Configuration method for radio frequency signal generation device, and computer-readable storage medium

By communicating with the catheter device, the target treatment method is identified and the catheter treatment parameters are obtained, which solves the problem of increased equipment costs for different treatment directions and realizes the versatility and reliability of the radiofrequency signal generation device.

WO2026114180A1PCT designated stage Publication Date: 2026-06-04SHANGHAI GOLDEN LEAF MED TEC CO LTD

Patent Information

Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
SHANGHAI GOLDEN LEAF MED TEC CO LTD
Filing Date
2025-11-24
Publication Date
2026-06-04

AI Technical Summary

Technical Problem

Existing radiofrequency signal generating equipment requires corresponding treatment devices for catheters with different treatment directions, which increases costs.

Method used

By communicating with the catheter device, the target treatment method is identified based on the catheter type information, and the corresponding catheter treatment parameters are obtained. This enables customized configuration of one control device with multiple different types of catheter devices. Different treatments can be performed simply by changing the catheter device on the control device.

Benefits of technology

This allows catheter devices with different treatment directions to be configured with only the corresponding treatment equipment, saving costs and improving the versatility and reliability of the control equipment for radiofrequency signal generation devices.

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Abstract

A configuration method for a radio frequency signal generation device, and a computer-readable storage medium. The method comprises: a control device communicating with a catheter device; on the basis of catheter type information transmitted by the catheter device, identifying a target treatment mode corresponding to the catheter; on the basis of the identified target treatment mode, acquiring a catheter treatment parameter corresponding to the type of the catheter device; and on the basis of the catheter treatment parameter, controlling the catheter device to execute the catheter treatment parameter for treatment. Therefore, customized configuration between one control device and a plurality of different types of catheter devices can be achieved; thus, simply replacing the catheter devices on the control device suffices to meet the need of different treatments, thereby saving costs and improving the universality of the control device for the radio frequency signal generation device.
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Description

Configuration method of radio frequency signal generating equipment and computer-readable storage medium

[0001] Cross-reference to related applications

[0002] This application claims priority to Chinese Patent Application No. 202411706404.2, filed on November 26, 2024, entitled "Configuration Method of Radio Frequency Signal Generating Device and Computer-Readable Storage Medium", the entire contents of which are incorporated herein by reference. Technical Field

[0003] This application relates to the field of radio frequency signal generating equipment technology, and specifically to a configuration method for radio frequency signal generating equipment and a computer-readable storage medium. Background Technology

[0004] The main function of radiofrequency signal generating devices (such as ablation devices) is to insert electrode catheters into the target tissue site through veins or arteries, release radiofrequency current to cause local coagulative necrosis of nerves, thereby achieving the therapeutic effect.

[0005] Currently, radiofrequency signal generating devices on the market include devices for treating arrhythmias, herniated discs, hypertension, tumors, and so on. The parameter requirements for devices for different treatment directions are also different. This means that each catheter for different treatment directions needs to be equipped with a corresponding treatment device, such as a radiofrequency signal generator / ablation device, which increases costs. Summary of the Invention

[0006] In view of the above problems, this application provides a configuration method for a radio frequency signal generating device and a computer-readable storage medium, which can solve the problem of increased costs caused by the need to configure a corresponding treatment device for each catheter for different treatment directions.

[0007] In a first aspect, this application provides a configuration method for a radio frequency signal generating device, the radio frequency signal generating device including a control device and a catheter device connected to the control device; the catheter device is provided with multiple radio frequency electrodes, which are used to release radio frequency current to achieve radio frequency ablation; the method is applied to the control device and includes: acquiring catheter information transmitted by the connected catheter device; wherein the catheter information includes catheter type information; determining the target treatment mode corresponding to the catheter type information based on the catheter type information; wherein the control device stores multiple treatment modes, and each catheter type information corresponds to a corresponding treatment mode; determining the catheter treatment parameters configured by the catheter device connected to the control device based on the target treatment mode; wherein the control device stores multiple catheter treatment parameters, and each catheter instruction parameter corresponds to a corresponding treatment mode.

[0008] The configuration method of the radio frequency signal generating device described above involves communication between the control device and the catheter device. Based on the catheter type information transmitted by the catheter device, the target treatment mode corresponding to the catheter is identified. Then, the catheter treatment parameters corresponding to the identified target treatment mode are obtained. Based on the catheter treatment parameters, the catheter device is controlled to execute the catheter instruction parameters for treatment. This enables customized configuration between one control device and multiple different types of catheter devices. Furthermore, it allows for the configuration of only the corresponding treatment device for catheters with different treatment directions. In addition, when performing different treatments, only the catheter device needs to be replaced based on the control device, thereby saving costs and improving the versatility of the control device for the radio frequency signal generating device.

[0009] In an optional implementation of this embodiment, the treatment methods corresponding to different catheter type information are all different; determining the target treatment method corresponding to the catheter type information based on the catheter type information includes: finding the treatment method corresponding to the catheter type information based on the catheter type information to obtain the target treatment method.

[0010] In the above implementation method, when one type of catheter information corresponds to one treatment method, this solution can quickly find the target treatment method by pre-storing the one-to-one correspondence between catheter type information and the corresponding treatment method, thereby improving the efficiency of the treatment method that matches the catheter type information.

[0011] In an optional implementation of this embodiment, the same catheter type information corresponds to multiple treatment methods; determining the target treatment method corresponding to the catheter type information based on the catheter type information includes: searching for multiple treatment methods corresponding to the catheter type information based on the catheter type information to obtain multiple candidate treatment methods; displaying the candidate treatment methods on the display screen of the control device; obtaining the treatment method selected by the user from the multiple candidate treatment methods based on the user's selection operation to obtain the target treatment method.

[0012] In the above embodiments, when one catheter type information corresponds to multiple treatment methods, this solution displays the corresponding multiple treatment methods on the display screen of the control device. Thus, the user selects and determines the target treatment method corresponding to the catheter type information, thereby enabling catheter devices with one catheter type information corresponding to multiple treatment methods to be adapted to the configuration method designed in this solution, thereby improving the versatility and reliability of the configuration method of this solution.

[0013] In an optional embodiment of this example, the catheter information further includes catheter ownership information; the method further includes: determining whether the catheter device belongs to compliant devices based on the catheter ownership information; if it is determined that the catheter device does not belong to compliant devices, an alarm is generated.

[0014] In the above implementation, the catheter information designed in this solution also includes catheter ownership information, and then the catheter ownership information is used to determine whether the catheter device is a compliant device, thereby ensuring the quality of the catheter device and the reliability and compliance of the radio frequency signal generating device.

[0015] In an optional embodiment of this example, the catheter information further includes catheter activation time information; the method further includes: determining whether the catheter device is a used device and / or an expired device based on the catheter activation time information; if the catheter device is determined to be a used device and / or an expired device, an alarm is generated.

[0016] In the above implementation method, this solution reminds expired or used catheter devices based on catheter activation time information, ensuring the cleanliness and safety of the ablation process performed by the radiofrequency signal generating device.

[0017] In an optional embodiment of this example, after determining the catheter treatment parameters configured for the catheter device connected to the control device according to the target treatment method, the method further includes: obtaining the number of electrode channels of the configured catheter device and displaying the number of configured motor channels on the display screen of the control device.

