Cellular perianal treatment equipment for anal fistula

Abstract

The crissum treatment equipment comprises a main body, a probe, a cleaning tube and an aspirator, the probe is connected with the cleaning tube through a connecting block, the aspirator is connected with the cleaning tube through a connecting block, the probe is wirelessly connected with the main body, the cleaning tube is connected with the main body through a sealing block, and the sealing block is connected with the main body through a connecting block. The aspirator is connected with the main body through a sealing block, the diameter of the middle of the connecting block is consistent with that of the outer circle of the probe body, and the two ends of the connecting block are consistent with that of the inner circle of the probe body. And the operation difficulty is reduced. Meanwhile, due to the modular design, part replacement, cleaning and disinfection are facilitated, resource waste and infection risks are reduced, personalized treatment requirements can be met, and the anal fistula treatment effect is improved.

Description

Technical Field

[0001] The present invention belongs to the field of medical device technology, and in particular relates to an anal perianal treatment device for honeycomb anal fistula.

[0002] Anal fistula is a common anorectal condition that plagues many patients. Its pathological characteristic is the formation of an abnormal channel between the anal canal or rectum and the perianal skin, leading to recurrent infection and pus discharge, seriously affecting the patient's quality of life and physical health. Effective treatment of anal fistula relies on precise exploration, thorough cleaning, and disinfection of the fistula to avoid recurrence and reduce the risk of recurrence. Therefore, appropriate treatment devices play a vital role in the treatment of anal fistula.

[0003] At present, the clinical treatment technologies for anal fistula mainly include traditional probe exploration, surgical resection, and drug-assisted treatment. Traditional probe exploration relies on the experience of medical staff. A hard metal probe is used to tentatively enter the fistula to determine the direction and internal opening of the fistula. However, this method lacks visual assistance and it is difficult to fully grasp the complex internal morphology of the fistula. During surgical resection, due to insufficient preoperative understanding of the fistula, it is very easy to damage the normal tissue around the fistula during the operation, increasing the patient's postoperative pain and recovery time. During the cleaning and disinfection process, existing cleaning tools are difficult to penetrate deep into the narrow and curved fistula and cannot effectively remove dirt and pus attached to the wall of the fistula. Conventional disinfection methods often have blind spots in disinfection, making it difficult to achieve the ideal sterilization effect. In addition, the existing treatment process lacks a tightly coordinated integrated device for each link, resulting in a cumbersome operation process. Medical staff need to frequently change different instruments, which not only reduces treatment efficiency but also increases the risk of cross-infection.

[0004] These defects and problems in existing technologies have greatly reduced the effectiveness of anal fistula treatment. Inaccurate fistula exploration leads to the omission of some branch fistulas, which lays the hidden danger of recurrence of the disease; damage to normal tissues during surgery may cause serious complications such as anal incontinence; incomplete cleaning and disinfection cannot effectively eliminate the source of infection, prolonging the patient's recovery period; and the cumbersome nature of the treatment process also places higher demands on the operational proficiency of medical staff. A slight carelessness may lead to medical errors and increase the risk of medical disputes. Therefore, there is an urgent need to develop a new anal fistula treatment device to overcome the shortcomings of existing technologies and improve the safety and effectiveness of anal fistula treatment. Summary of the Invention

[0005] In order to solve the above problems, the purpose of the present invention is to provide an anal perianal treatment device for honeycomb anal fistula, including a main body, a probe, a cleaning tube and an aspirator, the probe and the cleaning tube are connected by a connecting block, the aspirator and the cleaning tube are connected by a connecting block, the probe and the subject are wirelessly connected, the cleaning tube and the main body are connected by a sealing block, the aspirator and the main body are connected by a sealing block, the middle part of the connecting block is consistent with the outer circle diameter of the probe, and the two ends of the connecting block are consistent with the inner circle of the probe.

[0006] In one example, a transparent silicone top is set on the top of the probe, and the lower side of the silicone top is a hollow cylindrical probe. An LED light is installed inside the probe, and a miniature camera is installed under the LED light. The miniature camera is wirelessly connected to the display set on the top of the main shell through a wireless transmission module.

