Gastrointestinal bleeding and endoscopic findings in critically and non-critically ill patients with corona virus disease 2019 (COVID-19): Results from Lean European Open Survey on SARS-CoV-2 (LEOSS) and COKA registries.


Journal

United European gastroenterology journal
ISSN: 2050-6414
Titre abrégé: United European Gastroenterol J
Pays: England
ID NLM: 101606807

Informations de publication

Date de publication:
11 2021
Historique:
received: 02 07 2021
accepted: 23 08 2021
pubmed: 17 10 2021
medline: 1 12 2021
entrez: 16 10 2021
Statut: ppublish

Résumé

Corona virus disease 2019 (COVID-19) patients are at increased risk for thromboembolic events. It is unclear whether the risk for gastrointestinal (GI) bleeding is also increased. We considered 4128 COVID-19 patients enrolled in the Lean European Open Survey on SARS-CoV-2 (LEOSS) registry. The association between occurrence of GI bleeding and comorbidities as well as medication were examined. In addition, 1216 patients from COKA registry were analyzed focusing on endoscopy diagnostic findings. A cumulative number of 97 patients (1.8%) with GI bleeding were identified in the LEOSS registry and COKA registry. Of 4128 patients from the LEOSS registry, 66 patients (1.6%) had a GI bleeding. The rate of GI bleeding in patients with intensive care unit (ICU) admission was 4.5%. The use of therapeutic dose of anticoagulants showed a significant association with the increased incidence of bleeding in the critical phase of disease. The Charlson comorbidity index and the COVID-19 severity index were significantly higher in the group of patients with GI bleeding than in the group of patients without GI bleeding (5.83 (SD = 2.93) vs. 3.66 (SD = 3.06), p < 0.01 and 3.26 (SD = 1.69) vs. 2.33 (SD = 1.53), p < 0.01, respectively). In the COKA registry 31 patients (2.5%) developed a GI bleeding. Of these, the source of bleeding was identified in upper GI tract in 21 patients (67.7%) with ulcer as the most frequent bleeding source (25.8%, n = 8) followed by gastroesophageal reflux (16.1%, n = 5). In three patients (9.7%) GI bleeding source was located in lower GI tract caused mainly by diverticular bleeding (6.5%, n = 2). In seven patients (22.6%) the bleeding localization remained unknown. Consistent with previous research, comorbidities and disease severity correlate with the incidence of GI bleeding. Also, therapeutic anticoagulation seems to be associated with a higher risk of GI bleeding. Overall, the risk of GI bleeding seems not to be increased in COVID-19 patients.

Sections du résumé

BACKGROUND
Corona virus disease 2019 (COVID-19) patients are at increased risk for thromboembolic events. It is unclear whether the risk for gastrointestinal (GI) bleeding is also increased.
METHODS
We considered 4128 COVID-19 patients enrolled in the Lean European Open Survey on SARS-CoV-2 (LEOSS) registry. The association between occurrence of GI bleeding and comorbidities as well as medication were examined. In addition, 1216 patients from COKA registry were analyzed focusing on endoscopy diagnostic findings.
RESULTS
A cumulative number of 97 patients (1.8%) with GI bleeding were identified in the LEOSS registry and COKA registry. Of 4128 patients from the LEOSS registry, 66 patients (1.6%) had a GI bleeding. The rate of GI bleeding in patients with intensive care unit (ICU) admission was 4.5%. The use of therapeutic dose of anticoagulants showed a significant association with the increased incidence of bleeding in the critical phase of disease. The Charlson comorbidity index and the COVID-19 severity index were significantly higher in the group of patients with GI bleeding than in the group of patients without GI bleeding (5.83 (SD = 2.93) vs. 3.66 (SD = 3.06), p < 0.01 and 3.26 (SD = 1.69) vs. 2.33 (SD = 1.53), p < 0.01, respectively). In the COKA registry 31 patients (2.5%) developed a GI bleeding. Of these, the source of bleeding was identified in upper GI tract in 21 patients (67.7%) with ulcer as the most frequent bleeding source (25.8%, n = 8) followed by gastroesophageal reflux (16.1%, n = 5). In three patients (9.7%) GI bleeding source was located in lower GI tract caused mainly by diverticular bleeding (6.5%, n = 2). In seven patients (22.6%) the bleeding localization remained unknown.
CONCLUSION
Consistent with previous research, comorbidities and disease severity correlate with the incidence of GI bleeding. Also, therapeutic anticoagulation seems to be associated with a higher risk of GI bleeding. Overall, the risk of GI bleeding seems not to be increased in COVID-19 patients.

