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To print: Select File and then Print from your browser's menu Title: Statins Do Not Improve Outcome of End-Stage Renal Disease Dialysis Patients: Presented at ACC |
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"Statins Do Not Improve Outcome of End-Stage Renal Disease Dialysis Patients: Presented at ACC" By Em Brown ORLANDO, Fla -- April 1, 2009 -- Rosuvastatin does not improve cardiovascular outcomes in patients with end-stage renal disease (ESRD) who are on haemodialysis, despite improvements in lipid profile and inflammatory markers. Those are the results of A Study to Evaluate the Use of Rosuvastatin in Subjects on Regular Hemodialysis: An Assessment of Survival and Cardiovascular Events (AURORA), presented during a late-breaking clinical trials session here on March 30 at the American College of Cardiology (ACC) 58th Annual Scientific Session. "Renal insufficiency is a very strong cardiovascular risk factor -- on the order of hypercholesterolaemia," noted principal investigator Bengt C. Fellström, MD, Renal Unit, Department of Medicine, University Hospital, Uppsala, Sweden. He pointed out that atherogenic lipid abnormalities are found in most ESRD patients on haemodialysis. AURORA was a large, international, double-blind, placebo-controlled study of 2,773 patients with ESRD on dialysis, with the objective to assess the effect of rosuvastatin 10 mg daily on cardiovascular morbidity and mortality in statin-naïve dialysis patients. Patients were between 50 and 80 years of age (mean age, 64.2 years) and had been on haemodialysis for at least 3 months. The primary endpoint was time to cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke. Secondary endpoints were all-cause mortality, cardiovascular event-free survival, and thrombosis of the dialysis vascular access site. The mean length of follow-up was 3.2 years. During follow-up, there were 1,296 deaths, and cause was established in 1,164 cases. Of these, 648 were from cardiovascular causes. Overall, 396 patients in the rosuvastatin group and 408 patients in the placebo group reached the primary endpoint. There were 9.2 events per 100 patient-years with rosuvastatin and 9.5 events per 100 patient-years with placebo (hazard ratio [HR] for the combined endpoint in the rosuvastatin group versus the placebo group, 0.96; confidence interval [CI], 0.84-1.11; [P = .59). Rosuvastatin had no effect on individual components of the primary endpoint. There was also no significant effect on all-cause mortality (13.5 vs 14.0 events/100 patient-years; HR, 0.96; CI, 0.86-1.07; P = .51). |
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