Skin pressure sensing device
By designing a skin pressure sensing device including mounting panels, vacuum components and elastic connecting belts, the problem of wound tearing during disassembly of traditional medical bandages is solved, and the formation of an aerobic environment and efficient wound recovery is achieved.
Patent Information
- Application Number
- CN202510032480.8
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-01-09
- Publication Date
- 2025-03-18
AI Technical Summary
Traditional medical bandages can easily cause wound tear when disassembled, affecting the patient's recovery process.
A skin pressure sensing device is designed, including mounting panels, vacuum components and elastic connecting belts, which create an oxygen-free environment through vacuum and utilize the design of elastic connecting belts to reduce the risk of wound tearing.
It effectively avoids the tear of wounds during the removal of medical bandages, reduces bacterial growth, and improves the rehabilitation efficiency of wounds.
Smart Images

Figure CN119632762A_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of auxiliary rehabilitation, and in particular to a skin pressure sensing device. Background Art
[0002] Traditionally, after a skin burn, a medical bandage is usually used to bandage the wound. However, when the medical bandage is removed, the wound is easily torn during the removal process due to the fixed scab on the surface of the patient's skin.
[0003] Therefore, we propose a skin pressure sensing device that is easy to remove, which effectively avoids tearing of the wound caused by removing the medical bandage. Summary of the invention
[0004] In view of the defects in the prior art, the present invention provides a skin pressure sensing device to avoid tearing of the wound caused during the removal of the medical bandage.
[0005] In the first aspect, the present invention provides a skin pressure sensing device, comprising: a mounting plate assembly, the mounting plate assembly is provided with at least one connecting plate and a connecting belt; wherein any two adjacent connecting plates are connected by a connecting belt; the connecting plate is also provided with at least one ventilation hole, and the ventilation holes are evenly distributed on the connecting plate; wherein the connecting plate is located on the surface of the patient's skin; and a vacuum component, the vacuum component is arranged above the mounting plate assembly and covers the skin; the vacuum component includes a vacuum sleeve, and the vacuum sleeve is provided with a tightening port, and the vacuum sleeve is fastened to the patient through the tightening port and can form a vacuum.
[0006] Furthermore, the connecting plate is also provided with abutment sections, and the abutment sections are provided at two locations, and are respectively provided on one side of the connecting plate and close to the upper and lower ends of the connecting plate; wherein the abutment sections abut against the skin. In actual use, the abutment sections in this design are convenient for abutting against a normal arm, so that a cavity can be formed between the wound and the connecting plate, so that it is convenient for the patient to loosen and stretch the skin during exercise and daily life, reducing the impact of traditional bandages on the patient's life.
[0007] Furthermore, there are multiple connecting straps, and any adjacent connecting plates are provided with two connecting straps. In actual use, the purpose of this design is to facilitate the connection of two connecting plates, so that it is convenient to disassemble. Only one of the connecting plates needs to be disassembled to quickly and conveniently disassemble the other connecting plates. In this way, the influence of traditional bandaging methods on wound tearing can be reduced.
[0008] Furthermore, the connecting belt is made of an elastic belt. In actual use, this design makes it easy to place the device on the patient's arm; in actual work, the patient's arm is firstly medicated, and then the connecting plate is sequentially installed on the patient's arm, thus forming external protection for the patient's wound after the medication is applied. The design of the connecting belt as an elastic belt makes it easy to wrap the device around the patient's body, thereby increasing its degree of deformation.
[0009] Furthermore, the mounting plate assembly also includes a magnetic strip, which is provided at one location and installed on the side of the connecting plate. In actual use, the rack is provided on the outermost connecting plate, and the design is convenient for connecting into a cylindrical shape. Of course, in order to facilitate fixing, a medical bandage is also used to pass through the vent hole for fixing.
