CN113515561A - Parameter comparison method and device, electronic equipment and computer readable storage medium - Google Patents
Parameter comparison method and device, electronic equipment and computer readable storage medium Download PDFInfo
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Abstract
The application provides a parameter comparison method, a parameter comparison device, an electronic device and a computer readable storage medium, wherein the device comprises: the configuration acquisition module is used for acquiring historical configuration information of a target patient, wherein the historical configuration information comprises a plurality of single configuration information; the selection receiving module is used for receiving selection operation of at least two single configuration information; an information determination module, configured to determine, in response to the selection operation, the at least two pieces of single configuration information as parameter comparison information of the target patient; a comparison display module, configured to control a display device to display a parameter comparison table and/or a parameter comparison graph of the target patient based on the parameter comparison information, where the parameter comparison graph includes at least one of the following: a 2D parameter comparison graph and a 3D parameter comparison graph. The method and the device can enable a doctor to know the variation trend of the stimulation parameters corresponding to the target patient.
Description
Technical Field
The present application relates to the field of data processing technologies, and in particular, to a parameter comparison method and apparatus, an electronic device, and a computer-readable storage medium.
Background
When programming a patient, the physician sets the stimulation parameters using the corresponding device, however, the data generated for each programming procedure regarding the stimulation parameters is not effectively used, and the physician does not have the corresponding stimulation parameters as a reference for setting the stimulation parameters.
Disclosure of Invention
The application aims to provide a parameter comparison method, a parameter comparison device, electronic equipment and a computer readable storage medium, so that a doctor can know the variation trend of a stimulation parameter corresponding to a target patient.
The purpose of the application is realized by adopting the following technical scheme:
in a first aspect, the present application provides a parameter comparison method applied to an electronic device, where the method includes: obtaining historical configuration information of a target patient, wherein the historical configuration information comprises a plurality of single configuration information, and the single configuration information comprises at least one stimulation parameter identifier and a parameter value corresponding to each stimulation parameter identifier; receiving selection operation of at least two single configuration information; in response to the selection operation, determining the at least two pieces of single configuration information as parameter comparison information of the target patient; controlling a display device to display a parameter comparison table and/or a parameter comparison graph of the target patient based on the parameter comparison information, wherein the parameter comparison graph comprises at least one of the following: a 2D parameter comparison graph and a 3D parameter comparison graph. The technical scheme has the advantages that on one hand, historical configuration information can be reasonably utilized, and parameter comparison information is obtained according to the historical configuration information, so that a doctor can know the variation trend of the stimulation parameters corresponding to a target patient; on one hand, the selection mode of the single configuration information is not limited, at least two pieces of single configuration information can be arbitrarily selected from historical configuration information as parameter comparison information of the target patient according to actual needs, the parameter comparison information can be part or all of the historical configuration information, when the parameter comparison information is all the historical configuration information, the change trend of stimulation parameters corresponding to the target patient can be reflected on the whole, when the parameter comparison information is part of the historical configuration information, for example, the single configuration information corresponding to the electrical stimulation applied to the target patient for the last 5 times, generally speaking, the recent single configuration information is more concerned in practical application, the data operation amount can be reduced under the condition that the comparison requirement is met, and the intelligent degree is higher; on the other hand, parameter comparison information can be displayed in a form of a table and/or a graph by using the display device, and a comparison result is displayed in a digital mode, so that the display effect is vivid and visual, and the use experience of a user is improved.
In some optional embodiments, the method further comprises: when detecting that the parameter comparison information meets a preset condition, generating prompt information and sending the prompt information to doctor equipment, wherein the preset condition is used for indicating at least one of the following conditions: the difference degree of the parameter values of the same stimulation parameter identification of the at least two single configuration information is greater than a preset difference degree threshold value; the parameter value of at least one stimulation parameter identification of the at least one single configuration information is not within the preset range of the parameter value of the corresponding stimulation parameter identification. The technical scheme has the advantages that when the parameter ratio pair information meets the preset condition, the condition that the change fluctuation between two single configuration information is too large or at least one single configuration information is abnormal exists, and the prompt information can be sent to the doctor equipment at the moment, so that the doctor can know the abnormal condition of the configuration information of the target patient in time.
In some optional embodiments, the generating a prompt message and sending the prompt message to a doctor device when it is detected that the parameter comparison information satisfies a preset condition includes: calculating parameter values corresponding to target stimulation parameter identifications of every two pieces of single configuration information in the parameter comparison information to obtain at least one comparison value; and when the maximum value of the at least one comparison value is larger than a preset threshold value corresponding to the target stimulation parameter identification, generating prompt information and sending the prompt information to doctor equipment, wherein the prompt information comprises the target stimulation parameter identification. The technical scheme has the advantages that the parameter value corresponding to the target stimulation parameter identification of every two single configuration information in the parameter comparison information can be calculated to obtain at least one comparison value, when the maximum value in the comparison values is larger than the preset threshold value corresponding to the target stimulation parameter identification, the situation that the parameter setting is abnormal is possible due to the fact that two single configuration information with overlarge difference exist in the parameter comparison information, and the prompt information can be sent to the doctor equipment at the moment, so that the doctor can timely know the abnormal situation of the configuration information of the target patient.
