Phlebitis timing hydropathic compress device
By designing a phlebitis timing wet compressor and automatically humidifying gauze blocks with water pumps and humidity sensors, the problem of frequent monitoring of humidity in existing wet compress methods is solved, reducing the workload of medical staff and improving the treatment effect.
Patent Information
- Application Number
- CN202420590794.0
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-03-26
- Publication Date
- 2025-01-03
- Estimated Expiration
- 2034-03-26
AI Technical Summary
The existing wet compression methods for phlebitis require medical staff to continuously monitor the humidity of the gauze, which leads to a large workload and affects the treatment effect, and it is difficult to maintain the wet compression effect.
A phlebitis timing wet compressor is designed, including a liquid storage box, a fixing belt and a wet compressor. It adopts a water pump, a humidity sensor and a timing module to automatically humidify the gauze block to prevent the seepage of the medicine liquid, and facilitate the use of the observation window and the operating panel. Medicinal solution addition and function settings.
The automatic humidification function is realized, which reduces the workload of medical staff, ensures the treatment effect, and prevents the seepage of the drug liquid through viscose and airbags, enhancing the fixity and humidity monitoring capabilities of the wet compressing mechanism.
Smart Images
Figure CN222286215U_ABST
Abstract
Description
Technical Field
[0001] The utility model belongs to the technical field of medical equipment, and in particular relates to a phlebitis timing wet compress. Background Art
[0002] Phlebitis refers to an inflammatory phenomenon that occurs in the veins. It may be caused by a long-term lack of exercise, which leads to obstructed blood circulation in the blood vessels, or local trauma, which leads to coagulation dysfunction. It may also cause local swelling, muscle soreness, limited movement and other symptoms. At present, magnesium sulfate is often used clinically to soak sterile gauze for local wet compresses. However, since the wet compress solution soaked in the gauze is volatile, medical staff need to constantly observe the patient's wet compress condition to avoid the inability to maintain wet compress treatment due to drying of the gauze. However, this not only greatly increases the workload of medical staff, but also affects the treatment effect. Utility Model Content
[0003] In view of the above problems, the purpose of the present utility model is to provide a phlebitis timed wet compress to solve the problems raised in the above background technology.
[0004] To achieve the above purpose, the utility model adopts the following technical solution: a phlebitis timed wet compress, comprising a liquid storage box, a fixing belt and a wet compress mechanism, the liquid storage box is provided with an operation panel, a protective pad 1, a sealing cover, an observation window, a charging hole, a connecting pipe A and a wire, the liquid storage box is provided with a liquid inlet, a liquid storage cavity, a cavity and a perforation, and a battery, a water pump, a buzzer and a timing module are arranged in the cavity, and the fixing belt is inserted into the perforation, the water pump is connected to the liquid storage cavity and the connecting pipe A through a water delivery pipeline The connecting tube A is connected, a connector A is provided at the other end away from the liquid storage box, and a mounting block is provided at the other end of the wire away from the liquid storage box, and a humidity sensor and a spring block are provided in the mounting block, the wet compress mechanism is composed of a film, an air bag, a gauze block, a nozzle and a mounting seat, the nozzle is connected to one end of the connecting tube B, and a connector B is provided at the other end of the connecting tube B, and the connector B is screwed to the connector A, the mounting seat is snap-fitted to the mounting block, and a snap hole is provided on the mounting seat.
[0005] The beneficial effect of the utility model is that the gauze piece can be automatically humidified during use, which can save the workload of medical staff and ensure the treatment effect.
[0006] In order to facilitate the filling of the liquid reservoir with wet compress solution and to check and confirm the remaining amount of wet compress solution:
[0007] As a further improvement of the above technical solution: the liquid storage chamber is located above the inside of the liquid storage box, and the liquid inlet is located at the top of the liquid storage box and is connected to the liquid storage chamber, and the screw-on cover at the liquid inlet is provided with a sealing cover, and the observation window is arranged at the outer end of the liquid storage box corresponding to the opening position of the liquid storage chamber.
[0008] The beneficial effect of this improvement is that by setting up the liquid inlet, the sealing cover can be unscrewed to open the liquid inlet, and then the liquid storage chamber can be filled with wet compress liquid, and the setting up of the observation window can facilitate medical staff to observe and confirm the amount of liquid in the liquid storage chamber.
[0009] In order to prevent excess liquid from seeping out of the gauze block and to humidify the gauze block:
[0010] As a further improvement of the above technical solution: the airbag, gauze block and nozzle are all arranged at the bottom end of the film, and the gauze block is located in the middle of the film, the airbag is located at the outer end of the gauze block, and the nozzle is located between the gauze block and the film.
