The present disclosure relates to the field of biomedical engineering, in more detail, a technology of non-invasively monitoring a hemodynamic variable of an examinee.
A pulmonary artery, which is an artery connecting the right ventricle of a heart and lungs to each other, is difficult to approach. Accordingly, an invasive method of inserting a catheter into a pulmonary artery through a central vein and the right atrium and the right ventricle of a heart is used to measure pulmonary artery pressure (PAP). In this case, Swan-Ganz catheter is the most generally used, a skillful clinician is required for a surgical procedure of inserting Swan-Ganz catheter through the right atrium and the right ventricle, and it has been known that even though a catheter is successfully inserted, a heart is burdened, which causes various side effects.
It is possible to solve this problem when measuring PAP using an invasive method, so many studies have been conducted. In particular, various methods using echocardiography have been proposed. However, according to echocardiography, since a user manually puts an ultrasound probe on the skin and measures PAP, the result depends on the skillfulness of users and fluctuation when the same user repeatedly measures PAP is also large. Further, continuous measurement is difficult, so these methods are very inconvenient when they are used for monitoring.
In order to solve these problems, many studies about hemodynamic monitoring method including PAP that uses electrical impedance tomography (EIT) have been conducted. When EIT data are measured from the chest of a human body, a signal about respiration by the lungs and a signal about the blood flow in the heart are mixed in the data. Since the intensity of a respiration signal is generally over 10 times the intensity of a blood flow signal, it is very difficult to extract a blood flow signal. Further, since blood flow quickly changes in comparison to respiration, it is required to increase the EIT data collection speed.
One of the difficult subjects of hemodynamic monitoring is to invasively measure PAP. Some techniques of invasively measuring PAP have been known in the art, but these techniques are all evaluated as causing errors in PAP measurement. According to knowledge known in the field of hemodynamics, PAP depends on a right ventricular ejection time (RVET) that is time that the right ventricle of a heart takes to send blood to a pulmonary artery through contraction, a pulmonary perfusion time for which blood is supplied to the lungs, one-time stroke volume (SV) of a ventricle, a variation of a one-time stroke volume (DSV), etc., but existing techniques do not consider this fact.
An aspect provides a method of calculating a hemodynamic variable of an examinee on the basis of Electrical Impedance Tomography (EIT). The method includes: obtaining EIT images of a chest of an examinee at discrete points in time in a cardiac cycle of the examinee; recognizing values of a first pixel (position) in a region corresponding to a heart in the EIT images and values of a second pixel (position) in a region corresponding to lungs—the values of the first pixel are related to the discrete points in time, respectively, and the values of the second pixel are related to the discrete points in time, respectively; and calculating at least one hemodynamic value on the basis of a first point in time related to a minimum value of the recognized values of the first pixel and a second point in time related to a maximum value of the recognized values of the second pixel.
In an embodiment, the obtaining of EIT images of a chest of an examinee at discrete points in time in a cardiac cycle of the examinee may include: attaching a plurality of electrodes to the chest of the examinee and obtaining impedance data for the chest of the examinee; and restoring the EIT images from the impedance data.
In an embodiment, the recognizing of values of a first pixel in a region corresponding to a heart in the EIT images and values of a second pixel in a region corresponding to lungs—the values of the first pixel are related to the discrete points in time, respectively, and the values of the second pixel are related to the discrete points in time, respectively—, may include designating the region corresponding to the heart in the EIT images as a first region of interest and selecting the first pixel in the first region of interest, and designating the region corresponding to the lungs in the EIT images as a second region of interest and selecting the second pixel in the second region of interest.
In an embodiment, the first point in time may be ventricular ejection time and the second point in time may be pulmonary perfusion time.
In an embodiment, the calculating of at least one hemodynamic value on the basis of a first point in time related to a minimum value of the recognized values of the first pixel and a second point in time related to a maximum value of the recognized values of the second pixel may include calculating pulmonary artery pressure (PAP) on the basis of the first point in time and the second point in time.
In an embodiment, the calculating of pulmonary artery pressure (PAP) on the basis of the first point in time and the second point in time may include calculating the pulmonary artery pressure on the basis of the first point in time, the second point in time, the minimum value, and the maximum value.