In some optional embodiments, the single configuration information further comprises a stimulation application time; calculating parameter values corresponding to target stimulation parameter identifications of every two pieces of single configuration information in the parameter comparison information to obtain at least one comparison value, wherein the calculation comprises the following steps: determining single configuration information of which the stimulation application time is in a preset stimulation application time range in the parameter comparison information as information to be compared; when the number of the single configuration information in the information to be compared is at least two, calculating parameter values corresponding to the target stimulation parameter identifications of every two single configuration information in the information to be compared to obtain at least one comparison value. The technical scheme has the advantages that generally speaking, in practical application, the difference degree between the single configuration information with the stimulation application time in the same range is concerned, the single configuration information with the stimulation application time in the preset stimulation application time range in the parameter comparison information can be used as the information to be compared, calculation is carried out aiming at the information to be compared, and the obtained comparison value can reflect the difference degree between the single configuration information in the preset stimulation application time range, so that the requirement in practical application is met.
In some optional embodiments, when it is detected that the parameter comparison information satisfies a preset condition, generating a prompt message and sending the prompt message to a doctor device further includes: acquiring a difference value of stimulus application time of two corresponding single configuration information based on a target comparison value, wherein the target comparison value is one of the at least one comparison value; and when the ratio of the target comparison value to the difference value is greater than a preset ratio, generating prompt information and sending the prompt information to doctor equipment. The technical scheme has the advantages that when the ratio of the target comparison value to the difference value of the stimulus application time of the two corresponding single configuration information is larger than the preset ratio, the parameter value corresponding to the target stimulus parameter identification of the target patient changes and fluctuates greatly in a short time, the target patient is easy to have tolerance to the stimulus under the condition, and at the moment, the prompt information can be sent to the doctor equipment, so that the doctor can know the relevant conditions of the target patient in time, and therefore corresponding measures are taken, and the target patient is prevented from having tolerance to the stimulus.
In some optional embodiments, the method further comprises: reference configuration information is acquired. The technical scheme has the advantages that the parameter comparison information can be used as a reference to acquire the reference configuration information, and the obtained reference configuration information is more scientific and reasonable.
In some optional embodiments, the obtaining of the reference configuration information includes: based on each stimulation parameter identification of all single configuration information in the parameter comparison information, executing the following processing: and calculating the average value of all parameter values corresponding to the stimulation parameter identification, and taking the average value as the parameter value corresponding to the stimulation parameter identification of the reference configuration information. The technical scheme has the advantages that the average value of all parameter values corresponding to a certain stimulation parameter identifier can be calculated, the average value is used as the parameter value corresponding to the stimulation parameter identifier of the reference configuration information, and the corresponding parameter value of the reference configuration information determined by the method cannot be too high or too low, so that the method is reasonable.
In some optional embodiments, the obtaining of the reference configuration information includes: acquiring training data of a plurality of sample objects, wherein the training data of each sample object comprises parameter comparison information and configuration information; training by using a deep neural network according to the training data of the plurality of sample objects to obtain a parameter configuration model; inputting the parameter comparison information of the target patient into the parameter configuration model to obtain the configuration information of the target patient as the reference configuration information. The technical scheme has the advantages that the configuration information of the target patient can be acquired in real time as long as the parameter comparison information of the target patient is input into the parameter configuration model, particularly, when the number of samples is large enough, the accuracy is expected to reach a high level, compared with a mode of manually inputting the configuration information or importing the configuration information, the intelligent degree is high, and human errors can be avoided.
In a second aspect, the present application provides a parameter ratio pair apparatus applied to an electronic device, the apparatus including: the system comprises a configuration acquisition module, a data processing module and a data processing module, wherein the configuration acquisition module is used for acquiring historical configuration information of a target patient, the historical configuration information comprises a plurality of single configuration information, and the single configuration information comprises at least one stimulation parameter identifier and a parameter value corresponding to each stimulation parameter identifier; the selection receiving module is used for receiving selection operation of at least two single configuration information; an information determination module, configured to determine, in response to the selection operation, the at least two pieces of single configuration information as parameter comparison information of the target patient; a comparison display module, configured to control a display device to display a parameter comparison table and/or a parameter comparison graph of the target patient based on the parameter comparison information, where the parameter comparison graph includes at least one of the following: a 2D parameter comparison graph and a 3D parameter comparison graph.
In some optional embodiments, the apparatus further comprises: the prompt generation module is used for generating prompt information and sending the prompt information to doctor equipment when detecting that the parameter comparison information meets a preset condition, wherein the preset condition is used for indicating at least one of the following conditions: the difference degree of the parameter values of the same stimulation parameter identification of the at least two single configuration information is greater than a preset difference degree threshold value; the parameter value of at least one stimulation parameter identification of the at least one single configuration information is not within the preset range of the parameter value of the corresponding stimulation parameter identification.
