Restraint device for neurology nursing

By adopting the circulating filling and deflation technology with the principle of air pressure in the restraining device, the adaptive restraint force adjustment of the patient's limbs is achieved, which solves the problem that the restraint force is difficult to adjust in the existing restraint device, and improves the comfort and safety of the patient.

CN120203906AActive Publication Date: 2025-06-27THE SIXTH MEDICAL CENT OF THE CHINESE PEOPLES LIBERATION ARMY GENERAL HOSPITAL
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Patent Information

Application Number
CN202510445218.6
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-04-10
Publication Date
2025-06-27
Estimated Expiration
2045-04-10

AI Technical Summary

Technical Problem

When existing constraint devices restrain patients, the constraint strength is not easy to adjust, which easily leads to excessive tightness or looseness of the constraints, affecting the patient's comfort and safety.

Method used

Using the air pressure principle, the first airbag bag and the second airbag bag are circulated and deflated, so that the adaptive constraint force adjustment of the patient's limbs is achieved, and space for movement is reserved on the bed to relieve the discomfort caused by the constraint.

Benefits of technology

It improves the patient's comfort, solves the contradictory problem of the constraints, avoids long-term constraints affecting blood circulation, and increases the freedom of patient's movement.

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Abstract

The invention belongs to the technical field of medical instruments, and particularly provides a neurology nursing restraining device which comprises a bed body, an upper limb limiting mechanism, a hand restraining assembly and a leg restraining assembly are arranged on the bed body, and the hand restraining assembly and the leg restraining assembly are symmetrically arranged. The hand restraining assembly and the leg restraining assembly are each provided with a circulation type restraining assembly. According to the device, the whole patient can be restrained, by means of the air pressure principle, after the patient is restrained, the first air bag and the second air bag are circularly inflated to be tightly attached to and restrain the four limbs of the patient, the technical effect that the restraining force of the four limbs of the patient is adjusted in a self-adaptive mode is achieved, and the use comfort of the patient is improved; the contradictory technical problem that the constraining force of the four limbs of the patient is tight and loose is solved, and meanwhile, the phenomenon that the same part is restrained for a long time to affect blood circulation is avoided by adopting a circulating inflation and deflation structure; in addition, the activity space of the patient is reserved, and discomfort of the patient caused by constraint is relieved.
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Description

Technical Field

[0001] The present invention belongs to the technical field of medical devices, and specifically refers to a restraint device for neurology nursing. Background Art

[0002] Neurological diseases mainly include Parkinson's disease, epilepsy, cerebral thrombosis, Alzheimer's disease, etc. When nursing neurological patients, especially epilepsy or Parkinson's patients, in order to prevent patients from causing harm to themselves or others, restraint chairs or beds are often used to control the patient's limbs. When in use, restraint belts are often used to restrain the patient on the chair or bed.

[0003] When the existing restraint devices restrain and fix patients, they only restrain the patient's limbs. After restraint, the patient's body can still move around at will, which poses a safety hazard; and during the restraint process, it is not easy to adjust the restraint strength of the patient. If the restraint is too tight, it will compress the restraint part of the patient, and long-term restraint will also cause discomfort to the patient, affecting blood circulation. If the restraint is too loose, it is easy to cause the restraint to fail, and the patient is more likely to break free. Moreover, after restraint, the patient's activity space cannot be adjusted, increasing the discomfort caused by restraint to the patient. Summary of the Invention

[0004] To solve the above existing problems, the present invention provides a restraint device for neurology nursing that restrains the patient as a whole and can autonomously adjust the restraint strength. Using the air pressure principle, after restraining the patient, the first airbag and the second airbag are cyclically inflated to closely adhere to and bind the patient's limbs, achieving the technical effect of adaptively adjusting the restraint strength of the patient's limbs, improving the patient's comfort, and solving the contradictory technical problem of the restraint force of the patient's limbs being both tight and loose. At the same time, the structure of cyclic inflation and deflation is adopted to avoid affecting blood circulation due to long-term restraint of the same part; in addition, a patient activity space is reserved on the bed to relieve the discomfort caused by restraint to the patient.

[0005] To achieve the above object, the technical solution adopted by the present invention is as follows: A restraint device for neurology nursing provided by the present invention includes a bed body. An upper limb restriction mechanism is provided at one end of the bed body. Hand restraint components and leg restraint components are respectively provided on the bed body. The hand restraint components and the leg restraint components are symmetrically arranged. The leg restraint components are arranged on the side of the hand restraint components away from the upper limb restriction mechanism. Cyclic restraint components are respectively provided on the hand restraint components and the leg restraint components; The leg restraint component includes a sliding frame, a bracket mechanism, and a leg locking mechanism. The sliding frames are symmetrically arranged at the lower part of the bed body. The bracket mechanism is slidably arranged in the sliding frame. The leg locking mechanism is arranged on the bracket mechanism; The cyclic restraint assembly includes a first airbag, a second airbag, and an intermittent inflation mechanism. The first airbag and the second airbag are symmetrically arranged at the inner ends of both sides of the leg locking mechanism and inside the hand restraint assembly respectively. The intermittent inflation mechanism is arranged on the leg locking mechanism and the hand restraint assembly respectively. An inflation tube is connected between the intermittent inflation mechanism and the first airbag and the second airbag respectively.

[0006] Further, hand activity grooves and leg activity grooves are symmetrically arranged on the bed body respectively, and the hand activity grooves and the leg activity grooves penetrate through the bed body respectively. The sliding frame is arranged below the leg activity groove. The leg locking mechanism includes a first bracket, a first cover plate, and a first magnet. The first bracket is movably arranged above the leg activity groove. The first cover plate is rotatably arranged on the first bracket. The inner walls of the first bracket and the first cover plate are combined to form a cylindrical shape. The first magnet is slidably arranged on the outer side wall of the first bracket. A first electromagnetic plate is arranged at the end of the first cover plate away from its rotating end. The first electromagnetic plate is inserted into the first bracket. A groove is arranged on the first electromagnetic plate. The first electromagnetic plate is movably engaged with the groove. When the first electromagnetic plate is energized, it generates magnetism, and its magnetic pole is different from that of the first magnet. The first electromagnetic plate adsorbs the first magnet to fix the first bracket and the first cover plate. When the first electromagnetic plate loses magnetism after being powered off, pulling the first magnet can release the fixation of the first bracket and the first cover plate.

