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The Local Damage and Systemic Inflammation Induced by a Biodegradable Polydioxanone Stent Implanted in the Rabbit
Carolina Serrano-Casorran1,2, Sergio Rodriguez-Zapater1,3, Francisco Rodriguez-Panadero4,5
1Minimally Invasive Research Group (GITMI), Universidad de Zaragoza, 50009 Zaragoza, Spain.
Biodegradable polydioxanone tracheal stents reduce airway inflammation and symptoms in rabbits. Inflammatory markers like interleukin-8 (IL-8) decreased significantly after the stent degraded, indicating a safe and effective biodegradable option.
Area of Science:
- Biomaterials Science
- Respiratory Medicine
- Inflammation Research
Background:
- Metallic and removable tracheal stents have limitations in treating benign airway diseases.
- Biodegradable tracheal stents offer a potential alternative to overcome these limitations.
Purpose of the Study:
- To evaluate the local and systemic inflammatory response to a biodegradable polydioxanone tracheal stent in a rabbit model.
- To assess the impact of stent degradation on airway inflammation and clinical outcomes.
Main Methods:
- Twenty-one rabbits received polydioxanone tracheal stents or underwent sham procedures, with follow-up at 30, 60, and 90 days.
- Clinical status, respiratory symptoms, and serial peripheral blood interleukin-8 (IL-8) levels were monitored.
- Tracheoscopy, IL-8 quantification in tracheal lavage, and necropsy were performed post-procedure.
Main Results:
- Tracheoscopic findings showed significantly reduced congestion, inflammation, and secretions after stent degradation (p < 0.05).
- Mean IL-8 expression in tracheal lavage decreased dramatically post-degradation (p = 0.003).
- Peripheral blood IL-8 levels showed a transient increase on day 1, followed by a decrease.
Conclusions:
- Biodegradable polydioxanone tracheal stents induce a transient inflammatory response that significantly decreases after stent degradation.
- These findings suggest that biodegradable tracheal stents are a safe and effective option for benign airway disease, with reduced long-term inflammatory effects.
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