[0010] Furthermore, the vacuum sleeve is also provided with a suction pipe port, which is connected to an external air pump, wherein a protective gas is first introduced to evacuate the gas in the vacuum sleeve, and then the vacuum sleeve is sucked, and the suction pipe port is tightly closed by a cable tie. In actual use, the purpose of this design is to facilitate the emptying. In actual work, the protective gas is first injected into the vacuum sleeve to exhaust the internal gas, especially oxygen, and then the vacuum sleeve is evacuated and the entirety is wrapped around the connecting plate to form an outer protective sleeve; of course, the vacuum sleeve is made of silicone material, which can effectively increase the actual service life. At the same time, this operation realizes an anaerobic environment in the wound part through the later cable tie, effectively avoiding the growth of bacteria in an aerobic environment, thereby improving the efficiency of wound recovery.
[0011] Furthermore, the protective gas is nitrogen. In practical application, the gas is easy to obtain and can achieve effective protection.
[0012] It can be seen from the above technical solution that the skin pressure sensing device provided by the present invention has the following beneficial effects:
[0013] (1) In actual use, the purpose of this design is to facilitate the separation of wounds and reduce the tearing sensation of the patient's skin;
[0014] (2) The vacuum component used can effectively create an oxygen-free environment, which can reduce bacterial growth and effectively improve recovery efficiency. BRIEF DESCRIPTION OF THE DRAWINGS
[0015] In order to more clearly illustrate the specific embodiments of the present invention, the following will briefly introduce the drawings required for the specific embodiments or the prior art description. In all the drawings, each element or part is not necessarily drawn according to the actual scale.
[0016] Figure 1A three-dimensional schematic diagram of a mounting assembly of a skin pressure sensing device provided by an embodiment of the present invention, which is mounted on an arm;
[0017] Figure 2 for Figure 1 A schematic diagram of the structure of a vacuum sleeve in a skin pressure sensing device is shown;
[0018] Figure 3 for Figure 1 A three-dimensional schematic diagram of a connecting plate in a skin pressure sensing device is shown;
[0019] Figure 4 A schematic diagram of the structure of a flexible abutting section made of silicone material provided by another embodiment of the present invention;
[0020] Figure 5 A schematic diagram of the structure of a flexible abutment section made of a liquid jacket provided by another embodiment of the present invention;
[0021] Figure 6 A schematic structural diagram of a vacuum sleeve for convenient inflation and exhaust provided by another embodiment of the present invention;
[0022] Reference numerals:
[0023] Install the assembly plate 1, the connecting plate 11, the connecting belt 12, the magnetic strip 13, the vent hole 101, the abutment section 102, the vacuum component 2, the vacuum sleeve 21, the tightening port 201, the suction tube port 202, the flexible abutment section 300, the inflation head 400, the end cover 401, and the inflation tube 402. DETAILED DESCRIPTION
[0024] The following embodiments of the technical solution of the present invention are described in detail in conjunction with the accompanying drawings. The following embodiments are only used to more clearly illustrate the technical solution of the present invention, and are therefore only used as examples, and cannot be used to limit the protection scope of the present invention.
[0025] The embodiment is basically as shown in the attached Figures 1 to 3 As shown:
[0026] Embodiment 1:
[0027] like Figure 1 - Figure 3 As shown, a skin pressure sensing device provided in this embodiment can avoid tearing of the wound caused during the process of removing the medical bandage.
[0028] The present invention provides a skin pressure sensing device, comprising: a mounting plate 1, wherein the mounting plate 1 is provided with at least one connecting plate 11 and a connecting belt 12; wherein any two adjacent connecting plates 11 are connected by a connecting belt 12; wherein the connecting plate 11 is also provided with at least one vent hole 101, wherein the vent hole 101 is evenly distributed on the connecting plate 11; wherein the connecting plate 11 is located on the surface of the patient's skin; and a vacuum component 2, wherein the vacuum component 2 is arranged above the mounting plate 1 and covers the skin; the vacuum component 2 includes a vacuum sleeve 21, and the vacuum sleeve 21 is provided with a tightening port 201, wherein the vacuum sleeve 21 is fastened to the patient through the tightening port 201, and a vacuum can be formed. In actual use, the purpose of this design is to facilitate the separation of the wound and ensure the reduction of the tearing sensation of the patient's skin; at the same time, the vacuum component 2 used can effectively form an anaerobic environment, so that the growth of bacteria can be reduced and the rehabilitation efficiency can be effectively improved.
