Detumescence and analgesia mask used after oral implantation

Abstract

The utility model discloses a detumescence and analgesia mask used after oral implantation, which comprises a mask body, and the two sides of the mask body are connected with laces; the mask body is composed of an inner layer close to the face, an outer layer away from the face and a filtering layer located between the inner layer and the outer layer. The ice compress bag comprises a refrigerant, a water bag and an accommodating space for accommodating the ice compress bag; the accommodating space is divided into six independent placing areas, namely a nose base area, a lower jaw area, a left cheek area, a right cheek area, a left submandibular area and a right submandibular area which correspond to the oral implant operation area; at least part of the puncturing part extends into the ice compress bag, and the puncturing part is used for puncturing the water bag so that the refrigerant and the water can be mixed to achieve refrigeration ice compress; and the puncturing pieces are in one-to-one correspondence with the six placing areas. According to the detumescence and analgesia mask used after oral implantation, one or more subareas can be selected, the water bag is punctured by pressing the puncture piece of each subarea, water and refrigerant are mixed, and ice compress can be carried out by utilizing endothermic reaction for cooling without hand holding and squeezing.

Description

Technical Field

[0001] This utility model relates to the field of medical devices, and in particular to a mask for reducing swelling and relieving pain after dental implant surgery. Background Technology

[0002] After dental implant surgery, blood and tissue exudate can seep into surrounding tissues through the loose subcutaneous tissue, causing postoperative swelling, bruising, and discoloration in the implant area and corresponding cheek area. In severe cases, the bruising can extend to the infraorbital region and the lower border of the mandible. Swelling and bruising usually subside within one to two weeks, but to facilitate faster absorption, intermittent ice application after surgery is currently recommended.

[0003] Currently, cryogenic ice packs are commonly used in clinical practice. These are made by freezing ice packs filled with water or gel in a refrigerator before use. Due to their simplicity, ease of operation, and low production cost, they are adopted by many hospitals and clinics.

[0004] After freezing, ice packs become hard and angular. Patients often experience poor results because the ice packs don't fit the face properly, cannot be accurately applied to the cheek corresponding to the transplanted area, and cannot be secured. This leads to persistent bruising and swelling on the cheeks that is difficult to reduce, affecting the patient's daily life. Furthermore, because ice packs need to be frozen, patients cannot use them anytime and anywhere, limiting their application. Utility Model Content

[0005] This invention aims to solve at least one of the technical problems existing in the prior art. To this end, this invention proposes a mask for reducing swelling and pain after dental implant surgery. Patients can choose the appropriate ice pack area based on their postoperative condition. A puncture device is used to puncture the water bag to achieve mixed heat absorption and cooling, allowing for precise ice application anytime, anywhere.

[0006] A swelling-reducing and pain-relieving mask according to a first aspect of the present invention includes a mask body with straps on both sides; the mask body consists of an inner layer close to the face, an outer layer away from the face, and a filter layer located between the inner and outer layers; an ice pack including a refrigerant and a water bag, with a receiving space formed between the filter layer and the inner layer to accommodate the ice pack; the receiving space is divided into six independent placement areas for placing the ice pack, the placement areas being the nasal floor area, mandibular area, left cheek area, right cheek area, left submandibular area, and right submandibular area corresponding to the oral implantation surgery area; a puncture device, at least partially inserted into the ice pack, the puncture device being used to puncture the water bag to mix the refrigerant with water to achieve cooling and ice application; the puncture device is provided in a one-to-one correspondence with the six placement areas.

[0007] According to an embodiment of this utility model, a swelling-reducing and pain-relieving mask for post-oral implant surgery has at least the following technical effects: After the patient's implant surgery, different zones can be selected according to the implantation area, one or more zones can be selected. By pressing the puncture device of each zone, the water bag is punctured, and the water and refrigerant mix. Cooling and ice application can be performed by utilizing the endothermic reaction without squeezing. After the inside of the mask is fitted to the face, the straps are tied to the head and back of the head to secure the mask.

[0008] According to some embodiments of this utility model, the ice pack has an opening on the side away from the face, the puncture member passes through the opening, and the inner wall of the opening is coated with sealant for fixing the puncture member.

[0009] According to some embodiments of the present invention, the puncture head of the puncture member is blunt and faces the water bag.

[0010] According to some embodiments of the present invention, a pressure block is provided on the side of the puncture member away from the water bag, and the pressure block is located on the outside of the ice pack and is fixedly connected to the puncture member.

