Infusion monitoring device system and method

• US 20060276748A1
• Filed: 05/17/2006
• Published: 12/07/2006
• Est. Priority Date: 05/17/2005
• Status: Abandoned Application

• Current Assignee: Infussafe LLC
• Original Assignee: Infussafe LLC
• Inventors: Durand, Kevin, Grinnell, Charles
• Application Number:
  US11/436,110
• Publication Number:
  US 20060276748A1
• Time in Patent Office: Days
• US Class Current: 604/131
• CPC Class Codes: A61M 2005/1404 Keep vein-open rate [KVO], i.e. low flow rate
• CPC Class Codes: A61M 2005/1588 having means for monitoring, controlling or visual inspection, e.g. for patency check, avoiding extravasation
• CPC Class Codes: A61M 2205/18 with alarm
• CPC Class Codes: A61M 2205/52 with memories providing a history of measured variating parameters of apparatus or patient
• CPC Class Codes: A61M 2205/583 by visual feedback
• 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

The present invention provides a manual or automated device, system, and method for the monitoring and administration of fluids into a patient. The invention determines if a proper infusion site is being maintained by stopping the infusion fluid, creating a negative pressure differential between the device and the patient, and observing either manually or automatically the fluid being drawn into the device. The presence or absence of blood in the device is an indication of a failed or faulty infusion site depending on the condition being monitored. The system may also be used to inspect the patient'"'"'s blood for certain characteristics, and to monitor the characteristics of the infusate being delivered to the patient. The invention may be used for either intermittent or continuous injection and may be used separately of other patient care devices, or integrated into or with them.

Claims

1. An infusion monitoring device, for monitoring infusion in a patient from a fluid source, the device comprising:

a fluid valve, disposed in a fluid connection between said fluid source and said patient, and operable for preventing or allowing the flow of fluid from said fluid source to said patient;

a variable volume chamber, fluidly coupled between said fluid valve and said patient, for allowing the fluid volume contained in the infusion monitoring device to increase and decrease;

a fluid inspection window, disposed in said fluid connection between said variable volume chamber and said patient, for allowing a view of fluid in said infusion monitoring device.

2. The device of claim 1 wherein the view of said fluid in said fluid inspection window allows a determination of whether said needle or catheter in said patient is correctly positioned with respect to a patient'"'"'s venous system.

3. The device of claim 1 wherein said fluid inspection window allows for manual, visual inspection of the fluid in the window.

4. The device of claim 1 wherein said fluid valve is a manually operated fluid valve.

5. The device of claim 1 wherein said fluid valve is normally closed or normally open.

6. The device of claim 1 wherein said fluid valve does not require power to stay in either the open or closed position.

7. The device of claim 1 further including a sensor, disposed proximate said fluid inspection window, for facilitating automated inspection of said fluid in said fluid inspection window.

8. The device of claim 7 further including a controller, coupled to at least said sensor, for automatically inspecting said fluid in said fluid inspection window and for providing a signal indicative of said sensing selected from the group consisting of an audible signal, a visible signal and an electronic signal.

9. The device of claim 8 wherein said signal indicative of said sensing is an alarm.

10. The device of claim 8 wherein said signal indicative of said sensing is provided locally to said device and said patient.

11. The device of claim 8 wherein said signal indicative of said sensing is provided remotely from said device and said patient.

12. The device of claim 1 wherein said fluid valve is automatically controllable.

13. The device of claim 12 further including a controller, coupled to said fluid valve, for automatically controlling operation of said fluid valve between an open and a closed position.

14. The device of claim 13 further including a sensor, disposed proximate said fluid inspection window, for facilitating automated inspection of said fluid in said fluid inspection window and further including a controller, coupled to said sensor, for automatically inspecting said fluid in said fluid inspection window and coupled to said fluid valve, for controlling operation of said fluid valve between said open and said closed position, for closing said fluid valve for facilitating automated inspection of said fluid by said sensor, and responsive to said sensor inspection of said fluid for either opening said fluid valve or for maintaining said fluid valve in said closed position.

15. The device of claim 14 wherein said controller records the current state and/or history of said sensor inspection data and alarms.

16. The device of claim 15 wherein said controller reports said recorded data.

17. The device of claim 14 wherein said controller is user programmable.

18. The device of claim 14 wherein said controller may be user programmable with regard to one or more of the group of elements consisting of:

inspection times, intervals or periods;

alarm trigger thresholds;

what is to be recorded;

how long is recorded information to be kept;

reporting format, criterion and frequency;

acceptable range of sensor values; and

volumes and pressure for drawing fluid from the patient.

19. The device of claim 5 wherein said sensor is selected from the group consisting of ultrasonic sensors, light sensors, optical sensors, cameras and probes.

20. The device of claim 5 wherein said sensor is adapted to detect one or more conditions selected from the group consisting of:

presence or absence of blood in said fluid inspection window, composition and/or characteristics of patient'"'"'s blood, and composition and/or characteristics of fluid being infused.

21. The device of claim 1 wherein said device further includes one or more features for securing said infusion monitoring device to said patient.

22. The device of claim 1 wherein the volume of said variable volume chamber is selected based on the volume of said fluid connection between said variable volume chamber and said patient.

23. The device of claim 1 further including an actuator, coupled to said variable volume chamber, for causing said variable volume chamber to expand and contract for creating a negative or positive pressure differential between said patient and said variable volume chamber.

