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对于无法手术的恶性肝门部胆管梗阻患者,在Oddi括约肌上方放置支架是一种有效的选择。

Stent placement above the sphincter of Oddi is a useful option for patients with inoperable malignant hilar biliary obstruction.

作者信息

Kurita Akira, Uza Norimitsu, Asada Masanori, Yoshimura Kenichi, Takemura Tadamasa, Yazumi Shujiro, Kodama Yuzo, Seno Hiroshi

机构信息

Department of Gastroenterology and Hepatology, Kitano Hospital, Tazuke Kofukai Medical Research Institute, 2-4-20 Ohgimachi, Kita-ku, Osaka, 530-8480, Japan.

Department of Gastroenterology and Hepatology, Kyoto University Graduate School of Medicine, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto, 606-8507, Japan.

出版信息

Surg Endosc. 2022 May;36(5):2869-2878. doi: 10.1007/s00464-021-08576-x. Epub 2021 Jun 2.

Abstract

BACKGROUND AND AIMS

Endoscopic biliary drainage (EBD) is essential for the management of malignant hilar biliary obstruction (MHBO). We prospectively evaluated the efficacy and safety of "inside-stent" therapy, where a plastic stent is placed above the sphincter of Oddi without endoscopic sphincterotomy, in patients with inoperable MHBO.

METHODS

This study was a multicenter, single-blinded, randomized controlled trial at three centers. Patients with inoperable MHBO were enrolled in this study, and randomly assigned to receive an inside-stent or conventional-stent therapy. The primary endpoint was cumulative stent patency of the initial stent. The secondary endpoints were second stent patency, technical and clinical success rate, adverse events, re-intervention rate, and overall patient survival.

RESULTS

Forty-three patients were randomly assigned to the inside-stent group (n = 21) or the conventional-stent group (n = 22). The median cumulative stent patency of the initial stent was 123 days in the inside-stent group and 51 days in the conventional-stent group (P = .031). For patients with the initial stent dysfunction in the conventional-stent group, the inside-stent was placed as a second stent, and its patency was significantly longer than that of the initial stent (P = .0001). The technical and clinical success rate, re-intervention rate, second stent patency, adverse events, and survival probability did not differ between the groups.

CONCLUSIONS

Inside-stent therapy appears to be useful not only as an initial stent but also as a second stent for patients with inoperable MHBO.

TRIAL REGISTRATION NUMBER

UMIN000004587.

摘要

背景与目的

内镜下胆道引流(EBD)对于恶性肝门部胆管梗阻(MHBO)的治疗至关重要。我们前瞻性评估了“内置支架”疗法的疗效和安全性,即在不进行内镜括约肌切开术的情况下,将塑料支架置于Oddi括约肌上方,用于治疗无法手术的MHBO患者。

方法

本研究是一项在三个中心进行的多中心、单盲、随机对照试验。纳入无法手术的MHBO患者,并随机分配接受内置支架或传统支架治疗。主要终点是初始支架的累积通畅时间。次要终点包括第二枚支架的通畅时间、技术和临床成功率、不良事件、再次干预率以及患者总体生存率。

结果

43例患者被随机分配至内置支架组(n = 21)或传统支架组(n = 22)。内置支架组初始支架的中位累积通畅时间为123天,传统支架组为51天(P = 0.031)。对于传统支架组中初始支架功能障碍的患者,置入内置支架作为第二枚支架,其通畅时间明显长于初始支架(P = 0.0001)。两组在技术和临床成功率、再次干预率、第二枚支架通畅时间、不良事件及生存概率方面无差异。

结论

对于无法手术的MHBO患者,内置支架疗法似乎不仅可作为初始支架,也可作为第二枚支架使用。

试验注册号

UMIN000004587。

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