Effect of Acute Coronary Syndrome Probability on Diagnostic and Prognostic Performance of High-Sensitivity Cardiac Troponin

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Effect of Acute Coronary Syndrome Probability on Diagnostic and Prognostic Performance of High-Sensitivity Cardiac Troponin. / Badertscher, Patrick; Boeddinghaus, Jasper; Nestelberger, Thomas; Twerenbold, Raphael; Wildi, Karin; Sabti, Zaid; Puelacher, Christian; Rubini Giménez, Maria; Pfäffli, Julian; Flores, Dayana; du Fay de Lavallaz, Jeanne; Miró, Òscar; Martin-Sanchez, F Javier; Morawiec, Beata; Lohrmann, Jens; Buser, Andreas; Keller, Dagmar I; Geigy, Nicolas; Reichlin, Tobias; Mueller, Christian.

In: CLIN CHEM, Vol. 64, No. 3, 03.2018, p. 515-525.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Badertscher, P, Boeddinghaus, J, Nestelberger, T, Twerenbold, R, Wildi, K, Sabti, Z, Puelacher, C, Rubini Giménez, M, Pfäffli, J, Flores, D, du Fay de Lavallaz, J, Miró, Ò, Martin-Sanchez, FJ, Morawiec, B, Lohrmann, J, Buser, A, Keller, DI, Geigy, N, Reichlin, T & Mueller, C 2018, 'Effect of Acute Coronary Syndrome Probability on Diagnostic and Prognostic Performance of High-Sensitivity Cardiac Troponin', CLIN CHEM, vol. 64, no. 3, pp. 515-525. https://doi.org/10.1373/clinchem.2017.279513

APA

Badertscher, P., Boeddinghaus, J., Nestelberger, T., Twerenbold, R., Wildi, K., Sabti, Z., Puelacher, C., Rubini Giménez, M., Pfäffli, J., Flores, D., du Fay de Lavallaz, J., Miró, Ò., Martin-Sanchez, F. J., Morawiec, B., Lohrmann, J., Buser, A., Keller, D. I., Geigy, N., Reichlin, T., & Mueller, C. (2018). Effect of Acute Coronary Syndrome Probability on Diagnostic and Prognostic Performance of High-Sensitivity Cardiac Troponin. CLIN CHEM, 64(3), 515-525. https://doi.org/10.1373/clinchem.2017.279513

Vancouver

Bibtex

@article{8227732f79134dbfa0b527ee0bc1bd9b,
title = "Effect of Acute Coronary Syndrome Probability on Diagnostic and Prognostic Performance of High-Sensitivity Cardiac Troponin",
abstract = "BACKGROUND: There is concern that high-sensitivity cardiac troponin (hs-cTn) may have low diagnostic accuracy in patients with low acute coronary syndrome (ACS) probability.METHODS: We prospectively stratified patients presenting with acute chest discomfort to the emergency department (ED) into 3 groups according to their probability for ACS as assessed by the treating ED physician using a visual analog scale: ≤10%, 11% to 79%, and ≥80%, reviewing all information available at 90 min. hs-cTnT and hs-cTnI concentrations were determined in a blinded fashion. Two independent cardiologists adjudicated the final diagnosis.RESULTS: Among 3828 patients eligible for analysis, 1189 patients had low (≤10%) probability for ACS. The incidence of non-ST-segment elevation myocardial infarction (NSTEMI) increased from 1.3% to 12.2% and 54.8% in patients with low, intermediate, and high ACS probability, respectively. The positive predictive value of hs-cTnT and hs-cTnI was low in patients with low ACS probability and increased with the incidence of NSTEMI, whereas the diagnostic accuracy of hs-cTnT and hs-cTnI for NSTEMI as quantified by the area under the curve (AUC) was very high and comparable among all 3 strata, e.g., AUC hs-cTnI, 0.96 (95% CI, 0.94-0.97); 0.87 (95% CI, 0.85-0.89); and 0.89 (95% CI, 0.87-0.92), respectively. Findings were validated using bootstrap analysis as an alternative methodology to define ACS probability. Similarly, higher hs-cTnT/I concentrations independently predicted all-cause mortality within 2 years (e.g., hs-cTnT hazard ratio, 1.39; 95% CI, 1.27-1.52), irrespective of ACS probability.CONCLUSIONS: Diagnostic and prognostic accuracy and utility of hs-cTnT and hs-cTnI remain high in patients with acute chest discomfort and low ACS probability.ClinicalTrials.gov Identifier: NCT00470587.",
keywords = "Acute Coronary Syndrome/blood, Adult, Aged, Biomarkers/blood, Female, Humans, Incidence, Male, Middle Aged, Myocardial Infarction/blood, Probability, Sensitivity and Specificity, Troponin I/blood, Troponin T/blood",
author = "Patrick Badertscher and Jasper Boeddinghaus and Thomas Nestelberger and Raphael Twerenbold and Karin Wildi and Zaid Sabti and Christian Puelacher and {Rubini Gim{\'e}nez}, Maria and Julian Pf{\"a}ffli and Dayana Flores and {du Fay de Lavallaz}, Jeanne and {\`O}scar Mir{\'o} and Martin-Sanchez, {F Javier} and Beata Morawiec and Jens Lohrmann and Andreas Buser and Keller, {Dagmar I} and Nicolas Geigy and Tobias Reichlin and Christian Mueller",
note = "{\textcopyright} 2017 American Association for Clinical Chemistry.",
year = "2018",
month = mar,
doi = "10.1373/clinchem.2017.279513",
language = "English",
volume = "64",
pages = "515--525",
journal = "CLIN CHEM",
issn = "0009-9147",
publisher = "American Association for Clinical Chemistry Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Effect of Acute Coronary Syndrome Probability on Diagnostic and Prognostic Performance of High-Sensitivity Cardiac Troponin