[0011] The beneficial effects of this improvement are as follows: through the establishment of the air bag at the outer end of the gauze block, when the wet compress mechanism is located at the lesion for wet compress treatment, the air bag can effectively prevent excess medicine in the gauze block from seeping outwards; through the establishment of the nozzle, when the connecting tube A and the connecting tube B are connected by the screw connection of the connecting head A and the connecting head B, the water pump can start the humidification function, and the medicine in the liquid storage cavity can be transported to the nozzle through the infusion tube and the connecting tube A and the connecting tube B, and the medicine is sprayed outwards from the nozzle to humidify the gauze block.
[0012] In order to facilitate the fixation of the wet compress mechanism to the lesion:
[0013] As a further improvement of the above technical solution: adhesive is provided at the edge of the bottom wall of the film, and the adhesive is medical non-allergenic adhesive.
[0014] The beneficial effect of this improvement is that through the establishment of the adhesive, when the wet compress mechanism is located at the lesion, the adhesive adheres to the skin around the lesion and can fix the position of the wet compress mechanism, thereby preventing the wet compress mechanism from slipping and falling during the wet compress process, thereby affecting the treatment effect.
[0015] In order to facilitate the monitoring of the humidity of the gauze block:
[0016] As a further improvement of the above technical solution: the mounting seat is arranged on the gauze block through the film, and clamping holes are opened on both sides of the mounting seat, and the clamping holes are clamped and connected with spring clamping blocks arranged at corresponding positions on both sides of the mounting block.
[0017] The beneficial effect of this improvement is that by installing the mounting block in the mounting seat and locking the spring clamping block in the clamping hole to fix the mounting block in position, the sensing end of the humidity sensor contacts the gauze block, thereby being able to monitor the humidity of the gauze block.
[0018] In order to facilitate the operation and setting of various function modes:
[0019] As a further improvement of the above technical solution: the operation panel is electrically connected to the battery, the water pump, the buzzer, the timing module, and the humidity sensor.
[0020] The beneficial effect of this improvement is that by setting up the operation panel, it is convenient to operate and set various function modes.
[0021] To facilitate the fixation of the liquid storage box:
[0022] As a further improvement of the above technical solution: one side of the fixing belt is connected with a through loop, and the other side thereof is provided with a Velcro, and the rest of the fixing belt where the Velcro is provided is provided with an adhesive layer, and the Velcro and the adhesive layer are bonded together.
[0023] The beneficial effect of this improvement is: after the fixing belt is passed through the perforation, the liquid storage box is placed on the limb near the lesion, the fixing belt is used to surround the limb, and then passed through the ring, folded back and tightened, so that the Velcro adheres to the adhesive layer at an appropriate distance, and the position of the liquid storage box can be fixed.
[0024] To enhance the comfort and stability of the reservoir when it is fixed:
[0025] As a further improvement of the above technical solution: the protective pad 1 is arranged at the bottom end of the liquid storage box, and the protective pad 2 is arranged on the other end surface of the fixing belt away from the Velcro, and the protective pad 1 and the protective pad 2 are both soft and elastic.
[0026] The beneficial effect of this improvement is: by setting up the protection pad one and the protection pad two, and the protection pad one and the protection pad two are both made of soft and elastic silicone material, it can not only increase the comfort when surrounding and fixing, but also increase the friction coefficient, enhance the stability of the liquid storage box when it is fixed, and prevent sliding displacement caused by patient activities. BRIEF DESCRIPTION OF THE DRAWINGS
[0027] Figure 1 It is the front view of the utility model;
[0028] Figure 2 It is a schematic diagram of the disassembly structure of the fixing belt and the wet compress mechanism of the utility model;
[0029] Figure 3 This is a schematic diagram of the wet compress mechanism structure of the utility model;
[0030] Figure 4 It is a schematic diagram of the internal structure of the utility model;
[0031] Figure 5 This is a bottom view of the wet compress mechanism of the utility model;
[0032] Figure 6 A top view of the nozzle of the utility model;
[0033] In the figure: 1. liquid storage box; 2. operation panel; 3. protective pad 1; 4. sealing cover; 5. observation window; 6. charging port; 7. connecting tube A; 8. wire; 9. liquid inlet; 10. liquid storage chamber; 11. cavity; 12. perforation; 13. battery; 14. water pump; 15. buzzer; 16. timing module; 17. fixing belt; 18. protective pad 2; 19. Velcro; 20. adhesive layer; 21. ring; 22. film; 23. air bag; 24. gauze block; 25. nozzle; 26. mounting seat; 27. adhesive; 28. connecting tube B; 29. connector B; 30. connector A; 31. mounting block; 32. humidity sensor; 33. spring clamp block; 34. clamp hole. DETAILED DESCRIPTION
[0034] In order to enable those skilled in the art to better understand the technical solution of the utility model, the utility model is described in detail below in conjunction with the accompanying drawings. The description in this part is only exemplary and explanatory and should not have any limiting effect on the protection scope of the utility model.
