Pulmonary lesion volume ratio and laboratory parameters as risk factors for plastic bronchitis in pediatric

Jiahui Wu1, Fangfang Cheng1, Xiaoxing Kong1

  • 1Department of Infectious Diseases, Children's Hospital of Soochow University, No. 92, Zhongnan Street, Suzhou, 215025, China.

BMC Pediatrics
|November 22, 2025
PubMed

Insights

Refractory Mycoplasma pneumoniae pneumonia (RMPP) can lead to plastic bronchitis (PB). Key risk factors for PB in children include elevated neutrophil-to-lymphocyte ratio (NLR), lactate dehydrogenase (LDH), and alanine aminotransferase (ALT), along with increased pulmonary lesion volume and reduced activated partial thromboplastin time (APTT).

Area of Science:

  • Pediatric Pulmonology
  • Infectious Diseases
  • Critical Care Medicine

Background:

  • Refractory Mycoplasma pneumoniae pneumonia (RMPP) is a severe respiratory illness in children.
  • Plastic bronchitis (PB) is a known complication of RMPP, necessitating identification of predictive factors.
  • Early detection of PB risk can improve patient outcomes and guide treatment strategies.

Purpose of the Study:

  • To identify clinical risk factors associated with the development of plastic bronchitis (PB) in pediatric patients diagnosed with refractory Mycoplasma pneumoniae pneumonia (RMPP).
  • To develop a predictive model for early risk stratification of PB in pediatric RMPP cases.

Main Methods:

  • A cohort of 361 pediatric RMPP patients undergoing bronchoscopy was divided into PB and non-PB groups.
  • Clinical characteristics, laboratory markers (including NLR, LDH, ALT, APTT), and chest CT findings were analyzed.
  • Multivariate logistic regression and ROC analysis identified independent predictors and assessed diagnostic performance; a scoring system was developed.

Main Results:

  • PB patients exhibited higher rates of extrapulmonary lesions, pleural effusion, and treatment resistance.
  • Independent predictors for PB included elevated NLR (≥3.30), LDH (≥451.0 U/L), ALT (≥21.75 U/L), pulmonary lesion volume ratio (≥8.23%), and reduced APTT (≤35.95s).
  • A combined predictive model achieved 85.70% sensitivity and 84.90% specificity (AUC=0.92), enabling effective risk stratification into high, middle, and low-risk groups.

Conclusions:

  • Elevated NLR, LDH, ALT, increased pulmonary lesion volume, and reduced APTT are significant independent risk factors for PB in pediatric RMPP.
  • A scoring system integrating these factors allows for early identification and risk stratification of PB.
  • This facilitates timely clinical intervention for pediatric RMPP patients at risk of developing PB.
Abstract