Biocompatible silicone bronchial stent. It follows the general design of the Stening® Tracheal, with variations adapted to its wall thickness and dimensions for use in the bronchial airway.
Product code: ST




Code ST
The Stening® Bronchial —also known as a bronchial stent or bronchial prosthesis— is a silicone bronchial stent that follows the general design of the Stening® Tracheal, with variations applied to its wall thickness and dimensions.
It comes in a wide range of diameters and lengths, sharing many of the indications described for the tracheal version.
Check indications, available dimensions, usage, care and warnings for the Stening® Bronchial.
The Stening® Bronchial is indicated for a wide range of bronchial pathologies, including stenosis, compression and neoplastic lesions of the airway.
The Stening® Bronchial is manufactured in a wide range of diameters and lengths, allowing the most suitable size to be selected for each clinical case.


All sizes are always available. For specific inquiries about instrumentation, bronchoscopes or introducers, contact us at (+54) 11 4553-5070 or (+54) 11 4551-2333.
The procedure is performed under general anesthesia. The implant can be performed directly through the working channel of the tracheoscope or bronchoscope, or by using a conventional introducer for silicone prostheses. The airway is accessed with a rigid endoscope.
The length and diameter of the area to be covered by the stent must be properly established. A simple method to determine the length of the affected area is to mark the tracheoscope when its tip is at the end of the lesion, and repeat the marking after withdrawing it to the beginning of the lesion. The diameter of the trachea or bronchus should be estimated by comparison with the known diameter of the endoscope used.
The prosthesis is thus released. If necessary, it can be repositioned with alligator forceps; the maneuver is simpler if the stent is located “below” the lesion.
Steps 1, 2 and 3 are repeated. Then the tracheoscope containing the introducer and prosthesis is stopped 5 mm before the lesion to be treated, and the ejector plunger is pressed slowly. The prosthesis is thus ejected into the affected trachea.
Some stent loader models are not inserted into the tracheoscope, but are simply coupled to it at its proximal end, from where the stent is propelled. For this, the endoscope will have been stopped proximally or distally to the lesion as explained above, to push the prosthesis with the plunger provided by the endoscopic instrumentation. The stent will then travel through the entire interior of the tracheoscope until it reaches the trachea. At this point, a sudden reduction in the resistance to the pressure applied on the plunger will be perceived, indicating that the stent has begun to leave the interior of the endoscope.
The stent may require additional maneuvers to correct or adjust its final position. It is preferable to correct a stent that has been deployed beyond the desired position rather than the opposite, since advancing a prosthesis that has been released “before” the affected area is highly inconvenient.
To move a stent proximally, it can be grasped by its edge and gently pulled. We strongly recommend, for its precision, a maneuver that consists of grasping the stent by its edge as mentioned, and then advancing the direct-vision optics inside the stent until its distal end is visualized. Then pull the forceps and you will see how the stent ascends through the airway. Stop pulling when you consider the position optimal.
Intubation is performed with a rigid tracheoscope or bronchoscope as appropriate. Easy to extract, the silicone stent should be grasped firmly by its edge with alligator-tooth forceps. The forceps is rotated approximately 360° so that the stent folds, taking on an omega shape and thereby losing its radial resistance to compression. The forceps is then pulled to extract the prosthesis along with the tracheoscope.
The proximal end of the stent can be inserted into the tracheoscope. This maneuver protects the vocal cords during extraction. Other implantation and removal methods are possible depending on the operator’s experience and preferences.
Recommendations for the follow-up of patients with a bronchial stent.
The product must not be reused, to avoid cross-contamination.
Contact us for personalized technical advice, size selection, custom manufacturing or international shipping inquiries.