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新型可取出的全内置式自膨式金属食管支架:人体中的可行性、取出技术及组织反应

Novel removable internally fully covered self-expanding metal esophageal stent: feasibility, technique of removal, and tissue response in humans.

作者信息

Eloubeidi Mohamad A, Lopes Tercio L

机构信息

Department of Gastroenterology and Hepatology, the University of Alabama in Birmingham, 1530 3rd Ave. S., Birmingham, AL 35294-0007, USA.

出版信息

Am J Gastroenterol. 2009 Jun;104(6):1374-81. doi: 10.1038/ajg.2009.133. Epub 2009 Apr 28.

Abstract

OBJECTIVES

Internally fully covered self-expandable metal stents (FCSEMSs) have recently become available offering the possibility of removal. However, to our knowledge, the feasibility, techniques for endoscopic removal, and tissue reaction to FCSEMS have not been reported in humans. Our aims are (1) to report reasons for and success of FCSEMS removal in consecutive patients, (2) to describe methods of esophageal stent retrieval, and (3) to describe stent reactions induced by FCSEMS in humans.

METHODS

Removable FCSEMSs (ALIMAXX-E, Alveolus Inc., Charlotte, NC) were placed in consecutive patients requiring palliation of dysphagia symptoms with locally advanced esophageal or gastro-esophageal junction cancers, refractory benign esophageal strictures, postoperative mediastinal leaks, or tracheoesophageal fistulas. Dysphagia scores were assessed at 1, 3, and 6 months. Esophagogram and endoscopy follow-up were performed routinely at 1 month or to assess new symptoms.

RESULTS

A total of 36 stents were placed in 31 patients over 16 months (mean age 62.8 years, 61% white, 58% male). Indications included the following: malignant strictures (n=17), refractory benign strictures (n=7), tracheoesophageal fistulas (n=8), postoperative mediastinal leaks (n=2), and iatrogenic perforations (n=2). Dysphagia scores improved (decreased) significantly at 1 (mean difference 2.09; 95% confidence interval (CI) 1.65-2.52, P=0.0001), 3 (mean difference 2.1; 95% CI 1.57-2.62, P=0.0001), and 6 months (mean difference of 2; 95% CI 1.28-2.73, P<0.0001). Clinical success rates for various indications were: malignant strictures 88%, refractory benign strictures 29%, tracheoesophageal fistula 88%, postoperative mediastinal leaks 100%, and iatrogenic perforations 50%. Sixty one percent (n=22) of the stents were removed (removal was successful in 100% of cases attempted). Twenty three percent (n=5 stents in four patients) were removed due to chest pain or abdominal pain. The stents satisfied their purposes in all of these four patients. The remainder were removed on schedule or had satisfied their purpose and/or migrated. Fifty percent of removed stents had ulcers (median size=2 cm) at the distal edge of the stent, whereas 23% had ulcers at the proximal edge of the stent. Pseudo-polyps formed at either the proximal or distal edge of the stent in four patients. Tissue reaction was severe in only two patients. Stents were embedded in four cases but were easily lifted from tissue. Our preferred method of retrieval was the double-channel therapeutic endoscope with two rat-tooth forceps or rat-tooth forceps with a snare.

CONCLUSIONS

FCSEMSs palliate dysphagia from both benign and malignant conditions and seal postoperative tracheoesophageal fistulas and mediastinal leaks. Tissue reaction to the stents was common but remained clinically insignificant in the majority of patients. Close follow-up of patients with FCSEMS is required and repeat endoscopy with stent retrieval might be necessary with the development of new symptoms or complications from the stent.

摘要

目的

内部完全覆盖的自膨式金属支架(FCSEMS)最近已上市,提供了可取出的可能性。然而,据我们所知,FCSEMS在人体中的取出可行性、内镜取出技术以及组织反应尚未见报道。我们的目的是:(1)报告连续患者中FCSEMS取出的原因及成功率;(2)描述食管支架取出的方法;(3)描述FCSEMS在人体中引起的支架反应。

方法

将可取出的FCSEMS(ALIMAXX-E,Alveolus公司,北卡罗来纳州夏洛特)置入连续的患者体内,这些患者因局部晚期食管癌或胃食管交界癌、难治性良性食管狭窄、术后纵隔瘘或气管食管瘘导致吞咽困难症状需要缓解。在1、3和6个月时评估吞咽困难评分。在1个月时常规进行食管造影和内镜随访,或评估新出现的症状。

结果

在16个月内,共31例患者置入了36枚支架(平均年龄62.8岁,61%为白人,58%为男性)。适应证包括:恶性狭窄(n = 17)、难治性良性狭窄(n = 7)、气管食管瘘(n = 8)、术后纵隔瘘(n = 2)和医源性穿孔(n = 2)。吞咽困难评分在1个月(平均差值2.09;95%置信区间(CI)1.65 - 2.52,P = 0.0001)、3个月(平均差值2.1;95% CI 1.57 - 2.62,P = 0.0001)和6个月(平均差值2;95% CI 1.28 - 2.73,P < 0.0001)时显著改善(降低)。各种适应证的临床成功率为:恶性狭窄88%,难治性良性狭窄29%,气管食管瘘88%,术后纵隔瘘100%,医源性穿孔50%。61%(n = 22)的支架被取出(所有尝试取出的病例均成功)。23%(4例患者中的5枚支架)因胸痛或腹痛被取出。这4例患者中,支架均达到了预期目的。其余的支架按计划取出,或已达到预期目的和/或发生移位。50%的取出支架在支架远端边缘有溃疡(中位大小 = 2 cm),而23%在支架近端边缘有溃疡。4例患者在支架近端或远端边缘形成假息肉。仅2例患者组织反应严重。4例支架嵌入组织,但很容易从组织中提起。我们首选的取出方法是使用双通道治疗内镜,配备两把鼠齿钳或带圈套器的鼠齿钳。

结论

FCSEMS可缓解良性和恶性疾病引起的吞咽困难,并封闭术后气管食管瘘和纵隔瘘。支架的组织反应很常见,但在大多数患者中临床意义不大。需要对FCSEMS患者进行密切随访,随着新症状或支架并发症的出现,可能需要重复内镜检查并取出支架。

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