A pulse microwave treatment device for obstetrics and gynecology

Through the design of guide support and sliding support components, the problem of treatment head angle and distance deviation is solved, ensuring the effectiveness and efficiency of obstetrics and gynecological microwave therapy, and reducing energy waste and operator fatigue.

CN120361432BActive Publication Date: 2025-08-29GENERAL HOSPITAL OF NUCLEAR IND
View PDF 2 Cites 0 Cited by

Patent Information

Application Number
CN202510868730.1
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2025-06-26
Publication Date
2025-08-29
Estimated Expiration
2045-06-26

AI Technical Summary

Technical Problem

In the existing manual treatment heads, in obstetrics and gynecology microwave treatment, the angle and distance of the treatment head are prone to deviation, resulting in an increase in the treatment time in non-lesion areas and a shortened treatment time in the target lesion areas, affecting the treatment effect and increasing energy waste.

Method used

The guide support and sliding support assembly are used to connect to the microwave therapy device main unit through the assist arm to provide sliding support to ensure that the treatment head moves back and forth along the guide support, covering the target area, avoiding misalignment and energy waste, and improving treatment efficiency.

Benefits of technology

Full coverage of the treatment area is achieved, radiation and energy waste in non-target areas are avoided, fatigue of the operator is reduced, and treatment efficiency and equipment adaptability are improved.

✦ Generated by Eureka AI based on patent content.

Smart Images

  • Figure CN120361432B_ABST
    Figure CN120361432B_ABST
Patent Text Reader

Abstract

The present invention discloses a pulse microwave treatment device for obstetrics and gynecology, specifically relating to the technical field of medical equipment, including a microwave therapy device main unit, a first detection head provided on the microwave therapy device main unit, a treatment head guide assembly provided on the first detection head, a sliding support assembly provided on the outside of the first detection head, the sliding support assembly being used to slide with a guide support member, the guide support member being an adjustable guide support member, and the adjustable guide support member including a plurality of unit support blocks. The present invention provides sliding support for the first detection head through the guide support member and the sliding support assembly, and during treatment, the first detection head is manually manipulated to move back and forth along the guide support member, thereby ensuring that the treatment area can fully cover the target area, forming effective treatment, avoiding unnecessary mismovement that causes the first detection head to radiate to other non-target areas, causing accidental damage and energy waste, thereby improving treatment efficiency.
Need to check novelty before this filing date? Find Prior Art

Description

Technical Field

[0001] The present invention relates to the technical field of medical equipment, and more particularly to a pulse microwave treatment device for obstetrics and gynecology. Background Art

[0002] Microwave therapy device is a therapeutic device that uses microwaves as a therapeutic factor. Due to its strong penetrating power, microwaves can directly penetrate the human body to a certain depth and have become one of the most effective devices for improving tissue blood circulation.

[0003] Pulsed microwave refers to a treatment method in which microwave energy is output intermittently in a pulsed mode. Therefore, the treatment time is divided into two periods: energy output and non-energy output. The advantage of this is that while keeping the average microwave output power unchanged, the patient can receive high-power microwave irradiation in a short period of time. Therefore, the main effect of pulsed microwave is to improve the blood circulation of deep-seated inflammatory tissues much better than ordinary microwaves. Clinical practice in recent years has shown that for diseases with deep lesions such as osteoarthritis, prostatitis, and gynecological inflammation, the effect of using pulsed microwaves is significantly better than continuous microwaves.

[0004] Because pulsed microwave therapy is designed to treat specific areas deep within the human body, if the microwave coverage area exceeds the actual lesion being treated, surrounding healthy tissue will absorb the microwave energy and heat up. This can easily lead to unnecessary thermal damage, such as skin burns and muscle or nerve damage. Therefore, during actual treatment, the pulsed microwave transmitter's transmission range should not be too large and should be targeted at the actual lesion area.

[0005] In obstetrics and gynecology treatment, microwave therapy technology is used for cervical diseases, pelvic inflammatory diseases, postoperative recovery and postpartum rehabilitation. Microwave therapy is especially widely used in postoperative recovery and postpartum rehabilitation. For example, after certain gynecological surgeries, such as the recovery stage after hysterectomy, microwave therapy can help reduce swelling, accelerate wound healing and prevent infection; in the postpartum rehabilitation process, microwave therapy can also help restore the function of the pelvic floor muscles, improve blood circulation, relieve perineal discomfort and promote physical recovery.

[0006] Unlike other departments where injuries such as arthritis, muscle strain or sprain are relatively small and continuous treatment can be carried out by simply fixing the treatment head of the microwave therapy device, some lesion areas in obstetrics and gynecology are relatively large, and the lesion areas are relatively different in different situations. Therefore, in actual use, the patient or other personnel such as the patient's family members are required to hold the treatment head and control its movement back and forth to ensure that the energy can be evenly and effectively distributed in the entire treatment area and the target area is evenly heated. Especially during the treatment process, if a certain part begins to feel overheated or painful, the operator can immediately adjust the position of the treatment head or pause the treatment, thereby improving the overall treatment experience.

