Lim Ki-Dong, Yan Andrew T, Casanova Amparo, Yan Raymond T, Mendelsohn Aurora, Jolly Sanjit, Fitchett David H, Langer Anatoly, Goodman Shaun G
Terrence Donnelly Heart Centre, Division of Cardiology, St Michael's Hospital, University of Toronto, Toronto, Ontario, Canada.
Am Heart J. 2008 Apr;155(4):718-24. doi: 10.1016/j.ahj.2007.11.012. Epub 2008 Feb 21.
The aim of this study was to evaluate whether quantitative cardiac troponin (cTn) assessment can improve risk stratification in a spectrum of patients with non-ST-segment elevation (NSTE) acute coronary syndrome (ACS) using the validated Global Registry of Acute Cardiac Events (GRACE) risk model.
The Canadian ACS Registry II is a prospective, multicenter study that enrolled patients admitted to hospital with a suspected NSTE ACS within 24 hours of symptom onset. Of the total 2297 patients, those with elevated cTn (n = 1013) were further stratified into tertiles of cTn ranges. Our primary end point was death and our secondary end point was a composite of death or/and recurrent myocardial infarction at 1-year follow-up.
Multivariable analysis adjusting for validated predictors of death confirmed the independent prognostic value of any abnormal cTn (vs normal) for death (adjusted odds ratio 2.28, 95% CI 1.49-3.49, P < .001) and for the composite outcome (adjusted odds ratio 2.18, 95% CI 1.61-2.95, P < .001) at 1 year. With quantitative assessment, the gradient of mortality risk with increasing cTn level was not evident after adjusting for other prognosticators. Quantitative (compared to qualitative) assessment of cTn level did not improve either the GRACE risk model discrimination for 1-year death.
Any cTn elevation is associated with higher rate of death at 1 year, but its quantitative assessment did not prove as important as its mere presence as an independent long-term prognosticator in a nonclinical trial, "real-world" NSTE ACS population.
本研究旨在评估使用经过验证的急性心脏事件全球注册研究(GRACE)风险模型,定量检测心肌肌钙蛋白(cTn)是否能改善非ST段抬高(NSTE)急性冠状动脉综合征(ACS)患者的风险分层。
加拿大ACS注册研究II是一项前瞻性、多中心研究,纳入症状发作后24小时内因疑似NSTE ACS入院的患者。在总共2297例患者中,cTn升高的患者(n = 1013)进一步按cTn范围分为三分位数。我们的主要终点是死亡,次要终点是1年随访时死亡或/和再发心肌梗死的复合终点。
对已验证的死亡预测因素进行多变量分析,证实任何异常cTn(与正常相比)对1年时的死亡(调整后的优势比为2.28,95%CI为1.49 - 3.49,P <.001)和复合结局(调整后的优势比为2.18,95%CI为1.61 - 2.95,P <.001)具有独立的预后价值。通过定量评估,在调整其他预后因素后,随着cTn水平升高的死亡风险梯度并不明显。cTn水平的定量(与定性相比)评估也未改善GRACE风险模型对1年死亡的判别能力。
任何cTn升高都与1年时较高的死亡率相关,但在非临床试验的“真实世界”NSTE ACS人群中,其定量评估并未证明像其单纯存在那样作为独立的长期预后因素那么重要。