Short-term high-dose atorvastatin for periprocedural myocardial infarction prevention in patients with renal dysfunction

J Cardiovasc Med (Hagerstown). 2011 May;12(5):318-21. doi: 10.2459/JCM.0b013e328341024f.

Abstract

Objectives: Short-term high-dose atorvastatin administered before percutaneous coronary intervention (PCI) reduces the rate of periprocedural myocardial infarction (pMI) in high-risk patients, such as those with acute coronary syndromes and those with elevated high-sensitivity C-reactive protein. It is unknown whether short-term high-dose administration reduces the rate of pMI in patients with chronic kidney disease. Recently, we observed that in 304 patients with estimated creatinine clearance less than 60 ml/min randomized to receive 80 mg/day of atorvastatin or placebo for 48 h before elective coronary angiography and/or angioplasty, statin administration did not reduce contrast-induced nephropathy (CIN). In this post-hoc analysis, we evaluate the pMI in the subgroup of 161 patients who underwent PCI.

Methods: In all patients, creatine kinase myocardial isoenzyme (CK-MB) [upper reference limit (URL) 5 ng/ml] was assessed before and at 12 and 24 h after PCI. The pMI, defined as CK-MB elevation more than three times the URL, occurred in 27 (17%) patients.

Results: The incidence of pMI was 10.4% (of 77 patients) in the atorvastatin and 23% (of 84 patients) in the placebo group (P < 0.05). Multivariate analysis identified the pretreatment with high-dose atorvastatin as an independent predictor of reduced risk of pMI [odds ratio 0.39, 95% confidence interval 0.16-0.96, P < 0.05].

Conclusion: This post-hoc analysis shows that short-term high-dose atorvastatin administration reduced pMI in patients with renal dysfunction submitted to elective PCI, but without benefit regarding CIN prevention.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Analysis of Variance
  • Angioplasty, Balloon, Coronary / adverse effects*
  • Atorvastatin
  • Biomarkers / blood
  • Chi-Square Distribution
  • Coronary Angiography / adverse effects
  • Coronary Artery Disease / complications
  • Coronary Artery Disease / diagnostic imaging
  • Coronary Artery Disease / therapy*
  • Creatine Kinase, MB Form / blood
  • Creatinine / blood
  • Drug Administration Schedule
  • Female
  • Glomerular Filtration Rate
  • Heptanoic Acids / administration & dosage*
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / administration & dosage*
  • Italy
  • Kidney Diseases / blood
  • Kidney Diseases / complications*
  • Kidney Diseases / physiopathology
  • Logistic Models
  • Male
  • Myocardial Infarction / blood
  • Myocardial Infarction / etiology
  • Myocardial Infarction / prevention & control*
  • Odds Ratio
  • Pyrroles / administration & dosage*
  • Randomized Controlled Trials as Topic
  • Retrospective Studies
  • Risk Assessment
  • Risk Factors
  • Time Factors
  • Treatment Outcome
  • Up-Regulation

Substances

  • Biomarkers
  • Heptanoic Acids
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Pyrroles
  • Atorvastatin
  • Creatinine
  • Creatine Kinase, MB Form