Atomization respiratory therapy device for lung cancer

Abstract

The utility model discloses a lung cancer atomization breathing treatment device in the technical field of medical equipment, which comprises a device assembly, a cooling assembly, a breathing assembly and a protection assembly, the device assembly comprises a device main body, a base and a heating rod, and the cooling assembly comprises a storage block, a top cover, an ice block, a liquid adding port, a spiral pipe and a discharging port. The breathing assembly comprises a breathing tube and a breathing mask, the protection assembly comprises an elastic block, a connecting spring, a movable block, a threaded lead screw, a bevel gear and a toothed rod, a storage block and a spiral tube are arranged in the device body, ice blocks in the storage block cool medicine in the spiral tube, and due to the spiral structure of the spiral tube, the medicine in the spiral tube is cooled; the medicine cooling device is simple in structure, medicine stays in ice cubes for a long time, a better cooling effect is achieved, the medicine cannot be mixed with the ice cubes due to isolation of the spiral tube, the treatment effect of the medicine cannot be affected, the medicine is at a proper temperature, and a patient is prevented from being scalded.

Description

Technical Field

[0001] The utility model relates to the technical field of medical equipment, in particular to a lung cancer atomization breathing treatment device. Background Art

[0002] With the development of society, various waste gases in life pollute our environment. The air is full of automobile exhaust and industrial dust particles. These harmful gases threaten our health and increase our chances of developing lung cancer. At the same time, many men like to smoke. Long-term smoking will threaten the lung health of smokers and greatly increase the chances of developing lung cancer. Therefore, the number of lung cancer patients in life is gradually increasing. Generally, chemotherapy and other methods are selected for the treatment of lung cancer patients to inhibit the growth of cancer cells, and some oral nebulizers are used for nebulization treatment. However, this nebulizer is not convenient for patients to use, and cannot provide long-term nebulization treatment for patients, and the effect of nebulization treatment is not obvious.

[0003] For example, patent application number CN201720785174.2 discloses a lung cancer atomization breathing treatment device, which can continuously and slowly treat the patient's lungs through hot mist. The design of the ice storage box can prevent the mist from being too hot and scalding the patient. The device is more convenient to use and can be used for long-term atomization treatment. However, this technical solution still has shortcomings, as follows:

[0004] The treatment device cools down the medicine through the ice storage box, but the ice will melt and mix with the medicine during the cooling process, which will make the treatment effect of the mist worse and affect the treatment of the patient. Secondly, the breathing mask is easily entangled when it is stretched during use, which affects the mist when it passes through the breathing mask, and it is also easy to be stepped on by the outside world. To this end, we propose a lung cancer atomization breathing treatment device to solve the above-mentioned problems. Utility Model Content

[0005] The purpose of this section is to summarize some aspects of the embodiments of the utility model and briefly introduce some preferred embodiments. Some simplifications or omissions may be made in this section and the abstract of the specification and the name of the utility model to avoid blurring the purpose of this section, the abstract of the specification and the name of the utility model, and such simplifications or omissions cannot be used to limit the scope of the utility model.

[0006] Therefore, the purpose of the utility model is to provide a lung cancer atomization breathing treatment device, which can solve the problems that when the existing drugs are cooled by ice cubes, the ice cubes melt and mix with the drugs, thereby reducing the drug treatment effect, and the breathing tube is easily entangled or stepped on during use, affecting the inhalation of mist.

[0007] In order to solve the above technical problems, the utility model provides a lung cancer atomization breathing treatment device, which adopts the following technical solution: comprising a device assembly, which also includes a device body, wherein a base is arranged inside the device body, and a heating rod is arranged above the base;

[0008] The cooling assembly further comprises a storage block, the storage block is located above the inside of the device body, a top cover is connected to the top of the storage block, ice cubes are arranged inside the storage block, a liquid filling port is arranged at the center of the ice cubes, a spiral tube is connected below the liquid filling port, and a material discharge port is arranged below the spiral tube;

[0009] The breathing assembly further comprises a breathing tube, the breathing tube is located on the right side of the device body, a limiting block is arranged at the bottom of the breathing tube, a rubber block is arranged on the outside of the breathing tube, a fixing block is connected to the outside of the rubber block, and a breathing mask is connected to the top of the breathing tube;

[0010] The protective component also includes an elastic block, which is located on the outside of the breathing tube. The other side of the elastic block is connected to a connecting spring. A movable block is also provided on the left side of the breathing tube. The left side of the movable block is connected to a threaded screw. The left side of the threaded screw is connected to a bevel gear. A toothed rod is connected above the bevel gear.

