As determined by the monitor, 45 patients (24.5%) had at least one day per month with no administrations of pilocarpine; 56 subjects (30.4%) compressed the doses during the daytime hours, leaving an interval between the night dose and the morning dose the next day of 12 hours or more. The rate of compliance was significantly higher (P less than .0001) in the 24-hour period preceding the return appointment than in the entire observation period.

摘要

我们使用一种不引人注意的眼药水用药监测器,对184名患者样本中局部使用毛果芸香碱治疗的依从性进行了测量。眼药水监测器以电子方式记录了四至六周内每次使用毛果芸香碱的日期和时间。受试者使用的毛果芸香碱剂量平均为规定剂量的76.0%±24.3%。11名患者(6%)使用的剂量不到规定剂量的四分之一,28名患者(15.2%)使用的剂量不到规定剂量的一半。相比之下,当对受试者进行访谈时,他们报告使用的毛果芸香碱剂量平均为规定剂量的97.1%±5.9%。根据监测器的测定,45名患者(24.5%)每月至少有一天未使用毛果芸香碱;56名受试者(30.4%)在白天时段压缩了用药剂量,使得夜间用药剂量与次日早晨用药剂量之间的间隔达到12小时或更长时间。复诊前24小时内的依从率显著高于整个观察期(P<0.0001)。

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