Bohnacker S, Thonke F, Hinner M, Seitz U, Binmoeller K F, Brand B, Rathod V D, Soehendra N
Dept. of Endoscopic Surgery, University Hospital Eppendorf, Hamburg, Germany.
Endoscopy. 1998 Aug;30(6):524-31. doi: 10.1055/s-2007-1001338.
Endoscopic palliative treatment of malignant esophageal stenosis using conventional plastic stents has been reported to be associated with a considerable risk of perforation. Stenoses with a distance of less than 2cm from the upper esophageal sphincter (UES) have generally been excluded from treatment. Using self-expandable metal stents, procedure-related complications are rare. However, the rates of late complications necessitating retreatment appear to be as high as those of plastic stents. This study describes our stent placement technique and our results using a modified Tygon plastic stent.
Over a two-year period, 71 consecutive patients with incurable malignant esophageal stenosis were prospectively studied. Tygon plastic stents of diameter 9-14 mm were individually tailored according to length and location of the stenosis. Prior to stenting, stepwise bougienage was performed, if necessary over several sessions. After endoscopic placement of a guide wire, the stent was inserted over a bougie without fluoroscopic monitoring.
A total of 71 patients (54 men and 17 women, median age 69, range 34-93), were treated with Tygon plastic stents (14 mm: 19 patients; 12 mm: 50 patients; 9 mm: 2 patients). Median length of the strictures and of the stents were 7 (range 2-18) and 10 (range 6-25) cm, respectively. Four patients had an associated esophago-respiratory fistula. After a median of 2 (range 1-5) bougienage sessions, stent insertion was technically successful in all patients. Forty-one stents were placed across the cardia, 13 were positioned 0.5-1 cm below the UES. Three patients had to undergo retreatment within 24 hours because of pain or stent migration and the stents were repositioned or exchanged. No procedure-related perforation, hemorrhage or respiratory problems were observed. During a median follow-up of 63 (range 2-388) days, 82% of the patients died. Improvement or stabilization of dysphagia allowing for oral nutrition could be achieved in 89%. Dislocation occurred in eight patients, bolus obstruction in five patients and tumor overgrowth in four patients. Three of the four fistulas could be covered by the stent. In one patient with a fistula located at the level of the UES, a stent was placed but migrated after 5 days. Overall, 27 patients (38%) required reinterventions, mainly for dysphagia or nutritional problems.
In our experience, Tygon plastic stents with a diameter of 9-14 mm can be safely placed after stepwise, less extensive bougienage. Effective palliation is possible even for lesions located close to the UES. Perforation can be avoided. Reintervention rates seem to be comparable to those seen with self-expanding metal stents.
据报道,使用传统塑料支架对恶性食管狭窄进行内镜姑息治疗会有相当高的穿孔风险。距食管上括约肌(UES)小于2cm的狭窄通常被排除在治疗范围之外。使用自膨式金属支架时,与操作相关的并发症很少见。然而,需要再次治疗的晚期并发症发生率似乎与塑料支架一样高。本研究描述了我们使用改良泰贡塑料支架的支架置入技术及结果。
在两年期间,对71例连续的无法治愈的恶性食管狭窄患者进行了前瞻性研究。根据狭窄的长度和位置,分别定制直径为9 - 14mm的泰贡塑料支架。在置入支架前,必要时进行多次逐步探条扩张术。在内镜置入导丝后,在无荧光透视监测的情况下,将支架套在探条上插入。
共有71例患者(54例男性和17例女性,中位年龄69岁,范围34 - 93岁)接受了泰贡塑料支架治疗(14mm:19例患者;12mm:50例患者;9mm:2例患者)。狭窄和支架的中位长度分别为7(范围2 - 18)cm和10(范围6 - 25)cm。4例患者伴有食管 - 呼吸道瘘。经过中位2(范围1 - 5)次探条扩张术后,所有患者的支架置入在技术上均获成功。41个支架置于贲门处,13个位于UES下方0.5 - 1cm处。3例患者因疼痛或支架移位在24小时内必须接受再次治疗,支架被重新定位或更换。未观察到与操作相关的穿孔、出血或呼吸问题。在中位随访63(范围2 - 388)天期间,82%的患者死亡。89%的患者吞咽困难得到改善或稳定,可允许经口营养。8例患者出现支架移位,5例患者出现团块梗阻,4例患者出现肿瘤过度生长。4例瘘管中有3例可被支架覆盖。1例位于UES水平的瘘管患者置入了支架,但5天后支架移位。总体而言,27例患者(38%)需要再次干预,主要是因为吞咽困难或营养问题。
根据我们的经验,在进行逐步、范围较小的探条扩张术后,可安全置入直径为9 - 14mm的泰贡塑料支架。即使对于靠近UES的病变,也可实现有效的姑息治疗。可避免穿孔。再次干预率似乎与自膨式金属支架相当。