A monitoring method and system for radial artery

By designing a monitoring system for radial artery, using connecting cables and signal transmitters to monitor patient location in real time, the limited problem of medical staff is solved, safe and effective monitoring of patients after radial artery PCI surgery is achieved, and the risk of rebleeding is reduced and security risks.

CN118845370BActive Publication Date: 2025-01-07湖南爱立达医疗科技有限公司
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Patent Information

Application Number
CN202411019664.2
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2024-07-29
Publication Date
2025-01-07
Estimated Expiration
2044-07-29

AI Technical Summary

Technical Problem

Medical staff are limited and cannot take care of patients after radial artery PCI for a long time, resulting in increased safety risks.

Method used

Design a monitoring system for the radial artery, including a controller, communicator, restriction mechanism and hemostasis, to monitor the patient's position and activity in real time through connecting cables and signal transmitters, and send alarm information if the distance exceeds the alert distance. Ensure that medical staff respond quickly.

Benefits of technology

It effectively reduces the risk of patients bleeding again after radial artery hemostasis, reduces safety hazards caused by insufficient medical staff, and improves the convenience and safety of patient monitoring.

✦ Generated by Eureka AI based on patent content.

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Abstract

The present invention relates to the technical field of medical devices, and discloses a monitoring system for radial artery, including a controller, a communicator, a limiting mechanism, a connecting cable and a hemostat, wherein the limiting mechanism drives one end of the connecting cable, and the hemostat is detachably connected to the other end of the connecting cable; the limiting mechanism is used to retract and release the connecting cable, and adjust the spacing distance between the limiting mechanism and the hemostat; the hemostat is provided with a signal transmitter; the communicator and the controller are both provided on the limiting mechanism; the controller is used to control the signal transmitter to send a position signal to the outside world; the controller is also used to obtain the position signal through the communicator, and determine the spacing distance between the hemostat and the limiting mechanism according to the position signal, so that when the spacing distance is greater than or equal to the warning distance, an alarm message is sent to the outside world through the communicator. The present invention proposes a technical solution in which the patient's position is monitored in real time by a signal transmitter, which is convenient for medical staff to quickly find patients and reduce safety risks.
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Description

Technical Field

[0001] The present invention relates to the technical field of medical devices, and in particular to a monitoring method and system for radial artery. Background Art

[0002] The radial artery is one of the terminal branches of the brachial artery. It first passes between the brachioradialis and pronator teres muscles, then between the radial flexor carpi and the brachioradialis muscles, to the lower end of the radius, obliquely passes deep to the tendons of the abductor pollicis longus and extensor pollicis brevis, to the back of the hand and enters the anterior nasopharyngeal fossa.

[0003] After transradial PCI, elastic bandage pressure hemostasis or elastic band pressure hemostat is mainly used for hemostasis. The pressure is usually relieved within 24 to 72 hours after the operation. During the release, the pressure cannot be completely released at one time, and multiple stages of pressure relief are required. During the process of hemostasis and pressure relief, the patient is generally required to lie still and reduce the activity of the injured part to reduce the risk of re-bleeding. However, some patients are more energetic and do not follow the doctor's instructions, which increases the risk of re-bleeding. Due to the limited medical staff, medical staff cannot provide close care for a long time, which poses a certain safety risk. Summary of the invention

[0004] The main purpose of the present invention is to provide a monitoring method and system for the radial artery, aiming to solve the problem that medical staff is limited, close care cannot be performed for a long time, and there are certain safety risks.

[0005] To achieve the above purpose, the technical solution proposed by the present invention is:

[0006] A monitoring system for radial artery comprises a controller, a communicator, a limiting mechanism, a connecting cable and a hemostat, wherein the limiting mechanism is driven to connect one end of the connecting cable, the hemostat is detachably connected to the other end of the connecting cable, and the hemostat is used to be worn on the wrist of a patient to stop bleeding in radial artery; the limiting mechanism is used to retract and release the connecting cable and adjust the spacing distance between the limiting mechanism and the hemostat; the hemostat is provided with a signal transmitter; the communicator and the controller are both provided at the limiting mechanism; the controller is electrically connected to the communicator, and the communicator signal is connected to the signal transmitter, and the controller is used to control the communicator to send a start signal to the signal transmitter when the connecting cable and the hemostat are disconnected, so that the signal transmitter sends a position signal to the outside; the controller is also used to obtain the position signal through the communicator, and determine the spacing distance between the hemostat and the limiting mechanism according to the position signal obtained by the communicator, so that when the spacing distance is greater than or equal to the warning distance, an alarm message is sent to the outside through the communicator.