[0007] Further, the support mechanism includes a follower rotating rod, a limit rotating rod, a telescopic sliding plate, a limit adjusting plate, and an adjusting insertion rod. The follower rotating rod and the limit rotating rod are respectively rotatably arranged at both lower ends of the first bracket. The limit rotating rod is arranged at one end of the first bracket close to the hand activity groove. A limiting groove is penetrated through the limit rotating rod. The follower rotating rod and the limit rotating rod are movably arranged in the leg activity groove. The telescopic sliding plate is horizontally arranged at the lower end of the follower rotating rod. The telescopic sliding plate is perpendicular to the follower rotating rod. The telescopic sliding plate slides inside the sliding frame. The limit adjusting plates are symmetrically arranged at the telescopic ends of the telescopic sliding plate. The limit rotating rod slides inside the symmetric limit adjusting plates. A plurality of adjusting holes are penetrated through the limit adjusting plates evenly. The adjusting insertion rod is movably inserted into the adjusting holes, and the adjusting insertion rod penetrates through the limiting groove.

[0008] During use, the height of the limiting rotating rod is restricted by adjusting the insertion rod. The insertion rod is inserted into the adjustment hole on the limiting adjustment plate, so that the movement range of the limiting rotating rod is between the insertion rod and the telescopic sliding plate. The patient can move by bending the leg. During the process of bending the leg, the lower leg drives the first bracket to rotate around the upper end of the follower rod. Driven by the upward movement of one end of the first bracket of the limiting rotating rod, it slides upward between the limiting adjustment plates. The first bracket slides towards the patient's hip, driving the entire bracket mechanism to slide in the leg activity groove. The telescopic sliding plate slides in the sliding frame and adapts to expand and contract. The patient can only perform up and down bending movements, restricting the left and right movement of the patient's leg and avoiding accidental injuries caused by the patient's violent activities.

[0009] Furthermore, the hand restraint assembly includes a second bracket and a second cover plate. The second bracket is movably arranged above the hand activity groove, and the second cover plate is rotatably arranged on the second bracket; the first airbag and the second airbag are respectively attached to both ends of the inner walls of the first bracket and the first cover plate and both ends of the inner walls of the second bracket and the second cover plate. The intermittent inflation mechanism is respectively arranged on the upper parts of the first cover plate and the second cover plate. The first airbag is circumferentially and uniformly communicated with a first insertion pocket on the side facing the second airbag. The second airbag is circumferentially and uniformly communicated with a second insertion pocket on the side facing the first airbag. The first insertion pocket and the second insertion pocket are staggered in the circumferential direction. A pressure strip is arranged inside the first insertion pocket and the second insertion pocket. The first airbag, the second airbag, the first insertion pocket, the second insertion pocket and the pressure strip are all made of rubber material, and soft materials are used to reduce the harm caused to the patient during restraint; Furthermore, the intermittent inflation mechanism includes a reversing motor, a turntable and an air pump. The reversing motor is respectively embedded in the upper parts of the first cover plate and the second cover plate. The turntable is arranged at the output end of the reversing motor, and the air pump is arranged on the upper part of the turntable; an air release channel and an inflation channel are respectively arranged inside the turntable. The air release channel and the inflation channel respectively penetrate the side wall and the upper wall of the turntable. The inflation channel is communicated with the output end of the air pump. The air release channel and the inflation channel are respectively communicated with symmetric inflation pipes. A compression cavity is communicated on the side of the inflation channel close to the air release channel. A pneumatic push plate is slidably arranged in the compression cavity. A spring is connected between the pneumatic push plate and the inner wall of the compression cavity. A pressure sensor is arranged on the inner wall of the compression cavity. The model of the pressure sensor is MS5803 pressure sensor. The spring is sleeved outside the pressure sensor; the air release channel penetrates the upper wall of the turntable and extends to be provided with an air release pipe. An air release groove is arranged on the outer wall of the air release pipe. An air release floating plate is slidably arranged in the air release pipe; When in use, the inflation channel and the deflation channel are respectively connected to the symmetric inflation tubes. If the inflation channel is connected to the second airbag bag at this time and the air pump works, air is inflated into the second airbag bag and the second insertion bag through the inflation channel. The second airbag bag and the second insertion bag gradually expand. During the expansion process, they squeeze the first insertion bag and gradually fit with the patient's limbs. The rubber strip presses tightly against the patient's skin, providing strong friction and strengthening the fixation effect on the patient's limbs. The gas squeezed out from the first insertion bag flows through the deflation channel to the deflation tube. The gas lifts the deflation float plate and is discharged from the deflation slot. During this period, after the second airbag bag and the second insertion bag are inflated and tightly attached to the patient's limbs, the gas gradually saturates, and then squeezes the pneumatic push plate, pushing the pneumatic push plate to slide in the compression cavity against the elasticity of the spring. When the pneumatic push plate slides to the pressure sensor, the flipping motor starts, causing the turntable to rotate 180 degrees. As a result, the inflation tube connecting the inflation channel to the first airbag bag is connected, and the deflation tube connecting the deflation channel to the second airbag bag is connected. The deflation float plate falls to the lower end of the deflation tube under the action of gravity, blocking the deflation channel to prevent the instantaneous deflation of the gas in the second airbag bag and the second insertion bag, weakening the restraint force. The pneumatic push plate returns to the end of the compression cavity away from the pressure sensor under the elastic action of the spring. Immediately afterwards, the air pump inflates the first airbag bag and the first insertion bag through the inflation channel. The first airbag bag and the first insertion bag inflate and expand. During this process, the first insertion bag squeezes the second insertion bag, and the gas in the second insertion bag pushes the deflation float plate to move up and then flows out from the deflation slot. At this time, the strip on the first insertion bag presses tightly against the patient's skin, and the first insertion bag squeezes the patient's limbs for fixation. This cycle repeats; the structure of cyclic inflation and deflation avoids affecting blood circulation by restraining the same part for a long time, and at the same time avoids the large restraint force on the patient's limbs caused by the continuous inflation of the air pump, which affects the blood circulation of the patient. Through the change of air pressure, the restraint force on the patient's limbs is adaptively adjusted, improving the comfort of the patient's use and solving the contradictory technical problem of the restraint force on the patient's limbs being both tight and loose.