In an embodiment, the values of the second pixel may show two or more peak patterns, and the calculating of pulmonary artery pressure (PAP) on the basis of the first point in time and the second point in time may include calculating the pulmonary artery pressure on the basis of the first point in time, the second point in time, the minimum value, the maximum value, peak values of the second pixel at the other peak patterns excluding a peak pattern related to the maximum value of the two or more peak patterns, and points in time related to the peak values.
In an embodiment, the values of the first pixel may show two or more peak patterns, and the calculating of pulmonary artery pressure (PAP) on the basis of the first point in time and the second point in time may include calculating the pulmonary artery pressure on the basis of the first point in time, the second point in time, the minimum value, the maximum value, peak values of the first pixel at the other peak patterns excluding a peak pattern related to the minimum value of the two or more peak patterns, and points in time related to the peak values.
In an embodiment, the calculating of pulmonary artery pressure (PAP) on the basis of the first point in time and the second point in time may include calculating the pulmonary artery pressure on the basis of the first point in time, the second point in time, electrocardiography (ECG) of the examinee, blood pressure of the examinee, photoplethysmography (PPG) of the examinee, and seismocardiography (SCG) of the examinee.
In an embodiment, the calculating of at least one hemodynamic value on the basis of a first point in time related to a minimum value of the recognized values of the first pixel and a second point in time related to a maximum value of the recognized values of the second pixel may further include calculating pulmonary vascular resistance (PVR) using the calculated pulmonary artery pressure.
In an embodiment, the calculating of at least one hemodynamic value on the basis of a first point in time related to a minimum value of the recognized values of the first pixel and a second point in time related to a maximum value of the recognized values of the second pixel may include calculating myocardial contractility on the basis of the minimum value and the first point in time.
In another aspect, a method of calculating a hemodynamic variable of an examinee on the basis of EIT is provided. The method includes: obtaining EIT images of a chest of an examinee at discrete points in time in a plurality of cardiac cycles of the examinee; recognizing a pixel value corresponding to a first point in time of pixel values in a region corresponding to a heart in EIT images obtained at discrete points in times in a first cardiac cycle of a plurality of cardiac cycles, and a pixel value corresponding a second point in time of pixel values in a region corresponding to the heart of EIT images obtained at discrete points in time in a second cardiac cycle of the plurality of cardiac cycles—the first point in time is advanced further than the second point in time in terms of time by time corresponding to the cardiac cycle; and calculating at least one hemodynamic value on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time.
In an embodiment, the first point in time and the second point in time may be end diastole points in time, and the calculating of at least one hemodynamic value on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time may include calculating a variation of end-diastolic ventricular volume (EDVV) on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time.
In an embodiment, the calculating of at least one hemodynamic value on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time may further include calculating myocardial contractility using the calculated variation of end-diastolic ventricular volume and a variation of a one-time stroke volume (SV) between cardiac cycles.
In an embodiment, the first point in time and the second point in time may be end systole points in time, and the calculating of at least one hemodynamic value on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time may include calculating a variation of end-systolic ventricular volume (ESVV) on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time.
In an embodiment, the calculating of at least one hemodynamic value on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time may further include calculating ejection fraction (EF) using the calculated variation of end-systolic ventricular volume and a variation of a one-time stroke volume between cardiac cycles.
In another aspect, an apparatus for calculating a hemodynamic variable of an examinee on the basis of EIT is provided. The apparatus includes: a storage configured to store EIT images—the EIT images are images of a chest of an examinee obtained at discrete points in time in a cardiac cycle of the examinee; and a controller configured to recognize values of a first pixel in a region corresponding to a heart in the EIT images and values of a second pixel in a region corresponding to lungs—the values of the first pixel are related to the discrete points in time, respectively, and the values of the second pixel are related to the discrete points in time, respectively—, and configured to calculate at least one hemodynamic value on the basis of a first point in time related to a minimum value of the recognized values of the first pixel and a second point in time related to a maximum value of the recognized values of the second pixel.
In an embodiment, the first point in time may be ventricular ejection time and the second point in time may be pulmonary perfusion time.
