Radio frequency postoperative inguinal artery and vein wound compression device

By designing a radiofrequency postoperative arteriovenous wound compression device using adhesive bonding and adjusting structure, the problem of skin damage and reduced use effect caused by strap fixation in the prior art is solved, and a higher compression effect and use comfort is achieved.

CN222899213UActive Publication Date: 2025-05-27ZHEJIANG UNIV
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Patent Information

Application Number
CN202421763030.3
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-07-24
Publication Date
2025-05-27
Estimated Expiration
2034-07-24

AI Technical Summary

Technical Problem

The existing inguinal arteriovenous wound compression device after radiofrequency surgery needs to be fixed to the patient's body through a strap, resulting in poor comfort in the patient, prone to strangulation, damage to the skin, and reduce the effectiveness of use.

Method used

A compression device for inguinal arteriovenous wounds after radiofrequency surgery is designed, using a buffer layer and the compression piece body as an integrated structure. The bottom of the buffer layer is coated with adhesive, which is tightly fixed with the patient's skin through the adhesive to reduce damage to the skin, and the compression degree adjustment of the compression block is achieved through the adjustment structure.

Benefits of technology

The device is tightly fixed by adhesive, which reduces damage to the patient's skin, avoids discomfort caused by strap fixation, and improves the compression effect and comfort of use.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model discloses a radio frequency postoperative inguinal artery and vein wound compression device which comprises a compression piece body and a buffer layer arranged on the inner side of the compression piece body. A protective layer is arranged on the lower surface of the buffer layer, fixing grooves are formed in the buffer layer and the compression part body, and compression blocks are arranged on the inner sides of the fixing grooves; the inner side of the fixing groove is further provided with an adjusting structure capable of adjusting the pressing degree of the pressing block, and the adjusting structure comprises a connecting block. The upper surface of the compression part body is provided with a protective sleeve, and the bottom of the protective sleeve is connected with a non-stick block. According to the radio frequency postoperative inguinal artery and vein wound compression device, the connecting screw rod is in threaded connection with the protective sleeve, and the connecting screw rod is in threaded connection with the pushing block, so that when the connecting screw rod rotates, the pushing block is driven to move, the purpose of adjusting the compression force of the compression block can be achieved, and different compression requirements can be better met.
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Description

Technical Field

[0001] The utility model relates to the technical field of wound compression, in particular to a wound compression device for the groin arteriovenous after radiofrequency surgery. Background Technique

[0002] Radiofrequency technique is a technology that uses radiofrequency energy to generate heat for treating diseases or achieving other medical purposes. It is commonly used in fields such as neurointerventional therapy, tumor therapy, cardiac electrophysiology, etc. And the wound compression device for the groin arteriovenous after radiofrequency surgery is a device used to compress the surgical site, helping to reduce bleeding and relieve pain.

[0003] For example, the publication number is CN213940848U, which discloses a postoperative wound compression device, including: a strap main body, the bandage main body is wound and fixed around the hip joint of the human body; a compression bag, the compression bag is arranged on the strap main body corresponding to the postoperative wound position; a compression adjustment component, the compression adjustment component passes through the compression bag and performs compression treatment on the wound position. The utility model provides a postoperative wound compression device with convenient fixation, convenient operation, not easy to slip, the sandbag is not easy to fall or shift, so that the patient has no worry about the sandbag falling when translating or moving in bed, which is convenient for medical staff to observe, and can be applicable to patients of different body types;

[0004] However, there are still some deficiencies in the above-mentioned compression device during use. For example, it is necessary to fix the device to the patient's body through a strap, so that the patient's comfort is poor, and obvious indentations will appear, causing damage to the patient's skin, thereby reducing the use effect of the compression device. Therefore, we propose a wound compression device for the groin arteriovenous after radiofrequency surgery to solve the problems raised above. Content of the Utility Model

[0005] The purpose of the utility model is to provide a wound compression device for the groin arteriovenous after radiofrequency surgery to solve the problem that the current compression devices on the market need to fix the device to the patient's body through a strap, so that the patient's comfort is poor, and obvious indentations will appear, causing damage to the patient's skin, thereby reducing the use effect of the compression device as mentioned in the above background technique.

