Special dressing for breast shaping

Abstract

The utility model relates to a special dressing for breast shaping, which belongs to the field of medical instruments and comprises a base layer, avoidance holes are arranged on the base layer, a contact layer is arranged on one side of the base layer and comprises a plurality of water-ripple-shaped strips which are uniformly arranged, a groove is arranged between every two adjacent strips, and the grooves are communicated with the avoidance holes. A medicine area is arranged on the periphery of the receding hole in the side where the contact layer is located. The utility model has the beneficial effects that traction force or pressure is generated on the skin through the dressing, the skin of the epidermal layer is pulled up or wrinkles are formed, the subcutaneous tissue gap can be enlarged, the grooves are formed between the strips, pressure difference can be formed, subcutaneous blood and lymph backflow can be promoted, and the avoiding holes can prevent nipples from being pressed, prevent nipples from necrosis and accelerate healing; the edema is relieved.

Description

Technical Field

[0001] This utility model relates to medical devices, specifically a dressing for breast augmentation. Background Art

[0002] With the increasing popularity of breast augmentation surgery, the nipple is often in a period of ischemia and remodeling after the surgery. The pressure during bandaging can affect the blood supply and shape of the nipple, which can seriously affect the surgical outcome. Therefore, postoperative bandaging and care are particularly important.

[0003] Currently, after breast augmentation surgery, the dressing for the areola incision is made by manually cutting ordinary sterile gauze and securing it with regular adhesive tape. This method has poor breathability, easily causing skin allergies, itching, and discomfort. It is inconvenient to use, provides a poor patient experience, and puts significant pressure on the nipple, hindering postoperative recovery. Utility Model Content

[0004] The technical problem to be solved by this utility model is to provide a dressing specifically for breast augmentation.

[0005] The technical solution of this utility model to solve the above-mentioned technical problems is as follows: A special dressing for breast augmentation includes a base layer, on which clearance holes are provided, and a contact layer is provided on one side of the base layer. The contact layer is a plurality of evenly arranged water ripple-shaped strips, with a groove between two adjacent strips. A drug area is provided around the clearance holes on the side where the contact layer is located.

[0006] The beneficial effects of this invention are: by applying traction or pressure to the skin through the dressing, the epidermis is pulled up or wrinkled, which can increase the interstitial space. Furthermore, the grooves between the strips can create a pressure difference, promoting blood and lymph return from the subcutaneous tissue. The avoidance holes prevent compression of the nipple, thus preventing nipple necrosis, accelerating healing, and reducing edema.

[0007] Based on the above technical solution, the present invention can be further improved as follows.

[0008] Furthermore, each of the strips is provided with adhesive.

[0009] The beneficial effect of adopting the above-mentioned further solutions is that it enables the dressing to adhere stably to human skin.

[0010] Furthermore, the adhesive is medical-grade acrylic adhesive.

[0011] The beneficial effects of adopting the above-mentioned further solutions are: medical acrylic adhesive has strong adhesion, good durability and no irritation.

[0012] Furthermore, an outer film is provided on the side of the base layer opposite to the contact layer.

[0013] The beneficial effect of adopting the above-mentioned further solution is that the outer film is used to protect the outer side of the base layer.

[0014] Furthermore, the outer film is made of a breathable and waterproof material.

[0015] The beneficial effects of adopting the above-mentioned further solution are: the outer film prevents external water splashes from contaminating the dressing, and also prevents the drug from seeping out from the inside of the dressing.

[0016] Furthermore, the base layer is an absorbent foam pad.

[0017] The beneficial effects of adopting the above-mentioned further solutions are: the base layer has strong water absorption and can absorb the medicine, body fluid and tissue fluid that seep out from the dressing.

[0018] Furthermore, the radius of the clearance hole is 1.5cm.

[0019] The beneficial effect of adopting the above-mentioned further solution is that it fits the size of the nipple and prevents pressure on the nipple.

[0020] Furthermore, the radius of the drug region is 1.5cm to 2.5cm.

[0021] The beneficial effect of adopting the above-mentioned further approach is that the surgical incision is aligned with the areola for drug application.

[0022] Furthermore, the edges of the base layer are petal-shaped.

[0023] The advantages of adopting the above-mentioned further solution are: it prevents curling after use and allows for adjustment of the adhesion position.

[0024] Furthermore, a protective film is attached to one side of the contact layer.

[0025] The beneficial effect of adopting the above-mentioned further measures is that it protects the contact layer and the drug area from contamination before the dressing is used. Attached Figure Description

[0026] Figure 1 This is a schematic diagram of the contact layer of this utility model.

[0027] Figure 2 This is a schematic diagram of the base layer of this utility model.