[0007] In one example, a cooling chamber is provided inside the probe. The cooling chamber is a cylindrical and closed structure. Coolant is stored inside the cooling chamber. There are through holes between the bottoms of the cooling chamber. A cooling fan is provided at the bottom of the cooling chamber.

[0008] In one example, the bottom of the probe is fixedly connected to the probe body, and a precise scale is provided on the outer surface of the probe body.

[0009] In one example, a disinfection box is provided on the top of the main body, and an ultraviolet disinfection lamp and a high-temperature disinfection device are provided inside the disinfection box.

[0010] In one example, the cleaning tube is connected to the bottom of the probe, a cleaning brush is provided inside the cleaning tube, one end of the cleaning brush is fixedly connected to the inside of the retention tube, the length of the bristles of the cleaning brush is greater than the radius of the cleaning tube, and a blocking plate is provided at the position of the bristles of the cleaning brush, and a strip-shaped moving block is connected to the bottom of the blocking plate, and the thickness of the blocking block is less than the thickness of the cleaning tube.

[0011] In one example, a liquid spray head is provided on the surface of the cleaning brush rod, the interior of the cleaning brush rod is hollow, the bottom of the cleaning brush rod is open, a liquid storage bottle is installed on one side of the interior of the main shell, hydrogen peroxide disinfectant is stored in the liquid storage bottle, a liquid pump is placed at the bottom of the liquid storage bottle, the liquid pump is connected to one end of the disinfectant tube, and the other end of the disinfectant tube is connected to a sealing block, and the sealing block is consistent with the inner diameter of the cleaning brush rod.

[0012] In one example, a connecting block is installed at the bottom of the cleaning tube, and the other end of the connecting block is connected to a suction tube. The suction device is in the shape of a hollow cylinder, and there are suction holes on the surface of the suction tube. The bottom end of the suction tube is connected to the sealing block at one end of the guide tube, and the other end of the guide tube is connected to the bottom of the liquid collecting tube. The top position of the liquid collecting tank is connected to an air pipe, and the other end of the air pipe is connected to an air pump.

[0013] In one example, the connecting block is solid.

[0014] In one example, the liquid collecting tank is installed on one side inside the main body, the liquid collecting tank is transparent, there is a scale on the surface of the liquid collecting tank, the side of the main body corresponding to the liquid collecting tank is transparent, the side of the main body is cabinet-shaped, and a slide rail and a card slot are provided inside the main body.

[0015] The perianal treatment device for honeycomb anal fistula proposed by the present invention can bring the following beneficial effects:

[0016] 1. The main body, probe, cleaning tube and aspirator of the present invention are cleverly connected. The transparent silicone top, built-in LED light and miniature camera on the top of the probe constitute a precise exploration structure. The cooling chamber in the probe ensures the stable operation of the components, and the ruler on the probe body is convenient for measurement. The cleaning tube cooperates with the indwelling tube and the cleaning brush, and the spray head and the liquid storage bottle are disinfected. The aspirator is connected to the cleaning tube to form a negative pressure suction structure. This modular and detachable structural design makes the functions of each component clear, and can be flexibly assembled and disassembled according to actual treatment needs during use. For example, the probe can be easily removed for disinfection after the exploration is completed, and the connection between the cleaning tube and the aspirator can also be quickly achieved, which greatly improves the convenience of operation.

[0017] 2. The present invention uses a combination of a transparent silicone top, an LED light, and a miniature camera to allow medical staff to clearly observe the internal conditions of the fistula, avoid damaging normal tissue, accurately grasp the direction of the fistula and the position of the internal opening, reduce the omission of branch fistulas, and reduce the recurrence rate of anal fistulas; the setting of the cooling chamber solves the problem of heat generation of components and ensures the safety of patients. The ruler assists in accurately measuring fistula-related data, providing a reliable basis for the formulation of treatment plans. In the cleaning, disinfection, and suction links, the cleaning brush, spray head, and liquid storage bottle effectively disinfect and clean the fistula, and the negative pressure environment formed by the suction device can thoroughly absorb pus and disinfectant. Overall, the present invention realizes the integration of multiple links in anal fistula treatment, significantly shortens the treatment time, reduces the pain and treatment costs of patients, and at the same time reduces the difficulty of operation for medical staff and reduces the occurrence of medical errors. BRIEF DESCRIPTION OF THE DRAWINGS

[0018] The drawings described herein are used to provide a further understanding of the present invention and constitute a part of the present invention. The exemplary embodiments of the present invention and their descriptions are used to explain the present invention and do not constitute an improper limitation of the present invention. In the drawings:

[0019] Figure 1 This is a schematic diagram of the overall structure of an anal perianal treatment device for honeycomb anal fistula according to the present invention.

