Device and method for monitoring orthopedic implants and rehabilitation
By combining a device with components such as a fixed base plate, a telescopic sealing plate, and a fluid storage bladder, the position of the orthopedic implant is monitored in real time, solving the problem of secondary injury caused by implant deviation during patient rehabilitation training, and achieving effective management of patient bones and non-Newtonian fluids.
Patent Information
- Application Number
- CN202510873340.3
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-06-27
- Publication Date
- 2025-09-12
AI Technical Summary
When a patient undergoes rehabilitation training, if the implant of an existing monitoring orthopedic implant device deviates out of a controllable range, it may easily cause the patient's bones to come into contact with the implant surface, resulting in secondary damage.
A device including a fixed base plate, a telescopic sealing plate, a sealing cover plate, a telescopic infusion tube, a fluid storage bladder and other components is used. Through the cooperation of a pressure sensor and a non-Newtonian fluid, the position of the orthopedic implant is monitored in real time, and the patient's bones are protected to avoid direct contact when the implant is offset.
It protects the patient's bones when the orthopedic implant is offset, avoids secondary damage, and prolongs the storage time of the non-Newtonian fluid, ensuring real-time monitoring and timely adjustment of the orthopedic implant within a controllable range.
Smart Images
Figure CN120616449A_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of monitoring orthopedic implants, and in particular to a device and method for monitoring orthopedic implants and rehabilitation. Background Art
[0002] Joint replacement surgery is a common orthopedic procedure for a joint. In cases where a patient has a worn or damaged joint, the joint can be replaced with an implant that integrates with the bone structure and restores painless movement and function. Before a prosthetic component is implanted in a patient's joint, the surgeon typically removes at least a portion of the patient's natural bone to create a platform, recess, or cavity to accommodate at least a portion of the prosthetic component being implanted. During the process of implanting the prosthetic component, muscles and tendons must be repositioned and reattached.
[0003] Most existing devices for monitoring orthopedic implants and rehabilitation can only monitor orthopedic implants in real time. If the orthopedic implant deviates from the controllable range during rehabilitation training, the patient's bones will directly touch the surface of the orthopedic implant. If the patient still needs to move at this time, it will cause secondary damage to the patient's bones.
[0004] To this end, the present invention provides an apparatus and method for monitoring orthopedic implants and rehabilitation to solve the above problems. Summary of the Invention
[0005] In view of the deficiencies of the prior art, the present invention provides a device and method for monitoring orthopedic implants and rehabilitation, which solve the above problems.
[0006] To achieve the above objectives, the present invention is implemented through the following technical solutions: a device for monitoring orthopedic implants and rehabilitation, comprising a fixed base plate, a telescopic sealing plate fixedly connected to the top of the fixed base plate, a sealing cover plate movably connected to the top of the telescopic sealing plate, a telescopic bladder movably connected to the top of the sealing cover plate, a telescopic infusion tube connected to the bottom of the sealing cover plate, a limiting cross bar fixedly connected to the inner wall of the telescopic infusion tube, a skin-breaking cone fixedly connected to the bottom of the limiting cross bar, a liquid storage bladder fixedly connected to the bottom of the telescopic infusion tube, a battery compartment fixedly connected to the bottom of the sealing cover plate, and a rotating The bottom of the liquid storage bladder is movably connected to the top of the fixed base plate, the bottom of the rotating ring is rotatably connected to the top of the fixed base plate, the inner wall of the fixed base plate is fixedly connected to a fixed vertical tube, the side wall of the fixed vertical tube is slidably connected to a sliding vertical tube, the bottom of the battery compartment is fixedly connected to a limiting spring, the inner wall of the fixed vertical tube is fixedly connected to a fixed round rod, one end of the fixed round rod is fixedly connected to a pressure sensor, the bottom of the battery compartment is fixedly connected to a trigger cylinder, the bottom of the trigger cylinder is movably connected to the top of the pressure sensor, the inner wall of the liquid storage bladder is movably connected to the side wall of the sliding vertical tube, and the bottom of the breaking cone is movably connected to the top of the liquid storage bladder.
[0007] Preferably, the inner wall of the telescopic bladder is movably connected to a fixed circular plate, the bottom of the fixed circular plate is fixedly connected to a micro electric push rod, the bottom of the micro electric push rod is fixedly connected to a liquid pushing plate, and the side wall of the liquid pushing plate is movably connected to the inner wall of the telescopic bladder.