[0018] In the above implementation method, the number of configured motor channels is displayed on the display screen of the control device, thereby making the number of electrode channels explicit and improving the user's controllability over the electrode channels.

[0019] In an optional embodiment of this example, after determining the catheter treatment parameters configured in the catheter device connected to the control device according to the target treatment method, the method further includes: obtaining surgical guidance information corresponding to the target treatment method; wherein each treatment method corresponds to a surgical guidance information, and the surgical guidance information includes surgical step prompts for the target treatment method; and displaying the surgical guidance information on the display screen of the control device.

[0020] The above implementation method searches for the corresponding stored surgical guidance information by targeting the treatment method, and then displays the surgical guidance information corresponding to the target treatment method on the display screen of the control device, thereby achieving the effect of guiding the user through the surgery. In this way, even doctors who are new to the relevant surgery can obtain the corresponding instructions based on such guidance, thereby improving surgical efficiency and reducing the learning cost for doctors.

[0021] In an optional embodiment of this example, the method further includes: performing state detection on the control device itself.

[0022] In an optional embodiment of this example, the status detection of the control device itself includes: performing status detection of the control device itself after the control device is initially started; and / or, periodically performing status detection of the control device itself during the operation of the control device.

[0023] In the above-described implementation, this solution can perform status detection on the control device after initial startup and periodically perform status detection on the control device during operation, thereby enabling real-time monitoring of the control device's status and improving the stability and reliability of the control device's operation.

[0024] In an optional embodiment of this example, the status detection of the control device itself includes: detecting the communication status of the control device by detecting the peripheral information of the control device; and / or, detecting the power status of the control device based on the voltage acquisition value at the power supply of the control device; and / or, detecting the power amplifier power supply of each channel based on the voltage acquisition value of each channel; and / or, detecting the fan status based on the fan operating signal; and / or, detecting the usage status of the electrode channels of the control device.

[0025] The above-described implementation scheme covers all key points of the control equipment, thus providing complete control equipment testing. It can comprehensively test the equipment, including power supply testing, channels, RF voltage, fans, temperature, impedance, and power. Furthermore, this scheme can automatically issue alarms when problems are detected, thereby improving the timeliness of equipment failure reminders and repairs.

[0026] In an optional embodiment of this example, after performing status detection on the control device itself, the method further includes: detecting the connection status of the conduit device connected to the control device and the electrode temperature measurement performance of the conduit device.

[0027] In an optional embodiment of this example, the connection performance of the catheter device connected to the control device is detected, including: sending a test signal to the catheter device; determining whether a return signal corresponding to the test signal transmitted by the catheter device is received; if it is determined that a return signal corresponding to the test signal transmitted by the catheter device is received, then the connection status of the catheter device is determined to be normal; acquiring the temperature information of each electrode transmitted by the catheter device; determining whether the temperature information of each electrode transmitted by the catheter device is greater than a temperature threshold; if it is determined that the temperature information of each electrode transmitted by the catheter device is not greater than the temperature threshold, then the temperature measurement performance of the multiple electrodes of the catheter device is determined to be normal.

[0028] In the above-described implementation, this solution detects the connection status of the catheter device and the temperature measurement performance of the electrodes on it, thereby enabling the detection of catheter connection quality and catheter performance. This avoids time loss caused by catheter performance defects during surgery, thus ensuring the safety and timeliness of treatment.

[0029] In an optional embodiment of this example, the method further includes: after determining that the connection status of the catheter device is normal and the temperature measurement performance of the multiple electrodes of the catheter device is normal, controlling the channel corresponding to each electrode in the catheter device to open; controlling the channel corresponding to each electrode to output a first energy value; collecting the first temperature value and the first impedance value of the channel corresponding to each electrode; collecting the second temperature value and the second impedance value of the channel corresponding to each electrode after a preset time interval; and determining whether the corresponding electrode meets the wall adhesion requirements based on the first temperature value, the first impedance value, the second temperature value, and the second impedance value of the channel corresponding to the electrode.

[0030] In an optional embodiment of this example, determining whether the corresponding electrode meets the wall adhesion requirement based on the first temperature value, the first impedance value, the second temperature value, and the second impedance value of the channel corresponding to the electrode includes: calculating the temperature difference between the second temperature value and the first temperature value of the channel corresponding to the electrode; calculating the impedance difference between the second impedance value and the first impedance value of the channel corresponding to the electrode; if the temperature difference is greater than a preset temperature threshold and the impedance difference is less than a preset impedance threshold, then the corresponding electrode is determined to meet the wall adhesion requirement; wherein, the preset temperature threshold is greater than 0 and the preset impedance threshold is less than 0; if the temperature difference is not greater than the preset temperature threshold and / or the impedance difference is not less than the preset impedance threshold, then the corresponding electrode is determined not to meet the wall adhesion requirement.

[0031] In the above-described implementation, this solution performs electrode adhesion detection before radiofrequency ablation, which can automatically detect channels with poor adhesion. This can effectively eliminate electrodes with poor adhesion during the subsequent radiofrequency ablation process, thereby avoiding poor ablation results and improving the accuracy and reliability of radiofrequency ablation.

[0032] In an optional embodiment of this example, after determining that the corresponding electrode does not meet the wall adhesion requirements, the method further includes: controlling the channel corresponding to the electrode that does not meet the wall adhesion requirements to close, and displaying the status of the electrode with the closed channel on the display.

[0033] In the above-described embodiments, this solution can automatically close the channel of electrodes that do not meet the adhesion requirements and display it on the display, thereby automatically eliminating electrodes with poor adhesion during the subsequent radiofrequency ablation process. The display also prompts the operator about the electrodes that do not meet the adhesion requirements, for example, which specific electrode does not meet the adhesion requirements, thereby improving the accuracy and reliability of radiofrequency ablation for the operator.

[0034] Secondly, this application provides a configuration device for a radio frequency signal generating device. The device is disposed within the radio frequency signal generating device, which includes a control device and a catheter device connected to the control device. The catheter device is provided with multiple radio frequency electrodes, which are used to release radio frequency current to achieve radio frequency ablation. The device includes an acquisition module for acquiring catheter information transmitted by the connected catheter device, wherein the catheter information includes catheter type information; and a determination module for determining the target treatment method corresponding to the catheter type information based on the catheter type information. The control device stores multiple treatment methods, with each catheter type information corresponding to a specific treatment method. Based on the target treatment method, the device determines the catheter treatment parameters configured on the catheter device connected to the control device. The control device stores multiple catheter treatment parameters, with each catheter instruction parameter corresponding to a specific treatment method.

[0035] The configuration device for the radio frequency signal generating equipment described above communicates with the catheter device through a control device. Based on the catheter type information transmitted by the catheter device, it identifies the target treatment method corresponding to the catheter. Then, it obtains the catheter treatment parameters corresponding to the identified target treatment method and controls the catheter device to execute the catheter instruction parameters for treatment. This allows for customized configuration between one control device and multiple different types of catheter devices. Furthermore, it enables the configuration of only the corresponding treatment device for catheters with different treatment directions. In addition, when performing different treatments, only the catheter device needs to be replaced based on the control device, thereby saving costs and improving the versatility of the control device for the radio frequency signal generating equipment.

