Hospital discharge preparation device with monitoring and reminding functions

Abstract

The utility model discloses a hospital discharge preparation device with monitoring and reminding functions, which belongs to the technical field of medical instruments and comprises a shell, the shell comprises a monitoring structure fixedly mounted in the shell, and the surface of the upper limb of a patient is observed in real time through the monitoring structure. The monitoring structure comprises an illumination structure slidably connected to the interior of the shell, the outer wall of the shell is rotationally connected with a limiting structure which is clamped to the outer walls of the two sets of rod bodies to limit the device, and the shell and the limiting structure are connected through a folding structure; when the upper limb rehabilitation device is used, the limiting structures are arranged, the strip-shaped rods drive the lantern rings to be arranged between any two sets of rod bodies in guardrails at the two ends of a sickbed in a sleeved mode when the upper limb rehabilitation device is used, and therefore the upper limb rehabilitation device and the upper limb of a patient are limited; looseness of the monitoring structure caused by unconscious overturning of the upper limbs of the patient in the using process is avoided.

Description

Technical Field

[0001] The utility model relates to the field of medical instruments, in particular to a discharge preparation device with monitoring and reminding functions. Background Art

[0002] Some patients with chronic diseases, such as hypertension and diabetes, must take long-term medication after discharge. Before discharge, medical staff need to observe the patients after taking the medication to ensure that the medication is effective for the patients and that no adverse reactions occur during subsequent medication.

[0003] The skin on the arms is relatively thin and tender, and more open areas are exposed, making them more likely to show rash symptoms. As a result, rashes caused by drug allergies often start on the arms. In addition, metabolites produced during drug metabolism sometimes cause an overreaction of the immune system, resulting in allergic rashes in other parts of the body such as the arms.

[0004] In the prior art, when a patient is waiting for a reaction after taking medicine, the patient can only be observed by the patient's family or medical staff. However, since some drugs take a long time to take effect, when the patient is resting during the waiting process, the upper limbs may shake unconsciously, which may cause the instruments bound to the upper limbs to loosen, making it impossible to monitor the patient in real time, resulting in the inability to treat the patient in time. Utility Model Content

[0005] The purpose of the utility model is to provide a discharge preparation device with monitoring and reminder functions to solve the problems raised in the above background technology.

[0006] To achieve the above-mentioned purpose, the utility model provides the following technical solution: it includes a shell, the shell includes a monitoring structure fixedly installed inside the shell, and the surface of the patient's upper limb is observed in real time through the monitoring structure, so as to facilitate the first-time discovery of drug allergy on the patient's skin, the monitoring structure includes a lighting structure slidably connected to the inside of the shell, the outer wall of the shell is rotatably connected to a limiting structure that limits the device by being clamped on the outer walls of two groups of rods, the shell and the limiting structure are connected by a folding structure, and the limiting structure can be folded at the side end of the shell through the folding structure.

[0007] Furthermore, the folding structure includes a cover body, which is fixedly connected to one end of the shell body close to the limiting structure. A special-shaped pull plate is slidably connected to the inside of the cover body, and the end of the special-shaped pull plate away from the cover body is rotatably connected to a sleeve plate. The limiting structure is slidably inserted into the sleeve plate, thereby supporting the outside of the limiting structure.

[0008] Furthermore, the limiting structure comprises a strip rod, the outer wall of the strip rod is clamped in the inner cavity of the special-shaped pull plate, and one end of the strip rod away from the special-shaped pull plate is fixedly connected with a ring for sleeved on the outer wall of the rod body.

[0009] Furthermore, the shell also includes annular airbags fixed at both ends thereof, and the annular airbags improve the comfort of the patient when the patient's upper limbs are inserted into the shell.

[0010] Furthermore, the monitoring structure includes a camera, the top of which is fixedly mounted on the top of the inner cavity of the shell, and a wireless transmission module for transmitting the captured images is installed inside the camera.

[0011] Furthermore, the lighting structure comprises a lighting lamp, and the lighting lamp is slidably installed in the inner cavity of the shell.

[0012] Beneficial Effects

[0013] Compared with the prior art, the beneficial effects of the utility model are:

[0014] 1. When the utility model is used, a limiting structure is set. When in use, the strip rod drives the ring to be set between any two groups of rods in the guardrails at both ends of the bed, so as to limit the device and the patient's upper limbs, avoiding the loosening of the monitoring structure due to the unconscious turning of the patient's upper limbs during use.

[0015] 2. When the utility model is used, a camera assembly is provided to monitor the external skin of the patient's upper limbs, and when the patient's skin initially shows adverse reactions such as rashes, the medical staff is notified in the first time, so that the patient can be rescued in time. BRIEF DESCRIPTION OF THE DRAWINGS

[0016] Figure 1 It is a schematic diagram of the overall structure of the utility model;

[0017] Figure 2 This is a cross-sectional view of the sleeve structure of the utility model;

[0018] Figure 3 It is a schematic diagram of the lighting structure of the utility model;

[0019] Figure 4 This is a schematic diagram of module connection of the present utility model.

