PAEDIATRIC
PAEDIATRIC
ORTHOPAEDIC INFECTIONS
In this topic:
Common organisms according to age groups:
≤ 3 months
S. aureus
Streptococcus agalactiae
Gram-negative enteric organism
>3 months to 5 years old
Staphylococcus aureus
Streptococcus pyogenes
Streptococcus pneumoniae
Non-typeable Haemophilus spp.
Kingella kingae
Older than 5 years
Staphylococcus aureus
Streptococcus pyogenes
Polymicrobial infection: More likely with penetrating trauma or contagious spread
Preferred
0 - 3 months old
Cloxacillin 200mg/kg/day IV in 4-6 divided doses (max. 2g/dose)
PLUS
Cefotaxime 200mg/kg/day IV in 4 divided doses (max. 2g/dose)
>3 months to 5 years old
Cloxacillin 200mg/kg/day IV in 4-6 divided doses (max. 2g/dose)
MAY ADD
Cefuroxime 100-200mg/kg/day IV in 3 divided doses (max. 1.5g/dose) (monotherapy)
OR
Cefotaxime 200mg/kg/day IV in 4 divided doses (max. 2g/dose)
Older than 5 years old
Cloxacillin 200 mg/kg/day IV in 4-6 divided doses (max. 2g/dose)
Alternative
0 - 3 months old
Cefazolin is alternative anti-staphylococcal agent for infants age 1-3 months if no CNS involvement
>3 months
Cefazolin 100-150mg/kg/day IV in 3 divided doses (max. 1g/dose)
(Can be used in children with suspected S. aureus or S. pyogenes. Less hypersensitivity reaction compared to cloxacillin & more convenient dosing)
Kingella kingae: uncommon organism causing infection in <5 years old; indolent onset; preceding oral ulcers; may affect nontubular bones; sensitive to β-lactam antibiotics e.g., cefuroxime or amoxicillin/clavulanate
Comments
Empiric antibiotics should be started based on clinical diagnosis of SA or OM.
CBC, blood cultures and CRP +/- ESR should be taken prior to antibiotic therapy.
Optimise antimicrobial treatment based on C&S.
Surgical debridement often not required in OM.
Urgent wash out & drainage is needed in SA in hip and other joints to reduce pressure on growth plate.
Synovial fluid and bone culture/analysis is part of diagnostic work up if child is subjected to drainage or debridement.
Duration of antibiotics:
SA: total of 3-4 weeks (*4-6 weeks if hip is involved)
OM: 4-6 weeks
For both SA and OM, transition to oral antibiotic is based on clinical and laboratory improvement if compliance and follow up is assured.
Shorter duration of 3-4 weeks antibiotics for uncomplicated MSSA or culture negative OM responded to initial therapy for children > 3 months old.
Neonatal OM: Similar duration for other age group but at least 4 weeks of IV antibiotics.
Choice of oral regimen is based on culture and susceptibility results. If cultures are negative, oral therapy is directed toward the most likely pathogen with similar spectrum of activity as parenteral therapy. Higher doses are generally given to ensure adequate bone penetration.
Uncomplicated OM is defined as single bone involvement, rapid resolution of bacteremia, rapid clinical response to medical and surgical treatment, rapid fall of CRP with no identified acute or late sequalae of infection.
Complex OM (multifocal, significant bone destruction, immunocompromised host & resistant/unusual pathogens), prolonged IV antibiotics are needed & duration might exceed 6 weeks.
References:
David W. Kimberlin, Elizabeth D. Barnett, Ruth Lynfield, Mark H. Sawyer, American Academy of Pediatrics: Red Book 2021-2024 Report of the committee on Infectious Diseases.
Woods CR, Bradley JS, Chatterjee A, et al. Guideline on diagnosis and management of acute hematogenous osteomyelitis in pediatrics. Clinical practice guideline by the Pediatric Infectious Diseases Society (PIDS) and Infectious Diseases Society of America (IDSA): 2020
Manual of childhood infections-Blue Book 4th edition; Oxford University Press
Annaleise R Howard-Jones1 and David Isaacs1. Systematic review of duration and choice of systemic antibiotic therapy for acute haematogenous bacterial osteomyelitis in children. Journal of Paediatrics and Child Health © 2013 Paediatrics and Child Health Division
Cornelia M Donders, Anne J Spaans, Herbert van Wering, Christiaan JA van Bergen, Developments in diagnosis and treatment of paediatric septic arthritis. World J Orthop 2022 February 18; 13(12):122-130