In some optional embodiments, the prompt generation module comprises: the comparison value unit is used for calculating parameter values corresponding to target stimulation parameter identifications of every two pieces of single configuration information in the parameter comparison information to obtain at least one comparison value; and the first generating unit is used for generating prompt information and sending the prompt information to doctor equipment when the maximum value in the at least one comparison value is greater than a preset threshold value corresponding to the target stimulation parameter identifier, wherein the prompt information comprises the target stimulation parameter identifier.
In some optional embodiments, the single configuration information further comprises a stimulation application time; the comparison value unit comprises: the comparison subunit is used for determining that the single configuration information of which the stimulation application time is within the preset stimulation application time range in the parameter comparison information is the comparison information; and the calculating subunit is configured to, when the number of the single configuration information in the information to be compared is at least two, calculate a parameter value corresponding to the target stimulation parameter identifier of every two single configuration information in the information to be compared, so as to obtain the at least one comparison value.
In some optional embodiments, the prompt generation module further comprises: a target comparison value unit, configured to obtain a difference between stimulus application times of two corresponding single configuration information based on a target comparison value, where the target comparison value is one of the at least one comparison value; and the second generating unit is used for generating prompt information and sending the prompt information to doctor equipment when the ratio of the target comparison value to the difference value is greater than a preset ratio.
In some optional embodiments, the apparatus further comprises: and the reference configuration module is used for acquiring the reference configuration information.
In some optional embodiments, the reference configuration module is to: based on each stimulation parameter identification of all single configuration information in the parameter comparison information, executing the following processing: and calculating the average value of all parameter values corresponding to the stimulation parameter identification, and taking the average value as the parameter value corresponding to the stimulation parameter identification of the reference configuration information.
In some optional embodiments, the reference configuration module comprises: the training data unit is used for acquiring training data of a plurality of sample objects, and the training data of each sample object comprises parameter comparison information and configuration information; the model training unit is used for training by utilizing a deep neural network according to the training data of the plurality of sample objects to obtain a parameter configuration model; and the configuration information unit is used for inputting the parameter comparison information of the target patient into the parameter configuration model to obtain the configuration information of the target patient as the reference configuration information.
In a third aspect, the present application provides an electronic device comprising a memory and a processor, the memory storing a computer program, the processor implementing the steps of any of the above methods when executing the computer program.
In a fourth aspect, the present application provides a computer readable storage medium having stored thereon a computer program which, when executed by a processor, carries out the steps of any of the methods described above.
Drawings
The present application is further described below with reference to the drawings and examples.
Fig. 1 is a schematic flowchart of a parameter comparison method according to an embodiment of the present disclosure;
FIG. 2 is a schematic flow chart of another parameter comparison method provided in the embodiments of the present application;
fig. 3 is a schematic flowchart of a process for generating a prompt message according to an embodiment of the present application;
FIG. 4 is a schematic diagram of a process for obtaining at least one alignment value according to an embodiment of the present disclosure;
FIG. 5 is a schematic flow chart of another example of generating a prompt message according to the present disclosure;
fig. 6 is a partial schematic flow chart of a parameter comparison method according to an embodiment of the present application;
fig. 7 is a schematic flowchart of acquiring reference configuration information according to an embodiment of the present application;
FIG. 8 is a schematic structural diagram of a parameter ratio apparatus according to an embodiment of the present application;
FIG. 9 is a schematic structural diagram of another parameter comparison apparatus provided in the embodiments of the present application;
fig. 10 is a schematic structural diagram of a prompt generation module according to an embodiment of the present application;
fig. 11 is a schematic structural diagram of a comparison value unit according to an embodiment of the present application;
fig. 12 is a schematic structural diagram of another prompt generation module provided in the embodiment of the present application;
FIG. 13 is a schematic diagram of a partial structure of a parameter comparison apparatus according to an embodiment of the present application;
fig. 14 is a schematic structural diagram of a reference configuration module according to an embodiment of the present application;
fig. 15 is a schematic structural diagram of an electronic device according to an embodiment of the present application;
fig. 16 is a schematic structural diagram of a program product for implementing a parameter comparison method according to an embodiment of the present application.
Detailed Description
The present application is further described with reference to the accompanying drawings and the detailed description, and it should be noted that, in the present application, the embodiments or technical features described below may be arbitrarily combined to form a new embodiment without conflict.
Referring to fig. 1, an embodiment of the present application provides a parameter comparison method applied to an electronic device, where the method includes steps S101 to S104.
Step S101: obtaining historical configuration information of a target patient, wherein the historical configuration information comprises a plurality of single configuration information, and the single configuration information comprises at least one stimulation parameter identifier and a parameter value corresponding to each stimulation parameter identifier.