[0010] Further, a second magnet is slidably provided on the outer side wall of the second bracket, and a second electromagnetic plate is provided at a position far from the rotation end of the second cover plate. The second magnet is movably engaged with the second electromagnetic plate. The hand restraint assembly further includes a hand pad, a pressure pad, a transition rod, a movable cover, a fixing plate, and a fixing insertion rod. The hand pad is provided at the end of the second bracket, and the pressure pad is provided at the end of the second cover plate. The pressure pad is arranged above the hand pad. A nursing groove is penetrated through the inner side of the pressure pad. The hand pad and the pressure pad clamp the patient's hand to prevent the patient's hand from moving around randomly and increasing the difficulty of infusion care. When the patient needs infusion care, the infusion operation can be performed on the back of the hand through the nursing groove on the pressure pad. The transition rod is movably arranged at the lower part of the second bracket and slides in the hand activity groove. A return spring is connected between the transition rod and the inner wall of the hand activity groove. The movable cover is arranged at the lower end of the transition rod. The fixing plate is arranged at the lower part of the bed body and symmetrically arranged on both sides of the hand activity groove. The fixing insertion rod is movably inserted into the fixing plate. A rotating shaft is rotatably arranged inside the movable cover, and a fixing convex block is arranged inside the rotating shaft. A torsion spring is connected between the rotating shaft and the movable cover. An activity belt is wound around the rotating shaft. The activity belt penetrates through the inside of the transition rod and is connected to the second bracket. The activity belt does not have elasticity, and the length of the activity belt does not exceed the normal activity range of the patient. In the initial state, the movable cover is inside the symmetric fixing plates, the torsion spring makes the activity belt taut, the fixing insertion rod penetrates through the inside of the rotating shaft, and the upper part of the fixing insertion rod is engaged with the fixing convex block to fix the rotating shaft. Further, the upper limb restricting mechanism includes a fixed cylinder, a connecting rod, a telescopic pull plate, a chest and abdomen pressing plate, a pull rod, a restricting plate, and a limiting bolt. The restricting plate is arranged at the end of the bed body far from the leg activity groove. The restricting plate is L-shaped, and a plurality of jacks are vertically and uniformly penetrated through the restricting plate. The limiting bolt is movably engaged in the jacks. The fixed cylinders are symmetrically sleeved on the ends of the bed body, and the fixed cylinders are rotatably connected to the bed body. The connecting rod is arranged on the outer wall of the fixed cylinder. The chest and abdomen pressing plate is connected to the end of the connecting rod far from the fixed cylinder. The chest and abdomen pressing plate is arranged in an I-shaped manner, and a cotton pad is arranged on the side of the chest and abdomen pressing plate facing the bed body. The telescopic pull plate is arranged on the outer side wall of the fixed cylinder, and the telescopic pull plate and the connecting rod are centrosymmetrically arranged. The pull rod is connected to the telescopic end of the telescopic pull plate, and the pull rod is rotatably connected to the telescopic pull plate. The pull rod is slidably sleeved on the restricting plate, and the limiting bolt penetrates through the pull rod. The pull rod is positioned by inserting the limiting bolt into the jack.

[0011] Preferably, a main controller is provided on the bed body. The model of the main controller is S7-200. The first electromagnetic plate, the second electromagnetic plate, the flipping motor, the air pump, and the pressure sensor are respectively electrically connected to the main controller.

[0012] The beneficial effects achieved by the present invention with the above structure are as follows: 1. A restraint device for neurology nursing provided by the present invention preliminarily limits the overall body of the patient through the upper limb limiting mechanism, and restrains the limbs of the patient through the hand restraint component and the leg restraint component respectively. After the overall restraint of the patient, the patient cannot move around randomly, avoiding harm to the patient himself and the medical staff; 2. A cyclic restraint component is provided. Using the principle of air pressure, after restraining the patient, the first airbag and the first insertion bag and the second airbag and the second insertion bag are cyclically inflated to tightly adhere to and restrain the limbs of the patient. When the first insertion bag is inflated, the second insertion bag is squeezed to deflate, and when the second insertion bag is inflated, the first insertion bag is squeezed to deflate. The first insertion bag and the second insertion bag are cyclically tightened against the patient's limbs. The structure of cyclic inflation and deflation is adopted to avoid affecting blood circulation by restraining the same part for a long time, and the pneumatic push plate automatically judges inflation and deflation, achieving the technical effect of adaptively adjusting the restraint force on the limbs of the patient, improving the comfort of the patient's use, and solving the contradictory technical problem of the restraint force on the patient's limbs being both tight and loose; The soft first airbag and the first insertion bag and the second airbag and the second insertion bag are used together to restrain the limbs of the patient, reducing the harm caused to the patient during restraint; 3. A nursing groove is provided on the hand restraint component to press and limit the finger part of the patient, facilitating the infusion operation of the medical staff during nursing and avoiding the situation where the finger part of the patient moves randomly and makes it difficult to infuse; 4. To prevent the patient from always maintaining one state during restraint, which may cause poor blood circulation in the patient and make the patient more irritable, an activity belt is provided on the hand restraint component and a bracket mechanism is provided on the leg restraint component. When the patient needs to move the limbs during restraint, the patient can move under the restriction of the activity belt and the limit rotating rod, enabling the patient to move the limbs within the restricted range adjusted by the medical staff, relieving the irritable psychology caused by restraint, avoiding discomfort caused to the patient during restraint, and at the same time restricting the patient's movement so that the patient will not cause harm to others and himself during movement. BRIEF DESCRIPTION OF THE DRAWINGS

