Sleep monitoring first-aid device for neurology department

Abstract

The invention belongs to the technical field of medical instruments, particularly relates to a sleep monitoring first-aid device for the neurology department, and aims to solve the problems that in the prior art, first-aid pills are easily clamped in the throat of a patient, and a first-aid scheme is not comprehensive enough, the sleep monitoring first-aid device for the neurology department comprises a bed board, U-shaped frames are slidably connected to the two sides of the bed board, and extrusion rods slidably penetrate through the U-shaped frames; a hollow rotating shaft rotationally penetrates through the interior of the extrusion rod, and pressing plates are fixedly connected to the two ends of the hollow rotating shaft; the cardiopulmonary resuscitation first-aid structure is arranged at the bottom of the pressing plate and used for carrying out cardiopulmonary resuscitation first-aid on According to the first-aid device, cardio-pulmonary resuscitation first aid and click first aid can be sequentially carried out on the patient through pressing the air bag and electric defibrillation, the first-aid function is complete, effective first aid is provided for the patient in time, pills and warm water can be rapidly mixed during first aid, and the first-aid device is convenient to use and high in practicability. The medicine can be safely and stably taken for patients.

Description

Technical Field

[0001] This invention relates to the field of medical device technology, and in particular to a neurological sleep monitoring and emergency device. Background Technology

[0002] Patients in the neurology department often experience myocardial ischemia, myocardial infarction, and corresponding electrocardiogram changes during stroke. They usually present with difficulty breathing and irregular breathing, especially during sleep, and may not receive timely rescue, which can easily lead to sudden death.

[0003] For example, invention publication CN110946721B discloses a neurological sleep monitoring and emergency device, including a bed board, an electroencephalogram (EEG) monitor, an oxygen mask, and a sleep apnea monitor. The EEG monitor is located on one side of the bed board and has an EEG patch. The EEG monitor includes a programmer, an alarm, and a flashing light. The alarm and flashing light are connected to the programmer via wires. The sleep apnea monitor is connected to the EEG monitor via wires. The oxygen mask has an oxygen tube and an outlet tube, with the other end of the oxygen tube connected to the hospital's oxygen supply pipeline. This invention can issue an audible and flashing light alarm when a patient experiences sudden cardiac arrest or a sudden decrease in breathing or heart rate. Simultaneously, it can automatically administer emergency medication and promptly perform cardiac resuscitation, thereby saving the patient's life. This invention is suitable for widespread application.

[0004] The above technical solution still has some shortcomings in its use:

[0005] 1. The above technical solution involves directly placing the emergency pill into the patient's mouth and then performing chest compressions to provide first aid. However, when the patient is in critical condition, it is difficult for the patient to swallow the emergency pill, and the pill is likely to get stuck in the patient's throat. This not only fails to provide first aid but also affects the patient's breathing.

[0006] 2. The above-mentioned technical solution can only perform emergency resuscitation by using an electric push rod to drive the airbag to compress the patient's heart and lungs. When cardiopulmonary resuscitation cannot be effectively performed, other methods cannot be used to effectively resuscitate the patient. Therefore, the emergency resuscitation solution is not comprehensive enough.

[0007] To address the aforementioned problems, this invention proposes a neurological sleep monitoring and emergency device. Summary of the Invention

[0008] This invention provides a neurological sleep monitoring emergency device that solves the shortcomings of existing technologies, such as the ease with which emergency pills can get stuck in a patient's throat and the lack of comprehensive emergency treatment plans.

[0009] This invention provides the following technical solution:

[0010] A neurological sleep monitoring emergency device includes: a bed board, with U-shaped frames slidably connected to both sides of the bed board, a squeezing rod slidably passing through the U-shaped frame, a hollow rotating shaft rotatably passing through the squeezing rod, and pressing plates fixedly connected to both ends of the hollow rotating shaft;

[0011] The cardiopulmonary resuscitation (CPR) emergency device is located at the bottom of the compression plate and is used to perform CPR on patients.

[0012] The defibrillation emergency device is located on top of the compression plate and is used to resuscitate the patient.

[0013] The medication delivery mechanism, located at the top of the U-shaped frame, is used to securely administer emergency pills to the patient.

[0014] In one possible design, the cardiopulmonary resuscitation (CPR) emergency structure includes two compression bags fixedly connected to the bottom of two compression plates, and ventilation tubes fixedly connected to both sides of the bottom of the hollow rotating shaft, with the ventilation tubes communicating with the compression bags. The compression rod has a cavity coaxial with the hollow rotating shaft, and the hollow rotating shaft has multiple through holes communicating with the cavity. The compression rod has a flexible tube communicating with the cavity, with one end of the flexible tube extending to one side of the compression rod. Air is injected into the cavity through the flexible tube, and then the air enters the compression bags through the through holes, the hollow rotating shaft, and the ventilation tubes. The compression bags inflate, and then the compression rod drives the compression bags to move up and down reciprocally to perform CPR on the patient's chest.

[0015] In one possible design, the cardiopulmonary resuscitation (CPR) emergency structure further includes a fixed plate fixedly connected to the top of the U-shaped frame. A gas-storage airbag is fixedly connected to the fixed plate near the compression rod. A compression plate is fixedly connected to the gas-storage airbag near the compression rod, and the compression plate is slidably connected to the top of the U-shaped frame. The end of the hose away from the cavity passes through the compression plate and communicates with the gas-storage airbag. Multiple return springs are fixedly connected between the compression plate and the gas-storage airbag. A trapezoidal block is fixedly connected to the side of the compression rod near the compression plate. When the compression rod and trapezoidal block move downwards, the trapezoidal block compresses the gas-storage airbag through the compression plate. Air from the gas-storage airbag enters the cavity through the hose to inflate the compression airbag, facilitating subsequent emergency treatment of the patient.

[0016] In one possible design, the defibrillation emergency structure includes two defibrillators respectively mounted on top of two compression plates. Two one-way bearings are fitted onto the outer wall of the hollow rotating shaft, and spur gears are fixedly fitted onto the outer wall of each one-way bearing. Two racks are fixedly connected to the bottom of the U-shaped frame, with the racks located on either side of the compression rod and meshing with the spur gears. When the compression rod moves upward to a certain height, the spur gears mesh with the racks, and the one-way bearings and hollow rotating shaft are locked. As the compression rod moves upward, the hollow rotating shaft rotates 180° under the action of the spur gears and racks, switching between the compression bag and the defibrillator. Then, the compression rod drives the compression plates downward, releasing the one-way bearings from the hollow rotating shaft. The compression rod then drives the compression plates and defibrillator downward until the defibrillator is in contact with the patient's chest, and defibrillation is then used to provide emergency treatment.

