Methods and devices for forming an auxiliary airway for treating obstructive sleep apnea

• US 8,678,008 B2
• Filed: 07/30/2008
• Issued: 03/25/2014
• Est. Priority Date: 07/30/2008
• Status: Active Grant

• Current Assignee: Ethicon Incorporated (Johnson & Johnson)
• Original Assignee: Ethicon Incorporated (Johnson & Johnson)
• Inventors: Rousseau, Robert A., Weadock, Kevin
• Primary Examiner(s): Bianco, Patricia
• Assistant Examiner(s): NELSON, KERI JESSICA
• Application Number:
  US12/182,402
• Publication Number:
  US 20100024830A1
• Time in Patent Office: 2,064 Days
• Field of Search: 128/848, 623/9, 623/1.11, 623/1.23, 623/1.27, 604/8, 604/9, 604 11- 18
• US Class Current: 128/848
• CPC Class Codes: A61F 2/20 Epiglottis; Larynxes; Tracheae combined with larynxes or for use therewith tracheae, bronchi per se A61F2/04 ; tracheostomy tubes A61M16/0465
• CPC Class Codes: A61F 2/82 Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents stent-grafts for tubular structures of the body other than blood vessels A61F2/04; stent-grafts for blood vessels A61F2/07; instruments specially adapted for placement or removal of stents or stent-grafts A61F2/95; for closing wounds, or holding wounds closed A61B17/04 - A61B17/115; dilators A61M29/00
• CPC Class Codes: A61F 2/94 Stents retaining their form, i.e. not being deformable, after placement in the predetermined place
• CPC Class Codes: A61F 2230/0008 elliptical or oval
• CPC Class Codes: A61F 2230/0013 Horseshoe-shaped, e.g. crescent-shaped, C-shaped, U-shaped
• CPC Class Codes: A61F 5/566 Intra-oral devices

Abstract

An auxiliary airway for treating obstructive sleep apnea is formed by implanting an elongated conduit beneath a pharyngeal wall of a pharynx. The elongated conduit has a proximal end in communication with a first region of the pharynx, a distal end in communication with a second region of the pharynx, and a section extending beneath the pharyngeal wall for bypassing an oropharynx region of the pharynx. The system includes a first opening in the pharyngeal wall in communication with a first opening in the elongated conduit, and a second opening in the pharyngeal wall in communication with a second opening in the elongated conduit. The system has a first anastomotic connector for coupling the first opening in the pharyngeal wall with the first opening in the conduit, and a second anastomotic connector for coupling the second opening in the pharyngeal wall with the second opening in the conduit.

Claims

1. A system for treating obstructive sleep apnea comprising:

an elongated conduit adapted to be implanted beneath a pharyngeal wall of a pharynx;

said elongated conduit having a proximal end adapted to be in communication with a first region of the pharynx and a distal end adapted to be in communication with a second region of the pharynx, wherein a section of said elongated conduit is adapted to extend beneath the pharyngeal wall for bypassing an oropharynx region of the pharynx, and wherein said elongated conduit includes a central lumen defining an inner surface extending along the length of said elongated conduit between the proximal and distal ends thereof; and

a mandrel insertable within the central lumen of said elongated conduit, said mandrel having an outer surface that contacts the inner surface of the central lumen of said elongated conduit along the length of said elongated conduit for supporting said elongated conduit when implanted beneath the pharyngeal wall, wherein said mandrel has a length that is greater than or equal to the length of said elongated conduit, and wherein the entire length of said elongated conduit is directly supported by said mandrel via contact between the outer surface of said mandrel and the inner surface of the central lumen of said elongated conduit.

2. The system as claimed in claim 1, wherein said elongated conduit has a first opening adjacent the proximal end thereof and a second opening adjacent the distal end thereof, said system further comprising:

the first opening adjacent the proximal end of said elongated conduit adapted to be in communication with the first opening in the pharyngeal wall; and

the second opening adjacent the distal end of said elongated conduit adapted to be in communication with the second opening in the pharyngeal wall.