[0007] Preferably, a connecting connector is provided on a side of the connecting cable away from the limiting mechanism; a connecting mechanism is provided on the outer wall surface of the hemostat, and the connecting mechanism is used to detachably fix the connecting connector so that the hemostat and the connecting cable are fixedly connected.

[0008] Preferably, the connecting mechanism includes a fixed shell and a push-pull electromagnet, a slot is provided on the side of the fixed shell facing away from the hemostat, a mounting through hole is provided on the slot wall, the push-pull electromagnet is arranged in the mounting through hole, and the output end of the push-pull electromagnet is arranged opposite to the slot; a limiting through hole is provided on the outer wall surface of the connecting joint, and the connecting joint is used to be inserted into the slot so that the limiting through hole is arranged opposite to the mounting through hole; the controller is electrically connected to the push-pull electromagnet, and the controller is used to control the output end of the push-pull electromagnet to be inserted into the limiting through hole when the limiting through hole is opposite to the mounting through hole, so that the connecting joint is fixed in the slot.

[0009] Preferably, a fixing hole is provided in the side wall of the slot away from the mounting through hole, and the fixing hole, the limiting through hole and the mounting through hole are coaxially arranged; a limiting structure is provided in the limiting through hole, and the limiting structure is used to be pushed by the output end of the push-pull electromagnet when the output end of the push-pull electromagnet is inserted into the limiting through hole, and inserted into the fixing hole through the limiting through hole.

[0010] Preferably, the limiting structure includes a first tension spring, a connecting column, an insertion column and a limiting plate, the limiting plate is arranged at the end of the limiting plate away from the push-pull electromagnet, and the limiting plate has a connecting through hole along the thickness of the plate; one end of the connecting column is connected to one end of the insertion column, and the insertion column is located between the limiting plate and the connecting column; the diameter of the connecting column is larger than the diameter of the insertion column; the first tension spring is sleeved on the insertion column, one end of the first tension spring abuts the connecting column, and the other end of the first tension spring abuts the limiting plate; the output end of the push-pull electromagnet is used to insert into the end of the limiting through hole away from the fixing hole, so that the output end of the push-pull electromagnet pushes the connecting column and the insertion column in turn, and drives the insertion column to pass through the connecting through hole and insert into the fixing hole.

[0011] Preferably, the limiting mechanism includes a box body and a fixing structure, the fixing structure is arranged on one side of the box body, and the fixing structure is used to detachably fix the box body to one side of the bed; a accommodating space is provided inside the box body, and a connecting port connected to the accommodating space is provided outside the box body; a servo motor, a wire pulley and a connecting shaft are provided in the accommodating space, the output end of the servo motor is connected to the connecting shaft, the wire pulley is sleeved on the connecting shaft, and the end of the connecting cable away from the hemostat is connected to the wire pulley; the controller is electrically connected to the servo motor, and the controller is used to control the servo motor to drive the wire pulley to rotate, so that the wire pulley retracts and releases the connecting cable.

[0012] Preferably, the connecting cable includes a first cable, a second cable and a detection mechanism, one end of the first cable is connected to the detection mechanism, and the other end of the first cable is detachably connected to the hemostat; one end of the second cable is connected to the detection mechanism, and the other end of the second cable is connected to the wire wheel; the controller is electrically connected to the detection mechanism, and the detection mechanism is used to detect the tension data between the first cable and the second cable and send it to the controller; the controller is used to control the servo motor according to the tension data, so that the servo motor drives the wire wheel to retract and release the connecting cable.

[0013] Preferably, the detection mechanism includes a tube body, a column, a pressure sensor and a second tension spring, one end of the tube body is a closed end, and the other end of the tube body is an open end; the end of the first cable away from the hemostat is connected to the closed end; the pressure sensor and the second tension spring are both arranged in the tube body, the pressure sensor is located on the inner wall surface of the tube body close to the first cable, and one end of the second tension spring is connected to the pressure sensor; one end of the column is connected to the end of the second cable away from the reel, and the other end of the column is inserted into the tube body from the open end and connected to the end of the second tension spring away from the pressure sensor; the communicator signal is connected to the pressure sensor, and the pressure sensor is used to detect tension data when the first cable pulls the tube body or the second cable pulls the column, and send it to the controller through the communicator.

[0014] Preferably, the fixing structure includes a connecting plate, a bottom plate, a pressing plate, a screw and a handle, the bottom plate and the box body are spaced apart, the connecting plate is located between the bottom plate and the box body, and the connecting plate connects the bottom plate and the box body respectively; the pressing plate is located between the bottom plate and the box body, and a clamping gap is formed between the bottom plate and the box body; the handle is arranged on the side of the bottom plate away from the pressing plate, and the bottom plate has a threaded through hole along the thickness of the plate; one end of the screw is connected to the handle, the screw is threadedly connected to the threaded through hole, and the end of the screw away from the handle passes through the threaded through hole to connect to the pressing plate.

