Cold and hot comparison treatment equipment

By designing a hot and cold comparison treatment equipment including energy storage warehouse, buffer warehouse and heating component, it solves the problem of muscle rigidity and temperature discomfort that high -intensity athletes may occur during cold and hot compresses, achieving safe and effective cold cold Hot -alternative treatment.

CN222399102UActive Publication Date: 2025-01-28BEIJING RUIJINGFOUNDER SCI & TRADE CO LTD
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Patent Information

Application Number
CN202420962473.9
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-05-07
Publication Date
2025-01-28
Estimated Expiration
2034-05-07

AI Technical Summary

Technical Problem

Existing cold and hot compress treatments may cause irreversible muscle stiffness in high-intensity athletes, and the temperature adjustment of ice bags and hot water bags is inconvenient, which can easily cause frostbite or scalds.

Method used

A hot and cold comparison treatment equipment is designed, including the main body and application pads. The device main body is equipped with an energy storage warehouse, buffer warehouse and working warehouse. By heating the temperature, the ice water temperature is adjusted to ensure that the cold and hot compress temperature are in the safe interval.

Benefits of technology

By accurately regulating cold compresses and hot compress temperatures, the muscle rigidity and too high temperature or too high temperature are avoided, and the safety and effectiveness of treatment are ensured.

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Abstract

The utility model provides cold and hot contrast treatment equipment which comprises an equipment main body and a dressing pad, the equipment body comprises an inner cavity, an energy storage bin, a buffering bin, a working bin and a heating assembly. The working bin is communicated with the application pad through a second infusion tube and a liquid return tube; the heating assembly is located in the working bin. A plurality of filter holes communicated with the surge bin are formed in the side wall of one side, close to the surge bin, of the energy storage bin; a first water pump and a first infusion tube are arranged in the surge bin, one end of the first infusion tube communicates with the first water pump, and the other end of the first infusion tube extends to the top of the working bin; a one-way overflow assembly and a second water suction pump are arranged in the working bin; the one-way overflow assembly is communicated with the energy storage bin, and the second water suction pump is communicated with the application pad through a second infusion tube; and the application pad is communicated with the working bin through a liquid return pipe. According to the application, ice blocks can be prevented from being in direct contact with the skin, the hot compress temperature is more accurate, and frostbite or scald is avoided through alternate cooling and heating treatment.
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Description

Technical Field

[0001] The utility model relates to the technical field of therapeutic instruments, in particular to a cold-heat contrast therapeutic device. Background Art

[0002] When an acute sprain or collision occurs during exercise, it will cause local congestion and edema of the soft tissue. At this time, cold or hot compress therapy can reduce the congestion and edema of the soft tissue. However, for high-intensity professional athletes, cold compress alone may cause irreversible stiffness of muscle tissue and affect athletic ability, so cold and hot compresses need to be used alternately for treatment. Usually, cold and hot compresses are applied with ice packs and hot water bags on the affected area. Not only will cold compresses cause the ice to come into direct contact with the skin, but the temperature of hot compresses cannot be adjusted, which can easily cause secondary frostbite or burns to the patient. Utility Model Content

[0003] In order to solve the above problems, the purpose of the embodiments of the present utility model is to provide a cold and hot contrast treatment device.

[0004] In a first aspect, an embodiment of the utility model provides a cold-heat contrast therapy device, characterized in that it comprises: a device body and a pad;

[0005] The equipment body comprises: an inner cavity, an energy storage chamber, a buffer chamber, a working chamber and a heating component;

[0006] The buffer bin is fixed on the side wall of the energy storage bin, and the buffer bin and the working bin are arranged side by side; the working bin and the pad are connected through a second infusion tube and a liquid reflux tube;

[0007] The heating component is located in the working chamber;

[0008] A plurality of filter holes communicating with the buffer bin are arranged on the side wall of the energy storage bin close to the buffer bin;

[0009] A first water pump and a first infusion tube are arranged in the buffer bin, one end of the first infusion tube is connected to the first water pump, and the other end of the first infusion tube extends to the top of the working bin;

[0010] The working chamber is provided with: a one-way overflow component and a second water pump; the one-way overflow component is connected to the energy storage chamber, and the second water pump is connected to the pad through the second infusion tube;

[0011] The pad is communicated with the working chamber through the liquid reflux pipe.

