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无名动脉横断术治疗严重胸廓畸形患者:最佳适应证及时机

Innominate artery transection for patients with severe chest deformity: optimal indication and timing.

作者信息

Hisamatsu Chieko, Okata Yuichi, Zaima Azusa, Yasufuku Masao, Maeda Kosaku, Okita Yutaka, Nishijima Eiji

机构信息

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

出版信息

Pediatr Surg Int. 2012 Sep;28(9):877-81. doi: 10.1007/s00383-012-3138-y.

Abstract

PURPOSE

The innominate artery sometimes compresses the trachea, leading to tracheomalacia and highly fatal tracheoinnominate fistula in patients with severe chest deformity. This study is focused on the indication of innominate artery transection for the definitive treatment of these complications.

PATIENTS AND METHODS

We retrospectively analyzed the medical records of eight patients who underwent transection of innominate artery.

RESULTS

All patients had developed severe chest deformity and their symptoms were life-threatening anoxic spell or endotracheal hemorrhage. Bronchoscopy showed tracheomalacia with or without pulsatile granulations on the anterior wall of the trachea underlying the innominate artery. In six cases who had previously undergone tracheostomy or laryngotracheal separation, the tracheal tube tip made granulations or tracheoinnominate fistulas. In addition to transection of innominate artery, the tracheoinnominate fistula was closed in two cases and the artery was transposed in one. All patients survived without neurologic complications and airway symptoms postoperatively.

CONCLUSIONS

For patients with severe chest deformity, innominate artery transection is indicated when they have tracheal compression by the artery and need to be intubated through the compressed part of trachea to secure the airway. This would be the best timing to schedule the prophylactic operation.

摘要

目的

无名动脉有时会压迫气管,导致严重胸壁畸形患者出现气管软化和极具致命性的气管无名动脉瘘。本研究聚焦于无名动脉横断术在这些并发症确定性治疗中的适应证。

患者与方法

我们回顾性分析了8例行无名动脉横断术患者的病历。

结果

所有患者均有严重胸壁畸形,其症状为危及生命的缺氧发作或气管内出血。支气管镜检查显示气管软化,无名动脉下方气管前壁有或无搏动性肉芽组织。6例曾行气管切开术或喉气管分离术的患者,气管导管尖端形成肉芽组织或气管无名动脉瘘。除无名动脉横断术外,2例患者的气管无名动脉瘘得以闭合,1例患者的动脉被移位。所有患者术后均存活,无神经并发症及气道症状。

结论

对于严重胸壁畸形患者,当无名动脉压迫气管且需要经气管受压部位插管以确保气道安全时,应行无名动脉横断术。这将是安排预防性手术的最佳时机。

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