A humidifying and heating pulse therapy device

Abstract

This application relates to the field of pulse therapy technology, specifically providing a humidified and heated pulse therapy device, comprising: a therapy device body, with a tank mounting section and a compressed air channel; a humidifier tank, detachably mounted on the tank mounting section, the humidifier tank having an inlet pipe and an outlet pipe, the inlet of the inlet pipe being connected to the compressed air channel; and a handle, one end of which is connected to the outlet pipe. By setting a tank mounting section on the therapy device body and using a detachable humidifier tank, humidification and heating of the compressed airflow are achieved, solving the respiratory discomfort caused by dry airflow and low temperature in the prior art, thus improving treatment comfort and clinical efficacy; the stable connection and detachable design of the humidifier tank and the tank mounting section facilitates cleaning and maintenance, avoids the problems of complex structure, air leakage, and high maintenance costs of traditional external humidification devices, and optimizes the overall size and reliability of the device.

Description

Technical Field

[0001] This application relates to the field of pulse therapy technology, and more particularly to a humidified and heated pulse therapy device. Background Technology

[0002] Pulse breathing therapy is a medical device used to improve patients' respiratory function. It mainly works by generating specific pulsed airflow to act on the respiratory tract to promote sputum expectoration, improve lung ventilation, and relieve symptoms such as dyspnea. It is widely used in the treatment of patients with chronic obstructive pulmonary disease, bronchiectasis, and postoperative lung rehabilitation.

[0003] In clinical applications, existing pulsed respiratory therapy devices primarily work by directly applying compressed pulsed airflow to the patient's respiratory system. However, in some cases, the dry, low-temperature airflow, without humidification or heating, can easily cause discomfort during treatment. Some patients experience symptoms such as respiratory dryness, sore throat, and worsened cough, especially during long-term treatment, where these discomforts become more pronounced. Furthermore, the dry airflow can easily cause the evaporation of moisture from the respiratory mucosa, making sputum thicker and harder to expel, thus affecting the effectiveness of pulsed therapy and potentially damaging the respiratory mucosa, increasing the risk of infection.

[0004] Currently, while some medical devices are equipped with external humidification devices for humidifying and heating the airflow, these structures are typically quite complex. This not only increases the size and maintenance costs of the equipment, but also makes the connection between the external humidification device and the main unit unstable, prone to leaks and malfunctions, thus affecting the effectiveness of the device. Therefore, existing pulse breathing therapy devices still have significant shortcomings in humidification and heating functions, failing to meet the patient's needs for comfort and clinical efficacy during treatment.

[0005] Therefore, existing technologies have defects and shortcomings, and need further improvement and development. Summary of the Invention

[0006] In view of the shortcomings of the prior art, the purpose of this application is to provide a humidifying and heating pulse therapy device, which aims to solve the problems that the pulse breathing therapy devices in the prior art cannot humidify or heat, or are prone to leakage when using existing humidifying and heating equipment.

[0007] The technical solution adopted by this application to solve the technical problem is as follows: A humidifying and heating pulse therapy device, comprising:

[0008] The therapeutic device body is provided with a tank mounting part and a compressed air channel;

[0009] A humidifying tank is detachably mounted on the tank body mounting part. The humidifying tank is provided with an air inlet pipe and an air outlet pipe. The inlet of the air inlet pipe is connected to the compressed air passage.

[0010] A handle, one end of which is connected to the air outlet pipe.

[0011] Optionally, the humidifying tank includes:

[0012] A heating base, which is detachably connected to the tank mounting part;

[0013] The tank body is sealed to the heating base to form a humidification and heating chamber, and the air inlet pipe and air outlet pipe are both located on the top of the tank body away from the heating base;

[0014] A liquid filling pipe is disposed on the top of the tank body away from the heating base;

[0015] The medicine compartment is disposed on the air inlet pipe and is connected to the air inlet pipe in an openable and closable manner.

[0016] Optionally, the intake pipe includes:

[0017] An intake pipe section, one end of which is used to connect to the compressed air passage;

[0018] The tank section has one end connected to the humidification and heating chamber and the other end connected to the air inlet pipe section.

[0019] The medicine compartment section has a detachable medicine compartment and a connection port at one end opposite to the tank section. The medicine compartment is connected to the junction of the tank section and the air inlet pipe section, and the connection port is used to connect external power cords and control lines.

