Anesthesia recovery room monitoring and early warning device

By using limit components and winding seats in the monitoring equipment of the anesthesia recovery room, the error warning problem caused by the connection line in the prior art is solved, and the accurate judgment of the connection line status and the effect of saving medical resources is achieved.

CN120130967AInactive Publication Date: 2025-06-13TONGJI HOSPITAL ATTACHED TO TONGJI MEDICAL COLLEGE HUAZHONG SCI TECH
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Patent Information

Application Number
CN202510249029.1
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-03-04
Publication Date
2025-06-13
Estimated Expiration
Not applicable · inactive patent

AI Technical Summary

Technical Problem

The automatic alarm device of existing anesthesia recovery room monitoring equipment is prone to abnormal reminders due to the fall off of the connecting line or the bending of the pressure, resulting in wasting medical resources.

Method used

A monitoring and early warning device for anesthesia recovery room is designed to detect limit and abnormal conditions of the connecting line through the limiting component, and use the winding seat to wind the pull rope and pull the connecting line to move it, so as to determine the connecting line problem or patient problem, so as to take corresponding solutions.

Benefits of technology

It effectively avoids error warnings due to problems of the instrument itself, saves medical resources, and improves the accurate judgment and handling of the connection line status.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention provides anesthesia recovery room monitoring and early warning equipment, and relates to the technical field of medical monitoring equipment.The anesthesia recovery room monitoring and early warning equipment comprises a monitor, a display screen is installed at the top of the monitor, a connecting box is arranged on the side face of the monitor, a plurality of connecting ends are arranged on the outer surface of the connecting box at equal intervals, and connecting wires are inserted into the connecting ends; the monitor is provided with a limiting assembly on the side surface of each connecting line, the limiting assembly comprises a sliding rod, the top of the sliding rod is provided with an alarm lamp, and the top of the sliding rod is internally provided with a small motor for driving the alarm lamp to rotate. The pull rope is wound through the winding seat, meanwhile, the connecting line is pulled to move, and in the state, whether a problem occurs on the connecting line or a problem of a patient is judged according to whether the connecting line can be pulled or not, so that a corresponding solution is made, and waste of medical resources can be avoided.
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Description

Technical Field

[0001] The present invention relates to the technical field of medical monitoring equipment, and particularly to a monitoring and warning device for an anesthesia recovery room. Background Art

[0002] The post-anesthesia care unit is a ward where patients after anesthesia are closely observed and monitored until they are fully awake and their vital signs return to stability. It is generally open during the day, and patients with unstable emergency vital signs can be transferred to the surgical intensive care unit for further treatment. The recovery room works under the leadership of the director of the anesthesia department. The daily monitoring and treatment work is responsible by anesthesiologists and nurses. The anesthesiologist is responsible for formulating the monitoring and treatment plan for the patient and determining the indication for transfer to the general ward or ICU. The items that need to be detected for anesthetic patients include activity, respiration, circulation, consciousness, and oxygen saturation.

[0003] Currently, the common detection device is an integrated monitor. By attaching electrode patches to the patient's body, multiple data can be monitored and fed back to an instrument screen for the doctor to uniformly observe each value. For the existing technology, the monitoring instrument has an automatic alarm device. When a certain data is abnormal, it will emit an alarm sound and light up to remind the medical staff. However, since the detection instrument is connected to the human body through a connecting wire and electrode patches, during this process, connection detachment, the connecting wire being squeezed or bent may occur, which may cause the instrument to give an abnormal reminder, and this kind of reminder is likely to waste medical resources. Summary of the Invention

[0004] Aiming at the deficiencies of the existing technology, the purpose of the present invention is to provide a monitoring and warning device for an anesthesia recovery room to solve the problems raised in the above background art. The structure of the present invention is novel. The connecting wire is limited and the detection of abnormal conditions is carried out through a limiting component. The pulling rope is wound by a winding seat, and at the same time, the connecting wire is pulled to move. In this state, according to whether the connecting wire can be pulled, it is determined whether the problem is with the connecting wire or the patient himself, and then corresponding solutions are made, which can avoid the waste of medical resources.