[0008] Preferably, a plurality of stirring blades are fixedly connected to the top of the rotating ring, and the plurality of stirring blades are arranged at equal intervals. An annular slide rail is fixedly connected to the top of the fixed base plate, and the annular slide rail is slidably connected to the rotating ring through an electronic slider.
[0009] Preferably: the inner wall of the sliding vertical tube is provided with a plurality of receiving grooves, the interiors of the plurality of receiving grooves are fixedly connected with alarm devices, the inner walls of the plurality of receiving grooves are fixedly connected with return springs, and one end of the plurality of return springs is fixedly connected with a sliding cylinder.
[0010] Preferably, a temperature control plate is fixedly connected to the inner wall of the fixed bottom plate, the top of the temperature control plate is fixedly connected to the bottom of the annular slide rail, and the top of the temperature control plate is rotatably connected to the bottom of the rotating ring.
[0011] Preferably, the side wall of the rotating ring is fixedly connected with a sealing strip, the bottom of the sealing cover plate is fixedly connected with a sealing strip, and the side wall of the fixed circular plate is fixedly connected with a sealing strip.
[0012] Preferably, the plurality of receiving grooves are arranged at equal intervals, and the plurality of sliding cylinders are all slidably connected to the inner walls of the plurality of receiving grooves.
[0013] A method for monitoring orthopedic implants and rehabilitation, comprising the steps of: S1. The staff first places the battery into the battery compartment, then installs the device inside the orthopedic implant, and finally places the orthopedic implant into the patient's body; S2. When the patient needs rehabilitation training, the position of the orthopedic implant in the patient's body can be monitored through the cooperation of the telescopic bladder, the sealing cover, the fixed vertical tube, the sliding vertical tube, the limit spring, the fixed round rod, the pressure sensor and the trigger cylinder; S3. When the orthopedic implant is deflected due to rehabilitation training, the sealing cover, telescopic bladder, fixed circular plate, micro electric push rod, liquid push plate, telescopic infusion tube, limit cross bar, skin-breaking cone and liquid storage bladder can be used to input non-Newtonian fluid into the telescopic bladder to avoid secondary damage caused by direct contact between the patient's bones and the sealing cover. S4. When the orthopedic implant is placed in the patient's body, the non-Newtonian fluid inside the liquid storage bladder can be stirred and the temperature controlled by cooperating with the rotating ring, stirring blades, annular slide rail, liquid storage bladder and temperature control plate, thereby extending the storage time of the non-Newtonian fluid. Beneficial effects
[0014] The present invention provides a device and method for monitoring orthopedic implants and rehabilitation. Compared with the prior art, it has the following advantages: (1) The device and method for monitoring orthopedic implants and rehabilitation can monitor the position of the orthopedic implant through the cooperation of a telescopic bladder, a sealing cover, a telescopic infusion tube, a limit cross bar, a skin-breaking cone, a liquid storage bladder, a telescopic sealing plate, a fixed vertical tube, a sliding vertical tube, a trigger cylinder, a fixed round rod and a pressure sensor. When the orthopedic implant deviates from the controllable range, the non-Newtonian fluid in the liquid storage bladder can be input into the telescopic bladder to protect the patient's bones, thereby avoiding direct contact with the patient's bones due to the hard surface of the sealing cover and causing secondary damage.
[0015] (2) The device and method for monitoring orthopedic implants and rehabilitation, through the cooperation of the micro electric push rod, the liquid pushing plate, the telescopic bladder, the telescopic infusion tube, the liquid storage bladder, the rotating ring, the temperature control plate, the stirring blade and the annular slide rail, can make the micro electric push rod drive the leg plate to squeeze the non-Newtonian fluid inside the telescopic bladder into the liquid storage bladder when the staff takes out the orthopedic implant, and seal the telescopic infusion tube to prevent the telescopic bladder from rupturing and the non-Newtonian fluid from flowing into the patient's body. At the same time, the annular slide rail drives the non-Newtonian fluid inside the liquid storage bladder to rotate slowly through the stirring blade, so as to prevent the non-Newtonian fluid from being left in the liquid storage bladder for a long time and coagulating and deteriorating, thereby extending the storage time of the non-Newtonian fluid and not affecting the position of the orthopedic implant.