[0020] Optionally, the air outlet pipe includes:

[0021] The air outlet includes a plurality of radially tapered baffles evenly spaced apart, and an outlet gap is provided between the radially tapered baffles;

[0022] A liquid baffle is disposed axially on the outside of the outlet gap to follow liquid particles in the compressed airflow in the outlet gap.

[0023] Optionally, the treatment device body includes:

[0024] A compression body, wherein a compressor is disposed within the compression body, and the compression air passage includes a first compression air passage and a second compression air passage, wherein the first compression air passage is disposed within the compression body and is connected to the compressor;

[0025] The humidifier body, the second compressed air passage and the tank mounting part are disposed on the humidifier body, and the second compressed air passage is used to connect the first compressed air passage and the air inlet pipe.

[0026] Optionally, the compressor includes:

[0027] The outer casing has a receiving cavity, and a partition is provided inside the receiving cavity, which divides the receiving cavity into a main unit area and a current stabilization and noise reduction area;

[0028] A current stabilizing and noise reduction component, wherein the current stabilizing and noise reduction component is detachably disposed within the current stabilizing and noise reduction zone;

[0029] The flow stabilizing and noise reduction component is provided with a plurality of flow stabilizing and noise reduction through holes, and the openings of the plurality of flow stabilizing and noise reduction through holes are all provided with arc-shaped transition sections, which are used to reduce turbulent gas flow.

[0030] Optionally, the tank mounting part includes a limiting groove and a limiting baffle. The heating base is limited along the height direction with the limiting groove, and the limiting baffle is limited along the front-back direction with the heating base. The limiting groove and the limiting baffle cooperate to fix the humidifying tank.

[0031] Optionally, the humidified and heated pulse therapy device further includes:

[0032] A filter, which is detachably connected to the outlet of the compressed air passage, is used to connect the compressed air passage and the outlet pipe.

[0033] Optionally, the handle includes a handle body, a pulse airway, and a sensor assembly; the pulse airway is detachably mounted on the handle body, one end of the pulse airway is used to connect to the air outlet pipe, and the other end of the pulse airway is used to connect to the user's mouth; the sensor assembly is mounted on the handle body and is used to detect airflow parameters within the pulse airway.

[0034] Optionally, the pulse airway includes a ventilation circuit, a filter chamber, a pulse generator, and a gas output assembly connected in sequence. The filter chamber, pulse generator, and gas output assembly are detachably connected to the handle body. The ventilation circuit is used to connect to the air outlet pipe. The pulse generator is used to convert compressed airflow into pulsed airflow. The pulsed airflow is transmitted to the user via the gas output assembly. The sensor assembly is connected to the filter chamber and is used to detect the airflow parameters in the filter chamber.

[0035] Compared with existing technologies, this application provides a humidified and heated pulse therapy device. By setting a tank mounting part on the main body of the therapy device and using a detachable humidification tank, it achieves humidification and heating of compressed airflow, solving the problems of respiratory discomfort and thick sputum that are difficult to expel caused by dry airflow and low temperature in existing technologies, thus improving treatment comfort and clinical efficacy. The stable connection and detachable design of the humidification tank and the tank mounting part facilitates cleaning and maintenance, and avoids the problems of complex structure, air leakage and high maintenance costs of traditional external humidification devices. At the same time, it optimizes the overall size and reliability of the device, and further expands the applicable scenarios of the therapy device, especially in cold or dry environments, providing patients with humidified and appropriately warm airflow, effectively improving the treatment experience. Attached Figure Description

[0036] Figure 1 This is a three-dimensional structural diagram of the humidified and heated pulse therapy device provided in this application;

[0037] Figure 2 This is a three-dimensional exploded structural diagram of the humidified and heated pulse therapy device provided in this application;

[0038] Figure 3 This is a top view of the air outlet pipe of the humidified and heated pulse therapy device provided in this application;

[0039] Figure 4 This is a three-dimensional structural diagram of the compressor of the humidifying and heating pulse therapy device provided in this application;

[0040] Figure 5 This is a three-dimensional exploded structural diagram of the compressor of the humidifying and heating pulse therapy device provided in this application;

[0041] Figure 6 This is a three-dimensional structural diagram of the current stabilization and noise reduction component of the compressor of the humidifying and heating pulse therapy device provided in this application;

[0042] Figure 7 This is a three-dimensional cross-sectional view of the compressor of the humidifying and heating pulse therapy device provided in this application;

[0043] Figure 8 This is a three-dimensional structural diagram of the handle of the humidifying and heating pulse therapy device provided in this application.

