A semi-implantable IDDS wound dressing waterproof device

Abstract

The utility model discloses a kind of semi-implantable IDDS wound dressing waterproof devices, it is related to semi-implantable IDDS wound dressing waterproof technical field, and include: silica gel paste;Pressure regulating component, the pressure regulating component is wrapped in the inside of silica gel paste, and extend to the outside of silica gel paste;The utility model is blocked to the edge of silica gel paste by the setting of water-blocking turnup, avoid water to enter the inside of silica gel paste, can effectively prevent the transparent dressing hemming, water seepage, fall off covered at butterfly needle, prevent the occurrence of infection;Relied on the feature of silica gel paste self-adhesion is bonded on the skin of patient, and by the setting of pressure regulating component, form negative pressure between silica gel paste and patient skin, increase the firmness of silica gel paste after bonding, avoid patient when washing, mistake touch silica gel paste, cause silica gel paste to fall off, simultaneously, pressure regulating component can also adjust the negative pressure between silica gel paste and patient skin, so that silica gel paste can be normally disassembled and cleaned and used again.

Description

Technical Field

[0001] This utility model relates to the field of waterproof semi-implantable IDDS wound dressing technology, and in particular to a waterproof semi-implantable IDDS wound dressing device. Background Technology

[0002] 10% to 20% of cancer patients develop refractory cancers, severely impacting their quality of life. When oral analgesia is ineffective, the NCCN Cancer Pain Guidelines recommend intrathecal drug delivery systems (IDDS) for pain relief. An IDDS consists of an infusion pump and a connecting thin catheter. The infusion pump delivers medication directly into the cerebrospinal fluid surrounding the brain and spinal cord, bypassing the blood-brain barrier to deliver drugs to the central nervous system. IDDS are available in fully implantable and semi-implantable versions. Due to the high cost of fully implantable devices, they are not currently covered by medical insurance; therefore, semi-implantable devices are more common in clinical practice.

[0003] A semi-implantable IDDS consists of an implantable infusion port, a catheter, and ancillary devices[4]. The infusion port of a semi-implantable IDDS is usually located in the lower left or lower right abdomen of the patient. Then, a butterfly needle is inserted into the infusion port placed in the lower left or lower right abdomen of the patient, the catheter is connected, analgesic drugs are pumped in, and finally, sterile gauze and transparent dressing are used to cover the port to keep it clean and dry and prevent infection.

[0004] Although the patient's abdomen was covered with a waterproof transparent dressing, the dressing was prone to curling, seeping water, and falling off during the bath, which could lead to redness and inflammation of the skin around the puncture site, and in severe cases, intracranial infection. Utility Model Content

[0005] This invention provides a semi-implantable IDDS waterproof wound dressing device to solve the problem in the prior art where, although the abdomen is covered with a waterproof transparent dressing, the transparent dressing is prone to curling, seepage, and falling off during the patient's bathing process, which can lead to redness and inflammation of the skin around the puncture site, and in severe cases, intracranial infection.

[0006] The technical problem solved by this utility model is achieved by the following technical solution:

[0007] A semi-implantable IDDS waterproof wound dressing device includes:

[0008] Silicone stickers;

[0009] A voltage regulating component, which is enclosed inside a silicone pad and extends to the outside of the silicone pad;

[0010] Water-resistant flange, which is bonded to the outer edge of the silicone sticker.

[0011] Optionally, the outer center of the silicone patch is provided with a binding sleeve, the binding sleeve is provided with a blocking edge away from the opening of the silicone patch, and the center of the silicone patch is provided with a through hole communicating with the voltage regulating component.

[0012] Optionally, the voltage regulating component includes:

[0013] The outer casing, which is wrapped inside the edge binding sleeve;

[0014] The first sealing ring is bonded to the outer side of the outer shell and contacts the inner surface of the edge sleeve;

[0015] Two baffles are provided and fixed to the openings at both ends of the outer casing, respectively;

[0016] A sliding assembly, which is installed inside the housing.

[0017] Optionally, the sliding component includes:

[0018] A sliding plate, which is slidably mounted inside the housing;

[0019] The second sealing ring is bonded to the outside of the sliding plate and contacts the inner surface of the housing;

[0020] An extension rod, which is fixed to the sliding plate and passes through the blocking plate;

[0021] A control button is fixed at the end of the extension rod away from the sliding plate.

