Method and system for processing the correspondence between patient perception and treatment measures

Abstract

The present application discloses a method and system for processing the correspondence between patient perception and treatment measures, the method comprising: obtaining a first parameter from a patient, wherein the first parameter is obtained when the patient is treated, and the first parameter is a physiological parameter of the patient; determining the patient's perception based on the first parameter, wherein the perception is used to indicate the degree of pain perceived by the patient during treatment; obtaining the treatment measures taken when treating the patient; and determining a first correspondence between the treatment measures and the patient's perception. This application solves the problem caused by the prior art not involving how to use the degree of pain perceived by the patient, establishes a correspondence between pain and treatment measures, and provides data support for further processing.

Description

Technical Field

[0001] The present application relates to the medical field, and more specifically, to a method for processing the correspondence between patient perception and treatment measures. Background Art

[0002] In the prior art, after a patient is treated, the treatment measures are generally evaluated based on the effects after the treatment. This evaluation method is a relatively common method.

[0003] In some treatment processes, the patient does not need to be fully or partially anesthetized. At this time, the inventors found that in this case, the patient has a perception of the treatment process, for example, the patient can feel the pain during the treatment process.

[0004] Doctors usually understand patients' feelings about the measures taken during treatment by talking to them. For example, doctors can ask patients during treatment: Does this operation hurt? When answering questions like this, patients usually have certain subjective factors, which cannot objectively reflect their true feelings during the treatment.

[0005] In the existing technology, although there are some technologies that can objectively evaluate the patient's pain, how to use the patient's perceived pain has not been mentioned in the existing technology, resulting in the patient's perception not being well utilized to improve treatment measures, improve the doctor's treatment effect, and effectively reduce the patient's pain during treatment. Summary of the invention

[0006] The embodiments of the present application provide a method and system for processing the correspondence between patient perception and treatment measures, so as to at least solve the problem that the prior art does not involve how to utilize the pain perceived by the patient.

[0007] According to one aspect of the present application, a method for processing the correspondence between patient perception and treatment measures is provided, including: obtaining a first parameter from a patient, wherein the first parameter is obtained when the patient is treated, and the first parameter is a physiological parameter of the patient; determining the patient's perception based on the first parameter, wherein the perception is used to indicate the pain perceived by the patient during treatment; obtaining the treatment measures taken when treating the patient; and determining a first correspondence between the treatment measures and the patient's perception.

[0008] Furthermore, determining the correspondence between the treatment measures and the patient's perception includes: determining the correspondence between the perception and time; obtaining the correspondence between the treatment measures taken when treating the patient and time; and establishing the correspondence between the treatment measures and the perception based on the time.

[0009] Furthermore, it also includes: obtaining a second correspondence between a pre-configured treatment measure and the perception corresponding to the treatment measure; using the second correspondence as a comparison benchmark, obtaining a portion of the first correspondence relative to the second correspondence perception where the difference exceeds a threshold; and prompting the portion of the perception that exceeds the threshold.

[0010] Furthermore, it also includes: obtaining treatment measures corresponding to the portion of the perception exceeding the threshold, wherein the treatment measures are treatment performed by intervening a treatment pen in the patient's soft tissue, and obtaining the patient's condition information; saving the treatment measures and the condition information, wherein the saved information is used as a basis for improving the treatment measures.

[0011] Furthermore, the first parameter includes at least one of the following: skin resistance value, muscle current value, pulse, respiration, blood pressure, pupil size, and electrocardiogram information.

[0012] According to another aspect of the present application, there is also provided a device for processing the correspondence between patient perception and treatment measures, including: a first acquisition module, used to acquire a first parameter from the patient, wherein the first parameter is acquired when the patient is treated, and the first parameter is a physiological parameter of the patient; a first determination module, used to determine the patient's perception based on the first parameter, wherein the perception is used to indicate the degree of pain perceived by the patient during treatment; a second acquisition module, used to acquire the treatment measures taken when treating the patient; and a second determination module, used to determine a first correspondence between the treatment measures and the patient's perception.

