Flores-Ríos Xacobe, Marzoa-Rivas Raquel, Abugattás-de Torres Juan Pablo, Piñón-Esteban Pablo, Aldama-López Guillermo, Salgado-Fernández Jorge, Calviño-Santos Ramón, Vázquez-Rodríguez José Manuel, Vázquez-González Nicolás, Castro-Beiras Alfonso
Department of Cardiology, Complexo Hospitalario Universitario Juan Canalejo y Marítimo de Oza, A Coruña, Spain.
Am Heart J. 2008 Apr;155(4):648-53. doi: 10.1016/j.ahj.2007.11.027. Epub 2008 Feb 21.
Late thrombosis is the major safety concern of drug-eluting stents, but its incidence in common clinical practice remains controversial to date, especially beyond the first year after stent implantation. We sought to investigate the incidence, clinical consequences, and risk factors of late thrombosis after drug-eluting stent implantation.
Consecutive patients (N = 604) who received > or = 1 paclitaxel-eluting stent(s) (PES) between June 2003 and February 2005 at our institution were enrolled. Clinical characteristics and major outcomes were reviewed to detect cases and predictors of late and very late definite PES thrombosis (LDT) of PES, as currently defined by the Academic Research Council.
During long-term follow-up (median 34.3 months, IQR 8.6), 17 cases of LDT were noted (cumulative incidence 2.8%, 95% CI 1.7%-4.5%). Most of LDT were very late thromboses (14 cases, 82%). Late and very late definite PES thrombosis appeared at a steady rate (incidence density 1.1% patient-years). Late and very late definite PES thrombosis was related to a high risk of all-cause death (HR 3.2, 95% CI 1.3-7.9) and cardiac death (HR 6.0, 95% CI 2.3-15.6). Withdrawal of antiplatelet therapy, left ventricular ejection fraction, and average stent diameter per patient were independent predictors of LDT in multivariate analysis.
Late and very late definite PES thrombosis may be more frequent in a real setting than anticipated by initial experimental and observational studies but is keeping with more recent scientific evidence. It seems to occur at a constant rate during long-term follow-up and is associated with a high risk of overall and cardiac death.
晚期血栓形成是药物洗脱支架的主要安全问题,但在目前的临床实践中,其发生率仍存在争议,尤其是在支架植入后的第一年之后。我们旨在研究药物洗脱支架植入后晚期血栓形成的发生率、临床后果及危险因素。
纳入2003年6月至2005年2月在我院接受≥1枚紫杉醇洗脱支架(PES)的连续患者(N = 604例)。回顾临床特征和主要结局,以检测目前由学术研究委员会定义的PES晚期和极晚期明确血栓形成(LDT)的病例及预测因素。
在长期随访(中位时间34.3个月,四分位间距8.6)期间,共发现17例LDT(累积发生率2.8%,95%可信区间1.7% - 4.5%)。大多数LDT为极晚期血栓形成(14例,82%)。晚期和极晚期明确PES血栓形成以稳定的速率出现(发病密度为1.1%患者-年)。晚期和极晚期明确PES血栓形成与全因死亡高风险(HR 3.2,95%可信区间1.3 - 7.9)及心源性死亡高风险(HR 6.0,95%可信区间2.3 - 15.6)相关。在多变量分析中,停用抗血小板治疗、左心室射血分数及每位患者的平均支架直径是LDT的独立预测因素。
在实际临床中,晚期和极晚期明确PES血栓形成可能比最初的实验和观察性研究所预期的更为常见,但与更多近期科学证据相符。在长期随访期间,其似乎以恒定速率发生,并且与总体和心源性死亡高风险相关。