Methods and systems for determining fluid administration

• US 10,328,202 B2
• Filed: 01/25/2016
• Issued: 06/25/2019
• Est. Priority Date: 02/04/2015
• Status: Active Grant

• Current Assignee: Covidien LP (Medtronic Plc)
• Original Assignee: Covidien LP (Medtronic Plc)
• Inventors: Doyle, Peter, Addison, Paul S., Watson, James N.
• Primary Examiner(s): Osinski, Bradley J
• Application Number:
  US15/006,018
• Publication Number:
  US 20160220756A1
• Time in Patent Office: 1,247 Days
• CPC Class Codes: A61B 5/02416 using photoplethysmograph signals, e.g. generated by infrared radiation A61B5/14552 takes precedence
• CPC Class Codes: A61B 5/02438 with portable devices, e.g. worn by the patient
• CPC Class Codes: A61B 5/08 Detecting, measuring or recording devices for evaluating the respiratory organs A61B5/0205 takes precedence
• CPC Class Codes: A61B 5/0816 Measuring devices for examining respiratory frequency measuring frequency of electric signals G01R23/00
• CPC Class Codes: A61B 5/14551 for measuring blood gases
• CPC Class Codes: A61B 5/4848 Monitoring or testing the effects of treatment, e.g. of medication
• CPC Class Codes: A61B 5/4875 Hydration status, fluid retention of the body
• CPC Class Codes: A61M 5/1723 using feedback of body parameters, e.g. blood-sugar, pressure measurement of body parameters A61B5/00

Abstract

Methods and systems are provided for determining fluid administration. The system may determine fluid administration based on the fluid responsiveness and regional oxygen saturation of a subject. The system may receive the fluid responsiveness and regional oxygen saturation from external sources or may determine one or both based on received physiological signals. In some embodiments, the system may determine whether to administer fluid based on the fluid responsiveness and regional oxygen saturation. In some embodiments, the system may determine the amount of fluid to administer based on the fluid responsiveness and regional oxygen saturation. In some embodiments, the system may determine the effectiveness of fluid administration. In some embodiments, the system may provide an indication of the determined fluid administration so that a care-giver can implement the appropriate fluid administration. In some embodiments, the system may control the fluid administration based on its determination.

Claims

1. A physiological monitoring system comprising:

a pulse oximetry sensor configured to;

detect at least one first wavelength of light from a first tissue of a subject; and

generate a photoplethysmograph (PPG) signal based on the detected at least one first wavelength of light;

a regional oxygen saturation sensor configured to detect at least one second wavelength of light from a second tissue of the subject and determine a value indicative of regional oxygen saturation in the second tissue; and

a processor coupled to the pulse oximetry sensor and the regional oxygen saturation sensor, wherein the processor is configured to;

receive the PPG signal;

determine a value indicative of fluid responsiveness of the subject based on a change in the PPG signal over time;

receive the value indicative of regional oxygen saturation in the second tissue; and

determine whether to administer fluid to the subject based on the value indicative of regional oxygen saturation and the value indicative of fluid responsiveness.

2. The system of claim 1, wherein the value indicative of fluid responsiveness is determined based on respiratory variations identified in the PPG signal.

3. The system of claim 1, wherein the value indicative of fluid responsiveness is determined based on amplitude variations in the PPG signal.

4. The system of claim 1, wherein the value indicative of fluid responsiveness is determined based on variations of a percent modulation of the PPG signal.

5. The system of claim 1, wherein the value indicative of regional oxygen saturation is indicative of oxygen saturation in at least one of the subject'"'"'s brain, kidney, and abdomen.

6. The system of claim 1 further comprising a fluid administration mechanism coupled to the processor configured to administer fluid to the subject based on the processor'"'"'s determination of whether to administer fluid.

7. The system of claim 6, wherein the fluid administration mechanism comprises a syringe and an automated pump mechanism coupled to the syringe that actuates the syringe to administer fluid to the subject based on the processor'"'"'s determination of whether to administer fluid.

8. The system of claim 1, wherein the processor is configured to determine whether to administer fluid to the subject by:

comparing the value indicative of fluid responsiveness to a fluid responsiveness threshold;

comparing the value indicative of regional oxygen saturation to a regional oxygen saturation threshold; and

determining whether to administer fluid to the subject based on both comparisons.

9. The system of claim 8, wherein the regional oxygen saturation threshold is indicative of adequate perfusion of a region associated with the value indicative of regional oxygen saturation.

10. The system of claim 1, wherein the processor is configured to determine the amount of fluid to administer to the subject based on the value indicative of regional oxygen saturation and the value indicative of fluid responsiveness.

11. The system of claim 1, comprising a display configured to display the value indicative of fluid responsiveness and an indication of fluid administration upon a determination to administer fluid to the subject.

12. A physiological monitoring system comprising:

a monitor configured to receive a first plurality of physiological signals generated by a pulse oximetry sensor coupled to the physiological monitoring system and a second plurality of physiological signals generated by a regional oxygen saturation sensor coupled to the physiological monitoring system, wherein the first plurality of physiological signals are indicative of light detected from a first tissue of a subject and the second plurality of physiological signals are indicative of light detected from a second tissue of the subject, the monitor comprising a processor configured to;

calculate regional oxygen saturation in the second tissue of the subject based on the second plurality of physiological signals, wherein the second plurality of physiological signals comprise signals from a first detector and a second detector spaced apart from the first detector, and wherein the regional oxygen saturation is calculated based on a differential absorption of light in the second tissue as detected at the first detector relative to the second detector;

calculate a parameter indicative of fluid responsiveness based on the first plurality of physiological signals; and

provide an indication to administer fluid to the subject based on the regional oxygen saturation and the parameter indicative of fluid responsiveness.

13. The system of claim 12, wherein the processor is configured to calculate the parameter indicative of fluid responsiveness based on respiratory-induced amplitude variations identified in one of the first plurality of physiological signals.

14. The system of claim 12, wherein the processor is configured to calculate the parameter indicative of fluid responsiveness based on variations of a percent modulation of the first plurality of physiological signals.

15. The system of claim 12, wherein the processor is configured to determine whether to administer fluid to the subject based on the regional oxygen saturation and the parameter indicative of fluid responsiveness.

16. The system of claim 12, wherein the processor is configured to determine an amount of fluid to be administered to the subject based on the regional oxygen saturation and the parameter indicative of fluid responsiveness.

17. The system of claim 12, wherein the processor is configured to determine the effectiveness of fluid administration based on a change in at least one of the regional oxygen saturation and the parameter indicative of fluid responsiveness.

18. The system of claim 17, wherein the processor is configured to control the fluid administration of the subject based on the effectiveness of the fluid administration.

19. The system of claim 12, wherein the second tissue for which regional oxygen saturation is calculated is at least one of the subject'"'"'s brain, kidney, and abdomen.

20. The system of claim 12, wherein the processor is configured to control the fluid administration of the subject based on the regional oxygen saturation and the parameter indicative of fluid responsiveness.