[0035] like Figure 1-6As shown, a phlebitis timing wet compress device comprises a liquid storage box 1, a fixing belt 17 and a wet compress mechanism, wherein the liquid storage box 1 is provided with an operation panel 2, a protective pad 3, a sealing cover 4, an observation window 5, a charging hole 6, a connecting tube A7 and a wire 8, the liquid storage box 1 is provided with a liquid inlet 9, a liquid storage cavity 10, a cavity 11 and a perforation 12, and a battery 13, a water pump 14, a buzzer 15 and a timing module 16 are arranged in the cavity 11, and the fixing belt 17 is penetrated in the perforation 12, the water pump 14 is connected to the liquid storage cavity 10 and the connecting tube A7 through a water delivery pipeline, the other end of the connecting tube A7 away from the liquid storage box 1 is provided with a connector A30, and the other end of the wire 8 away from the liquid storage box 1 is provided with a mounting block 31, and the mounting block 31 is provided with a humidity sensor The sensor 32 and the spring block 33, the wet compress mechanism is composed of a film 22, an air bag 23, a gauze block 24, a nozzle 25 and a mounting seat 26, the nozzle 25 is connected to one end of the connecting tube B28, and the other end of the connecting tube B28 is provided with a connector B29, and the connector B29 and the connector A30 are screwed together, the mounting seat 26 and the mounting block 31 are snap-fitted, and a card hole 34 is provided on the mounting seat 26. During use, the utility model can automatically humidify the gauze block 24, which can save the workload of medical staff and ensure the treatment effect. The liquid storage chamber 10 is located above the inside of the liquid storage box 1, and the liquid inlet 9 is located at the top of the liquid storage box 1 and is connected to the liquid storage chamber 10, and the screw-on cover at the liquid inlet 9 is provided with a sealing cover 4, and the observation window 5 corresponds to the opening position of the liquid storage chamber 10, which is arranged at the outer end of the liquid storage box 1. Through the establishment of the liquid inlet 9, the sealing cover 4 can be unscrewed to open the liquid inlet 9, and the wet compress liquid can be added to the liquid storage chamber 10. The establishment of the observation window 5 can facilitate medical personnel to observe and confirm the amount of liquid in the liquid storage chamber 10. The air bag 23, gauze block 24 and nozzle 25 are all arranged at the bottom end of the film 22, and the gauze block 24 is located in the middle of the film 22. The air bag 23 is located at the outer end of the gauze block 24, and the nozzle 25 is located between the gauze block 24 and the film 22. Through the establishment of the air bag 23 at the outer end of the gauze block 24, when the wet compress mechanism is located at the lesion for wet compress treatment, the air bag 23 can effectively prevent the excess liquid in the gauze block 24 from seeping out. Through the establishment of the nozzle 25, when When the connecting tube A7 and the connecting tube B28 are connected by the screw connection of the connecting head A30 and the connecting head B29, the water pump 14 can transport the liquid in the liquid storage chamber 10 to the nozzle 25 through the infusion tube and the connecting tube A7 and the connecting tube B28 when the humidification function is started, and the liquid is sprayed outward by the nozzle 25 to humidify the gauze block 24. The edge of the bottom wall of the film 22 is provided with adhesive 27, and the adhesive 27 is medical non-sensitive adhesive 27. Through the establishment of the adhesive 27, when the wet compress mechanism is located at the lesion, the adhesive 27 adheres to the skin around the lesion, and the position of the wet compress mechanism can be fixed, thereby preventing the wet compress mechanism from slipping and falling during the wet compress process, thereby affecting the treatment effect. The mounting seat 26 penetrates the film 22 and is arranged on the gauze block 24.And both sides of the mounting seat 26 are provided with card holes 34, and the card holes 34 are card-engaged with the spring card blocks 33 arranged at the corresponding positions on both sides of the mounting block 31. When the mounting block 31 is installed in the mounting seat 26 and the spring card blocks 33 are carded in the card holes 34 to fix the mounting block 31 in position, the sensing end of the humidity sensor 32 contacts the gauze block 24, and the humidity of the gauze block 24 can be monitored. The operation panel 2 is electrically connected to the battery 13, the water pump 14, the buzzer 15, the timing module 16, and the humidity sensor 32. Through the establishment of the operation panel 2, it is convenient to operate and set various functional modes. One side of the fixing belt 17 is connected to the ring 21, and the other side thereof is provided with a Velcro 19, and the fixing belt 17 on