[0017] In one possible design, the medication feeding structure includes a dissolving tank and an insulated water tank fixedly connected to the top of a U-shaped frame. Multiple heating elements for maintaining water temperature are fixedly connected to the inner wall of the insulated water tank. A water pump is located at the top of the insulated water tank. An inlet pipe extending into the insulated water tank is fixedly fitted onto the inlet of the water pump, and an outlet pipe communicating with the dissolving tank is fixedly fitted onto the outlet of the water pump. A fixing rod is fixedly connected to the side of the extrusion plate away from the extrusion rod. One end of the fixing rod passes through the air storage bladder and the fixing plate and is fixedly connected to a nut plate. A stirring rod rotatably passes through the dissolving tank, and a [missing information - likely a device or component] is fixedly connected to the outer wall of the stirring rod. Multiple stirring blades are located in the dissolving tank. The outer wall of the stirring rod is provided with a threaded section, and the stirring rod is threadedly connected to the nut plate through the threaded section. A storage box for dispensing emergency pills into the dissolving tank is fixedly connected to the top of the dissolving tank. Warm water from an insulated water tank is pumped into the dissolving tank by a water pump. When the trapezoidal block squeezes the extrusion plate, the extrusion plate pushes the nut plate to the left side through a fixed rod. The nut plate is threadedly connected to the stirring rod. When the nut plate moves, the stirring rod rotates. The stirring rod can fully mix the emergency pills dispensed from the storage box with the warm water, enabling the emergency pills to be absorbed quickly and effectively by the patient, avoiding the risk of the emergency pills getting stuck in the throat.

[0018] In one possible design, a baffle is fixedly connected to one inner wall of the storage box, and a lead screw is threaded through the other side of the storage box. A guide rod and a sliding rod are slidably connected to both ends of the lead screw. A grinding plate for crushing emergency pills is fixedly connected to one end of the guide rod near the baffle, and a third spring is fixedly connected to the other end of the guide rod. The other end of the third spring is fixedly connected to one inner wall of the lead screw. The sliding rod drives the lead screw to rotate, and the lead screw drives the grinding plate to rotate and move to the left. The grinding plate and the baffle cooperate to crush the emergency pills on the plate. The crushed emergency pills can be quickly dissolved in the warm water pumped into the dissolving tank, so that the patient can be given emergency medication safely and reliably in a timely manner.

[0019] In one possible design, the inner walls of the storage box on both sides away from each other are provided with grooves. A single placement plate for holding the emergency pills is slidably connected within the two grooves, and the top of the placement plate slides into the bottom of the baffle. A fourth spring is fixedly connected to the inner wall of the two grooves on the side away from the grinding plate, and the other end of the fourth spring is fixedly connected to the placement plate. The emergency pills are placed between the baffle and the grinding plate, and the placement plate is positioned between the baffle and the grinding plate to hold the emergency pills. When the grinding plate crushes the emergency pills, it pushes the placement plate to the left and below the baffle. The baffle can then scrape off any residual powder at the bottom of the placement plate, preventing powder residue from causing insufficient efficacy.

[0020] In one possible design, a gearbox is fixedly connected to the top of the dissolving tank, and a first synchronous pulley is fixedly connected to the output shaft of the gearbox. A second synchronous pulley is fixedly sleeved on the outer wall of the stirring rod. The first and second synchronous pulleys are connected by a synchronous belt. The output shaft of the gearbox is fixedly connected to a sliding rod. A liquid guide tube is fixedly connected to the bottom of the dissolving tank, and a solenoid valve is sleeved on the outer wall of the liquid guide tube. The bottom end of the dissolving tank is connected to a drug storage tube. When the fixed rod pushes the nut plate to move, the nut plate cooperates with the stirring rod to drive the stirring rod to rotate. The gearbox can make reasonable use of the stirring rod's rotation speed through the cooperation of the first synchronous pulley, the second synchronous pulley, and the synchronous belt to reasonably drive the sliding rod to rotate, crushing the emergency pills. The mixture of the pills and warm water is injected into the drug storage tube through the liquid guide tube for easy administration by the patient later.

[0021] In one possible design, a screw is rotatably connected to the top of the U-shaped frame via a base. A nut block is threaded onto the outer wall of the screw and slidably connected to the top of the U-shaped frame. A connecting rod is rotatably connected to the top of the nut block, and the top of the connecting rod is rotatably connected to one side of the compression rod. A drive motor is fixedly connected to the top of the U-shaped frame, and the output shaft of the drive motor is fixedly connected to one end of the screw. The drive motor drives the screw to rotate, the screw drives the nut block to rotate, and the nut block drives the compression rod to move up and down via the connecting rod. This allows control of the cardiopulmonary resuscitation (CPR) and defibrillation emergency structures to provide emergency care to patients. It also allows emergency pills to dissolve quickly in warm water, facilitating safe administration to patients.

[0022] In one possible design, a plurality of first springs are fixedly connected to the bottom inner wall of the pressure plate, the top ends of which are fixedly connected to the bottom of the defibrillator, which is slidably connected within the pressure plate. A second spring is fixedly connected to the bottom of the defibrillator, and a pressure plate is fixedly connected to the bottom end of the second spring. A pressure sensor is fixedly connected to the bottom inner wall of the pressure plate, and the pressure sensor cooperates with the pressure plate. When the squeezing rod moves the pressure plate and the defibrillator downward, the defibrillator initially contacts the patient's chest. The squeezing rod moves the pressure plate further downward. The first springs act as a buffer for the defibrillator, preventing it from squeezing the patient. As the pressure plate moves downward, the pressure plate exerts a certain squeezing force on the pressure sensor under the action of the second spring. When the pressure signal detected by the pressure sensor reaches a certain value, the defibrillator is activated to provide emergency treatment to the patient.

[0023] It should be understood that the above general description and the following detailed description are merely exemplary and do not limit the invention.

[0024] In this invention, two one-way bearings are fitted on the outer wall of the hollow rotating shaft, and spur gears are fixedly fitted on the outer wall of the one-way bearings. Two racks are fixedly connected to the bottom of the U-shaped frame. The spur gears mesh with the racks, and the one-way bearings and the hollow rotating shaft are locked. When the squeezing rod moves upward, the hollow rotating shaft rotates 180° under the action of the spur gears and racks, switching between the airbag and defibrillation. Then, the squeezing rod drives the squeezing plate downward, at which point the one-way bearings and the hollow rotating shaft are unlocked. Then, the squeezing rod drives the defibrillator downward until it is in contact with the patient's chest. Then, the patient is given first aid through defibrillation.

