June 2021
Volume 62, Issue 8
Open Access
ARVO Annual Meeting Abstract  |   June 2021
Group-based trajectory modeling in electronically monitored adherence data in patients with glaucoma
Author Affiliations & Notes
  • Shervonne Poleon
    Optometry and Vision Science, The University of Alabama at Birmingham School of Optometry, Birmingham, Alabama, United States
  • Sampson Abu
    Department of Ophthalmology and Visual Sciences, The University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, United States
  • Tracy Thomas
    Department of Ophthalmology and Visual Sciences, The University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, United States
  • Lyne Racette
    Department of Ophthalmology and Visual Sciences, The University of Alabama at Birmingham School of Medicine, Birmingham, Alabama, United States
  • Footnotes
    Commercial Relationships   Shervonne Poleon, None; Sampson Abu, None; Tracy Thomas, None; Lyne Racette, Olleyes Inc (C)
  • Footnotes
    Support  NIH Grant EY025756; Unrestricted grant from Research to Prevent Blindness
Investigative Ophthalmology & Visual Science June 2021, Vol.62, 1586. doi:
  • Views
  • Share
  • Tools
    • Alerts
      ×
      This feature is available to authenticated users only.
      Sign In or Create an Account ×
    • Get Citation

      Shervonne Poleon, Sampson Abu, Tracy Thomas, Lyne Racette; Group-based trajectory modeling in electronically monitored adherence data in patients with glaucoma. Invest. Ophthalmol. Vis. Sci. 2021;62(8):1586.

      Download citation file:


      © ARVO (1962-2015); The Authors (2016-present)

      ×
  • Supplements
Abstract

Purpose : Group-Based Trajectory Modeling (GBTM) is a statistical approach that clusters persons with similar behavioral and developmental trajectories. When applied to administrative claims data which document the frequency of ocular hypotensive prescription refills, GBTM has revealed distinct patterns of medication adherence. In this study, we applied GBTM to electronically monitored data which document daily eye drop use in order to identify distinct patterns of medication adherence in glaucoma patients.

Methods : We performed GBTM with ancillary adherence data from 100 participants enrolled in an NIH-funded glaucoma progression study at the University of Alabama at Birmingham. Participants were included if they were above age 18, used hypotensive eye drops, had 2 or more reliable visual field tests, and had visual acuity better than 20/40 at baseline. Adherence was monitored for 6 months using Medication Event Monitoring Systems (Aardex, Switzerland) which record the date and time at which the devices are opened to use the eye drops stored inside. Using the Proc Traj macro (SAS Institute, Cary NC), quadratic functions [RL(1] [sp2] were fitted to weekly mean adherence data to estimate trajectory models with 2, 3, 4, 5, and 6 groups. The trajectory model that included 5% or more of participants in each group and had the highest Bayesian Information Criterion (BIC) was identified as optimal.

Results : Mean age was 68.6 ± 8.3 years, and mean baseline intraocular pressure was 25 ± 4.8 mmHg (right eye) and 23.9 ± 6.5 mmHg (left eye). Mean adherence was 80 ± .21% and the BIC for the final model was -437.5. Five trajectory groups were estimated: Near-perfect adherence (30.7% of participants), Good adherence (32.7%), Initially Good but Declining adherence (6% of participants), Consistently Poor adherence (18.7% of participants), and Poor and Declining adherence (11.9% of participants).

Conclusions : We identified “Near-perfect” adherence and “Initially Good but Declining” adherence as two patterns that had not been previously captured in administrative data. Utilizing different metrics to quantify adherence may provide additional insight into the dynamic nature of medication adherence, which may help to predict adherence to prescribed hypotensive therapy.

This is a 2021 ARVO Annual Meeting abstract.

×
×

This PDF is available to Subscribers Only

Sign in or purchase a subscription to access this content. ×

You must be signed into an individual account to use this feature.

×