A Control Method, Device, Equipment and Medium for a Millimeter-Wave Therapy Instrument

Abstract

The present application relates to a control method, device, equipment and medium for a millimeter wave therapy instrument, and relates to the field of medical equipment. It includes obtaining the first temperature information and the second temperature information of a patient, where the first temperature information is the temperature information of the normal part of the patient, and the second temperature information is the temperature information of the uncomfortable part of the patient. Then, it determines the first temperature difference between the first temperature information and the second temperature information, and judges whether the first temperature difference reaches or exceeds the first temperature difference threshold. When the first temperature difference reaches or exceeds the first temperature difference threshold, it generates an instrument start instruction to control the automatic start of the instrument equipment. The present application has the effect of solving the problems of slow diagnosis process and untimely treatment, and can perform preventive treatment.

Description

Technical Field

[0001] The present application relates to the technical field of medical devices, and in particular, to a control method, device, equipment and medium for a millimeter wave therapy instrument. Background Art

[0002] A millimeter wave therapy instrument is an instrument that uses millimeter wave high-frequency electromagnetic waves with wavelengths of 10 - 1 mm and frequencies of 30 - 300 GHz to treat diseases. Millimeter waves are high-frequency electromagnetic waves belonging to the microwave band. As an electromagnetic wave, it can penetrate the biological epidermis and act on deep tissues. Since the frequency of millimeter waves is relatively high, the power can be effectively limited to a small range and only act on specific parts.

[0003] For various currently known millimeter wave therapy instruments, the principle of treating diseases is mainly based on the doctor's diagnosis, the patient's reaction, and the control of medical equipment. Among them, the control method of medical equipment is to manually control the millimeter wave therapy instrument by medical staff. Since the medical staff manually control the millimeter wave therapy instrument, it is necessary for the medical staff to monitor the patient's physical condition in real time, so as to timely and effectively treat the patient's uncomfortable parts.

[0004] Regarding the above related technologies, the inventor believes that when using a millimeter wave therapy instrument to treat a patient, once the medical staff fails to monitor in time, the millimeter wave therapy instrument cannot be controlled in a timely and effective manner, resulting in slow diagnosis and untimely treatment. Summary of the Invention

[0005] In order to solve the problems of slow diagnosis and untimely treatment, the present application provides a control method, device, equipment and medium for a millimeter wave therapy instrument.

[0006] In a first aspect, the present application provides a control method for a millimeter wave therapy instrument, which is achieved through the following technical solutions:

[0007] A control method for a millimeter wave therapy instrument, characterized by comprising:

[0008] Obtain the first temperature information and the second temperature information of the patient, where the first temperature information is the temperature information of the normal part of the patient, and the second temperature information is the temperature information of the uncomfortable part of the patient;

[0009] Determine the temperature difference information between the first temperature information and the second temperature information;

[0010] Judge whether the temperature difference information reaches or exceeds a first temperature difference threshold;

[0011] If the temperature difference information reaches or exceeds the first temperature difference threshold, an instrument activation instruction is generated to control the automatic activation of the instrument device.

[0012] By adopting the above technical solution, the temperature information of the normal part and the uncomfortable part on the patient's skin surface is obtained. The temperature information of the normal part is the first temperature information, and the temperature information of the uncomfortable part is the second temperature information. The temperature information of the two parts is used as the standard of the patient's physical sign information. By performing calculations on it, the temperature difference information between the two can be obtained. The temperature difference information is compared with the first temperature difference threshold. If the temperature difference information reaches or exceeds the set first temperature difference threshold, it proves that the uncomfortable part of the patient needs treatment, that is, an activation instruction is generated to control the automatic activation of the instrument device, so that the patient can receive treatment in the shortest time, ensuring the timeliness of treatment, thereby solving the problems of slow diagnosis process and untimely treatment.

[0013] In another possible implementation manner, the obtaining of the first temperature information and the second temperature information of the patient includes:

[0014] Obtain the uncomfortable area, the instrument treatment area, and the instrument detection area of the patient. The instrument treatment area is used to treat the uncomfortable part of the patient, and the instrument detection area is used to detect the normal part around the uncomfortable part;

[0015] Determine whether the uncomfortable area exceeds the instrument treatment area;

[0016] If the uncomfortable area does not exceed the instrument treatment area, obtain the first temperature information and the second temperature information of the patient;

[0017] If the uncomfortable area exceeds the instrument treatment area, determine whether the uncomfortable area exceeds the instrument detection area;

[0018] If the uncomfortable area does not exceed the instrument detection area, obtain the first temperature information and the second temperature information of the patient;

[0019] If the uncomfortable area exceeds the instrument detection area, perform threshold analysis on the uncomfortable area and the instrument treatment area, generate an instrument combination plan, and determine the combined treatment area and the combined detection area according to the instrument combination plan. Based on the combined treatment area and the combined detection area, detect the uncomfortable area to obtain the first temperature information and the second temperature information of the patient;

[0020] Among them, the combined treatment area covers the uncomfortable area.

[0021] Through the above technical solutions, when obtaining the first temperature information and the second temperature information of the patient, the uncomfortable area of the patient, the instrument treatment area of the instrument, and the instrument detection area of the instrument are respectively obtained, and then it is determined whether the current uncomfortable area exceeds the instrument treatment area. When the uncomfortable area does not exceed the treatment area of the instrument device, it means that the instrument treatment area can detect the uncomfortable area to obtain the temperature of the uncomfortable part, and the instrument detection area can obtain the temperature of the normal part of the patient. Therefore, the first temperature information and the second temperature information of the patient are directly obtained. When the uncomfortable area exceeds the treatment area but is smaller than the instrument detection area, it means that the instrument treatment area can detect the uncomfortable area to obtain the temperature of the uncomfortable part, and the instrument detection area can still obtain the temperature of the local normal part, that is, the instrument detection area can work normally. Therefore, the first temperature information and the second temperature information of the patient are directly obtained. When the uncomfortable area exceeds the instrument detection area, the uncomfortable area and the instrument treatment area are compared, and the uncomfortable area and the instrument treatment area are respectively calculated and analyzed to obtain the required threshold result. According to the threshold result, an instrument combination plan is generated. By analyzing the threshold result, the instrument devices are combined so that the combined treatment area exceeds the uncomfortable part. The device combination based on the instrument combination plan can obtain the first temperature information and the second temperature information of the patient, thereby achieving the effect of accurately controlling the uncomfortable area and improving the treatment efficiency.

[0022] In another possible implementation manner, the obtaining of the uncomfortable part information of the patient includes any of the following methods:

[0023] Obtain the part description information of the patient, and perform area division according to the part description information to obtain the uncomfortable part information of the patient;

[0024] Obtain the doctor's diagnosis information, and perform area division according to the doctor's diagnosis information to obtain the uncomfortable part information of the patient;

[0025] Obtain the device diagnosis information, and perform area division according to the device diagnosis information to obtain the uncomfortable part information of the patient, where the device diagnosis information is obtained by a medical device diagnosing the patient.

[0026] Through the above technical solutions, when obtaining the uncomfortable part information of the patient, the uncomfortable part information of the patient can be obtained according to the patient's description of their own illness, the doctor's diagnosis of the patient, and the result obtained after the medical device measures the patient, thereby improving the diversity of information acquisition and facilitating the subsequent accurate treatment of the uncomfortable part.

