AI Article Synopsis

  • E. coli bloodstream infections (BSI) among children in Africa are increasing, with limited prior studies on antibiotic resistance in this context.
  • A 10-year study analyzed 583 E. coli BSI cases, revealing a 2.7 incidence risk per 1,000 hospital admissions, with 29.9% caused by extended-spectrum β-lactamase (ESBL)-producing strains.
  • Key risk factors for severe disease included recent hospitalization, chronic illnesses, and high fever, with a 5.9% mortality rate and intensive care admission required for 12.3% of cases; overall findings can help shape treatment and prevention strategies.

Article Abstract

Introduction: There are few studies describing Escherichia coli (E. coli) bloodstream infection (BSI) among children in Africa, yet E.coli is increasing in importance as a cause of antibiotic resistant infection in paediatric settings.

Methods: In this retrospective, descriptive study aspects of E. coli BSI epidemiology are described over a 10-year period including incidence risk, risk factors for extended-spectrum β-lactamase (ESBL)-producing E. coli BSI, antibiotic susceptibility of the bacterial isolates and outcome including risk factors for severe disease.

Results: There were 583 new E. coli BSI episodes among 217,483 admissions, an overall incidence risk of 2.7 events/1,000 hospital admissions. Of 455 of these E. coli BSI episodes that were analysed, 136 (29.9%) were caused by ESBL-producing isolates. Risk factors for ESBL-producing E. coli BSI included hospitalization in the 28-day period preceding E. coli BSI episodes, having an underlying chronic illness other than HIV infection at the time of the E. coli BSI and having a temperature of 38° Celsius or higher at the time of the E. coli BSI. None of the E. coli isolates were resistant to carbapenems or colistin. The mortality rate was 5.9% and admission to the intensive care unit was required in 12.3% of BSI episodes. Predictors of severe disease included age less than 1 month, hospitalization in the 28-day period preceding E. coli BSI and BSI without a definable focus.

Conclusions: These findings extend our understanding of E. coli BSI in a sub-Saharan African setting, provide useful information that can guide empiric treatment choices for community- and hospital-acquired BSI and help inform prevention strategies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759190PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0222675PLOS

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