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用于缓解食管癌或贲门癌吞咽困难的新型设计食管支架:一项随机试验。

New design esophageal stents for the palliation of dysphagia from esophageal or gastric cardia cancer: a randomized trial.

作者信息

Verschuur Els M L, Repici Alessandro, Kuipers Ernst J, Steyerberg Ewout W, Siersema Peter D

机构信息

Department of Gastroenterology & Hepatology, Erasmus MC University Medical Center Rotterdam, Rotterdam, The Netherlands.

出版信息

Am J Gastroenterol. 2008 Feb;103(2):304-12. doi: 10.1111/j.1572-0241.2007.01542.x. Epub 2007 Sep 25.

Abstract

BACKGROUND & AIM: Stents are often used for the palliation of inoperable esophageal or gastric cardia cancer. One of the drawbacks of the currently used stents is the high percentage of recurrent dysphagia due to stent migration and tissue growth. New stents have been designed to overcome this unwanted sequela of stent placement. In the present study, we investigated whether results of stent placement could be improved with newer stent designs.

METHODS

Between June 2004 and May 2006, 125 patients with dysphagia from inoperable carcinoma of the esophagus or gastric cardia were randomized to placement of an Ultraflex stent (N = 42), Polyflex stent (N = 41), or Niti-S stent (N = 42). Patients were followed by scheduled telephone calls at 14 days after treatment, and then monthly for 6 months or until death. Technical and functional outcome, complications, recurrent dysphagia, and survival were analyzed with, chi(2) tests, Kaplan-Meier curves, and log-rank tests.

RESULTS

Stent placement was technically successful in all patients with an Ultraflex stent, in 34/41 (83%) patients with a Polyflex stent, and in 40/42 (95%) patients treated with a Niti-S stent (P= 0.008). Dysphagia score improved from a median of 3 (liquids only) to 1 (ability to eat some solid food) in all patients. There were no differences in complications among the three stent types. Recurrent dysphagia, caused by tissue in- or overgrowth, migration, or food obstruction, was significantly different between patients with an Ultraflex stent and patients with a Polyflex stent or Niti-S stent (22 [52%]vs 15 [37%]vs 13 [31%], P= 0.03). Stent migration occurred more frequently with Polyflex stents, whereas tissue in- or overgrowth was more frequently seen with Ultraflex stents, and to a lesser degree, Niti-S stents. No differences were found in survival (median survival: Ultraflex stent 132 days vs Polyflex stent 102 days vs Niti-S stent 159 days) among the three stent types.

CONCLUSIONS

All three stents are safe and offer adequate palliation of dysphagia from esophageal or gastric cardia cancer. Nonetheless, Polyflex stents seem the least preferable in this patient group, as placement of this device is technically demanding and associated with a high rate of stent migrations.

摘要

背景与目的

支架常用于无法手术切除的食管癌或贲门癌的姑息治疗。当前使用的支架的缺点之一是由于支架移位和组织生长导致吞咽困难复发的比例较高。已设计出新的支架以克服支架置入这一不良后遗症。在本研究中,我们调查了采用更新的支架设计是否能改善支架置入的效果。

方法

2004年6月至2006年5月期间,125例因无法手术切除的食管癌或贲门癌导致吞咽困难的患者被随机分为置入Ultraflex支架组(N = 42)、Polyflex支架组(N = 41)或Niti - S支架组(N = 42)。在治疗后14天通过定期电话随访患者,然后每月随访6个月或直至死亡。采用卡方检验、Kaplan - Meier曲线和对数秩检验分析技术和功能结局、并发症、吞咽困难复发情况及生存率。

结果

所有置入Ultraflex支架的患者支架置入技术均成功,置入Polyflex支架的患者中有34/41(83%)成功,置入Niti - S支架组的患者中有40/42(95%)成功(P = 0.008)。所有患者的吞咽困难评分从中位数3(仅能吞咽液体)改善至1(能吃一些固体食物)。三种支架类型的并发症无差异。由组织内生或过度生长、移位或食物阻塞引起的吞咽困难复发在置入Ultraflex支架的患者与置入Polyflex支架或Niti - S支架的患者之间有显著差异(22 [52%]对15 [37%]对13 [31%],P = 0.03)。Polyflex支架的移位更频繁,而Ultraflex支架的组织内生或过度生长更常见,Niti - S支架的组织内生或过度生长程度较轻。三种支架类型的生存率无差异(中位生存期:Ultraflex支架132天对Polyflex支架102天对Niti - S支架159天)。

结论

所有三种支架都是安全的,并且能为食管癌或贲门癌导致的吞咽困难提供充分的姑息治疗。尽管如此,在该患者群体中Polyflex支架似乎是最不理想的,因为该装置的置入技术要求高且与较高的支架移位率相关。

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