[0027] In another possible implementation manner, the threshold analysis of the uncomfortable area and the instrument treatment area to generate an instrument combination plan includes:

[0028] Perform shape detection on the discomfort area to obtain area shape information;

[0029] Input the area shape information into the trained area combination network for training to obtain at least one area combination feature;

[0030] Perform feature recognition and analysis on the at least one area combination feature to generate at least one instrument combination plan;

[0031] Calculate the instrument quantity information of the at least one instrument combination plan, and detect the instrument quantity information to generate an instrument combination plan.

[0032] Through the above technical solution, analyze the discomfort area of the patient to obtain the exact shape of the discomfort area. Compare the obtained area information with the working range of the instrument to generate an instrument combination plan. In order to treat the discomfort area of the patient in different situations, obtain its area characteristics according to the shape information of the discomfort area, and perform targeted treatment on it using a variety of combination plans according to the actual situation, so as to achieve an accurate and efficient treatment effect.

[0033] In another possible implementation manner, the generating the instrument startup instruction to control the instrument device to automatically start, and then further includes:

[0034] Obtain a set treatment time, where the set treatment time is the cycle time of temperature detection;

[0035] Based on the set treatment time, determine the updated first temperature information and second temperature information;

[0036] Determine the second temperature difference between the first temperature information and the second temperature information;

[0037] Judge whether the second temperature difference reaches or exceeds the second temperature difference threshold;

[0038] If the second temperature difference does not reach or exceed the second temperature difference threshold, generate an instrument shutdown instruction to control the instrument device to automatically shut down.

[0039] Through the above technical solution, by setting a periodic temperature detection time, it is possible to achieve automatic detection and treatment of the patient's discomfort area. A new round of temperature detection will be carried out on the discomfort area every cycle. After the instrument and equipment perform a new round of temperature detection on the patient, a second temperature difference will be obtained, that is, the latest temperature difference between the patient's discomfort area and the normal area. The obtained latest temperature difference is compared with the pre-set second temperature difference threshold. If the latest temperature difference does not reach or exceed the set second temperature difference threshold, an instrument shutdown instruction will be generated to control the instrument and equipment to automatically shut down. Thus, there is no need for the patient to manually detect and treat the discomfort area, realizing the intelligence of the instrument and equipment for the diagnosis and treatment of the patient. Through the accurate calculation of the cycle detection time and temperature difference data by the instrument and equipment, unnecessary resource waste during the treatment process can be minimized as much as possible.

[0040] In another possible implementation, before determining whether the temperature difference information reaches or exceeds the first temperature difference threshold, it further includes:

[0041] Obtain clinical test data and disease information, where the clinical test data is the data generated from historical clinical medical records, and the disease information is the patient's disease information;

[0042] Screen the clinical test data to obtain disease category information and the corresponding part temperature difference information, where the part temperature difference information is the temperature difference information of different parts of the body;

[0043] Match the disease information with the disease category information to obtain part set information;

[0044] Match the discomfort part with multiple parts in the part set information to obtain matching part information;

[0045] Based on the matching part information and the part temperature difference information, determine the historical temperature difference data;

[0046] Calculate the average value of the historical temperature difference data to obtain the first temperature difference threshold.

[0047] Through the above technical solution, the clinically tested data and disease information obtained are statistically analyzed, and the clinically tested data are screened and classified to obtain disease category information and temperature difference information of different parts of the body corresponding to the disease. The disease information of the patient is matched with the disease category information to obtain the part set information corresponding to the disease category, and the uncomfortable area part is matched with the obtained part set information to obtain the matching part information. Then, based on the obtained matching part information and the temperature difference information of this part, the historical temperature difference data of this part is determined, and by calculating the average value of the historical temperature difference data, a first temperature difference threshold is obtained. Through a large amount of clinically tested data and precise analysis of the disease type and uncomfortable part of the patient, the temperature difference of the corresponding part of the disease is finally obtained as the first temperature difference threshold, so as to provide accurate data support for the temperature difference of the uncomfortable part and achieve an efficient treatment effect in a short time.

[0048] In another possible implementation manner, the method further includes:

[0049] Obtain the part position information of the uncomfortable part and the instrument position information of the instrument;

[0050] Determine the instrument offset value based on the part position information and the instrument position information;

[0051] Judge whether the instrument offset value exceeds a preset offset threshold;

[0052] If the instrument offset value exceeds the preset offset threshold, generate an offset warning instruction to control the warning device to give a warning.

[0053] Through the above technical solution, when detecting the offset of the instrument, the position information of the uncomfortable part and the instrument device is obtained, and then the instrument offset value is determined through the analysis of the uncomfortable part position information and the instrument device position information. The instrument offset value is compared with the preset offset threshold to judge whether the instrument offset value exceeds the offset threshold. If the instrument offset value exceeds the offset threshold, a warning instruction is generated to control the warning device to give a warning. Thus, the situation of reduced treatment efficiency caused by instrument offset is reduced.

[0054] In a second aspect, the present application provides a control device for a millimeter wave treatment instrument, adopting the following technical solution:

[0055] A control device for a millimeter wave treatment instrument, comprising:

[0056] A temperature acquisition module, configured to acquire the first temperature information and the second temperature information of the patient, where the first temperature information is the temperature information of the normal part of the patient, and the second temperature information is the temperature information of the uncomfortable part of the patient;

[0057] A first temperature difference determination module, configured to determine a first temperature difference between the first temperature information and the second temperature information;

[0058] A first temperature difference judgment module, configured to judge whether the first temperature difference reaches or exceeds a first temperature difference threshold;

[0059] A control start module, configured to generate an instrument start instruction and control the automatic start of the instrument device when the first temperature difference reaches or exceeds the first temperature difference threshold.

[0060] By adopting the above technical solution, the temperature information of the normal part and the uncomfortable part on the patient's skin surface is obtained. The temperature information of the normal part is the first temperature information, and the temperature information of the uncomfortable part is the second temperature information. The temperature information of the two parts is used as the standard of the patient's physical sign information. By performing operations on it, the temperature difference information between the two can be obtained. The temperature difference information is compared with the first temperature difference threshold. If the temperature difference information reaches or exceeds the set first temperature difference threshold, it proves that the uncomfortable part of the patient needs to be treated, that is, an opening instruction is generated to control the automatic start of the instrument device, so that the patient can receive treatment in the shortest time and ensure the timeliness of treatment.

[0061] In a possible implementation manner, when the temperature acquisition module acquires the first temperature information and the second temperature information of the patient, it is specifically configured to:

[0062] Acquire the uncomfortable area, the instrument treatment area and the instrument detection area of the patient. The instrument treatment area is used to treat the uncomfortable part of the patient, and the instrument detection area is used to detect the normal part around the uncomfortable part;

[0063] Determine whether the uncomfortable area exceeds the instrument treatment area;

[0064] If the uncomfortable area does not exceed the instrument treatment area, acquire the first temperature information and the second temperature information of the patient;

[0065] If the uncomfortable area exceeds the instrument treatment area, judge whether the uncomfortable area exceeds the instrument detection area;

[0066] If the uncomfortable area does not exceed the instrument detection area, acquire the first temperature information and the second temperature information of the patient;

[0067] If the uncomfortable area exceeds the instrument detection area, perform threshold analysis on the uncomfortable area and the instrument treatment area, generate an instrument combination plan, and determine a combined treatment area and a combined detection area according to the instrument combination plan. Based on the combined treatment area and the combined detection area, detect the uncomfortable area and acquire the first temperature information and the second temperature information of the patient;

[0068] Among them, the combined treatment area covers the discomfort area.