[0012] In the solution provided in the first aspect of the embodiment of the utility model, an energy storage bin, a buffer bin and a working bin are respectively arranged in the main body of the device, a filter hole is arranged between the energy storage bin and the buffer bin, a first water pump is arranged between the buffer bin and the working bin, a heating component is arranged in the working bin, and the working bin is connected to the pad through the second water pump; compared with the hot water bag and ice bag for hot and cold compresses in the related art, ice water is directly poured into the energy storage bin during cold compress, and when the ice water enters the working bin, the heating component can adjust the temperature of the ice water to avoid muscle damage caused by too low temperature during ice compress; during hot compress, the heating component is used to melt the ice water and accurately control the heating temperature, so that the hot compress temperature is more accurate, and through alternating hot and cold treatment, the cold compress temperature and the hot compress temperature will be maintained in the most scientific temperature range of clinical experiments, and frostbite or scalds can be avoided through alternating hot and cold treatment.

[0013] In order to make the above-mentioned objects, features and advantages of the present invention more obvious and easy to understand, preferred embodiments are given below and described in detail with reference to the accompanying drawings. BRIEF DESCRIPTION OF THE DRAWINGS

[0014] In order to more clearly illustrate the embodiments of the utility model or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the utility model. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying creative work.

[0015] Figure 1 The working principle diagram of the cold and heat contrast therapy device provided by the embodiment of the utility model is shown;

[0016] Figure 2 A schematic diagram of the three-dimensional structure of the cold and heat contrast therapy device provided by an embodiment of the utility model is shown;

[0017] Figure 3 A first cross-sectional view of the cold-heat contrast therapy device provided by an embodiment of the utility model is shown;

[0018] Figure 4 A second cross-sectional view of the cold-heat contrast therapy device provided by an embodiment of the utility model is shown;

[0019] Figure 5 A third cross-sectional view of the cold-heat contrast therapy device provided by an embodiment of the utility model is shown. DETAILED DESCRIPTION

[0020] In the description of the present invention, it should be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "up", "down", "front", "back", "left", "right", "vertical", "horizontal", "top", "bottom", "inside", "outside", "clockwise", "counterclockwise" and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the accompanying drawings, and are only for the convenience of describing the present invention and simplifying the description, and do not indicate or imply that the referred device or element must have a specific orientation, be constructed and operated in a specific orientation, and therefore should not be understood as a limitation on the present invention.

[0021] In addition, the terms "first" and "second" are used for descriptive purposes only and should not be understood as indicating or implying relative importance or implicitly indicating the number of the indicated technical features. Therefore, the features defined as "first" and "second" may explicitly or implicitly include one or more of the features. In the description of the present utility model, the meaning of "plurality" is two or more, unless otherwise clearly and specifically defined.

[0022] In the present invention, unless otherwise clearly specified and limited, the terms "install", "connect", "connect", "fix" and the like should be understood in a broad sense, for example, it can be a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection, or it can be an indirect connection through an intermediate medium, or it can be the internal communication of two components. For ordinary technicians in this field, the specific meanings of the above terms in the present invention can be understood according to specific circumstances.

[0023] Example

[0024] Cold compress and hot compress are often used in medical care as auxiliary treatment methods.

[0025] Cold compress: Applying a low-temperature object (the medically effective temperature is usually 5-10°C) to the injured part of the patient's body can cause the blood vessels to contract and reduce blood flow. This can effectively reduce inflammation, inhibit pain nerves and thus reduce pain.

[0026] Hot compress: Applying warm objects (the effective temperature for medical students is usually 38-42°C) to the injured part of the patient's body can dilate blood vessels and speed up blood flow. This can increase the flow of oxygen and essential nutrients to the injured part of the body and speed up recovery and healing.

[0027] By alternating between the two states of cold and hot compresses, hot and cold contrast therapy can produce a "pumping" effect to help expel metabolic waste from body tissues and enhance the delivery of oxygen and nutrients, thereby helping muscle tissue to recover and regenerate, and avoiding muscle tissue stiffness, muscle weakness, etc.

