Method and Apparatus For Acute Cardiac Monitoring

• US 20100056881A1
• Filed: 08/25/2009
• Published: 03/04/2010
• Est. Priority Date: 08/29/2008
• Status: Abandoned Application

• Current Assignee: Medtronic Monitoring, Inc. (Medtronic Plc)
• Original Assignee: Corventis Inc (Medtronic Plc)
• Inventors: Manicka, Yatheendhar D., Libbus, Imad, Mazar, Scott T.
• Application Number:
  US12/546,918
• Publication Number:
  US 20100056881A1
• Time in Patent Office: Days
• US Class Current: 600/301
• CPC Class Codes: A61B 2560/0412 Low-profile patch shaped housings
• CPC Class Codes: A61B 5/0537 Measuring body composition by impedance, e.g. tissue hydration or fat content
• CPC Class Codes: A61B 5/085 Measuring impedance of respiratory organs or lung elasticity
• CPC Class Codes: A61B 5/318 Heart-related electrical modalities, e.g. electrocardiography [ECG]
• CPC Class Codes: A61B 5/6833 Adhesive patches

Abstract

A device for monitoring a patient from the back of the patient comprises a support configured to adhere to the back of the patient, at least two electrodes supported with the support, circuitry coupled to the at least two electrodes to measure a signal from the at least two electrodes, and circuitry to transmit the signal wirelessly. The support and the at least two electrodes may be placed on at least one of a lower back or between shoulder blades of the patient, which can help to reduce pressure on the patient when the device is worn for an extended period, for example 1 week. Placement of the adherent device in at least one of these locations can improve patient comfort, for example by decreasing pressure to the skin of the patient from the device when the patient lies supine. The device may also provide lumbar support, for example when placed on the lumbar of the patient.

Claims

1. A method of monitoring a patient having a back and a spine disposed along a midline of the patient, the method comprising:

placing a first electrode and a second electrode on the back of the patient; and

measuring a signal from the first electrode and the second electrode.

2. The method of claim 1 wherein the first electrode and the second electrode are placed such that the first electrode is placed on a first side of the midline and the second electrode is placed on a second side of the midline opposite the first side

3. The method of claim 1 wherein the first electrode and the second electrode are placed along the midline and aligned with the spine.

4. The method of claim 1 wherein the first electrode and the second electrode are placed on at least one of a lower back or between shoulder blades of the patient.

5. The method of claim 4 wherein the first electrode is placed a first distance from the midline of the patient and the second electrode is placed a second distance from the midline of the patient, the first distance substantially similar to the second distance such that the first electrode and the second electrode are symmetrically disposed on opposite sides of the midline of the patient.

6. The method of claim 1 wherein the signal comprises at least one of an electrocardiogram signal or a bioimpedance signal.

7. The method of claim 6 wherein the signal comprises the bioimpedance signal and at least one of a hydration or a respiration of the patient is determined from the bioimpedance signal.

8. The method of claim 1 wherein the first electrode and the second electrode are supported with a flexible adherent device comprising a support adhered to the back of the patient.

9. The method of claim 8 wherein the support comprises a midline and the midline of the support is aligned with the midline of the patient when the support is adhered to the back of the patient.

10. The method of claim 9 wherein the support supports rigid circuitry components disposed on each side of the support away from the midline of the support to minimize pressure to the spine of the patient when the patient is placed in the supine position.

11. The method of claim 10 wherein the rigid circuitry components comprise at least one of an integrated circuit or a rigid printed circuitry board.

12. The method of claim 8 wherein the flexible adherent device is adhered to at least one of a lower back of the patient or an upper back of the patient.

13. The method of claim 12 wherein the device is adhered to the lower back of the patient and at least partially supports a lumbar of the spine of the patient when the patient sits and/or is placed in a supine position.

14. The method of claim 12 wherein the support is adhered to the back between shoulder blades of the patient.

15. The method of claim 1 wherein the flexible adherent device comprises a central portion supported on the back with the skin of the patient, the central portion comprising a midline aligned with the midline of the patient.

16. The method of claim 15 wherein the flexible adherent device comprises peripheral portions adhered to the back and extending from the central portion.

17. The method of claim 16 wherein the central portion comprises a thickness of no more than about 10 mm from an inner surface configured to adhere to the skin to an outer surface opposite the inner surface and wherein the peripheral portions each comprise a thickness of no more than about 5 mm from the inner surface configured to adhere to the skin of the patient to the outer surface opposite the inner surface.

18. The method of claim 17 wherein the thickness of the central portion comprises no more than about 5 mm and the thickness of each peripheral portion comprises no more than about 3 mm.

19. The method of claim 15 wherein the central portion comprises the midline aligned with the spine and wherein the peripheral portions comprise the electrodes and extend along at least one of trapezius muscles or latissimus dorsi muscles of the patient.

20. The method of claim 1 wherein a second signal is measured and comprises at least one of an activity signal, a posture signal, a temperature signal or an oxygen saturation signal.

21. The method of claim 1 further comprising transmitting the signal wirelessly to a monitoring station in a hospital such that hospital personnel can monitor a status of the patient.

