Nasal cannula, conduit and securement system

• US 10,238,828 B2
• Filed: 10/18/2011
• Issued: 03/26/2019
• Est. Priority Date: 10/18/2010
• Status: Active Grant

• Current Assignee: Fisher & Paykel Healthcare Limited
• Original Assignee: Fisher & Paykel Healthcare Limited
• Inventors: O'Connor, Mark Thomas, Eaton-Evans, Jimmy Edward, Duthie, Neil Gray, Laing, Brent Ian, Korner, Steven Charles, Gulliver, Laurence, Zhang, Puqing, Niccol, Andrew Grant, Irving, Charles William Douglas, White, Craig Karl, Hopkins, Caroline Geraldine, Ronayne, Michael Paul, Spence, Callum James Thomas
• Primary Examiner(s): Ditmer, Kathryn E
• Application Number:
  US13/880,036
• Publication Number:
  US 20140000626A1
• Time in Patent Office: 2,716 Days
• Field of Search: None
• CPC Class Codes: A61M 16/0666 Nasal cannulas or tubing devices for improving normal breathing through the nose A61F5/08; nose filters A62B23/06; outside holding devices A61M25/02
• CPC Class Codes: A61M 16/0683 Holding devices therefor
• CPC Class Codes: A61M 16/0688 by means of an adhesive
• CPC Class Codes: A61M 16/0875 Connecting tubes
• CPC Class Codes: A61M 2205/0216 Materials providing elastic properties, e.g. for facilitating deformation and avoid breaking
• CPC Class Codes: A61M 2205/0238 the material being a coating or protective layer
• CPC Class Codes: A61M 2205/7536 allowing gas passage, but preventing liquid passage, e.g. liquophobic, hydrophobic, water-repellent membranes
• CPC Class Codes: A61M 2207/10 Device therefor
• CPC Class Codes: A61M 2210/0618 Nose

Abstract

Medical breathing tubes have a tubular body that defines a lumen extending between open terminal ends of the tubular body. An internal form is enclosed within the lumen and supportive of the tubular body. The internal form may be a coated encapsulated internal form where the coating secures the internal form to the tubular body. The internal form may provide for a series of alternative crests and troughs of the tubular body. A patient interface and/or a securement system may be attached to the tubular body.

Claims

1. An interface assembly comprising:

a user interface comprising a nasal cannula arrangement comprising;

at least one nasal prong, said prong having a gas outlet adapted to be inserted into a user'"'"'s nare and a gas inlet fluidly connected to the gas outlet,

a patient facing rear surface extending generally laterally outward from the at least one nasal prong, and a lip extending about at least a portion of a perimeter of the rear surface; and

a securement system for at least one of the user interface and a component associated with the user interface, the securement system comprising a two-part releasable attachment arrangement, the two-part releasable attachment arrangement comprising;

a dermal patch and a user interface patch,

the dermal patch comprising a patient side and an interface side,

the patient side of the dermal patch configured to attach to the skin of a user,

the interface side of the dermal patch comprising a first part of the two-part releasable attachment arrangement, and

the user interface patch comprising an interface side and patient side,

the patient side of the user interface patch comprising a second part of the two-part releasable attachment arrangement, the second part being complementary to the first part,

the interface side of the user interface patch being attachable to at least one of the user interface and the component associated with the user interface,

the rear surface of the user interface configured for receiving or retaining the user interface patch such that the user interface patch is capable of being releasably attachable or connectable to, or with, the dermal patch and the lip at least partially bounds the user interface patch, wherein the dermal patch is configured to be affixed to a user'"'"'s face.

2. The interface assembly as claimed in claim 1, wherein the interface includes one or a pair of nasal prongs.

3. The interface assembly as claimed in claim 1, wherein the lip is a barrier.

4. The interface assembly as claimed in claim 1, wherein the lip is deformable.

5. The interface assembly as claimed in claim 1, wherein the lip is a continuous lip extending about the perimeter of the rear surface.

6. The interface assembly as claimed in claim 1, wherein the lip is a series of one or more separate lips.

7. The interface assembly as claimed in claim 1, wherein, in use, the lip substantially forms a fluid (e.g. liquid) seal, or barrier to fluid, between the rear surface of the nasal cannula arrangement and a cannula-facing surface of the user interface patch.

8. The interface assembly as claimed in claim 1, wherein the rear surface is contoured and configured to conform to a user'"'"'s face.

9. The interface assembly as claimed in claim 1, wherein the lip is hydrophobic.

10. The interface assembly as claimed in claim 1, wherein the lip comprises at least one outer perimeter lip portion and at least one inner perimeter lip portion, each of said lip portions provided for contacting with a user'"'"'s face.

11. The interface assembly as claimed in claim 1, wherein the first part of the two-part releasable attachment arrangement has a first of a hook and a loop, and the second part of the two-part releasable attachment arrangement has a second of the hook and the loop, such that the first and second parts are releasably attachable to each other.