[0028] The attached diagram lists the components represented by each number as follows:

[0029] 1. Base layer; 2. Avoidance hole; 3. Strip; 4. Drug zone; 5. Outer film. DETAILED DESCRIPTION

[0030] The principles and features of this utility model are described below with reference to the accompanying drawings. The examples given are only for explaining this utility model and are not intended to limit the scope of this utility model.

[0031] Example 1

[0032] like Figures 1 to 2 As shown, a special dressing for breast augmentation includes a base layer 1, on which clearance holes 2 are provided. A contact layer is provided on one side of the base layer 1. The contact layer consists of several evenly arranged water ripple-shaped strips 3, with grooves between adjacent strips 3. A drug area 4 is provided around the clearance holes 2 on the side where the contact layer is located.

[0033] The beneficial effects of this embodiment are: by applying traction or pressure to the skin through the dressing, the epidermal layer is lifted or wrinkled, which can increase the subcutaneous tissue gap, and the grooves between the strips 3 can create a pressure difference, promote subcutaneous blood and lymph return, prevent nipple necrosis, accelerate healing, and reduce edema.

[0034] Specifically, after a patient undergoes breast reduction or lift surgery, the surgical incision is usually made at the areola, and the nipple is often in a period of ischemia and remodeling, requiring the use of dressings for postoperative care.

[0035] In this embodiment, the avoidance hole 2 is used to avoid the nipple and reduce pressure. It can not only maintain the original upright shape of the nipple, but also increase the patient's comfort and reduce the probability of nipple necrosis. The dressing exerts traction or pressure on the skin through its own elasticity and adhesion to achieve the effects of fixation, support, promotion and relaxation, thereby promoting wound healing. Anti-inflammatory drugs are placed in the drug area 4, corresponding to the surgical incision at the areola.

[0036] The water ripple pattern creates a pressure difference between the strips 3. Compared to a smooth surface or a straight strip 3, the water ripple pattern can better integrate with the skin, make it easier to form wrinkles, increase the interstitial space, and evenly distribute pressure, which can reduce postoperative pain and speed up recovery.

[0037] Based on this embodiment, both the base layer 1 and the contact layer are made of sterile, highly breathable fabric with a certain degree of elasticity.

[0038] Example 2

[0039] like Figures 1 to 2 As shown, preferably, based on Example 1, each strip 3 is provided with adhesive.

[0040] The beneficial effect of adopting the preferred solution in the above embodiments is that it enables the dressing to adhere stably to human skin.

[0041] Preferably, the adhesive is medical grade acrylic adhesive.

[0042] The beneficial effects of adopting the above-mentioned further solutions are: medical acrylic adhesive has strong adhesion, good durability and no irritation.

[0043] As a parallel technical solution in this embodiment, medical acrylic adhesive can also be replaced with other medical adhesive materials such as acrylic adhesive.

[0044] Example 3

[0045] like Figures 1 to 2 As shown, preferably, based on Embodiments 1-2, the base layer 1 is provided with an outer film 5 on the other side of the contact layer.

[0046] The beneficial effect of adopting the preferred solution in the above embodiments is that the outer film 5 is used to protect the outer side of the base layer 1.

[0047] Preferably, the outer film 5 is made of a breathable and waterproof material.

[0048] The beneficial effects of the preferred solution in the above embodiments are: the outer film 5 prevents external water splashes from contaminating the dressing and also prevents the drug from seeping out from the inside of the dressing.

[0049] In this embodiment, when the contact layer is applied to human skin, the areola wound may secrete sweat and tissue fluid, and the medication may also become wetted and leak out, so isolation is necessary.

[0050] Example 4

[0051] like Figures 1 to 2 As shown, preferably, based on Examples 1-3, the base layer 1 is an absorbent foam pad.

[0052] The beneficial effects of the preferred scheme in the above embodiments are: the base layer 1 has strong water absorption and can absorb the medicine, body fluid and tissue fluid that seep out from the dressing.

[0053] Example 5

[0054] like Figures 1 to 2 As shown, preferably, based on embodiments 1-4, the radius of the clearance hole 2 is 1.5cm.

[0055] The beneficial effect of adopting the preferred solution in the above embodiments is that it fits the size of the nipple and prevents pressure on the nipple.

[0056] Example 6

[0057] like Figures 1 to 2 As shown, preferably, based on Examples 1-5, the radius of the drug region 4 is 1.5cm to 2.5cm.

[0058] The beneficial effect of adopting the preferred solution in the above embodiments is that the drug area 4 is aligned with the surgical incision at the areola.

[0059] Example 7

[0060] like Figures 1 to 2 As shown, preferably, based on embodiments 1-6, the edge of the base layer 1 is petal-shaped.

[0061] The advantages of the preferred solution in the above embodiments are: it prevents curling after use and allows for adjustment of the adhesion position.