[0013] Figure 1 It is a schematic structural diagram of a restraint device for neurology nursing provided by the present invention; Figure 2 It is a schematic combined structural diagram of the bed body and the upper limb limiting mechanism; Figure 3 It is a schematic combined structural diagram of the leg restraint component and the cyclic restraint component; Figure 4 It is a schematic combined structural diagram of the leg locking mechanism and the bracket mechanism; Figure 5 It is a front view of the combined structure of the leg locking mechanism and the bracket mechanism; Figure 6 For Figure 5Schematic diagram of the sectional structure at A-A in [the figure]; Figure 7 Schematic diagram of the structure of the cyclic restraint assembly; Figure 8 Front view of the cyclic restraint assembly; Figure 9 For Figure 8 Schematic diagram of the sectional structure at B-B in [the figure]; Figure 10 Schematic diagram of the structure of the intermittent inflation mechanism; Figure 11 For Figure 9 Schematic diagram of the enlarged partial structure at C in [the figure]; Figure 12 Schematic diagram of the structure of the hand restraint assembly; Figure 13 Front view of the hand restraint assembly; Figure 14 For Figure 13 Schematic diagram of the enlarged partial structure at D in [the figure].

[0014] Wherein, 1. Bed body, 11. Leg activity groove, 12. Hand activity groove, 2. Leg restraint assembly, 21. Bracket mechanism, 211. Follow-up rotating rod, 212. Limit rotating rod, 213. Telescopic sliding plate, 214. Limit adjusting plate, 215. Adjusting hole, 216. Adjusting insertion rod, 22. Leg locking mechanism, 221. First bracket, 222. First cover plate, 223. First magnet, 224. First electromagnetic plate, 23. Sliding frame, 3. Hand restraint assembly, 31. Second bracket, 32. Second cover plate, 33. Hand pad, 34. Pressure pad, 35. Nursing groove, 36. Second magnet, 37. Transition rod, 38. Activity cover, 39. Fixed plate, 310. Fixed insertion rod, 311. Return spring, 312. Rotating shaft, 313. Activity belt, 314. Fixed convex block, 4. Cyclic restraint assembly, 41. First airbag, 42. Second airbag, 43. First insertion pocket, 44. Second insertion pocket, 45. Inflation tube, 46. Intermittent inflation mechanism, 461. Reversing motor, 462. Turntable, 463. Air pump, 464. Inflation channel, 465. Deflation channel, 466. Deflation groove, 467. Deflation floating plate, 468. Pneumatic push plate, 469. Compression chamber, 4610. Pressure sensor, 47. Pressure strip, 5. Upper limb restriction mechanism, 51. Fixed cylinder, 52. Connecting rod, 53. Chest and abdomen pressing plate, 54. Telescopic pulling plate, 55. Pull rod, 56. Restriction plate, 57. Limit bolt. Detailed implementation mode

[0015] The technical solutions of the present invention will be further described in detail below in conjunction with specific embodiments. Parts of the technical features or connection relationships of the present invention that are not described in detail are all prior arts adopted.

[0016] The present invention will be further described in detail below in conjunction with the accompanying drawings.

[0017] As Figures 1 - 14 shown, a restraint device for neurology nursing provided by the present invention includes a bed body 1. An upper limb restriction mechanism 5 is provided at one end of the bed body 1. A hand restraint assembly 3 and a leg restraint assembly 2 are respectively provided on the bed body 1. The hand restraint assembly 3 and the leg restraint assembly 2 are symmetrically arranged respectively. The leg restraint assembly 2 is arranged on the side of the hand restraint assembly 3 away from the upper limb restriction mechanism 5. A circular restraint assembly 4 is respectively provided on the hand restraint assembly 3 and the leg restraint assembly 2; Hand activity grooves 12 and leg activity grooves 11 are symmetrically provided on the bed body 1 respectively. The hand activity grooves 12 and the leg activity grooves 11 penetrate through the bed body 1 respectively. The hand restraint assembly 3 is arranged on the hand activity groove 12, and the leg restraint assembly 2 is arranged on the leg activity groove 11.

[0018] The upper limb restriction mechanism 5 includes a fixed cylinder 51, a restriction plate 56 and a limit bolt 57. The restriction plate 56 is arranged at the end of the bed body 1 away from the leg activity groove 11. The restriction plate 56 is L-shaped. A plurality of jacks are vertically and uniformly penetrated through the restriction plate 56. The limit bolt 57 is movably engaged in the jacks. The fixed cylinders 51 are symmetrically sleeved on the ends of the bed body 1. The fixed cylinders 51 are rotatably connected to the bed body 1. Connecting rods 52 and telescopic pull plates 54 are respectively provided on the outer walls of the fixed cylinders 51. The telescopic pull plates 54 and the connecting rods 52 are centrosymmetrically arranged. One end of the connecting rod 52 away from the fixed cylinder 51 is connected with a chest and abdomen pressing plate 53. The chest and abdomen pressing plate 53 is I-shaped. A cotton pad is provided on the side of the chest and abdomen pressing plate 53 facing the bed body 1. The telescopic end of the telescopic pull plate 54 is connected with a pull rod 55. The pull rod 55 is rotatably connected to the telescopic pull plate 54. The pull rod 55 is slidably sleeved on the restriction plate 56. The limit bolt 57 penetrates through the pull rod 55. The pull rod 55 is positioned by inserting the limit bolt 57 into the jack.

[0019] The leg restraint assembly 2 includes a sliding frame 23, a bracket mechanism 21 and a leg locking mechanism 22. The sliding frames 23 are symmetrically arranged at the lower part of the bed body 1. The sliding frames 23 are arranged below the leg activity grooves 11. The bracket mechanism 21 is slidably arranged in the sliding frames 23. The leg locking mechanism 22 is arranged on the bracket mechanism 21; The leg locking mechanism 22 includes a first bracket 221. The first bracket 221 is movably arranged above the leg activity groove 11. A first cover plate 222 is rotatably arranged on the first bracket 221. The inner walls of the first bracket 221 and the first cover plate 222 are combined to form a cylindrical shape. A first magnet 223 is slidably arranged on the outer side wall of the first bracket 221. A first electromagnetic plate 224 is provided at the end of the first cover plate 222 away from its rotating end. The first electromagnetic plate 224 is inserted into the first bracket 221. A groove is provided on the first electromagnetic plate 224. The first electromagnetic plate 224 is movably engaged with the groove.

