Institute for Clinical Evaluative Sciences, Division of Cardiology, Schulich Heart Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Circ Cardiovasc Interv. 2010 Apr;3(2):140-7. doi: 10.1161/CIRCINTERVENTIONS.109.928721. Epub 2010 Mar 23.
Previous data on bleeding after percutaneous coronary intervention (PCI) have been obtained primarily from randomized trials that focused on in-hospital bleeding. The incidence of late bleeding after PCI, its independent predictors, and its prognostic importance in clinical practice has not been fully addressed.
We evaluated 22 798 patients aged >65 years who underwent PCI from December 1, 2003, to March 31, 2007, in Ontario, Canada. Cox proportional hazard models were used to determine factors associated with late bleeding, which was defined as hospitalization for bleeding after discharge from the index PCI, and to estimate risk of death or myocardial infarction associated with late bleeding. We found that 2.5% of patients were hospitalized for bleeding in the year after PCI, with 56% of bleeding episodes due to gastrointestinal bleed. The most significant predictor of late bleeding was warfarin use after PCI (hazard ratio [HR], 3.12). Other significant predictors included age (HR, 1.41 per 10 years), male sex (HR, 1.24), cancer (HR, 1.80), previous bleeding (HR, 2.42), chronic kidney disease (HR, 1.93), and nonsteroidal antiinflammatory drug use (HR, 1.73). After adjusting for baseline covariates, hospitalization for a bleeding episode was associated with a significantly increased 1-year hazard of death or myocardial infarction (HR, 2.39; 95% CI, 1.93 to 2.97) and death (HR, 3.38; 95% CI, 2.60 to 4.40).
Hospitalization for late bleeding after PCI is associated with substantially increased risk of death and myocardial infarction. The use of triple therapy (i.e., aspirin, thienopyridine, and warfarin) is associated with the highest risk of late bleeding.
先前关于经皮冠状动脉介入治疗(PCI)后出血的资料主要来源于关注住院期间出血的随机试验。PCI 后迟发性出血的发生率、其独立预测因子以及其在临床实践中的预后意义尚未得到充分阐述。
我们评估了 2003 年 12 月 1 日至 2007 年 3 月 31 日期间在加拿大安大略省接受 PCI 的 22798 名年龄>65 岁的患者。Cox 比例风险模型用于确定与迟发性出血相关的因素,迟发性出血定义为 PCI 出院后因出血住院,并估计迟发性出血与死亡或心肌梗死相关的风险。我们发现,2.5%的患者在 PCI 后 1 年内因出血住院,56%的出血事件归因于胃肠道出血。迟发性出血的最显著预测因子是 PCI 后使用华法林(风险比[HR],3.12)。其他显著预测因子包括年龄(HR,每增加 10 岁 1.41)、男性(HR,1.24)、癌症(HR,1.80)、既往出血(HR,2.42)、慢性肾脏病(HR,1.93)和非甾体抗炎药的使用(HR,1.73)。在校正基线协变量后,因出血事件住院与 1 年内死亡或心肌梗死(HR,2.39;95%CI,1.93 至 2.97)和死亡(HR,3.38;95%CI,2.60 至 4.40)的风险显著增加相关。
PCI 后迟发性出血与死亡和心肌梗死风险显著增加相关。三联疗法(即阿司匹林、噻吩吡啶和华法林)的使用与迟发性出血的风险最高相关。