MEDICAL DEVICE MECHANICAL PUMP

• US 20110319861A1
• Filed: 06/22/2011
• Published: 12/29/2011
• Est. Priority Date: 06/29/2010
• Status: Abandoned Application

• Current Assignee: Animas Corporation (Johnson & Johnson)
• Original Assignee: Animas Corporation (Johnson & Johnson)
• Inventors: Wilk, Robert
• Application Number:
  US13/166,100
• Publication Number:
  US 20110319861A1
• Time in Patent Office: Days
• US Class Current: 604/500
• CPC Class Codes: A61M 2005/14252 with needle insertion means
• CPC Class Codes: A61M 2205/3569 sublocal, e.g. between console and disposable
• CPC Class Codes: A61M 2205/3592 using telemetric means, e.g. radio or optical transmission
• CPC Class Codes: A61M 2205/6054 Magnetic identification systems
• CPC Class Codes: A61M 2230/201 Glucose concentration
• CPC Class Codes: A61M 5/14224 Diaphragm type
• CPC Class Codes: A61M 5/1424 Manually operated pumps
• CPC Class Codes: A61M 5/14248 of the skin patch type
• CPC Class Codes: A61M 5/38 using hydrophilic or hydrophobic filters

Abstract

A medical device pump with a housing with a compartment for removably receiving a cartridge containing a therapeutic agent, a conduit configured to operatively provide a fluid flow path for therapeutic agent to exit from the cartridge, a user activated delivery button, a trigger mechanism, and a mechanical pump mechanism. The trigger mechanism, user activated delivery button and mechanical pump mechanism of the medical device pump are configured such that the trigger mechanism is activated by a user fully activating the user activated delivery button. Moreover, such full activation generates mechanical power employed by, and sufficient for, the mechanical pump mechanism to pump a predetermined volume of therapeutic agent from the cartridge and through the fluid flow path.

Claims

1. A medical device pump comprising:

a housing with a compartment therein, the compartment configured for accommodating a cartridge containing a therapeutic agent;

a conduit configured to operatively provide a fluid flow path for therapeutic agent to exit from the cartridge;

a user activated delivery button;

a trigger mechanism, and

a mechanical pump mechanism,

wherein the trigger mechanism, user activated delivery button and mechanical pump mechanism are configured such that the trigger mechanism is activated by a user fully activating the user activated delivery button and such full activation generates mechanical power employed by, and sufficient for, the mechanical pump mechanism to pump a predetermined volume of therapeutic agent from the cartridge into the fluid flow path.

2. The medical device pump of claim 1 wherein the trigger mechanism is configured such that partial activation of the user activated delivery button by a user is insufficient to activate the trigger mechanism to generate mechanical power for the mechanical pump mechanism and, therefore, results in zero volume of therapeutic agent being pumped by the mechanical pump mechanism.

3. The medical device pump of claim 1 wherein the trigger mechanism is configured such that once a user has fully activated the user activated delivery button and the trigger mechanism has been activated, the user activated delivery button must be fully released before the trigger mechanism can be again activated.

4. The medical device pump of claim 1 further including:

a user activated safety release button configured such that pressing of the safety release button by a user enables the user activated delivery button to be fully activated by a user.

5. The medical device pump of claim 1 wherein the housing is configured for attachment to an adhesive patch platform.

6. The medical device pump of claim 1 further including a bubble trap disposed in the fluid flow path, the bubble trap configured to prevent inadvertent bubbles in the cartridge from reaching the mechanical pump mechanism.

7. The medical device pump of claim 1 further including:

a one-way communication means, the one-way communication means configured to operatively send a communication signal from the medical device pump to an associated meter configured to detect the communication signal.

8. The medical device pump of claim 7 wherein the one-way communication means includes at least one Radio Frequency Identification (RFID) tag.

9. The medical device pump of claim 7 wherein full activation of the user activated delivery button interrupts the sending of a communication signal from the one-way communication means to the associated meter.

10. The medical device pump of claim 7 wherein full activation of the user activated delivery button initiates the sending of a communication signal from the one-way communication means to the associated meter.

11. The medical device pump of claim 7 wherein the one-way communication means is configured to be externally powered by the associated meter.

12. The medical device pump of claim 7 wherein the one-way communication means includes at least two RFID tags, and

wherein full activation of the user activated delivery button interrupts the sending of a communication signal from one of the at least two RFID tags to the associated meter, and

wherein full activation of the user activated delivery button also initiates the sending of a communication signal from another of the at least two RFID tags to the associated meter.