[0044] Explanation of reference numerals in the attached figures:

[0045] 10. Humidifying and heating pulse therapy device; 11. Therapy device body; 12. Humidifier tank; 13. Handle; 14. Filter; 111. Tank mounting part; 112. Compressed air passage; 113. Compressor body; 114. Humidifier body; 115. Compressor; 1111. Limiting slide groove; 1112. Limiting baffle; 1151. Outer shell; 1152. Separator; 1153. Main unit area; 1154. Flow stabilization and noise reduction area; 1155. Flow stabilization and noise reduction component; 1156. Flow stabilization and noise reduction through hole; 1157. Arc-shaped transition section; 1158. Receptacle; 1121. First compressed air passage; 1122. Second compressed air passage; 121. Inlet pipe; 122. Outlet pipe; 123. Heating base; 124. Tank body; 126. Liquid filling pipe; 127. Medicine compartment; 1211. Inlet pipe section; 1212. Tank body section; 1213. Medicine compartment section; 1214. Connection port; 1221. Outlet pipe port; 1222. Radial conical baffle; 1223. Outlet gap; 1224. Liquid baffle; 131. Handle body; 132. Pulse air passage; 133. Sensor assembly; 1321. Ventilation circuit; 1322. Filter chamber; 1323. Pulse generator; 1324. Gas output assembly. Detailed Implementation

[0046] The embodiments of this application 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 application, and should not be construed as limiting this application.

[0047] In the description of this application, it should be understood that the terms "center," "longitudinal," "lateral," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," and "outer," etc., indicating orientation or positional relationships based on the orientation or positional relationships shown in the accompanying drawings, are used only for the convenience of describing this application 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, and therefore should not be construed as a limitation on this application. Furthermore, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of indicated technical features. Thus, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of this application, unless otherwise stated, "a plurality of" means two or more.

[0048] In the description of this application, it should be noted that, unless otherwise expressly specified and limited, the terms "installation," "connection," and "linking" 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 between two components. Those skilled in the art can understand the specific meaning of the above terms in this application based on the specific circumstances.

[0049] Please refer to the following: Figure 1 and Figure 2 The first embodiment of this application provides a humidified and heated pulse therapy device 10, which includes a therapy device body 11, a humidification tank 12, and a handle 13 to achieve efficient humidification and heating of compressed airflow and improve treatment comfort and device practicality. The therapy device body 11 is provided with a tank mounting part 111 and a compressed air channel 112. By designing the tank mounting part 111 on the therapy device body 11, the humidification tank 12 can be integrated and installed on the therapy device body 11, making the installation of the humidification tank 12 more stable and providing a reliable air channel connection path for the airflow to be delivered from the compressed air source to the humidification tank 12, thereby ensuring the overall airtightness and operational stability of the device.

[0050] The humidifier tank 12 is detachably mounted on the tank mounting part 111. The humidifier tank 12 is equipped with an air inlet pipe 121 and an air outlet pipe 122. The inlet of the air inlet pipe 121 is connected to the compressed air channel 112. This facilitates the cleaning and maintenance of the humidifier tank 12 and allows for easy replacement or upgrading of the humidifier device according to different treatment needs, effectively avoiding the problems of complex structure and high maintenance cost of traditional external humidification devices. At the same time, the connection between the air inlet pipe 121 and the compressed air channel 112 allows compressed airflow to smoothly enter the humidifier tank 12 for humidification and heating, thereby providing patients with humidified and appropriately warm airflow in cold or dry environments.

[0051] One end of the handle 13 is connected to the air outlet pipe 122 of the humidifier 12. By transmitting the humidified airflow through the air outlet pipe 122 to the handle 13, the pulsed airflow is effectively transmitted from inside the device to the user's mouth. Furthermore, the humidified airflow improves the patient's respiratory discomfort and enhances treatment comfort. In addition, the design of the handle 13 ensures ease of operation and safety for the user during treatment.

[0052] In summary, the humidified and heated pulse therapy device 10 of this application, through the coordinated arrangement of the therapy device body 11, the humidification tank 12, and the handle 13, achieves humidification and heating of compressed airflow, solving the problems of respiratory discomfort and thick sputum that are difficult to expel due to dry airflow and low temperature in the prior art. The device has a compact design, which optimizes the size, improves the applicability and ease of maintenance of the device, and significantly improves the treatment experience.