[0025] In this invention, a gas-storing airbag is fixedly connected to the side of the fixed plate near the squeezing rod, and a squeezing plate is fixedly connected to the side of the gas-storing airbag near the squeezing rod. The end of the hose away from the cavity passes through the squeezing plate and communicates with the gas-storing airbag. A fixed rod passing through the fixed plate and the gas-storing airbag is fixedly connected to one side of the squeezing plate. A trapezoidal block is fixedly connected to the side of the squeezing rod near the squeezing plate. The squeezing rod and the trapezoidal block move downward, and the trapezoidal block squeezes the gas-storing airbag through the squeezing plate to inflate the airbag for later emergency treatment of the patient. The movement of the squeezing plate can also drive the medication delivery structure to turn the emergency pill into a liquid medicine for safe and reliable administration to the patient.

[0026] In this invention, a stirring rod is rotatably inserted inside the dissolving tank. The stirring rod is threadedly connected to a nut plate via a threaded section. A lead screw is threaded through the other side of the storage tank. One end of the lead screw is slidably connected to a grinding plate via a guide rod, and the other end of the lead screw is slidably connected to a sliding rod. The movement of the nut plate drives the stirring rod to rotate, which in turn drives the lead screw to rotate. The lead screw is used to crush the pills, and the stirring rod can quickly mix the crushed pills with warm water, enabling the rapid, safe, and reliable administration of emergency medication to patients.

[0027] In this invention, a plurality of first springs are fixedly connected to the bottom inner wall of the pressing plate, and the top ends of the plurality of first springs are fixedly connected to the bottom of the defibrillator. A second spring is fixedly connected to the bottom of the defibrillator, and a pressing plate is fixedly connected to the bottom end of the second spring. A pressure sensor is fixedly connected to the bottom inner wall of the pressing plate. When the squeezing rod moves the pressing plate and the defibrillator downward, the first springs buffer the defibrillator to prevent it from squeezing the patient. The squeezing force generated by the pressing plate on the pressure sensor under the action of the second spring reaches a certain value, and when it reaches a certain value, the defibrillator provides emergency treatment to the patient, enabling timely emergency treatment.

[0028] In this invention, cardiopulmonary resuscitation and defibrillation can be performed on the patient sequentially by pressing the airbag and then by applying a defibrillator. The emergency rescue functions are relatively complete, providing timely and effective emergency care to the patient. In addition, during emergency care, the pills can be quickly mixed with warm water to safely and reliably administer the medication to the patient, avoiding the risk of the medication getting stuck in the throat and being unable to be taken by the patient. Attached Figure Description

[0029] Figure 1 This is a three-dimensional structural diagram of a neurological sleep monitoring and emergency device provided in Embodiment 1 of the present invention;

[0030] Figure 2 This is a three-dimensional exploded view of the U-shaped frame of a neurological sleep monitoring and emergency device provided in Embodiment 1 of the present invention;

[0031] Figure 3 This is a three-dimensional cross-sectional view of the squeezing rod of a neurological sleep monitoring emergency device provided in Embodiment 1 of the present invention;

[0032] Figure 4 This is a three-dimensional cross-sectional view of the hollow rotating shaft, spur gear, and one-way bearing of a neurological sleep monitoring and emergency device provided in Embodiment 1 of the present invention.

[0033] Figure 5 This is a three-dimensional exploded structural diagram of the spur gear, rack, and one-way bearing of a neurological sleep monitoring emergency device provided in Embodiment 1 of the present invention;

[0034] Figure 6 This is a three-dimensional cross-sectional exploded structural diagram of the defibrillator, pressure plate, and pressure airbag of a neurological sleep monitoring emergency device provided in Embodiment 1 of the present invention.

[0035] Figure 7 This is a three-dimensional cross-sectional view of the dissolution box, air storage bag, and fixing plate of a neurological sleep monitoring emergency device provided in Embodiment 1 of the present invention.

[0036] Figure 8 This is a three-dimensional cross-sectional view of the dissolution box and storage box of a neurological sleep monitoring emergency device provided in Embodiment 1 of the present invention;

[0037] Figure 9 This is a three-dimensional cross-sectional view of the storage box, grinding plate, and baffle of a neurological sleep monitoring emergency device provided in Embodiment 1 of the present invention.

[0038] Figure 10 This is a three-dimensional cross-sectional view of the lead screw of a neurological sleep monitoring and emergency device provided in Embodiment 1 of the present invention;

[0039] Figure 11 This is a three-dimensional cross-sectional view of the insulated water tank of a neurological sleep monitoring emergency device provided in Embodiment 1 of the present invention;

[0040] Figure 12 This is a three-dimensional exploded cross-sectional view of the defibrillator, pressure plate, and cavity of a neurological sleep monitoring emergency device provided in Embodiment 2 of the present invention.

[0041] Figure label:

[0042] 1. Bed board; 2. U-shaped frame; 3. Compression rod; 4. Screw; 5. Nut block; 6. Connecting rod; 7. Drive motor; 8. Hollow rotating shaft; 9. Pressing plate; 10. Pressing airbag; 11. Ventilation tube; 12. Cavity; 13. Through hole; 14. Hose; 15. Fixing plate; 16. Compression plate; 17. Air storage airbag; 18. One-way bearing; 19. Spur gear; 20. Rack; 21. Defibrillator; 22. First spring; 23. Second spring; 24. Pressing plate; 25. Pressure sensor; 26. Insulated water tank; 27. Water 28. Pump; 29. ​​Inlet pipe; 30. Outlet pipe; 31. Dissolving tank; 32. Stirring rod; 33. Guide pipe; 34. Nut plate; 35. Fixing rod; 36. Gearbox; 37. First synchronous pulley; 38. Second synchronous pulley; 39. Synchronous belt; 40. Storage tank; 41. Baffle; 42. Lead screw; 43. Sliding rod; 44. Guide rod; 45. Grinding plate; 46. Third spring; 47. Slide groove; 48. Placement plate; 49. Fourth spring; 50. Heating element; 51. Solenoid valve; 52. Trapezoidal block; 53. Return spring. Detailed Implementation

[0043] The embodiments of the present invention will now be described with reference to the accompanying drawings.

[0044] In the description of the embodiments of the present invention, it should be noted that, unless otherwise explicitly specified and limited, the terms "connection" and "installation" should be interpreted broadly. For example, "connection" can be a detachable connection or a non-detachable connection; it can be a direct connection or an indirect connection through an intermediate medium. Furthermore, "connection" can be a direct connection or an indirect connection through an intermediate medium. "Fixed" means that the devices are connected to each other and their relative positional relationship remains unchanged after the connection. The directional terms mentioned in the embodiments of the present invention, such as "inner," "outer," "top," and "bottom," are only for reference to the directions in the accompanying drawings. Therefore, the directional terms used are for better and clearer explanation and understanding of the embodiments of the present invention, and are not intended to indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, they should not be construed as limitations on the embodiments of the present invention.

[0045] In this embodiment of the invention, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of indicated technical features. Therefore, a feature defined with "first" and "second" may explicitly or implicitly include one or more of that feature.

