Outcomes of iodine-125 seed strips combined with double self-expandable metallic stent for Bismuth type III and IV malignant biliary obstruction.

IF 1.7 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Chuan-Guo Zhou, Yong Zhang, Hui Li, Ke-Yun Liu, Xiang-Yu Yang, Kun Gao
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Abstract

Background: No reports have been published on the use of iodine-125 (125I) seed strips combined with double biliary self-expandable metallic stent (SEMS) for the treatment of type III and IV hilar malignant biliary obstruction (MBO).

Aim: To evaluate effectiveness and safety of 125I seed trips combined with double SEMS in treating Bismuth type III and IV hilar MBO.

Methods: This was a retrospective, observational study conducted from April 2017 to December 2022. Patients with Bismuth-Corlette type III and IV hilar MBO who underwent 125I seed strip implantation combined with double SEMS placement were analyzed. Patient demographics, clinical characteristics, SEMS implantation methods, procedural and clinical outcomes, overall survival, stent patency duration, and complications were evaluated.

Results: Four types of stent implantation were utilized: (1) Type X; (2) Type T; (3) Type Y; and (4) Tandem type. The technical success rate was 94.1% (16/17), and the clinical success rate was 100% (17/17). The median overall survival time was 189.00 days ± 47.27 days (95%CI: 96.35-281.66). The median stent fluency time was 154.00 days ± 12.19 days (95%CI: 130.11-177.89). No serious complications were observed.

Conclusion: This retrospective, observational study suggests that the combination of 125I seed strips with double SEMS may be a safe and potentially effective approach for managing type III and IV hilar MBO patients.

125碘粒子条联合双自膨胀金属支架治疗铋III型和IV型恶性胆道梗阻的疗效。
背景:碘-125 (125I)粒子条联合双胆道自膨胀金属支架(SEMS)治疗III型和IV型肝门恶性胆道梗阻(MBO)的报道尚未发表。目的:评价125I种子脱粒联合双SEMS治疗铋型、IV型肺源性MBO的有效性和安全性。方法:这是一项回顾性观察性研究,于2017年4月至2022年12月进行。对Bismuth-Corlette III型和IV型肝门部MBO患者行125I粒子条植入术联合双SEMS植入术进行分析。评估患者人口统计学、临床特征、SEMS植入方法、手术和临床结果、总生存期、支架通畅时间和并发症。结果:采用四种支架植入术:(1)X型;(2) T型;(3) Y型;(4)串联式。技术成功率为94.1%(16/17),临床成功率为100%(17/17)。中位总生存时间为189.00天±47.27天(95%CI: 96.35 ~ 281.66)。中位支架通畅时间为154.00天±12.19天(95%CI: 130.11-177.89)。无严重并发症。结论:这项回顾性观察性研究表明,125I种子条联合双SEMS可能是治疗III型和IV型肝门部MBO患者的一种安全且潜在有效的方法。
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