[0029] In order to reduce direct contact, in this embodiment, the connecting plate 11 is further provided with abutment sections 102. The abutment sections 102 are provided at two locations, and are respectively provided on one side of the connecting plate 11 and close to the upper and lower ends of the connecting plate 11; wherein the abutment sections 102 abut against the skin. In actual use, the abutment sections 102 in this design are convenient for abutting against a normal arm, so that a cavity can be formed between the wound and the connecting plate 11, so that it is convenient for the patient to loosen and stretch the skin during exercise and daily life, reducing the impact of traditional bandages on the patient's life.
[0030] At the same time, in order to facilitate the connection stability of the connecting plate 11, in this embodiment, the connecting belt 12 is provided with multiple roots, wherein any adjacent connecting plates 11 are provided with two connecting belts 12. In actual use, the purpose of this design is to facilitate the connection of two connecting plates 11, so that it is convenient to disassemble. Only one of them needs to be disassembled to quickly and conveniently disassemble the other connecting plates 11. In this way, the influence of traditional bandaging methods on wound tearing can be reduced. And in order to facilitate deformation, in this embodiment, the connecting belt 12 is made of an elastic belt. In actual use, this design facilitates the placement of the device on the patient's arm; in actual work, the patient's arm is firstly applied with medicine, and then the connecting plate 11 is installed on the patient's arm in turn, so that the external protection of the patient's wound after the medicine is applied is formed. By designing the connecting belt 12 as an elastic belt, it is convenient to wrap the device around the patient's body and improve its degree of deformation.
[0031] In order to facilitate the quick connection effect, in this embodiment, the mounting plate 1 further includes a magnetic strip 13, which is provided at one place and installed on the side of the connecting plate 11. In actual use, the rack is provided on the outermost connecting plate 11, and this design is convenient for connecting into a cylindrical shape. Of course, in order to facilitate fixing, a medical bandage is also used to pass through the vent hole 101 for fixed connection.
[0032] In this embodiment, the vacuum sleeve 21 is also provided with a suction pipe port 202, and the suction pipe port 202 is connected to an external air pump, wherein a protective gas is first introduced to evacuate the gas in the vacuum sleeve 21, and then the vacuum sleeve 21 is sucked, and the suction pipe port 202 is tightly closed by a cable tie. In actual use, the purpose of this design is to facilitate the emptying. In actual work, the protective gas is first injected into the vacuum sleeve 21 to discharge the internal gas, especially oxygen, and then the vacuum sleeve 21 is evacuated and the whole is wrapped around the connecting plate 11 to form an outer protective sleeve; of course, the vacuum sleeve 21 is made of silicone material, which can effectively increase the actual service life. At the same time, this operation realizes an anaerobic environment in the wound part through the later cable tie, effectively avoiding the growth of bacteria in an aerobic environment, thereby improving the efficiency of wound recovery.
[0033] In this embodiment, the protective gas is nitrogen. In practical use, this gas is easy to obtain and can achieve effective protection.
[0034] Embodiment 2:
[0035] like Figure 4 - Figure 5 As shown, the flexible abutting section 300 provided in this embodiment is a further improvement of the abutting section 102 provided in the first embodiment, and the flexible abutting section 300 can effectively contact the skin, so that the contact stability can be maintained, and at the same time, a certain airtightness can be maintained to prevent the drug from spilling out of the wound. Of course, the design of the above-mentioned flexible abutting section 102 can be made of a liquid jacket or a silicone flexible material.
