Tonsil postoperative cold compress device

Abstract

The utility model discloses a tonsil postoperation cold compress device which comprises a bag body, an open groove is formed in the upper surface of the bag body, the tonsil postoperation cold compress device further comprises mesh cloth, the mesh cloth is fixedly installed on the upper surface of the open groove, the bag body is connected with a limiting structure, and a biological ice bag can be wrapped and limited in the open groove through the limiting structure. The limiting structure comprises a moisture absorption pad, a gap is formed between the mesh cloth and the opening in the upper surface of the bag body, the moisture absorption pad is inserted between the mesh cloth and the bag body in a penetrating mode, an opening is formed in the front surface of the bag body and penetrates through the front surface of the open groove, and an elastic opening is formed in the opening in the front surface of the bag body. According to the tonsil postoperative cold compress device, the limiting structure is arranged, the biological ice bag is limited through the open groove, displacement of the biological ice bag is avoided, a patient wears the device more comfortably, the connecting structure is further arranged, a second connecting belt can be adjusted by pressing a sliding buckle, the bag body is made to be matched with the head of the patient, and ice compress is more stable through an anti-skid pad.

Description

Technical Field

[0001] This utility model relates to the field of tonsil cold compress technology, specifically a post-tonsilar cold compress device. Background Technology

[0002] Tonsillectomy is a common surgical procedure mainly used to treat recurrent tonsillitis, tonsillar hypertrophy causing difficulty breathing and swallowing. Applying ice after tonsillectomy can constrict local blood vessels, reduce blood flow to the surgical site, thereby reducing the risk of bleeding. Low temperature can reduce nerve sensitivity at the surgical site, thus effectively relieving pain and reducing swelling, which helps patients recover faster, reduces postoperative discomfort, and is also conducive to wound healing.

[0003] When using ice packs after tonsillectomy, condensation forms on the surface due to the heat of the ice pack coming into contact with the skin. This condensation runs down the neck, causing discomfort to the patient and affecting the effectiveness of the ice pack. Furthermore, existing tonsillectomy ice packs are of a fixed size, which cannot provide a proper fit for people with different face shapes and sizes. After prolonged use, the ice pack softens and is prone to falling off. Utility Model Content

[0004] The purpose of this invention is to provide a post-tonsillar ablation device to solve the problem mentioned in the background art where condensation from contact between the ice pack and the skin affects the effectiveness of the ablation.

[0005] To achieve the above objectives, this utility model provides the following technical solution: a post-tonsillar ablation cold compress device, comprising a bag body, the upper surface of which is provided with a groove, and a mesh cloth, the mesh cloth being fixedly installed on the upper surface of the groove, the bag body being connected to a limiting structure, the limiting structure being able to wrap and restrict the biological ice pack within the groove.

[0006] Preferably, the limiting structure includes a moisture-absorbing pad, a gap is provided between the mesh fabric and the opening on the upper surface of the bag body, the moisture-absorbing pad is inserted through the mesh fabric and the bag body, the front surface of the bag body is provided with an opening that penetrates the slotted front surface, and the opening on the front surface of the bag body is provided with an elastic opening.

[0007] Using the above technical solution, cold air from the biological ice pack is allowed to penetrate through the mesh fabric for ice application.

[0008] Preferably, there are two symmetrically arranged slots.

[0009] The above technical solution facilitates simultaneous ice application to both sides.

[0010] Preferably, the front end of the biological ice pack is provided with a connecting strip, which is located between the elastic opening.

[0011] Using the above technical solution, the biological ice pack is removed via a connecting strip.

[0012] Preferably, the bag body is further provided with a connecting structure, which enables the connecting strap one and connecting strap two to be adjusted and fixed to the head.

[0013] The above technical solution facilitates a stable fit between the bag and the patient's skin.

[0014] Preferably, the connecting structure includes a first connecting strap, which is fixedly installed at one end of the bag body. A second connecting strap is fixedly connected to the other end of the bag body. A rope buckle is fixedly connected to the other end of the first connecting strap. A sliding buckle is slidably installed on the inner wall surface of the rope buckle. A spring is fixedly connected to one end of the sliding buckle, and the other end of the spring is fixedly installed on the inner wall surface of the rope buckle. Anti-slip pads are provided on the upper surfaces of both the first connecting strap and the second connecting strap.

[0015] Using the above technical solution, connecting strap one and connecting strap two are connected by a sliding buckle and a rope buckle.

[0016] Preferably, the upper and lower surfaces of the cord buckle are provided with openings corresponding to each other, and the upper surface of the sliding buckle is provided with an opening that corresponds to the opening position of the cord buckle.

[0017] The above technical solution facilitates the clamping of the connecting strap by the sliding buckle and the rope buckle.

[0018] Compared with the prior art, the beneficial effects of this utility model are: the post-tonsillar ablation cold compress device:

[0019] 1. The post-tonsillar surgery cold compress device is equipped with a limiting structure. When the biological ice pack is placed into the pre-set slot, the slot will limit the biological ice pack, which can accurately fix the biological ice pack around the tonsil surgery site, ensuring that the cold compress acts on the target area and maximizes the effect of the cold compress.