[0007] However, the distance between the treatment head (microwave probe, built-in radiator) and the actual target area also affects the actual treatment effect, such as the energy density effect (when the treatment head is close to the skin or treatment area, the energy density increases, which means that more energy can be concentrated in a smaller area, which may enhance the local treatment effect. As the treatment head moves away from the skin or treatment area, the energy density decreases, causing the microwave energy to be dispersed over a larger area, which may weaken the effect on the specific target area), the depth penetration effect (a closer distance helps to transmit energy more concentratedly to the deep tissue, while a too long distance may cause the energy to be absorbed too much by the surface tissue before reaching the target depth, reducing the energy that can be received by the deep tissue energy) and thermal effect control effect (controlling thermal effect is an important consideration in microwave therapy. Proper adjustment of the distance between the treatment head and the skin can help accurately control the heating range and degree, avoid unnecessary overheating of surface tissue, and ensure that the target area receives sufficient thermal stimulation), etc. When operating the movement of the treatment head, the angle and distance of the treatment head will deviate greatly, resulting in increased treatment time in non-lesion areas, while the target lesion area will suffer from errors such as shortening of the actual effective treatment time due to reasons such as the skewed movement of the treatment head, thereby affecting the actual treatment effect, and necessitating a longer actual treatment time to compensate for the above errors, thereby increasing the overall treatment time and generating a certain amount of energy waste. Summary of the Invention

[0008] The present invention provides a pulse microwave treatment device for obstetrics and gynecology, and aims to solve the problem that when the existing manually operated treatment head is used for microwave treatment, the angle and distance of the treatment head will deviate greatly, resulting in an increase in the treatment time of the non-lesion area, while the target lesion area will suffer from an error such as shortening of the actual effective treatment time due to reasons such as the movement of the treatment head, thereby affecting the actual treatment effect, and a longer actual treatment time needs to be set to compensate for the above error, thereby increasing the overall treatment time and causing a certain amount of energy waste.

[0009] To achieve the above object, the present invention provides the following technical solution: a pulsed microwave therapeutic device for obstetrics and gynecology, comprising a microwave therapeutic device main unit, the microwave therapeutic device main unit is provided with a first detection head, and the first detection head is connected to the microwave therapeutic device main unit via a power-assisting arm;

[0010] The first detection head is also provided with a treatment head guide assembly, which includes a guide support and a support leg. The outside of the first detection head is provided with a sliding support assembly, which is used to slide with the guide support;

[0011] The guide support is an adjustable guide support, which includes multiple unit support blocks. Two adjacent unit support blocks are vertically slidably fitted together, and both ends of the adjustable guide support are connected to edge fixing frames, which are connected to the support legs. A unit fastener is provided between two adjacent guide supports, and the unit fastener is used to fix the two adjacent unit support blocks.

[0012] In a preferred embodiment, the boost arm consists of a mounting base, a rotating base, a first support arm, a second support arm and a mounting arm. The mounting base is fixedly mounted on the microwave therapy device main unit, the rotating base is rotatably mounted on the mounting base, and the rotating base and the mounting base have rotating axes arranged vertically. The first support arm is rotatably mounted on the rotating base, the second support arm is rotatably mounted on the first support arm, the mounting arm is rotatably mounted on the second support arm, the first detection head is rotatably mounted in the mounting arm, and a damping structure is provided in the rotating pairs of each corresponding structure.

[0013] Sliding slots and sliding blocks are respectively provided on both sides of the unit support block. When matched, the sliding block of one guide support member is slidably mounted in the sliding slot of the other guide support member, and a sliding damping structure is provided between each adjacent unit support block. The edge fixing frame is slidably installed on the support leg, and a tightening structure is provided between the edge fixing frame and the support leg.

[0014] In a preferred embodiment, the sliding support assembly includes a guide card base, a rotating sleeve is rotatably installed on the outside of the first detection head, the guide card base is fixedly installed on the rotating sleeve, a groove is provided inside the guide card base, and the groove is used to slide and adapt with the guide support member, and an opening is provided at the bottom of the guide card base, and the opening is used to allow the guide support member to enter the groove in the guide card base, two sets of guide wheels are rotatably installed in the guide card base, and a rubber buffer sleeve is provided on the outside of the guide wheel.

[0015] In a preferred embodiment, a deformable relief strip is provided above the adjustable guide support, and the guide wheel rolls with the deformable relief strip. The deformable relief strip is an elastic flat belt structure, and the two ends of the deformable relief strip extend to two edge fixing frames respectively and slide with the edge fixing frames. A cylindrical pad is provided on the top of the unit support block, and a cylindrical groove is provided on the top of the unit support block. The cylindrical pad is rotatably installed in the cylindrical groove, and the top of the cylindrical pad is provided as a planar support portion. The planar support portion slides with the bottom wall of the deformable relief strip, and the cylindrical pad is a flexible structure.

[0016] In a preferred embodiment, a deformable support bone is provided through each unit support block, and the two ends of the deformable support bone respectively pass through two edge fixing frames and slide with the edge fixing frames, and the edge fixing frames are provided with an external pulling mechanism for fixing and pulling the deformable support bone.

[0017] In a preferred embodiment, the unit fastener is an expansion clip, which includes a locking plate and a locking control airbag. The locking plate is slidably installed in one side wall of the unit support block, and the surface of the locking plate and the surface of the unit support block away from the locking plate are provided with mutually compatible convex tooth structures, and the interior of the unit support block is provided with an active cavity, the locking control airbag is installed in the active cavity, and the locking control airbag is in contact with the side of the locking plate located inside the unit support block. The expansion clip also includes an inflation and deflation control tube, and a branch tube is provided on the inflation and deflation control tube at a position corresponding to each locking control airbag. The branch tube is used to connect the locking control airbag with the inflation and deflation control tube. The inflation and deflation control tube is also connected to an inflation and deflation control component, and the inflation and deflation control component is used to inflate or deflate the locking control airbag.