[0028] Usually, cold and hot compresses are chosen by applying ice bags and hot water bags to the affected area. Not only will cold compresses cause the ice to come into direct contact with the skin, but the temperature of hot compresses cannot be adjusted, which can easily cause frostbite and burns to the patient.

[0029] Based on this, see Figure 1 The working principle diagram of the hot and cold contrast therapy device shown and refer to Figure 2 The three-dimensional structural diagram of the cold and heat contrast therapy device shown in the figure, this embodiment proposes a cold and heat contrast therapy device, which includes: a device body 10 and a pad; the device body 10 includes: an inner cavity, an energy storage bin 13, a buffer bin 14, a working bin 15 and a heating component; the energy storage bin, the buffer bin and the working bin are all located in the inner cavity; the buffer bin 14 is fixed on the side wall of the energy storage bin 13, and the buffer bin 14 and the working bin 15 are arranged side by side; the working bin 15 is connected to the pad through a second infusion tube and a liquid reflux tube; the heating component is located in the working bin 15; the storage bin 13 A plurality of filter holes 16 connected to the buffer bin 14 are arranged on the side wall of the energy bin 13 close to the buffer bin 14; a first water pump and a first infusion tube are arranged in the buffer bin 14, one end of the first infusion tube is connected to the first water pump, and the other end of the first infusion tube extends to the top of the working bin 15; the working bin 15 is provided with: a one-way overflow component and a second water pump 19; the one-way overflow component is connected to the energy storage bin 13, and the second water pump 19 is connected to the pad through the second infusion tube; the pad is connected to the working bin 15 through the liquid reflux pipe.

[0030] In this embodiment, both the first infusion tube and the second infusion tube are flexible hoses. A delivery port connected to the outside is provided on the top of the energy storage bin 13, and a device cover 11 is installed on the delivery port. When the device cover 11 is opened, only the energy storage bin 13 is directly exposed to the outside, and a sealing plate is additionally installed on the top of the buffer bin 14 and the working bin 15. The filter hole 16 is provided at the bottom of the buffer bin 14, and the one-way overflow component is provided at the top of the working bin 15.

[0031] It should be noted that due to the presence of the filter hole 16, the energy storage bin 13 and the buffer bin 14 are equivalent to communicating vessels, and the liquid level of the energy storage bin 13 is always consistent with the liquid level of the buffer bin 14. However, the buffer bin 14 and the working bin 15 are independent of each other, and the liquid inside them cannot flow freely. The liquid in the buffer bin 14 can only be transported to the working bin 15 in one direction through the first pump. When pouring room temperature water and ice cubes into the energy storage bin 13, it should be noted that the liquid level in the energy storage bin 13 should be lower than the height of the one-way overflow component. Therefore, a water filling scale line lower than the one-way overflow component is set on the side wall of the energy storage bin 13, and the volume of the energy storage bin 13 needs to be greater than the volume of the working bin 15.

[0032] In particular, a first liquid level monitor linked to the first water pump is provided in the buffer bin 14 , a second liquid level monitor linked to the second water pump 19 is provided in the working bin 15 , and a temperature monitor linked to the heating assembly is also provided in the working bin 15 .

[0033] Specifically, when performing a cold compress, first pour room temperature water and ice cubes into the energy storage bin 13. At this time, the room temperature water and ice cubes are exchanged for heat and become cold water. The cold water flows into the buffer bin 14 through the filter hole 16, and the impurities such as crushed ice in the cold water are isolated outside the buffer bin 14 by the filter hole 16. When the liquid level of the cold water in the buffer bin 14 is higher than the height of the first liquid level monitor, the first liquid level monitor triggers and controls the first pump to start, and the first pump delivers the cold water in the buffer bin 14 to the working bin 15 through the first infusion tube. When the liquid level of the cold water in the working bin 15 is higher than the second liquid level monitor again, the second liquid level monitor is triggered and controls the second pump 19 to start, and the second pump 19 delivers the cold water in the working bin 15 to the pad through the second infusion tube. The pad is in direct contact with human skin, and the cold water in the pad directly performs a cold compress operation on the skin. After absorbing the heat of the skin, the cold water in the pad flows back to the working bin 15 through the liquid reflux tube. The first pump continuously injects cold water into the working chamber 15. The subsequently injected cold water will neutralize the liquid in the pad that absorbs a small amount of skin heat and flows back to the working chamber 15. After neutralization, the liquid in the working chamber 15 will always remain at a low temperature. Therefore, the liquid in the pad that flows back to the working chamber 15 through the liquid return pipe will not change the overall liquid temperature in the working chamber 15. The liquid delivered to the pad by the second pump 19 is still cold water. When the liquid level in the working chamber 15 rises to the height of the one-way overflow component, the excess liquid in the working chamber 15 will be discharged to the energy storage chamber 13 through the one-way overflow component. At this point, the cold compress is completed.

