Improved Stratification of Autonomic Regulation for risk prediction in post-infarction patients with preserved left ventricular function (ISAR-Risk).

Improved Stratification of Autonomic Regulation for risk prediction in post-infarction patients with preserved left ventricular function (ISAR-Risk).
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DOI:
10.1093/eurheartj/ehn540
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发表时间:
2009-03
影响因子:
39.3
通讯作者:
Schmidt G
Schmidt G
中科院分区:
医学1区
文献类型:
--
作者:
Bauer A;Barthel P;Schneider R;Ulm K;Müller A;Joeinig A;Stich R;Kiviniemi A;Hnatkova K;Huikuri H;Schömig A;Malik M;Schmidt G

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探讨窦性心率震荡(HRT)和减速能力(DC)联合应用对心肌梗死后左室射血分数(LVEF)> 30%患者的危险预测作用。我们纳入了2343例窦性心律的急性心肌梗死(MI)(<76岁)连续幸存者。从24 h霍尔特记录中获得HRT和DC。HRT异常(斜率≤ 2.5 ms/RR且发作≥ 0%)和DC异常(≤4.5 ms)的患者被视为患有重度自主神经功能衰竭(SAF),并前瞻性归类为高风险。主要和次要终点是随访前5年内的全因死亡、心源性死亡和心源性猝死。随访期间,181例患者死亡; LVEF ≤ 30%的120例患者中有39例死亡,LVEF>30%的2223例患者中有142例死亡(累积5年死亡率分别为37.9%和7.8%)。在LVEF > 30%的患者中,SAF确定了另一个高风险组117例患者,其中37例死亡(累积5年死亡率分别为38.6%和6.1%)。合并两个高风险组(即LVEF ≤ 30%和/或SAF)与LVEF ≤ 30%相比,死亡率预测的灵敏度增加了一倍(21.1% vs. 42.1%,P < 0.001),同时保持了5年死亡率(38.2%)。在LVEF> 30%的MI后患者中,SAF确定了一个高风险组,其规模和死亡风险与LVEF ≤ 30%的患者相当。
To investigate the combination of heart rate turbulence (HRT) and deceleration capacity (DC) as risk predictors in post-infarction patients with left ventricular ejection fraction (LVEF) > 30%. We enrolled 2343 consecutive survivors of acute myocardial infarction (MI) (<76 years) in sinus rhythm. HRT and DC were obtained from 24 h Holter recordings. Patients with both abnormal HRT (slope ≤ 2.5 ms/RR and onset ≥ 0%) and abnormal DC (≤4.5 ms) were considered suffering from severe autonomic failure (SAF) and prospectively classified as high risk. Primary and secondary endpoints were all-cause, cardiac, and sudden cardiac mortality within the first 5 years of follow-up. During follow-up, 181 patients died; 39 deaths occurred in 120 patients with LVEF ≤ 30%, and 142 in 2223 patients with LVEF>30% (cumulative 5-year mortality rates of 37.9% and 7.8%, respectively). Among patients with LVEF > 30%, SAF identified another high-risk group of 117 patients with 37 deaths (cumulative 5-year mortality rates of 38.6% and 6.1%, respectively). Merging both high-risk groups (i.e. LVEF ≤ 30% and/or SAF) doubled the sensitivity of mortality prediction compared with LVEF ≤ 30% alone (21.1% vs. 42.1%, P < 0.001) while preserving 5-year mortality rate (38.2%). In post-MI patients with LVEF>30%, SAF identifies a high-risk group equivalent in size and mortality risk to patients with LVEF ≤ 30%.
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