[0036] Thirdly, this application provides an electronic device, including a memory and a processor, wherein the memory stores a computer program, and the processor executes the computer program to perform the method described in the first aspect or any optional implementation thereof.

[0037] Fourthly, this application provides a computer-readable storage medium storing a computer program, which, when executed by a processor, performs the method described in the first aspect or any optional implementation thereof.

[0038] Fifthly, this application provides a computer program product that, when run on a computer, causes the computer to perform the method described in the first aspect or any optional implementation thereof.

[0039] The above description is only an overview of the technical solution of this application. In order to better understand the technical means of this application and to implement it in accordance with the contents of the specification, and to make the above and other objects, features and advantages of this application more obvious and understandable, specific embodiments of this application are given below. Attached Figure Description

[0040] Various other advantages and benefits will become apparent to those skilled in the art upon reading the detailed description of the preferred embodiments below. The accompanying drawings are for illustrative purposes only and are not intended to limit the scope of this application. Furthermore, the same reference numerals denote the same parts throughout the drawings. In the drawings:

[0041] Figure 1 is a first flowchart of the configuration method of the radio frequency signal generating device provided in an embodiment of this application;

[0042] Figure 2 is a second flowchart of the configuration method of the radio frequency signal generating device provided in the embodiment of this application;

[0043] Figure 3 is a third flowchart of the configuration method of the radio frequency signal generating device provided in the embodiment of this application;

[0044] Figure 4 is a fourth flowchart of the configuration method of the radio frequency signal generating device provided in the embodiments of this application;

[0045] Figure 5 is a structural diagram of the configuration device of the radio frequency signal generating device provided in the embodiment of this application;

[0046] Figure 6 is a schematic diagram of the structure of the electronic device provided in an embodiment of this application.

[0047] Icons: 500 - Acquisition Module; 510 - Confirmation Module; 520 - Judgment Module; 530 - Alarm Module; 540 - Display Module; 550 - Detection Module; 560 - Control Module; 570 - Acquisition Module; 6 - Electronic Equipment; 601 - Processor; 602 - Memory; 603 - Communication Bus. Detailed Implementation

[0048] The embodiments of the technical solution of this application will now be described in detail with reference to the accompanying drawings. These embodiments are only used to more clearly illustrate the technical solution of this application and are therefore merely examples, and should not be used to limit the scope of protection of this application.

[0049] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this application pertains; the terminology used herein is for the purpose of describing particular embodiments only and is not intended to limit the application; the terms “comprising” and “having”, and any variations thereof, in the specification, claims, and foregoing description of the drawings are intended to cover non-exclusive inclusion.

[0050] In the description of the embodiments of this application, technical terms such as "first" and "second" are used only to distinguish different objects and should not be construed as indicating or implying relative importance or implicitly specifying the number, specific order, or primary and secondary relationship of the indicated technical features. In the description of the embodiments of this application, "multiple" means two or more, unless otherwise explicitly defined.

[0051] In this document, the term "embodiment" means that a particular feature, structure, or characteristic described in connection with an embodiment may be included in at least one embodiment of this application. The appearance of this phrase in various places throughout the specification does not necessarily refer to the same embodiment, nor is it a separate or alternative embodiment mutually exclusive with other embodiments. It will be explicitly and implicitly understood by those skilled in the art that the embodiments described herein can be combined with other embodiments.

[0052] In the description of the embodiments in this application, the term "and / or" is merely a description of the relationship between related objects, indicating that three relationships can exist. For example, A and / or B can represent: A existing alone, A and B existing simultaneously, and B existing alone. Additionally, the character " / " in this document generally indicates that the preceding and following related objects have an "or" relationship.

[0053] In the description of the embodiments of this application, the term "multiple" refers to two or more (including two), similarly, "multiple sets" refers to two or more (including two sets), and "multiple pieces" refers to two or more (including two pieces).

[0054] In the description of the embodiments of this application, the technical terms "center," "longitudinal," "lateral," "length," "width," "thickness," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," "outer," "clockwise," "counterclockwise," "axial," "radial," and "circumferential" indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings. They are only for the convenience of describing the embodiments of this application and simplifying the description, and are not intended to indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, they should not be construed as limitations on the embodiments of this application.

[0055] In the description of the embodiments of this application, unless otherwise expressly specified and limited, technical terms such as "installation," "connection," "joining," and "fixing" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral part; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; they can refer to the internal communication of two components or the interaction between two components. For those skilled in the art, the specific meaning of the above terms in the embodiments of this application can be understood according to the specific circumstances.

[0056] The main function of radiofrequency signal generating devices (such as ablation devices) is to insert electrode catheters into the target tissue site through veins or arteries, release radiofrequency current to cause local coagulative necrosis of nerves, thereby achieving the therapeutic effect.

[0057] Currently, radiofrequency signal generating devices on the market include devices for treating arrhythmias, herniated discs, hypertension, tumors, and so on. The parameter requirements for devices for different treatment directions are also different. This means that each catheter for different treatment directions needs to be equipped with a corresponding treatment device, which increases costs.

[0058] To address the aforementioned issues, this application presents a configuration method for a radio frequency (RF) signal generating device and a computer-readable storage medium. The method involves communication between a control device and a catheter device. Based on the catheter type information transmitted by the catheter device, the target treatment method corresponding to the catheter is identified. Then, the corresponding catheter treatment parameters for that type of catheter device are obtained. Based on these parameters, the catheter device is controlled to execute the corresponding treatment instructions. This allows for customized configuration between a single control device and multiple different types of catheter devices. Furthermore, only the corresponding treatment device needs to be configured for catheters with different treatment directions. In addition, for different treatments, only the catheter device needs to be replaced with the control device, thus saving costs and improving the versatility of the RF signal generating device's control device. Moreover, this solution displays different surgical guidance functions on different interfaces depending on the catheter. The control device in this solution can also detect its own status and the status of connected catheter devices, improving the reliability of the RF signal generating device.

[0059] Based on the above ideas, this application first provides a radio frequency signal generating device, which may include a control device and a conduit device connected to the control device. The conduit device is provided with multiple radio frequency electrodes. The control device can control the radio frequency electrodes to release radio frequency current to achieve radio frequency ablation. The control device can control the radio frequency frequency, temperature value, power value and impedance range value of the radio frequency released by the radio frequency electrodes. Furthermore, the control device can realize the conduction control of different radio frequency electrodes among the multiple radio frequency electrodes through a control channel.

[0060] Based on the aforementioned radio frequency signal generating device, this solution designs a configuration method for the radio frequency signal generating device. This configuration method can be applied to the control device described above. As shown in Figure 1, this method can be implemented in the following ways, including:

[0061] Step S100: Obtain catheter information transmitted by the connected catheter device, including catheter type information.

[0062] Step S110: Determine the target treatment method corresponding to the catheter type information based on the catheter type information.

[0063] Step S120: Determine the catheter treatment parameters configured for the catheter device connected to the control device according to the target treatment method.