[0005] To achieve the above object, the present invention is implemented through the following technical solutions: An anesthesia recovery room monitoring and warning device includes a monitor. A display screen is installed on the top of the monitor, and a connection box is provided on the side of the monitor. A plurality of connection ends are equidistantly arranged on the outer surface of the connection box, and connection lines are inserted into the connection ends. The monitor is provided with a limiting component on the side of each connection line. The limiting component includes a sliding rod. An alarm lamp is installed on the top of the sliding rod, and a small motor for driving the alarm lamp to rotate is built into the top of the sliding rod. A connecting plate is slidably sleeved on the surface of the sliding rod, and a supporting frame is fixed on one side of the connecting plate where the connection line is located. The connection line is placed inside the supporting frame. A third fixing ring is fixed at the bottom of the supporting frame where the connection line is located. The front end of the connection line is fixed with a first fixing ring and a second fixing ring, and the part of the connection line between the first fixing ring and the second fixing ring is bent into a U shape. A pulling rope is fixed at the top of the third fixing ring, and the pulling rope is attached to the rear end surface of the connection line. A winding seat is provided at the bottom of the sliding rod, and the pulling rope is wound on the winding shaft of the winding seat.

[0006] Further, a storage box is fixed at the bottom of the monitor where the connection box is located. A cover plate is provided at the upper end of the storage box, and electrode sheets connected to the connection lines are placed inside the storage box.

[0007] Further, limiting frames are fixed at adjacent ends of the first fixing ring and the second fixing ring, and a plurality of first springs are fixed between the two groups of limiting frames.

[0008] Further, the limiting component further includes a second spring. The second spring is sleeved on the outer surface of the sliding rod, and a bottom plate is fixed at the bottom of the sliding rod. The bottom plate is fixedly connected to the side surface of the monitor. The two ends of the second spring are respectively fixedly connected to the connecting plate and the bottom plate.

[0009] Further, a collar is rotatably installed around the sliding rod on the connecting plate. The collar is slidably sleeved on the sliding rod. A vertical plate is fixed at the bottom of the alarm lamp, and the vertical plate slidably passes through the collar. A supporting ring is fixed at the bottom of the vertical plate, and the top of the supporting ring is in pressing contact with an arc plate.

[0010] Further, an installation frame is fixedly connected to the outer end of the arc plate. A telescopic rod is fixed at the bottom of the installation frame, and the bottom of the telescopic rod is fixed on the bottom plate. The extended end of the telescopic rod is sleeved with a third spring, and the bottom of the third spring is fixedly connected to the retracted end of the telescopic rod.

[0011] Further, a socket is fixed on the winding shaft of the winding seat. A driving motor is fixed at one end of the installation frame facing the socket, and a convex block is fixed at the output end of the driving motor. The convex block is slidably inserted into the slot of the socket.

[0012] Furthermore, fixing blocks are equidistantly fixed on the surface of the connecting line at the rear end of the third fixing ring, and the pull rope is fixed through the fixing blocks.

[0013] Furthermore, a contact plate is fixed to a side of the bottom of the supporting frame facing the third fixing ring, and a contact module is arranged at the bottom of the contact plate.

[0014] Furthermore, an adhesive tape is fixed on the outer surface of the storage box where the connecting wire is inserted.

[0015] Beneficial effects of the present invention:

[0016] 1. The present invention reels the pull rope by driving the motor. Since one end of the pull rope is fixed to the third fixing ring and the pull rope is attached to the surface of the connecting line through the fixing block, it will not affect the normal wiring of the connecting line. At the same time, it will give the connecting line a traction force to detect whether the connecting line will move.

[0017] 2. The support frame of the present invention slides along the slide rod through the connecting plate, and the slide rod guides its moving path. When the connecting wire is not in use, it can be restricted to the upper end by the support frame through the elastic force of the second spring, so as to bundle the connecting wires and avoid confusion between the connecting wires. When in use, the connecting wire can be manually pulled to make the support frame and the connecting plate slide downward along the slide rod, or the connecting wire can be directly removed from the support frame, depending on the length of the connecting wire to be used.

[0018] 3. When a certain data of the monitor is abnormal, the alarm light on the side of the corresponding connecting line is turned on by an electrical signal, and the alarm light is driven to rotate by a small motor built into the top of the slide bar, making the warning effect more obvious.

[0019] 4. The present invention can prevent the electrode sheets from being contaminated and damaged by storing the electrode sheets connected to the connecting wires in a storage box. After the electrode sheets are attached to the human body, the tape at the front end of the connecting wires is attached to the skin, which has a certain fixing effect on the connecting wires. This effect can be used to distinguish between the first and third situations.