[0046] In this embodiment of the invention, "and / or" is merely a description of the relationship between related objects, indicating that three relationships can exist. For example, A and / or B can represent three cases: A existing alone, A and B existing simultaneously, and B existing alone. Additionally, the character " / " in this document generally indicates that the preceding and following related objects have an "or" relationship.

[0047] References to "one embodiment" or "some embodiments" as used in this specification mean that a particular feature, structure, or characteristic described in connection with that embodiment is included in one or more embodiments of the invention. Therefore, the phrases "in one embodiment," "in some embodiments," "in other embodiments," "in still other embodiments," etc., appearing in different parts of this specification do not necessarily refer to the same embodiment, but rather mean "one or more, but not all, embodiments," unless otherwise specifically emphasized. The terms "comprising," "including," "having," and variations thereof mean "including, but not limited to," unless otherwise specifically emphasized.

[0048] Example 1

[0049] Reference Figures 1-11This embodiment of a neurological sleep monitoring emergency device includes a bed board 1, with a U-shaped frame 2 slidably connected to both sides of the bed board 1. A compression rod 3 slides through the U-shaped frame 2, and a hollow rotating shaft 8 rotatably passes through the compression rod 3. Both ends of the hollow rotating shaft 8 are fixedly connected to a pressing plate 9 by bolts. A cardiopulmonary resuscitation (CPR) emergency structure is located at the bottom of the pressing plate 9 for performing CPR on the patient. A defibrillation emergency structure is located at the top of the pressing plate 9 for performing emergency treatment on the patient again. A medication delivery structure is located at the top of the U-shaped frame 2 for securely administering emergency medication to the patient.

[0050] Reference Figure 2 , Figure 3 and Figure 4 The cardiopulmonary resuscitation (CPR) emergency structure includes two compression bags 10 fixedly connected to the bottom of two compression plates 9 by bolts. Air tubes 11 are fixedly connected to both sides of the bottom of a hollow rotating shaft 8, and the air tubes 11 are connected to the compression bags 10. A cavity 12 coaxial with the hollow rotating shaft 8 is provided inside the compression rod 3. Multiple through holes 13 connected to the cavity 12 are provided inside the hollow rotating shaft 8. A flexible hose 14 connected to the cavity 12 is provided inside the compression rod 3, with one end of the hose 14 extending to one side of the compression rod 3. Air is injected into the cavity 12 through the hose 14, and then the air enters the compression bags 10 through the through holes 13, the hollow rotating shaft 8, and the air tubes 11. The compression bags 10 inflate, and then the compression rod 3 drives the compression bags 10 to move up and down repeatedly to perform CPR on the patient's chest.

[0051] Reference Figure 2 , Figure 3 , Figure 4 and Figure 7 The cardiopulmonary resuscitation (CPR) emergency structure also includes a fixing plate 15 bolted to the top of the U-shaped frame 2. A gas-storage airbag 17 is fixedly connected to the side of the fixing plate 15 near the compression rod 3. A compression plate 16 is fixedly connected to the side of the gas-storage airbag 17 near the compression rod 3, and the compression plate 16 is slidably connected to the top of the U-shaped frame 2. The end of the hose 14 away from the cavity 12 passes through the compression plate 16 and is connected to the gas-storage airbag 17. Multiple return springs 52 are fixedly connected between the compression plate 16 and the gas-storage airbag 17. A trapezoidal block 51 is bolted to the side of the compression rod 3 near the compression plate 16. When the compression rod 3 and the trapezoidal block 51 move down, the trapezoidal block 51 compresses the gas-storage airbag 17 through the compression plate 16. The air in the gas-storage airbag 17 enters the cavity 12 through the hose 14 to inflate the compression airbag 10 for later emergency treatment of the patient.

[0052] Reference Figure 2 , Figure 3 , Figure 4 , Figure 5 and Figure 6The defibrillation emergency structure includes two defibrillators 21 respectively installed on top of two compression plates 9. Two one-way bearings 18 are fitted onto the outer wall of the hollow rotating shaft 8. A spur gear 19 is fixedly fitted onto the outer wall of each one-way bearing 18. Two racks 20 are bolted to the bottom of the U-shaped frame 2, and the racks 20 are located on both sides of the compression rod 3. The racks 20 mesh with the spur gear 19. When the compression rod 3 moves to a certain height, the spur gear 19 meshes with the racks 20, at which point the one-way bearings... 18 is locked to the hollow rotating shaft 8. As the squeezing rod 3 moves upward, the hollow rotating shaft 8 rotates 180° under the action of the spur gear 19 and the rack 20, switching the compression bag 10 and the defibrillator 21. Then, the squeezing rod 3 drives the compression plate 9 to move downward. At this time, the one-way bearing 18 is unlocked from the hollow rotating shaft 8. Then, the squeezing rod 3 drives the compression plate 9 and the defibrillator 21 to move downward until the defibrillator 21 is in contact with the patient's chest. Then, the patient is given first aid through the defibrillator 21.

[0053] Reference Figure 2 , Figure 7 , Figure 8 , Figure 9 and Figure 11 The feeding structure includes a dissolving tank 30 and an insulated water tank 26, which are bolted to the top of the U-shaped frame 2. Multiple heating elements 49 for maintaining water temperature are bolted to the inner wall of the insulated water tank 26. A water pump 27 is located on the top of the insulated water tank 26. An inlet pipe 28 extending into the insulated water tank 26 is fixedly fitted to the inlet of the water pump 27, and an outlet pipe 29 connected to the dissolving tank 30 is fixedly fitted to the outlet of the water pump 27. A fixing rod 34 is bolted to the side of the extrusion plate 16 away from the extrusion rod 3. One end of the fixing rod 34 passes through the air storage bladder 17 and the fixing plate 15 and is bolted to a nut plate 33. A stirring rod 31 rotates through the dissolving tank 30. Multiple heating elements located on the outer wall of the stirring rod 31 are fixedly connected to the outer wall of the dissolving tank 30. The dissolving tank 30 has stirring blades, and the outer wall of the stirring rod 31 is provided with a threaded section. The stirring rod 31 is threadedly connected to the nut plate 33 through the threaded section. The top of the dissolving tank 30 is fixedly connected to a storage box 39 for dispensing emergency pills into the dissolving tank 30 by bolts. The warm water pump 27 in the insulated water tank 26 is pumped into the dissolving tank 30 by the water pump 27. When the trapezoidal block 51 squeezes the squeezing plate 16, the squeezing plate 16 pushes the nut plate 33 to the left side through the fixing rod 34. The nut plate 33 is threadedly connected to the stirring rod 31. When the nut plate 33 moves, the stirring rod 31 rotates. The stirring rod 31 can fully mix the emergency pills dispensed from the storage box 39 with the warm water, so that the emergency pills can be absorbed by the patient quickly and effectively, avoiding the risk of the emergency pills getting stuck in the throat.