[0069] In another possible implementation, when the temperature acquisition module acquires the discomfort site information of the patient, it specifically includes any one of the following methods:

[0070] Acquire the site description information of the patient, perform area division according to the site description information, and acquire the discomfort site information of the patient;

[0071] Acquire the doctor's diagnosis information, perform area division according to the doctor's diagnosis information, and acquire the discomfort site information of the patient;

[0072] Acquire the device diagnosis information, perform area division according to the device diagnosis information, and acquire the discomfort site information of the patient, where the device diagnosis information is obtained by a medical device diagnosing the patient.

[0073] In another possible implementation, when the temperature acquisition module performs threshold analysis on the discomfort area and the instrument treatment area to generate an instrument combination plan, it is specifically used for:

[0074] Perform shape detection on the discomfort area to obtain area shape information;

[0075] Input the area shape information into the trained area combination network for training to obtain at least one area combination feature;

[0076] Perform feature recognition analysis on the at least one area combination feature to generate at least one instrument combination plan;

[0077] Calculate the instrument quantity information of the at least one instrument combination plan, and detect the instrument quantity information to generate an instrument combination plan.

[0078] In another possible implementation, the device further includes: a time acquisition module, a temperature determination module, a second temperature difference determination module, a second temperature difference judgment module, and a control shutdown module, where

[0079] The time acquisition module is used to acquire the set treatment time, and the set treatment time is the cycle time of temperature detection;

[0080] The temperature determination module is used to determine the updated first temperature information and second temperature information based on the set treatment time;

[0081] The second temperature difference determination module is used to determine the second temperature difference between the first temperature information and the second temperature information;

[0082] The second temperature difference judgment module is used to judge whether the second temperature difference reaches or exceeds a second temperature difference threshold value;

[0083] The control shutdown module is used to generate an instrument shutdown instruction and control the automatic shutdown of the instrument device if the second temperature difference does not reach or exceed the second temperature difference threshold value.

[0084] In another possible implementation manner, the device further includes: a data information acquisition module, a data screening module, a disease matching module, a part matching module, a historical temperature difference determination module, and a data calculation module, where,

[0085] The data information acquisition module is used to acquire clinical test data and disease information, where the clinical test data is data generated by historical clinical medical records, and the disease information is the disease information of the patient;

[0086] The data screening module is used to screen the clinical test data to obtain disease category information and part temperature difference information corresponding to the disease category information, where the part temperature difference information is the temperature difference information of different parts of the body;

[0087] The disease matching module is used to match the disease information with the disease category information to obtain part set information;

[0088] The part matching module is used to match the uncomfortable part with multiple parts in the part set information to obtain matching part information;

[0089] The historical temperature difference determination module is used to determine historical temperature difference data based on the matching part information and the part temperature difference information;

[0090] The data calculation module is used to calculate the average value of the historical temperature difference data to obtain a first temperature difference threshold value.

[0091] In another possible implementation manner, the device further includes: a position acquisition module, an offset determination module, an offset judgment module, and a control warning module,

[0092] The position acquisition module is used to acquire the part position information of the uncomfortable part and the instrument position information of the instrument;

[0093] The offset determination module is used to determine an instrument offset value based on the part position information and the instrument position information;

[0094] The offset judgment module is used to judge whether the instrument offset value exceeds a preset offset threshold value;

[0095] The control and warning module is used to generate an offset warning instruction when the instrument offset value exceeds a preset offset threshold, and control the warning device to give a warning.

[0096] In a third aspect, the present application provides an electronic device, adopting the following technical solution:

[0097] An electronic device, which includes:

[0098] One or more processors;

[0099] A memory;

[0100] One or more applications, wherein the one or more applications are stored in the memory and are configured to be executed by the one or more processors, and the one or more programs are configured to: execute a control method of a millimeter wave therapy instrument according to any one of the first aspect.

[0101] In a fourth aspect, the present application provides a computer-readable storage medium, adopting the following technical solution:

[0102] A computer-readable storage medium, on which a computer program is stored, characterized in that the program is executed by a processor to perform a control method of a millimeter wave therapy instrument according to any one of the first aspect.

[0103] In summary, the present application includes at least one of the following beneficial technical effects:

[0104] 1. Obtain the temperature information of the normal part and the uncomfortable part on the patient's skin surface. The temperature information of the normal part is the first temperature information, and the temperature information of the uncomfortable part is the second temperature information. The temperature information of the two parts is used as the standard of the patient's physical sign information. By performing operations on it, the temperature difference information between the two can be obtained. The temperature difference information is compared with the first temperature difference threshold. If the temperature difference information reaches or exceeds the set first temperature difference threshold, it proves that the uncomfortable part of the patient needs to be treated, that is, an opening instruction is generated to control the instrument device to automatically start, so that the patient can receive treatment in the shortest time, ensuring the timeliness of treatment, thereby solving the problems of slow diagnosis process and untimely treatment;

[0105] 2. Analyze the uncomfortable area of the patient to obtain the exact shape of the uncomfortable area, and generate an instrument combination plan by comparing the obtained area information with the working range of the instrument. In order to treat the uncomfortable areas of the patient in different situations, the area characteristics are obtained according to the shape information of the uncomfortable area, and targeted treatment is carried out on it using a variety of combination plans according to the actual situation, so as to achieve accurate and efficient treatment effects. Description of the Drawings

[0106] Figure 1It is a schematic flowchart of a control method for a millimeter wave therapy instrument according to an embodiment of the present application;

[0107] Figure 2 It is a schematic structural diagram of a control device for a millimeter wave therapy instrument according to an embodiment of the present application;

[0108] Figure 3 It is a schematic structural diagram of an electronic device according to an embodiment of the present application;

[0109] Figure 4 It is intended to show a schematic diagram of the instrument treatment area and the instrument detection area of the millimeter wave therapy instrument according to an embodiment of the present application. Detailed implementation manners

[0110] The following will further describe the present application in detail with reference to the Figures 1-4 accompanying drawings.

[0111] Those skilled in the art can make modifications to this embodiment without creative contributions according to their needs after reading this specification, but as long as they are within the scope of the claims of the present application, they are protected by the patent law.

[0112] To make the objectives, technical solutions, and advantages of the embodiments of the present application clearer, the technical solutions in the embodiments of the present application will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present application. Apparently, the described embodiments are some, but not all, of the embodiments of the present application. All other embodiments obtained by those of ordinary skill in the art based on the embodiments of the present application without creative efforts shall fall within the scope of protection of the present application.

[0113] In addition, the term "and / or" in this article is only a description of the association relationship of associated objects, indicating that there can be three relationships. For example, A and / or B can represent: A exists alone, A and B exist simultaneously, and B exists alone. In addition, the character " / " in this article generally represents an "or" relationship between the associated objects before and after, unless otherwise specified.

