Choi Jin Ho, Cho In Rae, Lee Sang Hyub, Kim Joo Seong, Park Namyoung, Lee Min Woo, Jang Dong Kee, Paik Woo Hyun, Ahn Dong Won, Ryu Ji Kon, Kim Yong-Tae, Kim Eunji, Lee Jaeyoung
Department of Internal Medicine, Liver Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea.
Department of Internal Medicine, Liver Research Institute, Seoul National University Hospital, Seoul National University College of Medicine, 101 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea.
Dig Liver Dis. 2023 Apr;55(4):527-533. doi: 10.1016/j.dld.2023.01.157. Epub 2023 Feb 1.
Endoscopists often experience obstacles with traditional hemostasis using the side-viewing duodenoscope for bleeding after endoscopic sphincterotomy (EST) or endoscopic papillectomy (EP).
In this randomized controlled trial, we evaluated the efficacy and safety of a novel hemostatic gel for post-EST or post-EP bleeding.
A randomized trial was conducted from November 2020 to December 2021 at two tertiary centers in South Korea. Patients who experienced bleeding immediately after EST or EP were enrolled in the study, and primary hemostasis was achieved with either the novel hemostatic gel or epinephrine spray.
A total of 84 patients were enrolled in this study, and 41 patients were finally analyzed in each group. Hemostatic gel was significantly superior to epinephrine spray for successful primary hemostasis (100% vs. 85.4%; P = 0.026). ). In terms of delayed bleeding, no significant difference was observed between the hemostatic gel and epinephrine spray (2.4% vs. 7.3%; P = 0.329). The mean procedural time was significantly higher for the hemostatic gel than epinephrine spray (3.23 ± 1.94 vs. 1.76 ± 0.99 min; P < 0.001), and no differences were observed in the adverse events.
The novel hemostatic gel is expected to achieve satisfactory results with easier hemostasis for immediate bleeding after EST or EP. (Registered in Clinical Research Information Service: KCT0005607).
内镜医师在使用侧视十二指肠镜对内镜括约肌切开术(EST)或内镜乳头切除术(EP)后出血进行传统止血时常常遇到障碍。
在这项随机对照试验中,我们评估了一种新型止血凝胶用于EST或EP后出血的有效性和安全性。
2020年11月至2021年12月在韩国的两个三级中心进行了一项随机试验。纳入EST或EP后立即出血的患者,使用新型止血凝胶或肾上腺素喷雾实现初步止血。
本研究共纳入84例患者,每组最终分析41例患者。在成功实现初步止血方面,止血凝胶显著优于肾上腺素喷雾(100%对85.4%;P = 0.026)。在延迟出血方面,止血凝胶与肾上腺素喷雾之间未观察到显著差异(2.4%对7.3%;P = 0.329)。止血凝胶的平均操作时间显著长于肾上腺素喷雾(3.23±1.94对1.76±0.99分钟;P < 0.001),且在不良事件方面未观察到差异。
新型止血凝胶有望在EST或EP后立即出血的止血过程中更轻松地取得满意效果。(在临床研究信息服务中心注册:KCT0005607)