SUPRAGLOTTIC TUBE FOR INSERTING A LARYNX MASK

Abstract

The invention discloses a supraglottic tube, which despite certain softness has high compressive strength in the proximal distal direction and the radius of curvature can be adjusted. For this purpose, the supraglottic tube comprises at least three lumens. A guiding lumen is located between a lateral respiration lumen and a further lateral esophageal lumen. Said lumens are separated from each other by separating walls. A guiding means, which comprises a pressure element and a tractive element, is located in the guiding lumen. A tractive force can be applied to the tractive element by way of a feed connector and an adjustment unit, in which the pressure element is supported, whereby the radius of curvature of the supraglottic tube is adjusted and it can be better introduced into the patient in the bent state and thereafter the radius of curvature thereof can be adapted to the anatomy of the patient or the position of the patient, thereby maintaining the sealing pressure of the larynx mask around the larynx.

Description

The present invention relates to a supraglottic tube for inserting a larynx mask via the pharynx whereby the supraglottic tube has several lumens, of which a respiration lumen serves to supply respiration air and is used for instrumentation, whereby at least one further lumen is present as a guide lumen, in which a guide means is positioned for changing the bending radius of the tube.

Supraglottic tubes are tubes inserted into the pharynx to keep open the airways and to ventilate a patient. A classic example are so-called larynx masks. By means of the tube a larynx mask is introduced through the central pharynx via the epiglottis into the lower pharynx and placed behind or around the larynx. Such larynx masks are used to ventilate a patient who is anaesthetised. They allow the insertion of tubes, probes, optical instruments and other instruments into the airways. At the same time larynx masks can have an oesophageal access. This allows the introduction of probes into the oesophagus and the stomach in order to remove gastric juices and other fluids as well as air from the stomach. In anaesthetised patients emptying of the stomach is intended to prevent the stomach contents flowing back into the upper respiratory tract and being aspirated into the unprotected airways (windpipe, bronchi and lungs). A further advantage of an oesophageal access is the removal of passively or actively regurgitated stomach contents from the upper oesophagus to outside, which thereby represents limited, and thus inadequate, aspiration protection.

A large number of different larynx masks are known on the market. A typical example is set out in U.S. Pat. No. 5,878,745. This shows a gastro-laryngeal mask in which the supraglottic tube is a pipe through which several tubes can be fed. These tubes have lumens which are used for ventilation and for an oesophageal access.

The combination of a larynx mask with an oesophageal passage is becoming more and more available. U.S. Pat. No. 7,040,322 also shows such a larynx mask and the supraglottic tube here is divided by means of an intermediately well running ventral-dorsally whereby in the larger of the two lumens produced by the division a separate tube is inserted which is used to inflate or deflate a proximal of the larynx mask.

A larynx mask with a relatively rigid supraglottic tube can be introduced more easily, whereby the rigidity of the supraglottic tube prevents adaptation of the position of the larynx mask to the anatomical conditions. Insertion into the pharyngeal cavity by means of a relatively rigid supraglottic tube can result in injury, and positioning in the pharyngeal cavity is not always reliable.

Highly flexible larynx masks tube (ProSeal® LMA, Flexible® LMA) allow better positioning in the larynx but are more difficult and therefore occasionally more traumatic to insert and more difficult to position in the pharynx.

In the last decade anatomically curved supraglottic tubes for inserting the larynx mask have proven themselves. They not only allow simple introduction of the larynx mask into the pharynx and good positioning, but they also exhibit better sealing. Such larynx masks with a rigid, curved tube are used particularly in emergency situations. Due the anatomically preformed shape they can also be inserted by paramedics in emergencies.

Typical examples of such larynx masks are sold under the name LMA Fastrach® (U.S. Pat. No. 5,896,858) and LMA CTrach®, both by the company LMA Inc. However, because of their rigidity these bent supragottic rigid tubes cannot be left in the patient over a longer period of time and are not therefore suitable for the routine treatment of patients.

As similar design is also supplied by the company Ambu GmbH, whereby the version is sold under the name Ambu Aura 40™. The curve angle of the supraglottic tube is however greater and wider and the tube softer in consistency. The latter allows this larynx mask to be used routinely over longer periods.

Particularly when an intervention in the neck and head area has to take place, the position of the head can vary greatly and accordingly a larynx mask with a preformed relatively rigid tube can hardly be used. However if the larynx mask is correctly positioned on the larynx fixing in such position is desirable.

