Pulse oximeter probe-off detection system

• US 6,526,300 B1
• Filed: 06/16/2000
• Issued: 02/25/2003
• Est. Priority Date: 06/18/1999
• Status: Expired due to Term

• Current Assignee: Masimo Corporation
• Original Assignee: Masimo Corporation
• Inventors: Kiani, Massi E., Diab, Mohamed K.
• Primary Examiner(s): Winakur, Eric F.
• Assistant Examiner(s): KREMER, MATTHEW J
• Application Number:
  US09/595,081
• Time in Patent Office: 984 Days
• Field of Search: 600/309-310, 600/322-324, 600/316, 600/344, 356/39-42
• US Class Current: 600/322
• CPC Class Codes: A61B 5/14552 Details of sensors specially adapted therefor
• CPC Class Codes: A61B 5/6843 Monitoring or controlling sensor contact pressure

Abstract

The present invention provides a number of improvements that can be incorporated into a pulse oximeter probe to detect when a probe has become dislodged from a patient and/or to prevent a probe-off condition. A probe-off condition occurs when the optical probe becomes partially or completely dislodged from the patient, but continues to detect an AC signal within the operating region of the pulse oximeter. In one aspect, the present invention provides electrical contacts that contact the skin of a patient when the probe is properly attached. In another aspect, the present invention provides a number of louvers placed in front of the sensor'"'"'s photodetector to filter out oblique light rays that do not originate from a point in front of the detector. Accordingly, if the emitter and photodetector are not properly aligned, the photodetector will not produce a signal within the valid operating range of the pulse oximeter. In accordance with a method of the present invention the pulse oximeter can sound an alarm or display a warning if it determines that the probe is not properly attached to the patient.

Claims

1. A method for verifying attachment of an optical probe to a patient, the method comprising:

providing an optical probe, the optical probe having at least two contacts configured to contact a patient'"'"'s skin when the optical probe is properly attached;

applying a voltage across the at least two contacts; and

determining, based upon a measured resistance of a coding resistor, whether the at least two contacts are in contact with the patient'"'"'s skin.

2. The method of claim 1, wherein the at least two contacts comprise metallic contacts.

3. The method of claim 1, wherein the at least two contacts comprise conductive adhesive contacts.

4. The method of claim 1, wherein the at least two contacts comprise gel-based contacts.

5. The method of claim 1, wherein the at least two contacts are positioned on the patient'"'"'s skin proximate to a detector aperture in the optical probe.

6. The method of claim 1, wherein the at least two contacts are positioned on the patient'"'"'s skin proximate to an emitter aperture in the optical probe.

7. The method of claim 1, wherein one of the at least two contacts is positioned on the patient'"'"'s skin proximate to a detector aperture in the optical probe and the other of the at least two contacts is positioned on the patient'"'"'s skin proximate to an emitter aperture in the optical probe.

8. The method of claim 1, further comprising generating a visual alarm when the at least two contacts are not in contact with the patient'"'"'s skin.

9. The method of claim 1, further comprising generating a audible alarm when the at least two contacts are not in contact with the patient'"'"'s skin.

10. The method of claim 1, further comprising generating at least one of a visual or audible indicator when the at least two contacts are in contact with the patient'"'"'s skin.

11. A method of detecting that a pulse oximetry probe may not be properly attached to a tissue site, the method comprising:

providing a pulse oximetry probe having a light emitter, a light detector configured to detect light from the light emitter when the pulse oximetry probe is properly attached, and at least two contacts configured to make contact to a patient'"'"'s skin when the pulse oximetry probe is properly attached;

emitting light from the light emitter;

checking for continuity across the at least two contacts by measuring a resistance of a coding resistor;

checking for a valid signal from the light detector; and

determining whether the pulse oximetry probe is properly attached based upon the continuity check and the valid signal check.

12. The method of claim 11, wherein the light detector further includes at least one louver.

13. The method of claim 11, wherein the measuring the resistance of the coding resistor includes measuring the resistance of the patient'"'"'s skin.

14. The method of claim 11, wherein the measuring the resistance of the coding resistor does not include measuring the resistance of the patient'"'"'s skin.

15. The method of claim 11, wherein the at least two contacts comprise metallic contacts.

16. The method of claim 11, wherein the at least two contacts comprise conductive adhesive contacts.

17. The method of claim 11, wherein the at least two contacts comprise gel-based contacts.

18. The method of claim 11 wherein the at least two contacts are positioned on the patient'"'"'s skin proximate to the light detector.