[0013] Furthermore, the first determination module is used to: determine the correspondence between the perception and time; obtain the correspondence between the treatment measures taken when treating the patient and time; and establish the correspondence between the treatment measures and the perception according to the time.

[0014] Furthermore, it also includes: a third acquisition module, used to obtain a second correspondence between a pre-configured treatment measure and the perception corresponding to the treatment measure; a fourth acquisition module, used to use the second correspondence as a comparison benchmark to obtain the part of the first correspondence relative to the second correspondence perception that exceeds a threshold; and a prompt module, used to prompt the part of the perception that exceeds the threshold.

[0015] Furthermore, it also includes: a fifth acquisition module, used to obtain the treatment measures corresponding to the part of the perception exceeding the threshold, wherein the treatment measures are treatments performed by intervening a treatment pen in the patient's soft tissue, a sixth acquisition module, used to obtain the patient's medical condition information; a saving module, used to save the treatment measures and the medical condition information, wherein the saved information is used as a basis for improving the treatment measures.

[0016] According to another aspect of the present application, a system for processing the correspondence between patient perception and treatment measures is also provided, including: a treatment device for treating a patient; and software for executing the above method when the treatment device is used to treat the patient.

[0017] In the embodiment of the present application, a first parameter from a patient is obtained, wherein the first parameter is obtained when the patient is treated, and the first parameter is a physiological parameter of the patient; the patient's perception is determined based on the first parameter, wherein the perception is used to indicate the pain perceived by the patient during treatment; the treatment measures taken when treating the patient are obtained; and a first correspondence between the treatment measures and the patient's perception is determined. This application solves the problem caused by the prior art not involving how to use the pain perceived by the patient, establishes a correspondence between pain and treatment measures, and provides data support for further processing. BRIEF DESCRIPTION OF THE DRAWINGS

[0018] The drawings constituting a part of the present application are used to provide a further understanding of the present application. The illustrative embodiments and descriptions of the present application are used to explain the present application and do not constitute an improper limitation on the present application. In the drawings:

[0019] Figure 1 It is a flowchart of a method for processing the correspondence between patient perception and treatment measures according to an embodiment of the present application. DETAILED DESCRIPTION

[0020] It should be noted that, in the absence of conflict, the embodiments and features in the embodiments of the present application can be combined with each other. The present application will be described in detail below with reference to the accompanying drawings and in combination with the embodiments.

[0021] It should be noted that the steps shown in the flowcharts of the accompanying drawings can be executed in a computer system such as a set of computer executable instructions, and that, although a logical order is shown in the flowcharts, in some cases, the steps shown or described can be executed in an order different from that shown here.

[0022] In this embodiment, a method for processing the correspondence between patient perception and treatment measures is provided. Figure 1is a flow chart of a method for processing the correspondence between patient perception and treatment measures according to an embodiment of the present application, such as Figure 1 As shown, the process includes the following steps:

[0023] Step S102, obtaining a first parameter from a patient, wherein the first parameter is obtained when the patient is treated, and the first parameter is a physiological parameter of the patient;

[0024] Step S104, determining the patient's perception according to the first parameter, wherein the perception is used to indicate the pain felt by the patient during treatment;

[0025] Step S106, obtaining treatment measures taken when treating the patient;

[0026] Step S108: determining a first corresponding relationship between the above treatment measure and the patient's perception.

[0027] Pain can be divided into two types. One is the pain during illness, which can include three parts: pain during onset, pain at peak, and pain during recovery. The second is the pain during treatment, which is mainly caused by the intervention of medical devices. According to the order of treatment, it can also include three stages: pain in the skin and muscles during intervention, pain at the lesion point when entering the lesion site, and continued pain after the medical device is removed. In this embodiment, it is necessary to capture the pain value during treatment (i.e., the pain in the second stage). The pain at this stage is related to the patient's treatment experience, treatment effect, and the doctor's prescription and operating specifications for treating similar diseases.

