Treatment module with quick drug replacement and head therapy instrument

Abstract

The utility model provides a kind of treatment module and head therapy instrument of quick medicine change.The quick medicine changeable treatment module includes cover body, medicine package and medicine package frame.The cover body is equipped with accommodating cavity inside;The medicine package includes medicine package base material and the medicine component kept by the medicine package base material;The medicine package frame can be detachably installed in the accommodating cavity, and is configured to be kept in detachable manner The medicine package.The utility model is matched with detachable medicine package frame by prefabricated medicine package, realizes the quick installation and replacement of medicine package.The design completely avoids the cumbersome process of manual smearing and scraping medicine in traditional mode, significantly reduces operation difficulty and time cost, and is more conducive to clinical popularization and application.Meanwhile, the modular medicine package design supports quick replacement when different prescriptions or for different patients, so as to flexibly adapt to diversified treatment schemes, meet the individualized treatment needs.

Description

Technical Field

[0001] This utility model relates to the field of head treatment medical device technology, specifically to a treatment module and head therapy device with rapid dressing changes. Background Technology

[0002] With social development, scientific and technological advancements, and increased health awareness, head health and wellness will play an increasingly important role in the future, becoming a crucial link in promoting overall societal health. Head therapy devices require a heater to cover the patient's head, thus they are typically designed as a cover structure. In existing technology, a common head therapy device operates as follows: a drug is coated onto the inner wall of the cover; the heat from the cover then promotes the release of the active pharmaceutical ingredients, allowing them to diffuse throughout the cover's cavity. The patient's head, within this cavity, can then absorb these active pharmaceutical ingredients. A larger coating area generally results in a faster evaporation rate of the active pharmaceutical ingredients, thus contributing to a higher drug concentration within the cavity. To support this evaporation process, the area requiring an effective temperature also needs to be expanded. Therefore, according to industry practice, in actual operation, the entire cover (except for localized areas such as the ports) typically needs to be maintained at a high temperature (generally above 60°C) to meet the thermal conditions for large-area drug evaporation.

[0003] However, this existing drug application method has several significant drawbacks, severely restricting its clinical application and promotion. First, before and after each treatment, operators must manually apply the powder or ointment to the inner wall of the treatment chamber, and then manually clean the medication after treatment. This process is difficult, cumbersome, and time-consuming. Second, because the medication is applied to the inner wall of the treatment chamber, it is difficult to quickly and conveniently change the type of medication based on the actual condition and treatment needs of different patients using a single device. This "one machine, one medication" model cannot meet the personalized needs of modern treatment and is detrimental to the clinical promotion of this technology.

[0004] Therefore, there is an urgent need in this field for a new head therapy solution that can overcome the above-mentioned shortcomings in order to solve the core problems of inconvenient drug replacement, cumbersome operation, and inability to meet personalized needs. Utility Model Content

[0005] To overcome the problems existing in related technologies, this utility model provides a treatment module and head therapy device that can quickly change dressings, thereby solving the defects in related technologies.

[0006] According to a first aspect of this utility model, a treatment module with rapid dressing changes is provided, comprising:

[0007] The cover has an internal cavity for receiving the contents;

[0008] A medicine packet, the medicine packet comprising a medicine packet substrate and a drug ingredient held by the medicine packet substrate;

[0009] The medicine pack holder can be detachably installed within the receiving cavity;

[0010] The medicine bag holder is configured to hold the medicine bag in a detachable manner.

[0011] In one embodiment, the medicine pack and the medicine pack holder are provided with a matching connecting structure, through which the medicine pack is detachably fixed to the medicine pack holder. This fixing operation can be completed before the medicine pack holder is inserted into the receiving cavity, facilitating unobstructed operation in a spacious area. The medicine pack and medicine pack holder are pre-fixed before being installed into the receiving cavity, making the entire operation simple and easy to perform.

[0012] Based on the previous embodiment, when the medicine pack holder is installed in the receiving cavity, the medicine pack is in contact with the inner wall of the receiving cavity, so that the heat of the receiving cavity can be directly conducted to the medicine pack through its inner wall, thereby achieving efficient heating.

[0013] In another embodiment, the medicine pack holder is constructed as a support frame; when the medicine pack holder is installed in the receiving cavity, the medicine pack is located between the support frame and the inner wall of the receiving cavity and is fixed by compression. This structure supports the following installation method: first, the medicine pack is placed directly into the receiving cavity (at this time, the treatment module needs to be flipped so that the opening faces upward), and then the medicine pack holder is installed. This method is simple to operate, and the medicine pack and medicine pack holder themselves have simple structures. In addition, the medicine pack can adhere to the inner wall of the receiving cavity, which is conducive to heat being directly conducted to the medicine pack through the inner wall, improving heat transfer efficiency.

[0014] Preferably, the substrate of the medicine pack is a flexible, breathable sheet material. In the embodiment where "the medicine pack is detachably fixed to the medicine pack frame via the connecting structure," the "flexibility" allows the medicine pack to conform to the complex shape of the medicine pack frame (such as a mesh or grid structure). In the embodiment where the medicine pack is in contact with the inner wall of the receiving cavity, the "flexibility" ensures that the medicine pack can fully conform to the curved surface of the inner wall, thereby achieving efficient heat conduction. The "breathability" ensures that the active pharmaceutical ingredients in the medicine pack can effectively volatilize and diffuse through the medicine pack substrate into the receiving cavity under heating, thus guaranteeing the therapeutic effect.

[0015] Building upon the previous point, the medication pack can be further configured as a sheet-like sandwich structure, comprising two layers of the medication pack substrate and the drug component situated between the two layers. The sheet-like shape provides a larger specific surface area, facilitating the uniform and efficient volatilization of the drug component under heating, thereby enhancing therapeutic efficacy. Since the sheet-like structure is easily processed into large-area medication packs with "small dosage but large coverage area," and the area of ​​the medication pack is positively correlated with the release rate of the active drug component, using a large-area medication pack directly meets the high standard requirement of this therapy for rapidly establishing and maintaining a high drug concentration environment within the containment cavity. This sandwich structure effectively prevents the drug component from spilling or adhering to equipment components during the handling and installation of the medication pack, providing a stable storage space for the drug component. During heating, the active drug component can be continuously volatilized and released through the "breathable" medication pack substrate. This structure is particularly suitable for powdered drug components.

[0016] Preferably, the substrate of the medicine package is non-woven fabric or gauze. These materials are low in cost and easy to process and seal: non-woven fabric can be sealed by heat sealing, sewing, etc., and gauze can also be sealed by common processes such as sewing.

[0017] Preferably, the pharmaceutical ingredient is in powder form. Powder has a larger specific surface area, allowing for more complete heating and release of the active pharmaceutical ingredient. Powder is also easier to fill and dispense, and is more adaptable to various packaging structures.