[0020] 2. Furthermore, the post-tonsillar surgery cold compress device has a moisture-absorbing pad between the mesh fabric and the bag body. The moisture-absorbing pad can absorb the condensation generated during the cold compress process, preventing the condensation from wetting the mesh fabric and contacting the patient's skin, thereby keeping the area around the patient's neck dry and improving the patient's comfort.

[0021] 3. Furthermore, a connecting structure is provided, through which the second connecting strap is inserted into the slots of the rope buckle and the sliding buckle. The second connecting strap can be clamped by the rope buckle and the sliding buckle. When the sliding buckle is pressed, the length of the second connecting strap can be adjusted to ensure that the ice pack device can fit snugly and comfortably on the patient's neck, thereby improving the patient's comfort. Attached Figure Description

[0022] Figure 1This is a schematic diagram of the axial surface structure of this utility model;

[0023] Figure 2 This is a top view sectional structural diagram of the present invention;

[0024] Figure 3 This is a schematic diagram of the surface structure of this utility model from a bottom view;

[0025] Figure 4 This is a schematic diagram of the side cross-sectional structure of this utility model;

[0026] Figure 5 This is a schematic diagram of the connection structure between the connecting strip 2 and the sliding buckle of this utility model;

[0027] Figure 6 This is a schematic diagram of the front cross-sectional structure of the rope buckle of this utility model.

[0028] In the diagram: 1. Bag body; 2. Mesh fabric; 3. Moisture-absorbing pad; 4. Groove; 5. Bio-ice pack; 6. Connecting strip; 7. Elastic opening; 8. Connecting strap one; 9. Connecting strap two; 10. Anti-slip pad; 11. Rope buckle; 12. Sliding buckle; 13. Spring. Detailed Implementation

[0029] 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.

[0030] Please see Figure 1-6 This utility model provides a technical solution: a cold compress device for tonsil surgery, including a bag body 1, a mesh cloth 2, a moisture-absorbing pad 3, a groove 4, a biological ice pack 5, a connecting strip 6, an elastic opening 7, a connecting strap one 8, a connecting strap two 9, an anti-slip pad 10, a rope buckle 11, a sliding buckle 12, and a spring 13.

[0031] Example 1: This post-tonsillar ablation cold compress device is equipped with a limiting structure, which can restrict the biological ice pack 5 to fit the cold compress position, specifically:

[0032] The upper surface of the bag body 1 has a slot 4 and also includes a mesh fabric 2, which is fixedly installed on the upper surface of the slot 4. The bag body 1 is connected to a limiting structure, which can wrap and restrict the biological ice pack 5 within the slot 4. The limiting structure includes a moisture-absorbing pad 3. A gap is provided between the mesh fabric 2 and the opening on the upper surface of the bag body 1. The moisture-absorbing pad 3 is inserted through the mesh fabric 2 and the bag body 1. The front surface of the bag body 1 has an opening that penetrates the front surface of the slot 4. The front surface opening of the bag body 1 has an elastic opening 7. Two slots 4 are symmetrically provided. The front end of the biological ice pack 5 is provided with a connecting strip 6, which is located between the elastic openings 7.

[0033] When using this post-tonsillar ablation cold compress device, first open the elastic opening 7 on the front surface of the bag body 1, then insert the biological ice pack 5 into the slot 4 through the elastic opening 7, leaving the connecting strip 6 of the biological ice pack 5 between the elastic opening 7. When the biological ice pack 5 needs to be replaced, simply open the elastic opening 7 to easily remove the used biological ice pack 5 and insert a new one. This operation is simple and quick, saving time, especially for patients who need frequent changes of the biological ice pack 5, thus improving the efficiency of nursing care. Because the connecting strip 6 of the biological ice pack 5 is left between the elastic opening 7, direct contact with the surgical site can be avoided when removing the biological ice pack 5, reducing irritation to the wound caused by improper operation. To mitigate the risk of injury, the slot 4 limits the placement of the biological ice pack 5, ensuring it is accurately fixed around the tonsil surgery site. This prevents the ice pack from shifting unnecessarily, which could lead to inaccurate cold compress placement and affect postoperative recovery. The cold compress effect is more concentrated, effectively cooling and relieving pain at the surgical site, thus aiding in faster patient recovery. A mesh fabric 2 is positioned on the upper surface of the bag 1, corresponding to the slot 4. A gap exists between the mesh fabric 2 and the opening on the upper surface of the bag 1, allowing the moisture-absorbing pad 3 to be inserted. The moisture-absorbing pad 3 absorbs condensation generated by the biological ice pack 5 during the cold compress process, preventing condensation from seeping through the mesh fabric 2 and contacting the patient's skin, thus keeping the area around the patient's neck dry.

[0034] The biological ice pack 5 in this application is an existing commercially available ice pack, whose internal filling is absorbent resin, which will not cause frostbite to the skin.

