Risk factors for postgastric endoscopic submucosal dissection bleeding in direct oral anticoagulant users

Author:

Kagawa Tomo1,Ishikawa Shigenao1,Hidaka Yu2,Colvin Hugh Shunsuke1,Nakanishi Akira1,Ohkawa Jumpei1,Negishi Shin1,Yasutomi Eriko1,Yamauchi Kenji1,Okamoto Kunio13,Sakakihara Ichiro1,Izumikawa Koichi1,Yamamoto Kumiko1,Takahashi Sakuma1,Tanaka Shigetomi1,Matsuura Mihoko1,Wato Masaki1,Hasui Toshimi1,Inaba Tomoki1

Affiliation:

1. Department of Gastroenterology Kagawa Prefectural Central Hospital Kagawa Japan

2. Department of Medical Statistics and Bioinformatics, Graduate School of Medicine Kyoto University Kyoto Japan

3. Department of Medical Oncology Kagawa Prefectural Central Hospital Kagawa Japan

Abstract

ObjectivesBleeding after endoscopic submucosal dissection (ESD) for gastric tumors in patients taking antithrombotic drugs, in particular direct oral anticoagulants (DOACs), remains unresolved; therefore, we evaluated the risk factors for post‐ESD bleeding and drug differences in patients taking DOACs.MethodsWe included 278 patients taking antithrombotic drugs who underwent gastric ESD between January 2017 and March 2022. Antithrombotic drugs were withdrawn following the 2017 guidelines (Appendix on anticoagulants including DOACs). To further clarify differences in antithrombotic agents' effects, the peri‐cancerous mucosa in the resected specimen was pathologically evaluated according to the Updated Sydney System. Multivariate analysis was performed to assess the risk of post‐ESD bleeding.ResultsThe incidence of post‐ESD bleeding in patients taking DOACs was 19.6% (10/51). Among patients taking antithrombotic drugs, DOACs were identified as a possible factor involved in post‐ESD bleeding (odds ratio [OR] 4.92). Among patients taking DOACs, possible factors included resection length diameter ≥30 mm (OR 3.72), presence of neutrophil infiltration (OR 2.71), lesions occurring in the lower third of stomach (OR 2.34), and preoperative antiplatelet use (OR 2.22). Post‐ESD bleeding by DOAC type was 25.0% of patients (4/16) receiving apixaban, in 20.0% (3/15) receiving edoxaban, in 21.4% (3/14) receiving rivaroxaban, and in none of those receiving dabigatran.ConclusionsThe administration of DOACs was shown to be a possible factor involved in post‐ESD bleeding, and risk factors for patients taking DOACs included neutrophil infiltration. The pharmacological differences in the effects of DOACs contributing to bleeding in gastric ulcers suggest comparatively less bleeding with dabigatran after ESD.

Publisher

Wiley

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