TY - JOUR
T1 - Software reproducibility of myocardial blood flow and flow reserve quantification in ischemic heart disease
T2 - A 13N-ammonia PET study
AU - Monroy-Gonzalez, Andrea G.
AU - Juarez-Orozco, Luis Eduardo
AU - Han, Chunlei
AU - Vedder, Issi R.
AU - Vállez García, David
AU - Borra, Ronald
AU - Slomka, Piotr J.
AU - Nesterov, Sergey V.
AU - Knuuti, Juhani
AU - Slart, Riemer H.J.A.
AU - Alexanderson-Rosas, Erick
N1 - Funding Information:
This project was supported with public funds of the National Mexican Council of Science and Technology (CONACYT) and the University of Groningen/University Medical Center Groningen (RuG/UMCG). We thank Andres Sanabria Rodríguez for assisting in the PET/CCTA data acquisition.
Publisher Copyright:
© 2019, American Society of Nuclear Cardiology.
PY - 2020/8/1
Y1 - 2020/8/1
N2 - Background: We explored agreement in the quantification of myocardial perfusion by cross-comparison of implemented software packages (SPs) in three distinguishable patient profile populations. Methods: We studied 91 scans of patients divided into 3 subgroups based on their semi-quantitative perfusion findings: patients with normal perfusion, with reversible perfusion defects, and with fixed perfusion defects. Rest myocardial blood flow (MBF), stress MBF, and myocardial flow reserve (MFR) were obtained with QPET, SyngoMBF, and Carimas. Agreement between SPs was considered adequate when a pairwise standardized difference was found to be < 0.20 and its corresponding intraclass correlation coefficient was ≥ 0.75. Results: In patients with normal perfusion, two out of three comparisons of global stress MBF quantifications were outside the limits of agreement. In ischemic patients, all comparisons of global stress MBF and MFR were outside the limits of established agreement. In patients with fixed perfusion defects, all SP comparisons of perfusion quantifications were within the limit of agreement. Regionally, agreement of these perfusion estimates was mostly found for the left anterior descending artery vascular territory. Conclusion: Reversible defects demonstrated the worst agreement in global stress MBF and MFR and discrepancies showed to be regional dependent. Reproducibility between SPs should not be assumed.
AB - Background: We explored agreement in the quantification of myocardial perfusion by cross-comparison of implemented software packages (SPs) in three distinguishable patient profile populations. Methods: We studied 91 scans of patients divided into 3 subgroups based on their semi-quantitative perfusion findings: patients with normal perfusion, with reversible perfusion defects, and with fixed perfusion defects. Rest myocardial blood flow (MBF), stress MBF, and myocardial flow reserve (MFR) were obtained with QPET, SyngoMBF, and Carimas. Agreement between SPs was considered adequate when a pairwise standardized difference was found to be < 0.20 and its corresponding intraclass correlation coefficient was ≥ 0.75. Results: In patients with normal perfusion, two out of three comparisons of global stress MBF quantifications were outside the limits of agreement. In ischemic patients, all comparisons of global stress MBF and MFR were outside the limits of established agreement. In patients with fixed perfusion defects, all SP comparisons of perfusion quantifications were within the limit of agreement. Regionally, agreement of these perfusion estimates was mostly found for the left anterior descending artery vascular territory. Conclusion: Reversible defects demonstrated the worst agreement in global stress MBF and MFR and discrepancies showed to be regional dependent. Reproducibility between SPs should not be assumed.
KW - diagnostic and prognostic application
KW - image interpretation
KW - image reconstruction
KW - myocardial blood flow
KW - Myocardial ischemia and infarction
KW - PET
UR - http://www.scopus.com/inward/record.url?scp=85073955317&partnerID=8YFLogxK
U2 - 10.1007/s12350-019-01620-3
DO - 10.1007/s12350-019-01620-3
M3 - Article
C2 - 30903608
AN - SCOPUS:85073955317
SN - 1532-6551
VL - 27
SP - 1225
EP - 1233
JO - Journal of Nucleair Cardiology
JF - Journal of Nucleair Cardiology
IS - 4
ER -