4.5 Article

Very early diagnosis of chest pain by point-of-care testing: comparison of the diagnostic efficiency of a panel of cardiac biomarkers compared with troponin measurement alone in the RATPAC trial

Journal

HEART
Volume 98, Issue 4, Pages 312-318

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/heartjnl-2011-300723

Keywords

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Funding

  1. National Institute for Health Research (NIHR) [06/302/19]
  2. University of Sheffield
  3. National Institute for Health Research [09/22/16, 06/302/19] Funding Source: researchfish

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Objective To assess the impact of triple marker testing on patient management and the diagnostic efficiencies of different biomarker strategies examined. Design A prospective randomised trial of triple marker testing by point-of-care testing (POCT); the Randomised Assessment of Panel Assay of Cardiac markers (RATPAC) study. Setting Six emergency departments. Patients Low-risk patients presenting with chest pain to diagnostic assessment with a cardiac panel measured by POCT or to diagnosis when biomarker measurement was based on central laboratory testing. Interventions 1125 patients were randomly assigned to POCT measurement of the triple marker panel of cardiac troponin I (cTnI), myoglobin and the MB isoenzyme of creatine kinase (CK-MB) on admission and 90 min from admission. Main Outcome Measures Myocardial infarction (MI) was defined by the universal definition of MI. The following diagnostic strategies were compared by receiver operator characteristic (ROC) curve analysis and comparison of area under the curve (AUC): individual marker values, change (Delta) in CK-MB and myoglobin and the combination of presentation or 90 min value plus Delta value. Results Admission sample measurement of cTnI was the most diagnostically efficient AUC 0.96 (0.93-0.98) with areas under the ROC curve statistically significantly greater than CK-MB 0.85 (0.80-0.90) and myoglobin 0.75 (0.68-0.81). At 90 min cTnI measurement had the highest AUC 0.95 (0.87-1.00) but was statistically significantly different only from Delta myoglobin and Delta CK-MB. Conclusion Measurement of cTnI alone is sufficient for diagnosis. Measurement of a marker panel does not facilitate diagnosis.

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