EP1570378A1 - Method for evaluating a sequence of discrete readings - Google Patents
Method for evaluating a sequence of discrete readingsInfo
- Publication number
- EP1570378A1 EP1570378A1 EP02808173A EP02808173A EP1570378A1 EP 1570378 A1 EP1570378 A1 EP 1570378A1 EP 02808173 A EP02808173 A EP 02808173A EP 02808173 A EP02808173 A EP 02808173A EP 1570378 A1 EP1570378 A1 EP 1570378A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- measured values
- measured value
- measured
- sequence
- attribute
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Ceased
Links
- 238000000034 method Methods 0.000 title claims description 30
- 230000009466 transformation Effects 0.000 claims description 29
- 238000011156 evaluation Methods 0.000 claims description 7
- 230000036772 blood pressure Effects 0.000 claims description 6
- 230000010355 oscillation Effects 0.000 claims description 6
- 238000005259 measurement Methods 0.000 claims description 3
- 101100225106 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) EDC2 gene Proteins 0.000 description 14
- 238000002565 electrocardiography Methods 0.000 description 9
- 230000007774 longterm Effects 0.000 description 6
- 206010061216 Infarction Diseases 0.000 description 5
- 230000007574 infarction Effects 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 4
- 230000001133 acceleration Effects 0.000 description 3
- 208000010125 myocardial infarction Diseases 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000004083 survival effect Effects 0.000 description 2
- 238000012935 Averaging Methods 0.000 description 1
- 208000010201 Exanthema Diseases 0.000 description 1
- 108091008698 baroreceptors Proteins 0.000 description 1
- 230000035581 baroreflex Effects 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009530 blood pressure measurement Methods 0.000 description 1
- 210000001715 carotid artery Anatomy 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 201000005884 exanthem Diseases 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 230000007257 malfunction Effects 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 230000008288 physiological mechanism Effects 0.000 description 1
- 210000001774 pressoreceptor Anatomy 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 238000013517 stratification Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
- A61B5/316—Modalities, i.e. specific diagnostic methods
- A61B5/318—Heart-related electrical modalities, e.g. electrocardiography [ECG]
- A61B5/346—Analysis of electrocardiograms
- A61B5/349—Detecting specific parameters of the electrocardiograph cycle
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
- A61B5/316—Modalities, i.e. specific diagnostic methods
- A61B5/318—Heart-related electrical modalities, e.g. electrocardiography [ECG]
- A61B5/333—Recording apparatus specially adapted therefor
- A61B5/335—Recording apparatus specially adapted therefor using integrated circuit memory devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/72—Signal processing specially adapted for physiological signals or for diagnostic purposes
- A61B5/7235—Details of waveform analysis
- A61B5/7253—Details of waveform analysis characterised by using transforms
- A61B5/7257—Details of waveform analysis characterised by using transforms using Fourier transforms
Definitions
- the invention relates to a method for evaluating a sequence of discrete measured values according to the preamble of claim 1.
- the invention has for its object to provide a method for evaluating a sequence of discrete measured values, such. B. to specify measured values based on vibration patterns, repetitive processes or processes that change over time, with which parameters can be determined which define characteristic properties, including hidden ones, of the measured value sequence.
- the method for evaluating a sequence of discrete measured values has the following features:
- a chain of a certain length is selected from the sequence of discrete measured values
- partial chains are formed from this selected chain, each of which has a selected event as the center, the remaining measured values of the partial chains being arranged in the original sequence on both sides of the central event;
- the measured values of the individual partial chains are assigned to one another according to their position in the respective partial chain, namely the measured values of the central events are assigned to one another and the measured values that are in the same place around the respective central event;
- all measured values of the signal are thus assigned a certain attribute in a first step, which characterizes the measured values in any desired property.
- any kind of attribute is conceivable, in a simple case e.g. the attribute can consist of the difference to the previous measured value.
- the attribute does not necessarily have to be derivable from the signal to be analyzed. It is also possible to assign an attribute from a synchronously recorded second signal to the measured values of the signal to be analyzed, e.g. the measured values of an EKG signal with attributes from a blood pressure signal recorded at the same time.
- At least some measured values are selected from the measured values thus assigned attributes, the attribute of which fulfills a certain criterion. If, for example, all measured values were assigned the attribute of the difference to the previous measured value, the selection criterion could be that the attribute is negative, ie the measured value is larger than al? the previous one is.
- the selected measured values are to be called “events” in the following.