[0064] As described above, the control device is connected to the catheter device. In this case, the control device communicates with the catheter device. Specifically, as one possible implementation, the catheter device is equipped with a communication storage module (such as an EEPROM module). The communication interface of this communication storage module is a single-wire encrypted communication interface. The control device can connect to the communication storage module through this communication interface. The catheter device can upload catheter information to the control device through the communication storage module, so that the control device receives the catheter information. The catheter information can be stored in the communication storage module. Different types of catheter devices store different catheter information in their communication storage modules.

[0065] The catheter information mentioned above may include one or more types of catheter information. Specifically, the catheter information may include catheter type information, which characterizes the type of catheter, such as whether the catheter is an ultrasound catheter or a radiofrequency catheter, or whether the catheter is suitable for the kidneys or for the abdominal aorta.

[0066] Upon obtaining the catheter type information transmitted by the catheter device, this solution determines the target treatment method corresponding to that catheter type information. The control device stores multiple treatment methods, with each catheter type information corresponding to a specific treatment method. Specifically, each catheter type information can correspond to one or more corresponding treatment methods. In the case of multiple corresponding treatment methods, this solution allows the operator to manually select the target treatment method corresponding to the catheter type information.

[0067] Since different treatment methods require different catheter treatment parameters, this solution, after obtaining the corresponding target treatment method based on catheter type information, determines the catheter treatment parameters configured for the catheter device connected to the control device according to the target treatment method. Based on these parameters, the solution controls the catheter device to perform corresponding radiofrequency therapy. These parameters may include radiofrequency frequency, number of channels, temperature, power, and impedance range, etc. The radiofrequency frequency is the frequency at which each radiofrequency electrode on the catheter device generates a radiofrequency signal; the temperature is the temperature of each radiofrequency electrode when it generates a radiofrequency signal; the power is the power of the radiofrequency signal generated by each radiofrequency electrode; and the impedance range is the impedance range of the radiofrequency signal generated by each radiofrequency electrode. Each channel corresponds to one radiofrequency electrode, and the number of channels represents the number of electrodes on the catheter device that transmit radiofrequency signals.

[0068] For example, based on the target treatment method, the catheter treatment parameters obtained are as follows: The number of channels is 4; the radiofrequency electrode corresponding to the first channel has a radiofrequency frequency of H1 Hz, a temperature of T1, a power of N1, and an impedance range of R1; the radiofrequency electrode corresponding to the second channel has a radiofrequency frequency of H2 Hz, a temperature of T2, a power of N2, and an impedance range of R2; the radiofrequency electrode corresponding to the third channel has a radiofrequency frequency of H3 Hz, a temperature of T3, a power of N3, and an impedance range of R3; and the radiofrequency electrode corresponding to the fourth channel has a radiofrequency frequency of H4 Hz, a temperature of T4, a power of N4, and an impedance range of R4. In this case, the control device is controllable. The electrodes corresponding to the first, second, third, and fourth channels of the catheter fabrication device are activated. The radiofrequency electrode corresponding to the first channel has a radiofrequency frequency of H1 Hz, a temperature of T1, a power of N1, and an impedance range of R1. The radiofrequency electrode corresponding to the second channel has a radiofrequency frequency of H2 Hz, a temperature of T2, a power of N2, and an impedance range of R2. The radiofrequency electrode corresponding to the third channel has a radiofrequency frequency of H3 Hz, a temperature of T3, a power of N3, and an impedance range of R3. The radiofrequency electrode corresponding to the fourth channel has a radiofrequency frequency of H4 Hz, a temperature of T4, a power of N4, and an impedance range of R4, thereby achieving radiofrequency ablation.

[0069] Different treatment methods require different catheter treatment parameters. For example, the catheter treatment parameters for treating hypertension and diabetes, as described above, are different. Furthermore, multiple catheter treatment parameters can be pre-configured and stored in the control device. Each catheter treatment parameter corresponds to a specific treatment method, and different catheter treatment methods require different catheter treatment parameters. The control device can find the corresponding catheter treatment parameters based on the obtained target treatment method.

[0070] The configuration method of the radio frequency signal generating device described above involves communication between the control device and the catheter device. Based on the catheter type information transmitted by the catheter device, the target treatment method corresponding to the catheter is identified. Then, the catheter treatment parameters corresponding to the identified target treatment method are obtained. Based on the catheter treatment parameters, the catheter device is controlled to execute the catheter instruction parameters for treatment. This allows for customized configuration between one control device and multiple different types of catheter devices. Furthermore, it enables the configuration of only the corresponding treatment device for catheters with different treatment directions. In addition, when performing different treatments, only the catheter device needs to be replaced based on the control device, thereby saving costs and improving the versatility of the control device for the radio frequency signal generating device.

[0071] In an optional implementation of this embodiment, as described above, each catheter type information may correspond to one or more corresponding treatment methods. As one possible implementation, each catheter type information may correspond to one treatment method. Different catheter type information corresponds to different treatment methods. For example, a catheter type suitable for the kidneys may correspond to hypertension treatment, and a catheter type suitable for the abdominal aorta may correspond to diabetes treatment, etc.

[0072] In this case, for step S110, this solution can search for the treatment method corresponding to the catheter type information in the storage, thereby obtaining the target treatment method. For example, assuming that the catheter type information is a catheter type applicable to the kidneys, this solution can search for the corresponding treatment method of hypertension treatment in the storage content based on the catheter type applicable to the kidneys, and thus obtain the target treatment method as hypertension treatment.

[0073] As another possible implementation, the same catheter type may correspond to multiple treatment methods. For example, a radiofrequency catheter type may correspond to two treatment methods: hypertension treatment and diabetes treatment; another example is a catheter type applicable to the kidneys, which may correspond to two treatment methods: hypertension treatment and renal tumor treatment; yet another example is that, based on the catheter type, the corresponding treatment methods may be radiofrequency ablation and microwave ablation. Based on this, this solution can be configured with an ablation device that includes both radiofrequency ablation sources and microwave ablation sources. The control device can switch between radiofrequency ablation sources and microwave ablation sources based on the treatment method identified by the catheter type.

[0074] In this case, for step S110, this solution first searches for multiple treatment methods corresponding to the catheter type information in the storage database to obtain multiple candidate treatment methods. Then, these multiple candidate treatment methods are displayed on the control device's screen. The operator can select from the displayed multiple candidate treatment methods. The control device then obtains the treatment method selected by the user from the multiple candidate treatment methods based on the user's selection, thereby obtaining the target treatment method. As one possible implementation, the user can select from the multiple candidate treatment methods displayed on the screen via a touchscreen. The control device can receive the treatment method information selected by the user via touchscreen, thereby obtaining the target treatment method. As another possible implementation, the control device has selection buttons. The user can select and confirm from the displayed multiple candidate treatment methods via the selection buttons. The control device can obtain the target treatment method by receiving the user's confirmation information.

[0075] For example, assuming the catheter type is suitable for kidney treatment, the corresponding treatment methods may be hypertension treatment and kidney tumor treatment. In this case, the control device's display screen will show hypertension treatment and kidney tumor treatment. The user selects hypertension treatment, and the control device will confirm that the target treatment method is hypertension treatment.

