Surgery – Respiratory method or device – Respiratory gas supply means enters mouth or tracheotomy...
Reexamination Certificate
2001-12-28
2004-11-09
Flynn, Amanda R. (Department: 3743)
Surgery
Respiratory method or device
Respiratory gas supply means enters mouth or tracheotomy...
C128S207150, C128S207160
Reexamination Certificate
active
06814077
ABSTRACT:
BACKGROUND OF THE INVENTION
This invention relates to a tracheal cannula for insertion into the trachea following a tracheotomy, with this cannula having a shaft and a cuff for blocking the tracheal cross-sectional area surrounding the shaft.
Following a tracheotomy, a cannula is inserted into the trachea in order to keep open the lumen thereby created. Available to this end are cannulas in diverse forms and made of various materials. Thus, thin-walled silver cannulas are familiar that are constructed in a double-barreled form, namely, they have an outer cannula and an inner cannula that is easy to remove. Furthermore, there are also more thick-walled plastic cannulas that, in contrast to metal cannulas, are not as rigid and that at body temperature conform roughly to the shape of the surrounding space, without their lumen thereby changing.
When there is an increased risk of aspiration, a tracheal cannula with a so-called blocker cuff is used, which is intended to prevent any entering of saliva, gastric juice, or other fluids or food (aspiration). These cuffs are normally positioned around the shaft of the cannula or are integrated within it, and can be inflated in order to conform to the surrounding space of the trachea.
Finally there are artificial larynxes, which are equipped with a valve mechanism and a hole or a screen on their shaft in order to make it possible for the patient to vocalize. When the patient inhales, the valve mechanism at the cannula entrance opens up and permits the intake of air through the cannula into the lungs. On the other hand, in exhalation the valve closes and the air stream is led out through the larynx in a normal way via the cannula hole or window, thus enabling both a normal air intake and also the use of the voice. However, such artificial larynxes can be used only in patients who are not at risk for aspiration, so that those who are at such a risk have no way to speak. Whereas this is still tolerable for patients in the transitional stage immediately after a tracheotomy, the inability to vocalize over a long period of time is quite difficult to accept, especially in the case of neurologically impaired patients with a protracted risk for aspiration (for example, following a stroke).
Known from U.S. Pat. No. 4,459,984 is a tracheal cannula of this species for insertion into the trachea. This device comprises a curved cannula that has an inflatable cuff positioned around the end of the cannula that is within the trachea. Above the cuff, the tracheal cannula has an escape nozzle or opening that can be closed by a flap valve and that can be opened by increasing the air pressure in the tracheal cannula, so that air escapes into the upper esophagus and the patient can speak during the mechanical evacuation of air. However, because of this valve, which is intended to prevent aspiration when in the closed state, the air stream is deflected and slowed down considerably. This causes the natural vocalization characteristics in the larynx to be impaired. Furthermore, when the inner pressure in the tracheal cannula slackens, the valve is abruptly closed and thereby prevents vocalization from continuing. Moreover, due to the possibility that the flap of the valve may jam, a risk of aspiration cannot be excluded with certainty.
Therefore, one object of the invention is to make possible in a reliable way a vocalization that is as natural as possible in patients equipped with tracheal cannulas that have a cuff.
SUMMARY OF THE INVENTION
By means of the invention, this object is essentially achieved by constructing a window in the section of the shaft lying above the cuff, with this window being covered by a membrane that is permeable to air. This membrane thereby prevents the entry of saliva and food particles into the cannula and thus into the lower airways. But on the other hand, speaking is made possible because of the air permeability of the membrane.
In accordance with one preferred embodiment of the invention, the membrane is not permeable to water, so as to ensure that no saliva or nutrient components enter into the cannula. It has turned out to be especially advantageous in this connection to use a membrane made of polytetrafluoroethylene (PTFE), especially a fabric made of PTFE such as can be obtained on the commercial market under the trade name of Gore-Tex®.
In the inhalation process the air is carried through the cannula into the lungs, whereas for speaking purposes the patient can hold closed the cannula in order for the air to go through the membrane into the larynx. However, in accordance with one preferred embodiment of the invention, a provision is made to have a valve situated at the entrance of the cannula, with this valve automatically opening with inhalation and closing with exhalation.
In one improvement of the invention, the cuff is connected via a line to a pilot balloon or the like for the inflation of the cuff and for controlling the cuff pressure.
Other aims, advantages, and possible applications of the invention appear from the following description of an exemplary embodiment and from the drawings. Here all the described and/or graphically represented features form the subject of the invention by themselves or in any given combination, regardless of how they are summarized in the claims or of any of their back-references.
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TESS trademark record for Teflon Reg. # 1111147, filed Jun. 15, 1978.*
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Flynn Amanda R.
Zylka-Eistert Maria
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