[0053] In some preferred embodiments, the humidifying tank 12 includes a heating base 123, a tank body 124, a liquid inlet pipe 126, and a medicine container 127. The heating base 123 is detachably connected to the tank body mounting part 111. The tank body 124 is sealed to the heating base 123 to form a humidifying heating chamber. The air inlet pipe 121 and the air outlet pipe 122 are both located on the top of the tank body 124 away from the heating base 123. The liquid inlet pipe 126 is located on the top of the tank body 124 away from the heating base 123. The medicine container 127 is located on the air inlet pipe 121 and is closable and connected to the air inlet pipe 121.

[0054] The drug chamber 127 is uniquely arranged on the air inlet pipe 121. The compressed airflow in the air inlet pipe 121 flows at high speed, causing the drug in the drug chamber 127 to be atomized and flow out due to negative pressure. It then enters the humidification tank 12 with the compressed airflow, and may partially dissolve and mix with the water in the humidification tank 12. When the heating base 123 heats the water in the humidification heating chamber, the water and the mixed drug vaporize together, so that the airflow output from the air outlet pipe 122 not only contains moist and appropriately warm water vapor, but also carries drug components in the form of tiny evaporated droplets.

[0055] Furthermore, compared to the traditional approach where the drug chamber 127 is located inside the handle 13, the drug liquid particles do not undergo sufficient heating and humidification before entering the patient's mouth, potentially causing the patient to inhale colder, drier drug particles, reducing treatment comfort and drug absorption efficiency. By placing the drug chamber 127 on the air inlet pipe 121, the humidification tank 12 allows the drug to evaporate and heat up along with water after being atomized or dissolved. The humidified and heated airflow output through the air outlet pipe 122 carries sufficient drug components. When it enters the handle 13 and is finally delivered to the patient's mouth, the atomized drug is in a suitable temperature and humid state, reducing irritation and discomfort to the user and facilitating effective drug absorption. This meets the dual needs of drug delivery and gas humidification and heating in various respiratory therapy scenarios.

[0056] In some preferred embodiments, the present application includes an air inlet pipe section 1211, a tank section 1212, and a drug compartment section 1213 in the air inlet pipe 121, thereby improving the operability, flexibility, and efficiency of drug delivery and humidification heating of the equipment. One end of the air inlet pipe section 1211 is used to connect to the compressed air channel 112, which ensures that the airflow delivered from the compressed air source can smoothly enter the humidification tank 12 structure. While reducing the number of connecting pipe interfaces, it is beneficial to improve the transmission efficiency and airtightness of the airflow, providing a stable airflow basis for subsequent humidification heating and drug atomization treatment.

[0057] One end of the tank section 1212 is connected to the humidification and heating chamber, and the other end of the tank section 1212 is connected to the air inlet pipe section 1211. Placing the tank section 1212 between the air inlet pipe section 1211 and the humidification and heating chamber allows for a certain amount of space and structural layout before the airflow enters the humidification and heating chamber, ensuring a stable flow state before the airflow enters the humidification and heating chamber. It also provides convenient conditions for the installation and disassembly of the medicine compartment section 1213. When the airflow enters the humidification and heating chamber through the tank section 1212, it can better contact the water heated by the heating base 123 and achieve sufficient humidification and heating, improving the comfort and effectiveness of the output airflow.

[0058] The end of the medicine compartment section 1213 opposite to the tank section 1212 is detachably equipped with a medicine compartment 127 and a connection port 1214. The medicine compartment 127 is connected to the junction of the tank section 1212 and the air inlet pipe section 1211, and the connection port 1214 is used for connecting an external power cord and control line. By providing a detachable medicine compartment 127 on the medicine compartment section 1213, it is convenient to clean and replace the medicine, and the medicine compartment 127 can be quickly disassembled or the type of medicine can be changed when necessary. Unlike the prior art in which the medicine compartment 127 is fixed to the handle 13, in this embodiment, the medicine compartment 127 is placed at the junction of the tank section 1212 and the air inlet pipe section 1211, so that the medicine enters the airflow channel before entering the humidification and heating chamber, and is heated and humidified together with the compressed airflow. When the heated medicine and the humidified compressed gas are output to the patient's mouth through the air outlet pipe 122, the drug absorption efficiency and patient comfort are further improved.

