Swiss Cardiovascular Center Bern, Bern University Hospital, Bern, Switzerland; Erasmus University Medical Center, Rotterdam, Netherlands; Department of Clinical and Experimental Medicine, Policlinic "G Martino", University of Messina, Messina, Italy.
Erasmus University Medical Center, Rotterdam, Netherlands; Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, Boston, MA, USA.
Lancet. 2017 Mar 11;389(10073):1025-1034. doi: 10.1016/S0140-6736(17)30397-5.
Dual antiplatelet therapy (DAPT) with aspirin plus a P2Y inhibitor prevents ischaemic events after coronary stenting, but increases bleeding. Guidelines support weighting bleeding risk before the selection of treatment duration, but no standardised tool exists for this purpose.
A total of 14 963 patients treated with DAPT after coronary stenting-largely consisting of aspirin and clopidogrel and without indication to oral anticoagulation-were pooled at a single-patient level from eight multicentre randomised clinical trials with independent adjudication of events. Using Cox proportional hazards regression, we identified predictors of out-of-hospital Thrombosis in Myocardial Infarction (TIMI) major or minor bleeding stratified by trial, and developed a numerical bleeding risk score. The predictive performance of the novel score was assessed in the derivation cohort and validated in patients treated with percutaneous coronary intervention from the PLATelet inhibition and patient Outcomes (PLATO) trial (n=8595) and BernPCI registry (n=6172). The novel score was assessed within patients randomised to different DAPT durations (n=10 081) to identify the effect on bleeding and ischaemia of a long (12-24 months) or short (3-6 months) treatment in relation to baseline bleeding risk.
The PRECISE-DAPT score (age, creatinine clearance, haemoglobin, white-blood-cell count, and previous spontaneous bleeding) showed a c-index for out-of-hospital TIMI major or minor bleeding of 0·73 (95% CI 0·61-0·85) in the derivation cohort, and 0·70 (0·65-0·74) in the PLATO trial validation cohort and 0·66 (0·61-0·71) in the BernPCI registry validation cohort. A longer DAPT duration significantly increased bleeding in patients at high risk (score ≥25), but not in those with lower risk profiles (p=0·007), and exerted a significant ischaemic benefit only in this latter group.
The PRECISE-DAPT score is a simple five-item risk score, which provides a standardised tool for the prediction of out-of-hospital bleeding during DAPT. In the context of a comprehensive clinical evaluation process, this tool can support clinical decision making for treatment duration.
None.
双联抗血小板治疗(DAPT)联合阿司匹林和 P2Y 抑制剂可预防冠状动脉支架置入后的缺血事件,但会增加出血风险。指南支持在选择治疗持续时间之前权衡出血风险,但目前尚无用于此目的的标准化工具。
共纳入 14963 例在冠状动脉支架置入后接受 DAPT 治疗的患者,这些患者主要接受阿司匹林和氯吡格雷治疗,且无口服抗凝指征。在单患者水平上,对来自 8 项多中心随机临床试验的数据进行了汇总,这些试验均对事件进行了独立裁决。采用 Cox 比例风险回归分析,我们根据试验分层确定了场外血栓形成的预测因子(TIMI)大出血或小出血,并开发了一个数值出血风险评分。在推导队列中评估了新评分的预测性能,并在接受经皮冠状动脉介入治疗的患者中进行了验证(PLATO 试验[n=8595]和 BernPCI 登记处[n=6172])。在随机接受不同 DAPT 持续时间的患者中评估了新评分(n=10081),以确定与基线出血风险相关的长(12-24 个月)或短(3-6 个月)治疗对出血和缺血的影响。
PRECISE-DAPT 评分(年龄、肌酐清除率、血红蛋白、白细胞计数和既往自发性出血)在推导队列中用于场外 TIMI 大出血或小出血的 c 指数为 0.73(95%CI 0.61-0.85),在 PLATO 试验验证队列中为 0.70(0.65-0.74),在 BernPCI 登记处验证队列中为 0.66(0.61-0.71)。较长的 DAPT 持续时间显著增加了高危患者(评分≥25)的出血风险,但在低危患者中则没有(p=0.007),且仅在后者中产生了显著的缺血获益。
PRECISE-DAPT 评分是一种简单的五因素风险评分,可为 DAPT 期间场外出血的预测提供标准化工具。在全面的临床评估过程中,该工具可支持治疗持续时间的临床决策。
无。