[0020] Figure 2 This is a schematic structural diagram of the perianal treatment device for honeycomb anal fistula of the present invention, excluding the outer shell.

[0021] Figure 3 This is a schematic structural diagram of a probe and a cleaning tube of an anal perianal treatment device for honeycomb anal fistula according to the present invention.

[0022] Figure 4 This is a schematic structural diagram of a probe and a cleaning tube of an anal perianal treatment device for honeycomb anal fistula according to the present invention when the blocking plate is opened.

[0023] Figure 5 This is a schematic diagram of the internal structure of a probe of an anal perianal treatment device for honeycomb anal fistula according to the present invention.

[0024] Figure 6 This is a schematic diagram of the connection block structure of an anal perianal treatment device for honeycomb anal fistula according to the present invention.

[0025] Figure 7 This is a schematic structural diagram of the perianal treatment device A for honeycomb anal fistula of the present invention.

[0026] Reference numerals:

[0027] 1. Main body; 2. Display; 3. Disinfection box; 4. Probe; 401. Camera; 402. Lamp; 403. Probe; 404. Probe body; 405. Ruler; 406. Cooling chamber; 407. Cooling fan; 5. Connecting block; 6. Cleaning pipe; 601. Cleaning brush; 602. Spray head; 603. Disinfectant pipe; 604. Liquid storage bottle; 605. Liquid pump; 7. Blocking plate; 8. Moving block; 9. Aspirator; 901. Liquid collecting tank; 902. Air pipe; 903. Air pump; 904. Diversion pipe; 905. Suction pipe; 11. Sealing block. DETAILED DESCRIPTION

[0028] In order to more clearly illustrate the overall concept of the present invention, a detailed description is given below in an exemplary manner in conjunction with the accompanying drawings.

[0029] In the description of the present invention, it should be understood that the terms "center", "up", "down", "front", "back", "left", "right", "vertical", "horizontal", "top", "bottom", "inside", "outside", "axial", "radial", "circumferential", etc., indicating the orientation or position relationship, are based on the orientation or position relationship shown in the accompanying drawings, and are only for the convenience of describing the present invention and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operate in a specific orientation, and therefore cannot be understood as limiting the present invention.

[0030] Furthermore, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of the technical features being referred to. Thus, a feature identified as "first" or "second" may explicitly or implicitly include one or more of the features. In the description of the present invention, "plurality" means two or more, unless otherwise specifically defined.

[0031] In the present invention, unless otherwise expressly specified or limited, terms such as "mounted," "connected," "connect," and "fixed" should be understood broadly. For example, they may refer to fixed connection, detachable connection, or integration; mechanical connection, electrical connection, or communication; direct connection or indirect connection through an intermediate medium; and internal communication between two components or interaction between two components. Those skilled in the art will understand the specific meanings of the above terms in the present invention based on specific circumstances.

[0032] In the present invention, unless otherwise clearly specified and limited, a first feature "above" or "below" a second feature may be such that the first and second features are in direct contact, or the first and second features are in indirect contact through an intermediate medium. In the description of this specification, the descriptions with reference to the terms "one scheme", "some schemes", "examples", "specific examples" or "some examples" etc. mean that the specific features, structures, materials or characteristics described in conjunction with the scheme or example are included in at least one scheme or example of the present invention. In this specification, the schematic expressions of the above terms do not necessarily refer to the same scheme or example. Moreover, the specific features, structures, materials or characteristics described may be combined in an appropriate manner in any one or more schemes or examples.

