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Incorporation of biomarkers into a prediction model for paediatric radiographic pneumonia
Sriram Ramgopal1, Lilliam Ambroggio2, Douglas Lorenz3
1Division of Emergency Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, Department of Pediatrics, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Insights
C-reactive protein (CRP) can help predict pneumonia in children with lower respiratory tract infections (LRTI). Combining CRP with clinical factors improves diagnostic accuracy for radiographic pneumonia.
Area of Science:
- Pediatric Medicine
- Infectious Diseases
- Diagnostic Biomarkers
Background:
- Lower respiratory tract infections (LRTI) are common in children.
- Accurate diagnosis of radiographic pneumonia is crucial for appropriate treatment.
- Existing clinical models may have limitations in predicting pneumonia.
Purpose of the Study:
- To evaluate the predictive value of biomarkers for radiographic pneumonia in children with suspected LRTI.
- To assess the performance of C-reactive protein (CRP) and other biomarkers in conjunction with a clinical model.
Main Methods:
- Prospective cohort study of 580 children (3 months to 18 years) with suspected LRTI.
- Evaluation of white blood cell count, absolute neutrophil count, CRP, and procalcitonin.
- Multivariable logistic regression analysis incorporating biomarkers and a clinical model.
Main Results:
- 36.7% of children had radiographic pneumonia.
- CRP showed the strongest association with radiographic pneumonia (OR 1.79).
- A model with CRP and clinical variables improved sensitivity (70.0%) and diagnostic performance (c-index 0.812) compared to clinical variables alone.
Conclusions:
- A combined model of clinical variables and CRP enhances the identification of pediatric radiographic pneumonia.
- CRP is a valuable biomarker for predicting pneumonia in children with LRTI.
Objective:
The aim of this study was to evaluate biomarkers to predict radiographic pneumonia among children with suspected lower respiratory tract infections (LRTI).
Methods:
We performed a single-centre prospective cohort study of children 3 months to 18 years evaluated in the emergency department with signs and symptoms of LRTI. We evaluated the incorporation of four biomarkers (white blood cell count, absolute neutrophil count, C-reactive protein (CRP) and procalcitonin), in isolation and in combination, with a previously developed clinical model (which included focal decreased breath sounds, age and fever duration) for an outcome of radiographic pneumonia using multivariable logistic regression. We evaluated the improvement in performance of each model with the concordance (c-) index.
Results:
Of 580 included children, 213 (36.7%) had radiographic pneumonia. In multivariable analysis, all biomarkers were statistically associated with radiographic pneumonia, with CRP having the greatest adjusted odds ratio of 1.79 (95% CI 1.47-2.18). As an isolated predictor, CRP at a cut-off of 3.72 mg·dL-1 demonstrated a sensitivity of 60% and a specificity of 75%. The model incorporating CRP demonstrated improved sensitivity (70.0% versus 57.7%) and similar specificity (85.3% versus 88.3%) compared to the clinical model when using a statistically derived cutpoint. In addition, the multivariable CRP model demonstrated the greatest improvement in concordance index (0.780 to 0.812) compared with a model including only clinical variables.
Conclusion:
A model consisting of three clinical variables and CRP demonstrated improved performance for the identification of paediatric radiographic pneumonia compared with a model with clinical variables alone.
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