Department of Cardiovascular Medicine, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Circ Cardiovasc Interv. 2012 Apr;5(2):237-46. doi: 10.1161/CIRCINTERVENTIONS.111.963728. Epub 2012 Mar 6.
There still remain safety concerns on surgical procedures after coronary drug-eluting stents (DES) implantation, and optimal management of perioperative antiplatelet therapy (APT) has not been yet established.
During 3-year follow-up of 12 207 patients (DES=6802 patients and bare-metal stent [BMS] only=5405 patients) who underwent coronary stent implantation in the CREDO-Kyoto registry cohort-2, surgical procedures were performed in 2398 patients (DES=1295 patients and BMS=1103 patients). Surgical procedures (early surgery in particular) were more frequently performed in the BMS group than in the DES group (4.4% versus 1.9% at 42-day and 23% versus 21% at 3-year, log-rank P=0.0007). Cumulative incidences of death/myocardial infarction (MI)/stent thrombosis (ST) and bleeding at 30 days after surgery were low, without differences between BMS and DES (3.5% versus 2.9%, P=0.4 and 3.2% versus 2.1%, P=0.2, respectively). The adjusted risks of DES use relative to BMS use for death/MI/ST and bleeding were not significant (hazard ratio: 1.63, 95% confidence interval: 0.93 to 2.87, P=0.09 and hazard ratio: 0.6, 95% confidence interval: 0.34 to 1.06, P=0.08, respectively). The risks of perioperative single- and no-APT relative to dual-APT for both death/MI/ST and bleeding were not significant; single-APT as compared with dual-APT tended to be associated with lower risk for death/MI/ST (hazard ratio: 0.4, 95% confidence interval: 0.13 to 1.01, P=0.053).
Surgical procedures were commonly performed after coronary stent implantation, and the risk of ischemic and bleeding complications in surgical procedures was low. In patients selected to receive DES or BMS, there were no differences in outcomes. Perioperative administration of dual-APT was not associated with lower risk for ischemic events.
在冠状动脉药物洗脱支架(DES)植入后,手术过程仍存在安全问题,围手术期抗血小板治疗(APT)的最佳管理尚未确定。
在 CREDO-Kyoto 注册队列-2 的 12207 例接受冠状动脉支架植入的患者(DES=6802 例,仅裸金属支架[BMS]=5405 例)的 3 年随访期间,2398 例患者(DES=1295 例,BMS=1103 例)进行了手术。与 DES 组相比,BMS 组更频繁地进行手术(42 天的 4.4%比 1.9%,3 年的 23%比 21%,对数秩 P=0.0007)。手术后 30 天的死亡/心肌梗死(MI)/支架血栓形成(ST)和出血的累积发生率较低,BMS 和 DES 之间无差异(3.5%比 2.9%,P=0.4 和 3.2%比 2.1%,P=0.2)。DES 与 BMS 相比,死亡/MI/ST 和出血的调整风险无显著差异(风险比:1.63,95%置信区间:0.93 至 2.87,P=0.09 和风险比:0.6,95%置信区间:0.34 至 1.06,P=0.08)。与双 APT 相比,围手术期单 APT 和无 APT 对死亡/MI/ST 和出血的风险无显著差异;与双 APT 相比,单 APT 倾向于降低死亡/MI/ST 的风险(风险比:0.4,95%置信区间:0.13 至 1.01,P=0.053)。
冠状动脉支架植入后常进行手术,手术过程中缺血和出血并发症的风险较低。在选择接受 DES 或 BMS 的患者中,结局无差异。围手术期使用双 APT 与缺血事件风险降低无关。