Protective application for high-exudation wound incision

By introducing drainage fluid collection system and antibacterial biological layer into the protective patch, the problem that existing patches cannot add drugs is solved, effective contact between drugs and wounds is achieved and healing is accelerated, the risk of infection is reduced, and the application is improved Practical and safe.

CN222130380UInactive Publication Date: 2024-12-10THE THIRD AFFILIATED HOSPITAL OF PLA NAVAL MEDICAL UNIVERSITY
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Patent Information

Application Number
CN202322777319.2
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2023-10-17
Publication Date
2024-12-10
Estimated Expiration
Not applicable · inactive patent

AI Technical Summary

Technical Problem

The existing protective patches used for minimally invasive facial surgery or after injection cannot add drugs to the patch, which affects the healing effect of the wound and limits its usefulness.

Method used

A protective patch including drainage fluid collection bags, drainage hoses, catheters and drainage fluid drain valves was designed to allow the addition of drugs to the inside of the patch, and ensure that the drugs only go to the wound through a one-way guide membrane and an antibacterial bioparticle layer. Flow to avoid bacterial growth.

Benefits of technology

Accelerating wound healing with medication assistance improves the practicality of the patch, and reduces the risk of wound infection through antibacterial biological particles, improving safety and healing rate.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model discloses a protective application for a high-exudation wound incision, which relates to the technical field of medical instruments and comprises a drainage liquid collecting bag, a catheter is arranged in the middle of the front of the drainage liquid collecting bag, a drainage liquid discharge valve is arranged in the middle of the catheter, and the drainage liquid collecting bag, a drainage hose, the catheter and the drainage liquid discharge valve are arranged. A traditional protective application can only protect a wound, the situation that the wound is infected due to the fact that the wound touches water and the wound recovery effect is affected is avoided, a drainage liquid discharging valve is opened, medicine is injected into a catheter, the medicine is injected into a drainage liquid collecting bag and flows into the bottom of a breathable waterproof outer film through a drainage hose, and the medicine makes contact with the wound; when the medicine is replaced, the drainage liquid discharge valve is opened, the medicine overflows through the catheter, and therefore the medicine is replaced, the structure is simple, use is more convenient, the wound healing rate is increased through assistance of the medicine, and the practicability of the device is improved.
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Description

Technical Field

[0001] The utility model relates to the technical field of medical devices, in particular to a protective dressing for high exudative wound incisions. Background Art

[0002] At present, facial minimally invasive surgery or injection beauty is widely used, so choosing a wound dressing that is beneficial to wound healing and disease recovery has become one of the important issues that the people and medical workers are increasingly concerned about. The physiological, psychological, and economic acceptance of the patient for the dressing is also very important. With the progress of society and the improvement of people's quality of life, patients' requirements for wound healing and comfort have also increased accordingly. However, postoperative wound compression generally uses traditional gauze compression to stop bleeding. In this way, although the operation of medical staff is simple and convenient, the patient's compression is prone to displacement or falling off, and there will be a series of situations that affect the effect of facial surgery and injections, such as uneven strength control.

[0003] For example, a medical dressing is proposed in publication number CN204636717U, which includes an absorbent pad and a sticky pad made of a sticky material; the sticky pad is arranged on the outer edge of the absorbent pad, and the absorbent pad is placed on the inner side thereof, and a plurality of tear strips are arranged on the sticky pad, and the plurality of tear strips can be detachably adhered to the sticky pad to form a separation structure for protecting the stickiness of the sticky pad. The medical dressing of the utility model is simple to use, and can effectively compress and stop bleeding, protect the wound surface, prevent infection, and promote healing after minimally invasive facial surgery or injection. At the same time, it has many advantages such as shape fitting, simple use, easy to carry, good breathability, and reliable efficacy.

[0004] However, in the implementation of relevant technologies, it was found that the above-mentioned medical dressings still have the following problems: the above-mentioned device can effectively compress and stop bleeding, protect the wound surface, prevent infection and promote healing after minimally invasive facial surgery or injection, but since it is impossible to add medicine to the inside of the dressing when using it on the wound, the healing effect of the wound is affected, resulting in a certain degree of limitation in the practicality of the device. Utility Model Content

[0005] The utility model proposes a protective dressing for high exudative wound incisions, which solves the problem in the related art that when the dressing is used on the wound, drugs cannot be added into the dressing, which affects the healing effect of the wound:

[0006] The technical solution of the utility model is as follows: a protective dressing for high exudative wound incisions, comprising a drainage fluid collection bag, a catheter is arranged in the middle of the front of the drainage fluid collection bag, a drainage fluid discharge valve is arranged in the middle of the catheter, a drainage hose is arranged inside the drainage fluid collection bag, the rear end of the catheter is connected to the drainage hose, and a breathable and waterproof outer film is arranged on the surface of the drainage fluid collection bag.

