Division of Vascular and Endovascular Surgery, Duke University Health System, Durham, NC, USA.
Division of Cardiology, Department of Medicine Duke University Health System, USA; Duke Clinical Research Institute, Durham, NC, USA.
Atherosclerosis. 2020 Dec;315:10-17. doi: 10.1016/j.atherosclerosis.2020.11.001. Epub 2020 Nov 6.
Polyvascular disease (PVD) affects approximately 20% of patients with atherosclerosis and is a strong independent risk factor for ischemic outcomes. However, guidelines do not address screening or treatment for PVD, and there have been no PVD-specific trials. We reviewed subgroup analyses of large randomized controlled trials of more intense antithrombotic therapy to determine whether increased intensity of therapy improved ischemic outcomes in patients with PVD.
MEDLINE, MEDLINE in-Process, EMBASE, and the Cochrane Library were queried for randomized controlled trials larger than 5000 patients evaluating secondary prevention therapies in patients with coronary artery disease or lower extremity peripheral artery disease.
Thirteen trials were included ranging in size from 7243 to 27,395 patients. In 9 trials (CHARISMA, TRA 2°P-TIMI 50, PEGASUS-TIMI 54, VOYAGER PAD, TRACER, EUCLID, TRILOGY ACS, PLATO, and COMPASS), patients in the PVD subgroup treated with increased-intensity antithrombotic therapy had similar or greater relative risk reductions for ischemic events in comparison with the general trial cohorts. In four trials (DAPT, THEMIS, APPRAISE-2, and ATLAS ACS 2 TIMI 51), the PVD subgroup had an increased hazard of ischemic events with increased-intensity therapy compared with the general trial cohorts.
More intense antithrombotic therapy in patients with PVD was associated with a similar relative risk reduction for ischemic events compared with patients without PVD. Therefore, patients with PVD benefit from a larger absolute risk reduction because of their higher baseline risk. Future trials in patients with atherosclerotic cardiovascular disease should intentionally include PVD patients to adequately assess treatment options for this under-studied, under-treated population.
多血管疾病(PVD)影响约 20%的动脉粥样硬化患者,是缺血性结局的一个强有力的独立危险因素。然而,指南并未涉及 PVD 的筛查或治疗,也没有专门针对 PVD 的试验。我们对更强化抗栓治疗的大型随机对照试验的亚组分析进行了回顾,以确定在 PVD 患者中增加治疗强度是否能改善缺血结局。
通过 MEDLINE、MEDLINE 正在处理、EMBASE 和 Cochrane 图书馆检索了超过 5000 例评估冠心病或下肢外周动脉疾病二级预防治疗的随机对照试验。
纳入了 13 项试验,规模从 7243 例到 27395 例不等。在 9 项试验(CHARISMA、TRA 2°P-TIMI 50、PEGASUS-TIMI 54、VOYAGER PAD、TRACER、EUCLID、TRILOGY ACS、PLATO 和 COMPASS)中,与一般试验队列相比,接受强化抗栓治疗的 PVD 亚组患者发生缺血事件的相对风险降低相似或更大。在 4 项试验(DAPT、THEMIS、APPRAISE-2 和 ATLAS ACS 2 TIMI 51)中,与一般试验队列相比,PVD 亚组患者接受强化治疗与缺血事件的风险增加相关。
与无 PVD 的患者相比,PVD 患者接受更强化的抗栓治疗与缺血事件的相对风险降低相似。因此,由于基线风险较高,PVD 患者受益于更大的绝对风险降低。未来针对动脉粥样硬化性心血管疾病患者的试验应有意纳入 PVD 患者,以充分评估这一研究不足、治疗不足的人群的治疗选择。