Genova Gaia Luca, Moscatelli Andrea, Sacco Oliviero, Guerriero Vittorio, Rizzo Francesca, Santoro Francesco, Torre Michele
Division of Pediatric Surgery, Department of Surgery, IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini 5, 16147, Genova, Italy; Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, DINOGMI, Università di Genova, Largo Paolo Daneo 3, 16132, Genova, Italy.
Neonatal and Pediatric Intensive Care Unit, Emergency Department IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini 5, 16147, Genova, Italy.
J Pediatr Surg. 2025 Mar;60(3):162085. doi: 10.1016/j.jpedsurg.2024.162085. Epub 2024 Dec 5.
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.
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.
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.
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 IV.
Original Article.
先天性气管狭窄(CTS)合并完整软骨环是儿科患者中一种罕见但可能危及生命的疾病。目前,最常见的方法是在体外循环(CPB)下通过胸骨切开术进行滑动气管成形术(ST)。为了使手术创伤更小,并考虑到各种相关情况,我们为患者量身定制了手术方法,由多学科气道团队进行治疗。
纳入2012年至2022年在加斯利尼研究所接受手术治疗的CTS患者。回顾性收集并分析术前、手术及术后的详细资料。所有患者在手术前均进行了血管计算机断层扫描(CT)、超声心动图以及支气管造影支气管镜检查。每个患者和每个手术都在气道团队会议上进行了讨论。
20例CTS患者中,15例行ST,5例行气管切除吻合术(TRA)。60%的患者年龄小于12个月。30%的患者曾接受过气管/心脏手术。8例患者同时进行了心脏手术。4例患者采用颈部切开术和体外膜肺氧合(ECMO)治疗。30天内死亡率为5%。8例患者(40%)术后需要内镜扩张,1例接受了翻修手术。术后无患者行气管造口术。我们未发现接受颈部切开术和ECMO治疗的患者有更高的死亡率和发病率。
我们为CTS患者提出一种多学科且量身定制的治疗方法。通过详细的术前研究,包括支气管造影,对每个患者进行评估后,团队可以选择CPB下传统ST的替代方法,如TRA、颈部入路和ECMO。
IV级。
原创文章。