[0022] Optionally, a compression spring is installed between the sliding plate and the blocking plate, and the compression spring is compressed and stores force when the sliding plate slides.

[0023] Optionally, the water-blocking flange includes:

[0024] A water-blocking strip is disposed at the outer edge of the pressure regulating assembly;

[0025] An adhesive pad, wherein the two sides of the adhesive pad are respectively bonded to a water-blocking strip and a silicone sticker.

[0026] Optionally, the silicone sticker is a pure silicone product with high self-adhesion.

[0027] The beneficial effects of this utility model are:

[0028] By using a water-resistant, rolled-up edge design to block water from entering the silicone patch, the transparent dressing covering the butterfly needle area can be effectively prevented from curling, seeping, or falling off, thus preventing infection.

[0029] Relying on the self-adhesive properties of silicone patches, they adhere to the patient's skin. The pressure regulating component creates negative pressure between the silicone patch and the patient's skin, increasing the patch's adhesion and preventing accidental contact during cleaning, which could cause the patch to fall off. The pressure regulating component also adjusts the negative pressure between the silicone patch and the patient's skin, allowing the patch to be easily removed, cleaned, and reused. Attached Figure Description

[0030] To more clearly illustrate the technical solutions in the embodiments of this utility model or the prior art, the drawings used in the description of the embodiments or the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this utility model. For those skilled in the art, other drawings can be obtained from these drawings without creative effort.

[0031] Figure 1 This is a schematic diagram of the structure of this utility model;

[0032] Figure 2 This is a schematic diagram of the internal structure of the outer shell of this utility model;

[0033] Figure 3 This utility model Figure 2 Enlarged schematic diagram of the structure at point A in the middle;

[0034] Figure 4 This utility model Figure 2 Enlarged schematic diagram of the structure at point B;

[0035] Figure 5 This is a schematic diagram of the silicone sticker structure of this utility model.

[0036] In the diagram: 100, silicone sticker; 110, edge banding; 120, blocking edge; 130, through hole;

[0037] 200, Pressure regulating assembly; 210, Housing; 220, First sealing ring; 230, Baffle plate; 240, Sliding assembly; 241, Sliding plate; 242, Second sealing ring; 243, Extension rod; 244, Control button; 250, Compression spring;

[0038] 300, Water-blocking flange; 310, Water-blocking strip; 320, Adhesive pad. Detailed Implementation

[0039] To make the technical means, creative features, objectives and effects of this utility model easier to understand, the following description, in conjunction with specific illustrations, further elaborates on this utility model.

[0040] Reference Figure 1-5 The semi-implantable IDDS waterproof wound dressing device shown includes:

[0041] Silicone sticker 100;

[0042] The voltage regulating component 200 is wrapped inside the silicone pad 100 and extends to the outside of the silicone pad 100;

[0043] Water-resistant flange 300 is bonded to the outer edge of silicone sticker 100.

[0044] In use, firstly, the water-blocking flange 300 is bonded to the outer edge of the pressure regulating component 200. Then, the pressure regulating component 200 is squeezed to compress and store force. The silicone patch 100 is then placed over the outside of the semi-implantable IDDS and the transparent dressing. Finally, the force on the pressure regulating component 200 is released, and the stress on the pressure regulating component 200 is released, creating negative pressure by drawing air out between the silicone patch 100 and the patient's skin.

[0045] During disassembly, press the pressure regulating component 200 to store force and restore the air pressure between the silicone patch 100 and the patient's skin to atmospheric pressure. Then, remove the silicone patch 100 from the semi-implantable IDDS and transparent dressing.

[0046] The silicone patch 100 adheres to the patient's skin due to its self-adhesive properties. The pressure regulating component 200 creates negative pressure between the silicone patch 100 and the patient's skin, increasing the adhesion of the silicone patch 100 and preventing the patient from accidentally touching it during cleaning, which could cause the silicone patch 100 to fall off. At the same time, the pressure regulating component 200 can also adjust the negative pressure between the silicone patch 100 and the patient's skin, allowing the silicone patch 100 to be easily removed, cleaned, and reused.

