DEVICE AND METHOD FOR ASSESSING MORTALITY RISK OF A CARDIAC PATIENT

• US 20160063207A1
• Filed: 03/28/2014
• Published: 03/03/2016
• Est. Priority Date: 04/02/2013
• Status: Active Application

• Current Assignee: Georg Schmidt
• Original Assignee: Georg Schmidt
• Inventors: Schmidt, Georg
• Application Number:
  US14/782,036
• Publication Number:
  US 20160063207A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: A61B 5/0205 Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition
• 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 5/245 specially adapted for magnetoencephalographic [MEG] signals
• CPC Class Codes: A61B 5/352 Detecting R peaks, e.g. for synchronising diagnostic apparatus; Estimating R-R interval
• CPC Class Codes: A61B 5/369 Electroencephalography [EEG] devices for psychotechnics A61B5/16
• CPC Class Codes: A61B 5/389 Electromyography [EMG]
• CPC Class Codes: A61B 5/6826 Finger
• CPC Class Codes: A61B 5/7264 Classification of physiological signals or data, e.g. using neural networks, statistical classifiers, expert systems or fuzzy systems neural networks per se G06N3/00; expert systems per se G06N5/00
• CPC Class Codes: A61B 5/7275 Determining trends in physiological measurement data; Predicting development of a medical condition based on physiological measurements, e.g. determining a risk factor
• CPC Class Codes: G16H 40/63 for local operation
• CPC Class Codes: G16H 50/30 for calculating health indices; for individual health risk assessment

Abstract

Device and method for assessing a mortality risk of a cardiac patient based on at least one vital sign or biosignal of said patient The invention relates to a device and method for assessing a mortality risk of a cardiac patient based on at least one vital sign or biosignal of said patient. In order to improve the quality of risk stratification for cardiac patients as compared to conventional mortality risk assessment concepts, the invention provides a device for assessing a mortality risk of a cardiac patient based on at least one vital sign or biosignal of said patient, said device comprising a data provision unit being configured to provide at least one data function of at least one vital sign or biosignal of said patient, a data processing unit being configured to process data of said at least one data function for assessing a mortality risk of said patient by performing the following actions: selecting at least one data sequence from said at least one data function according to a predetermined routine; computing a specific behavior of at least one parameter of said at least one data function based on said at least one selected data sequence; and assessing a mortality risk of said patient based on said computed behavior. A corresponding method and computer readable medium, which, when loaded, performs steps of said method, are also disclosed.

Claims

1. Device for assessing a mortality risk of a cardiac patient based on at least one vital sign or biosignal of said patient, said device comprising:

a. A data provision unit being configured to provide at least one data function of at least one vital sign or biosignal of said patient.

b. A data processing unit being configured to process data of said at least one data function for assessing a mortality risk of said patient by performing the following actions;

i. Selecting at least one data sequence from said at least one data function according to a predetermined routine.

ii. Computing a specific behavior of at least one parameter of said at least one data function based on said at least one selected data sequence.

iii. Assessing a mortality risk of said patient based on said computed behavior.

2. Device according to claim 1, characterized by said data provision unit being configured to perform at least one of the following actions:

a. Recording said at least one vital sign or biosignal, preferably in digital form.

b. Recording said at least one vital sign or biosignal continuously for a predetermined period of time, preferably for at least 30 minutes.

c. Recording said at least one vital sign or biosignal with non-invasive recording means, preferably using at least one of the following devices;

i. A finger photoplethysmographic device, preferably for continuously recording a blood pressure of said patient.

ii. An electrocardiogram recorder, preferably a high resolution electrocardiogram recorder with at least 1.6 kHz in orthogonal XYZ leads, preferably for continuously recording an electrocardiogram of said patient.

d. Recording said at least one vital sign or biosignal in a resting position of said patient, preferably in a supine resting position of said patient.

e. Recording at least two different vital signs or biosignals simultaneously, preferably an electrocardiogram and blood pressure, preferably continuous arterial blood pressure.

f. Storing the recorded data in data storage means, preferably in digital form.

g. Providing, as at least one data function, at least one recording of at least one of the following vital signs of said patient;

i. Body temperature

ii. Pulse rate or heart rate

iii. Blood pressure, preferably arterial blood pressure

iv. Respiratory rate

h. Providing, as at least one data function, at least one recording of at least one of the following biosignals of said patient;

i. Electroencephalogram (EEG)

ii. Magnetoencephalogram (MEG)

iii. Galvanic skin response (GSR)

iv. Electrocardiogram (ECG)

v. Mechanocardiogram (MCG)

vi. Electromyogram (EMG)

i. Providing said at least one data function as a function of said at least one vital sign or biosignal of said patient over the time.

j. Enabling verification and/or review and/or manual correction of said at least one data function, preferably including the elimination of artefacts, more preferably enabling review and/or manual correction of QRS classifications so as to differentiate sinus and ventricular premature complexes (VPC).

k. Providing at least one data function as a function of blood pressure, preferably continuous arterial blood pressure, over the time, preferably in the units mmHg over ms.

l. Providing at least two different data functions from simultaneous recordings of at least two different vital signs or biosignals, preferably simultaneous recordings of electrocardiogram and blood pressure.

m. Storing said at least one data function in data storage means, preferably in digital form.

n. Loading said at least one data function from data storage means, preferably in digital form.