- a chain of measured values is now created for each event, the central element of which is the event itself, surrounded by the measured values which are arranged in the output signal before or after the event Chains formed in this way for each event, the lengths of which can be freely defined, are arranged “one below the other” in a table, each row of the table corresponding to a chain of measured values. It is important that the Measured values of the same positions with respect to the
- the table Represent the table multiple times, i.e. the table contains redundant information according to the methodology.
- the averages of each column in the table are formed, i.e. the measured values of the same position with respect to the selected one
- SBT Schot-Bauer transformation
- the method according to the invention can be used particularly advantageously in medical technology, e.g. B. for the evaluation of long-term ECGs, long-term blood pressure measurements etc.
- the method can be used as follows.
- the sequence of beat-to-beat intervals of the long-term ECG serves as the output signal, which is the basis of most evaluation methods of long-term ECGs.
- An attribute is first assigned to each measured value.
- the comparison to the previous measured value should serve as an attribute, more precisely the quotient between the measured value itself and the previous measured value.
- the criterion for the selection of a measured value could be a value between 1 and 1.05 According to this criterion, all measured values would be selected as an event, which are larger, but not larger than 5% of the previous measured value .. In an average long-term ECG approximately 30% of all measured values correspond to this criterion.
- the SBT corresponds to the average course of the measured values before, during and after the event (here: rise in the measured values in the output signal).
- the SBT can be quantified in many ways: For the Estimating future risk in patients
- EDC2 value can be seen as a measure of the central increase and allows a statement regarding the patient's chance of survival. The bigger this
- an attribute was assigned to the measured values of the original signal, which establishes the relation to the immediately preceding measured value, whereby the SBT emphasizes above all the shorter frequencies of the output signal.
- An emphasis on longer frequencies can be achieved by assigning attributes to the measured values that compare the measured values over a longer period of time, e.g. compare the sum of the values of a certain period after the measured value with the sum of the values of a certain period before the measured value.
- the SBT is therefore also suitable for the detection or exclusion of
- Figure 1 with lines a to f is a schematic representation of the method for evaluating a sequence of discrete measured values according to the invention
- FIG. 2 shows a so-called tachogram in which the time intervals between two successive heartbeats are plotted for a patient over a period of 24 hours;
- FIG. 3 shows the frequency spectrum of the tachogram in FIG. 2, which was formed using a simple Fourier transformation
- Figure 4 shows the Schmidt-Bauer transformation of the tachogram in Figure 2 according to the invention
- FIG. 5 shows a detail from FIG. 4, which illustrates the calculation of the parameter EDC2;
- FIG. 6 shows the frequency spectrum of the Schmidt-Bauer transformation in FIG. 4 7 shows the Schmidt-Bauer transformation similar to FIG. 4 of a risk-prone infarct patient;
- FIG. 8 shows the frequency spectrum of the Schmidt-Bauer transformation according to FIG. 7;
- FIG. 9 shows the distributions of the EDC2 parameter for infarct patients who have survived for a longer period and for infarct patients who have died within a certain period of time;
- FIG. 10 shows the amplitude of an oscillation over time, in this case a rotational acceleration of a truck wheel with unbalance
- FIG. 11 shows a simple Fourier transformation of the oscillation according to FIG. 10
- FIG. 12 shows the Schmidt-Bauer transformation of the vibration according to FIG. 10 on the basis of an evaluation using a method according to the invention.
- FIG. 13 shows a Fourier transformation of the Schmidt-Bauer transformation shown in FIG. 12.
- FIG. 1 The general principle of the invention is shown in FIG. 1 with lines a), b), c), d), e) and f).
- a criterion is defined which is applied to the attributes assigned to the measured values.
- Measured values whose attributes meet the defined criteria are defined as events.
- the events, together with the previous and following measured values, are entered as event chains in a table, in such a way that measured values of the same position are related to one another for the event.
- the Schmidt-Bauer transformation is determined by averaging the event chains. In this way, the events themselves and the measured values of the same position with respect to the event are averaged.
- This tachogram is from a patient after a myocardial infarction who has survived it for over two years.
- FIG. 3 shows the frequency spectrum of the tachogram shown in FIG. 2, which can be calculated using a simple Fourier transformation as a function of Amplitude was determined depending on the frequency.
- FIG. 4 shows the Schmidt-Bauer transformation of the tachogram in FIG. 2 according to the invention.
- the quotient between the measured value itself and the previous measured value was used as an attribute, and a value between 1 and 1.5 was used as the criterion.
- the chain length of the Schmidt-Bauer transformation was set to 200 here, i.e. 100 values before and 100 values after the central event.
- the values of the transformation fluctuate around the value 1000 ms, whereby considerable dynamics can be determined around the center at the value zero. Fast modulations of the beat-to-beat intervals can be distinguished from slower ones.