[0114] An embodiment of the present application provides a control method for a millimeter wave therapy instrument, which is executed by an electronic device. The electronic device can be a server or a terminal device. Among them, the server can be an independent physical server, a server cluster or a distributed system composed of multiple physical servers, or a cloud server providing cloud computing services. The terminal device can be a smart phone, a tablet computer, a laptop computer, a desktop computer, etc., but is not limited thereto. The terminal device and the server can be directly or indirectly connected through wired or wireless communication methods, and the embodiments of the present application do not make limitations here. For example Figure 1As shown, the method includes step S10, step S11, step S12, and step S13, where

[0115] Step S10: Obtain the first temperature information and the second temperature information of the patient.

[0116] Among them, the first temperature information is the temperature information of the normal part of the patient, and the second temperature information is the temperature information of the uncomfortable part of the patient.

[0117] Specifically, temperature sensors are installed at equal intervals in the white area and the yellow (refer to Figure 4 the shaded part) area of the instrument and equipment. The temperature sensors in the white area will detect the temperature information of the normal part of the patient as the first temperature information, and the temperature sensors in the yellow area will detect the temperature information of the uncomfortable part of the patient as the second temperature information.

[0118] Step S11: Determine the first temperature difference between the first temperature information and the second temperature information.

[0119] Specifically, the temperature value of the first temperature information obtained by testing the normal part of the patient in the white area is operated with the temperature value of the second temperature information obtained by testing the uncomfortable part of the patient in the yellow area, and the difference between the two is used as the first temperature difference. For example, if the detected first temperature information is 36.5°C and the second temperature information is 39°C, the obtained first temperature difference is 2.5°C.

[0120] Step S12: Determine whether the first temperature difference reaches or exceeds the first temperature difference threshold.

[0121] In the embodiments of the present application, the first temperature difference threshold is determined according to the actual condition and actual part of the patient.

[0122] Specifically, the obtained first temperature difference is numerically compared with the first temperature difference threshold, and the first temperature difference threshold is the critical temperature value for whether the device can be started. For example, if the first temperature difference threshold is 0.1°C and the first temperature difference is 0.2°C, it proves that the first temperature difference exceeds the first temperature difference threshold.

[0123] Step S13: If the first temperature difference reaches or exceeds the first temperature difference threshold, generate an instrument activation instruction to control the automatic activation of the instrument and equipment.

[0124] Specifically, when the first temperature difference reaches or exceeds the set first temperature difference threshold, an instrument activation instruction is generated and sent to the instruction receiving end of the instrument and equipment. After receiving the instruction, the instrument and equipment changes from the closed state to the open state to treat the uncomfortable part of the patient.

[0125] An embodiment of the present application provides a control method for a millimeter-wave therapy instrument. The temperature information of the normal part and the uncomfortable part on the patient's skin surface is obtained. The temperature information of the normal part is the first temperature information, and the temperature information of the uncomfortable part is the second temperature information. The temperature information of the two parts is used as the standard of the patient's physical sign information. By performing operations on it, the temperature difference information between the two can be obtained. The temperature difference information is compared with the first temperature difference threshold. If the temperature difference information reaches or exceeds the set first temperature difference threshold, it proves that the uncomfortable part of the patient needs to be treated, that is, an opening instruction is generated to control the instrument device to automatically turn on, so that the patient can receive treatment in the shortest time and ensure the timeliness of treatment, thereby solving the problems of slow diagnosis process and untimely treatment.

[0126] In a possible implementation manner of the embodiment of the present application, step S10 specifically includes step S101 (not shown in the figure), step S102 (not shown in the figure), step S103 (not shown in the figure), step S104 (not shown in the figure), step S105 (not shown in the figure), and step S106 (not shown in the figure), where

[0127] Step S101, obtain the uncomfortable area of the patient, the instrument treatment area, and the instrument detection area.

[0128] Among them, the instrument treatment area is used to treat the uncomfortable part of the patient, and the instrument detection area is used to detect the normal part around the uncomfortable part.

[0129] Specifically, according to the diagnosis information and the patient's description information, determine the uncomfortable part of the patient, perform infrared scanning on the uncomfortable part of the patient to obtain the thermal images of the uncomfortable part and the normal part, and determine the uncomfortable area according to the thermal images.

[0130] Specifically, scan and identify the production barcode of the millimeter-wave therapy instrument device through a scanning device, obtain the production information of the therapy instrument, and screen the specification information of the instrument treatment area and the instrument detection area in the production information, so as to obtain the specification sizes of the instrument treatment area and the instrument detection area.

[0131] Step S102, determine whether the uncomfortable area exceeds the instrument treatment area.

[0132] Step S103, if the uncomfortable area does not exceed the instrument treatment area, obtain the first temperature information and the second temperature information of the patient.

[0133] Specifically, when the uncomfortable area of the patient does not exceed the instrument device treatment area, it means that the instrument treatment area completely covers the uncomfortable area of the patient, so that the uncomfortable area of the patient can be treated in a covering manner. The white area temperature sensor and the yellow area temperature sensor of the instrument device can detect the first temperature information and the second temperature information respectively.

[0134] Step S104, if the uncomfortable area exceeds the instrument treatment area, determine whether the uncomfortable area exceeds the instrument detection area.

[0135] In the embodiment of the present application, the white area of the instrument device is the instrument detection area, and the yellow area is the instrument treatment area. When the uncomfortable area of the patient exceeds the instrument treatment area and also exceeds the instrument detection area, the first temperature detected in the white area and the second temperature detected in the yellow area are always the same. Therefore, there is no temperature difference, which means that the millimeter wave therapeutic instrument cannot work properly. When the uncomfortable area of the patient exceeds the instrument treatment area but does not exceed the instrument detection area, there is a temperature difference between the first temperature detected in the white area and the second temperature detected in the yellow area, that is, the millimeter wave therapeutic instrument can work properly.

[0136] Step S105, if the uncomfortable area does not exceed the instrument detection area, obtain the first temperature information and the second temperature information of the patient.

[0137] Specifically, when the uncomfortable area of the patient is smaller than the instrument detection area, that is, the temperature sensor in the white area can detect the temperature of the normal part of the patient to obtain the first temperature information, and the temperature sensor in the yellow area can detect the temperature of the uncomfortable part of the patient to obtain the second temperature information.

[0138] Step S106, if the uncomfortable area exceeds the instrument detection area, perform threshold analysis on the uncomfortable area and the instrument treatment area to generate an instrument combination plan, and determine the combined treatment area and the combined detection area according to the instrument combination plan. Based on the combined treatment area and the combined detection area, detect the uncomfortable area to obtain the first temperature information and the second temperature information of the patient.

[0139] Specifically, for the case where the uncomfortable area exceeds the instrument detection area, analyze the corresponding thresholds of the uncomfortable area and the instrument treatment area to generate an instrument combination plan. For example, the length of the uncomfortable area is 20 cm and the width is 10 cm, and the threshold of the corresponding uncomfortable area is 200 square centimeters. The instrument treatment area of the millimeter wave therapeutic instrument is 5 cm long and 4 cm wide, and the threshold of the corresponding instrument treatment area is 20 square centimeters. When two millimeter wave therapeutic instruments are combined and spliced, the interval between the two instrument treatment areas is 4 cm. Combine 6 millimeter wave therapeutic instruments, splice the three instrument longitudinal surfaces, divide them into two rows, and form a treatment area with a threshold of 276 square centimeters. Since the instrument treatment area with a threshold of 276 square centimeters in the combination plan exceeds the uncomfortable area with a threshold of 200 square centimeters, this combination plan can be used to detect the normal part of the patient in the instrument detection side area to obtain the first temperature information, and use the instrument treatment area to detect the uncomfortable part of the patient to obtain the second temperature information.