13. The medical device pump of claim 7 wherein the communication signal enables the associated meter to create a time record of therapeutic agent pumped by the mechanical pump mechanism.

14. The medical device pump of claim 1 wherein the compartment of the housing is configured to accommodate a cartridge in the form of a user-filled reservoir.

15. The medical device pump of claim 1 wherein the compartment of the housing compartment is configured to removably accommodate the cartridge.

16. The medical device pump of claim 1 wherein the compartment of the housing is configured to accommodate a disposable pre-filled cartridge.

17. The medical device pump of claim 1 wherein the medical device is configured for multiple full activations of the user activated delivery button.

18. The medical device pump of claim 1 wherein the conduit and mechanical pump mechanism have a predetermined compliance that is sufficiently low that the user activated delivery button cannot be fully activated by a user in the event of an operative occlusion in at least one of the conduit and mechanical pump mechanism.

19. A method for transcutaneously delivering a therapeutic agent to a patient comprising:

inserting a cartridge pre-filled with a therapeutic agent into a cartridge compartment of a medical device pump;

priming the medical device pump; and

transcutaneously delivering the therapeutic agent to a patient by action of the patient fully activating a user activated delivery button of the medical device pump, thus activating a trigger mechanism of the medical device pump and generating mechanical power employed by, and sufficient for, a mechanical pump mechanism of the medical device pump to pump a predetermined volume of therapeutic agent from the cartridge and into a fluid flow path of the medical device pump.

20. The method of claim 19 wherein the therapeutic agent is insulin.

21. The method of claim 19 further including the step of:

attaching the medical device pump to a disposable infusion set prior to the delivering step.

22. The method of claim 20 wherein the attaching step includes attaching the medical device pump to an adhesive patch platform of a disposable infusion set.

23. The method of claim 19 further including, prior to the delivering step, the step of:

pressing, by the patient, of a user activated safety release button of the medical device pump, the user activated safety release button configured such that pressing of the safety release button by a user enables the user activated delivery button to be activated by a user.

24. The method of claim 19 further including, following the delivering step, the step of:

releasing fully the user activated delivery button by the patient; and

subsequently

transcutaneously delivering a further predetermined volume of therapeutic agent to the patient by action of the patient again fully activating the user activated delivery button of the medical device pump, thus activating the trigger mechanism of the medical device pump and generating mechanical power employed by, and sufficient for, the mechanical pump mechanism of the medical device pump to again pump the predetermined volume of therapeutic agent from the cartridge and into the fluid flow path of the medical device pump.

25. The method of claim 19 further including the step of:

sending a communication signal from the medical device pump to an associated meter using a one-way communication means of the medical device pump.

26. The method of claim 25 wherein during the sending step, full activation of the user activated delivery button interrupts the sending of the communication signal from the one-way communication means to the associated meter.

27. The method of claim 25 wherein the sending step is initiated by the patient'"'"'s full activation of the user activated delivery button.

28. The method of claim 25 wherein during the sending step, the one-way communication means is externally powered by the associated meter.

29. The method of claim 19 wherein the fluid flow path includes a bubble trap and the transcutaneously delivering step includes subcutaneously delivering the therapeutic agent.

30. The method of claim 19 wherein the fluid flow path includes a bubble trap and the transcutaneously delivering step includes intradermally delivering the therapeutic agent.

31. A medical device kit comprising:

a medical device pump that includes;

a housing with a compartment therein, the compartment configured for removably receiving a cartridge containing a therapeutic agent;

a conduit configured to operatively provide a fluid flow path for therapeutic agent to exit from the cartridge;

a user activated delivery button;

a trigger mechanism, and

a mechanical pump mechanism,

wherein the trigger mechanism, user activated delivery button and mechanical pump mechanism are configured such that the trigger mechanism is activated by a user fully activating the user activated delivery button and such full activation generates mechanical power employed by, and sufficient for, the mechanical pump mechanism to pump a fixed volume of therapeutic agent from the cartridge into the fluid flow path; and

a meter configured to detect a communication signal from the medical device pump.

32. The medical device kit of claim 31 further including an adhesive patch platform and wherein the housing is configured for removable attachment to the adhesive patch platform.

33. The medical device kit of claim 32 wherein the adhesive patch platform includes a flexible cannula inserter and a flexible cannula.

34. The medical device kit of claim 33 wherein the trigger mechanism, user activated delivery button and mechanical pump mechanism are configured such that the trigger mechanism is activated by a user fully activating the user activated delivery button and such full activation generates mechanical power employed by, and sufficient for, the mechanical pump mechanism to pump a predetermined volume of therapeutic agent from the cartridge, through the fluid flow path into the flexible cannula.

