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Published on: November 10, 2017
Comparative efficacy of ezetimibe/simvastatin, rosuvastatin, and atorvastatin in uncontrolled hyperlipidemia patients
Amy Furman1, Joy L Meier, Robert A Malmstrom
1Department of Veterans Affairs, Northern California Health Care System, Mather, CA 95655, USA.
Insights
Ezetimibe/simvastatin demonstrated superior low-density lipoprotein (LDL) reduction compared to rosuvastatin or atorvastatin in high-risk patients. Further research is needed to determine the clinical impact of these findings.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Practice
Background:
- Dyslipidemia treatment in high-risk patients aims for low-density lipoprotein (LDL) cholesterol <100 mg/dL.
- Efficacy of potent lipid-lowering regimens in patients not achieving goals on generic therapy requires further characterization.
Purpose of the Study:
- To determine the LDL-lowering efficacy of higher-potency statin strategies (ezetimibe/simvastatin, rosuvastatin, atorvastatin) in high-risk patients switched from simvastatin.
- To evaluate patient adherence, effects on other lipid parameters, and adverse events.
Main Methods:
- Retrospective analysis of Veterans Affairs Health Care System data (3-year period).
- Lipid data assessed pre- and post-conversion from simvastatin (2-6 months).
- Medication refill data used to determine therapy adherence.
Main Results:
- Ezetimibe/simvastatin achieved significantly greater LDL reduction (37 mg/dL) versus rosuvastatin (25 mg/dL) or atorvastatin (26 mg/dL) (P <0.05).
- Adherence to therapy was 51%.
- All interventions lowered total cholesterol, HDL, and triglycerides compared to simvastatin; no significant difference in adverse events between groups.
Conclusions:
- Ezetimibe/simvastatin demonstrated superior LDL reduction compared to rosuvastatin or atorvastatin at the doses used.
- The clinical significance of these observed LDL reduction differences remains undetermined.
Objective:
Treatment of dyslipidemia in high-risk patients specifies a low-density lipoprotein (LDL) cholesterol <100 mg/dL. The efficacy of higher-potency regimens in clinical practice in patients who have not achieved their LDL goal on generic therapy is not well characterized. The primary objective of this study was to determine the LDL-lowering efficacy of higher-potency strategies (ezetimibe/simvastatin, rosuvastatin, and atorvastatin) in high-risk patients who were switched from simvastatin therapy. Secondary objectives were to evaluate patient adherence to these therapies, determine the efficacy of these interventions on other lipid parameters, and define the incidence of adverse effects.
Study Design:
Retrospective data analysis derived from the Veterans Affairs Health Care System VISN 21 over a 3-year time period.
Methods:
Lipid data were assessed prior to and within 2 to 6 months following the conversion from simvastatin. Adherence to therapy was determined by medication refill data.
Results:
Treatment with ezetimibe/simvastatin resulted in significantly greater reductions in LDL compared with rosuvastatin or atorvastatin (37 vs 25 and 26 mg/dL, respectively; P <0.05). Adherence to therapy was 51% of all patients studied. All treatments significantly lowered total cholesterol, high-density lipoprotein, and triglycerides when compared with simvastatin. There was no difference between treatment groups in the number of adverse events.
Conclusions:
At the doses used in this population, ezetimibe/simvastatin resulted in greater LDL reductions than rosuvastatin or atorvastatin. The clinical impact of these differences is as yet undetermined.
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