[0018] In a preferred embodiment, a pre-positioning strut is provided on the outer side of the unit support block, and the top end of the pre-positioning strut is fixedly connected to an insert structure, which extends into the unit support block and slides with the unit support block. An elastic member is provided between the top of the insert structure and the unit support block, and the bottom of the insert structure is provided in contact with the locking control airbag, and a cushion structure is provided at the bottom end of the pre-positioning strut.

[0019] In a preferred embodiment, protective plates are provided on both sides of the first detection head, and the protective plates are tilted downward at one end corresponding to the bottom of the first detection head. A guide plate is also fixedly connected below the protective plate, and the guide plate is tilted upward at one end close to the bottom of the first detection head, and the guide plate is located in the area of ​​the bottom end of the protective plate away from the first detection head, and the guide plate and the protective plate form a trumpet mouth opening outward.

[0020] In a preferred embodiment, a second detection head is also provided on the microwave therapy device host, and the second detection head is connected to the microwave therapy device host only through corresponding wires. The microwave therapy device host is equipped with a hook structure for placing the second detection head. A walking chassis is provided at the bottom of the microwave therapy device host. The walking chassis is a cabinet structure, and walking wheels are provided at the bottom of the walking chassis.

[0021] The beneficial effects of the present invention are: the present invention provides sliding support for the first detection head through the guide support and the sliding support assembly. During the treatment process, the first detection head is manually controlled to move back and forth along the guide support, thereby ensuring that the treatment area can fully cover the target area, forming effective treatment, avoiding unnecessary mismovement and causing accidental injury and energy waste caused by the first detection head radiating to other non-target areas, thereby improving treatment efficiency. During operation, the operator does not need to apply additional adjustment force in other directions, thereby reducing the operator's fatigue and making the equipment easier to use. During actual use, the positional relationship between each unit support block can be pre-adjusted according to the patient's body shape and the body shape of the required treatment position, thereby improving the adaptability of the equipment, eliminating the need to use multiple types of guide supports, and reducing production costs. BRIEF DESCRIPTION OF THE DRAWINGS

[0022] Figure 1 It is a schematic diagram of the overall structure of the present invention.

[0023] Figure 2 This is a schematic diagram from another perspective of the present invention.

[0024] Figure 3 It is a schematic diagram of the overall structure of the power-assisting arm of the present invention.

[0025] Figure 4 This is a schematic diagram of the process of controlling the movement of the first treatment head during the treatment process of the present invention.

[0026] Figure 5 This is a schematic diagram of the treatment head guide assembly of the present invention when it is installed above the human body.

[0027] Figure 6 It is a structural schematic diagram of the adjustable guide support member of the present invention.

[0028] Figure 7 Schematic diagram of the cooperation between the guide holder on the outside of the treatment head of the present invention and the adjustable guide support.

[0029] Figure 8 It is a partial cross-sectional view of the interconnected state between the unit support blocks of the present invention.

[0030] Figure 9 It is a top view of the connection position between each unit support block of the present invention.

[0031] Figure 10 This is a schematic structural diagram of the present invention when a set screw is used as a unit fastener.

[0032] Figure 11 This is a partial cross-sectional view of the expansion clip of the present invention when used as a unit fastener.

[0033] Figure 12 This is a structural schematic diagram of the present invention using a hand-held inflatable ball as an inflation and deflation control component.

[0034] Figure 13 This is a schematic structural diagram of the adjustable guide support member after adding a pre-positioning strut in the present invention.

[0035] Figure 14 This is a state diagram of the present invention when the locking and controlling airbag expands to lift the interpolated structure.

[0036] Figure 15 This is a schematic structural diagram of the present invention when an anti-touch structure is added to the outside of the first treatment head.

[0037] The accompanying drawings are marked as follows: 1. Microwave therapy device host; 11. First detection head; 12. Second detection head; 13. Walking chassis; 2. Power-assisting arm; 21. Mounting seat; 22. Rotating seat; 23. First support arm; 24. Second support arm; 25. Mounting arm; 26. Telescopic lever; 3. Treatment head guide assembly; 31. Guide support member; 311. Unit support block; 3111. Sliding card slot; 3112. Sliding card block; 3113. Active cavity; 312. Edge fixing frame; 313. Column Pad; 3131, plane support part; 32, support leg; 33, deformable relief strip; 34, deformable support bone; 35, external pulling mechanism; 36, pre-positioning support rod; 361, internal insertion structure; 4, sliding support assembly; 41, guide seat; 42, guide wheel; 5, set screw; 6, expansion clamp; 61, locking plate; 62, locking control airbag; 63, inflation and deflation control tube; 64, branch pipe; 65, inflation and deflation control assembly; 7, protective plate; 71, drainage plate; 72, installation bracket. DETAILED DESCRIPTION

[0038] The present application is described in further detail below in conjunction with the accompanying drawings. It is necessary to point out that the following specific implementation methods are only used to further illustrate the present application and cannot be understood as limiting the scope of protection of the present application. Technicians in this field can make some non-essential improvements and adjustments to the present application based on the above application content.

