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新型可生物降解支架在肺移植后支气管狭窄治疗中的应用。

Novel biodegradable stents in the treatment of bronchial stenosis after lung transplantation.

机构信息

University Hospital Motol, Prague, Czech Republic.

出版信息

Eur J Cardiothorac Surg. 2011 Sep;40(3):619-24. doi: 10.1016/j.ejcts.2010.12.047. Epub 2011 Feb 21.

Abstract

OBJECTIVE

To evaluate the safety and effectiveness of novel biodegradable (BD) stents to treat bronchial anastomotic stenosis in patients after lung transplantation.

METHODS

Twenty BD stents were implanted endoscopically in six patients (median age 41.5 years (range 35-57 years)) with post-transplant bronchial anastomotic stenoses, between 2006 and 2010. All stents were custom-made from bio-absorbable polydioxanone (PDS). The median stent diameter was 12 mm (8-17 mm) and median length was 20mm (12-30 mm). All patients were evaluated clinically, by bronchoscopy and high-definition computed tomography (CT).

RESULTS

The stenosis was initially relieved in all cases. There was no bleeding, perforation or displacement after BD stent implantation. Four patients needed multiple stenting for anastomotic re-stenosis. Median time to any re-stenting was 5 months (2-15 months). There was one sudden death, 1 year after the last BD stent implantation, from a pulmonary embolus. All five survivors are in good clinical condition up to 4 years' follow-up (median 40 months, range 7-48 months) since first stenting and intervention-free up to 44 months (median 24 months, range 7-44 months).

CONCLUSIONS

This small pilot study shows that BD stents are a safe, effective and reliable alternative to classical metallic stents in patients with anastomotic stenosis after lung transplantation, and may avoid the need for permanent stenting.

摘要

目的

评估新型可生物降解(BD)支架治疗肺移植后支气管吻合口狭窄患者的安全性和有效性。

方法

2006 年至 2010 年间,6 例(中位年龄 41.5 岁(范围 35-57 岁))肺移植后支气管吻合口狭窄患者接受了 20 个 BD 支架的内镜下植入。所有支架均由可生物吸收的聚二氧杂环已酮(PDS)定制而成。支架直径中位数为 12mm(8-17mm),长度中位数为 20mm(12-30mm)。所有患者均接受临床、支气管镜和高分辨率计算机断层扫描(CT)评估。

结果

所有病例的狭窄均得到初步缓解。BD 支架植入后无出血、穿孔或移位。4 例患者因吻合口再狭窄需要多次支架置入。中位再狭窄支架置入时间为 5 个月(2-15 个月)。1 例患者在最后一次 BD 支架植入后 1 年因肺栓塞突然死亡。5 例存活者在最后一次支架置入后 4 年的随访中(中位随访时间 40 个月,范围 7-48 个月)均处于良好的临床状态,无干预情况下随访时间达 44 个月(中位 24 个月,范围 7-44 个月)。

结论

这项小型初步研究表明,BD 支架是肺移植后吻合口狭窄患者的一种安全、有效和可靠的金属支架替代物,可避免永久性支架置入的需要。

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