Medication infusion set

• US 7,303,543 B1
• Filed: 12/03/2004
• Issued: 12/04/2007
• Est. Priority Date: 12/03/2004
• Status: Active Grant

• Current Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Inventors: Kavazov, Julian D., Griffin, Christopher G., Moberg, Sheldon B, Holecek, Arin N., Kovelman, Paul H., Maule, Susie E.
• Primary Examiner(s): Lucchesi; Nicholas D.
• Assistant Examiner(s): KOHARSKI, CHRISTOPHER
• Application Number:
  US11/003,225
• Time in Patent Office: 1,096 Days
• Field of Search: 604/164.01, 604/158, 604/174, 604/93.01, 604/533, 604/192, 604263-264, 604/177, 604/164.04
• US Class Current: 604/93.01
• CPC Class Codes: A61M 2005/1587 suitable for being connected to an infusion line after insertion into a patient
• CPC Class Codes: A61M 2025/024 having a clip or clamp system
• CPC Class Codes: A61M 2025/0266 using pads, patches, tapes or the like
• CPC Class Codes: A61M 2025/028 having a mainly rigid support structure
• CPC Class Codes: A61M 25/02 Holding devices, e.g. on the body
• CPC Class Codes: A61M 5/158 Needles for infusions; Accessories therefor, e.g. for inserting infusion needles, or for holding them on the body

Abstract

An infusion set is provided for use in delivering fluid through a cannula, which is housed on a cannula housing, to a selected subcutaneous infusion site on a patient. The fluid is generally a medication, for example, insulin. The cannula is in fluid communication with a fluid passageway surrounded by a projection on the cannula housing that includes one or more rail-like extensions acting as connection guides. A connector connects the cannula housing to a fluid delivery system, such as an infusion pump. The connector includes a connecting needle and one or more guide arms that slide over the rail-like extensions to guide the needle into the self-sealing septum. The connector includes one or more locking arms, with barbs at the end, to connect with one or more recesses that are provided in the cannula housing.

Claims

1. An infusion set for subcutaneous administration of a fluid, comprising:

a cannula housing including

a projection,

a passageway formed through the projection,

a first convex-shaped guide rail formed on a first external surface of the projection;

a second convex-shaped guide rail formed on a second external surface of the projection, and

a cannula adapted to be placed into the skin of a patient and in fluid communication with the passageway in the projection; and

a connector adapted to be connected to the cannula housing, the connector including

a first guide arm having a first concave portion adapted to slide over the first convex-shaped guide rail,

a second guide arm having a second concave portion adapted to slide over the second convex-shaped guide rail, and

a first locking arm, wherein the first locking arm includes a first barb, and wherein the cannula housing further includes a first recess adapted to receive the first barb.

2. The infusion set of claim 1, wherein the connector further includes a second locking arm, wherein the second locking arm includes a barb, and wherein the cannula housing further includes a second recess adapted to receive the second barb.

3. The infusion set of claim 1, wherein the connector is reversible.

4. The infusion set of claim 1, wherein the first guide rail and the second guide rail are each substantially triangular shaped.

5. The infusion set of claim 1, wherein the fluid is insulin.

6. The infusion set of claim 1, further comprising fluid tubing connected to the connector and adapted to be connected to a fluid delivery device.

7. The infusion set of claim 6, wherein the fluid delivery device is an infusion pump.

8. The infusion set of claim 1, wherein the connector is composed of polycarbonate.

9. The infusion set of claim 1, wherein the cannula housing is composed of polycarbonate.

10. The infusion set of claim 1, wherein the connector is composed of polypropylene.

11. The infusion set of claim 1, wherein the cannula housing is composed of polypropylene.

12. The infusion set of claim 1, further comprising a self-sealing septum at the end of the fluid passageway opposite the cannula.

13. The infusion set of claim 12, wherein the self-sealing septum is a substantially beer-barrel shaped septum.

14. The infusion set of claim 12, wherein the self-sealing septum is a substantially disc shaped septum.

15. The infusion set of claim 12, wherein the connector further includes a the connecting needle mounted thereon and adapted to pierce the self-sealing septum.

16. The infusion set of claim 15, wherein the first guide arm and the second guide arm extend past the tip of the connecting needle.

17. The infusion set of claim 1, wherein the cannula housing further includes a needle guide adapted to guide the connecting needle into the fluid passageway.

18. The infusion set of claim 17, wherein the needle guide is metal.

19. The infusion set of claim 1, wherein the cannula housing further includes a base and adhesive on the base adapted to adhere the base to a skin surface of the patient.

20. The infusion set of claim 19, wherein the adhesive is on a patch.

21. The infusion set of claim 20, wherein the patch is composed of colored material.

22. The infusion set of claim 21, wherein the color of the colored material changes appearance over a predetermined period of time.

23. The infusion set of claim 1, wherein the projection is substantially cylindrical.

24. The infusion set of claim 1, wherein the first locking arm is distinct from the first and second guide arms.

25. The infusion set of claim 1, wherein at least a portion of the projection is not covered by the first and second guide arms when the cannula housing is connected to the connector.

26. The infusion set of claim 1, wherein the projection contacts the first guide arm only at the first concave portion when the connector is connected to the cannula housing.

27. The infusion set of claim 1, wherein the projection contacts the second guide arm only at the second concave portion when the connector is connected to the cannula housing.

28. The infusion set of claim 1, wherein the first concave portion of the first guide arm and the second concave portion of the second guide arm face each other.

