Utilization of chest tube as an esophagus stent in pediatric caustic injuries: A retrospective study

Maryam Salimi1, Hamidreza Hosseinpour2, Reza Shahriarirad3

  • 1Department of Orthopaedic Surgery, Shiraz University of Medical Sciences, Shiraz 7138433608, Iran.

Insights

This study introduces an esophageal chest tube (ECT) stent for pediatric caustic esophageal burns, offering an accessible and cost-effective solution. The novel ECT stent method demonstrated no complications and avoided the need for gastrostomy or jejunostomy in treated patients.

Area of Science:

  • Pediatric Surgery
  • Gastroenterology
  • Medical Devices

Background:

  • Pediatric caustic esophageal burns management remains controversial regarding optimal effectiveness, availability, and cost.
  • Evolving treatment strategies necessitate innovative and accessible solutions.

Purpose of the Study:

  • To describe a method for utilizing a chest tube as an esophageal stent in pediatric patients.
  • To evaluate the feasibility and outcomes of this esophageal chest tube (ECT) stent technique.

Main Methods:

  • Retrospective data collection on pediatric caustic esophageal injury over 10 years.
  • Preparation and placement of a modified chest tube (esophageal chest tube - ECT) as a stent.
  • Analysis of patient demographics, injury etiology, treatment, and follow-up for ECT stenting.

Main Results:

  • Seven pediatric patients (mean age 2 years) with Grade IIB or III esophageal burns were treated with ECT stents.
  • The ECT stent was inserted within a mean of 3.8 days for 5 patients, and later for 2 patients with delayed referrals.
  • No complications or stent failures were observed; none of the 7 patients required gastrostomy or jejunostomy.

Conclusions:

  • The esophageal chest tube (ECT) stent is a broadly available, economic, and easy-to-use option for esophageal stenting in pediatric caustic esophageal burns.
  • This method is particularly suitable for resource-limited settings and emergency departments.
  • Further multicenter studies are recommended to validate this technique with larger patient cohorts.
Abstract

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