[0039] Refer to the instruction manual Figures 1 to 15, a pulse microwave therapy device for obstetrics and gynecology, including a microwave therapy device host 1, a first detection head 11 and a second detection head 12 are provided on the microwave therapy device host 1, and a walking case 13 is provided at the bottom of the microwave therapy device host 1, and the walking case 13 is a cabinet structure for storing medical devices related to microwave therapy, and the walking case 13 is provided with walking wheels and corresponding push handles to facilitate the movement of the device and convenient use. The first detection head 11 is connected to the microwave therapy device host 1 through a power-assisting arm 2, and the second detection head 12 is only connected to the microwave therapy device host 1 through corresponding wires. At the same time, the microwave therapy device host 1 is equipped with a hook structure for placing the second detection head 12, and the power-assisting arm 2 is used to assist in supporting the movement of the first detection head 11, and the power-assisting arm 2 is composed of a mounting seat 21, a rotating seat 22, a first supporting arm 23, a second supporting arm 24 and a mounting arm 25. The mounting seat 21 is fixedly mounted on the microwave therapy device host 1, and the rotating seat 22 rotates The first detection head 11 is rotatably mounted on the mounting base 21, and the rotating base 22 is vertically arranged with respect to the rotating axis of the mounting base 21. The first support arm 23 is rotatably mounted on the rotating base 22, the second support arm 24 is rotatably mounted on the first support arm 23, and the mounting arm 25 is rotatably mounted on the second support arm 24. The first detection head 11 is rotatably mounted in the mounting arm 25, and a damping structure (such as a damping device such as a rubber pad) and a corresponding fastening structure (such as a fastening bolt) are provided in the rotating pair of each structure. The damping structure provides resistance for the rotation of the two relative groups of structures, and then after manually adjusting the position of the first detection head 11, it can be positioned with the help of the damping between the structures of the power-assisting arm 2, and the fastening structure can directly lock the rotation between the structures when necessary, so that the first detection head 11 is in a fixed posture for fixed treatment, and the second detection head 12 is a movable treatment head, which is suitable for handheld use, thereby providing users with more choices and improving the functionality and practicality of the device.

[0040] In addition, in view of the use in obstetrics and gynecology departments, the device is also equipped with a treatment head guide assembly 3 for the first detection head 11, that is, the first detection head 11 is also provided with a treatment head guide assembly 3, the treatment head guide assembly 3 includes a guide support 31, both ends of the guide support 31 are connected with legs 32, and the outside of the first detection head 11 is provided with a sliding support assembly 4, which is used to slide with the guide support 31 to provide sliding support for the first detection head 11. Specifically, in actual use, the patient lies on the bed, and the medical staff or the patient's accompanying person moves the first detection head 11 above the patient's body, and makes the legs 32 contact with the bed to form support, and determines the reciprocating movement required by the first detection head 11 according to the patient's lesion area and position. After moving the direction, adjust the placement position of the treatment head guide assembly 3, and then turn on the equipment for microwave treatment. During the treatment process, the medical staff or accompanying personnel manually control the first detection head 11 to move it back and forth along the guide support 31, thereby ensuring that the treatment area can fully cover the target area, forming effective treatment, and avoiding unnecessary mismovement that causes the first detection head 11 to radiate to other non-target areas and cause accidental injuries and energy waste, thereby improving treatment efficiency. At the same time, using pulse maintenance treatment in conjunction with the equipment can avoid damage caused by excessive treatment of fixed areas or excessive power to a greater extent. If the patient feels uncomfortable during the treatment, the first detection head 11 can be pushed away in time, away from the patient, to provide maximum safety protection for the patient.

[0041] It should be noted that the above-mentioned power-assisting arm 2 is a commonly used support rod structure on the market. Under the action of the damping structure and other balancing structures, it can hover, that is, when there is no external force pushing the first detection head 11, the first detection head 11 can hover motionless to perform fixed area treatment. Therefore, when actually manipulating the first detection head 11 to move, although the power-assisting arm 2 can produce adaptive changes, it can still provide part of the supporting force for the first detection head 11. However, in the case of long-term use, the operator needs to keep the first detection head 11 moving as much as possible according to the corresponding height. Therefore, during the operation process, if there is no treatment head guide assembly 3, the operator still needs to adjust the force of the first detection head 11 up and down at all times, and the operator's arm is also in a suspended state, lacking support, which makes the operator easily fatigued. With the auxiliary support of the treatment head guide assembly 3, during actual operation, it is only necessary to slightly press the first detection head 11 to make it move along the guide The support member 31 only needs to be moved, and the operator does not need to apply additional adjustment force in other directions. The treatment head guide assembly 3 can provide support for the first detection head 11 while also providing a certain support force to the operator, thereby reducing the operator's fatigue and making the equipment easier to use. At the same time, if the patient has no accompanying personnel during actual use, based on the above scheme, a telescopic lever 26 can be added to the first detection head 11, that is, the end of the telescopic lever 26 corresponding to the first detection head 11 is connected to the first detection head 11 through a ball joint structure, and the end of the telescopic lever 26 facing away from the first detection head 11 is set as a handle structure, and the telescopic lever 26 itself is a telescopic tube structure, and its length can be adjusted. Therefore, in actual use, based on the above-mentioned medical staff having prepared the equipment in place, the patient can hold the telescopic lever 26 by himself during the remaining treatment period to move the first detection head 11 on the guide support member 31.