[0016] (3) The device and method for monitoring orthopedic implants and rehabilitation can monitor the displacement of the orthopedic implant within a controllable range in real time through the cooperation of the fixed vertical tube, the sliding vertical tube, the receiving groove, the alarm device, the reset spring and the sliding cylinder, and send the displacement degree of the orthopedic implant to the staff in real time, so that the staff can always pay attention to the location of the orthopedic implant and provide treatment to the patient as soon as the orthopedic implant deviates from the controllable range. BRIEF DESCRIPTION OF THE DRAWINGS
[0017] Figure 1 is a schematic structural diagram of an apparatus and method for monitoring orthopedic implants and rehabilitation according to the present invention; Figure 2 Schematic diagram of the position structure of the micro electric push rod of the present invention; Figure 3 This is a schematic diagram of the internal structure of the telescopic infusion tube of the present invention; Figure 4 Schematic diagram of the internal structure of the liquid storage bladder of the present invention; Figure 5 yes Figure 4 A magnified view of point A in the figure; Figure 6 It is a schematic diagram of the position structure of the annular slide rail of the present invention; Figure 7 It is a schematic diagram of the internal structure of the fixed vertical pipe of the present invention.
[0018] In the figure: 1. Fixed bottom plate; 2. Telescopic sealing plate; 3. Trigger cylinder; 4. Sealing cover; 5. Telescopic bladder; 6. Fixed circular plate; 7. Micro electric push rod; 8. Liquid pushing plate; 9. Battery compartment; 10. Telescopic infusion tube; 11. Limiting cross bar; 12. Skin-breaking cone; 13. Liquid storage bladder; 14. Rotating ring; 15. Stirring blade; 16. Annular slide rail; 17. Temperature control plate; 18. Sealing strip; 19. Fixed vertical tube; 20. Sliding vertical tube; 21. Limiting spring; 22. Fixed circular rod; 23. Pressure sensor; 24. Storage slot; 25. Alarm device; 26. Reset spring; 27. Sliding cylinder. DETAILED DESCRIPTION
[0019] The following will clearly and completely describe the technical solutions in the embodiments of the present invention in conjunction with the accompanying drawings. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without making creative efforts are within the scope of protection of the present invention. Example
[0020] See also Figure 1 - Figure 7A device for monitoring orthopedic implants and rehabilitation comprises a fixed base plate 1, a telescopic sealing plate 2 is fixedly connected to the top of the fixed base plate 1, a sealing cover plate 4 is movably connected to the top of the telescopic sealing plate 2, a telescopic bladder 5 is movably connected to the top of the sealing cover plate 4, a telescopic infusion tube 10 is connected to the bottom of the sealing cover plate 4, a limiting cross bar 11 is fixedly connected to the inner wall of the telescopic infusion tube 10, a skin-breaking cone 12 is fixedly connected to the bottom of the limiting cross bar 11, a liquid storage bladder 13 is fixedly connected to the bottom of the telescopic infusion tube 10, a battery compartment 9 is fixedly connected to the bottom of the sealing cover plate 4, a rotating ring 14 is movably connected to the inner wall of the liquid storage bladder 13, and the bottom of the liquid storage bladder 13 is connected to the fixed The top of the base plate 1 is movably connected, the bottom of the rotating ring 14 is rotatably connected to the top of the fixed base plate 1, the inner wall of the fixed base plate 1 is fixedly connected to a fixed vertical tube 19, and the side wall of the fixed vertical tube 19 is slidably connected to a sliding vertical tube 20, the bottom of the battery compartment 9 is fixedly connected to a limiting spring 21, the inner wall of the fixed vertical tube 19 is fixedly connected to a fixed round rod 22, and one end of the fixed round rod 22 is fixedly connected to a pressure sensor 23, the bottom of the battery compartment 9 is fixedly connected to a trigger cylinder 3, the bottom of the trigger cylinder 3 is movably connected to the top of the pressure sensor 23, the inner wall of the liquid storage bladder 13 is movably connected to the side wall of the sliding vertical tube 20, and the bottom of the skin-breaking cone 12 is movably connected to the top of the liquid storage bladder 13.
