Ventilator-associated events in children: A review of literature
Noor Azizah Mohd Ali1, Jacqueline Jauncey-Cooke2, Fiona Bogossian3
1School of Nursing, Midwifery and Social Work, The University of Queensland, Australia; Department of Critical Care Nursing, Faculty of Nursing, International Islamic University Malaysia (IIUM), Malaysia.
Insights
The new ventilator-associated event (VAE) surveillance definition shows promise for children but requires specific paediatric criteria. Further research is needed before clinical implementation to address challenges in VAE identification.
Area of Science:
- Pediatric critical care medicine
- Infectious disease surveillance
- Respiratory care
Background:
- Existing ventilator-associated pneumonia (VAP) definitions in children lack consistency, impacting reliable VAP identification.
- The adult ventilator-associated event (VAE) surveillance definition was revised to address these issues.
- Evidence for applying the VAE definition in pediatric populations is currently lacking.
Purpose of the Study:
- To systematically review the evidence on the application of the VAE surveillance definition in children.
- To identify potential challenges in the clinical practice of VAE surveillance in pediatric settings.
Main Methods:
- A systematic literature search was conducted to identify relevant pediatric studies.
- Studies were appraised using the epidemiological appraisal instrument (EAI).
- The quality of evidence was assessed using National Health Medical Research Council (NHMRC) guidelines.
Main Results:
- Seven studies met inclusion criteria, with above 50% quality on EAI and an overall evidence grade of C (satisfactory).
- Pediatric VAE incidence varied widely (1.1–20.9 per 1000 ventilator days) due to differing surveillance criteria.
- Limited agreement exists between VAE and VAP definitions in identifying VAP in children. Challenges include differing ventilation modes, inconclusive pediatric-specific criteria, and lack of automated data extraction support.
Conclusions:
- The VAE surveillance definition shows potential for defining VAE in children, but the current evidence level is low.
- Further consideration of pediatric-specific VAE criteria and the value of automated data collection is necessary before clinical implementation.
Background:
The complexity and variation in ventilator associated pneumonia (VAP) definitions in paediatrics may pose threats to the reliable identification of VAP. The revision of the surveillance definition to ventilator-associated event (VAE) has been mandated in adult populations, to overcome these issues. However, the evidence for application of the definition is unknown in children.
Objectives:
To review the evidence on the application of the new VAE surveillance definition in paediatric population and examine the potential challenges in clinical practice.
Review Methods:
A systematic approach was used to locate and synthesise the relevant paediatric literature. Studies were appraised according to epidemiological appraisal instrument (EAI) and the grades of evidence in the National Health Medical Research Council (NHMRC) guidelines.
Results:
Seven studies met the inclusion criteria. Quality of study methods was above 50% on the EAI. The overall grade of evidence was assessed as C (satisfactory). The incidence of VAE in children ranged from 1.1 to 20.9 per 1000 ventilator days as a result of variations in surveillance criteria across included studies. There is little agreement between the new VAE and PNU/VAP surveillance definition in the identification of VAP. Challenges in the application of VAE surveillance were related to; the difference in modes of ventilation used in children versus adults, inconclusive criteria tailored to paediatric samples and a lack of data that support for automatic data extraction applied in paediatric studies.
Conclusion:
This review demonstrated promising evidence using the new VAE surveillance definition to define the VAE in children, but the level of the evidence is low. Before the possibility of real implementation in clinical settings, challenges related to VAE paediatric specific criteria' and the value of automated data collection need to be considered.
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