The worldwide pandemic of novel coronavirus disease 2019 (COVID-19) in 2020 has caused significant changes in clinical practice of medicine, including gastroenterology.¹ Severe acute respiratory syndrome-related coronavirus 2, which can transmit from human to human, poses a higher risk of infection among healthcare professionals than among the general population.^2,3 Wearing face masks and eye protection in the healthcare setting reduced this high risk of virus infection in healthcare professionals.⁴ Therefore, the U.S. Centers for Disease Control and Prevention recommended that healthcare professionals should use appropriate personal protective equipment (PPE) as a routine infection prevention and control practice during the COVID-19 pandemic.⁵

In the gastrointestinal endoscopy unit, healthcare professionals are in close contact with patients and gastrointestinal endoscopies, such as esophagogastroduodenoscopy, endoscopic retrograde cholangiopancreatography, and colonoscopy, are potentially aerosol-generating procedures, with increased risk of transmission of COVID-19.⁶ Therefore, professional societies of gastroenterology worldwide have recommended strategies for infection prevention and control in the gastrointestinal endoscopy unit and appropriate protocol utilizing PPE for healthcare professionals during the COVID-19 pandemic.^7-10 Representative PPE includes surgical masks, face shields, isolation gowns, and disposable gloves.

Colonoscopy is the principal diagnostic tool for various colorectal diseases. In addition, colonoscopy is one of the most important screening methods for colorectal cancer. The fundamental role of screening colonoscopy is detection of colorectal neoplasms, including cancers and polyps. Another important function of colonoscopy is endoscopic resection of colorectal polyps and T1 colorectal cancers with low risk of lymph node metastasis. The quality of colonoscopy is of utmost importance to satisfy the goals of screening and therapeutic colonoscopies,¹¹ such as qualified detection of colorectal neoplasm, without missed lesions and complete endoscopic resection of colorectal neoplasm, without serious adverse events. Several quality indicators, such as the adenoma detection rate (ADR) and withdrawal time, have been implemented to monitor the quality of colonoscopy.^12,13 Because the face shield is a PPE that was not used frequently in endoscopy units before the COVID-19 pandemic, endoscopists are not accustomed to it. Thus, there can be a reasonable concern that wearing a face shield may be cumbersome and induce impaired visibility to endoscopists, thereby worsening the quality of colonoscopy.

In this study, we investigated whether wearing the face shield might affect the quality of colonoscopy, by assessing ADR and withdrawal time with and without the face shield. We also evaluated the effect of the face shield on therapeutic colonoscopies, such as polypectomy.

1. Study design and patients

This was a single center, retrospective cohort study that compared the quality of colonoscopy depending on whether a face shield was added as a PPE. Disposable latex gloves, isolation gown, and surgical mask were worn as PPE before the COVID-19 pandemic at Asan Medical Center, Seoul, Korea. Since the COVID-19 outbreak in Daegu, Korea in late February 2020, the KF94 mask (Dr. Puri^Ⓡ KF [Korea Filter] 94, KM Healthcare Corp, Seoul, Korea), which has equivalent efficacy to the N95 mask, was worn instead of the surgical mask.¹⁴ Because a nationwide outbreak continued, a face shield (Sview, RoitsNine Corp., Seoul, Korea) was added, from April 13, 2020, to reinforce the PPE. The face shield, Sview, is made of transparent polyethylene terephthalate material (Fig. 1). Thus, at our institution, disposable latex gloves, an isolation gown, and a KF94 mask were worn as PPE between late February and April 12, 2020 whereas a face shield was added to this from April 13, 2020.

Figure 1. Wearing of a face shield (Sview, RoitsNine Corp.).

We reviewed the medical records and colonoscopy results of consecutive subjects who underwent colonoscopies at the Department of Gastroenterology and Health Screening and Promotion Center in our institution from March 10 to May 31, 2020. Of these, we included colonoscopies conducted by five 2nd-year gastroenterology fellows as the trainee endoscopist group at the Department of Gastroenterology, who had previously performed 300 to 500 colonoscopy procedures before March 2020. As the expert endoscopist group, we included colonoscopies performed at the Health Screening and Promotion Center by four board-certified gastroenterologists with experience of 4,000 or more colonoscopies over a period of 6 years or longer. As described above, colonoscopies performed between March 10 and April 12, 2020 were included in the no-face shield group and those performed between April 13 to May 31, 2020 were included in the face shield group. We compared colonoscopy quality indicators between the face shield and no-face shield groups.

