AI Article Synopsis

  • - The study highlights the challenge of insufficient diagnostic tools for nuclear medicine imaging in newborns, particularly those with extremely low birth weight, and suggests investigating new technology to address this issue.
  • - Researchers created a phantom model of a 500-g infant to test cardiac PET imaging with SiPM technology, assessing its ability to visualize a 3-mm myocardial defect using two different tracers (F-FDG and F-flurpiridaz).
  • - Results showed that while SiPM PET could effectively image the heart, both tracers overestimated defect accumulation, with F-flurpiridaz providing better contrast, suggesting its preference for future studies if limited to one tracer.

Article Abstract

The lack of pediatrics-specific equipment for nuclear medicine imaging has resulted in insufficient diagnostic information for newborns, especially low-birth-weight infants. Although PET offers high spatial resolution and low radiation exposure, its use in newborns is limited. This study investigated the feasibility of cardiac PET imaging using the latest silicon photomultiplier (SiPM) PET technology in infants of extremely low birth weight (ELBW) using a phantom model. The study used a phantom model representing a 500-g ELBW infant with brain, cardiac, liver, and lung tissues. The cardiac tissue included a 3-mm-thick defect mimicking myocardial infarction. Organ tracer concentrations were calculated assuming F-FDG myocardial viability scans and F-flurpiridaz myocardial perfusion scans and were added to the phantom organs. Imaging was performed using an SiPM PET/CT scanner with a 5-min acquisition. The data acquired in list mode were reconstructed using 3-dimensional ordered-subsets expectation maximization with varying iterations. Image evaluation was based on the depiction of the myocardial defect compared with normal myocardial accumulation. Increasing the number of iterations improved the contrast of the myocardial defect for both tracers, with F-flurpiridaz showing higher contrast than F-FDG. However, even at 50 iterations, both tracers overestimated the defect accumulation. A bull's-eye image can display the flow metabolism mismatch using images from both tracers. SiPM PET enabled cardiac PET imaging in a 500-g ELBW phantom with a 1-g heart. However, there were limitations in adequately depicting these defects. Considering the image quality and defect contrast,F-flurpiridaz appears more desirable than F-FDG if only one of the two can be used.

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http://dx.doi.org/10.2967/jnmt.124.267826DOI Listing

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