Publication

An upright eyedrop bottle: Accuracy, usage of excess drops, and contamination compared to a conventional bottle

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Last modified
  • 05/22/2025
Type of Material
Authors
    Isaiah J Davies, Duke UniversityNinita H Brown, Metrolina Nephrology AssociatesJoanne C Wen, University of WashingtonSandra Sstinnett, Duke UniversityKelsey Kubelick, Emory UniversityRoma P Patel, University of California Davis Health System Eye CenterKristin L Benokraitis, EG-GILEROLatoya Greene, Duke UniversityCurry Cheek, Duke UniversityKelly W Muir, Duke University
Language
  • English
Date
  • 2016-07-28
Publisher
  • Dove Medical Press Limited
Publication Version
Copyright Statement
  • © 2016 Davies et al. This work is published and licensed by Dove Medical Press Limited
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 10
Start Page
  • 1411
End Page
  • 1417
Grant/Funding Information
  • Dr Muir receives salary support from a VA HSR&D Career Development Award.
  • This work was funded in part by 1R43EY022515-01A1 (PI: Mosler).
Abstract
  • Purpose: This study tested the feasibility of using an upright eyedrop bottle (UEB), a device designed to assist patients with eyedrop placement without reclining their head. Patients and methods: Experienced eyedrop users were enrolled who answered “yes” to the question, “Do you ever have trouble getting your eyedrops in?” After being shown a multimedia presentation and answering a questionnaire regarding eyedrop usage, participants were observed instilling eyedrops. Participants were instructed to instill a single eyedrop in each eye with both a standard bottle and the UEB. They repeated this process three times. With each trial, the amount of time taken to instill drops was recorded, as well as whether a drop landed in the eye (accuracy), if excess drops were used, and if the bottle tip was contaminated. Results: Forty participants were enrolled, with an average age of 72.4±8.9 years; the majority were females (24 females). Thirty-four participants had been using eyedrops for at least 1 year. The time required to instill eyedrops was significantly less with the UEB in the second and third trials. There was no difference in accuracy between the conventional bottle and the UEB in the left or right eye in any trials. Significantly more participants used excess number of drops while using the conventional bottle in both the left and right eyes in all three trials. The bottle tip was never contaminated with the UEB. Depending on the trial and the eye, the conventional bottle was contaminated by between 42% and 53% of participants. Conclusion: The UEB has the potential to assist patients with eyedrop placement. Although there was no difference in accuracy between the UEB and the conventional bottle, the UEB was associated with less use of excess drops and less contamination of the bottle tip, compared to the conventional bottle.
Author Notes
  • Kelly W Muir, Duke University School of Medicine, Duke University Medical Center, Box 3802, Durham, NC 27710, USA, Tel +1 919 684 3283, Fax +1 919 681 8267, Email: kelly.muir@duke.edu
Keywords
Research Categories
  • Engineering, Biomedical

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