Recombinant Tissue Plasminogen Activator: The New Concept for Dissolving Septae in Loculated Peri-pancreatic Fluid Collection prior to Endoscopic Drainage. A Case Report

IF 2.1 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of Gastrointestinal and Liver Diseases Pub Date : 2023-12-22 DOI:10.15403/jgld-4798
Cătălina Vlăduț, Mădălina Stan-Ilie, Adrian Săftoiu, R. Tutuian, Gabriel Constantinescu
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Abstract

Peri-pancreatic fluid collections are late complications of acute pancreatitis. Loculated peri-pancreatic fluid collections, even rare, remain the „black sheep” in terms of drainage, due to difficulty to puncture all compartments, thus prohibiting proper drainage of all compartments. Recombined tissue plasminogen activator (r-tPA) has been advocated as treatment of the loculated collections, due to its ability to dissolve the fibrinous strands and thus facilitate proper drainage. We report the case of a 58 years-old male presenting with a painful loculated peri-pancreatic fluid collection secondary to acute pancreatitis. We performed Alteplase injection, followed by successful endosonographic drainage with lumen apposing metal stent of the collection after 48 hours. Our observation suggests that r-tPA could be a new strategy for loculated collections management, ensuring better drainage and limiting the indication for surgical treatment.
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重组组织蛋白酶原激活剂:内镜引流前溶解定位胰周积液隔膜的新概念。病例报告
胰周积液是急性胰腺炎的晚期并发症。定位性胰周积液即使非常罕见,但仍是引流方面的 "害群之马",原因是难以穿刺所有腔室,因此无法对所有腔室进行适当引流。重组组织纤溶酶原激活剂(r-tPA)能够溶解纤维蛋白股,从而促进适当的引流,因此一直被提倡用于治疗定位性积液。我们报告了一例 58 岁男性的病例,他因急性胰腺炎继发胰周定位性积液,疼痛难忍。我们为患者注射了阿替普酶,48 小时后成功地用腔内金属支架引流了积液。我们的观察结果表明,r-tPA 可以作为处理定位性积液的一种新策略,确保更好的引流并限制手术治疗的适应症。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
61
审稿时长
6-12 weeks
期刊介绍: The Journal of Gastrointestinal and Liver Diseases (formerly Romanian Journal of Gastroenterology) publishes papers reporting original clinical and scientific research, which are of a high standard and which contribute to the advancement of knowledge in the field of gastroenterology and hepatology. The field comprises prevention, diagnosis and management of gastrointestinal and hepatobiliary disorders, as well as related molecular genetics, pathophysiology, and epidemiology. The journal also publishes reviews, editorials and short communications on those specific topics. Case reports will be accepted if of great interest and well investigated.
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