[0076] In the above-described embodiments, when one catheter type corresponds to one treatment method, this solution quickly finds the target treatment method by pre-storing the one-to-one correspondence between catheter type information and the corresponding treatment method, thereby improving the efficiency of adapting the treatment method to the catheter type information. Furthermore, when one catheter type corresponds to multiple treatment methods, this solution displays the corresponding multiple treatment methods on the display screen of the control device, so that the user can select and determine the target treatment method corresponding to the catheter type information. This allows catheter devices with one catheter type corresponding to multiple treatment methods to also be adapted to the configuration method designed in this solution, thereby improving the versatility and reliability of the configuration method of this solution.

[0077] In an optional embodiment of this example, the catheter information described above may include one or more types of information. In this application, the catheter information may include not only the catheter type information described above, but also catheter ownership information. The catheter ownership information represents the manufacturing ownership of the guide rail. For example, each catheter has a corresponding number, which is the catheter ownership information.

[0078] Based on the above, the control device can determine whether the catheter device is a compliant device according to the catheter ownership information. If the catheter device is determined not to be a compliant device, an alarm is generated. Specifically, the control device can verify whether the catheter number in the catheter ownership information is pre-stored in the control device itself. If the catheter ownership information is not stored in the control device, it means that the catheter device may not be a catheter from a legitimate channel, and the quality of the catheter cannot be fully guaranteed. Therefore, the control device is determined not to be a compliant device, and an alarm is generated.

[0079] In the above implementation, the catheter information designed in this solution also includes catheter ownership information, and then the catheter ownership information is used to determine whether the catheter device is a compliant device, thereby ensuring the quality of the catheter device and the reliability and compliance of the radio frequency signal generating device.

[0080] In an optional embodiment of this solution, the catheter information may further include catheter activation time information, which may include the catheter's usage time and expiration date. In this case, the control device can determine whether the catheter device is a used device and / or an expired device based on the catheter activation time information. Specifically, this solution can determine whether the catheter has been used based on the catheter's usage time and whether the catheter is an expired device based on the catheter's expiration date. If the catheter device is determined to be a used device and / or an expired device, an alarm is generated, so that if the user does not remind the user whether the catheter device has been used or expired, the expired or used catheter device will be reminded, thus ensuring the cleanliness and safety of the radio frequency signal generating device during the ablation process.

[0081] In an optional embodiment of this invention, as described above, the control device designed in this solution also includes a display screen. In this case, the solution can display the number of electrode channels of the configured catheter device on the display screen of the control device. Specifically, this solution can display the radio frequency, temperature value, power value, and impedance range value of the electrode corresponding to each channel on the display screen. For example, as described above, this solution can display the radio frequency of the radio frequency electrode corresponding to the first channel as H1 Hz, the temperature value as T1, the power value as N1, and the impedance range value as R1; the radio frequency of the radio frequency electrode corresponding to the second channel as H2 Hz, the temperature value as T2, the power value as N2, and the impedance range value as R2; the radio frequency of the radio frequency electrode corresponding to the third channel as H3 Hz, the temperature value as T3, the power value as N3, and the impedance range value as R3; and the radio frequency of the radio frequency electrode corresponding to the fourth channel as H4 Hz, the temperature value as T4, the power value as N4, and the impedance range value as R4 on the display screen of the control device.

[0082] In an optional embodiment of this example, the control device also stores surgical guidance information corresponding to each treatment method. This surgical guidance information includes surgical step prompts corresponding to the treatment method, such as surgical step prompts for hypertension treatment and surgical step prompts for renal tumor treatment as described above.

[0083] Once the target treatment method corresponding to the catheter type information is obtained, this solution can search for the corresponding stored surgical guidance information through the target treatment method, and then display the surgical guidance information corresponding to the target treatment method on the display screen of the control device, thereby achieving the effect of guiding the user through the surgery. In this way, even doctors who are new to the relevant surgery can obtain the corresponding instructions based on such guidance, thereby improving surgical efficiency and reducing the learning cost for doctors.

[0084] In addition, the surgical guidance information can also include information recording the ablation sites and displaying the recorded ablation sites. For example, in the hypertension treatment described above, radiofrequency ablation of the renal artery branches of both kidneys is required. Assuming that radiofrequency ablation of the renal artery branch of the left kidney has been completed, the control device can mark the renal artery branch of the left kidney and then display the marked renal artery branch of the left kidney on the display screen, thereby reminding the user that the renal artery branch of the left kidney has been ablated, thus achieving a reminder and guidance effect.

[0085] In an optional implementation of this embodiment, as shown in FIG2, the solution may further include the following steps:

[0086] Step S200: Perform status detection on the control device itself.

[0087] In the above embodiments, to ensure the reliability and operational stability of the control equipment, the control equipment can perform status monitoring on itself. As one possible implementation, this solution can perform status monitoring on the control equipment upon initial startup. As another possible implementation, this solution can periodically perform status monitoring on the control equipment during operation.

[0088] In the above-described implementation, this solution can perform status detection on the control device after initial startup and periodically perform status detection on the control device during operation, thereby enabling real-time monitoring of the control device's status and improving the stability and reliability of the control device's operation.

[0089] In an optional implementation of this embodiment, as one possible approach, the aforementioned status detection of the control device itself may specifically include communication detection, power supply detection, power amplifier power supply detection, fan detection, and electrode detection, etc. Specifically, the following detection method is adopted: the communication status of the control device is detected based on the peripheral information of the control device. Specifically, this solution can detect the communication status of the control device by checking whether each module of the control device receives communication data from the peripheral device through the communication bus. If each module can receive communication data from the peripheral device through the communication bus, then it is determined that each module is in normal condition.

[0090] This solution can also detect the power status of the control equipment based on the voltage acquisition value at the power supply point. Specifically, this solution can determine the power status by comparing the acquisition value of the ADC at the power detection point with the standard value of the power supply voltage detection point. If the difference between the ADC acquisition value and the standard value is greater than a preset threshold, the power status is determined to be abnormal; if it is not greater than the preset threshold, the power status is determined to be normal.

[0091] This solution can also detect the power amplifier power supply of each channel based on the voltage acquisition value of each channel. Specifically, this solution compares the voltage acquisition value of each channel with the standard value of the corresponding channel voltage detection point. If the difference between the voltage acquisition value of the channel and the standard value is greater than a preset threshold, the power amplifier power supply is determined to be abnormal; if it is not greater than the preset threshold, the power amplifier power supply is determined to be normal.

[0092] This solution can also detect the fan status based on the fan operating signal. Specifically, if the control device does not receive a fan operating signal, it determines that the fan is malfunctioning; if it receives a fan operating signal, it determines that the fan is functioning normally.

[0093] This solution can also detect the usage status of the electrode channels of the control device. Specifically, this solution can open the relay of the dummy load, connect the onboard resistor and the RF circuit to form a dummy load loop, and then detect whether the electrode channel can be used through the dummy load loop.

[0094] In addition, this solution can also detect and verify whether the data communication protocol is correct based on the communication data frame, and use ADC acquisition data to determine whether the ADC acquisition module is working properly, etc., to detect its own status.