[0042] In the above embodiment, the sliding support assembly 4 is mainly composed of a guide holder 41, and a rotating sleeve is installed on the outside of the first detection head 11, and the guide holder 41 is fixedly installed on the rotating sleeve, that is, the guide holder 41 can generate rotational motion relative to the outer circumference of the microwave therapy device host 1. A groove is provided inside the guide holder 41, and the groove is used to slide and adapt with the guide support 31. An opening is provided at the bottom of the guide holder 41, and the opening is used to allow the guide support 31 to enter the groove inside the guide holder 41. That is to say, the actual guide support 31 can be disassembled and separated from the sliding support assembly 4. Therefore, the treatment head guide assembly 3 can be selectively installed and used according to needs.

[0043] In the above embodiment, the guide support member 31 can directly adopt a hard structure integrated with the support leg 32, for example, it can be formed by bending a metal rod, wherein, in order to adapt to the curve shape of the human body, the guide support member 31 should be bent to form a certain curvature. Due to the different body shapes of different patients (fat or thin), the shapes of the corresponding guide supports 31 are also slightly different. Therefore, multiple specifications of guide supports 31 can be set, and they can be detachably matched with the guide holder 41. In actual use, different models of guide supports 31 can be used for different patients.

[0044] However, in the above embodiment, if the number of guide support members 31 is large, although it is relatively convenient to use, it requires a higher cost, and the department also needs to be equipped with a corresponding storage area, which takes up more space. For this reason, this embodiment also provides an adjustable guide support member as the guide support member 31. For details, refer to the attached manual. Figures 6 to 11 The adjustable guide support member includes a plurality of unit support blocks 311, and two adjacent unit support blocks 311 are vertically slidably matched through a sliding structure (for example, sliding slots 3111 and sliding blocks 3112 are respectively provided on both sides of the unit support block 311. When matched, the sliding block 3112 of one guide support member 31 is slidably mounted in the sliding slot 3111 of another guide support member 31, thereby forming a sliding connection). Both ends of the adjustable guide support member formed by the plurality of unit support blocks 311 are connected to edge fixing frames 312 (that is, in a group of unit support blocks 311, the two unit support blocks 311 located at the two end positions are respectively connected to an edge fixing frame 312), the edge fixing frame 312 is connected to the support leg 32, and a unit fastener is provided between two adjacent guide support members 31. The unit fastener is used to fix the two adjacent unit support blocks 311.

[0045] In actual use, the positional relationship between the unit support blocks 311 can be pre-adjusted according to the patient's body shape and the body shape of the desired treatment position, for example, Figure 6 By controlling the sliding between two adjacent unit support blocks 311, the bending of a group of adjustable guide supports can be adjusted to adapt to the patient, wherein sliding damping is provided between each adjacent unit support block 311 to ensure that a temporary positioning can be formed after the position of the unit support block 311 is manually adjusted, and it will not collapse, so as to facilitate the adjustment operation. After the adjustment is completed, all the unit support blocks 311 are fixed by unit fasteners to form a whole with sufficient strength, thereby forming a stable structure that can support the first detection head 11.

[0046] Among them, refer to the instructions attached Figure 10The unit fasteners in this embodiment can directly adopt the set screws 5, that is, by tightening the set screws 5 to squeeze the other unit support block 311, a vertical friction resistance can be formed, thereby fixing the unit support block 311. It should be noted that, based on the fact that the unit support blocks 311 can slide relative to each other to adjust the overall shape of the guide support member 31, there will be a difference in the top height of each unit support block 311, thereby forming an uneven top wall. At this time, in order to reduce the shaking generated when moving the first detection head 11, the original direct sliding friction of the guide card seat 41 can be changed to rolling friction, that is, two sets of guide wheels 42 are rotatably installed in the guide card seat 41, and a rubber buffer sleeve is provided on the outside of the guide wheel 42. In actual design, the shape of the guide wheel 42 can be set to be relatively large, so that the height difference of the unit support block 311 appears smaller under the large circumferential curvature of the guide wheel 42, thereby reducing the vibration generated during movement. However, this solution will greatly increase the diameter of the guide wheel 42. Therefore, this embodiment also provides the following The technical solution is that a deformable relief strip 33 is provided above the adjustable guide support formed by the unit support block 311, and the guide wheel 42 rolls with the deformable relief strip 33. The deformable relief strip 33 is an elastic flat belt structure (such as a flat steel belt or a flat plastic belt). The two ends of the deformable relief strip 33 extend to the two edge fixing frames 312 respectively and slide with the edge fixing frames 312. After adjustment based on each guide support member 31, the deformable relief strip 33 is directly supported, and then the guide wheel 42 is indirectly supported by the deformable relief strip 33. After adjusting each unit support block 311, the deformable relief strip 33 is directly attached to the top of the unit support block 311 to form a shape adaptation with all the unit support blocks 311. At the same time, the deformable relief strip 33 compensates for the stepped structure caused by the height difference between the two adjacent guide supports 31, thereby making the movement trajectory of the guide wheel 42 smoother. When the first detection head 11 is actually operated to move, no large shaking will occur, making the equipment more stable to use.

[0047] Further, refer to the instructions for Figure 8 The top of the unit support block 311 is provided with a cylindrical pad 313, and the top of the unit support block 311 is provided with a cylindrical groove. The cylindrical pad 313 is rotatably installed in the cylindrical groove. The top of the cylindrical pad 313 is provided with a planar support portion 3131, and the planar support portion 3131 slides with the bottom wall of the deformable relief strip 33, and the cylindrical pad 313 is preferably a rubber structure. Therefore, in actual use, when each unit support block 311 adjusts its posture, the cylindrical pad 313 can provide support for the deformable relief strip 33, and the deformable relief strip 33 has a curvature change. Therefore, the cylindrical pads 313 at different positions can produce corresponding rotations, thereby being able to provide more and more stable support for the deformable relief strip 33.

