Methods and apparatus for patient monitoring

• US 20050222502A1
• Filed: 03/29/2005
• Published: 10/06/2005
• Est. Priority Date: 03/30/2004
• Status: Active Grant

• Current Assignee: Port-A-Nirs Pty Ltd.
• Original Assignee: Philip George Cooper
• Inventors: Cooper, Philip George
• Granted Patent: US 7,570,979 B2
• Time in Patent Office: Days
• US Class Current: 600/323
• CPC Class Codes: A61B 2560/0247 for compensation or correction of the measured physiological value
• CPC Class Codes: A61B 5/1116 Determining posture transitions
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: A61B 5/14553 specially adapted for cerebral tissue
• CPC Class Codes: A61B 5/1495 Calibrating or testing of in-vivo probes
• CPC Class Codes: A61B 5/4818 Sleep apnoea
• CPC Class Codes: A61B 5/6814 Head

Abstract

A respiratory monitoring apparatus that detects changes in physiological parameters relevant to respiration, including blood oxygen and blood volume, using near infrared spectroscopy. Methods for diagnosing respiratory-related events including hypoxia index, hypopnea, arousal, tissue oxygen debt, and respiratory muscle events or distinguishing central from obstructive sleep apnea are also disclosed.

Claims

1. A method of detecting disordered respiration in a patient, the method comprising:

(a) exposing the patient'"'"'s cerebral tissue to radiation, the radiation having at least first and second predetermined wavelengths, the first and second predetermined wavelengths being between about 730 nm to 770 nm, and 790 nm to 830 nm, respectively;

(b) sensing the levels of radiation reflected by the cerebral tissue at the first and second predetermined wavelengths;

(c) in a calibration step;

(i) determining reflection levels for first and second patient orientations; and

,

(ii) using the determined reflection levels to determine a calibration factor; and

(d) in a monitoring step;

(i) calculating a blood oxygen index in accordance with the sensed reflected radiation and the calibration factor; and

,

(ii) detecting a presence or absence of disordered respiration in the patient based at least in part on changes in the blood oxygen index determined in accordance with the calibration factor.

2. The method according to claim 1, wherein the disordered respiration is a sleep-related respiratory deregulation

3. The method according to claim 2, wherein the sleep-related respiratory deregulation is obstructive sleep apnea, central sleep apnea or both.

4. The method according to claim 1, wherein the first and second patient orientations include:

(e) the patient lying on their back; and

,

(f) the patient lying on their side.

5. The method according to claim 1, wherein the blood oxygen index is determined in accordance with the equation:

|B−

A|

wherein;

A is the reflected level at the first predetermined frequency; and

,

B is the reflected level at the second predetermined frequency.

6. The method according to claim 1, wherein the blood oxygen index is determined in accordance with one of the following equations:

|B−

kA| or [Ak−

B]

wherein;

k is the calibration factor.

7. The method according to claim 6, wherein the calibration factor is determined empirically so as to reduce effects of a hydrostatic head change effect on the blood oxygen index.

8. The method according to claim 1, wherein first and second light-emitting diodes (LEDs) are used to generate the first and second wavelengths respectively.

9. The method according to claim 8, wherein the method further includes a photodiode to sense absorbed radiation.

10. The method according to claim 1, said method further including:

a) selectively exposing the patient'"'"'s cerebral tissue to radiation;

b) sensing reflected radiation when the patient'"'"'s cerebral tissue is exposed, to determine an exposed level;

c) sensing radiation when the patient'"'"'s cerebral tissue is not exposed to determine an ambient radiation level; and

,

d) determining a reflected level by subtracting the ambient radiation level from the exposed level.

11. The method according to claim 1, wherein the reflected values for the first and second wavelengths and ambient light are consecutively sampled at least 30 times per second.

12. The method according to claim 1, wherein the method includes using algorithms to calculate parameters selected from the group consisting of oxygen debt accumulation value during insufficient respiration, hypoxic value of apnea events, pulsatile flow, blood volume cycling, diaphragm movements during respiration patient wherein a movement is indicative of obstructive, central or mixed type sleep apnea, arousals during an unconscious state and recovery time to quiescent saturation.