To increase the sealing of the larynx mask on the larynx, the “Proseal patent” (GB 9 821 771) describes a dorsal cuff which on the highly flexible supraglottic tube pushes the larynx mask away from the posterior wall of the pharynx and onto the larynx.

Finally a larynx mask is known from US 2007/0028923 is known with a supraglottic tube in which a further lumen in formed in the wall of the respiration for passing through a cord as simple traction means. The traction means grips the distal end of the larynx mask whereby it is also bent. Controlled and active resetting is not possible.

It is therefore the aim of the present invention to create a supraglottic tube which in a relatively rigid state allows improved, simple, anatomical insertion of the larynx mask, after correct positioning then allows the supraglottic tube to become flexible and, if required, allows bending of the supraglottic tube with transmission of the bending onto the larynx mask in order, in the relevant position, to be able to exert a desired pressing force around the larynx.

This objective is achieved by a supraglottic tube for inserting a larynx mask via the epiglottis with the features of claim 1 and alternatively with the features of claim 13. As a result of the design in accordance with claim 13 it is ensured that a guide means does not deform the tube in a random direction.

Further advantageous forms of embodiment of the supraglottic tube in accordance with the invention are set out in the other dependent claims. Their relevance and action is explained in the following description with reference to the attached drawings.

FIG. 1 shows a diametric section through the supraglottic tube in accordance with the invention with a guide means arranged in the guide lumen;

FIG. 2 shows an identical diametric section through a supraglottic tube with a dorsally reinforce wall areas which forms the casing of a Bowden cable.

FIG. 3 shows a longitudinal section through a supraglottic tube with a proximally mounted larynx mask and a distal adjusting device

FIG. 4 shows the same arrangement as in FIG. 3, whereby the supraglottic tube is bent more strongly;

FIG. 5 shows the proximal end of a supraglottic tube in a diametric section with a supporting element inserted into the larynx mask and

FIG. 6 shows a side view of the supraglottic tube with a similarly designed supporting element

FIG. 7 shows a diametric longitudinal section through a supraglottic tube and the larynx mask with a supporting element.

The overall situation is shown with reference to FIG. 3. The supraglottic tube is designated with 1. At its proximal end the larynx mask 2 is attached. The distal end of the supraglottic tube is provided with a feed connector and adjusting unit 2. In relation to introduction into the patient, the side with the smaller, concave inner radius is designated as the ventral side, while the side with the outer, convex, larger radius is designated as the dorsal side. The actual larynx mask 2, which is here shown in diametric longitudinal section, has a passage section 29 which ends in a holder sleeve 21 on the distal side. In this holder sleeve 21 the proximal end of the supraglottic tube 1 is firmly held.

On the lower, ventral side of the larynx mask there is a circumferential sealing collar 22, usually known as a cuff 22. The oesophageal passage 23 passes over the cuff 22. This oesophageal passage is connected in sealed manner with a corresponding lumen of the supraglottic tube 1. The respiration air flows through laterally to the oesophageal passage and enters the inner chamber 24 which is sealed off by the cuff 22 and from which the respiration air can flow in or out of the trachea.

The actual design of the larynx mask 2 is of secondary importance for the invention. Only if a supporting element is formed on the proximal end of the supraglottic tube 1 does the larynx mask 2 have to be designed so that this supporting element can correctly held therein. This supporting element 60 essentially serves to reinforce the larynx mask in order, in particular, to prevent bending over of the tip 25 of the larynx mask during intubation. The supporting element 60 also helps to transfer the bending of the supraglottic tube to the larynx mask and prevent kinking in the area of the holder sleeve 21. The precise design of the adjusting unit and the feed connection 3 will be set out in more detail later after the description of the supraglottic tube and the guiding means.

FIG. 1 show a cross-section through the actual supraglottic tube. As usual this is made of a plastic approved for this. The supraglottic tube 1 can be produced by way of continuous extrusion or injection moulding. In the diametric cross-section in accordance with FIG. 1 the three provided lumens can be clearly seen. However it is perfectly possible that more than three lumens may be envisaged, whereby through one lumen any necessary surgical equipment, measuring probes and or an optical system, so example a fibre optic and/or an endoscope of both can be introduced.

