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验证主要使用第二代药物洗脱支架后随机接受 6 或 12 个月氯吡格雷治疗的患者的 DAPT 评分。

Validation of the DAPT score in patients randomized to 6 or 12 months clopidogrel after predominantly second-generation drug-eluting stents.

机构信息

Stefanie Schüpke, MD, Deutsches Herzzentrum München, Lazarettstr. 36, 80636 Munich, Germany, Tel.: +49 89 1218 0, Fax: +49 89 1218 1538, E-mail:

出版信息

Thromb Haemost. 2017 Oct 5;117(10):1989-1999. doi: 10.1160/TH17-02-0101. Epub 2017 Jul 27.

Abstract

The DAPT score is a recently-proposed decision tool for guiding optimal duration of dual antiplatelet therapy (DAPT). It showed modest accuracy in prior derivation and validation cohorts of patients with ≥12 months DAPT. This study was aimed to evaluate the validity of the DAPT score in a cohort of patients with 6 or 12 months DAPT after implantation of predominantly second-generation drug-eluting stents. We analyzed data of patients enrolled in the ISAR-SAFE trial. Patients were classified into low (<2) or high (≥2) DAPT score groups. Primary ischaemic (all-cause death, myocardial infarction, definite stent thrombosis or stroke) and bleeding (TIMI major or minor) outcomes were analyzed in the low and high DAPT score groups. Data of 3976 patients were available for DAPT score calculation. 2407 patients (60.5 %) were classified in the low DAPT score group and 1569 patients (39.5 %) in the high DAPT score group. In the low DAPT score group there were no significant differences between 6 and 12 months DAPT regarding ischaemic (1.0 % vs. 1.4 %, HR=0.74, 95 % CI, 0.35-1.57; p=0.43) or bleeding outcomes (0.3 % vs. 0.8 %, HR=0.44, 95 % CI, 0.13-1.42; p=0.17). In the high DAPT score group there were also no significant differences between 6 and 12 months DAPT regarding ischaemic (1.9 % vs. 1.8 %, HR=1.02, 95 % CI, 0.49-2.14; p=0.96) or bleeding (0.3 % vs. 0.5 %, HR=0.51, 95 % CI, 0.09-2.78; p=0.44) outcomes. In conclusion, the DAPT score failed to show a differential treatment effect in patients receiving 6 or 12 months DAPT after contemporary drug-eluting stent implantation.

摘要

DAPT 评分是一种新提出的决策工具,用于指导双重抗血小板治疗(DAPT)的最佳持续时间。它在接受≥12 个月 DAPT 的患者的先前推导和验证队列中显示出适度的准确性。本研究旨在评估 DAPT 评分在植入主要为第二代药物洗脱支架后接受 6 或 12 个月 DAPT 的患者队列中的有效性。我们分析了 ISAR-SAFE 试验中入组患者的数据。患者分为低(<2)或高(≥2)DAPT 评分组。在低和高 DAPT 评分组中分析了主要缺血(全因死亡、心肌梗死、明确的支架血栓形成或中风)和出血(TIMI 主要或次要)结局。有 3976 例患者可用于 DAPT 评分计算。2407 例(60.5%)患者被归类为低 DAPT 评分组,1569 例(39.5%)患者被归类为高 DAPT 评分组。在低 DAPT 评分组中,6 个月和 12 个月 DAPT 之间在缺血方面无显著差异(1.0%比 1.4%,HR=0.74,95%CI,0.35-1.57;p=0.43)或出血结局(0.3%比 0.8%,HR=0.44,95%CI,0.13-1.42;p=0.17)。在高 DAPT 评分组中,6 个月和 12 个月 DAPT 之间在缺血方面也无显著差异(1.9%比 1.8%,HR=1.02,95%CI,0.49-2.14;p=0.96)或出血(0.3%比 0.5%,HR=0.51,95%CI,0.09-2.78;p=0.44)结局。总之,在接受当代药物洗脱支架植入后接受 6 或 12 个月 DAPT 的患者中,DAPT 评分未能显示出差异治疗效果。

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