[0059] Furthermore, the connection port 1214 can be used to connect external power and control cables, facilitating the monitoring, heating, or fine-tuning of the drug chamber 127's status, enabling precise drug delivery and equipment control. Moreover, the combined structure of the air inlet section 1211, the tank section 1212, and the drug chamber section 1213 of the air inlet pipe 121 organically integrates the humidified and heated pulse therapy device 10 of this application in terms of airflow layout, pre-nebulization and dissolution of drugs, and energy and data transmission. The overall operation, maintenance, and debugging of the equipment become simpler, while significantly improving the quality of airflow processing and the effect of drug delivery, providing a more flexible and efficient structural configuration for diverse treatment needs.

[0060] Please refer to further details. Figure 3 In some preferred embodiments, the vent pipe 122 includes a vent outlet 1221 and a liquid baffle 1224; the vent outlet 1221 includes a plurality of radially tapered baffles 1222 evenly spaced, and an outlet gap 1223 is provided between the radially tapered baffles 1222; the liquid baffle 1224 is correspondingly arranged axially on the outside of the outlet gap 1223 to follow the liquid particles in the compressed airflow in the outlet gap 1223.

[0061] By employing the arrangement of radial conical baffles 1222, the humidified airflow to be output can be effectively diverted and guided at the outlet 1221. The inclined and evenly spaced distribution of the conical baffles helps stabilize the airflow field, allowing the gas in a high-temperature, humid state to be ejected in a more stable and orderly manner. At the same time, the outlet gap 1223 formed between multiple radial conical baffles 1222 provides a suitable channel for the atomized drug droplets or water vapor, ensuring that the liquid components carried in the airflow do not undergo violent turbulence or disorderly aggregation when passing through the outlet, thereby improving the patient's comfort during inhalation.

[0062] A liquid baffle 1224 is provided at the outer axial position corresponding to the radial conical baffle 1222 to follow the liquid particles in the compressed airflow in the outlet gap 1223. It should be noted that the liquid particles here do not include drug atomized particles and water vapor, because they are all at the micron level; the liquid particles here refer to the water droplets that may be carried out by the high-speed flow of the compressed airflow. By setting the liquid baffle 1224 on the outside of the outlet gap 1223, unnecessary turbulence, droplet accumulation or local condensation of the airflow at the outlet is effectively avoided.

[0063] In some preferred embodiments, this application achieves a reasonable layout and isolation of the compression and humidification functional modules by setting a compression main body 113 and a humidification main body 114 in the treatment device body 11, thereby reducing mutual interference and improving the operating efficiency and maintenance convenience of the device.

[0064] The compression body 113 houses a compressor 115, and the compression duct 112 includes a first compression duct 1121 and a second compression duct 1122. The first compression duct 1121 is located within the compression body 113 and communicates with the compressor 115. The arrangement of the compressor 115 and the first compression duct 1121 within the compression body 113 allows external air to quickly obtain sufficient pressure and flow under the action of the compressor 115. Directly connecting the first compression duct 1121 to the compressor 115 helps reduce pipeline length and connection points, thereby reducing airflow transmission losses, maintaining high-speed and stable airflow output, reducing the possibility of airflow leakage, and providing a stable air source foundation for subsequent humidification and heating treatment.

[0065] The humidifying body 114 is provided with a second compressed air duct 1122 and a tank mounting part 111. The second compressed air duct 1122 is used to connect the first compressed air duct 1121 and the air inlet pipe 121. The humidifying body 114 is connected to the first compressed air duct 1121 through the second compressed air duct 1122, realizing the orderly transmission of compressed airflow from the compression body 113 to the humidifying body 114. The tank mounting part 111 is provided in the humidifying body 114, which can seamlessly integrate components such as the humidifying tank 12. This allows the compressed airflow to be stably introduced into the humidifying tank 12 for humidification and heating treatment through the second compressed air duct 1122 and the air inlet pipe 121 before entering the humidification and heating chamber. This reduces mutual interference between the humidifying component and the compression component, and also provides flexible space in the structure.

[0066] In summary, by integrating the compressor 115 and the first compressed air duct 1121 into the compressor body 113, efficient and stable compressed air output is ensured. The second compressed air duct 1122 on the humidification body 114 then transmits the airflow to the inlet pipe 121 and the humidification tank 12 for humidification, heating, and drug atomization. Compared to the traditional structure that integrates all functions into a single body, this embodiment improves the overall operational flexibility, maintenance-friendliness, and quality and reliability of treatment output through functional module separation and optimized airflow stage transmission.

