Shifts in unidentified-pathogen acute hematogenous osteomyelitis incidence after nonpharmaceutical interventions highlight the role of seasonal viruses: An interrupted time-series analysis - Scorecard - MDSpire
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Changes in the Incidence of Acute Hematogenous Osteomyelitis from Unidentified Pathogens Following Nonpharmaceutical Interventions: Insights from an Interrupted Time-Series Study on Seasonal Viral Impact
Clinical Scorecard: Changes in the Incidence of Acute Hematogenous Osteomyelitis from Unidentified Pathogens Following Nonpharmaceutical Interventions: Insights from an Interrupted Time-Series Study on Seasonal Viral Impact
Acute hematogenous osteomyelitis develops as a complication of bacteremia. In young children, Kingella kingae is considered a leading cause of UP-AHO, and viral infections may facilitate bacterial translocation from the oropharynx into the bloodstream.
Target Population
Children aged 1 to <5 years hospitalized with UP-AHO in mainland France
Care Setting
Hospital-based pediatric care in France
Key Highlights
Osteoarticular infections have an estimated incidence of approximately 22 cases per 100,000 children in France, and AHO accounts for about 40% of osteoarticular infections in children younger than 5 years.
In France, Israel, and Switzerland, K. kingae is considered to be involved in 50%-80% of AHO cases in young children and is probably the leading pathogen in UP-AHO.
Blood cultures are positive in only approximately 20%-30% of AHO cases, making the underlying epidemiology difficult to establish.
UP-AHO incidence decreased 57.6% immediately after COVID-19-related NPIs were implemented in March 2020 and increased 101.0% after school reopening in September 2020.
Human rhinovirus accounted for an estimated 21.3% of UP-AHO incidence and varicella-zoster virus for 9.8%; no significant associations were found for the other viruses studied.
Guideline-Based Recommendations
The study was an observational interrupted time-series analysis rather than a clinical guideline. The following reflects diagnostic, management, and surveillance considerations described in the study and cited guidance.
Diagnosis
The study identified UP-AHO using ICD-10 codes M860, M861, M862, and M869 while excluding cases associated with S. aureus, S. pyogenes, or S. pneumoniae, as well as sickle cell disease and prosthesis-related infections.
Because microbiological confirmation is often limited, the authors note that K. kingae may be underrecognized, particularly in milder disease that does not require surgical intervention or deep sampling.
Management
French guidance cited by the authors recommends intravenous antibiotic therapy for at least the first 3 days of osteomyelitis treatment, which is typically administered in hospitals.
K. kingae should be considered an important potential pathogen in young children with UP-AHO because it is probably the leading cause in this age group in the study setting.
Monitoring & Follow-up
Population-level monitoring of seasonal virus circulation may help clarify changes in UP-AHO incidence over time.
The authors found the strongest temporal associations with human rhinovirus and, to a lesser extent, varicella-zoster virus.
Risks
K. kingae can colonize the oropharynx and may enter the bloodstream; viral infections may compromise the mucosal barrier and facilitate bacterial translocation.
Patient & Prescribing Data
The study included 5,619 children aged 1 to <5 years hospitalized with UP-AHO from January 2015 through August 2023. The median age was 2 years, and 73.9% were aged 1 to <3 years.
Joint aspiration was performed in 4.1% of patients and bone biopsy in 8.0%. The authors note that K. kingae often causes mild AHO forms that rarely require surgical intervention or deep sampling.
Clinical Best Practices
Use comprehensive hospital-based surveillance to monitor UP-AHO incidence and changes over time.
Consider the possible contribution of seasonal viral circulation when evaluating epidemiological shifts in UP-AHO among young children.
Interpret associations cautiously because viral circulation was assessed at the population level rather than through individual virologic testing in children with UP-AHO.
Related Resources & Content
Clinical Practice Guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 Guideline on Diagnosis and Management of Acute Hematogenous Osteomyelitis in Pediatrics — Woods CR, Bradley JS, Chatterjee A, et al; Journal of the Pediatric Infectious Diseases Society; 2021; 10:801-844.
Temporal Association Between Rhinovirus Activity and Kingella kingae Osteoarticular Infections — Droz N, Enouf V, Bidet P, et al; Journal of Pediatrics; 2018; 192:234-239.e2.
High Respiratory Virus Oropharyngeal Carriage Rate During Kingella kingae Osteoarticular Infections in Children — Basmaci R, Bonacorsi S, Ilharreborde B, et al; Future Microbiology; 2015; 10:9-14.
Antibiotic Therapy for Osteoarticular Infections in 2023: Proposals From the Pediatric Infectious Pathology Group (GPIP) — Lorrot M, Gillet Y, Basmaci R, et al; Infectious Diseases Now; 2023; 53:104789.