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Distinguishing Kingella kingae from Pyogenic Acute Septic Arthritis in Young Portuguese Children
Catarina Gouveia1,2, Ana Subtil3,4, Susana Norte5
1Infectious Diseases Unit, Hospital de Dona Estefânia, Centro Hospitalar Universitário Lisboa Central, 1169-045 Lisbon, Portugal.
Insights
Kingella kingae septic arthritis (SA) in children under 5 presents with lower fever and inflammatory markers compared to pyogenic SA. Key predictors include age between 6 months and 2 years, absence of fever, and C-reactive protein (CRP) levels under 100 mg/L.
Area of Science:
- Pediatric Infectious Diseases
- Microbiology
- Clinical Diagnostics
Background:
- Distinguishing Kingella kingae septic arthritis (SA) from pyogenic SA in young children is clinically important.
- Kingella kingae is an increasingly recognized cause of pediatric SA.
Purpose of the Study:
- To identify clinical and laboratory parameters differentiating Kingella kingae from pyogenic SA in children under 5 years old.
- To develop a predictive model for Kingella kingae SA.
Main Methods:
- A longitudinal, observational, single-center study included 75 children (<5 years) with microbiologically confirmed SA.
- Clinical and laboratory data were collected at admission, 48 hours, and during treatment.
- Multivariate analysis and ROC curves were used to identify predictive factors.
Main Results:
- 44 cases of Kingella kingae SA and 31 of pyogenic SA were identified.
- Kingella kingae SA was associated with younger age, absence of fever, and lower inflammatory markers (CRP, ESR).
- A predictive model (age >6 months ≤2 years, apyrexia, CRP ≤100 mg/L) showed high accuracy (AUC 0.861) in differentiating Kingella kingae SA.
Conclusions:
- Age between 6 months and 2 years, absence of fever, and CRP ≤100 mg/L are key predictors for Kingella kingae SA in children under 5.
- These findings can aid in early diagnosis and management of pediatric SA.
- Further validation in larger studies is recommended.
Abstract:
(1) Background: We aim to identify clinical and laboratorial parameters to distinguish Kingella kingae from pyogenic septic arthritis (SA). (2) Methods: A longitudinal, observational, single-centre study of children < 5 years old with microbiological positive SA admitted to a paediatric hospital from 2013−2020 was performed. Clinical and laboratorial data at admission and at 48 h, as well as on treatment and evolution, were obtained. (3) Results: We found a total of 75 children, 44 with K. kingae and 31 with pyogenic infections (mostly MSSA, S. pneumoniae and S. pyogenes). K. kingae affected younger children with low or absent fever, low inflammatory markers and a favourable prognosis. In the univariate analyses, fever, septic look, CRP and ESR at admission and CRP at 48 h were significantly lower in K. kingae SA. In the multivariate analyses, age > 6 months ≤ 2 years, apyrexy and CRP ≤ 100 mg/L were significative, with an overall predictive positive value of 86.5%, and 88.4% for K. kingae. For this model, ROC curves were capable of differentiating (AUC 0.861, 95% CI 0.767−0.955) K. kingae SA from typical pathogens. (4) Conclusions: Age > 6 months ≤ 2 years, apyrexy and PCR ≤ 100 mg/L were the main predictive factors to distinguish K. kingae from pyogenic SA < 5 years. These data need to be validated in a larger study.
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