Publication:
Optimization of imaging protocols for myocardial blood flow (MBF) quantification with <sup>18</sup>F-flurpiridaz PET

dc.contributor.authorKanyalak Wiyapornen_US
dc.contributor.authorChiraporn Tocharoenchaien_US
dc.contributor.authorPawana Pusuwanen_US
dc.contributor.authorTakahiro Higuchien_US
dc.contributor.authorGeorge S.K. Fungen_US
dc.contributor.authorTao Fengen_US
dc.contributor.authorMin Jae Parken_US
dc.contributor.authorBenjamin M.W. Tsuien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherFaculty of Medicine, Siriraj Hospital, Mahidol Universityen_US
dc.contributor.otherUniversitätsklinikum Würzburgen_US
dc.contributor.otherJohns Hopkins Universityen_US
dc.contributor.otherPhilips Healthcare Nederlanden_US
dc.date.accessioned2018-12-21T06:41:55Z
dc.date.accessioned2019-03-14T08:02:46Z
dc.date.available2018-12-21T06:41:55Z
dc.date.available2019-03-14T08:02:46Z
dc.date.issued2017-10-01en_US
dc.description.abstract© 2017 Associazione Italiana di Fisica Medica The new PET tracer, 18F-flurpiridaz, with high myocardial extraction allows quantitative myocardial blood flow (MBF) estimation from dynamic PET data and tracer kinetic modeling. The goal of this study is to determine the optimal imaging protocols and parameters using a realistic simulation study. The time activity curves (TACs) of different tissue organs from a 30-s infusion time (IT) of 18F-flurpiridaz in a dynamic PET study were extracted from a previous study. The TACs at different time points were incorporated in a series of realistic 3D XCAT phantoms from which the parameters of a 2-compartment model and the ‘true’ MBF of 18F-flurpiridaz were determined. The compartmental model was used to generate TACs from 7 additional ITs. PET projection data from the XCAT phantoms were generated using Monte Carlo simulation. They were reconstructed using an OS-EM reconstruction algorithm with different update number (N) to obtain dynamic PET images. The blood and myocardial TACs were derived from the dynamic images from which the MBF and %MBF error was estimated. The %MBF error decreases with increasing N of the OS-EM and levels off after ∼42. The 30-s IT gave the smallest %MBF error that decreases from ∼0.57% to ∼19.40%. The MBF for 2-min, 4-min, 8-min and 16-min IT were statistically significant different from the MBF for 30-s IT (P < 0.05). Too fast or too slow infusion time gave higher %MBF error. The optimal imaging protocol in dynamic 18F-flurpiridaz PET for accurate quantitative MBF estimation was 30-s IT and N of ∼42 for the OS-EM.en_US
dc.identifier.citationPhysica Medica. Vol.42, (2017), 127-134en_US
dc.identifier.doi10.1016/j.ejmp.2017.08.002en_US
dc.identifier.issn1724191Xen_US
dc.identifier.issn11201797en_US
dc.identifier.other2-s2.0-85035113652en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/41777
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85035113652&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleOptimization of imaging protocols for myocardial blood flow (MBF) quantification with <sup>18</sup>F-flurpiridaz PETen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85035113652&origin=inwarden_US

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