Centre Hospitalier Universitaire de Caen, Caen, France; Faculté de Médecine de Caen, Caen, France.
Centre Hospitalier Régional et Universitaire de Lille, Lille, France; Inserm U744, Institut Pasteur de Lille, Université Lille Nord de France, Lille, France; Faculté de Médecine de Lille, Lille, France.
J Am Coll Cardiol. 2014 Oct 7;64(14):1430-6. doi: 10.1016/j.jacc.2014.07.957.
Although there is evidence that patients who experience major bleeding after an acute coronary event are at higher risk of death in the months after the event, the incidence and impact on outcome of bleeding beyond 1 year of follow-up in patients with stable coronary artery disease (CAD) are largely unknown.
The goal of this study was to assess the incidence, source, determinants, and prognostic impact of major bleeding in stable CAD.
We prospectively included 4,184 consecutive CAD outpatients who were free from any myocardial infarction (MI) or coronary revascularization for >1 year at inclusion. Follow-up was performed at 2 years, with major bleeding defined as a type ≥3 bleed using the Bleeding Academic Research Consortium (BARC) definition.
There were 51 major bleeding events during follow-up (0.6%/year). Most events were BARC type 3a bleeds with 12 fatal bleeds (type 5). In most cases (54.9%), the site of bleeding was gastrointestinal. Major bleeding was significantly associated with mortality (adjusted hazard ratio: 2.89; 95% confidence intervals: 1.73 to 4.83; p < 0.0001). The increased risk of bleeding associated with vitamin K antagonist (VKA) treatment was particularly evident when VKA was combined with an antiplatelet therapy (APT). In contrast, the risk of cardiovascular death, MI, or nonhemorrhagic stroke did not differ in patients who received VKA + APT versus patients on VKA alone.
In patients with stable CAD (i.e., >1 year, with no acute events), major bleeding events are rare, but such events are an independent predictor of death. When oral anticoagulation is required, concomitant APT should not be prescribed in the absence of a recent cardiovascular event.
尽管有证据表明急性冠脉事件后发生大出血的患者在事件发生后数月内死亡风险更高,但稳定型冠状动脉疾病(CAD)患者在 1 年以上随访期间出血的发生率和对预后的影响在很大程度上尚不清楚。
本研究旨在评估稳定型 CAD 中主要出血的发生率、来源、决定因素和预后影响。
我们前瞻性纳入了 4184 例连续的 CAD 门诊患者,他们在纳入时已无任何心肌梗死(MI)或冠状动脉血运重建超过 1 年。随访时间为 2 年,主要出血定义为采用 Bleeding Academic Research Consortium(BARC)定义的≥3 级出血。
随访期间发生了 51 例主要出血事件(0.6%/年)。大多数事件为 BARC 3a 型出血,其中 12 例为致命性出血(类型 5)。在大多数情况下(54.9%),出血部位为胃肠道。主要出血与死亡率显著相关(调整后的危险比:2.89;95%置信区间:1.73 至 4.83;p<0.0001)。与华法林(VKA)治疗相关的出血风险增加,在 VKA 联合抗血小板治疗(APT)时尤为明显。相比之下,在接受 VKA+APT 的患者与单独接受 VKA 的患者之间,心血管死亡、MI 或非出血性卒中的风险无差异。
在稳定型 CAD 患者(即,>1 年,无急性事件)中,主要出血事件罕见,但此类事件是死亡的独立预测因素。当需要口服抗凝治疗时,在无近期心血管事件的情况下,不应联合使用 APT。