[0067] Please refer to further details. Figures 4 to 7In some embodiments, the compressor 115 with stabilizing flow and reducing noise includes a housing body 1151 and a stabilizing and noise-reducing component 1155. The housing body 1151 has a receiving cavity 1158, and a partition 1152 is disposed within the receiving cavity 1158, dividing the receiving cavity 1158 into a main unit area 1153 and a stabilizing and noise-reducing area 1154. A removable stabilizing and noise-reducing component 1155 is disposed within the stabilizing and noise-reducing area 1154. The flow stabilization and noise reduction component 1155 is provided with a plurality of flow stabilization and noise reduction through holes 1156. All of the plurality of flow stabilization and noise reduction through holes are used to stabilize and reduce noise in the airflow. That is, the plurality of flow stabilization and noise reduction through holes 1156 are used to stabilize and reduce noise in the airflow introduced into the main unit area 1153, thereby improving the uniformity and stability of the airflow, improving the flow stabilization and noise reduction capability of the compressor 115, solving the noise problem caused by vibration of the compressor 115 in the prior art, and improving the comfort and reliability of the ventilator.

[0068] Meanwhile, the openings of several of the flow stabilization and noise reduction through holes 1156 are all provided with arc-shaped transition sections 1157. The arc-shaped transition sections 1157 are used to reduce turbulent gas, thereby helping the airflow to flow more smoothly when passing through the flow stabilization and noise reduction through holes 1156, reducing turbulence in the airflow, and thus effectively reducing the noise generated by the airflow.

[0069] Please refer to the reference again. Figure 1 and Figure 2In some preferred embodiments, this application provides a limiting groove 1111 and a limiting baffle 1112 on the tank mounting portion 111. The heating base 123 is limited along the height direction by the limiting groove 1111, and the limiting baffle 1112 is limited along the front-rear direction by the heating base 123. The limiting groove 1111 and the limiting baffle 1112 cooperate to fix the humidifying tank 12. This achieves multi-directional limiting and fixing of the heating base 123 and the humidifying tank 12, thereby ensuring that the humidifying tank 12 has a stable and reliable installation state during equipment operation. By providing mutually cooperating limiting structures on the tank mounting portion 111, a clear installation path and positioning reference can be provided for the heating base 123 and the humidifying tank 12 during equipment assembly, avoiding deviations or loosening during installation. In the height direction, the limiting groove 1111 provides stable vertical positioning for the heating base 123. When the heating base 123 is inserted into the limiting slide groove 1111, the heating base 123 is constrained in the height direction, ensuring that the heating base 123 will not be vertically displaced due to vibration or external force during operation, maintaining tight contact between the heating base 123 and the tank mounting part 111, and improving the airtightness and heating efficiency of the humidification heating chamber. In the front-back direction, the limiting baffle 1112 constrains the heating base 123, effectively preventing the heating base 123 from sliding in the horizontal direction, keeping the heating base 123 and the tank mounting part 111 stable and fixed in the front-back direction, thereby reducing the displacement of the heating base 123 that may be caused by airflow fluctuations, vibration, or moving equipment during operation. Through the synergistic effect of the limiting slide groove 1111 and the limiting baffle 1112, the heating base 123 and the humidification tank 12 are constrained and supported in multiple directions. This not only improves the stability of the humidifier tank 12 itself, but also ensures that the relative position of the heating base 123 and the humidifier tank 12 remains consistent over a long period of time. This helps to ensure sufficient contact between the airflow and water and a stable heating effect during the humidification and heating process, thereby improving the overall equipment performance and treatment effect.

[0070] In some preferred embodiments, the humidifying and heating pulse therapy device 10 further includes a filter 14, which is detachably connected to the outlet of the compressed air duct 112. The filter 14 connects the compressed air duct 112 and the air outlet pipe 122. By providing a detachably connected filter 14 at the outlet of the compressed air duct 112, this application can effectively filter the compressed airflow, removing dust, particulate matter, or other impurities from the airflow. This prevents these impurities from entering the subsequent humidification tank 12 and air outlet pipe 122 with the airflow, ensuring the cleanliness of the airflow during humidification and heating. Simultaneously, the filter 14 prevents impurities from accumulating inside the device, reducing wear on components such as the humidification tank 12 and air outlet pipe 122, and extending the device's service life. The detachable design of the filter 14 allows users to easily clean, replace, or maintain it, ensuring long-term stable filtration performance.

