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Influenza virus RNA recovered from droplets and droplet nuclei emitted by adults in an acute care setting.
Yip, Lily; Finn, Mairead; Granados, Andrea; Prost, Karren; McGeer, Allison; Gubbay, Jonathan B; Scott, James; Mubareka, Samira.
Afiliação
  • Yip L; a Biological Sciences , Sunnybrook Research Institute , Toronto , Ontario , Canada.
  • Finn M; a Biological Sciences , Sunnybrook Research Institute , Toronto , Ontario , Canada.
  • Granados A; b Public Health Ontario , Toronto , Ontario , Canada.
  • Prost K; c Department of Laboratory Medicine and Pathobiology , University of Toronto , Toronto , Ontario , Canada.
  • McGeer A; a Biological Sciences , Sunnybrook Research Institute , Toronto , Ontario , Canada.
  • Gubbay JB; c Department of Laboratory Medicine and Pathobiology , University of Toronto , Toronto , Ontario , Canada.
  • Scott J; d Sinai Health System , Toronto , Ontario , Canada.
  • Mubareka S; b Public Health Ontario , Toronto , Ontario , Canada.
J Occup Environ Hyg ; 16(5): 341-348, 2019 05.
Article em En | MEDLINE | ID: mdl-31050610
ABSTRACT
Transmission in hospital settings of seasonal influenza viruses and novel agents such as the Middle East respiratory syndrome coronavirus (MERS-CoV) is well-described but poorly understood. The characterization of potentially infectious bio-aerosols in the healthcare setting remains an important yet ill-defined factor in the transmission of respiratory viruses. Empiric data describing the distribution of bio-aerosols enable discernment of potential exposure risk to respiratory viruses. We sought to determine the distribution of influenza virus RNA emitted into the air by participants with laboratory-confirmed influenza, and whether these emissions had the potential to reach healthcare workers' breathing zones. Two-stage cyclone bio-aerosol samplers from the Centers for Disease Control and Prevention - National Institute for Occupational Safety and Health were placed 0.5-1.0 m (near field) and 2.1-2.5 m (far field) from infected patient participants, as well as in the corridor immediately outside their rooms. In addition, healthcare worker participants providing care to infected participants were recruited to wear a polytetrafluoroethylene (PTFE) filter cassette in their breathing zones. Viral RNA was detected from the air emitted by 37.5% of the 16 participants infected with influenza virus and distributed both in near and far fields and in all tested particle sizes (<1 µm, 1-4 µm, and >4 µm). Viral RNA was recovered in droplet nuclei and beyond 1 m from naturally-infected participants in the healthcare setting and from the breathing zone of one healthcare worker. There was no correlation between patient participant nasal viral load and recovery of viral RNA from the air, and we did not identify any significant association between RNA detection from the air and patient demographics or clinical presentation. A more substantial study is required to identify patient determinants of virus emission into the air and delineate implications for evidence-based policy for prevention and control.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Orthomyxoviridae / RNA Viral / Aerossóis / Influenza Humana Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Orthomyxoviridae / RNA Viral / Aerossóis / Influenza Humana Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article