AU - Badertscher, Patrick

AU - Boeddinghaus, Jasper

AU - Nestelberger, Thomas

AU - Twerenbold, Raphael

AU - Wildi, Karin

AU - Sabti, Zaid

AU - Puelacher, Christian

AU - Rubini Giménez, Maria

AU - Pfäffli, Julian

AU - Flores, Dayana

AU - du Fay de Lavallaz, Jeanne

AU - Miró, Òscar

AU - Martin-Sanchez, F Javier

AU - Morawiec, Beata

AU - Lohrmann, Jens

AU - Buser, Andreas

AU - Keller, Dagmar I

AU - Geigy, Nicolas

AU - Reichlin, Tobias

AU - Mueller, Christian

N1 - © 2017 American Association for Clinical Chemistry.

PY - 2018/3

Y1 - 2018/3

N2 - BACKGROUND: There is concern that high-sensitivity cardiac troponin (hs-cTn) may have low diagnostic accuracy in patients with low acute coronary syndrome (ACS) probability.METHODS: We prospectively stratified patients presenting with acute chest discomfort to the emergency department (ED) into 3 groups according to their probability for ACS as assessed by the treating ED physician using a visual analog scale: ≤10%, 11% to 79%, and ≥80%, reviewing all information available at 90 min. hs-cTnT and hs-cTnI concentrations were determined in a blinded fashion. Two independent cardiologists adjudicated the final diagnosis.RESULTS: Among 3828 patients eligible for analysis, 1189 patients had low (≤10%) probability for ACS. The incidence of non-ST-segment elevation myocardial infarction (NSTEMI) increased from 1.3% to 12.2% and 54.8% in patients with low, intermediate, and high ACS probability, respectively. The positive predictive value of hs-cTnT and hs-cTnI was low in patients with low ACS probability and increased with the incidence of NSTEMI, whereas the diagnostic accuracy of hs-cTnT and hs-cTnI for NSTEMI as quantified by the area under the curve (AUC) was very high and comparable among all 3 strata, e.g., AUC hs-cTnI, 0.96 (95% CI, 0.94-0.97); 0.87 (95% CI, 0.85-0.89); and 0.89 (95% CI, 0.87-0.92), respectively. Findings were validated using bootstrap analysis as an alternative methodology to define ACS probability. Similarly, higher hs-cTnT/I concentrations independently predicted all-cause mortality within 2 years (e.g., hs-cTnT hazard ratio, 1.39; 95% CI, 1.27-1.52), irrespective of ACS probability.CONCLUSIONS: Diagnostic and prognostic accuracy and utility of hs-cTnT and hs-cTnI remain high in patients with acute chest discomfort and low ACS probability.ClinicalTrials.gov Identifier: NCT00470587.

AB - BACKGROUND: There is concern that high-sensitivity cardiac troponin (hs-cTn) may have low diagnostic accuracy in patients with low acute coronary syndrome (ACS) probability.METHODS: We prospectively stratified patients presenting with acute chest discomfort to the emergency department (ED) into 3 groups according to their probability for ACS as assessed by the treating ED physician using a visual analog scale: ≤10%, 11% to 79%, and ≥80%, reviewing all information available at 90 min. hs-cTnT and hs-cTnI concentrations were determined in a blinded fashion. Two independent cardiologists adjudicated the final diagnosis.RESULTS: Among 3828 patients eligible for analysis, 1189 patients had low (≤10%) probability for ACS. The incidence of non-ST-segment elevation myocardial infarction (NSTEMI) increased from 1.3% to 12.2% and 54.8% in patients with low, intermediate, and high ACS probability, respectively. The positive predictive value of hs-cTnT and hs-cTnI was low in patients with low ACS probability and increased with the incidence of NSTEMI, whereas the diagnostic accuracy of hs-cTnT and hs-cTnI for NSTEMI as quantified by the area under the curve (AUC) was very high and comparable among all 3 strata, e.g., AUC hs-cTnI, 0.96 (95% CI, 0.94-0.97); 0.87 (95% CI, 0.85-0.89); and 0.89 (95% CI, 0.87-0.92), respectively. Findings were validated using bootstrap analysis as an alternative methodology to define ACS probability. Similarly, higher hs-cTnT/I concentrations independently predicted all-cause mortality within 2 years (e.g., hs-cTnT hazard ratio, 1.39; 95% CI, 1.27-1.52), irrespective of ACS probability.CONCLUSIONS: Diagnostic and prognostic accuracy and utility of hs-cTnT and hs-cTnI remain high in patients with acute chest discomfort and low ACS probability.ClinicalTrials.gov Identifier: NCT00470587.

KW - Acute Coronary Syndrome/blood

KW - Adult

KW - Aged

KW - Biomarkers/blood

KW - Female

KW - Humans

KW - Incidence

KW - Male

KW - Middle Aged

KW - Myocardial Infarction/blood

KW - Probability

KW - Sensitivity and Specificity

KW - Troponin I/blood

KW - Troponin T/blood

U2 - 10.1373/clinchem.2017.279513

DO - 10.1373/clinchem.2017.279513

M3 - SCORING: Journal article

C2 - 29343534

VL - 64

SP - 515

EP - 525

JO - CLIN CHEM

JF - CLIN CHEM

SN - 0009-9147

IS - 3

ER -