Method for monitoring blood flow and volume using photoplethysmography

• US 9,717,836 B2
• Filed: 07/27/2011
• Issued: 08/01/2017
• Est. Priority Date: 09/15/2006
• Status: Active Grant

• Current Assignee: University of Florida Research Foundation, Incorporated (State University System of Florida)
• Original Assignee: University of Florida Research Foundation, Incorporated (State University System of Florida)
• Inventors: Melker, Richard J.
• Primary Examiner(s): Zalukaeva, Tatyana
• Assistant Examiner(s): TREYGER, ILYA Y
• Application Number:
  US13/191,790
• Publication Number:
  US 20120053469A1
• Time in Patent Office: 2,197 Days
• Field of Search: 604 504, 604 611, 604 9
• CPC Class Codes: A61B 5/02007 Evaluating blood vessel condition, e.g. elasticity, compliance
• CPC Class Codes: A61B 5/0261 using optical means, e.g. infrared light
• CPC Class Codes: A61B 5/0295 using plethysmography, i.e. measuring the variations in the volume of a body part as modified by the circulation of blood therethrough, e.g. impedance plethysmography
• CPC Class Codes: A61B 5/6819 Nose
• CPC Class Codes: A61M 1/34 Filtering material out of the blood by passing it through a membrane, i.e. hemofiltration or diafiltration
• CPC Class Codes: A61M 1/3403 Regulation parameters
• CPC Class Codes: A61M 1/341 by measuring the filtrate rate or volume
• CPC Class Codes: A61M 1/3609 Physical characteristics of the blood, e.g. haematocrit, urea
• CPC Class Codes: A61M 2205/3306 Optical measuring means
• CPC Class Codes: A61M 2205/50 with microprocessors or computers

Abstract

Disclosed herein are methods, systems and devices to monitor vascular volume status utilizing at least one oximetry/photoplethysmography sensor. The methods, systems and devices provide an alternative to conventional vascular volume monitoring methods while enabling reliable, non-invasive, and automatic monitoring of vascular volume to avert patient hypotension. The methods, systems and devices may be employed in the context of both inpatient and outpatient facilities and may also be incorporated into conventional monitoring devices, techniques and equipment.

Claims

1. A method of monitoring and adjusting volume status in a subject, said method comprising

positioning a first photoplethysmography sensor on a central source site of said subject and positioning a second photoplethysmography sensor on a peripheral source site of said subject;

obtaining a first area under the curve (AUC) and/or first amplitude of a pulsatile cardiac component (PCC) of a photoplethysmographic (PPG) signal from said first photoplethysmography sensor on said central source site;

obtaining a second area under the curve (AUC) and/or second amplitude of a pulsatile cardiac component (PCC) of a photoplethysmographic (PPG) signal from said second photoplethysmography sensor on said peripheral source site; and

comparing said first AUC and/or amplitude and said second AUC and/or amplitude;

wherein if said second AUC and/or amplitude decreases relative to said first AUC and/or amplitude, fluids are administered to the subject or fluid removal is decreased, and if said second AUC and/or amplitude increases relative to said first AUC and/or amplitude, fluid removal is increased or fluid administration to the subject is decreased.

2. The method of claim 1, wherein said central source site is a nasal septum, nasal alar, lip or cheek of said subject.

3. The method of claim 1, wherein said peripheral source site is a finger or toe of said subject.

10. The method of claim 1, wherein at least one processing module calculates the first AUC and/or first amplitude of the PCC of the first PPG signal, and wherein the at least one processing module calculates the second AUC and/or second amplitude of the PCC of a second PPG signal.

11. The method of claim 10, wherein the at least one processing module generates a report indicating the subject'"'"'s blood flow and/or volume status.

4. A method of monitoring and treating hypovolemia in a subject, said method comprising

positioning a first photoplethysmography sensor on a central source site of said subject and positioning a second photoplethysmography sensor on a peripheral source site of said subject;

comparing a first AUC and/or amplitude obtained from a PPG signal from said first photoplethysmography sensor on said central source site and a second AUC and/or amplitude obtained from a PPG signal from said second photoplethysmography sensor on said peripheral source site of said subject;

wherein if said second AUC and/or amplitude decreases relative to said first AUC and/or amplitude, fluids are administered to the subject or fluid removal to the subject is decreased.

5. The method of claim 4, wherein said central source site is a nasal alar, nasal septum, cheek or lip of said subject.

6. The method of claim 4, wherein said central source site is a nasal alar of said subject.

7. The method of claim 4, wherein said central source site is a nasal septum of said subject.

8. The method of claim 4, wherein said peripheral source site is an extremity of said subject.

9. The method of claim 4, wherein said peripheral source site is a finger or toe of said subject.