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Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery

AIM: We investigated the effect of perioperative management of direct oral anticoagulants (DOACs) on bleeding and thromboembolic complications during gastroenterological (GE) surgery. METHODS: A total of 334 patients receiving anticoagulants and undergoing elective GE surgery between 2012 and 2018 w...

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Detalles Bibliográficos
Autores principales: Fujikawa, Takahisa, Takahashi, Ryo, Naito, Shigetoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240147/
https://www.ncbi.nlm.nih.gov/pubmed/32490344
http://dx.doi.org/10.1002/ags3.12328
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author Fujikawa, Takahisa
Takahashi, Ryo
Naito, Shigetoshi
author_facet Fujikawa, Takahisa
Takahashi, Ryo
Naito, Shigetoshi
author_sort Fujikawa, Takahisa
collection PubMed
description AIM: We investigated the effect of perioperative management of direct oral anticoagulants (DOACs) on bleeding and thromboembolic complications during gastroenterological (GE) surgery. METHODS: A total of 334 patients receiving anticoagulants and undergoing elective GE surgery between 2012 and 2018 were enrolled. The patients were divided into three groups: patients receiving warfarin (WF, n = 231), patients receiving DOACs with heparin bridging (DOAC‐HB, n = 34), and patients receiving DOAC without heparin bridging (DOAC‐NHB, n = 69). Outcome variables were compared between the groups and the risk factors of postoperative bleeding were assessed using logistic multivariate analysis. RESULTS: No significant differences were observed in background characteristics between the groups. There were similarities between the groups in surgical blood loss (P = .772) and rate of intraoperative transfusion (P = .952). Thromboembolic complications only occurred in two patients in the WF group (0.9%), and no thromboembolism occurred in the DOAC groups. The incidence of major postoperative bleeding was significantly higher in DOAC‐HB group than in the other groups (14.7% vs 4.8% vs 1.4%, P = .011). Multivariate analysis showed DOAC with heparin bridging to be the most significant risk factor of major postoperative bleeding (odds ratio = 11.60, P = .028). CONCLUSIONS: Elective GE surgery can be safely performed in patients receiving DOACs without heparin bridging. Perioperative heparin bridging during DOAC interruption is not recommended even for patients undergoing major GE surgery due to increased postoperative bleeding.
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spelling pubmed-72401472020-06-01 Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery Fujikawa, Takahisa Takahashi, Ryo Naito, Shigetoshi Ann Gastroenterol Surg Original Articles AIM: We investigated the effect of perioperative management of direct oral anticoagulants (DOACs) on bleeding and thromboembolic complications during gastroenterological (GE) surgery. METHODS: A total of 334 patients receiving anticoagulants and undergoing elective GE surgery between 2012 and 2018 were enrolled. The patients were divided into three groups: patients receiving warfarin (WF, n = 231), patients receiving DOACs with heparin bridging (DOAC‐HB, n = 34), and patients receiving DOAC without heparin bridging (DOAC‐NHB, n = 69). Outcome variables were compared between the groups and the risk factors of postoperative bleeding were assessed using logistic multivariate analysis. RESULTS: No significant differences were observed in background characteristics between the groups. There were similarities between the groups in surgical blood loss (P = .772) and rate of intraoperative transfusion (P = .952). Thromboembolic complications only occurred in two patients in the WF group (0.9%), and no thromboembolism occurred in the DOAC groups. The incidence of major postoperative bleeding was significantly higher in DOAC‐HB group than in the other groups (14.7% vs 4.8% vs 1.4%, P = .011). Multivariate analysis showed DOAC with heparin bridging to be the most significant risk factor of major postoperative bleeding (odds ratio = 11.60, P = .028). CONCLUSIONS: Elective GE surgery can be safely performed in patients receiving DOACs without heparin bridging. Perioperative heparin bridging during DOAC interruption is not recommended even for patients undergoing major GE surgery due to increased postoperative bleeding. John Wiley and Sons Inc. 2020-04-01 /pmc/articles/PMC7240147/ /pubmed/32490344 http://dx.doi.org/10.1002/ags3.12328 Text en © 2020 The Authors. Annals of Gastroenterological Surgery published by John Wiley & Sons Australia, Ltd on behalf of The Japanese Society of Gastroenterological Surgery This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Fujikawa, Takahisa
Takahashi, Ryo
Naito, Shigetoshi
Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery
title Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery
title_full Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery
title_fullStr Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery
title_full_unstemmed Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery
title_short Perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery
title_sort perioperative antithrombotic management of patients who receive direct oral anticoagulants during gastroenterological surgery
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7240147/
https://www.ncbi.nlm.nih.gov/pubmed/32490344
http://dx.doi.org/10.1002/ags3.12328
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