Kokkoz Çağrı, Bilge Adnan, Irik Mehmet, Dayangaç Halil I, Hayran Mustafa, Akarca Funda Karbek, Erdem Nimet Bilal, Çavuş Musa
Department of Emergency Medicine, Izmir Cigli State Education Hospital, Izmir, Turkey.
Department of Emergency Medicine, Faculty of Medicine, Celal Bayar University, Manisa, Turkey.
Turk J Emerg Med. 2018 Feb 9;18(2):62-66. doi: 10.1016/j.tjem.2018.01.003. eCollection 2018 Jun.
The aim of this study is to detect plasma ST2 levels in patients who were admitted to emergency department with chest pain and diagnosed with non st segment elevation myocardial infarction (NSTEMI) and to research the relationship between 28-day mortality and ST2 levels.
The present study was conducted at Emergency Department of Celal Bayar University Hafsa Sultan Hospital between September 2015 and January 2016 as a prospective, single-center, cross-sectional study. Plasma ST2 levels were detected in patients who were diagnosed with NSTEMI based on physical examination, ECG and troponin. The eligible patients were followed up with regard to mortality during 28 days.
A total of 88 patients diagnosed with NSTEMI were included in the study and followed up for 28 days. While 18 (20.5%) patients died at the end of 28 days, 70 (79.5%) patients survived. Mean ST2 level of surviving 70 patients was 651.37 ± 985.66 pg/mL and mean ST2 level of dying 18 patients was 2253.66 ± 1721.15 pg/mL (p < 0.001). ST2 value was higher among the dying (non-survivors) compared to the survivors at the end of 28 days and this was found related to mortality. ST2 cut-off value was found as 1000 pg/mL with 72.2% sensitivity and 20.0% specificity.
Among the patients who were diagnosed with NSTEMI at the emergency department, ST2 levels on admission were found significantly higher among the non-survivors compared to the survivors. ST2 level was accepted as a reliable biomarker for prediction of 28 mortality in patients diagnosed with NSTEMI.
本研究旨在检测因胸痛入院并被诊断为非ST段抬高型心肌梗死(NSTEMI)患者的血浆ST2水平,并研究28天死亡率与ST2水平之间的关系。
本研究于2015年9月至2016年1月在切拉尔·贝亚尔大学哈夫萨·苏丹医院急诊科进行,为一项前瞻性、单中心横断面研究。对根据体格检查、心电图和肌钙蛋白诊断为NSTEMI的患者检测血浆ST2水平。对符合条件的患者进行28天的死亡率随访。
本研究共纳入88例诊断为NSTEMI的患者并进行了28天的随访。28天结束时,18例(20.5%)患者死亡,70例(79.5%)患者存活。70例存活患者的平均ST2水平为651.37±985.66 pg/mL,18例死亡患者的平均ST2水平为2253.66±1721.15 pg/mL(p<0.001)。28天结束时,死亡(非存活)患者的ST2值高于存活患者,且发现这与死亡率相关。ST2临界值为1000 pg/mL,敏感性为72.2%,特异性为20.0%。
在急诊科诊断为NSTEMI的患者中,发现入院时非存活患者的ST2水平显著高于存活患者。ST2水平被认为是预测NSTEMI患者28天死亡率的可靠生物标志物。