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Rosuvastatin and cardiovascular events in patients undergoing hemodialysis.

Fellström, Bengt (author)
Uppsala universitet,Institutionen för medicinska vetenskaper,Renal Medicine
Jardine, Alan G (author)
Schmieder, Roland E (author)
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Holdaas, Hallvard (author)
Bannister, Kym (author)
Beutler, Jaap (author)
Chae, Dong-Wan (author)
Chevaile, Alejandro (author)
Cobbe, Stuart M (author)
Grönhagen-Riska, Carola (author)
De Lima, José J (author)
Lins, Robert (author)
Mayer, Gert (author)
McMahon, Alan W (author)
Parving, Hans-Henrik (author)
Remuzzi, Giuseppe (author)
Samuelsson, Ola, 1952 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine
Sonkodi, Sandor (author)
Sci, D (author)
Süleymanlar, Gultekin (author)
Tsakiris, Dimitrios (author)
Tesar, Vladimir (author)
Todorov, Vasil (author)
Wiecek, Andrzej (author)
Wüthrich, Rudolf P (author)
Gottlow, Mattis, 1973 (author)
Johnsson, Eva (author)
Zannad, Faiez (author)
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 (creator_code:org_t)
2009
2009
English.
In: The New England journal of medicine. - 1533-4406 .- 0028-4793. ; 360:14, s. 1395-407
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • BACKGROUND: Statins reduce the incidence of cardiovascular events in patients at high cardiovascular risk. However, a benefit of statins in such patients who are undergoing hemodialysis has not been proved. METHODS: We conducted an international, multicenter, randomized, double-blind, prospective trial involving 2776 patients, 50 to 80 years of age, who were undergoing maintenance hemodialysis. We randomly assigned patients to receive rosuvastatin, 10 mg daily, or placebo. The combined primary end point was death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke. Secondary end points included death from all causes and individual cardiac and vascular events. RESULTS: After 3 months, the mean reduction in low-density lipoprotein (LDL) cholesterol levels was 43% in patients receiving rosuvastatin, from a mean baseline level of 100 mg per deciliter (2.6 mmol per liter). During a median follow-up period of 3.8 years, 396 patients in the rosuvastatin group and 408 patients in the placebo group reached the primary end point (9.2 and 9.5 events per 100 patient-years, respectively; hazard ratio for the combined end point in the rosuvastatin group vs. the placebo group, 0.96; 95% confidence interval [CI], 0.84 to 1.11; P=0.59). Rosuvastatin had no effect on individual components of the primary end point. There was also no significant effect on all-cause mortality (13.5 vs. 14.0 events per 100 patient-years; hazard ratio, 0.96; 95% CI, 0.86 to 1.07; P=0.51). CONCLUSIONS: In patients undergoing hemodialysis, the initiation of treatment with rosuvastatin lowered the LDL cholesterol level but had no significant effect on the composite primary end point of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke. (ClinicalTrials.gov number, NCT00240331.)

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)

Keyword

Aged
Aged
80 and over
C-Reactive Protein
analysis
Cardiovascular Diseases
mortality
prevention & control
Cholesterol
blood
Double-Blind Method
Female
Fluorobenzenes
adverse effects
therapeutic use
Follow-Up Studies
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
adverse effects
therapeutic use
Kaplan-Meiers Estimate
Kidney Failure
Chronic
blood
drug therapy
mortality
therapy
Male
Middle Aged
Prospective Studies
Pyrimidines
adverse effects
therapeutic use
Renal Dialysis
adverse effects
Sulfonamides
adverse effects
therapeutic use
Treatment Failure
Kidney diseases
Medicine

Publication and Content Type

ref (subject category)
art (subject category)

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