[0054] Reference Figure 8 , Figure 9 and Figure 10A baffle 40 is bolted to one inner wall of the storage box 39. A screw rod 41 is threaded through the other side of the storage box 39. A guide rod 43 and a sliding rod 42 are slidably connected to both ends of the screw rod 41. A grinding plate 44 for crushing emergency pills is bolted to one end of the guide rod 43 near the baffle 40. A third spring 45 is fixedly connected to the other end of the guide rod 43, and the other end of the third spring 45 is fixedly connected to one inner wall of the screw rod 41. The sliding rod 42 drives the screw rod 41 to rotate, and the screw rod 41 drives the grinding plate 44 to rotate and move to the left. The grinding plate 44 and the baffle 40 cooperate to crush the emergency pills on the placement plate 47. The crushed emergency pills can be quickly dissolved in the warm water pumped into the dissolving tank 30, so that the patient can take emergency medication safely and reliably in a timely manner.

[0055] Reference Figure 9 The storage box 39 has grooves 46 on its two outer walls that are far apart from each other. A single placement plate 47 for holding the emergency pills is slidably connected in the two grooves 46. The top of the placement plate 47 is slidably engaged with the bottom of the baffle 40. A fourth spring 48 is fixedly connected to the inner wall of the two grooves 46 on the side away from the grinding plate 44. The other end of the fourth spring 48 is fixedly connected to the placement plate 47. The emergency pills are placed between the baffle 40 and the grinding plate 44. The placement plate 47 is located between the baffle 40 and the grinding plate 44 to hold the emergency pills. When the grinding plate 44 crushes the emergency pills, it pushes the placement plate 47 to the left and below the baffle 40. The baffle 40 can scrape off the residual powder at the bottom of the placement plate 47 to avoid powder residue and insufficient efficacy.

[0056] Reference Figure 7 , Figure 8 and Figure 10 The top of the dissolving tank 30 is bolted to a gearbox 35, the output shaft of which is fixedly connected to a first synchronous pulley 36. A second synchronous pulley 37 is fixedly sleeved on the outer wall of the stirring rod 31. The first synchronous pulley 36 and the second synchronous pulley 37 are connected by a synchronous belt 38. The output shaft of the gearbox 35 is fixedly connected to the sliding rod 42 by a coupling. A liquid guide tube 32 is fixedly connected to the bottom of the dissolving tank 30, and a solenoid valve 50 is sleeved on the outer wall of the liquid guide tube 32. The bottom end of the dissolving tank 30 is connected to the drug storage tube. When the fixed rod 34 pushes the nut plate 33 to move, the nut plate 33 cooperates with the stirring rod 31 to drive the stirring rod 31 to rotate. The gearbox 35 can make reasonable use of the rotation speed of the stirring rod 31 through the cooperation of the first synchronous pulley 36, the second synchronous pulley 37 and the synchronous belt 38 to reasonably drive the sliding rod 42 to rotate, crush the emergency pills, and inject the mixture of pills and warm water into the drug storage tube through the liquid guide tube 32 for later patient administration.

[0057] Reference Figure 2 and Figure 3The top of the U-shaped frame 2 is rotatably connected to a screw 4 via a base. A nut block 5 is threaded onto the outer wall of the screw 4 and slidably connected to the top of the U-shaped frame 2. A connecting rod 6 is rotatably connected to the top of the nut block 5, and the top of the connecting rod 6 is rotatably connected to one side of the compression rod 3. A drive motor 7 is fixedly connected to the top of the U-shaped frame 2 via bolts, and the output shaft of the drive motor 7 is fixedly connected to one end of the screw 4 via a coupling. The drive motor 7 drives the screw 4 to rotate, the screw 4 drives the nut block 5 to rotate, and the nut block 5 drives the compression rod 3 to move up and down via the connecting rod 6. This allows control of the cardiopulmonary resuscitation and defibrillation emergency structures to provide emergency care for patients. It also allows emergency pills to dissolve quickly in warm water, making it convenient for patients to take them safely.

[0058] Example 2

[0059] Reference Figures 1-12 This embodiment of a neurological sleep monitoring emergency device includes a bed board 1, with a U-shaped frame 2 slidably connected to both sides of the bed board 1. A compression rod 3 slides through the U-shaped frame 2, and a hollow rotating shaft 8 rotatably passes through the compression rod 3. Both ends of the hollow rotating shaft 8 are fixedly connected to a pressing plate 9 by bolts. A cardiopulmonary resuscitation (CPR) emergency structure is located at the bottom of the pressing plate 9 for performing CPR on the patient. A defibrillation emergency structure is located at the top of the pressing plate 9 for performing emergency treatment on the patient again. A medication delivery structure is located at the top of the U-shaped frame 2 for securely administering emergency medication to the patient.

[0060] Reference Figure 2 , Figure 3 and Figure 4 The cardiopulmonary resuscitation (CPR) emergency structure includes two compression bags 10 fixedly connected to the bottom of two compression plates 9 by bolts. Air tubes 11 are fixedly connected to both sides of the bottom of a hollow rotating shaft 8, and the air tubes 11 are connected to the compression bags 10. A cavity 12 coaxial with the hollow rotating shaft 8 is provided inside the compression rod 3. Multiple through holes 13 connected to the cavity 12 are provided inside the hollow rotating shaft 8. A flexible hose 14 connected to the cavity 12 is provided inside the compression rod 3, with one end of the hose 14 extending to one side of the compression rod 3. Air is injected into the cavity 12 through the hose 14, and then the air enters the compression bags 10 through the through holes 13, the hollow rotating shaft 8, and the air tubes 11. The compression bags 10 inflate, and then the compression rod 3 drives the compression bags 10 to move up and down repeatedly to perform CPR on the patient's chest.

[0061] Reference Figure 2 , Figure 3 , Figure 4 and Figure 7The cardiopulmonary resuscitation (CPR) emergency structure also includes a fixing plate 15 bolted to the top of the U-shaped frame 2. A gas-storage airbag 17 is fixedly connected to the side of the fixing plate 15 near the compression rod 3. A compression plate 16 is fixedly connected to the side of the gas-storage airbag 17 near the compression rod 3, and the compression plate 16 is slidably connected to the top of the U-shaped frame 2. The end of the hose 14 away from the cavity 12 passes through the compression plate 16 and is connected to the gas-storage airbag 17. Multiple return springs 52 are fixedly connected between the compression plate 16 and the gas-storage airbag 17. A trapezoidal block 51 is bolted to the side of the compression rod 3 near the compression plate 16. When the compression rod 3 and the trapezoidal block 51 move down, the trapezoidal block 51 compresses the gas-storage airbag 17 through the compression plate 16. The air in the gas-storage airbag 17 enters the cavity 12 through the hose 14 to inflate the compression airbag 10 for later emergency treatment of the patient.