3. The system as claimed in claim 2, wherein the first opening in the pharyngeal wall is in the nasopharynx region of the pharynx and the second opening in the pharyngeal wall is in the hypopharynx region of the pharynx.

4. The system as claimed in claim 2, further comprising:

a first anastomotic connector adapted for coupling the first opening in the pharyngeal wall with the first opening adjacent the proximal end of said elongated conduit; and

a second anastomotic connector adapted for coupling the second opening in the pharyngeal wall with the second opening adjacent the distal end of said elongated conduit.

5. The system as claimed in claim 2, wherein said elongated conduit is selected from the group consisting of biocompatible conduits, stents, polymer tubes, and tubes.

6. The system as claimed in claim 1 wherein said elongated conduit has a length of about 5-20 cm and a diameter of about 2-8 mm.

7. The system as claimed in claim 1, further comprising:

an applicator instrument including an outer sheath with a proximal end and a distal end, the distal end of said outer sheath having a central opening;

said mandrel is flexible and has a guide wire lumen extending along the length thereof;

a pusher insertable into said outer sheath for deploying said elongated conduit and said flexible mandrel from the central opening at the distal end of said outer sheath, said pusher having a proximal end, a distal end coupled with a proximal end of said flexible mandrel, and a central lumen extending between the proximal and distal ends of said pusher;

wherein said flexible mandrel is positioned within said elongated conduit with the guide wire lumen of said flexible mandrel aligned with the central opening at the distal end of said outer sheath and the central lumen of said pusher aligned with both the guide wire lumen of said flexible mandrel and the central opening at the distal end of said outer sheath.

8. The system as claimed in claim 7, wherein the central lumen of said pusher, the guide wire lumen of said flexible mandrel, and the central opening at the distal end of said outer sheath are aligned with one another, and wherein said system further comprises a guide wire insertable into the aligned central lumen of said pusher, the guide wire lumen of said flexible mandrel, and the central opening at the distal end of said outer sheath.

9. The system as claimed in claim 7, further comprising slits extending outwardly from the central opening at the distal end of said outer sheath, wherein said slits define flaps at the distal end of the outer sheath that are normally closed but that are adapted to flex away from one another to provide a larger opening for deploying said elongated conduit and said flexible mandrel.

10. The system as claimed in claim 7, wherein said flexible mandrel has an end having at least one eyelet formed therein and said system further comprises a tether secured to said eyelet for removing said flexible mandrel from said elongated conduit.

11. The system as claimed in claim 7, wherein said flexible mandrel is a modular structure comprising multiple parts that are adapted to be removed individually from inside said elongated conduit for reducing friction as said parts are removed from said elongated conduit.

12. An auxiliary airway for treating obstructive sleep apnea comprising:

an elongated conduit;

said elongated conduit having a first opening adapted to be in communication with a first region of a pharynx and a second opening adapted to be in communication with a second region of the pharynx, said elongated conduit including a central lumen having an inner surface that extends along the length of said elongated conduit; and

a mandrel disposed within said elongated conduit, said mandrel having an outer surface that contacts the inner surface of the central lumen of said elongated conduit along the length of said elongated conduit for supporting said elongated conduit when implanting said elongated conduit beneath the pharyngeal wall, wherein said mandrel has a length that is greater than or equal to the length of said elongated conduit, and wherein the entire length of said elongated conduit is directly supported by said mandrel via contact between the outer surface of said mandrel and the inner surface of the central lumen of said elongated conduit.

13. The auxiliary airway as claimed in claim 12, wherein the first region is the nasopharynx region of the pharynx and the second region is the hypopharynx region of the pharynx.

14. The auxiliary airway as claimed in claim 12, wherein said elongated conduit is adapted to be implanted beneath a pharyngeal wall.

15. The auxiliary airway as claimed in claim 14, wherein said elongated conduit is adapted to be implanted in a lateral section of the pharyngeal wall.

