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Adherence with topical glaucoma medication monitored electronically the Travatan Dosing Aid study.

AbstractPURPOSE:
To assess patient adherence and behaviors with topical once-daily therapy for glaucoma.
DESIGN:
Prospective, observational cohort study.
PARTICIPANTS:
One hundred ninety-six patients with glaucoma who were being treated with a prostaglandin analog in 1 or both eyes at the Scheie or Wilmer Eye Institutes between August 2006 and June 2007.
METHODS:
Detailed medical history was obtained from each patient. All subjects used the Travatan Dosing Aid (DA; Alcon, Fort Worth, TX) to administer travoprost as prescribed. Devices were collected at 3 months and the data of drop usage was downloaded using software provided with the dosing aid. Data were analyzed for the 8-week period starting 2 weeks after the enrollment visit and ending 2 weeks before the 3-month visit.
MAIN OUTCOME MEASURES:
Assessment of adherence and patterns of drop usage as indicated by the DA.
RESULTS:
A total of 282 subjects consented to be in the study and 86 (30%) withdrew before study completion or had device errors, leaving 196 subjects (70%) with evaluable data at 3 months. The overall mean (+/-standard deviation) adherence rate was 0.71 (+/-0.24), ranging from 0.02 to 0.97. One hundred nine of these patients (55.6%) took greater than 75% of the expected doses. Those with adherence of less than 50% of expected doses showed substantially increased dose taking immediately after the office visit and just before the return visit at 3 months (P = 0.03). The mean adherence rate estimates of the physician and patient self-report were 0.77 and 0.95, respectively. The agreement between the physician assessment and DA-recorded adherence rate showed poor correlation for individual cases (intraclass correlation coefficient, 0.09; 95% confidence interval, 0.00-0.19).
CONCLUSIONS:
Nearly 45% of patients using an electronic monitoring device who knew they were being monitored and were provided free medication used their drops less than 75% of the time. Patients reported far higher medication use than their actual behavior. The ability of the physician to identify which persons are poorly adherent from their self-report or from other subjective clues is poor.
FINANCIAL DISCLOSURE(S):
Proprietary or commercial disclosure may be found after the references.
AuthorsConstance O Okeke, Harry A Quigley, Henry D Jampel, Gui-shuang Ying, Ryan J Plyler, Yuzhen Jiang, David S Friedman
JournalOphthalmology (Ophthalmology) Vol. 116 Issue 2 Pg. 191-9 (Feb 2009) ISSN: 1549-4713 [Electronic] United States
PMID19084273 (Publication Type: Journal Article, Multicenter Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Antihypertensive Agents
  • Ophthalmic Solutions
  • Cloprostenol
  • Travoprost
Topics
  • Administration, Topical
  • Adult
  • Aged
  • Aged, 80 and over
  • Antihypertensive Agents (administration & dosage)
  • Attitude to Health
  • Cloprostenol (administration & dosage, analogs & derivatives)
  • Cohort Studies
  • Drug Monitoring (instrumentation)
  • Female
  • Follow-Up Studies
  • Glaucoma, Angle-Closure (drug therapy)
  • Glaucoma, Open-Angle (drug therapy)
  • Humans
  • Intraocular Pressure (drug effects)
  • Male
  • Middle Aged
  • Ocular Hypertension (drug therapy)
  • Ophthalmic Solutions (administration & dosage)
  • Patient Compliance (statistics & numerical data)
  • Prospective Studies
  • Surveys and Questionnaires
  • Travoprost

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