Ventilator-associated pneumonia in PICU - how are we doing?

L van Wyk1, J T Applegate2, S Salie1,2

  • 1Department of Paediatrics and Child Health, Faculty of Health Sciences, University of Cape Town, South Africa.

Insights

Ventilator-associated pneumonia (VAP) rates in pediatric intensive care units remain unchanged. Improving adherence to VAP bundles is crucial for reducing infection rates and enhancing patient outcomes.

Area of Science:

  • Pediatric Intensive Care
  • Infection Control
  • Hospital-Acquired Infections

Background:

  • Ventilator-associated pneumonia (VAP) is a significant cause of morbidity and mortality in pediatric intensive care units (PICUs).
  • Previous interventions in 2013, including a VAP bundle and coordinator, initially reduced VAP rates.
  • Ongoing evaluation is necessary to assess the sustained efficacy of these quality improvement initiatives.

Purpose of the Study:

  • To evaluate the VAP rate in a PICU between 2017 and 2018.
  • To identify the primary causative microorganisms of VAP during this period.
  • To analyze antibiotic sensitivity and resistance patterns for effective treatment strategies.

Main Methods:

  • A retrospective, descriptive study design was employed.
  • Data were collected from the existing PICU VAP database and patient clinical records.
  • Analysis included VAP incidence, causative organisms, and antibiotic susceptibility.

Main Results:

  • A total of 31 VAP cases were identified over the two-year study period.
  • VAP rates were 4.0/1000 ventilator days in 2017 and 5.4/1000 ventilator days in 2018.
  • Extended-spectrum beta-lactamase (ESBL) *Klebsiella pneumoniae* was the most common organism, sensitive to amikacin and carbapenems.

Conclusions:

  • VAP rates have not decreased since 2013, indicating a need for improved interventions.
  • Enhanced compliance with the VAP bundle is essential to effectively reduce VAP incidence.
  • *Klebsiella pneumoniae* and *Pseudomonas aeruginosa* remain common pathogens, supporting the empiric use of piptazobactam and amikacin.
Abstract

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