[0006] To achieve the above purpose, the utility model provides the following technical solution: A wound compression device for the groin arteriovenous after radiofrequency surgery, including a compression member body and a buffer layer arranged inside the compression member body;

[0007] It further includes:

[0008] A protective layer is arranged on the lower surface of the buffer layer, and fixing grooves are opened inside both the buffer layer and the compression member body, and compression blocks are arranged inside the fixing grooves;

[0009] An adjusting structure for adjusting the pressing degree of the pressing block is further provided inside the fixing groove, and the adjusting structure includes a connecting block;

[0010] A protective sleeve is installed on the upper surface of the pressing member body, and a non-sticking block is connected to the bottom of the protective layer.

[0011] Preferably, the buffer layer and the pressing member body are of an integral structure, the buffer layer is made of silica gel, and an adhesive is coated on the bottom surface of the buffer layer.

[0012] Preferably, the protective layer and the buffer layer are adhesively connected, the protective layer is release paper, and the protective layer and the non-sticking block are of an integral structure.

[0013] Preferably, the connecting block is arranged inside the fixing groove, a sealing block is installed on the outer surface of the connecting block, and the top of the connecting block is connected to the pushing block.

[0014] Preferably, the sealing block and the connecting block are adhesively connected, the sealing block is made of rubber, and the sealing block is slidably connected to the inner wall of the fixing groove.

[0015] Preferably, a connecting screw is arranged inside the protective sleeve, and a rotating block is installed at the top of the connecting screw.

[0016] Preferably, the connecting screw is in threaded connection with the protective sleeve, and the connecting screw is in threaded connection with the pushing block.

[0017] Compared with the prior art, the beneficial effects of the present utility model are as follows: for this radiofrequency postoperative groin arteriovenous wound compression device, through the adhesive provided at the bottom of the buffer layer, the patient's skin can be tightly fixed, without the need for fixation by a bandage, reducing damage to the patient's skin, as shown in the following content:

[0018] (1) The buffer layer and the pressing member body are of an integral structure, the buffer layer is made of silica gel, and an adhesive is coated on the bottom surface of the buffer layer, which can make the connection between the buffer layer and the pressing member body more firm, and at the same time can be tightly fixed to the patient's skin through the adhesive;

[0019] Furthermore, the protective layer and the buffer layer are adhesively connected, the protective layer is release paper, and the protective layer and the non-sticking block are of an integral structure, which can protect the buffer layer through the protective layer, and under the action of the non-sticking block, it is convenient to tear the protective layer;

[0020] Furthermore, the connecting block is arranged inside the fixing groove, a sealing block is installed on the outer surface of the connecting block, and the top of the connecting block is connected to the pushing block, so that when the pushing block moves, it will drive the connecting block to move together;

[0021] Furthermore, the sealing block and the connecting block are adhesively connected. The sealing block is made of rubber, and the sealing block is slidably connected to the inner wall of the fixing groove. When the connecting block moves, it will drive the sealing block to move together. The setting of the sealing block can make the connecting block move more smoothly, thus enabling the pushing block to move stably.

[0022] (2) The connecting screw and the protective sleeve are threadedly connected, and the connecting screw and the pushing block are threadedly connected. In this way, when the connecting screw rotates, it will drive the pushing block to move, so as to achieve the purpose of adjusting the pressing force of the pressing block and better adapt to different pressing needs. Description of the Drawings

[0023] Figure 1 It is a schematic top view structure diagram of the whole utility model;

[0024] Figure 2 It is a schematic bottom view structure diagram of the pressing block of the utility model;

[0025] Figure 3 It is a schematic front sectional structure diagram of the whole utility model;

[0026] Figure 4 It is a schematic connection structure diagram of the pressing member body and the pressing block of the utility model;

[0027] Figure 5 It is a schematic structure diagram of the whole utility model;

[0028] Figure 6 It is a schematic connection structure diagram of the connecting block and the sealing block of the utility model.