[0095] It should be noted that the self-state detection under the initial startup condition and the periodic self-state detection process during operation described above are the same as the state detection process described above.

[0096] The above-described implementation scheme covers all key points of the control equipment, thus providing complete control equipment testing. It can comprehensively test the equipment, including power supply testing, channels, RF voltage, fans, temperature, impedance, and power. Furthermore, this scheme can automatically issue alarms when problems are detected, thereby improving the timeliness of equipment failure reminders and repairs.

[0097] In an optional embodiment of this example, this solution can not only detect the status of the control device itself, but also detect the connection status of the connected conduit device, the electrode temperature measurement performance of the conduit device, and the contact status of the conduit.

[0098] Specifically, as one possible implementation method, as shown in Figure 3, this solution may also include the following implementation methods:

[0099] Step S300: Detect the connection status of the conduit equipment connected to the control device and the electrode temperature measurement performance of the conduit equipment.

[0100] In some cases, although the catheter device and the control device have established an electrical connection in hardware, communication between the two devices may fail due to interface incompatibility or wiring problems. In such situations, this solution requires detecting the connection status of the catheter device connected to the control device. Specifically, the control device can send a test signal to the catheter device. If the catheter device receives the test signal, it will return a corresponding feedback signal to the control device based on the test signal. Therefore, the control device can determine the connection status of the catheter device by judging whether it receives the feedback signal corresponding to the test signal transmitted by the catheter device. If the control device receives the feedback signal corresponding to the test signal transmitted by the catheter device, it determines that the connection status of the catheter device is normal; if the control device does not receive the feedback signal corresponding to the test signal transmitted by the catheter device, it indicates that the connection status between the control device and the catheter device is abnormal, and an alarm can be triggered.

[0101] In some cases, the temperature of the electrodes on the catheter device may be abnormal, affecting the ablation performance and accuracy of the radio frequency signal generating device. Therefore, this solution also needs to detect the temperature measurement performance of the electrodes on the catheter device connected to the control device. Specifically, the control device can acquire the temperature information of each electrode transmitted by the catheter device and determine whether the temperature information of each electrode transmitted by the catheter device is greater than a temperature threshold. If it is determined that the temperature information of each electrode transmitted by the catheter device is not greater than the temperature threshold, then the temperature measurement performance of multiple electrodes on the catheter device is normal; if it is determined that the temperature information of the electrodes on the catheter device is greater than the temperature threshold, then the temperature measurement performance of the electrodes with temperature information greater than the temperature threshold is abnormal. Multiple temperature sensors can be installed on the catheter device to acquire the temperature information of each electrode. The acquired temperature information can be transmitted to the communication storage module of the catheter device. The catheter device then transmits the acquired electrode temperature information to the control device through the communication storage module, enabling the control device to acquire the temperature information of each electrode transmitted by the catheter device.

[0102] In the above-described implementation, this solution detects the connection status of the catheter device and the temperature measurement performance of the electrodes on it, thereby enabling the detection of catheter connection quality and catheter performance. This avoids time loss caused by catheter performance defects during surgery, thus ensuring the safety and timeliness of treatment.

[0103] In an optional embodiment of this example, this solution can not only detect the connection status of the catheter device and the temperature measurement performance of the electrodes, but also detect the catheter contact performance. Specifically, as shown in Figure 4, this method can also detect the catheter contact performance in the following ways:

[0104] Step S400: Open the channel corresponding to each electrode in the catheter device.

[0105] Step S410: Control the output of the first energy value of the channel corresponding to each electrode.

[0106] Step S420: Collect the first temperature value and the first impedance value of the channel corresponding to each electrode.

[0107] Step S430: After a preset time interval, collect the second temperature value and the second impedance value of the channel corresponding to each electrode.

[0108] Step S440: Determine whether the corresponding electrode meets the wall adhesion requirements based on the first temperature value, first impedance value, second temperature value, and second impedance value of the channel corresponding to the electrode.

[0109] The above-described implementation involves testing the accuracy of the catheter's placement before the formal ablation procedure, after the catheter device is inserted into the ablation site. This is known as catheter placement performance testing. In this case, the solution first activates all electrode channels and then controls the output of a first energy value for each electrode's corresponding channel. This first energy value can be a low energy value (e.g., 0.5W or less). After outputting the first energy value, the solution collects the first temperature value and first impedance value of each electrode's corresponding channel. Then, after a preset time interval, it collects the second temperature value and second impedance value of each electrode's corresponding channel again. Based on the first temperature value, first impedance value, second temperature value, and second impedance value of the electrode's corresponding channel, it is determined whether the electrode meets the wall adhesion requirements.

[0110] Specifically, this solution calculates the temperature difference between the second temperature value and the first temperature value of the channel corresponding to the electrode, and then calculates the impedance difference between the second impedance value and the first impedance value of the channel corresponding to the electrode. If the temperature difference is greater than a preset temperature threshold and the impedance difference is less than a preset impedance threshold, then the corresponding electrode is determined to meet the wall adhesion requirement. If the temperature difference is not greater than the preset temperature threshold and / or the impedance difference is not less than the preset impedance threshold, then the corresponding electrode is determined not to meet the wall adhesion requirement. Here, the preset temperature threshold is greater than 0 and the preset impedance threshold is less than 0.

[0111] For example, suppose an electrode has a first temperature value of T2, a second temperature value of T3, a first impedance value of Z1, a second impedance value of Z2, a preset temperature threshold of 3 degrees Celsius, and a preset impedance value of 0. If T2-T3 > 3 degrees Celsius and Z1-Z2 < 0, then the electrode is determined to meet the wall adhesion requirements. If T2-T3 ≤ 3 degrees Celsius and / or Z1-Z2 ≥ 0, then the electrode is determined to not meet the wall adhesion requirements.

[0112] In the above-described implementation, this solution performs electrode adhesion detection before radiofrequency ablation, which can automatically detect channels with poor adhesion. This can effectively eliminate electrodes with poor adhesion during the subsequent radiofrequency ablation process, thereby avoiding poor ablation results and improving the accuracy and reliability of radiofrequency ablation.

[0113] In an optional embodiment of this example, for electrodes that do not meet the wall adhesion requirements described above, this solution can control the channel corresponding to the electrode that does not meet the wall adhesion requirements to be closed, and display the status of the closed electrode on the display.

[0114] In the above-described embodiments, this solution can automatically close the channel of electrodes that do not meet the adhesion requirements and display it on the display, thereby automatically eliminating electrodes with poor adhesion during the subsequent radiofrequency ablation process. The display also prompts the operator about the electrodes that do not meet the adhesion requirements, for example, which specific electrode does not meet the adhesion requirements, thereby improving the accuracy and reliability of radiofrequency ablation for the operator.