[0036] Embodiment 3:
[0037] like Figure 6 As shown, the present embodiment provides a convenient inflation and exhaust vacuum sleeve 21, the structure of which is basically the same as the vacuum sleeve 21 of the above-mentioned embodiment 1, except that it also includes an inflation head 400, and the inflation head 400 is fixedly mounted on the suction pipe mouth 202. In actual design, the inflation head adopts the design of an end cover 401 and an inflation tube 402, wherein the end cover 401 is mounted at the pipe mouth of the suction pipe mouth 202 and is sealed and connected to the suction pipe mouth 202; the inflation tube 402 is fixedly mounted on the end cover 401, passes through the end cover 401, and is used to communicate with an external air source.
[0038] In actual work, firstly, the medicine is applied to the patient's burn area, and then the connecting plate 11 is placed on the wound in turn and covered in a ring shape; then the vacuum sleeve 21 is covered on the wound and on the outside of the connecting plate 11; at this time, nitrogen is first filled into the vacuum sleeve 21 through the suction pipe port; then, after seeing that the vacuum sleeve 21 is expanded, the gas in the vacuum sleeve 21 is extracted and tied tightly to achieve sealing; in this way, the medicine application process is completed; when it is necessary to change the dressing, it is only necessary to fill the gas into the vacuum sleeve 21 first; then remove the vacuum sleeve 21, and then remove the connecting plate 11; finally, the dressing can be changed.
[0039] In summary, a skin pressure sensing device is not only reasonably designed but also easy to operate. It can reduce the growth of wound bacteria by achieving an anaerobic environment and effectively improve the efficiency of wound recovery. Therefore, the device is suitable for industry promotion.
[0040] The above embodiments are only used to illustrate the technical solutions of the present invention, rather than to limit it. Although the present invention has been described in detail with reference to the aforementioned embodiments, those skilled in the art should understand that they can still modify the technical solutions described in the aforementioned embodiments, or replace some or all of the technical features therein with equivalents. These modifications or replacements do not deviate the essence of the corresponding technical solutions from the scope of the technical solutions of the embodiments of the present invention, and they should all be included in the scope of the claims and specification of the present invention.
Claims
1. A skin pressure sensing device, characterized in that: include: An installation panel assembly, wherein the installation panel assembly is provided with at least one connection plate and a connection belt; wherein any two adjacent connection plates are connected by a connection belt; the connection plate is also provided with at least one ventilation hole, and the ventilation holes are evenly distributed on the connection plate; wherein the connection plate is located on the patient's skin surface; and A vacuum component is arranged above the mounting assembly plate and covers the skin; the vacuum component includes a vacuum sleeve, and the vacuum sleeve is provided with a tightening port, and the vacuum sleeve is fastened to the patient through the tightening port and can form a vacuum.
2. A skin pressure sensing device according to claim 1, characterized in that: The connecting plate is also provided with abutment sections, and the abutment sections are provided at two locations, and are respectively arranged on one side of the connecting plate and close to the upper and lower ends of the connecting plate; wherein the abutment sections abut against the skin.
3. The skin pressure sensing device according to claim 1, characterized in that: There are a plurality of connecting belts, wherein any adjacent connecting plates are provided with two connecting belts.
4. The skin pressure sensing device according to claim 1, characterized in that: The connecting belt is made of an elastic belt.
5. The skin pressure sensing device according to claim 1, characterized in that: The mounting plate assembly also includes a magnetic strip, which is provided at one location and mounted on the side of the connecting plate.
6. The skin pressure sensing device according to claim 1, characterized in that: The vacuum jacket is also provided with a suction pipe opening, which is communicated with an external air pump, wherein protective gas is first introduced to evacuate the gas in the vacuum jacket, and then the vacuum jacket is sucked, and the suction pipe opening is tightly closed by a cable tie.
7. The skin pressure sensing device according to claim 6, characterized in that: The protective gas is nitrogen.