[0028] In the above steps, the pain perceived by the patient when each treatment measure is taken can be found, and these pains are evaluated based on the patient's physiological parameters, so that an objective correspondence between pain and treatment measures can be established. These correspondences can provide effective data support for the next step of processing.

[0029] When establishing the correspondence between the treatment measures and the patient's perception, it can be established based on the timeline. When obtaining the first parameter, the time when the first parameter is obtained can be recorded, so that the correspondence between perception and time can be determined; when treating patients with similar symptoms, the time when different treatment measures are taken for the patients can also be recorded, that is, the correspondence between the treatment measures taken when treating patients with similar symptoms and time can be obtained; then the correspondence between the treatment measures and perception is established according to time.

[0030] Time can also be retained in the correspondence. As an optional additional implementation, a video recording of the doctor using the treatment measure to perform treatment can be performed during treatment, and the time in the recorded video is consistent with the time when the correspondence between the treatment measure and the perception is established. In this way, the patient's perception, treatment measure, and treatment video can be presented on a timeline.

[0031] Through the above steps, based on the time point or time period when the doctor takes treatment measures for the patient, and the patient's perception of the treatment measures at the time point or time period, and establishing a corresponding relationship between these perceptions and the treatment measures, these data are of great significance. For example, it helps to improve the treatment measures; for example, it helps to establish better communication with the patient.

[0032] After retaining the correspondence between treatment measures and perception, a curve graph of time and perception (the curve graph is related to the time and first parameter change graph) can be established, and the treatment measures taken in different time periods are marked on the curve graph according to the time periods on the curve graph. Under normal conditions, the pain perceived by the patient should not change dramatically, and the curve in the curve graph should be relatively flat. If the change amplitude of the curve in the curve graph exceeds the threshold, the treatment measures taken at that time point or time period are recorded, and the treatment video at that time point or time period is obtained and saved. These saved data serve as the basis for future evaluation and / or improvement of treatment measures.

[0033] Alternatively, the correspondence between multiple perceptions and treatment measures of patients with the same disease under the same treatment measure can also be collected. These patients have similar perceptions during the treatment process, that is, the curves in the generated curve graph are similar. By averaging multiple curve graphs, a benchmark correspondence can be obtained, and the benchmark correspondence is called a second correspondence. In an optional embodiment, a second correspondence between a pre-configured treatment measure and the perception corresponding to the treatment measure can be obtained; the second correspondence is used as a comparison benchmark to obtain the portion of the first correspondence relative to the perception of the second correspondence that exceeds a threshold; and a prompt is given for the portion of the perception that exceeds the threshold.

[0034] That is, the curve graph corresponding to the first correspondence relationship and the curve graph corresponding to the second correspondence relationship can be compared to determine the part of the two curve graphs in which the difference between the curve graph corresponding to the first correspondence relationship and the curve graph corresponding to the second correspondence relationship exceeds a threshold, obtain the time point or time period corresponding to the part, and then obtain the measures taken at the time point or time period, and the treatment video corresponding to the time point or time period can also be saved together.

[0035] For example, when using the treatment pen described below in this embodiment for treatment, the treatment measures corresponding to the portion of the perception exceeding the threshold can be obtained, wherein the treatment measures are treatment performed by intervening the treatment pen in the patient's body to obtain the patient's condition information; the treatment measures and the condition information are saved, wherein the saved information is used as a basis for improving the treatment measures.

[0036] The treatment measure may include at least one of the following: the value of the physical energy output by the treatment pen, the frequency of the treatment pen intervening in the patient's body, the number of times the treatment pen intervenes in the patient's body, the direction and / or position of the treatment pen intervening in the patient's body, etc.

[0037] In another optional implementation, the proportion of patients with similar symptoms whose perception exceeds the threshold under the same treatment measures is obtained. For example, when the predetermined treatment measures are adopted, more than half of the patients have perceptions beyond expectations. At this time, the treatment measures can be adjusted, and then the adjusted treatment measures can be monitored again. If the proportion of patients with subsequent treatment who perceive the threshold exceeds the threshold is reduced, the treatment measures before and after the adjustment are recorded. These measures provide data support for the formulation and adjustment of future treatment plans.

