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Title
Lipid-altering efficacy and safety of simvastatin 80
mg/day: long term experience in a large group of patients
with hypercholesterolemia. World Wide Expanded Dose
Simvastatin Study Group
Purpose
To evaluate the long-term lipid-altering efficacy and
safety of simvastatin 80 mg/day in patients with hypercholesterolemia
Design
Two randomized, multicenter, double-blind, parallel
group studies
Patients
1105 hypercholesterolemic patients
Follow-up
48 weeks
Treatment regimen
Simvastatin 80 mg daily vs simvastatin 40 mg daily
Results
Mean percentage reductions from baseline in
LDL cholesterol in the 40 and 80 mg groups were 41%
and 46%, respectively.
Larger reductions in total cholesterol and triglycerides
were also observed with the 80 mg dose compared to the
40 mg dose.
Both doses were well tolerated .
Conclusion
Compared with the 40 mg dose, simvastatin 80 mg produced
greater reductions in LDL cholesterol, total cholesterol
and triglycerides. Both doses were well tolerated.
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