急诊科N端前脑钠肽对呼吸困难的研究(PRIDE研究)

The N-terminal Pro-BNP investigation of dyspnea in the emergency department (PRIDE) study.

作者信息

Januzzi James L, Camargo Carlos A, Anwaruddin Saif, Baggish Aaron L, Chen Annabel A, Krauser Daniel G, Tung Roderick, Cameron Renee, Nagurney J Tobias, Chae Claudia U, Lloyd-Jones Donald M, Brown David F, Foran-Melanson Stacy, Sluss Patrick M, Lee-Lewandrowski Elizabeth, Lewandrowski Kent B

机构信息

Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA.

出版信息

Am J Cardiol. 2005 Apr 15;95(8):948-54. doi: 10.1016/j.amjcard.2004.12.032.

Abstract

The utility of aminoterminal pro-brain natriuretic peptide (NT-proBNP) testing in the emergency department to rule out acute congestive heart failure (CHF) and the optimal cutpoints for this use are not established. We conducted a prospective study of 600 patients who presented in the emergency department with dyspnea. The clinical diagnosis of acute CHF was determined by study physicians who were blinded to NT-proBNP results. The primary end point was a comparison of NT-proBNP results with the clinical assessment of the managing physician for identifying acute CHF. The median NT-proBNP level among 209 patients (35%) who had acute CHF was 4,054 versus 131 pg/ml among 390 patients (65%) who did not (p <0.001). NT-proBNP at cutpoints of >450 pg/ml for patients <50 years of age and >900 pg/ml for patients >or=50 years of age were highly sensitive and specific for the diagnosis of acute CHF (p <0.001). An NT-proBNP level <300 pg/ml was optimal for ruling out acute CHF, with a negative predictive value of 99%. Increased NT-proBNP was the strongest independent predictor of a final diagnosis of acute CHF (odds ratio 44, 95% confidence interval 21.0 to 91.0, p <0.0001). NT-proBNP testing alone was superior to clinical judgment alone for diagnosing acute CHF (p = 0.006); NT-proBNP plus clinical judgment was superior to NT-proBNP or clinical judgment alone. NT-proBNP measurement is a valuable addition to standard clinical assessment for the identification and exclusion of acute CHF in the emergency department setting.

摘要

氨基末端脑钠肽前体(NT-proBNP)检测在急诊科用于排除急性充血性心力衰竭(CHF)的效用以及该用途的最佳切点尚未确定。我们对600例因呼吸困难到急诊科就诊的患者进行了一项前瞻性研究。急性CHF的临床诊断由对NT-proBNP结果不知情的研究医生确定。主要终点是将NT-proBNP结果与主治医生对急性CHF的临床评估进行比较。209例(35%)患有急性CHF的患者中NT-proBNP水平中位数为4054 pg/ml,而390例(65%)未患急性CHF的患者中为131 pg/ml(p<0.001)。对于<50岁的患者,NT-proBNP切点>450 pg/ml,对于≥50岁的患者,切点>900 pg/ml,对急性CHF的诊断具有高度敏感性和特异性(p<0.001)。NT-proBNP水平<300 pg/ml最适合排除急性CHF,阴性预测值为99%。NT-proBNP升高是急性CHF最终诊断的最强独立预测因素(比值比44,95%置信区间21.0至91.0,p<0.0001)。单独进行NT-proBNP检测在诊断急性CHF方面优于单独的临床判断(p = 0.006);NT-proBNP加临床判断优于单独的NT-proBNP或临床判断。在急诊科环境中,NT-proBNP检测是标准临床评估中用于识别和排除急性CHF的一项有价值的补充。

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