[0035] Example 2: This post-tonsillar ablation cold compress device also has a connecting structure, which allows the bag body 1 to fit snugly against the patient's skin by adjusting the connecting strap 2 9. Specifically:

[0036] The bag body 1 is also provided with a connecting structure, which allows the connecting strap 8 and connecting strap 9 to be adjusted and fixed to the head. The connecting structure includes connecting strap 8, which is fixedly installed at one end of the bag body 1. Connecting strap 9 is fixedly connected to the other end of the bag body 1. A rope buckle 11 is fixedly connected to the other end of connecting strap 8. A sliding buckle 12 is slidably installed on the inner wall surface of the rope buckle 11. A spring 13 is fixedly connected to one end of the sliding buckle 12, and the other end of the spring 13 is fixedly installed on the inner wall surface of the rope buckle 11. Anti-slip pads 10 are provided on the upper surfaces of both connecting strap 8 and connecting strap 9. Openings are provided on the upper and lower surfaces of the rope buckle 11. The opening on the upper surface of the sliding buckle 12 corresponds to the opening position of the rope buckle 11.

[0037] When securing the device to the head, wrap connecting strap 8 and connecting strap 9 around both sides of the head. Then, insert one end of connecting strap 9 into the opening between the cord buckle 11 and the sliding buckle 12. When the sliding buckle 12 is pressed, the corresponding opening between the sliding buckle 12 and the cord buckle 11 will widen, allowing adjustment of the length of connecting strap 9. After releasing the pressure on the sliding buckle 12, the other end of the spring 13, which is fixedly connected to one end of the sliding buckle 12, is fixedly installed on the inner wall surface of the cord buckle 11. Therefore, the sliding buckle 12 and the cord buckle 11 will clamp the connecting strap 9. The cord buckle 11 and the sliding buckle 12 can firmly clamp the connecting strap 9, preventing the ice pack device from loosening or slipping during use. Especially for postoperative patients, there may be slight movements or head rotations. A stable fixation ensures that the biological ice pack 5 remains in the correct position and continues to provide cooling. In the early postoperative period, a tighter fit may be needed to ensure that the biological ice pack 5 is fixed in the accurate position. The anti-slip pads 10 on the upper surfaces of the connecting strap 1 8 and connecting strap 2 9 make the position of the ice pack more stable. As the recovery process progresses, the length of connecting strap 2 9 can be appropriately loosened to adapt to changes in the patient. Adjusting the length of connecting strap 2 9 is very convenient; it can be easily achieved by simply pressing the sliding buckle 12 without complicated operating steps, thus improving the ease of use.

[0038] Working principle: When using this post-tonsil surgery cold compress device, a limiting structure is set up. The slot 4 restricts the biological ice pack 5 to fit the cold compress position. A connecting structure is also set up, which can be adjusted by pressing the sliding buckle 12 to make the connecting strap 9 fit the patient's skin, thus increasing the overall practicality.

[0039] Although embodiments of the present invention have been shown and described, it will be understood by those skilled in the art that various changes, modifications, substitutions and alterations can be made to these embodiments without departing from the principles and spirit of the present invention, the scope of which is defined by the appended claims and their equivalents.

Claims

1. A post-tonsillar ablation cold compress device, comprising a bag (1), wherein the upper surface of the bag (1) is provided with a groove (4), characterized in that: It also includes a mesh fabric (2), which is fixedly installed on the upper surface of the slot (4). The bag body (1) is connected to a limiting structure, which can wrap and restrict the biological ice pack (5) in the slot (4). The limiting structure includes a moisture-absorbing pad (3). A gap is provided between the mesh fabric (2) and the opening on the upper surface of the bag body (1). The moisture-absorbing pad (3) is inserted through the mesh fabric (2) and the bag body (1). The front surface of the bag body (1) is provided with an opening that penetrates the front surface of the slot (4). The front surface opening of the bag body (1) is provided with an elastic opening (7).

2. The post-tonsillar ablation cold compress device according to claim 1, characterized in that: The slot (4) has two symmetrical openings.

3. The post-tonsillar ablation cold compress device according to claim 1, characterized in that: The front end of the biological ice pack (5) is provided with a connecting strip (6), which is located between the elastic opening (7).

4. The post-tonsillar ablation cold compress device according to claim 1, characterized in that: The bag body (1) is also provided with a connecting structure, which enables the connecting strap one (8) and connecting strap two (9) to be adjusted and fixed to the head.

5. The post-tonsillar ablation cold compress device according to claim 4, characterized in that: The connecting structure includes a connecting strap one (8), which is fixedly installed at one end of the bag body (1). The other end of the bag body (1) is fixedly connected to a connecting strap two (9). The other end of the connecting strap one (8) is fixedly connected to a rope buckle (11). A sliding buckle (12) is slidably installed on the inner wall surface of the rope buckle (11). A spring (13) is fixedly connected to one end of the sliding buckle (12), and the other end of the spring (13) is fixedly installed on the inner wall surface of the rope buckle (11). Anti-slip pads (10) are provided on the upper surfaces of both the connecting strap one (8) and the connecting strap two (9).

6. The post-tonsillar ablation cold compress device according to claim 5, characterized in that: The upper and lower surfaces of the rope buckle (11) are provided with openings, and the upper surface of the sliding buckle (12) is provided with an opening that corresponds to the opening position of the rope buckle (11).

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