US2022400962A1PendingUtilityA1

Plethysmographic respiration rate detection

Assignee: MASIMO CORPPriority: Mar 30, 2010Filed: Jul 27, 2022Published: Dec 22, 2022
Est. expiryMar 30, 2030(~3.7 yrs left)· nominal 20-yr term from priority
A61B 5/725A61B 5/0261A61B 5/7278A61B 5/02007A61B 5/029G16H 50/30A61B 5/7253A61B 5/0816A61B 5/7475G16H 50/00A61B 5/08A61B 5/6826A61B 5/14552A61B 5/7405A61B 5/7264A61B 5/7225A61B 5/0205A61B 5/0806A61B 5/0295A61B 5/7203G16H 15/00A61B 5/742A61B 5/7246A61B 5/7228A61B 5/746G06F 18/21A61B 5/02416G06F 2218/16G06F 2218/10
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Claims

Abstract

A plethysmographic respiration processor is responsive to respiratory effects appearing on a blood volume waveform and the corresponding detected intensity waveform measured with an optical sensor at a blood perfused peripheral tissue site so as to provide a measurement of respiration rate. A preprocessor identifies a windowed pleth corresponding to a physiologically acceptable series of plethysmograph waveform pulses. Multiple processors derive different parameters responsive to particular respiratory effects on the windowed pleth. Decision logic determines a respiration rate based upon at least a portion of these parameters.

Claims

exact text as granted — not AI-modified
1 - 20 . (canceled) 
     
     
         21 . A method for determining a respiration rate from a plethysmograph waveform, the method comprising:
 receiving a plethysmograph waveform from a noninvasive sensor monitoring a patient;   identifying a plurality of portions of the plethysmograph waveform which include physiologically acceptable series of plethysmograph waveform pulses;   deriving, by one or more processors, a first set of frequencies from a first respiratory-induced modulation in a portion of the plurality of portions;   deriving, by the one or more processors, a second set of frequencies from a second respiratory-induced modulation in the portion, the second respiratory-induced modulation being different from the first respiratory-induced modulation;   comparing, by the one or more processors, the first set of frequencies and the second set of frequencies to determine whether any of the first set of frequencies matches any of the second set of frequencies within a tolerance;   generating and outputting, by the one or more processors, a respiration rate in real time to a display from determining that one of the first set of frequencies matches one of the second set of frequencies within the tolerance; and   activating, by the one or more processors, an alarm in real time if the respiration rate satisfies an alarm threshold.   
     
     
         22 . The method of  claim 21 , wherein said comparing comprises comparing individual frequencies of the first set of frequencies and individual frequencies of the second set of frequencies in an order that depends on a pulse rate for the patient. 
     
     
         23 . The method of  claim 21 , wherein said comparing comprises comparing the first set of frequencies and the second set of frequencies until at least determining that none of at least two of the first set of frequencies match none of at least two of the second set of frequencies within the tolerance. 
     
     
         24 . The method of  claim 21 , further comprising deriving, by the one or more processors, a third set of frequencies from a third respiratory-induced modulation in the portion, the third respiratory-induced modulation being different from the first respiratory-induced modulation and the second respiratory-induced modulation,
 wherein said comparing comprises comparing the first set of frequencies, the second set of frequencies, and the third set of frequencies to determine whether any of the first set of frequencies matches any of the second set of frequencies and any of the third set of frequencies within the tolerance, and   wherein said generating and outputting comprises generating and outputting the respiration rate in real time to the display from determining that the one of the first set of frequencies matches the one of the second set of frequencies and one of the third set of frequencies within the tolerance.   
     
     
         25 . The method of  claim 21 , wherein the portion comprises plethysmograph data captured from monitoring the patient over a period less than 120 seconds. 
     
     
         26 . The method of  claim 21 , further comprising:
 deriving a third set of frequencies from the first respiratory-induced modulation in another portion of the plurality of portions;   deriving a fourth set of frequencies from the second respiratory-induced modulation in the another portion;   comparing the third set of frequencies and the fourth set of frequencies to determine whether any of the third set of frequencies matches any of the fourth set of frequencies within the tolerance;   generating another respiration rate from determining that one of the third set of frequencies matches one of the fourth set of frequencies within the tolerance; and   deriving a combined respiration rate from the respiratory rate and the another respiratory rate.   
     
     
         27 . The method of  claim 26 , further comprising:
 deriving a fifth set of frequencies from the first respiratory-induced modulation in yet another portion of the plurality of portions;   deriving a sixth set of frequencies from the second respiratory-induced modulation in the yet another portion;   comparing the fifth set of frequencies and the sixth set of frequencies to determine whether any of the fifth set of frequencies matches any of the sixth set of frequencies within the tolerance;   generating yet another respiration rate from determining that one of the fifth set of frequencies matches one of the sixth set of frequencies within the tolerance;   determining that the yet another respiration rate differs from the combined respiration rate by more than an amount; and   rejecting the yet another respiration rate in response to determining that the yet another respiration rate differs from the combined respiration rate by more than the amount.   
     
     
         28 . The method of  claim 29 , wherein the portion comprises plethysmograph data captured from monitoring the patient over a different period than the another portion. 
     
     
         29 . The method of  claim 21 , wherein said generating and outputting comprises generating and outputting the respiration rate in real time to the display from determining that the one of the first set of frequencies matches the one of the second set of frequencies within the tolerance and from determining that an additional condition is met. 
     
     
         30 . The method of  claim 29 , wherein the additional condition is met when the respiration rate differs from a value by less than an amount. 
     
     
         31 . The method of  claim 21 , wherein the first respiratory-induced modulation comprises a respiratory-induced baseline shift of the portion, and the second respiratory-induced modulation comprises a respiratory-induced amplitude modulation of the portion. 
     
     
         32 . The method of  claim 21 , wherein the first respiratory-induced modulation comprises a respiratory-induced baseline shift of the portion, and the second respiratory-induced modulation comprises a respiratory-induced shape modulation of the portion. 
     
     
         33 . The method of  claim 21 , wherein the first respiratory-induced modulation comprises a respiratory-induced amplitude modulation of the portion, and the second respiratory-induced modulation comprises a respiratory-induced shape modulation of the portion. 
     
     
         34 . The method of  claim 21 , further comprising presenting the respiration rate by the display. 
     
     
         35 . The method of  claim 34 , wherein the one or more processors and the display are part of a patient monitor. 
     
     
         36 . The method of  claim 21 , wherein the respiration rate comprises the one of the first set of frequencies. 
     
     
         37 . The method of  claim 21 , further comprising generating the plethysmograph waveform with the noninvasive sensor. 
     
     
         38 . The method of  claim 37 , further comprising attaching the noninvasive sensor to a finger of the patient.

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