[0018] Preferably, the medicine pack holder is a mesh or grid-like frame structure adapted to the shape of the receiving cavity. This frame structure provides stable physical support for the large-area sheet-like medicine pack, which significantly increases the release rate of the active pharmaceutical ingredient, thus facilitating the rapid achievement and maintenance of the high drug concentration environment required for therapy within the receiving cavity. For designs where the medicine pack contacts the inner wall of the receiving cavity, this structure allows the medicine pack to adhere more stably and tightly to the inner wall, thereby improving heat conduction efficiency. The mesh or grid-like structure has good permeability and does not significantly hinder the release of the active pharmaceutical ingredient within the medicine pack. The mesh or grid-like structure of the medicine pack holder creates a physical barrier between the patient's head and the inner wall of the receiving cavity; the actual temperature of the medicine pack holder is much lower than that of the inner wall of the receiving cavity, therefore, even if the patient's head accidentally touches the medicine pack holder, the perceived burning sensation is significantly reduced.

[0019] According to a second aspect of the present invention, a head therapy device is provided, comprising a treatment module with rapid dressing change capability as described in the first aspect.

[0020] The technical solution provided by this utility model can include the following beneficial effects:

[0021] This invention provides a treatment module with rapid medication replacement, which achieves quick installation and replacement of medication packs through the combination of prefabricated medication packs and a detachable medication pack holder. This completely avoids the cumbersome process of manually applying and scraping off medication in traditional methods, significantly reducing operational difficulty and time costs, and thus making it more conducive to clinical promotion.

[0022] The modular design of the medicine pack allows for flexible switching of treatment plans by quickly changing the medicine pack when using different prescriptions or for different patients, thus meeting personalized treatment needs. Attached Figure Description

[0023] The accompanying drawings, which are incorporated in and form part of this specification, illustrate embodiments consistent with the present invention and, together with the description, serve to explain the principles of the present invention.

[0024] Figure 1 This is a schematic diagram of the overall structure of a treatment module capable of rapid dressing changes, as shown in an exemplary embodiment of this utility model.

[0025] Figure 2 This is an exploded view of a treatment module capable of rapid dressing changes, as illustrated in an exemplary embodiment of this utility model.

[0026] Figure 3 This is a schematic diagram illustrating the connection structure between the medicine pack and the medicine pack holder, as shown in an exemplary embodiment of this utility model;

[0027] Figure 4 This is a schematic diagram of the medicine package structure shown in an exemplary embodiment of the present invention;

[0028] Figure 5 This is a schematic diagram of the cross-sectional outline of the cover shown in an exemplary embodiment of the present invention;

[0029] Figure 6 This is an exploded schematic diagram of the medicine pack holder locking structure shown in an exemplary embodiment of this utility model;

[0030] Figure 7 This is a schematic diagram of the heating system structure shown in an exemplary embodiment of the present invention;

[0031] Figure 8 This is a schematic diagram of the gripping part structure of a medicine pack holder according to an exemplary embodiment of the present invention.

[0032] In the attached diagram, 100-cover body, 200-medicine bag rack, 201-hook, 202-grip, 300-medicine bag, 301-hanging hole, 302-medicine compartment, 400-knob, 401-protrusion, 500-fixing block, 600-screw, 700-end cover, 701-mounting hole, 800-outer cover, 900-far-infrared heating tube, 1000-tube clamp, 1100-reflector. Detailed Implementation

[0033] Exemplary embodiments will now be described in detail, examples of which are illustrated in the accompanying drawings. In the following description, when referring to the drawings, unless otherwise indicated, the same numerals in different drawings denote the same or similar elements. The embodiments described in the following exemplary embodiments do not represent all embodiments consistent with this invention. Rather, they are merely examples of apparatuses and methods consistent with some aspects of this invention as detailed in the appended claims.

[0034] The terminology used in this invention is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. The singular forms “a,” “the,” and “the” used in this invention and the appended claims are also intended to include the plural forms unless the context clearly indicates otherwise. It should also be understood that the term “and / or” as used herein refers to and includes any or all possible combinations of one or more of the associated listed items.

[0035] It should be understood that although the terms first, second, third, etc., may be used in this invention to describe various information, this information should not be limited to these terms. These terms are only used to distinguish information of the same type from one another. For example, without departing from the scope of this invention, first information may also be referred to as second information, and similarly, second information may also be referred to as first information. Depending on the context, the word "if" as used herein may be interpreted as "when," "when," or "in response to determination."

[0036] In a first aspect, this utility model provides a treatment module capable of rapid dressing changes, comprising:

[0037] Example 1

[0038] This embodiment provides a treatment module with rapid dressing changes. It mainly includes:

[0039] The cover 100 has an internal cavity. The size and shape of this cavity are designed to accommodate the human head and provide adequate space for movement. During normal use, it creates a restricted, enclosed space around the user's head, allowing for limited exchange of internal and external air. This structure, similar to the near-sealed space of a hair treatment device, effectively inhibits the drastic exchange between internal hot air and volatile active pharmaceutical ingredients and external cold air, thus significantly reducing the loss of active ingredients. This design aims to maintain a relatively stable treatment environment in terms of temperature, humidity, and drug concentration around the user's head, thereby significantly enhancing the effects of thermotherapy and drug therapy.

[0040] The medicine package 300 includes a medicine package substrate and a drug ingredient held by the medicine package substrate.

[0041] It is understood that the drug ingredients described in this utility model cover a variety of types, including but not limited to traditional Chinese medicinal materials and their effective extracts, as well as chemical drug ingredients such as methyl salicylate and synthetic capsaicin.

[0042] It is understood that the drug packaging substrate of this utility model can "retain" drug components in various physical forms. Specifically, this includes, but is not limited to: powdered or paste-like drug components being carried on the surface of the drug packaging substrate through adhesion, coating, or other methods; liquid drug components (such as medicinal oils) being stored in the internal pores of a porous drug packaging substrate (such as non-woven fabric or sponge) through adsorption, impregnation, or other methods; or solid or semi-solid drug components being sealed in a sandwich cavity formed by heat sealing or pressing two or more layers of drug packaging substrates. Those skilled in the art can select or combine one or more suitable retention methods based on the drug's form, release characteristics, and manufacturing process.

[0043] The medicine pack holder 200 can be detachably installed in the receiving cavity.

[0044] The medicine bag holder 200 is configured to hold the medicine bag 300 in a detachable manner.

[0045] The treatment module achieves its therapeutic effect in the following ways: (Method 1) Heating the medicine pack placed near the inner wall of the cavity to promote the release of the active pharmaceutical ingredients, and the warm environment generated by the heat convection can promote blood circulation in the user's scalp, thereby improving the absorption efficiency of the released active pharmaceutical ingredients; and / or, (Method 2) Emitting heat radiation through the inner wall of the cavity to directly produce a physiotherapy effect on the user's head and body surface, which usually coexists with the heat convection effect.