[0020] 5. Compared with the prior art, the present invention limits the connection line and detects abnormal conditions through a limiting component, reels the pull rope through a reel-up seat, and pulls the connection line to move at the same time. In this state, whether the connection line can be pulled can be used to determine whether the problem is with the connection line or with the patient himself, so as to make corresponding solutions and avoid wasting medical resources. BRIEF DESCRIPTION OF THE DRAWINGS

[0021] Figure 1 This is a schematic diagram of the overall structure of an anesthesia recovery room monitoring and early warning device of the present invention;

[0022] Figure 2Schematic diagram of the connection between the limit component and the connecting wire of a monitoring and warning device for an anesthesia recovery room according to the present invention;

[0023] Figure 3 Schematic diagram of the structure of the limit component of a monitoring and warning device for an anesthesia recovery room according to the present invention;

[0024] Figure 4 Schematic diagram of the top structure of the sliding rod of a monitoring and warning device for an anesthesia recovery room according to the present invention;

[0025] Figure 5 Schematic diagram of the bottom structure of the sliding rod of a monitoring and warning device for an anesthesia recovery room according to the present invention;

[0026] Figure 6 Schematic diagram of the positions of the first fixing ring and the second fixing ring of a monitoring and warning device for an anesthesia recovery room according to the present invention;

[0027] Figure 7 Schematic diagram of the connection between the winding seat and the driving motor of a monitoring and warning device for an anesthesia recovery room according to the present invention;

[0028] Figure 8 Schematic diagram of the connection between the alarm lamp and the vertical plate of a monitoring and warning device for an anesthesia recovery room according to the present invention.

[0029] In the figure: 1. Monitor; 11. Display screen; 2. Connection box; 21. Connecting wire; 22. Connection end; 23. First fixing ring; 24. Second fixing ring; 25. Limit frame; 26. First spring; 27. Adhesive tape; 3. Storage box; 4. Limit component; 41. Sliding rod; 42. Second spring; 43. Alarm lamp; 44. Connection plate; 45. Support frame; 46. Third fixing ring; 47. Pulling rope; 48. Bottom plate; 49. Contact plate; 410. Fixed block; 411. Vertical plate; 412. Support ring; 413. Telescopic rod; 414. Winding seat; 415. Collar; 416. Contact module; 417. Socket; 418. Convex block; 419. Driving motor; 420. Mounting frame; 421. Arc plate; 422. Third spring. Detailed implementation manners

[0030] In order to make the technical means, creative features, achieved purposes and effects of the present invention easy to understand, the present invention will be further described below in conjunction with the detailed implementation manners.

[0031] Please refer to Figures 1 to 8, the present invention provides a technical solution: an anesthesia recovery room monitoring and warning device, including a monitor 1. A display screen 11 is installed on the top of the monitor 1, and a connection box 2 is arranged on the side of the monitor 1. A plurality of connection terminals 22 are equidistantly arranged on the outer surface of the connection box 2, and a connection wire 21 is inserted into the connection terminal 22. A limiting component 4 is arranged on the side of the monitor 1 for each connection wire 21. The limiting component 4 includes a sliding rod 41. An alarm lamp 43 is installed on the top of the sliding rod 41. A small motor for driving the alarm lamp 43 to rotate is built into the top of the sliding rod 41. A connecting plate 44 is slidably sleeved on the surface of the sliding rod 41. A supporting frame 45 is fixed on one side of the connecting plate 44 and located at the connection wire 21. The connection wire 21 is placed inside the supporting frame 45. A third fixing ring 46 is fixed at the bottom of the supporting frame 45 for the connection wire 21. The front end of the connection wire 21 is fixed with a first fixing ring 23 and a second fixing ring 24. The part of the connection wire 21 between the first fixing ring 23 and the second fixing ring 24 is bent into a U shape. A pulling rope 47 is fixed at the top of the third fixing ring 46, and the pulling rope 47 is attached to the surface of the rear end of the connection wire 21. A winding base 414 is arranged at the bottom of the sliding rod 41, and the pulling rope 47 is wound on the winding shaft of the winding base 414. In this application, the usage methods of the monitor 1, the connection wire 21, and the electrode patch are the same as those of existing medical monitors 1, and will not be described in detail here. When the device is not in use, each connection wire 21 is stored on one side of the monitor 1. When in use, the connection wire 21 corresponding to the monitoring item to be monitored is taken out and connected to the human body. When an abnormal signal is sent out for a certain item monitored by the monitor 1, a preliminary self-check is carried out through the limiting component 4 to avoid false warnings caused by problems with the instrument itself and save medical resources.

