Nasopharyngeal Carriage and Antibiotic Resistance in Children With Sickle Cell Disease: The DREPANOBACT French

Luu-Ly Pham1,2, Emmanuelle Varon3,4, Stéphane Bonacorsi2,4,5

  • 1From the Pediatrics Department, Jean Verdier Hospital, AP-HP, Sorbonne Paris-Nord University, Bondy.

Insights

Children with sickle cell disease (SCD) have high rates of resistant Streptococcus pneumoniae nasopharyngeal carriage. Surveillance is crucial to monitor evolving serotypes and resistance patterns in this vulnerable population.

Area of Science:

  • Pediatric Infectious Diseases
  • Microbiology
  • Hematology

Background:

  • Children with sickle cell disease (SCD) face increased risk of invasive bacterial infections, especially from Streptococcus pneumoniae.
  • Limited data exist on nasopharyngeal carriage of bacteria in children with SCD, a group prone to resistant strains due to antibiotic use and hospitalizations.

Purpose of the Study:

  • To assess the nasopharyngeal carriage rate of Streptococcus pneumoniae in children with SCD.
  • To determine serotype distribution and penicillin resistance of S. pneumoniae.
  • To evaluate carriage and antibiotic resistance rates for Staphylococcus aureus, Moraxella catarrhalis, and Haemophilus influenzae.

Main Methods:

  • Prospective trial (DREPANOBACT) conducted in 7 French hospitals.
  • Enrolled 300 children aged 6 months to 15 years with SCD.
  • Collected data on bacterial carriage, serotypes, and antibiotic resistance patterns.

Main Results:

  • Streptococcus pneumoniae carriage found in 11% of children, with 66% of strains being penicillin-nonsusceptible.
  • Predominant serotypes were often non-PCV13, with limited coverage by PCV20 and PCV21.
  • Carriage rates for S. aureus (31%), M. catarrhalis (17%), and H. influenzae (11%) were reported, with 5% MRSA.
  • Younger age (≤5 years) associated with S. pneumoniae, M. catarrhalis, and H. influenzae carriage; older age (≥11 years) associated with S. aureus.

Conclusions:

  • Nasopharyngeal carriage surveillance in children with SCD is essential.
  • Monitoring changes in predominant serotypes and antibiotic resistance is critical for this high-risk group.
Abstract

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