The inclusion criteria of this study were patients who underwent screening and surveillance colonoscopies. Patients who underwent diagnostic colonoscopies because of mild gastrointestinal symptoms, such as vague low abdominal discomfort, were also included. The exclusion criteria were (1) patients under 18 years of age, (2) patients with previous colectomy, (3) patients with inflammatory bowel disease and colorectal polyposis syndrome, (4) patients with moderate to severe symptoms such as overt gastrointestinal bleeding, (5) patients referred from a primary clinic for treatment of colorectal polyp and/or cancer, and (6) patients with a screening colonoscopy within 5 years. Patients whose colonoscopy was incomplete because of inadequate bowel preparation (Boston Bowel Preparation Scale <6)¹⁵ were also excluded. The Institutional Review Board of Asan Medical Center (IRB number: 2020-1228) approved this study and waived the requirement for informed consent.

2. Colonoscopy procedure

All colonoscopies were performed using an Olympus CF-HQ290I or CF-HQ290L colonoscope (Olympus Optical, Co., Ltd., Tokyo, Japan). Bowel preparation was performed with 2 L polyethylene glycol plus ascorbic acid solution (Coolprep^Ⓡ; Taejoon Pharm, Seoul, Korea). After observing the anus and taking a picture, the colonoscope was inserted in a standard method up to the cecum. After a photograph of the cecum was taken, the observation of colonic mucosa was made during the colonoscope withdrawal. The size, location, number, and morphology of all colonic lesions were documented during colonoscopy. When a polyp was detected, endoscopists could use narrow band imaging at his or her discretion for detailed assessment of real-time histological diagnosis. The size of a polyp was estimated by open biopsy forceps or the diameter of the snare catheter. Polypectomy was performed using cold forceps polypectomy, cold snare polypectomy, and endoscopic mucosal resection depending on the size and morphology of polyps and the endoscopist’s preference. Histological evaluation of resected polyp was performed by board-certified gastrointestinal pathologists.

3. Study outcomes

The primary outcomes of interest were ADR and withdrawal time. ADR was defined as the proportion of colonoscopies with at least one adenoma detected. Withdrawal time was defined as the time to observe the colon lumen from the cecum to the rectum, excluding the polypectomy time. Secondary outcomes included the polyp detection rate (PDR), advanced adenoma detection rate (AADR), mean number of polyps per colonoscopy, mean number of adenomas per colonoscopy (APC), and cecal insertion time. Advanced adenomas were defined as adenomas larger than 10 mm and adenomas containing a villous component, high-grade dysplasia, or carcinoma. Insertion time was defined as the time for the colonoscope to reach the cecum from the anus. Polypectomy-associated indicators were also investigated, which included endoscopically complete resection, polypectomy time, and postpolypectomy adverse events. Polypectomy time was defined as the time from polyp detection to completion of its resection. Procedural time data were investigated by using the time recorded at colonoscopy photographs.

4. Statistical analysis

The primary study goal was to compare the mean withdrawal time and ADR between the face shield and no-face shield groups. To calculate the number of study patients, we assumed the mean withdrawal time was 7.8 minutes based on previous studies in which colonoscopy was performed without the face shield.^16,17 Increase of withdrawal time by 0.5 minutes or less was considered clinically non-inferior. Enrollment of 1,200 patients, i.e., 600 in each arm, were needed to detect such a difference between groups assuming a standard deviation of 3.1 with 80% power and a 5% level of significance.

Descriptive statistics were used for the demographic characteristics. Normally distributed variables were presented as means with standard deviation, and non-normally distributed variables were presented as medians with interquartile ranges (IQRs). Continuous variables were compared using the Student t test or the Mann-Whitney U test as appropriate. Categorical variables were presented as proportion of the total study population. Proportions were compared using the chi-squared test or the Fisher exact test as appropriate. A p-value of <0.05 was considered statistically significant. All data were analyzed using the IBM SPSS version 21 software (IBM Corp., Armonk, NY, USA).