[0021] It should be noted that the staff first placed the glucose biofuel cell into the battery compartment 9. The glucose biofuel cell is a device that uses glucose as fuel to generate electricity through an enzyme-catalyzed reaction. This type of cell relies on enzymes in the human body to carry out chemical reactions and is typically used to provide power for implantable medical devices in the human body and power subsequent equipment. The staff then installed the device within an orthopedic implant, which was then placed in the patient's body for rehabilitation treatment. When the patient needs to move for rehabilitation, the device monitors the orthopedic implant once it deviates. The bones in the affected area will press the fixed circular plate 6, and the fixed circular plate 6 will press the sealing cover plate 4 through the micro-electric push rod 7 and the liquid push plate 8. When the sealing cover plate 4 is under pressure, the battery compartment 9 drives the sliding vertical tube 20 to slide downward. When the battery compartment 9 drives the sliding vertical rod 20 downward, the battery compartment 9 drives the trigger cylinder 3 downward. The trigger cylinder 3 is pressed down until it hits the surface of the pressure sensor 23. The trigger pressure sensor 23 issues a warning to the staff so that the staff can promptly discover that the orthopedic implant has deviated from the established position and can adjust the orthopedic implant in time. When the sealing cover plate 4 is forced to be pressed down, the sealing cover plate 4 drives the telescopic sealing plate 2 to contract, and at the same time, the sealing cover plate 4 drives the telescopic infusion tube 10 to contract. When the telescopic infusion tube 10 contracts, the limit cross bar 11 drives the skin-breaking cone 12 to be pressed down until the skin-breaking cone 12 moves to the surface of the liquid storage bag 13 and punctures the liquid storage bag 13. The non-Newtonian liquid inside the liquid storage bag 13 enters the interior of the telescopic bag 5 through the telescopic infusion tube 10, so that the interior of the telescopic bag 5 is filled with the non-Newtonian liquid, supporting the patient's bones, and preventing the orthopedic implant from causing secondary damage to the patient's bones when the patient still has to move a distance after the orthopedic implant deviates; When the orthopedic implant needs to be removed, the staff adjusts the patient's bones. When the orthopedic implant loses bone pressure, the limit spring 21 elastically drives the sealing cover plate 4 to rise. When the sealing cover plate 4 rises, the non-flowing fluid inside the telescopic bag 5 is squeezed into the liquid storage bag 13, avoiding the telescopic bag 5 from rupturing when the staff removes the orthopedic implant, and the non-Newtonian fluid inside the telescopic bag 5 flowing into the patient's body, causing a medical accident.
[0022] In an optional embodiment: the inner wall of the telescopic bladder 5 is movably connected to a fixed circular plate 6, the bottom of the fixed circular plate 6 is fixedly connected to a micro electric push rod 7, the bottom of the micro electric push rod 7 is fixedly connected to a liquid pushing plate 8, and the side wall of the liquid pushing plate 8 is movably connected to the inner wall of the telescopic bladder 5.
[0023] It should be noted that when the orthopedic implant needs to be removed, the micro electric push rod 7 is started, and the micro electric push rod 7 drives the liquid pushing plate 8 to squeeze all the non-Newtonian fluid inside the telescopic bladder 5 into the liquid storage bladder 13, and at the same time seal the telescopic infusion tube 10 to prevent the non-Newtonian fluid from still existing inside the telescopic bladder 5.
[0024] In an optional embodiment: a plurality of stirring blades 15 are fixedly connected to the top of the rotating ring 14, and the plurality of stirring blades 15 are arranged at equal intervals. An annular slide rail 16 is fixedly connected to the top of the fixed base plate 1, and the annular slide rail 16 is slidably connected to the rotating ring 14 through an electronic slider.
[0025] It should be noted that when the orthopedic implant is placed in the patient's body, the annular slide 16 is started. The annular slide 16 drives the stirring blade 15 to rotate slowly inside the liquid storage bag 13 by rotating the ring 14, so that the non-Newtonian fluid flows slowly inside the liquid storage bag 13, avoiding the non-Newtonian fluid inside the liquid storage bag 13 from solidifying and deteriorating due to long-term standing, thereby extending the storage time of the non-Newtonian fluid. Since 16 drives 15 to rotate slowly, the position of the orthopedic implant will not change.
