Diagnostic performance of a rapid, novel, whole blood, point of care high-sensitivity cardiac troponin I assay for myocardial infarction

Abstract

BackgroundWe evaluated the diagnostic performance of a whole blood, point of care (POC) high-sensitivity cardiac troponin I (hs-cTnI) assay for myocardial infarction (MI) compared to central laboratory assays. MethodsConsecutive patients presenting to the emergency department with symptoms of ischemia were studied. Serial hs-cTnI testing was based on clinical indication at presentation. Parallel measurements were made using fresh whole blood on Siemens Atellica VTLi POC assay, EDTA plasma on Abbott ARCHITECT i2000 used in practice, and heparin plasma on Siemens Atellica. MI was determined according to the Fourth Universal Definition of MI using 99th percentiles. Sensitivities and negative predictive values (NPV) were calculated using 99th percentile URLs. Results1089 Patients, 418 females and 671 males, were enrolled. There were 91 (8.4%) MIs. At baseline (0 h), POC hs-cTnI assay had a sensitivity of 65.7% (95% CI 47.8–80.9) for females and 67.9% (54.0–79.7) for males and NPV of 96.4% (93.9–98.1) for females and 96.7% (94.9–98.0) for males. At 2 h, sensitivity improved to 82.9% (66.4–93.4) for females and 80.4% (67.6–89.8) for males, while NPV improved to 98.2% (96.1–99.3) and 97.9% (96.3–99.0), respectively. For central laboratory assays, comparable diagnostics were observed at 2 h: females - sensitivity 94.3% (80.8–99.3) for ARCHITECT and 79.4% (62.1–91.3) for Atellica, and NPV 99.3% (97.6–99.9) and 98.0% (95.8–99.2), respectively; males - sensitivity 87.5% (75.9–94.8) for ARCHITECT and 80.4% (67.6–89.8) for Atellica, NPVs of 98.7% (97.3–99.5) and 97.9% (96.3–99.0), respectively. ConclusionsThe POC, whole blood Atellica VTLi hs-cTnI assay demonstrated comparable diagnostic accuracy for MI to central laboratory assays using 99th percentiles.