Here too the supraglottic tube is designated with 1 overall. In the example shown here this has three different lumens. 11 is a respiration lumen for the passage of respiration air. This lumen normally has the largest cross-section. Between the respiration lumen 11 and the oesophageal lumen 12 there is a guiding lumen 13. Guiding means 4 are arranged in the guiding lumen 13. These guiding means 4 can be fixed or be interchangeable in the guiding lumen 13. This depends on whether the supraglottic tube is to be a disposable part of a sterilisable reusable part. The guiding means 4 lead to a certain reinforcement of the supraglottic tube 1 and thus to improved introduction of the larynx mask into the patient and on the other hand permit the bending radius of the supraglottic tube to be changed, thereby also improving the introduction of the larynx mask into the patient and adaptation of the position of the larynx mask to the anatomy and the position of the patient. Accordingly the guiding means 4 have two elements, namely a spring-back and/or adjustable pressure element 40 and a flexible traction element 41. The design of these two elements 40, 41 can vary greatly. The traction element 41 always comprises a flexible rope, wire or cable, which does not stretch at the forces occurring here and which can be mono- or multifilar. The materials used for this can also be very different, the only essential feature being that they are approved from medical purposes.

In a particularly simple form of embodiment as shown in FIG. 1, the pressure element 40 can be a relatively flat metal profile, square in cross-section, with relatively high elasticity, whereby this flat profile is designated 42 as a special example of embodiment of a pressure element. This flat profile 42 exhibits a bend which corresponds to the minimum bending of the supraglottic tube 1. The traction element 41 is attached directly or indirectly on the pressure element or on the flat profile 42 at its proximal end. In the simplest case the traction element 41 can loosely project from the end of the supraglottic tube 1 and the surgeon could bring about bending by pulling on this traction element 41 with simultaneous counter-pressure on the tube at its distal end or counterpressure on the feed connector or the adjusting unit 3. For fixing in the end position the traction element 41 can be fixed at the required bending position to a corresponding fixing means, for example a simple hook. However, in the example shown here the traction element 41 is firmly attached to a part of the feed connector and adjusting unit 3. This will be set out in below in the detailed description of the feed connector and adjusting unit 3.

FIG. 2 shows a further form of embodiment of the guiding means 4. Whereas the traction element 41 is again in the form of a simple wire or cable, the pressure element is designated as 40′ here and is an integral part of the supraglottic tube 1. The supraglottic tube 1 has a relatively thin outer wall 10 and the individual lumens 11, 12, 13 are separated from each other by separating walls 14.

In the embodiment in accordance with FIG. 2 the outer wall is strongly thickened in the area of the guiding lumen. In this way this outer wall area forms a pressure element 40′. Such an injection moulded or extruded supraglottic tube can be preformed with the minimum bend or can be produced as a straight part and then bent through pretensioning or after thermal treatment. The pressure element 40, 40′, i.e. the thickened wall area or the flat profile 42, is always arranged on the dorsal side of the supraglottic tube, while the traction element lies on the ventral side of the supraglottic tube. As has already been stated, pulling on the traction element 41 leads to bending of the supraglottic tube 1; once this pulling ceases the supraglottic tube 1 returns to its original shape either through its own elasticity or with the aid of the elastic pressure element 40, 40′.

A particularly preferred form of embodiment of the guiding element 4 is shown in FIGS. 3 and 7. Here the pressure element 40 is in the form of a preferably one-piece link chain 43. This link chain 43 has chain links 44 which can be of different sizes and are all connected via a dorsally continuous wall 45. Parallel to this dorsal wall 45 are two parallel ventral wall, namely and inner ventral wall 46 and an outer ventral wall 47. Both the inner ventral wall 46 and the outer ventral wall 47 have interruptions 48 which arranged so that they overlap. Between the inner ventral wall 46 and the outer ventral wall 47 there is an intermediate space 49 in which the traction element 41 is arranged. At the proximal end of the link chain 43 there is an anchoring sleeve 50. This anchoring sleeve 50 is formed by a projection of the inner and outer ventral walls 46, 47. The traction element 41 is here a monofilar string onto which a head 51 is formed. At the distal end of the traction element 41 a cylindrical bearing head 52 is formed. The link chain 43 in the guiding lumen 13 also serves as compression/bite protection for the distal supraglottic tube area.

In FIGS. 3 and 7 the combined feed connector and adjusting unit 3 is again seen in diametric section. The actual feed connector is designated as 30. Although it is in one piece, this feed connector 30 has two different connectors, namely the respiration air supply connector 31 and the oesophageal connector 32. The respiration air supply connector 31 is in communicating connection with the respiration lumen 11 and the oesophageal connector 32 is in communicating connection with the oesophageal lumen 12. The air supply connector 31 is straight and flush with distal end of the respiration lumen 11 or the supraglottic tube 1. The oesophageal connector 32 in the direct connection area to the oesophageal lumen 12 is also straight and flush therewith, but has a crimped, mounted end 33. In FIG. 3 only the air supply connector 31 is seen as in the shown position the oesophageal connector 32 is arranged directly behind it in the direction of view.