[0046] The use of the word "and / or" here reflects that this treatment module can flexibly select the following working modes according to treatment needs:

[0047] Mode 1: When the medicine pack completely covers the inner wall of the receiving cavity, the inner wall heats the medicine pack, causing the active ingredients of the medicine to volatilize. In this case, the medicine pack significantly blocks the heat radiation emitted by the inner wall, so the direct therapeutic effect of the heat radiation is weak. This is primarily Mode 1.

[0048] Mode 2: When the medication pack only partially covers the inner wall of the cavity, the inner wall simultaneously heats the medication pack to promote drug evaporation, and the uncovered area of ​​the inner wall directly applies heat radiation to the head and body surface. That is, Mode 1 and Mode 2 coexist.

[0049] Mode 3: When the medication pack is not placed near the inner wall of the receiving cavity. In this case, it is mainly Mode 2.

[0050] The combination of Method 1 and Method 2 can produce a synergistic effect. Specifically, thermal radiation can further promote local blood circulation in the user's head, thereby significantly improving the absorption efficiency of the released active pharmaceutical ingredients.

[0051] In Method 2, the intensity of thermal radiation is significantly affected by the material and surface treatment of the inner wall of the cavity. Specifically, when materials with inherently high infrared radiation efficiency, such as ceramics, are used, or when the inner wall of the cavity is metal but has a coating that enhances radiation, such as enamel, the resulting thermal radiation intensity is higher; conversely, if the inner wall of the cavity is only made of metal and does not have any special coating designed to improve radiation efficiency, its thermal radiation intensity is relatively weaker. It should be understood that the above embodiments are not intended to limit the scope of protection of this utility model.

[0052] In summary, this treatment module allows users to select the "heating the medicine pack (synergistically enhancing drug efficacy through thermal convection)" and "applying thermal radiation (accompanied by thermal convection)" functions independently or in combination, which precisely corresponds to the optional technology combination described by the word "and / or".

[0053] Example 2

[0054] In this embodiment, the medicine pack 300 and the medicine pack rack 200 are provided with mutually matching connection structures, and the medicine pack 300 is detachably fixed to the medicine pack rack 200 through the connection structures.

[0055] As an optional embodiment for connecting and fixing the medicine pack and the medicine pack holder, the specific description is as follows:

[0056] The medicine bag rack 200 is provided with several hooks 201, and the medicine bag 300 is provided with hanging holes 301 corresponding to the position and number of hooks 201. During installation, the hanging holes 301 on the medicine bag 300 are aligned with the hooks 201 on the medicine bag rack 200, allowing for quick installation and fixation of the medicine bag 300. When it is necessary to replace or remove the medicine bag 300, simply detach the hanging holes 301 from the hooks 201 to complete the disassembly. This cooperation between the hooks 201 and hanging holes 301 achieves detachable fixation of the medicine bag 300 on the medicine bag rack 200, resulting in a simple structure and convenient operation. The hooks 201 shown in the figure are arranged in a back-to-back configuration (the hook opening of the upper hook faces upwards, and the hook opening of the lower hook faces downwards). The advantage of this configuration is that the medicine bag 300 is unlikely to fall off the hooks 201 even with slight pulling from either direction. During installation, the medicine pack 300 should be stretched using its own material's moderate elasticity and then hung on the opposite hook 201. After releasing, the medicine pack 300 will spring back and be reliably secured. This method provides a firm fixation and resists accidental pulling.

[0057] In another alternative embodiment, the hooks 201 can also be configured with all hook openings facing upwards. This method is simpler to operate when hanging the medicine packs 300, as it eliminates the need to stretch the medicine packs. However, its drawback is that if the medicine packs 300 are subjected to an upward force, they may come off. Considering that the probability of the medicine packs 300 being subjected to such directional external forces during normal loading and use is low, this method is still applicable. Removing the medicine pack rack 200 may cause the medicine packs 300 to fall off, but this impact is minimal and within acceptable limits. Therefore, the technical meaning of "the medicine pack 300 is detachably fixed to the medicine pack holder 200 through the connecting structure" in this utility model does not mean that the connecting structure must absolutely lock the medicine pack 300 to the medicine pack holder 200 in any state. Rather, it means that when neither the medicine pack holder 200 nor the medicine pack 300 is inserted into the receiving cavity, and the medicine pack holder 200 is in its working position (i.e., the treatment angle with the opening facing downwards), the connecting structure can work in conjunction with gravity, friction, the elasticity of the medicine pack itself, and other forces to ensure that the medicine pack 300 is stably maintained on the medicine pack holder 200 without loosening. The specific embodiments listed in the specification should not be construed as limiting the scope of protection of the claims.

[0058] It is understood that this utility model does not limit the specific form of the hooking mechanism. The shape of the connecting hole can be circular, elliptical, elongated, or other geometric shapes suitable for hanging, and its number and position can be adjusted according to the size of the medicine bag and the fixing requirements. The hook can also be a spring, a curved hook, or other different structures, as long as it can form an effective hook with the connecting hole.

[0059] It is understood that the form of the connection structure is not limited to the combination of hooks and hanging holes. Those skilled in the art can adopt other common detachable connection methods according to actual needs. For example, the rough and barbed sides of Velcro can be respectively provided at corresponding positions on the medicine pack 300 and the medicine pack holder 200, achieving detachable fixation through hook and loop fasteners. Alternatively, the combination of snaps and slots, magnetic adsorption components, adhesive backing on the medicine pack, or snap fasteners can also be used. Furthermore, making the medicine pack 300 into a cap shape and directly fitting it onto the medicine pack holder 200, as long as it can be reliably held in the pre-installed state, also falls under the connection structure described herein.

[0060] It is understood that the number of the medicine packs 300 can be one, two, or more. Their placement can cover any area suitable for the corresponding head treatment region, such as the side or top of the cavity wall. The specific number and layout of the medicine packs 300 can be adapted and combined according to the surface area of ​​the cavity wall, the size of a single medicine pack 300, and the area requiring drug coverage for treatment.

[0061] It is understood that the fixed position and fixing method of the medicine pack 300 on the medicine pack rack 200 can be varied. For example, the medicine pack 300 can be fixed to the outside of the medicine pack rack 200, or it can be fixed to the inside of it by setting multiple connection points, or it can be combined with the medicine pack rack 200 by weaving or other methods. This utility model does not limit the specific fixed position and combination method of the medicine pack 300 on the medicine pack rack 200, and any arrangement that can achieve reliable and detachable fixing is within the protection scope of this utility model.

