A breast cancer patient postoperative rehabilitation device

Abstract

The utility model relates to breast cancer rehabilitation technical field especially, it is a kind of breast cancer patient postoperative rehabilitation device, solve the problem that existing technology is difficult to replace and gauze is insufficient for the adsorption of permeate problem.One kind of breast cancer patient postoperative rehabilitation device, including wrapping cover, wrapping cover one side is fixedly connected with drug-loading bag, wrapping cover is provided with two, two the wrapping cover adjacent side is elastically connected by elastic band, two the wrapping cover outside is fixedly connected with bandage.The utility model can obviously improve the operation speed of medical staff, improve its work efficiency, and through the absorption of permeate of absorbent, can significantly reduce the outflow condition of permeate.

Description

Technical Field

[0001] This utility model relates to the field of breast cancer rehabilitation technology, and in particular to a postoperative rehabilitation device for breast cancer patients. Background Technology

[0002] Breast cancer patients typically require a combination of treatments, including surgery, radiotherapy, chemotherapy, endocrine therapy, and targeted therapy. These treatments aim to eliminate cancer cells and prevent recurrence and metastasis. However, these treatments can also cause varying degrees of side effects, such as pain, limited mobility, lymphedema, sensory disturbances, and cognitive impairment. These side effects severely impact patients' daily lives and work abilities; therefore, rehabilitation medicine plays an increasingly important role in the recovery process for breast cancer patients.

[0003] Most breast cancer treatments involve surgery. Because surgery damages local tissues, it can cause tissue fluid leakage. Additionally, since most surgical procedures include axillary lymph node dissection, this disrupts the lymphatic circulation system, hindering lymphatic fluid return and causing leakage from the wound. Therefore, in the early postoperative recovery process, it is necessary to apply medication to the wound and simultaneously monitor wound drainage.

[0004] However, in current rehabilitation treatments, postoperative care typically involves applying medication to the wound site by wrapping it with gauze. This method presents several problems in practice and during rehabilitation. First, during lymphatic drainage, gauze is the only means to absorb the exudate. However, the gauze commonly used in current technology lacks sufficient absorbency to handle large amounts of lymphatic drainage. Current solutions typically involve frequent gauze changes, which is wasteful of manpower and resources. Second, the primary purpose of applying medication to the wound is to promote healing, meaning fresh granulation tissue will grow. However, the gauze often adheres to the granulation tissue after becoming soaked with exudate, requiring separation during dressing changes. This undoubtedly causes significant psychological and physiological trauma to the patient. Furthermore, in rehabilitation medicine, this method of dressing changes indirectly hinders wound healing and is detrimental to postoperative rehabilitation.

[0005] Therefore, we propose a postoperative rehabilitation device for breast cancer patients to address the aforementioned issues. Utility Model Content

[0006] The purpose of this invention is to provide a postoperative rehabilitation device for breast cancer patients, which solves the problems of difficulty in changing dressings and insufficient absorption of permeable fluid by gauze in the prior art.

[0007] To achieve the above objectives, the present invention adopts the following technical solution:

[0008] A postoperative rehabilitation device for breast cancer patients includes a wrap-around cover, with a drug-carrying bag fixedly connected to one side of the wrap-around cover. Two wrap-around covers are provided, and the adjacent sides of the two wrap-around covers are elastically connected by an elastic band. Straps are fixedly connected to the outer sides of both wrap-around covers.

[0009] Preferably, an absorbent bag is fixedly connected to the side of the package cover near the drug-carrying bag.

[0010] Preferably, one end of one of the two straps is fixedly connected with a row of buckles, and the other end of the strap is fixedly connected with a row of hooks.

[0011] Preferably, the top and bottom of the cover are fixedly connected with plastic strips.

[0012] Preferably, the absorbent bag is located between the drug-carrying bag and the plastic strip at the bottom of the packaging cover.

[0013] Preferably, the drug-carrying bag contains a dressing, and the absorbent bag contains absorbent material, wherein the absorbent material is made of hydrophilic colloidal particles.

[0014] This utility model has the following beneficial effects:

[0015] 1. To meet the needs of patients who require frequent dressing changes, we have adopted a row of buckles and hooks for the dressing cover. This design allows medical staff to quickly untie and re-secure the dressing when changing it, which can significantly improve the speed of operation and increase their work efficiency.

[0016] 2. At the same time, considering that different patients have different body shapes, in order to meet the needs of most patients as much as possible, we designed shaping strips on both sides of the cover. The shaping strips are very easy to use. By pinching the shaping strips, they can be made to fit patients with different body shapes. At the same time, it is equipped with elastic bands and straps made of elastic material. With its good elasticity, it can flexibly adapt to the body shape of patients with different chest sizes, fit the patient's skin better, and reduce the discomfort of wearing it.

[0017] 3. Finally, we added absorbent material to the bottom of the dressing to absorb the permeable fluid. This absorbent material addresses the problem of existing gauze's inability to absorb large amounts of permeable fluid. The absorption of permeable fluid by the absorbent material significantly reduces outflow. This reduction in permeable fluid outflow significantly prevents the gauze from sticking tightly to the skin due to permeable fluid soaking, alleviating patient discomfort during dressing changes. It also greatly reduces the risk of bacterial growth and infection caused by permeable fluid remaining on the skin surface for extended periods or seeping into the external environment. Attached Figure Description

[0018] To more clearly illustrate the technical solutions of the embodiments of this utility model, the drawings used in the description of the embodiments will be briefly introduced below. Obviously, the drawings described below are some embodiments of this utility model. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.

