RESPIRATORY DISEASE MONITORING SYSTEM

• US 20110125044A1
• Filed: 11/24/2010
• Published: 05/26/2011
• Est. Priority Date: 11/25/2009
• Status: Active Grant

• Current Assignee: University of Rochester
• Original Assignee: University of Rochester
• Inventors: RHEE, Hyekyun, BOCKO, Mark
• Granted Patent: US 8,758,262 B2
• Time in Patent Office: Days
• US Class Current: 600/534
• CPC Class Codes: A61B 5/113 occurring during breathing
• CPC Class Codes: A61B 5/7267 involving training the classification device
• CPC Class Codes: A61B 7/003 Detecting lung or respiration noise
• CPC Class Codes: A61B 7/04 Electric stethoscopes microphones, acoustic transducers therefor H04R

Abstract

An automated system for monitoring respiratory diseases, such as asthma, provides noninvasive, multimodal monitoring of respiratory signs and symptoms that can include wheeze and cough. Some embodiments employ a mobile device, such as a cell phone, in which raw data from a microphone and an accelerometer are processed, analyzed, and stored. Data can be collected continuously. Time domain and frequency domain analyses of signals to determine, e.g., energy, duration, and spectral content of candidate sounds can be employed to discriminate symptoms of interest from background sounds and to establish significance. Accelerometer signals are analyzed to determine activity levels. Analyses of a user'"'"'s symptoms and activity level prior to, during, and after an event can provide meaningful determinations of disease severity and predict future respiratory events. The system can provide a summary of data, as well as an alarm when symptom severity reaches a threshold.

Claims

1. A method of monitoring a respiratory illness, comprising:

detecting a patient sound, comprising at least one of an abnormal breath sound of a patient and a cough sound of the patient;

detecting a movement of at least part of the patient;

determining a correlation between an indicator of the patient sound and an indicator of the movement;

outputting to an output device an indicator, based on the correlation, of at least one of a severity of the respiratory illness and a probability of a respiratory illness-related event of the patient.

2. The method of claim 1, wherein the respiratory illness comprises asthma.

3. The method of claim 1, wherein the abnormal breath sound comprises at least one of a wheeze, a rhonchus, a diminished breath sound, and stridor.

4. The method of claim 1, wherein the indicator of the movement comprises an acceleration.

5. An asthma monitoring system, comprising:

a sound sensing device that detects sound over at least a portion of the audible spectrum and converts the detected sound to a sound signal;

an acceleration sensing device that detects acceleration and converts the detected acceleration to an acceleration signals;

an output device; and

a computation module, operably connected to the sound sensing device, the acceleration sensing device, and the output device, the computation module comprising;

a memory, containing instructions for processing the sound signal and the acceleration signal;

a communication module configured to transmit signals to an external device; and

a processor module, operably connected to the memory, the communication module, and the output device, and configured to receive the sound signal and the acceleration signal;

wherein the processor module retrieves the instructions from the memory, processes the sound signal and the acceleration signal according to the instructions, stores data generated according to the instructions, sends at least one signal generated according to the instructions to the output device, and sends data through the communication module to the external device according to the instructions.

6. The system of claim 5, wherein the instructions comprise at least one algorithm that converts a time waveform of the sound signal into a frequency representation and performs time-domain analysis and frequency-domain analysis of at least one of the sound signal and the acceleration signal.

7. The system of claim 6, wherein the instructions further comprise at least one algorithm capable of discriminating an asthma symptom from another sonic event in the sound signal.

8. The system of claim 6, wherein the instructions further comprise an algorithm that measures peaks of the frequency representation at frequencies in about the 200-800 Hz range, and compares these to a predetermined value associated with wheezing that is stored in the memory.

9. The system of claim 6, wherein the instructions further comprise an algorithm that measures an amplitude and duration of a sonic event of the sound signal and measures a power spectral density over a selected band of frequencies, and compares the power spectral density to a predetermined value associated with coughing that is stored in the memory.

10. The system of claim 6, wherein the instructions further comprise an algorithm that measures a spectral centroid of the sound signal.

11. The system of claim 6, wherein the instructions further comprise an algorithm that measures a spectral-peak-to-noise ratio of the sound signal.

12. The system of claim 6, wherein the instructions further comprise an algorithm that measures a time characteristic and a spectral characteristic of the acceleration signal and compares these measurements to predetermined values associated with at least one level of activity stored in the memory.

13. The system of claim 12, wherein the instructions further comprise an algorithm that detects a sonic event in a time waveform of the sound signal, discriminates an asthma symptom from another sonic event, measures an amplitude and a duration of the symptom, measures a power spectral density over a selected band of frequencies, and compares the amplitude and the duration and the power spectral density of the symptom to predetermined values associated with coughing that are stored in the memory, measures a peak of a frequency representation of the symptom at frequencies in about the 200-800 Hz range, and compares the measured peak to a predetermined value associated with wheezing that is stored in the memory, and uses a combination of the cough comparison, the wheezing comparison, and the activity level to produce an indication of at least one of an asthma severity and a likelihood of worsening of an asthma condition.

14. The system of claim 5, wherein the computation module further comprises a circuit that measures power of the sound signal and of the acceleration signal at selected frequencies and passes the power measurements to the processor module.

15. The system of claim 5, wherein the output device comprises an audio speaker.

16. The system of claim 5, wherein the acceleration sensing device measures acceleration in more than one non-parallel axis and produces signals representing accelerations in three orthogonal axes.

17. The system of claim 5, wherein the computation module is contained in at least one of a cell phone, a personal digital assistant (PDA), a handheld computer, a pager, and a portable media player.

18. The system of claim 17, wherein the acceleration sensing device communicates wirelessly with the computation module.

19. The system of claim 17, wherein the acceleration sensing device is contained in the same cell phone, personal digital assistant (PDA), handheld computer, pager, or portable media player.

20. The system of claim 5, further comprising the external device.

21. A method of monitoring asthma of a patient, comprising:

generating a sound signal, from detected sound in at least a portion of an audible spectrum;

generating an acceleration signal, from detected acceleration of at least part of the patient'"'"'s body;

determining a correlation between the sound signal and the acceleration signal, according to program instructions stored in a computer-readable memory;

sending an indicator signal to an output device when the correlation is indicative of at least one of (a) exceeding a threshold value of a severity of asthma, and (b) exceeding a threshold value of a probability of an asthma-related event,

wherein the indicator signal results in the output device indicating at least one of the severity of asthma and the probability.

22. The method of claim 21, wherein the detected sound comprises at least one of a sound of a cough and an abnormal breath sound of the patient.

23. The method of claim 21, wherein the abnormal breath sound comprises at least one of a wheeze, a rhonchus, a diminished breath sound, and stridor.