[0029] In the figure: 1. Pressing member body; 2. Buffer layer; 3. Protective layer; 4. Fixing groove; 5. Pressing block; 6. Connecting block; 7. Sealing block; 8. Pushing block; 9. Protective sleeve; 10. Connecting screw; 11. Rotating block; 12. Non-stick block. Detailed Embodiment

[0030] Next, the technical solutions in the embodiments of the present utility model will be clearly and completely described in conjunction with the accompanying drawings in the embodiments of the present utility model. Obviously, the described embodiments are only a part of the embodiments of the present utility model, rather than all the embodiments. Based on the embodiments of the present utility model, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present utility model.

[0031] Embodiment 1:

[0032] In this embodiment, it is disclosed that by pressing the whole pressing member body 1, the pressing member body 1 presses the buffer layer 2, so that the buffer layer 2 is tightly fixed to the skin. Specifically, as Figure 2 and Figure 4 shown:

[0033] A protective layer 3 is arranged on the lower surface of the buffer layer 2. Fixing grooves 4 are formed inside both the buffer layer 2 and the pressing member body 1, and pressing blocks 5 are arranged inside the fixing grooves 4. A non-sticking block 12 is connected to the bottom of the protective layer 3;

[0034] The buffer layer 2 and the pressing member body 1 are of an integral structure. The buffer layer 2 is made of silica gel, and an adhesive is coated on the bottom surface of the buffer layer 2. The protective layer 3 and the buffer layer 2 are adhesively connected, and the protective layer 3 is release paper. The protective layer 3 and the non-sticking block 12 are of an integral structure;

[0035] A protective sleeve 9 is installed on the upper surface of the pressing member body 1;

[0036] When using this radiofrequency postoperative groin arteriovenous wound compression device, since a buffer layer 2 is arranged inside the pressing member body 1, an adhesive is coated on the bottom surface of the buffer layer 2, and the protective layer 3 and the buffer layer 2 are adhesively connected, and a non-sticking block 12 is arranged at the bottom of the protective layer 3, when it is necessary to compress the patient's wound, the non-sticking block 12 can be pulled to tear the protective layer 3, so that the surface of the buffer layer 2 coated with the adhesive is exposed. Since a pressing block 5 is arranged at the middle position of the buffer layer 2, the pressing block 5 can be aligned with the affected area, and then the whole pressing member body 1 is pressed, so that the pressing member body 1 presses the buffer layer 2, so that the buffer layer 2 is tightly fixed to the skin, and the pressing block 5 compresses the wound, achieving the effect of hemostasis.

[0037] Embodiment Two:

[0038] In this embodiment, it is disclosed that when the connecting screw 10 rotates and extends in, it will drive the pushing block 8 to move together. Since the pushing block 8 and the connecting block 6 are connected to each other, when the pushing block 8 moves, it will drive the connecting block 6 to move. Specifically, as Figure 1 , Figure 3 and Figure 5 shown:

[0039] An adjusting structure for adjusting the pressing degree of the pressing block 5 is further arranged inside the fixing groove 4, and the adjusting structure includes a connecting block 6;

[0040] The connecting block 6 is arranged inside the fixing groove 4. A sealing block 7 is installed on the outer surface of the connecting block 6, and the top of the connecting block 6 is connected to the pushing block 8;

[0041] On the inner side of the protective sleeve 9, a connecting screw rod 10 is provided, and a rotating block 11 is installed at the top end of the connecting screw rod 10. The connecting screw rod 10 and the protective sleeve 9 are in threaded connection, and the connecting screw rod 10 and the pushing block 8 are in threaded connection;

[0042] When it is necessary to increase the pressing force on the wound, the rotating block 11 can be rotated. The rotating block 11 is fixed at the top end of the connecting screw rod 10. Therefore, when the rotating block 11 rotates, it will drive the connecting screw rod 10 to rotate together. Since the connecting screw rod 10 and the protective sleeve 9 are in threaded connection, when the protective sleeve 9 is fixed, the connecting screw rod 10 will gradually extend into the protective sleeve 9 when it rotates. Moreover, the connecting screw rod 10 and the pushing block 8 are in threaded connection. Therefore, when the connecting screw rod 10 rotates and extends, it will drive the pushing block 8 to move together. The pushing block 8 and the connecting block 6 are connected to each other. Therefore, when the pushing block 8 moves, it will drive the connecting block 6 to move, causing the connecting block 6 to descend.

