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Paeds Vivasrheumatology-musculoskeletal-and-sports

Paeds Vivas · rheumatology-musculoskeletal-and-sports

Transient synovitis and the irritable hip — branching viva

Branching viva on transient synovitis and the irritable hip: excluding septic arthritis with the Kocher criteria, interpreting the ultrasound effusion and the inflammatory markers, choosing between watchful waiting and aspiration, recognising the Kingella kingae mimic in the under-four, and applying the safety-net review for the persistent limp.

branching clinical structured oral2 min readVerification in progress

Target exams

RACP DCEMRCPCH ClinicalRCPSC Pediatrics
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Target exams

RACP DCEMRCPCH ClinicalRCPSC Pediatrics
Prompt
A five-year-old boy is brought in with a one-day limp and a sore hip, two days after a runny nose. He is afebrile, well-looking, and walks with an antalgic gait. The examiner asks: what is your differential, how do you exclude septic arthritis, what is your single most important investigation, and what is your management — then branches to the Kocher criteria and the Caird CRP refinement, the ultrasound effusion, the Kingella kingae mimic in the younger child, the safety-net review, and finally the persistent limp as the signal of a declaring mimic.

Branching framework

Open with the one-sentence problem representation. This is a well-looking child in the peak age group with an acute post-viral limp, and transient synovitis is the likely diagnosis once septic arthritis has been excluded. State the principle aloud — transient synovitis is a diagnosis of exclusion, made only after the Kocher criteria and the inflammatory markers have lowered the probability of pus — before you discuss anything else. The examiner is listening for whether you reach for the score and the markers before you reach for the reassurance. [1] [3]

Apply the Kocher criteria to exclude sepsis. The four predictors are a fever above 38.5 degrees, an inability to bear weight, an ESR above 40, and a white cell count above 12,000, with the Caird addition of a CRP above 20 milligrams per litre. State the rising probability with each predictor — below one per cent with none, forty per cent with two, ninety-three per cent with three — and be ready for the calibration probe, because the Caird prospective study found the original Kocher probabilities may overestimate. The child with zero or one predictor and a well appearance fits transient synovitis, while two or more predictors demand aspiration. [1] [3]

Branch to the single most important investigation. Ultrasound is the first-line investigation, confirming the hip effusion and guiding an aspiration when one is needed. State that the markers frame the probability and that the ultrasound confirms the effusion, and be ready to explain that a normal ultrasound does not exclude early septic arthritis. If the examiner probes a culture-negative effusion in the under-four, name Kingella kingae and the blood-culture-bottle inoculation and the polymerase chain reaction, because the young child with a culture-negative effusion is not safely reassured. [6] [9]

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References4ShowHide
  1. [1]Kocher MS, Zurakowski D, Kasser JR. Differentiating between septic arthritis and transient synovitis of the hip in children: an evidence-based clinical prediction algorithm. J Bone Joint Surg Am, 1999.PMID 10608376
  2. [3]Caird MS, Flynn JM, Leung YL, et al. Factors distinguishing septic arthritis from transient synovitis of the hip in children. A prospective study. J Bone Joint Surg Am, 2006.PMID 16757758
  3. [6]Nouri A, Walmsley D, Pruszczynski B, Synder M. Transient synovitis of the hip: a comprehensive review. J Pediatr Orthop B, 2014.PMID 23812087
  4. [9]Ryan DD. Differentiating Transient Synovitis of the Hip from More Urgent Conditions. Pediatr Ann, 2016.PMID 27294495
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