[0007] Preferably, a one-way liquid guide film is provided at the bottom of the drainage fluid collection bag, and a waterproof coating is sprayed on the surface of the one-way liquid guide film.

[0008] Preferably, a first antibacterial biological particle layer is provided at the bottom of the one-way liquid guide membrane. The first antibacterial biological particle layer is amoxicillin particles, which can kill bacteria by inhibiting the synthesis of cell walls.

[0009] Preferably, a first two-way flow guide membrane is disposed at the bottom of the first antibacterial biological particle layer, and a two-way channel is disposed inside the first two-way flow guide membrane to increase the flow rate of the fluid.

[0010] Preferably, a second antibacterial biological particle layer is disposed at the bottom of the first two-way flow-guiding membrane, and a second two-way flow-guiding membrane is disposed at the bottom of the second antibacterial biological particle layer.

[0011] Preferably, a skin self-adhesive edge is provided at the bottom of the second two-way flow guide membrane, and an antibacterial coating slip film is provided at the middle of the bottom end of the second two-way flow guide membrane.

[0012] Preferably, the thickness of the skin self-adhesive edge is higher than the thickness of the antibacterial coating synovial membrane, and the skin self-adhesive edge surrounds the outer side of the antibacterial coating synovial membrane.

[0013] Preferably, an adhesive paper is provided at the bottom of the second two-way flow-guiding membrane.

[0014] The working principle and beneficial effects of the utility model are:

[0015] 1. In this embodiment, a drainage fluid collection bag, a drainage hose, a catheter, and a drainage fluid discharge valve are provided. The traditional protective dressing can only protect the wound to prevent the wound from contacting water and causing wound infection, which affects the wound recovery effect. By opening the drainage fluid discharge valve, the drug is added to the catheter. The drug is added to the drainage fluid collection bag and flows through the drainage hose to the bottom of the breathable and waterproof outer membrane, so that the drug contacts the wound. When the drug is replaced, the drainage fluid discharge valve is opened, and the drug overflows through the catheter, thereby replacing the drug. The structure is simple and the use is more convenient. With the assistance of the drug, the healing rate of the wound is accelerated, and the practicality of the device is improved.

[0016] 2. In this embodiment, a unidirectional liquid guide membrane, a first antibacterial biological particle layer, a first bidirectional flow guide membrane, a second antibacterial biological particle layer, and a second bidirectional flow guide membrane are provided. The infused drugs will pass through the unidirectional liquid guide membrane respectively. Since the unidirectional liquid guide membrane can only conduct unidirectional flow, the drug liquid can only flow to the wound, so that the drug liquid contacts the wound, and the bacteria grown in the wound are mixed with the drug and retained in the first bidirectional flow guide membrane and the second bidirectional flow guide membrane. The first antibacterial biological particle layer is arranged in the middle of the unidirectional liquid guide membrane and the first bidirectional flow guide membrane, and the second antibacterial biological particle layer is located in the middle of the first bidirectional flow guide membrane and the second bidirectional flow guide membrane. The mixture of bacteria and drugs will be sterilized under the action of the first antibacterial biological particle layer and the second antibacterial biological particle layer, thereby avoiding bacterial growth, reducing wound infection, and improving the safety of the device. BRIEF DESCRIPTION OF THE DRAWINGS

[0017] The utility model is further described in detail below in conjunction with the accompanying drawings and specific implementation methods.

