Prognostic value of combining high sensitive troponin T and N-terminal pro B-type natriuretic peptide in chest pain patients with no persistent ST-elevation

被引:14
|
作者
Melki, Dina [1 ]
Lind, Suzanne [2 ]
Agewall, Stefan [3 ,4 ]
Jernberg, Tomas [1 ]
机构
[1] Cardiol Sect, Dept Med, Huddinge, Sweden
[2] Karolinska Univ Hosp, Karolinska Inst, Div Clin Chem, Dept Lab Med, S-14186 Stockholm, Sweden
[3] Oslo Univ Hosp, Dept Cardiol, Oslo, Norway
[4] Univ Oslo, Oslo, Norway
关键词
Chest pain; Myocardial infarction; Troponin; Natriuretic peptide; Prognosis; ACUTE CORONARY SYNDROMES; MYOCARDIAL-INFARCTION; ASSAY; PREDICTION; PERFORMANCE; MORTALITY;
D O I
10.1016/j.cca.2012.02.008
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The aim was to examine whether high sensitive troponin T (Hs-TnT) is better than conventional troponins to risk stratify chest pain patients, in particular when applying early serial measurements or combining with natriuretic peptides. Samples were obtained on admission and after 2 h in 231 chest pain patients who were followed for a median time of 22 months. Troponin levels were determined by Hs-TnT, conventional TnT (Roche Diagnostics) and troponin I (Beckman Coulter) assays. N-terminal pro B-type natriuretic peptide (NT-proBNP) was determined by the assay from Roche Diagnostics. The combined endpoint was death, MI or heart failure. When predefined decision limits were used, Hs-TnT (14 ng/L), TnT (0.04 mu g/L), and TnI (0.06 mu g/L) identified 63%, 46%, and 52% of the patients with positive troponin. In those with negative TnT, Hs-TnT identified 36 patients of whom 19% had subsequent events. In those with negative TnI, Hs-TnT identified 26 patients of whom 23% had subsequent events. After adjusting for differences in baseline characteristics, both Hs-TnT and NT-proBNP were independently associated with short-term (3 months) risk of combined endpoint and long-term risk of death or MI. By combining Hs-TnT and NT-proBNP patients could be divided into low-, intermediate- and high-risk groups. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:933 / 937
页数:5
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