MEDICAL DEVICE SYSTEM INCLUDING A TRACHEAL TUBE AND METHOD
20180326170 ยท 2018-11-15
Inventors
Cpc classification
A61M16/0427
HUMAN NECESSITIES
A61M16/208
HUMAN NECESSITIES
A61M16/0463
HUMAN NECESSITIES
A61M16/0465
HUMAN NECESSITIES
A61M2205/0216
HUMAN NECESSITIES
International classification
Abstract
A method and apparatus for accomplishing placement and removal of an inner cannula with in an outer cannula endotracheal or other tracheal tube circuit for a critically ill patient without having to disconnect the patient from a respirator machine. An inner cannula is positioned in the outer cannula of an endotracheal or other tracheal tube through a wall of the respirator tubing set in a manner that maintains the integrity of the respiration system.
Claims
1. A medical device system, comprising: a tracheal tube configured for insertion into an opening of a patient, comprising: an outer cannula extending from a proximal end to a distal end configured to be positioned between in a patient's trachea, the outer cannula including a lumen extending from a first opening defined in the proximal end to a second opening defined in the distal end, and an inner cannula removably positioned in the lumen of the outer cannula, the inner cannula having a proximal end that extends outwardly from the first opening of the outer cannula, a distal end positioned adjacent to the distal end of the outer cannula, and a passageway extending through the distal and proximal ends, and a manifold removably coupled to the proximal end of the outer cannula, the manifold including an outlet connected to the first opening of the lumen of the outer cannula, a first inlet sized to receive and permit the passage of the inner cannula through the manifold into the first opening of the lumen of the outer cannula, and a second inlet configured to be coupled to an outlet of a respirator machine to permit airflow from the second inlet into the outlet, and a cover positioned over the first inlet, the cover including at least one valve flap operable to be moved between a first position in which the first inlet is sealed and a second position in which the inner cannula is permitted to enter the first inlet.
2. The medical device system of claim 1, wherein: the inner cannula includes a curved outer surface that extends between its distal end and its proximal end, and the at least one flap is configured to engage the curved outer surface to create a seal between the inner cannula and the at least one valve flap when the inner cannula is positioned in the first inlet.
3. The medical device system of claim 1, wherein the cover and the at least one valve flap are formed from an elastomeric material.
4. The medical device system of claim 3, wherein the elastomeric material is at least one of rubber and silicone.
5. The medical device system of claim 1, wherein the at least one valve flap includes a plurality of triangular valve flaps extending from an outer rim of the cover, the outer rim being coupled to the manifold.
6. The medical device system of claim 1, wherein the manifold includes a first housing and a second housing movable coupled to the first housing.
7. The medical device system of claim 6, wherein the second housing is movable between a first position in which the first inlet is aligned with the outlet and a second position in which the first inlet is positioned transverse to the outlet.
8. The medical device system of claim 7, wherein when the second housing is the second position, a section of the first housing is positioned over the first inlet.
9. The medical device system of claim 7, wherein the second inlet is in fluid communication with the outlet when the second housing is in the second position.
10. The medical device system of claim 9, wherein the second inlet is positioned transverse to the outlet when the second housing is in the first position and the second inlet is aligned with the outlet when the second housing is in the second position.
11. The medical device system of claim 10, further comprising a connector having a first end sized to be positioned in the opening defined in the proximal end of the outer cannula and a second end sized to be positioned over the outlet of the manifold.
12. A medical device system, comprising: a tracheal tube configured for insertion into an opening of a patient, the tracheal tube including an outer cannula, a conduit configured to be coupled to a proximal end of the tracheal tube, the conduit including (i) a manifold comprising an outlet connected to the outer cannula, a first inlet sized to receive and permit the passage of an inner cannula through the manifold into the outer cannula, and a second inlet configured to be coupled to an outlet of a respirator machine to permit airflow from the second inlet into the tracheal tube, and (ii) a cover positioned over the first inlet, the cover including at least one valve flap operable to selectively seal the first inlet.
13. The medical device system of claim 12, wherein the inner cannula is one of a plurality of inner cannulas is sized to be positioned in the outer cannula.
14. The medical device system of claim 12, wherein the at least one flap includes a plurality of triangular flaps extending from an outer rim of the cover, the outer rim being coupled to the manifold.
15. The medical device system of claim 12, wherein the manifold includes a first housing and a second housing movable coupled to the first housing.
16. The medical device system of claim 15, wherein the second housing is movable between a first position in which the first inlet is aligned with the outlet and a second position in which the first inlet is positioned transverse to the outlet.
17. The medical device system of claim 16, wherein when the second housing is the second position, a section of the first housing is positioned over the first inlet.
18. The medical device system of claim 16, wherein the second inlet is in fluid communication with the outlet when the second housing is in the second position.
