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A Novel Tracheobronchial Stent Loaded with 125 I Seeds in Patients with Malignant Airway Obstruction Compared to a Conventional Stent: A Prospective Randomized Controlled Study

机译:与传统支架相比,恶性气道阻塞患者中装有125 I种子的新型气管支气管支架:一项前瞻性随机对照研究

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Background To evaluate the safety and efficacy of a novel radioactive bare metal stent (RBMS) compared with a conventional bare metal stent (CBMS) in patients with inoperable malignant airway obstruction. Methods This prospective study was approved by the Institutional Ethics Committee, and informed consent was obtained from each participant. Patients with malignant airway obstruction who had dyspnea were randomly assigned to receive RBMS or CBMS placement. The primary endpoint was stenosis grade, while the secondary endpoints were technical success, overall survival, and complications. A p value of Results Between September 2013 and July 2015, 66 patients with inoperable malignant airway obstruction received stent placement fluoroscopically (33 in either group). The median follow-up time was 154?days (range, 15–335?days). The baseline stenosis was immediately relieved in both groups after stent placement, and the stenosis grades in the RBMS group were significantly lower than that in the CBMS group since the second month ( p Conclusions The placement of RBMS in patients with inoperable malignant airway obstruction is feasible and safe, and it significantly reduces restenosis and improves overall survival compared with the placement of CBMS.
机译:背景技术为了评估新型放射性裸金属支架(RBMS)与常规裸金属支架(CBMS)在无法手术的恶性气道阻塞患者中的安全性和有效性。方法这项前瞻性研究获得了机构伦理委员会的批准,并获得了每个参与者的知情同意。呼吸困难的恶性气道阻塞患者被随机分配接受RBMS或CBMS放置。主要终点为狭窄等级,次要终点为技术成功,总体生存率和并发症。结果的p值在2013年9月至2015年7月之间,对66例无法手术的恶性气道阻塞患者进行了透视置管(两组均33例)。中位随访时间为154天(范围15-335天)。自第二个月起,两组患者的基线狭窄立即得到缓解,RBMS组的狭窄程度明显低于CBMS组(p结论不能手术切除恶性气道阻塞患者的RBMS放置是可行的且安全,与放置CBMS相比,它可显着减少再狭窄并改善总体生存率。

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