- FIG. 5 shows a section around the center of the Schmidt-Bauer transformation according to FIG. 4 and illustrates the calculation of the parameter EDC2, which is used for risk stratification.
- the values RRI (-2), RRI (-l) and RRI (+1) are entered around the central event RRI (0). From these values, a character, static value EDC2 can be calculated, namely
- EDC2 (RRI (0) + RRI (+ l)) - (RRI (-l) + RRI (-2)
- FIG. 6 shows a simple Fourier transformation of the Schmidt-Bauer transformation according to FIG. 4. You can see clear swings at around 0.003Hz, at 0.03Hz and at 0.3Hz, which in the simple Fourier transform of
- FIG. 7 shows a Schmidt-Bauer transformation of a tachogram of a patient who suddenly died within two years of a heart attack. You can see that the dynamic around the central event is clearly limited. The EDC2 value is significantly lower at 6 ms.
- FIG. 8 shows the Fourier transformation of the Schmidt-Bauer transformation according to FIG. 7 (the Fourier transformation according to FIG. 6 is shown as a dotted line for comparison).
- the deflection at 0.3 Hz that can be seen in FIG. 6 is not present, but there is a deflection at approximately 0.75 Hz. This corresponds to the modulation of the heartbeat by the pressure receptors of the carotid artery, the so-called baroreceptors.
- FIG. 9 shows the differences in the distribution of the EDC2 values calculated for over 1000 patients for patients who had a monitoring interval of two Have survived for years (group 0) and for patients who have died during this period (group 0).
- FIG. 10 shows the time behavior of the amplitude of an oscillation, in this case the oscillation in connection with the rotational acceleration of a truck wheel with an imbalance.
- the amplitude as a function of time is plotted in this figure.
- FIG. 12 shows the Schmidt-Bauer transformation of the vibration according to FIG. 10. The difference to the previous measured value was used as an attribute and a value above zero was used as the criterion.
- FIG. 13 shows the Fourier transformation of the Schmidt-Bauer transformation according to FIG. 10. It can be seen that this representation essentially corresponds to the diagram according to FIG. 11.
- a decisive advantage is that the transformation represents a relatively short signal, which, however, does not lose any information in comparison to a long output signal.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Cardiology (AREA)
- Physics & Mathematics (AREA)
- Molecular Biology (AREA)
- Public Health (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Medical Informatics (AREA)
- Biophysics (AREA)
- Surgery (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Pathology (AREA)
- Veterinary Medicine (AREA)
- Mathematical Physics (AREA)
- Artificial Intelligence (AREA)
- Computer Vision & Pattern Recognition (AREA)
- Physiology (AREA)
- Psychiatry (AREA)
- Signal Processing (AREA)
- Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
Description
Claims
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/DE2002/004349 WO2004049190A2 (en) | 2002-11-27 | 2002-11-27 | Method for evaluating a sequence of discrete readings |
Publications (1)
Publication Number | Publication Date |
---|---|
EP1570378A1 true EP1570378A1 (en) | 2005-09-07 |
Family
ID=32332085
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP02808173A Ceased EP1570378A1 (en) | 2002-11-27 | 2002-11-27 | Method for evaluating a sequence of discrete readings |
Country Status (3)
Country | Link |
---|---|
US (1) | US7200528B2 (en) |
EP (1) | EP1570378A1 (en) |
WO (1) | WO2004049190A2 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090177102A1 (en) | 2008-01-07 | 2009-07-09 | The General Electric Company | System, method and device for predicting sudden cardiac death risk |
WO2010070640A1 (en) | 2008-12-15 | 2010-06-24 | Ariel Medical K.L. Ltd. | Method and system for measuring heart rate variability |
DE102017119301A1 (en) * | 2017-08-23 | 2019-02-28 | Iwis Antriebssysteme Gmbh & Co. Kg | Device and method for determining the state of wear of a chain |
DE102017119300A1 (en) * | 2017-08-23 | 2019-02-28 | Iwis Antriebssysteme Gmbh & Co. Kg | Device and method for determining the state of wear of a chain |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6016462A (en) * | 1997-08-29 | 2000-01-18 | Exxon Production Research Company | Analysis of statistical attributes for parameter estimation |
-
2002
- 2002-11-27 EP EP02808173A patent/EP1570378A1/en not_active Ceased
- 2002-11-27 WO PCT/DE2002/004349 patent/WO2004049190A2/en not_active Application Discontinuation
- 2002-11-27 US US10/535,921 patent/US7200528B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
WO2004049190A2 (en) | 2004-06-10 |
US20060064285A1 (en) | 2006-03-23 |
US7200528B2 (en) | 2007-04-03 |
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