Step-Up Strategy for Endoscopic Hemostasis Using PuraStat After Endoscopic Sphincterotomy Bleeding (STOP Trial)

IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY Techniques and Innovations in Gastrointestinal Endoscopy Pub Date : 2024-01-01 DOI:10.1016/j.tige.2024.03.005
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Abstract

Background and Aims

Recently, a novel self-assembling peptide hemostatic gel (PuraStat) has become available. Although PuraStat for endoscopic sphincterotomy (EST) bleeding has been evaluated and reported mainly in case reports and several retrospective studies, no prospective evaluation has been reported. The aim of the present study was to prospectively evaluate the safety and efficacy of PuraStat for persistent EST bleeding >120 seconds as a first-line endoscopic hemostasis technique.

Methods

This single-arm, prospective study was conducted between November 2022 and August 2023. As the primary technique for endoscopic hemostasis, PuraStat was applied first. If hemostasis failed, other techniques were used. The primary outcome of the present study was to evaluate the technical success rate of the application of PuraStat to the bleeding site. Clinical success was defined as the absence of oozing for 180 seconds after PuraStat application. Adverse events associated with procedures and secondary hemorrhage were secondary outcomes. PuraStat application was performed using the embankment method.

Results

During the study period, 1080 endoscopic retrograde cholangiopancreatography procedures were performed. A total of 108 patients experienced complications with EST bleeding. Among them, endoscopic hemostasis was required in 51 patients. These patients enrolled in this prospective study. All patients successfully underwent PuraStat application without PuraStat dislocation into the third part of the duodenum. The technical success rate of endoscopic hemostasis using PuraStat was 98% (50/51). As possible factors associated with secondary hemorrhage, biliary stents, including plastic or metal stents, were deployed in 60.7% (31/51). Finally, severe adverse events associated with the procedures were not observed in any patients, although mild acute pancreatitis was observed in 2 patients, and conservative treatment was successful.

Conclusion

In conclusion, PuraStat application may be safe for oozing after EST without increasing the frequency of acute pancreatitis.

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内镜括约肌切开术出血后使用 PuraStat 的内镜止血阶梯策略(STOP 试验)
背景和目的最近,一种新型自组装多肽止血凝胶(PuraStat)问世。虽然 PuraStat 用于内镜括约肌切开术(EST)出血的评估和报告主要见于病例报告和几项回顾性研究,但尚未见前瞻性评估报告。本研究旨在前瞻性地评估 PuraStat 作为一线内镜止血技术在治疗EST持续出血>120 秒的安全性和有效性。作为内镜止血的主要技术,首先应用 PuraStat。如果止血失败,则使用其他技术。本研究的主要结果是评估在出血部位应用 PuraStat 的技术成功率。临床成功的定义是使用 PuraStat 后 180 秒内无渗血。与手术相关的不良事件和继发性出血是次要结果。研究期间共进行了 1080 例内镜逆行胰胆管造影术。共有 108 名患者出现EST出血并发症。其中 51 例患者需要内镜止血。这些患者参加了这项前瞻性研究。所有患者都成功应用了 PuraStat,且 PuraStat 没有移位到十二指肠的第三部分。使用 PuraStat 进行内镜止血的技术成功率为 98%(50/51)。60.7%(31/51)的患者使用了胆道支架,包括塑料或金属支架,这可能是继发性出血的相关因素。最后,尽管有 2 名患者出现了轻微的急性胰腺炎,但没有发现任何与手术相关的严重不良事件,保守治疗也取得了成功。
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来源期刊
CiteScore
2.10
自引率
50.00%
发文量
60
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