Key result
Fixed-dose rosuvastatin-ezetimibe is linked to ~46% lower risk of discontinuation versus free-combination therapy.
Why the study?
Does a fixed-dose combination of rosuvastatin and ezetimibe improve treatment adherence and persistence compared to free-combination therapy in adults?
Cohort (n=15,643)
Yes
Does a fixed-dose combination of rosuvastatin and ezetimibe improve treatment adherence and persistence compared to free-combination therapy in adults?
Answers are grounded in this paper and cite their sources.
Fixed-dose combination of rosuvastatin and ezetimibe significantly improves treatment adherence and persistence compared to free-combination therapy, which is associated with greater LDL-C reductions.
Background: Guidelines for dyslipidemia management recommend adding ezetimibe for patients with dyslipidemia inadequately controlled with statin monotherapy. A fixed-dose combination (FDC) of statin and ezetimibe may improve persistence and adherence and hence reduce LDL-C further compared to free-combination treatment (FCT). The primary aim was to compare persistence/adherence with FDC versus FCT of rosuvastatin and ezetimibe (R/E); the secondary aim was to assess the impact of treatment adherence and persistence to LDL-C percentage reduction from baseline. An exploratory analysis assessed the impact of treatment adherence and persistence to incidence of major adverse cardiovascular events (MACEs). A subgroup analysis of patients on FDC of rosuvastatin 10 mg and ezetimibe 10 mg was also conducted. Methods: A retrospective analysis was performed using the THIN® database from Belgium and France in individuals (aged ≥18 years who received R/E as FDC or FCT between January 01, 2017, and November 30, 2022). Persistence (time from landmark date to discontinuation, with the latter defined as >45 days gap between prescription fills) and adherence (having a proportion of days covered ≥80%) were defined. Subsequent analyses adopted propensity score matching or weighting, followed by Cox and logistic regression models. Results: A total of 15,643 treatment episodes (FDC: 11,300; FCT: 4,343) were selected. FDC R/E was associated with greater persistence (HR: 0.54, 95% CI: 0.51-0.58) and higher odds of adherence (OR: 3.00, 95% CI: 2.70-3.30) than FCT R/E. Based on the regression analysis results, patients who were persistent to treatment had a 10% higher reduction in LDL-C values from baseline than those non persistent. Similarly, patients who were adherent had 9.6% higher reduction in LDL-C levels from baseline than those not adherent. No significant difference was observed in association between persistence/adherence and MACEs. A consistent trend was also observed in the subgroup analysis. Conclusions: In conclusion, FDC of R/E use was associated with higher treatment persistence and adherence than FCT of R/E. Patients persistent/adherent to treatment had greater LDL-C reductions than those who discontinued or did not follow treatment schedule. The limited number of MACEs suggests a cautious interpretation of exploratory MACE findings.
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Samnaliev et al. (2025) conducted a cohort in Dyslipidemia (n=15,643). Fixed-dose combination of rosuvastatin and ezetimibe vs. Free-combination treatment of rosuvastatin and ezetimibe was evaluated on Persistence (time to discontinuation) (HR 0.54, 95% CI 0.51-0.58). Fixed-dose combination of rosuvastatin and ezetimibe was associated with greater persistence and higher odds of adherence compared to free-combination therapy.
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