A clinical observational analysis of aerosol emissions from dental procedures.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 08 11 2021
accepted: 22 02 2022
entrez: 10 3 2022
pubmed: 11 3 2022
medline: 4 5 2022
Statut: epublish

Résumé

Aerosol generating procedures (AGPs) are defined as any procedure releasing airborne particles <5 μm in size from the respiratory tract. There remains uncertainty about which dental procedures constitute AGPs. We quantified the aerosol number concentration generated during a range of periodontal, oral surgery and orthodontic procedures using an aerodynamic particle sizer, which measures aerosol number concentrations and size distribution across the 0.5-20 μm diameter size range. Measurements were conducted in an environment with a sufficiently low background to detect a patient's cough, enabling confident identification of aerosol. Phantom head control experiments for each procedure were performed under the same conditions as a comparison. Where aerosol was detected during a patient procedure, we assessed whether the size distribution could be explained by the non-salivary contaminated instrument source in the respective phantom head control procedure using a two-sided unpaired t-test (comparing the mode widths (log(σ)) and peak positions (DP,C)). The aerosol size distribution provided a robust fingerprint of aerosol emission from a source. 41 patients underwent fifteen different dental procedures. For nine procedures, no aerosol was detected above background. Where aerosol was detected, the percentage of procedure time that aerosol was observed above background ranged from 12.7% for ultrasonic scaling, to 42.9% for 3-in-1 air + water syringe. For ultrasonic scaling, 3-in-1 syringe use and surgical drilling, the aerosol size distribution matched the non-salivary contaminated instrument source, with no unexplained aerosol. High and slow speed drilling produced aerosol from patient procedures with different size distributions to those measured from the phantom head controls (mode widths log(σ)) and peaks (DP,C, p< 0.002) and, therefore, may pose a greater risk of salivary contamination. This study provides evidence for sources of aerosol generation during common dental procedures, enabling more informed evaluation of risk and appropriate mitigation strategies.

Identifiants

pubmed: 35271682
doi: 10.1371/journal.pone.0265076
pii: PONE-D-21-35581
pmc: PMC8912243
doi:

Substances chimiques

Aerosols 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0265076

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Tom Dudding (T)

MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Bristol Dental Hospital and School, University of Bristol, Bristol, United Kingdom.

Sadiyah Sheikh (S)

Bristol Aerosol Research Centre, School of Chemistry, University of Bristol, Bristol, United Kingdom.

Florence Gregson (F)

Bristol Aerosol Research Centre, School of Chemistry, University of Bristol, Bristol, United Kingdom.

Jennifer Haworth (J)

Bristol Dental Hospital and School, University of Bristol, Bristol, United Kingdom.
Royal United Hospital Bath, Combe Park, Bath, United Kingdom.

Simon Haworth (S)

MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Bristol Dental Hospital and School, University of Bristol, Bristol, United Kingdom.

Barry G Main (BG)

Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Bristol Dental Hospital and School, University of Bristol, Bristol, United Kingdom.
Bristol Centre for Surgical Research, Population Health Sciences, Bristol Medical School, Bristol, United Kingdom.

Andrew J Shrimpton (AJ)

School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, United Kingdom.

Fergus W Hamilton (FW)

MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Infection Sciences, Southmead Hospital, North Bristol NHS Trust, Bristol, United Kingdom.

Anthony J Ireland (AJ)

Bristol Dental Hospital and School, University of Bristol, Bristol, United Kingdom.
Royal United Hospital Bath, Combe Park, Bath, United Kingdom.

Nick A Maskell (NA)

Academic Respiratory Unit, North Bristol NHS Trust, Bristol, United Kingdom.

Jonathan P Reid (JP)

Bristol Aerosol Research Centre, School of Chemistry, University of Bristol, Bristol, United Kingdom.

Bryan R Bzdek (BR)

Bristol Aerosol Research Centre, School of Chemistry, University of Bristol, Bristol, United Kingdom.

Mark Gormley (M)

MRC Integrative Epidemiology Unit, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Department of Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
Bristol Dental Hospital and School, University of Bristol, Bristol, United Kingdom.

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