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金属支架置入术治疗大肠梗阻的疗效

The efficacy of metallic stent placement in the treatment of colorectal obstruction.

作者信息

Kang Sung Gwon, Jung Gyu Sik, Cho Soon Gu, Kim Jae Gyu, Oh Joo Hyung, Song Ho Young, Kim Eun Sang

机构信息

Department of Diagnostic Radiology, Chosun University Medical College, Gwangju, South Korea.

出版信息

Korean J Radiol. 2002 Apr-Jun;3(2):79-86. doi: 10.3348/kjr.2002.3.2.79.

Abstract

OBJECTIVE

To evaluate the efficacy of newly designed covered and non-covered coated colorectal stents for colonic decompression.

MATERIALS AND METHODS

Twenty-six patients, (15 palliative cases and 11 preoperative) underwent treatment for the relief of colorectal obstruction using metallic stents positioned under fluoroscopic guidance. In 24 of the 26, primary colorectal carcinoma was diagnosed, and in the remaining two, recurrent colorectal carcinoma. Twenty-one patients were randomly selected to receive either a type A or type B stent; for the remaining five, type C was used. Type A, an uncovered nitinol wire stent, was lightly coated to ensure structural integrity. Type B (flare type) and C (shoulder type) stents were polyurethane covered and their diameter was 24 and 26 mm, respectively. The rates of technical success, clinical success, and complications were analyzed using the chi-square test, and to analyse the mean period of patency, the Kaplan-Meier method was used.

RESULTS

Thirty of 31 attempted placements in 26 patients were successful, with a technical success rate of 96.8% (30/31) and a clinical success rate of 80.0% (24/30). After clinically successful stent placement, bowel decompression occurred within 1-4 (mean, 1.58+/-0.9) days. Five of six clinical failures involved stent migration and one stent did not expand after successful placement. In the preoperative group, 11 stents, one of which migrated, were placed in ten patients, in all of whom bowel preparation was successful. In the palliative group, 19 stents were placed in 15 patients. The mean period of patency was 96.25+/-105.12 days: 146.25+/-112.93 for type-A, 78.82+/-112.26 for type-B, and 94.25+/-84.21 for type-C. Complications associated with this procedure were migration (n=6, 20%), pain (n=4, 13.3%), minor bleeding (n=5, 16.7%), incomplete expansion (n=1, 3.3%), and tumor ingrowth (n=1, 3.3%). The migration rate was significantly higher in the type-B group than in other groups (p=0.038).

CONCLUSION

Newly designed covered and non-covered metallic stents of a larger diameter are effective for the treatment of colorectal obstruction. The migration rate of covered stents with flaring is higher than that of other types. For evaluation of the ideal stent configuration for the relief of colorectal obstruction, a clinical study involving a larger patient group is warranted.

摘要

目的

评估新设计的有覆膜和无覆膜的结肠直肠支架用于结肠减压的疗效。

材料与方法

26例患者(15例姑息治疗病例和11例术前病例)在透视引导下使用金属支架进行治疗以缓解结直肠梗阻。26例中的24例被诊断为原发性结直肠癌,其余2例为复发性结直肠癌。随机选择21例患者接受A型或B型支架;其余5例使用C型支架。A型为无覆膜镍钛合金丝支架,轻度涂层以确保结构完整性。B型(喇叭口型)和C型(肩部型)支架为聚氨酯覆膜,其直径分别为24mm和26mm。使用卡方检验分析技术成功率、临床成功率和并发症发生率,并使用Kaplan-Meier方法分析平均通畅期。

结果

26例患者31次置入尝试中有30次成功,技术成功率为96.8%(30/31),临床成功率为80.0%(24/30)。临床成功置入支架后,肠减压在1 - 4天内(平均1.58±0.9天)出现。6例临床失败中有5例涉及支架移位,1例支架成功置入后未扩张。术前组中,10例患者置入11个支架,其中1个移位,所有患者肠道准备均成功。姑息治疗组中,15例患者置入19个支架。平均通畅期为96.25±105.12天:A型为146.25±112.93天,B型为78.82±112.26天,C型为94.25±84.21天。该操作相关的并发症有移位(n = 6,20%)、疼痛(n = 4,13.3%)、少量出血(n = 5,16.7%)、扩张不完全(n = 1,3.3%)和肿瘤长入(n = 1,3.3%)。B型组的移位率显著高于其他组(p = 0.038)。

结论

新设计的大直径有覆膜和无覆膜金属支架对结直肠梗阻的治疗有效。喇叭口型覆膜支架的移位率高于其他类型。为评估缓解结直肠梗阻的理想支架构型,有必要开展一项纳入更大患者群体的临床研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4aac/2713840/96666233f247/kjr-3-79-g001.jpg

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