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先天性气管食管瘘的宫颈修复术:潜伏的并发症!

Cervical repair of congenital tracheoesophageal fistula: Complications lurking!

作者信息

Conforti Andrea, Iacusso Chiara, Valfrè Laura, Trozzi Marilena, Bottero Sergio, Bagolan Pietro

机构信息

Neonatal Surgery Unit, Department of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Rome, Italy.

Neonatal Surgery Unit, Department of Medical and Surgical Neonatology, Bambino Gesù Children's Hospital, Rome, Italy.

出版信息

J Pediatr Surg. 2016 Oct;51(10):1623-6. doi: 10.1016/j.jpedsurg.2016.06.010. Epub 2016 Jun 21.

Abstract

AIM

Esophageal atresia (EA) and tracheoesophageal fistula (TEF) consist of a spectrum of rare congenital abnormalities. Although EA surgical treatment is well established, the outcome of EA with proximal fistula (type B and D EA) or isolated H-type fistula (type E EA) is poorly explored. These forms of EA shared a common surgical step: the need of a cervical approach to close the fistula. Therefore, the aim of present study is to evaluate postoperative outcomes of patients treated for Gross type B-D and E EA, on regards of their cervical surgery.

MATERIALS AND METHODS

A retrospective case series analysis of all patients affected by type B-D and E EA, and admitted to our tertiary care center between January 2003 and December 2014 was performed. All patients underwent preoperative flexible laryngo-tracheobronchoscopy (LTBS) as part of our standardized preoperative diagnostic assessment to define the diagnosis, evaluate preoperative vocal cord motility and to cannulate the fistula when required. Fistula closure was always performed through a right cervical access. Analysis of all cases and comparison between type B-D and E EA were performed. Mann-Whitney test, Chi-squared test and unpaired t test were used as appropriate; p<0.05 was considered significant.

RESULTS

During the study period, 180 EA newborns were treated. Proximal or isolated TEF was found in 18 patients (10%): 7 type B, 11 type E EA. Patients affected by type B and E EA/TEF frequently present associated major malformations (27%), and major cardiac abnormalities (44%). Major postoperative complications were: vocal cord paralysis (5 patients), bilateral in 2 infants requiring tracheostomy, cerebral ischemia (1 patient), and cardiac failure (1 patient).

CONCLUSION

Patients affected by type B and E EA have a high rate of associated abnormalities, and risk of possible sequelae. Postoperative complications are common, with possible transient vocal cord dismotility, but in some cases persistent paralysis may require tracheostomy. Therefore, both preoperative and postoperative LTBS is highly recommended to evaluate the presence of a proximal fistula, and vocal cord motility, even in asymptomatic patients, to rule out any possible intraoperative "surprise" and any vocal cord abnormality and to possibly define its pathogenesis (congenital vs. iatrogenic).

摘要

目的

食管闭锁(EA)和气管食管瘘(TEF)是一系列罕见的先天性异常疾病。尽管EA的外科治疗已很成熟,但对于近端瘘型EA(B型和D型EA)或孤立H型瘘(E型EA)的治疗效果仍探索不足。这些类型的EA有一个共同的手术步骤:需要通过颈部入路来闭合瘘管。因此,本研究的目的是评估接受B-D型和E型EA治疗的患者颈部手术后的结局。

材料与方法

对2003年1月至2014年12月间入住我们三级医疗中心的所有B-D型和E型EA患者进行回顾性病例系列分析。所有患者均接受术前软性喉镜-气管支气管镜检查(LTBS),作为我们标准化术前诊断评估的一部分,以明确诊断、评估术前声带活动度,并在必要时插入瘘管。瘘管闭合总是通过右侧颈部入路进行。对所有病例进行分析,并对B-D型和E型EA进行比较。根据情况使用曼-惠特尼检验、卡方检验和非配对t检验;p<0.05被认为具有统计学意义。

结果

在研究期间,共治疗了180例EA新生儿。18例患者(10%)发现有近端或孤立性TEF:7例B型,11例E型EA。B型和E型EA/TEF患者常伴有严重畸形(27%)和严重心脏异常(44%)。主要术后并发症有:声带麻痹(5例患者),其中2例婴儿双侧麻痹需要气管切开,脑缺血(1例患者),以及心力衰竭(1例患者)。

结论

B型和E型EA患者伴有异常的发生率高,且有发生后遗症的风险。术后并发症很常见,可能出现短暂的声带运动障碍,但在某些情况下,持续性麻痹可能需要气管切开。因此,强烈建议术前和术后均进行LTBS,以评估近端瘘的存在以及声带活动度,即使是无症状患者,以排除任何可能的术中“意外”和任何声带异常,并可能确定其发病机制(先天性与医源性)。

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