[0038] There are many ways to obtain the user's pain perception, and the user's perception can be obtained based on a combination of at least one of the following parameters: skin resistance value, muscle current value, pulse, respiration, blood pressure, pupil size, and electrocardiogram information. This is illustrated below with an example.

[0039] Example 1

[0040] This can be done by combining an electrocardiogram with a skin conductivity sensor or an electromyography sensor.

[0041] In this example, electrocardiographic information may be acquired, and pain may be determined based on fluctuations associated with the wave height correlation value of the electrocardiographic information; and then the determination result of the pain determination unit may be output.

[0042] The fluctuations associated with the wave height correlation value may be fluctuations in characteristic values ​​of P wave, Q wave, R wave, S wave, T wave or ST, and therefore, accurate pain judgment may be made based on these clear values ​​of the characteristic points.

[0043] Specifically, the wave height correlation value obtained as time series data can be subjected to frequency analysis; based on the frequency component of the wave height correlation value obtained by the wave height correlation value frequency analysis unit, the LF component is calculated and the wave height correlation value LF component is obtained as the wave height correlation value LF component as the characteristic of the fluctuation of the wave height correlation value. The degree of pain is determined by the wave height correlation value LF component. When the wave height correlation value LF component increases, it is determined that pain exists.

[0044] Alternatively, the intervals of the waveform feature points of the electrocardiographic information obtained as time series data may be subjected to frequency analysis; based on the frequency components of the intervals of the waveform feature points obtained by the interval frequency analysis unit, the HF component is calculated as the interval HF component, and the interval HF component is obtained as a feature of the fluctuation of the interval. The accuracy of pain determination may be improved by the interval HF component. When the interval HF component does not decrease, but the wave height correlation value LF component increases, it is determined that pain exists. The interval HF component is an indicator of the respiratory variation component obtained from the frequency components of the intervals of the waveform feature points obtained by the interval frequency analysis unit.

[0045] In this example, the fluctuation of the interval of the characteristic points of the electrocardiogram waveform, myoelectric information, skin resistance, or skin potential may be used as an index to determine whether to exclude noise.

[0046] Example 2

[0047] The corresponding relationship between the user's perception and the first parameter can also be obtained through machine learning. A machine learning model can be obtained by training using multiple sets of training data, each set of training data includes an input data and an output data, the input data can measure the user's physiological parameters (i.e., the first parameter), and the output data is the pain perceived by the user, and the pain can be characterized by a number input by the user to characterize the pain; or the output data can also be characterized by letting the user press the pressure sensor to obtain the pressure value, so that a number used to characterize the feature can be obtained. After training, such a model can be obtained. When in use, the first parameter is input into the machine learning model, and the model can output a number used to characterize the pain. This number can be used as the basis for drawing a curve graph.

[0048] In this embodiment, an electronic device is provided, including a memory and a processor. The memory stores a computer program, and the processor is configured to run the computer program to execute the method in the above embodiment.

[0049] These computer programs can also be loaded onto a computer or other programmable data processing device so that a series of operating steps are executed on the computer or other programmable device to produce a computer-implemented process, so that the instructions executed on the computer or other programmable device provide instructions for implementing the process. Figure 1 A process or multiple processes and / or boxes Figure 1 The steps of the functions specified in one or more boxes can be implemented by different modules corresponding to different steps. In one embodiment, such a device is provided, which is called a device for processing the correspondence between patient perception and treatment measures, and the device includes: a first acquisition module, used to obtain a first parameter from the patient, wherein the first parameter is obtained when the patient is treated, and the first parameter is a physiological parameter of the patient; a first determination module, used to determine the patient's perception based on the first parameter, wherein the perception is used to indicate the pain perceived by the patient during treatment; a second acquisition module, used to obtain the treatment measures taken when treating the patient; a second determination module, used to determine the first correspondence between the treatment measures and the patient's perception.