The implanted nerve stimulation system mainly comprises a stimulator implanted in a body, an electrode and program control equipment in vitro. The existing nerve regulation and control technology is mainly characterized in that an electrode is implanted in a specific structure (namely a target spot) in a body through a three-dimensional operation, and a stimulator implanted in the body of a patient sends electric pulses to the target spot through the electrode to regulate and control the electric activity and the function of a corresponding nerve structure and network, so that symptoms are improved, and pain is relieved. The stimulator may be any one of an Implantable nerve electrical stimulation device, an Implantable cardiac electrical stimulation System (also called a cardiac pacemaker), an Implantable Drug Delivery System (I DDS for short), and a lead switching device. Examples of the implantable neural electrical Stimulation device include Deep Brain Stimulation (DBS), Cortical Brain Stimulation (CNS), Spinal Cord Stimulation (SCS), Sacral Nerve Stimulation (SNS), and Vagal Nerve Stimulation (VNS).
The stimulation parameters may include at least one of: frequency (number of pulses per unit time in 1s, in Hz), pulse width (duration of each pulse, in mus), amplitude (typically expressed in voltage, i.e. the intensity of each pulse, in V), stimulation pattern (including timed and cyclic stimulation patterns), and upper and lower patient control limits (the range within which the patient can autonomously adjust).
In a particular application, the individual stimulation parameters of the stimulator may be adjusted in either current mode or voltage mode.
Wherein, the stimulation parameter identification can be represented by at least one of Chinese, letter, number and special symbol. Such as "a 01", "amplitude", or "# 01".
In one embodiment, the single configuration information is, for example: the frequency was 130Hz, the pulse width was 60 mus and the amplitude was 3V.
In some embodiments, the step S101 may include: receiving an entry operation, and responding to the entry operation to obtain historical configuration information of the target patient; alternatively, historical configuration information for the target patient is imported using a data interface. Thus, the doctor can select a suitable way to acquire the historical configuration information.
Step S102: a selection operation of at least two single configuration information is received. The at least two pieces of single configuration information are, for example, 2 pieces of single configuration information, 3 pieces of single configuration information, or 5 pieces of single configuration information, and one piece of single configuration information is generated in each program control process.
In a specific application, a doctor performs program control on a target patient 3 times from 6 months to 9 months, performs program control on the target patient 1 st time in 6 months, and obtains 1 piece of single configuration information; the 2 nd program control is carried out on the target patient in 7 months, and 1 piece of single configuration information is obtained; the 3 rd program was performed on the target patient in 9 months, resulting in 1 single configuration message.
In a specific application, the at least two single shots of configuration information may be single shots of configuration information corresponding to the last N electrical stimulations applied to the target patient, where N is, for example, a positive integer such as 2, 3, 4, 5, etc.
Step S103: in response to the selection operation, determining the at least two single configuration information as parameter alignment information of the target patient.
Step S104: controlling a display device to display a parameter comparison table and/or a parameter comparison graph of the target patient based on the parameter comparison information, wherein the parameter comparison graph comprises at least one of the following: a 2D parameter comparison graph and a 3D parameter comparison graph. The form of the parameter comparison graph is not limited in the present application, and the form of the parameter comparison graph may include at least one of the following: pie charts, graphs, wave charts, bar charts, and bar charts.
Therefore, on one hand, the historical configuration information can be reasonably utilized, and parameter comparison information is obtained according to the historical configuration information, so that a doctor can know the variation trend of the stimulation parameters corresponding to the target patient; on one hand, the selection mode of the single configuration information is not limited, at least two pieces of single configuration information can be arbitrarily selected from historical configuration information as parameter comparison information of the target patient according to actual needs, the parameter comparison information can be part or all of the historical configuration information, when the parameter comparison information is all the historical configuration information, the change trend of stimulation parameters corresponding to the target patient can be reflected on the whole, when the parameter comparison information is part of the historical configuration information, for example, the single configuration information corresponding to the electrical stimulation applied to the target patient for the last 5 times, generally speaking, the recent single configuration information is more concerned in practical application, the data operation amount can be reduced under the condition that the comparison requirement is met, and the intelligent degree is higher; on the other hand, parameter comparison information can be displayed in a form of a table and/or a graph by using the display device, and a comparison result is displayed in a digital mode, so that the display effect is vivid and visual, and the use experience of a user is improved.
Referring to fig. 2, in some embodiments, the method may further include step S105.
Step S105: when detecting that the parameter comparison information meets a preset condition, generating prompt information and sending the prompt information to doctor equipment, wherein the preset condition is used for indicating at least one of the following conditions: the difference degree of the parameter values of the same stimulation parameter identification of the at least two single configuration information is greater than a preset difference degree threshold value; the parameter value of at least one stimulation parameter identification of the at least one single configuration information is not within the preset range of the parameter value of the corresponding stimulation parameter identification.
The doctor equipment is for example cell-phone, panel computer, notebook computer, desktop, intelligent wearing equipment etc..
The stimulation parameter identification may include an amplitude and a frequency, and the parameter values of the amplitude and the parameter values of the frequency of the parameter comparison information may be compared respectively.
When the comparison target is a parameter value of the amplitude of the parameter comparison information, the difference may be a difference value of the parameter value of the amplitude, and the preset difference threshold is, for example, 2V; the degree of difference may also be a ratio of parameter values of the amplitude, and the preset degree of difference threshold is, for example, 3.
