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Molecular imaging agent coupled with 'motion frozen' processing improves heart imaging

Date:
June 7, 2010
Source:
Society of Nuclear Medicine
Summary:
Molecular imaging of the heart just got better, according to a new study. Combining a potential new imaging agent with a molecular imaging technique that reduces blur caused by the motion of the heart and lungs could lead to unprecedented image quality when conducting myocardial perfusion imaging, a procedure used to evaluate blood flow to the heart.
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Molecular imaging of the heart just got better, according to a study revealed at the Society of Nuclear Medicine's 57th Annual Meeting. Combining a potential new imaging agent with a molecular imaging technique that reduces blur caused by the motion of the heart and lungs could lead to unprecedented image quality when conducting myocardial perfusion imaging, a procedure used to evaluate blood flow to the heart.

"Both cardiac and respiratory motion degrade image quality by adding some unwanted blur," said Ludovic Le Meunier, Ph.D., lead researcher and staff scientist for Siemens Healthcare, Knoxville, Tenn., based at Cedars-Sinai Medical Center, Los Angeles, Calif. "Our objective in this work was to provide the highest myocardial perfusion image quality by using a promising heart imaging agent and correcting the motion of those organs. In conjunction, these tools can provide unprecedented diagnostic capability for clinicians evaluating heart disease."

The new imaging agent, called flurpiridaz F 18 injection, uses a fluorine-18 (F-18) based radioisotope, and while it is still in clinical trials, the compound has been shown to facilitate very high-quality imaging of the heart. Other positron emission tomography (PET) agents used to image the heart have a much shorter half-life and need to be produced within an on-site cyclotron, which limits access. Some agents can be produced on-site with a generator, but image quality appears not to be as high. F-18 has a half-life of 108 minutes and therefore can be delivered to imaging centers located within a wider radius, with no compromise to image quality.

The technology used in this study included high-definition, or "HD" PET, a technique that images the body's physiological functions and automatically corrects distortions that occur during scanning. Next, researchers used post-scan image processing tools called respiratory gating and "motion-frozen" cardiac gating, which cut out or otherwise compensate for the motion of these organs during scanning. The result is virtually motion-free myocardial perfusion imaging.

This clinical trial was led by Daniel Berman, M.D., director of cardiac imaging and nuclear cardiology at Cedars-Sinai Medical Center. Motion-frozen technology was developed in collaboration with Piotr Slomka, Ph.D., a research scientist at Cedars-Sinai and professor of medicine at the University of California, Los Angeles.

Scientific Paper 522: L. Le Meunier, Siemens Healthcare, Knoxville, Tenn.; P.J. Slomka, A. Ramesh, L.E. Thomson, S.W. Hayes, B. Tamarappoo, V. Cheng, G. Germano, D.S. Berman, Cedars-Sinai Medical Center, Los Angeles, Calif.; J. Lazewatsky, Lantheus Medical Imaging, North Billerica, Mass.; "Enhanced dual gated cardiac perfusion PET using a new F-18 imaging agent (BMS747158)," SNM's 57th Annual Meeting, June 5-9, 2010, Salt Lake City, Utah.


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The above post is reprinted from materials provided by Society of Nuclear Medicine. Note: Materials may be edited for content and length.


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Society of Nuclear Medicine. "Molecular imaging agent coupled with 'motion frozen' processing improves heart imaging." ScienceDaily. ScienceDaily, 7 June 2010. <www.sciencedaily.com/releases/2010/06/100607142007.htm>.
Society of Nuclear Medicine. (2010, June 7). Molecular imaging agent coupled with 'motion frozen' processing improves heart imaging. ScienceDaily. Retrieved July 31, 2015 from www.sciencedaily.com/releases/2010/06/100607142007.htm
Society of Nuclear Medicine. "Molecular imaging agent coupled with 'motion frozen' processing improves heart imaging." ScienceDaily. www.sciencedaily.com/releases/2010/06/100607142007.htm (accessed July 31, 2015).

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