经导管边缘到边缘二尖瓣修复后的指导药物治疗

Tetsu Tanaka, R. Kavsur, M. Spieker, C. Iliadis, C. Metze, Birthe M Brachtendorf, P. Horn, C. Zachoval, A. Sugiura, M. Kelm, S. Baldus, G. Nickenig, R. Westenfeld, R. Pfister, M. Becher
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引用次数: 2

摘要

目的相当大比例的继发性二尖瓣返流(SMR)患者未接受心力衰竭(HF)的指导药物治疗(GDMT)。我们调查了接受经导管边缘到边缘修复(TEER)的SMR患者使用GDMT与死亡率之间的关系。方法我们回顾性分析了在三个中心接受TEER治疗的SMR和左心室射血分数<50%的患者。根据目前的HF指南,GDMT被定义为由β受体阻滞剂、肾素-血管紧张素系统(RAS)抑制剂和矿皮质激素受体拮抗剂(MRAs)组成的三联疗法。患者分为GDMT组和非GDMT组。我们计算倾向得分,并进行治疗加权逆概率(IPTW)分析,比较两组的2年死亡率。结果463例患者中,228例(49.2%)在出院时接受了GDMT治疗。经iptw校正的Kaplan-Meier曲线显示,GDMT患者的死亡率低于未GDMT患者(19.8% vs 31.1%, p=0.011)。在iptw校正的Cox比例风险分析中,GDMT与2年死亡风险降低相关(HR: 0.58;95% CI: 0.35 ~ 0.95;P =0.030),这在临床亚组中是一致的。此外,与没有GDMT的患者相比,有GDMT的患者在TEER后1年的左心室反向重构率更高。结论GDMT,定义为由β受体阻滞剂、RAS抑制剂和MRAs组成的三联疗法,与SMR患者TEER后2年死亡率降低相关。优化药物治疗对于改善因SMR而接受TEER治疗的患者的临床结果至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Guideline-directed medical therapy after transcatheter edge-to-edge mitral valve repair
Objective A sizeable proportion of patients with secondary mitral regurgitation (SMR) do not receive guideline-directed medical therapy (GDMT) for heart failure (HF). We investigated the association between the use of GDMT and mortality in patients with SMR who underwent transcatheter edge-to-edge repair (TEER). Methods We retrospectively analysed patients with SMR and a left ventricular ejection fraction of <50% who underwent TEER at three centres. According to current HF guidelines, GDMT was defined as triple therapy consisting of beta-blockers, renin–angiotensin system (RAS) inhibitors and mineralocorticoid receptor antagonists (MRAs). Patients were divided into two groups: GDMT and non-GDMT groups. We calculated the propensity scores and carried out inverse probability of treatment weighting (IPTW) analyses to compare 2-year mortality between the two groups. Results Of 463 patients, 228 (49.2%) were treated with GDMT upon discharge. IPTW-adjusted Kaplan-Meier curve showed patients with GDMT had a lower incidence of mortality than those without GDMT (19.8% vs 31.1%, p=0.011). In IPTW-adjusted Cox proportional hazards analysis, GDMT was associated with a reduced risk of 2-year mortality (HR: 0.58; 95% CI: 0.35 to 0.95; p=0.030), which was consistent among clinical subgroups. Moreover, patients with GDMT had a higher rate of left ventricular reverse remodelling at 1 year after TEER than those without GDMT. Conclusion GDMT, defined as triple therapy consisting of beta-blockers, RAS inhibitors and MRAs, was associated with a reduced risk of 2-year mortality after TEER for SMR. Optimisation of medical therapy is crucial to improve clinical outcomes in patients undergoing TEER for SMR.
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