[0026] In an optional embodiment: a plurality of receiving grooves 24 are opened on the inner wall of the sliding vertical tube 20, an alarm device 25 is fixedly connected inside the plurality of receiving grooves 24, a return spring 26 is fixedly connected to the inner wall of the plurality of receiving grooves 24, and a sliding cylinder 27 is fixedly connected at one end of the plurality of return springs 26.
[0027] It should be noted that when the orthopedic implant deviates within a controllable range, the patient's bones will press the fixed circular plate 6 downward, and the fixed circular plate 6 drives the sliding vertical tube 20 downward through the battery compartment 9 through the micro-electric push rod 7, the liquid pushing plate 8 and the sealing cover plate 4. When the sliding vertical tube 20 is pressed down, the fixed vertical tube 19 squeezes the sliding cylinder 27, and the sliding cylinder 27 contracts until the alarm device 25 is triggered. The alarm device 25 provides the staff with an orthopedic implant deviation signal, so that the staff can continue to pay attention to the position of the orthopedic implant and deal with it as soon as possible when the orthopedic implant deviates out of the controllable range.
[0028] In an optional embodiment: a temperature control plate 17 is fixedly connected to the inner wall of the fixed base plate 1 , the top of the temperature control plate 17 is fixedly connected to the bottom of the annular slide rail 16 , and the top of the temperature control plate 17 is rotatably connected to the bottom of the rotating ring 14 .
[0029] It should be noted that the temperature of the non-Newtonian fluid inside the liquid storage bladder 13 is adjusted by setting the temperature control plate 17 so that the internal temperature of the liquid storage bladder 13 is moderately between minus two degrees and eight degrees, further extending the storage time of the non-Newtonian fluid.
[0030] In an optional embodiment, a sealing strip 18 is fixedly connected to the side wall of the rotating ring 14 , a sealing strip 18 is fixedly connected to the bottom of the sealing cover plate 4 , and a sealing strip 18 is fixedly connected to the side wall of the fixed circular plate 6 .
[0031] It should be noted that the rotating ring 14, the sealing cover plate 4 and the fixed circular plate 6 are sealed by the provision of multiple sealing strips 18 to avoid non-Newtonian flow leakage inside the device and improve the sealing performance of the device.
[0032] In an optional embodiment, the plurality of receiving grooves 24 are arranged at equal intervals, and the plurality of sliding cylinders 27 are all slidably connected to the inner walls of the plurality of receiving grooves 24 .
[0033] It should be noted that by arranging the multiple receiving slots 24 at equal intervals, the degree of displacement of the orthopedic implant can be monitored in real time. Example
[0034] See also Figure 1 - Figure 7 , a method for monitoring orthopedic implants and rehabilitation, comprising the steps of: S1. The staff first places the battery into the battery compartment 9, then installs the device inside the orthopedic implant, and finally the staff places the orthopedic implant into the patient's body; S2. When the patient needs rehabilitation training, the position of the orthopedic implant in the patient's body can be monitored through the cooperation of the telescopic bladder 5, the sealing cover 4, the fixed vertical tube 19, the sliding vertical tube 20, the limit spring 21, the fixed round rod 22, the pressure sensor 23 and the trigger cylinder 3; S3. When the orthopedic implant is deflected due to rehabilitation training, the sealing cover 4, the telescopic bladder 5, the fixed circular plate 6, the micro electric push rod 7, the liquid pushing plate 8, the telescopic infusion tube 10, the limit cross bar 11, the skin-breaking cone 12 and the liquid storage bladder 13 can cooperate to input the non-Newtonian fluid into the telescopic bladder 5, so as to avoid the patient's bones from directly contacting the sealing cover 4 and causing secondary damage. S4. When the orthopedic implant is placed in the patient's body, the non-Newtonian fluid inside the liquid storage bladder 13 can be stirred and the temperature controlled by rotating the ring 14, the stirring blade 15, the annular slide 16, the liquid storage bladder 13 and the temperature control plate 17, thereby extending the storage time of the non-Newtonian fluid.
[0035] Meanwhile, the contents not described in detail in this specification belong to the prior art known to those skilled in the art.