[0020] The bracket mechanism 21 includes a follower rotating rod 211 and a limit rotating rod 212. The follower rotating rod 211 and the limit rotating rod 212 are respectively rotatably arranged at both lower ends of the first bracket 221. The limit rotating rod 212 is arranged at one end of the first bracket 221 close to the hand activity groove 12. A limiting groove is penetrated through the limit rotating rod 212. The follower rotating rod 211 and the limit rotating rod 212 are movably arranged in the leg activity groove 11. A telescopic sliding plate 213 is horizontally arranged at the lower end of the follower rotating rod 211. The telescopic sliding plate 213 is perpendicular to the follower rotating rod 211. The telescopic sliding plate 213 slides inside the sliding frame 23. Limiting adjusting plates 214 are symmetrically arranged at the telescopic end of the telescopic sliding plate 213. The limit rotating rod 212 slides inside the symmetrically arranged limiting adjusting plates 214. Adjusting holes 215 are penetrated and evenly distributed on the limiting adjusting plates 214. Adjusting inserting rods 216 are movably inserted into the adjusting holes 215. The adjusting inserting rods 216 penetrate through the limiting groove.

[0021] The hand restraint assembly 3 includes a second bracket 31 and a second cover plate 32. The second bracket 31 is movably arranged above the hand activity groove 12. The second cover plate 32 is rotatably arranged on the second bracket 31. A second magnet 36 is slidably arranged on the outer side wall of the second bracket 31. A second electromagnetic plate is arranged at the end of the second cover plate 32 far from its rotating end. The second magnet 36 is movably engaged with the second electromagnetic plate. A hand pad 33 is arranged at the end of the second bracket 31. A pressure pad 34 is arranged at the end of the second cover plate 32. The pressure pad 34 is arranged above the hand pad 33. A nursing groove 35 is penetrated through the inner side of the pressure pad 34. A transition rod 37 is movably arranged at the lower part of the second bracket 31. The transition rod 37 slides in the hand activity groove 12. A return spring 311 is connected between the transition rod 37 and the inner wall of the hand activity groove 12. An activity cover 38 is arranged at the lower end of the transition rod 37. A rotating shaft 312 is rotatably arranged inside the activity cover 38. A fixed convex block 314 is arranged inside the rotating shaft 312. A torsion spring is connected between the rotating shaft 312 and the activity cover 38. An activity belt 313 is wound around the rotating shaft 312. The activity belt 313 penetrates through the inside of the transition rod 37 and is connected with the second bracket 31; A fixing plate 39 is arranged at the lower part of the bed body 1. The fixing plates 39 are symmetrically arranged on both sides of the hand activity groove 12. Fixing inserting rods 310 are movably inserted into the fixing plates 39; In the initial state, the activity cover 38 is inside the symmetric fixing plates 39. The torsion spring makes the activity belt 313 taut. The fixing inserting rod 310 penetrates through the inside of the rotating shaft 312. The upper part of the fixing inserting rod 310 is engaged with the fixed convex block 314.

[0022] The cyclic restraint assembly 4 includes a first airbag 41 and a second airbag 42. The first airbag 41 and the second airbag 42 are respectively attached to both ends of the inner walls of the first bracket 221 and the first cover plate 222, and both ends of the inner walls of the second bracket 31 and the second cover plate 32. Intermittent inflation mechanisms 46 are respectively provided on the upper parts of the first cover plate 222 and the second cover plate 32. Inflation tubes 45 are connected between the intermittent inflation mechanisms 46 and the first airbag 41 and the second airbag 42 respectively; a plurality of first insertion pockets 43 are evenly distributed and communicated on the side of the first airbag 41 facing the second airbag 42 in the circumferential direction, and a plurality of second insertion pockets 44 are evenly distributed and communicated on the side of the second airbag 42 facing the first airbag 41 in the circumferential direction. The first insertion pockets 43 and the second insertion pockets 44 are staggered in the circumferential direction. A pressure strip 47 is provided inside the first insertion pockets 43 and the second insertion pockets 44. The first airbag 41, the second airbag 42, the first insertion pockets 43, the second insertion pockets 44 and the pressure strip 47 are all made of rubber material.

[0023] The intermittent inflation mechanism 46 includes a flipping motor 461. The flipping motor 461 is respectively embedded in the upper parts of the first cover plate 222 and the second cover plate 32. A turntable 462 is provided at the output end of the flipping motor 461. An air pump 463 is provided on the upper part of the turntable 462; an air release channel 465 and an inflation channel 464 are respectively provided inside the turntable 462. The air release channel 465 and the inflation channel 464 respectively penetrate through the side wall and the upper wall of the turntable 462. The inflation channel 464 is communicated with the output end of the air pump 463. The air release channel 465 and the inflation channel 464 are respectively communicated with the symmetric inflation tubes 45. A compression cavity 469 is communicated on the side of the inflation channel 464 close to the air release channel 465. A pneumatic push plate 468 is slidably provided in the compression cavity 469. A spring is connected between the pneumatic push plate 468 and the inner wall of the compression cavity 469. A pressure sensor 4610 is provided on the inner wall of the compression cavity 469. The spring is sleeved outside the pressure sensor 4610; the air release channel 465 penetrates through the upper wall of the turntable 462 and extends to be provided with an air release pipe. An air release groove 466 is provided on the outer wall of the air release pipe. An air release floating plate 467 is slidably provided in the air release pipe.

[0024] A main controller is provided on the bed body 1. The model of the main controller is S7-200. The first electromagnetic plate 224, the second electromagnetic plate, the flipping motor 461, the air pump 463 and the pressure sensor 4610 are respectively electrically connected to the main controller.

