Neonatal Colonization With Antibiotic-Resistant Pathogens in Low- and Middle-Income Countries: A Systematic Review

Anne-Lise Beaumont1,2, Elsa Kermorvant-Duchemin3, Sébastien Breurec4,5,6,7

  • 1Anti-Infective Evasion and Pharmacoepidemiology Team, Center for Epidemiology and Population Health, Université Paris-Saclay, UVSQ, INSERM, Montigny-le-Bretonneux, France.

JAMA Network Open
|November 5, 2024
PubMed

Insights

Neonatal colonization with antibiotic-resistant bacteria like third-generation cephalosporin-resistant Enterobacterales (3GCRE) is common in LMICs. Hospital birth and neonatal antibiotic use increase the risk of 3GCRE colonization, highlighting the need for preventive strategies.

Area of Science:

  • Medical Microbiology
  • Public Health
  • Infectious Diseases

Background:

  • Neonatal bacterial infections in low- and middle-income countries (LMICs) are primarily caused by Enterobacterales and Staphylococcus aureus.
  • These pathogens are leading causes of mortality linked to antimicrobial resistance (AMR).
  • Understanding bacterial colonization patterns is crucial for preventing antibiotic-resistant neonatal sepsis.

Purpose of the Study:

  • To synthesize evidence on the prevalence of and factors associated with colonization by third-generation cephalosporin-resistant Enterobacterales (3GCRE), carbapenem-resistant Enterobacterales (CRE), and methicillin-resistant S. aureus (MRSA).
  • To assess colonization in neonates and infants up to 3 months of age in LMICs.

Main Methods:

  • Systematic review and meta-analysis of studies published between 2000 and 2024.
  • Searched PubMed, Scopus, Web of Science, and WHO Global Index Medicus.
  • Included studies from LMICs reporting prevalence or associated factors for 3GCRE, CRE, or MRSA colonization in infants up to 3 months; excluded outbreak reports.

Main Results:

  • Pooled prevalence of 3GCRE colonization was 30.2%, higher in hospitalized (48.2%) versus non-hospitalized (18.2%) individuals.
  • Prevalence of CRE colonization was 2.6%, and MRSA colonization was 2.7%.
  • Increased risk of 3GCRE colonization was associated with hospital birth (OR 1.87), neonatal antibiotic use (OR 2.96), and prolonged rupture of membranes (OR 3.86).

Conclusions:

  • A substantial prevalence of antibiotic-resistant pathogen colonization exists in neonates and young infants in LMICs.
  • High heterogeneity among studies limits broad extrapolation.
  • Further research is needed to identify transmission routes and develop targeted preventive measures against neonatal sepsis.
Abstract

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