22. The method of claim 1 wherein an algorithm is configured to determine a condition of the patient in response to the signal and generate an alarm in response to the condition.

23. The method of claim 22 wherein the condition comprises an arrhythmia of the patient.

24. A device for monitoring a patient having a back, the device comprising:

a support comprising an adhesive, the support configured to adhere to a skin of the back of the patient;

at least two electrodes supported with the support; and

circuitry supported with the support and coupled to the at least two electrodes, the circuitry configured to measure a signal from the electrodes and transmit the signal wirelessly.

25. The device of claim 24 wherein support is configured to flex and conform to the surface contour of the skin of the patient when the support is adhered to the skin and wherein the support comprises at least one of a breathable tape or a flex printed circuit board configured to flex with the surface contour of the skin of the patient when the support is adhered to the skin of the patient.

26. The device of claim 24 wherein support comprises a midline configured for alignment with a spine of the patient.

27. The device of claim 26 wherein support comprises a visible indicia to align the support with the midline of the patient along the spine.

28. The device of claim 24 wherein a first portion of the circuitry is disposed on first side of the midline and a second portion of the circuitry is disposed on a second side of the midline opposite the first side.

29. The device of claim 24 wherein the device comprises a thickness profile comprising a distance extending from a lower surface of the device configured for placement against the skin of the patient to an outer surface of the device opposite the lower surface and wherein the thickness profile comprises a first central dimension at a first location configured for placement on the midline of the patient and a second peripheral dimension at a second location configured for placement away from the midline of the patient, the first central dimension greater than the second peripheral dimension.

30. The device of claim 29 wherein the thickness profile comprises a third distance at a third location, the third location located away from the midline and between the first location and the second location, the third distance greater than the first distance and the second distance.

31. The device of claim 24 further comprising:

a cover having an outer surface, the cover disposed over the electronics and supported with the support and wherein the cover and support comprise a central portion of the device and peripheral portions of the device, each portion having a thickness extending from the adhesive to the outer surface of the cover, the central portion comprising the midline configured for alignment with the spine of the patient and having a maximum thickness no more than about 10 mm, the peripheral portions extending from the central portion and having a maximum thickness of no more than about 5 mm.

32. The device of claim 31 wherein the cover comprises at least one of a coating, a dip coating, a molding, a housing, a casing or a stretchable fabric.

33. The device of claim 31 wherein the maximum thickness of the central portion comprises no more than about 5 mm and the maximum thickness of each peripheral portion comprises no more than about 3 mm.

34. The device of claim 31 wherein the maximum thickness of the central portion is disposed away from a midline of the central portion and wherein the central portion comprises a second thickness along the midline less than the maximum thickness of the central portion to decrease pressure on a spine of the patient when the patient lies in a supine position.

35. The device of claim 24 wherein the support comprises a midline and extends away from the midline symmetrically to an outer boundary disposed symmetrically about the midline and wherein the at least two electrodes are positioned on the support symmetrically about the midline such that the electrodes are positioned on opposite sides of the spine at equal distances from the midline when the supported is adhered to the back of the patient and the midline of the support is aligned with the spine of the patient.

36. The device of claim 24 wherein support comprises at least one of a breathable tape or a flex printed circuit board configured to stretch with the skin of the patient.

37. The device of claim 24 wherein the support is shaped for lumbar support of the patient.

38. A system for monitoring a patient having a back, the system comprising:

at least one support comprising an adhesive, the at least one support configured to adhere to a skin of the back of the patient;

at least two electrodes supported with the at least one support;

circuitry supported with the at least one support and coupled to the at least two electrodes, the circuitry configured to measure a signal from the electrodes and transmit a wireless signal comprising the signal from the electrodes; and

a gateway configured to receive the wireless signal.

39. The system of claim 38 wherein the circuitry is configured to monitor and transmit wirelessly to the gateway at least one of an electrocardiogram signal, a respiration rate signal, body fluid signal, an activity signal, a posture signal, a temperature signal or an oxygen saturation signal.

40. The system of claim 38 further comprising:

at least one processor comprising a tangible medium configured to receive the signal from the gateway; and

a display located at a station to monitor the patient and coupled to the at least one processor to display the signal.

41. The system of claim 38 wherein the at least one support comprises a first support and a second support and the circuitry comprises first circuitry supported with the first support and second circuitry supported with the second support, the first circuitry configured to measure a first signal from the patient, the second circuitry configured to measure a second signal from the patient, the first circuitry and the second circuitry each configured to transmit signals to the gateway, the first support configured to adhere to at least one of a lower back of the patient or between shoulder blades of the patient.

42. The system of claim 41 wherein the first circuitry is coupled to a first at least two electrodes configured to measure the first signal comprising a first cardiac vector in a direction extending between the first at least two electrodes, the second circuitry coupled to a second at least two electrodes configured to measure the second signal comprising a second cardiac vector in a direction extending between the second at least two electrodes.

43. The system of claim 42 wherein the first at least two electrodes extend substantially laterally across the back of the patient and the second at least two electrodes extend substantially vertically along at least one of the back or the side of the patient.