[0025] Working principle and working process: In the initial state, the pull rod 55 is located at the lower end of the limiting plate 56. By pulling the telescopic pull plate 54, the connecting rod 52 rotates around the axis of the fixed cylinder 51, causing the chest and abdomen pressing plate 53 to lift. The return spring 311 is in a free state, making the movable cover 38 located inside the symmetric fixed plate 39. The torsion spring makes the movable belt 313 taut, pulling the second bracket 31 tightly. The fixed insertion rod 310 passes through the inner side of the rotating shaft 312, and the upper part of the fixed insertion rod 310 is engaged with the fixed convex block 314, thus positioning the rotating shaft 312 and preventing it from rotating, making the second bracket 31 fit with the upper end of the transition rod 37. The adjusting insertion rod 216 is inserted into the lowermost adjusting hole 215, and the adjusting insertion rod 216 passes through the limiting groove of the limiting rotating rod 212. At this time, the adjusting insertion rod 216 is at the lowermost end of the limiting groove, further making the first bracket 221 in a horizontal state. The first cover plate 222 and the first bracket 221, as well as the second cover plate 32 and the second bracket 31, are all in a state of being rotatably opened. The first airbag 41, the second airbag 42, the first insertion pocket 43, and the second insertion pocket 44 are not inflated and are all in a deflated state.

[0026] During specific use, medical staff guide the patient to lie flat on the bed body 1. First, the limit bolt 57 is pulled out from the limiting plate 56, and the connecting rod 52 is flipped so that the chest and abdomen pressing plate 53 presses down to the patient's chest and abdomen. The cotton pad on the chest and abdomen pressing plate 53 naturally fits with the patient's chest and abdomen, while the telescopic pull plate 54 symmetrically located with the connecting rod 52 lifts, driving the pull rod 55 to slide on the limiting plate. The telescopic pull plate 54 adapts and expands or contracts. Subsequently, the limit bolt 57 is passed through the pull rod 55 and inserted into the jack on the limiting plate 56, thereby positioning the position of the chest and abdomen pressing plate 53 and preliminarily restraining the patient.

[0027] Immediately start the main controller, spread the patient's limbs, place the patient's hands on the second bracket 31 respectively, and place the patient's legs on the first bracket 221 respectively. Among them, it is necessary to place the patient's hands on the pressure pad 34, and place the part of the patient's lower leg near the ankle on the first bracket 221. Then rotate the first cover plate 222 and the second cover plate 32 respectively, so that the first electromagnetic plate 224 and the second electromagnetic plate are inserted into the first bracket 221 and the second bracket 31 respectively. After being energized, the first electromagnetic plate 224 and the second electromagnetic plate generate magnetism, and then adsorb the first magnet 223 and the second magnet 36, so that the first magnet 223 is engaged with the first electromagnetic plate 224, and the second magnet 36 is engaged with the second electromagnetic plate. Under the adsorption of magnetic force, it is more difficult for the patient to break free. At this time, the first bracket 221 and the first cover plate 222 clamp the patient's lower leg part, the second bracket 31 and the second cover plate 32 clamp the patient's forearm part, and the hand pad 33 and the pressure pad 34 clamp the patient's hand to prevent the patient's hand from moving around and increasing the difficulty of infusion care. When the patient needs infusion care, the back of the hand can be infused through the care groove 35 on the pressure pad 34 to complete the preliminary restraint of the patient. Compared with the restraint process in which medical staff wrap the restraint belt around the patient multiple times and then tie the restraint belt, this restraint process takes less time and reduces the harm caused to medical staff or the patient himself during restraint.

[0028] The main controller starts the air pump 463, the flipping motor 461 and the pressure sensor 4610. The inflation channel 464 and the deflation channel 465 are respectively connected to the symmetric inflation tubes 45. If the inflation channel 464 is connected to the second airbag 42 at this time, the air pump 463 works, and inflates the second airbag 42 and the second insertion pocket 44 through the inflation channel 464. The second airbag 42 and the second insertion pocket 44 gradually expand, and squeeze the first insertion pocket 43 during the expansion process and gradually fit with the patient's limbs. The rubber strip 47 closely adheres to the patient's skin, providing strong friction and strengthening the fixing effect on the patient's limbs. At the same time, the soft second airbag 42 and the second insertion pocket 44 reduce the harm caused to the patient during restraint. The gas squeezed out from the first insertion pocket 43 flows through the deflation channel 465 to the deflation tube, the gas lifts the deflation floating plate 467, and is discharged from the deflation groove 466. During this period, after the second airbag 42 and the second insertion pocket 44 are inflated and closely adhere to the patient's limbs, the gas gradually saturates, and then squeezes the pneumatic push plate 468, pushing the pneumatic push plate 468 to slide in the compression chamber 469 against the elasticity of the spring. When the pneumatic push plate 468 slides to the pressure sensor 4610, the flipping motor 461 starts, rotates the turntable 462 by 180 degrees, and then connects the inflation channel 464 to the inflation tube 45 connected to the first airbag 41, and the deflation channel 465 to the inflation tube 45 connected to the second airbag 42. The deflation floating plate 467 falls to the lower end of the deflation tube under the action of gravity, blocking the deflation channel 465 to prevent the gas in the second airbag 42 and the second insertion pocket 44 from instantaneously deflating and weakening the restraint force. The pneumatic push plate 468 returns to the end of the compression chamber 469 away from the pressure sensor 4610 under the elastic action of the spring. Immediately afterwards, the air pump 463 inflates the first airbag 41 and the first insertion pocket 43 through the inflation channel 464. The first airbag 41 and the first insertion pocket 43 inflate and expand. During this process, the first insertion pocket 43 squeezes the second insertion pocket 44, and the gas in the second insertion pocket 44 pushes the deflation floating plate 467 to move up and then flows out from the deflation groove 466. At this time, the strip 47 on the first insertion pocket 43 closely adheres to the patient's skin, and the first insertion pocket 43 squeezes the patient's limbs for fixation, and so on in a cycle; the structure of cyclic inflation and deflation avoids affecting blood circulation by restraining the same part for a long time, and at the same time avoids the continuous inflation of the air pump 463 from causing a large restraint force on the patient's limbs and affecting the blood circulation of the patient. By changing the air pressure, the restraint force on the patient's limbs is adaptively adjusted, improving the comfort of the patient's use, and solving the contradictory technical problem that the restraint force on the patient's limbs needs to be both tight and loose.

