Development and Internal Validation of a Prediction Model to Risk Stratify Children With Suspected Community-Acquired Pneumonia

Author:

Florin Todd A12ORCID,Ambroggio Lilliam34,Lorenz Douglas5,Kachelmeyer Andrea67,Ruddy Richard M67,Kuppermann Nathan8,Shah Samir S69

Affiliation:

1. Department of Pediatrics, Northwestern University Feinberg School of Medicine and Division of Emergency Medicine, Chicago, Illinois, USA

2. Ann and Robert H. Lurie Children’s Hospital of Chicago, Chicago, Illinois, USA

3. Department of Pediatrics, University of Colorado School of Medicine, Aurora, Colorado, USA

4. Section of Emergency Medicine, Children’s Hospital Colorado, Aurora, Colorado, USA

5. Department of Bioinformatics and Biostatistics, University of Louisville, Louisville, Kentucky, USA

6. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, Ohio, USA

7. Division of Emergency Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, USA

8. Departments of Emergency Medicine and Pediatrics, University of California, Davis School of Medicine and UC Davis Health, Sacramento, California, USA

9. Divisions of Hospital Medicine and Infectious Diseases, Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, USA

Abstract

Abstract Background Although community-acquired pneumonia (CAP) is one of the most common infections in children, no tools exist to risk stratify children with suspected CAP. We developed and validated a prediction model to risk stratify and inform hospitalization decisions in children with suspected CAP. Methods We performed a prospective cohort study of children aged 3 months to 18 years with suspected CAP in a pediatric emergency department. Primary outcome was disease severity, defined as mild (discharge home or hospitalization for <24 hours with no oxygen or intravenous [IV] fluids), moderate (hospitalization <24 hours with oxygen or IV fluids, or hospitalization >24 hours), or severe (intensive care unit stay for >24 hours, septic shock, vasoactive agents, positive-pressure ventilation, chest drainage, extracorporeal membrane oxygenation, or death). Ordinal logistic regression and bootstrapped backwards selection were used to derive and internally validate our model. Results Of 1128 children, 371 (32.9%) developed moderate disease and 48 (4.3%) severe disease. Severity models demonstrated excellent discrimination (optimism-corrected c-indices of 0.81) and outstanding calibration. Severity predictors in the final model included respiratory rate, systolic blood pressure, oxygenation, retractions, capillary refill, atelectasis or pneumonia on chest radiograph, and pleural effusion. Conclusions We derived and internally validated a score that accurately predicts disease severity in children with suspected CAP. Once externally validated, this score has potential to facilitate management decisions by providing individualized risk estimates that can be used in conjunction with clinical judgment to improve the care of children with suspected CAP.

Funder

National Institute of Allergy and Infectious Diseases

National Institutes of Health

National Center for Research Resources

Cincinnati Center for Clinical and Translational Science and Training

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

Reference31 articles.

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2. British Thoracic Society guidelines for the management of community acquired pneumonia in children: update 2011;Harris;Thorax,2011

3. Wide geographic variation between Pennsylvania counties in the population rates of hospital admissions for pneumonia among children with and without comorbid chronic conditions;Gorton;Pediatrics,2006

4. Variation in emergency department diagnostic testing and disposition outcomes in pneumonia;Florin;Pediatrics,2013

5. Biomarkers and disease severity in children with community-acquired pneumonia;Florin;Pediatrics,2020

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