3. Device according to claim 1, characterized by said data processing unit being configured to select said at least one data sequence from said at least one data function by performing at least one of the following actions:

a. Identifying periodic patterns within said at least one data function, preferably QRS-complexes of an electrocardiogram.

b. Identifying data points of said at least one data function correlating with at least one of the following;

i. Cardiac activities, preferably cardiac activities of the same kind

ii. R-peaks of the QRS complexes of an electrocardiogram

iii. Ventricular systoles

c. Measuring the intervals between each subsequent two data points, preferably between successive two R-peaks of QRS complexes of an electrocardiogram.

d. Calculating a quotient between an interval of interest, preferably an interval terminated by or initiated by a ventricular extrasystole, and a mean interval, wherein the mean interval is preferably calculated from at least one of the following;

i. A number of consecutive intervals preceding and/or succeeding the interval of interest, wherein the number of consecutive intervals is preferably two, three, four, five, six, seven, eight, nine or ten

ii. A number of consecutive intervals preceding and/or succeeding a ventricular extrasystole, wherein the number of consecutive intervals is preferably two, three, four, five, six, seven, eight, nine or ten

e. Selecting a data sequence for further processing in at least one of the following cases;

i. The data sequence contains at least one data point correlating with a ventricular extrasystole

ii. The data sequence contains at least a number of consecutive data points correlating with regular ventricular systoles preceding and/or succeeding a ventricular extrasystole, preferably without interruption by any further ventricular extrasystole, wherein the number of consecutive data points correlating with regular ventricular systoles preceding and/or succeeding a ventricular extrasystole is preferably two, three, four, five, six, seven, eight, nine or ten

iii. The quotient calculated for at least one interval fulfills at least one mathematical criterion

iv. The quotients calculated for at least two subsequent intervals fulfill different mathematical criteria

v. The quotients calculated for at least two subsequent intervals are out of a predetermined range of values

vi. The quotient calculated for a first interval of said data sequence is equal to or less than a first value, preferably 0.99, 0.97, 0.9 or 0.8 and/or the quotient calculated for a second interval subsequent to the first interval is equal to or greater than a second value, preferably 1, 0.1, 1.03, 1.3 or 1.4

vii. The quotient calculated for an interval of said data sequence is equal to or less than a first value, preferably 0.99, 0.97, 0.9 or 0.8 and/or the quotient calculated for a number of subsequent consecutive intervals is equal to or greater than said first value, wherein the number of subsequent consecutive intervals is preferably two, three, four, five, six, seven, eight, nine or ten.

4. Device according to claims 1, characterized by said data processing unit being configured to compute a specific blood pressure response to a ventricular extrasystole based on said at least one data sequence, preferably by performing at least one of the following actions:

a. Identifying the systolic blood pressure corresponding to at least one cardiac contraction based on said at least one data sequence.

b. Identifying the systolic blood pressure for each one of a number of consecutive cardiac contractions preceding and/or succeeding said ventricular extrasystole, wherein the number of consecutive cardiac contractions preceding and/or succeeding said ventricular extrasystole is preferably two, three, four, five, six, seven, eight, nine or ten.

c. Calculating the mean systolic blood pressure for a number of consecutive cardiac contractions preceding and/or succeeding said ventricular extrasystole, wherein the number of consecutive cardiac contractions preceding and/or succeeding said ventricular extrasystole is preferably two, three, four, five, six, seven, eight, nine or ten.

d. Calculating a blood pressure quotient between a systolic blood pressure corresponding to one cardiac contraction and a mean systolic blood pressure for other cardiac contractions.

e. Calculating a blood pressure quotient between the systolic blood pressure corresponding to the first post-extrasystolic cardiac contraction and a mean systolic blood pressure, preferably corresponding to the second to ninth or second to tenth post-extrasystolic cardiac contractions.

f. Storing the calculated blood pressure quotient or the mean of a plurality of calculated blood pressure quotients under the variable PESP1.

g. Storing the number of calculated blood pressure quotients per time.