[0062] Reference Figure 2 , Figure 3 , Figure 4 , Figure 5 and Figure 6 The defibrillation emergency structure includes two defibrillators 21 respectively installed on top of two compression plates 9. Two one-way bearings 18 are fitted onto the outer wall of the hollow rotating shaft 8. A spur gear 19 is fixedly fitted onto the outer wall of each one-way bearing 18. Two racks 20 are bolted to the bottom of the U-shaped frame 2, and the racks 20 are located on both sides of the compression rod 3. The racks 20 mesh with the spur gear 19. When the compression rod 3 moves to a certain height, the spur gear 19 meshes with the racks 20, at which point the one-way bearings... 18 is locked to the hollow rotating shaft 8. As the squeezing rod 3 moves upward, the hollow rotating shaft 8 rotates 180° under the action of the spur gear 19 and the rack 20, switching the compression bag 10 and the defibrillator 21. Then, the squeezing rod 3 drives the compression plate 9 to move downward. At this time, the one-way bearing 18 is unlocked from the hollow rotating shaft 8. Then, the squeezing rod 3 drives the compression plate 9 and the defibrillator 21 to move downward until the defibrillator 21 is in contact with the patient's chest. Then, the patient is given first aid through the defibrillator 21.

[0063] Reference Figure 2 , Figure 7 , Figure 8 , Figure 9 and Figure 11The feeding structure includes a dissolving tank 30 and an insulated water tank 26, which are bolted to the top of the U-shaped frame 2. Multiple heating elements 49 for maintaining water temperature are bolted to the inner wall of the insulated water tank 26. A water pump 27 is located on the top of the insulated water tank 26. An inlet pipe 28 extending into the insulated water tank 26 is fixedly fitted to the inlet of the water pump 27, and an outlet pipe 29 connected to the dissolving tank 30 is fixedly fitted to the outlet of the water pump 27. A fixing rod 34 is bolted to the side of the extrusion plate 16 away from the extrusion rod 3. One end of the fixing rod 34 passes through the air storage bladder 17 and the fixing plate 15 and is bolted to a nut plate 33. A stirring rod 31 rotates through the dissolving tank 30. Multiple heating elements located on the outer wall of the stirring rod 31 are fixedly connected to the outer wall of the dissolving tank 30. The dissolving tank 30 has stirring blades, and the outer wall of the stirring rod 31 is provided with a threaded section. The stirring rod 31 is threadedly connected to the nut plate 33 through the threaded section. The top of the dissolving tank 30 is fixedly connected to a storage box 39 for dispensing emergency pills into the dissolving tank 30 by bolts. The warm water pump 27 in the insulated water tank 26 is pumped into the dissolving tank 30 by the water pump 27. When the trapezoidal block 51 squeezes the squeezing plate 16, the squeezing plate 16 pushes the nut plate 33 to the left side through the fixing rod 34. The nut plate 33 is threadedly connected to the stirring rod 31. When the nut plate 33 moves, the stirring rod 31 rotates. The stirring rod 31 can fully mix the emergency pills dispensed from the storage box 39 with the warm water, so that the emergency pills can be absorbed by the patient quickly and effectively, avoiding the risk of the emergency pills getting stuck in the throat.

[0064] Reference Figure 8 , Figure 9 and Figure 10 A baffle 40 is bolted to one inner wall of the storage box 39. A screw rod 41 is threaded through the other side of the storage box 39. A guide rod 43 and a sliding rod 42 are slidably connected to both ends of the screw rod 41. A grinding plate 44 for crushing emergency pills is bolted to one end of the guide rod 43 near the baffle 40. A third spring 45 is fixedly connected to the other end of the guide rod 43, and the other end of the third spring 45 is fixedly connected to one inner wall of the screw rod 41. The sliding rod 42 drives the screw rod 41 to rotate, and the screw rod 41 drives the grinding plate 44 to rotate and move to the left. The grinding plate 44 and the baffle 40 cooperate to crush the emergency pills on the placement plate 47. The crushed emergency pills can be quickly dissolved in the warm water pumped into the dissolving tank 30, so that the patient can take emergency medication safely and reliably in a timely manner.

[0065] Reference Figure 9The storage box 39 has grooves 46 on its two outer walls that are far apart from each other. A single placement plate 47 for holding the emergency pills is slidably connected in the two grooves 46. The top of the placement plate 47 is slidably engaged with the bottom of the baffle 40. A fourth spring 48 is fixedly connected to the inner wall of the two grooves 46 on the side away from the grinding plate 44. The other end of the fourth spring 48 is fixedly connected to the placement plate 47. The emergency pills are placed between the baffle 40 and the grinding plate 44. The placement plate 47 is located between the baffle 40 and the grinding plate 44 to hold the emergency pills. When the grinding plate 44 crushes the emergency pills, it pushes the placement plate 47 to the left and below the baffle 40. The baffle 40 can scrape off the residual powder at the bottom of the placement plate 47 to avoid powder residue and insufficient efficacy.

[0066] Reference Figure 7 , Figure 8 and Figure 10 The top of the dissolving tank 30 is bolted to a gearbox 35, the output shaft of which is fixedly connected to a first synchronous pulley 36. A second synchronous pulley 37 is fixedly sleeved on the outer wall of the stirring rod 31. The first synchronous pulley 36 and the second synchronous pulley 37 are connected by a synchronous belt 38. The output shaft of the gearbox 35 is fixedly connected to the sliding rod 42 by a coupling. A liquid guide tube 32 is fixedly connected to the bottom of the dissolving tank 30, and a solenoid valve 50 is sleeved on the outer wall of the liquid guide tube 32. The bottom end of the dissolving tank 30 is connected to the drug storage tube. When the fixed rod 34 pushes the nut plate 33 to move, the nut plate 33 cooperates with the stirring rod 31 to drive the stirring rod 31 to rotate. The gearbox 35 can make reasonable use of the rotation speed of the stirring rod 31 through the cooperation of the first synchronous pulley 36, the second synchronous pulley 37 and the synchronous belt 38 to reasonably drive the sliding rod 42 to rotate, crush the emergency pills, and inject the mixture of pills and warm water into the drug storage tube through the liquid guide tube 32 for later patient administration.

[0067] Reference Figure 2 and Figure 3 The top of the U-shaped frame 2 is rotatably connected to a screw 4 via a base. A nut block 5 is threaded onto the outer wall of the screw 4 and slidably connected to the top of the U-shaped frame 2. A connecting rod 6 is rotatably connected to the top of the nut block 5, and the top of the connecting rod 6 is rotatably connected to one side of the compression rod 3. A drive motor 7 is fixedly connected to the top of the U-shaped frame 2 via bolts, and the output shaft of the drive motor 7 is fixedly connected to one end of the screw 4 via a coupling. The drive motor 7 drives the screw 4 to rotate, the screw 4 drives the nut block 5 to rotate, and the nut block 5 drives the compression rod 3 to move up and down via the connecting rod 6. This allows control of the cardiopulmonary resuscitation and defibrillation emergency structures to provide emergency care for patients. It also allows emergency pills to dissolve quickly in warm water, making it convenient for patients to take them safely.

