Use of the HEART Pathway with high sensitivity cardiac troponins: A secondary analysis
Simon A Mahler1, Jason P Stopyra1, Fred S Apple2
1Department of Emergency Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Insights
The HEART Pathway demonstrates 100% sensitivity for major adverse cardiac events (MACE) when using either cardiac troponin I (cTnI) or high-sensitivity troponin I (hs-cTnI). High-sensitivity troponin T (hs-cTnT) was associated with a missed MACE event.
Area of Science:
- Cardiology
- Biomarker Analysis
- Clinical Diagnostics
Background:
- The HEART Pathway utilizes cardiac troponin I (cTnI) for early detection of major adverse cardiac events (MACE).
- Integration of high-sensitivity troponin (hs-cTn) assays into the HEART Pathway requires evaluation.
Purpose of the Study:
- To compare the diagnostic performance of the HEART Pathway using high-sensitivity troponin I (hs-cTnI), high-sensitivity troponin T (hs-cTnT), and conventional cTnI.
- To assess early discharge rates and test characteristics for MACE within 30 days.
Main Methods:
- Secondary analysis of a HEART Pathway randomized controlled trial cohort.
- Risk stratification using serial cTnI (Siemens TnI-Ultra) and 3-hour hs-cTnI (Abbott) or hs-cTnT (Roche).
- Calculation of sensitivity, specificity, negative predictive value (NPV), and early discharge rate for MACE.
Main Results:
- No significant difference in test characteristics between cTnI and hs-cTnI HEART Pathway protocols; both achieved 100% sensitivity and NPV.
- hs-cTnI and cTnI protocols yielded identical specificity (49%) and early discharge rates (45%).
- The hs-cTnT HEART Pathway protocol resulted in one missed MACE event (myocardial infarction), with 91% sensitivity and 98% NPV.
Conclusions:
- The HEART Pathway maintains excellent test characteristics, including 100% sensitivity and NPV, when employing hs-cTnI instead of cTnI.
- Use of hs-cTnT in the HEART Pathway is associated with a potential reduction in sensitivity for detecting MACE.
- Both cTnI and hs-cTnI are suitable for the HEART Pathway, supporting early patient discharge while ensuring high sensitivity for MACE.
Objectives:
The HEART Pathway combines a decision aid and serial contemporary cardiac troponin I (cTnI) measures to achieve >99% sensitivity for major adverse cardiac events (MACE) at 30days and early discharge rates >20%. However, the impact of integrating high-sensitivity troponin (hs-cTn) measures into the HEART Pathway has yet to be determined. In this analysis we compare test characteristics of the HEART Pathway using hs-cTnI, hs-cTnT, or cTnI.
Design & Methods:
A secondary analysis of participants enrolled in the HEART Pathway RCT was conducted. Each patient was risk stratified by the cTn-HEART Pathway (Siemens TnI-Ultra at 0- and 3-h) and a hs-cTn-HEART Pathway using hs-cTnI (Abbott) or hs-cTnT (Roche) at 3-h. The early discharge rate, sensitivity, specificity, and negative predictive value (NPV) for MACE (death, myocardial infarction, or coronary revascularization) at 30days were calculated.
Results:
hs-cTnI measures were available on 133 patients. MACE occurred in 11/133 (8%) of these patients. Test characteristics for the HEART Pathway using serial cTnI vs 3hour hs-cTnI were the same: sensitivity (100%, 95%CI: 72-100%), specificity (49%, 95%CI: 40-58%), NPV (100%, 95%CI: 94-100%), and early discharge rate (45%, 95%CI: 37-54%). The HEART Pathway using hs-cTnT missed one MACE event (myocardial infarction): sensitivity (91%, 95%CI: 59-100%), specificity (48%, 95%CI: 39-57%), NPV (98%, 95%CI: 91-100%), and early discharge rate (45%, 95%CI: 37-54%).
Conclusions:
There was no difference in the test characteristics of the HEART Pathway whether using cTnI or hs-cTnI, with both achieving 100% sensitivity and NPV. Use of hs-cTnT with the HEART Pathway was associated with one missed MACE.
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