35. The medical device kit of claim 31 wherein the therapeutic agent is insulin.

36. The medical device kit of claim 31 further including a cartridge containing a therapeutic agent.

37. The medical device kit of claim 36 wherein the cartridge is configured to be pre-filled prior to being provided to the user.

38. The medical device kit of claim 36 wherein the cartridge is configured to be filled by a user of the kit.

39. The medical device kit of claim 31 wherein the trigger mechanism is configured such that partial activation of the user activated delivery button by a user is insufficient to activate the trigger mechanism to generate mechanical power for the mechanical pump mechanism and, therefore, results in zero volume of therapeutic agent being pumped by the mechanical pump mechanism.

40. The medical device kit of claim 31 wherein the trigger mechanism is configured such that once a user has fully activated the user activated delivery button and the trigger mechanism has been activated, the user activated delivery button must be fully released before the trigger mechanism can be again activated.

41. The medical device kit of claim 31 further including:

a user activated safety release button configured such that pressing of the safety release button by a user provides for the user activated delivery button to be activated by a user.

42. The medical device kit of claim 31 wherein the housing is configured for attachment to an adhesive patch platform.

43. The medical device kit of claim 31 further including a bubble trap disposed in the fluid flow pathway, the bubble trap configured to prevent inadvertent bubbles in the cartridge from reaching the mechanical pump mechanism.

44. The medical device kit of claim 31 further including:

a one-way communication means, the one-way communication means configured to operatively send a communication signal from the medical device pump to the associated meter.

45. The medical device kit of claim 44 wherein the one-way communication means includes at least one Radio Frequency Identification (RFID) tag.

46. The medical device kit of claim 44 wherein full activation of the user activated delivery button interrupts the sending of a communication signal from the one-way communication means to the associated meter.

47. The medical device kit of claim 44 wherein full activation of the user activated delivery button initiates the sending of a communication signal from the one-way communication means to the associated meter.

48. The medical device kit of claim 44 wherein the one-way communication means is configured to be externally powered by the associated meter.

49. The medical device kit of claim 44 wherein the one-way communication means includes at least two RFID tags, and

wherein full activation of the user activated delivery button interrupts the sending of a communication signal from one of the at least two RFID tags to the associated meter, and

wherein full activation of the user activated delivery button initiates the sending of a communication signal from another of the at least two RFID tags to the associated meter.

50. A hand-held medical fluid delivery device comprising:

a housing with a compartment therein, the compartment configured for removably receiving a cartridge containing a therapeutic agent;

a conduit configured to operatively provide a fluid flow path for therapeutic agent to exit from the cartridge;

a user activated delivery button,

a mechanical pump mechanism, and

a one-way communication means, the one-way communication means configured to operatively send a communication signal from the hand-held medical fluid delivery device to an associated meter configured to detect the communication signal,

wherein the user activated delivery button and mechanical pump mechanism are configured such that a user fully activating the user activated delivery button generates mechanical power employed by, and sufficient for, the mechanical pump mechanism to pump a predetermined volume of therapeutic agent from the cartridge into the fluid flow path.

51. The hand-held medical fluid delivery device of claim 50 wherein the conduit and fluid path are configured to subcutaneously deliver therapeutic agent to the user.

52. The hand-held medical fluid delivery device of claim 50 wherein the conduit and fluid path are configured to intradermally deliver therapeutic agent to the user.

53. The hand-held medical fluid delivery device of claim 50 further including a bubble trap disposed in the fluid flow path, the bubble trap configured to prevent inadvertent bubbles in the cartridge from reaching the mechanical pump mechanism.

54. The hand-held medical fluid delivery device of claim 50 further including a priming sensor configured to detect priming and distinguish priming from subsequent fluid delivery.

55. A medical fluid delivery device comprising:

a housing with a compartment therein, the compartment configured for accommodating a therapeutic agent reservoir;

a conduit configured to operatively provide a fluid flow path for therapeutic agent to exit from the reservoir;

a mechanical pump mechanism; and

a bubble trap disposed in the fluid flow path, the bubble trap configured to prevent inadvertent bubbles in the cartridge from reaching the mechanical pump mechanism.

56. The medical fluid delivery device of claim 55 wherein the conduit and fluid path are configured to subcutaneously deliver therapeutic agent to the user.

57. The medical fluid delivery device of claim 55 wherein the conduit and fluid path are configured to intradermally deliver therapeutic agent to the user.