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Impact of anticoagulation therapy on valve haemodynamic deterioration following transcatheter aortic valve replacement

医学 倾向得分匹配 内科学 心脏病学 阀门更换 冲程(发动机) 主动脉瓣 血流动力学 入射(几何) 主动脉瓣置换术 外科 狭窄 机械工程 光学 物理 工程类
作者
María Del Trigo,Antonio J. Muñoz-García,Azeem Latib,Vincent Auffret,Harindra C. Wijeysundera,Luis Nombela‐Franco,Enrique Gutiérrez‐Ibañes,Asim N. Cheema,Violeta Serra,Ignacio J. Amat‐Santos,Joëlle Kefer,Luis Benítez,Florence Leclercq,Antonio Mangieri,Hervé Breton,Pilar Jiménez‐Quevedo,Bruno García del Blanco,Antonio Dager,Omar Abdul‐Jawad Altisent,Rishi Puri,Philippe Pîbarot,Josep Rodés‐Cabau
出处
期刊:Heart [BMJ]
卷期号:104 (10): 814-820 被引量:31
标识
DOI:10.1136/heartjnl-2017-312514
摘要

To evaluate the changes in transvalvular gradients and the incidence of valve haemodynamic deterioration (VHD) following transcatheter aortic valve replacement (TAVR), according to use of anticoagulation therapy.This multicentre study included 2466 patients (46% men; mean age 81±7 years) who underwent TAVR with echocardiography performed at 12-month follow-up. Anticoagulation therapy was used in 707 patients (28.7%) following TAVR (AC group). A total of 663 patients received vitamin K antagonists, and 44 patients received direct oral anticoagulants. A propensity score matching analysis was performed to adjust for intergroup (AC vs non-AC post-TAVR) differences. A total of 622 patients per group were included in the propensity-matched analysis. VHD was defined as a ≥10 mm Hg increase in the mean transprosthetic gradient at follow-up (vs hospital discharge). The mean clinical follow-up was 29±18 months. The mean transvalvular gradient significantly increased at follow-up in the non-AC group within the global cohort (P=0.003), whereas it remained stable over time in the AC group (P=0.323). The incidence of VHD was significantly lower in the AC group (0.6%) compared with the non-AC group (3.7%, P<0.001), and these significant differences remained within the propensity-matched populations (0.6% vs 3.9% in the AC and non-AC groups, respectively, P<0.001). The occurrence of VHD did not associate with an increased risk of all-cause death (P=0.468), cardiovascular death (P=0.539) or stroke (P=0.170) at follow-up.The lack of anticoagulation therapy post-TAVR was associated with significant increments in transvalvular gradients and a greater risk of VHD. VHD was subclinical in most cases and did not associate with major adverse clinical events. Future randomised trials are needed to determine if systematic anticoagulation therapy post-TAVR would reduce the incidence of VHD.

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