Open Access
CC BY-NC-ND 4.0 · Endosc Int Open 2022; 10(09): E1188-E1192
DOI: 10.1055/a-1896-4376
Original article

External nasal dilator decreases N95 respirator-related respiratory effort and symptoms in gastrointestinal endoscopy unit staff

Asif Khalid
1   VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, United States
,
Christopher Thomas
1   VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, United States
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
Michael Kingsley
1   VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, United States
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
Kishore Vipperla
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
Jeffrey Dueker
1   VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, United States
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
Christianna Kreiss
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
Anna Evans Phillips
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
Rohit Das
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
Kenneth Fasanella
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
,
James Ibinson
1   VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, United States
2   University of Pittsburgh Medical Center. Pittsburgh, Pennsylvania, United States
› Author Affiliations
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Abstract

Background and study aims N95-filtering facepiece respirators (FFR) use is associated with physiological changes and symptoms due to impaired nasal airflow and increased breathing resistance. We prospectively studied the effect of using an external nasal dilator (END) in gastroenterology laboratory (gastrointestinal lab) staff using N95FFR.

Patients and methods N95FFR qualitative saccharine fit testing was performed on study participants with and without an END. Prospective data collection and comparisons included: 1) survey of perceived symptoms and difficulty of performing one day of gastrointestinal procedures with N95FFR and 1 day of gastrointestinal procedures with END plus N95FFR in random sequence; and 2) vitals and respiratory belt plethysmography in ten gastroenterologists performing simulated colonoscopy while wearing a surgical mask (SM), N95FFR plus SM, END plus N95FFR plus SM for 20 minutes each in random sequence and rapid succession.

Results Twenty-nine of 31 participants passed the N95FFR and the END plus N95FFR fit test. Twenty-two participants (12 physicians; 11 males; mean age 44.1 years, range 31–61) performed 1 day of gastrointestinal procedures with an N95FFR and 1 day of gastrointestinal procedures with an END plus N95FFR. Significantly less difficulty with nasal breathing and severity of symptoms including breathing difficulty, headache, fatigue and frustration, occurred while using an END plus N95FFR. Respiratory plethysmography peak-to-trough measurement showed an increase during the N95FFR stage compared to the END plus N95FFR stage and the SM stage.

Conclusions N95FFR related respiratory changes and symptom development may be mitigated by END use.

Supplementary material



Publication History

Received: 29 July 2021

Accepted after revision: 25 May 2022

Accepted Manuscript online:
11 July 2022

Article published online:
14 September 2022

© 2022. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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