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Jenifer Wogen, Charles A. Kreilick, Richard C. Livornese, Feride Frech, P-249: A population-based study of compliance and persistency with cardiovascular agents used in hypertension management, American Journal of Hypertension, Volume 14, Issue S1, April 2001, Page 112A, https://doi.org/10.1016/S0895-7061(01)01439-X
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Abstract
Purpose: To conduct a head to head comparison of persistency and compliance associated with representative agents used in the pharmacologic management of hypertension including lisinopril (Zestril), valsartan (Diovan), amlodipine (Norvasc) in a usual care setting.
Methods: This retrospective database study utilized patients continuously benefit-eligible from the Merck-Medco pharmacy claims database from 8/1997 through 7/2000 (N=14.6M). Patients who received an initial (no prescription filled within class during prior 12 months) prescription for lisinopril, valsartan, or amlodipine between 8/1998 through 7/1999 (N=142,945) were included and followed for 12 months. Compliance was assessed using the medication possession ratio (MPR), or the percentage of time a patient had drug available over a 1-year time period. Persistency was defined as having drug on hand at least one day in the month. To control for differences in overall baseline chronic disease burden, a Chronic Disease Score (CDS), which uses drug markers to identify chronic conditions, was used to classify the cohort as mild, moderate, or severe.
Results: Mean age of the study cohort was 63.1 years and 53% were female. Over half (51%) of the cohort used amlodipine as initial therapy, 21% valsartan, and 28% lisinopril. More valsartan patients remained persistent on therapy at 12-months post-therapy initiation (66%) compared to amlodipine (57%) and lisinopril (55%) (p<.0001, both comparisons). Mean duration of therapy was 266 days for valsartan patients versus 246 days for amlodipine and 240 days for lisinopril (p<.0001, both comparisons). Compliance was also greatest for valsartan patients, reflecting a mean MPR of 76% vs. 67% for amlodipine, 65% for lisinopril (p<.0001, both comparisons). While a slightly greater proportion of valsartan patients had a lower CDS (31% classified as severe, vs. 35% for both lisinopril and amlodipine), compliance and duration of therapy remained greater for valsartan patients across all CDS strata. Valsartan patients classified as severe via CDS had a mean duration of therapy of 266 days, compared to 245 for amlodipine and 237 for lisinopril (p<.0001, both comparisons). These patients also had a mean MPR of 75% as compared to 67% and 64% for amlodipine and lisinopril patients, respectively (p<.0001, both comparisons).
Conclusion: These preliminary results suggest that patients receiving valsartan in a typical managed care setting for the treatment of hypertension may be more adherent to therapy. These differences appear to be independent of baseline CDS.
Research funded by Novartis Pharmaceuticals