Postoperative fixing bag for bromhidrosis operation

Abstract

The utility model discloses a bromhidrosis postoperative fixing bag which comprises a fixing bag body, the fixing bag body comprises a connecting band and bag bodies, two ends of the connecting band are respectively connected with a group of detachable bag bodies, the connecting band is detachably connected with the bag bodies in a penetrating mode, and the connecting band can penetrate through the connecting band. By means of the adjustable locking assemblies, the fixing bag can adapt to patients with different body types, operation positions and wound conditions, the best bearing effect and comfort degree are guaranteed, and the fixing bag has the advantages of being simple in structure, convenient to use and high in practicability. The interpenetrating type connection design enables the wearing process to be simpler, more convenient and faster, complex binding steps are not needed, the difficulty and time cost of postoperative care are reduced, the tightness of the bag body and the connecting band can be adjusted, the comfort of a patient in the postoperative recovery period is jointly ensured, and pain and discomfort are reduced.

Description

Technical Field

[0001] This utility model relates to the field of fixation bag technology, specifically a fixation bag for postoperative fixation after axillary osmidrosis surgery. Background Technology

[0002] Axillary odor surgery is a common surgical procedure that reduces or eliminates body odor by removing or destroying apocrine glands. After the surgery, in order to promote wound healing and reduce complications, the patient's armpits need to be fixed and bandaged, usually using bandages or similar materials.

[0003] Traditional postoperative fixation methods for axillary osmidrosis surgery mainly rely on bandages to bind the arm and support the arm by hanging it around the neck. While this method provides some fixation and support, it has the following drawbacks: using bandages requires certain skills and time, especially in ensuring both fixation effectiveness and patient comfort, and ensuring the bandage is neither too tight nor too loose. This increases the difficulty and complexity of postoperative care. Therefore, it is necessary to design a postoperative fixation bag for axillary osmidrosis surgery to solve the above problems. Utility Model Content

[0004] The purpose of this invention is to provide a fixation bag after axillary osmidrosis surgery to solve the problems mentioned in the background art.

[0005] To achieve the above objectives, this utility model provides the following technical solution: a fixation bag after axillary odor surgery, comprising a fixation bag, the fixation bag including a connecting strap and a bag body, each end of the connecting strap being connected to a detachable bag body, the detachable connection between the connecting strap and the bag body being an insert connection, the connecting strap being able to penetrate the connecting strap, and both ends of the connecting strap being provided with locking components that can be adjusted for tightness, which can lock the bag body.

[0006] Preferably, the locking component includes a limiting block and a limiting seat. Two sets of the limiting blocks are installed on one side of the connecting strip, and multiple sets of the limiting seats are installed at equal intervals at the end of the connecting strip corresponding to the limiting blocks. The limiting blocks and the limiting seats are plugged into each other.

[0007] Preferably, the limiting block is a T-shaped cylindrical component, and the limiting seat has two sets of slots that are interconnected and respectively adapted to the head and tail of the limiting block.

[0008] Preferably, the bag body includes a support strap and connecting blocks, with a set of connecting blocks installed at each end of the support strap, and both sets of connecting blocks can be penetrated by the connecting strap.

[0009] Preferably, the width of the support strip is greater than the width of the connecting strip.

[0010] Preferably, a set of protective pads is fitted over the outside of the connecting strip, and the two are slidably connected.

[0011] Compared with the prior art, the beneficial effects of this utility model are:

[0012] 1. This utility model, through its adjustable locking components, allows the fixed bag to adapt to patients of different body types, surgical sites, and wound conditions, ensuring optimal support and comfort. The interlocking connection design makes the wearing process simpler and faster, eliminating the need for complicated binding steps, thus reducing the difficulty and time cost of postoperative care. The adjustable tightness of the bag and connecting straps together ensures the patient's comfort during postoperative recovery, reducing pain and discomfort.

[0013] 2. The plug-in snap-fit ​​design of this utility model ensures a firm connection between the connecting strap and the bag body, avoiding the loosening and detachment problems that may occur with traditional bandage fixation methods. By selecting different limiting seats and limiting blocks for snap-fit, patients can easily adjust the tightness of the connecting strap. This design allows the fixation bag to adapt to patients with different body types, arm sizes, and comfort needs, improving personalized adaptability. The plug-in snap-fit ​​design simplifies the wearing process, allowing patients to complete the installation of the fixation bag without complicated binding steps, improving the convenience and efficiency of wearing, and reducing the burden on patients.