[0048] In addition, in order to improve the self-positioning ability of the unit support block 311 during initial adjustment, the present embodiment also provides the following scheme. Specifically, a deformable support bone 34 is provided through each unit support block 311. The two ends of the deformable support bone 34 respectively pass through two edge fixing frames 312 and slide with the edge fixing frames 312. The edge fixing frames 312 are provided with an external pulling mechanism 35 for fixing and pulling the deformable support bone 34 (for example, a threaded sleeve, the threaded sleeve is threadedly engaged with the deformable support bone 34, and traction can be formed by controlling the relative rotation of the two). The deformable support bone 34 is a deformable plastic structure (refer to structures such as iron bars or copper bars. After bending the iron bar, the iron bar can maintain the shape), serving as the keel structure of all unit support blocks 311. After manually adjusting each unit support block 311, the deformable support bone 34 also deforms accordingly and provides temporary support for the unit support block 311.

[0049] Based on the above embodiment, since at least two groups of legs 32 are provided, and are positioned on either side of the patient's body during actual use, to enhance the support effect of the legs 32, the two groups of legs 32 can be connected by a set of crossbars to provide greater stability. The edge fixing frame 312 can be slidably mounted on the legs 32, and a fastening structure, such as the aforementioned set screw 5, is provided between the edge fixing frame 312 and the legs 32, thereby making the edge fixing frame 312 height adjustable. Based on the above solution, if there is no direct scar on the patient's treatment area or if contact with the patient's body is permitted, the legs 32 can be first placed outside the patient, and then all the unit support blocks 311 can be simultaneously lowered so that the unit support blocks 311 contact the patient's body (clothing can be used to block the unit support blocks 311, but the clothing should not be too thick). The unit support blocks 311 can then be adjusted according to the patient's actual body shape. After adjustment, the edge fixing frame 312 can be controlled to move upward and secure, thereby moving the unit support blocks 311 away from the patient's body. This allows for more convenient adjustment of the guide support member 31 to suit different patients.

[0050] It should be noted that the guide support member 31 formed by the unit support block 311 in the above scheme is used to guide the sliding of the first detection head 11. Therefore, the unit support block 311 does not need to be too far away from the patient, and the corresponding spacing in the drawings of this application specification is relatively large for ease of understanding. In actual design and use, the unit support block 311 can maintain a relatively small distance from the patient, and it is only necessary to ensure that it does not contact the patient. Therefore, after the initial contact with the patient's body for shaping (avoiding contact with the patient's injured part, for example, setting two groups of guide support members 31, and the two groups of guide support members 31 are set on both sides of the injured part), the guide support member 31 is slightly raised to basically maintain a support trajectory that is adapted to the patient's body, thereby further improving the accuracy of the movement of the first detection head 11, and keeping the distance between the first detection head 11 and the patient as stable as possible, further improving the treatment effect.

[0051] In the above embodiment, if the number of unit support blocks 311 is large, the number of corresponding set screws 5 is also relatively large, and the actual fixing operation is relatively cumbersome. Therefore, this embodiment also provides the following technical solutions. For details, refer to the attached manual. Figure 11 The unit fastener is an expansion card member 6, which includes a locking plate 61 and a locking control airbag 62. The locking plate 61 is slidably installed in one side wall of the unit support block 311, and the surface of the locking plate 61 and the surface of the unit support block 311 facing away from the locking plate 61 are provided with small convex tooth structures that adapt to each other, and the interior of the unit support block 311 is provided with an active cavity 3113, the locking control airbag 62 is installed in the active cavity 3113, and the locking control airbag 62 and the side of the locking plate 61 located inside the unit support block 311 are in contact with each other, the expansion card member 6 also includes an inflation and deflation control tube 63, and the inflation and deflation control tube 63 is provided with a branch tube 64 at the position corresponding to each locking control airbag 62. The branch tube 64 is used to connect the locking control airbag 62 with the inflation and deflation control tube 63, and the inflation and deflation control tube 63 is also connected to an inflation and deflation control component 65, which is used to inflate or deflate the locking control airbag 62.

[0052] Specifically, in actual use, before adjusting each guide support member 31, the locking control airbag 62 does not expand, and the locking plate 61 does not contact the corresponding other unit support block 311. After the adjustment is completed, all the locking control airbags 62 are inflated at the same time by the inflation and deflation control component 65 to expand, so that all the locking plates 61 can be pushed out synchronously, and the small protruding teeth on the locking plate 61 are engaged with the small protruding teeth on the corresponding other unit support block 311, so that all the unit support blocks 311 can be fixed. Among them, the inflation and deflation control component 65 can be used as follows Figure 12The hand-held inflatable ball shown is similar to the inflation device of a blood pressure monitor and can be operated by the patient himself. Although this solution has relatively more structures, each structure can be reused, and the operation is simple and easy to use.