[0068] Reference Figure 6 and Figure 8Multiple first springs 22 are fixedly connected to the bottom inner wall of the compression plate 9. The top ends of the multiple first springs 22 are fixedly connected to the bottom of the defibrillator 21, and the defibrillator 21 is slidably connected inside the compression plate 9. A second spring 23 is fixedly connected to the bottom of the defibrillator 21, and a compression plate 24 is fixedly connected to the bottom end of the second spring 23. A pressure sensor 25 is fixedly connected to the bottom inner wall of the compression plate 9 by bolts, and the pressure sensor 25 cooperates with the compression plate 24. When the squeezing rod 3 moves the compression plate 9 and the defibrillator 21 downward, the defibrillator 21 initially contacts the patient's chest. The squeezing rod 3 moves the compression plate 9 further downward. The first springs 22 buffer the defibrillator 21 to prevent it from squeezing the patient. As the compression plate 9 moves downward, the compression plate 24 exerts a certain squeezing force on the pressure sensor 25 under the action of the second spring 23. When the pressure signal detected by the pressure sensor 25 reaches a certain value, the defibrillator 21 is activated to provide emergency treatment to the patient.

[0069] Instructions for use of a neurological sleep monitoring emergency device:

[0070] S1. The device monitors the patient's core sleep parameters such as blood oxygen, heart rate, and nasal breathing airflow. The principle of this invention is consistent with that of CN110946721B, so it will not be elaborated here. When the patient needs emergency treatment, the drive motor 7 drives the screw 4 to rotate. The screw 4 drives the nut block 5 to rotate. The nut block 5 drives the compression rod 3 and the trapezoidal block 51 to move down through the connecting rod 6. The trapezoidal block 51 compresses the air storage bag 17 through the compression plate 16. The air in the air storage bag 17 enters the cavity 12 through the hose 14. Then the air enters the compression bag 10 through the through hole 13, the hollow rotating shaft 8 and the ventilation tube 11. The compression bag 10 inflates. Then the compression rod 3 drives the compression bag 10 to move up and down repeatedly to perform cardiopulmonary resuscitation on the patient's chest.

[0071] S2, the water pump 27 pumps the pre-stored warm water in the insulated water tank 26 into the dissolving tank 30. When the trapezoidal block 51 squeezes the extrusion plate 16, the extrusion plate 16 pushes the nut plate 33 to the left side through the fixing rod 34. The nut plate 33 is threadedly connected to the stirring rod 31. When the nut plate 33 moves, the stirring rod 31 rotates. The stirring rod 31 drives the sliding rod 42 to rotate through the first synchronous wheel 36, the second synchronous wheel 37, the synchronous belt 38, and the gearbox 35. The sliding rod 42 drives the lead screw 41 and the grinding plate 44 to rotate. The lead screw 41 drives the grinding plate 44 to rotate and move to the left. The grinding plate 44 cooperates with the baffle 40 to crush the emergency pills on the placement plate 47. When the grinding plate 44 moves, it pushes the placement plate 47 to the left and below the baffle 40. The baffle 40 can just scrape off the residual powder at the bottom of the placement plate 47 to avoid powder residue and insufficient efficacy.

[0072] S3. The powder falls and mixes with the crystal in the dissolving tank 30. In addition, the nut plate 33 drives the stirring rod 31 to rotate, which can quickly mix the powder with warm water to form a medicine solution. Then, the solenoid valve 50 is opened, and the medicine solution is injected into the patient's mouth through the liquid guide tube 32 and the medicine storage tube (the medicine storage tube is a component in the invention with announcement number CN110946721B, which is not shown here). By crushing the emergency pill and mixing it with warm water, the emergency pill can be quickly and effectively absorbed by the patient, avoiding the risk of the emergency pill getting stuck in the throat.

[0073] S4. When the emergency pills and the compression bag 10 cannot effectively perform cardiopulmonary resuscitation, the screw 4 rotates, driving the compression rod 3 upward through the nut block 5 and the connecting rod 6. When the compression rod 3 moves to a certain height, the spur gear 19 meshes with the rack 20. At this time, the one-way bearing 18 and the hollow shaft 8 are locked. As the compression rod 3 moves upward, the hollow shaft 8 rotates 180° under the action of the spur gear 19 and the rack 20, switching the compression bag 10 and the defibrillator 21. Then, the compression rod 3 drives the compression plate 9 downward. At this time, the one-way bearing 18 and the hollow shaft 8 are unlocked. Then, the compression rod 3 drives the compression plate 9 and the defibrillator 21 downward until the defibrillator 21 is in contact with the patient's chest. Then, the patient is given emergency treatment through the defibrillator 21.

[0074] S5. When the squeezing rod 3 moves the compression plate 9 and the defibrillator 21 downwards, the defibrillator 21 initially contacts the patient's chest. The squeezing rod 3 moves the compression plate 9 downwards as well. The first spring 22 acts as a buffer for the defibrillator 21, preventing it from squeezing the patient. As the compression plate 9 moves downwards, the compression disc 24 exerts a certain squeezing force on the pressure sensor 25 under the action of the second spring 23. When the pressure signal detected by the pressure sensor 25 reaches a certain value, the defibrillator 21 is activated, and the defibrillator 21 provides emergency treatment to the patient.

[0075] S6. When the patient is resting at night, the emergency pills are placed between the baffle 40 and the grinding plate 44 in advance. The placement plate 47 is located between the baffle 40 and the grinding plate 44 to place the emergency pills. The elastic force of the third spring 45 on the grinding plate 44 can hold the emergency pills and prevent them from falling into the dissolving box 30.

[0076] However, as is well known to those skilled in the art, the working principles and wiring methods of the pressure sensor 25, heating element 49, water pump 27, solenoid valve 50, defibrillator 21 and drive motor 7 are commonplace and belong to conventional means or common knowledge. They will not be described in detail here. Those skilled in the art can make any selections according to their needs or convenience.

[0077] The above are merely specific embodiments of the present invention, but the scope of protection of the present invention is not limited thereto. Any variations or substitutions that can be easily conceived by those skilled in the art within the technical scope disclosed in the present invention should be included within the scope of protection of the present invention. In the absence of conflict, the embodiments and features of the embodiments of the present invention can be combined with each other. Therefore, the scope of protection of the present invention should be determined by the scope of the claims.