The predetermined range of parameter values for the amplitude is, for example, 3V to 4V.
When the number of the at least two single configuration information is two, taking the difference degree of the two single configuration information as the difference degree of the at least two single configuration information; and when the quantity of the at least two single configuration information is more than two, comparing one single configuration information with the other single configuration information one by taking one single configuration information as a reference to obtain a plurality of difference degrees, and taking the maximum difference degree as the difference degree of the at least two single configuration information.
Therefore, when the parameter ratio information meets the preset condition, the condition that the variation fluctuation between two single configuration information is too large or at least one single configuration information is abnormal exists, and the prompt information can be sent to the doctor equipment at the moment, so that the doctor can know the abnormal condition of the configuration information of the target patient in time.
Referring to fig. 3, in some embodiments, the step S105 may include steps S201 to S202.
Step S201: and calculating parameter values corresponding to the target stimulation parameter identifications of every two pieces of single configuration information in the parameter comparison information to obtain at least one comparison value.
In a specific application, the calculation method for obtaining at least one comparison value is, for example, calculation of a difference value or calculation of a ratio.
Step S202: and when the maximum value of the at least one comparison value is larger than a preset threshold value corresponding to the target stimulation parameter identification, generating prompt information and sending the prompt information to doctor equipment, wherein the prompt information comprises the target stimulation parameter identification.
For example, the following steps are carried out: the parameter comparison information comprises 3 pieces of single configuration information which are respectively the 1 st configuration information to the 3 rd configuration information, the target stimulation parameter identifier is a pulse width, the preset threshold corresponding to the pulse width is 20 mus, and the parameter values of the pulse widths of the 1 st configuration information to the 3 rd configuration information are as follows: and performing difference calculation on the parameter values corresponding to the pulse widths for 50 mus, 60 mus and 80 mus to obtain 3 comparison values (absolute values) which are respectively 10 mus, 30 mus and 20 mus, wherein the maximum value of the 3 comparison values is greater than a preset threshold value corresponding to the pulse widths. At this point, a prompt message may be generated and sent to the physician device, the prompt message including the pulse width.
In a particular application, the prompting message may also include an identification of the target patient and/or an identification of the stimulator. Thereby, the doctor can know the corresponding target patient and/or the corresponding stimulator when the configuration information is abnormal.
Therefore, the parameter values corresponding to the target stimulation parameter identifications of every two pieces of single configuration information in the parameter comparison information can be calculated to obtain at least one comparison value, when the maximum value of the comparison values is larger than the preset threshold value corresponding to the target stimulation parameter identification, the situation that two pieces of single configuration information with overlarge difference exist in the parameter comparison information and the parameter setting is abnormal possibly exists is explained, and at the moment, the prompt information can be sent to the doctor equipment, so that the doctor can know the abnormal situation of the configuration information of the target patient in time.
Referring to fig. 4, in some embodiments, the single configuration information may also include a stimulation application time; the step S201 may include steps S301 to S302.
Step S301: and determining the single configuration information of which the stimulation application time is in the preset stimulation application time range in the parameter comparison information as the information to be compared. The preset stimulus application time range is, for example, 9: 00-9: 30. 10: 00-10: 30 or 12: 00-12: 30.
step S302: when the number of the single configuration information in the information to be compared is at least two, calculating parameter values corresponding to the target stimulation parameter identifications of every two single configuration information in the information to be compared to obtain at least one comparison value.
Therefore, generally speaking, in practical application, attention is paid to the difference between the single configuration information with the stimulation application time in the same range, the single configuration information with the stimulation application time in the preset stimulation application time range in the parameter comparison information can be used as the information to be compared, and the information to be compared is calculated, so that the obtained comparison value can reflect the difference between the single configuration information in the preset stimulation application time range, and the requirement in practical application is met.
Referring to fig. 5, in some embodiments, the step S105 may further include steps S401 to S402.
Step S401: and acquiring a difference value of the stimulus application time of the corresponding two single configuration information based on a target comparison value, wherein the target comparison value is one of the at least one comparison value.
Step S402: and when the ratio of the target comparison value to the difference value is greater than a preset ratio, generating prompt information and sending the prompt information to doctor equipment.
The target alignment value is, for example, 10 μ s, 30 μ s or 20 μ s, the difference between the stimulus application times of the corresponding two single configuration information is, for example, 30min, 60min or 90min, and the preset ratio is, for example, 0.5 μ s/min, 0.6 μ s/min or 0.8 μ s/min.
Therefore, when the ratio of the target comparison value to the difference value of the stimulus application time of the two corresponding single configuration information is greater than the preset ratio, it is indicated that the parameter value corresponding to the target stimulus parameter identification of the target patient has large variation and fluctuation in a short time, the target patient is easy to have tolerance to the stimulus under the condition, and at the moment, the prompt information can be sent to the doctor equipment, so that the doctor can know the relevant condition of the target patient in time, and therefore corresponding measures are taken, and the target patient is prevented from having tolerance to the stimulus.
