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Rapid detection of human infections with fluorine-18 fluorodeoxyglucose and positron emission tomography: preliminary results

dc.contributor.authorSugawara, Yoshifumien_US
dc.contributor.authorRusso, Joseph E.en_US
dc.contributor.authorWahl, Richard L.en_US
dc.contributor.authorBraun, Daniel K.en_US
dc.contributor.authorKison, Paul V.en_US
dc.contributor.authorZasadny, Kenneth R.en_US
dc.date.accessioned2006-09-08T19:56:34Z
dc.date.available2006-09-08T19:56:34Z
dc.date.issued1998-09en_US
dc.identifier.citationSugawara, Yoshifumi; Braun, Daniel K.; Kison, Paul V.; Russo, Joseph E.; Zasadny, Kenneth R.; Wahl, Richard L.; (1998). "Rapid detection of human infections with fluorine-18 fluorodeoxyglucose and positron emission tomography: preliminary results." European Journal of Nuclear Medicine 25(9): 1238-1243. <http://hdl.handle.net/2027.42/42074>en_US
dc.identifier.issn0340-6997en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42074
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=9724371&dopt=citationen_US
dc.description.abstractThe purpose of this study was to evaluate the feasibility of 2-[fluorine-18]fluoro-2-deoxy- d -glucose (FDG) and positron emission tomography (PET) for rapid detection of human infections. Eleven patients who were known or suspected to be harboring various infections were studied with FDG-PET. Dynamic scans over the putative infection sites were performed immediately after FDG (370 MBq) injection through 60 min, and static images including multiple projection images were then obtained. FDG uptake was assessed visually into four grades (0, normal; 1, probably normal; 2, probably abnormal; 3, definitely abnormal). For the semiquantitative index of FDG uptake in infections, the standardized uptake value of FDG normalized to the predicted lean body mass (SUV-lean, SUL) was determined from the images obtained at 50–60 min after FDG injection. PET results were compared with final clinical diagnoses. Eleven lesions in eight patients, which were interpreted as grade 2 or 3 by FDG-PET, were all concordant with active infectious foci. The SUL values of infections ranged from 0.97 to 6.69. In two patients, FDG-PET correctly showed no active infection. In one patient, it was difficult to detect infectious foci by FDG-PET due to substantial normal background uptake of FDG. In total, FDG-PET correctly diagnosed the presence or absence of active infection in 10 of 11 patients. Fusion images of PET with computed tomography showed the most intense FDG uptake to be within an abscess wall. In conclusion, FDG-PET appears to be a promising modality for rapid imaging of active human infections. More extensive clinical evaluation is warranted to determine the accuracy of this method.en_US
dc.format.extent321484 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherSpringer-Verlag; Springer-Verlag Berlin Heidelbergen_US
dc.subject.otherPositron Emission Tomographyen_US
dc.subject.otherKey Words: Fluorine-18 Fluorodeoxyglucoseen_US
dc.subject.otherInfectionen_US
dc.subject.otherLegacyen_US
dc.titleRapid detection of human infections with fluorine-18 fluorodeoxyglucose and positron emission tomography: preliminary resultsen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelRadiologyen_US
dc.subject.hlbsecondlevelPhysicsen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Nuclear Medicine, The University of Michigan Medical Center, Ann Arbor, Michigan, USA, USen_US
dc.contributor.affiliationumDivision of Nuclear Medicine, The University of Michigan Medical Center, Ann Arbor, Michigan, USA, USen_US
dc.contributor.affiliationumDepartment of Internal Medicine, The University of Michigan Medical Center, Ann Arbor, Michigan, USA, USen_US
dc.contributor.affiliationumDivision of Nuclear Medicine, The University of Michigan Medical Center, Ann Arbor, Michigan, USA, USen_US
dc.contributor.affiliationumDivision of Nuclear Medicine, The University of Michigan Medical Center, Ann Arbor, Michigan, USA, USen_US
dc.contributor.affiliationumDivision of Nuclear Medicine, The University of Michigan Medical Center, Ann Arbor, Michigan, USA, USen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid9724371en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42074/1/259-25-9-1238_80251238.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/s002590050290en_US
dc.identifier.sourceEuropean Journal of Nuclear Medicineen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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