Pulmonary embolism in children with mycoplasma pneumonia: can it be predicted?

Jiapu Hou1,2, Ruiyang Sun1,2, Xue Zhang1,2

  • 1Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan, 450052, China.

Abstract

Insights

Pediatric Mycoplasma pneumoniae pneumonia (MPP) with pulmonary embolism (PE) can present with unusual symptoms. Elevated D-dimer, IL-6, CRP, and LDH levels may indicate a higher risk of PE in children with MPP.

Area of Science:

  • Pediatric Pulmonology
  • Infectious Diseases
  • Cardiovascular Medicine

Background:

  • Mycoplasma pneumoniae pneumonia (MPP) is a common childhood respiratory infection.
  • Pulmonary embolism (PE) is a serious complication that can occur in children with MPP.
  • Understanding the clinical characteristics of combined MPP and PE is crucial for early diagnosis and management.

Purpose of the Study:

  • To investigate the clinical characteristics of pediatric Mycoplasma pneumoniae pneumonia (MPP) complicated with pulmonary embolism (PE).
  • To identify potential biomarkers for predicting PE in children with MPP.

Main Methods:

  • A retrospective study of 291 hospitalized pediatric cases with MPP was conducted.
  • Cases were divided into a PE group (141) and a non-PE control group (150).
  • Clinical data, including laboratory markers and symptoms, were analyzed and compared between the groups.

Main Results:

  • The PE group exhibited significantly higher levels of C-reactive protein (CRP), D-dimer, lactate dehydrogenase (LDH), and interleukin-6 (IL-6) compared to the non-PE group.
  • Key indicators for PE prediction included D-dimer (AUC=0.964), LDH (AUC=0.765), CRP (AUC=0.690), and IL-6 (AUC=0.632).
  • Pulmonary necrosis was observed in 63.12% of the PE group, with hemoptysis and chest pain also noted.

Conclusions:

  • Pediatric MPP with PE can manifest with atypical clinical symptoms.
  • Elevated D-dimer, IL-6, CRP, and LDH levels are associated with an increased risk of PE in children with MPP.
  • These findings aid in identifying high-risk pediatric patients for timely PE diagnosis and intervention.