[0050] The device can be understood as a device in software. The modules in the device are used to respectively implement the steps in the above method embodiment. Those that have been explained in the method will not be repeated here.

[0051] For example, the first determination module is used to: determine the correspondence between the perception and time; obtain the correspondence between the treatment measures taken when treating the patient and time; and establish the correspondence between the treatment measures and the perception according to the time.

[0052] For another example, the device may also include: a third acquisition module, used to acquire a second correspondence between a pre-configured treatment measure and the perception corresponding to the treatment measure; a fourth acquisition module, used to use the second correspondence as a comparison benchmark to acquire the portion of the first correspondence relative to the second correspondence perception that exceeds a threshold; a prompt module, used to prompt the portion of the perception that exceeds the threshold. And / or, the device may also include: a fifth acquisition module, used to acquire the treatment measure corresponding to the portion of the perception that exceeds the threshold, wherein the treatment measure is a treatment performed by intervening in the patient's body with a treatment pen, a sixth acquisition module, used to acquire the patient's condition information; a storage module, used to store the treatment measure and the condition information, wherein the stored information is used as a basis for improving the treatment measure.

[0053] In this embodiment, a system for processing the correspondence between patient perception and treatment measures is also provided, including: a treatment device for treating a patient; and software for executing the above method when the treatment device is used to treat the patient. The software in the system may also be a program, a service, or an application.

[0054] The above program (or the above device) can be run in a processor, or can be stored in a memory (or computer-readable medium), which includes permanent and non-permanent, removable and non-removable media. Information storage can be implemented by any method or technology. Information can be computer-readable instructions, data structures, program modules or other data. Examples of computer storage media include, but are not limited to, phase change memory (PRAM), static random access memory (SRAM), dynamic random access memory (DRAM), other types of random access memory (RAM), read-only memory (ROM), electrically erasable programmable read-only memory (EEPROM), flash memory or other memory technology, read-only compact disk read-only memory (CD-ROM), digital versatile disk (DVD) or other optical storage, magnetic cassettes, magnetic tape magnetic disk storage or other magnetic storage devices or any other non-transmission media that can be used to store information that can be accessed by a computing device. As defined herein, computer-readable media does not include temporary computer-readable media (transitory media), such as modulated data signals and carrier waves.

[0055] The above embodiments can be applied to a variety of therapeutic devices. For example, as a typical tool, the therapeutic device can be a therapeutic pen, and the therapeutic pen can implement the above method. Alternatively, the therapeutic device can also be a combination of a therapeutic pen and a therapeutic device, and the therapeutic device can run the above software, that is, execute the method steps in the above embodiments. The therapeutic device can also be called a therapeutic device host or host.

[0056] In the present embodiment, a therapeutic pen for a limb pain therapeutic device including a host that outputs a vibration prescription signal to the therapeutic pen is provided, the therapeutic pen comprising: a pen body and a pen cap detachably connected to the distal end of the pen body, the pen body can be installed with a therapeutic needle after the pen cap is removed, and a switch button is provided on the surface of the pen body, the needle tube of the therapeutic needle extends out of the distal end of the pen cap, and a vibrator that can be controlled to start and stop by the switch button is provided inside the pen body, and the vibrator is used to transfer physical kinetic energy corresponding to the vibration prescription signal to the therapeutic needle in the interventional lesion site when it is turned on.

[0057] Optionally, an elastic ball is provided at the distal end of the pen shaft for installing and releasing the pen cap; a contact surface is provided inside the pen cap, and the contact surface is located at the distal end of the pen cap, and the treatment needle also includes a needle tube seat fixedly connected to the needle tube, and when the treatment needle is fixed on the pen shaft, the distal end surface of the needle tube seat contacts the contact surface.

