J Neurol Surg B Skull Base 2021; 82(S 02): S65-S270
DOI: 10.1055/s-0041-1725262
Presentation Abstracts
Live Session Abstracts

Topical Therapies to Prevent Aerosolization of Respiratory Viral Particles during Endonasal Skull Base Surgery: A Practical Review

Katherine Tai
1   Department of Otolaryngology - Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States
,
Leila J. Mady
2   Department of Otorhinolaryngology, University of Pennsylvania, Philadelphia, Pennsylvania, United States
,
Debraj Mukherjee
3   Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States
,
Nicholas Rowan
1   Department of Otolaryngology - Head and Neck Surgery, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States
› Author Affiliations
 

Background: The potential reservoir of severe acute respiratory syndrome coronavirus (SARS-CoV-2) in the nasopharynx and upper airway of infected or asymptomatic patients undergoing endonasal procedures amid the ongoing coronavirus disease 2019 (COVID-19) pandemic may put skull base surgeons and their teams at high risk of exposure to aerosolized viral particles during endonasal procedures. Strategies to mitigate the risk of potential aerosol-generating procedures (AGPs) have been promoted at a feverish pace, and significant effort has been made to optimize guidelines limiting aerosolization. This review summarizes the use of topical therapies as a perioperative infection control strategy, detailing efficacy, safety, and delivery options.

Methods: A PubMed/MEDLINE and Scopus database review of articles was conducted querying topical therapies, including povidone-iodine (PVP-I), chlorhexidine, saline, surfactants, alcohols, and interferon activity against coronaviruses, and safety for peri-operative use.

Results: Few clinical studies specifically investigate the in vivo viricidal activity of topical agents against SARS-CoV-2 in the perioperative setting. Of topical agents with viricidal potential, PVP-I is supported by the most robust investigations—in vitro studies have shown that PVP-I solutions as low as 0.5% can completely inactivate SARS-CoV-2 with 15 seconds of contact time, and solutions as low as 0.23% may neutralize SARS-CoV-2 homologues. Regarding safety, PVP-I concentrations of 2.5% and greater are associated with ciliotoxicity effects on human respiratory epithelial cells, but can be tolerated up to 5% when administered intraorally, and up to 1% as a sinus irrigation formulation. As for other agents, preliminary studies show that chlorhexidine mouthwash may transiently decrease the SARS-CoV-2 virus load below the detectable limit in saliva for 2 to 4 hours, but in isolation it is less effective than PVP-I in vitro studies. Furthermore, chlorhexidine and other antiseptics including ethanol have a worse safety profile than PVP-I, including increased flammability and ototoxicity. Studies also show that hypertonic saline nasal irrigation and gargling leads to decreased duration of illness, transmission, and viral shedding among patients with the common cold, including coronaviruses, and was well tolerated barring some reports of nasal irritation, epistaxis, and headache.

Conclusions: Several topical therapies, including PVP-I and hypertonic saline, may be at least temporarily effective at inactivating SARS-CoV-2 in the perioperative setting. However, these interventions are not without potential risks, including ciliotoxicity, which adversely impacts the mucociliary clearance of pathogens, and the efficacy of these agents is limited by available clinical data. However, thoughtful, evidence-based approaches should be considered as a sustainable option to reduce the risk of respiratory viral particle aerosolization in AGPs, such as endonasal skull base surgery.



Publication History

Article published online:
12 February 2021

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