[0140] Another possible implementation of the embodiment of the present application, step S101 specifically includes step S1011 (not shown in the figure), step S1012 (not shown in the figure), and step S1013 (not shown in the figure), where

[0141] Step S1011, obtain the part description information of the patient, and perform area division according to the part description information to obtain the discomfort part information of the patient.

[0142] For the implementation of the present application, the patient can, according to the actual diagnosis situation, independently describe the part through the hospital self-service device. For example, when the patient needs to wait for a long time for diagnosis, the patient can input the part description information of their own discomfort part into the self-service device, and then the self-service device sends the part description information to the electronic device. The electronic device screens and disassembles the part fields in the part description information to obtain the final diagnosis part, and then divides the area of the diagnosis part from the area of the normal part. When the patient receives the instrument diagnosis, the diagnosis can be directly performed on the diagnosis part to obtain the discomfort part information of the patient.

[0143] Step S1012, obtain the doctor's diagnosis information, and perform area division according to the doctor's diagnosis information to obtain the discomfort part information of the patient.

[0144] Specifically, when the patient is unsure about the discomfort area, the doctor diagnoses the discomfort area of the patient and imports the obtained doctor's diagnosis information into the electronic device. Then the electronic device screens and disassembles the part fields in the doctor's diagnosis information to obtain the final diagnosis part, and then divides the area of the diagnosis part from the area of the normal part. When the patient receives the instrument diagnosis, the diagnosis can be directly performed on the diagnosis part to obtain the discomfort part information of the patient.

[0145] Step S1013, obtain the device diagnosis information, and perform area division according to the device diagnosis information to obtain the discomfort part information of the patient. The device diagnosis information is obtained by a medical device diagnosing the patient.

[0146] For the embodiment of the present application, the medical device includes: an infrared detector, a thermal imager, etc. The medical device performs image detection on the discomfort part of the patient to generate device diagnosis information, and then sends the generated device diagnosis information to the electronic device for processing. The electronic device divides the areas of the images of different colors in the device diagnosis information to obtain the final discomfort part information of the patient.

[0147] In a possible implementation of the embodiment of the present application, step S106 specifically includes step S1061 (not shown in the figure), step S1062 (not shown in the figure), step S1063 (not shown in the figure), and step S1064 (not shown in the figure), where

[0148] Step S1061: Detect the shape of the discomfort area to obtain area shape information.

[0149] Specifically, determine the thermal imaging map of the patient's discomfort area according to the medical device, and then detect the shape of the area shown in the thermal imaging map to obtain area shape information. For example, the shape corresponding to the thermal imaging map is circular, and the radius of the circle is 8 cm.

[0150] Step S1062: Input the area shape information into the trained area combination network for training to obtain at least one area combination feature.

[0151] In the embodiment of the present application, different area shape information is collected as training samples, where the different area shape information includes area shape, area size, and instrument combination layout. Then, an area combination network is created, and the training samples are imported into the area combination network for training to obtain a trained area combination network. Then, the area shape information of the patient's discomfort area is input into the area combination network for training to obtain at least one area combination feature corresponding to the area shape information.

[0152] Step S1063: Perform feature recognition and analysis on at least one area combination feature to generate at least one instrument combination plan.

[0153] Specifically, each area combination feature corresponds to an instrument combination plan. Therefore, perform feature recognition and analysis on each area combination feature to obtain the instrument combination plan in the area combination feature.

[0154] Step S1064: Calculate the instrument quantity information of at least one instrument combination plan, and detect the instrument quantity information to generate an instrument combination plan.

[0155] Specifically, detect the instrument quantity of each obtained instrument combination plan. For example, there are three instrument combination plans obtained by feature recognition and analysis in step S1063. In the first instrument combination plan, the number of instruments is 4, and the arrangement is two in a row. The second instrument combination plan is 6, and the arrangement is a two-row combination, with three instruments arranged horizontally in each row. The third combination plan is 7, and the arrangement is a two-row combination, with three instruments arranged horizontally in the first row and four instruments arranged horizontally in the second row. Based on the detection of the quantities in the above three plans, determine the instrument combination plan with the least quantity, that is, the first instrument combination plan.

[0156] In another possible implementation manner of the embodiment of the present application, after step S13, steps S131 (not shown in the figure), S132 (not shown in the figure), S133 (not shown in the figure), S134 (not shown in the figure), and S135 (not shown in the figure) are further included, where,

[0157] Step S131: Obtain the set treatment time.

[0158] Wherein, the set treatment time is the cycle time of temperature detection.

[0159] Specifically, calculate by combining the patient's local signs and historical clinical data to obtain the recovery time period after the patient is treated by the instrument device, and set this time period as the set treatment time.

[0160] Step S132: Based on the set treatment time, determine the updated first temperature information and second temperature information.

[0161] Specifically, after the set treatment time has passed, perform a new round of temperature detection on the patient's uncomfortable part and normal part. The instrument switches from the treatment stage to the temperature detection stage. The temperature sensor in the white area detects the temperature of the patient's normal part to obtain the first temperature information within this set treatment time, and the temperature sensor in the yellow area detects the temperature of the patient's uncomfortable area to obtain the second temperature information within this set treatment time. For example: The initial temperature of the patient's uncomfortable part is 37°C, the initial temperature of the normal part is 36.7°C, and the set treatment time is 30 minutes. When the treatment time of the millimeter wave therapeutic instrument on the patient's uncomfortable part reaches 30 minutes, update the temperature of the uncomfortable part and the normal part.

[0162] Step S133: Determine the second temperature difference between the first temperature information and the second temperature information.

[0163] Specifically, perform a difference operation on the temperature value of the first temperature information obtained by the temperature sensor in the white area for testing the patient's normal part and the temperature value of the second temperature information obtained by the yellow area for testing the patient's uncomfortable part, and use the obtained difference as the second temperature difference. Taking the example in step S132 for elaboration, the updated first temperature information is 36.7°C, the second temperature information is 37°C, then the obtained second temperature difference is 0.3°C.

[0164] Step S134: Determine whether the second temperature difference reaches or exceeds the second temperature difference threshold.

[0165] Step S134: If the second temperature difference does not reach or exceed the second temperature difference threshold, generate an instrument shutdown instruction to control the instrument device to automatically shut down.

[0166] Specifically, the obtained second temperature difference is numerically compared with the second temperature difference threshold. When the second temperature difference does not reach or exceed the second temperature difference threshold, an instrument shutdown instruction is generated and sent to the instruction receiving end of the instrument device. After receiving the instruction, the instrument device changes from the on state to the off state and no longer treats the uncomfortable part of the patient. When the second temperature difference still exceeds the first temperature difference threshold, no operation is performed on the instrument device, that is, the instrument device continues to treat the uncomfortable part of the patient.