the end face of the Velcro 19 is provided with an adhesive layer 20 on the rest of the part, and the Velcro 19 and the adhesive layer 20 For bonding connection, after the fixing belt 17 passes through the perforation 12, the liquid storage box 1 is placed on the limb near the lesion, the fixing belt 17 is used to surround the limb, and then it passes through the ring 21, and is folded back and tightened, so that the Velcro 19 is bonded to the adhesive layer 20 at a suitable distance, that is, the liquid storage box 1 can be fixed in position, the protective pad 13 is arranged at the bottom of the liquid storage box 1, and the other end face of the fixing belt 17 away from the Velcro 19 is provided with a protective pad 2 18, and the protective pad 13 and the protective pad 2 18 are both soft and elastic. Through the establishment of the protective pad 13 and the protective pad 2 18, and the protective pad 13 and the protective pad 2 18 are both made of soft and elastic silicone material, it can not only increase the comfort when surrounding and fixing, but also increase the friction coefficient, enhance the stability of the liquid storage box 1 when fixed, and prevent the sliding displacement phenomenon accompanying the patient's activities.
[0036] The working principle of the utility model is as follows: through the establishment of the liquid inlet 9, the sealing cover 4 can be unscrewed to open the liquid inlet 9, and the wet compress liquid can be added to the liquid storage chamber 10, and the establishment of the observation window 5 can facilitate the medical staff to observe and confirm the amount of liquid in the liquid storage chamber 10. Through the establishment of the adhesive 27, when the wet compress mechanism is located at the lesion, the adhesive 27 is adhered to the skin around the lesion, and the position of the wet compress mechanism can be fixed, thereby preventing the wet compress mechanism from slipping and falling during the wet compress process, thereby affecting the treatment effect. After the fixing belt 17 passes through the perforation 12, the liquid storage box 1 is placed on a limb near the lesion, the fixing belt 17 is used to surround the limb, and then The liquid storage box 1 is fixed in position by passing through the loop 21, folding back and tightening, so that the Velcro 19 is adhered to the adhesive layer 20 at an appropriate distance. After the wet compress mechanism and the liquid storage box 1 are both fixed on the patient, it is convenient for the patient to perform wet compress treatment during bed rest, and it is also convenient for the patient to get up and move around during wet compress treatment. By setting up the air bag 23 at the outer end of the gauze block 24, when the wet compress mechanism is located at the lesion for wet compress treatment, the air bag 23 can effectively prevent the excess liquid in the gauze block 24 from seeping out. By setting up the nozzle 25, when the connecting tube A7 and the connecting tube B28 are connected by the screw connection of the connecting head A30 and the connecting head B29, the liquid storage box 1 and the wet compress mechanism can be completed. The connection operation is performed so that when the operation button on the operation panel 2 is pressed to start the humidification function, the water pump 14 can transport the liquid in the liquid storage chamber 10 to the nozzle 25 through the infusion tube and the connecting tube A7 and the connecting tube B28, and the liquid is sprayed outward by the nozzle 25 to humidify the gauze block 24. After the connector A30 and the connector B29 are separated, the liquid storage box 1 and the wet compress mechanism can be separated to replace the wet compress mechanism. By installing the mounting block 31 in the mounting seat 26 and making the spring clamping block 33 clamped in the clamping hole 34 to fix the mounting block 31 in position, the sensing end of the humidity sensor 32 contacts with the gauze block 24, so that the humidity of the gauze block 24 can be monitored. When the humidity sensor When the sensor 32 senses that the humidity of the gauze block 24 is lower than the set minimum humidity value, the operation panel 2 can immediately control the water pump 14 to start the conveying function after receiving the electrical signal from the temperature sensor 32, and humidify the gauze block 24. When the temperature sensor 32 senses that the humidity of the gauze block 24 is higher than the set maximum humidity value, the operation panel 2 can immediately control the water pump 14 to turn off the conveying function and stop the humidification operation of the gauze block 24 after receiving the electrical signal from the humidity sensor 32. Through the establishment of the timing module 16, when the end time of the wet compress is reached, the operation panel 2 can immediately control the buzzer 15 to turn on and emit a buzzer sound after receiving the electrical signal to warn the patient and medical staff.