The combined feed connector 30 has a sealing sleeve 34 in which the supraglottic tube 1 is firmly held in sealed manner. As no large forces or high pressures occur in this area and the material of the supraglottic tube 1 is elastic, a pure frictional connection should suffice. However an adhesive connection may also be present or the sealing sleeve 34 can additionally be provided with one or more circumferential radial lips and corresponding circumferential radial grooves can be provided in the supraglottic tube 1 in order to thereby produce a form-fitted connection. A proximally extended sealing sleeve 34 over the straight, distal part of the supraglottic tube 1 also provides bite protection. Formed on the distal end of the sealing sleeve 34 is a radially projecting sliding collar 35. This sliding collar 35 engages in a circumferential slide groove 37 which is formed in the proximal end area of a union nut 36. In the union nut 36 is a traction pin 38, which is most clearly seen in FIG. 3. On rotation of the union nut 36 the traction pin 38 only moves in the axial direction relative to the distal end of the supraglottic tube 1. The traction pin 39 has a bearing cup 39 in which the cylindrical bearing head 52 is firmly held. As the traction pin 38 is only moved axially and does not rotate, the air supply connector 31 can easily pass through the traction pin 38. The oesophageal connector 32 also passes through the traction pin 3 while the crimped end 33 is formed on the traction pin 38. A sliding seal therefore exists between the oesophageal connector 32 and the traction pin 38.

The supraglottic tube 1 in accordance with the invention can therefore be made of a relatively soft and flexible material which easily adapts to the anatomy. Due to the pressure element relatively high compressive strength comes about. In the inserted state, the guiding means 4 then allow the bending radius of the supraglottic tube 1 to be adjusted simply by turning the union nut 36. This stiffens the supraglottic tube and allows it to be introduced and positioned more easily due to its bent form. Secondarily, the bending radius of the supraglottic tube can be adapted to the anatomy or position of the patient so that the larynx mask 2 or its cuff 22 remain pressed around the larynx.

Once the supraglottic tube 1 has been inserted into the patient it is hardly noticeably whether the shape or the bending radius has already adjusted to the anatomy of the patient or not. Although at the minimum bending radius the respiration air supply connector 31 still projects from the traction pin 38, this not evident to the eye. It is therefore proposed to apply a scale 28 (FIG. 3) to the respiration air supply connector in order to be able to read off the relative bending.

In FIG. 4 the supraglottic tube 1 together with the larynx mask 2 and the feed connector 3 is again shown in principle, but in a more curved state, whereby the traction pin 38 is accordingly moved in the distal direction, whereby the section of the traction element 41 is pulled out further from the supraglottic tube 1 and thereby relatively shortened, while the length of the pressure element 40 remains unchanged.

As, as has already been stated, the pressure that can absorbed by the supraglottic tube 1 is relatively high, it makes sense to also provide means that could serve to reinforce the larynx mask 2, in order, in particular, to largely prevent kinking of the larynx mask 2 in the area of the holding sleeve 21 of the larynx mask 2 itself and its tip 25. For this two solutions are shown schematically in FIGS. 5 and 6. FIGS. 5 and 6 show the supragottic tube 1 in a view from above and from the side respectively, whereby only their proximal end is shown schematically. In both cases a supporting element 60 is formed on the proximal end of the link chain 43. In the view in accordance with FIG. 5 this supporting element 60 is designed as a vertical supporting wall. This supporting wall can be formed as an extension of the foremost, proximal chain link. The height of the supporting wall 60 is reduced on both sides by the wall thickness of the outer wall 10 in order to facilitate introduction of the supporting element 60 into the larynx mask in the area of the holding sleeve 21. Naturally the larynx mask 2 must be designed accordingly so that the supporting well 60 can be introduced as far as possible into the area of the tip 25.

As, as shown in FIG. 5, the supporting wall runs practically perpendicularly to any possible bending of the larynx mask 2, the supporting force is correspondingly great and therefore this form of embodiment is preferred. While the supraglottic tube itself is made of a soft plastic, the pressure element 40, here in the form of a link chain 43, is made of hard plastic and is therefore extremely suitable as a supporting element 60. The entire guiding means 4 with the supporting wall or the supporting element 60 can be easily inserted in to the supraglottic tube 1.