[0115] Figure 5 shows a schematic structural block diagram of a configuration device for a radio frequency signal generating device provided in this application. It should be understood that this device is used in accordance with the methods described above. This device corresponds to the method embodiments executed in Figures 1 to 4 and is capable of executing the steps involved in the aforementioned methods. The specific functions of this device can be found in the description above. To avoid repetition, detailed descriptions are appropriately omitted here. The device includes at least one software function module that can be stored in a memory or embedded in the device's operating system (OS) in the form of software or firmware. Specifically, the device includes: an acquisition module 500, used to acquire catheter information transmitted by a connected catheter device; wherein the catheter information includes catheter type information; a determination module 510, used to determine the target treatment method corresponding to the catheter type information based on the catheter type information; wherein the control device stores multiple treatment methods, and each catheter type information corresponds to a corresponding treatment method; and determines the catheter treatment parameters configured for the catheter device connected to the control device based on the target treatment method; wherein the control device stores multiple catheter treatment parameters, and each catheter instruction parameter corresponds to a corresponding treatment method.

[0116] The configuration device for the radio frequency signal generating equipment described above communicates with the catheter device through a control device. Based on the catheter type information transmitted by the catheter device, it identifies the target treatment method corresponding to the catheter. Then, it obtains the catheter treatment parameters corresponding to the identified target treatment method and controls the catheter device to execute the catheter instruction parameters for treatment. This allows for customized configuration between one control device and multiple different types of catheter devices. Furthermore, it enables the configuration of only the corresponding treatment device for catheters with different treatment directions. In addition, when performing different treatments, only the catheter device needs to be replaced based on the control device, thereby saving costs and improving the versatility of the control device for the radio frequency signal generating equipment.

[0117] In an optional implementation of this embodiment, the treatment methods corresponding to different catheter type information are all different. The determining module 510 is specifically used to find the treatment method corresponding to the catheter type information based on the catheter type information and obtain the target treatment method.

[0118] In an optional embodiment of this example, where the same catheter type information corresponds to multiple treatment methods, the determining module 510 is further specifically used to search for multiple treatment methods corresponding to the catheter type information based on the catheter type information, obtain multiple candidate treatment methods; display the candidate treatment methods on the display screen of the control device; and obtain the treatment method selected by the user from the multiple candidate treatment methods based on the user's selection operation, thereby obtaining the target treatment method.

[0119] In an optional embodiment of this example, the catheter information also includes catheter ownership information. The device further includes a judgment module 520, which is used to determine whether the catheter device belongs to compliant devices based on the catheter ownership information; and an alarm module 530, which is used to generate an alarm when the judgment module determines that the catheter device does not belong to compliant devices.

[0120] In an optional embodiment of this example, the catheter information also includes catheter activation time information. The judgment module 520 is further configured to determine whether the catheter device is a used device and / or an expired device based on the catheter activation time information. The alarm module 530 is further configured to generate an alarm when the judgment module determines that the catheter device is a used device and / or an expired device.

[0121] In an optional embodiment of this example, the acquisition module 500 is further configured to acquire the number of electrode channels of the configured catheter device; the display module 540 is configured to display the number of configured motor channels on the display screen of the control device.

[0122] In an optional embodiment of this example, the acquisition module 500 is further configured to acquire surgical guidance information corresponding to the target treatment method; wherein each treatment method corresponds to a surgical guidance information, and the surgical guidance information includes surgical step prompts for the target treatment method; the display module 540 is further configured to display the surgical guidance information on the display screen of the control device.

[0123] In an optional embodiment of this example, the device further includes a detection module 550 for detecting the status of the control device itself.

[0124] In an optional embodiment of this example, the detection module 550 is specifically used to perform status detection on the control device itself after the control device is initially started; and / or, to periodically perform status detection on the control device itself during the operation of the control device.

[0125] In an optional embodiment of this example, the detection module 550 is further specifically used to detect the communication status of the control device by detecting peripheral information of the control device; and / or to detect the power status of the control device based on the voltage acquisition value at the power supply of the control device; and / or to detect the power amplifier power supply of each channel based on the voltage acquisition value of each channel; and / or to detect the fan status based on the fan working signal; and / or to detect the usage status of the electrode channels of the control device.

[0126] In an optional embodiment of this example, the detection module 550 is also used to detect the connection status of the conduit device connected to the control device and the electrode temperature measurement performance of the conduit device.

[0127] In an optional embodiment of this example, the detection module 550 is further specifically used to send a test signal to the catheter device; determine whether a return signal corresponding to the test signal transmitted by the catheter device is received; if it is determined that a return signal corresponding to the test signal transmitted by the catheter device is received, then it is determined that the connection status of the catheter device is normal; acquire the temperature information of each electrode transmitted by the catheter device; determine whether the temperature information of each electrode transmitted by the catheter device is greater than a temperature threshold; if it is determined that the temperature information of each electrode transmitted by the catheter device is not greater than the temperature threshold, then it is determined that the temperature measurement performance of the multiple electrodes of the catheter device is normal.

[0128] In an optional embodiment of this example, the device further includes a control module 560, which is used to control the opening of the channel corresponding to each electrode in the catheter device after determining that the connection status of the catheter device is normal and the temperature measurement performance of the multiple electrodes of the catheter device is normal; and to control the output of a first energy value of the channel corresponding to each electrode; the acquisition module 570 is used to acquire the first temperature value and the first impedance value of the channel corresponding to each electrode; and to acquire the second temperature value and the second impedance value of the channel corresponding to each electrode after a preset time interval; the determination module 510 is also used to determine whether the corresponding electrode meets the wall adhesion requirements based on the first temperature value, the first impedance value, the second temperature value, and the second impedance value of the channel corresponding to the electrode.

[0129] In an optional embodiment of this example, the determining module 510 is further specifically used to calculate the temperature difference between the second temperature value and the first temperature value of the channel corresponding to the electrode; calculate the impedance difference between the second impedance value and the first impedance value of the channel corresponding to the electrode; if the temperature difference is greater than a preset temperature threshold and the impedance difference is less than a preset impedance threshold, then the corresponding electrode is determined to meet the wall adhesion requirement; wherein, the preset temperature threshold is greater than 0 and the preset impedance threshold is less than 0; if the temperature difference is not greater than the preset temperature threshold and / or the impedance difference is not less than the preset impedance threshold, then the corresponding electrode is determined not to meet the wall adhesion requirement.

[0130] In an optional embodiment of this example, the control module 560 is further configured to control the channel corresponding to the electrode that does not meet the wall adhesion requirement to be closed, and display the status of the closed electrode on the display.

[0131] According to some embodiments of this application, as shown in FIG6, this application provides an electronic device 6, including: a processor 601 and a memory 602. The processor 601 and the memory 602 are interconnected and communicate with each other through a communication bus 603 and / or other forms of connection mechanism (not shown). The memory 602 stores a computer program executable by the processor 601. When the computing device is running, the processor 601 executes the computer program to perform any optional implementation method, such as steps S100 and S120: obtaining catheter information transmitted by the connected catheter device, the catheter information including catheter type information; determining the target treatment mode corresponding to the catheter type information based on the catheter type information; and determining the catheter treatment parameters configured by the catheter device connected to the control device based on the target treatment mode.

[0132] This application provides a computer-readable storage medium storing a computer program that, when executed by a processor, performs the method in any of the aforementioned optional implementations.