[0167] In another possible implementation manner of the embodiment of the present application, before step S12, there are also steps S121 (not shown in the figure), step S122 (not shown in the figure), step S123 (not shown in the figure),

[0168] step S124 (not shown in the figure), step S125 (not shown in the figure), and step S126 (not shown in the figure), where

[0169] Step S121, obtain clinical test data and disease information.

[0170] Among them, the clinical test data is the data generated by historical clinical medical records, and the disease information is the disease information of the patient.

[0171] Specifically, by statistically analyzing and classifying a large amount of data from historical clinical tests, the clinical test data of the uncomfortable area of the patient is obtained. The diagnosing physician determines the disease information based on the symptoms of the uncomfortable area of the patient and historical symptoms, and then inputs the disease information into the electronic device.

[0172] Step S122, screen the clinical test data to obtain disease category information and part temperature difference information corresponding to the disease category information. The part temperature difference information is the temperature difference information of different parts of the body.

[0173] In the embodiment of the present application, the clinical test data includes disease category information, disease part information, part temperature difference information, disease lethality, and disease transmissibility. Among them, the disease category information is associated with the disease part information, and the disease part information is associated with the part temperature difference information. For example: the disease category information is rheumatoid joint pain, and the corresponding disease part information includes: knee joint, finger joint, and arm joint. At the same time, the part temperature difference information corresponding to the disease part information includes: the knee joint is 0.1 degree Celsius to 0.4 degree Celsius, the finger joint is 0.3 degree Celsius to 0.6 degree Celsius, and the arm joint is 0.2 degree Celsius to 0.5 degree Celsius.

[0174] Specifically, by screening the tags of the clinical test data, the disease category information and the part temperature difference information are obtained.

[0175] Step S123: Match the disease information with the disease category information to obtain the site set information.

[0176] Specifically, perform field matching on the disease information diagnosed by the diagnosing physician and the disease category information to obtain the corresponding disease category information, then obtain the disease site information associated therewith according to the disease category information, and collect the disease site information to obtain the site set information.

[0177] Step S124: Match the uncomfortable site with multiple sites in the site set information to obtain the matching site information.

[0178] Specifically, split the site information in the site set information to obtain multiple site information, and then, according to the principle of field matching, perform field matching on the uncomfortable site and the multiple site information to obtain the matching site information.

[0179] Step S125: Determine the historical temperature difference data based on the matching site information and the site temperature difference information.

[0180] Specifically, determine the site temperature difference information associated therewith according to the matching site information, and then use the site temperature difference information as the historical temperature difference data.

[0181] Step 126: Calculate the average value of the historical temperature difference data to obtain the first temperature difference threshold.

[0182] Specifically, determine the historical temperature difference data of the site according to the matching site information and the site temperature difference information, and calculate the average value of the data set of the site in the historical temperature difference data to obtain the first temperature difference threshold. For example: the historical temperature difference data is 0.1 degree Celsius, 0.2 degree Celsius, 0.3 degree Celsius, and 0.4 degree Celsius. Input the historical temperature difference data into the average value calculation formula, that is, (0.1 + 0.2 + 0.3 + 0.4) / 4, to obtain the first temperature difference threshold of 0.225 degree Celsius.

[0183] Compared with the embodiments of the present application, the method for obtaining the second temperature difference threshold in step S134 is the same as the principle for obtaining the first temperature difference threshold, that is, clinical test data and disease information are obtained, and then the clinical test data is screened to obtain the frequency information of the set treatment time and the disease category information and the site temperature difference information matching the frequency information of the set treatment time. Among them, the site temperature difference information is the site temperature difference information corresponding to the disease category information. Then, the disease information is matched with the disease category information to obtain the site set information, and then the uncomfortable site is matched with multiple sites in the site set information to obtain the matching site information. Then, according to the frequency information, the matching site information, and the site temperature difference information, historical temperature difference data is determined, and by calculating the average value of the historical temperature difference data, the second temperature difference threshold is obtained. For example, the set treatment time is half an hour. After half an hour, the frequency information of the set treatment time is once. After one hour, the frequency information of the set treatment time is twice.

[0184] In another possible implementation manner of the embodiments of the present application, step S11 specifically includes step S111 (not shown in the figure), step S112 (not shown in the figure), step S113 (not shown in the figure), and step S114 (not shown in the figure), where

[0185] Step S111, obtain the site position information of the uncomfortable site and the instrument position information of the instrument.

[0186] In the embodiments of the present application, the method for obtaining the site position information includes: obtaining the thermal images of the uncomfortable site and the normal site of the patient through an infrared scanner and a thermal imaging instrument, then marking the site position information of the uncomfortable site according to the thermal images, and sending the marked site position information to the electronic device. The method for obtaining the instrument position information includes: pre-installing a positioning chip in the millimeter wave therapy instrument, and obtaining the instrument position information of the instrument in real time through the positioning function of the positioning chip, and sending the instrument position information to the electronic device.

[0187] Step S112, determine the instrument offset value based on the site position information and the instrument position information.

[0188] Specifically, obtain the initial position distance between the millimeter wave therapy instrument and the uncomfortable site, and then calculate the relative distance between the millimeter wave therapy instrument and the site position information in real time according to the site position information and the instrument position information to obtain the offset position distance. Perform a difference operation on the offset position distance and the initial position distance to determine the final instrument offset value.

[0189] Step S113, determine whether the instrument offset value exceeds a preset offset threshold.

[0190] In the embodiments of the present application, the preset offset threshold is set according to the specifications of the millimeter wave therapeutic instrument. For example, if the specifications of the millimeter wave therapeutic instrument are 50 cm * 40 cm and the specifications of the instrument treatment area are 40 cm * 30 cm, then the preset offset threshold is a horizontal relative distance of 40 cm and a vertical relative distance of 30 cm.

[0191] Step S114, if the instrument offset value exceeds the preset offset threshold, an offset warning instruction is generated to control the warning device to give a warning.

[0192] Specifically, when the instrument offset value reaches or exceeds the offset threshold, a warning instruction will be generated and sent to the instruction receiving end of the instrument device. After receiving the instruction, the instrument device will change from the normal working state to the warning state to remind the patient that the instrument has shifted.

[0193] For the embodiments of the present application, when the instrument offset value reaches or exceeds the offset threshold, the offset can also be corrected by changing the combination mode of the millimeter wave therapeutic instrument, that is, increasing the combination quantity of the millimeter wave therapeutic instrument, thereby increasing the threshold value of the instrument treatment area.

[0194] The above embodiments introduce a control method of a millimeter wave therapeutic instrument from the perspective of the method flow. The following embodiments introduce a control device of a millimeter wave therapeutic instrument from the perspective of virtual modules or virtual units. For details, see the following embodiments.

[0195] The embodiments of the present application provide a control device for a millimeter wave therapeutic instrument, as Figure 2 shown. The control device 20 of the millimeter wave therapeutic instrument may specifically include: a temperature acquisition module 21, a first temperature difference determination module 22, a first temperature difference judgment module 23, and a control start module 24, where

[0196] The temperature acquisition module 21 is used to acquire the first temperature information and the second temperature information of the patient. The first temperature information is the temperature information of the normal part of the patient, and the second temperature information is the temperature information of the uncomfortable part of the patient;

[0197] The first temperature difference determination module 22 is used to determine the first temperature difference between the first temperature information and the second temperature information;

[0198] The first temperature difference judgment module 23 is used to judge whether the first temperature difference reaches or exceeds the second temperature difference threshold;

[0199] The control start module 24 is used to generate an instrument start instruction and control the instrument device to automatically start when the first temperature difference reaches or exceeds the first temperature difference threshold.

