Takotsubo综合征微血管功能的预后价值:个体患者资料的汇总分析。

Rob Eerdekens,Mohamed El Farissi,Giovanni Luigi De Maria,Aviel Shetrit,Robert Sykes,Christina Ekenbäck,Jonas Persson,Jonas Spaak,Liam S Couch,Fernando Alfonso,Fernando Rivero,Nieves Gonzalo,Javier Escaned,Iván J Núñez Gil,Oscar Vedia Cruz,Reut Amar Shamir,Ophir Freund,Marc Vanderheyden,Marta Belmonte,Emanuele Barbato,Pim A L Tonino,Adrian Banning,Ole Geir Solberg,Colin Berry,William F Fearon,Frederik M Zimmermann
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引用次数: 0

摘要

背景冠状动脉微血管功能障碍似乎在Takotsubo综合征(TTS)的发病机制中起主要作用。然而,在TTS急性期测量微血管功能的预后价值尚不清楚。方法对来自9个前瞻性TTS队列的个体患者数据进行协作、汇总分析,对冠状动脉微血管功能进行有创评估,包括微循环阻力指数(IMR)、冠状动脉血流储备(CFR)和微血管阻力储备(MRR)。主要终点是全因死亡率。次要终点包括主要心脑血管不良事件(MACCE),定义为全因死亡、TTS复发、卒中、短暂性脑缺血发作或心肌梗死的复合。结果本组共纳入166例TTS患者,其中典型(根尖)TTS变异130例(78%),非典型变异36例(22%)。在中位随访20.6[4.3 - 60.0]个月期间,17例(10.2%)患者出现全因死亡,29例(17.5%)患者出现MACCE。IMR、CFR和MRR与全因死亡率相关。调整基线差异后,IMR是两种全因死亡率的唯一独立预测因子(aHR 3.9;95% ci: 1.39 ~ 10.88, p = 0.010;c-statistic 0.817 (95% CI: 0.711-0.923))和MACCE (aHR 2.6;95% ci: 1.17-5.67;P = 0.018;c-statistic 0.719 (95% CI: 0.612-0.826))。结论:在对来自9个前瞻性TTS队列的个体患者数据的汇总分析中,急性期测量的微血管功能障碍与全因死亡率相关。特别是,根据IMR评估,微血管阻力升高是死亡率和MACCE的唯一独立预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic Value of Microvascular Function in Takotsubo Syndrome: a Pooled Analysis of Individual Patient Data.
BACKGROUND Coronary microvascular dysfunction appears to play a major role in the pathogenesis of Takotsubo Syndrome (TTS). However, the prognostic value of microvascular function measured in the acute phase of TTS is unclear. METHODS In a collaborative, pooled analysis of individual patient data from nine prospective TTS cohorts, invasive assessment of coronary microvascular function was performed, including the index of microcirculatory resistance (IMR), coronary flow reserve (CFR), and microvascular resistance reserve (MRR). The primary endpoint was all-cause mortality. Secondary endpoints included major adverse cardiac and cerebrovascular events (MACCE) defined as the composite of all-cause death, recurrence of TTS, stroke, transient ischemic attack, or myocardial infarction. RESULTS One hundred and sixty six patients with TTS were included, in whom 130 (78%) had the typical (apical) TTS variant and 36 (22%) an atypical variant. During a median follow-up of 20.6 [4.3 - 60.0] months, all-cause mortality occurred in 17 patients (10.2%) and MACCE in 29 patients (17.5%). IMR, CFR, and MRR were associated with all-cause mortality. After adjustment for baseline differences, IMR was the only independent predictor of both all-cause mortality (aHR 3.9; 95% CI: 1.39-10.88, P = 0.010; c-statistic 0.817 (95% CI: 0.711-0.923)) and MACCE (aHR 2.6; 95% CI: 1.17-5.67; P = 0.018; c-statistic 0.719 (95% CI: 0.612-0.826)). CONCLUSIONS In this pooled analysis of individual patient data from nine prospective TTS cohorts, microvascular dysfunction measured in the acute phase, was associated with all-cause mortality. In particular, an elevated microvascular resistance, as assessed by IMR, was the only independent predictor of both mortality and MACCE.
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