1. Baseline characteristics

The nine endoscopists who participated in this study performed 2,817 colonoscopies in 2,817 patients from March 10 to May 31, 2020. We excluded 1,473 patients based on the exclusion criteria. Therefore, a total of 1,344 colonoscopies were included in the final analysis of this study. Of these, 715 colonoscopies were performed before introduction of the face shield, and 629 colonoscopies after introduction of the face shield (Fig. 2). Baseline characteristics, such as age, sex, and family history of colorectal cancer, were similar between the face shield and no-face shield groups. The proportions of screening, surveillance, and diagnostic colonoscopy were also not different between the two groups. They were also similar between subgroups according to the expertise level of endoscopists (Table 1). We investigated the average number of total colonoscopy examinations per day at our center before and after wearing the face shield during the study period. The numbers were not different between the two periods (39.2±3.2 vs 40.4±3.7, p=0.233). The average numbers of colonoscopies by one endoscopist in one session (270 to 300 minutes) were also not different before and after wearing the face shield (4.0±1.6 vs 3.9±1.5, p=0.626). Moreover, there were no patients with COVID-19 symptoms and/or confirmed COVID-19 during the study period.

Table 1 . Baseline Characteristics of the Study Patients and Colonoscopies.

Characteristics	Overall patients group (n=1,344)				Expert endoscopists group (n=636)				Trainee endoscopists group (n=708)
	Face shield group (n=629)	No-face shield group (n=715)	p-value		Face shield group (n=280)	No-face shield group (n=356)	p-value		Face shield group (n=349)	No-face shield group (n=359)	p-value
Age, yr	56.9±12.5	55.7±13.3	0.102		54.2±11.0	52.9±12.6	0.161		59.0±13.3	58.5±13.5	0.613
Sex			0.215				0.166				0.789
Male	284 (45.2)	347 (48.5)			130 (46.4)	185 (52.0)			154 (44.1)	162 (45.1)
Female	345 (54.8)	368 (51.5)			150 (53.6)	171 (48.0)			195 (55.9)	197 (54.9)
BMI, kg/m2	23.7±3.4	23.7±3.6	0.920		23.3±3.5	23.7±3.6	0.143		24.0±3.3	23.7±3.5	0.199
Family history of colorectal cancer	39 (6.2)	35 (4.9)	0.361		18 (6.4)	15 (4.2)	0.286		21 (6.0)	20 (5.9)	0.842
Current smoking	146 (23.2)	185 (25.9)	0.109		114 (40.7)	142 (39.9)	0.512		32 (9.2)	43 (12.0)	0.246
Antiplatelet use	74 (11.8)	78 (10.9)	0.617		25 (8.9)	26 (7.3)	0.459		49 (14.0)	52 (14.5)	0.924
Anticoagulant use	17 (2.7)	11 (1.5)	0.141		2 (0.7)	4 (1.1)	0.869		15 (4.3)	7 (1.9)	0.086
Colonoscopy under sedation	580 (92.2)	662 (92.6)	0.794		269 (96.1)	342 (96.1)	0.998		311 (89.1)	320 (89.1)	0.992
Colonoscopy indication			0.192				0.420				0.658
Screening	468 (74.4)	562 (78.6)			259 (92.5)	335 (94.1)			209 (59.9)	227 (63.2)
Surveillance	36 (5.7)	35 (4.9)			21 (7.5)	21 (5.9)			15 (4.3)	14 (3.9)
Diagnostic	125 (19.9)	118 (16.5)			0	0			125 (35.8)	118 (32.9)
Bowel preparation			0.693				0.460				0.398
Excellent (BBPS 8–9)	521 (82.8)	598 (83.6)			247 (88.2)	307 (86.2)			274 (78.5)	291 (81.1)
Good (BBPS 6–7)	108 (17.2)	117 (16.4)			33 (11.8)	49 (13.8)			75 (21.5)	68 (18.9)

Data are presented as the mean±SD or number (%)..