[0036] During operation, the staff first places the glucose biofuel cell into the battery compartment 9. The glucose biofuel cell is a device that uses glucose as fuel to generate electricity through enzyme-catalyzed reactions. This cell relies on enzymes in the human body to carry out chemical reactions and is typically used to provide power for implantable medical devices in the human body and power subsequent equipment. The staff then installs the device within an orthopedic implant, which is then placed in the patient's body for rehabilitation treatment. When the patient needs to move for rehabilitation, the device monitors the orthopedic implant once it deviates. The bones in the affected area will press the fixed circular plate 6, and the fixed circular plate 6 will press the sealing cover plate 4 through the micro-electric push rod 7 and the liquid push plate 8. When the sealing cover plate 4 is under pressure, the battery compartment 9 drives the sliding vertical tube 20 to slide downward. When the battery compartment 9 drives the sliding vertical rod 20 downward, the battery compartment 9 drives the trigger cylinder 3 downward. The trigger cylinder 3 is pressed down until it hits the surface of the pressure sensor 23. The trigger pressure sensor 23 issues a warning to the staff so that the staff can promptly discover that the orthopedic implant has deviated from the established position and can adjust the orthopedic implant in time. When the sealing cover plate 4 is forced to be pressed down, the sealing cover plate 4 drives the telescopic sealing plate 2 to contract, and at the same time, the sealing cover plate 4 drives the telescopic infusion tube 10 to contract. When the telescopic infusion tube 10 contracts, the limit cross bar 11 drives the skin-breaking cone 12 to be pressed down until the skin-breaking cone 12 moves to the surface of the liquid storage bag 13 and punctures the liquid storage bag 13. The non-Newtonian liquid inside the liquid storage bag 13 enters the interior of the telescopic bag 5 through the telescopic infusion tube 10, so that the interior of the telescopic bag 5 is filled with the non-Newtonian liquid, supporting the patient's bones, and preventing the orthopedic implant from causing secondary damage to the patient's bones when the patient still has to move a distance after the orthopedic implant deviates; When the orthopedic implant needs to be removed, the staff adjusts the patient's bones. When the orthopedic implant loses bone pressure, the limit spring 21 elastically drives the sealing cover plate 4 to rise. When the sealing cover plate 4 rises, the non-flowing fluid inside the telescopic bag 5 is squeezed into the liquid storage bag 13, avoiding the telescopic bag 5 from rupturing when the staff removes the orthopedic implant, and the non-Newtonian fluid inside the telescopic bag 5 flowing into the patient's body, causing a medical accident.
[0037] It should be noted that, in this document, relational terms such as first and second, etc., are used only to distinguish one entity or operation from another entity or operation, and do not necessarily require or imply any actual relationship or order between these entities or operations. Moreover, the terms "comprises," "comprising," or any other variations thereof are intended to cover non-exclusive inclusion, such that a process, method, article, or apparatus that includes a list of elements includes not only those elements but also other elements not explicitly listed, or elements inherent to such process, method, article, or apparatus.
[0038] While embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions, and variations may be made to these embodiments without departing from the principles and spirit of the invention, and that the scope of the invention is defined by the appended claims and their equivalents.
Claims
1. A device for monitoring orthopedic implants and rehabilitation, comprising a fixing base plate (1), characterized in that: The top of the fixed base plate (1) is fixedly connected to a telescopic sealing plate (2), the top of the telescopic sealing plate (2) is movably connected to a sealing cover plate (4), the top of the sealing cover plate (4) is movably connected to a telescopic leather bag (5), the bottom of the sealing cover plate (4) is connected to a telescopic infusion tube (10), the inner wall of the telescopic infusion tube (10) is fixedly connected to a limiting cross bar (11), the bottom of the limiting cross bar (11) is fixedly connected to a skin-breaking cone (12), the bottom of the telescopic infusion tube (10) is fixedly connected to a liquid storage bag (13), the bottom of the sealing cover plate (4) is fixedly connected to a battery compartment (9), the inner wall of the liquid storage bag (13) is movably connected to a rotating ring (14), the bottom of the liquid storage bag (13) is movably connected to the top of the fixed base plate (1), the rotating ring (14) The bottom of the circular ring (14) is rotatably connected to the top of the fixed base plate (1); the inner wall of the fixed base plate (1) is fixedly connected to a fixed vertical tube (19); the side wall of the fixed vertical tube (19) is slidably connected to a sliding vertical tube (20); the bottom of the battery compartment (9) is fixedly connected to a limit spring (21); the inner wall of the fixed vertical tube (19) is fixedly connected to a fixed round rod (22); one end of the fixed round rod (22) is fixedly connected to a pressure sensor (23); the bottom of the battery compartment (9) is fixedly connected to a trigger cylinder (3); the bottom of the trigger cylinder (3) is movably connected to the top of the pressure sensor (23); the inner wall of the liquid storage sac (13) is movably connected to the side wall of the sliding vertical tube (20); and the bottom of the skin-breaking cone (12) is movably connected to the top of the liquid storage sac (13).