[0034] When performing hot compress, set the starting temperature of the temperature monitor. After turning on the hot compress mode, the temperature monitor monitors the temperature of the liquid in the working chamber 15. When the temperature of the liquid in the working chamber 15 is lower than the set temperature, the temperature monitor controls the heating component to start, and the heating component heats the liquid in the working chamber 15 until the liquid in the working chamber 15 meets the set temperature. At this time, the temperature monitor controls the heating component to stop heating and starts the second water pump 19, and the second water pump 19 delivers hot water to the pad through the second infusion tube. The process of the liquid in the pad flowing back to the energy storage chamber 13 is the same as that of cold compress. Please refer to the above-mentioned cold compress reflux process, so it will not be repeated.

[0035] Among them, see Figure 5As shown in the third cross-sectional view of the cold and hot contrast therapy device, the one-way overflow assembly comprises: a one-way valve and an overflow port 21; the overflow port 21 is arranged at the top of the side wall of the working bin 15 close to the energy storage bin 13; the one-way valve is installed in the overflow port 21, and the overflow port 21 is also connected to the energy storage bin 13.

[0036] In this embodiment, the one-way valve is a conventional reverse water check valve. In order to facilitate the discharge of excess liquid in the working chamber 15 to the energy storage chamber 13, the overflow port 21 is tilted downward toward the side of the energy storage chamber 13 to facilitate the liquid to quickly fall to the energy storage chamber 13 when passing through the overflow port 21.

[0037] See also Figure 3 The first cross-sectional view of the thermal contrast therapy device shown and the Figure 4 In the second cross-sectional view of the cold and hot contrast therapy device shown in the figure, the above-mentioned heating component includes: a box body 18, a circuit board 17, a resistance wire and a hollow heat-conducting plate 20; the box body 18 is installed on the side wall of the working chamber 15, and the hollow heat-conducting plate 20 is fixed to the bottom of the box body 18; the circuit board 17 is located in the box body 18; one end of the resistance wire is located in the hollow heat-conducting plate 20, and the other end extends into the box body 18 and is connected to the circuit board 17.

[0038] Specifically, in addition to the above structure, the heating assembly can also be replaced by a heating rod. Therefore, the specific heating structure of the heating assembly is not limited here.

[0039] In one embodiment, the working chamber 15 further includes: a secondary filter assembly; the secondary filter assembly includes: a frame and a filter; the frame is installed on the side wall of the working chamber 15, and the frame is located below the first infusion tube; the filter is fixed in the frame.

[0040] Specifically, the first pump drains the liquid in the buffer bin 14 downward from the top of the working bin 15 through the first water delivery pipe, and the liquid first passes through the filter screen and then enters the working bin 15 during the falling process. The filter screen will filter the liquid again.

[0041] Furthermore, an interlayer is formed between the equipment body 10 and the inner cavity, and a drainage component is arranged at the bottom of the equipment body 10; the drainage component includes: a first down liquid pipe, a second down liquid pipe, a liquid outlet pipe 22 and a cover body 12; the liquid outlet pipe 22 is installed at the bottom of the equipment body 10, one end of the liquid outlet pipe 22 is connected to the outside, and the other end is connected to the interlayer; one end of the first down liquid pipe is connected to the working bin 15, and the other end extends to the interlayer and is connected to the liquid outlet pipe 22; one end of the second down liquid pipe is connected to the energy storage bin 13, and the other end extends to the interlayer and is connected to the liquid outlet pipe 22; the cover body 12 is sleeved on one end of the liquid outlet pipe 22 connected to the outside, and is threadedly connected to the liquid outlet pipe 22.

