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FDG-PET/CT for differentiating between aseptic and septic delayed union in the lower extremity. | LitMetric

FDG-PET/CT for differentiating between aseptic and septic delayed union in the lower extremity.

Arch Orthop Trauma Surg

Trauma Unit, Department of Surgery, Maasstad ziekenhuis, Rotterdam, The Netherlands.

Published: February 2018

Background: F-fluorodeoxyglucose (F-FDG) positron emission tomography (PET)/computed tomography (CT) has proven to have a high diagnostic accuracy for the detection of bone infections. In patients with delayed union it may be clinically important to differentiate between aseptic and septic delayed union. The aim of this study was to evaluate the efficacy and to assess the optimal diagnostic accuracy of FDG-PET/CT in differentiating between aseptic and septic delayed union in the lower extremity.

Methods: This is a retrospective study of consecutive patients who underwent FDG-PET/CT scanning for suspicion of septic delayed union of the lower extremity. Diagnosis of aseptic delayed union or septic delayed union was made based on surgical deep cultures following PET/CT scanning and information on clinical follow-up. FDG-uptake values were measured at the fractured site by use of the maximum standardized uptake value (SUV). Sensitivity, specificity and diagnostic accuracy of FDG-PET/CT were calculated at various SUV cut-off points.

Results: A total of 30 patients were included; 13 patients with aseptic delayed unions and 17 patients with septic delayed unions. Mean SUV in aseptic delayed union patients was 3.23 (SD ± 1.21). Mean SUV in septic delayed union patients was 4.77 (SD ± 1.87). A cut-off SUV set at 4.0 showed sensitivity, specificity and diagnostic accuracy of FDG-PET/CT were 65, 77 and 70% to differentiate between aseptic and septic delayed union, respectively.

Conclusion: Using a semi-quantitative measure (SUV) for interpretation of FDG-PET/CT imaging seems to be a promising tool for the discrimination between aseptic and septic delayed union.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773632PMC
http://dx.doi.org/10.1007/s00402-017-2806-8DOI Listing

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