[0020] In the figure: 1. shell; 2. monitoring structure; 3. lighting structure; 4. limiting structure; 5. folding structure; 6. annular airbag; 201. camera; 301. lighting lamp; 302. strip groove; 303. slider; 401. strip rod; 402. collar; 403. block; 404. second spring; 501. cover; 502. special-shaped pull plate; 503. elliptical groove; 504. column; 505. sleeve plate; 506. first support shaft; 507. connecting block; 508. second support shaft; 509. limiting baffle; 510. first spring. DETAILED DESCRIPTION

[0021] The following will be combined with the drawings in the embodiments of the utility model to clearly and completely describe the technical solutions in the embodiments of the utility model. Obviously, the described embodiments are only part of the embodiments of the utility model, not all of the embodiments. Based on the embodiments in the utility model, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the utility model.

[0022] Example 1: Please refer to Figure 1-3 , a discharge preparation device with monitoring and reminder functions, comprising a shell 1, the shell 1 comprising a monitoring structure 2 fixedly installed therein, and the monitoring structure 2 is used to observe the surface of the patient's upper limb in real time, so as to facilitate the first time to find the condition of drug allergy on the patient's skin, the monitoring structure 2 comprises a lighting structure 3 slidably connected to the shell 1, the outer wall of the shell 1 is rotatably connected with a limiting structure 4 that limits the device by being clamped on the outer walls of two groups of rods, the limiting structure 4 is adjusted according to the width between any two groups of rod bodies in the guardrails at both ends of the bed, so that the limiting structure 4 is clamped on the outer walls of the two groups of tube bodies to limit the device, thereby avoiding the situation that when a group of rod bodies are fixed, because the rod bodies are cylindrical and the surface is relatively smooth, when the patient's upper limbs swing during use, the limiting structure 4 rotates around the rod bodies, the shell 1 and the limiting structure 4 are connected with a folding structure 5, and the limiting structure 4 can be folded at the side end of the shell 1 through the folding structure 5.

[0023] See also Figure 1-2 The folding structure 5 includes a cover body 501, which is fixedly connected to one end of the shell 1 close to the limiting structure 4. A special-shaped pull plate 502 is slidably connected inside the cover body 501. An elliptical groove 503 is provided inside the special-shaped pull plate 502. A column 504 is inserted inside the elliptical groove 503. Both ends of the column 504 are fixedly connected to the inside of the cover body 501. One end of the special-shaped pull plate 502 away from the cover body 501 is rotatably connected to a sleeve plate 505. The limiting structure 4 is slidably inserted inside the sleeve plate 505, thereby supporting the outside of the limiting structure 4.

[0024] Specifically, the special-shaped pull plate 502 is internally rotatably connected to the first support shaft 506, the first support shaft 506 is externally rotatably connected to the connecting block 507, the end of the connecting block 507 away from the first support shaft 506 is internally rotatably connected to the second support shaft 508, and the second support shaft 508 is rotatably inserted in the inner cavity of the sleeve plate 505. More specifically, a limit baffle 509 for limiting the limit structure 4 is slidably inserted in the inner cavity of the sleeve plate 505, and the sleeve plate 505 and the limit baffle 509 are fixedly connected by a first spring 510.

[0025] See also Figure 1-2 The limiting structure 4 includes a strip rod 401, and the outer wall of the strip rod 401 is clamped in the inner cavity of the special-shaped pull plate 502. There are two groups of strip rods 401 and they are symmetrically clamped in the inner cavity of the special-shaped pull plate 502. The end of the strip rod 401 away from the special-shaped pull plate 502 is fixedly connected with a ring 402 for being sleeved on the outer wall of the rod body. Specifically, the ring 402 includes a block 403 slidably connected to the inner cavity of the strip rod 401, and abuts against the outer wall of the rod body through the block 403, thereby increasing the stability of the ring 402. More specifically, a square groove is opened inside the strip rod 401, and the strip rod 401 is fixedly connected with a second spring 404 through the square groove, and the end of the block 403 close to the strip rod 401 is fixedly connected to the second spring 404.

[0026] See also Figure 1 and 3 The shell 1 also includes annular airbags 6 fixed at both ends thereof, and the annular airbags 6 improve the patient's comfort when the patient's upper limb is inserted into the shell 1.