[0032] In this embodiment, a storage box 3 is fixed at the bottom of the monitor 1 and located at the connection box 2. A cover plate is arranged at the upper end of the storage box 3. Electrode patches connected to the connection wire 21 are placed inside the storage box 3. An adhesive tape 27 is fixed on the outer surface of the connection wire 21 inserted into the storage box 3. Storing the electrode patches connected to the connection wire 21 in the storage box 3 can prevent the electrode patches from being contaminated and damaged. After the electrode patch is attached to the human body, it is pasted on the skin through the adhesive tape 27 at the front end of the connection wire 21, which plays a certain fixing effect on the connection wire 21. This effect can be used to distinguish the first and third situations.

[0033] In this embodiment, a limiting frame 25 is fixed to one end of each of the adjacent first fixing ring 23 and second fixing ring 24. A plurality of first springs 26 are fixed between the two groups of limiting frames 25. A collar 415 is rotatably mounted around the outer periphery of the sliding rod 41 of the connecting plate 44. The collar 415 is slidably sleeved on the sliding rod 41. A vertical plate 411 is fixed to the bottom of the warning lamp 43, and the vertical plate 411 slidably passes through the collar 415. A supporting ring 412 is fixed to the bottom of the vertical plate 411. The top of the supporting ring 412 is in pressing contact with an arc plate 421. The outer end of the arc plate 421 is fixedly connected to a mounting bracket 420. A telescopic rod 413 is fixed to the bottom of the mounting bracket 420, and the bottom of the telescopic rod 413 is fixed to the bottom plate 48. A third spring 422 is sleeved on the extending end of the telescopic rod 413, and the bottom of the third spring 422 is fixedly connected to the receiving end of the telescopic rod 413. A socket 417 is fixed to the winding shaft of the winding base 414. A driving motor 419 is fixed to one end of the mounting bracket 420 facing the socket 417, and a convex block 418 is fixed to the output end of the driving motor 419. The convex block 418 is slidably inserted into the slot of the socket 417. Fixing blocks 410 are equidistantly fixed to the surface of the connecting wire 21 at the rear end of the third fixing ring 46, and the pull rope 47 is fixedly passed through the fixing blocks 410. A contact plate 49 is fixed to one side of the bottom of the support frame 45 facing the third fixing ring 46, and a contact module 416 is arranged at the bottom of the contact plate 49. The front end of the connecting wire 21 becomes a U-shaped structure under the action of the first fixing ring 23, the second fixing ring 24, the limiting frame 25 and the first spring 26. This structure is not too large and will not affect the normal use of the connecting wire 21 and the monitoring. When a certain data of the monitor 1 is abnormal, the warning lamp 43 on the side of the corresponding connecting wire 21 is turned on by an electric signal. The small motor built into the top of the sliding rod 41 drives the warning lamp 43 to rotate, making the warning effect more obvious. Originally, the arc block is located on the top of the supporting ring 412. At this time, the telescopic rod 413 is in the extended state, driving the driving motor 419 to separate from the winding base 414. When the warning lamp 43 rotates, the vertical plate 411 will rotate along the collar 415. At the same time, the supporting ring 412 at the bottom of the vertical plate 411 will also rotate. After the arc plate 421 is not subjected to the downward resistance, it moves downward along with the mounting bracket 420 and the telescopic rod 413 under the elastic force of the third spring 422. At this time, the convex block 418 of the driving motor 419 is inserted into the socket 417. The driving motor 419 winds up the pull rope 47. Because one end of the pull rope 47 is fixed to the third fixing ring 46, and the pull rope 47 is attached to the surface of the connecting wire 21 through the fixing blocks 410, it will not affect the normal wiring of the connecting wire 21. At the same time, a traction force will be given to the connecting wire 21 to detect whether the connecting wire 21 will move. There are three structures in this state. First, because there is a reserved length at the front end of the connecting wire 21, the winding of the pull rope 47 will drive the connecting wire 21 to have a certain displacement, but it cannot continue to move afterwards. This state is determined that the connecting wire 21 has not separated from the human body or been squeezed, indicating that it is a problem of the patient himself.Remind medical staff in a timely manner. In the second case, the second drawstring 47 cannot be wound up and the connection line 21 cannot move. This state may be that the connection line 21 is pressed by the patient's body or other objects, affecting the monitoring signal. In the third case, the drawstring 47 can be continuously wound up and the connection line 21 can also move continuously until the third fixing ring 46 contacts the contact plate 49. At this time, an electrical signal is transmitted through the contact module 416, indicating that the part of the connection line 21 connected to the human body has become detached. The second and third cases can be solved after inspection by medical staff. The first case is a problem of the patient himself and requires timely assistance.

