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Updated: Apr 1, 2026

Signal Acquisition, Score Interpretation, and Economics of a Non-Invasive Point-of-Care Test for Coronary Artery Disease
Published on: August 9, 2024
Diagnostic yield of second-line functional imaging after an abnormal coronary computed tomography angiography: an
Laust D Rasmussen1,2, Roel Hoek3, Jelmer Westra4
1Department of Cardiology, Gødstrup Hospital, Hospitalsparken 15, Herning DK-7400, Denmark.
Aims:
Second-line functional imaging is recommended following an abnormal coronary computed tomography angiography (CCTA). However, evidence guiding the choice of imaging modality is limited. We assessed the diagnostic performance of second-line functional imaging using different invasive reference standards.
Methods And Results:
We conducted an individual patient-data meta-analysis of seven prospective diagnostic studies including 1410 patients (mean age 62 ± 8.1 years, 67% male) with abnormal CCTA [≥50% diameter stenosis (DS)], who underwent second-line functional imaging tests (dobutamine stress ECHO, SPECT, CMR, and/or PET) followed by invasive angiography with fractional flow reserve (FFR) and quantitative coronary angiography (QCA). Haemodynamically obstructive coronary artery disease (CAD) was defined as invasive FFR ≤0.80 or >90% visual DS; anatomically severe CAD as ≥70% DS by QCA. Pooled and per test, 904/1906 (47.2%) functional imaging tests had haemodynamically obstructive CAD, and 504/1906 (26.3%) functional imaging tests had anatomically severe CAD. In total, 730/1906 (38.3%) functional imaging tests were abnormal. Pooled sensitivity and specificity were 63% and 84% for haemodynamically obstructive CAD, and 81% and 77% for anatomically severe CAD. Findings were generally stable across sex and age. More advanced second-line functional imaging tests showed higher sensitivities, but lower specificities compared to less advanced techniques.
Conclusion:
Second-line functional imaging after an abnormal CCTA enables identification of patients with anatomically severe CAD. In contrast, moderate stenoses (<70% DS) with FFR ≤0.80 do not consistently result in myocardial ischaemia detectable by functional imaging tests. Substantial diagnostic accuracy differences were found between non-invasive diagnostic test which need further investigation.
Clinical Trial Identifiers:
NCT02264717, NCT03481712, NCT04707859, NCT01521468.
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