13. The method according to claim 1, wherein the monitoring step is performed for a predetermined time period.

14. A method of monitoring flow response times to hydrostatic pressure adjustments in a patient, the method comprising:

(a) exposing the patient'"'"'s cerebral tissue to radiation, the radiation having at least first and second predetermined wavelengths, the first and second predetermined wavelengths being between about 730 nm to 770 nm, and 790 nm to 830 nm respectively;

(b) sensing the levels of radiation absorbed by the cerebral tissue at the first and second predetermined wavelengths;

(c) in a calibration step;

(i) determining absorption levels for first and second patient orientations; and

,

(ii) using the determined absorption levels to determine a calibration factor; and

(d) in a monitoring step;

(i) calculating a blood oxygen index in accordance with the sensed absorbed radiation and the calibration factor; and

,

detecting a flow response time to a hydrostatic pressure adjustment in the patient based at least in part on changes in the blood oxygen index determined in accordance with the calibration factor.

15. An apparatus for detecting disordered respiration or a flow response time to a hydrostatic pressure adjustment in a patient, the apparatus comprising:

(a) a radiation source for exposing the patient'"'"'s cerebral tissue to radiation, the radiation having at least first and second predetermined wavelengths, the first and second predetermined wavelengths being between about 730 nm to 770 nm, and 790 nm to 830 nm respectively;

(b) a sensor for sensing the level of radiation reflected by the cerebral tissue at the first and second predetermined wavelengths; and

,

(c) a processor for;

(i) in a calibration step;

(a) determining reflected radiation levels for first and second patient orientations; and

,

(b) using the determined absorption levels to determine a calibration factor; and

(ii) in a monitoring step;

(a) calculating a blood oxygen index in accordance with the sensed absorbed radiation and the calibration factor; and

,

(b) detecting a presence or absence of disordered respiration in the patient based at least in part on changes in the blood oxygen index determined in accordance with the calibration factor.

16. The apparatus according to claim 15, wherein the radiation source includes first and second LEDs for generating the first and second predetermined wavelengths, respectively.

17. The apparatus according to claim 16, wherein the sensor includes a photodiode for sensing the reflected radiation.

18. The apparatus according to claim 15, further including a controller for controlling the operation of the radiation source and the sensor.

19. The apparatus according to claim 18, wherein the controller is adapted to:

(a) selectively activate the radiation source to thereby expose the patient'"'"'s cerebral tissue to radiation;

(b) selectively sample signals from the sensor to thereby sense radiation when;

(i) the patient'"'"'s cerebral tissue is exposed to determine an exposed radiation level;

(ii) the patient'"'"'s cerebral tissue is not exposed to determine an ambient radiation level; and

,

(c) determine a reflected level by subtracting the ambient level from the exposed level.

20. The apparatus according to claim 19, wherein the controller is adapted to cause reflected values for the first and second wavelengths and ambient light to be consecutively sampled at least 30 times per second.

21. The apparatus according to claim 20, wherein the controller includes:

(a) a processor for controlling the radiation source and a sampling time interval of the sensor; and

,

(b) a memory for storing reflected level signal values.

22. The apparatus according to claim 21, wherein the processor is adapted to control a pulsed radiation source.

23. The apparatus according to claim 21, wherein the processor is adapted to perform at least some processing of the reflected level signal values.

24. The apparatus according to claim 21, wherein the controller includes a communication means for transferring data to a remote processing system, the remote processing system being adapted to perform at least some processing of the reflected level signal values.

25. The apparatus according to claim 24, wherein the remote processing system is adapted to display a reflected level.

26. The apparatus according to claim 18, wherein the apparatus includes a user input for controlling the controller.

27. The apparatus according to claim 26, wherein the user input is used for selectively activating at least one of the calibration step and the monitoring step.

28. The apparatus according to claim 27, wherein the controller is provided in a housing.

29. The apparatus according to claim 28, wherein the housing is suitable for home use by a patient.

30. The apparatus according to claim 28, wherein the radiation source and the sensor are provided in a probe coupled to the housing, the probe being adapted for attachment to the patient in use.

31. The apparatus according to claim 30, wherein the probe is formed from silicon rubber.

32. (canceled)