Processing venous oxygen saturation and hematocrit information in an implantable sensor

• US 8,385,999 B1
• Filed: 02/08/2008
• Issued: 02/26/2013
• Est. Priority Date: 02/08/2008
• Status: Active Grant

• Current Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Pacesetter Incorporated (Abbott Laboratories Incorporated)
• Inventors: Nabutovsky, Yelena, Bornzin, Gene A., Farazi, Taraneh Ghaffari, Poore, John W.
• Primary Examiner(s): Hindenburg, Max
• Assistant Examiner(s): DANEGA, RENEE A
• Application Number:
  US12/028,261
• Time in Patent Office: 1,845 Days
• Field of Search: 600/323, 600/508, 607/22
• US Class Current: 600/323
• CPC Class Codes: A61B 5/0031 Implanted circuitry
• CPC Class Codes: A61B 5/14535 for measuring haematocrit
• CPC Class Codes: A61B 5/14551 for measuring blood gases
• CPC Class Codes: A61B 5/4836 Diagnosis combined with treatment in closed-loop systems or methods A61B5/0036 takes precedence

Abstract

Methods of processing venous oxygen saturation and hematrocrit information in an implantable sensor are provided. In an embodiment a method for collecting data from an implantable multi-wavelength SvO2 sensor having multiple light sources is provided. The method includes receiving a frame signal that indicates a beginning of the light sources being turned on and receiving a light source signal that indicates a light source is on. The output of a photodetector is sampled to measure the intensity of the transmitted light. The process is repeated for each light source to gather intensity measurements that then can be used to generate venous oxygen saturation and hematocrit measurements.

Claims

1. A method for collecting data from an implantable multi-wavelength venous oxygen (SvO₂) sensor having multiple light sources, comprising:

(a) receiving a first signal in response to a peak of a pulsatile action of a blood vessel;

(b) turning on a light source of the multiple light sources in response to the first signal;

(c) receiving a second signal that indicates the light source is on;

(d) sampling, in response to the second signal, an output of a photodetector to measure the intensity of the light source that is on, such that the sampling occurs during the peak of the pulsatile action; and

(e) repeating steps (b) through (d) until outputs corresponding to each of the multiple light sources have been sampled.

2. The method of claim 1, wherein the second signal is a light source signal.

3. The method of claim 1, wherein the first signal and the second signal are the same signal.

4. The method of claim 1, farther comprising turning on each of the multiple light sources in a series.

5. The method of claim 1, further comprising inserting a blanking interval prior to the sampling, wherein the blanking interval ensures that data is collected during the same condition each time data is sampled.

6. The method of claim 1, further comprising delaying sampling an output of a photodetector associated with the light source that is on for a predetermined time interval following receiving the second signal that indicates the light source is on.

7. The method of claim 1, wherein sampling an output of a photodetector associated with the light source includes sampling a predefined number of sample points.

8. The method of claim 1, wherein sampling an output of a photodetector associated with the light source includes taking samples from the photodetector until the second signal indicates that the light source is off.

9. The method of claim 1, wherein a sampling interval for sampling an output of a photodetector varies as a function of respiration information.

10. The method of claim 1, further comprising combining data collected during sampling from each light source into a single data point by averaging the collected data or by generating a median of the collected data.

11. The method of claim 1, further comprising storing data collected during sampling from each light source until data based on all light sources has been collected.

12. The method of claim 1, further comprising combining the data received from each of the light sources into ratios for O₂ saturation and hematocrit calculations.

13. The method of claim 12, further comprising:

(i) accumulating data received from each of the light sources for a predetermined period of time; and

(ii) filtering data received from each of the light sources.

14. The method of claim 13, wherein filtering data received from each of the light sources includes applying a median filter to the received data for each light source.