[0034] In this embodiment, the limiting component 4 further includes a second spring 42. The second spring 42 is sleeved on the outer surface of the sliding rod 41, and a bottom plate 48 is fixed to the bottom of the sliding rod 41. The bottom plate 48 is fixedly connected to the side surface of the monitor 1. The two ends of the second spring 42 are respectively fixedly connected to the connecting plate 44 and the bottom plate 48. The support frame 45 slides along the sliding rod 41 through the connecting plate 44. The sliding rod 41 guides its moving path. When the connection line 21 is not in use, it can be restricted to the upper end by the support frame 45 through the elastic force of the second spring 42 to bundle the connection line 21 and prevent the connection lines 21 from being chaotic with each other. When in use, the connection line 21 can be manually pulled to make the support frame 45 and the connecting plate 44 slide down along the sliding rod 41, or the connection line 21 can be directly removed from the support frame 45, depending on the length of the connection line 21 required for use.

[0035] When the device is not in use, each connecting wire 21 is stored on one side of the monitor 1. When in use, the connecting wire 21 corresponding to the item to be monitored is taken out and connected to the human body. The front end of the connecting wire 21 becomes a U-shaped structure under the action of the first fixing ring 23, the second fixing ring 24, the limiting frame 25 and the first spring 26. This structure is not too large and will not affect the normal use of the connecting wire 21 and the monitoring. When a certain data of the monitor 1 is abnormal, the alarm light 43 on the side of the corresponding connecting wire 21 is turned on through an electrical signal. The small motor built into the top of the slide bar 41 drives the alarm light 43 to rotate, making the warning effect more obvious. Originally, the arc block is located on the top of the supporting ring 412. At this time, the telescopic rod 413 is in the extended state, driving the drive motor 419 to separate from the winding base 414. When the alarm light 43 rotates, the vertical plate 411 will rotate along the collar 415. At the same time, the supporting ring 412 at the bottom of the vertical plate 411 will also rotate. After the arc plate 421 is not subjected to the downward resistance, it moves downward along with the mounting frame 420 and the telescopic rod 413 under the elastic force of the third spring 422. At this time, the convex block 418 of the drive motor 419 is inserted into the socket 417. The drive motor 419 winds the pull rope 47. Because one end of the pull rope 47 is fixed to the third fixing ring 46 and the pull rope 47 is attached to the surface of the connecting wire 21 through the fixing block 410, it will not affect the normal wiring of the connecting wire 21. At the same time, it will give the connecting wire 21 a traction force to detect whether the connecting wire 21 will move. There are three structures in this state. First, because there is a reserved length at the front end of the connecting wire 21, the winding of the pull rope 47 will drive the connecting wire 21 to have a certain displacement, but it cannot continue to move later. This state is determined that the connecting wire 21 is not separated from the human body or squeezed, indicating that it is a problem of the patient himself, and a reminder is sent to the medical staff in time. The second is that the pull rope 47 cannot be wound and the connecting wire 21 cannot move. This state may be that the connecting wire 21 is pressed by the patient's body or other objects, affecting the monitoring signal. The third is that the pull rope 47 can be continuously wound and the connecting wire 21 can also move continuously until the third fixing ring 46 contacts the contact plate 49. At this time, an electrical signal is transmitted through the contact module 416, indicating that the part of the connecting wire 21 connected to the human body has become detached. The second and third situations can be solved after being checked by the medical staff. The first situation is a problem of the patient himself and needs to be rescued in time to avoid false warnings due to problems with the instrument itself and save medical resources.

[0036] The above shows and describes the basic principles, main features and advantages of the present invention. For those skilled in the art, it is obvious that the present invention is not limited to the details of the above exemplary embodiments, and without departing from the spirit or basic features of the present invention, the present invention can be implemented in other specific forms.

[0037] In addition, it should be understood that although this specification is described in terms of embodiments, not every embodiment contains only one independent technical solution. This narrative manner of the specification is only for clarity. Those skilled in the art should regard the specification as a whole, and the technical solutions in each embodiment can also be appropriately combined to form other embodiments that can be understood by those skilled in the art.