[0043] Embodiment 3:

[0044] In this embodiment, it is disclosed that the descent of the connecting block 6 will squeeze the pressing block 5, thereby increasing the pressing force of the pressing block 5 on the wound and improving the pressing effect. Specifically, as Figure 6 shown:

[0045] The sealing block 7 and the connecting block 6 are adhesively connected. The sealing block 7 is made of rubber material, and the sealing block 7 and the inner wall of the fixing groove 4 are in sliding connection;

[0046] A sealing block 7 is provided on the outer surface of the connecting block 6. The sealing block 7 is made of rubber material, and the sealing block 7 and the inner wall of the fixing groove 4 are in sliding connection. Therefore, when the connecting block 6 descends, it will drive the sealing block 7 to descend together, causing the sealing block 7 to slide downward along the inner wall of the fixing groove 4. Under the action of the sealing block 7, the connecting block 6 will move more smoothly. The descent of the connecting block 6 will squeeze the pressing block 5, thereby increasing the pressing force of the pressing block 5 on the wound and improving the pressing effect, improving the use effect of the pressing device. Moreover, the pasting method is more convenient, reducing the damage to the patient's skin. The above is the working process of the entire device. The content not described in detail in this specification belongs to the prior art well-known to those skilled in the art.

[0047] Although the present invention has been described in detail with reference to the foregoing embodiments, for those skilled in the art, they can still modify the technical solutions described in the foregoing embodiments, or perform equivalent replacements for some of the technical features. Any modifications, equivalent replacements, improvements, etc. made within the spirit and principle of the present invention shall be included in the protection scope of the present invention.

Claims

1. A post-operative radiofrequency inguinal artery and vein wound compression device, comprising a compression member body (1) and a buffer layer (2) arranged on the inner side of the compression member body (1); It is characterized in that Also includes: A protective layer (3) is provided on the lower surface of the buffer layer (2), a fixing groove (4) is provided inside the buffer layer (2) and the compression member body (1), and a compression block (5) is provided inside the fixing groove (4); An adjusting structure capable of adjusting the compression degree of the pressing block (5) is also provided on the inner side of the fixing groove (4), and the adjusting structure includes a connecting block (6); A protective sleeve (9) is installed on the upper surface of the compression member body (1), and a non-stick block (12) is connected to the bottom of the protective layer (3).

2. A radiofrequency postoperative inguinal arteriovenous wound compression device according to claim 1, characterized in that: The buffer layer (2) and the compression member body (1) are of an integrated structure, the buffer layer (2) is made of silicone material, and the bottom surface of the buffer layer (2) is coated with adhesive.

3. The radiofrequency postoperative inguinal arteriovenous wound compression device according to claim 1, characterized in that: The protective layer (3) and the buffer layer (2) are bonded together, the protective layer (3) is release paper, and the protective layer (3) and the non-stick block (12) are an integrated structure.

4. The radiofrequency postoperative inguinal arteriovenous wound compression device according to claim 1, characterized in that: The connecting block (6) is arranged on the inner side of the fixing groove (4), a sealing block (7) is installed on the outer surface of the connecting block (6), and the top of the connecting block (6) is connected to the pushing block (8).

5. The radiofrequency postoperative inguinal arteriovenous wound compression device according to claim 4, characterized in that: The sealing block (7) and the connecting block (6) are bonded together, the sealing block (7) is made of rubber, and the sealing block (7) and the inner wall of the fixing groove (4) are slidably connected.

6. The radiofrequency postoperative inguinal artery and vein wound compression device according to claim 1, characterized in that: A connecting screw (10) is arranged on the inner side of the protective sleeve (9), and a rotating block (11) is installed on the top end of the connecting screw (10).

7. A radiofrequency postoperative inguinal arteriovenous wound compression device according to claim 6, characterized in that: The connecting screw rod (10) and the protective sleeve (9) are connected by threads, and the connecting screw rod (10) and the pushing block (8) are connected by threads.

Citation Information

Patent Citations

  • Postoperative wound compression device

    CN213940848U