Pediatric Tracheal Surgery: A 25-Year Review of Slide Tracheoplasty and Tracheal Resection.

Ann Thorac Surg

Division of Cardiovascular-Thoracic Surgery, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois; Department of Surgery, Northwestern University Feinberg School of Medicine, Chicago, Illinois. Electronic address:

Published: January 2020

Background: The purpose of this study was to assess the outcomes of slide tracheoplasty and tracheal resection in pediatric patients and analyze the data for predictors of outcomes.

Methods: A retrospective review of tracheal surgery from January 1, 1993 to May 1, 2018 was performed. Demographic data, operative details, perioperative data, and clinical outcomes were collected. The study investigators' management strategy has evolved over time, with less rigid bronchoscopy, more reliance on postoperative computed tomographic imaging, and the use of inhaled Ciprodex (combination of ciprofloxacin and dexamethasone) since 2007.

Results: The study included 41 patients, with a median age of 4.1 months and a median weight of 4.2 kg. There were 6 neonates and 24 infants. Slide tracheoplasty was performed in 27 patients (66%), and resection with end-to-end anastomosis was performed in 14 (34%). Eleven patients (27%) had a pulmonary artery sling. Simultaneous intracardiac repairs requiring cross-clamp and cardioplegia were performed in 9 patients (22%). Lung agenesis (n = 6) or severe hypoplasia (n = 2) was present in 8 patients (20%). Complications included tracheostomy in 5 patients (12%) and in-hospital death in 3 patients (7%). There were no cases of mediastinitis. Inhaled Ciprodex was used to decrease granulation tissue at suture lines. Median intubation time was 7 days, and median length of stay was 25.0 days. There was no difference in outcomes when comparing intracardiac repairs with the remaining patients, lung agenesis or hypoplasia vs the remaining cohort, or neonates vs infants.

Conclusions: Slide tracheoplasty and tracheal resection are effective operative strategies for infants and children with tracheal stenosis, including patients with lung agenesis/hypoplasia. Simultaneous repair of intracardiac anomalies and pulmonary artery sling is recommended.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.athoracsur.2019.06.042DOI Listing

Publication Analysis

Top Keywords

slide tracheoplasty
16
tracheoplasty tracheal
12
tracheal resection
12
patients
10
tracheal surgery
8
inhaled ciprodex
8
performed patients
8
pulmonary artery
8
artery sling
8
intracardiac repairs
8

Similar Publications

Background: Long segmental congenital tracheal stenosis and long segmental congenital tracheobronchial stenosis are rare congenital airway anomalies with variable arborizations. This study aimed to analyze presentations and outcomes of slide tracheoplasty in long segmental congenital tracheal and tracheobronchial stenosis with variable arborizations.

Methods: Retrospective analysis included all patients who underwent slide tracheoplasty between March 1995 and February 2023 for long segmental congenital tracheal and tracheobronchial stenosis at the Great Ormond Street Hospital for Children (London, United Kingdom).

View Article and Find Full Text PDF

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

J Pediatr Surg

December 2024

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; Pediatric Thoracic and Airway Surgery Unit, Department of Surgery, IRCCS Istituto Giannina Gaslini, Via Gerolamo Gaslini 5, 16147, Genova, Italy.

Article Synopsis
  • Congenital Tracheal Stenosis (CTS) is a rare but serious condition in children, often treated with slide tracheoplasty (ST) involving sternotomy and cardiopulmonary bypass.
  • The study analyzed surgical outcomes of 20 CTS patients treated from 2012 to 2022, revealing a 5% mortality rate post-surgery, with 40% requiring further interventions, but no need for tracheostomy.
  • A tailored, multidisciplinary approach is recommended for treating CTS, allowing for alternative procedures based on individual patient evaluations, rather than relying solely on the traditional ST method.
View Article and Find Full Text PDF

Retrospective analysis of factors contributing to poor prognosis among 271 pediatric patients with tracheal stenosis treated with slide tracheoplasty.

J Thorac Cardiovasc Surg

November 2024

Department of Laboratory Medicine, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, P.R. China. Electronic address:

Article Synopsis
  • The study aimed to identify factors that lead to negative postsurgical outcomes in children with congenital tracheal stenosis (CTS) who underwent slide tracheoplasty (STP).
  • It found that conditions like unilateral lung hypoplasia and bilateral bronchomalacia significantly increased the risk of airway complications, mechanical ventilation time, and longer hospital stays.
  • Key factors influencing patient survival included weight and tracheal diameter, highlighting the importance of thorough assessment and tailored management for these patients.
View Article and Find Full Text PDF
Article Synopsis
  • The study investigates airway management techniques and demographic data of patients with congenital tracheal stenosis (CTS) during preoperative, intraoperative, and postoperative periods, based on a review of patient charts from a pediatric medical center from 2001 to 2018.
  • Out of 148 patients analyzed, the majority had congenital tracheal rings as the cause of their CTS, with a median age of 9 months at surgery and most experiencing 50% to 80% stenosis.
  • Findings emphasize the importance of coordinated airway management between surgical and anesthesia teams during slide tracheoplasty, which is shown to be an effective treatment for CTS.
View Article and Find Full Text PDF

Achieving normal pulmonary function following tracheoplasty in infancy.

Interdiscip Cardiovasc Thorac Surg

September 2024

Department of Respiratory Medicine, Royal Children's Hospital, Melbourne, Australia.

Infant long-segment congenital tracheal stenosis (LTS) is rare and presents a challenging clinical scenario. We describe the management of a child who required extracorporeal membrane oxygenation following a respiratory arrest and underwent slide tracheoplasty in infancy for severe LTS and required repeated bronchoscopic reinterventions for recurrent tracheal granulations. At 9 years of age, the child has normal pulmonary function testing and a normal exercise tolerance.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!