[0062] Example 3

[0063] This embodiment is a preferred implementation based on the treatment module described in Embodiment 2. Specifically, when the medicine pack holder 200 is installed in the receiving cavity, the medicine pack 300 is in contact with the inner wall of the receiving cavity.

[0064] In one specific implementation, the medicine pack 300 is fixed to the outside of the medicine pack holder 200. By adapting the structure and dimensions of the medicine pack holder 200 to the thickness of the medicine pack 300, it can be ensured that the medicine pack 300 maintains contact with the inner wall of the receiving cavity when the medicine pack holder 200 is installed in place. This contact allows the inner wall of the receiving cavity to efficiently heat the medicine pack 300 through direct heat conduction, thereby significantly improving the heating efficiency of the medicine pack 300 and promoting the release of drug components.

[0065] The above describes the configuration where "the medicine pack 300 is in contact with the inner wall of the receiving cavity". Correspondingly, as another variation of this utility model, the configuration where "a predetermined gap is maintained between the medicine pack 300 and the inner wall of the receiving cavity" will be described below:

[0066] The predetermined gap is achieved by fixing the medicine pack 300 to the inside of the medicine pack holder 200, or by adapting the structure and size of the medicine pack holder 200 to the thickness of the medicine pack 300, so that when the medicine pack holder 200 is installed, the gap is formed and maintained between the medicine pack 300 and the inner wall of the receiving cavity.

[0067] The core of this configuration lies in changing the primary heating method of the medicine pack 300 from high-efficiency heat conduction (when the medicine pack is in direct contact with the inner wall) to the less efficient heat radiation and convection (when there is a gap between the medicine pack and the inner wall) by setting the gap. Since the latter's overall heat transfer intensity is significantly lower than that of direct contact heat conduction, and further decreases as the gap distance increases, the actual temperature of the medicine pack 300 is reduced and can be effectively controlled by the gap size.

[0068] This differentiated design is particularly important for medicine packs containing heat-sensitive substances such as plant essential oils as active ingredients. To achieve flexible control, multiple medicine pack racks 200 and / or medicine packs 300 of different sizes can be equipped for the same treatment module, thus creating different gaps after installation to meet diverse drug release temperature requirements.

[0069] It should be noted that the overall operating temperature setting of the receiving cavity is primarily based on the user's head comfort and treatment needs, rather than on the temperature tolerance of the medicine pack. Therefore, physically adjusting the distance between the medicine pack 300 and the heat source (inner wall of the receiving cavity) is a more effective and practical technical means to independently and precisely control the temperature of the medicine pack.

[0070] In the above-described variant embodiments, since the medicine pack 300 does not contact the inner wall of the receiving cavity, but is only installed on the medicine pack holder 200, this highlights the necessity of the technical feature in the claim that "the medicine pack is detachably fixed to the medicine pack holder through the connecting structure".

[0071] Example 4

[0072] This embodiment provides an alternative technical solution for maintaining the position of the medicine pack using the medicine pack holder. Specifically, the medicine pack holder 200 is constructed as a support frame; when the medicine pack holder 200 is installed in the receiving cavity, the medicine pack 300 is located between the support frame and the inner wall of the receiving cavity, and is fixed by compression.

[0073] Specifically, the medicine pack holder 200 is configured as a support frame structure.

[0074] The installation method of the medicine pack 300 involved in this embodiment is as follows: First, adjust the treatment module so that the opening faces upward, pre-place the medicine pack 300 in a predetermined area on the inner wall of the receiving cavity, and then install the support frame (medicine pack holder 200) into place. The structure and size of the support frame (medicine pack holder 200) are adapted to the thickness of the medicine pack 300, which can ensure that when the support frame (medicine pack holder 200) is installed in place, the medicine pack 300 is stably pressed between the support frame and the inner wall of the receiving cavity, and is reliably fixed mainly by the compression action it receives, without relying on additional connecting structures.

[0075] According to the above description, the "holding" as defined in the claim "the medicine pack holder is configured to hold the medicine pack in a detachable manner" does not specifically mean that there must be a separate connection structure (such as hooks, Velcro, etc.) between the medicine pack holder 200 and the medicine pack 300. Its core is to achieve a structural state in which, when the medicine pack holder 200 is installed in the receiving cavity, the medicine pack 300 can be held in a predetermined position near the inner wall of the receiving cavity by means of the medicine pack holder 200.

[0076] It is understood that the technical focus of this embodiment is on the final state of the medicine pack 300 after the medicine pack holder 200 is installed, where it is either "in contact with the inner wall of the receiving cavity" or "compressed". The technical focus of Embodiment 2, however, is on the reliable fixation of the medicine pack holder 200 and the medicine pack 300 before they are inserted into the receiving cavity. The two embodiments have different technical focuses.

[0077] The "detachable" aspect, defined in the claim that "the medicine pack holder is constructed to hold the medicine pack in a detachable manner," emphasizes the ease of separation between the medicine pack 300 and the medicine pack holder 200. Whether through hooks and holes, clips and slots, magnetic adsorption components, adhesive backing, snap fasteners, or other connection methods, or even by using the medicine pack holder 200 to press the medicine pack 300 against the inner wall of the receiving cavity in this embodiment, the medicine pack 300 can be easily, quickly, and non-destructively removed from the medicine pack holder 200. The core of this definition is ensuring that the replacement of the medicine pack as a consumable is simple and easy, rather than being limited to a specific connection structure. Therefore, any mechanical or physical connection method that enables convenient detachment falls within the scope of this feature.

[0078] Example 5

[0079] In this embodiment, the substrate of the medicine package is a flexible, breathable sheet material.

[0080] Specifically, the medicine package 300 includes a medicine package substrate made of a flexible and breathable sheet material. For example, the medicine package substrate can be non-woven fabric, cotton fabric, breathable composite film, or other materials with similar properties.

[0081] The "flexible" characteristic provides adaptation advantages in different implementations: In the scheme where "the medicine pack is detachably fixed to the medicine pack holder via the connecting structure," when the medicine pack 300 is fixed to the medicine pack holder 200, its flexibility allows it to conform to the complex configuration of the medicine pack holder 200 (e.g., a mesh or grid structure), facilitating the fixation of the medicine pack 300 to the medicine pack holder 200. In the scheme where the medicine pack 300 contacts the inner wall of the receiving cavity, its flexibility ensures that the medicine pack 300 can fully conform to the curved surface of the inner wall of the receiving cavity, thereby increasing the effective contact area and achieving efficient heat conduction.

[0082] The breathable property allows heat, moisture, and volatile active pharmaceutical ingredients to effectively pass through the drug pack substrate, facilitating the release and diffusion of the active pharmaceutical ingredients. The sheet-like form of the drug pack substrate provides convenience for diverse designs in terms of shape, size, and structure. By using this type of flexible, breathable sheet material as the drug pack substrate, the drug pack 300 achieves its drug-carrying function while also possessing good fit and breathability, helping to ensure the overall therapeutic effect.

