HANDHELD PHYSIOLOGICAL SENSOR

• US 20170188859A1
• Filed: 01/05/2016
• Published: 07/06/2017
• Est. Priority Date: 01/05/2016
• Status: Abandoned Application

• Current Assignee: OtoSense, Inc. (Analog Devices, Inc.)
• Original Assignee: OtoSense, Inc. (Analog Devices, Inc.)
• Inventors: BANET, Matthew, DHILLON, Marshal Singh, PEDE, Susan Meeks, DEPTALA, Arthur, HAYWARD, Lauren Nicole Miller, COCHRAN, Jonas Dean
• Application Number:
  US14/988,692
• Publication Number:
  US 20170188859A1
• Time in Patent Office: Days
• CPC Class Codes: A61B 5/02055 Simultaneously evaluating both cardiovascular condition and temperature
• CPC Class Codes: A61B 5/021 Measuring pressure in heart or blood vessels A61B5/0205 takes precedence
• CPC Class Codes: A61B 5/02405 Determining heart rate variability
• CPC Class Codes: A61B 5/02433 for infrared radiation
• CPC Class Codes: A61B 5/0245 by using sensing means generating electric signals, i.e. ECG signals
• CPC Class Codes: A61B 5/029 Measuring or recording blood output from the heart, e.g. minute volume A61B8/065 takes precedence
• CPC Class Codes: A61B 5/0535 Impedance plethysmography for measuring blood flow A61B5/0295
• CPC Class Codes: A61B 5/14551 for measuring blood gases
• CPC Class Codes: A61B 5/349 Detecting specific parameters of the electrocardiograph cycle
• CPC Class Codes: A61B 5/6824 Arm or wrist
• CPC Class Codes: A61B 5/6826 Finger

Abstract

A handheld device measures all vital signs and some hemodynamic parameters from the human body and transmits measured information wirelessly to a web-based system, where the information can be analyzed by a clinician to help diagnose a patient. The system utilizes our discovery that bio-impedance signals used to determine vital signs and hemodynamic parameters can be measured over a conduction pathway extending from the patient'"'"'s wrist to a location on their thoracic cavity, e.g. their chest or navel. The device'"'"'s form factor can include re-usable electrode materials to reduce costs. Measurements made by the handheld device, which use the belly button as a ‘fiducial’ marker, facilitate consistent, daily measurements, thereby reducing positioning errors that reduce accuracy of standard impedance measurements. In this and other ways, the handheld device provides an effective tool for characterizing patients with chronic diseases, such as heart failure, renal disease, and hypertension.

Claims

1. A biometric sensor configured to measure a set of physiological parameters from a patient, comprising:

an arm-receiving portion comprising a first opening configured to receive a distal portion of one of the patient'"'"'s arms and a first electrode configured and arranged to contact the distal portion of the patient'"'"'s arm when it is inserted in the first opening;

a body-contacting portion comprising an exterior-facing surface and a second electrode configured and arranged to contact a second body location that is one of the patient'"'"'s torso, legs, opposing arm, and neck when the body-contacting portion is pressed against the second body location while the distal portion of the patient'"'"'s arm is inserted in the first opening;

a first analog system configured to receive biometric signals from the first electrode and the second electrode and to process the biometric signals to generate a first analog physiological waveform;

a finger-receiving portion comprising a second opening, configured and arranged to receive a finger of said one of the patient'"'"'s arms while the distal portion thereof is received by the arm-receiving portion, and an optical system, the optical system comprising a first light source configured to irradiate the finger and a photodetector configured to receive radiation after it irradiates the finger;

a second analog system configured to receive signals from the photodetector and to process them to generate a second analog physiological waveform;

a first digital system configured to digitize the first analog physiological waveform and process it with computer code to determine a first physiological parameter in the set of physiological parameters; and

a second digital system configured to digitize the second physiological waveform and process it with computer code to determine a second physiological parameter in the set of physiological parameters.

2. The biometric sensor of claim 1, wherein the second analog physiological waveform comprises heartbeat-induced pulsations.

3. The biometric sensor of claim 2, wherein the second analog physiological waveform is a photoplethysmogram waveform.

4. The biometric sensor of claim 3, wherein the photoplethysmogram waveform comprises a set of heartbeat-induced pulses, and the computer code is configured to calculate a time difference between the pulses to determine the patient'"'"'s heart rate.

5. The biometric sensor of claim 1, wherein the optical system further comprises a second light source configured to irradiate the finger and the photodetector is configured to receive radiation from both the first and second light sources after they irradiate the finger.

6. The biometric sensor of claim 5, wherein the second analog system is configured 1) to receive signals from the photodetector that are generated with radiation from the first light source and to process them to generate the second physiological waveform;

and

     2) to receive signals from the photodetector that are generated with radiation from the second light source and to process them to generate a third physiological waveform.

7. The biometric sensor of claim 6, wherein the first light source is configured to emit optical radiation between 880 and 920 nm.

8. The biometric sensor of claim 7, wherein the first light source is configured to emit optical radiation around 905 nm.

9. The biometric of claim 6, wherein the second light source is configured to emit optical radiation between 640 and 680 nm.

10. The biometric sensor of claim 9, wherein the second light source is configured to emit optical radiation around 660 nm.

11. The biometric sensor of claim 6, wherein the first and second light sources and the photodetector are connected to a common surface of the optical system.

12. The biometric sensor of claim 11, wherein the photodetector is configured to receive infrared radiation from the first and second light sources after it reflects off of the patient'"'"'s finger.

13. The biometric sensor of claim 1, wherein the first and second light sources are connected to a top surface of the optical system so as to irradiate an upper surface of the patient'"'"'s finger when it is positioned within the second opening.

14. The biometric sensor of claim 13, wherein the photodetector is connected to a bottom surface of the optical system so as to irradiate a lower surface of the patient'"'"'s finger when it is positioned within the second opening.

15. The biometric sensor of claim 14, wherein the photodetector is configured to receive infrared radiation from the first and second light sources after it is transmitted through the patient'"'"'s finger.

16. The biometric sensor of claim 6, wherein the second digital system comprises computer code configured to analyze the second analog physiological waveform to determine an AC infrared component thereof (infrared(AC)) and a DC infrared component thereof (infrared(DC)).

17. The biometric sensor of claim 16, wherein the second digital system comprises computer code configured to analyze the third physiological waveform to determine a red AC component thereof (red(AC)) and a red DC component thereof (red(DC)).

18. The biometric sensor of claim 17, wherein the second digital system comprises computer code configured to collectively analyze the infrared(AC), infrared(DC), red(AC), and red(DC) components to determine a pulse oximetry value.

19. The biometric sensor of claim 18, wherein the second digital system comprises computer code configured to collectively analyze the infrared(AC), infrared(DC), red(AC), and red(DC) components according to the following equation to determine a ratio of ratios (RoR):

20. The biometric sensor of claim 19, wherein the second digital system comprises computer code configured to process the RoR according to the following equation to determine said pulse oximetry value:

pulse oximetry value=(a+b×

RoR+c×

RoR)×

100

wherein a, b, and c are pre-determined constants.