Referring to fig. 6, in some embodiments, the method may further include step S106.
Step S106: reference configuration information is acquired.
Therefore, the parameter comparison information can be used as reference to acquire the reference configuration information, and the obtained reference configuration information is more scientific and reasonable.
In some embodiments, the step S106 may include: based on each stimulation parameter identification of all single configuration information in the parameter comparison information, executing the following processing: and calculating the average value of all parameter values corresponding to the stimulation parameter identification, and taking the average value as the parameter value corresponding to the stimulation parameter identification of the reference configuration information.
Therefore, the average value of all parameter values corresponding to a certain stimulation parameter identifier can be calculated, the average value is used as the parameter value corresponding to the stimulation parameter identifier of the reference configuration information, and the corresponding parameter value of the determined reference configuration information is not too high or too low, so that the method is reasonable.
Referring to fig. 7, in some embodiments, the step S106 may include steps S501 to S503.
Step S501: training data of a plurality of sample objects is obtained, and the training data of each sample object comprises parameter comparison information and configuration information.
Step S502: and training by using a deep neural network according to the training data of the plurality of sample objects to obtain a parameter configuration model.
Step S503: inputting the parameter comparison information of the target patient into the parameter configuration model to obtain the configuration information of the target patient as the reference configuration information.
Therefore, the configuration information of the target patient can be acquired in real time as long as the parameter comparison information of the target patient is input into the parameter configuration model, particularly when the number of samples is large enough, the accuracy is expected to reach a very high level, the intelligent degree is high compared with a mode of manually inputting the configuration information or importing the configuration information, and human errors can be avoided.
Referring to fig. 8, an embodiment of the present application further provides a parameter comparison apparatus, and a specific implementation manner of the parameter comparison apparatus is consistent with the implementation manner and the achieved technical effect described in the embodiment of the parameter comparison method, and a part of the contents are not described again.
The device is applied to the electronic equipment, and the device comprises: a configuration obtaining module 101, configured to obtain historical configuration information of a target patient, where the historical configuration information includes a plurality of single configuration information, and the single configuration information includes at least one stimulation parameter identifier and a parameter value corresponding to each stimulation parameter identifier; a selection receiving module 102, configured to receive a selection operation on at least two pieces of single configuration information; an information determining module 103, configured to determine, in response to the selecting operation, the at least two pieces of single configuration information as parameter comparison information of the target patient; a comparison display module 104, configured to control a display device to display a parameter comparison table and/or a parameter comparison graph of the target patient based on the parameter comparison information, where the parameter comparison graph includes at least one of the following: a 2D parameter comparison graph and a 3D parameter comparison graph.
Referring to fig. 9, in some embodiments, the apparatus may further include: a prompt generating module 105, configured to generate a prompt message and send the prompt message to a doctor device when it is detected that the parameter comparison information meets a preset condition, where the preset condition is used to indicate at least one of the following situations: the difference degree of the parameter values of the same stimulation parameter identification of the at least two single configuration information is greater than a preset difference degree threshold value; the parameter value of at least one stimulation parameter identification of the at least one single configuration information is not within the preset range of the parameter value of the corresponding stimulation parameter identification.
Referring to fig. 10, in some embodiments, the prompt generation module 105 may include: a comparison value unit 201, configured to calculate a parameter value corresponding to a target stimulation parameter identifier of every two pieces of single configuration information in the parameter comparison information to obtain at least one comparison value; a first generating unit 202, configured to generate a prompt message and send the prompt message to a doctor device when a maximum value of the at least one comparison value is greater than a preset threshold corresponding to the target stimulation parameter identifier, where the prompt message includes the target stimulation parameter identifier.
Referring to fig. 11, in some embodiments, the single configuration information may also include a stimulation application time; the alignment value unit 201 may include: a to-be-compared subunit 301, configured to determine that, in the parameter comparison information, the single configuration information whose stimulation application time is within a preset stimulation application time range is to be compared; a calculating subunit 302, configured to, when the number of the single configuration information in the information to be compared is at least two, calculate a parameter value corresponding to a target stimulation parameter identifier of every two single configuration information in the information to be compared, so as to obtain the at least one comparison value.
Referring to fig. 12, in some embodiments, the prompt generation module 105 may further include: a target comparison value unit 401, configured to obtain a difference between stimulation application times of two corresponding single configuration information based on a target comparison value, where the target comparison value is one of the at least one comparison value; a second generating unit 402, configured to generate a prompt message and send the prompt message to a doctor device when a ratio of the target comparison value to the difference value is greater than a preset ratio.
Referring to fig. 13, in some embodiments, the apparatus may further include: and a reference configuration module 106, configured to obtain reference configuration information.
In some embodiments, the reference configuration module 106 may be configured to: based on each stimulation parameter identification of all single configuration information in the parameter comparison information, executing the following processing: and calculating the average value of all parameter values corresponding to the stimulation parameter identification, and taking the average value as the parameter value corresponding to the stimulation parameter identification of the reference configuration information.