[0011] By adopting the above technical scheme, this scheme prolongs the residence time of the medicine inside the ice cube by providing a spiral tube, thereby achieving a better cooling effect, while preventing the ice cube from melting into the medicine. Secondly, a limiting block is provided to limit the breathing tube to prevent the breathing tube from getting tangled into a knot during use. At the same time, a rubber block is used to smooth the breathing tube, so that the breathing tube is in a flat state when entering and exiting the device body, further reducing the occurrence of knots.

[0012] Optionally, the device body and the base are installed in an integrated manner, the base and the heating rod are installed in an integrated manner, and the heating rod is located at the bottom center of the device body.

[0013] By adopting the above technical solution, the present invention heats the medicine by means of a heating rod to avoid excessively cold medicine irritating the patient.

[0014] Optionally, the storage block is connected to the top cover by a rotational connection, ice cubes are evenly and equidistantly distributed inside the storage block, and the storage block is connected to the device body by a sliding connection.

[0015] By adopting the above technical solution, the present solution uses storage blocks to limit the storage of ice cubes, making it convenient for ice cubes to cool down overheated medicines and avoid scalding patients.

[0016] Optionally, the liquid adding port is integrally installed with the storage block through a cross bar, the liquid adding port is connected to the spiral tube by hot-melt connection, and the center of the spiral tube is aligned with the center of the feed port.

[0017] By adopting the above technical solution, the solution isolates the medicine from the ice cubes through the cooperation of the liquid adding port and the spiral tube, and at the same time prolongs the contact time with the ice cubes to ensure the cooling effect.

[0018] Optionally, the breathing tube is connected to the limit block by sliding connection, the limit block is connected to the device body by hot-melt connection, and the breathing tube is installed in an integrated manner with the breathing mask.

[0019] By adopting the above technical solution, the present invention limits the breathing tube by means of a limiting block, thereby ensuring the normal use of the breathing tube.

[0020] Optionally, the rubber block is connected to the breathing tube by a sliding connection, the rubber block is installed in an integrated manner with the fixed block, and the fixed block forms a fixed structure with the device body through a side panel.

[0021] By adopting the above technical solution, the present solution limits the breathing tube by means of a rubber block, thereby ensuring that the breathing tube is smoothed when entering and exiting the device body.

[0022] Optionally, the elastic block is connected to the breathing tube by a sliding connection, and the elastic block forms a spring reset structure with the device body via a connecting spring, and the elastic blocks are symmetrically distributed on both sides of the breathing tube.

[0023] By adopting the above technical solution, the present solution pulls the breathing tube to form an S-shaped structure inside the device body by connecting the spring and the elastic block, thereby preventing entanglement.

[0024] Optionally, the movable block is connected to the side panel by a sliding connection, the movable block is integrally installed with the rubber block, the movable block is connected to the threaded screw by a threaded connection, the threaded screw and the bevel gear are connected by a hot-melt connection, the bevel gear and the toothed rod are connected by a meshing connection, and a grip block is provided above the toothed rod.

[0025] By adopting the above technical solution, the present solution uses the toothed rod to drive the movable block to press against the breathing tube, thereby completing the limiting fixation of the breathing tube and ensuring the use of the breathing tube.

[0026] In summary, the present invention has at least one of the following beneficial effects:

[0027] By arranging a storage block and a spiral tube inside the device body, the ice inside the storage block cools down the medicine inside the spiral tube, and due to the spiral structure of the spiral tube, the medicine stays in the ice block for a longer time, achieving a better cooling effect. Secondly, due to the isolation of the spiral tube, the medicine will not mix with the ice, thereby not affecting the therapeutic effect of the medicine, and the medicine is kept at a suitable temperature to prevent scalding of the patient.

[0028] By arranging a rubber block and an elastic block on the outside of the breathing tube, the rubber block makes the breathing tube in a smooth state when in the main body of the device to avoid knotting, and the elastic block pulls the breathing tube into an S-shaped structure when the breathing tube is stored to prevent the breathing tube from getting knotted when stored inside the main body of the device. Secondly, a movable block is arranged on the left side of the rubber block to limit the breathing tube, so that the breathing tube can be freely fixed in length according to the patient's use, ensuring easy use. BRIEF DESCRIPTION OF THE DRAWINGS

[0029] In order to more clearly illustrate the technical solutions of the embodiments of the utility model, the drawings required for describing the embodiments are 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 creative work.