[0011] According to some embodiments of this utility model, the ice pack is made of non-PVC composite film soft bag material, and the puncture device and water bag are both made of plastic.

[0012] According to some embodiments of the present invention, a dressing layer is provided on the side of the inner layer near the face, and the dressing layer includes a gel, wherein the gel is a polymer material with good compatibility with traditional Chinese medicine ingredients.

[0013] According to some embodiments of the present invention, the dressing layer further includes a solvent, a co-solvent, and a penetration enhancer mixed with the gel.

[0014] According to some embodiments of the present invention, a removable isolation layer is provided on the surface of the dressing layer to protect the gel.

[0015] According to some embodiments of the present invention, the mask body covers the entire lower 1 / 3 of the face and the area under the chin, but does not cover the nose; the placement area does not cover the lips.

[0016] According to some embodiments of this utility model, the outer layer is made of non-woven fabric coated with waterproof material, the filter layer is made of meltblown non-woven fabric, and the inner layer is made of elastic non-woven fabric; the straps are made of non-woven fabric and are heat-pressed and bonded to both sides of the mask body.

[0017] Additional aspects and advantages of this invention will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the invention. Attached Figure Description

[0018] The present invention will be further described below with reference to the accompanying drawings and embodiments.

[0019] Figure 1 This is a structural schematic diagram of an embodiment of the present utility model;

[0020] Figure 2 This is a schematic diagram illustrating the use of an embodiment of this utility model;

[0021] Figure 3 This is an exploded view of an embodiment of the present invention;

[0022] Figure 4 This is a structural diagram of the puncture device and the ice pack;

[0023] Figure 5 This is a cross-sectional view of the inner layer of the mask.

[0024] Figure label:

[0025] The mask body is 100, the inner layer is 110, the dressing layer is 111, the isolation layer is 112, the outer layer is 120, the filter layer is 130, and the straps are 140.

[0026] Nasal base area 200, mandibular area 210, left cheek area 220, right cheek area 230, left submandibular area 240, right submandibular area 250;

[0027] Ice pack 300, opening 301, sealant 302, refrigerant 310, water bag 320;

[0028] Piercing part 400, pressing block 410. Detailed Implementation

[0029] The embodiments of this utility model are described in detail below. Examples of these embodiments are shown in the accompanying drawings, wherein the same or similar reference numerals denote the same or similar elements or elements having the same or similar functions throughout. The embodiments described below with reference to the accompanying drawings are exemplary and are only used to explain this utility model, and should not be construed as limiting this utility model.

[0030] 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," "axial," "radial," and "circumferential," etc., indicating orientation or positional relationships, are based on the orientation or positional relationships shown in the accompanying drawings and are only for the convenience of describing this utility model and simplifying the description. They do not 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. Furthermore, features defined with "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of this utility model, unless otherwise stated, "a plurality of" means two or more.

[0031] In the description of this utility model, it should be noted that, unless otherwise explicitly specified and limited, the terms "installation," "connection," and "joining" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral connection; 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; and they can refer to the internal connection of two components. Those skilled in the art can understand the specific meaning of the above terms in this utility model based on the specific circumstances.

[0032] Reference Figures 1 to 5 An embodiment of the present invention provides a mask for reducing swelling and relieving pain after oral implant surgery, comprising a mask body 100, a tie 140, an ice pack 300, and a puncture device 400.

[0033] The mask body 100 consists of an inner layer 110 close to the face, an outer layer 120 away from the face, and a filter layer 130 located between the inner layer 110 and the outer layer 120.

[0034] The mask body 100 has straps 140 on both sides. The straps 140 on the mask are used to fix the ice pack 300 to the head and the back of the head, thus fixing the ice pack 300. This eliminates the need to hold the ice pack 300 for a long time, and the straps 140 are more comfortable than the ear loops.

[0035] The ice pack 300 includes a refrigerant 310 and a water bag 320. The filter layer 130 and the inner layer 110 form a space for accommodating the ice pack 300. The space is divided into six independent placement areas for placing the ice pack 300. The placement areas are the nasal base area 200, mandibular area 210, left cheek area 220, right cheek area 230, left submandibular area 240, and right submandibular area 250, which correspond to the oral implant surgery area. The coverage area is large and precise, and different areas can be selected for precise ice application after surgery.

[0036] Specifically, the ice pack 300 contains refrigerant 310 particles (such as ammonium salts like ammonium sulfate) and a water bag 320. The piercing element 400 extends at least partially into the ice pack 300 to puncture the water bag 320, allowing the refrigerant 310 particles to mix with the water. The endothermic reaction between the water and the refrigerant 310 rapidly cools the ice pack, eliminating the need to pre-freeze the ice pack 300 or pre-place the frozen ice pack 300 into the ice pack device, making it convenient to use.