BMI, body mass index; BBPS, Boston Bowel Preparation Scale..

Figure 2. Inclusion and exclusion of study participants.

2. Quality indicators associated with colonoscopy observation

ADR was similar between the face shield and no-face shield groups (41.5% vs 39.8%, p=0.605). Additionally, ADR was calculated only in the screening colonoscopy populations in the face shield (n=468) and no-face shield groups (n=562), which showed similar ADR (38.9% [30.2% to 45.8%] vs 37.9% [30.6% to 44.6%], p=0.880). There was no significant difference in PDR between both groups (48.3% vs 50.5%, p=0.863). AADR was also similar (5.1% vs 3.8%, p=0.387) (Table 2). The distribution of ADR, PDR, and AADR of nine endoscopists according to wearing and non-wearing of a face shield is presented in Fig. 3. The APC (0.72±1.27 vs 0.77±1.38, p=0.510) and polyps per colonoscopy (1.06±1.61 vs 1.14±1.75, p=0.386) were also not different between both groups.

Table 2 . Quality Indicators Associated with Colonoscopy Observation.

Variable	Face shield group (n=629)	No-face shield group (n=715)	p-value
Cecal intubation rate	629 (100)	713 (99.7)	0.184
Cases with withdrawal time <6 min	5 (0.8)	11 (1.5)	0.210
Insertion time, min	5.57 (3.83–8.65)	5.40 (3.53–8.30)	0.131
Withdrawal time, min	8.72 (7.32–10.87)	8.68 (7.37–10.93)	0.816
Polyp detection rate, %	48.3 (38.7–57.3)	50.5 (40.4–58.7)	0.863
Adenoma detection rate, %	41.5 (32.8–44.9)	39.8 (30.5–43.6)	0.605
Advanced adenoma detection rate, %	5.1 (2.8–8.0)	3.8 (2.6–5.6)	0.387
Polyps per colonoscopy	1.06±1.61	1.14±1.75	0.386
Adenomas per colonoscopy	0.72±1.27	0.77±1.38	0.510

Data are presented as the number (%), median (interquartile range), or mean±SD..

Figure 3. Distribution of PDR, ADR, and AADR according to whether a face shield was worn.
PDR, polyp detection rate; ADR, adenoma detection rate; AADR, advanced adenoma detection rate; FS, face shield; No-FS, no-face shield.

The median withdrawal time was similar between the face shield and no-face shield groups (8.72 minutes [IQR, 7.32 to 10.87] vs 8.68 minutes [IQR, 7.37 to 10.93], p=0.816). The proportion of cases with withdrawal time <6 minutes was not different between the two groups (0.8% vs 1.5%, p=0.210). The cecal intubation rate was similar between the two groups (100% vs 99.7%, p=0.184). The median cecal insertion time was also not different between the groups (Table 2).

Colonoscopy quality indicators were compared between the face shield and no-face shield groups according to the colonoscopy expertise level. There was no significant difference in all quality indicators such as insertion time, withdrawal time, PDR, ADR, and AADR between the face shield and no-face shield groups of four experienced board-certified gastroenterologists. Similarly, all quality indicators were not different between the face shield and no-face shield groups of trainee endoscopists, i.e., five 2nd-year gastroenterology fellows (Table 3, Fig. 4).

Table 3 . Comparison of Quality Indicators between the Face Shield and No-Face Shield Groups According to the Colonoscopy Expertise Level.