[0027] See also Figure 1 and 3 -4, the monitoring structure 2 includes a camera 201, the top of the camera 201 is fixedly installed on the top of the inner cavity of the shell 1, and a wireless transmission module for transmitting the collected images is installed inside the camera 201. The wireless transmission module is connected to a detection module. After the wireless transmission module transmits the collected images to the detection module, the detection module can detect the patient's skin. When the patient's skin is abnormal, a prompt can be issued to the medical staff through the connected wireless alarm module, so that the patient can be treated as soon as possible.

[0028] See also Figure 1 and 3 -4, the lighting structure 3 includes a lighting lamp 301, which is slidably installed in the inner cavity of the shell 1. The lighting lamp 301 can illuminate the patient's upper limbs from the inner side of the shell 1, thereby helping the camera 201 to photograph the patient's skin. Specifically, a strip groove 302 for providing sliding of the lighting lamp 301 is opened inside the shell 1, and a slider 303 is fixedly connected to one end of the lighting lamp 301 close to the strip groove 302, and the slider 303 is located in the inner cavity of the strip groove 302.

[0029] Working principle: First, adjust the height of the lighting lamp 301 according to the thickness of the patient's upper limbs. When the patient's upper limbs are thicker, the lighting lamp 301 can be pushed upward inside the strip groove 302, and then the shell 1 is set on the patient's upper limbs, and the special-shaped pull plate 502 is pulled downward, and the cover plate 505 is turned over at the same time to make the cover plate 505 horizontal. By pressing the limit baffle 509, it retracts into the inside of the cover plate 505, and then the limit structure 4 is placed inside the cover plate 505, and the width between any two groups of rods in the guardrails at both ends of the bed is adjusted. The limiting structure 4 is adjusted so that it is clamped on the outer walls of the two groups of tube bodies to limit the device, and the lighting lamp 301 is driven to illuminate the inside of the shell 1. At the same time, the monitoring structure 2 is driven to make the camera 201 collect the patient's skin and monitor the patient's upper limb skin through the detection module. When the patient develops rashes or other adverse reactions on the upper limbs after taking the medicine, the detection module can identify it and send a prompt to the medical staff through the wireless alarm module, so that the medical staff can treat the patient as soon as possible.

[0030] The above description is only a preferred specific implementation manner of the present utility model, but the protection scope of the present utility model is not limited thereto. Any technician familiar with the technical field can make equivalent replacements or changes within the technical scope disclosed by the present utility model according to the technical scheme and utility model concept of the present utility model, which should be covered by the protection scope of the present utility model.

Claims

1. A discharge preparation device with monitoring and reminder functions, comprising a housing (1), characterized in that: The shell (1) comprises a monitoring structure (2) fixedly mounted therein, and the monitoring structure (2) is used to observe the surface of the patient's upper limb in real time, thereby facilitating the discovery of drug allergy on the patient's skin at the first opportunity. The monitoring structure (2) comprises an illumination structure (3) slidably connected to the shell (1). The outer wall of the shell (1) is rotatably connected to a limiting structure (4) for limiting the device by being clamped on the outer walls of two groups of rods. A folding structure (5) is connected between the shell (1) and the limiting structure (4), and the limiting structure (4) can be folded at the side end of the shell (1) by the folding structure (5).

2. A discharge preparation device with monitoring and reminder functions according to claim 1, characterized in that: The folding structure (5) comprises a cover body (501), wherein the cover body (501) is fixedly connected to one end of the shell (1) close to the limiting structure (4), a special-shaped pull plate (502) is slidably connected inside the cover body (501), and one end of the special-shaped pull plate (502) away from the cover body (501) is rotatably connected to a sleeve plate (505), and the limiting structure (4) is slidably inserted into the sleeve plate (505), thereby supporting the outside of the limiting structure (4).

3. The discharge preparation device with monitoring and reminder functions according to claim 1, characterized in that: The limiting structure (4) comprises a strip rod (401), the outer wall of which is clamped in the inner cavity of the special-shaped pull plate (502), and one end of the strip rod (401) away from the special-shaped pull plate (502) is fixedly connected to a ring (402) for being sleeved on the outer wall of the rod body.

4. The discharge preparation device with monitoring and reminder functions according to claim 1, characterized in that: The shell (1) further comprises annular air bags (6) fixed at two ends thereof, and the annular air bags (6) improve the comfort of the patient when the patient's upper limbs are inserted into the shell (1).

5. The discharge preparation device with monitoring and reminder functions according to claim 1, characterized in that: The monitoring structure (2) comprises a camera (201), the top of the camera (201) being fixedly mounted on the top of the inner cavity of the housing (1), and a wireless transmission module for transmitting captured images being installed inside the camera (201).

6. The discharge preparation device with monitoring and reminder functions according to claim 1, characterized in that: The lighting structure (3) comprises a lighting lamp (301), and the lighting lamp (301) is slidably mounted in the inner cavity of the housing (1).

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