Loading…
Feasibility and diagnostic performance of fractional flow reserve measurement derived from coronary computed tomography angiography in real clinical practice
Non-invasive fractional flow reserve measured by coronary computed tomography angiography (FFR CT ) has demonstrated a high diagnostic accuracy for detecting coronary artery disease (CAD) in selected patients in prior clinical trials. However, feasibility of FFR CT in unselected population have not...
Saved in:
Published in: | International Journal of Cardiovascular Imaging 2017-02, Vol.33 (2), p.271-281 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Non-invasive fractional flow reserve measured by coronary computed tomography angiography (FFR
CT
) has demonstrated a high diagnostic accuracy for detecting coronary artery disease (CAD) in selected patients in prior clinical trials. However, feasibility of FFR
CT
in unselected population have not been fully evaluated. Among 60 consecutive patients who had suspected significant CAD by coronary computed tomography angiography (CCTA) and were planned to undergo invasive coronary angiography, 48 patients were enrolled in this study comparing FFR
CT
with invasive fractional flow reserve (FFR) without any exclusion criteria for the quality of CCTA image. FFR
CT
was measured in a blinded fashion by an independent core laboratory. FFR
CT
value was evaluable in 43 out of 48 (89.6 %) patients with high prevalence of severe calcification in CCTA images [calcium score (CS) >400: 40 %, and CS > 1000: 19 %). Per-vessel FFR
CT
value showed good correlation with invasive FFR value (Spearman’s rank correlation = 0.69, P 1000), per-vessel FFR
CT
value showed a diagnostic performance similar to that in patients with CS ≤ 1000 (Spearman’s rank correlation = 0.81, P |
---|---|
ISSN: | 1569-5794 1573-0743 1875-8312 |
DOI: | 10.1007/s10554-016-0995-9 |