Evaluation of the aerosol generating potential of endoscopic dacryocystorhinostomy.

Autor: Chen DA; Weill Cornell Medical College New York New York USA., Lee M; Weill Cornell Medicine Otolaryngology New York New York USA., Lelli GJ; Weill Cornell Medicine Ophthalmology New York New York USA., Kacker A; Weill Cornell Medicine Otolaryngology New York New York USA.
Jazyk: angličtina
Zdroj: Laryngoscope investigative otolaryngology [Laryngoscope Investig Otolaryngol] 2021 Aug 17; Vol. 6 (5), pp. 948-951. Date of Electronic Publication: 2021 Aug 17 (Print Publication: 2021).
DOI: 10.1002/lio2.639
Abstrakt: Purpose: The COVID-19 pandemic gave rise to renewed concerns of the transmission risks posed by surgeries on sites of high viral colonization such as the nasopharynx. Endoscopic dacryocystorhinostomy (DCR) involves the creation of a new tear duct from the lacrimal sac to the nasal cavity. The purpose of this project is to determine if endoscopic DCR is an aerosol generating procedure (AGP).
Methods: An optical particle sizer (OPS) was used to intraoperatively quantify aerosol concentrations during four cases of endoscopic DCR. The OPS sampled the air once every 60 seconds throughout the operations. The time of important operative steps were documented and correlated with OPS readings. Particle concentrations during each major surgical step were compared to baseline readings by the Mann Whitney U Test.
Results: There were statistically significant increases in median particle concentrations during laryngeal mask airway intubations for both particles 0.3 to 5.0 μm and >5.0 μm ( P  < .001 and P  = .023, respectively). Median particle concentrations during nasolacrimal duct probing, middle meatal debridement, drilling, balloon insertion, tube insertion, and Posisef insertion were not statistically different from baseline.
Conclusions: Endoscopic DCR in itself does not appear to be an AGP. It is, however, associated with other aerosol generating events such as laryngeal mask intubation, and thus requires appropriate personal protective equipment. Cautious interpretation of the results is encouraged given the limitations of OPS.
Level of Evidence: 4.
Competing Interests: Provisional patent EFS ID 39386708, Application #63021722 submitted by Cornell University on May 8, 2020. The authors report no conflicts of interest.
(© 2021 The Authors. Laryngoscope Investigative Otolaryngology published by Wiley Periodicals LLC on behalf of The Triological Society.)
Databáze: MEDLINE