Key result
Adding objective cardiac testing to serial troponin I and physician risk assessment did not significantly improve prediction of 30-day AMI or revascularization in women (AUC 0.89 vs 0.85; p=0.053).
Why the study?
Does the addition of objective cardiac testing improve the prediction of 30-day AMI or revascularization in women presenting to the ED with chest pain evaluated with serial troponin I and physician risk assessment?
Observational (n=460)
Yes
Does the addition of objective cardiac testing improve the prediction of 30-day AMI or revascularization in women presenting to the ED with chest pain evaluated with serial troponin I and physician risk assessment?
In women presenting to the ED with chest pain, adding objective cardiac testing to serial troponin I and physician risk assessment does not improve the prediction of 30-day AMI or revascularization and may increase false positives.
Answers are grounded in this paper and cite their sources.
Objective testing adds no predictive value in women; leaves open whether serial troponin and physician assessment alone suffice.
OBJECTIVES: Guidelines recommend that patients presenting to the emergency department (ED) with chest pain who are at low risk for acute coronary syndrome (ACS) receive an objective cardiac evaluation with a stress test or coronary imaging. It is uncertain whether all women derive benefit from this process. The study aim was to determine the incremental value of objective cardiac testing after serial cardiac markers and physician risk assessment. METHODS: Women enrolled in the 18-site Myeloperoxidase in the Diagnosis of Acute Coronary Syndrome (MIDAS) study had serial troponin I measured at time 0 and 90 minutes and physician risk assessment for the presence of ACS. Risk estimates obtained at the time of ED evaluation were dichotomized as high or non-high risk. The primary outcome was the composite of acute myocardial infarction (AMI) or revascularization at 30 days. Logistic regression with receiver operator characteristic (ROC) curves and net reclassification index were used to determine the diagnostic accuracy for the composite outcome of 30-day MI or revascularization for two models: 1) troponin I results and physician risk assessment alone and 2) troponin I results, physician risk assessment, and objective cardiac testing. RESULTS: A total of 460 women with a median age 58 years (interquartile range [IQR] = 48.5 to 68 years) were included, and 32 (6.9%) experienced AMI or revascularization by 30 days. Comparison of the area under the ROC curves (AUC) showed that the addition of objective cardiac testing to the combination of troponin I results and physician risk assessment did not significantly improve prediction of 30-day AMI or revascularization (AUC = 0.85 vs. 0.89; p = .053). Using a threshold of 1%, net reclassification index showed that the addition of objective cardiac testing to troponin I results and physician risk assessment worsened the prediction for 30-day AMI and revascularization. All of the reclassified patients were false positives, with nine (2.1%) patients incorrectly reclassified from <1% risk to ≥ 1% risk of 30-day AMI or revascularization. CONCLUSIONS: In the era of contemporary troponin assays, objective cardiac testing after an ED clinician risk assessment of non-high risk and negative troponin I results at 0 and 90 minutes does not improve the prediction of 30-day AMI or revascularization in women presenting with chest pain or other symptoms of cardiac ischemia.
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Diercks et al. (2013) conducted an observational in Chest pain or symptoms of cardiac ischemia (n=460). Objective cardiac testing vs. Physician risk assessment and serial troponin I alone was evaluated on Composite of acute myocardial infarction (AMI) or revascularization at 30 days (p=0.053). Adding objective cardiac testing to serial troponin I and physician risk assessment did not significantly improve prediction of 30-day AMI or revascularization in women (AUC 0.89 vs 0.85; p=0.053).
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