PT - JOURNAL ARTICLE AU - Robert Hatherly AU - Fredrik Brolin AU - Åsa Oldner AU - Anders Sundin AU - Henrik Lundblad AU - Gerald Q. Maguire, Jr. AU - Cathrine Jonsson AU - Hans Jacobsson AU - Marilyn E. Noz TI - Technical Requirements for Na<sup>18</sup>F PET Bone Imaging of Patients Being Treated Using a Taylor Spatial Frame AID - 10.2967/jnmt.113.133082 DP - 2014 Mar 01 TA - Journal of Nuclear Medicine Technology PG - 33--36 VI - 42 IP - 1 4099 - http://tech.snmjournals.org/content/42/1/33.short 4100 - http://tech.snmjournals.org/content/42/1/33.full SO - J. Nucl. Med. Technol.2014 Mar 01; 42 AB - Diagnosis of new bone growth in patients with compound tibia fractures or deformities treated using a Taylor spatial frame is difficult with conventional radiography because the frame obstructs the images and creates artifacts. The use of Na18F PET studies may help to eliminate this difficulty. Methods: Patients were positioned on the pallet of a clinical PET/CT scanner and made as comfortable as possible with their legs immobilized. One bed position covering the site of the fracture, including the Taylor spatial frame, was chosen for the study. A topogram was performed, as well as diagnostic and attenuation correction CT. The patients were given 2 MBq of Na18F per kilogram of body weight. A 45-min list-mode acquisition was performed starting at the time of injection, followed by a 5-min static acquisition 60 min after injection. The patients were examined 6 wk after the Taylor spatial frame had been applied and again at 3 mo to assess new bone growth. Results: A list-mode reconstruction sequence of 1 × 1,800 and 1 × 2,700 s, as well as the 5-min static scan, allowed visualization of regional bone turnover. Conclusion: With Na18F PET/CT, it was possible to confirm regional bone turnover as a means of visualizing bone remodeling without the interference of artifacts from the Taylor spatial frame. Furthermore, dynamic list-mode acquisition allowed different sequences to be performed, enabling, for example, visualization of tracer transport from blood to the fracture site.