US2012078069A1PendingUtilityA1

Blood Flow Monitoring

51
Assignee: MELKER RICHARD JPriority: Jun 20, 2002Filed: Jul 27, 2011Published: Mar 29, 2012
Est. expiryJun 20, 2022(expired)· nominal 20-yr term from priority
A61M 16/085A61B 5/0816A61B 5/0836A61B 5/6826A61B 5/6829A61M 16/0666A61B 2562/247A61M 2230/06A61B 5/14551A61M 16/0672A61M 2202/03A61M 2205/3561A61B 5/0873A61M 2230/30A61M 2205/3569A61M 16/0051A61B 5/14552A61M 2230/205A61M 2230/432A61B 5/6819A61M 2202/0208A61M 2210/0662A61B 2560/0276A61M 16/021A61B 5/682A61M 2210/0618A61M 2210/0625A61M 2230/42A61B 5/0295A61B 5/0261A61M 16/08A61B 5/02427A61M 16/20A61B 5/087A61B 5/7282A61B 5/0205A61B 5/4836A61M 16/0057A61B 5/7278A61B 5/036A61B 5/4818A61M 16/0003A61B 5/02416
51
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Claims

Abstract

The present invention relates to a method of utilizing photoplethysmography obtained from a central site and a non-central site to detect a low blood flow or low blood volume condition. Also disclosed are apparatuses and systems designed to acquire and process physiological information based on photoplethysmograpy signal information from dual sites.

Claims

exact text as granted — not AI-modified
1 . A method of determining hypovolemia in a subject, said method comprising obtaining a first photoplethysmographic (PPG) signal from a central source site of said subject;
 obtaining a second PPG signal from a non-central site of said subject; and   monitoring for a difference between said first PPG signal relative to said second PPG signal;   
       wherein a change between said second PPG signal relative to said first PPG signal indicates a low blood volume condition in the subject. 
     
     
         2 . The method of  claim 1 , wherein said central source site is a nasal alar, nasal septum, cheek or lip of said subject. 
     
     
         3 . The method of  claim 1 , wherein said central source site is a nasal alar of said subject. 
     
     
         4 . The method of  claim 1 , wherein said central source site is a nasal septum of said subject. 
     
     
         5 . The method of  claim 1 , wherein said non-central site is an extremity of said subject. 
     
     
         6 . The method of  claim 1 , wherein said non-central site is a finger or toe of said subject. 
     
     
         7 . The method of  claim 1 , wherein a decrease of said second PPG signal relative to said first PPG signal indicates a low blood flow/low blood volume condition in the subject. 
     
     
         8 . A method of determining hypovolemia in a subject, said method comprising
 monitoring for a difference between a first PPG signal obtained from a central source site of said subject and a second PPG signal obtained from a non-central site of said subject;   
       wherein a decrease of said second PPG signal relative to said first PPG signal indicates a low blood flow/low blood volume condition in the subject. 
     
     
         9 . The method of  claim 8 , wherein said central source site is a nasal alar, nasal septum, cheek or lip of said subject. 
     
     
         10 . The method of  claim 8 , wherein said central source site is a nasal alar of said subject. 
     
     
         12 . The method of  claim 8 , wherein said central source site is a nasal septum of said subject. 
     
     
         13 . The method of  claim 8 , wherein said non-central source site is an extremity of said subject. 
     
     
         14 . The method of  claim 8 , wherein said non-central source site is a finger or toe of said subject. 
     
     
         15 . An apparatus for analyzing photoplethysmography signals from at least two sites on a living vertebrate, to determine the presence or absence of, or to monitor changes in, impaired peripheral perfusion or volume status comprising:
 a. means for receiving pulse oximeter probe signals from at least two sites on a living vertebrate, wherein at least one said site is a central source site and at least one said site is a non-central site; and   
       means for determining a change in blood volume at at least one non-central site based on the extent to which said at least one non-central site has a lower photoplethysmography signal than said central source site or the photoplethysmograpy signal from one non-central site decreases relative to the signal at the central site over time. 
     
     
         16 . The apparatus of  claim 15 , further comprising a means for presenting results to a user of said apparatus. 
     
     
         17 . A monitor system for analyzing photoplethysmography signals from at least two sites on a living vertebrate, to monitor changes in blood flow, comprising:
 a. output circuitry to deliver timed signals to energize light generating components of at least two pulse oximeter probes;   b. input circuitry to receive signals from said at least two pulse oximeter probes positioned said at least two sites on a living vertebrate, wherein at least one said site is a central source site and at least one said site is a non-central site;   c. a computer loaded with software to
 1. provide timed signals to energize said light generating components; 
 2. average sufficient signals from each pulse oximeter probe site to obtain a statistically reliable average; 
 3. calculate a time-set estimate of a photoplethysmography signal based on said statistically reliable average; 
 4. repeat steps 2 and 3 to obtain sequential time-set estimates of a photoplethysmography signal from each site; 
 5. compare a sequential time-set estimate of the photoplethysmography signal from the central source site with a sequential time-set estimate, taken at a similar time, of the photoplethysmography signal from the at least one non-central site; and 
 6. determine a change in blood volume to said at least one non-central site based on the extent to which said non-central site has a lower photoplethsymography signal than said central source site. 
   
     
     
         18 . A monitor system of  claim 17 , further comprising a read-out device to provide results to a user of said system. 
     
     
         19 . The monitor system of  claim 17 , further comprising software in said computer for estimating blood pressure through analysis of pulse time delay between said at least two sites. 
     
     
         20 . A method of observing respiration in a patient, said method comprising monitoring changes in the envelope of a PPG signal from a central source site of said patient.

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