Variable	Expert endoscopists (n=636)				Trainee endoscopists (n=708)
	Face shield group (n=280)	No-face shield group (n=356)	p-value		Face shield group (n=349)	No-face shield group (n=359)	p-value
Cecal intubation rate	280 (100)	355 (99.7)	0.375		349 (100)	358 (99.7)	0.324
Cases with withdrawal time <6 min	3 (1.1)	5 (1.4)	0.708		2 (0.6)	6 (1.7)	0.167
Insertion time, min	4.38 (3.30–5.97)	4.00 (3.05–5.52)	0.259		7.15 (4.97–10.83)	7.33 (5.22–11.22)	0.833
Withdrawal time, min	7.73 (6.88–8.97)	7.87 (6.92–9.12)	0.855		9.80 (8.25–12.12)	10.08 (8.17–12.87)	0.711
Polyp detection rate, %	56.4 (47.8–64.7)	52.0 (43.8–60.8)	0.686		43.1 (34.1–50.4)	44.9 (37.1–58.7)	0.421
Adenoma detection rate, %	42.0 (41.5–50.9)	40.1 (35.5–45.3)	0.200		36.8 (27.2–43.2)	33.3 (27.7–46.9)	0.882
Advanced adenoma detection rate, %	5.0 (2.2–8.2)	3.9 (2.8–5.7)	0.686		5.1 (2.1–8.3)	3.8 (2.5–5.6)	0.548
Polyps per colonoscopy	1.20±1.59	1.22±1.87	0.896		0.94±1.61	1.05±1.62	0.353
Adenomas per colonoscopy	0.80±1.24	0.87±1.55	0.520		0.66±1.28	0.67±1.17	0.918

Data are presented as the number (%), median (interquartile range), or mean±SD..

Figure 4. Comparison of withdrawal time between the face shield (FS) and no-face shield (No-FS) groups according to the endoscopist expertise levels. The dotted line in each dot plot represents the mean level. The black line in each dot plot represents the median level. The grey lines in each dot plot represent the 25% and 75% quartile levels.

3. Polypectomy-associated quality indicators

A total of 590 and 734 polyps were detected and resected endoscopically in 306 patients of the face shield group and 355 patients of the no-face shield group, respectively. Distribution of polyp size was similar between the groups (polyps ≤5 mm, 81.9% vs 82.0%; polyps of 6‒9 mm, 14.4% vs 15.3%; polyps ≥10 mm, 3.7% vs 2.7%; p=0.549). Cold forceps polypectomy was the most frequently used resection technique in both groups (72.4% vs 73.3%), followed by cold snare polypectomy (13.6% vs 12.3%) and endoscopic mucosal resection (14.0% vs 14.4%). The proportion of each polypectomy technique was similar between the groups (p=0.779). All polyps were endoscopically completely resected in both groups.

Median procedure time of cold forceps polypectomy was similar between the face shield and no-face shield groups (0.80 minutes [IQR, 0.60 to 1.16] vs 0.83 minutes [IQR, 0.63 to 1.23], p=0.475). Median cold snare polypectomy time and endoscopic mucosal resection time were also not different between the face shield and no-face shield groups (Table 4). In addition, there were no cases of adverse events, including perforation and delayed bleeding, in either group.

Table 4 . Polypectomy-Associated Variables.

Variable	Face shield group (590 polyps in 306 patients)	No-face shield group (734 polyps in 355 patients)	p-value
Polyp size			0.549
≤5 mm	483 (81.9)	602 (82.0)
6–9 mm	85 (14.4)	112 (15.3)
≥10 mm	22 (3.7)	20 (2.7)
Mean polyp size, mm	4.11±2.10	4.04±1.90	0.545
Endoscopically complete resection	590 (100)	734 (100)	NA
Polypectomy technique			0.779
Cold forceps	427 (72.4)	538 (73.3)
Cold snare	80 (13.6)	90 (12.3)
EMR	83 (14.0)	106 (14.4)
Mean polyp size in each polypectomy method, mm
Cold forceps polypectomy	3.20±0.95	3.28±1.03	0.254
Cold snare polypectomy	4.96±1.28	4.82±1.15	0.455
EMR	7.94±2.50	7.24±2.30	0.054
Procedure time, min
Cold forceps polypectomy	0.80 (0.60–1.16)	0.83 (0.63–1.23)	0.475
Cold snare polypectomy	1.66 (1.50–2.55)	1.95 (1.38–3.02)	0.301
EMR	3.83 (3.13–5.5)	3.65 (3.07–5.35)	0.567
Adverse events
Perforation	0	0	NA
Delayed bleeding	0	0	NA

Data are presented as the number (%), mean±SD, or median (interquartile range)..

EMR, endoscopic mucosal resection; NA, not applicable..