[0062] Specifically, if the dressing edge is round, the edge of the base layer 1 may curl after use. The curling will gradually extend to the entire circumference, resulting in reduced adhesion and a worse patient experience.

[0063] In this embodiment, the edge of the base layer 1 is changed to a petal-shaped polygon, which fits the shape of the breast better and reduces the possibility of curling. Even if a certain edge curls, it will not extend to other petal positions due to the limitation of the petal outline.

[0064] Because the base layer 1 is elastic, each petal can be pulled. Depending on the location of the surgical incision, the adhesion position of the end of each petal can be adjusted. The further the pulling is, the greater the pulling force can be provided in that direction, ensuring good pressure on the wound and strong targeting.

[0065] Example 8

[0066] like Figures 1 to 2 As shown, preferably, based on Examples 1-7, a protective film is attached to one side of the contact layer.

[0067] The beneficial effect of adopting the preferred solution in the above embodiments is that it protects the contact layer and the drug area from contamination before the dressing is used.

[0068] Specifically, to use it, simply tear off the protective film and attach it to the patient's body.

[0069] In the description of this utility model, it should be understood that the terms "center", "longitudinal", "transverse", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", "axial", "radial", "circumferential", etc., indicating the orientation or positional relationship are based on the orientation or positional relationship shown in the accompanying drawings, and are only for the convenience of describing this utility model and simplifying the description, and are not intended to indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation, and therefore should not be construed as a limitation of this utility model.

[0070] 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 indicated technical features. Thus, a feature defined as "first" or "second" may explicitly or implicitly include at least one of that feature. In the description of this utility model, "a plurality of" means at least two, such as two, three, etc., unless otherwise explicitly specified.

[0071] In this utility model, unless otherwise explicitly specified and limited, the terms "installation," "connection," "joining," and "fixing," etc., should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral part; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; they can refer to the internal communication of two components or the interaction between two components, unless otherwise explicitly limited. Those skilled in the art can understand the specific meaning of the above terms in this utility model according to the specific circumstances.

[0072] In this utility model, unless otherwise explicitly specified and limited, "above" or "below" the second feature can mean that the first feature is in direct contact with the second feature, or that the first feature is in indirect contact with the second feature through an intermediate medium. Furthermore, "above," "on top of," and "over" the second feature can mean that the first feature is directly above or diagonally above the second feature, or simply that the first feature is at a higher horizontal level than the second feature. "Below," "below," and "under" the second feature can mean that the first feature is directly below or diagonally below the second feature, or simply that the first feature is at a lower horizontal level than the second feature.

[0073] In the description of this specification, the references to terms such as "one embodiment," "some embodiments," "example," "specific example," or "some examples," etc., indicate that a specific feature, structure, material, or characteristic described in connection with that embodiment or example is included in at least one embodiment or example of the present invention. In this specification, the illustrative expressions of the above terms do not necessarily refer to the same embodiment or example. Furthermore, the specific features, structures, materials, or characteristics described may be combined in any suitable manner in one or more embodiments or examples. Moreover, without contradiction, those skilled in the art can combine and integrate the different embodiments or examples described in this specification, as well as the features of different embodiments or examples.

[0074] Although embodiments of the present invention have been shown and described above, it is understood that the above embodiments are exemplary and should not be construed as limiting the present invention. Those skilled in the art can make changes, modifications, substitutions and variations to the above embodiments within the scope of the present invention.

Claims

1. A dressing specifically for breast augmentation, characterized in that, It includes a base layer (1), on which a clearance hole (2) is provided. A contact layer is provided on one side of the base layer (1). The contact layer consists of several uniformly arranged water ripple-shaped strips (3). There is a groove between two adjacent strips (3). A drug area (4) is provided around the clearance hole (2) on the side where the contact layer is located.

2. The breast augmentation dressing according to claim 1, characterized in that, Adhesive is provided on each of the strips (3).

3. The dressing for breast augmentation according to claim 2, characterized in that, The adhesive is medical-grade acrylic adhesive.

4. The dressing for breast augmentation according to claim 1, characterized in that, The base layer (1) has an outer film (5) on the other side of the contact layer.

5. The breast augmentation dressing according to claim 4, characterized in that, The outer film (5) is made of breathable and waterproof material.

6. The dressing for breast augmentation according to claim 1, characterized in that, The base layer (1) is an absorbent foam pad.

7. The dressing for breast augmentation according to claim 1, characterized in that, The radius of the clearance hole (2) is 1.5cm.

8. The dressing for breast augmentation according to claim 7, characterized in that, The radius of the drug zone (4) is 1.5cm to 2.5cm.

9. A dressing for breast augmentation according to any one of claims 1 to 8, characterized in that, The edges of the base layer (1) are petal-shaped.

10. A dressing for breast augmentation according to any one of claims 1 to 8, characterized in that, A protective film is attached to one side of the contact layer.

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