[0083] Example 6

[0084] This embodiment is based on "using flexible and breathable sheet material as the drug packaging substrate", and further makes the drug packaging 300 a sheet sandwich structure, which includes two layers of the drug packaging substrate and the drug component between the two layers of the drug packaging substrate.

[0085] In this embodiment, the following two medicine pack solutions are provided:

[0086] (1) A continuous sealed boundary is formed around the periphery of the medicine pack substrate through heat sealing and other processes, constituting the sealed physical outline of the medicine pack. Within the area enclosed by this sealed boundary, multiple partition seams formed by sewing are also provided. These partition seams divide the interior of the medicine pack into multiple independent compartments arranged in an array (e.g., a rectangular grid of 3 rows × 5 columns), namely medicine compartments 302. The outer sealed boundary and the inner partition seams together constitute a composite binding structure: the sealed boundary ensures the overall airtightness of the medicine pack and prevents leakage of drug components; while the partition seams effectively restrict the migration of drug components in each compartment, thereby significantly reducing the problem of uneven thickness caused by drug component accumulation during transportation, compression, or hanging, which is conducive to the full release of active drug components. Furthermore, one or more connecting holes are provided on the sealed boundary of the medicine pack. The connecting holes are used to cooperate with the hooks 201 and other connecting structures on the medicine pack rack 200 to realize the quick hanging and fixing of the medicine pack on the medicine pack rack 200.

[0087] It is understood that the array layout, specific shape (such as rectangle, rhombus, etc.) and quantity of the grid areas can be designed according to specific needs; the width and sealing strength of the sealing boundary can be adjusted according to the size, material and strength requirements of the medicine pack; the shape (such as circle, ellipse, etc.), quantity and position on the sealing boundary of the connecting holes can be set according to the actual connection and cooperation requirements with the medicine pack rack 200.

[0088] The drug packaging structure can be prepared using various processes. As an exemplary, and not limiting, preparation method, its main process flow is as follows:

[0089] A. Bag forming: For example, heat-seal three sides of two separate pieces of non-woven fabric; or fold a piece of non-woven fabric in half and heat-seal its two sides to form a bag-shaped preform with one end open.

[0090] B. Quantitative drug filling: A predetermined dose of drug components is filled into the bag-shaped preform using a quantitative filling device.

[0091] C. Sealing and forming: The opening of the bag-shaped preform is heat-sealed to form a closed, flat medicine package with a complete sealed boundary.

[0092] D. Uniform drug distribution: The drug pack is passed through a vibrating plate and a spiral track, etc., and the vibration is used to make the drug components inside evenly distributed.

[0093] E. Partitioned Structure Forming: Using sewing technology, the partitioned seams are sewn onto the medicine package according to a predetermined pattern to form a composite binding structure.

[0094] F. Connecting hole machining: Punching is performed at predetermined positions on the sealing boundary of the medicine package to form one or more connecting holes for connection.

[0095] (2) The periphery of the medicine package substrate is formed into a complete sealed boundary through a heat-sealing process. Its internal partitioning structure consists of crisscrossing heat-sealing partition lines formed by the heat-sealing process, which divide the interior of the medicine package into multiple independent sealed compartments. The heat-sealing partition lines have a certain width, thus forming a processable strip-shaped area on the surface of the medicine package. Based on this structure, the connecting holes for attaching to the medicine package holder 200 can be opened either on the sealed boundary of the medicine package periphery or directly on the strip-shaped area of ​​the heat-sealing partition lines with sufficient width. This structure, through physical isolation, confines the drug components within each independent sealed compartment, effectively preventing their migration and ensuring uniform thickness of the medicine package.

[0096] The drug packaging structure can be prepared using various processes. As an exemplary, and not limiting, preparation method, the process flow is as follows:

[0097] A. Bag Body and Vertical Segmentation Forming: First, a bag-shaped structure with one open end is formed through a heat-sealing process. Then, multiple longitudinal heat-sealing segmentation lines are hot-pressed onto the bag body, forming multiple parallel, vertically elongated open compartments.

[0098] B. Step-by-step filling and lateral sealing: The drug package is placed in a specialized forming device, and the drug components are sequentially and quantitatively filled into each vertical compartment. After the drug components fall to the bottom of the compartment, a lateral heat-sealing section line is hot-pressed at a predetermined height, thereby sealing the upper end of the current compartment and forming an independent, sealed chamber.

[0099] C. Iterative molding: Repeat the above steps of filling the drug and horizontal heat sealing to form and seal multiple cells in the vertical compartment in sequence, and finally make a drug pack containing multi-dimensional array cells.

[0100] D. Connecting hole processing: Finally, punching is performed on the sealing boundary around the medicine pack and / or on the strip area with a sufficiently wide intermediate heat-sealing partition line to form connecting holes.

[0101] It is understood that this utility model does not limit the specific implementation of the above structure: the array layout, specific shape and number of compartments can be designed according to the drug distribution requirements. The number, shape and location of the connecting holes (sealing boundary or middle heat-sealing partition line) can be flexibly set according to the hanging and fixing requirements with the medicine pack rack 200.

[0102] Understandably, the flake-like shape provides a larger specific surface area, which is beneficial for the uniform and efficient volatilization of drug components under heating, thereby improving the therapeutic effect.

[0103] It is understandable that sheet-like structures are easy to process into large-area drug packs that "use less medication but cover a large area". The area of ​​the drug pack is positively correlated with the release rate of the active drug ingredient. Therefore, using large-area drug packs can directly meet the high standard requirements of this therapy for the release rate in order to quickly establish and maintain a high drug concentration environment in the cavity.

[0104] It is understood that this sandwich structure can effectively prevent drug components from spilling or adhering to equipment parts during the handling and installation of the drug pack, and provides a stable storage space for the drug components.

[0105] It is understood that, when heated, the active pharmaceutical ingredients can be continuously volatilized and released through the "breathable" substrate of the pharmaceutical packaging.

[0106] It is understandable that the two aforementioned packaging structures are particularly suitable for encapsulating powdered drug components.

[0107] Example 7

[0108] In this embodiment, the substrate for the medicine pack is non-woven fabric or gauze. Both materials meet the requirements of "flexible and breathable sheet material." In terms of process and cost, non-woven fabric and gauze offer the following advantages as medicine pack substrates: non-woven fabric is particularly suitable for sealing and shaping processes such as heat sealing or sewing; gauze is especially suitable for processing using sewing and other similar techniques. The processing technologies for both materials are mature, simple, and easy to implement. Furthermore, non-woven fabric and gauze have lower costs, which is beneficial for the large-scale production and application of medicine packs.

