Best Patricia J M, Steinhubl Steven R, Berger Peter B, Dasgupta Arijit, Brennan Danielle M, Szczech Lynda A, Califf Robert M, Topol Eric J
Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN 55905, USA.
Am Heart J. 2008 Apr;155(4):687-93. doi: 10.1016/j.ahj.2007.10.046. Epub 2008 Feb 21.
Mild and moderate chronic kidney disease (CKD) is associated with decreased survival and increased adverse events after a percutaneous coronary intervention (PCI). Therapy with clopidogrel decreases adverse events in large patient populations. Therefore, we sought to determine the efficacy and safety of long-term clopidogrel therapy in patients with CKD.
Two thousand two patients from the CREDO trial in whom an elective PCI of a single or multiple vessels was planned were analyzed. Patients were randomly assigned to a 300-mg loading dose of clopidogrel before PCI followed by clopidogrel 75 mg/d for a year versus a placebo loading dose at the time of the PCI procedure and clopidogrel 75 mg/d for 28 days and placebo for the remainder of a year. Patients were categorized by their estimated creatinine clearance (>90 [normal, n = 999], 60-89 [mild CKD, n = 672], <60 mL/min [moderate CKD, n = 331]).
Diminished renal function was associated with worse outcomes. Patients with normal renal function who received 1 year of clopidogrel had a marked reduction in death, myocardial infarction, or stroke compared with those who received placebo (10.4% vs 4.4%, P < .001), whereas patients with mild and moderate CKD did not have a significant difference in outcomes with clopidogrel therapy versus placebo (mild: 12.8% vs 10.3%, P = .30; moderate: 13.1% vs 17.8%, P = .24). Clopidogrel use was associated with an increased relative risk of major or minor bleeding, but this increased risk was not different based on renal function (relative risk 1.2, 1.3, 1.1).
Clopidogrel in mild or moderate CKD patients may not have the same beneficial effect as it does in patients with normal renal function, but was not associated with a greater relative risk of bleeding based on renal function. Further studies are needed to define the role of clopidogrel therapy in patients with CKD.
轻度和中度慢性肾脏病(CKD)与经皮冠状动脉介入治疗(PCI)后生存率降低及不良事件增加相关。氯吡格雷治疗可降低大量患者群体中的不良事件。因此,我们试图确定氯吡格雷长期治疗对CKD患者的疗效和安全性。
分析了CREDO试验中计划进行单支或多支血管择期PCI的2200例患者。患者被随机分为两组,一组在PCI前给予300mg负荷剂量氯吡格雷,随后每日服用75mg氯吡格雷,持续一年;另一组在PCI时给予安慰剂负荷剂量,28天内每日服用75mg氯吡格雷,之后一年服用安慰剂。患者根据估算的肌酐清除率进行分类(>90[正常,n = 999],60 - 89[轻度CKD,n = 672],<60 mL/min[中度CKD,n = 331])。
肾功能减退与更差的预后相关。肾功能正常且接受一年氯吡格雷治疗的患者与接受安慰剂治疗的患者相比,死亡、心肌梗死或中风显著减少(10.4%对4.4%,P <.001),而轻度和中度CKD患者接受氯吡格雷治疗与接受安慰剂治疗的预后无显著差异(轻度:12.8%对10.3%,P =.30;中度:13.1%对17.8%,P =.24)。使用氯吡格雷与大出血或小出血的相对风险增加相关,但这种增加的风险在肾功能方面并无差异(相对风险1.2、1.3、1.1)。
轻度或中度CKD患者使用氯吡格雷可能不像肾功能正常的患者那样具有相同的有益效果,但基于肾功能,其出血相对风险并未增加。需要进一步研究来确定氯吡格雷治疗在CKD患者中的作用。