Journal of cardiovascular medicine (Hagerstown, Md.) · 2011
Short-term high-dose atorvastatin for periprocedural myocardial infarction prevention in patients with renal dysfunction.
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Toso Anna, Leoncini Mario, Maioli Mauro, Gallopin Michela, Tedeschi Delio, Amato Marcello, Bellandi Francesco
Аннотация
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.
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.
Предметные рубрики MeSH
AgedAged, 80 and overAnalysis of VarianceAngioplasty, Balloon, CoronaryAtorvastatinBiomarkersChi-Square DistributionCoronary AngiographyCoronary Artery DiseaseCreatine Kinase, MB FormCreatinineDrug Administration ScheduleFemaleGlomerular Filtration RateHeptanoic AcidsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsItalyKidney DiseasesLogistic ModelsMaleMyocardial InfarctionOdds RatioPyrrolesRandomized Controlled Trials as TopicRetrospective StudiesRisk AssessmentRisk FactorsTime FactorsTreatment OutcomeUp-Regulation