2. A device for monitoring orthopedic implants and rehabilitation according to claim 1, characterized in that: The inner wall of the telescopic leather bag (5) is movably connected to a fixed circular plate (6), the bottom of the fixed circular plate (6) is fixedly connected to a micro electric push rod (7), the bottom of the micro electric push rod (7) is fixedly connected to a liquid pushing plate (8), and the side wall of the liquid pushing plate (8) is movably connected to the inner wall of the telescopic leather bag (5).
3. A device for monitoring orthopedic implants and rehabilitation according to claim 1, characterized in that: A plurality of stirring blades (15) are fixedly connected to the top of the rotating ring (14), and the plurality of stirring blades (15) are arranged at equal intervals. An annular slide rail (16) is fixedly connected to the top of the fixed base plate (1), and the annular slide rail (16) is slidably connected to the rotating ring (14) via an electronic slider.
4. The device for monitoring orthopedic implants and rehabilitation according to claim 1, characterized in that: The inner wall of the sliding vertical tube (20) is provided with a plurality of receiving grooves (24), the interiors of the plurality of receiving grooves (24) are fixedly connected to an alarm device (25), the inner walls of the plurality of receiving grooves (24) are fixedly connected to a return spring (26), and one end of the plurality of return springs (26) is fixedly connected to a sliding cylinder (27).
5. The device for monitoring orthopedic implants and rehabilitation according to claim 1, characterized in that: A temperature control plate (17) is fixedly connected to the inner wall of the fixed base plate (1), the top of the temperature control plate (17) is fixedly connected to the bottom of the annular slide rail (16), and the top of the temperature control plate (17) is rotatably connected to the bottom of the rotating ring (14).
6. The device for monitoring orthopedic implants and rehabilitation according to claim 1, characterized in that: The side wall of the rotating ring (14) is fixedly connected with a sealing strip (18), the bottom of the sealing cover plate (4) is fixedly connected with a sealing strip (18), and the side wall of the fixed circular plate (6) is fixedly connected with a sealing strip (18).
7. The device for monitoring orthopedic implants and rehabilitation according to claim 1, characterized in that: The plurality of receiving grooves (24) are arranged at equal intervals, and the plurality of sliding cylinders (27) are all slidably connected to the inner walls of the plurality of receiving grooves (24).
8. A method for monitoring orthopedic implants and rehabilitation, applied to the device for monitoring orthopedic implants and rehabilitation as claimed in any one of claims 1 to 7, characterized in that: The following steps are involved: S1. The staff first places the battery into the battery compartment (9), then installs the device inside the orthopedic implant, and finally the staff places the orthopedic implant into the patient's body; S2. When the patient needs to undergo rehabilitation training, the position of the orthopedic implant in the patient's body can be monitored by cooperating with the telescopic leather bag (5), the sealing cover plate (4), the fixed vertical tube (19), the sliding vertical tube (20), the limit spring (21), the fixed round rod (22), the pressure sensor (23) and the trigger cylinder (3); S3. When the orthopedic implant is deflected due to the patient's rehabilitation training, the non-Newtonian fluid can be input into the telescopic bladder (5) through the cooperation of the sealing cover (4), the telescopic bladder (5), the fixed circular plate (6), the micro-electric push rod (7), the liquid pushing plate (8), the telescopic infusion tube (10), the limit cross bar (11), the skin-breaking cone (12) and the liquid storage bladder (13), so as to avoid the patient's bones from directly contacting the sealing cover (4) and causing secondary damage. S4. When the orthopedic implant is placed in the patient's body, the non-Newtonian fluid inside the liquid storage sac (13) can be stirred and the temperature controlled by rotating the ring (14), the stirring blade (15), the annular slide rail (16), the liquid storage sac (13) and the temperature control plate (17), thereby extending the storage time of the non-Newtonian fluid.