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Updated: Aug 1, 2026

Subcutaneous Infection of Methicillin Resistant Staphylococcus Aureus MRSA
Published on: February 9, 2011
Predictive value of AFR and UCR for the methicillin-resistant Staphylococcus aureus infection in children with bone
Chaochen Zhao1, Chenghui Ke1, Zhiye Guan1
1Department of Orthopedics, Shanghai Children's Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Abstract:
Methicillin-resistant Staphylococcus aureus (MRSA) poses diagnostic and therapeutic challenges in pediatric bone and joint infections (BJIs). This two-center retrospective study evaluated the admission albumin-to-fibrinogen ratio (AFR) and urea-to-creatinine ratio (UCR) as predictors of MRSA among children with culture-confirmed S. aureus BJIs. Seventy-seven patients (MRSA, n = 23; MSSA, n = 54) admitted from 2015 to 2024 were analyzed. Clinical data and laboratory tests obtained before antibiotic initiation were reviewed. Compared with MSSA, the MRSA group had significantly lower AFR and UCR values. Using Firth's penalized logistic regression, AFR and UCR were incorporated as continuous covariates to construct a composite indicator (AFR + UCR). The model showed acceptable discrimination (AUC = 0.724, 95% CI 0.612-0.854) and good calibration (Hosmer-Lemeshow P = 0.273; Brier score = 0.184), with internal validation by stratified 10-fold cross-validation and 1,000 bootstrap resamples. At a prespecified probability cutoff of 0.293, sensitivity and specificity were 0.826 and 0.611, respectively. Decision curve analysis indicated net clinical benefit across threshold probabilities of approximately 10-60%. In pediatric BJIs, lower AFR and UCR at admission are associated with increased MRSA risk, and their combination may serve as an adjunctive tool for early risk assessment and empirical treatment planning. Findings pertain to culture-positive S. aureus infections; external validation in larger multicenter cohorts is warranted to confirm generalizability and clinical utility.
Insights
Lower admission albumin-to-fibrinogen ratio (AFR) and urea-to-creatinine ratio (UCR) predict methicillin-resistant Staphylococcus aureus (MRSA) in pediatric bone and joint infections. These ratios can aid early risk assessment for MRSA in children.
Area of Science:
- Pediatric Infectious Diseases
- Clinical Diagnostics
- Biomarker Research
Background:
- Pediatric bone and joint infections (BJIs) caused by Staphylococcus aureus present diagnostic and treatment challenges, particularly with methicillin-resistant Staphylococcus aureus (MRSA) strains.
- Early identification of MRSA is crucial for effective empirical antibiotic selection and improved patient outcomes.
Purpose of the Study:
- To evaluate the admission albumin-to-fibrinogen ratio (AFR) and urea-to-creatinine ratio (UCR) as predictors of MRSA in pediatric patients with culture-confirmed S. aureus BJIs.
- To develop and validate a composite indicator using AFR and UCR for early MRSA risk assessment.
Main Methods:
- Retrospective analysis of 77 pediatric patients with S. aureus BJIs (23 MRSA, 54 MSSA) from two centers (2015-2024).
- Clinical data and laboratory values (AFR, UCR) obtained before antibiotic initiation were reviewed.
- Firth's penalized logistic regression was used to construct a composite indicator (AFR + UCR), with model performance assessed by discrimination (AUC) and calibration (Hosmer-Lemeshow, Brier score), and validated using 10-fold cross-validation and bootstrap resampling.
Main Results:
- The MRSA group exhibited significantly lower admission AFR and UCR values compared to the methicillin-sensitive Staphylococcus aureus (MSSA) group.
- The composite AFR + UCR model demonstrated acceptable discrimination (AUC = 0.724) and good calibration.
- At a probability cutoff of 0.293, the model achieved a sensitivity of 0.826 and specificity of 0.611, indicating clinical utility across a range of threshold probabilities.
Conclusions:
- Lower admission AFR and UCR are associated with an increased risk of MRSA in pediatric S. aureus BJIs.
- The combination of AFR and UCR serves as a valuable adjunctive tool for early risk stratification and guiding empirical treatment decisions in pediatric BJIs.
- Further external validation in larger, multicenter cohorts is recommended to confirm generalizability and clinical utility.
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