[0033] like Figures 1 to 7As shown, the present invention mainly includes a main body 1, a probe 4, a cleaning tube 6, and an aspirator 9. The probe 4 and the cleaning tube 6 are connected in a detachable manner, which not only facilitates assembly and disassembly but also allows for flexible adjustment according to actual needs during use. The cleaning tube 6 and the main body 1 are also detachably connected, facilitating individual maintenance and replacement of each component. The aspirator 9 is fixedly connected to the side of the main body 1 and can be connected to the cleaning tube 6 and the aspirator 9 via a specially designed sealing connection structure, thus forming a complete and tight anal fistula treatment system.

[0034] Probe 4 is a key component used in this invention for fistula exploration. Its transparent silicone tip is made of medical-grade, highly transparent silicone. This material not only offers excellent flexibility, preventing damage to the fistula wall during insertion, but also boasts excellent light transmittance, minimizing light refraction and scattering. This ensures uniform and stable transmission of light from the internal LED lamp 402, providing a clear field of view for camera 401. Underneath the silicone tip is a hollow cylindrical probe 403, within which is meticulously installed an LED lamp 402. This LED lamp utilizes a low-power, high-brightness medical lighting chip. Its strategically positioned position within the silicone tip ensures optimal illumination of the fistula interior at the optimal angle and intensity. Below this LED lamp 402 is a miniature camera 401, featuring a high-resolution, ultra-wide-angle lens with autofocus and image stabilization, enabling real-time capture of the fistula's internal microstructure and pathological conditions. Miniature camera 401 connects wirelessly to the display 2 mounted on top of the housing via an advanced wireless transmission module. Utilizing 5G communication technology, it ensures real-time and stable image transmission, with a transmission delay of less than 0.1 second. Once medical personnel insert probe 403 into the external opening of the anal fistula and turn on LED light 402, camera 401 provides a clear and comprehensive view of the fistula's interior through the silicone top, projecting the image in real time onto display 2 in high-definition quality. This design helps medical personnel accurately determine the fistula's direction, shape, and internal opening, preventing probe 4 from penetrating surrounding tissue. This allows for accurate tracking of the entire fistula, effectively avoiding missing branches and significantly reducing the likelihood of fistula recurrence. Furthermore, the combination of camera 401 and LED light 402 significantly improves the accuracy of fistula shape and location, easing operational complexity for medical personnel and significantly reducing the likelihood of medical errors.

[0035] Considering that LED lamp 402 and camera 401 generate a significant amount of heat during prolonged operation, and the confined space within the fistula makes it difficult to effectively dissipate this heat, excessive heat buildup can easily cause burns within the patient's fistula, leading to new infections. Therefore, the present invention innovatively incorporates a cooling chamber 406 within probe 403. Cooling chamber 406 is a cylindrical, enclosed structure, its outer shell constructed from a medical-grade aluminum alloy with excellent thermal conductivity, enabling rapid heat transfer. Cooling chamber 406 contains a coolant, specifically a medical-grade cooling liquid with a high specific heat capacity and a low freezing point, capable of absorbing a large amount of heat within a relatively small volume. The bottom of cooling chamber 406 is perforated with holes. The size and distribution of these holes have been precisely calculated and experimentally verified to ensure structural strength while maximizing air circulation. A cooling fan 407 is located at the bottom of cooling chamber 406. This quiet, efficient turbofan features an automatic speed adjustment based on the temperature monitored in real time by a temperature sensor. When the temperature rises, the cooling fan 407 automatically increases its speed to accelerate air circulation, so that the cold air near the cooling chamber 406 flows quickly to the LED lamp 402 and the camera 401. At the same time, the cooling chamber 406 also absorbs the nearby heat through heat conduction and heat convection, which can effectively reduce the temperature and avoid excessive heat accumulation, providing a stable working environment for the LED lamp 402 and the camera 401, while ensuring the safety of patients and effectively preventing the risk of burns.

