Evidence map›Paper›PMID 41501764›Full record

ArticleBMC musculoskeletal disorders2026

Decision-making after joint aspiration: C-reactive protein and synovial white blood cell count as laboratory indicators for surgical joint lavage in pediatric septic arthritis.

Manuel Kramer, Michael Strässle, Niko Keller, Stefan Schmid, Claus Egidy, Christoph Matissek, Johannes Cip, Harry Klima, Christian Kahlert, Harald Lengnick

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Article in BMC musculoskeletal disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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10 authors.

Manuel Kramer *Department of Orthopaedics and Traumatology, HOCH Health Ostschweiz, Cantonal Hospital St. Gallen, Rorschacherstr. 95, St. Gallen, 9007, Switzerland. manuel.kramer@kssg.ch.ORCID http://orcid.org/0000-0001-6267-1609
Michael Strässle *Department of Orthopaedics and Traumatology, HOCH Health Ostschweiz, Cantonal Hospital St. Gallen, Rorschacherstr. 95, St. Gallen, 9007, Switzerland.
Niko KellerDepartment of Pediatric Surgery, Ostschweizer Kinderspital, St. Gallen, Switzerland.
Stefan SchmidDepartment of Pediatric Orthopaedics, Ostschweizer Kinderspital, St. Gallen, Switzerland.
Claus EgidyDepartment of Pediatric Orthopaedics, Ostschweizer Kinderspital, St. Gallen, Switzerland.
Christoph MatissekDepartment of Pediatric Surgery, Ostschweizer Kinderspital, St. Gallen, Switzerland.
Johannes CipDepartment of Pediatric Orthopaedics, Ostschweizer Kinderspital, St. Gallen, Switzerland.
Harry KlimaDepartment of Pediatric Orthopaedics, Ostschweizer Kinderspital, St. Gallen, Switzerland.
Christian KahlertDepartment of Pediatric Infectiology, Ostschweizer Kinderspital, St. Gallen, Switzerland.
Harald LengnickDepartment of Pediatric Orthopaedics, Ostschweizer Kinderspital, St. Gallen, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPediatric septic arthritis requires immediate recognition, as delayed diagnosis can cause severe joint damage and long-term dysfunction. In the absence of guideline-based cut-off values for laboratory markers, surgical decisions are often made on a case-by-case basis. Due to the scarcity of evidence specific to the pediatric population, treatment strategies are often based on adult data, highlighting the need for targeted research in this population. To address this gap, we developed a diagnostic algorithm that incorporated reliable predictive factors.

methodsOf 443 joint aspirations performed in our clinic (2014-2024), 132 (29.8%) were for suspected septic arthritis. After applying exclusion criteria, 80 cases were included. Clinical (fever, pain with movement, comorbidities), laboratory parameters at the time of joint aspiration (serum CRP, synovial white blood cell count [syWBC], serum white blood cell count [seWBC], synovial neutrophil perventage [syN%] and radiological data (radiographs, CT and MRI if available) were collected. Septic arthritis was defined by detection of pathogens in joint aspirate via culture or PCR.

resultsA pathogen was identified in 25% (20/80) of cases, with Kingella kingae (30%) being the most frequently detected organism, followed by Staphylococcus aureus (25%). Regression analysis revealed CRP (p < 0.01), syWBC (p = 0.04), but not syN% (p = 0.51) as predictors. ROC analysis yielded optimal cutoff values for CRP (69 mg/L; AUC = 0.82; 95% CI 0.71-0.93) and syWBC (65,000 cells/µL; AUC = 0.79; 95% CI 0.66-0.92). A diagnostic algorithm using CRP > 69 mg/L alone, or CRP < 69 mg/L combined with syWBC > 110,000 cells/µL, predicted septic arthritis with a sensitivity of 85% (95% CI 0.62-0.97; p < 0.01) and a specificity of 90% (95% CI 0.79-0.96; p < 0.01).

conclusionCRP was slightly more accurate than syWBC in predicting septic arthritis. When combined in an recursive partitioning model, these parameters demonstrated strong diagnostic performance. In cases where CRP measurements may be unreliable, an elevated syWBC count represents a CRP-independent alternative, although with reduced specificity. LEVEL OF EVIDENCE: Level III: a retrospective case-control study.

Indexed as

Arthritis, InfectiousArthrocentesisClinical Decision-MakingC-Reactive ProteinSynovial FluidTherapeutic IrrigationAdolescentAlgorithmsBiomarkersChildChild, PreschoolFemaleHumansLeukocyte CountMalePredictive Value of TestsBiomarkersC-Reactive ProteinCRPCutoff valueDiagnostic algorithm for septic arthritisPediatric septic arthritisSynovial white blood cell count

Identifiers

PMID41501764
PMCPMC12870044

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.