[0058] Optionally, the needle tube seat includes a needle tube fixing portion and a clamping portion fixedly connected to the needle tube fixing portion, the needle tube fixing portion is penetrated by a needle tube mounting hole, the needle tube is inserted and fixed in the needle tube mounting hole, the clamping portion is annular and hollow, and the cavity of the clamping portion is connected to the needle tube mounting hole; a needle tube outlet hole is provided at the distal end of the pen cap, and the needle tube can pass through the needle tube outlet hole and extend out of the distal end of the pen cap; the therapeutic pen also includes a mounting bracket arranged inside the pen shaft, the mounting bracket includes a bracket body extending along the length direction of the pen shaft and a mastoid fixedly connected to the distal end of the bracket body, and the clamping portion is sleeved and fixed on the mastoid.

[0059] Optionally, the bracket body includes a first body portion and a second body portion that are relatively arranged and fixedly connected, and the vibrator is fixedly connected between the first body portion and the second body portion; the mounting bracket also includes a side wall fixed to the distal ends of the first body portion and the second body portion and surrounding the mastoid, and the side wall is in contact with the outer side surface of the needle tube seat.

[0060] Optionally, an ultraviolet disinfection band LED emitter that emits light toward the treatment needle is provided at the distal end inside the pen shaft, for performing ultraviolet disinfection on the treatment needle and the pen cap.

[0061] Optionally, the pen cap is provided with at least one viewing window along the circumference, and the needle tube seat is a needle tube seat made of a transparent material, and the needle tube seat can be observed through each viewing window.

[0062] Optionally, a printed circuit board (PCB) is also provided inside the pen body, and an LED backlight, a vibration indicator light and the switch button are integrated on the PCB control board. The LED backlight and the switch button are exposed on the surface of the pen body. A working observation hole is also provided on the surface of the pen body, and the working observation hole corresponds to the position of the vibration indicator light. The LED backlight is closer to the far end of the pen body than the vibration indicator light. The PCB control board is also electrically connected to the vibrator.

[0063] Optionally, the therapeutic pen satisfies at least one of the following features: (a) the trajectory of the vibration output by the vibrator is in a plane perpendicular to or parallel to the axis of the pen shaft, and the vibration trajectory includes: a trajectory of reciprocating motion in a single direction, and / or a trajectory of reciprocating motion in multiple angular directions centered on the axis of the pen shaft; (b) the amplitude of the vibrator is designed to be between 2μm-500μm, and the vibration frequency of the vibrator is designed to be between 5Hz-500Hz; (c) the therapeutic needle is a special therapeutic needle or a disposable syringe needle, which is used to intervene in the diagnosis and / or treatment of lesions formed by soft tissue damage.

[0064] Optionally, the therapeutic pen also includes: a negative pressure pump detachably connected to the distal end of the pen shaft; the pen cap is a pen cap made of transparent material; a joint is fixed on the surface of the pen cap, the negative pressure pump is connected to the joint through a drainage tube, the joint is connected to the pen cap and the therapeutic needle, and the negative pressure pump is used to provide negative pressure for drawing out the accumulated fluid in the lesion site when started, so that the accumulated fluid is drawn out from the lesion site.

[0065] Optionally, a connecting tube connecting the drainage tube and the connector is also included; the control signal for starting and stopping the negative pressure pump comes from the host, and the host generates the corresponding control signal based on detecting whether there is fluid accumulation at the position where the sensor is located in the connecting tube.

[0066] Optionally, the sensor is a liquid level sensor, which includes two electrodes fixed to the inner wall of the connecting tube and having a gap, and a control circuit board electrically connected to the two electrodes respectively, wherein the control circuit board is arranged in the host, and the control circuit board is also electrically connected to the CPU main control board; when there is liquid accumulation at the position where the two electrodes are located in the connecting tube, the two electrodes are turned on, and the control circuit board transmits the electrical signal corresponding to the conduction of the two electrodes to the CPU main control board; or, when there is no liquid accumulation at the position where the two electrodes are located in the connecting tube, the two electrodes are turned off, and the control circuit board transmits the electrical signal corresponding to the disconnection and conduction of the two electrodes to the CPU main control board.

[0067] Optionally, the vibrator comprises a rotary centrifugal vibrator.