[0037] The puncture device 400 is set up one-to-one with the six placement areas. After the patient's implantation, one or more areas can be selected to puncture the water bag 320 for ice application according to the implantation area.

[0038] Reference Figure 4 In some embodiments of this utility model, the ice pack 300 has an opening 301 on the side away from the face, through which the puncture member 400 passes. The inner wall of the opening 301 is coated with sealant 302 for fixing and connecting the puncture member 400.

[0039] In other embodiments, the outer layer 120 and filter layer 130 of the mask body 100 may also have through clearance holes corresponding to the opening 301, and these holes are connected to form a channel. The piercing member 400 enters the channel from the outside of the mask body 100 and extends into the ice pack 300. The inner wall of the channel is coated with sealant 302 to fix the piercing member 400 to the mask body 100.

[0040] Reference Figure 4 In a further embodiment of this utility model, the puncture head of the puncture member 400 is blunt and faces the water bag 320. The needle will only puncture the water bag 320 when an external force is applied, thus preventing the water bag 320 from breaking during transportation.

[0041] Reference Figure 4 In a further embodiment of this utility model, a pressure block 410 is provided on the side of the puncture member 400 away from the water bag 320. The pressure block 410 is located on the outside of the ice pack 300 and is made of silicone material, and is fixedly connected to the puncture member 400. When in use, pressing the pressure block 410 on the surface of the ice pack 300 will allow the puncture member 400 connected to the pressure block 410 to puncture the water bag 320.

[0042] In some embodiments of this utility model, the ice pack 300 is made of non-PVC composite film soft bag material, which is soft and skin-friendly, waterproof and frost-resistant, lightweight, high mechanical strength, and not easy to burst; the puncture part 400 and the water bag 320 are both made of plastic.

[0043] Reference Figure 5In some embodiments of this invention, a dressing layer 111 is provided on the side of the inner layer 110 closest to the face. The dressing layer 111 includes a gel, which is a polymer material with good compatibility with traditional Chinese medicine ingredients, ensuring uniform and stable dispersion of the active substances in the traditional Chinese medicine. The gel mainly contains a functional ingredient, which can be, but is not limited to, traditional Chinese medicine ingredients with anti-inflammatory, analgesic, and blood-activating functions such as Yunnan Baiyao and anti-inflammatory tincture. The drug is absorbed through the facial skin into the bloodstream to achieve an effective blood drug concentration, thereby realizing the effects of anti-inflammatory, analgesic, and blood-activating effects.

[0044] Reference Figure 5 In a further embodiment of the present invention, the dressing layer 111 also includes a solvent, a cosolvent, and a penetration enhancer mixed with the gel, which helps the functional components to be more evenly distributed in the gel, improves the transdermal absorption efficiency of the drug, and enhances the therapeutic effects of reducing swelling, relieving pain, and dispersing blood stasis.

[0045] Furthermore, adhesives and stabilizers are added to the gel to make it have a suitable texture, a certain degree of adhesion, and make it easy to apply to the inner layer 110 of the mask. It also fits the face well and is not easy to fall off, maintaining a stable structure and function.

[0046] Reference Figure 5 In a further embodiment of the present invention, a removable isolation layer 112 is provided on the surface of the dressing layer 111. A specially treated plastic film (such as polyethylene film) can be selected, which can adhere to the gel layer and is easy to remove, and is used to protect the gel layer and prevent it from being contaminated or dried.

[0047] Reference Figure 2 In some embodiments of this utility model, the mask body 100 covers the entire lower 1 / 3 of the face and the area under the chin, but does not cover the nose.

[0048] The placement area does not cover the lips, allowing the patient to breathe easily and preventing the exhaled hot air from melting the ice pack (300).

[0049] In some embodiments of this utility model, the outer layer 120 is made of non-woven fabric coated with waterproof material, the filter layer 130 is made of meltblown non-woven fabric, and the inner layer 110 is made of elastic non-woven fabric. The three layers, outer layer 120, filter layer 130 and inner layer 110, are sewn and fixed at the separation points of each ice application area, and the outermost edge is fixed by hot pressing.

[0050] The straps 140 are made of non-woven fabric and are heat-pressed and bonded to both sides of the mask body 100.

