Department of Cardiology and Internal Diseases, Military Institute of Medicine, Warszawa, Poland.
3rd Department of Internal Diseases and Cardiology, Second Faculty of Medicine, Medical University of Warsaw, Warszawa, Poland.
Kardiol Pol. 2021;79(5):546-553. doi: 10.33963/KP.15917.
Neuron-specific enolase (NSE) is a biomarker for neurological outcomes after cardiac arrest with the most evidence collected thus far; however, recommended prognostic cutoff values are lacking owing to the discrepancies in the published data.
The aim of the study was to establish NSE cutoff values for prognostication in the environment of a cardiac intensive care unit following out-of-hospital cardiac arrest (OHCA).
A consecutive series of 82 patients admitted after OHCA were enrolled. Blood samples for the measurement of NSE levels were collected at admission and after 1 hour, 3, 12, 24, 48, and 72 hours. Neurological outcomes were quantified using the cerebral performance category (CPC) index. Each patient was classified into either the good (CPC ≤2) or poor prognosis (CPC ≥3) group.
Median NSE concentrations were higher in the poor prognosis group, and the difference reached statistical significance at 48 and 74 hours (84.4 ng/ml vs 22.9 ng/ml at 48 hours and 152.1 ng/ml vs 18.7 ng/ml at 72 hours; P <0.001, respectively). Moreover, in the poor prognosis group, NSE increased significantly between 24 and 72 hours (P <0.001). NSE cutoffs for the prediction of poor prognosis after OHCA were 39.8 ng/ml, 78.7 ng/ml, and 46.2 ng/ml for 24, 48, and 72 hours, respectively. The areas under the curve were significant at each time point, with the highest values at 48 and 72 hours after admission (0.849 and 0.964, respectively).
Elevated NSE concentrations with a rise in levels in serial measurements may be utilized in the prognostication algorithm after OHCA.
神经元特异性烯醇化酶(NSE)是心脏骤停后神经预后的生物标志物,迄今为止已有最多的证据支持;然而,由于发表的数据存在差异,目前仍缺乏推荐的预后截断值。
本研究旨在建立心脏骤停后在心脏重症监护病房(CICU)环境下 NSE 的截断值,以进行预后判断。
连续纳入了 82 名因院外心脏骤停(OHCA)后入院的患者。在入院时和入院后 1 小时、3 小时、12 小时、24 小时、48 小时和 72 小时采集血样,以测量 NSE 水平。使用脑功能预后评分(CPC)指数来量化神经功能结局。将每个患者分为预后良好(CPC ≤2)或预后不良(CPC ≥3)组。
预后不良组的 NSE 浓度中位数较高,在 48 小时和 74 小时时差异具有统计学意义(48 小时时为 84.4ng/ml 比 22.9ng/ml,72 小时时为 152.1ng/ml 比 18.7ng/ml;P<0.001)。此外,在预后不良组中,NSE 在 24 小时至 72 小时之间显著增加(P<0.001)。OHCA 后预测预后不良的 NSE 截断值为 24、48 和 72 小时时的 39.8ng/ml、78.7ng/ml 和 46.2ng/ml。每个时间点的曲线下面积均具有统计学意义,入院后 48 小时和 72 小时时的 AUC 值最高(分别为 0.849 和 0.964)。
连续测量时升高的 NSE 浓度及其水平升高可用于 OHCA 后的预后算法。