1999
DOI: 10.1016/s0021-9150(99)00062-3
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The effect of fluvastatin on cardiac events in patients with symptomatic coronary artery disease during one year of treatment

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Cited by 107 publications
(49 citation statements)
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“…The results were consistent with previously observed positive effects of long-term fluvastatin treatment in patients with coronary heart disease or undergoing coronary intervention [38][39][40] . Because the parasympathomimetic activity reflected by the baroreflex activity in turn exerts an antiarrythmogenic effect counteracting the proarrhythmic effect of the sympathetic nervous system, the fluvastatin-ameliorated BRS can contribute to a reduction in cardiac mortality [38][39][40][41] . Undoubtedly, these findings will result in increased interest in the use of fluvastatin to treat diabetic patients with cardiac complications, and the mechanisms behind these effects deserve further study.…”
Section: Discussionsupporting
confidence: 92%
“…The results were consistent with previously observed positive effects of long-term fluvastatin treatment in patients with coronary heart disease or undergoing coronary intervention [38][39][40] . Because the parasympathomimetic activity reflected by the baroreflex activity in turn exerts an antiarrythmogenic effect counteracting the proarrhythmic effect of the sympathetic nervous system, the fluvastatin-ameliorated BRS can contribute to a reduction in cardiac mortality [38][39][40][41] . Undoubtedly, these findings will result in increased interest in the use of fluvastatin to treat diabetic patients with cardiac complications, and the mechanisms behind these effects deserve further study.…”
Section: Discussionsupporting
confidence: 92%
“…Thus, three of the four fluvastatin studies (FLARE, FLORIDA, LIPS) used the maximum dose of 80 mg; the LiSA study increased the starting dose of 40 mg to 80 mg 6 weeks after randomisation if the decrease in LDL-C was less than 30%. 93 Similarly, all but two of the pravastatin studies used the maximum dose of 40 mg; in the remaining two (PLAC II and PMSG), the dose could be increased to 40 mg in participants whose LDL-C levels had not responded to the starting dose of 20 mg. 95,96 Three of the simvastatin studies (Aronow 2003, 101 By contrast, the atorvastatin studies generally used doses well below the maximum dose of 80 mg: ASCOT-LLA and CARDS used a fixed dose of 10 mg, 102,103 and the 4D study a fixed dose of 20 mg. 84 Only the small DALI 86 and Mohler 21 studies used an 80-mg dose: each had two treatment arms, one on a fixed dose of 10 mg and the other on 80 mg.…”
Section: Placebo-controlled Studiesmentioning
confidence: 99%
“…Recommendations ) used the maximum dose of 80 mg/day whereas the LiSA study 218 increased the starting dose of 40 mg/day to 80 mg/day 6 weeks after randomisation if the decrease in LDL-c was less than 30%. All but two of the pravastatin studies used the maximum dose of 40mg/day (CAIUS, 219 CARE, 220 PLAC-I, 221 REGRESS 222 ).…”
Section: Chaptermentioning
confidence: 99%