Pourhosseini HamidReza, Lashkari Reza, Aminorroaya Arya, Soltani Danesh, Jalali Arash, Tajdini Masih
Tehran Heart Center and School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Tehran Heart Center, Tehran University of Medical Sciences, North Kargar Ave., Tehran, Iran.
Int J Cardiol Heart Vasc. 2019 Jan 10;22:96-101. doi: 10.1016/j.ijcha.2018.12.003. eCollection 2019 Mar.
Some studies have demonstrated that post-PCI elevated cardiac enzymes are associated with worse outcomes. In this study, we aimed to determine if high-dose treatment with atorvastatin before planned elective PCI reduces PMI or MACE at 1-year median follow-up.
Eligible participants were randomly allocated to group A (80 mg atorvastatin 12 h and 40 mg 2 h before PCI) and group B (40 mg atorvastatin daily). Blood samples were obtained before and at 24 h after PCI to measure hsTnT. All patients were followed regarding MACE (combination of death, re-hospitalizations for ACS, and unplanned coronary revascularization) during one year after PCI.
207 patients randomly assigned to Group A (n = 97) or group B (n = 110). The rate of PMI was lower in group A (5.2%) compared to group B (10.9%); despite near to 50% lower rate of PMI in group A, binary logistic regression showed no significant association between atorvastatin recapture and PMI. The occurrence of MACE in 97 patients of group A was 11 (11.3%), higher than 11 (10%) cases of 110 patients in group B. Cox proportional hazards regression model shows no significant difference in MACE of study groups.
Pretreatment of patients with stable angina who were planned to undergo an elective PCI with 120 mg of atorvastatin before the procedure confer them the same benefit in terms of PMI and MACE as 40 mg routine daily dosage of this statin does.
一些研究表明,经皮冠状动脉介入治疗(PCI)后心脏酶升高与更差的预后相关。在本研究中,我们旨在确定在计划进行的择期PCI之前给予大剂量阿托伐他汀治疗是否能在1年的中位随访期内降低主要不良心肌梗死(PMI)或主要不良心血管事件(MACE)。
符合条件的参与者被随机分配到A组(PCI前12小时服用80毫克阿托伐他汀,PCI前2小时服用40毫克)和B组(每日服用40毫克阿托伐他汀)。在PCI前和PCI后24小时采集血样以测量高敏肌钙蛋白T(hsTnT)。在PCI后的一年内,对所有患者进行MACE(死亡、因急性冠状动脉综合征(ACS)再次住院和非计划冠状动脉血运重建的组合)随访。
207例患者被随机分配到A组(n = 97)或B组(n = 110)。A组的PMI发生率(5.2%)低于B组(10.9%);尽管A组的PMI发生率低近50%,但二元逻辑回归显示阿托伐他汀再捕获与PMI之间无显著关联。A组97例患者中发生MACE的有11例(11.3%),高于B组110例患者中的11例(10%)。Cox比例风险回归模型显示研究组在MACE方面无显著差异。
对于计划进行择期PCI的稳定型心绞痛患者,在手术前用120毫克阿托伐他汀进行预处理,在PMI和MACE方面给予他们与该他汀类药物每日40毫克常规剂量相同的益处。