Endoscopic Biopsy Technique using an Alcohol Swab to Prevent Transmission through the Instrument Channel in the COVID-19 Era

Article information

Clin Endosc. 2021;54(5):771-773
Publication date (electronic) : 2021 May 11
doi : https://doi.org/10.5946/ce.2021.027
Department of Gastroenterology, Osaka City University Graduate School of Medicine, Osaka, Japan
Correspondence: Yasuaki Nagami Department of Gastroenterology, Osaka City University Graduate School of Medicine, 1-4-3, Asahimachi, Abeno-ku, Osaka 545-8585, Japan Tel: +81-6-6645-3811, Fax: +81-6-6645-3813, E-mail: yasuaki-75@med.osaka-cu.ac.jp
Received 2020 December 22; Revised 2021 January 24; Accepted 2021 February 1.

According to reports, the potential transmission routes of the Coronavirus Disease 2019 (COVID-19) infection include contact, droplet, and airborne transmission [1,2]. Therefore, many strategies to reduce aerosol spread by patient coughs during endoscopy have been reported, such as plastic cube barrier, vinyl-box, modified surgical mask, and glove-covered mouthpiece [3-6]. Endoscopic biopsy for suspected malignancies should be performed for diagnosis confirmation even in the COVID-19 era [7,8]. However, to our knowledge, there are no reports of precautions focusing on potential contamination during biopsy. First, a patient’s contaminated fluids, which potentially exist in the instrument channel of the endoscope, could splash from the biopsy valve on the channel port into the endoscopist’s face. Moreover, infection risk is higher because of the close distance to the endoscopist’s face [9]. Second, it should also be considered that long and elastic biopsy forceps have an unexpected risk of contact transmission when the forceps are pulled out from the channel port. Here, we present a method without harmful effects of using an alcohol swab not only to prevent contaminated fluid splash during biopsy, but also to deactivate severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) for the reduction of contact transmission after biopsy. We performed a demonstration to inspect the protective effect of the swab using an upper gastrointestinal training simulator (LM-022; KOKEN CO., LTD., Tokyo, Japan) and fluorescent dye (see Supplementary Video 1).

The first demonstration shows the endoscopic biopsy procedure using a training simulator without precaution for potential contamination. After the forceps were pulled out by an assistant, many fluorescent dye droplets were identified on the right forearm, chest, neck, and mask of the endoscopist by illuminating with ultraviolet light (Fig. 1A, B).

Fig. 1.

(A) Droplets of fluorescent dye illuminated with ultraviolet light identified on the neck and mask of an endoscopist. (B) Droplets of fluorescent dye found on endoscopist’s chest.

Next, we present the alcohol swab technique during biopsy to reduce contamination. Ahead of biopsy, an alcohol swab package was placed with a cellophane tape near the instrument channel port in order to quickly obtain the swab (Fig. 2A). The endoscopist removes the swab and continues to hold down the top of the biopsy valve, “sandwiching” the forceps to stabilize until the forceps are slowly pulled out by an assistant (Fig. 2B).

Fig. 2.

(A) Ahead of biopsy, an alcohol swab package taped near the instrument channel port. (B) The endoscopist continues to hold down the top of the biopsy valve, “sandwiching” the forceps by the swab to stabilize until the forceps are slowly pulled out by an assistant.

The last demonstration shows the endoscopic biopsy procedure with an alcohol swab. After the assistant pulled out the forceps, the fluorescent dye was absorbed in the swab. Ultraviolet light illumination revealed no scattering of dye on the endoscopist.

For further clinical examination, we evaluated the aerosol spread using the portable HHPC6 + Handheld Particle Counter (Beckman Coulter, Inc., Brea, CA, USA), while actual biopsies were performed using esophagogastroduodenoscopy (EGD). This device was positioned at the face height of the endoscopist and recorded the quantity of particles (0.3-2.0 μm) per cubic feet every 5 seconds in order to verify the endoscopist’s exposure to the aerosol. All values were normalized against the background particle count in the endoscopy room at the start of measurement. Fig. 3 shows the temporal changes in particle counts for each size during EGD. Most notably, the quantity of particles (0.3 µm) did not increase after the biopsy with alcohol swab compared to that without alcohol swab. The total number of particles (0.3–2.0 μm) measured for 30 s after two biopsies while using the alcohol swab was reduced to 59.4% compared to that without the alcohol swab (94,470/ft3 and 159,060/ft3).

Fig. 3.

The temporal changes of particle counts in each size per cubic feet during esophagogastroduodenoscopy. The red and blue arrows are the timing of biopsies without and with alcohol swab, respectively.

Our demonstration using the simulator and fluorescent dye suggested that the alcohol swab technique could prevent contaminated fluid splash and contact with SARS-CoV-2 on the forceps. In particular, we believe that droplet infection via the instrument channel can be almost completely controlled by this technique. However, this simulation did not demonstrate the preventive effect of small aerosol particles that cause airborne infections. Therefore, using a particle counter, we showed that our alcohol swab technique could limit the spread of aerosol to approximately 60% during endoscopic biopsies; however, the actual protective effect against airborne SARS-CoV-2 infection remains to be ascertained. Additional experiments are needed to investigate the effects of alcohol swabs on the disinfection of SARS-CoV-2 and the prevention of contact transmission. However, we consider that alcohol swabs can inactivate SARS-CoV-2 more effectively than simple gauze because of the disinfection effect of ethanol itself [10]. Our technique using an alcohol swab, an easy, low-cost option, can prevent viral transmission by the avoidance of fluid and aerosol blowout from the channel and by disinfection of the forceps. This technique can be applied to any endoscope or a similar device. Therefore, a further protective effect might be obtained for essential endoscopic procedures during the COVID-19 pandemic, and this novel technique can be accepted as a standard precaution to ensure infection control during routine endoscopy even after the COVID-19 era.

Notes

Conflicts of Interest: The authors have no potential conflicts of interest.

Funding:None.

Author Contributions

Conceptualization: Shusei Fukunaga, Taku, Manabe, Yasuaki Nagami

Data curation: Akira Higashimori

Formal analysis: AH, SF

Investigation: SF, Taku Manabe, Tadashi Ochiai, Mitsuhiro Kono, Masaki Ominami

Methodology: SF, YN

Project administration: SF, YN

Supervision: Yasuhiro Fujiwara

Validation: SF, YN, AH

Writing-original draft: SF

Writing-review&editing: YN

Supplementary Material

Video 1. A new method using an alcohol swab to reduce contamination during biopsy and simple demonstrations using fluorescent dye to inspect the protective effect. (https://doi.org/10.5946/ce.2021.027.v001).

ce-2021-027-v001.mp4

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Article information Continued

Fig. 1.

(A) Droplets of fluorescent dye illuminated with ultraviolet light identified on the neck and mask of an endoscopist. (B) Droplets of fluorescent dye found on endoscopist’s chest.

Fig. 2.

(A) Ahead of biopsy, an alcohol swab package taped near the instrument channel port. (B) The endoscopist continues to hold down the top of the biopsy valve, “sandwiching” the forceps by the swab to stabilize until the forceps are slowly pulled out by an assistant.

Fig. 3.

The temporal changes of particle counts in each size per cubic feet during esophagogastroduodenoscopy. The red and blue arrows are the timing of biopsies without and with alcohol swab, respectively.