In this retrospective cohort study, we found that colonoscopy with the face shield worn did not increase the withdrawal time or decrease the ADR. In addition, insertion time, PDR, AADR, and mean numbers of polyps per colonoscopy and APC were not different between the face shield and no-face shield groups. Furthermore, the polypectomy time and incidence of post-polypectomy adverse events were also not different between both groups. These findings suggest that wearing the face shield may not unfavorably affect the quality of colonoscopy.

High-quality colonoscopy and quality improvement programs are of paramount importance to accomplish the goal of colonoscopy effectively, including complete detection and removal of colorectal neoplasm.¹⁸ Several quality indicators were developed to measure the quality of colonoscopy, which include ADR, PDR, AADR, APC, and withdrawal time. Because increased ADR is associated with a reduced risk of interval colorectal cancer and death,¹⁹ ADR has been the most widely used quality indicator.^12,20 ADR levels (41.5% and 39.8%, respectively) in both groups in our study were higher than the target level (25%; 30% for men and 20% for women) recommended by American Society for Gastrointestinal Endoscopy and American College of Gastroenterology.¹² However, they were similar to those in previous screening colonoscopy studies performed in Korea (37.2% to 45.3%),^16,17 which suggests that endoscopists and patients in our study were not skewed or biased and that our findings can be generalized to other endoscopy units. We believe recent education about the importance of colonoscopy quality in the gastroenterology society may be the main reason for the high ADR. In previous studies, ADR was reported to be associated with factors such as a patient’s age, sex, bowel preparation adequacy, and the endoscopist-related technical factors, including cecal intubation rate and withdrawal time.^21-25 These factors did not differ between the face shield and no-face shield groups in our study. Furthermore, the number of colonoscopies at our center was not different before and after wearing the face shield, which suggests no difference in the workload, a possible confounding variable in the analysis of ADR, between the two periods. In addition, the proportion of diagnostic colonoscopy for patients with gastrointestinal symptoms was also not different between the face shield and no-face shield groups, which decreases the risk of selection bias. As a corollary, we suggest that fair comparison of ADR was made, which may objectively imply the absence of an unfavorable effect of the face shield on ADR.

Other quality indicators, such as PDR, AADR, APC, and withdrawal time, were also similar between the face shield and no-face shield groups. PDR is an easily obtainable quality indicator, because it does not require histopathology results, unlike ADR. AADR is another important quality indicator because advanced adenoma was reported to transit to colorectal cancer by 2.6% to 5.8% annually.²⁶ APC was raised as another quality indicator that might complement ADR, because there was a concern that concentration on detecting additional adenomas after detection of the first adenoma could decrease, and that ADR could not reflect the quality of the entire colonic examination. American Society for Gastrointestinal Endoscopy and American College of Gastroenterology recommended a mean withdrawal time >6 minutes for adequate observation and detection of colorectal neoplasms.¹² Although there were a few colonoscopy cases with withdrawal time <6 minutes in the face shield and no-face shield groups, the proportions were similar (0.8% vs 1.5%, p=0.210). This suggests that the discomfort from face shield may not have shortened the colonoscopy withdrawal time, which implies no negative effect of the face shield on colonoscopy quality indicators. Because not only ADR but also all these other important quality indicators, did not differ between the face shield and no-face shield groups, we suggest with high confidence that the face shield may not unfavorably affect the quality of colonoscopy. The similar insertion time between the two groups in our study further supports the absence of a negative effect from the face shield.

We investigated polypectomy-associated indicators to evaluate the effect of the face shield not only on the quality of screening/surveillance/diagnostic colonoscopy but also on that of therapeutic colonoscopy. All polyps could be completely resected endoscopically in both groups. Endoscopic resection procedure times were not different between the groups. In addition, polypectomy-associated adverse events did not occur in either group. These findings suggest that both the efficacy and safety of polypectomy may be similar between the face shield and no-face shield groups, implying that the face shield may not interfere with colonoscopic polypectomy.

