Key result
Patients initiated on loose-dose amlodipine/ARBs were at greater risk of a cardiovascular event composite compared with fixed-dose amlodipine/olmesartan.
Why the study?
Does fixed-dose combination amlodipine/olmesartan improve adherence, cardiovascular outcomes, and costs compared to amlodipine/benazepril or loose-dose amlodipine plus ARBs in patients with hypertension?
Cohort
Does fixed-dose combination amlodipine/olmesartan improve adherence, cardiovascular outcomes, and costs compared to amlodipine/benazepril or loose-dose amlodipine plus ARBs in patients with hypertension?
Fixed-dose combination amlodipine/olmesartan is associated with better adherence, lower costs, and reduced cardiovascular events compared to loose-dose amlodipine plus ARBs in hypertensive patients.
Answers are grounded in this paper and cite their sources.
Loose-dose amlodipine/ARBs associated with higher CV events; leaves open fixed-dose superiority pending randomized trials.
OBJECTIVES: Since treatment regimen type can influence adherence and other outcomes, this study examined adherence, cardiovascular events, and economic outcomes in patients with hypertension treated with fixed-dose combination (FDC) amlodipine/olmesartan (AML/OM), FDC AML/benazepril (AML/BEN), and loose-dose combination AML plus angiotensin II receptor blockers (LDC AML/ARBs). METHODS: Commercial health plan enrollees aged at least 18 years with index claim(s) for AML/OM, AML/BEN, or LDC AML/ARB were identified. Absence of study drug 6 months pre index, and continuous enrollment for at least 12 months post index were required. Descriptive analyses were executed to make comparisons between treatments, as well as multivariate models adjusting for baseline demographic and clinical characteristics, including propensity for assignment to study drug. RESULTS: Descriptive results suggested mean follow-up adherence was higher in the AML/OM cohort [proportion of days covered (PDC) = 0.63] compared with the AML/BEN (PDC = 0.55; p < 0.001) and LDC AML/ARB cohorts (PDC = 0.34; p < 0.001). The proportion of individuals with an incident follow-up cardiovascular event composite was lower in the AML/OM cohort versus the AML/BEN and LDC AML/ARB cohorts (5.94% versus 7.85% and 16.89% respectively). Adjusted Cox models suggested that patients initiated on LDC AML/ARB (hazard ratio 1.35; p < 0.001), but not on AML/BEN, were at greater risk of a follow-up cardiovascular event (composite) compared with AML/OM. Adjusted generalized linear models suggested that mean follow-up per-member-per-month overall costs were higher in the AML/BEN (cost ratio = 1.169; p < 0.001; unadjusted mean cost US$780) and LDC AML/ARB cohorts (cost ratio = 1.286; p < 0.001; unadjusted mean cost US $1394) compared with the AML/OM cohort (unadjusted mean cost US $740). CONCLUSION: The results suggested that treatment with FDC AML/OM was associated with greater likelihood of adherence and lower overall costs than with FDC AML/BEN and LDC AML/ARB, and lower risk of cardiovascular event composite versus LDC AML/ARB.
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Ferrario et al. (2013) conducted a cohort in hypertension. Fixed-dose combination amlodipine/olmesartan (AML/OM) vs. Fixed-dose amlodipine/benazepril (AML/BEN) and loose-dose amlodipine plus ARBs (LDC AML/ARBs) was evaluated on incident follow-up cardiovascular event composite (HR 1.35, p=<0.001). Patients initiated on loose-dose amlodipine/ARBs were at greater risk of a cardiovascular event composite compared with fixed-dose amlodipine/olmesartan.
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