scholarly journals Cardiac Troponin-T in Unstable Angina Pectoris

1996 ◽  
Vol 6 (2) ◽  
pp. 178-181
Author(s):  
Ziya Günal ◽  
Bilgin Özmen ◽  
Sinan Erten ◽  
Aysel Akgüner ◽  
Bülent Ildız ◽  
...  
1995 ◽  
Vol 76 (12) ◽  
pp. 970-972 ◽  
Author(s):  
Alan H.B. Wu ◽  
Syed A. Abbas ◽  
Sol Green ◽  
Lisa Pearsall ◽  
Sajid Dhakam ◽  
...  

2018 ◽  
Vol 122 (7) ◽  
pp. 1142-1147 ◽  
Author(s):  
Vegard Vavik ◽  
Eva Kristine Ringdal Pedersen ◽  
Gard Frodahl Tveitevåg Svingen ◽  
Grethe Seppola Tell ◽  
Hall Schartum-Hansen ◽  
...  

1998 ◽  
Vol 135 (2) ◽  
pp. 281-286 ◽  
Author(s):  
Wolfram Terres ◽  
Petra Kümmel ◽  
Anja Sudrow ◽  
Hilke Reuterb ◽  
Thomas Meinertz ◽  
...  

2010 ◽  
Vol 56 (4) ◽  
pp. 642-650 ◽  
Author(s):  
Evangelos Giannitsis ◽  
Meike Becker ◽  
Kerstin Kurz ◽  
Georg Hess ◽  
Dietmar Zdunek ◽  
...  

Abstract Background: We sought to determine the diagnostic performance of the new high-sensitivity cardiac troponin T (hs-cTnT) assay for early detection of non–ST-segment myocardial infarction (NSTEMI) in patients with acute coronary syndrome. Methods: We enrolled patients with retrospectively confirmed unstable angina or NSTEMI and an initially negative cTnT concentration and compared the performance of baseline concentrations and serial changes in concentration within 3 and 6 h. Percentage change criteria included ≥20% δ change and ROC-optimized value. Results: Based on the standard fourth-generation cTnT result of ≥0.03 μg/L, an evolving NSTEMI was diagnosed in 26 patients, and 31 patients were classified as having unstable angina. With the use of the hs-cTnT assay at the 99th-percentile cutoff, the percentage of NSTEMI cases detected increased gradually from 61.5% on presentation to 100% within 6 h, and the overall number of MI diagnoses increased by 34.6% (35 vs 26 cases). A δ change ≥20% or ≥ROC-optimized value of >117% within 3 h or ≥243% within 6 h yielded a specificity of 100% at sensitivities between 69% and 76%. The standard cTnT at the 99th percentile was less sensitive than hs-cTnT for early diagnosis of MI on presentation, and follow-up samples obtained within the initial 3 h demonstrated very low specificity of cTnT compared with hs-cTnT. Conclusions: The high-sensitivity cTnT assay increases the number of NSTEMI diagnoses and enables earlier detection of evolving NSTEMI. A doubling of the hs-cTnT concentration within 3 h in the presence of a second concentration ≥99th percentile is associated with a positive predictive value of 100% and a negative predictive value of 88%.


1997 ◽  
Vol 80 (4) ◽  
pp. 510-511 ◽  
Author(s):  
Trent L Pettijohn ◽  
Thomas Doyle ◽  
A. Michael Spiekerman ◽  
Linley E Watson ◽  
Mark W Riggs ◽  
...  

2000 ◽  
Vol 83 (02) ◽  
pp. 224-228 ◽  
Author(s):  
Margit Bardorff ◽  
Sybille Schweikart ◽  
Uwe Wiegand ◽  
Markus Kampmann ◽  
Hugo Katus ◽  
...  

SummaryThe present study sought to determine the incidence of increased procoagulant activity in patients with unstable angina (UAP), and to evaluate the relationship between cardiac troponin T (cTnT) and molecular markers of hemostatic activation.We studied 44 patients with UAP further classified by plasma cTnT levels. All patients received an antithrombotic therapy consisting of therapeutic doses of unfractionated heparin and acetylsalicylic acid. Quantitative levels of cTnT and plasma concentrations of fibrin monomers (FM), prothrombin fragments F1+2, thrombin antithrombin III complexes (TAT), plasminogen and α2-antiplasmin were sampled serially within the first 48 h.Increased plasma concentrations of FM were detected in 45.5% of patients and were more frequently present among those with cTnT concentrations >0.1 ng/ml (13 of 18 vs 7 of 26 patients, p = 0.003). In these patients, mean plasma concentrations of FM were significantly higher than in patients with cTnT <0.1 ng/ml (7.93 ± 2.3 vs 3.12 ± 0.6 µg/ml, p = 0.02). There was a close relationship between plasma levels of cTnT and FM (r = 0.74, p <0.004), prothrombin fragments F1+2 (r = 0.71, p = 0.046) and a trend to significance was noted for TAT (r = 0.42, p = 0.055). No significant correlation was observed with markers of the fibrinolytic system (plasminogen and α2-antiplasmin). Plasma levels of cTnT >0.1 ng/ml identified a concomitant increase of hemostatic markers with a sensitivity, specificity and positive predictive value of 65, 79, and 72% for FM, 63, 76, and 67% for prothrombin fragments F1+2, and 58, 66, and 39% for TAT, respectively.In patients with UAP, cTnT identifies patients with increased procoagulant activity and is closely related to plasma levels of molecular markers of hemostatic activation. Therefore, cTnT alone or in combination with one of these markers may be helpful to identify patients requiring more potent antithrombin or antiplatelet therapy.


2020 ◽  
Vol 127 ◽  
pp. 30-35
Author(s):  
Vegard Vavik ◽  
Eva Kristine Ringdal Pedersen ◽  
Gard FT Svingen ◽  
Eivind Solheim ◽  
Kristin Moberg Aakre ◽  
...  

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