[0047] The water-resistant flange 300 blocks water from entering the silicone patch 100, effectively preventing the transparent dressing covering the butterfly needle from curling, seeping, or falling off, thus preventing infection.

[0048] In some embodiments of this utility model, in order to ensure the proper installation of the voltage regulating component 200, refer to Figure 5 As shown, a binding sleeve 110 is provided at the center of the outer side of the silicone patch 100, and a blocking edge 120 is provided at the opening of the binding sleeve 110 away from the silicone patch 100. A through hole 130 communicating with the pressure regulating component 200 is provided at the center of the silicone patch 100.

[0049] When installing the pressure regulating component 200, the blocking edge 120 is opened and the pressure regulating component 200 is installed inside the edge sleeve 110, so that the pressure regulating component 200 corresponds to the through hole 130.

[0050] The edging sleeve 110 and the blocking edge 120 provide space for the installation of the pressure regulating assembly 200.

[0051] The through-hole 130 allows the pressure regulating component 200 to properly extract air between the silicone patch 100 and the patient's skin.

[0052] In some embodiments of this utility model, in order to maintain a seal with the edge-sealing sleeve 110, refer to Figure 2 and Figure 3 As shown, the voltage regulating assembly 200 includes:

[0053] The outer casing 210 is enclosed inside the binding sleeve 110;

[0054] The first sealing ring 220 is bonded to the outer side of the outer shell 210 and contacts the inner surface of the edge sleeve 110;

[0055] There are two baffle plates 230, which are detachably fixed to the openings at both ends of the housing 210, and the baffle plates 230 are circular.

[0056] Sliding assembly 240 is installed inside housing 210.

[0057] In use, pressure is first applied to the sliding component 240 to make it slide and compress the energy storage structure, simultaneously expelling air from inside the outer shell 210. After the silicone patch 100 is applied to the skin, the pressure on the sliding component 240 is released, and the energy storage structure pushes the sliding component 240 back to its original position, extracting air from between the silicone patch 100 and the skin. For removal, the sliding component 240 is squeezed again to push the air from inside the outer shell 210 into the space between the silicone patch 100 and the skin.

[0058] The outer shell 210 supports the edge banding 110 and provides space for the sliding component 240 to slide.

[0059] The first sealing ring 220 ensures the airtightness between the outer shell 210 and the edge sleeve 110, preventing gas from entering or leaking from the connection between the outer shell 210 and the edge sleeve 110.

[0060] Specifically, the sliding component 240 is blocked by the blocking plate 230, thereby limiting the sliding range of the sliding component 240.

[0061] In some embodiments of this utility model, in order to adjust the air pressure between the silicone patch 100 and the skin, refer to Figure 2 and Figure 3 As shown, the sliding component 240 includes:

[0062] Sliding plate 241 is slidably installed inside housing 210;

[0063] The second sealing ring 242 is bonded to the outside of the sliding plate 241 and contacts the inner surface of the housing 210.

[0064] Extension rod 243 is fixed on sliding plate 241 and passes through blocking plate 230;

[0065] Control button 244 is fixed to the end of extension rod 243 away from sliding plate 241.

[0066] In this process, the air between the silicone patch 100 and the skin is extracted by sliding the sliding plate 241, which will push the air into the space between the silicone patch 100 and the skin.

[0067] The second sealing ring 242 is used to seal the sliding plate 241 and the outer shell 210, preventing gas leakage or entry when the sliding plate 241 slides.

[0068] The extension rod 243 and the control button 244 work together to enable the sliding plate 241 to slide under external pressure, thus realizing the function of the sliding plate 241.

[0069] In some embodiments of this utility model, in order to push the sliding plate 241 to reset, refer to Figure 2 and Figure 3 As shown, a compression spring 250 is installed between the sliding plate 241 and the blocking plate 230. The compression spring 250 is compressed and stores force when the sliding plate 241 slides.

[0070] The spring 250 is compressed and stores force when the sliding plate 241 slides, and pushes the sliding plate 241 to reset after the squeezing force on the control button 244 disappears.