[0029] When it is necessary to release the restraint, the medical staff pumps air through the air pump 463 to extract the gas in the first airbag 41 or the second airbag 42. After the gas decreases, the first airbag 41, the first insertion bag 43, the second airbag 42, and the second insertion bag 44 are compressed. Subsequently, the main controller is turned off, causing the first electromagnetic plate 224 and the second electromagnetic plate to lose power and magnetism, and no longer attracting the first magnet 223 and the second magnet 36. The medical staff pulls the first magnet 223 and the second magnet 36 outwards respectively, no longer restricting the first electromagnetic plate 224 and the second electromagnetic plate. Then, the first cover plate 222 and the second cover plate 32 are rotated and opened respectively to release the restraint on the patient's limbs. Finally, the limit bolt 57 is pulled out, and the chest and abdomen pressing plate 53 is flipped up to release the restraint on the patient's upper body.

[0030] To prevent the patient from always maintaining one position during restraint and making the patient more irritable, the activity ranges of the hand restraint assembly 3 and the leg restraint assembly 2 can be appropriately adjusted; by adjusting the insertion rod 216 to limit the activity height of the limit rotating rod 212, the insertion rod 216 is inserted into the adjustment hole 215 on the limit adjustment plate 214, so that the activity range of the limit rotating rod 212 is within the distance between the adjustment insertion rod 216 and the telescopic sliding plate 213. The patient can move by bending the legs. During the process of bending the legs, the lower leg drives the first bracket 221 to rotate around the upper end of the follower rod 211. Driven by the upward movement of one end of the limit rotating rod 212 on the first bracket 221, it slides upward between the limit adjustment plates 214. The first bracket 221 slides towards the patient's buttocks, driving the entire bracket mechanism 21 to slide in the leg activity groove 11. The telescopic sliding plate 213 slides in the sliding frame 23 and adapts to telescopic movement. The patient can only make up and down bending movements, restricting the left and right movement of the patient's legs and avoiding accidental injuries caused by the patient's violent activities. The fixed insertion rod 310 is pulled out from the fixed plate 39. The fixed insertion rod 310 no longer restricts the rotating shaft 312 and the movable cover 38. Thus, the movable belt 313 can be pulled out from the transition rod 37. The rotating shaft 312 rotates, and the torsion spring is compressed. The movable belt 313 has no elasticity. The patient's arm can move within the range where the movable belt 313 extends while being restrained by the second bracket 31 and the second cover plate 32. The length of the movable belt 313 does not exceed the normal activity range of the patient, alleviating the irritable psychology caused by restraint, avoiding discomfort caused to the patient during restraint, and at the same time preventing the patient from causing harm to others and himself during activities. When the patient does not need to move, the patient's arm is pressed down. Under the action of the torsion spring, the rotating shaft 312 winds up the movable belt 313, causing the second bracket 31 to fit with the transition rod 37 again. Under the elastic action of the return spring 311, the movable cover 38 slides between the fixed plates 39, and the fixed insertion rod 310 is inserted again to position the rotating shaft 312.

[0031] It should be noted that flexible sealing sleeves are provided at the ends of the inflation channel 464 and the deflation channel 465, so that no gas leakage will occur when they rotate to the inflation tube 45 for inflation and deflation. This is prior art and will not be elaborated here.

[0032] The above is the overall working process of the present invention. Just repeat these steps the next time it is used.

[0033] It should be noted that in this text, relational terms such as first and second are only used 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 term "comprising", "including" or any other variant thereof is intended to cover non-exclusive inclusion, so that a process, method, article or device comprising a series of elements includes not only those elements but also other elements not expressly listed, or elements inherent to such process, method, article or device.

[0034] The present invention and its embodiments have been described above. Such description is not restrictive. What is shown in the drawings is only one of the embodiments of the present invention, and the actual structure is not limited thereto. Generally speaking, if those of ordinary skill in the art are inspired by it and, without departing from the gist of the present invention, design similar structural modes and embodiments to this technical solution without creative efforts, they shall fall within the protection scope of the present invention.

Claims

1. A restraint device for neurology nursing, comprising a bed, characterized in that: An upper limb restraint mechanism is provided at one end of the bed body, and a hand restraint assembly and a leg restraint assembly are respectively provided on the bed body, the hand restraint assembly and the leg restraint assembly are respectively arranged symmetrically, the leg restraint assembly is arranged on a side of the hand restraint assembly away from the upper limb restraint mechanism, and a circulating restraint assembly is respectively provided on the hand restraint assembly and the leg restraint assembly; The leg restraint assembly includes a sliding frame, a bracket mechanism and a leg locking mechanism, wherein the sliding frame is symmetrically arranged at the lower part of the bed body, the bracket mechanism is slidably arranged in the sliding frame, and the leg locking mechanism is arranged on the bracket mechanism; The circulating restraint assembly includes a first airbag bag, a second airbag bag and an intermittent inflation mechanism. The first airbag bag and the second airbag bag are symmetrically arranged at the inner ends of the leg locking mechanism and the inner side of the hand restraint assembly, respectively. The intermittent inflation mechanism is respectively arranged on the leg locking mechanism and the hand restraint assembly, and an inflation tube is connected between the intermittent inflation mechanism and the first airbag bag and the second airbag bag, respectively.

2. A restraint device for neurology nursing according to claim 1, characterized in that; The bed body is symmetrically provided with hand movable grooves and leg movable grooves, which respectively penetrate the bed body; the sliding frame is arranged below the leg movable groove, and the leg locking mechanism includes a first bracket, a first cover plate and a first magnet, the first bracket is movably arranged above the leg movable groove, the first cover plate is rotatably arranged on the first bracket, the first magnet is slidably arranged on the outer wall of the first bracket, the first cover plate is provided with a first electromagnetic plate away from its rotating end, the first electromagnetic plate is provided with a groove, and the first electromagnetic plate is movably engaged with the groove.