[0071] Please refer to further details. Figure 8 In some preferred embodiments, the handle 13 includes a handle body 131, a pulse airway 132, and a sensor assembly 133. The pulse airway 132 is detachably mounted on the handle body 131. One end of the pulse airway 132 is connected to the air outlet pipe 122, and the other end is connected to the user's mouth. The sensor assembly 133 is mounted on the handle body 131 and is used to detect airflow parameters within the pulse airway 132. By using the handle body 131 as the basic structure supporting the pulse airway 132 and the sensor assembly 133, multifunctional integration can be achieved in the handle 13. The handle body 131 can be made of lightweight, wear-resistant, and easy-to-clean materials, ensuring the durability of the handle 13 during long-term use and providing stable support for the transmission and detection of pulsed airflow. The pulse airway 132 is detachably mounted on the handle body 131, with one end connected to the outlet pipe 122 and the other end connected to the user's mouth. The pulse airway 132 serves as a crucial channel for transmitting humidified and heated airflow from inside the device to the user's mouth, converting compressed airflow into pulsed airflow. Its detachable design allows users and medical personnel to quickly replace, clean, disinfect, or upgrade the pulse airway 132 components as needed, reducing daily maintenance difficulty and downtime, and meeting the ergonomic requirements of different patients and clinical scenarios. Simultaneously, by integrating a sensor component 133 on the handle body 131, airflow parameters (such as pressure, flow rate, humidity, or temperature) within the pulse airway 132 can be monitored in real time. This enables the device to quickly respond to changes in airflow characteristics during operation and promptly fine-tune and optimize humidification, heating, or drug delivery parameters, thereby improving the accuracy and personalization of clinical treatment and ensuring patient comfort and efficacy throughout the treatment process.

[0072] In some preferred embodiments, the pulse airway 132 includes a ventilation circuit 1321, a filter chamber 1322, a pulse generator 1323, and a gas output assembly 1324 connected in sequence. The filter chamber 1322, the pulse generator 1323, and the gas output assembly 1324 are detachably connected to the handle body 131. The ventilation circuit 1321 is used to connect to the air outlet pipe 122. The pulse generator 1323 is used to convert compressed airflow into pulsed airflow. The pulsed airflow is transmitted to the user via the gas output assembly 1324. The sensor assembly 133 is connected to the filter chamber 1322 and is used to detect the airflow parameters within the filter chamber 1322. By detachably connecting the ventilation circuit 1321, filter chamber 1322, pulse generator 1323, and gas output assembly 1324 to the handle body 131, the aforementioned components can be removed from the handle body 131 for thorough cleaning and disinfection. This avoids the problem of bacteria and impurities remaining due to the components being integrated with the handle body 131 and unable to be disassembled, thus ensuring safe use and preventing cross-infection. Furthermore, any component can be replaced, maintained, or repaired as needed without replacing the entire handle body 131, thereby reducing usage costs and maintenance difficulty.

[0073] In summary, this application provides a humidified and heated pulse therapy device, comprising: a therapy device body, wherein the therapy device body is provided with a tank mounting part and a compressed air channel; a humidifier tank, wherein the humidifier tank is detachably mounted on the tank mounting part, the humidifier tank is provided with an air inlet pipe and an air outlet pipe, the inlet of the air inlet pipe being connected to the compressed air channel; and a handle, one end of the handle being connected to the air outlet pipe. By setting a tank mounting part on the therapy device body and cooperating with a detachable humidifier tank, humidification and heating of the compressed airflow are achieved, solving the problems of respiratory discomfort and thick sputum that are difficult to expel caused by dry airflow and low temperature in the prior art, thus improving treatment comfort and clinical efficacy. The stable connection and detachable design of the humidifier tank and the tank mounting part facilitate cleaning and maintenance, and avoid the problems of complex structure, air leakage and high maintenance costs of traditional external humidification devices. At the same time, it optimizes the overall size and reliability of the device, and further expands the applicable scenarios of the therapy device, especially in cold or dry environments, providing patients with humid and temperature-appropriate airflow, effectively improving the treatment experience.

[0074] It should be understood that the application of this application is not limited to the examples above. Those skilled in the art can make improvements or modifications based on the above description, and all such improvements and modifications should fall within the protection scope of the appended claims.