[0068] Optionally, in the case where a rotary centrifugal vibrator that can be started and stopped by the switch button is provided inside the pen shaft, the therapeutic pen also includes: a printed circuit board PCB control board electrically connected to the rotary centrifugal vibrator and used to output a vibration prescription signal to the rotary centrifugal vibrator, and a common mode filter is also integrated on the PCB control board.

[0069] Optionally, at least one of the treatment needle, the pen cap and the pen body has terahertz energy, and the frequency of the terahertz energy is 0.1THz-10THz.

[0070] In this embodiment, a host for a limb pain therapeutic device is also provided, the host comprising: a chassis, a touch screen arranged on the surface of the chassis, and a central processing unit CPU main control board arranged in the chassis and electrically connected to the touch screen, the CPU main control board is used to supply power to the vibrator and output the vibration prescription signal, the touch screen is used for the user to select the vibration prescription, wherein the vibration prescription signal is output to the above-mentioned treatment pen.

[0071] Optionally, it also includes: at least one intermediate frequency output interface arranged on the surface of the chassis; the limb pain therapeutic device also includes at least one group of electrode sheets electrically connected to the at least one intermediate frequency output interface through cables, and the CPU main control board is also electrically connected to the at least one intermediate frequency output interface for outputting current prescription signals to the at least one group of electrode sheets.

[0072] Optionally, the characteristic parameters of the vibration prescription signal include: continuous vibration of the vibrator and the vibration frequency and amplitude of the continuous vibration; or intermittent vibration of the vibrator and the duty cycle, vibration frequency and amplitude of the intermittent vibration.

[0073] Optionally, the vibration prescription includes: stored default fixed parameters for each treatment part and individual vibration intensity levels manually adjusted for the same treatment part; the touch display screen is used for the user to select a corresponding vibration prescription for the treatment part, and to jointly generate target characteristic parameters based on the default fixed parameters included in the selected vibration prescription and the individual vibration intensity levels manually adjusted by the user for the same treatment part, and to send the target characteristic parameters generated according to the vibration prescription selected by the user to the CPU main control board; the CPU main control board is used to generate a corresponding vibration prescription signal based on the target characteristic parameters.

[0074] Optionally, the CPU main control board includes: a microcomputer chip and a transistor; the microcomputer chip is used to receive the target characteristic parameter, and determine the target duty cycle according to the amplitude in the target characteristic parameter and the correspondence between the amplitude and the duty cycle stored in advance; generate the vibration prescription signal according to the target duty cycle and the vibration frequency in the target characteristic parameter, and send the vibration prescription signal to the transistor; the transistor is used to output the vibration prescription signal to the treatment pen, and control the vibration prescription signal to drive the vibrator.

[0075] Optionally, a timer and a counter are integrated in the touch display screen, and the timer is used to shut down the host or issue an alarm when the duration of the host outputting the vibration prescription signal to the therapeutic pen reaches a preset duration threshold; the counter is used to record the number of times the host outputs the vibration prescription signal to the therapeutic pen.

[0076] The method in the above embodiment may be executed in a host, or may also be used in a server connected to the host or the treatment pen.

[0077] The above embodiment provides an optional application implementation of the fourth correspondence. In this optional implementation, a fifth correspondence between a pre-configured treatment measure and the perception corresponding to the treatment measure can be obtained. The fifth correspondence is the treatment measure expected by the doctor and the perception corresponding to the treatment measure. In this way, there is a basis for comparison. According to the basis for comparison, the patient's perception that exceeds expectations can be determined, so that the degree of pain caused by the treatment measure can be confirmed. In this implementation, the part of the perception difference exceeding the threshold in the same time period or time point in the treatment measure in the fourth correspondence and the fifth correspondence is determined; the part of the perception exceeding the threshold is prompted. This implementation can be applied to a treatment pen. The following describes the implementation applied to the treatment pen.

[0078] When using the above-mentioned treatment pen, the needle of the treatment pen is inserted into the patient's affected part. Under normal circumstances, the patient should not feel obvious pain, and generally only feels soreness and swelling. At this time, according to the corresponding relationship between the treatment measures and the perception of a normal sore patient and whether the patient's real-time perception exceeds the threshold, it is determined that the patient feels pain. As a further processing method, the patient can be prompted with sound and light on the treatment pen or the host to feel pain.

