Suppr超能文献

先天性气管狭窄治疗的新方法:球囊气管成形术和可扩张金属支架置入术。

A new approach to the treatment of congenital tracheal stenosis: Balloon tracheoplasty and expandable metallic stenting.

作者信息

Maeda K, Yasufuku M, Yamamoto T

机构信息

Department of Surgery, Division II, Kobe University, School of Medicine, 7-5-2, Kusunoki-cho, Chuo-ku, Kobe, Japan 650-0017.

出版信息

J Pediatr Surg. 2001 Nov;36(11):1646-9. doi: 10.1053/jpsu.2001.27940.

Abstract

BACKGROUND/PURPOSE: Many surgical procedures have been unsatisfactory for the treatment of congenital tracheal stenosis. The authors used intraluminal balloon dilatation and expandable metallic airway stent for this condition.

METHODS

From 1997 to 2000, balloon expandable stents (Palmaz) were inserted into the trachea in 5 infants, aged 7 days to 12 months who had severe airway obstruction caused by tracheal stenosis. Tracheal stents were placed after intraluminal balloon dilatation of complete tracheal rings. The stents were placed on balloon catheters and were inserted into the desired position bronchoscopically using x-ray control. They were expanded and fixed in place by inflating the balloon to appropriate diameter. The stents were 10 to 40 mm long and 6 to 8 mm in diameter.

RESULTS

Four patients have been relieved of airway obstruction after this procedure. One patient died after 9 months of palliation. In all patients, granulation tissue developed over the stents and could be managed by scraping or balloon compression. Stents have been in place for 9 to 36 months after insertion without any other complication.

CONCLUSIONS

Airway stents after balloon tracheoplasty can be left for prolonged periods to relieve tracheal obstruction. This technique may provide an important remedy in infants and children with congenital tracheal stenosis.

摘要

背景/目的:许多外科手术治疗先天性气管狭窄的效果并不理想。作者采用腔内球囊扩张术和可扩张金属气道支架来治疗这种疾病。

方法

1997年至2000年,对5名年龄在7天至12个月的婴儿实施了气管支架置入术,这些婴儿因气管狭窄导致严重气道阻塞。在对完整气管环进行腔内球囊扩张后放置气管支架。支架放置在球囊导管上,在X线控制下通过支气管镜插入到所需位置。通过将球囊膨胀至合适直径使其扩张并固定在原位。支架长度为10至40毫米,直径为6至8毫米。

结果

4例患者经此手术后气道阻塞得到缓解。1例患者在姑息治疗9个月后死亡。所有患者的支架上均出现肉芽组织,可通过刮除或球囊压迫处理。支架置入后已在位9至36个月,无任何其他并发症。

结论

球囊气管成形术后的气道支架可长期留置以缓解气管阻塞。该技术可为先天性气管狭窄的婴幼儿提供一种重要的治疗方法。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验