[0014] 3. The width of the support strap of this utility model is greater than that of the connecting strap, ensuring sufficient support for the arm and reducing the pulling of arm movements on the surgical site. The rigid material design of the connecting block makes the bag more stable and less prone to deformation, further improving the support effect. The addition of the pad reduces the pressure on the neck and shoulders when the connecting strap is hung around the neck, improving wearing comfort. The soft material and sliding connection design of the pad allow patients to experience a smoother and more comfortable wearing experience during activities. The connecting strap can be connected to the bag by passing through the connecting block, without complicated binding steps. This design simplifies the wearing process and improves the convenience and efficiency of wearing. Attached Figure Description

[0015] Figure 1 This is an anatomical view of the overall structure of this utility model;

[0016] Figure 2 This is an enlarged view of section A of the structure of this utility model;

[0017] Figure 3 This is an enlarged view of section B of the structure of this utility model;

[0018] Figure 4 This is a schematic diagram of the overall structure of this utility model.

[0019] In the diagram: 1. Connecting strap, 2. Bag body, 3. Limiting block, 4. Limiting seat, 5. Supporting strap, 6. Connecting block, 7. Pad, 8. Card slot. Detailed Implementation

[0020] The technical solutions of the present utility model will be clearly and completely described below with reference to the accompanying drawings of the embodiments. Obviously, the described embodiments are only some embodiments of the present utility model, and not all embodiments. Based on the embodiments of the present utility model, all other embodiments obtained by those of ordinary skill in the art without creative effort are within the protection scope of the present utility model.

[0021] Example 1

[0022] Please refer to Figure 1-4 As shown, this utility model provides a fixation bag after axillary odor surgery, including a fixation bag, which includes a connecting strap 1 and a bag body 2. Each end of the connecting strap 1 is connected to a set of detachable bag bodies 2. The detachable connection between the connecting strap 1 and the bag body 2 is an interlocking connection, whereby the connecting strap 1 can penetrate the connecting strap 1. Both ends of the connecting strap 1 are provided with locking components that can be adjusted for tightness, which can lock the bag body 2.

[0023] The patient first wraps the connecting strap 1 around their neck, threading both ends through the corresponding loops of the two sets of bags 2. The bags 2 then support the arm. The locking mechanism is used to adjust the tightness of the connecting strap 1, preventing the bags 2 from detaching from the strap 1 while simultaneously adjusting the length of the strap 1 to fit different patients, ensuring it's not too tight and causes discomfort. Once the locking mechanism is engaged, the bag is installed, providing stable support for the arm.

[0024] Compared to existing technologies, the adjustable locking components allow the fixation bag to adapt to patients of different body types, surgical sites, and wound conditions, ensuring optimal support and comfort. The interlocking connection design makes the wearing process simpler and faster, eliminating the need for complicated binding steps and reducing the difficulty and time cost of postoperative care. The adjustable tightness of the bag and connecting straps together ensures patient comfort during postoperative recovery, reducing pain and discomfort.

[0025] Specifically, the locking component includes a limiting block 3 and a limiting seat 4. Two sets of limiting blocks 3 are installed on one side of the connecting belt 1, and multiple sets of limiting seats 4 are installed at equal intervals at the end of the connecting belt 1 corresponding to the limiting blocks 3. The limiting blocks 3 and the limiting seats 4 are plugged in and snapped together. The limiting blocks 3 are T-shaped cylindrical parts. The limiting seats 4 have two sets of slots 8, which are interconnected and are adapted to the head and tail of the limiting blocks 3 respectively.

[0026] When installing the fixation bag, the patient first wraps the connecting strap 1 around the neck and passes it through the loop of the bag body 2. Then, the head of the limiting block 3 is aligned with the larger slot 8 in the limiting seat 4 and inserted. After the head of the limiting block 3 has completely passed through this set of slots 8, the limiting block 3 is slid to one side so that its tail enters another set of smaller slots 8 that fit it, completing the engagement. By selecting different limiting seats 4 and limiting blocks 3 for engagement, the patient can flexibly adjust the tightness of the connecting strap 1. After the connecting strap 1 is locked, it forms a closed cavity to limit the bag body 2, ensuring a stable connection between the connecting strap 1 and the bag body 2 and preventing the bag body 2 from accidentally detaching.

[0027] The plug-in snap-fit ​​design ensures a secure connection between the connecting strap 1 and the bag body 2, avoiding the loosening and detachment problems that may occur with traditional bandage fixation methods. By selecting different limiting seats 4 and limiting blocks 3 for snap-fit, patients can easily adjust the tightness of the connecting strap 1. This design allows the fixation bag to adapt to patients with different body types, arm sizes, and comfort needs, improving personalized fit. The plug-in snap-fit ​​design simplifies the wearing process, allowing patients to complete the installation of the fixation bag without complicated binding steps, improving the convenience and efficiency of wearing and reducing the burden on patients.