[0030] Figure 1 It is a schematic diagram of the overall front view structure of the utility model;

[0031] Figure 2 This is a schematic diagram of the top view structure of the storage block of the utility model;

[0032] Figure 3 This is a schematic diagram of the top view of the rubber block of the utility model;

[0033] Figure 4 This is a schematic diagram of the front view structure of the protection component of the utility model;

[0034] Figure 5 It is a schematic diagram of the top view structure of the protection component of the utility model.

[0035] Description of reference numerals:

[0036] 100, device assembly; 101, device body; 102, base; 103, heating rod;

[0037] 200, cooling assembly; 201, storage block; 202, top cover; 203, ice cubes; 204, liquid filling port; 205, spiral tube; 206, feed port;

[0038] 300, breathing assembly; 301, breathing tube; 302, limit block; 303, fixing block; 304, rubber block; 305, breathing mask;

[0039] 400, protective assembly; 401, elastic block; 402, connecting spring; 403, movable block; 404, threaded screw; 405, bevel gear; 406, toothed rod. DETAILED DESCRIPTION

[0040] The following is combined with Figure 1-5 The utility model is described in further detail.

[0041] Embodiment 1, refer to Figure 1-2 In order to solve the problem that the ice cubes 203 in the existing ice storage box are easily melted and mixed with the medicine in contact with each other, thus affecting the treatment effect, the utility model discloses a lung cancer atomization breathing treatment device.

[0042] The device assembly 100 includes a device body 101, a base 102 is disposed inside the device body 101, and a heating rod 103 is disposed above the base 102;

[0043] The cooling assembly 200 also includes a storage block 201, which is located above the inside of the device body 101. A top cover 202 is connected to the top of the storage block 201, and the storage block 201 is closed by the top cover 202 to prevent the ice block 203 from melting. The ice block 203 is arranged on the inner side of the storage block 201, and a liquid filling port 204 is arranged at the center of the ice block 203. Medicines are stored through the liquid filling port 204 to prevent the medicines from dripping on the outside. A spiral tube 205 is connected below the liquid filling port 204. The spiral tube 205 is used to extend the cooling effect of the ice block 203 while preventing it from mixing with the medicine. A discharge port 206 is arranged below the spiral tube 205.

[0044] The device body 101 and the base 102 are installed in an integrated manner, and the base 102 and the heating rod 103 are installed in an integrated manner. The heating rod 103 is located at the bottom center of the device body 101. The heating rod 103 heats the medicine to prevent the medicine from being too cold to stimulate the patient.

[0045] The storage block 201 is connected to the top cover 202 in a rotating manner, and ice cubes 203 are evenly and equidistantly distributed inside the storage block 201. The storage block 201 is connected to the device body 101 in a sliding manner. The storage block 201 is used to limit the storage of the ice cubes 203, so that the ice cubes 203 can cool down the overheated medicine and avoid scalding the patient.

[0046] The liquid adding port 204 is integrated with the storage block 201 through a cross bar. The liquid adding port 204 and the spiral tube 205 are connected by hot melt connection. The center of the spiral tube 205 is aligned with the center of the discharge port 206. The liquid adding port 204 cooperates with the spiral tube 205 to isolate the medicine from the ice cube 203, and at the same time prolong the contact time with the ice cube 203 to ensure the cooling effect.

[0047] The specific working principle is: first, when in use, open the top cover 202, place the medicine inside the liquid filling port 204, and then the medicine enters the inside of the spiral tube 205 through the liquid filling port 204. When the medicine passes through the spiral tube 205, it contacts the ice cube 203 on the outside thereof, so that the ice cube 203 cools the medicine. Finally, the medicine enters the inside of the device body 101 through the discharge port 206. If it is too cold, it is heated by the heating rod 103 until it enters the patient's body through the breathing tube 301 for treatment. When adding medicine, if the ice cube 203 is seen to melt too much, the storage block 201 can be taken out and the ice cube 203 can be replaced.