[0109] Example 8

[0110] In this embodiment, the drug component is in powder form. Using powdered drugs has several advantages:

[0111] Easy to fill and quantify: The powder has good flowability, which makes it easy to fill the independent compartments or closed compartments formed by the drug packaging substrate with precise and quantitative filling through automated equipment, which is conducive to achieving standardized production and dosage control.

[0112] Facilitates heat volatilization: The powder has a large specific surface area. Under the heating effect of the inner wall of the container, its active ingredients can be heated more quickly and evenly and volatilized and released into the treatment environment, thereby improving drug utilization.

[0113] Adaptive structural design: The powder form is highly compatible with the sheet-like sandwich structure and the partitioned (grid area or compartment) design. The partitioned structure can effectively prevent uneven distribution of powdered drugs due to migration and aggregation during storage and transportation, ensuring the overall flatness of the 300-pack, thereby ensuring heat transfer efficiency and facilitating the full release of active pharmaceutical ingredients.

[0114] It is understood that limiting the drug ingredient to "powder" is a further specific and preferred description of its physical form. In practical applications, "powder" may include powders with a certain particle size range made from Chinese medicinal materials or chemical raw materials through processes such as pulverization and grinding.

[0115] Example 9

[0116] In this embodiment, the medicine pack holder 200 is a mesh or grid-like frame structure adapted to the shape of the receiving cavity.

[0117] In this embodiment, the medicine pack holder 200 is specifically constructed as a mesh or grid-like frame structure, the main structure of which is made of plastic. Its overall shape is adapted to the shape of the internal receiving cavity of the cover 100; for example, it can be presented as an approximately dome-shaped, arched, or cylindrical mesh structure. This structure has the following advantages:

[0118] Good permeability: The mesh or grid gaps allow hot air, moisture and volatile drug components to pass freely without hindering heat convection and drug diffusion.

[0119] Stable support and fixation: The frame structure provides stable physical support for the large-area sheet-like drug pack, which significantly increases the release rate of the active drug ingredient, thus facilitating the rapid achievement and maintenance of the high drug concentration environment required for therapy within the cavity. For designs where the drug pack contacts the inner wall of the cavity, the mesh or grid structure reliably compresses and fixes the drug pack 300 by cooperating with the inner wall, ensuring a tight and uniform fit between the drug pack 300 and the inner wall, thus promoting efficient heat conduction.

[0120] Preventing bumps and burns: The medicine pack holder 200, made of plastic with a mesh or grid structure, forms a physical barrier between the patient's head and the inner wall of the cover 100. On one hand, this structure prevents burns: because plastic is a poor conductor of heat, and the actual temperature of the medicine pack holder 200 is much lower than the continuously heated inner wall of the cover 100, the perceived burning sensation is significantly reduced even if the patient's head accidentally touches the medicine pack holder 200. On the other hand, this structure cushions impacts: the plastic material has a certain degree of softness and elasticity, which can cushion contact, thereby reducing direct impact and discomfort to the head.

[0121] Lightweight and rigidity balance: The mesh or grid design ensures sufficient structural rigidity while achieving lightweight design of the medicine pack rack 200, making it easy to operate and install.

[0122] Although the medicine bag holder 200 in this embodiment is described using plastic as an example, the scope of protection of this utility model is not limited thereto. It is understood that the mesh or grid-like structure can be achieved through various manufacturing processes such as wire welding, sheet metal stamping, engineering plastic injection molding, or 3D printing. It is understood that "mesh or grid-like" is a general term encompassing its regular or irregular perforated structural features, and the scope of protection of this utility model is not limited to the specific mesh shape, size, and arrangement shown in the figures.

[0123] In this embodiment, the medicine pack rack 200 is also exemplarily provided with a gripping part 202. The gripping part 202 is located at the top of the inner wall of the medicine pack rack 200 (based on the treatment angle with the treatment module facing downwards), which facilitates the operator's gripping. By gripping the gripping part 202, a series of operations can be conveniently performed, such as taking and placing the medicine pack rack 200, installing the medicine pack rack 200 into the receiving cavity, and detachably installing the medicine pack 300 onto the medicine pack rack 200.

[0124] It is understood that the structural form of the medicine pack holder 200 described in this utility model is not limited to the mesh or grid structure shown in this embodiment, and may also be other structures that can be conceived by those skilled in the art. For example, the medicine pack holder 200 may also be a claw-type structure composed of several elastic arms. When such a structure is adopted, its elastic arms can deform using their own elasticity, thereby abutting and pressing the medicine pack 300 between the medicine pack holder 200 and the inner wall of the cover 100. Although this embodiment exemplarily uses a mesh or grid structure, the protection scope of this utility model is not limited to this.

[0125] Example 10

[0126] This utility model also provides a knob mechanism for locking the medicine pack holder 200. This mechanism is located at the end of the end cover 700 of the treatment module, and its structure, installation, and function are as follows:

[0127] 1. Core structural components

[0128] The knob mechanism mainly consists of the following components:

[0129] Knob 400: Located outside the end cover 700, its end facing the interior of the mechanism has at least one protrusion 401. This embodiment uses one protrusion 401 as an example, but the number and layout of protrusions 401 (e.g., two symmetrically arranged) can be designed according to actual needs.

[0130] Fixing block 500: Located inside end cover 700.

[0131] Anti-rotation structure: It is set on the mating surfaces of the knob 400 and the fixing block 500, and is composed of mutually fitting convex keys and grooves to prevent the two from rotating relative to each other.

[0132] Screw 600: Passes through the center of knob 400 and fixing block 500 to connect and fasten the two.

[0133] It is understood that the above structure is an exemplary implementation. In an alternative, the fixing block 500 may have integrated threads or be fixed to the knob 400 via a snap-fit ​​structure, thus eliminating the need for a separate screw 600.

[0134] 2. Mechanism Installation Method

[0135] The installation relationship of the knob mechanism is as follows:

[0136] The end cover 700 has a mounting hole 701. During installation, the knob 400 is inserted into the mounting hole 701 from the outside, and the fixing block 500 is placed inside the end cover 700. The two are connected and clamped onto the end cover 700 by the screw 600. Through the cooperation of the anti-rotation structure (convex key and groove) and the locking force of the screw 600, it is ensured that there is no relative rotation between the knob 400 and the fixing block 500. This installation method restricts the knob 400 to rotate only around the axis of the mounting hole 701, and prevents significant axial movement. The knob mechanism can be symmetrically arranged on the left and right sides of the end cover 700, and its specific number and position (e.g., front and back arrangement or more) can be set according to actual fixing requirements.

