MONITORING OF USE STATUS AND AUTOMATIC POWER MANAGEMENT IN MEDICAL DEVICES

• US 20090030285A1
• Filed: 07/25/2007
• Published: 01/29/2009
• Est. Priority Date: 07/25/2007
• Status: Abandoned Application

• Current Assignee: 3M Innovative Properties Company (3M Company)
• Original Assignee: 3M Innovative Properties Company (3M Company)
• Inventors: ANDERSEN, Bjorn K.
• Application Number:
  US11/782,837
• Publication Number:
  US 20090030285A1
• Time in Patent Office: Days
• US Class Current: 600/300
• CPC Class Codes: A61B 2560/0209 adapted for power saving
• CPC Class Codes: A61B 2562/0257 Proximity sensors
• CPC Class Codes: A61B 5/6843 Monitoring or controlling sensor contact pressure
• CPC Class Codes: A61B 7/04 Electric stethoscopes microphones, acoustic transducers therefor H04R

Abstract

A method is provided for automatically determining the use status of an electronic medical device (e.g., an electronic stethoscope) and/or activating such a device. The method includes providing a patient portion of the device, i.e., one or more portions of the device that, in use, are brought into contact with a patient, with a contact or proximity detector. The detector provides an output signal when the patient portion is proximate to, or in contact with, a portion of a patient. This output signal, after signal processing, is used in determining the use status of the device.

Claims

1. A method for automatically determining use status of an electronic medical device and/or activating said electronic medical device, such as an electronic stethoscope, the method comprising providing a patient portion of the device, i.e. one or more portions of the device that during use is brought into contact with portions of a patient, with contact or proximity detector means that provides an output signal when said patient portion is proximate to or in contact with a portion of a patient, said output signal, optionally after a predetermined signal processing, providing a signal-processed version of said output signal, determining the use status of the device.

2. A method according to claim 1, where said output signal or said signal-processed version hereof is used for activating electronic signal-processing circuitry, such as amplifiers, filters, signal analysis means, etc., whereby said electronic medical device becomes active when said patient portion is brought into contact with a portion of a patient or brought into close proximity of a patient.

3. A method according to claim 2, where said signal processing of said output signal comprises low pass filtration of said output signal, whereby a low pass filtered version of said output signal is provided.

4. A method according to claim 3, where said low pass filtered version of said output signal is processed by RMS (root mean square) determining means with a suitable time constant, whereby a RMS value of said low pass filtered version of said output signal is provided.

5. A method according to claim 2, where said signal processing of said output signal comprises evaluation of the balance between the levels of a high-frequency portion of the power spectral density of said output signal and a low frequency portion of the power spectral density of said output signal, whereby the presence of frictional noise components in said output signal can be evaluated.

6. A method according to claim 1, where said detector means is a vibration sensor.

7. A method according to claim 1, where said vibration sensor is a piezoelectric sensor.

8. A method according to claim 7, where said piezoelectric sensor provides an output signal that is amplified by a low-power amplifier, such as a FET, MOSFET, bipolar operational amplifier.

9. A method according to claim 1, where said detector means is a capacitance proximity sensor.

10. A method according to claim 1, where said detector means is a bio-impedance sensor.

11. A method according to claim 10, where said bio-impedance sensor is a two-pole sensor.

12. A method according to claim 10, where said bio-impedance sensor is a four-pole sensor.

13. A method according to claim 1, where said medical device is an electronic stethoscope.

14. A method according to claim 1, where said medical device is an electronic auto-injector device.

15. A method according to claim 1, where said medical device is an electronic inhaler device.

16. An electronic stethoscope comprising a chestpiece comprising a stethoscope sensor for picking up sounds from a patient'"'"'s body, where said chestpiece is provided with contact or proximity detector means that provides an output signal when said chestpiece is proximate to or in contact with a surface portion of a patient, said output signal, or a signal-processed version of said output signal, determining the use status of the device and/or activating the stethoscope when said chestpiece is proximate to or in contact with said surface portion of a patient.

17. An electronic stethoscope according to claim 16, furthermore comprising amplification means and/or other electronic signal-processing means for amplifying/processing output signals from said stethoscope sensor, where said amplification means/processing means are turned on when said contact or proximity detector means determines that said chestpiece is in contact with said surface portion of a patient or when said chestpiece is in proximity to said surface portion of a patient.

18. An electronic stethoscope according to claim 16, where said contact detector means is a vibration sensor, where the vibration sensor will generate a voltage or charge upon physical contact with the body of the patient, which voltage/charge can be used to trigger status setting of the electronic stethoscope.

19. An electronic stethoscope according to claim 18, where said vibration sensor is a piezoelectric vibration sensor.

20. An electronic stethoscope according to claim 19, where said piezoelectric vibration sensor is in combination with a low-power amplifier means, such as a FET, MOSFET, bipolar operational amplifier, where the piezoelectric sensor will generate a voltage/charge upon physical contact with the skin of the patient, which voltage/charge is amplified by said low-power amplifier means.

21. An electronic stethoscope according to claim 16, where said detector means is a capacitance proximity sensor, where the capacitance increases when the sensor approaches the body of a patient.

22. An electronic stethoscope according to claim 16, where said use status of the stethoscope is determined by means capable of determining the bio-impedance at an interface area between the chestpiece of the stethoscope and a surface portion of a patient, where said bio-impedance is reduced when the patient chestpiece of the stethoscope touches said surface portion of the patient.

