Richard A. and Susan F. Smith Center for Outcomes Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Catheter Cardiovasc Interv. 2021 Mar;97(4):569-578. doi: 10.1002/ccd.29352. Epub 2020 Oct 28.
The dual antiplatelet therapy (DAPT) score, one of the first prediction tools to attempt to uncouple bleeding and ischemic risk following percutaneous coronary intervention, can help guide antiplatelet duration after coronary intervention. Evaluating the generalizability of the score is important to understand its utility in clinical practice.
We conducted a systematic review and meta-analysis of studies that validated the DAPT score. A random effect meta-analysis was performed of ischemic and bleeding risk based on DAPT score. A secondary analysis assessed the risk of longer versus shorter P2Y inhibitor duration on ischemic and bleeding risk in randomized controlled trials of DAPT duration.
We identified 10 patient cohorts involving 88,563 patients. Compared with a low DAPT score, a high DAPT score was associated with increased ischemic risk (RR: 1.62, 95% CI: 1.41-1.87) and reduced bleeding risk (RR: 0.80, 95% CI: 0.70-0.92). In three randomized trials of DAPT duration that contained information on the DAPT score, the relative risk of net adverse clinical events (combined ischemic and bleeding events) with longer duration of DAPT was 1.56 (95% CI: 0.77-3.19) for low DAPT score patients, and 0.86 (95% CI: 0.61-1.21) for high DAPT score patients (p = .14).
In this large meta-analysis, the DAPT score consistently stratified bleeding and ischemic risk in opposing directions across several different study populations. More evaluation is needed to understand if the effect of longer DAPT duration on NACE is modified by the DAPT score in current practice.
双联抗血小板治疗(DAPT)评分是尝试分离经皮冠状动脉介入治疗后出血和缺血风险的首个预测工具之一,可帮助指导冠状动脉介入治疗后的抗血小板治疗时间。评估评分的普遍性对于了解其在临床实践中的效用很重要。
我们对验证 DAPT 评分的研究进行了系统评价和荟萃分析。基于 DAPT 评分,对缺血和出血风险进行了随机效应荟萃分析。二次分析评估了在 DAPT 持续时间的随机对照试验中,与较短的 P2Y 抑制剂持续时间相比,较长的 P2Y 抑制剂持续时间对缺血和出血风险的影响。
我们确定了 10 项涉及 88563 名患者的患者队列研究。与低 DAPT 评分相比,高 DAPT 评分与缺血风险增加(RR:1.62,95%CI:1.41-1.87)和出血风险降低(RR:0.80,95%CI:0.70-0.92)相关。在包含 DAPT 评分信息的三项 DAPT 持续时间随机试验中,较长的 DAPT 持续时间与净不良临床事件(缺血和出血事件的组合)的相对风险为低 DAPT 评分患者为 1.56(95%CI:0.77-3.19),高 DAPT 评分患者为 0.86(95%CI:0.61-1.21)(p=0.14)。
在这项大型荟萃分析中,DAPT 评分在几个不同的研究人群中一致地分层出血和缺血风险,朝着相反的方向发展。需要进一步评估以了解在当前实践中,较长的 DAPT 持续时间对 NACE 的影响是否受 DAPT 评分的影响。