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Clinical update · 01 of 06

Fifty years of periprosthetic joint infection, and what actually changed

Audit your own periprosthetic joint infection pathway against the modern framework - validated criteria rather than impression, multiple held cultures rather than one, and a surgical choice made on host and organism rather than habit.

This JBJS review takes the long view on periprosthetic joint infection, tracing how management moved from empirical, procedure-centred practice to something structured around host, organism and disease.

Three shifts are identified. Diagnosis moved from clinical suspicion plus culture to a multimodal framework: validated diagnostic criteria, serological and synovial fluid biomarkers, and molecular techniques for the cases where culture stays negative. Surgical strategy moved from a default operation to a decision - debridement with implant retention, one-stage revision, two-stage revision, or salvage - chosen by the characteristics of the patient and the pathogen rather than by unit habit. And the microbiology moved, with the recognition of biofilm explaining why a course of antibiotics against a sensitive organism reliably fails around retained hardware, and the microbiome now entering the picture.

The honest framing is that this is a narrative review with no new data, and reviews of progress tend to flatter the field. But it is a useful audit against your own practice, and the questions it prompts are concrete. Are you applying validated diagnostic criteria or an impression? Is a negative culture being treated as an absence of infection? Is the choice between debridement with retention and two-stage revision made on the organism and the host, or on what your unit does? In Indian practice, where synovial biomarker assays and molecular diagnostics are unevenly available and culture-negative infection is common, the diagnostic half of this is the part with the most room in it.

  • Apply a validated diagnostic criteria set rather than an overall impression - write down which criteria you used
  • Do not read a negative culture as absence of infection; send multiple samples and hold them long enough for indolent organisms
  • Choose between debridement with implant retention and staged revision on symptom duration, organism and host, not on unit convention
  • Where synovial biomarkers are available, use them for the equivocal case rather than as routine
  • Remember biofilm is why antibiotics alone fail around retained hardware, whatever the sensitivities say

Why it matters

It gives a reference standard for a pathway most units assembled piecemeal over years.

Don't overread it

A narrative review of progress in a field, not new evidence or a guideline - it summarises direction rather than establishing practice.

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