[0028] Wherein: the bag body 2 includes a support belt 5 and a connecting block 6. A set of connecting blocks 6 is installed at each end of the support belt 5. Both sets of connecting blocks 6 can be penetrated by the connecting belt 1. The width of the support belt 5 is greater than the width of the connecting belt 1. A set of protective pads 7 are sleeved on the outside of the connecting belt 1, and the two are slidably connected.

[0029] When installing the fixation bag, the patient first wraps the connecting strap 1 around the neck. Then, both ends of the connecting strap 1 are passed through the holes in the connecting blocks 6 at both ends of the support strap 5, completing the connection between the connecting strap 1 and the bag body 2. The pad 7 is placed over the connecting strap 1. When the connecting strap 1 is hanging around the neck, the pad 7 provides cushioning and protection.

[0030] The support strap 5 is wider than the connecting strap 1, ensuring sufficient support for the arm and reducing the pulling of arm movements on the surgical site. The rigid material design of the connecting block 6 makes the bag body 2 more stable and less prone to deformation, further improving the support effect. The addition of the pad 7 reduces the pressure on the neck and shoulders when the connecting strap 1 is hung around the neck, improving wearing comfort. The soft material and sliding connection design of the pad 7 allow patients to experience a smoother and more comfortable wearing experience during activities. The connecting strap 1 can be connected to the bag body 2 by passing through the connecting block 6, without complicated binding steps. This design simplifies the wearing process and improves the convenience and efficiency of wearing.

[0031] Working principle: When installing the fixation bag, the patient first wraps the connecting strap 1 around the neck. Then, the two ends of the connecting strap 1 are passed through the holes of the connecting blocks 6 at both ends of the support strap 5 to complete the connection between the connecting strap 1 and the bag body 2. The pad 7 is placed on the outside of the connecting strap 1. When the connecting strap 1 is hanging around the neck, the pad 7 plays a role in cushioning and protection. Then, the head of the limiting block 3 is aligned with the larger-sized slot 8 in the limiting seat 4 and inserted. After the head of the limiting block 3 has completely passed through this set of slots 8, the limiting block 3 is slid to one side so that its tail enters another set of smaller-sized slots 8 that are compatible with it, thus completing the locking. By selecting different limiting seats 4 and limiting blocks 3 for locking, the patient can flexibly adjust the tightness of the connecting strap 1. After the connecting strap 1 is locked, it can form a closed cavity to limit the bag body 2, ensuring a stable connection between the connecting strap 1 and the bag body 2 and preventing the bag body 2 from accidentally detaching.

[0032] The contents not described in detail in this specification are existing technologies known to those skilled in the art.

[0033] Although the present invention has been described in detail with reference to the foregoing embodiments, those skilled in the art can still modify the technical solutions described in the foregoing embodiments or make equivalent substitutions for some of the technical features. Any modifications, equivalent substitutions, improvements, etc., made within the spirit and principles of the present invention should be included within the protection scope of the present invention.

Claims

1. A postoperative fixation bag for axillary osmidrosis surgery, comprising a fixation bag, characterized in that: The fixed bag includes a connecting strap (1) and a bag body (2). Each end of the connecting strap (1) is connected to a set of detachable bag bodies (2). The detachable connection between the connecting strap (1) and the bag body (2) is an interlocking connection. The connecting strap (1) can penetrate the connecting strap (1). Both ends of the connecting strap (1) are provided with locking components that can be adjusted to lock the bag body (2).

2. The postoperative fixation bag for axillary osmidrosis surgery according to claim 1, characterized in that: The locking component includes a limiting block (3) and a limiting seat (4). Two sets of the limiting blocks (3) are installed on one side of the connecting strip (1). Multiple sets of the limiting seats (4) are installed at equal intervals at the end of the connecting strip (1) corresponding to the limiting blocks (3). The limiting blocks (3) and the limiting seats (4) are plugged into each other.

3. The postoperative fixation bag for axillary osmidrosis surgery according to claim 2, characterized in that: The limiting block (3) is a T-shaped cylindrical part, and the limiting seat (4) has two sets of slots (8). The two sets of slots (8) are interconnected and are respectively adapted to the head and tail of the limiting block (3).

4. The postoperative fixation bag for axillary osmidrosis surgery according to claim 1, characterized in that: The bag body (2) includes a support strap (5) and a connecting block (6). A set of the connecting block (6) is installed at each end of the support strap (5), and both sets of the connecting blocks (6) can be penetrated by the connecting strap (1).

5. The postoperative fixation bag for axillary osmidrosis surgery according to claim 4, characterized in that: The width of the support strip (5) is greater than the width of the connecting strip (1).

6. The postoperative fixation bag for axillary osmidrosis surgery according to claim 1, characterized in that: The connecting strip (1) is covered with a set of protective pads (7), and the two are slidably connected.

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