Abstract

Objective: To present 8-year follow-up outcomes, treatment of complications, and prognosis in children with congenital tracheal stenosis after metallic airway stent implantation.Methods: Retrospective analysis was performed on the clinical records of children who had airway stents placed between May 20, 2011 and May 31, 2016, and on their follow-up records collected on November 31, 2019.Results: During the 8 years follow-up, 41 children underwent airway stenting under flexible bronchoscopy and participated in the follow-up investigation. There were 26 cases with left main bronchus (LMB) stenosis (63.4%), 16 cases with congenital tracheal stenosis (CTS, 39.0%), 12 cases with right main bronchus (RMB) stenosis (29.3%), and 1 case of subglottic stenosis (2.4%). A total of 76 stents were implanted, and 21 patients died after implantation. There were 34 children (82.9%) with congenital heart disease (CHD), while other diseases accounted for <5%. Among children with CHD and those with other conditions, the number of death cases was 19 and 2, respectively; no significant differences were observed between the two groups (P>0.05). The most frequent complications were increased airway secretion (75.8%), stent deformation (66.7%), and granulation tissue hyperplasia (60.6%). The airway stenosis (45.5%) and stent migration (12.1%) occurred at a moderate rate. The less common complications were airway softening (6.1%), and stent breakage (6.1%).Conclusions: The placement and removal of the metallic stent are convenient and quick procedures that can relieve the symptoms of dyspnea caused by airway stenosis in the case of an emergency. After stent implantation, the primary disease should be actively treated, and the stent should be removed as soon as possible after the cause of airway stenosis is successfully removed. Larger stents are more likely to cause complications; thus, a good follow-up system should be established to timely address all the complications.

Highlights

  • Congenital tracheal stenosis and tracheomalacia are congenital tracheal stenosis that causes airway obstruction [1] and are commonly encountered in pediatric intensive care units (PICU), especially in infants [2]

  • A retrospective analysis was performed on the clinical records of children who had airway stents placed at Bayi Children’s Hospital (Beijing, China) between May 20, 2011 and May 31, 2016, and on their follow-up records collected by November 31, 2019

  • A total of 41 children were diagnosed with severe central airway stenosis by fiberoptic bronchoscopy combined with CT and three-dimensional airway reconstruction, and all underwent airway stenting under soft bronchoscopy

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Summary

Introduction

Congenital tracheal stenosis and tracheomalacia are congenital tracheal stenosis that causes airway obstruction [1] and are commonly encountered in pediatric intensive care units (PICU), especially in infants [2]. In these children, pleural pressure exceeds intraluminal pressure resulting in airway collapse during dynamic expiration and coughing at low lung volume [3]. An attractive non-surgical option is endoscopic airway stenting [5] These stents can provide rapid relief of dyspnea in children, and tend to improve clinical symptoms within a few hours after the patient is taken off the ventilator. The goal of this study is to report the 8-year follow-up outcomes, treatment of complications, and prognosis in children with congenital tracheal stenosis after metallic airway stent implantation

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