[0019] Figure 1 This is a schematic diagram of the front structure of this utility model;

[0020] Figure 2 This is a schematic diagram of the rear structure of the present invention;

[0021] Figure 3 This is a side view of the present invention.

[0022] Figure 4 This is a schematic diagram of the structure of the protective cover of this utility model;

[0023] Figure 5 This is a schematic diagram of the structure of the drug-carrying bag and absorbent bag of this utility model.

[0024] In the diagram: 1. Wrapping cover; 2. Elastic band; 3. Straps; 4. Hook and loop; 5. Buckle and loop; 6. Medicine bag; 7. Absorbent bag; 8. Plastic strip; 9. Dressing; 10. Absorbent material. Detailed Implementation

[0025] To make the objectives, technical solutions, and advantages of this utility model clearer, the present utility model will be further described in detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the present utility model and are not intended to limit the present utility model.

[0026] Reference Figure 1-5 A postoperative rehabilitation device for breast cancer patients includes a wrap 1 made of cotton material with good breathability. A drug-carrying bag 6 is fixedly connected to one side of the wrap 1. The drug-carrying bag 6 is made of polyurethane material with good flexibility, breathability and waterproofness, which can prevent the seepage fluid from entering the dressing 9 and avoid the dressing 9 from becoming ineffective. There are two wrap 1s in total. The two wrap 1s are elastically connected on adjacent sides by elastic bands 2. Both wrap 1s are fixedly connected to the outside of the outer side by straps 3. Both straps 3 and elastic bands 2 are made of medical-grade silicone-coated spandex blend material.

[0027] Furthermore, an absorbent bag 7 is fixedly connected to the side of the cover 1 near the drug-carrying bag 6. The absorbent bag 7 is made of porous silicone material to ensure that it does not absorb water but does not affect the effect of the internal absorbent material 10.

[0028] Furthermore, one end of one of the two straps 3 is fixedly connected to a buckle 5, and the other end of the strap 3 is fixedly connected to a hook 4. The buckle 5 and the hook 4 can be quickly combined and separated.

[0029] Furthermore, the top and bottom of the cover 1 are fixedly connected with plastic strips 8, which can be shaped by hand to ensure that the cover 1 can fit the patient's skin.

[0030] Furthermore, the absorbent bag 7 is located between the drug-carrying bag 6 and the plastic strip 8 at the bottom of the cover 1. The absorbent bag 7 being located at the bottom of the cover 1 can prevent the permeate from flowing out of the cover 1.

[0031] Furthermore, the dressing 9 is installed inside the drug-loaded bag 6, and the absorbent material 10 is installed inside the absorbent bag 7. The absorbent material 10 is made of hydrophilic colloidal particles, which have excellent adsorption properties and can meet the needs of adsorbing a large amount of permeate.

[0032] In summary:

[0033] When medication is needed after surgery, medical staff can select a suitable dressing 9 based on the patient's individual condition, place it in the medication bag 6, and put absorbent material 10 in the absorbent bag 7, then apply it to the patient's wound. The elastic band 2 and the strap 3 are made of high-quality, highly elastic material, allowing for flexible stretching and adaptation according to different patient body characteristics. Considering the differences in patient body contours, plastic strips 8 are installed on both sides of the cover 1. Medical staff can pinch the plastic strips 8 to ensure a close fit to the patient's skin, according to the different patient's body characteristics. This fit not only helps enhance the patient's comfort but also creates a relatively sealed environment to a certain extent, providing good conditions for wound healing. Medical staff only need to fasten the hooks 4 into the buckles 5 to ensure the device is securely fixed to the patient's body. The dressing 9 in the medication bag 6 can accelerate wound healing, while the tissue fluid exuded from the wound is absorbed by the absorbent material 10 at the bottom of the medication bag 6, preventing exudate from flowing out, wetting the patient's clothing, reducing patient discomfort, and also reducing the risk of infection caused by exudate.

[0034] 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 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 claimed utility model. The scope of protection of this utility model is defined by the appended claims and their equivalents.

Claims

1. A postoperative rehabilitation device for breast cancer patients, comprising a protective cover (1), characterized in that, A medicine bag (6) is fixedly connected to one side of the package cover (1). There are two packages cover (1). The two packages cover (1) are elastically connected on adjacent sides by an elastic band (2). The outer sides of the two packages cover (1) are fixedly connected with straps (3). An absorbent bag (7) is fixedly connected to the side of the package cover (1) near the drug-carrying bag (6); The drug-carrying bag (6) contains a dressing (9), and the absorbent bag (7) contains an absorbent material (10). The absorbent material (10) is made of hydrophilic colloidal particles.

2. The postoperative rehabilitation device for breast cancer patients according to claim 1, characterized in that, One end of the two straps (3) is fixedly connected to a buckle (5), and the other end of the strap (3) is fixedly connected to a hook (4).

3. The postoperative rehabilitation device for breast cancer patients according to claim 1, characterized in that, Plastic strips (8) are fixedly connected to the top and bottom of the cover (1).

4. The postoperative rehabilitation device for breast cancer patients according to claim 3, characterized in that, The absorbent bag (7) is located between the drug-carrying bag (6) and the plastic strip (8) at the bottom of the cover (1).

Images