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Published on: February 25, 2022
Changing aetiology of paediatric septic arthritis
1Clinical Microbiology Laboratory, Soroka University Medical Center, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Insights
Kingella kingae is now the leading cause of septic arthritis in young children, often missed by traditional diagnostics. Improved molecular methods are crucial for accurate identification and management of this infection.
Area of Science:
- Pediatric Infectious Diseases
- Microbiology
- Rheumatology
Background:
- Septic arthritis in children traditionally involved Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae, and Haemophilus influenzae type b.
- Conventional bacteriologic cultures often failed to identify the causative pathogen in a significant number of pediatric joint infections.
- Vaccination programs and improved detection methods have significantly altered the understanding of pediatric infectious arthritis etiology.
Purpose of the Study:
- To highlight the changing landscape of causative agents in pediatric septic arthritis.
- To emphasize the emerging role of Kingella kingae as a primary cause of infectious arthritis in young children.
- To discuss the diagnostic challenges and advancements in identifying Kingella kingae infections.
Main Methods:
- Review of historical and recent data on pediatric septic arthritis etiology.
- Implementation of blood culture vial inoculation for synovial fluid aspirates.
- Advancement and utilization of sensitive molecular diagnostic techniques, particularly nucleic acid amplification tests (NAATs).
Main Results:
- Kingella kingae has emerged as the predominant cause of septic arthritis in children aged 6-48 months, identified in 30-93% of cases.
- The clinical presentation of Kingella kingae arthritis is often subtle, with normal or near-normal inflammatory markers and white blood cell counts.
- Molecular methods, especially NAATs targeting K. kingae-specific genes, have significantly improved pathogen detection rates and reduced culture-negative infections.
Conclusions:
- Kingella kingae is the leading etiology of septic arthritis in children under four years old.
- The subtle clinical presentation and frequent normality of standard laboratory tests necessitate high clinical suspicion for Kingella kingae.
- Advanced molecular detection methods are essential for accurate diagnosis and effective management of pediatric septic arthritis caused by Kingella kingae.
Abstract:
The management of septic arthritis in children requires the prompt administration of antibiotic therapy and the identification of the causative pathogen. In the past, Staphylococcus aureus, Streptococcus pyogenes, Streptococcus pneumoniae and Haemophilus influenzae type b were considered the main causative agents of the disease, but a substantial fraction of presumptive joint infections remained unconfirmed by conventional bacteriologic cultures. In the last two decades, our knowledge of the aetiology of paediatric infectious arthritis has substantially changed as the result of the implementation of vaccination programmes against H. influenzae type b and pneumococci, and by the use of improved detection methods. In 1988, the inoculation of synovial fluid aspirates into blood culture vials revealed that Kingella kingae, a commensal member of the oropharyngeal microbiota, was the prime aetiology of skeletal system infections in children aged 6-48 months. The clinical presentation of K. kingae arthritis is subtle, and the disease is frequently missed by classic clinical and laboratory diagnostic criteria. Many children are afebrile, the acute phase reactants levels and the white blood cell counts in the blood and synovial fluid specimens are frequently normal, requiring a high clinical acumen. Increasing use of sensitive molecular methods in recent years, and particularly nucleic acid amplification tests that target K. kingae-specific genes, has further improved the detection of this elusive pathogen, demonstrated that it is responsible for 30-93% of all cases of septic arthritis below 4 years of age and reduced the fraction of culture-negative infections.
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