心肌肌钙蛋白升高对非心脏疾病的预后意义。试点研究

A. Ibrahim, Hassan Walid, S. Nadia, Lhmdi Mohammed, Nazzal Alaa, Mohamed Mohammed J, Dar Farhan, Sharafeldin Sahar, A. Amr, B. Hasan, Alshengiti Basema, H. Ehab, Waez Heba, Bahnshal Sarah, Nassani Momen, Alaa Mohammed, AL-Ammari Maha, Elabidinm Hala Zein, Mansour G. Ibrahim
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引用次数: 5

摘要

背景:一些研究已经将心肌肌钙蛋白升高与急性冠状动脉综合征患者的总体风险增加联系起来,但在非心脏疾病中,肌钙蛋白升高的预后意义仍然很少。目的:本研究的主要目的是探讨高敏感性肌钙蛋白T (TnT-HS)升高在急性冠脉综合征(ACS)范围以外的非心脏疾病中的预后意义。其次,我们的目的是研究心血管合并症和其他临床表现对非心脏疾病中心脏生物标志物释放的影响。方法:这是一项回顾性电子病历试点研究,所有在三个月内没有急性冠状动脉综合征、近期血管成形术或心力衰竭的TnT-HS升高的患者被纳入研究,随后前瞻性随访6个月。2016年1月1日至2016年6月30日,共筛查2535例患者,其中306例患者TnT-HS升高,162例患者符合研究纳入标准。数据以Google数据库格式加密收集,导出为excel电子表格,使用SPSS (version 24)进行分析和计算,以确定TnT-HS值升高与临床的关联。结果:大多数肌钙蛋白TnT-HS样本(77.1%)来自急诊室(ER)就诊的患者,63.4%的患者为男性。平均年龄为72岁,经Spearman秩序相关分析,年龄与肌钙蛋白水平无相关性(rs = -0.18, p = 0.816)。急性冠状动脉综合征患者的nt - hs值明显高于其他组,但其他临床情况的患者也出现了nt - hs阳性(> 40 ng/l)。在多变量分析中,基线慢性肾脏疾病(CKD)、急性感染性疾病(主要是尿路感染)和脑血管事件(CVA)与入院时TnT-HS阳性独立相关。整个队列的观察结果;TnT-HS阳性具有高敏感性和阴性预测值,但特异性较低,阳性预测值有限。6个月内的主要不良心脑事件(MACCE)显著,包括;死亡(13.7%),心肌梗死(3.9%),卒中(缺血性4.6%,出血性2.3%,TIA 0.8%) p值< 0.02。结论:在表现出CKD、感染和cva相关的非急性心脏病的患者中,应谨慎解释TnT-HS阳性。非心脏疾病的肌钙蛋白升高仍有明显的不良预后。在调整了年龄和肾功能不全因素后,我们建议在非心脏疾病中,如果新的nt - hs临界值> 30 ng/l,则180天内MACCE风险增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Prognostic Significance of Elevated Cardiac Troponin in Non-Cardiac Medical Disorders. Pilot Study
Background: Several studies have linked elevated cardiac troponin to increased overall risk in patients with acute coronary syndrome but the prognostic significance of elevated troponin in non-cardiac conditions remains scanty. Objectives: The primary aim of this study was to investigate the prognostic significance of elevated high sensitivity troponin T (TnT-HS) in non-cardiac disorders outside the remit of an acute coronary syndrome (ACS). Secondarily we aimed to investigate the impact of cardiovascular comorbidities and other clinical presentations in the release of cardiac biomarkers in non-cardiac disorders. Methodology: This was a retrospective electronic patient record pilot review where all patients with elevated TnT-HS without acute coronary syndrome, recent angioplasty or heart failure within a three month period were enrolled into the study and subsequently followed prospectively for a six month period. From January 1, 2016 to June 30, 2016, a total of 2535 patients were screened of which 306 patients had elevated TnT-HS and 162 patients met the study inclusion criteria. Data were encrypted and collected in Google database format, exported into excel spreadsheet, analyzed and computed using SPSS (version 24) to identify clinical associations with increased values of TnT-HS. Results: Most troponin TnT-HS samples (77.1%) were obtained from emergency room (ER) attendance and 63.4% of patients were male. The mean age was 72 years and no correlation were found between age and troponin levels (rs = -0.18, p = 0.816) by Spearman Rank-order correlation. Although expectedly patients with diagnosis of acute coronary syndrome displayed TnT-HS values significantly higher than those of other groups, positivity to TnT-HS (> 40 ng/l) was also observed in patients with other clinical conditions. In multivariate analysis, baseline chronic kidney disease (CKD), acute infectious diseases mainly urinary tract infection and cerebrovascular events (CVA) were independently associated with TnT-HS positivity at admission. Observations from the cohort as a whole; TnT-HS positivity exhibited high sensitivity and negative predictive value, counterbalanced by low specificity and limited positive predictive value. Major adverse cardiac and cerebral events (MACCE) were significant within 6 months including; Death (13.7%), MI (3.9%), Stroke (ischemic 4.6%, hemorrhagic 2.3%, TIA 0.8%) p value < 0.02. Conclusions: TnT-HS positivity should be cautiously interpreted in patients exhibiting non acute cardiac conditions associated CKD, infections, and CVAs. This troponin elevation in non-cardiac conditions still carries a significant adverse prognosis. After adjusting for age and renal insufficiency, we can suggest a new cut off level of TnT-HS > 30 ng/l to have increased risk of MACCE within 180 days in non-cardiac conditions.
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