[0037] It should be noted that, in this article, the terms "comprises", "includes" or any other variations thereof are intended to cover non-exclusive inclusion, so that a process, method, article or apparatus that includes a series of elements includes not only those elements, but also other elements not explicitly listed, or also includes elements inherent to such process, method, article or apparatus.
[0038] This article uses specific examples to illustrate the principles and implementation methods of the utility model. The above examples are only used to help understand the method and core ideas of the utility model. The above is only the preferred implementation method of the utility model. It should be pointed out that due to the limitations of textual expression, there are objectively infinite specific structures. For ordinary technicians in this technical field, without departing from the principle of the utility model, they can make several improvements, embellishments or changes, and can also combine the above technical features in an appropriate manner; these improvements, embellishments, changes or combinations, or the direct application of the concept and technical solution of the utility model to other occasions without improvement, should be regarded as the protection scope of the utility model.
Claims
1. A phlebitis timed wet compress device, comprising a liquid storage box (1), a fixing belt (17) and a wet compress mechanism, wherein the liquid storage box (1) is provided with an operation panel (2), a protective pad (3), a sealing cover (4), an observation window (5), a charging hole (6), a connecting tube A (7) and a wire (8), characterized in that: The liquid storage box (1) is provided with a liquid inlet (9), a liquid storage cavity (10), a cavity (11) and a through hole (12), and a battery (13), a water pump (14), a buzzer (15) and a timing module (16) are arranged in the cavity (11), and a fixing belt (17) is passed through the through hole (12). The water pump (14) is connected to the liquid storage cavity (10) and a connecting pipe A (7) through a water delivery pipeline, and a connector A (30) is arranged at the other end of the connecting pipe A (7) away from the liquid storage box (1), and a mounting block is arranged at the other end of the wire (8) away from the liquid storage box (1). (31), and a humidity sensor (32) and a spring clamp (33) are arranged in the mounting block (31), the wet compress mechanism is composed of a film (22), an air bag (23), a gauze block (24), a nozzle (25) and a mounting seat (26), the nozzle (25) is connected to one end of a connecting pipe B (28), and a connector B (29) is arranged at the other end of the connecting pipe B (28), and the connector B (29) and the connector A (30) are screwed together, the mounting seat (26) and the mounting block (31) are snap-fitted, and a clamping hole (34) is opened on the mounting seat (26).
2. A phlebitis timed wet compress according to claim 1, characterized in that: The liquid storage chamber (10) is located at the upper part of the liquid storage box (1), and the liquid inlet (9) is located at the top of the liquid storage box (1) and is connected to the liquid storage chamber (10). The screw-on cover at the liquid inlet (9) is provided with a sealing cover (4), and the observation window (5) is arranged at the outer end of the liquid storage box (1) corresponding to the opening position of the liquid storage chamber (10).
3. The phlebitis timed wet compress according to claim 1, characterized in that: The air bag (23), the gauze block (24) and the nozzle (25) are all arranged at the bottom end of the film (22), and the gauze block (24) is located in the middle of the film (22), the air bag (23) is located at the outer end of the gauze block (24), and the nozzle (25) is located between the gauze block (24) and the film (22).
4. The phlebitis timed wet compress according to claim 1, characterized in that: The bottom wall edge of the film (22) is provided with adhesive (27), and the adhesive (27) is medical non-allergenic adhesive (27).
5. The phlebitis timed wet compress according to claim 1, characterized in that: The mounting seat (26) passes through the film (22) and is arranged on the gauze block (24), and both sides of the mounting seat (26) are provided with clamping holes (34), and the clamping holes (34) are clamped and connected with spring clamping blocks (33) arranged at corresponding positions on both sides of the mounting block (31).
6. The phlebitis timed wet compress according to claim 1, characterized in that: The operation panel (2) is electrically connected to the battery (13), the water pump (14), the buzzer (15), the timing module (16), and the humidity sensor (32).
7. The phlebitis timed wet compress according to claim 1, characterized in that: One side of the fixing belt (17) is connected to a through ring (21), and the other side thereof is provided with a Velcro (19), and the remaining part of the fixing belt (17) where the end face of the Velcro (19) is provided is provided with an adhesive layer (20), and the Velcro (19) and the adhesive layer (20) are connected by bonding.
8. The phlebitis timed wet compress according to claim 1, characterized in that: The protective pad 1 (3) is arranged at the bottom end of the liquid storage box (1), and the other end surface of the fixing belt (17) away from the Velcro (19) is provided with a protective pad 2 (18), and both the protective pad 1 (3) and the protective pad 2 (18) are soft and elastic.