5. Device according to claim 1, characterized by said data processing unit being configured to compute a blood pressure inclination during a characteristic sequence of heart rate intervals based on said at least one data sequence, preferably by performing at least one of the following actions:

a. Identifying the systolic blood pressure corresponding to two consecutive intervals, wherein preferably the quotient between the first one of the two consecutive intervals and the mean of a number of consecutive intervals preceding and/or succeeding said first interval is equal to or less than a first value, preferably 0.99, 0.97, 0.9 or 0.8, and/or the quotient between the second one of the two consecutive intervals and the mean of a number of consecutive intervals preceding and/or succeeding said second interval is equal to or greater than a second value, preferably 1.01, 1.03, 1.3 or 1.4, wherein the number of consecutive intervals preceding and/or succeeding said interval of interest is preferably two, three, four, five, six, seven, eight, nine or ten.

b. Calculating, as a blood pressure inclination, the inclination of a linear function defined by a first data point indicating a systolic blood pressure corresponding to the first interval and a second data point indicating a systolic blood pressure corresponding to the second interval.

c. Storing the calculated blood pressure inclination or the mean of a plurality of calculated blood pressure inclinations under the variable PESP2.

d. Storing the number of calculated blood pressure inclinations, preferably per time.

6. Device according to claim 1, characterized by said data processing unit being configured to compute a T-wave response to a ventricular extrasystole based on said data sequence, preferably by performing at least one of the following actions:

a. Calculating the mean of T-wave amplitudes corresponding to a number of regular ventricular systoles preceding and/or succeeding the first post-extrasystolic T-wave amplitude, preferably without interruption by any further ventricular extrasystole, wherein the number of consecutive ventricular systoles preceding and/or succeeding said first post-extrasystolic T-wave amplitude is preferably two, three, four, five, six, seven, eight, nine or ten.

b. Calculating the T-wave amplitude quotient between the first post-extrasystolic T-wave amplitude and the mean of T-wave amplitudes preceding and/or succeeding said first post-extrasystolic T-wave amplitude.

c. Storing the calculated T-wave amplitude quotient or the mean of a plurality of calculated T-wave amplitude quotient quotients under the variable PEST.

d. Storing the number of calculated T-wave amplitudes, preferably per time.

7. Device according to claim 1, characterized by said data processing unit being configured to assess a mortality risk for said patient by providing at least one of the following functions:

a. Allocating said patient to a low risk group under the following conditions;

i. The number of data sequences selected per 30 minutes recording of said at least one data function is less than five; and

ii. The number of blood pressure quotients calculated to be greater than 1 per 30 minutes recording of said at least one data function is zero;

or

iii. The number of blood pressure inclinations calculated to be greater than 4.5 mmHg/s per 30 minutes recording of said at least one data function is zero;

or

iv. The number of T-wave amplitude quotients calculated to be less than 1 per 30 minutes recording of said at least one data function is zero.

b. Allocating said patient to a medium risk group under the following conditions;

i. The number of data sequences selected per 30 minutes recording of said at least one data function is greater than five; and

ii. The number of blood pressure quotients calculated to be greater than 1 per 30 minutes recording of said at least one data function is zero;

or

iii. The number of blood pressure inclinations calculated to be greater than 4.5 mmHg/s per 30 minutes recording of said at least one data function is zero;

or

iv. The number of T-wave amplitude quotients calculated to be less than 1 per 30 minutes recording of said at least one data function is zero.

c. Allocating said patient to a high risk group under at least one of the following conditions;

i. The number of data sequences selected per 30 minutes recording of said at least one data function is greater than five

ii. The number of T-wave amplitude quotients calculated to be less than 1 per 30 minutes recording of said at least one data function is greater than zero

iii. PESP1 is greater than one

iv. PESP2 greater than 4.5 mmHg/s

v. PEST is less than one

d. Assessing mortality risk for said patient by calculating a prognostic score based on at least one of the following;

i. PESP1

ii. PESP2

iii. PEST

iv. VPC

v. Heart Rate Turbulence, in particular HRT-TS<

2.5 ms/RRI and/or HRT-TO≧

0%

8. Device according to claim 1, characterized by said device comprising display means for displaying the result of mortality risk assessment.

9. Method for assessing a mortality risk of a cardiac patient based on at least one vital sign or biosignal of said patient, preferably using the device according to claims 1, said method comprising the following steps:

a. Providing at least one data function of at least one vital sign or biosignal of said patient.

b. Processing data of said at least one data function for assessing a mortality risk of said patient by performing the following actions;

i. Selecting at least one data sequence from said at least one data function according to a predetermined routine.

ii. Computing a specific behavior of at least one parameter of said at least one data function based on said at least one selected data sequence.

iii. Assessing a mortality risk of said patient based on said computed behavior.

10. Computer-readable medium containing a program, which, when loaded, performs a method for assessing a mortality risk of a cardiac patient based on at least one vital sign or biosignal of said patient comprising the following steps:

a. Selecting at least one data sequence from at least one data function of at least one vital sign or biosignal of said patient according to a predetermined routine.

b. Computing a specific behavior of at least one parameter of at least one data function based on said at least one selected data sequence.

c. Assessing a mortality risk of said patient based on said computed behavior.