[0048] Example 2, refer to Figure 1-3 In order to solve the problem that the existing breathing tube 301 is easily tangled and knotted during use, in this embodiment, based on the same concept as the above-mentioned embodiment 1, the lung cancer atomization breathing treatment device also includes:

[0049] The breathing assembly 300 also includes a breathing tube 301, which is located on the right side of the device body 101. A limit block 302 is set at the bottom of the breathing tube 301, and the breathing tube 301 is limited by the limit block 302 to prevent it from shaking. A rubber block 304 is also set on the outside of the breathing tube 301, and the rubber block 304 is used to smooth the breathing tube 301 to prevent it from getting tangled. The outside of the rubber block 304 is connected to a fixing block 303, and the top of the breathing tube 301 is connected to a breathing mask 305.

[0050] The breathing tube 301 is connected to the limit block 302 by sliding connection, the limit block 302 is connected to the device body 101 by hot-melt connection, the breathing tube 301 and the breathing mask 305 are installed in an integrated manner, and the breathing tube 301 is limited by the limit block 302 to ensure the normal use of the breathing tube 301.

[0051] The rubber block 304 is connected to the breathing tube 301 by sliding connection. The rubber block 304 and the fixed block 303 are installed in an integrated manner. The fixed block 303 forms a fixed structure with the device body 101 through the side plate. The rubber block 304 limits the breathing tube 301 to ensure that the breathing tube 301 is smoothed when entering and exiting the device body 101.

[0052] The specific working principle is: as mentioned above, when the breathing tube 301 needs to be used, grab the breathing tube 301 and pull it toward the outside. When the breathing tube 301 enters and exits the device body 101, it rubs against the rubber block 304. At the same time, the rubber block 304 fits tightly to the breathing tube 301, thereby smoothing the breathing tube 301, so that the breathing tube 301 pulled out of the device body 101 is in a smooth state. Then, the patient is given drug treatment through the breathing mask 305. When entering, the limit block 302 limits and fixes the breathing tube 301 to prevent the breathing tube 301 from shaking during storage and thus getting tangled.

[0053] Example 3, refer to Figure 4-5 In this embodiment, in order to solve the problem that the existing breathing tube 301 is easy to get tangled when it is inside the device body 101 and the fixing effect of the limit block 302 is limited, based on the same concept as the above-mentioned embodiment 1, the lung cancer atomization breathing treatment device also includes:

[0054] The protective component 400 also includes an elastic block 401, which is located on the outside of the breathing tube 301. The other side of the elastic block 401 is connected to a connecting spring 402. The elastic block 401 is pulled by the connecting spring 402 to better fix the breathing tube 301. A movable block 403 is also provided on the left side of the breathing tube 301. The rubber block 304 is limited and fixed by the movable block 403 to prevent it from falling off. A threaded screw 404 is connected to the left side of the movable block 403. A bevel gear 405 is connected to the left side of the threaded screw 404. A toothed rod 406 is connected above the bevel gear 405.

[0055] The elastic block 401 is connected to the breathing tube 301 by sliding connection. The elastic block 401 forms a spring reset structure with the device body 101 through the connecting spring 402. The elastic blocks 401 are symmetrically distributed on both sides of the breathing tube 301. The connecting spring 402 cooperates with the elastic block 401 to pull the breathing tube 301 to form an S-shaped structure inside the device body 101 to prevent entanglement.

[0056] The movable block 403 is connected to the side plate by sliding connection, the movable block 403 is installed in an integrated manner with the rubber block 304, the movable block 403 is connected to the threaded screw 404 by threaded connection, the threaded screw 404 is connected to the bevel gear 405 by hot-melt connection, the bevel gear 405 is connected to the toothed rod 406 by meshing connection, a grip block is provided above the toothed rod 406, and the movable block 403 is driven by the toothed rod 406 to press against the breathing tube 301, thereby completing the limiting fixation of the breathing tube 301 and ensuring the use of the breathing tube 301.

[0057] The specific working principle is as follows: as described above, when in use, the breathing tube 301 is pulled out, and as the breathing tube 301 is pulled out, it drives the elastic block 401 to move, and under the limit fixation of the connecting spring 402, the breathing tube 301 inside the device body 101 is always in an S-shaped structure, and will not accumulate and cause entanglement and knotting. After reaching the appropriate position, the grip block is rotated to drive the toothed rod 406 to rotate, and the rear toothed rod 406 is engaged with the bevel gear 405, so that the rotation of the bevel gear 405 drives the threaded screw 404 to rotate at the same time, and the rear threaded screw 404 and the movable block 403 perform threaded motion, and under the limit of the side plate, the movable block 403 is against the rubber block 304, so as to achieve the limit fixation of the breathing tube 301, and when the breathing tube 301 is reset after use, the connecting spring 402 pulls the elastic block 401 to reset, so that the breathing tube 301 always maintains a certain distance from others and will not be entangled and knotted.

