2014
DOI: 10.1016/j.ijcard.2014.09.026
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Comparison of new point-of-care troponin assay with high sensitivity troponin in diagnosing myocardial infarction

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Cited by 30 publications
(21 citation statements)
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“…These findings are consistent with the results of Aldous et, al. which demonstrated no significant difference in the sensitivity or specificity for MACE of an ADP when using a new generation point of care cTnI versus a hs-cTnI assay [27]. The finding from our study are significant given the current lack of availability of hs-cTn assays in the US and the concern that lack of these assays significantly hampers our ability to perform chest pain risk stratification.…”
Section: Discussionmentioning
confidence: 69%
“…These findings are consistent with the results of Aldous et, al. which demonstrated no significant difference in the sensitivity or specificity for MACE of an ADP when using a new generation point of care cTnI versus a hs-cTnI assay [27]. The finding from our study are significant given the current lack of availability of hs-cTn assays in the US and the concern that lack of these assays significantly hampers our ability to perform chest pain risk stratification.…”
Section: Discussionmentioning
confidence: 69%
“…Newer POC assays have been developed specifically for the troponin I subunit that are improved from older testing versions. 4,5 Similar studies have been carried out, but there is a divergence in results reported when POC testing is compared to laboratory testing, with most studies stating that POC testing is inferior. 6,7 Loten et al 8 compared the results in terms of experienced and inexperienced operators with their central laboratory and concluded the POC produced similar results for troponin levels.…”
Section: Discussionmentioning
confidence: 95%
“…41 Major adverse cardiac events at 30 days: death (excluding clearly noncardiac), cardiac arrest, acute myocardial infarction, emergency revascularization procedure, cardiogenic shock, ventricular arrhythmia requiring intervention, and high-degree atrioventricular block requiring intervention. †Aldous et al 42 Major adverse cardiac events at 30 days: defined as acute myocardial infarction, cardiac death, cardiogenic shock, emergency revascularization, ventricular arrhythmia or high degree heart block requiring treatment by 30 days post presentation. ‡Meller et al 43 Major adverse cardiac events at 30 days: defined as death (unless clearly noncardiac), cardiac arrest, urgent coronary revascularization, cardiogenic shock, ventricular arrhythmia needing intervention, high-degree atrioventricular block needing intervention, and acute myocardial infarction adjudicated as recommended by the Universal Definition.…”
Section: Advantages and Disadvantages Of High-sensitivity Cardiac Tromentioning
confidence: 99%