PMID- 30945100 OWN - NLM STAT- MEDLINE DCOM- 20200917 LR - 20220201 IS - 2509-9280 (Electronic) IS - 2509-9280 (Linking) VI - 3 IP - 1 DP - 2019 Apr 3 TI - Timing optimization of low-dose first-pass analysis dynamic CT myocardial perfusion measurement: validation in a swine model. PG - 16 LID - 10.1186/s41747-019-0093-6 [doi] LID - 16 AB - BACKGROUND: Myocardial perfusion measurement with a low-dose first-pass analysis (FPA) dynamic computed tomography (CT) perfusion technique depends upon acquisition of two whole-heart volume scans at the base and peak of the aortic enhancement. Hence, the objective of this study was to validate an optimal timing protocol for volume scan acquisition at the base and peak of the aortic enhancement. METHODS: Contrast-enhanced CT of 28 Yorkshire swine (weight, 55 +/- 24 kg, mean +/- standard deviation) was performed under rest and stress conditions over 20-30 s to capture the aortic enhancement curves. From these curves, an optimal timing protocol was simulated, where one volume scan was acquired at the base of the aortic enhancement while a second volume scan was acquired at the peak of the aortic enhancement. Low-dose FPA perfusion measurements (P(FPA)) were then derived and quantitatively compared to the previously validated retrospective FPA perfusion measurements as a reference standard (P(REF)). The 32-cm diameter volume CT dose index, [Formula: see text] and size-specific dose estimate (SSDE) of the low-dose FPA perfusion protocol were also determined. RESULTS: P(FPA) were related to the reference standard by P(FPA) = 0.95 . P(REF) + 0.07 (r = 0.94, root-mean-square error = 0.27 mL/min/g, root-mean-square deviation = 0.04 mL/min/g). The [Formula: see text] and SSDE of the low-dose FPA perfusion protocol were 9.2 mGy and 14.6 mGy, respectively. CONCLUSIONS: An optimal timing protocol for volume scan acquisition at the base and peak of the aortic enhancement was retrospectively validated and has the potential to be used to implement an accurate, low-dose, FPA perfusion technique. FAU - Hubbard, Logan AU - Hubbard L AD - Department of Radiological Sciences, Medical Sciences I, B-140, University of California, Irvine, Irvine, CA, 92697, USA. FAU - Malkasian, Shant AU - Malkasian S AD - Department of Radiological Sciences, Medical Sciences I, B-140, University of California, Irvine, Irvine, CA, 92697, USA. FAU - Zhao, Yixiao AU - Zhao Y AD - Department of Radiological Sciences, Medical Sciences I, B-140, University of California, Irvine, Irvine, CA, 92697, USA. FAU - Abbona, Pablo AU - Abbona P AD - Department of Radiological Sciences, Medical Sciences I, B-140, University of California, Irvine, Irvine, CA, 92697, USA. FAU - Molloi, Sabee AU - Molloi S AD - Department of Radiological Sciences, Medical Sciences I, B-140, University of California, Irvine, Irvine, CA, 92697, USA. symolloi@uci.edu. LA - eng GR - F30 HL137288/HL/NHLBI NIH HHS/United States GR - T32 GM008620/GM/NIGMS NIH HHS/United States GR - T32 HL116270/HL/NHLBI NIH HHS/United States PT - Journal Article PT - Research Support, N.I.H., Extramural PT - Research Support, Non-U.S. Gov't PT - Validation Study DEP - 20190403 PL - England TA - Eur Radiol Exp JT - European radiology experimental JID - 101721752 SB - IM MH - Animals MH - Models, Animal MH - Myocardial Perfusion Imaging/*methods MH - Radiation Dosage MH - Swine MH - Time Factors MH - *Tomography, X-Ray Computed/methods PMC - PMC6447643 OTO - NOTNLM OT - Animal experimentation OT - Coronary artery disease OT - Myocardium OT - Perfusion imaging OT - Tomography (x-ray computed) COIS- ETHICS APPROVAL: The study was approved by the Institutional Animal Care and Use Committee (#1997-1273-9). CONSENT FOR PUBLICATION: Not applicable COMPETING INTERESTS: Sabee Molloi has previously received grants from Toshiba America Medical Systems and Philips Medical Systems. The remaining authors do not have any conflicts of interest to disclose. PUBLISHER'S NOTE: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations. EDAT- 2019/04/05 06:00 MHDA- 2020/09/18 06:00 PMCR- 2019/04/03 CRDT- 2019/04/05 06:00 PHST- 2018/12/17 00:00 [received] PHST- 2019/02/21 00:00 [accepted] PHST- 2019/04/05 06:00 [entrez] PHST- 2019/04/05 06:00 [pubmed] PHST- 2020/09/18 06:00 [medline] PHST- 2019/04/03 00:00 [pmc-release] AID - 10.1186/s41747-019-0093-6 [pii] AID - 93 [pii] AID - 10.1186/s41747-019-0093-6 [doi] PST - epublish SO - Eur Radiol Exp. 2019 Apr 3;3(1):16. doi: 10.1186/s41747-019-0093-6.