Monitoring physiological status based on bio-vibrational and radio frequency data analysis
A patient monitoring device includes an ECG sensor coupled to a patient, a sensor coupled to the patient and configured to detect bio-vibrational signals, and a radiofrequency monitoring device configured to produce information responsive to electromagnetic energy reflected from the patient's thoracic cavity. A processor processes the ECG signals, the bio-vibrational signals, and the radio frequency information to generate a plurality of physiological parameters of the patient. The processor also performs at least one of a predictive analysis and a trend analysis of the plurality of physiological parameters to determine a current clinical condition of the patient. The trend analysis includes determining a substantial relationship between changes in the plurality of physiological parameters. The processor can also compare the current clinical condition of the patient to predetermined clinically actionable criteria to determine one or more clinically actionable events and provide an output relating to one or more clinically actionable events.
1 . A system for generating and processing physiological parameters, the system comprising:
an externally worn cardiac monitor configured to be worn by a patient during a prescribed period of use, the externally worn cardiac monitor comprising:
an electrocardiogram sensor configured to detect one or more electrocardiogram signals of the patient,
a cardio-vibrational sensor configured to detect one or more cardio-vibrational signals of the patient,
one or more radiofrequency antennas and associated radiofrequency circuitry to produce radiofrequency information responsive to radiofrequency energy reflected from within a thoracic cavity of the patient, and
one or more device processors configured to
process the one or more electrocardiogram signals and the one or more cardio-vibrational signals to generate electromechanical activation parameter data for the patient for a monitoring interval,
process the radiofrequency information to generate thoracic fluid content data for the patient for the monitoring interval,
perform a trend analysis on the electromechanical activation parameter data and the thoracic fluid content data to identify a substantial relationship between the electromechanical activation parameter data and the thoracic fluid content data, and
cause an output device to provide a first output representing at least a first portion of the monitoring interval, wherein the first output visually depicts the substantial relationship.
2 . The system of claim 1 , wherein the cardio-vibrational sensor comprises an accelerometer.
3 . The system of claim 1 , wherein the one or more device processors are further configured to:
determine a current clinical condition of the patient based on the trend analysis;
compare the current clinical condition of the patient to predetermined clinically actionable criteria to identify a clinically actionable event; and
cause the output device to provide a second output relating to the clinically actionable event.
4 . The system of claim 3 , wherein the clinically actionable event is either:
an automated event that is triggered without user input; or
a manual event that is triggered based upon a user response to the second output relating to the clinically actionable event.
5 . The system of claim 3 , wherein the second output relating to the clinically actionable event comprises an instruction to perform an action.
6 . The system of claim 1 , wherein the one or more device processors are further configured to:
input the electromechanical activation parameter data and the thoracic fluid content data into a machine learning algorithm; and
determine a current clinical condition of the patient based upon on output of the machine learning algorithm.
7 . The system of claim 6 , wherein:
the current clinical condition of the patient comprises a predictive score based upon the output of the machine learning algorithm; and
the predictive score indicates a likelihood of an occurrence of an adverse event for the patient.
8 . The system of claim 7 , wherein the adverse event for the patient comprises one or more of an arrhythmia event for the patient, a stroke event for the patient, a syncopal event for the patient, or a hospitalization event for the patient.
9 . The system of claim 1 , wherein the one or more device processors are further configured to process the one or more cardio-vibrational signals over at least a second portion of the monitoring interval to determine a cardiac vibrational metric of the patient.
10 . The system of claim 9 , wherein the one or more device processors are further configured to:
make a determination that the thoracic fluid content data exceeds a threshold during at least a third portion of the monitoring interval; and
after making the determination, monitor the cardiac vibrational metric during a subsequent monitoring interval.
11 . The system of claim 9 , wherein the cardiac vibrational metric is one or more of a heart vibration intensity value, a pulmonary vibration intensity value, or a left ventricular systolic time.
12 . A system for monitoring physiological parameters of a patient, the system comprising:
an externally worn cardiac monitor configured to be bodily-attached to a patient during a prescribed period of use, the externally worn cardiac monitor comprising:
an electrocardiogram sensor configured to detect one or more electrocardiogram signals of the patient,
a microphone configured to detect one or more cardio-vibrational signals of the patient,
a radiofrequency transceiver circuit comprising one or more antennas configured to direct radiofrequency energy into the patient, wherein the radiofrequency transceiver circuit is configured to produce radiofrequency information responsive to reflected radiofrequency energy that is reflected from within the patient and received through the one or more antennas, and
one or more device processors configured to
during a monitoring interval within the prescribed period of use, process the one or more electrocardiogram signals and the one or more cardio-vibrational signals to generate electromechanical activation parameter data for the monitoring interval, and
during the monitoring interval, process the radiofrequency information to generate thoracic fluid content data for the monitoring interval; and
a remote server comprising one or more server processors and a network interface, the one or more server processors configured to:
receive, via the network interface, the electromechanical activation parameter data and the thoracic fluid content data for the monitoring interval,
perform a trend analysis on the electromechanical activation parameter data and the thoracic fluid content data to identify a substantial relationship between the electromechanical activation parameter data and the thoracic fluid content data, and
cause an output device to provide a first output representing at least a first portion of the monitoring interval, wherein the first output visually depicts the substantial relationship.
13 . The system of claim 12 , wherein the one or more server processors are further configured to:
determine a current clinical condition of the patient based on the trend analysis;
compare the current clinical condition of the patient to predetermined clinically actionable criteria to identify a clinically actionable event; and
cause the output device to provide a second output relating to the clinically actionable event.
14 . The system of claim 13 , wherein the second output relating to the clinically actionable event comprises an instruction to perform an action.
15 . The system of claim 12 , wherein the one or more server processors are further configured to:
input the electromechanical activation parameter data and the thoracic fluid content data into a neural networks algorithm; and
determine a current clinical condition of the patient based upon on output of the neural networks algorithm.
16 . The system of claim 15 , wherein:
the current clinical condition of the patient comprises a predictive score based upon the output of the neural networks algorithm; and
the predictive score indicates a likelihood of an occurrence of an adverse event for the patient.
17 . The system of claim 16 , wherein the adverse event for the patient comprises one or more of an arrhythmia event for the patient, a stroke event for the patient, a syncopal event for the patient, or a hospitalization event for the patient.
18 . The system of claim 12 , wherein the one or more server processors are further configured to process the detected one or more cardio-vibrational signals over at least a second portion of the monitoring interval to determine a cardiac vibrational metric of the patient.
19 . The system of claim 18 , wherein the one or more server processors are further configured to:
make a determination that the thoracic fluid content data exceeds a threshold during at least a third portion of the monitoring interval; and
after making the determination, monitor the cardiac vibrational metric during a subsequent monitoring interval.
20 . The system of claim 18 , wherein the cardiac vibrational metric is one or more of a heart vibration intensity value, a pulmonary vibration intensity value, or a left ventricular systolic time.