Atelectasis predicts poor prognosis in pediatric macrolides-unresponsive Mycoplasma pneumoniae pneumonia with

Jie Cheng1, Ya Liu2, Guangli Zhang3

  • 1Department of Emergency, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Intelligent Application of Big Data in Pediatrics Engineering Research Center of Chongqing Education Commission of China, Children's Hospital of Chongqing Medical University, Chongqing, China.

Abstract

Insights

Atelectasis is a key indicator of poor prognosis in pediatric macrolides-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP) with A2063/2064G mutations. Early detection of atelectasis can help predict treatment failure and guide individualized interventions for better outcomes.

Area of Science:

  • Pediatric Infectious Diseases
  • Respiratory Medicine
  • Clinical Microbiology

Background:

  • Macrolides-unresponsive Mycoplasma pneumoniae pneumonia (MUMPP) with specific mutations (A2063/2064G) poses a treatment challenge in children.
  • Azithromycin is a common treatment, but resistance necessitates identifying prognostic indicators for adverse outcomes.

Purpose of the Study:

  • To investigate prognostic indicators for pediatric MUMPP cases with A2063/2064G mutations treated with azithromycin.
  • To identify risk factors for short-term (refractory MUMPP) and long-term (bronchiolitis obliterans or bronchiectasis) adverse prognosis.

Main Methods:

  • Retrospective observational cohort study of 82 children with MUMPP and A2063/2064G mutations treated with azithromycin.
  • Logistic regression analysis was employed to identify independent risk factors for adverse outcomes.
  • Results were visualized using forest plots.

Main Results:

  • Atelectasis was independently associated with both short-term (refractory MUMPP) and long-term (bronchiolitis obliterans or bronchiectasis) adverse prognosis.
  • The odds ratio for atelectasis predicting short-term adverse prognosis was 4.02 (95% CI 1.03-16.00, P=0.043).
  • The odds ratio for atelectasis predicting long-term adverse prognosis was 5.62 (95% CI 1.04-32.80, P=0.045).

Conclusions:

  • Atelectasis is a significant predictor of poor prognosis in pediatric patients with A2063/2064G MUMPP.
  • The presence of atelectasis may signal an increased risk of azithromycin treatment failure.
  • Enhanced disease monitoring and individualized intervention strategies are recommended for patients with atelectasis and drug-resistant MUMPP.