3. A restraint device for neurology nursing according to claim 2, characterized in that: The bracket mechanism includes a follow-up rotating rod, a limit rotating rod, a telescopic sliding plate, a limit adjustment plate and an adjusting plug rod, the follow-up rotating rod and the limit rotating rod are respectively rotatably arranged at the two ends of the lower part of the first bracket, the limit rotating rod is arranged at one end of the first bracket close to the hand movable groove, the limit rotating rod is penetrated with a limit groove, the follow-up rotating rod and the limit rotating rod are movably arranged in the leg movable groove, the telescopic sliding plate is horizontally arranged at the lower end of the follow-up rotating rod, the telescopic sliding plate is perpendicular to the follow-up rotating rod, the telescopic sliding plate slides on the inner side of the sliding frame, the limit adjustment plate is symmetrically arranged at the telescopic end of the telescopic sliding plate, the limit rotating rod slides on the inner side of the symmetrical limit adjustment plate, the limit adjustment plate is penetrated with adjustment holes evenly distributed, the adjusting plug rod is movably inserted in the adjustment hole, and the adjusting plug rod penetrates the limit groove.

4. A restraint device for neurology nursing according to claim 3, characterized in that: The hand restraint assembly includes a second bracket and a second cover plate, the second bracket is movably arranged above the hand movable slot, and the second cover plate is rotatably arranged on the second bracket; The first airbag bag and the second airbag bag are respectively attached to the two ends of the inner wall of the first bracket and the first cover plate and the two ends of the inner wall of the second bracket and the second cover plate, and the intermittent inflation mechanism is respectively arranged on the upper part of the first cover plate and the second cover plate, and the first airbag bag is connected to the second airbag bag with first insertion bags evenly distributed on the circumference on one side of the first airbag bag, and the second airbag bag is connected to the first airbag bag with second insertion bags evenly distributed on the circumference on one side of the second airbag bag, the first insertion bags and the second insertion bags are staggered in the circumferential direction, and the first insertion bags and the second insertion bags are provided with pressure strips on the inner sides.

5. A restraint device for neurology nursing according to claim 4, characterized in that: The intermittent inflation mechanism comprises a flip motor, a turntable and an air pump. The flip motor is respectively embedded in the upper part of the first cover plate and the second cover plate, the turntable is arranged at the output end of the flip motor, and the air pump is arranged on the upper part of the turntable.

6. A restraint device for neurology nursing according to claim 5, characterized in that: The turntable is provided with a deflation channel and an inflation channel, respectively, the deflation channel and the inflation channel respectively penetrate the side wall and the upper wall of the turntable, the inflation channel is connected with the output end of the air pump, the deflation channel and the inflation channel are respectively connected with symmetrical inflation tubes, the inflation channel is connected with a compression chamber on one side close to the deflation channel, a pneumatic push plate is slidably provided in the compression chamber, a spring is connected between the pneumatic push plate and the inner wall of the compression chamber, a pressure sensor is provided on the inner wall of the compression chamber, and the spring is sleeved on the outer side of the pressure sensor; The deflation channel extends through the upper wall of the turntable to be provided with a deflation pipe, the outer wall of the deflation pipe is penetrated by a deflation groove, and a deflation floating plate is slidably provided in the deflation pipe.

7. A restraint device for neurology nursing according to claim 6, characterized in that: A second magnet is slidably provided on the outer wall of the second bracket, and a second electromagnetic plate is provided on the second cover plate away from its rotating end, and the second magnet is movably engaged with the second electromagnetic plate. The hand restraint assembly also includes a hand pad, a pressure pad, a transition rod, a movable cover, a fixed plate and a fixed plug rod. The hand pad is arranged at the end of the second bracket, the pressure pad is arranged at the end of the second cover plate, the pressure pad is arranged above the hand pad, a nursing groove is penetrated on the inner side of the pressure pad, the transition rod is movably arranged at the lower part of the second bracket, the transition rod slides in the hand movable groove, a reset spring is connected between the transition rod and the inner wall of the hand movable groove, the movable cover is arranged at the lower end of the transition rod, the fixed plate is arranged at the lower part of the bed, the fixed plates are symmetrically arranged on both sides of the hand movable groove, and the fixed plug rod is movably inserted in the fixed plate.

8. A restraint device for neurology nursing according to claim 7, characterized in that: A rotating shaft is rotatably provided on the inner side of the movable cover, a fixed protrusion is provided on the inner side of the rotating shaft, a torsion spring is connected between the rotating shaft and the movable cover, a movable belt is wrapped around the rotating shaft, and the movable belt passes through the interior of the transition rod and is connected to the second bracket; in the initial state, the movable cover is on the inner side of the symmetrical fixed plate, the fixed plug rod passes through the inner side of the rotating shaft, and the upper part of the fixed plug rod is engaged with the fixed protrusion.

9. A restraint device for neurology nursing according to claim 8, characterized in that: The upper limb restriction mechanism comprises a fixed tube, a connecting rod, a telescopic pull plate, a chest and abdominal pressure plate, a pull rod, a restriction plate and a limit bolt. The restriction plate is arranged at the end of the bed body away from the leg movable groove, the restriction plate is L-shaped, and the restriction plate is vertically penetrated with holes evenly distributed, the limit bolt is movably engaged in the hole, the fixed tube is symmetrically sleeved on the end of the bed body, the fixed tube is rotatably connected to the bed body, the connecting rod is arranged on the outer wall of the fixed tube, the chest and abdominal pressure plate is connected to the end of the connecting rod away from the fixed tube, the chest and abdominal pressure plate is arranged in an I-shape, and a cotton pad is provided on the side of the chest and abdominal pressure plate facing the bed body, the telescopic pull plate is arranged on the outer wall of the fixed tube, the telescopic pull plate and the connecting rod are centrally symmetrically arranged, the pull rod is connected to the telescopic end of the telescopic pull plate, the pull rod is rotatably connected to the telescopic pull plate, the pull rod is slidably sleeved on the restriction plate, and the limit bolt passes through the pull rod.

Citation Information

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