Chyrchel Michał, Rakowski Tomasz, Rzeszutko Lukasz, Legutko Jacek, Dziewierz Artur, Dubiel Jacek S, Dudek Dariusz
II Klinika Kardiologii CM UJ, ul. Kopernika 17, 31-501 Kraków.
Kardiol Pol. 2006 Dec;64(12):1357-62; discussion 1363.
Statins given after acute coronary syndrome without ST elevation (NSTE-ACS) reduce the incidence of major adverse cardiac events (MACE) in long-term follow-up.
To evaluate the effects of high-dose statin administered in patients with NSTE ACS and increased CRP level prior to percutaneous coronary intervention (PCI) on the incidence of MACE in long-term follow-up.
The study involved 140 consecutive patients with NSTE ACS and increased CRP level at baseline. Patients from group A (n=54) did not receive statin before PCI, whereas subjects in group B (n=86) were given 80 mg of atorvastatin. Patients in both groups received typical cardiological therapy including aspirin, thienopyridine and low molecular weight heparin. After PCI all patients received 40 mg of atorvastatin. Incidence of MACE (death, myocardial infarction (MI), re-PCI) during long-term followup was evaluated in both groups.
Study groups did not differ with respect to demographic parameters and rate of ischaemic heart disease risk factors. Also, no differences occurred regarding CRP level (group A vs. B: hsCRP 10.8+/-1.8 mg/l vs. 8.2+/-2.8 mg/l; p=NS) and TIMI Risk Score (group A vs. B: 4.3+/-0.71 vs. 4.37+/-0.79; p=NS). During long-term follow-up the incidence of MI (9.25% vs. 1.2%, p=0.03), composite endpoint: death + MI (14.8% vs. 2.32%, p=0.013) and death + MI + re PCI (25.9% vs. 8.1%, p=0.006) was significantly higher in group A than group B.
Administration of high-dose statin in NSTE ACS patients before PCI was associated with significant reduction of MACE in long-term follow-up. This effect was observed despite the same therapy given after PCI.
非ST段抬高型急性冠状动脉综合征(NSTE-ACS)后给予他汀类药物可降低长期随访中主要不良心脏事件(MACE)的发生率。
评估在经皮冠状动脉介入治疗(PCI)前给予高剂量他汀类药物对NSTE-ACS且CRP水平升高患者长期随访中MACE发生率的影响。
该研究纳入了140例基线时NSTE-ACS且CRP水平升高的连续患者。A组(n = 54)患者在PCI前未接受他汀类药物治疗,而B组(n = 86)患者给予80 mg阿托伐他汀。两组患者均接受包括阿司匹林、噻吩吡啶和低分子量肝素在内的典型心脏病治疗。PCI后所有患者均接受40 mg阿托伐他汀治疗。评估两组患者长期随访期间MACE(死亡、心肌梗死(MI)、再次PCI)的发生率。
研究组在人口统计学参数和缺血性心脏病危险因素发生率方面无差异。此外,CRP水平(A组与B组:高敏CRP 10.8±1.8 mg/l对8.2±2.8 mg/l;p = 无统计学意义)和TIMI风险评分(A组与B组:4.3±0.71对4.37±0.79;p = 无统计学意义)也无差异。在长期随访中,A组的MI发生率(9.25%对1.2%,p = 0.03)、复合终点(死亡+MI,14.8%对2.32%,p = 0.013)以及死亡+MI+再次PCI发生率(25.9%对8.1%,p = 0.006)均显著高于B组。
在NSTE-ACS患者PCI前给予高剂量他汀类药物与长期随访中MACE的显著降低相关。尽管PCI后给予相同治疗,但仍观察到了这种效果。