D'Ascenzo Fabrizio, Saglietto Andrea, Ramakrishna Harish, Andreis Alessandro, Jiménez-Mazuecos Jesús M, Nombela-Franco Luis, Cerrato Enrico, Liebetrau Christoph, Alfonso-Rodríguez Emilio, Bagur Rodrigo, Alkhouli Mohamad, De Ferrari Gaetano M, Núñez-Gil Iván J
Cardiology, Città della Salute e della Scienza, Molinette Hospital, Torino, Italy.
Division of Cardiovascular Anesthesiology, Mayo Clinic Rochester, Arizona.
Catheter Cardiovasc Interv. 2021 Nov 1;98(5):864-871. doi: 10.1002/ccd.29243. Epub 2020 Sep 9.
To assess the Usefulness of oral anticoagulation therapy (OAT) in patients with coronary artery aneurysm (CAA).
Data on the most adequate antithrombotic CAA management is lacking.
Patients included in CAAR (Coronary Artery Aneurysm Registry, Clinical Trials.gov: NCT02563626) were selected. Patients were divided in OAT and non-OAT groups, according to anticoagulation status at discharge and 2:1 propensity score matching with replacement was performed. The primary endpoint of the analysis was a composite and mutual exclusive endpoint of myocardial infarction, unstable angina (UA), and aneurysm thrombosis (coronary ischemic endpoint). Net adverse clinical events, major adverse cardiovascular events, their single components, cardiovascular death, re-hospitalizations for heart failure, stroke, aneurysm thrombosis, and bleeding were the secondary ones.
One thousand three hundred thirty-one patients were discharged without OAT and 211 with OAT. In the propensity-matched sample (390 patients in the non-OAT group, 195 patients in the OAT group), after 3 years of median follow-up (interquartile range 1-6 years), the rate of the primary endpoint (coronary ischemic endpoint) was significantly less in the OAT group as compared to non-OAT group (8.7 vs. 17.2%, respectively; p = .01), driven by a significant reduction in UA (4.6 vs. 10%, p < .01) and aneurysm thrombosis (0 vs. 3.1%, p = .03), along with a non-significant reduction in MI (4.1 vs. 7.7%, p = .13). A non-significant increase in bleedings, mainly BARC type 1 (55%), was found in the OAT-group (10.3% in the non-OAT vs. 6.2% in the OAT group, p = .08).
OAT decreases the composite endpoint of UA, myocardial infarction, and aneurysm thrombosis in patients with CAA, despite a non-significant higher risk of bleeding.
评估口服抗凝治疗(OAT)在冠状动脉瘤(CAA)患者中的有效性。
缺乏关于CAA最适当抗栓治疗管理的数据。
选取纳入CAAR(冠状动脉瘤登记处,临床试验.gov:NCT02563626)的患者。根据出院时的抗凝状态将患者分为OAT组和非OAT组,并进行2:1倾向评分匹配及替换。分析的主要终点是心肌梗死、不稳定型心绞痛(UA)和动脉瘤血栓形成(冠状动脉缺血终点)的复合且相互排斥的终点。净不良临床事件、主要不良心血管事件、其单一组成部分、心血管死亡、因心力衰竭再次住院、中风、动脉瘤血栓形成和出血为次要终点。
1331例患者出院时未接受OAT,211例接受OAT。在倾向评分匹配样本中(非OAT组390例患者,OAT组195例患者),经过3年的中位随访(四分位间距1 - 6年),与非OAT组相比,OAT组的主要终点(冠状动脉缺血终点)发生率显著更低(分别为8.7%和17.2%;p = 0.01),这是由UA(4.6%对10%,p < 0.01)和动脉瘤血栓形成(0对3.1%,p = 0.03)的显著降低以及MI的非显著降低(4.1%对7.7%,p = 0.13)所驱动。在OAT组中发现出血有非显著增加,主要是BARC 1型(55%)(非OAT组为10.3%,OAT组为6.2%,p = 0.08)。
OAT可降低CAA患者中UA、心肌梗死和动脉瘤血栓形成的复合终点,尽管出血风险有非显著的升高。