High incidence of pulmonary bacterial co-infection in children with severe respiratory syncytial virus (RSV) bronchiolitis

K Thorburn, S Harigopal, V Reddy, N Taylor… - Thorax, 2006 - thorax.bmj.com
K Thorburn, S Harigopal, V Reddy, N Taylor, HKF Van Saene
Thorax, 2006thorax.bmj.com
Background: Respiratory syncytial virus (RSV) is the most common cause of viral lower
respiratory tract infections (LRTI). Viral LRTI is a risk factor for bacterial superinfection,
having an escalating incidence with increasing severity of respiratory illness. A study was
undertaken to determine the incidence of pulmonary bacterial co-infection in infants and
children with severe RSV bronchiolitis, using paediatric intensive care unit (PICU) admission
as a surrogate marker of severity, and to study the impact of the co-infection on morbidity …
Background: Respiratory syncytial virus (RSV) is the most common cause of viral lower respiratory tract infections (LRTI). Viral LRTI is a risk factor for bacterial superinfection, having an escalating incidence with increasing severity of respiratory illness. A study was undertaken to determine the incidence of pulmonary bacterial co-infection in infants and children with severe RSV bronchiolitis, using paediatric intensive care unit (PICU) admission as a surrogate marker of severity, and to study the impact of the co-infection on morbidity and mortality.
Methods: A prospective microbiological analysis was made of lower airways secretions on all RSV positive bronchiolitis patients on admission to the PICU during three consecutive RSV seasons.
Results: One hundred and sixty five children (median age 1.6 months, IQR 0.5–4.6) admitted to the PICU with RSV bronchiolitis were enrolled in the study. Seventy (42.4%) had lower airway secretions positive for bacteria: 36 (21.8%) were co-infected and 34 (20.6%) had low bacterial growth/possible co-infection. All were mechanically ventilated (median 5.0 days, IQR 3.0–7.3). Those with bacterial co-infection required ventilatory support for longer than those with only RSV (p<0.01). White cell count, neutrophil count, and C-reactive protein did not differentiate between the groups. Seventy four children (45%) received antibiotics prior to intubation. Sex, co-morbidity, origin, prior antibiotics, time on preceding antibiotics, admission oxygen, and ventilation index were not predictive of positive bacterial cultures. There were 12 deaths (6.6%), five of which were related to RSV.
Conclusions: Up to 40% of children with severe RSV bronchiolitis requiring admission to the PICU were infected with bacteria in their lower airways and were at increased risk for bacterial pneumonia.
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