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Biodistribution of the radionuclides (18)F-FDG, (11)C-methionine, (11)C-PK11195, and (68)Ga-citrate in domestic juvenile female pigs and morphological and molecular imaging of the tracers in hematogenously disseminated Staphylococcus aureus lesions

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  1. Kinetic Modelling of [68Ga]Ga-DOTA-Siglec-9 in Porcine Osteomyelitis and Soft Tissue Infections

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  2. Blood perfusion in osteomyelitis studied with [(15)O]water PET in a juvenile porcine model

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

  3. Diagnostik af inflammation og infektion

    Publikation: Bidrag til tidsskriftTidsskriftartikelFormidling

  • Pia Afzelius
  • Ole L Nielsen
  • Aage Ko Alstrup
  • Dirk Bender
  • Páll S Leifsson
  • Svend B Jensen
  • Henrik C Schønheyder
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Approximately 5-7% of acute-care patients suffer from bacteremia. Bacteremia may give rise to bacterial spread to different tissues. Conventional imaging procedures as X-ray, Computed Tomography (CT), Magnetic Resonance Imaging (MRI), and ultrasound are often first-line imaging methods for identification and localization of infection. These methods are, however, not always successful. Early identification and localization of infection is critical for the appropriate and timely selection of therapy. The aim of this study was thus; a head to head comparison of (18)F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography (PET) to PET with tracers that potentially could improve uncovering of infectious lesions in soft tissues. We chose (11)C-methionine, (11)C-PK11195, and (68)Ga-citrate as tracers and besides presenting their bio-distribution we validated their diagnostic utility in pigs with experimental bacterial infection. Four juvenile 14-15 weeks old female domestic pigs were scanned seven days after intra-arterial inoculation in the right femoral artery with a porcine strain of S. aureus using a sequential scanning protocol with (18)F-FDG, (11)C-methionine, (11)C-PK11195 and (68)Ga-citrate. This was followed by necropsy of the pigs consisting of gross pathology, histopathology and microbial examination. The pigs primarily developed lesions in lungs and neck muscles. (18)F-FDG had higher infection to background ratios and accumulated in most infectious foci caused by S. aureus, while (11)C-methionine and particularly (11)C-PK11195 and (68)Ga-citrate accumulated to a lesser extent in infectious foci. (18)F-FDG-uptake was seen in the areas of inflammatory cells and to a much lesser extent in reparative infiltration surrounding necrotic regions.

TidsskriftAmerican Journal of Nuclear Medicine and Molecular Imaging
Udgave nummer1
Sider (fra-til)42-58
Antal sider17
StatusUdgivet - 2016

ID: 46380808