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采用创新型跨声带支架进行声门下狭窄的内镜治疗。

Endoscopic management of subglottic stenosis with innovative transcordal stent.

作者信息

Teodonio Leonardo, Marinucci Beatrice Trabalza, Peritore Valentina, Cassiano Francesco, Hanna Amir, Argento Giacomo, Messina Gaetana, Leonardi Beatrice, Fiorelli Alfonso, Andreetti Claudio

机构信息

Department of Thoracic Surgery, Sant'Andrea Hospital-Sapienza University, Via Di Grottarossa 1035-1039, 00189, Rome, Italy.

Department of Thoracic Surgery, Centre Chirurgical Marie Lannelongue, Paris, France.

出版信息

Updates Surg. 2025 Jun 5. doi: 10.1007/s13304-025-02235-9.

Abstract

Single-stage tracheal resection and anastomosis represents the gold standard for benign subglottic stenosis' management. Nevertheless, also considering the complexity of the surgical procedure, some patients are considered unfit for tracheal surgery (stenosis involving vocal cords, comorbidities, and relapse after surgery). Until now, the only alternative was tracheostomy which represents the only real alternative to secure the patency of the airway. Thanks to the creation of "transcordal stents", patients considered unfit for surgery have a valid alternative to tracheostomy and the conformation of the stent reduces the risk of stent migration, preserving airway patency, swallowing, and phonation. This study aims to evaluate the use of a new custom-made transcordal stent, comparing its safeness with traditional transcordal stent. Between 2017 and 2021, 28 consecutive patients underwent transcordal stenting for benign tracheal stenosis in 3 centers. Patients were divided into 2 groups: 16 treated with the new custom-made stent (Group 1) and 12 treated with conventional stents (Group 2). Intra-, post-operative complications, swallowing capacity, quality of voice, granulation tissue, stent migration, and quality of life (QoL) were compared between the two groups. Group 2 showed reduced swallowing capacity (p = 0.0001), higher rate of stent migration (p = 0.0003), higher rate of granulation tissue (p = 0.0044), and higher rate of stent replacement (p = 0.0001). Voice reduction was not significantly different between the two groups. QoL was better in Group 1. Despite this represent the largest study analyzing transcordal stenting as definitive treatment of subglottic stenosis in patients unfit for surgery, results could not draw definitive conclusions because of the small number of patients, the lack of randomization, and the small follow-up. Nevertheless, the use of the new custom-made transcordal stent could be considered safe and effective, guaranteeing stable results with low rate of long-term complications and better QoL compared to the traditional stents.

摘要

一期气管切除吻合术是治疗良性声门下狭窄的金标准。然而,考虑到手术的复杂性,一些患者被认为不适合进行气管手术(狭窄累及声带、合并症以及术后复发)。到目前为止,唯一的替代方法是气管造口术,这是确保气道通畅的唯一真正替代方案。由于“跨声带支架”的发明,被认为不适合手术的患者有了替代气管造口术的有效选择,并且支架的构造降低了支架移位的风险,保持了气道通畅、吞咽功能和发声功能。本研究旨在评估一种新型定制跨声带支架的使用情况,并将其安全性与传统跨声带支架进行比较。2017年至2021年期间,3个中心的28例连续患者因良性气管狭窄接受了跨声带支架置入术。患者分为两组:16例接受新型定制支架治疗(第1组),12例接受传统支架治疗(第2组)。比较两组患者的术中、术后并发症、吞咽能力、嗓音质量、肉芽组织、支架移位和生活质量(QoL)。第2组患者的吞咽能力下降(p = 0.0001)、支架移位率更高(p = 0.0003)、肉芽组织发生率更高(p = 0.0044)以及支架置换率更高(p = 0.0001)。两组之间的嗓音减退无显著差异。第1组的生活质量更好。尽管这是分析跨声带支架置入术作为不适合手术患者声门下狭窄确定性治疗方法的最大规模研究,但由于患者数量少、缺乏随机分组以及随访时间短,结果未能得出明确结论。然而,新型定制跨声带支架的使用可被认为是安全有效的,与传统支架相比,能保证稳定的结果,长期并发症发生率低且生活质量更好。

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