1997
DOI: 10.1016/s0002-9149(97)00280-4
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A multicenter, double-blind, one-year study comparing safety and efficacy of atorvastatin versus simvastatin in patients witb hypercholesterolemia

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Cited by 174 publications
(68 citation statements)
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“…Furthermore, success rates differed among the statins, ranging from 24.8% for fluvastatin to 54.7% for atorvastatin. Several studies have revealed that atorvastatin was more effective in attaining the LDL-C target goal than four other statins (simvastatin, pravastatin, lovastatin, and fluvastatin) in patients with or without CAD (19)(20)(21)(22). Our results were compatible with previous findings in non-Japanese populations.…”
Section: Discussionsupporting
confidence: 91%
“…Furthermore, success rates differed among the statins, ranging from 24.8% for fluvastatin to 54.7% for atorvastatin. Several studies have revealed that atorvastatin was more effective in attaining the LDL-C target goal than four other statins (simvastatin, pravastatin, lovastatin, and fluvastatin) in patients with or without CAD (19)(20)(21)(22). Our results were compatible with previous findings in non-Japanese populations.…”
Section: Discussionsupporting
confidence: 91%
“…The LDL-C and TG reductions by atorvastatin and simvastatin observed in the present analysis were typical of what has been reported by others. [20][21][22] Atorvastatin produced slightly greater reductions in LDL-C (Ϫ37 to Ϫ54% for atorvastatin vs. Ϫ35 to Ϫ49% for simvastatin) and TG (Ϫ22 to Ϫ31% for atorvastatin vs. Ϫ22 to Ϫ26% for simvastatin). However, the overall pattern of response (dose-dependent reductions) was the same for both drugs and was maintained across all of the subgroups examined.…”
Section: Discussionmentioning
confidence: 99%
“…Tailoring the starting dose according to individual LDL-C reduction requirements may aid in the achievement of target LDL-C levels [12,15]. There is evidence to suggest that baseline LDL-C levels impact overall LDL-C reduction, [16][17][18] and that treatment with intensive lipid lowering therapy results in greater reductions in LDL-C and a higher proportion of subjects achieving targets compared with more moderate regimens [19][20][21][22][23][24][25][26][27][28][29]. Thus, selecting an initial starting dose calculated to achieve the required LDL-C reduction, may allow more patients to reach targets more quickly, reducing the need for dose increases, thus improving clinical outcomes and being more cost-effective in the long term [30,31].…”
Section: Introductionmentioning
confidence: 99%