19. A method of operating a medical device system, comprising: aligning an inner cannula with a first inlet of a manifold coupled to an outer cannula of a tracheal tube, inserting the inner cannula through a cover positioned over the first inlet, advancing the inner cannula through an outlet of the manifold into the outer cannula of the tracheal tube, and operating the manifold to rotate the first inlet from a first position that is traverse to the outlet of the manifold to a second position in which the first inlet is aligned with the outlet.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0019] The detailed description particularly refers to the following figures, in which:
[0020]
[0021]
[0022]
[0023]
[0024]
[0025]
[0026]
DETAILED DESCRIPTION OF THE DRAWINGS
[0027] While the concepts of the present disclosure are susceptible to various modifications and alternative forms, specific exemplary embodiments thereof have been illustrated by way of example in the drawings and will herein be described in detail. It should be understood, however, that there is no intent to limit the concepts of the present disclosure to the particular forms disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
[0028] Referring now to
[0029] The outer cannula 16 includes an elongated curved body 20 that extends from a proximal end 22 to a distal end 24. The curved body 20 has a circular opening 26 defined in the proximal end 22 and another circular opening 28 defined in the opposite distal end 24. A lumen 30 extends between the openings 26, 28 and has a curvature corresponding to the curvature of the body 20. In the illustrative embodiment, the lumen has a circular cross-section along its length. In other embodiments, the openings 26, 28 may be, for example, oval or oblong, and the lumen may have an oval or oblong cross-section. The cannula 16 is semi-rigid and formed from a biocompatible plastic resin such as, for example, polyvinyl carbonate, but it should be appreciated that in other embodiments other suitable materials may be used.
[0030] As shown in
[0031] In the illustrative embodiment, the connector 34 includes a proximal sleeve 44 that is sized to be received in the outlet 40 of the manifold and a distal sleeve 46 that is sized to be received in the opening 26 defined in the proximal end 22 of the outer cannula 16. An annular rim 48 extends outwardly from the distal end of the proximal sleeve 44, which acts a stop to prevent over insertion of the connector 34 into the manifold 32 or cannula 16.
[0032] As shown in
[0033] The inner cannula 18 has a proximal opening 60 defined in the port 56 and an opposite distal opening 62 defined in the end 54 of the body 50. A passageway 64 extends between the openings 60, 62 and is sized to permit the passage of oxygen and other gases from a respirator machine 12 or other medical device attached to the port 56 downward into the patient's lungs. The passageway 64 has a circular cross-section along its length. In other embodiments, the openings 60, 62 may be, for example, oval or oblong, and the passageway may have an oval or oblong cross-section. In the illustrative embodiment, the body 50 and the port 56 are formed as a single semi-flexible monolithic component from a biocompatible plastic resin. In that way, the body 50 conforms to the shape of the curved lumen 30 of the outer cannula 16 when the body 50 is positioned in the lumen 30. In the illustrative embodiment, the body 50 of the cannula 18 also has a curved outer surface 66 that extends from the proximal end 52 to the distal end 54. It should be appreciated that the endotracheal tube 14 includes multiple inner cannulas 18 so that the inner cannula may be replaced as needed without replacement of the outer cannula 16.
[0034] Referring now to
[0035] In the illustrative embodiment, the seal 42 is formed from an elastomeric material such as, for example, silicone or rubber. As shown in
[0036] The manifold 32 includes an inner component 80 and an outer component 82 that is pivotally coupled to the inner component 80. As shown in
[0037] The outer component 82 includes a main body 92 that is positioned over the central body 84. The main body 92 has an outer cylindrical surface 94, and a transverse slot 96 that is defined in a section of the surface 94. As shown in
[0038] The outer component 82 includes a port 98 that extends outwardly from the main body 92. An opening 100 is defined in the port 98 and a cylindrical inner wall 102 extends inwardly from the opening 100 to define the inlet 36 of the manifold 32. As described above, the opening 100 is sized to receive the inner cannula 18. As shown in
[0039] The outer component 82 includes another port 110 that extends outwardly from the main body 92 traverse to the port 98. An opening 112 is defined in the port 110 and a cylindrical inner wall 114 extends inwardly from the opening 112 to define the inlet 38 of the manifold 32. As described above, the opening 112 is sized to receive the connection tube of the respirator machine 12 to connect the respirator machine to the conduit 10.
[0040] As shown in
[0041] Referring now to
[0042] In use, a medical professional or other user may insert an outer cannula 16 into a patient's mouth, down the patient's pharynx, and through the patient's glottis so that the distal opening 28 of the cannula 16 is positioned in the patient's trachea above the patient's carina (not shown). The user may then connect the conduit 10 with the manifold 32 in the respirator operational position shown in
[0043] When the medical professional or other user desires to insert an inner cannula 18 into the outer cannula 16, the medical professional may rotate the outer component 82 relative to the inner component 80 of the manifold 32. As the component 82 is rotated, the outlet port 86 of the outer component 82 is moved along the transverse slot 96 defined in the outer component 82 and the inlet 38 is moved out of alignment with the outlet 40. As shown in
[0044] While the disclosure has been illustrated and described in detail in the drawings and foregoing description, such an illustration and description is to be considered as exemplary and not restrictive in character, it being understood that only illustrative embodiments have been illustrated and described and that all changes and modifications that come within the spirit of the disclosure are desired to be protected.
[0045] There are a plurality of advantages of the present disclosure arising from the various features of the method, apparatus, and system described herein. It will be noted that alternative embodiments of the method, apparatus, and system of the present disclosure may not include all of the features described yet still benefit from at least some of the advantages of such features. Those of ordinary skill in the art may readily devise their own implementations of the method, apparatus, and system that incorporate one or more of the features of the present invention and fall within the spirit and scope of the present disclosure as defined by the appended claims.