Procalcitonin, C-reactive protein and leukocyte count in children with lower respiratory tract infection

Cristina Prat1, Josep Domínguez, Carlos Rodrigo

  • 1Servei de Microbiologia, Hospital Universitari Germans Trias i Pujol, C/Canyet s/n, 08916 Badalona, Spain. crisprat@ns.hugtip.scs.es

Insights

Procalcitonin (PCT) and C-reactive protein (CRP) effectively help differentiate bacterial from viral lower respiratory tract infections in children. These biomarkers aid in guiding antibiotic treatment decisions when the specific pathogen is unclear.

Area of Science:

  • Pediatric Infectious Diseases
  • Clinical Biochemistry
  • Diagnostic Biomarkers

Background:

  • Lower respiratory tract infections (LRTI) are common in children, often leading to empirical antibiotic use.
  • Rapid etiological diagnosis of LRTI is challenging, with pathogens frequently unidentified.
  • Clinical and laboratory factors alone do not reliably distinguish bacterial from viral LRTI.

Purpose of the Study:

  • To assess the diagnostic accuracy of procalcitonin (PCT), C-reactive protein (CRP), and leukocyte count.
  • To differentiate between pneumococcal, atypical, and viral etiologies in pediatric LRTI.

Main Methods:

  • Measured PCT, CRP, and leukocyte counts in children with microbiologically confirmed LRTI.
  • Compared biomarker levels across different etiological groups (pneumococcal, atypical, viral).

Main Results:

  • PCT and CRP levels significantly correlated with bacterial LRTI etiology; leukocyte count did not.
  • PCT (cutoff 2 ng/ml) and CRP (cutoff 65 mg/l) showed moderate sensitivity and specificity for bacterial vs. viral LRTI.
  • PCT and CRP demonstrated high sensitivity (90.3%) for distinguishing pneumococcal from other LRTI causes.

Conclusions:

  • Elevated PCT and CRP levels are strongly associated with bacterial LRTI in children.
  • PCT and CRP are valuable tools for differentiating pneumococcal infections and guiding antibiotic therapy decisions.
  • PCT offers higher specificity than CRP in distinguishing bacterial from viral etiologies.
Abstract