[0018] Figure 1 This is a schematic diagram of the overall structure of a protective dressing for high exudative wound incisions proposed by the utility model;

[0019] Figure 2 This is a schematic top view of the overall structure of a protective dressing for high exudative wound incisions proposed by the utility model;

[0020] Figure 3 This is a schematic cross-sectional view of the overall structure of a protective dressing for high exudative wound incisions proposed by the utility model;

[0021] Figure 4 This is an enlarged schematic diagram of the structure of location A of a protective dressing for high exudative wound incision proposed by the utility model;

[0022] In the figure: 1. drainage fluid collection bag; 2. drainage hose; 3. breathable and waterproof outer membrane; 4. unidirectional liquid guiding membrane; 5. catheter; 6. drainage fluid discharge valve; 7. first antibacterial biological particle layer; 8. first two-way guiding membrane; 9. second antibacterial biological particle layer; 10. second two-way guiding membrane; 11. skin self-adhesive edge; 12. antibacterial coated synovial membrane. DETAILED DESCRIPTION

[0023] The following will be combined with the embodiments of the utility model to clearly and completely describe the technical solutions in the embodiments of the utility model. Obviously, the described embodiments are only part of the embodiments of the utility model, not all of the embodiments. Based on the embodiments of the utility model, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the utility model.

[0024] See also Figure 1 and Figure 2 , a protective dressing for high exudation wound incision, comprising a drainage fluid collection bag 1, a catheter 5 is arranged in the middle of the front of the drainage fluid collection bag 1, a drainage fluid discharge valve 6 is arranged in the middle of the catheter 5, a drainage hose 2 is arranged inside the drainage fluid collection bag 1, the rear end of the catheter 5 is connected to the drainage hose 2, and the surface of the drainage fluid collection bag 1 is provided with a breathable and waterproof outer film 3. By providing the drainage fluid collection bag 1, the drainage hose 2, the catheter 5, and the drainage fluid discharge valve 6, the traditional protective dressing can only protect the wound to prevent the wound from contacting water and causing wound infection and affecting the wound recovery effect. By opening the drainage fluid discharge valve 6, the catheter 5 is filled with medicine, the medicine is filled into the drainage fluid collection bag 1, and flows into the bottom of the breathable and waterproof outer film 3 through the drainage hose 2, so that the medicine contacts the wound, and when the medicine is replaced, the drainage fluid discharge valve 6 is opened, and the medicine overflows through the catheter 5, thereby replacing the medicine. The structure is simple and the use is more convenient. With the assistance of the medicine, the healing rate of the wound is accelerated.

[0025] See also Figure 1 , Figure 3 and Figure 4 A unidirectional liquid guide film 4 is arranged at the bottom of the drainage fluid collection bag 1, and a waterproof coating is sprayed on the surface of the unidirectional liquid guide film 4. A first antibacterial biological particle layer 7 is arranged at the bottom of the unidirectional liquid guide film 4. The first antibacterial biological particle layer 7 is amoxicillin particles, which kill bacteria by inhibiting the synthesis of cell walls. A first two-way guide film 8 is arranged at the bottom of the first antibacterial biological particle layer 7. A two-way channel is arranged inside the first two-way guide film 8 to improve the circulation speed of the fluid. A second antibacterial biological particle layer 9 is arranged at the bottom of the first two-way guide film 8. A second two-way guide film 10 is arranged at the bottom of the second antibacterial biological particle layer 9. A skin self-adhesive edge 11 is arranged at the bottom of the second two-way guide film 10. An antibacterial layer slip film 12 is arranged at the middle of the bottom end of the second two-way guide film 10. The thickness of the skin self-adhesive edge 11 is higher than the thickness of the antibacterial layer slip film 12, and the skin self-adhesive edge 11 surrounds the antibacterial layer slip film. On the outside of the membrane 12, an adhesive paper is provided at the bottom of the second two-way guide membrane 10. By providing a unidirectional liquid guide membrane 4, a first antibacterial biological particle layer 7, a first two-way guide membrane 8, a second antibacterial biological particle layer 9, and a second two-way guide membrane 10, the infused medicine will pass through the unidirectional liquid guide membrane 4 respectively. Since the unidirectional liquid guide membrane 4 can only conduct unidirectional flow, the medicine liquid can only flow to the wound, so that the medicine liquid contacts the wound, and the bacteria grown in the wound are mixed with the medicine and retained in the first two-way guide membrane 8 and the second two-way guide membrane 10. The first antibacterial biological particle layer 7 is arranged in the middle of the unidirectional liquid guide membrane 4 and the first two-way guide membrane 8, and the second antibacterial biological particle layer 9 is located in the middle of the first two-way guide membrane 8 and the second two-way guide membrane 10. The mixture of bacteria and medicine will be sterilized under the action of the first antibacterial biological particle layer 7 and the second antibacterial biological particle layer 9, thereby avoiding bacterial growth and reducing wound infection.