16. The auxiliary airway as claimed in claim 14, wherein said elongated conduit has a proximal end and a distal end, a proximal opening adjacent the proximal end thereof, and a distal opening adjacent the distal end thereof, and wherein the proximal opening is adapted to be in communication with a first opening in said pharyngeal wall located in the nasopharynx region of the pharynx and the distal opening is adapted to be in communication with a second opening in said pharyngeal wall located in the hypopharynx region of the pharynx.

17. The auxiliary airway as claimed in claim 16, further comprising a first anastomotic connector adapted for coupling the proximal opening of said elongated conduit and the first opening in said pharyngeal wall and a second anastomotic connector adapted for coupling the distal opening of said elongated conduit and the second opening in said pharyngeal wall.

18. The auxiliary airway as claimed in claim 14, wherein said elongated conduit has an intermediate section that is adapted to be implanted beneath the pharyngeal wall, and wherein the intermediate section of said elongated conduit is adapted for bypassing an oropharynx region of the pharynx.

19. The auxiliary airway as claimed in claim 12, wherein said elongated conduit comprises a biocompatible material.

20. The auxiliary airway as claimed in claim 12, wherein said elongated conduit is a structure selected from the group consisting of stents and tubes.

21. The auxiliary airway as claimed in claim 12, further comprising:

an elongated sheath having a proximal end and a distal end, the distal end of said elongated sheath having a central opening;

said mandrel is flexible and has a guide wire lumen extending along the length thereof;

a pusher insertable into said elongated sheath for deploying said elongated conduit and said flexible mandrel from the central opening at the distal end of said elongated sheath, said pusher having a proximal end, a distal end coupled with a proximal end of said flexible mandrel, and a central lumen extending between the proximal and distal ends of said pusher;

wherein said flexible mandrel is positioned within said elongated conduit so that the guide wire lumen of said flexible mandrel is in communication with the central opening at the distal end of said elongated sheath, and the central lumen of said pusher is aligned with both the guide wire lumen of said flexible mandrel and the central opening at the distal end of said outer sheath.

22. The auxiliary airway as claimed in claim 21, wherein the central lumen of said pusher, the guide wire lumen of said flexible mandrel, and the central opening at the distal end of said outer sheath are aligned with one another, and wherein said system further comprises a guide wire insertable into the aligned central lumen of said pusher, the guide wire lumen of said flexible mandrel, and the central opening at the distal end of said outer sheath.

23. The auxiliary airway as claimed in claim 21, further comprising slits extending outwardly from the central opening at the distal end of said elongated sheath, wherein said slits define flaps at the distal end of the elongated sheath that are normally closed but that are adapted to flex away from one another to provide a larger opening for deploying said elongated conduit and said flexible mandrel.

24. A system for treating obstructive sleep apnea comprising:

an applicator instrument including a flexible outer sheath having a proximal end and a distal end, the distal end of said flexible outer sheath having a central opening;

a flexible stent disposed within said flexible outer sheath and adjacent the distal end of said flexible outer sheath, said flexible stent being adapted for implantation beneath a pharyngeal wall of a pharynx, wherein said flexible stent has a proximal end, a distal end, and a central lumen extending between the proximal and distal ends thereof;

a pusher insertable into said flexible outer sheath, said pusher having a proximal end, a distal end, and a central lumen extending between the proximal and distal ends thereof; and

a flexible mandrel insertable within the central lumen of said flexible stent for supporting said flexible stent, said flexible mandrel having a guide wire lumen extending along the length thereof, wherein said flexible mandrel is positioned within said flexible stent so that the guide wire lumen of said flexible mandrel is in communication with the central opening at the distal end of said outer sheath, and the central lumen of said pusher is aligned with both the guide wire lumen of said flexible mandrel and the central opening at the distal end of said flexible outer sheath, the mandrel having an outer surface that continuously contacts an inner surface of the central lumen of said flexible stent, wherein the length of said mandrel is greater than or equal to the length of said flexible stent, and wherein the entire length of said flexible stent is directly supported by said mandrel via contact between the outer surface of said mandrel and the inner surface of the central lumen of said flexible stent.