It should be noted that, while the ADAPT can be used with contemporary cardiac troponin assays, it performs better with high-sensitivity cardiac troponin assays (hs-cTn), especially for the Fairly Low Risk category.
In the derivation study of Than et al. (2012) using contemporary (not high-sensitivity) troponin assays (Abbott ARCHITECT cTnI assay and DxI Access Accu cTnI assay)
Low Risk: 1 out of 392 patients had a Major Adverse Cardiac Event within 30 days (0.26% risk)
Fairly Low Risk: 8 out of 367 patients had a Major Adverse Cardiac Event within 30 days (2.18% risk)
High Risk: 293 out of 1216 patients had a Major Adverse Cardiac Event within 30 days (24.1% risk)
In a Validation study by Cullen et al. (2013) using the ARCHITECT High Sensitive STAT Troponin-I assay
Low Risk: 0 out of 550 patients had a Major Adverse Cardiac Event within 30 days (0% risk)
Fairly Low Risk: 3 out of 479 patients had a Major Adverse Cardiac Event within 30 days (0.63% risk)
High Risk: 400 out of 1515 patients had a Major Adverse Cardiac Event within 30 days (26.4% risk)
A pooled analysis of multiple studies containing 3163 patients with a total of 487 events found a sensitivity of 99.79% and a negative predictive value of 99.86% for the Low Risk category
A pooled analysis of multiple studies exclusively using hs-cTn assays containing 4021 patients with a total of 646 events found a sensitivity of 99.23% and a negative predictive value of 99.68% for the combined categories of Low Risk and Fairly Low Risk.
Calculations alone should never dictate patient care, and are no substitute for professional judgement. See our full disclaimer.
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