[0079] Alternatively, the treatment measures at that time, i.e., the location and depth of needle insertion, can also be obtained, for example, a video at that time point or time period can be obtained from video surveillance to identify the location and depth of needle insertion in the video. Alternatively, it can be determined whether the doctor's operation is different from the standard operation in the following manner.

[0080] The method for judging whether the standards are met may be as follows: a method for standardizing the use of tools, comprising: obtaining data from a distance sensor, wherein the distance sensor is arranged on the tool, and the needle of the tool is used to intervene in the muscles and / or tendons of a human limb, and the data is used to indicate the depth of the needle intervention in the muscles and / or tendons of a human limb; comparing the data with the depth of a predetermined lesion site for treatment, and obtaining the difference between the data and the depth of the predetermined lesion site; and determining whether the operation of intervening in the muscles and / or tendons of a human limb meets the needle use standards and specifications based on the difference.

[0081] For example, when the needle of the tool repeatedly enters and exits different lesion points of the muscle and / or tendon of the painful lesion site of the human limb, the data is a plurality of numerical values ​​of varying sizes, and the numerical value is the distance detected by the distance sensor; comparing the data with the depth of the predetermined lesion site for treatment and obtaining the difference between the data and the depth of the predetermined lesion site for treatment includes: finding the extreme value within each numerical change cycle; calculating the first length of the needle penetrating into the muscle and / or tendon of the painful lesion site of the human limb within the numerical change cycle according to the information of the predetermined lesion site for treatment, wherein the predetermined information includes: the extreme value of the data change cycle and at least one of the lengths of the needle and the tool; comparing the first length with the depth of the predetermined lesion site for treatment, and determining the difference between the first length and the depth of the predetermined lesion site for treatment.

[0082] Another example: obtaining the number of needle applications in the needle application standard for a pre-configured location; obtaining all the extreme values ​​within multiple numerical change cycles; determining whether the number of all the extreme values ​​is the same as the number of needle applications; if they are not the same, determining that the needle application this time does not meet the needle application standard and specification for treating the predetermined lesion location.

[0083] The above are only embodiments of the present application and are not intended to limit the present application. For those skilled in the art, the present application may have various changes and variations. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present application should be included within the scope of the claims of the present application.

Claims

1. A device for processing the correspondence between patient perception and treatment measures, characterized in that: include: A first acquisition module, used for acquiring a first parameter from a patient, wherein the first parameter is acquired when the patient is treated, and the first parameter is a physiological parameter of the patient; A first determination module is used to determine the patient's perception according to the first parameter, wherein the perception is used to indicate the degree of pain perceived by the patient during treatment; wherein the corresponding relationship between the perception and time is determined; the corresponding relationship between the treatment measure taken when treating the patient and time is obtained; and the corresponding relationship between the treatment measure and the perception is established according to the time; A second acquisition module is used to acquire the treatment measures taken when treating the patient; A second determination module, configured to determine a first corresponding relationship between the treatment measure and the patient's perception; A third acquisition module is used to acquire a second corresponding relationship between a pre-configured treatment measure and a perception corresponding to the treatment measure; A fourth acquisition module, configured to use the second corresponding relationship as a comparison reference to acquire a portion of the first corresponding relationship where the perceived difference between the first corresponding relationship and the second corresponding relationship exceeds a threshold; A prompt module is used to prompt the part where the perception exceeds the threshold.

2. The device according to claim 1, characterized in that Also includes: a fifth acquisition module, configured to acquire a treatment measure corresponding to the portion of the sensed state exceeding the threshold, wherein the treatment measure is a treatment performed by intervening a treatment pen into the patient's body, A sixth acquisition module, used to acquire the patient's condition information; The saving module is used to save the treatment measures and the condition information, wherein the saved information is used as a basis for improving the treatment measures.

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