In an embodiment, the controller may be further configured to calculate pulmonary artery pressure on the basis of the first point in time and the second point in time.
In an embodiment, the controller may be further configured to the pulmonary artery pressure on the basis of the first point in time, the second point in time, the minimum value, and the maximum value.
In an embodiment, the controller may be further configured to calculate myocardial contractility on the basis of the minimum value and the first point in time.
In another aspect, an apparatus for calculating a hemodynamic variable of an examinee on the basis of EIT is provided. The apparatus includes: a storage configured to store EIT images—the EIT images are images of a chest of an examinee obtained at discrete points in time in a plurality of cardiac cycles of the examinee; and a controller configured to recognize a pixel value corresponding to a first point in time of pixel values in a region corresponding to a heart in EIT images obtained at discrete points in times in a first cardiac cycle of a plurality of cardiac cycles, and a pixel value corresponding a second point in time of pixel values in a region corresponding to the heart of EIT images obtained at discrete points in time in a second cardiac cycle of the plurality of cardiac cycles—the first point in time is advanced further than the second point in time in terms of time by time corresponding to the cardiac cycle—, and configured to calculate at least one hemodynamic value on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time.
In an embodiment, the first point in time and the second point in time may be end diastole points in time, and the controller may be further configured to calculate a variation of end-diastolic ventricular volume on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time.
In an embodiment, the first point in time and the second point in time may be end diastole points in time, and the controller may be further configured to calculate a variation of end-systolic ventricular volume on the basis of the pixel value corresponding to the first point in time and the pixel value corresponding to the second point in time.
Other aspects, features, and techniques will be apparent to one skilled in the relevant art in view of the following detailed description of the embodiments.
The application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.
The features, objects, and advantages of the present disclosure will become more apparent from the detailed description set forth below when taken in conjunction with the drawings in which like reference characters identify correspondingly throughout and wherein:
An objective of the preset disclosure is to provide an improved method and apparatus for non-invasively monitoring a hemodynamic variable by using electrical impedance tomography.
The objectives of the present disclosure are not limited to the objects described above and other objectives will be clearly understood by those skilled in the art from the following description
According to embodiments of the present disclosure, there is an effect that it is possible to non-invasively monitor hemodynamic variables by using electrical impedance tomography.
The advantages and features of the present disclosure, and methods of achieving them will be clear by referring to the exemplary embodiments that will be describe hereafter in detail with reference to the accompanying drawings. However, the present disclosure is not limited to the exemplary embodiments described hereafter and may be implemented in various ways, and the exemplary embodiments are provided to complete the description of the present disclosure and let those skilled in the art completely know the scope of the present disclosure and the present disclosure is defined by claims.
Terms used in the present disclosure are used only in order to describe specific exemplary embodiments rather than limiting the present disclosure. For example, a component expressed as a singular should be understood as a concept including a plurality of components as long as it clearly means only a singular. Further, in the specification of the present disclosure, terms “include” or “have” only show that specific feature, number, step, operation, component, part, or a combination thereof described in the specification exist without excluding the possibility of existence or addition of one or more other features, numbers, steps, operations, components, parts, or combinations thereof. In embodiments described herein, a “module” or a “unit” may mean a functional part that performs at least one function or operation.
Unless otherwise defined, all terms including technical and scientific terms used herein have the same meaning as commonly understood by those skilled in the art to which the present disclosure belongs. It will be further understood that terms defined in dictionaries that are commonly used should be interpreted as having meanings that are consistent with their meanings in the context of the relevant art and will not be interpreted in an idealized or overly formal sense unless expressly so defined herein.
Hereinafter, embodiments of the present disclosure are described in detail with reference to the accompanying drawings. However, in the following description, it is to be noted that, when the functions of conventional elements and the detailed description of elements may make the gist of the present disclosure unclear, a detailed description of those elements will be omitted.
