Prospective cohort study reveals high accuracy of FDG-PET in suspected spinal infection with Modic changes, suggesting effective differentiation of pyogenic spondylitis from degenerative lesions.
In Brief Study Design. Prospective cohort study. Objective. To examine the utility of 18F-fluorodeoxyglucose-positron emission tomography (FDG-PET) to diagnose pyogenic spondylitis in patients showing Modic change. Summary of Background Data. Vertebral bone marrow infection may appear as Modic type 1 signal on magnetic resonance imaging, so it is difficult to distinguish between common Modic change and infection. In the current study, we aimed to examine the utility of 18F-FDG-PET to diagnose pyogenic spondylitis in patients showing Modic change. Methods. In a prospective assessment of 312 patients showing low back pain, 18 patients were suspected of having pyogenic vertebral osteomyelitis because of their symptoms, biopsy results, blood analysis, x-ray examination, magnetic resonance imaging, and FDG-PET during a 1-year follow-up. Results. Observers ultimately diagnosed 11 patients with pyogenic spondylitis (group 1 observers). FDG-PET evaluation by 2 radiologists (group 2 observers) showed isotope accumulation in the lumbar spine in 11 patients, and no accumulation in 7 patients. The evaluation by group 1 observers, who did not see the FDG-PET findings, was compared with the evaluation by group 2 observers. No patients were evaluated differently by group 1 and group 2 observers. Conclusion. In conclusion, the rate of detecting spondylodiscitis infection was very high if FDG-PET was additionally used. FDG-PET is recommended to distinguish between common Modic change and spinal infection. We sought to examine whether F-fluorodeoxyglucose-positron emission tomography (F-FDG-PET) could be used to diagnose pyogenic spondylitis in patients showing Modic change. Of 18 patients, 11 were finally diagnosed with pyogenic spondylitis, and FDG-PET showed isotope accumulation. FDG-PET is able to distinguish between common Modic change and spinal infection in some patients.
No takes yet. Share an insight, caveat, or question.
Ohtori et al. (2010) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: