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The COVID-19 pandemic has severely curtailed the practice of endoscopy (as an exemplar for outpatient diagnostic procedures) worldwide. Restart and recovery processes will be influenced by the need to protect patients and staff from disease transmission, but data on the risk of COVID-19 transmission after an endoscopy are sparse. This is of particular importance in later pandemic phases when the risk of harm from delayed or missed significant diagnoses is likely to far outweigh the risk of infection. The British Society of Gastroenterology guidance for restarting endoscopy included the stratification of diagnostic procedures according to aerosol generation or assessment of infectious risk as well as pragmatic guidance on the use of personal protective equipment (PPE). We sought to document the risk of COVID-19 transmission after endoscopy in this ‘COVID-minimised’ environment. Prospective data were collected from 18 UK centres for n=6208 procedures. Pre-endoscopy, 3 of 2611 (0.11%; 95% CI 0.00%–0.33%) asymptomatic patients tested positive for SARS-CoV-2 on nasopharyngeal swab. Based on follow-up telephone symptom screening of patients at 7 and 14 days, no cases of COVID-19 were detected by any centre after endoscopy in either patients or staff. Although these data cannot determine the relative contribution of each component of a COVID-minimised pathway, they provide clear support for such an approach. The rational use of PPE and infection control policies should be continued and will aid in planning for outpatient diagnostics in the COVID-19 recovery phase.
In more detail
The COVID-19 pandemic has had an extraordinary impact on the delivery of GI endoscopy, with an initial reduction to 12% of prepandemic levels in the UK.1 In the deceleration and early recovery phases (up to end July 2020), this had risen to 42% of repandemic levels.2 Recovery has been influenced by multiple factors including availability of staff, restrictions caused by longer room cleansing, physical distancing and the use of personal protective equipment (PPE) slowing lists. There are grave implications of this contraction in activity,3 with the delayed diagnosis of significant conditions like GI cancer or inflammatory bowel disease of particular concern.1 4
The risk around the inadvertent periprocedure transmission of COVID-19 infection to both patients and staff is a primary concern,4 5 but is not well described. Early data from northern Italy described low rates of infection in patients and staff, even during the peak phase of the pandemic.6
Upper GI endoscopy is widely accepted to be an aerosol-generating procedure (AGP); however, the relevance of small-volume aerosols (ie, 0.3 μm; which appear to predominate7) for virus transmission is unclear.8 Infectious potential appears to be confined to particles 0.5 µm or larger,8 but this is a complex subject with a number of variables. There are also direct data to support the effectiveness of masks, including surgical face masks most widely used in endoscopy units, in preventing viral transmission.9 10 COVID-19 infection rates have been demonstrated to be lower-than-expected in endoscopy staff (compared with other healthcare workers) even when the so-called ‘high-risk’ PPE, particularly face masks, were not universally available or applied.6 Whether lower GI endoscopy is an AGP is also important but has been pragmatically regarded as having low infectious potential as per British Society of Gastroenterology (BSG) guidance,11 whereas staff are still advised to use appropriate (stratified) PPE for all procedures.
Significant patient anxiety regarding the potential for contracting COVID-19 infection also exists and this has also been demonstrated to influence the ability to provide effective diagnostic services.12 We therefore sought to study prospectively the number of patient infections following GI endoscopy from multiple centres across the UK through the peak, deceleration and early recovery phases of the pandemic. Taking into account the complexities of infection control, aerosols, infectivity and abrogation of risk by PPE, it was felt that the ultimate determinant of risk would be whether any COVID-19 cases were actually detected after endoscopy (in either patients or staff). The purpose of this study was to enable the quantification of the potential risk to patients and to inform endoscopy departments regarding the likelihood of transmitting the infection to patients. These data could be used to help communicate with patients and staff as well as inform planning for future outbreaks.
This multicentre prospective study collected data for consecutive outpatients attending for elective diagnostic or therapeutic endoscopy from 18 UK centres. No patient identifiable data were collected, no treatment decisions were affected and no identifiable data were used, analysed or transferred. As such ethical approval was deemed not to be required by the Research Governance committee at the lead author’s institution.
Centres were selected to reflect differently sized units, tertiary and local, covering a wide range of demographics including those serving mixed socioeconomic populations and a mix of ethnicities. All centres prospectively completed an anonymised database of patients including procedure type, responses to preprocedure SCOTS criteria, preprocedure nasopharyngeal swab test result (if performed in that unit), source of referral and dates for all activities. The SCOTS criteria5 comprise telephone screening questions around Symptoms, infectious Contacts, Occupational risk, Travel risk, Shielding status13 and are recommended in BSG guidance.11 These were developed as an update to a pre-existing screening tool (FTOCC; developed in Hong Kong during the first SARS outbreak and proposed for using during the COVID-19 pandemic14), to take into account considerations specific to COVID-19.
All centres conducted patient follow-up by telephone consultation at 7 and 14 days after the procedure to check for symptoms of COVID-19. If symptoms were reported that could be consistent with COVID-19,5 then these patients were advised to undergo COVID-19 nasopharyngeal swab testing. Data were collected on any patients with positive COVID-19 swab undertaken for any reason in the 14 days postendoscopy. Where patients were COVID-19 swab tested preprocedure and found to be positive, those patients were excluded from the follow-up study.
Data were collected from 6208 patients undergoing endoscopy at 18 centres between 30 April and 30 June 2020 (mean±SD age 59.3±15.4 years and n=2973 (48%) were female individuals). The characteristics of the endoscopy units are shown in table 1. Follow-up data on symptoms were collected up to 14 July 2020. There were no cases of COVID-19 detected in the 2 weeks following endoscopy (0/6208, 95% CI 0.0%–0.08% with continuity correction).