A particularly preferred form of embodiment of the guiding means 4 consists in the guiding means 4 being a fixed preformed element and can be introduced into the supraglottic tube or is fixed therein, whereby the element can be flexible=adaptable or not flexible.

A particularly preferred from of embodiment to the supraglottic tube contains, in an insertable or firmly fixed manner:

• a. Inflation line for the cuff through the supraglottic tube
• b. Thermosensor through the supraglottic tube
• c. Respiration pressure measurement through the supraglottic tube
• d. Respiratory gas measurement through the supraglottic tube
• e. Optical image transmission through the supraglottic tube
• f. Measuring probe through the supraglottic tube

An additional function of the guiding means consists in the fact that it can serve as bite protection.

LIST OF REFERENCE NUMBERS

• 1. Supraglottic tube
• 2. Larynx mask
• 3. Feed connector and adjusting unit
• 4. Guiding means
• 10. Outer wall
• 11. Respiration lumen
• 12. Oesophageal lumen
• 13. Guide lumen
• 14. Separating walls
• 20. Passage section of the larynx mask
• 21. Holding sleeve
• 22. Cuff or sealing collar
• 24. Internal chamber
• 25. Tip of the larynx mask
• 29. Scale for bending radius
• 30. Feed connector
• 31. Respiration air supply connector
• 32. Oesophageal connector
• 33. Crimped end of 32
• 34. Sealing sleeve
• 35. Sliding collar
• 36. Union nut
• 37. Circumferential sliding groove
• 38. Traction pin
• 39. Bearing cup
• 40, 40′ Pressure element
• 41. Traction element
• 42. Flat profile
• 43. Link chain
• 44. Chain links
• 45. Dorsal wall of the link chain
• 46. Inner ventral wall
• 47. Outer ventral wall
• 48. Interruptions
• 49. Intermediate space
• 50. Anchoring sleeve
• 51. Head on traction element 41
• 52. Cylindrical bearing head
• 60. Supporting element

Claims

1. A supraglottic tube for inserting a larynx mask via the pharynx whereby the supraglottic tube comprises a plurality of lumens, wherein the plurality of lumens comprises a respiration lumen that serves to supply respiration air and is used for instrumentation, and a guide lumen, in which guide means are positioned for changing the bending radius of the tube, wherein the guide means (4) comprise a pressure element and a flexible traction element.

2. A supraglottic tube according to claim 1 further comprising an oesophageal lumen which serves as the oesophageal access.

3. A supraglottic tube according to claim 1 wherein the guide lumen is closed at the proximal end.

4. A supraglottic tube according to claim 1 wherein the guide lumen is arranged medially between the two adjoining respiration and oesophageal lumens.

5. A supraglottic tube according to claim 1 wherein the supraglottic tube is formed in one piece from a tube and the lumens are formed by ventral-dorsally running separating walls.

6. A supraglottic tube according to claim 5 wherein at least one separating wall is extended on the proximal end and engages in the larynx mask as a ventral-dorsally running supporting element.

7. A supraglottic tube according to claim 6 wherein the supporting element extends proximally to at least close to the tip of the larynx mask.

8. A supraglottic tube according to claim 1 wherein the flexible traction element is firmly anchored on the proximal end of the pressure element.

9. A supraglottic tube according to claim 1 wherein a union nut (36) is attached at its distal end in which a traction pin, holding an end of the traction element (41) can be moved relative to the distal end of the supraglottic tube.

10. A supraglottic tube according to claim 1 wherein the pressure element is a one-piece link chain with a continuous dorsal wall, and at least one ventral wall provided with interruptions.

11. A supraglottic tube according to claim 10 comprising two parallel ventral walls with interruptions and wherein the traction element runs between the two parallel ventral walls.

12. A supraglottic tube according to claim 10 further comprising a supporting element is formed on the proximal end of the pressure element, wherein the supporting element can inserted into the larynx mask (2) until approximately its tip (25).

13. A supraglottic tube for inserting a larynx mask via the pharynx wherein the supraglottic tube comprises a plurality of lumens, wherein the plurality of lumens comprises a respiration lumen that serves to supply respiration air and is used for instrumentation, and a further lumen that serves as the oesophageal access, wherein a guide lumen with insertable guiding means is positioned between the respiration lumen and the oesophageal lumen, wherein the supraglottic tube has a cross-section adapted to the pharynx and the respiration lumen and the oesophageal lumen are divided by ventral-dorsally running separating walls, and wherein the separating wall between the guide lumen and respiration lumen is arranged at least approximately in the centre of the supraglottic tube.