[0200] In a possible implementation manner of the embodiments of the present application, when the temperature acquisition module 21 acquires the first temperature information and the second temperature information of the patient, it is specifically used for:

[0201] Obtain the discomfort area, the instrument treatment area, and the instrument detection area of the patient. The instrument treatment area is used to treat the discomfort part of the patient, and the instrument detection area is used to detect the normal part around the discomfort part;

[0202] Determine whether the discomfort area exceeds the instrument treatment area;

[0203] If the discomfort area does not exceed the instrument treatment area, obtain the first temperature information and the second temperature information of the patient;

[0204] If the discomfort area exceeds the instrument treatment area, determine whether the discomfort area exceeds the instrument detection area;

[0205] If the discomfort area does not exceed the instrument detection area, obtain the first temperature information and the second temperature information of the patient;

[0206] If the discomfort area exceeds the instrument detection area, perform threshold analysis on the discomfort area and the instrument treatment area to generate an instrument combination plan, and determine the combined treatment area and the combined detection area according to the instrument combination plan. Detect the discomfort area based on the combined treatment area and the combined detection area, and obtain the first temperature information and the second temperature information of the patient;

[0207] Among them, the combined treatment area covers the discomfort area.

[0208] Another possible implementation manner of the embodiment of the present application. When the temperature acquisition module 21 acquires the discomfort part information of the patient, it specifically includes any one of the following methods:

[0209] Obtain the part description information of the patient, and perform area division according to the part description information to obtain the discomfort part information of the patient;

[0210] Obtain the doctor's diagnosis information, and perform area division according to the doctor's diagnosis information to obtain the discomfort part information of the patient;

[0211] Obtain the device diagnosis information, and perform area division according to the device diagnosis information to obtain the discomfort part information of the patient. The device diagnosis information is obtained by a medical device diagnosing the patient.

[0212] Another possible implementation manner of the embodiment of the present application. When the temperature acquisition module 21 performs threshold analysis on the discomfort area and the instrument treatment area to generate an instrument combination plan, it is specifically used for:

[0213] Perform shape detection on the discomfort area to obtain area shape information;

[0214] Input the area shape information into the trained area combination network for training to obtain at least one area combination feature;

[0215] Perform feature recognition and analysis on at least one regional combination feature to generate at least one instrument combination plan;

[0216] Calculate the instrument quantity information of at least one instrument combination plan, and detect the instrument quantity information to generate an instrument combination plan.

[0217] Another possible implementation manner of the embodiment of the present application, the device 20 further includes: a time acquisition module, a temperature determination module, a second temperature difference determination module, a second temperature difference judgment module, and a control shutdown module, wherein,

[0218] The time acquisition module is used to acquire a set treatment time, and the set treatment time is the cycle time of temperature detection;

[0219] The temperature determination module is used to determine the updated first temperature information and second temperature information based on the set treatment time;

[0220] The second temperature difference determination module is used to determine the second temperature difference between the first temperature information and the second temperature information;

[0221] The second temperature difference judgment module is used to judge whether the second temperature difference reaches or exceeds the second temperature difference threshold;

[0222] The control shutdown module is used to generate an instrument shutdown instruction and control the automatic shutdown of the instrument device if the second temperature difference does not reach or exceed the second temperature difference threshold.

[0223] Another possible implementation manner of the embodiment of the present application, the device 20 further includes: a data information acquisition module, a data screening module, a disease matching module, a part matching module, a historical temperature difference determination module, and a data calculation module, wherein,

[0224] The data information acquisition module is used to acquire clinical test data and disease information. The clinical test data is the data generated by historical clinical medical records, and the disease information is the disease information of the patient;

[0225] The data screening module is used to screen the clinical test data to obtain disease category information and part temperature difference information corresponding to the disease category information. The part temperature difference information is the temperature difference information of different parts of the body;

[0226] The disease matching module is used to match the disease information with the disease category information to obtain part set information;

[0227] The part matching module is used to match the uncomfortable part with multiple parts in the part set information to obtain matching part information;

[0228] A historical temperature difference determination module, configured to determine historical temperature difference data based on matching part information and part temperature difference information;

[0229] A data calculation module, configured to calculate an average value of the historical temperature difference data to obtain a first temperature difference threshold.

[0230] In another possible implementation manner of the embodiment of the present application, the apparatus 20 further includes: a position acquisition module, an offset determination module, an offset judgment module, and a control and warning module.

[0231] The position acquisition module is configured to acquire part position information of the uncomfortable part and instrument position information of the instrument;

[0232] The offset determination module is configured to determine an instrument offset value based on the part position information and the instrument position information;

[0233] The offset judgment module is configured to judge whether the instrument offset value exceeds a preset offset threshold;

[0234] The control and warning module is configured to generate an offset warning instruction and control a warning device to give a warning when the instrument offset value exceeds the preset offset threshold.

[0235] An electronic device is provided in an embodiment of the present application, as Figure 3 shown. Figure 3 The electronic device 300 shown includes: a processor 301 and a memory 303. Among them, the processor 301 and the memory 303 are connected, such as being connected through a bus 302. Optionally, the electronic device 300 may further include a transceiver 304. It should be noted that in practical applications, the transceiver 304 is not limited to one, and the structure of the electronic device 300 does not constitute a limitation on the embodiment of the present application.

[0236] The processor 301 may be a CPU (Central Processing Unit, central processor), a general-purpose processor, a DSP (Digital Signal Processor, data signal processor), an ASIC (Application Specific Integrated Circuit, application-specific integrated circuit), an FPGA (Field Programmable Gate Array, field programmable gate array), or other programmable logic devices, transistor logic devices, hardware components, or any combination thereof. It can implement or execute various exemplary logic blocks, modules, and circuits described in connection with the disclosure of the present application. The processor 301 may also be a combination that implements a computing function, such as a combination including one or more microprocessors, a combination of a DSP and a microprocessor, etc.

[0237] The bus 302 may include a path for transmitting information between the above components. The bus 302 can be a PCI (Peripheral Component Interconnect) bus, an EISA (Extended Industry Standard Architecture) bus, or the like. The bus 302 can be divided into an address bus, a data bus, a control bus, etc. For the sake of simplicity of representation, Figure 3 it is only represented by a thick line in Figure 3 , but it does not mean that there is only one bus or one type of bus.

[0238] The memory 303 can be a ROM (Read Only Memory) or other types of static storage devices that can store static information and instructions, a RAM (Random Access Memory) or other types of dynamic storage devices that can store information and instructions, or it can also be an EEPROM (Electrically Erasable Programmable Read Only Memory), a CD-ROM (Compact Disc Read Only Memory), or other optical disc storage, optical disc storage (including compact discs, laser discs, optical discs, digital versatile discs, Blu-ray discs, etc.), magnetic disk storage media, or other magnetic storage devices, or any other medium that can be used to carry or store the desired program code in the form of instructions or data structures and can be accessed by a computer, but is not limited thereto.

