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Short read · Infection & inflammation

Role of Nuclear Medicine in Prosthetic Joint Infection

Infection & inflammation · 2 min read

A painful hip or knee replacement asks one question: aseptic or septic loosening? The answer decides between one-stage revision and debridement with prolonged antibiotics and a second operation. Aspiration can be dry or equivocal, CRP and ESR non-specific, radiographs unhelpful. Nuclear medicine is asked precisely when the answer is not otherwise available — and it delivers only if the right study is chosen and the pattern read correctly.

When to image

  • Persistent pain or a loose prosthesis when infection remains uncertain after clinical assessment, blood tests and aspiration.
  • Distinguishing infection from aseptic loosening before revision surgery.
  • Localising infection and assessing its extent around the prosthesis, especially when other imaging is inconclusive.

With what to image

  • Three-phase bone scan screens; leucocyte + marrow decides; FDG PET/CT is the option.
  • SPECT/CT throughout, to place activity at the bone–prosthesis interface or in soft tissue.

Patterns of uptake

StudyPatternInterpretation
Three-phase bone scanNormalLargely excludes infection and loosening
Focal delayed uptake at stem tip or along the shaftAseptic loosening
Hyperaemia on flow and blood pool with diffuse periprosthetic uptakeSuggests infection
Leucocyte + marrowCongruent — white cells match marrowDisplaced or expanded marrow; not infection
Incongruent — white cells without matching marrowInfection
FDG PET/CTBone–prosthesis interface, soft tissue or sinus tractFavours infection
Synovium or head–neck junction onlyNon-specific
Pearl

Infection timing follows thirds — about a third early (<3 months), a third delayed (3–12 months) from surgical seeding; late (>1 year) is usually haematogenous.

Why leucocyte + marrow decides

  • Both tracers accumulate in marrow; infection recruits leucocytes while suppressing colloid uptake — hence the incongruence.
  • 99mTc-HMPAO or 111In-oxine leucocytes, paired with 99mTc-sulfur colloid, read in the same planes.
  • Sensitivity ≈100%, specificity ≈91%, accuracy ≈95% in failed replacements.
  • Pooled by site: hip 69% / 96%, knee 80% / 93%.
  • Allow time after surgery — early postoperative leucocyte uptake is physiological.
Pearl

Reporting the white-cell study without its marrow scan is the commonest error in this subject.

FDG PET/CT, and its limits

  • Convenient: one visit, no cell labelling, whole-body coverage.
  • Pooled sensitivity and specificity both ≈86% in lower-limb prostheses.
  • Head to head against leucocyte/marrow it reached only ≈71% accuracy on any criteria.
  • Particle-debris reaction and aseptic loosening stay FDG-avid for years — the whole specificity problem.
  • No standardised interpretation criteria, no usable SUV cut-off.
  • 68Ga-citrate PET was more specific than FDG (88% vs 38%) but remains investigational.

Fuller version, with performance and pitfalls: Prosthetic joint infection.

Take home
  • Bone scan excludes; leucocyte/marrow decides; FDG is the option, not the reference.
  • Infection is incongruent uptake — white cells where marrow is not.
  • Never report a white-cell study without its marrow scan.
Sources
  1. Signore A, Sconfienza LM, Borens O, et al. Consensus document for the diagnosis of prosthetic joint infections: a joint paper by the EANM, EBJIS, and ESR (with ESCMID endorsement). Eur J Nucl Med Mol Imaging. 2019;46(4):971-88.
  2. Signore A, Jamar F, Israel O, et al. Clinical indications, image acquisition and data interpretation for white blood cells and anti-granulocyte monoclonal antibody scintigraphy: an EANM procedural guideline. Eur J Nucl Med Mol Imaging. 2018;45(10):1816-31.
  3. Gheysens O, Jamar F, Glaudemans AWJM, et al. Summary: EANM/SNMMI joint guideline/procedure standard for [18F]FDG hybrid PET use in infection and inflammation in adults, version 2.0. J Nucl Med. 2025;66(3):480-1.