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Particle and bioaerosol characteristics in a paediatric intensive care unit

The paediatric intensive care unit (PICU) provides care to critically ill neonates, infants and children. These patients are vulnerable and susceptible to the environment surrounding them, yet there is little information available on indoor air quality and factors affecting it within a PICU. To addr...

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Detalles Bibliográficos
Autores principales: He, Congrong, Mackay, Ian M., Ramsay, Kay, Liang, Zhen, Kidd, Timothy, Knibbs, Luke D., Johnson, Graham, McNeale, Donna, Stockwell, Rebecca, Coulthard, Mark G., Long, Debbie A., Williams, Tara J., Duchaine, Caroline, Smith, Natalie, Wainwright, Claire, Morawska, Lidia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7172583/
https://www.ncbi.nlm.nih.gov/pubmed/28692913
http://dx.doi.org/10.1016/j.envint.2017.06.020
Descripción
Sumario:The paediatric intensive care unit (PICU) provides care to critically ill neonates, infants and children. These patients are vulnerable and susceptible to the environment surrounding them, yet there is little information available on indoor air quality and factors affecting it within a PICU. To address this gap in knowledge we conducted continuous indoor and outdoor airborne particle concentration measurements over a two-week period at the Royal Children's Hospital PICU in Brisbane, Australia, and we also collected 82 bioaerosol samples to test for the presence of bacterial and viral pathogens. Our results showed that both 24-hour average indoor particle mass (PM(10)) (0.6–2.2 μg m(− 3), median: 0.9 μg m(− 3)) and submicrometer particle number (PN) (0.1–2.8 × 10(3) p cm(− 3), median: 0.67 × 10(3) p cm(− 3)) concentrations were significantly lower (p < 0.01) than the outdoor concentrations (6.7–10.2 μg m(− 3), median: 8.0 μg m(− 3) for PM(10) and 12.1–22.2 × 10(3) p cm(− 3), median: 16.4 × 10(3) p cm(− 3) for PN). In general, we found that indoor particle concentrations in the PICU were mainly affected by indoor particle sources, with outdoor particles providing a negligible background. We identified strong indoor particle sources in the PICU, which occasionally increased indoor PN and PM(10) concentrations from 0.1 × 10(3) to 100 × 10(3) p cm(− 3), and from 2 μg m(− 3) to 70 μg m(− 3), respectively. The most substantial indoor particle sources were nebulization therapy, tracheal suction and cleaning activities. The average PM(10) and PN emission rates of nebulization therapy ranged from 1.29 to 7.41 mg min(− 1) and from 1.20 to 3.96 p min(− 1) × 10(11), respectively. Based on multipoint measurement data, it was found that particles generated at each location could be quickly transported to other locations, even when originating from isolated single-bed rooms. The most commonly isolated bacterial genera from both primary and broth cultures were skin commensals while viruses were rarely identified. Based on the findings from the study, we developed a set of practical recommendations for PICU design, as well as for medical and cleaning staff to mitigate aerosol generation and transmission to minimize infection risk to PICU patients.