Kurita Akira, Uza Norimitsu, Asada Masanori, Yoshimura Kenichi, Takemura Tadamasa, Yazumi Shujiro, Kodama Yuzo, Seno Hiroshi
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.
Surg Endosc. 2022 May;36(5):2869-2878. doi: 10.1007/s00464-021-08576-x. Epub 2021 Jun 2.
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.
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.
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.
Inside-stent therapy appears to be useful not only as an initial stent but also as a second stent for patients with inoperable MHBO.
UMIN000004587.
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。
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。
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。
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。
UMIN000004587。