29. A cannula housing for subcutaneous administration of a fluid, comprising:

a projection,

a first convex-shaped guide rail formed on a first external surface of the projection and adapted to mate with a first concave portion on a first guide arm on a connecting device,

a second convex-shaped guide rail formed on a second external surface of the projection and adapted to mate with a second concave portion on a second guide arm on the connecting device;

a first recess adapted to receive a first barb on a first locking arm that is included on the connecting device,

a passageway formed through the projection; and

a cannula adapted to be placed into the skin of a patient and in fluid communication with the passageway in the projection.

30. The cannula housing of claim 29, wherein the connecting device is a connector adapted to connect fluid from a fluid infusion device.

31. The cannula housing of claim 29, further comprising a second recess adapted to receive a second barb on a second locking arm that is included on the connecting device.

32. The cannula housing of claim 29, wherein the fluid is insulin.

33. The cannula housing of claim 29, wherein the cannula housing is composed of polycarbonate.

34. The cannula housing of claim 29, further comprising a self-sealing septum at the end of the fluid passageway opposite the cannula.

35. The cannula housing of claim 34, wherein the self-sealing septum is a substantially beer-barrel shaped septum.

36. The cannula housing of claim 34, wherein the self-sealing septum is a substantially disc shaped septum.

37. The cannula housing of claim 34, wherein the self-sealing septum is adapted to be pierced by a connecting needle mounted on the connector.

38. The cannula housing of claim 37, wherein the first guide arm and the second guide arm extend past the tip of the connecting needle.

39. The cannula housing of claim 29, wherein the cannula housing further includes a base and adhesive on the base adapted to adhere the base to a skin surface of the patient.

40. The cannula housing of claim 29, wherein the projection is substantially cylindrical.

41. The cannula housing of claim 29, wherein at least a portion of the projection is not covered by the first and second guide arms when the cannula housing is connected to the connecting device.

42. The cannula housing of claim 29, wherein projection contacts the first guide arm only at the first concave portion when the connecting device is connected to the cannula housing.

43. The cannula housing of claim 29, wherein projection contacts the second guide arm only at the second concave portion when the connecting device is connected to the cannula housing.

44. The cannula housing of claim 29, wherein the first concave portion of the first guide arm and the second concave portion of the second guide arm face each other.

45. An infusion set for subcutaneous administration of a fluid, comprising:

a cannula housing including

a projection,

a passageway formed through the projection,

a first guide rail formed on a first external surface of the projection;

a second guide rail formed on a second external surface of the projection,

a cannula adapted to be placed into the skin of a patient and in fluid communication with the passageway in the projection; and

a connector adapted to be connected to the cannula housing, the connector including

a first guide arm having a first guide portion adapted to slide over the first guide rail,

a second guide arm having a second guide portion adapted to slide over the second guide rail, and

a first locking arm, wherein the first locking arm includes a first barb, and wherein the cannula housing further includes a first recess adapted to receive the first barb,

wherein one of the first guide rail and the first guide portion is convex and the other is concave, and wherein one of the second rail and the second guide portion is convex and the other is concave.

46. The infusion set of claim 45, wherein the first guide rail is convex and the first guide portion is concave.

47. The infusion set of claim 46, wherein the second guide rail is convex and the first guide portion is concave.

48. The infusion set of claim 45, wherein the projection contacts the first guide arm only at the first guide portion when the connector is connected to the cannula housing.

49. The infusion set of claim 45, wherein the first guide rail and the second guide rail are each substantially triangular shaped.

50. The infusion set of claim 45, wherein the cannula housing further includes a needle guide adapted to guide the connecting needle into the fluid passageway and the first guide arm and the second guide arm extend past the tip of the connecting needle.

51. The infusion set of claim 45, wherein the projection is substantially cylindrical.

52. An infusion set for subcutaneous administration of a fluid, comprising:

a cannula housing including

a projection,

a passageway formed through the projection,

a first guide rail formed on a first external surface of the projection;

a second guide rail formed on a second external surface of the projection,

a cannula adapted to be placed into the skin of a patient and in fluid communication with the passageway in the projection; and

a connector adapted to be connected to the cannula housing, the connector including

a first guide arm having a first guide portion adapted to slide over the first guide rail,

a second guide arm having a second guide portion adapted to slide over the second guide rail,

wherein one of the first guide rail and the first guide portion is convex and the other is concave, wherein one of the second rail and the second guide portion is convex and the other is concave, and wherein the projection contacts the first guide arm only at the first guide portion when the connector is connected to the cannula housing.

53. The infusion set of claim 52, wherein the first guide rail is convex and the first guide portion is concave.

54. The infusion set of claim 52, wherein the second guide rail is convex and the first guide portion is concave.

55. The infusion set of claim 52, wherein the projection contacts the second guide arm only at the second guide portion when the connector is connected to the cannula housing.

56. The infusion set of claim 52, wherein the connector further includes a first locking arm, wherein the first locking arm includes a first barb, and wherein the cannula housing further includes a first recess adapted to receive the first barb.

57. The infusion set of claim 52, wherein the first guide rail and the second guide rail are each substantially triangular shaped.

58. The infusion set of claim 52, wherein the cannula housing further includes a needle guide adapted to guide the connecting needle into the fluid passageway and the first guide arm and the second guide arm extend past the tip of the connecting needle.

59. The infusion set of claim 52, wherein the projection is substantially cylindrical.