Hôpital de la Tour, Geneva, Switzerland.
London School of Hygiene and Tropical Medicine, London, United Kingdom.
JAMA Cardiol. 2021 Apr 1;6(4):410-419. doi: 10.1001/jamacardio.2020.6814.
Patients who are candidates for percutaneous coronary intervention (PCI) and are at high bleeding risk constitute a therapeutic challenge because they often also face an increased risk of thrombotic complications.
To develop and validate models to predict the risks of major bleeding (Bleeding Academic Research Consortium [BARC] types 3 to 5 bleeding) and myocardial infarction (MI) and/or stent thrombosis (ST) for individual patients at high bleeding risk and provide assistance in defining procedural strategy and antithrombotic regimens.
DESIGN, SETTING, AND PARTICIPANTS: This prognostic study used individual patient data from 6 studies conducted from July 1, 2009, to September 5, 2017, for 6641 patients at more than 200 centers in Europe, the US, and Asia who underwent PCI and were identified as being at high bleeding risk using the Academic Research Consortium criteria. In 1 year of follow-up (excluding periprocedural events), individual patient risks of MI and/or ST and major bleeding were evaluated using 33 baseline variables. To validate these models, a subgroup of 1458 patients at high bleeding risk from the ONYX ONE trial were analyzed. Statistical analysis was performed from February 1, 2019, to April 30, 2020.
All patients underwent PCI with bare metal, drug-coated, or drug-eluting stent implants.
Forward, stepwise multivariable proportional hazards models were used to identify highly significant predictors of MI and/or ST and BARC types 3 to 5 bleeding.
A total of 6641 patients (4384 men [66.0%]; median age, 77.9 years [interquartile range, 70.0-82.6 years]) were included in this study. Over 365 days, nonperiprocedural MI and/or ST occurred in 350 patients (5.3%), and BARC types 3 to 5 bleeding occurred in 381 patients (5.7%). Eight independent baseline predictors of risk of MI and/or ST and 8 predictors for risk of BARC types 3 to 5 bleeding were identified. Four of these predictors were in both risk models. Both risk models showed moderate discrimination: C statistic = 0.69 for predicting MI and/or ST and 0.68 for predicting BARC types 3 to 5 bleeding. Applying these same models to the validation cohort gave a similar strength of discrimination (C statistic = 0.74 for both MI and/or ST and BARC types 3-5 bleeding). Patients with MI and/or ST had a mortality hazard ratio of 6.1 (95% CI, 4.8-7.7), and those with BARC types 3 to 5 bleeding had a mortality hazard ratio of 3.7 (95% CI, 2.9-4.8) compared with patients free of both events. Taking these data into account, the risk scores facilitate investigation of the individual patient trade-off between these 2 risks: 2931 patients (44.1%) at high bleeding risk in the 6 studies had a greater risk of MI and/or ST than of BARC 3 to 5 bleeding, 1555 patients (23.4%) had a greater risk of BARC 3 to 5 bleeding than of MI and/or ST, and 2155 (32.4%) had a comparable risk of both events.
In a large cohort of patients at high bleeding risk undergoing PCI, 2 prognostic models have been developed to identify individual patients' risk of major coronary thrombotic and bleeding events. In future clinical practice, using an application on a smartphone to evaluate the trade-off between these 2 quantifiable risks for each patient may help clinicians choose the most appropriate revascularization strategy and tailor the duration and intensity of antithrombotic regimens.
对于接受经皮冠状动脉介入治疗(PCI)且出血风险较高的患者,这是一个治疗挑战,因为他们通常也面临着增加血栓并发症的风险。
开发和验证模型,以预测高出血风险患者的主要出血(BARC 3 至 5 型出血)和心肌梗死(MI)和/或支架血栓形成(ST)的风险,并为定义程序策略和抗血栓治疗方案提供帮助。
设计、地点和参与者:这项预后研究使用了来自 2009 年 7 月 1 日至 2017 年 9 月 5 日期间在欧洲、美国和亚洲的 200 多个中心进行的 6 项研究的个体患者数据,这些患者被确定为使用学术研究联合会标准存在高出血风险。在 1 年的随访期(不包括围手术期事件)中,使用 33 个基线变量评估了个体患者发生 MI 和/或 ST 和主要出血的风险。为了验证这些模型,分析了 ONYX ONE 试验中的高出血风险亚组的 1458 名患者。统计分析于 2019 年 2 月 1 日至 2020 年 4 月 30 日进行。
所有患者均接受了裸金属、药物涂层或药物洗脱支架植入的 PCI。
采用向前、逐步多变量比例风险模型来识别 MI 和/或 ST 和 BARC 3 至 5 型出血的高度显著预测因子。
本研究共纳入 6641 名患者(4384 名男性[66.0%];中位年龄 77.9 岁[四分位距 70.0-82.6 岁])。在 365 天内,350 名患者(5.3%)发生非围手术期 MI 和/或 ST,381 名患者(5.7%)发生 BARC 3 至 5 型出血。确定了 8 个独立的基线风险预测因子,用于预测 MI 和/或 ST 以及 BARC 3 至 5 型出血的风险,其中 8 个预测因子用于预测 BARC 3 至 5 型出血的风险。这四个预测因子在两个风险模型中都有。这两个风险模型都显示出中等的区分度:预测 MI 和/或 ST 的 C 统计量为 0.69,预测 BARC 3 至 5 型出血的 C 统计量为 0.68。将这些相同的模型应用于验证队列,得到了类似的区分强度(MI 和/或 ST 以及 BARC 3-5 出血的 C 统计量均为 0.74)。发生 MI 和/或 ST 的患者死亡风险比为 6.1(95%CI,4.8-7.7),发生 BARC 3 至 5 型出血的患者死亡风险比为 3.7(95%CI,2.9-4.8)与未发生两种事件的患者相比。考虑到这些数据,风险评分有助于调查个体患者在这两种风险之间的权衡:在 6 项研究中,3641 名高出血风险患者(44.1%)发生 MI 和/或 ST 的风险高于 BARC 3 至 5 型出血,1555 名患者(23.4%)发生 BARC 3 至 5 型出血的风险高于 MI 和/或 ST,2155 名患者(32.4%)发生 BARC 3 至 5 型出血的风险与 MI 和/或 ST 相当。
在接受 PCI 的高出血风险患者的大型队列中,已经开发了两种预测模型,以识别个体患者主要冠状动脉血栓形成和出血事件的风险。在未来的临床实践中,使用智能手机上的应用程序评估每个患者的这两种可量化风险之间的权衡,可能有助于临床医生选择最合适的血运重建策略,并调整抗血栓治疗方案的持续时间和强度。