Figure 1 shows the procedures performed and overall % of total. There was an approximate 40:60 split between upper and lower GI procedures (where combined oesophagogastroduodenoscopy and colonoscopy counted as upper GI—given the AGP status of the former procedure and therefore potential for greater risk).
Most centres were prioritising urgent symptomatic patients during this period with less than 4% (n=233) of procedures classed as ‘routine or surveillance’ and these were performed at the discretion of the performing centre, mostly within the last 2 weeks of the data collection period. Of the remainder, n=3166 (51%), were patients referred for suspected cancer on the pre-existing UK ‘2-week wait’15 pathways (again split 60:40 in favour of lower GI). There were 1193 (19.0%) in a ‘shielded’ category13 as determined by the preprocedure telephone questionnaire.
Preprocedure nasopharyngeal swab testing for SARS-CoV-2 was performed in 2611 patients from 13 sites, in line with BSG guidance, after the confirmation of the absence of COVID-19 symptoms or risks.5 Only 3 (0.11%, 95% CI 0.03%–0.36% with continuity correction) patients were positive. All had their investigation safely deferred with no complications.
Following their procedure, 12 patients reported symptoms that were potentially compatible with COVID-19 infection at either the 7-day or 14-day telephone contact. All then underwent nasopharyngeal swab testing and were found to be negative. All symptoms settled with none deemed to have COVID-19. There was, sadly, one reported death due to an entirely unrelated cerebrovascular event within 14 days of a colonoscopy.
This prospective multicentre study of 6208 patients provides a clear indication that GI endoscopy can be safely performed in the recovery phase of COVID-19, when a COVID-minimised pathway5 is instituted. A relative strength of the study is that it involved 18 UK tertiary and local centres with a combined capacity of over 300 000 procedures per year.
There was a low incidence of positive swabs for asymptomatic patients preprocedure, but telephone screening alone might have missed up to 1 in 300 cases attending for endoscopy (at the top end of the 95% CI).
Our data cannot determine the relative contribution of each component of a COVID-minimised pathway (preprocedure questionnaire, swab testing and use of PPE), but provides a broad vindication of such an approach (a majority of the units involved used the recommendations for a stratified approach to PPE and infection control policies (air exchange, room cleaning and so on)). The combined effect of all these measures had a beneficial impact and should be continued through the pandemic. We cannot determine, in particular, whether less stringent PPE recommendations are possible beyond that already included in national guidance,11 but at the levels used across the units involved in this study, there does not appear to be any excess risk.
New guidance in the UK, issued after the study period, now also recommends testing 48–72 hours preadmission for diagnostic tests requiring sedation,16 and this is likely a cost-effective strategy (in a US context).17 This data collection was performed in the deceleration/recovery phases of the COVID-19 pandemic in the UK18 and should therefore inform periods of activity where similar rates of infection are seen.
When a COVID-minimised pathway is in place, patients (including those in a high-risk ‘shielding’ category) can now be reassured that concerns over COVID-19 infection should not stop them attending for GI endoscopy.
Collaborators Amyn Haji, Shraddha Gulati: King’s College Hospital NHS Foundation Trust, London; Joel Mawdsley, Freya Parker: Guy’s & St Thomas’s Hospitals, London; Ed Seward, Melanie Corpus: University College London Hospital, London; Srisha Hebbar, Rajeev Desai: Royal Stoke University Hospital; Nick Kennedy, Bridget Cann: Royal Devon and Exeter Hospital, Exeter; Rajesh Rameshshankar, Aymer Postgate: Hillingdon Hospital, London; John Greenaway, Martin Fletcher: South Tees Hospitals NHS Foundation Trust; Mo Thoufeeq, Thomas Archer: Sheffield Teaching Hospitals NHS Foundation Trust; David Nylander, John Leeds: Newcastle-upon-Tyne Hospitals NHS Foundation Trust; Gareth Corbett, Huma Asmat: Addenbrookes Hospital, Cambridge; Mohammed Raheel Anjum, Aravinth Murugananthan: Royal Wolverhampton NHS Trust; Adam Humphries, Sarah Marshall, Angad Dhillon, Romanov Nable: St Mark’s Hospital, London; Sunil Dolwani, Lavanya Shenbagaraj: Cardiff and Vale University Health Board; Pradeep Bhandari, Michelle Baker-Moffat: Queen Alexandra Hospital, Portsmouth; Ajay Verma, Vicki Lewin: Kettering General Hospital, Kettering; Colin Noble, Nick Church: Royal Infirmary of Edinburgh; Aisling Murphy, Adam Bailey: John Radcliffe Hospital, Oxford; Sergio Coda, Sas Banerjee: Barking and Havering NHS Trust, London.
Contributors Data collation and analysis was performed by BHH. All authors contributed to the study concept and design, manuscript writing and editing.
Funding JEE was funded by the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre.
Disclaimer The views expressed are those of the author(s) and not necessarily those of the National Health Service, the NIHR or the Department of Health. James East has served on clinical advisory board for Lumendi and Boston Scientific; Clinical advisory board and ownership, Satisfai Health; Speaker fees, Falk.
Competing interests CR has received grant funding from ARC Medical, Norgine Pharmaceuticals UK, Olympus Medical UK, 3D Matrix and an expert witness for ARC Medical. BHH has received grant funding from Olympus Medical UK, Fujifilm Europe, Takeda Pharmaceuticals UK and AbbVie UK. Clinical advisory board and ownership: Ampersand Health, Surgease Medical Ltd. IP has received speaker fees from Medtronic and Boston Scientific, UK.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Patient consent for publication Not required.
Provenance and peer review Not commissioned; externally peer reviewed.
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