Predictors of Outcome in Pediatric Osteomyelitis: Five Years Experience in a Single Tertiary Center

Andrew C Martin1, Denise Anderson, Julie Lucey

  • 1From the *Department of General Paediatrics, Princess Margaret Hospital for Children, Perth, Australia; †School of Paediatrics and Child Health, The University of Western Australia, Perth, Australia, ‡Telethon Kids Institute, Perth, Australia; §Department of Orthopaedic Surgery, Princess Margaret Hospital for Children, Perth, Australia; ¶Murdoch Childrens Research Institute, Parkville, Australia; ‖Department of Paediatrics, University of Melbourne, Parkville, Australia; **Department of Paediatrics, Monash University, Clayton, Australia; ††PathWest Laboratory Medicine WA, Princess Margaret Hospital for Children, Perth, Australia; and ‡‡Department of Infectious Diseases, Princess Margaret Hospital for Children, Perth, Australia.

Insights

Predicting complicated osteomyelitis in children is challenging. A simple risk model using admission data like age and C-reactive protein can identify high-risk pediatric patients early.

Area of Science:

  • Pediatric infectious diseases
  • Bone infections
  • Clinical risk prediction

Background:

  • Acute haematogenous osteomyelitis is a common bone infection in children.
  • Most children recover well, but some develop complicated disease, posing a diagnostic challenge.
  • Early identification of complicated osteomyelitis is crucial, especially with short hospital stays.

Purpose of the Study:

  • To identify predictors of complicated acute haematogenous osteomyelitis in children.
  • To develop a risk prediction model for complicated pediatric osteomyelitis.
  • To enable early identification of children at high risk for severe outcomes.

Main Methods:

  • Retrospective review of case notes for children aged 3 months to 16 years diagnosed with acute haematogenous osteomyelitis.
  • Comparison of clinical and laboratory parameters between simple and complicated osteomyelitis cases.
  • Analysis of 299 pediatric patients over a 5-year period.

Main Results:

  • 80.6% of children had simple osteomyelitis, while 19.4% developed complicated disease.
  • Key predictors for complicated osteomyelitis included older age, fever >38.5°C, and elevated C-reactive protein (CRP) on admission.
  • These factors were identified from standardized clinical and laboratory data.

Conclusions:

  • A risk prediction model using readily available admission data can effectively identify children at high risk for complicated osteomyelitis.
  • Early risk stratification allows for timely intervention and tailored management strategies.
  • This model aids clinicians in developed countries with short hospitalizations to manage pediatric osteomyelitis.
Abstract

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