# Diagnostic Test Accuracy and Semi-Quantitative Metrics of 18F-FDG PET in Assessing Treatment Response in Skull Base Osteomyelitis and Necrotising Otitis Externa: A Systematic Review and Meta-Analysis

**Authors:** Mark Laidlaw, Maya Reid, Sukanya Rajiv, Jean-Marc Gerard

PMC · DOI: 10.3390/tomography12030032 · Tomography · 2026-03-02

## TL;DR

PET scans using 18F-FDG are highly accurate in detecting active infection during treatment for skull base osteomyelitis and necrotising otitis externa, helping doctors decide when to stop antibiotics.

## Contribution

This study provides the first meta-analysis on the diagnostic accuracy of 18F-FDG PET for monitoring treatment response in these infections.

## Key findings

- PET scans showed 95% sensitivity and 89% specificity in identifying active infection.
- SUVmax was the most commonly used metabolic parameter for assessment.
- Current evidence is limited by retrospective study designs and variability across studies.

## Abstract

Skull base osteomyelitis is a severe bone infection near the ear requiring prolonged antibiotic treatment. Clinicians face difficulty determining when to safely stop antibiotics, as stopping too early risks dangerous relapse, while continuing too long causes medication side effects. Traditional imaging cannot distinguish healing bone from active infection. This study analysed whether PET scans, which detect metabolic activity, can accurately identify persistent infection during treatment. Results showed PET scans effectively ruled out active infection with 95% sensitivity and 89% specificity. These findings suggest PET imaging could help clinicians make safer decisions about when to discontinue antibiotics, though larger prospective studies are needed to establish standardised guidelines.

Background/Objectives: Skull base osteomyelitis and necrotising otitis externa require prolonged antibiotic therapy, yet determining optimal treatment cessation timing remains challenging. Conventional imaging modalities demonstrate persistent abnormalities beyond infection resolution, confounding treatment decisions. This systematic review evaluated the diagnostic test accuracy of 18F-fluorodeoxyglucose positron emission tomography (18F-FDG PET) for treatment response monitoring in skull base osteomyelitis and necrotising otitis externa. Methods: We conducted a systematic review following PRISMA-DTA guidelines, searching MEDLINE, Embase, CENTRAL, CINAHL, Scopus, and Web of Science from inception to November 2025. Studies evaluating 18F-FDG PET diagnostic accuracy for treatment response assessment in confirmed skull base osteomyelitis or necrotising otitis externa were included. Two reviewers independently screened studies, extracted data, and assessed risk of bias using QUADAS-2. Bivariate random-effects meta-analysis was performed using MetaBayesDTA to obtain pooled sensitivity and specificity. Results: Eight studies comprising 154 lesions contributed to the primary analysis. Pooled sensitivity was 95.2% (95% credible interval 85.6–99.0%) and pooled specificity was 89.1% (95% credible interval 70.7–96.7%). The positive likelihood ratio was 8.7 (95% credible interval 3.2–28.4) and negative likelihood ratio was 0.05 (95% credible interval 0.01–0.17), with a diagnostic odds ratio of 172.0. Seven studies evaluating detection rate at initial presentation yielded a pooled rate of 96.1% (95% confidence interval 91.3–98.3%). SUVmax was the most frequently used metabolic parameter. Conclusions: 18F-FDG PET, specifically using SUVmax, demonstrates high sensitivity and good specificity for treatment response monitoring, with excellent capacity to rule out persistent infection. However, evidence quality is limited by retrospective designs and substantial heterogeneity. Prospective studies with standardised thresholds are needed to validate clinical utility.

## Linked entities

- **Chemicals:** 18F-fluorodeoxyglucose (PubChem CID 68614), 18F-FDG (PubChem CID 68614)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Diabetes (MESH:D003920), facial paralysis (MESH:D005158), head and neck (MESH:D006258), toxicity (MESH:D064420), bacterial infections (MESH:D001424), bone infection (MESH:D001847), fungal infection (MESH:D009181), Necrotising Otitis (MESH:D010031), necrotising (MESH:D019283), infection (MESH:D007239), injury to (MESH:D014947), external auditory canal infection (MESH:C566245), otalgia (MESH:D004433), diabetic foot (MESH:D017719), inflammatory (MESH:D007249), bony erosion (MESH:D014077), SBO (MESH:D019292), cranial nerve palsy (MESH:D003389), middle ear/mastoid infection (MESH:D010033), Osteomyelitis (MESH:D010019), MOE (MESH:D010032)
- **Chemicals:** 18F-FDG (MESH:D019788), NOE (-), Gallium (MESH:D005708), glucose (MESH:D005947), Tc-99m (MESH:D013667), 67Ga (MESH:C000615429)
- **Species:** Homo sapiens (human, species) [taxon 9606], Aspergillus flavus (species) [taxon 5059], Pseudomonas aeruginosa (species) [taxon 287]

## Full text

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## Figures

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## References

57 references — full list in the complete paper: https://tomesphere.com/paper/PMC13030614/full.md

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Source: https://tomesphere.com/paper/PMC13030614