[0036] The bottom of the probe 403 is fixedly connected to the probe body 404, the outer surface of which is provided with a precise scale 405. Scale 405 is laser-engraved, resulting in clear and accurate graduations, with a minimum graduation of 0.1 mm, meeting the high-precision requirements of clinical measurements. When medical personnel insert the probe 4 into the fistula tract, scale 405 accurately determines the insertion length and thus measures the distance between the internal and external openings. This data helps medical personnel determine the height of the anal fistula and, combined with CT scans and other examination results, more accurately determines the location and depth of the fistula, providing important evidence for subsequent treatment planning. In actual clinical applications, the measurement error of scale 405 is less than ±0.5 mm, demonstrating extremely high reliability.

[0037] After the probe 4 completes the determination of the fistula position, it continues to advance forward so that the probe 4 is completely exposed from the rectum. The probe body 404 is hollow, and a connecting block 5 is provided at the bottom of the probe body 404. The connecting block 5 is made of high-strength medical-grade plastic material with good wear resistance and corrosion resistance. The middle part of the connecting block 5 is consistent with the outer diameter of the probe body 404, and the two ends of the connecting block 5 are consistent with the inner circle of the probe body 404. This special size design enables the probe body 404 to be tightly sleeved on one end of the connecting block 5. The other end of the connecting block 5 is sleeved with an indwelling tube, which is ensured to be firmly connected to the connecting block 5 by an interference fit and is not easy to fall off. The connector and the probe 4 part are removed from the top of the indwelling tube. At this time, the indwelling tube is completely inside the fistula, and the probe 4 is placed in the disinfection box 3 on the top of the main body 1 shell for disinfection. The disinfection box 3 is equipped with an ultraviolet disinfection lamp 402 and a high-temperature disinfection device. The ultraviolet disinfection lamp 402 uses a high-intensity lamp 402 tube with a wavelength of 254 nanometers, which can kill 99.9% of bacteria and viruses within 15 minutes; the high-temperature disinfection device can accurately control the temperature at 132°C and continue disinfection for 30 minutes to ensure that the probe 4 meets the sterility standard.

[0038] A cleaning tube 6 is connected below the indwelling tube, and a cleaning brush 601 is provided inside the cleaning tube 6. One end of the cleaning brush 601 is fixedly connected to the inside of the indwelling tube to ensure a stable connection. The bristles of the cleaning brush 601 are longer than the radius of the cleaning tube 6. The bristles are flexible and made of soft and elastic medical nylon material. This material can ensure a clean effect on the inner wall of the fistula without damaging the inner wall of the fistula. The bristle surface has been specially treated to have good hydrophobicity and anti-adhesion properties, which can effectively prevent dirt and pus from adhering to the bristles. The cleaning brush 601 has a bristle position provided with a blocking plate 7. The bottom of the blocking plate 7 is connected to a strip-shaped movable block 8. The thickness of the blocking block is less than that of the cleaning tube 6, and the cleaning tube 6 below the blocking block can pass through the blocking block. When the cleaning tube 6 enters the fistula, the blocking block is pulled down, and a hollow area appears in the middle of the cleaning tube. The bristles extend from the hollow area and directly contact the inner wall of the fistula. When the cleaning tube 6 is moved inside the fistula, sufficient friction is provided between the bristles and the inner wall of the fistula for cleaning.

[0039] A liquid spray head 602 is provided on the surface of the cleaning brush rod. The cleaning brush rod is hollow inside and has an open bottom. A liquid storage bottle 604 is installed on one side of the main body 1 shell. The liquid storage bottle 604 is made of transparent medical-grade polycarbonate material, which is convenient for observing the remaining amount of internal disinfectant. Disinfectant such as hydrogen peroxide is stored in the liquid storage bottle 604. A liquid pump 605 is placed at the bottom of the liquid storage bottle 604. The liquid pump 605 is selected from a high-precision, low-noise micro-diaphragm pump for accurately controlling the output flow of the disinfectant. The liquid pump 605 is connected to one end of a disinfectant pipe 603. The other end of the disinfectant pipe 603 is connected to a sealing block 11. The sealing block 11 is consistent with the inner diameter of the cleaning brush rod and is made of rubber material, which has good sealing performance. The sealing block 11 is stuck into the inside of the cleaning brush rod. The liquid pump 605 is turned on. The disinfectant pump 605 enters the inside of the brush rod and sprays out from the liquid spray head 602 to disinfect and clean the fistula. The spray head 602 adopts a multi-porous atomization design, which can evenly spray the disinfectant on the inner wall of the fistula, ensuring that there are no dead corners in the disinfection.