[0053] In addition, this embodiment also provides another adjustment method for the guide support member 31. For details, refer to the attached manual. Figure 13 and Figure 14 The outer side of the unit support block 311 is provided with a pre-positioning strut 36, and the top of the pre-positioning strut 36 is fixedly connected with an insert structure 361, which extends into the unit support block 311 and slides with the unit support block 311. An elastic member, such as a spring, is provided between the top of the insert structure 361 and the unit support block 311. The bottom of the insert structure 361 is in contact with the locking control airbag 62, and the bottom end of the pre-positioning strut 36 is provided with a cushion structure. Specifically, in actual use, the edge fixing frame 312 is first lowered, so that the bottom end of each pre-positioning strut 36 is in contact with the patient's body, thereby supporting the unit support block 311 for posture adjustment. After adjustment, the edge fixing frame 312 is fixed, and then the locking control airbag is moved to the bottom end. The airbag 62 is inflated. At this time, since there is an elastic part above the inserted structure 361, the locking control airbag 62 preferentially expands toward the locking plate 61, and then squeezes the locking plate 61. After the unit support block 311 is fixed, the locking control airbag 62 continues to expand to push up the inserted structure 361. At this time, since the unit support block 311 is relatively fixed, the inserted structure 361 can lift the pre-positioning strut 36 upward and away from the patient. Compared with the previous solution of directly making all the unit support blocks 311 contact the patient and manually lifting them as a whole, this solution can automatically lift the pre-positioning strut 36, and the operation process only requires manually holding the inflation and deflation control component 65 to operate, which will not cause the support leg 32 to be offset.

[0054] In the above embodiment, since the first detection head 11 itself absorbs a certain amount of microwaves, especially when used continuously for a long time and with a high power, the probe itself may also accumulate heat. Therefore, in order to avoid the discomfort caused by the first detection head 11 directly contacting the patient's body due to accidental use, this embodiment also provides the following solution. For details, please refer to the attached manual. Figure 15 A protective plate 7 is provided on both sides of the first detection head 11. The bottom end of the protective plate 7 extends to the area below the bottom end surface of the first detection head 11 without blocking the first detection head 11. The protective plate 7 is detachably connected to the first detection head 11 through the mounting bracket 72, thereby further providing safety assurance.

[0055] In addition, the protective plate 7 is arranged to be tilted downward at one end corresponding to the bottom of the first detection head 11, and a guide plate 71 is fixedly connected to the bottom of the protective plate 7. The end of the guide plate 71 close to the bottom of the first detection head 11 is arranged to be tilted upward, and the guide plate 71 is located in the area of ​​the bottom end of the protective plate 7 away from the first detection head 11, and the guide plate 71 and the protective plate 7 form a trumpet opening outward, wherein the above-mentioned protective plate 7 and guide plate 71 can be made of thin-walled plastic plate or metal plate structure, which can save materials and avoid excessive weight. Specifically, when actually operating the first detection head 11 to move, refer to the attached manual. Figure 15 When the first detection head 11 moves to the left, the air on the surface of the first detection head 11 is guided by the protective plate 7 and discharged upward. At the same time, the trumpet mouth formed by the left protective plate 7 and the guide plate 71 accelerates the low-temperature air outside to the area below the first detection head 11, forming an effective air exchange. This reciprocating process can avoid the discomfort caused by the air temperature in the bottom area of ​​the first detection head 11 being too high.

[0056] It should be noted that the above equipment is only used in obstetrics and gynecology as an example, but is not limited to other usage scenarios that require the reciprocating movement of the first detection head 11, and the use of the unit support block 311 to form an adjustable guide support is also one of the examples of the present invention. In the specific design, other adjustable guide support schemes can also be adopted. In addition, although the robotic arm can be introduced into the microwave therapy device to automatically operate the movement of the first detection head 11 according to actual needs, the cost is too high. Moreover, different moving routes need to be set for different patients according to their body shape, which also involves the use of corresponding scanning equipment. In actual use, there is too much preliminary preparation work, which does not save treatment time, but is relatively inconvenient to use.

[0057] The above-described embodiments merely illustrate several implementations of the present invention. While the descriptions are relatively specific and detailed, they should not be construed as limiting the scope of the present invention. It should be noted that a person skilled in the art would be able to make numerous variations and improvements without departing from the spirit of the present invention, and all such variations and improvements fall within the scope of protection of the present invention.