Claims

1. A humidifying and heating pulse therapy device, characterized in that, include: The therapeutic device body is provided with a tank mounting part and a compressed air channel; A humidifying tank is detachably mounted on the tank body mounting part. The humidifying tank is provided with an air inlet pipe and an air outlet pipe. The inlet of the air inlet pipe is connected to the compressed air passage. A handle, one end of which is connected to the air outlet pipe; The humidifier includes a medicine compartment, which is disposed on the air inlet pipe and is closably connected to the air inlet pipe. The therapeutic device body includes: a compression main body, wherein a compressor is disposed within the compression main body; the compressor includes: a housing body, wherein the housing body has a accommodating cavity, wherein a partition is disposed within the accommodating cavity, the partition dividing the accommodating cavity into a main unit area and a flow stabilization and noise reduction area; a flow stabilization and noise reduction component, wherein the flow stabilization and noise reduction component is detachably disposed within the flow stabilization and noise reduction area; wherein the flow stabilization and noise reduction component is provided with a plurality of flow stabilization and noise reduction through holes, wherein the openings of the plurality of flow stabilization and noise reduction through holes are all surrounded by an arc-shaped transition section, the arc-shaped transition section being used to reduce turbulent gas.

2. The humidifying and heating pulse therapy device according to claim 1, characterized in that, The humidification tank also includes: A heating base, which is detachably connected to the tank mounting part; The tank body is sealed to the heating base to form a humidification and heating chamber, and the air inlet pipe and air outlet pipe are both located on the top of the tank body away from the heating base; A liquid filling pipe is located on the top of the tank body away from the heating base.

3. The humidifying and heating pulse therapy device according to claim 2, characterized in that, The intake pipe includes: An intake pipe section, one end of which is used to connect to the compressed air passage; The tank section has one end connected to the humidification and heating chamber and the other end connected to the air inlet pipe section. The medicine compartment section has a detachable medicine compartment and a connection port at one end opposite to the tank section. The medicine compartment is connected to the junction of the tank section and the air inlet pipe section, and the connection port is used to connect external power cords and control lines.

4. The humidifying and heating pulse therapy device according to claim 2, characterized in that, The air outlet pipe includes: The air outlet includes a plurality of radially tapered baffles evenly spaced apart, and an outlet gap is provided between the radially tapered baffles; A liquid baffle is disposed axially on the outside of the outlet gap to follow liquid particles in the compressed airflow in the outlet gap.

5. The humidifying and heating pulse therapy device according to claim 1, characterized in that, The main body of the therapeutic device also includes: The humidifier body includes a first compressed air passage and a second compressed air passage. The first compressed air passage is disposed inside the humidifier body and is connected to the compressor. The second compressed air passage and the tank mounting part are disposed on the humidifier body. The second compressed air passage is used to connect the first compressed air passage and the air inlet pipe.

6. The humidifying and heating pulse therapy device according to claim 2, characterized in that, The tank mounting part includes a limiting groove and a limiting baffle. The heating base is limited along the height direction with the limiting groove, and the limiting baffle is limited along the front-back direction with the heating base. The limiting groove and the limiting baffle cooperate to fix the humidifying tank.

7. The humidifying and heating pulse therapy device according to claim 1, characterized in that, The humidifying and heating pulse therapy device also includes: A filter, which is detachably connected to the outlet of the compressed air passage, is used to connect the compressed air passage and the outlet pipe.

8. The humidifying and heating pulse therapy device according to claim 1, characterized in that, The handle includes a handle body, a pulse airway, and a sensor assembly; the pulse airway is detachably mounted on the handle body, one end of the pulse airway is used to connect to the air outlet pipe, and the other end of the pulse airway is used to connect to the user's mouth; the sensor assembly is mounted on the handle body and is used to detect the airflow parameters within the pulse airway.

9. The humidifying and heating pulse therapy device according to claim 8, characterized in that, The pulse airway includes a ventilation circuit, a filter chamber, a pulse generator, and a gas output component connected in sequence. The filter chamber, pulse generator, and gas output component are detachably connected to the handle body. The ventilation circuit is used to connect to the air outlet pipe. The pulse generator is used to convert compressed airflow into pulsed airflow. The pulsed airflow is transmitted to the user through the gas output component. The sensor component is connected to the filter chamber and is used to detect the airflow parameters in the filter chamber.

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