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Prognostic usefulness of serial c-reactive protein measurements in st-elevation acute myocardial infarction

机译:c-反应蛋白系列检测在st段抬高急性心肌梗死中的预后价值

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摘要

It has been reported that increased levels of C-reactive protein are related to adverse long-term prognosis in the setting of ST-segment elevation acute myocardial infarction (MI). In previous studies, the timing of C-reactive protein determination has varied widely. In the present study, serial high-sensitivity C-reactive protein (hsCRP) measurements were performed to investigate if any of the measurements is superior regarding long-term prognosis. A total of 861 consecutive patients admitted for ST-segment elevation MI and treated with intravenous thrombolysis within the first 6 hours from the index pain were included. HsCRP levels were determined at presentation and at 24, 48, and 72 hours. The median follow-up time was 3.5 years. New nonfatal MI and cardiac death were the study end points. By the end of follow-up, cardiac death was observed in 22.4% and nonfatal MI in 16.1% of the patients. HsCRP levels were found to be increasing during the first 72 hours. Multivariate Cox regression analysis demonstrated that hsCRP levels at presentation were an independent predictor of the 2 end points (relative risk [RR] 2.8, p = 0.002, and RR 2.1, p = 0.03, for MI and cardiac death, respectively), while hsCRP levels at 24 hours did not yield statistically significant results (RR 1.4, p = 0.40, and RR 1.1, p = 0.80, for MI and cardiac death, respectively). The corresponding RRs at 48 hours were 1.2 (p = 0.5) for MI and 3.2 (p = 0.007) for cardiac death and at 72 hours were 1.6 (p = 0.30) for MI and 3.9 (p <0.001) for cardiac death. In conclusion, hsCRP levels at presentation represent an independent predictor for fatal and nonfatal events during long-term follow-up. HsCRP levels at 48 and 72 hours, which are close to peak hsCRP levels, independently predict only cardiac death. ? 2013 Elsevier Inc. All rights reserved.
机译:据报道,在ST段抬高急性心肌梗死(MI)的情况下,C反应蛋白水平升高与不良的长期预后有关。在以前的研究中,C反应蛋白测定的时机变化很大。在本研究中,进行了系列高敏C反应蛋白(hsCRP)测量,以研究任何一种测量在长期预后方面是否均优于其他测量。纳入总共861名连续的患者,这些患者入院ST段抬高MI,并在食指疼痛后的最初6小时内接受了静脉溶栓治疗。 HsCRP水平是在就诊时以及在24、48和72小时确定的。中位随访时间为3。5年。新的非致死性心肌梗死和心源性死亡是研究的终点。到随访结束时,在22.4%的患者中观察到心源性死亡,在16.1%的患者中观察到非致命性MI。发现HsCRP水平在头72小时内增加。多变量Cox回归分析表明,呈现时的hsCRP水平是两个终点的独立预测因子(MI和心源性死亡的相对危险度[RR] 2.8,p = 0.002,RR 2.1,p = 0.03),而hsCRP在24小时时的血脂水平未产生统计学上的显着性结果(MI和心源性死亡分别为RR 1.4,p = 0.40和RR 1.1,p = 0.80)。心梗的48小时相应心律为1.2(p = 0.5),心源性死亡的相应RR为3.2(p = 0.007),心梗患者72小时的相应RR为1.6(p = 0.30),心源性死亡为3.9(p <0.001)。总之,呈现的hsCRP水平代表了长期随访期间致命和非致命事件的独立预测因子。在48和72小时的hsCRP水平接近峰值hsCRP水平,仅独立预测心脏死亡。 ? 2013 Elsevier Inc.保留所有权利。

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