Congenital Tracheal Stenosis With Complete Cartilage Rings: Proposal of A Multidisciplinary and Tailored Surgical Approach

IF 2.5 2区 医学 Q1 PEDIATRICS Journal of pediatric surgery Pub Date : 2024-12-05 DOI:10.1016/j.jpedsurg.2024.162085
Luca Genova Gaia , Andrea Moscatelli , Oliviero Sacco , Vittorio Guerriero , Francesca Rizzo , Francesco Santoro , Michele Torre
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Abstract

Introduction

Congenital Tracheal Stenosis (CTS) with complete cartilaginous rings is a rare but potentially life-threatening condition in paediatric patients. Currently, the most common approach is slide tracheoplasty (ST) with sternotomy under cardiopulmonary bypass (CPB). Intending to make the procedure less invasive and consider the variety of associated conditions, we have tailored the approach to our patients, who were treated by a multidisciplinary airway team.

Methods

Patients with CTS treated surgically between 2012 and 2022 at Gaslini Institute were enrolled. Preoperative, surgical and postoperative details were collected and analysed retrospectively. All patients had angio-computerized tomography (CT) scan, echocardiography and bronchoscopy with bronchography before surgery. Each patient and each procedure have been discussed at Airway Team meetings.

Results

Among 20 patients with CTS, 15 underwent ST and 5 tracheal resection and anastomosis (TRA). 60 % were younger than 12 months. 30 % patients had previous tracheal/cardiac surgery. Combined cardiac surgery was performed in 8 patients. 4 patients were approached with cervicotomy and extracorporeal membrane oxygenation (ECMO). Mortality within 30 days was 5 %. 8 patients (40 %) needed endoscopic dilatation after the surgery and 1 underwent revision surgery. No patient had tracheostomy after the surgery. We did not find a higher rate of mortality and morbidity in patients who had cervicotomy and ECMO.

Conclusion

We propose a multidisciplinary and tailored approach for patients with CTS. After evaluating each patient through detailed preoperative studies, including bronchography, the team can choose alternatives to the traditional ST under CPB, such as TRA, cervical approach, and ECMO.

Level of Evidence

Level IV.

Type of Study

Original Article.
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先天性气管狭窄伴完全软骨环:多学科和量身定制手术方法的提案。
先天性气管狭窄(CTS)伴完整软骨环是一种罕见但可能危及生命的儿科疾病。目前,最常见的方法是体外循环(CPB)下胸骨切开气管成形术(ST)。为了减少手术的侵入性,并考虑到各种相关情况,我们为患者量身定制了治疗方法,这些患者由多学科气道团队治疗。方法:纳入2012年至2022年在Gaslini研究所接受手术治疗的CTS患者。回顾性分析术前、手术及术后细节。所有患者术前均行血管计算机断层扫描(CT)、超声心动图和支气管镜检查。每个病人和每个手术都在气道小组会议上进行了讨论。结果:20例CTS患者中,15例行ST, 5例行气管切除吻合术。60%的婴儿小于12个月。30%的患者既往有气管/心脏手术。8例患者行联合心脏手术。4例患者行宫颈切开加体外膜氧合(ECMO)治疗。30天内死亡率为5%。术后需内镜扩张8例(40%),翻修手术1例。术后无患者行气管切开术。我们没有发现宫颈切除术和ECMO患者有更高的死亡率和发病率。结论:我们为CTS患者提出了一种多学科和量身定制的治疗方法。在通过详细的术前研究(包括支气管造影)对每位患者进行评估后,团队可以在CPB下选择传统ST的替代方案,如TRA、宫颈入路和ECMO。证据等级:四级。研究类型:原创文章。
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来源期刊
CiteScore
1.10
自引率
12.50%
发文量
569
审稿时长
38 days
期刊介绍: The journal presents original contributions as well as a complete international abstracts section and other special departments to provide the most current source of information and references in pediatric surgery. The journal is based on the need to improve the surgical care of infants and children, not only through advances in physiology, pathology and surgical techniques, but also by attention to the unique emotional and physical needs of the young patient.
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