Stening® Tracheal Stent

Code ST

CE 0051


The Stening® Tracheal stent is the classic and straight stent for tracheal affections. It has a tubular structure, with flat surface anchoring studs on its outer wall to prevent stent migration.


  • Primary or secondary tracheal neoplasm.
  • Tracheoesophageal fistula.
  • Tracheal rupture.
  • After laser resection, cryotherapy or electrocautery, to maintain the airway opened.
  • Extrinsic compression or compromise of the submucosa.
  • Post intubation stenosis.
  • Post-traumatic stenosis.
  • Post infectious stenosis  (endobronchial tuberculosis, histoplasmosis mediastinal fibrosis, herpes virus, diphtheria).
  • Focal trachea-broncho-malacia: following tracheostomy or radiation therapy.
  • Diffuse trachea-broncho-malacia: idiopathic, polychondritis or Mounier-Kuhn syndrome.
  • Tracheal tumours.
  • Amyloidosis.
  • Excessive dynamic compression of the airway.
Stening® provides detailed instructions for each device, including insertion and removal techniques, precautions and postoperative cares.
Stening - Made in Europe
image/svg+xml(units mm) D L W
References Dimensions (mm)
Translucent Radiopaque Diameter (D)Length (L)Wall thickness (W)
ST10-20 STX10-20 10201
ST10-30 STX10-30 10301
ST10-40 STX10-40 10401
ST10-50 STX10-50 10501
ST10-60 STX10-60 10601
ST10-70 STX10-70 10701
ST10-80 STX10-80 10801
ST11-20 STX11-20 11201.1
ST11-30 STX11-30 11301.1
ST11-40 STX11-40 11401.1
ST11-50 STX11-50 11501.1
ST11-60 STX11-60 11601.1
ST11-70 STX11-70 11701.1
ST11-80 STX11-80 11801.1
ST12-20 STX12-20 12201.2
ST12-30 STX12-30 12301.2
ST12-40 STX12-40 12401.2
ST12-50 STX12-50 12501.2
ST12-60 STX12-60 12601.2
ST12-70 STX12-70 12701.2
ST12-80 STX12-80 12801.2
ST13-30 STX13-30 13301.5
ST13-40 STX13-40 13401.5
ST13-50 STX13-50 13501.5
ST13-60 STX13-60 13601.5
ST13-70 STX13-70 13701.5
ST13-80 STX13-80 13801.5
ST14-30 STX14-30 14301.5
ST14-40 STX14-40 14401.5
ST14-50 STX14-50 14501.5
ST14-60 STX14-60 14601.5
ST14-70 STX14-70 14701.5
ST14-80 STX14-80 14801.5
ST15-30 STX15-30 15301.5
ST15-40 STX15-40 15401.5
ST15-50 STX15-50 15501.5
ST15-60 STX15-60 15601.5
ST15-70 STX15-70 15701.5
ST15-80 STX15-80 15801.5
ST16-30 STX16-30 16¼301.5
ST16-40 STX16-40 16¼401.5
ST16-50 STX16-50 16¼501.5
ST16-60 STX16-60 16¼601.5
ST16-70 STX16-70 16¼701.5
ST16-80 STX16-80 16¼801.5
ST17-30 STX17-30 17½301.5
ST17-40 STX17-40 17½401.5
ST17-50 STX17-50 17½501.5
ST17-60 STX17-60 17½601.5
ST17-70 STX17-70 17½701.5
ST17-80 STX17-80 17½801.5
ST18-100 STX18-100 181001.5
ST18-40 STX18-40 18401.5
ST18-60 STX18-60 18601.5
ST18-80 STX18-80 18801.5
ST20-100 STX20-100 201001.5
ST20-40 STX20-40 20401.5
ST20-60 STX20-60 20601.5
ST20-80 STX20-80 20801.5

For custom made devices you can contact us

Due to the characteristics of the production process,
the sizes of the devices may vary by +/- 2%

  • Extrinsic compression caused by an aortic aneurysm.
  • Tracheal distortion caused by kyphoscoliosis.
  • Tracheal obstruction caused by an oesophageal stent.
  • In combination with an oesophageal stent.

The useful area for ventilation is just one part of the cross section of any stent.

If we take as an example the Stening® model with a diameter of 16mm, the area of its whole cross section is 207mm2, as it is shown in the graphic. However, the 33% of that area is occupied by the wall of the prosthesis leaving only 66% (137mm2) for the ventilation.