[0042] In the embodiment of the utility model, a water blocking member inserted into the liquid outlet pipe 22 is provided on the side of the cover body 12 facing the liquid outlet pipe 22 to enhance the water blocking effect of the cover body 12 on the liquid outlet pipe 22. The first lower liquid pipe and the second lower liquid pipe need to be inserted into the liquid outlet pipe 22.

[0043] Specifically, when it is necessary to drain the liquid in the device body 10, the cover body 12 is rotated to loosen the threads at the cover body 12 and the threads at the liquid outlet pipe 22 until the cover body 12 is separated from the liquid outlet pipe 22. At this time, the liquid in the working chamber 15 flows downward into the first lower liquid pipe due to the action of gravity, and the liquid in the energy storage chamber 13 flows downward into the second lower liquid pipe due to the action of gravity. The liquids in the first lower liquid pipe and the second lower liquid pipe merge in the liquid outlet pipe 22 and are discharged to the outside. In particular, one end of the liquid outlet pipe 22 extending to the outside can be fixedly connected to a lengthened rubber hose, and a plug is provided at one end of the rubber hose away from the liquid outlet pipe 22. When it is necessary to drain the energy storage chamber 13 and the working chamber 15, the drainage direction can be controlled by controlling the direction of the rubber hose.

[0044] Furthermore, the device body 10 is also provided with an air pump and an air delivery pipe connected to the air pump, and the air delivery pipe is a flexible hose; the pad includes: a liquid storage chamber and a pressurizing chamber; the pressurizing chamber is located at the periphery of the liquid storage chamber and an air pressure sensor is provided in the pressurizing chamber; the liquid storage chamber is connected to the working chamber 15 through the second liquid delivery pipe and the liquid return pipe respectively; the pressurizing chamber is connected to the air pump through the air delivery pipe. The pressurizing chamber is provided with an air release hole connected to the outside and a plug that cooperates with the air release hole.

[0045] In the embodiment of the utility model, the pad needs to be attached to the skin to achieve the cold compress and hot compress functions on the skin. Therefore, the two ends of the pad are fixedly connected with straps. The pad is tied to the affected part of the patient that needs cold compress and hot compress through the straps.

[0046] Specifically, the air pump is turned on and injects gas into the pressurized chamber through the air pipe. At this time, due to the restraint of the strap, the gap between the pad and the skin gradually decreases, making the pad fit more closely to the skin, so that the temperature penetrates into the affected area more evenly and enhances the treatment effect.

[0047] Furthermore, the air pump is controlled by an air pressure sensor, which monitors the air pressure in the pressurized chamber. When the air pressure in the pressurized chamber reaches a set value, the air pump stops working. In particular, the set value includes three gear modes: low, medium and high. The low-range air pressure value is 25 mmHg, the medium-range air pressure value is 50 mmHg, and the high-range air pressure value is 75 mmHg. In this embodiment, the default is low.

[0048] In summary, the utility model provides a cold and hot contrast therapy device, by respectively arranging an energy storage bin 13, a buffer bin 14 and a working bin 15 in the device body 10, a filter hole 16 is arranged between the energy storage bin 13 and the buffer bin 14, a first water pump is arranged between the buffer bin 14 and the working bin 15, a heating component is arranged in the working bin 15, and the working bin 15 is connected with the pad through the second water pump 19; compared with the hot water bag and the ice bag for hot and cold compresses in the related art, ice water is directly poured into the energy storage bin 13 during cold compress, and when the ice water enters the working bin 15, the heating component can adjust the temperature of the ice water to avoid muscle damage caused by too low temperature during ice compress; during hot compress, the heating component is used to melt the ice water and accurately control the heating temperature, so that the hot compress temperature is more accurate, and through alternating hot and cold treatment, the cold compress temperature and the hot compress temperature will be maintained in the most scientific temperature range of clinical experiments, and through alternating hot and cold treatment, frostbite or scalds can be avoided.