[0133] The storage medium can be implemented by any type of volatile or non-volatile storage device or a combination thereof, such as Static Random Access Memory (SRAM), Electrically Erasable Programmable Read-Only Memory (EEPROM), Erasable Programmable Read Only Memory (EPROM), Programmable Red-Only Memory (PROM), Read-Only Memory (ROM), magnetic storage, flash memory, magnetic disk, or optical disk.

[0134] This application provides a computer program product that, when run on a computer, causes the computer to perform a method in any of the optional implementations.

[0135] Finally, it should be noted that the above embodiments are only used to illustrate the technical solutions of this application, and not to limit them. Although this application has been described in detail with reference to the foregoing embodiments, those skilled in the art should understand that modifications can still be made to the technical solutions described in the foregoing embodiments, or equivalent substitutions can be made to some or all of the technical features therein. These modifications or substitutions do not cause the essence of the corresponding technical solutions to deviate from the scope of the technical solutions of the embodiments of this application, and they should all be covered within the scope of the claims and specification of this application. In particular, as long as there is no structural conflict, the various technical features mentioned in the embodiments can be combined in any way. This application is not limited to the specific embodiments disclosed herein, but includes all technical solutions falling within the scope of the claims.

Claims

1. A method for configuring a radio frequency signal generating device, characterized in that, The radio frequency signal generating device includes a control device and a catheter device connected to the control device; the catheter device is provided with a plurality of radio frequency electrodes, which are used to release radio frequency current to achieve radio frequency ablation. The method is applied to the control device, and the method includes: Acquire catheter information transmitted by the connected catheter device; wherein, the catheter information includes catheter type information; Based on the catheter type information, the target treatment method corresponding to the catheter type information is determined; wherein, the control device stores multiple treatment methods, and each catheter type information corresponds to a specific treatment method; Based on the target treatment method, the catheter treatment parameters configured for the catheter device connected to the control device are determined; wherein, the control device stores multiple catheter treatment parameters, each corresponding to a specific treatment method.

2. The method according to claim 1, characterized in that, in, Different catheter types correspond to different treatment methods; The step of determining the target treatment method corresponding to the catheter type information based on the catheter type information includes: Based on the catheter type information, the corresponding treatment method is found to obtain the target treatment method.

3. The method according to claim 1, characterized in that, in, The same catheter type information can correspond to multiple treatment methods; The step of determining the target treatment method corresponding to the catheter type information based on the catheter type information includes: Based on the catheter type information, multiple treatment methods corresponding to the catheter type information are searched to obtain multiple candidate treatment methods; The multiple candidate treatment methods are displayed on the screen of the control device; Based on the user's selection operation, the treatment method selected by the user from multiple candidate treatment methods is obtained, and the target treatment method is obtained.

4. The method according to claim 1, characterized in that, in, The catheter information also includes catheter attribution information; the method further includes: Based on the catheter ownership information, determine whether the catheter device is a compliant device; If the catheter device is determined to be non-compliant, an alarm will be generated.

5. The method of claim 1, wherein, in, The catheter information also includes catheter activation time information; The method further includes: Based on the catheter activation time information, determine whether the catheter device is a used device and / or an expired device; An alarm is generated if the catheter device is determined to be a used device and / or an expired device.

6. The method of claim 1, wherein, After determining the catheter treatment parameters configured for the catheter device connected to the control device according to the target treatment method, the method further includes: The number of electrode channels of the configured catheter device is obtained, and the number of motor channels is displayed on the display screen of the control device.

7. The method according to claim 1, characterized in that, After determining the catheter treatment parameters configured for the catheter device connected to the control device according to the target treatment method, the method further includes: Obtain surgical guidance information corresponding to the target treatment method; wherein, each treatment method corresponds to a surgical guidance information, and the surgical guidance information includes surgical step prompts for the target treatment method; The surgical guidance information is displayed on the screen of the control device.

8. The method according to claim 1, characterized in that, The method further includes: performing status detection on the control device itself.

9. The method according to claim 8, characterized in that, The step of performing status detection on the control device itself includes: After the control device is initially started, the control device itself undergoes status detection; and / or, During the operation of the control device, the status of the control device itself is periodically detected.

10. The method according to claim 9, characterized in that, The step of performing status detection on the control device itself includes: The communication status of the control device is detected based on the peripheral information of the control device; and / or... The power status of the control device is detected based on the voltage acquisition value at the power supply of the control device; and / or... The power amplifier power supply of each channel is tested based on the voltage acquisition value of each channel; and / or, The fan status is detected based on the fan operating signal; and / or, the usage status of the electrode channels of the control device is detected.

11. The method according to claim 8, characterized in that, After performing state detection on the control device itself, the method further includes: The connection status of the conduit equipment connected to the control device and the electrode temperature measurement performance of the conduit equipment are detected.

12. The method according to claim 11, characterized in that, The testing of the connection performance of the conduit equipment connected to the control device includes: Send a test signal to the catheter device; Determine whether a feedback signal corresponding to the test signal transmitted by the catheter device has been received; If it is determined that a return signal corresponding to the test signal transmitted by the catheter device is received, then it is determined that the connection status of the catheter device is normal. Acquire the temperature information of each electrode transmitted by the catheter device; Determine whether the temperature information transmitted by each electrode in the catheter device is greater than a temperature threshold; If it is determined that the temperature information transmitted by each electrode of the catheter device is not greater than the temperature threshold, then it is determined that the temperature measurement performance of the multiple electrodes of the catheter device is normal.

13. The method according to claim 12, characterized in that, The method further includes: After confirming that the connection status of the catheter device is normal and that the temperature measurement performance of the multiple electrodes of the catheter device is normal, the channel corresponding to each electrode in the catheter device is opened. Control the output of the first energy value of the channel corresponding to each electrode; Collect the first temperature value and the first impedance value of the channel corresponding to each electrode; After a preset time interval, the second temperature value and the second impedance value of the channel corresponding to each electrode are collected; Determine whether the corresponding electrode meets the wall adhesion requirements based on the first temperature value, first impedance value, second temperature value, and second impedance value of the channel corresponding to the electrode.

14. The method according to claim 13, characterized in that, The step of determining whether the corresponding electrode meets the wall adhesion requirements based on the first temperature value, first impedance value, second temperature value, and second impedance value of the channel corresponding to the electrode includes: Calculate the temperature difference between the second temperature value and the first temperature value of the channel corresponding to the electrode; Calculate the impedance difference between the second impedance value and the first impedance value of the channel corresponding to the electrode; If the temperature difference is greater than a preset temperature threshold and the impedance difference is less than a preset impedance threshold, then the corresponding electrode is determined to meet the wall adhesion requirement; wherein, the preset temperature threshold is greater than 0 and the preset impedance threshold is less than 0. If the temperature difference is not greater than the preset temperature threshold and / or the impedance difference is not less than the preset impedance threshold, then the corresponding electrode is determined not to meet the wall adhesion requirements.

15. The method according to claim 14, characterized in that, After determining that the corresponding electrode does not meet the wall adhesion requirements, the method further includes: The channel corresponding to the electrode that does not meet the wall adhesion requirements is closed, and the status of the closed electrode is displayed on the screen.

16. A computer-readable storage medium having a computer program stored thereon, characterized in that, When the computer program is executed by a processor, it implements the method of any one of claims 1 to 15.