  • Medical grade silicone
  • Bevelled edges to prevent granulomas
  • Spur system to prevent migration
  • Removable
  • Surface of maximum softness to avoid adherence of secretions
  • Transparent or Radiopaque

Introduction technique:

The procedure will take place under general anaesthesia.

The implant of these types of prostheses can be made directly through the work channel of the tracheoscope or bronchoscope.

A conventional introducer for silicone prostheses can be used as well. A rigid endoscope will be used to access the airway.

The length and diameter of the area that the stent will cover must be established correctly.

If you want to know the length of the area, you can mark the tracheoscope when its extreme is located at the end of the injury. Repeat the process once the tracheoscope is moved up to the beginning of the injury. The diameter of the trachea or bronchi must be estimated by comparing it with the diameter of the endoscope used.

Retrograde mode of Implant:

  1. Lubricate the introducer nozzle with lidocaine gel, preventing the lubricant from reaching the operator’s fingers.
  2. Fold the Stening® over its axial axis and put it inside the prostheses introducer through its nozzle.
  3. Remove the nozzle.
  4. Surpass the injured area with the tube of the tracheoscope and put its distal edge over the healthy mucosa, exceeding from 5 to 7 mm the affected zone.
  5. Put the introducer inside the tracheoscope.
  6. Press the ejector while the tracheoscope is removed and the ejector plunger progresses. That is, the plunger of the stents’ charger has to be pressed as the endoscope is removed.

In this way, the prosthesis will be released. If it is necessary, it can be moved to a better position with an alligator forceps. The manoeuvre is much easier when the stent is lower than the injury.

Antegrade mode of implant:

Steps 1 to 3 will be repeated.

You have to stop the tracheoscope that contains the introducer and the prosthesis 5 mm before the injury.

After that, you have to press the ejector plunger slowly. By doing this, the prosthesis will be expelled into the injured trachea.

Some stents’ charger models are not introduced inside the tracheoscope, but they are added to the proximal extreme, from where the stent is expelled. To accomplish this, the endoscope will have to be stopped in a proximal or distal way to the injury, as it was explained before, to push the prosthesis with the plunger that is provided with the endoscopic instrumental. In this way, the stent will travel through the tracheoscope until it reaches the trachea. At this point, we will feel a small reduction of the resistance in the pressure performed on the plunger, showing that the stent has begun to abandon the endoscope interior.

Correction of the stent position:

The stent may require some additional manoeuvres, focusing on correcting or adjusting its final position.

It is preferable to correct stent that has been installed beyond the desired position than the opposite, due to the arduousness of pushing a stent that has been released before the damaged zone.

To move a stent in a proximal way, it can be taken by its edge and then you must pull with kindness.

To be more accurate we recommend a manoeuvre that consists on taking the stent by its edge as it was mentioned before. After that, you have to advance with the optical vision through the stent’s inside until you see its ending. Now pull the forceps and you will be able to see how the stent ascends through the airway.

Stop the pulling as long as you consider that the position is correct.

Extraction technique:

We will proceed to the intubation with the tracheoscope or the rigid bronchoscope depending on the case.

Of easy extraction, the silicone stent must be taken by its proximal edge with a crocodile forceps, with enough steadiness. Rotate the forceps 360º so that the stent bends, acquiring an omega shape and losing its radial resistance to compression. Then, pull the forceps and extract the prosthesis together with the tracheoscope.

The stent proximal edge can be introduced inside the tracheoscope. With this manoeuvre the vocal chords are protected during the extraction.

Other implant and removal methods are also possible depending on the experiences and preferences of the surgeon.

  • When an increase in secretions is detected, perform nebulisations frequently with a warm isotonic saline solution.
  • Take care of your oral hygiene and treat cavities.
  • Perform endoscopic controls according to the frequency prescribed by the doctor.

The product should not be reused because this can cause cross contamination.

Polymeric tracheal/bronchial stent, non-bioabsorbable, sterile

A sterile non-bioabsorbable tubular device intended to be implanted into the trachea and/or a bronchus/bronchiole to maintain luminal patency, typically used in cases of obstructions/stenoses, fistulae, tumours, scarring, surgical resection and anastomosis, or pulmonary transplantation. It is made entirely of a synthetic polymer(s) [e.g., silicone] and may have various designs (e.g., semi-soft continuous tube, covered or non-covered mesh structure, straight or branched configuration) intended to conform to the endotracheal/endobronchial surface. It may be expandable in situ (e.g., self-expands) and disposable devices intended to assist implantation may be included.