As shown in
The storage 130 may be used to store image data of an intermediate result obtained through image processing in accordance with various embodiments of the present disclosure, result image data obtained through image processing in accordance with various embodiments of the present disclosure, variable values for image processing and/or operating according to various embodiment of the present disclosure, pixel data selected from EIT images in accordance with various embodiments of the present disclosure, and operating result values obtained by operating in accordance with various embodiment of the present disclosure. In various embodiments, the storage 130 may store EIT images in the format of Digital Imaging and Communications in Medicine (DICOM) or common image file formats (BMP, JPEC, TIFF, etc.). The storage 130 may further store software/firmware, etc. for implementing the controller 120. The storage may be any one storage medium of a flash memory type, a hard disk type, a MultiMedia Card (MMC) type, a card type memory (e.g., Secure Digital (SD) card or an xTream Digital (XD) card), a Random Access Memory (RAM), a Static Random Access Memory (SRAM), a Read-Only Memory (ROM), an Electrically Erasable Programmable Read-Only Memory (EEPROM), a Programmable Read-Only Memory (PROM), a magnetic memory, a magnetic disc, and an optical disc, but those skilled art would know that the storage 130 is not limited thereto.
The input interface 110 may be a hardware or software module for inputting user instructions to perform image processing and/or operating according to various embodiments of the present disclosure. The input interface 110 may be usefully used to input various necessary instructions to the controller 120, input various image data such as EIT image data obtained by an EIT imaging device to the controller 130, or and perform various types of image processing by designating some or all of displayed images. The input interface 110 may be usefully used to designate a specific region in an EIT image as a region of interest (ROI) and select any point in the designated region of interest. In an embodiment, the input interface 110 may include a keyboard, a keypad, a touchpad, a mouse, etc. of a computer, but the kind of the input interface is not limited thereto. For example, the input interface 110 may include a graphic user interface that can control the input devices described above. The display 140, which is for visually displaying various images and/or various data according to various embodiments of the present disclosure, may include various display devices such as an LCD display, an LED display, an AMOLED display, and a CRT display.
The controller 120 may configured to discriminate the values of a first pixel (position) in a region corresponding to a heart and the values of a second pixel (position) in regions corresponding to lungs in EIT images obtained at a plurality of discrete points in time, respectively. In an embodiment, the controller 120 may be configured to designate a region 220 showing a heart as a first region of interest 225 in EIT images and to select a first pixel 227 in the first region of interest 225. In an embodiment, the controller 120 may be configured to designate regions 210 showing lungs as a second region of interest 215 in EIT images and to select a second pixel 217 in the second region of interest 215. In an embodiment, the controller 120 can designate the first region of interest 225 and the second region of interest 215 using algorithms such as an edge detection algorithm and an image segmentation algorithm, but it should be noted that the method of designating first region of interest 225 and the second region of interest 215 is not limited thereto. For example, a user may manually designate the first region of interest 225 and the second region of interest 215 using the input interface 110. The values of a first pixel and the values of a second pixel are all associated with the discrete points in time at which EIT images were obtained. By this interrelation, it is possible to know the points in time at which the values of the first pixel (position) were obtained such as a first value of the first pixel (position) 227 is a value of the first pixel 227 selected from an EIT image obtained at 15 ms and a second value of the first pixel 227 is a value of the first pixel 227 selected from an EIT image obtained at 25 ms. Similarly, it is possible to know the points in time at which the values of the second pixel (position) 217 were obtained from the interrelation.
