Optimization of temporal sampling for 82rubidium PET myocardial blood flow quantification

Benjamin C. Lee*, Jonathan B. Moody, Richard L. Weinberg, James R. Corbett, Edward P. Ficaro, Venkatesh L. Murthy

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Background: Suboptimal temporal sampling of left ventricular (LV) blood pool and tissue time-activity curves (TACs) may introduce bias and increased variability in estimates of myocardial blood flow (MBF) and flow reserve (MFR) from dynamic PET myocardial perfusion images. We aimed to optimize temporal sampling for estimation of MBF and MFR. Methods: Twenty-four normal volunteers and 32 patients underwent dynamic stress/rest rubidium-82 chloride (82Rb) PET imaging. Fine temporal sampling was used to estimate the full width at half maximum (FWHM) of the LV blood pool TAC. Fourier analysis was used to determine the longest sampling interval, TS, as a function of FWHM, which preserved the information content of the blood phase. Dynamic datasets were reconstructed with frame durations varying from 2 to 20 seconds over the first 2 minutes for the blood phase and 30 to 120 seconds for the tissue phase. The LV blood pool and tissue TACs were sampled using regions of interest (ROI) and fit to a compartment model for quantification of MBF and MFR. The effects of temporal sampling on MBF and MFR were evaluated using clinical data and simulations. Results: TS increased linearly with input function FWHM (R = 0.93). Increasing the blood phase frame duration from 5 to 15 seconds resulted in MBF and MFR biases of 6-12% and increased variability of 14-24%. Frame durations <5 seconds had biases of less than 5% for both MBF and MFR values. Increasing the tissue phase frame durations from 30 to 120 seconds resulted in <5% biases. Conclusions: A two-phase framing of dynamic 82Rb PET images with frame durations of 5 seconds (blood phase) and 120 seconds (tissue phase) optimally samples the blood pool TAC for modern 3D PET systems.

Original languageEnglish (US)
Pages (from-to)1517-1529
Number of pages13
JournalJournal of Nuclear Cardiology
Volume24
Issue number5
DOIs
StatePublished - Oct 1 2017

Funding

The authors of this article have provided a PowerPoint file, available for download at SpringerLink, which summarizes the contents of the paper and is free for re-use at meetings and presentations. Search for the article DOI on SpringerLink.com. JNC thanks Erick Alexanderson MD, Carlos Guitar MD, and Diego Vences MD, UNAM, Mexico, for providing the Spanish abstract, and Haipeng Tang MS, Zhixin Jiang MD, and Weihua Zhou PhD, for providing the Chinese abstract. An audio interview was held January 25th, 2017 between the Associate Editor, Heinrich R. Schelbert, and Benjamin C. Lee, co-author of this article. An audio file of the interview is available as an.mp3 download at the article webpage on SpringerLink.com, and can be found by searching for the article title or DOI. Venkatesh L. Murthy and Edward P. Ficaro contributed equally to this work and are co-senior authors.

Keywords

  • Myocardial perfusion imaging: PET
  • Rubidium-82
  • myocardial blood flow
  • myocardial flow reserve
  • temporal sampling

ASJC Scopus subject areas

  • Cardiology and Cardiovascular Medicine
  • Radiology Nuclear Medicine and imaging

Fingerprint

Dive into the research topics of 'Optimization of temporal sampling for 82rubidium PET myocardial blood flow quantification'. Together they form a unique fingerprint.

Cite this