Published in:
Open Access
01-01-2018 | Original Article
Continued Use of a Single Antiplatelet Agent Does Not Increase the Risk of Delayed Bleeding After Colorectal Endoscopic Submucosal Dissection
Authors:
Jun Arimoto, Takuma Higurashi, Hideyuki Chiba, Noboru Misawa, Tsutomu Yoshihara, Takayuki Kato, Kenji Kanoshima, Akiko Fuyuki, Hidenori Ohkubo, Shungo Goto, Yuutaro Ishikawa, Jun Tachikawa, Keiichi Ashikari, Takashi Nonaka, Masataka Taguri, Hitoshi Kuriyama, Kazuhiro Atsukawa, Atsushi Nakajima
Published in:
Digestive Diseases and Sciences
|
Issue 1/2018
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Abstract
Background
With the aging of the population and rising incidence of thromboembolic events, the usage of antiplatelet agents is also increasing. There are few reports yet on the management of antiplatelet agents for patients undergoing colorectal endoscopic submucosal dissection (ESD).
Aims
The aim of this study is to evaluate whether continued administration of antiplatelet agents is associated with an increased rate of delayed bleeding after colorectal ESD.
Methods
A total of 1022 colorectal neoplasms in 927 patients were dissected at Yokohama City University Hospital and its three affiliate hospitals between July 2012 and June 2017. We included the data of 919 lesions in the final analysis. The lesions were divided into three groups: the no-antiplatelet group (783 neoplasms), the withdrawal group (110 neoplasms), and the continuation group (26 neoplasms).
Results
Among the 919 lesions, bleeding events occurred in a total of 31 (3.37%). The rate of bleeding after ESD was 3.3% (26/783), 4.5% (5/110), and 0% (0/26), respectively. There were no significant differences in the rate of bleeding after ESD among the three groups (the withdrawal group vs. the no-antiplatelet group, the continuation group vs. the no-antiplatelet group, and the withdrawal group vs. the continuation group).
Conclusions
Continued administration of antiplatelet agents is not associated with any increase in the risk of delayed bleeding after colorectal ESD. Prospective, randomized studies are necessary to determine whether treatment with antiplatelet agents must be interrupted prior to colorectal ESD in patients who are at a high risk of thromboembolic events.