Abstract
Objectives: The aim of this study was to characterize the safety and efficiency of a strategy employing the limit of detection (LoD) of high-sensitivity troponin T (hs-TnT) as a gatekeeper for coronary computed tomography angiography (CCTA) in suspected acute coronary syndrome (ACS) patients in the emergency department (ED). Methods: We included suspected ACS patients who underwent CCTA and were evaluated with hs-TnT. Patients were categorized as below the LoD and at or above the LoD. The primary outcome was 30-day major adverse cardiac events (MACEs), defined as all-cause mortality, ACS, or coronary revascularization. Results: The study population consisted of 177 patients (mean age 55 ± 10 years, 50.3% women), and 16 (9.0%) patients reached the primary outcome. None of the patients died, while 13 had an adjudicated diagnosis of ACS, and 3 underwent elective coronary revascularization. There were 77 patients (44%) with an hs-TnT value below the LoD (MACEs; n = 1 [1.3%]) and 100 (56%) with at or above the LoD levels (MACEs; n = 15 [15%]). None of 67 patients with an hs-TnT value below the LoD and <50% stenosis on CCTA experienced MACEs. Out of the 10 patients with an hs-TnT value below the LoD and ≥50% stenosis on CCTA, 1 patient underwent elective percutaneous coronary revascularization. In patients with an hs-TnT value at or above the LoD, 74 patients had <50% stenosis on CCTA, and 2 patients (3%) were diagnosed with myocardial infarction without obstructive coronary artery disease confirmed on invasive angiography. Thirteen (50%) patients with an hs-TnT value at or above the LoD and ≥50% stenosis on CCTA experienced MACEs (11 ACS and 2 elective percutaneous coronary revascularizations). Conclusion: Our findings support that implementing the LoD of hs-TnT as a gatekeeper may reduce the need for CCTA in suspected ACS patients in the ED.
Original language | English |
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Pages (from-to) | 713-719 |
Number of pages | 7 |
Journal | Cardiology (Switzerland) |
Volume | 146 |
Issue number | 6 |
DOIs | |
Publication status | Published - 1 Dec 2021 |
Bibliographical note
Funding Information:This work was supported by a grant from Erasmus MC and a research grant from the Erasmus MC Thorax Foundation (project grant B4). The sponsor had no role in study design; in the collection, analysis, and interpretation of data; in writing the report; and in the decision to submit the article for publication.
Funding Information:
Koen Nieman was supported by a grant from the Dutch Heart Foundation (NHS 2014T061) and received grants from Siemens Medical Solutions, GE Healthcare, Bayer Healthcare, and HeartFlow outside the submitted work. All the other authors report no relationships relevant to the contents of this study to disclose.
Publisher Copyright:
© 2021