术中胰漏可视化(ViP): SmartPAN的IDEAL I期首次人体单臂临床试验。

Thomas M Pausch, Magdalena Holze, Josefin El-Mahdy, Bodil Gesslein, Helena Ossmer Thedius, Anja Sander, Solveig Tenckhoff, Tom Sundermann, Jan Larmann, Pascal Probst, Frank Pianka, Rosa Klotz, Thilo Hackert
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引用次数: 0

摘要

背景:部分切除胰腺的不可见液体泄漏与术后胰瘘(POPF)等并发症相关,需要可视化术中泄漏的策略。这项单臂、单中心试验旨在评估SmartPAN的有效性和安全性,SmartPAN是一种水凝胶,通过改变颜色与碱性胰腺液发生反应,从而使外科医生能够立即采取措施关闭泄漏。方法:招募因任何指征等待部分胰腺切除术的患者接受术中SmartPAN应用。根据每次手术后外科医生完成的报告、体液中不可生物降解化合物的实验室测量以及30天随访期间的临床评估,试验终点涵盖了SmartPAN的可用性和安全性。结果:共有42例患者被招募到试验中,29例患者根据方案应用SmartPAN进行了部分胰腺切除术。所有16名主治外科医生都认为SmartPAN易于学习和使用,大多数人都认为它很有用,他们打算经常使用它。没有与SmartPAN相关的不良反应或并发症,也没有在血液或腹腔液体中检测到其化合物。10/29例手术渗漏反应阳性。7例发生POPF,其中术中发现渗漏2例,有针对性封堵1例,未发现渗漏5例。结论:该研究代表了SmartPAN的首次人体临床试验,也是随机对照试验的先驱。结果支持SmartPAN的临床可用性和安全性,并展示了该设备在术中可视化POPF前体的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Visualization of Intraoperative Pancreatic Leakage (ViP): The IDEAL Stage I First-in-human, Single-arm Clinical Pilot Trial of SmartPAN.

Visualization of Intraoperative Pancreatic Leakage (ViP): The IDEAL Stage I First-in-human, Single-arm Clinical Pilot Trial of SmartPAN.

Visualization of Intraoperative Pancreatic Leakage (ViP): The IDEAL Stage I First-in-human, Single-arm Clinical Pilot Trial of SmartPAN.

Visualization of Intraoperative Pancreatic Leakage (ViP): The IDEAL Stage I First-in-human, Single-arm Clinical Pilot Trial of SmartPAN.

Background: The invisible fluid leaking from a partially resected pancreas is associated with complications including postoperative pancreatic fistula (POPF), calling for strategies to visualize intraoperative leakage. This single-arm, monocentric trial aims to evaluate the usefulness and safety of SmartPAN, a hydrogel that reacts to alkali pancreatic fluids by changing color and thus enables the surgeon to take immediate action to close leakage.

Methods: Patients awaiting partial pancreatic resection for any indication were recruited to receive intraoperative SmartPAN application. Trial endpoints covered SmartPAN usability and safety according to reports completed by surgeons after each operation, laboratory measurements of nonbiodegradable compounds in body fluids, and clinical evaluations over 30 days of follow-up.

Results: In total 42 patients were recruited to the trial and 29 received partial pancreatic resection with SmartPAN application according to protocol. All 16 attending surgeons rated SmartPAN as easy to learn and use, mostly agreeing that it was useful and that they intended to use it frequently. No adverse effects or complications were associated with SmartPAN, nor were its compounds detected in blood or abdominal fluids. Positive leakage response was detected in 10/29 surgeries. POPF developed in 7 patients, including 2 intraoperatively detected leakages, thereof 1 with targeted closure as well as 5 with no leakage detected.

Conclusion: This study represents the first-in-human clinical trial of SmartPAN and the precursor to randomized controlled trials. The outcomes support SmartPAN's clinical usability and safety and showcase the device's potential to intraoperatively visualize precursors of POPF.

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