19. The method of claim 11, wherein the at least two contacts are positioned on the patient'"'"'s skin proximate to the light emitter.

20. The method of claim 11, wherein one of the at least two contacts is positioned on the patient'"'"'s skin proximate to the light detector and the other of the at least two contacts is positioned on the patient'"'"'s skin proximate to the light emitter.

21. The method of claim 11, further comprising generating a visual alarm when the pulse oximetry probe is not properly attached.

22. The method of claim 11, further comprising generating a audible alarm when the pulse oximetry probe is not properly attached.

23. The method of claim 11, further comprising generating at least one of a visual or audible indicator when the pulse oximetry probe is properly attached.

43. The pulse oximetry system of claim 16, further comprising an indicator for indicating when the pulse oximetry sensor is properly affixed to the measurement site.

44. The pulse oximetry system of claim 16, wherein the probe-off circuit comprises two contacts.

45. The pulse oximetry system of claim 44, wherein the two contacts are positioned on the measurement site proximate to a detector of the pulse oximetry sensor.

46. The pulse oximetry system of claim 44, wherein the two contacts are positioned on the measurement site proximate to an emitter of the pulse oximetry sensor.

47. The pulse oximetry system of claim 44, wherein one of the two contacts is positioned on the measurement site proximate to a detector of the pulse oximetry sensor and the other of the two contacts is positioned on the measurement site proximate to an emitter of the pulse oximetry sensor.

24. A pulse oximetry system comprising:

a pulse oximeter base unit;

an optical probe configured to be affixed to a body member of a patient;

at least two electrical contacts located on the optical probe, the electrical contacts configured to make contact to the body member of the patient when the optical probe is properly affixed to the patient; and

a probe-off detector module configured to check for acceptable continuity across the electrical contacts by measuring a resistance of a coding resistor, thereby determining whether the optical probe is properly affixed to the patient.

25. The pulse oximetry system of claim 24, wherein the coding resistor is in parallel with an emitter of the optical probe.

26. The pulse oximetry system of claim 24, wherein the coding resistor is not in parallel with an emitter of the optical probe.

27. The pulse oximetry system of claim 24, further comprising an indicator for indicating when the optical probe is not properly affixed to the patient.

28. The pulse oximetry system of claim 27, wherein the indicator comprises at least one of an audible or visual alarm.

29. The pulse oximetry system of claim 24, further comprising an indicator for indicating when the optical probe is properly affixed to the patient.

30. The pulse oximetry system of claim 24, wherein the at least two electrical contacts are positioned on the body member proximate to a detector of the optical probe.

31. The pulse oximetry system of claim 24, wherein the at least two electrical contacts are positioned on the body member proximate to an emitter of the optical probe.

32. The pulse oximetry system of claim 24, wherein one of the at least two electrical contacts is positioned on the body member proximate to a detector of t he optical probe and the other of the at least two electrical contacts is positioned on the body member proximate to an emitter of the optical probe.

33. The pulse oximetry system of claim 24, wherein the at least two electrical contacts comprise metallic contacts.

34. The pulse oximetry system of claim 24, wherein the at least two electrical contacts comprise conductive adhesive contacts.

35. The pulse oximetry system of claim 24, wherein the at least two electrical contacts comprise gel-based contacts.

36. A pulse oximeter system for determining proper attachment of a sensor, the pulse oximeter system comprising:

an oximeter base unit; and

a probe-off detector module configured to verify proper attachment of a pulse oximetry sensor to a measurement site of a patient by measuring a resistance associated with a coding resistor and a probe-off circuit of the pulse oximetry sensor.

37. The pulse oximetry system of claim 36, wherein the probe-off circuit comprises a contact sensor.

38. The pulse oximetry system of claim 37, wherein the contact sensor comprises a piezoelectric sensor.

39. The pulse oximetry system of claim 36, wherein the coding resistor is in parallel with an emitter of the pulse oximetry sensor.

40. The pulse oximetry system of claim 36, wherein the coding resistor is not in parallel with an emitter of the pulse oximetry sensor.

41. The pulse oximetry system of claim 36, further comprising an indicator for indicating when the pulse oximetry sensor is not properly affixed to the measurement site.

42. The pulse oximetry system of claim 41, wherein the indicator comprises at least one of an audible or visual alarm.