一种新型透视模式在介入内镜超声(带视频)中提高可视性的临床评价。

IF 3.4 3区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY
Therapeutic Advances in Gastroenterology Pub Date : 2025-06-27 eCollection Date: 2025-01-01 DOI:10.1177/17562848251349595
Naoto Aoyama, Takeshi Ogura, Saori Ueno, Atsushi Okuda, Nobu Nishioka, Jun Sakamoto, Yuki Uba, Mitsuki Tomita, Nobuhiro Hattori, Junichi Nakamura, Kimi Bessho, Takafumi Kanadani, Hiroki Nishikawa
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引用次数: 0

摘要

背景:介入内镜超声(I-EUS),包括eus引导的胆道引流,目前已被广泛应用,但如果设备的可视性不足,则变得具有挑战性。一种新的可见度增强模式,称为“口音模式”,最近可用于透视系统。目的:比较I-EUS中Accent模式与Original模式各设备及胰胆管的可见性。设计:单中心非随机评价研究。方法:前瞻性纳入在Accent模式下行I-EUS的患者。所有评价均使用录制的程序录像进行。可见度评分分为五项,由三名专家和七名学员进行评估。结果:共纳入20例(Accent组)和24例(Original组)患者。Accent组的平均导丝可视性评分(专家和实习观察员分别为4.95和4.95)显著高于Original组(分别为2.53和2.32);p p p p = 0.0012)。结论:综上所述,重音模式减少了I-EUS手术时间。有必要在前瞻性、随机对照试验中证实这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical evaluation of a novel fluoroscopic mode for improving visibility during interventional endoscopic ultrasound (with video).

Clinical evaluation of a novel fluoroscopic mode for improving visibility during interventional endoscopic ultrasound (with video).

Clinical evaluation of a novel fluoroscopic mode for improving visibility during interventional endoscopic ultrasound (with video).

Clinical evaluation of a novel fluoroscopic mode for improving visibility during interventional endoscopic ultrasound (with video).

Background: Interventional endoscopic ultrasound (I-EUS), including EUS-guided biliary drainage, is now widely performed, but it becomes challenging if the visibility of devices is inadequate. A novel visibility enhancement mode, termed "Accent mode," has recently become available for use with a fluoroscopic system.

Objective: To compare the visibility of each device and pancreato-biliary ducts between Accent mode and Original mode during I-EUS.

Design: A single-center non-randomized evaluation study.

Methods: Patients who underwent I-EUS under Accent mode were prospectively enrolled. All evaluations were performed using recorded procedural videos. The visibility score was graded on a five-item scale, with evaluations performed by three experts and seven trainees.

Results: Twenty patients (Accent group) and 24 patients (Original group) were enrolled. Mean guidewire visibility scores were significantly higher in the Accent group (4.95 and 4.95 in the expert and trainee observers, respectively) than in the Original group (2.53 and 2.32, respectively; p < 0.001). For the dilation device, visibility scores were significantly higher in the Accent group (4.47 and 4.58 in the expert and trainee observers, respectively) than in the Original group (2.68 and 2.53, respectively; p < 0.001). Stent visibility scores were significantly higher in the Accent group (4.16 and 4.32 in the expert and trainee observers, respectively) than in the Original group (2.89 and 2.68, respectively; p < 0.001). Procedure time was significantly shorter in the Accent group than in the Original group (10.3 vs 17.2 min, p = 0.0012).

Conclusion: In conclusion, Accent mode appears to reduce I-EUS procedure time. It is necessary to confirm these findings in a prospective, randomized, controlled trial.

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来源期刊
Therapeutic Advances in Gastroenterology
Therapeutic Advances in Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
6.70
自引率
2.40%
发文量
103
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Gastroenterology is an open access journal which delivers the highest quality peer-reviewed original research articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of gastrointestinal and hepatic disorders. The journal has a strong clinical and pharmacological focus and is aimed at an international audience of clinicians and researchers in gastroenterology and related disciplines, providing an online forum for rapid dissemination of recent research and perspectives in this area. The editors welcome original research articles across all areas of gastroenterology and hepatology. The journal publishes original research articles and review articles primarily. Original research manuscripts may include laboratory, animal or human/clinical studies – all phases. Letters to the Editor and Case Reports will also be considered.
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