[0026] The working principle and use process of this utility model:

[0027] When installing and using the protective dressing for high exudation wound incision, first clean the patient's wound and sterilize the wound, then tear off the adhesive paper, align the antibacterial coating synovial membrane 12 with the center of the wound, and adhere the skin self-adhesive edge 11 to the skin to prevent the wound from being exposed to the outside air and causing pollution. Traditional protective dressings can only protect the wound to prevent the wound from contacting water and causing wound infection and affecting the wound recovery effect. By opening the drainage fluid discharge valve 6, the drug is added to the catheter 5. The drug is filled into the drainage fluid collection bag 1 and flows into the bottom of the breathable and waterproof outer film 3 through the drainage hose 2, so that the drug contacts the wound. When the drug is replaced, the drainage fluid discharge valve 6 is opened, and the drug overflows through the catheter 5, thereby replacing the drug. The structure is simple. , it is more convenient to use. With the assistance of drugs, the healing rate of wounds is accelerated. The infused drugs will pass through the unidirectional liquid guide membrane 4 respectively. Since the unidirectional liquid guide membrane 4 can only conduct unidirectional flow, the drug solution can only flow to the wound, so that the drug solution contacts the wound, and the bacteria grown in the wound are mixed with the drugs and retained in the first two-way flow guide membrane 8 and the second two-way flow guide membrane 10. The first antibacterial biological particle layer 7 is arranged in the middle of the unidirectional liquid guide membrane 4 and the first two-way flow guide membrane 8, and the second antibacterial biological particle layer 9 is located in the middle of the first two-way flow guide membrane 8 and the second two-way flow guide membrane 10. The mixture of bacteria and drugs will be sterilized under the action of the first antibacterial biological particle layer 7 and the second antibacterial biological particle layer 9, so as to avoid bacterial growth, reduce wound infection, and improve the safety of the device.

[0028] The above description is only a preferred specific implementation method of the present utility model, and does not limit the protection scope of the present utility model. Therefore, all equivalent changes made based on the structure, shape, and principle of the present utility model should be included in the protection scope of the present utility model.

Claims

1. A protective dressing for a high exudative wound incision, comprising a drainage fluid collection bag (1), characterized in that: A catheter (5) is arranged in the middle of the front of the drainage fluid collection bag (1), a drainage fluid discharge valve (6) is arranged in the middle of the catheter (5), a drainage hose (2) is arranged inside the drainage fluid collection bag (1), the rear end of the catheter (5) is connected to the drainage hose (2), and a breathable and waterproof outer film (3) is arranged on the surface of the drainage fluid collection bag (1).

2. A protective dressing for high exudative wound incision according to claim 1, characterized in that: A one-way liquid guiding film (4) is provided at the bottom of the drainage fluid collection bag (1), and a waterproof coating is sprayed on the surface of the one-way liquid guiding film (4).

3. A protective dressing for high exudative wound incision according to claim 2, characterized in that: A first antibacterial biological particle layer (7) is arranged at the bottom of the one-way liquid guide membrane (4), and the first antibacterial biological particle layer (7) is amoxicillin particles, which play a role in killing bacteria by inhibiting the synthesis of cell walls.

4. A protective dressing for high exudative wound incision according to claim 3, characterized in that: A first two-way flow-guiding membrane (8) is arranged at the bottom of the first antibacterial biological particle layer (7), and a two-way channel is arranged inside the first two-way flow-guiding membrane (8) to increase the circulation speed of the fluid.

5. A protective dressing for high exudative wound incision according to claim 4, characterized in that: A second antibacterial biological particle layer (9) is arranged at the bottom of the first two-way flow-guiding membrane (8), and a second two-way flow-guiding membrane (10) is arranged at the bottom of the second antibacterial biological particle layer (9).

6. A protective dressing for high exudative wound incision according to claim 5, characterized in that: The bottom of the second two-way flow-guiding membrane (10) is provided with a skin self-adhesive edge (11), and the middle of the bottom end of the second two-way flow-guiding membrane (10) is provided with an antibacterial coating slip film (12).

7. A protective dressing for high exudative wound incision according to claim 6, characterized in that: The thickness of the skin self-adhesive edge (11) is greater than the thickness of the antibacterial coating slip film (12), and the skin self-adhesive edge (11) surrounds the outer side of the antibacterial coating slip film (12).

8. The protective dressing for high exudative wound incision according to claim 5, characterized in that: The bottom of the second two-way flow-guiding membrane (10) is provided with adhesive paper.