Referring to fig. 14, in some embodiments, the reference configuration module 106 may include: a training data unit 501, configured to obtain training data of a plurality of sample objects, where the training data of each sample object includes parameter comparison information and configuration information; a model training unit 502, configured to perform training using a deep neural network according to the training data of the plurality of sample objects to obtain a parameter configuration model; a configuration information unit 503, configured to input the parameter comparison information of the target patient into the parameter configuration model, and obtain the configuration information of the target patient as the reference configuration information.
Referring to fig. 15, an embodiment of the present application further provides an electronic device 200, where the electronic device 200 includes at least one memory 210, at least one processor 220, and a bus 230 connecting different platform systems.
The memory 210 may include readable media in the form of volatile memory, such as Random Access Memory (RAM)211 and/or cache memory 212, and may further include Read Only Memory (ROM) 213.
The memory 210 further stores a computer program, and the computer program can be executed by the processor 220, so that the processor 220 executes the steps of the parameter comparison method in the embodiment of the present application, and the specific implementation manner of the method is consistent with the implementation manner and the achieved technical effect described in the embodiment of the parameter comparison method, and some contents are not described again.
Accordingly, the processor 220 may execute the computer programs described above, and may execute the utility 214.
The electronic device 200 may also communicate with one or more external devices 240, such as a keyboard, pointing device, bluetooth device, etc., and may also communicate with one or more devices capable of interacting with the electronic device 200, and/or with any devices (e.g., routers, modems, etc.) that enable the electronic device 200 to communicate with one or more other computing devices. Such communication may be through input-output interface 250. Also, the electronic device 200 may communicate with one or more networks (e.g., a Local Area Network (LAN), a Wide Area Network (WAN), and/or a public network such as the Internet) via the network adapter 260. The network adapter 260 may communicate with other modules of the electronic device 200 via the bus 230. It should be appreciated that although not shown in the figures, other hardware and/or software modules may be used in conjunction with the electronic device 200, including but not limited to: microcode, device drivers, redundant processors, external disk drive arrays, RAID systems, tape drives, and data backup storage platforms, to name a few.
In one particular application, the electronic device 200 may be integrated with a physician's device.
The embodiment of the present application further provides a computer-readable storage medium, where the computer-readable storage medium is used for storing a computer program, and when the computer program is executed, the steps of the parameter comparison method in the embodiment of the present application are implemented, and a specific implementation manner of the method is consistent with the implementation manner and the achieved technical effect described in the embodiment of the parameter comparison method, and some contents are not described again.
Fig. 16 shows a program product 300 for implementing the parameter comparison method provided in this embodiment, which may employ a portable compact disc read only memory (CD-ROM) and include program codes, and may be executed on a terminal device, such as a personal computer. However, the program product 300 of the present invention is not so limited, and in this application, a readable storage medium may be any tangible medium that can contain, or store a program for use by or in connection with an instruction execution system, apparatus, or device. Program product 300 may employ any combination of one or more readable media. The readable medium may be a readable signal medium or a readable storage medium. A readable storage medium may be, for example, but not limited to, an electronic, magnetic, optical, electromagnetic, infrared, or semiconductor system, apparatus, or device, or any combination of the foregoing. More specific examples (a non-exhaustive list) of the readable storage medium include: an electrical connection having one or more wires, a portable disk, a hard disk, a Random Access Memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or flash memory), an optical fiber, a portable compact disc read-only memory (CD-ROM), an optical storage device, a magnetic storage device, or any suitable combination of the foregoing.
A computer readable storage medium may include a propagated data signal with readable program code embodied therein, for example, in baseband or as part of a carrier wave. Such a propagated data signal may take many forms, including, but not limited to, electro-magnetic, optical, or any suitable combination thereof. A readable storage medium may also be any readable medium that can communicate, propagate, or transport the program for use by or in connection with the instruction execution system, apparatus, or device. Program code embodied on a readable storage medium may be transmitted using any appropriate medium, including but not limited to wireless, wireline, optical fiber cable, RF, etc., or any suitable combination of the foregoing. Program code for carrying out operations for aspects of the present invention may be written in any combination of one or more programming languages, including an object oriented programming language such as Java, C + + or the like and conventional procedural programming languages, such as the C language or similar programming languages. The program code may execute entirely on the user's computing device, partly on the user's device, as a stand-alone software package, partly on the user's computing device and partly on a remote computing device, or entirely on the remote computing device or server. In the case of a remote computing device, the remote computing device may be connected to the user computing device through any kind of network, including a Local Area Network (LAN) or a Wide Area Network (WAN), or may be connected to an external computing device (e.g., through the internet using an internet service provider).