Claims

1. An anesthesia recovery room monitoring and early warning device, comprising a monitor (1), characterized in that: A display screen (11) is installed on the top of the monitoring instrument (1), and a connection box (2) is arranged on the side of the monitoring instrument (1). A plurality of connection ends (22) are arranged at equal intervals on the outer surface of the connection box (2), and a connection line (21) is plugged into the connection end (22). The monitoring instrument (1) is provided with a limit assembly (4) on the side of each connection line (21), and the limit assembly (4) includes a slide bar (41), an alarm light (43) is installed on the top of the slide bar (41), and a small motor for driving the alarm light (43) to rotate is built into the top of the slide bar (41), and a connection plate (44) is slidably sleeved on the surface of the slide bar (41), and the connection plate (44) is located on the connection line (21). A support frame (45) is fixed on one side of the slide bar (41), the connecting wire (21) is placed inside the support frame (45), a third fixing ring (46) is fixed on the bottom of the support frame (45) of the connecting wire (21), a first fixing ring (23) and a second fixing ring (24) are fixed on the front end of the connecting wire (21), and the portion of the connecting wire (21) located between the first fixing ring (23) and the second fixing ring (24) is bent into a U shape, a pull rope (47) is fixed on the top of the third fixing ring (46), and the pull rope (47) is attached to the rear end surface of the connecting wire (21), and a winding seat (414) is provided at the bottom of the slide bar (41), and the pull rope (47) is wound on the winding shaft of the winding seat (414).

2. The anesthesia recovery room monitoring and early warning device according to claim 1 is characterized in that: The monitor (1) is provided with a storage box (3) fixed at the bottom of the connection box (2), a cover plate is provided at the upper end of the storage box (3), and an electrode sheet connected to the connection line (21) is placed inside the storage box (3).

3. The anesthesia recovery room monitoring and early warning device according to claim 1 is characterized in that: A limiting frame (25) is fixed to one adjacent end of the first fixing ring (23) and the second fixing ring (24), and a plurality of first springs (26) are fixed between the two sets of limiting frames (25).

4. The anesthesia recovery room monitoring and early warning device according to claim 1 is characterized in that: The limit assembly (4) also includes a second spring (42), the second spring (42) is sleeved on the outer surface of the slide bar (41), and a bottom plate (48) is fixed to the bottom of the slide bar (41), the bottom plate (48) is fixedly connected to the side of the monitor (1), and the two ends of the second spring (42) are respectively fixedly connected to the connecting plate (44) and the bottom plate (48).

5. The anesthesia recovery room monitoring and early warning device according to claim 4 is characterized in that: The connecting plate (44) is rotatably mounted on the periphery of the sliding rod (41) and is provided with a shaft ring (415). The shaft ring (415) is slidably sleeved on the sliding rod (41). A vertical plate (411) is fixed to the bottom of the warning light (43), and the vertical plate (411) slides through the shaft ring (415). A supporting ring (412) is fixed to the bottom of the vertical plate (411), and the top of the supporting ring (412) is pressed and contacted with an arc plate (421).

6. The anesthesia recovery room monitoring and early warning device according to claim 5, characterized in that: The outer end of the arc plate (421) is fixedly connected to a mounting frame (420), a telescopic rod (413) is fixed to the bottom of the mounting frame (420), and the bottom of the telescopic rod (413) is fixed to the bottom plate (48), the extended end of the telescopic rod (413) is sleeved with a third spring (422), and the bottom of the third spring (422) is fixedly connected to the storage end of the telescopic rod (413).

7. The anesthesia recovery room monitoring and early warning device according to claim 6, characterized in that: The reeling shaft of the reeling seat (414) is fixed with a socket (417), the mounting frame (420) is fixed with a driving motor (419) at one end facing the socket (417), and the output end of the driving motor (419) is fixed with a protrusion (418), and the protrusion (418) is slidably inserted into the slot of the socket (417).

8. The anesthesia recovery room monitoring and early warning device according to claim 7, characterized in that: The surface of the connection line (21) located at the rear end of the third fixing ring (46) is equidistantly fixed with fixing blocks (410), and the pull rope (47) is fixedly passed through the fixing blocks (410).

9. The anesthesia recovery room monitoring and early warning device according to claim 8, characterized in that: A contact plate (49) is fixed to the bottom of the support frame (45) on one side facing the third fixing ring (46), and a contact module (416) is arranged at the bottom of the contact plate (49).

10. The anesthesia recovery room monitoring and early warning device according to claim 1, characterized in that: The connecting wire (21) is inserted into the outer surface of the storage box (3) and is fixed with an adhesive tape (27).