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抗反流支架减少恶性胆道狭窄患者胆管炎风险的随机试验。

Antireflux stents to reduce the risk of cholangitis in patients with malignant biliary strictures: a randomized trial.

机构信息

Department of Endoscopy, Eastern Hepatobiliary Hospital, Second Military Medical University, Shanghai, China.

出版信息

Endoscopy. 2014 Feb;46(2):120-6. doi: 10.1055/s-0034-1364872. Epub 2014 Jan 29.

Abstract

BACKGROUND AND STUDY AIMS

There are limited data on the role of antireflux biliary stents. This single-center randomized trial compared the endoscopic use of partly covered antireflux metal stents (pcARMS) with that of standard uncovered self-expandable metal stents (ucSEMS) for the palliation of nonhilar malignant biliary obstruction.

PATIENTS AND METHODS

Between August 2007 and February 2012, patients with nonhilar malignant biliary obstruction were randomly assigned to treatment with either pcARMS or ucSEMS. Subsequent follow-up was conducted in clinic or by phone. The primary outcome was onset of cholangitis within 12 months of stenting. Secondary outcomes included other morbidities, stent dysfunctions, and survival.

RESULTS

Altogether 112 patients were included, 56 in each group. The stents were successfully deployed in all patients. Satisfactory jaundice control was achieved in 49 cases in the pcARMS group, compared with 47 in the ucSEMS group (P = 0.135). Fewer patients experienced cholangitis in the pcARMS group than in the ucSEMS group (10 vs. 21 patients; P = 0.035), and the frequency of episodes was less (P = 0.022). Respectively, 17 and 29 stent dysfunctions before death were observed in the pcARMS and ucSEMS groups (P = 0.051) and the median stent patency was 13.0 (standard deviation [SD] 3.4) and 10.0 (1.2) months, respectively (P = 0.044). At final follow-up, in January 2013, 50 /52 and 52 /55 patients had died and no difference in median survival was seen between the two groups (8.0 vs. 9.0 months, P = 0.56).

CONCLUSIONS

Stenting with pcARMS compared with standard ucSEMS reduces risk of ascending cholangitis and has longer stent patency, but does not increase patient survival. Chictr.org. number, ChiCTR-TRC-11001800.

摘要

背景与研究目的

关于抗反流胆道支架的作用,目前的数据有限。本单中心随机试验比较了内镜使用部分覆膜抗反流金属支架(pcARMS)与标准 uncovered 自膨式金属支架(ucSEMS)治疗非肝门恶性胆道梗阻的效果。

患者与方法

2007 年 8 月至 2012 年 2 月,将非肝门恶性胆道梗阻患者随机分配至 pcARMS 或 ucSEMS 治疗组。随后在门诊或通过电话进行随访。主要结局为支架置入后 12 个月内胆管炎的发生。次要结局包括其他并发症、支架功能障碍和生存情况。

结果

共纳入 112 例患者,每组 56 例。所有患者均成功植入支架。pcARMS 组 49 例患者黄疸控制满意,ucSEMS 组 47 例(P=0.135)。pcARMS 组发生胆管炎的患者少于 ucSEMS 组(10 例比 21 例;P=0.035),且发作频率较低(P=0.022)。分别有 17 例和 29 例 pcARMS 组和 ucSEMS 组在死亡前出现支架功能障碍(P=0.051),支架中位通畅时间分别为 13.0(标准差 3.4)和 10.0(1.2)个月(P=0.044)。在 2013 年 1 月的最终随访中,50/52 例和 52/55 例患者死亡,两组中位生存时间无差异(8.0 个月比 9.0 个月,P=0.56)。

结论

与标准 ucSEMS 相比,pcARMS 支架置入可降低上行性胆管炎的风险,且支架通畅时间更长,但不能提高患者生存率。ChiCTR-TRC-11001800。

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