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논문 기본 정보

자료유형
학술저널
저자정보
Nozomi Okuno (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Kazuo Hara (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Nobumasa Mizuno (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Shin Haba (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Takamichi Kuwahara (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Hiroki Koda (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Masahiro Tajika (Departments of Endoscopy Aichi Cancer Center Hospital Nagoya Japan) Tsutomu Tanaka (Departments of Endoscopy Aichi Cancer Center Hospital Nagoya Japan) Sachiyo Onishi (Departments of Endoscopy Aichi Cancer Center Hospital Nagoya Japan) Keisaku Yamada (Departments of Endoscopy Aichi Cancer Center Hospital Nagoya Japan) Akira Miyano (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Daiki Fumihara (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan) Moaz Elshair (Departments of Gastroenterology Aichi Cancer Center Hospital Nagoya Japan)
저널정보
대한소화기내시경학회 Clinical Endoscopy Clinical Endoscopy 제54권 제4호
발행연도
2021.1
수록면
596 - 602 (7page)

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Background/Aims: The Japan Gastroenterological Endoscopy Society (JGES) has published guidelines for gastroenterologicalendoscopy in patients undergoing antithrombotic treatment. These guidelines classify endoscopic ultrasound-guided biliary drainage(EUS-BD) as a high-risk procedure. Nevertheless, the bleeding risk of EUS-BD in patients undergoing antithrombotic therapy isuncertain. Therefore, this study aimed to assess the bleeding risk in patients undergoing antithrombotic therapy. Methods: This single-center retrospective study included 220 consecutive patients who underwent EUS-BD between January 2013and December 2018. We managed the withdrawal and continuation of antithrombotic agents according to the JGES guidelines. Wecompared the bleeding event rates among patients who received and those who did not receive antithrombotic agents. Results: A total of 18 patients (8.1 %) received antithrombotic agents and 202 patients (91.8 %) did not. Three patients experiencedbleeding events, with an overall bleeding event rate of 1.3% (3/220): one patient was in the antithrombotic group (5.5%) and twopatients were in the non-antithrombotic group (0.9%) (p=0.10). All cases were moderate. The sole thromboembolic event (0.4%) wasa cerebral infarction in a patient in the non-antithrombotic group. Conclusions: The rate of EUS-BD-related bleeding events was low. Even in patients receiving antithrombotic therapy, the bleedingevent rates were not significantly different from those in patients not receiving antithrombotic therapy.

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