Lagerqvist Bo, James Stefan K, Stenestrand Ulf, Lindbäck Johan, Nilsson Tage, Wallentin Lars
Uppsala Clinical Research Center, Uppsala University Hospital, Uppsala, Sweden.
N Engl J Med. 2007 Mar 8;356(10):1009-19. doi: 10.1056/NEJMoa067722. Epub 2007 Feb 12.
Recent reports have indicated that there may be an increased risk of late stent thrombosis with the use of drug-eluting stents, as compared with bare-metal stents.
We evaluated 6033 patients treated with drug-eluting stents and 13,738 patients treated with bare-metal stents in 2003 and 2004, using data from the Swedish Coronary Angiography and Angioplasty Registry. The outcome analysis covering a period of up to 3 years was based on 1424 deaths and 2463 myocardial infarctions and was adjusted for differences in baseline characteristics.
The two study groups did not differ significantly in the composite of death and myocardial infarction during 3 years of follow-up. At 6 months, there was a trend toward a lower unadjusted event rate in patients with drug-eluting stents than in those with bare-metal stents, with 13.4 fewer such events per 1000 patients. However, after 6 months, patients with drug-eluting stents had a significantly higher event rate, with 12.7 more events per 1000 patients per year (adjusted relative risk, 1.20; 95% confidence interval [CI], 1.05 to 1.37). At 3 years, mortality was significantly higher in patients with drug-eluting stents (adjusted relative risk, 1.18; 95% CI, 1.04 to 1.35), and from 6 months to 3 years, the adjusted relative risk for death in this group was 1.32 (95% CI, 1.11 to 1.57).
Drug-eluting stents were associated with an increased rate of death, as compared with bare-metal stents. This trend appeared after 6 months, when the risk of death was 0.5 percentage point higher and a composite of death or myocardial infarction was 0.5 to 1.0 percentage point higher per year. The long-term safety of drug-eluting stents needs to be ascertained in large, randomized trials.
近期报告表明,与裸金属支架相比,使用药物洗脱支架可能会增加晚期支架血栓形成的风险。
我们利用瑞典冠状动脉造影和血管成形术登记处的数据,评估了2003年和2004年接受药物洗脱支架治疗的6033例患者以及接受裸金属支架治疗的13738例患者。长达3年的结局分析基于1424例死亡和2463例心肌梗死,并针对基线特征的差异进行了调整。
在3年的随访期间,两个研究组在死亡和心肌梗死的综合情况方面没有显著差异。在6个月时,药物洗脱支架患者的未调整事件发生率有低于裸金属支架患者的趋势,每1000例患者中此类事件少13.4例。然而,6个月后,药物洗脱支架患者的事件发生率显著更高,每年每1000例患者多12.7例事件(调整后的相对风险,1.20;95%置信区间[CI],1.05至1.37)。在3年时,药物洗脱支架患者的死亡率显著更高(调整后的相对风险,1.18;95%CI,1.04至1.35),并且从6个月到3年,该组死亡的调整后相对风险为1.32(95%CI,1.11至1.57)。
与裸金属支架相比,药物洗脱支架与死亡率增加相关。这种趋势在6个月后出现,此时死亡风险每年高0.5个百分点,死亡或心肌梗死综合情况每年高0.5至1.0个百分点。药物洗脱支架的长期安全性需要在大型随机试验中确定。