[0137] 3. Function Implementation Process

[0138] The mechanism achieves its locking function through the following steps:

[0139] After the medicine holder 200 is placed into the receiving cavity and installed in place, rotate the knob 400 located on the end cover 700. Rotation of the knob 400 will cause the protrusion 401 to rotate synchronously. When the protrusion 401 rotates to a specific angle range, it mechanically interferes with the medicine holder 200, forming an effective abutment. This mechanical limiting effect generated by the interference abutment reliably locks the medicine holder 200, preventing it from loosening during treatment. The frictional force generated by this interference abutment effectively prevents the knob 400 from rotating back, thus forming a self-locking mechanism and making the locking state more reliable.

[0140] This embodiment describes a specific structure for locking the medicine bag holder 200. It is understood that this locking structure is a preferred but not mandatory implementation. If the medicine bag holder 200, the medicine bag 300, and the receiving cavity can be reliably fixed through an interference fit or a pre-set snap-fit ​​structure, then the operation of "pressing the medicine bag holder 200 into the receiving cavity" itself can complete the installation and fixation, without relying on the additional locking structure and corresponding secondary fixing operation described in this embodiment. Whether the fixation is achieved through an interference fit between the medicine bag holder 200, the medicine bag 300, and the receiving cavity, or through a knob mechanism as described in this embodiment, it ensures that the user can easily install and remove the medicine bag holder 200, making the operation simple. This fully reflects the technical effect required by the feature in the claims that "the medicine bag holder can be detachably installed in the receiving cavity," namely, the convenience of installation and removal.

[0141] It is understood that the specific structural form for achieving "detachable installation" is not limited to the examples described above. Any mechanical connection method that can reliably fix the medicine pack holder 200 within the receiving cavity and allow for non-destructive removal, as conceivable to those skilled in the art, such as snaps, threads, magnetic adsorption, etc., falls within the technical solutions covered by this utility model. Therefore, the scope of protection of this utility model is not limited to the embodiments specifically shown in this example.

[0142] The phrase "installed within" as defined in the claim that "the medicine holder can be detachably installed within the receiving cavity" describes the spatial position of the medicine holder 200 after installation, meaning its main structure is located inside the receiving cavity, rather than specifying that its exact fixing point or connecting structure must be located within the cavity. For example, the fixing point may be located on the end cover 700 at the port of the receiving cavity, but the main body of the medicine holder 200 extends into and is located inside the receiving cavity after installation, which also meets the characteristic of "installed within the receiving cavity." Those skilled in the art will understand that the core of this feature is to clarify the final spatial inclusion relationship between the medicine holder 200 and the receiving cavity, rather than making an exclusive limitation on the type or position of its connecting structure.

[0143] Example 11

[0144] This utility model also provides a heat management scheme for the cover body. The cover body 100 is fixed to the outer cover 800. A plurality of far-infrared electric heating tubes 900 are arranged on the outer periphery of the cover body 100. The far-infrared electric heating tubes 900 are fixed to the reflector 1100 by pipe clamps 1000. The reflector 1100 is fixed to the outer cover 800.

[0145] Specifically, the far-infrared heating tube 900 generates far-infrared radiation after being energized, which is used to heat the cover 100. Since the far-infrared heating tubes 900 are relatively evenly distributed on the outside of the cover 100, the entire cover 100 (except for the port area) can achieve a relatively uniform and significant temperature rise. By controlling the energized time ratio (i.e., duty cycle) of the far-infrared heating tubes 900, the heating power can be flexibly adjusted, thereby indirectly controlling the overall operating temperature of the cover 100. Furthermore, a temperature switch (not shown in the figure) is attached to the cover 100. This temperature switch is connected in series in the power supply circuit and can automatically cut off the circuit when the temperature exceeds a safe set value, achieving overheat protection.

[0146] The characteristic that "the entire enclosure 100 (except for the ports) can almost achieve a significant temperature rise" is of great value for achieving efficient drug volatilization. The technical logic is that the larger the drug coating area on the inner wall of the enclosure 100, the faster the volatilization rate of the active drug components, which is more conducive to accumulating a higher drug concentration within the containment cavity. To support this volatilization process, the area requiring effective heating also needs to be expanded simultaneously. Therefore, according to common industry practice, in actual work, the entire enclosure 100 (except for local areas such as the ports) usually needs to be maintained at a relatively high temperature level (e.g., above 60°C) to meet the thermal conditions for large-area drug volatilization. The large-area heating capability provided by this solution for the enclosure 100 provides the necessary hardware foundation for this. The demonstration of "the entire enclosure 100 (except for the ports) can almost achieve a significant temperature rise" in this embodiment is merely an exemplary illustration of achieving the core function of "effective heating over a large area." It can be understood that the scope of protection of this utility model is "providing the hardware capability that enables the enclosure to achieve a large-area temperature rise" to ensure the thermal conditions required for efficient drug volatilization. Therefore, any technical solution that can achieve this function falls within the protection scope of this utility model.

[0147] Example 12

[0148] This invention provides a treatment module with rapid dressing changes, particularly suitable for a head treatment method that supports rapid dressing changes. The method uses a heated cover 100 to create a warm environment within the cavity, and heats the medication pack 300 to promote drug volatilization and / or apply heat radiation to the user's head, thus combining heat convection therapy, drug therapy, and heat radiation therapy for a combined effect on the head. By introducing operational steps centered on a detachable medication pack holder 200 and the medication pack 300, this method primarily solves the technical problem of inconvenience and inefficiency inherent in existing head treatment devices where medication is a consumable and requires periodic replacement. Its core lies in simplifying the necessary dressing change process for each treatment into a rapid, modular, and standardized operation. Furthermore, this method also allows for flexible switching between different medication prescriptions to adapt to the treatment needs of different patient types. The following detailed application examples illustrate the head treatment method.

[0149] This head treatment method is characterized by comprising the following steps:

[0150] (S1) Providing equipment and medicine pack 300 installation steps: Provide an equipment, the equipment includes at least one treatment module that can quickly change medicine, the treatment module includes a cover 100 and a medicine pack rack 200, and at least one medicine pack 300 is placed between the cover 100 and the medicine pack rack 200;

[0151] (S2) Treatment positioning step: Adjust the relative position between the treatment module and the patient's head to a preset treatment position;

[0152] (S3) Treatment execution steps: Start the equipment to raise the temperature of the cover 100;

[0153] (S4) Treatment completion and dressing change procedure: After treatment, replace the dressing pack 300 to achieve rapid dressing change.

[0154] To better understand the above method, the following detailed explanation of each step is provided through specific application examples:

[0155] (S1) Provide installation steps for equipment and medicine pack 300.