While the present application is described in terms of various aspects, including exemplary embodiments, the principles of the invention should not be limited to the disclosed embodiments, but are also intended to cover various modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Claims (11)
1. A parameter comparison apparatus, applied to an electronic device, the apparatus comprising:
the system comprises a configuration acquisition module, a data processing module and a data processing module, wherein the configuration acquisition module is used for acquiring historical configuration information of a target patient, the historical configuration information comprises a plurality of single configuration information, and the single configuration information comprises at least one stimulation parameter identifier and a parameter value corresponding to each stimulation parameter identifier;
the selection receiving module is used for receiving selection operation of at least two single configuration information;
an information determination module, configured to determine, in response to the selection operation, the at least two pieces of single configuration information as parameter comparison information of the target patient;
a comparison display module, configured to control a display device to display a parameter comparison table and/or a parameter comparison graph of the target patient based on the parameter comparison information, where the parameter comparison graph includes at least one of the following: a 2D parameter comparison graph and a 3D parameter comparison graph.
2. The apparatus according to claim 1, further comprising:
the prompt generation module is used for generating prompt information and sending the prompt information to doctor equipment when detecting that the parameter comparison information meets a preset condition, wherein the preset condition is used for indicating at least one of the following conditions: the difference degree of the parameter values of the same stimulation parameter identification of the at least two single configuration information is greater than a preset difference degree threshold value; the parameter value of at least one stimulation parameter identification of the at least one single configuration information is not within the preset range of the parameter value of the corresponding stimulation parameter identification.
3. The apparatus of claim 2, wherein the prompt generation module comprises:
the comparison value unit is used for calculating parameter values corresponding to target stimulation parameter identifications of every two pieces of single configuration information in the parameter comparison information to obtain at least one comparison value;
and the first generating unit is used for generating prompt information and sending the prompt information to doctor equipment when the maximum value in the at least one comparison value is greater than a preset threshold value corresponding to the target stimulation parameter identifier, wherein the prompt information comprises the target stimulation parameter identifier.
4. The apparatus according to claim 3, wherein the single configuration information further comprises a stimulus application time;
the comparison value unit comprises:
the comparison subunit is used for determining that the single configuration information of which the stimulation application time is within the preset stimulation application time range in the parameter comparison information is the comparison information;
and the calculating subunit is configured to, when the number of the single configuration information in the information to be compared is at least two, calculate a parameter value corresponding to the target stimulation parameter identifier of every two single configuration information in the information to be compared, so as to obtain the at least one comparison value.
5. The apparatus of claim 4, wherein the prompt generation module further comprises:
a target comparison value unit, configured to obtain a difference between stimulus application times of two corresponding single configuration information based on a target comparison value, where the target comparison value is one of the at least one comparison value;
and the second generating unit is used for generating prompt information and sending the prompt information to doctor equipment when the ratio of the target comparison value to the difference value is greater than a preset ratio.
6. The apparatus according to claim 1, further comprising:
and the reference configuration module is used for acquiring the reference configuration information.
7. The apparatus of claim 6, wherein the reference configuration module is configured to: based on each stimulation parameter identification of all single configuration information in the parameter comparison information, executing the following processing: and calculating the average value of all parameter values corresponding to the stimulation parameter identification, and taking the average value as the parameter value corresponding to the stimulation parameter identification of the reference configuration information.
8. The apparatus of claim 6, wherein the reference configuration module comprises:
the training data unit is used for acquiring training data of a plurality of sample objects, and the training data of each sample object comprises parameter comparison information and configuration information;
the model training unit is used for training by utilizing a deep neural network according to the training data of the plurality of sample objects to obtain a parameter configuration model;
and the configuration information unit is used for inputting the parameter comparison information of the target patient into the parameter configuration model to obtain the configuration information of the target patient as the reference configuration information.
9. A parameter comparison method is applied to electronic equipment, and the method comprises the following steps:
obtaining historical configuration information of a target patient, wherein the historical configuration information comprises a plurality of single configuration information, and the single configuration information comprises at least one stimulation parameter identifier and a parameter value corresponding to each stimulation parameter identifier;
receiving selection operation of at least two single configuration information;
in response to the selection operation, determining the at least two pieces of single configuration information as parameter comparison information of the target patient;
controlling a display device to display a parameter comparison table and/or a parameter comparison graph of the target patient based on the parameter comparison information, wherein the parameter comparison graph comprises at least one of the following: a 2D parameter comparison graph and a 3D parameter comparison graph.
10. An electronic device, characterized in that the electronic device comprises a memory and a processor, the memory storing a computer program, the processor realizing the steps of the method as claimed in claim 9 when executing the computer program.
11. A computer-readable storage medium, characterized in that the computer-readable storage medium stores a computer program which, when being executed by a processor, carries out the steps of the method as claimed in claim 9.
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| PCT/CN2022/092816 WO2023000788A1 (en) | 2021-07-20 | 2022-05-13 | Parameter comparison method and apparatus, electronic device, and computer readable storage medium |
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| WO2023000788A1 (en) * | 2021-07-20 | 2023-01-26 | 苏州景昱医疗器械有限公司 | Parameter comparison method and apparatus, electronic device, and computer readable storage medium |
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| CN116721764B (en) * | 2023-08-10 | 2023-10-27 | 武汉楚精灵医疗科技有限公司 | Preoperative prompting method and device |
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