TY - JOUR
T1 - In vitro validation of coronary CT angiography for the evaluation of complex lesions
AU - Collet, Carlos
AU - Onuma, Yoshinobu
AU - Grundeken, Maik J.
AU - Miyazaki, Yosuke
AU - Bittercourt, Marcio
AU - Kitslaar, Pieter
AU - Motoyama, Sadako
AU - Ozaki, Yukio
AU - Asano, Taku
AU - Wentzel, Jolanda J.
AU - Streekstra, Geert J.
AU - Serruys, Patrick W.
AU - De Winter, Robbert J.
AU - Planken, R. Nils
N1 - Publisher Copyright:
© Europa Digital & Publishing 2018. All rights reserved.
PY - 2018/2
Y1 - 2018/2
N2 - Aims: The aim of this study was to assess in vitro the diagnostic accuracy of computed tomography angiography (CTA) for the evaluation of complex coronary lesions. Methods and results: Five Plexiglas phantoms with three bifurcation lesions each were designed to mimic the anatomic variations and fractal phenomena of the coronary tree. In addition, luminal stenoses were scaled up with increases of 10% from 40% to 80%, corresponding to luminal areas ranging from 3.0 mm2 to 0.22 mm2. Third-generation dual-source computed tomography was used. Automated quantitative CTA analysis was performed according to the bifurcation segment model. The primary objective was to determine the diagnostic accuracy of quantitative CTA in assessing bifurcation lesions with the phantoms as a reference. The accuracy of CTA for the assessment of minimal luminal diameter was-0.07 mm (limits of agreement-0.75 to 0.61), for reference vessel diameter 0.19 mm (limits of agreement-0.25 to 0.63) and diameter stenosis 8.2% (limits of agreement-13.2 to 29.5) with no difference regarding the location within the bifurcation (i.e., proximal and distal main vessel and side branch). In stenosis with minimal luminal diameter ≥1 mm, CTA overestimated the lesion severity (bias 0.19 mm, limits of agreement-0.09 to 0.47), whereas in lesions with severe stenosis and minimal luminal diameter ≤1 mm, CTA underestimated the lesion severity (bias-0.48 mm, limits of agreement-0.55 to-0.41). CTA was able to identify the contrastfilled lumen in all degrees of lesion severity. Conclusions: In vitro, CTA is accurate for the evaluation of bifurcation lesions. CTA was able to distinguish contrast-filled lumen even in severe obstructive lesions. These findings require further validation in the clinical setting.
AB - Aims: The aim of this study was to assess in vitro the diagnostic accuracy of computed tomography angiography (CTA) for the evaluation of complex coronary lesions. Methods and results: Five Plexiglas phantoms with three bifurcation lesions each were designed to mimic the anatomic variations and fractal phenomena of the coronary tree. In addition, luminal stenoses were scaled up with increases of 10% from 40% to 80%, corresponding to luminal areas ranging from 3.0 mm2 to 0.22 mm2. Third-generation dual-source computed tomography was used. Automated quantitative CTA analysis was performed according to the bifurcation segment model. The primary objective was to determine the diagnostic accuracy of quantitative CTA in assessing bifurcation lesions with the phantoms as a reference. The accuracy of CTA for the assessment of minimal luminal diameter was-0.07 mm (limits of agreement-0.75 to 0.61), for reference vessel diameter 0.19 mm (limits of agreement-0.25 to 0.63) and diameter stenosis 8.2% (limits of agreement-13.2 to 29.5) with no difference regarding the location within the bifurcation (i.e., proximal and distal main vessel and side branch). In stenosis with minimal luminal diameter ≥1 mm, CTA overestimated the lesion severity (bias 0.19 mm, limits of agreement-0.09 to 0.47), whereas in lesions with severe stenosis and minimal luminal diameter ≤1 mm, CTA underestimated the lesion severity (bias-0.48 mm, limits of agreement-0.55 to-0.41). CTA was able to identify the contrastfilled lumen in all degrees of lesion severity. Conclusions: In vitro, CTA is accurate for the evaluation of bifurcation lesions. CTA was able to distinguish contrast-filled lumen even in severe obstructive lesions. These findings require further validation in the clinical setting.
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U2 - 10.4244/EIJ-D-17-00326
DO - 10.4244/EIJ-D-17-00326
M3 - Article
C2 - 28649954
AN - SCOPUS:85041696830
SN - 1774-024X
VL - 13
SP - e1823-e1830
JO - EuroIntervention
JF - EuroIntervention
IS - 15
ER -