May 2004
Volume 45, Issue 13
Free
ARVO Annual Meeting Abstract  |   May 2004
Glaucoma and Compliance: Comparison of objective patient compliance information with respect to "QD" dosing versus "BID" dosing on patient medication compliance.
Author Affiliations & Notes
  • D.J. Blair
    Ophthalmology, Indiana University School of Medicine, Indianapolis, IN
  • L. Cantor
    Ophthalmology, Indiana University School of Medicine, Indianapolis, IN
  • D. WuDunn
    Ophthalmology, Indiana University School of Medicine, Indianapolis, IN
  • J. Hoop
    Ophthalmology, Indiana University School of Medicine, Indianapolis, IN
  • V. Malinovsky
    Optometry, Indiana University School of Optometry, Bloomington, IN
  • Footnotes
    Commercial Relationships  D.J. Blair, None; L. Cantor, None; D. WuDunn, None; J. Hoop, None; V. Malinovsky, None.
  • Footnotes
    Support  Supported in part by Allergan, Inc. and in part by an unrestricted grant from RPB, Inc.
Investigative Ophthalmology & Visual Science May 2004, Vol.45, 4510. doi:
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      D.J. Blair, L. Cantor, D. WuDunn, J. Hoop, V. Malinovsky; Glaucoma and Compliance: Comparison of objective patient compliance information with respect to "QD" dosing versus "BID" dosing on patient medication compliance. . Invest. Ophthalmol. Vis. Sci. 2004;45(13):4510.

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

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Abstract

Abstract: : Purpose: To compare the effect of "once a day" versus "twice a day dosing’ on patient medication compliance with glaucoma topical therapy. Methods: 100 patients were enrolled in this prospective series utilizing two different medication regimens. Group A (50 patients) were on glaucoma topical medication dosed once a day "QD" and group B (50 patients) were on eyedrops dosed twice a day, "BID". All patients signed consent allowing release of their refill data from their local pharmacy. If a patient refilled their medication as expected given their prescribed dosing regimen and bottle size, their rate of compliance would be 100%. If they refilled their medications less frequently or more frequently than expected their compliance rate would be below or above 100% respectively Calculated drops per bottle were obtained from a national pharmacy benefit manager. Allowing for some variation in dosing, we considered 85% to 115% utilization to reflect acceptable compliance with the prescribed regimen. Results: 20 patients (10 from each group) either withdrew or were not included due to insufficient data collection. Compliance rates of Group A varied from 31.9% to 429.6 %. Compliance rates for group B varied from 33.7% to 230.3%. Average differences between the two groups were not significantly different. Group A patients (QD) exhibited a 25.0 % over utilization rate as compared with a 30.0% over utilization rate for group B patients (BID). Group A patients (QD) exhibited a 37.5 % under utilization rate as compared with a 27.5% under utilization rate for group B patients (BID). Conclusions: This study provides evidence that compliance rates between once a day dosing versus twice a day dosing is similar.

Keywords: clinical (human) or epidemiologic studies: biostatistics/epidemiology methodology • clinical (human) or epidemiologic studies: health care delivery/economics/manpower • pharmacology 
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