[0049] The above is only a specific implementation of the utility model, but the protection scope of the utility model is not limited thereto. Any technical solution that can be easily thought of by a person skilled in the art within the technical scope disclosed by the utility model should be included in the protection scope of the utility model. Therefore, the protection scope of the utility model shall be based on the protection scope of the claims.

Claims

1. A cold and hot contrast therapy device, characterized in that: include: Device body and padding; The equipment body comprises: an inner cavity, an energy storage chamber, a buffer chamber, a working chamber and a heating component; The buffer bin is fixed on the side wall of the energy storage bin, and the buffer bin and the working bin are arranged side by side; the working bin and the pad are connected through a second infusion tube and a liquid reflux tube; The heating component is located in the working chamber; A plurality of filter holes communicating with the buffer bin are arranged on the side wall of the energy storage bin close to the buffer bin; A first water pump and a first infusion tube are arranged in the buffer bin, one end of the first infusion tube is connected to the first water pump, and the other end of the first infusion tube extends to the top of the working bin; The working chamber is provided with: a one-way overflow component and a second water pump; the one-way overflow component is connected to the energy storage chamber, and the second water pump is connected to the pad through the second infusion tube; The pad is communicated with the working chamber through the liquid reflux pipe.

2. The cold and heat contrast therapy device according to claim 1, characterized in that: The working chamber also includes: a secondary filtering component; The secondary filter assembly comprises: a frame and a filter screen; The frame is installed on the side wall of the working chamber, and the frame is located below the first infusion tube; The filter screen is fixed in the frame.

3. The cold and heat contrast therapy device according to claim 1, characterized in that: The one-way overflow assembly comprises: a one-way valve and an overflow port; The overflow port is arranged at the top of the side wall of the working bin close to the energy storage bin; The one-way valve is installed in the overflow port, and the overflow port is also connected to the energy storage bin.

4. The cold and heat contrast therapy device according to claim 1, characterized in that: An interlayer is formed between the equipment body and the inner cavity, and a drainage component is arranged at the bottom of the equipment body; The drainage assembly comprises: a first down-flow liquid pipe, a second down-flow liquid pipe, a liquid outlet pipe and a cover body; The liquid outlet pipe is installed at the bottom of the equipment body, one end of the liquid outlet pipe is connected to the outside, and the other end is connected to the interlayer; One end of the first liquid down pipe is connected to the working chamber, and the other end extends to the interlayer and is connected to the liquid outlet pipe; One end of the second liquid down pipe is connected to the energy storage bin, and the other end extends to the interlayer and is connected to the liquid outlet pipe; The cover body is sleeved on one end of the liquid outlet pipe communicating with the outside, and is threadedly connected with the liquid outlet pipe.

5. The cold and heat contrast therapy device according to claim 4, characterized in that: Also includes: Water blocking parts; The cover body is provided with a water blocking member inserted into the liquid outlet pipe on one side thereof facing the liquid outlet pipe.

6. The cold and heat contrast therapy device according to claim 1, characterized in that: The heating assembly comprises: a box body, a circuit board, a resistance wire and a hollow heat-conducting plate; The box body is installed on the side wall of the working chamber, and the hollow heat-conducting plate is fixed to the bottom of the box body; the circuit board is located in the box body; one end of the resistance wire is located in the hollow heat-conducting plate, and the other end extends into the box body and is connected to the circuit board.

7. The cold and heat contrast therapy device according to claim 1, characterized in that: The device body is also provided with an air pump and an air delivery pipe connected to the air pump; the pad comprises: a liquid storage chamber and a pressurizing chamber; The liquid storage chamber is located at the periphery of the pressurizing chamber; The liquid storage chamber is communicated with the working chamber through the second liquid infusion tube and the liquid reflux tube respectively; The pressurizing chamber is communicated with the air pump through the air delivery pipe.

8. The cold and heat contrast therapy device according to claim 1, characterized in that: The volume of the energy storage bin is greater than the volume of the working bin.

9. The cold and heat contrast therapy device according to claim 7, characterized in that: The first liquid infusion tube, the second liquid infusion tube and the gas infusion tube are all flexible hoses.

10. The cold and heat contrast therapy device according to claim 1, characterized in that: The pad also includes: a strap; two ends of the strap are respectively fixedly connected to two ends of the pad.