key: cord-0814670-eqm01xby authors: Casper, M.; Reichert, M. C.; Rissland, J.; Lammert, F.; Krawczyk, M. title: Pre-endoscopy SARS-CoV-2 testing strategy during COVID-19 pandemic: The care must go on date: 2020-10-27 journal: nan DOI: 10.1101/2020.10.22.20217885 sha: 45cdad95975ac1841bf1abe6ec3109d7c0e13a25 doc_id: 814670 cord_uid: eqm01xby Background: In response to the COVID-19 pandemic, endoscopic societies have recommended reduction of endoscopic procedures. In particular non-urgent endoscopies should be postponed. However, this might lead to unnecessary delay in diagnosing gastrointestinal conditions. Methods: Retrospectively we analysed the gastrointestinal endoscopies performed at the Central Endoscopy Unit of Saarland University Medical Center during seven weeks from 23 March to 10 May 2020 and present our real-world single-center experience with an individualized rtPCR-based pre-endoscopy SARS-CoV-2 testing ("PECo") strategy. Results: Altogether 359 gastrointestinal endoscopies were performed. The PECo strategy enabled us to conservatively handle endoscopy program reduction (44% reduction as compared 2019). The results of COVID-19 rtPCR from nasopharyngeal swabs were available in 89% of patients prior to endoscopies. Apart from six patients with known COVID-19, all other tested patients were negative. The frequencies of endoscopic therapies and clinically significant findings did not differ between patients with or without SARS-CoV-2 tests. Conclusion: A reasonable reduction of the endoscopy program in the setting of structured SARS-CoV-2 testing is feasible and safe. The PECo strategy allows continuation of endoscopic procedures in a region with intermediate frequency of COVID-19 when hospital capacities are not overwhelmed by the pandemic. Thus, the study might help to develop new strategies during future waves of COVID-19 or local outbreaks. INTRODUCTION COVID-19 substantially affects health care systems worldwide. Gastroenterologists must balance the risk for SARS-CoV-2 virus transmission during endoscopy against the risk caused by the delay of the procedures. Endoscopic societies around the world have published recommendations to assist endoscopists in decision-making during the pandemic (1) . In most of these recommendations it is advised to use personal protective equipment (PPE) and to postpone non-urgent or routine procedures temporarily. However, urgent procedures are not uniformly defined, requiring case-by-case decisions from endoscopists in many patients. Following these recommendations, endoscopy programs were substantially reduced worldwide (on average by 83%) during the pandemic (2) . The short-and medium-term consequences of this approach are difficult to estimate. As an alternative we present here our real-world experience with the rtPCR-based pre-endoscopy SARS-CoV-2 testing ("PECo") strategy that enabled us to conservatively handle endoscopy program reduction. Retrospectively we analysed the gastrointestinal endoscopies performed at the Central Endoscopy Unit of Saarland University Medical Center during seven weeks from 23 March to 10 May 2020 (local peak period of the COVID-19 pandemic). This endoscopy unit is an academic tertiary referral centre serving all medical and surgical departments as well as state and regional health care providers. In Germany, more than 169.000 COVID-19 cases leading to more than 7.400 deaths (4.4%) had been reported until 10 May 2020. The current cumulative incidence in Saarland, which is one of the Federal states in Southwestern Germany at the border to France, is 279 cases per 100.000. Between 23 March and 10 May 2020, 2.514 individuals were tested positive for SARS-CoV-2 in Saarland, of whom 146 All rights reserved. No reuse allowed without permission. perpetuity. preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in The copyright holder for this this version posted October 27, 2020. ; https://doi.org/10.1101/2020.10.22.20217885 doi: medRxiv preprint The rtPCR-based pre-endoscopy SARS-CoV-2 testing (PECo) on nasopharyngeal swabs (Roche, Basel, Switzerlanld Altona Diagnostics, Hamburg, Germany) was broadly offered to in-patients in the Saarland University Medical Centre during the pandemic. Starting on 2 April 2020, structured rtPCR testing was also implemented for all out-patients scheduled for endoscopic procedures. Endoscopies were planned to be performed when the patient tested negative within 5 days prior to the procedure. In addition, all members of the endoscopy suite (nurses, physicians, endoscope reprocessing and cleaning staff) were tested weekly using pooling of samples, as described recently (3). Routine rtPCR test results were available within 3 -5 hours, when performed before 04:30 PM on weekdays or 02:00 PM on weekends, or on the next day when performed later. Emergency testing was available 24/7 within 3 hours. Patients were also inquired using questionnaires for typical COVID-19 symptoms prior to endoscopy. All necessary in-patient endoscopic procedures were performed as requested. For out-patients urgent procedures were unrestrictedly offered, non-urgent procedures were discussed on an individual basis with patients and referring physicians. Risk-stratified personal protective measures conformed with the published recommendations (4). Asymptomatic patients with a negative rtPCR test result