[0051] After the implantation procedure, different zones are selected based on the implantation site. One or more zones can be selected. By pressing the pressure block 410 of each zone, the puncture piece 400 connected to the pressure block 410 is pressurized, causing it to descend and contact the water bag 320. Finally, the water bag 320 is punctured, and the water and refrigerant 310 mix. Cooling is achieved through an endothermic reaction without the need for hand squeezing. The sealant 302 on the inner wall of the opening 301 prevents the liquid inside the ice pack 300 from leaking out of the opening 301. According to the selected zone, the patient peels off the corresponding isolation layer 112, applies the mask with the inside side against the face, and then ties the straps 140 around the head and back of the head to secure the mask. Intermittent ice application is performed within 24 hours after the procedure, for 15-20 minutes each time, with an interval of at least 30 minutes between applications. The mask can be changed afterward to accelerate the reduction of facial swelling and bruising.

[0052] In the description of this invention, it should be noted that the terms "vertical," "upper," "lower," "horizontal," etc., indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings. They are only for the convenience of describing this invention and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, they should not be construed as limitations on this invention.

[0053] In the description of this invention, it should also be noted that, unless otherwise explicitly specified and limited, the terms "set," "install," "connect," and "link" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral connection; 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; and they can refer to the internal connection of two components. Those skilled in the art can understand the specific meaning of the above terms in this invention according to the specific circumstances.

[0054] The above description is merely a preferred embodiment of the present invention and is not intended to limit the present invention. 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 mask for reducing swelling and relieving pain after oral implant surgery, characterized in that... include: The mask body (100) has straps (140) connected to both sides; the mask body (100) consists of an inner layer (110) close to the face, an outer layer (120) away from the face, and a filter layer (130) located between the inner layer (110) and the outer layer (120); An ice pack (300) includes a refrigerant (310) and a water bag (320). A receiving space for accommodating the ice pack (300) is formed between the filter layer (130) and the inner layer (110). The receiving space is divided into six independent placement areas for placing the ice pack (300). The placement areas are respectively the nasal floor area (200), mandibular area (210), left cheek area (220), right cheek area (230), left submandibular area (240), and right submandibular area (250) corresponding to the oral implant surgery area. A puncture device (400) extends at least partially into an ice pack (300). The puncture device (400) is used to puncture the water pack (320) so that the refrigerant (310) mixes with water to achieve cooling and ice application. The puncture device (400) is provided in a one-to-one correspondence with the six placement areas.

2. The anti-swelling and analgesic mask according to claim 1, characterized in that: The ice pack (300) has an opening (301) on the side away from the face, through which the puncture member (400) passes. The inner wall of the opening (301) is coated with sealant (302) for fixing the puncture member (400).

3. A swelling-reducing and analgesic mask for post-oral implant surgery as described in claim 2, characterized in that: The puncture head of the puncture device (400) is blunt and faces the water bag (320).

4. A swelling-reducing and analgesic mask for post-oral implant surgery as described in claim 2, characterized in that: The puncture member (400) has a pressure block (410) on the side away from the water bag (320). The pressure block (410) is located outside the ice pack (300) and is fixedly connected to the puncture member (400).

5. A swelling-reducing and analgesic mask for post-oral implant surgery as described in claim 1, characterized in that: The ice pack (300) is made of non-PVC composite film soft bag material, and the puncture device (400) and water bag (320) are both made of plastic.

6. A swelling-reducing and analgesic mask for post-oral implant surgery as described in claim 1, characterized in that: The inner layer (110) has a dressing layer (111) on the side near the face. The dressing layer (111) includes a gel, which is a polymer material with good compatibility with traditional Chinese medicine ingredients.

7. A swelling-reducing and analgesic mask for post-oral implant surgery as described in claim 6, characterized in that: The dressing layer (111) also includes a solvent, a cosolvent, and a penetration enhancer mixed with the gel.

8. A swelling-reducing and analgesic mask for post-oral implant surgery as described in claim 6, characterized in that: The dressing layer (111) has a removable isolation layer (112) on its surface to protect the gel.

9. A swelling-reducing and analgesic mask for post-oral implant surgery according to claim 1, characterized in that: The mask body (100) covers the entire lower 1 / 3 of the face and the area under the chin, but does not cover the nose; the placement area does not cover the lips.

10. A swelling-reducing and analgesic mask for post-oral implant surgery according to claim 1, characterized in that: The outer layer (120) is made of nonwoven fabric coated with waterproof material, the filter layer (130) is made of meltblown nonwoven fabric, the inner layer (110) is made of elastic nonwoven fabric, and the straps (140) are made of nonwoven fabric and are heat-pressed to both sides of the mask body (100).

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