[0156] A device is provided, comprising at least one treatment module capable of rapid medication change. The treatment module includes a cover 100 and a medication holder 200, with at least one medication pack 300 containing medication disposed between the inner wall of the cover 100 and the medication holder 200. This step specifically includes the following two optional installation methods:

[0157] (Method 1): First, flip the treatment module so that its opening faces upward; then, place the medicine pack 300 on the inner wall of the cover 100; next, press the medicine pack holder 200 into the cover 100 and fix it in a preset position (it can be understood that the fixation of the medicine pack holder 200 can be achieved in the following ways: if the medicine pack holder 200, the medicine pack 300 and the cover 100 are fixed by interference fit or snap-fit ​​structure, then the "pressing in" action itself can complete the fixation without additional operation; or, an independent fixing structure can also be used for fixation); finally, flip the treatment module with the medicine pack 300 installed back to the angle required for treatment.

[0158] (Method 2): First, the medicine pack 300 is initially fixed to the medicine pack rack 200 by using the pre-set connection structure (e.g., hook) on the medicine pack rack 200 to cooperate with the corresponding connection structure (e.g., round hole) on the medicine pack 300; then, the medicine pack rack 200 with the medicine pack 300 fixed is pressed into the cover 100 and fixed in a preset position (it can be understood that the medicine pack rack 200 is fixed in the same way as described in Method 1). At this time, the medicine pack 300 is tightly pressed between the inner wall of the cover 100 and the medicine pack rack 200.

[0159] (S2) Treatment Positioning Steps

[0160] The relative position between the treatment module with the pre-installed drug pack 300 and the patient's head is adjusted to a preset treatment position. At this time, the patient's head is in the receiving cavity, and a surrounding space with restricted free exchange between the internal air and the external atmosphere is formed around the patient's head to limit the escape of the active drug ingredient, thereby maintaining an effective concentration of the active drug ingredient environment around the head.

[0161] It is understood that the "adjustment of relative position" can be achieved, but is not limited to, adjusting the spatial coordinates of the treatment module, adjusting the position of the patient's seat, or a combination of both. Specifically, examples include, but are not limited to, the following:

[0162] The height of the treatment module can be adjusted by its own electric, hydraulic or manual lifting mechanism;

[0163] The treatment module is moved by the device's built-in horizontal movement mechanism (such as a slide or robotic arm) to adjust its horizontal position;

[0164] The horizontal position of the treatment device can be adjusted by directly moving the entire device with casters.

[0165] Adjust the height of the patient's seat using the lifting mechanism;

[0166] Adjust the patient's horizontal position by moving the patient chair with casters.

[0167] (S3) Treatment Execution Steps

[0168] The device is activated, raising the temperature of the cover 100 to a preset treatment temperature. The heated cover 100 creates a warm environment within the cavity, simultaneously heating the medicine pack 300, causing the active pharmaceutical ingredients in the pack to volatilize and release into the cavity; and / or, the cover 100 itself applies heat radiation to the user's head. The combined effects of thermal convection-induced thermotherapy, the pharmacological effects of the active pharmaceutical ingredients, and the combined effect of heat radiation therapy are applied to the patient's head.

[0169] (S4) Treatment completion and dressing change procedures

[0170] After the preset treatment time is reached, the heating is turned off. Treatment ends. When it is necessary to replace the medicine pack 300, the medicine pack holder 200 is easily removed by reversing the installation steps (S1), the medicine pack 300 is replaced, and then reinstalled. The entire medicine replacement process is clear and simple to operate, completely avoiding the tedious process of manually applying and scraping off the powder in the traditional method, significantly reducing the difficulty of operation and time cost, and making it more conducive to clinical promotion; the modular medicine pack design allows for flexible switching of treatment plans by quickly changing the medicine pack when using different prescriptions or for different patients, meeting personalized and diversified treatment needs.

[0171] According to a second aspect of the present invention, a head therapy device is provided, comprising a treatment module with quick dressing change capability as described in the first aspect.

[0172] In a typical application mode, the treatment module, as a core functional unit, is included in the head therapy device. The entire head therapy device is equipped with a corresponding mechanical adjustment mechanism (not shown in the figure) for adjusting the height and / or horizontal position and / or angle of the treatment module to suit user needs.

[0173] Furthermore, the scope of protection of this utility model also covers special application modes. In this mode, the treatment module itself constitutes a complete head therapy device product. For example, the treatment module can be directly manufactured as a cap-shaped structure, which can be used by the user after wearing it without the need for an additional support and adjustment mechanism. This integrated design also falls within the scope of the claims of this "head therapy device".

[0174] Other embodiments of the present invention will readily occur to those skilled in the art upon consideration of the specification and practice of the disclosure herein. This application is intended to cover any variations, uses, or adaptations of the present invention that follow the general principles of the present invention and include common knowledge or customary techniques in the art not disclosed herein. The specification and examples are to be considered exemplary only, and the true scope and spirit of the present invention are indicated by the following claims.

[0175] It should be understood that this invention is not limited to the precise structure described above and shown in the accompanying drawings, and various modifications and changes can be made without departing from its scope. The scope of this invention is limited only by the appended claims.

Claims

1. A treatment module with rapid dressing changes, characterized in that, include: The cover has an internal cavity for receiving the contents; A medicine packet, the medicine packet comprising a medicine packet substrate and a drug ingredient held by the medicine packet substrate; The medicine pack holder can be detachably installed within the receiving cavity; The medicine bag holder is configured to hold the medicine bag in a detachable manner.

2. The treatment module with rapid dressing change capability according to claim 1, characterized in that, The medicine pack and the medicine pack holder are provided with matching connection structures, and the medicine pack is detachably fixed to the medicine pack holder through the connection structures.

3. The treatment module with rapid dressing change capability according to claim 2, characterized in that, When the medicine pack holder is installed in the receiving cavity, the medicine pack is in contact with the inner wall of the receiving cavity.

4. The treatment module with rapid dressing change capability according to claim 1, characterized in that, The medicine pack holder is constructed as a support frame; when the medicine pack holder is installed in the receiving cavity, the medicine pack is located between the support frame and the inner wall of the receiving cavity and is fixed by compression.

5. The treatment module with rapid dressing change capability according to claim 1, characterized in that, The substrate of the medicine package is a flexible, breathable sheet material.

6. The treatment module with rapid dressing change capability according to claim 5, characterized in that, The medicine package has a sheet-like sandwich structure, comprising two layers of the medicine package substrate and the drug ingredient located between the two layers of the medicine package substrate.

7. The treatment module with rapid dressing change capability according to any one of claims 1 to 6, characterized in that, The substrate of the medicine package is non-woven fabric or gauze.

8. The treatment module with rapid dressing change capability according to any one of claims 1 to 6, characterized in that, The drug ingredient is in powder form.

9. The treatment module with rapid dressing change capability according to any one of claims 1 to 6, characterized in that, The medicine pack holder is a mesh or grid-like frame structure adapted to the shape of the receiving cavity.

10. A head therapy device, characterized in that, Includes the treatment module with rapid dressing change as described in claim 1.

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