were categorized as low-risk patients and PPE was adapted (surgical mask, goggles, single-use gown, gloves, hairnet). All rights reserved. No reuse allowed without permission. perpetuity. preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in respectively, for non-urgent procedures). For lower endoscopies, 27.3% of essential/emergent and urgent procedures were therapeutic and 50% altered management (23.1% and 9.6%, respectively, for non-urgent procedures). Five malignant tumours (frequency 1.4%) were diagnosed by upper (essential/urgent: 3; non-urgent: 2) or lower endoscopy (essential/urgent: 5; non-urgent: 0). Twelve non-urgent ERCPs were done to exchange biliary stents after maximal extension of exchange intervals, and all but two ERC(P)s were therapeutic. The results of SARS-CoV-2 rtPCR were available prior to endoscopy in 313 procedures (88.6%). After implementation of structured testing, only eight from 302 (2.6%) non-emergency procedures were performed without known COVID-19 status. No patient scheduled for endoscopy tested positive for SARS-CoV-2 either before or after endoscopy. There occurred no infection of any endoscopy team member during the described period. perpetuity. preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in The copyright holder for this this version posted October 27, 2020. ; https://doi.org/10.1101/2020.10.22.20217885 doi: medRxiv preprint The reduction of endoscopies performed during COVID-19 pandemic is thought to (i) safe resources needed for COVID-19 patients, and (ii) minimize the risk of infection for patients and endoscopy team members. However, lock-down of endoscopy units during pandemic might confront us with potentially unmanageable numbers of patients afterwards. This strategy also implies that the pandemic of COVID-19 will soon be over, and this assumption might not necessarily be correct. Thus, we are in-need of simple and reliable screening tools that will allow functioning of endoscopy units without posing risks to patients or to the endoscopy teams. Overall, gastrointestinal endoscopy appears to be relatively safe when adequate protective measures are used (4, 5) , but these measures significantly alter the workflow and potentially impair the quality of endoscopies. Here we show that a moderate reduction of the endoscopy volume based on the structured rtPCR-based SARS-CoV-2 testing on nasopharyngeal swabs is feasible. The PECo strategy seems to work well, at least in regions with low to intermediate frequency of COVID-19 infections. However, the retrospective design, the lack of a structured follow-up for COVID-19 after the endoscopic procedure limit validity of the study. The reduction of endoscopy volume by 43% is substantially lower than the reported reductions of about 80% (1). Most endoscopies without a test result were performed in the evening or on weekends when results of routine tests were not available until the next morning. Based on our data and recent publications on the timing of endoscopy for upper gastrointestinal bleeding (6), the majority of endoscopies (except for suspected variceal haemorrhage with hemodynamic instability and severe septic shock due to cholangitis) can be safely deferred until the rtPCR result is available. Since false-negative rtPCR results are possible (7), we additionally recommend the use of standardized questionnaires to assess patients for COVID-19 symptoms and to adapt PPE. Our results might help to develop new strategies during future waves of COVID-19 infection or local outbreaks. All rights reserved. No reuse allowed without permission. perpetuity. preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in The copyright holder for this this version posted October 27, 2020. ; https://doi.org/10.1101/2020.10.22.20217885 doi: medRxiv preprint This study was approved by the ethics committee of Ärztekammer des Saarlandes (Saarbrücken, Germany; #254/20). A waiver was obtained for the consent to participate in the study. The study was performed in accordance with the Declaration of Helsinki. The datasets used and analysed during the current study are available from the corresponding author on reasonable request. The authors declare that they have no competing interests There was no funding source relevant to this work. perpetuity. preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in The copyright holder for this this version posted October 27, 2020. ; https://doi.org/10.1101/2020.10.22.20217885 doi: medRxiv preprint preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in The copyright holder for this this version posted October 27, 2020. ; https://doi.org/10.1101/2020.10.22.20217885 doi: medRxiv preprint Gastrointestinal Endoscopy During the COVID-19 Pandemic: An updated review of guidelines and statements from international and national nocieties Global Impact of the COVID-19 Pandemic on Endoscopy: An International Survey of 252 Centers from 55 Countries Pooling of samples for testing for SARS-CoV-2 in asymptomatic people COVID-19) outbreak: what the department of endoscopy should know Low risk of covid-19 transmission in GI endoscopy Timing of Endoscopy for Acute Upper Gastrointestinal Bleeding All rights reserved. No reuse allowed without permission preprint (which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in The copyright holder for this this version posted