We initially assumed that the face shield might interfere with the quality of vision of endoscopists, thereby lengthening the withdrawal time and decreasing the ADR. We also hypothesized that less-experienced endoscopists, such as trainees, could be influenced more significantly by the face shield. Therefore, we performed subgroup analyses according to the expertise level of endoscopists. Unlike what was expected not only experienced endoscopists but also second-year gastroenterology fellows were unaffected by the face shield in terms of colonoscopy quality. Although we found the absence of colonoscopy quality deterioration by the face shield consistently in both observation and resection of colorectal neoplasm and in both expert and beginner endoscopists, the reason for this finding is not clear. A Turkish study investigated the effect of face shields on the field-of-view of neurosurgeons when using a surgical microscope.²⁷ The field-of-view significantly decreased from that of the naked eye (9,305.33±406.1 mm²) to that with a face shield (92.33±6.4 mm²). Another study in the United Kingdom evaluated the effect of face shields on the field-of-vision of otolaryngologists using a microscope.²⁸ The face shield reduced the field-of-vision up to 76.8%. These two studies suggest that the face shield is not compatible with the use of a surgical microscope, because it decreases the visual field by increasing the distance between the eye piece and pupil. Unlike the situation of microsurgeries utilizing a microscope, the distance between the endoscopy monitor and the endoscopist’s pupil is 1 to 2 m in colonoscopy rooms, thereby possibly minimizing the risk of a clinically relevant unfavorable effect of the face shield. We suggest that this may explain the absence of colonoscopy quality deterioration while wearing the face shield. A study in Colombia that investigated the effect of eye-protecting PPE on quality of vision of gastroenterologists supports this assumption.²⁹ In this study, the quality of vision assessed by an ophthalmological examination did not worsen when using the 3M 6800 full facepiece. However, wearing two types of eye protectors simultaneously (3M mono safety glasses and protective screen) decreased visual acuity up to 37%, color visualization up to 25%, and contrast sensitivity up to 75% within minutes of placement. Nevertheless, the lower quality of vision assessed by an ophthalmological examination cannot be directly translated into worse colonoscopy quality in real endoscopy practices, such as a lower ADR. Taking the findings of previous studies together with the findings of our present study, we suggest that a simple face shield may not interfere with qualified colonoscopy performance, although the effect of wearing complex eye-protecting PPE, such as simultaneously wearing two different types of glasses, a shield, and/or a screen, may need further research to clarify its potential for unfavorable effects on colonoscopy quality.

Our study had several limitations. First, there could be selection bias of patients because of the COVID-19 pandemic. Healthcare service-seeking behavior could be influenced by the COVID-19 pandemic and the characteristics of persons who visited our center during this pandemic may not represent those of the general population, which limits the generalizability of our study. Second, this was a retrospective study. Colonoscopy insertion time, withdrawal time, and polypectomy time were calculated based on the time recorded on the endoscopy pictures, which may not always be completely correct. Third, we investigated the polypectomy time and adverse events to assess the effect of face shields on therapeutic colonoscopy. However, the primary goal of polypectomy is complete resection of colorectal neoplasm. Therefore, the evaluation of histological complete resection that was not performed in our study may be the most relevant method for assessment of quality of polypectomy, although we confirmed endoscopically complete resection in all cases. Despite these limitations, we believe that our study is meaningful in terms that we confidently showed the absence of unfavorable effect by the face shield on colonoscopy quality indicators, thereby providing a rationale for PPE use against a pandemic caused by aerosol transmission, to improve the safety of endoscopists without loss of colonoscopy quality.

In conclusion, in our experience, colonoscopy performance was not affected by the face shield. Colonoscopy quality indicators, such as ADR, AADR, APC, and withdrawal time, did not worsen when a face shield was worn. In addition, polypectomy-associated indicators, such as polypectomy time and adverse events, were not worse. Therefore, use of the face shield as PPE can be recommended without any concern about colonoscopy performance reduction during this COVID-19 pandemic.

No potential conflict of interest relevant to this article was reported.

Conceptualization, methodology, and data curation: J.W.L., H.J.L., J.S.B. Resources: J.W.L., H.J.L, D.S.K., J.Y., S.W.H., H.W.H., J.S.L., G.U.K., S.L. Formal analysis and visualization: J.W.L., J.S.B. Critical revision: J.C., J.H.P., D.H.Y. Writing - original draft: J.W.L. Overall project administration, and supervision: J.S.B.