23. An electronic stethoscope according to claim 22, where said bio-impedance is determined by two-pole impedance-determining means.

24. An electronic stethoscope according to claim 22, where said bio-impedance is determined by four-pole impedance-determining means.

25. An electronic stethoscope according to claim 16, where said output signal that indicates when said chestpiece is proximate to or in contact with a surface portion of a patient is provided by the stethoscope sensor itself.

26. An electronic stethoscope according to claim 16, where said signal processing comprises low pass filtration of said output signal, whereby a low pass filtered version of said output signal is provided.

27. An electronic stethoscope according to claim 26, where said low pass filtered version of said output signal is processed by RMS (root mean square) determining means with a suitable time constant, whereby a RMS value of said low pass filtered version of said output signal is provided.

28. An electronic stethoscope according to claim 16, where said signal processing of said output signal comprises evaluation of the balance between the levels of a high-frequency portion or band of said output signal and a low frequency portion or band of said output signal, whereby the presence of frictional noise components in said output signal can be evaluated.

29. An electronic stethoscope according to claim 16, where said output signal, or a signal-processed version of said output signal, determines the use status of the device and/or activates the device when said output signal or processed version hereof exceeds a given threshold value.

30. An electronic stethoscope according to claim 29, where said threshold value is variable.

31. An electronic stethoscope according to claim 16, where the stethoscope after activation is automatically turned off after a given period of time.

32. An electronic auto-injection device comprising a main body and a needle, where the device is provided with detection means for detecting an electronically conductive pathway established between said needle and said main body of the device when the needle is inserted into the tissue of a patient, said detecting means providing an output signal, where the output signal, or a signal-processed version hereof, determines the use status, such as proper insertion of the needle into a patient'"'"'s tissue, of the auto-injection device.

33. An electronic auto-injection device according to claim 32, where said detection means comprises two-pole or four-pole impedance-sensing means.

41. An electronic auto-injection device according to claim 32, where said output signal, or said signal-processed version hereof, determines the time interval between insertion and retraction of the needle, whereby it can be monitored whether the needle has been kept in the tissue of a patient for a required period of time.

42. An electronic auto-injection device according to claim 32, where the device is furthermore provided with signal analysis means for discrimination between needle insertion into a patient'"'"'s muscles or fat or into an artery or vein, where said analysis means receives the measured impedance means from said detection means or two- or four-pole impedance-sensing means and based on these received impedance measurements differentiates between needle insertion in muscle, fat, arteries or veins.

34. An electronic auto-injection device comprising a main body and a needle, where the device is provided with vibration sensing means for sensing the vibration of the needle and/or the vibration of the device main body, said vibration sensing means providing an output signal, where the output signal, or a processed version hereof, determines the use status of the device.

43. An electronic auto-injection device according to claim 34, where said output signal, or said signal-processed version hereof, determines the time interval between insertion and retraction of the needle, whereby it can be monitored whether the needle has been kept in the tissue of a patient for a required period of time.

44. An electronic auto-injection device according to claim 34, where the device is furthermore provided with signal analysis means for discrimination between needle insertion into a patient'"'"'s muscles or fat or into an artery or vein, where said analysis means receives the measured impedance means from said detection means or two- or four-pole impedance-sensing means and based on these received impedance measurements differentiates between needle insertion in muscle, fat, arteries or veins.

35. An electronic auto-injection device comprising a main body, a needle and an interface plate for providing an interface between the device and a surface portion of a patient, where said interface plate is provided with capacitance proximity sensing means for sensing proximity of the interface plate to a surface portion of a patient, where the capacitance proximity sensing means provides an output signal, where the output signal, or a signal-processed version hereof, determines the use status of the device.

36. An electronic auto-injection device according to claim 35, where said output signal, or said signal-processed version hereof, determines the time interval between insertion and retraction of the needle, whereby it can be monitored whether the needle has been kept in the tissue of a patient for a required period of time.

37. An electronic auto-injection device according to claim 35, where the device is furthermore provided with signal analysis means for discrimination between needle insertion into a patient'"'"'s muscles or fat or into an artery or vein, where said analysis means receives the measured impedance means from said detection means or two- or four-pole impedance-sensing means and based on these received impedance measurements differentiates between needle insertion in muscle, fat, arteries or veins.

38. An electronic inhaler device comprising a mouthpiece, where the mouthpiece is provided with two- or four-pole impedance-measuring means formed for contact with the mouth or lip portion of a patient, wherein the measured impedance provides information about the use status, such as whether the lips of the patient are properly folded around the mouthpiece, of the inhaler device.

39. An electronic inhaler device comprising a mouthpiece, where the device is provided with vibration-sensing means for providing an output signal when the mouthpiece of the device is subjected to vibrations caused by contact of the mouthpiece with lip portions of a patient, where the vibration-sensing means provides an output signal indicating such vibration, and where the output signal, or a signal-processed version hereof, indicates use status of the device.

40. An electronic inhaler device comprising a mouthpiece and a hand grip portion, where the hand grip portion is provided with either two- or four-pole impedance-sensing means or with vibration-sensing means, said means providing an output signal indication when a person is holding said hand grip portion, where said output signal, or a signal-processed version hereof, is used for turning on an LCD display and/or for initiating a text guidance on the display relating for instance to proper inhalation technique and/or time elapsed since last dose of medicament provided by the device.