[0040] After disinfection is completed, the sealing head of the disinfectant pipe 603 is taken out from the top of the cleaning brush 601, and the mobile block 8 advances the cleaning brush toward the rectum. A connecting block 5 is installed at the bottom of the cleaning pipe 6, and the other end of the connecting block 5 is connected to the suction pipe 905 of the aspirator 9. Here, the connecting block 5 is solid, and the suction pipe 905 is hollow cylindrical, and there are suction holes on the surface of the suction pipe 905. The size and number of the suction holes are optimized and designed to avoid damaging the inner wall of the fistula while ensuring suction efficiency. When the suction hole enters the fistula inside, the sealing block 11 at one end of the diversion pipe 904 is installed at the bottom of the cleaning pipe, and the other end of the diversion pipe 904 is connected to the bottom of the liquid collecting pipe. The top position of the liquid collecting tank 901 is connected to the air pipe 902, and the other end of the air pipe 902 is connected to the air pump 903. The air pump 903 adopts variable frequency speed regulation technology, which can adjust the suction force according to actual needs. When the air pump 903 is turned on, the air pressure inside the liquid collection bottle decreases, and the pus and disinfectant inside the fistula can be sucked into the liquid collection tank 901. The liquid collection tank 901 is installed on one side inside the main body 1. The liquid collection tank 901 is transparent and has a scale on the surface with a scale accuracy of 1 ml. The side of the main body 1 corresponding to the liquid collection tank 901 is transparent, which makes it convenient for the operator to observe the state of the aspirated liquid in the liquid collection tank 901 and assess the patient's condition. The side of the main body 1 is cabinet-shaped, with slide rails and card slots inside to facilitate the drainage of pus inside the liquid collection tank 901 and the cleaning of the liquid collection tank 901. In actual operation, medical staff can quickly complete the disassembly and installation of the liquid collection tank 901.

[0041] After suction is complete, the air pump 903 is turned off, the sealing block 11 is removed, the connecting block 5 is installed at the bottom of the cleaning tube 6, and the retention tube is installed at the bottom of the connecting block 5. The retention tube is placed inside the fistula to facilitate subsequent operations. Throughout the treatment process, the various components of the present invention work closely together to form a complete treatment system.

[0042] The presence of the connecting block 5 enables flexible assembly and disassembly of various components, tightly connecting the probe 4 to the cleaning tube 6 and the aspirator 9. This allows for easy assembly and disassembly, saving treatment time, improving efficiency, and reducing operational difficulty. Furthermore, its modular design facilitates component replacement, cleaning, and disinfection, reducing resource waste and infection risks. It also meets personalized treatment needs and enhances the effectiveness of anal fistula treatment.

[0043] Compared to traditional anal fistula treatment devices, this invention improves fistula detection accuracy, cleaning efficiency, and disinfection effectiveness, significantly shortening treatment time and reducing patient pain and costs. Furthermore, the device's operating procedures have been optimized and ergonomically designed, allowing medical staff to operate it proficiently after simple training, demonstrating its high clinical application value and potential for widespread adoption.

[0044] The various embodiments in this specification are described in a progressive manner. Similar parts between the various embodiments can be referred to in conjunction with each other. Each embodiment focuses on the differences between the other embodiments. In particular, the system embodiments are generally similar to the method embodiments, so the description is relatively simple. For relevant parts, refer to the description of the method embodiments.

[0045] The foregoing is merely an embodiment of the present invention and is not intended to limit the present invention. It will be apparent to those skilled in the art that various modifications and variations of the present invention are possible. Any modifications, equivalent substitutions, improvements, etc. made within the spirit and principles of the present invention are intended to be included within the scope of the claims of the present invention.

