Shin Ji Hoon, Kim Sang-We, Shim Tae Sun, Jung Gyoo-Sik, Kim Tae-Hyung, Ko Gi-Young, Song Ho-Young
Department of Radiology, Asan Medical Center, University of Ulsan College of Medicine, 388-1 Pungnap-2dong, Songpa-gu, Seoul 138-736, Korea.
J Vasc Interv Radiol. 2003 Dec;14(12):1525-34. doi: 10.1097/01.rvi.0000099525.29957.34.
To evaluate the safety and clinical effectiveness of a covered retrievable expandable nitinol stent for the treatment of malignant tracheobronchial stricture and/or esophagorespiratory fistula (ERF).
With fluoroscopic guidance, stents were placed in 35 symptomatic patients with malignant tracheobronchial stricture and/or ERF in most cases caused by lung or esophageal cancer. The site of stricture was most commonly at the trachea or left main bronchus. If there were complications, the stent was removed with a retrieval set. Nine patients had combined symptomatic ERF.
A total of 47 tracheobronchial stents were placed and were technically successful and well-tolerated in all patients. Improvement of dyspnea was achieved in 92% of the patients (24 of 26 patients). Associated ERF in nine patients was effectively treated with tracheobronchial stent placement with or without esophageal stent placement. Stent migration, tumor overgrowth, symptomatic sputum retention, and hemoptysis occurred in 17% (6/35), 6% (2/35), 20% (7/35), and 17% (6/35) of patients, respectively. There were no documented cases of tumor ingrowth. Stent removal was performed easily in five patients when stent migration (n = 2), severe pain (n = 1), tumor overgrowth (n = 1), or persistent gastrobronchial fistula (n = 1) developed. All patients died 2 days to 26 weeks (mean, 9.62 weeks) after stent placement because of disease progression (n = 18), pneumonia (n = 9), hemoptysis (n = 5), or unknown cause (n = 3).
Use of a covered retrievable expandable nitinol stent is a safe and effective method for relieving dyspnea. This procedure contributed to improved quality of life for patients with malignant tracheobronchial stricture and/or ERF. Stent retrievability was useful in resolving stent-related complications.
评估一种覆膜可回收可扩张镍钛合金支架治疗恶性气管支气管狭窄和/或食管气管瘘(ERF)的安全性和临床有效性。
在透视引导下,为35例有症状的恶性气管支气管狭窄和/或ERF患者放置支架,多数情况下病因是肺癌或食管癌。狭窄部位最常见于气管或左主支气管。若出现并发症,使用回收装置取出支架。9例患者合并有症状的ERF。
共放置47个气管支气管支架,所有患者技术操作均成功且耐受性良好。92%(26例中的24例)的患者呼吸困难得到改善。9例合并ERF的患者通过放置气管支气管支架(有或无食管支架)得到有效治疗。支架移位、肿瘤过度生长、有症状的痰液潴留和咯血分别发生在17%(6/35)、6%(2/35)、20%(7/35)和17%(6/35)的患者中。无肿瘤长入的记录病例。当发生支架移位(n = 2)、严重疼痛(n = 1)、肿瘤过度生长(n = 1)或持续性胃支气管瘘(n = 1)时,5例患者的支架取出操作轻松。所有患者在支架置入后2天至26周(平均9.62周)因疾病进展(n = 18)、肺炎(n = 9)、咯血(n = 5)或不明原因(n = 3)死亡。
使用覆膜可回收可扩张镍钛合金支架是缓解呼吸困难的一种安全有效的方法。该方法有助于提高恶性气管支气管狭窄和/或ERF患者的生活质量。支架可回收性有助于解决与支架相关的并发症。