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Naproxen treatment prevents periprocedural inflammatory response but not myocardial injury after percutaneous coronary intervention
Authors:Ozdol Cagdas  Gulec Sadi  Rahimov Uzeyir  Atmaca Yusuf  Turhan Sibel  Erol Cetin
Affiliation:Ankara University School of Medicine, Cardiology Department, Ankara, Turkey. cagdas_2005@yahoo.com
Abstract:BACKGROUND AND AIM: Recent studies have documented that elevation of C-reactive protein (CRP) levels after percutaneous coronary intervention (PCI) have been predictive of adverse outcome. This study was performed to test the hypothesis that preprocedural use of naproxen sodium is associated with a reduction in the extent of inflammatory response and myocardial injury after PCI. METHODS: Ninety-seven patients who were scheduled for elective PCI were randomized either for naproxen sodium (500 mg bid) (n:39, 75% male, 59+/-10 years) or control (n:58, 76% male, 60+/-10 years). All patients were troponin negative before the procedure. Blood samples for CRP, Troponin I and CK-MB were collected at baseline and after the procedure. RESULTS: The characteristics were similar between the two groups. After coronary stenting, the rise in CRP levels was significantly higher in controls than those treated with naproxen (DeltaCRP=6.4 mg/L in the controls and 0.43 mg/L in the naproxen group, p<0.0001). The incidence of any troponin I elevation or CK-MB elevation above upper limit of normal was not statistically different between groups. During follow up (12+/-2 months), major cardiac adverse events (death, myocardial infarction, and revascularization of target lesion) was similar between groups. CONCLUSION: Our data show that naproxen pretreatment leads to significant suppression in PCI related CRP elevation. However this improvement in CRP levels was not associated with any significant reduction in post-PCI myonecrosis.
Keywords:PCI, percutaneous coronary intervention   CRP, C-reactive protein   NSAID, nonsteroidal anti-inflammatory drugs   TnI, troponin I   CK-MB, creatine kinase-myocardial band   MACE, major cardiac adverse events   MI, myocardial infarction   TLR, target lesion revascularization.
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