[0058] The above are all preferred embodiments of the present utility model, and are not intended to limit the protection scope of the present utility model. Therefore, any equivalent changes made based on the structure, shape, and principle of the present utility model should be included in the protection scope of the present utility model.

Claims

1. A lung cancer atomization breathing treatment device, characterized in that: include, A device assembly (100), further comprising a device body (101), wherein a base (102) is arranged inside the device body (101), and a heating rod (103) is arranged above the base (102); A cooling assembly (200), further comprising a storage block (201), the storage block (201) being located above the inside of the device body (101), the storage block (201) being connected to a top cover (202) above, an ice block (203) being arranged on the inner side of the storage block (201), a liquid filling port (204) being arranged at the center of the ice block (203), a spiral tube (205) being connected below the liquid filling port (204), and a discharge port (206) being arranged below the spiral tube (205); A breathing assembly (300), further comprising a breathing tube (301), wherein the breathing tube (301) is located to the right of the device body (101), a limiting block (302) is provided at the bottom of the breathing tube (301), a rubber block (304) is further provided on the outside of the breathing tube (301), a fixing block (303) is connected to the outside of the rubber block (304), and a breathing mask (305) is connected to the top of the breathing tube (301); The protection assembly (400) further comprises an elastic block (401), wherein the elastic block (401) is located outside the breathing tube (301), the other side of the elastic block (401) is connected to a connecting spring (402), a movable block (403) is further provided on the left side of the breathing tube (301), a threaded screw (404) is connected to the left side of the movable block (403), a bevel gear (405) is connected to the left side of the threaded screw (404), and a toothed rod (406) is connected above the bevel gear (405).

2. The aerosol breathing treatment device for lung cancer according to claim 1, characterized in that: The device body (101) and the base (102) are installed in an integrated manner, the base (102) and the heating rod (103) are installed in an integrated manner, and the heating rod (103) is located at the bottom center of the device body (101).

3. The aerosol breathing treatment device for lung cancer according to claim 2, characterized in that: The storage block (201) is connected to the top cover (202) in a rotating manner, ice cubes (203) are evenly and equidistantly distributed inside the storage block (201), and the storage block (201) is connected to the device body (101) in a sliding manner.

4. The aerosol breathing treatment device for lung cancer according to claim 3, characterized in that: The liquid adding port (204) is integrally mounted with the storage block (201) via a cross bar, the liquid adding port (204) is connected to the spiral tube (205) by hot-melt connection, and the center of the spiral tube (205) is aligned with the center of the feed port (206).

5. The aerosol breathing treatment device for lung cancer according to claim 4, characterized in that: The breathing tube (301) and the limit block (302) are connected in a sliding manner, the limit block (302) and the device body (101) are connected in a hot-melt manner, and the breathing tube (301) and the breathing mask (305) are installed in an integrated manner.

6. The aerosol breathing treatment device for lung cancer according to claim 5, characterized in that: The rubber block (304) and the breathing tube (301) are connected in a sliding manner. The rubber block (304) and the fixing block (303) are installed in an integrated manner. The fixing block (303) forms a fixing structure with the device body (101) via a side plate.

7. The aerosol breathing treatment device for lung cancer according to claim 6, characterized in that: The elastic block (401) is connected to the breathing tube (301) in a sliding manner. The elastic block (401) forms a spring return structure with the device body (101) via a connecting spring (402). The elastic blocks (401) are symmetrically distributed on both sides of the breathing tube (301).

8. The aerosol breathing treatment device for lung cancer according to claim 7, characterized in that: The movable block (403) is connected to the side plate by sliding connection, the movable block (403) is integrally mounted with the rubber block (304), the movable block (403) is connected to the threaded screw (404) by threaded connection, the threaded screw (404) is connected to the bevel gear (405) by hot melt connection, the bevel gear (405) is connected to the toothed rod (406) by meshing connection, and a grip block is provided above the toothed rod (406).

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