Daytime/nighttime respiration rate monitoring

Patent metadata

Field	Value
Publication number	US-9743859-B2
Application number	US-70865510-A
Country	US
Kind code	B2
Filing date	Feb 19, 2010
Priority date	Jun 15, 2007
Publication date	Aug 29, 2017
Grant date	Aug 29, 2017

Abstract

A device and method can monitor or trend a patient's respiration rate measurements according to the time of day. The device, which may be implantable or external, collects and classifies respiration rate measurements over time. The trended information about particular classes of respiration rate measurements is then communicated to a remote external device, which in turn provides an indication of heart failure decompensation. Examples of classes of respiration rate measurements include a daily maximum respiration rate value, a daily minimum respiration rate value, a daily maximum respiration rate variability value, a daily minimum respiration rate variability value, and a daily central respiration rate value. These respiration rate measurements can be further classified into daytime or nighttime respiration rate measurements.

First claim

What is claimed is:

1. A non-transitory device-readable storage medium including instructions that, when performed by one or more devices, cause the one or more devices to perform acts comprising:
detecting a respiration signal from a subject using a respiration sensor; determining respiration rate or interval measurements from the respiration signal;
classifying the respiration rate or interval measurements into daytime respiration rate or interval measurements or nighttime respiration rate or interval measurements using a first classifier circuit; classifying the daytime respiration rate or interval measurements into two or more daytime subclasses of statistical measurements of respiration rate or interval measurements, or classifying the nighttime respiration rate or interval measurements into two or more nighttime subclasses of statistical measurements of respiration rate or interval measurements using a second classifier circuit;
trending the classified daytime subclasses or nighttime subclasses of respiration rate or interval measurements over a period of multiple days;
generating a diagnostic indicator of heart failure decompensation using a statistical measure of the trended daytime subclasses or nighttime subclasses of respiration rate or interval measurements; and
providing instructions to display the diagnostic indicator to guide a heart failure therapy.

2. The non-transitory device-readable storage medium of claim 1 , including instructions that, when performed by the one or more devices, cause one of the one or more devices to perform acts comprising comparing the daytime or nighttime respiration rate or interval measurements.

3. The non-transitory device-readable storage medium of claim 1 , wherein determining respiration rate or interval measurements from the respiration signal comprises excluding a period of apneic breathing.

4. The non-transitory device-readable storage medium of claim 1 , wherein classifying the daytime or nighttime respiration rate or interval measurements includes (1) classifying the daytime respiration rate or interval measurements into at least one of the following subclasses:
a daytime maximum respiration rate value, a daytime minimum respiration rate value, a daytime maximum respiration rate variability value, a daytime minimum respiration rate variability value, and a daytime central tendency of respiration rate value, or (2) classifying the nighttime respiration rate or interval measurements into at least one of the following subclasses:
a nighttime maximum respiration rate value, a nighttime minimum respiration rate value, a nighttime maximum respiration rate variability value, a nighttime minimum respiration rate variability value, and a nighttime central tendency of respiration rate value.

5. The non-transitory device-readable storage medium of claim 1 , including instructions that, when performed by the one or more devices, cause one of the one or more devices to perform acts comprising providing the diagnostic indicator using a detected change over time in a measure of centrality of the trended daytime or nighttime subclasses of respiration rate or interval measurements.

6. The non-transitory device-readable storage medium of claim 1 , including instructions that, when performed by the one or more devices, cause one of the one or more devices to perform acts comprising providing the diagnostic indicator using a detected change over time in a measure of spread or variance of the trended daytime or nighttime subclasses of respiration rate or interval measurements.

7. The non-transitory device-readable storage medium of claim 1 , including instructions that, when performed by the one or more devices, cause one of the one or more devices to perform acts comprising:
integrating or otherwise lowpass filtering the respiration rate or interval measurements to obtain lowpass filtered respiration rate or interval measurements;
detecting a change in the lowpass filtered respiration rate or interval measurements over a period of time; and
providing a second diagnostic indicator using the detected change in the lowpass filtered respiration rate or interval measurements.

8. The non-transitory device-readable storage medium of claim 1 , including instructions that, when performed by the one or more devices, cause one of the one or more devices to perform acts including a second trending of the classified daytime subclasses or nighttime subclasses of respiration rate or interval measurements, the second trending comprising:
forming a histogram of the classified daytime subclasses or nighttime subclasses of respiration rate or interval measurements;
updating the histogram over time; and
detecting a change in the histogram over time; and
wherein the instruction to generate the diagnostic indicator using the statistical measure of the trended daytime or nighttime subclasses include an instruction that causes the one or more devices to generate a second diagnostic indicator using the detected change in the histogram over time.

9. The non-transitory device-readable storage medium of claim 1 , including instructions that, when performed by the one or more devices, cause one of the one or more devices perform acts comprising a second classifying of the respiration rate or interval measurements into one of: respiration rate or interval measurements determined at a specified sleep stage measure; respiration rate or interval measurements determined at an angle of reclination; respiration rate or interval measurements determined at a physical activity level; or respiration rate or interval measurements determined at a posture.

10. The non-transitory device-readable storage medium of claim 9 , including instructions that, when performed by the one or more devices, cause one of the one or more devices to perform acts comprising trending of the second classified respiration rate or interval measurements.

11. The non-transitory device-readable storage medium of claim 10 , wherein the trending of the second classified respiration rate or interval measurements includes at least one of:
trending a central tendency measure of a respiration rate or interval obtained when the subject is in a supine position;
trending a variability measure of a respiration rate or interval obtained when the subject is exhibiting non-rapid eye movement sleep; and
trending a maximum respiration rate or interval measurement obtained when the patient is exhibiting a physical activity level that is above a threshold value.

12. The non-transitory device-readable storage medium of claim 11 , wherein the instructions for generating the diagnostic indicator include instructions for generating an indicator of a worsening heart failure status in response to the trended central tendency exceeds a threshold, or the trended central tendency shift in time to an earlier occurrence.

13. The non-transitory device-readable storage medium of claim 11 , wherein the instruction for generating the diagnostic indicator include instructions for generating an indicator of a worsening heart failure status in response to the trended variability exceeds a threshold.

14. The non-transitory device-readable storage medium of claim 1 , including instructions that, when performed by the one or more devices, cause one of the one or more devices to perform acts comprising recording, in correspondence with the respiration rate or interval measurements, at least one of a heart rate, heart sound, heart rate variability, blood pressure, and impedance.

15. The non-transitory device-readable storage medium of claim 1 , including instructions that, when per

Assignees

• Lewicke Aaron
• Zhang Yi
• Hatlestad John D
• Cardiac Pacemakers Inc

Inventors

• Lewicke Aaron
• Zhang Yi
• Hatlestad John D

Classifications

• G16H50/20

  for computer-aided diagnosis, e.g. based on medical expert systems · CPC title

• A61B5/0205

  Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition · CPC title

• A61B5/0816 Primary

  Measuring devices for examining respiratory frequency (measuring frequency of electric signals G01R23/00) · CPC title

• A61B5/7264

  Classification of physiological signals or data, e.g. using neural networks, statistical classifiers, expert systems or fuzzy systems · CPC title

• A61B5/1116

  Determining posture transitions · CPC title