Identifiants

pubmed: 34655180
doi: 10.1002/ueg2.12165
pmc: PMC8598966
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1081-1090

Subventions

Organisme : Deutsches Zentrum für Infektionsforschung
Organisme : Willy Robert Pitzer Foundation

Informations de copyright

© 2021 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology.

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Auteurs

Stephan Zellmer (S)

Clinic for Internal Medicine III-Gastroenterology and Infectious Diseases, University Hospital Augsburg, Augsburg, Germany.

Frank Hanses (F)

Emergency Department, University Hospital Regensburg, Regensburg, Germany.
Department of Infection Prevention and Infectious Diseases, University Hospital Regensburg, Regensburg, Germany.

Anna Muzalyova (A)

Clinic for Internal Medicine III-Gastroenterology and Infectious Diseases, University Hospital Augsburg, Augsburg, Germany.

Johanna Classen (J)

Clinic for Internal Medicine III-Gastroenterology and Infectious Diseases, University Hospital Augsburg, Augsburg, Germany.

Georg Braun (G)

Clinic for Internal Medicine III-Gastroenterology and Infectious Diseases, University Hospital Augsburg, Augsburg, Germany.

Christiane Piepel (C)

Department of Hematooncology and Infectiology, Klinikum Bremen-Mitte, Bremen, Germany.

Johanna Erber (J)

Department of Internal Medicine II, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.

Lisa Pilgram (L)

Department of Internal Medicine, Hematology and Oncology, Goethe University Frankfurt, Frankfurt, Germany.

Lorenz Walter (L)

Clinic for Anesthesiology, Hospital St. Joseph-Stift Dresden, Dresden, Germany.

Siri Göpel (S)

Department of Internal Medicine I, University Hospital Tuebingen, Tuebingen, Germany.

Kai Wille (K)

University Clinic for Haematology, Oncology, Haemostaseology and Palliative Care, Johannes Wesling Klinikum, University of Bochum, Minden, Germany.

Martin Hower (M)

Department of Pneumology, Infectious Diseases and Internal Medicine, Klinikum Dortmund, Dortmund, Germany.

Maria Madeleine Rüthrich (MM)

Department of Internal Medicine II, Hematology and Medical Oncology, University Hospital Jena, Jena, Germany.

Jan Rupp (J)

Department of Infectious Diseases and Microbiology, University Hospital Schleswig-Holstein/Campus Luebeck, Luebeck, Germany.

Christian Degenhardt (C)

Department of Pharmacy, Municipal Hospital Karlsruhe, Karlsruhe, Germany.

Ingo Voigt (I)

Clinic for Acute and Emergency Medicine, Elisabeth Hospital, Essen, Germany.

Stefan Borgmann (S)

Department of Infectious Diseases and Infection Control, Ingolstadt Hospital, Ingolstadt, Germany.

Melanie Stecher (M)

Department I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
German Centre for Infection Research (DZIF), partner site Bonn-Cologne, Cologne, Germany.

Carolin Jakob (C)

Department I of Internal Medicine, University Hospital of Cologne, Cologne, Germany.
German Centre for Infection Research (DZIF), partner site Bonn-Cologne, Cologne, Germany.

Christine Dhillon (C)

COVID-19 Task Force, University Hospital Augsburg, Augsburg, Germany.

Helmut Messmann (H)

Clinic for Internal Medicine III-Gastroenterology and Infectious Diseases, University Hospital Augsburg, Augsburg, Germany.

Alanna Ebigbo (A)

Clinic for Internal Medicine III-Gastroenterology and Infectious Diseases, University Hospital Augsburg, Augsburg, Germany.

Christoph Römmele (C)

Clinic for Internal Medicine III-Gastroenterology and Infectious Diseases, University Hospital Augsburg, Augsburg, Germany.
COVID-19 Task Force, University Hospital Augsburg, Augsburg, Germany.

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