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Published on: April 7, 2021
Mechanical ventilation drives inflammation in severe viral bronchiolitis
Marije P Hennus1, Adrianus J van Vught1, Mark Brabander1
1Department of Paediatric Intensive Care, Wilhelmina Children's Hospital / University Medical Center Utrecht, Utrecht, The Netherlands.
Insights
Mechanical ventilation in infants with respiratory syncytial virus (RSV) bronchiolitis significantly increases pulmonary inflammation. This study found elevated inflammatory mediators after intubation, suggesting ventilation itself, not just disease severity, drives this inflammation.
Area of Science:
- Pediatric critical care medicine
- Respiratory viral infections
- Immunology
Background:
- Severe respiratory syncytial virus (RSV) infection is a leading cause of infant intensive care unit admissions.
- Mechanically ventilated children with viral bronchiolitis show higher airway inflammatory mediators than spontaneously breathing ones.
- Previous research indicated elevated inflammatory mediators in ventilated children, but the cause—disease severity versus mechanical ventilation—remained unclear.
Purpose of the Study:
- To investigate whether elevated inflammatory mediators in infants with RSV bronchiolitis are linked to disease severity or mechanical ventilation.
- To compare cytokine levels in mechanically ventilated infants versus non-ventilated controls.
Main Methods:
- Prospective observational multi-center study.
- Nasopharyngeal aspirates collected from 18 infants with RSV bronchiolitis requiring mechanical ventilation and 18 non-ventilated controls before intubation and 24 hours later.
- Measured concentrations of interleukin (IL)-1α, IL-1β, IL-6, monocyte chemotactic protein (MCP)-1, and macrophage inflammatory protein (MIP)-1α.
Main Results:
- Baseline cytokine levels were similar between ventilated and non-ventilated groups.
- After 24 hours of mechanical ventilation, mean levels of IL-1α, IL-1β, IL-6, and MCP-1 were significantly elevated compared to non-ventilated controls.
- MIP-1α levels did not show a significant difference between the groups after 24 hours.
Conclusions:
- Mechanical ventilation and endotracheal intubation induce significant pulmonary inflammation in infants with RSV bronchiolitis.
- The findings suggest that mechanical ventilation itself is a major contributor to increased pulmonary inflammation, beyond the initial disease severity.
Introduction:
Respiratory insufficiency due to severe respiratory syncytial virus (RSV) infection is the most frequent cause of paediatric intensive care unit admission in infants during the winter season. Previous studies have shown increased levels of inflammatory mediators in airways of mechanically ventilated children compared to spontaneous breathing children with viral bronchiolitis. In this prospective observational multi-center study we aimed to investigate whether this increase was related to disease severity or caused by mechanical ventilation.
Materials And Methods:
Nasopharyngeal aspirates were collected <1 hour before intubation and 24 hours later in RSV bronchiolitis patients with respiratory failure (n = 18) and non-ventilated RSV bronchiolitis controls (n = 18). Concentrations of the following cytokines were measured: interleukin (IL)-1α, IL-1β, IL-6, monocyte chemotactic protein (MCP)-1 and macrophage inflammatory protein (MIP)-1α.
Results:
Baseline cytokine levels were comparable between ventilated and non-ventilated infants. After 24 hours of mechanical ventilation mean cytokine levels, except for MIP-1α, were elevated compared to non-ventilated infected controls: IL-1α (159 versus 4 pg/ml, p<0.01), IL-1β (1068 versus 99 pg/ml, p<0.01), IL-6 (2343 versus 958 pg/ml, p<0.05) and MCP-1 (174 versus 26 pg/ml, p<0.05).
Conclusions:
Using pre- and post-intubation observations, this study suggests that endotracheal intubation and subsequent mechanical ventilation cause a robust pulmonary inflammation in infants with RSV bronchiolitis.
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