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Cardiac Troponin Thresholds and Kinetics to Differentiate Myocardial Injury and Myocardial Infarction.

Wereski, R; Kimenai, DM; Taggart, C; Doudesis, D; Lee, KK; Lowry, MTH; Bularga, A; Lowe, DJ; Fujisawa, T; Apple, FS; et al. Wereski, R; Kimenai, DM; Taggart, C; Doudesis, D; Lee, KK; Lowry, MTH; Bularga, A; Lowe, DJ; Fujisawa, T; Apple, FS; Collinson, PO; Anand, A; Chapman, AR; Mills, NL (2021) Cardiac Troponin Thresholds and Kinetics to Differentiate Myocardial Injury and Myocardial Infarction. Circulation, 144 (7). pp. 528-538. ISSN 1524-4539 https://doi.org/10.1161/CIRCULATIONAHA.121.054302
SGUL Authors: Collinson, Paul

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Abstract

BACKGROUND: Although the 99th percentile is the recommended diagnostic threshold for myocardial infarction, some guidelines also advocate the use of higher troponin thresholds to rule in myocardial infarction at presentation. It is unclear whether the magnitude or change in troponin concentration can differentiate causes of myocardial injury and infarction in practice. METHODS: In a secondary analysis of a multicenter randomized controlled trial, we identified 46 092 consecutive patients presenting with suspected acute coronary syndrome without ST-segment-elevation myocardial infarction. High-sensitivity cardiac troponin I concentrations at presentation and on serial testing were compared between patients with myocardial injury and infarction. The positive predictive value and specificity were determined at the sex-specific 99th percentile upper reference limit and rule-in thresholds of 64 ng/L and 5-fold of the upper reference limit for a diagnosis of type 1 myocardial infarction. RESULTS: Troponin was above the 99th percentile in 8188 patients (18%). The diagnosis was type 1 or type 2 myocardial infarction in 50% and 14% and acute or chronic myocardial injury in 20% and 16%, respectively. Troponin concentrations were similar at presentation in type 1 (median [25th-75th percentile] 91 [30-493] ng/L) and type 2 (50 [22-147] ng/L) myocardial infarction and in acute (50 [26-134] ng/L) and chronic (51 [31-130] ng/L) myocardial injury. The 99th percentile and rule-in thresholds of 64 ng/L and 5-fold upper reference limit gave a positive predictive value of 57% (95% CI, 56%-58%), 59% (58%-61%), and 62% (60%-64%) and a specificity of 96% (96%-96%), 96% (96%-96%), and 98% (97%-98%), respectively. The absolute, relative, and rate of change in troponin concentration were highest in patients with type 1 myocardial infarction (P<0.001 for all). Discrimination improved when troponin concentration and change in troponin were combined compared with troponin concentration at presentation alone (area under the curve, 0.661 [0.642-0.680] versus 0.613 [0.594-0.633]). CONCLUSIONS: Although we observed important differences in the kinetics, cardiac troponin concentrations at presentation are insufficient to distinguish type 1 myocardial infarction from other causes of myocardial injury or infarction in practice and should not guide management decisions in isolation. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01852123.

Item Type: Article
Additional Information: © 2021 The Authors. Circulation is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited.
Keywords: kinetics, myocardial infarction, predictive value of tests, troponin, PPV, pathways, rule-in, thresholds, Cardiovascular System & Hematology, 1103 Clinical Sciences, 1102 Cardiorespiratory Medicine and Haematology, 1117 Public Health and Health Services
SGUL Research Institute / Research Centre: Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Circulation
ISSN: 1524-4539
Language: eng
Dates:
DateEvent
17 August 2021Published
25 June 2021Published Online
9 June 2021Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
SP/12/10/29922British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
MR/V007017/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/V007254/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MR/N013166/1Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
FS/18/25/33454British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
HDR-5012Health Data Research UKUNSPECIFIED
SGL021/1075Academy of Medical Scienceshttp://dx.doi.org/10.13039/501100000691
FS/16/14/32023British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
RG/20/10/34966British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
RE/18/5/34216British Heart Foundationhttp://dx.doi.org/10.13039/501100000274
PubMed ID: 34167318
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/113468
Publisher's version: https://doi.org/10.1161/CIRCULATIONAHA.121.054302

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