24. A system for automatically monitoring an infusion in a patient receiving an infusion from a fluid source, the system comprising:

an infusion monitoring device comprising;

a fluid valve, disposed in a fluid connection between said fluid source and said patient, and operable for preventing or allowing the flow of fluid from said fluid source to said patient;

a variable volume chamber, fluidly coupled between said fluid valve and said patient, for allowing the creation of a pressure differential between said variable volume chamber and said patient; and

a fluid inspection window, disposed in said fluid connection between said variable volume chamber and said patient, for allowing a view of fluid drawn from said patient into said infusion monitoring device when said fluid valve is closed and said variable volume chamber creates a negative pressure differential between said variable volume chamber and said patient;

at least one sensor, disposed proximate with said fluid inspection window, for facilitating automated inspection of said fluid in said fluid inspection window; and

a controller, coupled to said fluid valve and to said at least one sensor, for controlling operation of said fluid valve between an open and a closed position and responsive to said sensor, for performing automated inspection of said fluid in said fluid inspection window and determining the status of said infusion.

25. The system of claim 24 wherein said controller causes an alarm to sound if said infusion is determined to be faulty.

26. The system of claim 25 wherein said alarm is sounded locally proximate said patient.

27. The system of claim 25 wherein said alarm is sounded remote from said patient.

28. The system of claim 25 wherein said controller records the current state and/or history of infusion inspection data and alarms.

29. The system of claim 28 wherein said controller reports said recorded data.

30. The system of claim 24 wherein said controller is programmable.

31. The system of claim 24 wherein said sensor is selected from the group consisting of ultrasonic sensors, light sensors, optical sensors, cameras and probes.

32. The system of claim 24 wherein said sensor is adapted to detect one or more conditions selected from the group consisting of:

presence or absence of blood in said fluid inspection window, composition and/or characteristics of patient'"'"'s blood, and composition and/or characteristics of fluid being infused.

33. The system of claim 24 wherein a sample of said fluid drawn from said patient is removed from the infusion monitoring device and processed with or without diluent, reagent, incubation enhancer or other standard sample preparation methods.

34. The system of claim 24 wherein the infusion monitoring device is integrated with one or more other patient care devices selected from the group consisting of:

infusion devices, patient monitoring devices, and diagnostics devices.

35. The system of claim 34 wherein the infusion monitoring device operates cooperatively with said integrated patient care device by sharing one or more functions from the group consisting of:

power source, user interface, alarm enunciation, control commands, data storage, and communications capabilities.

36. A method for monitoring and controlling the site of an infusion in a patient, said method comprising the acts of:

providing an infusion monitoring device, said infusion monitoring device including;

at least one fluid valve, coupled between the infusion fluid source and the patient, a variable volume chamber coupled between the at least one fluid valve and the patient, and a fluid inspection window disposed between the variable volume chamber and the patient;

closing said at least one fluid valve;

creating a pressure differential between said variable volume chamber and said patient causing the potential for fluid from said patient to flow into said fluid inspection window of said infusion monitoring device; and

monitoring said fluid in said fluid inspection window of said infusion monitoring device.

37. The method of claim 36 wherein said act of monitoring is performed manually by visual inspection.

38. The method of claim 36 wherein said act of monitoring is performed automatically by a sensor disposed proximate said fluid inspection window, and coupled to a controller.

39. The method of claim 36 wherein monitoring said fluid in said fluid inspection window includes monitoring blood drawn from a patient for one or more characteristics.

40. The method of claim 36 wherein said act of creating a pressure differential between said variable volume chamber and said patient is performed by changing the volume of said variable volume chamber with an actuator.

41. The method of claim 36 wherein said act of creating a pressure differential between said variable volume chamber and said patient is performed by the patient'"'"'s venous pressure, with or without the use of an actuator.

42. The method of claim 36 further including a controller, and wherein said controller is responsive to said act of monitoring for sounding an alarm if said controller determines that an infusion is faulty.

43. The method of claim 42 wherein said controller opens the valve and continues an infusion if said controller determines that said infusion is not faulty.

44. The method of claim 42 wherein said controller keeps the valve closed if said controller determines that said infusion is faulty.

45. The method of claim 42 wherein said controller determines if a clinician has responded within a predetermined time.

46. The method of claim 45 wherein if said controller determines that said clinician has responded within the predetermined time, said controller allows said clinician to either shut off the alarm and open the valve or shut off the alarm and keep the valve closed.

47. The method of claim 45 wherein if a clinician does not respond within the predetermined time the infusion monitoring device keeps the valve closed, power is shut off to the valve, and the alarm is maintained.

48. A method for monitoring an infusion in a patient, said method comprising the acts of:

providing an infusion monitoring device, said infusion monitoring device including a fluid inspection window disposed between the fluid valve and the patient; and

monitoring said fluid in said fluid inspection window of said infusion monitoring device.

49. The method of claim 48 wherein monitoring said fluid in said fluid inspection window includes monitoring the fluid being infused in said patient for one or more characteristics.

50. The method of claim 48 wherein a fluid valve is disposed in line with said fluid inspection window for the purpose of stopping the flow of infusion fluid as needed for inspection.

51. A method for keeping a patient infusion open comprising the acts of:

providing an infusion monitoring device, said infusion monitoring device including at least;

a fluid valve, disposed in a fluid connection between a fluid source and a patient, and operable for preventing or allowing the flow of fluid from said fluid source to said patient and a variable volume chamber, fluidly coupled between said fluid valve and said patient, for allowing the creation of a negative pressure differential between said variable volume chamber and said patient tending to draw fluid from the patient into the variable volume chamber and for allowing the creation of a positive pressure differential between said variable volume chamber and said patient tending to push fluid back from said variable volume chamber to said patient;

closing said fluid valve;

creating a negative pressure differential between said variable volume chamber and said patient causing fluid from said patient at an infusion site to be drawn into said variable volume chamber of said infusion monitoring device;

creating a positive pressure differential between said variable volume chamber and said patient causing fluid from variable volume chamber to be pushed into said patient at said infusion site; and

repeating the cycle of drawing fluid from and pushing fluid to the patient.