Claims

1. A pulsed microwave treatment device for obstetrics and gynecology, characterized by: The microwave therapeutic apparatus comprises a main unit (1), wherein the main unit (1) is provided with a first detection head (11), and the first detection head (11) is connected to the main unit (1) of the microwave therapeutic apparatus via a power-assisting arm (2); The first detection head (11) is further provided with a treatment head guide assembly (3), the treatment head guide assembly (3) comprising a guide support member (31) and a support leg (32), and the first detection head (11) is provided with a sliding support assembly (4) on the outside, the sliding support assembly (4) being used for slidingly cooperating with the guide support member (31); The guide support member (31) is an adjustable guide support member, comprising a plurality of unit support blocks (311), wherein two adjacent unit support blocks (311) are vertically slidably engaged with each other, and both ends of the adjustable guide support member are connected to edge fixing frames (312), wherein the edge fixing frames (312) are connected to the legs (32), and a unit fastener is provided between two adjacent guide support members (31), wherein the unit fastener is used to fix the two adjacent unit support blocks (311); The booster arm (2) is composed of a mounting base (21), a rotating base (22), a first support arm (23), a second support arm (24) and a mounting arm (25); the mounting base (21) is fixedly mounted on the microwave therapeutic apparatus host (1); the rotating base (22) is rotatably mounted on the mounting base (21); and the rotating axes of the rotating base (22) and the mounting base (21) are vertically arranged; the first support arm (23) is rotatably mounted on the rotating base (22); the second support arm (24) is rotatably mounted on the first support arm (23); the mounting arm (25) is rotatably mounted on the second support arm (24); the first detection head (11) is rotatably mounted in the mounting arm (25); and a damping structure is provided in the rotating pairs of each corresponding structure; A sliding slot (3111) and a sliding block (3112) are respectively provided on both sides of the unit support block (311); when engaged, the sliding block (3112) of one guide support member (31) is slidably mounted in the sliding slot (3111) of the other guide support member (31), and a sliding damping structure is provided between each adjacent unit support block (311); the edge fixing frame (312) is slidably mounted on the support leg (32), and a fastening structure is provided between the edge fixing frame (312) and the support leg (32); The sliding support assembly (4) includes a guide card seat (41), a rotating sleeve is rotatably mounted on the outside of the first detection head (11), the guide card seat (41) is fixedly mounted on the rotating sleeve, a groove is provided inside the guide card seat (41), the groove is used to slide and adapt with the guide support member (31), an opening is provided at the bottom of the guide card seat (41), the opening is used to allow the guide support member (31) to enter the groove in the guide card seat (41), two sets of guide wheels (42) are rotatably mounted in the guide card seat (41), and a rubber buffer sleeve is provided on the outside of the guide wheel (42); A deformable relief strip (33) is provided above the adjustable guide support, the guide wheel (42) and the deformable relief strip (33) are in rolling engagement, the deformable relief strip (33) is a flat belt structure with elasticity, the two ends of the deformable relief strip (33) respectively extend to two edge fixing frames (312) and are in sliding engagement with the edge fixing frames (312), a columnar pad (313) is provided on the top of the unit support block (311), a columnar groove is provided on the top of the unit support block (311), the columnar pad (313) is rotatably mounted in the columnar groove, the top of the columnar pad (313) is provided as a plane support portion (3131), the plane support portion (3131) is in sliding engagement with the bottom wall of the deformable relief strip (33), and the columnar pad (313) is a flexible structure; A deformable support bone (34) is provided through each of the unit support blocks (311), and both ends of the deformable support bone (34) respectively pass through two edge fixing frames (312) and are slidably engaged with the edge fixing frames (312), and an external pulling mechanism (35) for fixing and pulling the deformable support bone (34) is provided on the edge fixing frames (312).

2. The pulse microwave treatment device for obstetrics and gynecology according to claim 1, characterized in that: The unit fastener is an expansion clamp (6), and the expansion clamp (6) includes a locking plate (61) and a locking control airbag (62). The locking plate (61) is slidably installed in one side wall of the unit support block (311), and the surface of the locking plate (61) and the surface of the unit support block (311) away from the locking plate (61) are both provided with mutually adapted convex tooth structures, and the interior of the unit support block (311) is provided with an active cavity (3113), the locking control airbag (62) is installed in the active cavity (3113), and the locking control airbag (62) is installed in the active cavity (3113). The bag (62) and the locking plate (61) are in contact with each other on one side inside the unit support block (311). The expansion clamp (6) further includes an inflation and deflation control tube (63). A branch tube (64) is provided on the inflation and deflation control tube (63) at a position corresponding to each locking control air bag (62). The branch tube (64) is used to connect the locking control air bag (62) with the inflation and deflation control tube (63). The inflation and deflation control tube (63) is also connected to an inflation and deflation control component (65). The inflation and deflation control component (65) is used to inflate or deflate the locking control air bag (62).

3. The pulse microwave treatment device for obstetrics and gynecology according to claim 2, characterized in that: A pre-positioning support rod (36) is provided on the outer side of the unit support block (311), and the top end of the pre-positioning support rod (36) is fixedly connected to an insert structure (361), and the insert structure (361) extends into the unit support block (311) and is slidably matched with the unit support block (311), and an elastic member is provided between the top of the insert structure (361) and the unit support block (311), and the bottom of the insert structure (361) is provided in contact with the locking control airbag (62), and a cushion structure is provided at the bottom end of the pre-positioning support rod (36).

4. The pulse microwave treatment device for obstetrics and gynecology according to claim 3, characterized in that: A protective plate (7) is provided on both sides of the first detection head (11), and one end of the protective plate (7) corresponding to the bottom of the first detection head (11) is tilted downward. A guide plate (71) is fixedly connected below the protective plate (7), and one end of the guide plate (71) close to the bottom of the first detection head (11) is tilted upward. The guide plate (71) is located in an area of ​​the bottom end of the protective plate (7) away from the first detection head (11), and the guide plate (71) and the protective plate (7) form a bell mouth opening outward.

5. The pulse microwave treatment device for obstetrics and gynecology according to claim 4, characterized in that: The microwave therapeutic apparatus main unit (1) is further provided with a second detection head (12), which is connected to the microwave therapeutic apparatus main unit (1) only through corresponding wires. The microwave therapeutic apparatus main unit (1) is equipped with a hook structure for placing the second detection head (12). A walking case (13) is provided at the bottom of the microwave therapeutic apparatus main unit (1), and the walking case (13) is a cabinet structure. Walking wheels are provided at the bottom of the walking case (13).

Citation Information

Patent Citations

  • Digital solar microwave therapeutic apparatus

    CN118949281A

  • Microwave physiotherapy equipment

    CN219423583U