Claims

1. A neurological sleep monitoring and emergency device, characterized in that, include: A bed board (1) is slidably connected to two sides of the bed board (1). A pressing rod (3) is slidably passed through the U-shaped frame (2). A hollow rotating shaft (8) is rotatably passed through the pressing rod (3). Pressing plates (9) are fixedly connected to both ends of the hollow rotating shaft (8). The cardiopulmonary resuscitation (CPR) emergency structure is located at the bottom of the compression plate (9) and is used to perform CPR on the patient. The defibrillation emergency structure is located on top of the compression plate (9) for re-emergency treatment of the patient; The medication delivery mechanism, located at the top of the U-shaped frame (2), is used to securely administer emergency pills to the patient.

2. The neurological sleep monitoring and emergency device according to claim 1, characterized in that, The cardiopulmonary resuscitation emergency structure includes two compression airbags (10) fixedly connected to the bottom of two compression plates (9), and ventilation tubes (11) fixedly connected to both sides of the bottom of the hollow rotating shaft (8), and the ventilation tubes (11) are connected to the compression airbags (10). The compression rod (3) has a cavity (12) coaxial with the hollow rotating shaft (8), and the hollow rotating shaft (8) has multiple through holes (13) connected to the cavity (12). The compression rod (3) has a flexible tube (14) connected to the cavity (12), and one end of the flexible tube (14) extends to one side of the compression rod (3).

3. The neurological sleep monitoring and emergency device according to claim 2, characterized in that, The cardiopulmonary resuscitation emergency structure also includes a fixing plate (15) fixedly connected to the top of the U-shaped frame (2). An air-storage bag (17) is fixedly connected to the side of the fixing plate (15) near the compression rod (3). A compression plate (16) is fixedly connected to the side of the air-storage bag (17) near the compression rod (3), and the compression plate (16) is slidably connected to the top of the U-shaped frame (2). The end of the hose (14) away from the cavity (12) passes through the compression plate (16) and communicates with the air-storage bag (17). Multiple return springs (52) are fixedly connected between the compression plate (16) and the air-storage bag (17). A trapezoidal block (51) is fixedly connected to the side of the compression rod (3) near the compression plate (16).

4. The neurological sleep monitoring and emergency device according to claim 3, characterized in that, The defibrillation emergency structure includes two defibrillators (21) respectively set on the top of two pressing plates (9), two one-way bearings (18) are sleeved on the outer wall of the hollow rotating shaft (8), and a spur gear (19) is fixedly sleeved on the outer wall of the one-way bearing (18). Two racks (20) are fixedly connected to the bottom of the U-shaped frame (2), and the two racks (20) are located on both sides of the pressing rod (3). The racks (20) mesh with the spur gear (19).

5. The neurological sleep monitoring and emergency device according to claim 4, characterized in that, The feeding structure includes a dissolving tank (30) and a heat-insulating water tank (26) fixedly connected to the top of the U-shaped frame (2). Multiple heating elements (49) for maintaining water temperature are fixedly connected to the inner wall of the heat-insulating water tank (26). A water pump (27) is located on the top of the heat-insulating water tank (26). An inlet pipe (28) extending into the heat-insulating water tank (26) is fixedly fitted onto the inlet of the water pump (27). An outlet pipe (29) communicating with the dissolving tank (30) is fixedly fitted onto the outlet of the water pump (27). A pressure plate (16) is fixedly connected to the side away from the pressure rod (3). A fixed rod (34) is provided, one end of which passes through the gas storage bag (17) and the fixed plate (15) and is fixedly connected to a nut plate (33). A stirring rod (31) is rotatably passed through the dissolving tank (30). Multiple stirring blades located in the liquid of the dissolving tank (30) are fixedly connected to the outer wall of the stirring rod (31). The outer wall of the stirring rod (31) is provided with a threaded section. The stirring rod (31) is threadedly connected to the nut plate (33) through the threaded section. A storage box (39) for dispensing emergency pills into the dissolving tank (30) is fixedly connected to the top of the dissolving tank (30).

6. The neurological sleep monitoring and emergency device according to claim 5, characterized in that, A baffle (40) is fixedly connected to one side of the storage box (39), and a screw (41) is threaded through the other side of the storage box (39). A guide rod (43) and a sliding rod (42) are slidably connected to both ends of the screw (41). A grinding plate (44) for crushing emergency pills is fixedly connected to one end of the guide rod (43) near the baffle (40), and a third spring (45) is fixedly connected to the other end of the guide rod (43). The other end of the third spring (45) is fixedly connected to one side of the inner wall of the screw (41).

7. A neurological sleep monitoring and emergency device according to claim 6, characterized in that, The storage box (39) has grooves (46) on its two inner walls that are far apart from each other. The same placement plate (47) for preventing the use of emergency pills is slidably connected in the two grooves (46). The top of the placement plate (47) is slidably engaged with the bottom of the baffle (40). A fourth spring (48) is fixedly connected to the inner wall of the two grooves (46) on the side away from the grinding plate (44). The other end of the fourth spring (48) is fixedly connected to the placement plate (47).

8. A neurological sleep monitoring and emergency device according to claim 7, characterized in that, A gearbox (35) is fixedly connected to the top of the dissolving tank (30). A first synchronous pulley (36) is fixedly connected to the output shaft of the gearbox (35). A second synchronous pulley (37) is fixedly sleeved on the outer wall of the stirring rod (31). The first synchronous pulley (36) and the second synchronous pulley (37) are connected by a synchronous belt (38). The output shaft of the gearbox (35) is fixedly connected to the sliding rod (42). A liquid guide pipe (32) is fixedly connected to the bottom of the dissolving tank (30). A solenoid valve (50) is sleeved on the outer wall of the liquid guide pipe (32). The bottom end of the dissolving tank (30) is connected to the drug storage pipe.

9. A neurological sleep monitoring and emergency device according to claim 8, characterized in that, The top of the U-shaped frame (2) is rotatably connected to a screw (4) via a base. A nut block (5) is threaded on the outer wall of the screw (4), and the nut block (5) is slidably connected to the top of the U-shaped frame (2). A connecting rod (6) is rotatably connected to the top of the nut block (5), and the top end of the connecting rod (6) is rotatably connected to one side of the extrusion rod (3). A drive motor (7) is fixedly connected to the top of the U-shaped frame (2), and the output shaft of the drive motor (7) is fixedly connected to one end of the screw (4).

10. A neurological sleep monitoring and emergency device according to claim 9, characterized in that, The bottom inner wall of the pressing plate (9) is fixedly connected to a plurality of first springs (22), the top ends of the plurality of first springs (22) are fixedly connected to the bottom of the defibrillator (21), and the defibrillator (21) is slidably connected inside the pressing plate (9). The bottom of the defibrillator (21) is fixedly connected to a second spring (23), the bottom end of the second spring (23) is fixedly connected to a pressing plate (24), and the bottom inner wall of the pressing plate (9) is fixedly connected to a pressure sensor (25), and the pressure sensor (25) cooperates with the pressing plate (24).

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