[0071] In some embodiments of this invention, to further prevent water from entering, refer to Figure 2 and Figure 4 As shown, the water-blocking flange 300 includes:

[0072] Water-blocking strip 310 is disposed at the outer edge of pressure regulating component 200;

[0073] Adhesive pad 320, with its two sides respectively bonded to water-blocking strip 310 and silicone sticker 100.

[0074] The adhesive pad 320 ensures the proper installation and use of the water-blocking strip 310 and provides initial water-blocking protection.

[0075] In some embodiments of this utility model, reference is made to Figure 1 As shown, silicone sticker 100 is a pure silicone product with high self-adhesion.

[0076] Among them, the silicone patch 100 can adhere to the patient's skin by its own effect, ensuring stability while also playing a role in preventing water.

[0077] The working method of this utility model:

[0078] In use, first, attach the water-blocking strip 310 to the outer edge of the silicone patch 100 via the adhesive pad 320. Then, squeeze the control button 244 to push the sliding plate 241 to slide and expel the air inside the outer shell 210, and squeeze the compression spring 250 to compress and store force. Then, cover the outside of the semi-implantable IDDS and transparent dressing with the silicone patch 100. Then, release the pressure on the control button 244, and the elastic force of the compression spring 250 will be released, pushing the sliding plate 241 to reset and drawing out the air between the silicone patch 100 and the patient's skin to form a negative pressure.

[0079] During disassembly, press the control button 244 to push the sliding plate 241 to slide, pushing the air inside the outer shell 210 into the space between the silicone patch 100 and the patient's skin. Then, remove the silicone patch 100.

[0080] The foregoing has shown and described the basic principles, main features, and advantages of this utility model. Those skilled in the art should understand that this utility model is not limited to the above embodiments. The embodiments and descriptions in the specification are merely illustrative of the principles of this utility model. Various changes and modifications can be made to this utility model without departing from its spirit and scope, and all such changes and modifications fall within the scope of the claims. The scope of protection of this utility model is defined by the appended claims and their equivalents.

Claims

1. A semi-implantable IDDS waterproof wound dressing device, characterized in that, include: Silicone sticker (100); A voltage regulating assembly (200) is wrapped inside the silicone pad (100) and extends to the outside of the silicone pad (100); Water-blocking flange (300) is bonded to the outer edge of silicone sticker (100).

2. The semi-implantable IDDS waterproof wound dressing device according to claim 1, characterized in that: The outer center of the silicone patch (100) is provided with a binding sleeve (110), and the binding sleeve (110) is provided with a blocking edge (120) away from the opening of the silicone patch (100). The center of the silicone patch (100) is provided with a through hole (130) communicating with the voltage regulating component (200).

3. The semi-implantable IDDS waterproof wound dressing device according to claim 2, characterized in that: The voltage regulating assembly (200) includes: The outer shell (210) is enclosed inside the edging sleeve (110); The first sealing ring (220) is bonded to the outside of the outer shell (210) and contacts the inner surface of the edge sleeve (110); Two baffle plates (230) are provided and are respectively fixed at the openings at both ends of the outer casing (210); A sliding assembly (240) is mounted inside a housing (210).

4. The semi-implantable IDDS waterproof wound dressing device according to claim 3, characterized in that: The sliding component (240) includes: A sliding plate (241) is slidably mounted inside the housing (210); The second sealing ring (242) is bonded to the outside of the sliding plate (241) and contacts the inner surface of the housing (210); An extension rod (243) is fixed to a sliding plate (241) and passes through a baffle plate (230); A control button (244) is fixed to the end of the extension rod (243) away from the sliding plate (241).

5. A semi-implantable IDDS waterproof wound dressing device according to claim 4, characterized in that: A compression spring (250) is installed between the sliding plate (241) and the blocking plate (230), and the compression spring (250) is compressed and stores force when the sliding plate (241) slides.

6. The semi-implantable IDDS waterproof wound dressing device according to claim 1, characterized in that: The water-blocking flange (300) includes: A water-blocking strip (310) is disposed at the outer edge of the pressure regulating assembly (200); An adhesive pad (320) is bonded to a water-blocking strip (310) and a silicone sticker (100) on both sides, respectively.

7. The semi-implantable IDDS waterproof wound dressing device according to claim 1, characterized in that: The silicone sticker (100) is a pure silicone product with high self-adhesion.

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