In
According to qualitative analysis of the waveform shown in
The controller 120 shown in
In an embodiment, the controller 120 may be further configured to calculate pulmonary artery pressure on the basis of the first point in time, the second point in time, the minimum value of the values of the first pixel 227, and the maximum value of the values of the second pixel 217. Similar to the embodiment described above, the controller 120 can calculate pulmonary artery pressure on the basis of a first point in time, a second point in time, and a linear combination of a minimum value and a maximum value. In this embodiment, it is also possible to calculate coefficients for the first point in time, the second point in time, the minimum value, and the maximum value such that the square of the difference between pulmonary artery pressure expressed as a linear combination and pulmonary artery pressure measured through an invasive method is minimized by applying least square method. The controller 120 may be further configured to, when the values of the second pixel 217 show two or more peak patterns, calculate pulmonary artery pressure on the basis of the first point in time, the second point in time, the minimum value, the maximum value, peak values of the second pixel 217 at the other peak patterns excluding a peak pattern related to the maximum value of the two or more peak patterns, and points in time related to the peak values. Even in this case, similar to the embodiment described above, the controller 120 can calculate coefficients for the first point in time, the second point in time, the minimum value, the maximum value, the peak values of the second pixel 217, the points in time related to the peak values such that the square of the difference between pulmonary artery pressure expressed as a linear combination and pulmonary artery pressure measured through an invasive method is minimized by applying least square method. The controller 120 may be further configured to, when the values of the first pixel 227 show two or more peak patterns, calculate pulmonary artery pressure on the basis of the first point in time, the second point in time, the minimum value, the maximum value, peak values of the first pixel 227 at the other peak patterns excluding a peak pattern related to the minimum value of the two or more peak patterns, and points in time related to the peak values. Even in this case, similar to the embodiment described above, the controller 120 can calculate coefficients for the first point in time, the second point in time, the minimum value, the maximum value, the peak values of the first pixel 217, the points in time related to the peak values such that the square of the difference between pulmonary artery pressure expressed as a linear combination and pulmonary artery pressure measured through an invasive method is minimized by applying least square method. The controller 120 may be further configured to calculate pulmonary artery pressure on the basis of a first point in time, a second point in time, electrocardiography of an examinee, blood pressure of the examinee, photoplethysmography (PPG) of the examinee, and seismocardiography (SCG) of the examinee. When various data are complexly applied to calculate pulmonary artery pressure, a more accurate pulmonary artery pressure value can be obtained. The controller 120 may be further configured to calculate pulmonary vascular resistance (PVR) using the calculated pulmonary artery pressure. The controller 120 may be further configured to calculate myocardial contractility that is an index showing how much a heart can contract on the basis of the minimum value and the first point in time, that is, the ventricular ejection time TDH. In an embodiment, the controller 120 is configured to calculate myocardial contractility on the basis of a value obtained by dividing the minimum value by the value of the first point in time.
The controller 120 may be further configured to recognize a pixel value corresponding to a first point in time of pixel values in a region corresponding to a heart in EIT images obtained at discrete points in times in a first cardiac cycle of a plurality of cardiac cycles, and a pixel value corresponding a second point in time of pixel values in a region corresponding to the heart of EIT images obtained at discrete points in time in a second cardiac cycle of the plurality of cardiac cycles. In this case, the first point in time is advanced further than the second point in time in terms of time by time corresponding to the cardiac cycle. The controller 120 may be further configured to calculate at least one hemodynamic variable on the basis of a pixel value corresponding to a first point in time and a pixel value corresponding to a second point in time. As shown in
The controller 120 may be implemented, in terms of hardware, using at least one of Application Specific Integrated Circuits (ASICs), Digital Signal Processors (DSPs), Digital Signal Processing Devices (DSPDs), Programmable Logic Devices (PLDs), Field-Programmable Gate Arrays (FPGAs), processors, controllers, micro-controllers, and microprocessors. The controller 120 may be implemented as a firmware/software module that can be executed on the hardware platform described above. In this case, the firmware/software module may be implemented by one or more software applications written in an appropriate program language.
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In the above description, when a component is connected or coupled to another component, it should be understood that the component may be not only directly connected or coupled to another component, but may be connected or coupled to another component through one or more other components therebetween. Further, terms for describing the relationship of components (e.g., “between”, “among”, etc.) should also be analyzed in similar meanings.
In embodiments described herein, arrangement of components shown in the figures may depend on the environment in which the present disclosure is implemented, or requested matters. For example, some components may be omitted or may be combined into one component. The arrangement order or connection of some components may be changed.
Although exemplary embodiments of the present disclosure were illustrated and described above, the present disclosure is not limited to the specific exemplary embodiments, the exemplary embodiments described above may be modified in various ways by those skilled in the art without departing from the scope of the present disclosure described in claims, and the modified examples should not be construed independently from the spirit of the scope of the present disclosure. Accordingly, the technical range of the present disclosure should be determined by only claims.
The present disclosure can non-invasively monitor hemodynamic variables by using electrical impedance tomography.
Number | Date | Country | Kind |
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10-2020-0077738 | Jun 2020 | KR | national |
Filing Document | Filing Date | Country | Kind |
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PCT/KR2021/004458 | 4/9/2021 | WO |