Neck-worn physiological monitor

Patent metadata

Field	Value
Publication number	US-11229405-B2
Application number	US-201514975646-A
Country	US
Kind code	B2
Filing date	Dec 18, 2015
Priority date	Dec 18, 2015
Publication date	Jan 25, 2022
Grant date	Jan 25, 2022

Abstract

The invention provides a neck-worn sensor that is a single, body-worn system that measures the following parameters from an ambulatory patient: heart rate, pulse rate, pulse oximetry, respiratory rate, temperature, thoracic fluid levels, stroke volume, cardiac output, and a parameter sensitive to blood pressure called pulse transit time. From stroke volume, a first algorithm employing a linear model can estimate the patient's pulse pressure. And from pulse pressure and pulse transit time, a second algorithm, also employing a linear algorithm, can estimate systolic blood pressure and diastolic blood pressure. Thus, the sensor can measure all five vital signs along with hemodynamic parameters. It also includes a motion-detecting accelerometer, from which it can determine motion-related parameters such as posture, degree of motion, activity level, respiratory-induced heaving of the chest, and falls.

First claim

What is claimed is:

1. A sensor for measuring from a patient a systolic blood pressure (SYS), a diastolic blood pressure (DIA), and a pulse oximetry (SpO2), the sensor configured to be located on the patient's chest and comprising:
a sensing portion having a flexible housing configured to be located on the patient's chest and enclosing a battery, wireless transmitter, and all of the sensor's sensing and electronic components, including:
at least two pairs of electrode contact points disposed on a bottom surface of the flexible housing, with each pair of electrode contact points comprising a current-injecting electrode contact point and a voltage-sensing electrode contact point;
an analog electrocardiogram (ECG) circuit contained entirely within the flexible housing and in electrical contact with a first voltage-sensing electrode contact point from a first pair of electrode contact points and a second voltage-sensing electrode contact point from a second pair of electrode contact points, the analog ECG circuit configured to generate an analog ECG waveform based on sensed voltage;
an analog impedance circuit contained entirely within the flexible housing and in electrical contact with current-injecting and voltage-sensing electrode contact points in both the first and second pair of electrode contact points, the analog impedance circuit being configured to generate an analog impedance waveform based on sensed voltage;
an optical system located on a bottom surface of the flexible housing, the optical system comprising a light source configured to generate radiation in both the red and infrared spectral ranges that separately irradiates a portion of the patient's chest disposed underneath the flexible housing, and a photodetector configured to detect radiation in the red spectral range that reflects off the portion of the patient's chest to generate a first analog photoplethysmogram waveform (red-PPG), and to detect radiation in the infrared spectral range that reflects off the portion of the patient's chest to generate a second analog photoplethysmogram waveform (infrared-PPG), with the optical system located between a first electrode contact point and a second electrode contact point of one of the two pairs of electrode contact points and configured to be releasably connected to the patient's chest by the electrode contact points, such that the optical system irradiates the portion of the patient's chest between the first electrode contact point and the second electrode contact point of one of the two pairs of electrode contact points;
a digital processing system contained entirely within the housing and comprising a microprocessor and an analog-to-digital converter, the digital processing system being configured to: 1) digitize the analog ECG waveform to generate a digital ECG waveform, 2) digitize the analog impedance waveform to generate a digital impedance waveform, 3) digitize the analog red-PPG waveform to generate a digital red-PPG waveform, and 4) digitize the analog infrared-PPG waveform to generate a digital infrared-PPG waveform;
a first sensor for measuring stroke volume (SV) disposed within the flexible housing, the first sensor comprising a first processor configured to determine SV from a maximum value of a mathematical derivative of the digital impedance waveform and a baseline value of the digital impedance waveform;
a second sensor for measuring blood pressure contained entirely within the flexible housing, the second sensor comprising a second processor configured to collectively process the digital impedance waveform and one of the digital red-PPG and infrared-PPG waveforms to determine: 1) a first time point from one of the digital red-PPG and digital infrared-PPG waveforms, 2) a second time point from the digital impedance waveform, 3) a vascular transit time (VTT) from the temporal difference between the first and second time points, 4) a value of SYS from a linear equation that includes an inverse value of VTT, 5) a value of pulse pressure (PP) from the product of SV and a calibration parameter relating this to PP, and 6) a value of DIA from the mathematical difference between SYS and PP; and
a third sensor for measuring SpO2 contained entirely within the flexible housing, the third sensor comprising a third processor configured to determine a value of SpO2 from alternating and static components of both the digital red-PPG waveform and digital infrared-PPG waveform.

2. The sensor of claim 1 , wherein the flexible housing comprises two or more rigid housing segments that are connected to each other by means of one or more flexible connectors.

3. The sensor of claim 2 , wherein the analog ECG and analog impedance circuits and the digital processing system are located on rigid circuit boards disposed within the housing segments and the analog ECG circuit, analog impedance circuit, and digital processing system are interconnected via one or more flexible conductors located within the one or more flexible connectors.

4. The sensor of claim 3 , wherein each of the one or more flexible connectors comprises a flexible circuit.

5. The sensor of claim 4 , wherein the analog ECG circuit and the digital processing system are located on separate rigid circuit boards located in separate housing segments.

6. The sensor of claim 4 , wherein the analog impedance circuit and the digital processing system are located on separate rigid circuit boards located in separate housing segments.

7. The sensor of claim 4 , wherein the housing comprises three rigid housing segments, with the analog ECG circuit, the analog impedance circuit, and the digital processing system each being located in one of the three housing segments.

8. The sensor of claim 7 , wherein the digital processing system is located in a middle segment of said three housing segments, with each of the analog ECG circuit and the analog impedance circuit being located in a respective outboard housing segment and being connected to the digital processing system via a respective flexible circuit.

9. The sensor of claim 2 , wherein the sensing portion includes first and second pairs of electrode contact points, with 1) the first pair of electrode contact points including a first voltage-sensing electrode contact point that is located in a first housing segment arranged to contact a first side of the patient's chest, and 2) the second pair of electrode contact points including a second voltage-sensing electrode contact point that is located in a second housing segment arranged to contact a second side of the patient's chest that is laterally opposite to the first side of the patient's chest.

10. The sensor of claim 2 , wherein the sensing portion includes first and second pairs of electrode contact points, with 1) the first pair of electrode contact points including a first current-injecting electrode contact point that is located in a first housing segment arranged to contact a first side of the patient's chest, and 2) the second pair of electrode contact points including a second current-injecting electrode contact point that is located in a second housing segment arranged to contact a second side of the patient's chest that is laterally opposite to the first side of the patient's chest.

11. The sensor of claim 2 , wherein the sensing portion includes first and second pairs of electrode contact points, with 1) the first pair of electrode contact points including a first voltage-sensing electrode contact point and a first current-injecting electrode contact point that are both located in a first housing segment arranged to contact a first side of the patient's chest; and 2) the second pair of electrode contact points including a second voltage-sensing

Assignees

• Tosense Inc
• Baxter Int
• Baxter Healthcare Sa

Inventors

• Banet Matthew
• Dhillon Marshal Singh
• Pede Susan Meeks
• Hunt Kenneth Robert

Classifications

• A61B5/282

  Holders for multiple electrodes (for introduction into the body A61B5/287) · CPC title

• A61B5/02108

  from analysis of pulse wave characteristics · CPC title

• A61B5/0205

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

• A61B5/25

  Bioelectric electrodes therefor · CPC title

• A61B5/0816

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