2014
Effect of Rosuvastatin Therapy on Troponin I Release Following Percutaneous Coronary Intervention in Nonemergency Patients (from the TIP 3 Study)
VESELKA, Josef; Petr HÁJEK; Pavol TOMAŠOV; David TESAŘ; Hana BRŮHOVÁ et al.Základní údaje
Originální název
Effect of Rosuvastatin Therapy on Troponin I Release Following Percutaneous Coronary Intervention in Nonemergency Patients (from the TIP 3 Study)
Autoři
VESELKA, Josef; Petr HÁJEK; Pavol TOMAŠOV; David TESAŘ; Hana BRŮHOVÁ; Martin MATĚJOVIČ; Marian BRANNY; Martin STUDENČAN a David ZEMÁNEK
Vydání
American Journal of Cardiology, Bridgewater, Elsevier Science INC, 2014, 0002-9149
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30201 Cardiac and Cardiovascular systems
Stát vydavatele
Spojené státy
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 3.276
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/14:00081970
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
PERIPROCEDURAL MYOCARDIAL-INFARCTION; STATIN THERAPY; ATORVASTATIN PRETREATMENT; RANDOMIZED-TRIAL; UNIVERSAL DEFINITION; OUTCOMES; IMPACT; ANGIOPLASTY; REDUCTION; IMPROVES
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 25. 8. 2015 11:18, Ing. Mgr. Věra Pospíšilíková
Anotace
V originále
Several randomized studies have suggested that pretreatment with statins may reduce a periprocedural biomarker release in patients who underwent percutaneous coronary intervention (PCI); however, results remain controversial. The purpose of this study was to investigate the effect of a 1-day rosuvastatin therapy on troponin I release in patients who underwent nonemergency PCI. A total of 445 patients with angina pectoris were randomly assigned to therapy with rosuvastatin (20 mg 12 hours before coronary angiography + 20 mg immediately before PCI; rosuvastatin group, 220 patients) or PCI without statin therapy (control group, 225 patients). In patients taking statins (73%), rosuvastatin was added to their long-term statin therapy. The primary end point was the incidence of TnI microleak defined as TnI elevation >1.5 x upper limit of normal, and the secondary end point was the incidence of post-PCI TnI elevation >3 x upper limit of normal. The incidence of primary and secondary end point in the rosuvastatin versus control group was 13.6% versus 12% (p = 0.61) and 8.2% versus 7.1% (p = 0.67), respectively. Patients with C-reactive protein >= 2.0 mg/L had a decreased release of post-PCI TnI in the rosuvastatin group (0.032 [0.010 to 0.143] mu g/L vs 0.056 [0.018 to 0.241] mu g/L; p = 0.04). In conclusion, 1-day rosuvastatin therapy (20 mg twice a day) did not influence post-PCI TnI release in patients with angina. However, these results suggest that, in patients with an advanced inflammatory status, rosuvastatin loading therapy might have a cardioprotective effect.