Division of Cardiology, Pulmonology, and Vascular Medicine, Heinrich Heine University Medical Center Dusseldorf, Dusseldorf, Germany.
Institute for Pharmacology and Clinical Pharmacology, Heinrich Heine University, Dusseldorf, Germany.
Thromb Haemost. 2021 Oct;121(10):1310-1316. doi: 10.1055/s-0041-1725190. Epub 2021 Mar 23.
Transcatheter aortic valve implantation (TAVI) is an evolving treatment of severe aortic valve stenosis. However, thromboembolic events such as stroke are common, predominantly early after TAVI. Optimal periprocedural antithrombotic regime is unknown. Especially, as antithrombotic medication enhances bleeding risk, thrombin generation and platelet function are crucial in the pathogenesis of ischemic events. However, the impact of the TAVI procedure on thrombin formation and platelet reactivity is not known by now.
We evaluated thrombin levels using thrombin-antithrombin (TAT) complexes and prothrombin fragments (PTFs) using enzyme-linked immunosorbent assay. Furthermore, platelet reactivity was measured via light transmission aggregometry before and 2 hours after TAVI in 198 patients.
TAT complexes and PTF F1 + 2 substantially increased during TAVI. Postprocedurally, TAT complexes and PTF were significantly higher after TAVI compared with percutaneous coronary intervention due to acute myocardial infarction, while preprocedural TAT complexes and PTF F1 + 2 did not differ. In contrast, platelet reactivity was not altered early after TAVI. Only adenosine diphosphate-induced aggregation was reduced, reflecting preprocedural loading with clopidogrel.
In this pilot study, we were able to demonstrate that thrombin generation is significantly increased early after TAVI, while platelet function is not affected. Increased thrombin concentrations may contribute to the high risk of postprocedural thromboembolic events. This leads to the hypothesis that extended peri-interventional anticoagulation early after TAVI may be an approach to reduce thromboembolic events.
经导管主动脉瓣植入术(TAVI)是一种治疗严重主动脉瓣狭窄的新兴方法。然而,血栓栓塞事件(如中风)很常见,主要发生在 TAVI 后早期。目前尚不清楚最佳的围手术期抗血栓治疗方案。特别是,由于抗血栓药物会增加出血风险,因此凝血酶生成和血小板功能在缺血性事件的发病机制中至关重要。然而,目前尚不清楚 TAVI 手术对凝血酶形成和血小板反应性的影响。
我们使用酶联免疫吸附试验评估了 TAVI 期间的凝血酶水平(使用凝血酶-抗凝血酶(TAT)复合物和凝血酶原片段(PTFs))。此外,我们在 198 例患者中通过透光比浊法测量了 TAVI 前后 2 小时的血小板反应性。
TAVI 期间 TAT 复合物和 PTF F1+2 显著增加。与经皮冠状动脉介入治疗(由于急性心肌梗死)相比,TAVI 后即刻 TAT 复合物和 PTF 明显更高,而术前 TAT 复合物和 PTF F1+2 无差异。相反,TAVI 后早期血小板反应性没有改变。仅二磷酸腺苷诱导的聚集减少,反映了氯吡格雷的术前负荷。
在这项初步研究中,我们能够证明凝血酶生成在 TAVI 后早期显著增加,而血小板功能不受影响。增加的凝血酶浓度可能导致术后血栓栓塞事件的高风险。这导致了一个假设,即在 TAVI 后早期延长围手术期抗凝可能是减少血栓栓塞事件的一种方法。