Normal presenting levels of high-sensitivity troponin and myocardial infarction

被引:39
作者
Hoeller, Rebeca [1 ]
Rubini Gimenez, Maria [1 ,2 ]
Reichlin, Tobias [1 ,3 ,4 ]
Twerenbold, Raphael [1 ,5 ]
Zellweger, Christa [1 ]
Moehring, Berit [1 ]
Wildi, Karin [1 ]
Freese, Michael [1 ]
Stelzig, Claudia [1 ]
Hartmann, Beate [1 ]
Stoll, Melanie [1 ]
Mosimann, Tamina [1 ]
Reiter, Miriam [1 ]
Haaf, Philip [1 ]
Mueller, Mira [1 ]
Meller, Bernadette [1 ]
Hochgruber, Thomas [1 ]
Balmelli, Cathrin [1 ]
Sou, Seoung Mann [1 ]
Murray, Karsten [1 ]
Freidank, Heike [6 ]
Steuer, Stephan [7 ]
Minners, Jan [1 ]
Osswald, Stefan [1 ]
Mueller, Christian [1 ]
机构
[1] Univ Basel Hosp, Dept Cardiol, CH-4031 Basel, Switzerland
[2] Parc Salut Mar IMIM UPF CIBERES ISC Iii, Dept Pneumol, Barcelona, Spain
[3] Brigham & Womens Hosp, Dept Med, Div Cardiovasc, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
[5] Univ Herz Zentrum Bad Krozingen, Bad Krozingen, Germany
[6] Univ Basel Hosp, Dept Lab Med, CH-4031 Basel, Switzerland
[7] Spital Lachen, Emergency Dept, Lachen, Switzerland
基金
瑞士国家科学基金会;
关键词
CORONARY ARTERY DISEASE; ACUTE CORONARY SYNDROME; EARLY-DIAGNOSIS; T ASSAY; I ASSAY; NEXT-GENERATION; POPULATION; UTILITY; RISK;
D O I
10.1136/heartjnl-2013-303643
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective To analyse whether levels of high-sensitivity cardiac troponin (hs-cTn) below their respective 99th percentile can be used as a single parameter to rule out acute myocardial infarction (AMI) at presentation. Design Prospective, multicentre study. Main outcome measures We measured hs-cTn using four different methods (hs-cTnT Roche, hs-cTnI Siemens, hs-cTnI Beckman Coulter and hs-cTnI Abbott) in consecutive patients presenting to the emergency department with acute chest pain. Two independent cardiologists adjudicated the final diagnosis. Patients were followed for death or AMI during a mean period of 24months. Results Among 2072 consecutive patients with hs-cTnT measurements available, 21.4% had an adjudicated diagnosis of AMI (sensitivity 89.6%, 95% CI 86.4% to 92.3%, negative predictive value (NPV): 96.5%, 95% CI 95.4% to 97.4%). Among 1180 consecutive patients with hs-cTnI Siemens measurements available, 20.0% had AMI (sensitivity 94.1%, 95% CI 90.3% to 96.7%, NPV: 98.0%, 95% CI: 96.6% to 98.9%). Among 1151 consecutive patients with hs-cTnI Beckman Coulter measurements available, 19.7% had AMI (sensitivity 92.1%, 95% CI 87.8% to 95.2%, NPV: 97.5%, 95% CI 96.0% to 98.5%). Among 1567 consecutive patients with hs-cTnI Abbott measurements available, 20.0% had AMI (sensitivity 77.2%, 95% CI 72.1% to 81.7%, NPV: 94.3%, 95% CI 92.8% to 95.5%). Conclusions Normal hs-cTn levels at presentation should not be used as a single parameter to rule out AMI as 6%-23% of adjudicated AMI cases had normal levels of hs-cTn levels at presentation. Our data highlight the lack of standardisation among hs-cTnI assays resulting in substantial differences in sensitivity and NPV at the 99th percentile.
引用
收藏
页码:1567 / 1572
页数:6
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