AI Article Synopsis

  • Diagnosing infections in patients with autosomal dominant polycystic kidney disease (ADPKD) is challenging, and 18-fluorodeoxyglucose positron-emission tomography-computed tomography (F-FDG PET-CT) is often recommended, though its accuracy is debated.
  • Through a meta-analysis of seven studies, researchers evaluated the diagnostic performance of F-FDG PET-CT, finding a pooled sensitivity of 82.6% and specificity of 77.6% for identifying kidney and hepatic cyst infections.
  • Overall, results indicate that F-FDG PET-CT shows strong diagnostic performance, making it a valuable tool for detecting renal and hepatic cyst infections in patients with ADPKD

Article Abstract

Diagnosing suspected renal or hepatic infections in autosomal dominant polycystic kidney disease (ADPKD) is difficult. Although 18-fluorodeoxyglucose positron-emission tomography-computed tomography (F-FDG PET-CT) is recommended to aid in the diagnosis, there is no consensus about its diagnostic accuracy. We aimed to investigate its diagnostic performance. To further assess this, we performed a meta-analysis. A comprehensive literature search screening of PubMed/MEDLINE, Embase, and Cochrane library databases through February 2024 was performed. Pooled sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and C-reactive protein (CRP) were estimated using the random effects model. Heterogeneity between studies was estimated using Cochran Q and I2 statistics. A total of seven studies were included in the final analysis. The pooled sensitivity of F-FDG PET-CT in diagnosing kidney and hepatic cyst infection was 82.6% (95% CI: 73.8-88.9; I2 16.9%), specificity was 77.6% (95% CI: 66.7-85.7; I2 15.6%), PPV was 79.4% (95% CI: 62.4-89.9; I2 62.6%), and NPV was 81.3% (95% CI: 72.7-87.7; I2 0%). The mean CRP was 244.2 mg/L (95% CI: 209.1-279.1; I2 66%). The results showed that F-FDG PET-CT demonstrated excellent pooled diagnostic performance in diagnosing renal and hepatic cyst infections in ADPKD.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11531930PMC
http://dx.doi.org/10.7759/cureus.70863DOI Listing

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