Claims

1. An anal perianal treatment device for honeycomb anal fistula, comprising a main body (1), a probe (4), a cleaning tube (6) and a suction device (9), characterized in that: The probe (4) is connected to the cleaning tube (6) via a connecting block (5), the suction device (9) is connected to the cleaning tube (6) via a connecting block (5), the probe (4) is connected to the subject via a wireless connection, the cleaning tube (6) is connected to the main body (1) via a sealing block (11), the suction device (9) is connected to the main body (1) via a sealing block (11), the middle of the connecting block (5) is consistent with the outer diameter of the probe body (404), and the two ends of the connecting block (5) are consistent with the inner diameter of the probe body (404).

2. The perianal treatment device for honeycomb anal fistula according to claim 1, characterized in that: A transparent silicone top is provided on the top of the probe (4), and a hollow cylindrical probe (403) is provided on the lower side of the silicone top. An LED light (402) is installed inside the probe (403), and a miniature camera (401) is installed below the LED light (402). The miniature camera (401) is wirelessly connected to a display (2) provided on the top of the housing of the main body (1) via a wireless transmission module.

3. The perianal treatment device for honeycomb anal fistula according to claim 2, characterized in that: A cooling chamber (406) is provided inside the probe (403), the cooling chamber (406) is cylindrical, the cooling chamber (406) is a closed structure, a coolant is stored inside the cooling chamber (406), a through hole is provided between the bottoms of the cooling chamber (406), and a heat dissipation fan (407) is provided at the bottom of the cooling chamber (406).

4. The perianal treatment device for honeycomb anal fistula according to claim 2, characterized in that: The bottom of the probe (403) is fixedly connected to a probe body (404), and a precise scale (405) is provided on the outer surface of the probe body (404).

5. The perianal treatment device for honeycomb anal fistula according to claim 1, characterized in that: A disinfection box (3) is provided on the top of the main body (1), and an ultraviolet disinfection lamp (402) and a high-temperature disinfection device are provided inside the disinfection box (3).

6. The perianal treatment device for honeycomb anal fistula according to claim 1, characterized in that: The cleaning tube (6) is connected to the bottom of the probe (4), and a cleaning brush (601) is provided inside the cleaning tube (6). One end of the cleaning brush (601) is fixedly connected to the inside of the retention tube. The length of the bristles of the cleaning brush (601) is greater than the radius of the cleaning tube (6). A blocking plate (7) is provided at the position of the bristles of the cleaning brush (601). The bottom of the blocking plate (7) is connected to a strip-shaped moving block (8), and the thickness of the blocking block is less than the thickness of the cleaning tube (6).

7. The perianal treatment device for honeycomb anal fistula according to claim 6, characterized in that: A liquid spray head (602) is provided on the surface of the cleaning brush rod. The interior of the cleaning brush rod is hollow, and the bottom of the cleaning brush rod is open. A liquid storage bottle (604) is installed on one side of the inner shell of the main body (1). Hydrogen peroxide disinfectant is stored in the liquid storage bottle (604). A liquid pump (605) is placed at the bottom of the liquid storage bottle (604). The liquid pump (605) is connected to one end of the disinfectant pipe (603). The other end of the disinfectant pipe (603) is connected to a sealing block (11). The sealing block (11) has the same inner diameter as the cleaning brush rod.

8. The perianal treatment device for honeycomb anal fistula according to claim 1, characterized in that: A connecting block (5) is installed at the bottom of the cleaning tube (6), and the other end of the connecting block (5) is connected to the suction tube (905) of the suction device (9). The suction device (9) is in the shape of a hollow cylinder. There are suction holes on the surface of the suction tube (905). The bottom end of the suction tube (905) is connected to the sealing block (11) at one end of the guide tube (904). The other end of the guide tube (904) is connected to the bottom of the liquid collecting tank (901). The top position of the liquid collecting tank (901) is connected to the air pipe (902), and the other end of the air pipe (902) is connected to the air pump (903).

9. The perianal treatment device for honeycomb anal fistula according to claim 8, characterized in that: The connecting block (5) is solid.

10. The perianal treatment device for honeycomb anal fistula according to claim 8, characterized in that: The liquid collecting tank (901) is installed on one side of the interior of the main body (1). The liquid collecting tank (901) is transparent and has scales on its surface. The side of the main body (1) corresponding to the liquid collecting tank (901) is transparent. The side of the main body (1) is cabinet-shaped. A slide rail and a card slot are provided inside the main body (1).

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