12. The interface assembly as claimed in claim 11, wherein the first part of the two-part releasable attachment arrangement occupies less than about 90% of the interface side of the dermal patch.

13. The interface assembly as claimed in claim 1, wherein the first part of the two-part releasable attachment arrangement is adhered or adherable to the interface side of the dermal patch with an adhesive.

14. The interface assembly as claimed in claim 1, wherein the patient side of the dermal patch has a dermatologically sensitive adhesive capable of adhering the dermal patch to a user'"'"'s skin.

15. The interface assembly as claimed in claim 1, wherein the securement system is configured to receive and/or secure the nasal cannula arrangement and associated tubing, the tubing configured to extend from one or both sides of a user'"'"'s face.

16. The interface assembly as claimed in claim 1, wherein the securement system is configured for use with an infant or neonatal infant.

17. The interface assembly as claimed in claim 1, wherein the first part of the two-part releasable attachment arrangement includes a substrate portion secured to, or for securing to, the dermal patch.

18. The interface assembly as claimed in claim 17, wherein the substrate portion includes at least one slit or at least one slot with areas of the substrate portion separated by the slit or slot.

19. The interface assembly as claimed in claim 18, wherein the slits and/or slots are arranged in the substrate portion such that a first set of at least one set of slits or slots extends into the substrate portion from a first edge of the substrate portion and a second set of slits or slots extends into the substrate portion from a second edge of the substrate portion, the second edge opposing the first edge, the slits or slots of the first set being interleaved with the slits or slots of a second set such that a path along the substrate portion from a first end to a second end without crossing the slits or slots must follow a zigzag or serpentine path much longer than a direct line between the first end and the second end.

20. The interface assembly as claimed in claim 18, wherein the slits or slots are arranged in a herring bone pattern extending in from at least one edge of the substrate portion.

24. The interface assembly as claimed in claim 18, wherein the slit or slots divide the substrate portion into a plurality of islands, each joined to an adjacent island or islands by a narrow bridge.

25. The interface assembly as claimed in claim 17, wherein the substrate portion is divided into separated portions by a serpentine slit or slot.

26. The interface assembly as claimed in claim 17, wherein the substrate portion is divided into portions by a spiral slit or slot.

27. The interface assembly as claimed in claim 17, wherein the substrate portion is divided into sub-portions by slits or slots arranged on substantially concentric circles.

28. The interface assembly as claimed in claim 17, wherein the substrate portion covers at least 70% of the dermal patch.

29. The interface assembly as claimed in claim 1, further comprising a tube connected to the user interface providing at least a part of a breathing circuit for a user of the user interface, wherein the tube comprises:

a tubular body defining a lumen extending between open terminal ends of the tubular body,

an internal form enclosed within the lumen and supportive of the tubular body, and

a coating encapsulating the internal form, the coating securing the internal form to the tubular body.

30. The interface assembly as claimed in claim 29, wherein the tube is a medical breathing tube.

31. The interface assembly as claimed in claim 29, wherein the coating and the tubular body of the tube are plastically welded together along the tube.

32. The interface assembly as claimed in claim 29, wherein an outer-most perimeter of the internal form defines a plurality of alternating crests and troughs along a length of the tubular body.

33. The interface assembly as claimed in claim 29, wherein the internal form is one of, or a combination of, a helical spring or a helically wound element, a helically wound skeleton or a helically wound rib, annular disks, rings, or a plurality of discrete supports interconnected or inter-connectable by one or more connecting links.

34. The interface assembly as claimed in claim 29, herein the tubular body is a breathable tube, or is formed of or from a breathable material.

35. The interface assembly as claimed in claim 29, wherein the internal form is a helically wound element having a pitch between adjacent turns of about 1 mm to about 1.5 mm.

36. The interface assembly as claimed in claim 29, wherein the internal form is a helically wound element, the helically wound element having a diameter of about 0.1 mm to about 0.4 mm.

37. The interface assembly as claimed in claim 29, wherein the internal form is a conductive wire suitable for heating or sensing a property of gases within the tube.

38. The interface assembly as claimed in claim 29, wherein the internal form is a helically wound element having a pitch and wherein a ratio of pitch of the internal form to an outer diameter of the internal form is about 0.10 to about 0.50.

39. The interface assembly as claimed in claim 38, wherein the ratio of pitch of the internal form to an outer diameter of the internal form is about 0.28.

21. The interface assembly as claimed in 18, wherein the substrate portion includes a plurality of slits or slots or both which together divide the substrate portion into a serpentine body.

22. The interface assembly as claimed in claim 21, wherein at least one of the slits or slots of the plurality of slits or slots is curved.

23. The interface assembly as claimed in claim 21, wherein a plurality of the slits or slots is curved and the curved slits or slots are arranged substantially parallel.