[0239] The memory 303 is used to store the application program code for implementing the solution of this application, and is controlled by the processor 301 for execution. The processor 301 is used to execute the application program code stored in the memory 303 to implement the content shown in the foregoing method embodiments.

[0240] Among them, the electronic device includes but is not limited to: mobile terminals such as mobile phones, laptop computers, digital broadcast receivers, PDAs (Personal Digital Assistants), PADs (Tablet Computers), PMPs (Portable Multimedia Players), in-vehicle terminals (such as in-vehicle navigation terminals), etc., and fixed terminals such as digital TVs, desktop computers, etc. It can also be a server, etc. Figure 3 The electronic device shown is only an example and should not impose any limitations on the functions and usage scope of the embodiments of the present disclosure.

[0241] An embodiment of the present application provides a computer-readable storage medium, on which a computer program is stored. When it runs on a computer, the computer can execute the corresponding content in the foregoing method embodiment. Compared with the prior art, in the embodiment of the present application, the temperature information of the normal part and the uncomfortable part on the patient's skin surface is obtained. The temperature information of the normal part is the first temperature information, and the temperature information of the uncomfortable part is the second temperature information. The temperature information of the two parts is used as the standard of the patient's physical sign information. By performing operations on it, the temperature difference information between the two can be obtained. The temperature difference information is compared with the first temperature difference threshold. If the temperature difference information reaches or exceeds the set first temperature difference threshold, it proves that the uncomfortable part of the patient needs to be treated, that is, an opening instruction is generated to control the instrument and equipment to automatically turn on, so that the patient can receive treatment in the shortest time and ensure the timeliness of treatment, thus solving the problems of slow diagnosis process and untimely treatment.

[0242] It should be understood that although the steps in the flowchart of the accompanying drawings are shown in sequence according to the indication of the arrows, these steps are not necessarily executed in the order indicated by the arrows. Unless otherwise clearly stated in this article, the execution of these steps has no strict order limit, and they can be executed in other orders. Moreover, at least a part of the steps in the flowchart of the accompanying drawings may include multiple sub-steps or multiple stages. These sub-steps or stages are not necessarily executed at the same time, but can be executed at different times, and their execution order is not necessarily sequential, but can be executed alternately or alternately with at least a part of other steps or sub-steps or stages of other steps.

[0243] The above are only some embodiments of the present application. It should be noted that for those of ordinary skill in the art, without departing from the principle of the present application, several improvements and refinements can be made, and these improvements and refinements should also be regarded as the protection scope of the present application.

Claims

1. A control device for a millimeter-wave therapy instrument, characterized in that, it includes: a temperature acquisition module, configured to acquire the patient's discomfort area, the instrument treatment area, and the instrument detection area, where the instrument treatment area is used to treat the patient's discomfort site, and the instrument detection area is used to detect the normal site around the discomfort site; determine whether the discomfort area exceeds the instrument treatment area; if the discomfort area does not exceed the instrument treatment area, acquire the patient's first temperature information and second temperature information; if the discomfort area exceeds the instrument treatment area, determine whether the discomfort area exceeds the instrument detection area; if the discomfort area does not exceed the instrument detection area, acquire the patient's first temperature information and second temperature information; if the discomfort area exceeds the instrument detection area, perform threshold analysis on the discomfort area and the instrument treatment area to generate an instrument combination plan, and determine a combined treatment area and a combined detection area according to the instrument combination plan, and detect the discomfort area based on the combined treatment area and the combined detection area to acquire the patient's first temperature information and second temperature information, where the first temperature information is the temperature information of the patient's normal site, and the second temperature information is the temperature information of the patient's discomfort site; wherein, the combined treatment area covers the discomfort area; a first temperature difference determination module, configured to determine a first temperature difference between the first temperature information and the second temperature information; a first temperature difference judgment module, configured to judge whether the first temperature difference reaches or exceeds a first temperature difference threshold; a control start module, configured to generate an instrument start instruction and control the automatic start of the instrument device when the first temperature difference reaches or exceeds the first temperature difference threshold.

2. The device according to claim 1, characterized in that, when the temperature acquisition module acquires the patient's discomfort site information, it specifically includes any one of the following methods: acquire the patient's site description information, and perform area division according to the site description information to acquire the patient's discomfort site information; acquire the doctor's diagnosis information, and perform area division according to the doctor's diagnosis information to acquire the patient's discomfort site information; acquire device diagnosis information, and perform area division according to the device diagnosis information to acquire the patient's discomfort site information, where the device diagnosis information is obtained by a medical device diagnosing the patient.

3. The device according to claim 1, characterized in that, when the temperature acquisition module performs threshold analysis on the discomfort area and the instrument treatment area to generate an instrument combination plan, it is specifically used for: perform shape detection on the discomfort area to obtain area shape information; input the area shape information into a trained area combination network for training to obtain at least one area combination feature; perform feature recognition analysis on the at least one area combination feature to generate at least one instrument combination plan; Calculate the instrument quantity information of the at least one instrument combination plan, and detect the instrument quantity information to generate an instrument combination plan.

4. The device according to claim 1, wherein, the device further comprises: a time acquisition module, a temperature determination module, a second temperature difference determination module, a second temperature difference judgment module, and a control shutdown module, wherein, the time acquisition module is configured to acquire a set treatment time, and the set treatment time is the cycle time of temperature detection; the temperature determination module is configured to determine updated first temperature information and second temperature information based on the set treatment time; the second temperature difference determination module is configured to determine a second temperature difference between the first temperature information and the second temperature information; the second temperature difference judgment module is configured to judge whether the second temperature difference reaches or exceeds a second temperature difference threshold; the control shutdown module is configured to generate an instrument shutdown instruction and control the instrument device to automatically shut down if the second temperature difference does not reach or exceed the second temperature difference threshold.

5. The device according to claim 1, wherein, the device further comprises: a data information acquisition module, a data screening module, a disease matching module, a part matching module, a historical temperature difference determination module, and a data calculation module, wherein, the data information acquisition module is configured to acquire clinical test data and disease information, the clinical test data is data generated by historical clinical medical records, and the disease information is the disease information of a patient; the data screening module is configured to screen the clinical test data to obtain disease category information and part temperature difference information corresponding to the disease category information, and the part temperature difference information is temperature difference information of different parts of the body; the disease matching module is configured to match the disease information with the disease category information to obtain part set information; the part matching module is configured to match the uncomfortable part with multiple parts in the part set information to obtain matching part information; the historical temperature difference determination module is configured to determine historical temperature difference data based on the matching part information and the part temperature difference information; the data calculation module is configured to calculate an average value of the historical temperature difference data to obtain a first temperature difference threshold.

6. The device according to claim 1, wherein, the device further comprises: a position acquisition module, an offset determination module, an offset judgment module, and a control warning module, the position acquisition module is configured to acquire part position information of the uncomfortable part and instrument position information of the instrument; the offset determination module is configured to determine an instrument offset value based on the part position information and the instrument position information; the offset judgment module is configured to judge whether the instrument offset value exceeds a preset offset threshold; the control warning module is configured to generate an offset warning instruction and control a warning device to give a warning when the instrument offset value exceeds the preset offset threshold.

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