F-FDG PET/CT and Tc-HMPAO-WBC SPECT/CT effectively contribute to early diagnosis of infection of arteriovenous graft for hemodialysis.

Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub

Department of Vascular and Transplantation Surgery, University Hospital Olomouc, Czech Republic.

Published: December 2019

Objective: An arteriovenous graft (AVG) is indicated in hemodialysis patients with failed arteriovenous access. Early treatment of AVG infection is important because an advanced prosthetic infection leads to the removal of the prosthesis. The aim of this study was to evaluate the benefits of F-FDG PET/CT and Tc-HMPAO-WBC SPECT/CT in early detection of AVG infections.

Subjects And Methods: Fifty-one AVGs were evaluated. F-FDG PET/CT and Tc-HMPAO-WBC SPECT/CT studies were performed at intervals of 10, 20-30, and 40-50 weeks after AVG insertion. Agreement between the imaging methods and reference parameters (i.e. clinical presentation, C-reactive protein and microbiological findings on the hemodialysis cannula extracted after hemodialysis from AVG) was evaluated.

Results: The study results showed that focal accumulation of the radiopharmaceuticals can be considered a sign of AVG infection. At 10 weeks after AVG implantation, the focal F-FDG findings showed the best agreement with the reference parameters (agreement coefficients AC1 - clinical status: 0.693, CRP: 0.605, cannula microbiology: 0.518, respectively). At 20 to 30 weeks after AVG implantation, the diagnostic value of focal Tc-HMPAO-WBC accumulation increased (AC1 coefficients: 0.658, 0.658, 0.408) and was similar to that of focal F-FDG uptake (AC1s: 0.656, 0.570, 0.409). Between 40 and 50 weeks since AVG implantation, the diagnostic significance of focal Tc-HMPAO-WBC accumulation (AC1 coefficients: 0.771, 0.811, 0.611) slightly exceeded the diagnostic value of focal F-FDG accumulation (AC1 coefficients: 0.524, 0.456, 0.569).

Conclusion: F-FDG PET/CT and Tc-HMPAO-WBC SPECT/CT can both serve as important tools contributing to early diagnosis of AVG infection.

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Source
http://dx.doi.org/10.5507/bp.2019.025DOI Listing

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