[0015] To achieve the above object, the present invention further provides a monitoring method for radial artery, wherein the monitoring method for radial artery monitors a patient based on any of the above-mentioned monitoring systems for radial artery, and the method comprises:

[0016] When the connecting cable and the hemostat are disconnected, the signal transmitter sends position information;

[0017] determining, according to the position information, whether the spacing distance between the hemostat and the limiting mechanism is less than a warning distance;

[0018] When the interval distance is greater than or equal to the warning distance, an alarm message is sent to the outside world.

[0019] Compared with the prior art, the present invention has at least the following beneficial effects:

[0020] The restriction mechanism is fixed on one side of the bed, and the hemostat is used to stop bleeding in the patient's radial artery. The patient's activities are initially restricted through the connecting cable. When the patient needs to go to the toilet, the connecting cable and the hemostat are separated, and the patient's position is monitored in real time through the signal transmitter, which is convenient for medical staff to quickly find the patient and reduce safety risks. BRIEF DESCRIPTION OF THE DRAWINGS

[0021] In order to more clearly illustrate the embodiments of the present invention or the technical solutions in the prior art, the drawings required for use in the embodiments or the description of the prior art will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For ordinary technicians in this field, other drawings can be obtained based on the structures shown in these drawings without paying creative work.

[0022] Figure 1 It is a structural schematic diagram of an embodiment of a monitoring system for radial artery of the present invention;

[0023] Figure 2 It is a schematic diagram of the structure inside the box;

[0024] Figure 3This is a schematic diagram of the structure of the inspection agency;

[0025] Figure 4 It is a structural schematic diagram of the connection structure and the connection joint.

[0026] Description of Figure Numbers:

[0027] 1-limiting mechanism; 11-box body; 12-accommodating space; 13-connecting port; 14-servo motor; 15-reel; 16-connecting shaft;

[0028] 2-connecting cable; 21-connecting connector; 22-limiting through hole; 23-first cable; 24-second cable;

[0029] 3-connecting mechanism; 31-fixed housing; 32-push-pull electromagnet; 33-slot; 34-mounting through hole; 35-fixing hole;

[0030] 4-limiting structure; 41-first tension spring; 42-connecting column; 43-insertion column; 44-limiting plate;

[0031] 5-fixed structure; 51-connecting plate; 52-bottom plate; 53-pressing plate; 54-screw rod; 55-handle;

[0032] 6-detection mechanism; 61-tube body; 62-column; 63-pressure sensor; 64-second tension spring;

[0033] 7-Hemostat;

[0034] The realization of the purpose, functional features and advantages of the present invention will be further explained in conjunction with embodiments and with reference to the accompanying drawings. DETAILED DESCRIPTION

[0035] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

[0036] It should be noted that all directional indications in the embodiments of the present invention (such as up, down, left, right, front, back, etc.) are only used to explain the relative position relationship, movement status, etc. between the components under a certain specific posture (as shown in the accompanying drawings). If the specific posture changes, the directional indication will also change accordingly.

[0037] In addition, in the present invention, descriptions such as "first", "second", etc. are only used for descriptive purposes and cannot be understood as indicating or implying their relative importance or implicitly indicating the number of the indicated technical features. Therefore, the features defined as "first" or "second" may explicitly or implicitly include at least one of the features. In the description of the present invention, the meaning of "plurality" is at least two, such as two, three, etc., unless otherwise clearly and specifically defined.

[0038] In the present invention, unless otherwise clearly specified and limited, the terms "connection", "fixation", etc. should be understood in a broad sense. For example, "fixation" can be a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection or an indirect connection through an intermediate medium, it can be the internal connection of two elements or the interaction relationship between two elements, unless otherwise clearly defined. For ordinary technicians in this field, the specific meanings of the above terms in the present invention can be understood according to specific circumstances.

[0039] In addition, the technical solutions between the various embodiments of the present invention can be combined with each other, but it must be based on the fact that ordinary technicians in the field can implement it. When the combination of technical solutions is contradictory or cannot be implemented, it should be deemed that such combination of technical solutions does not exist and is not within the scope of protection required by the present invention.

[0040] The present invention proposes a monitoring system for the radial artery.

[0041] like Figures 1 to 4 A monitoring system for radial artery shown in the figure includes a controller, a communicator, a limiting mechanism 1, a connecting cable 2 and a hemostat 7, wherein the limiting mechanism 1 drives one end of the connecting cable 2, and the hemostat 7 is detachably connected to the other end of the connecting cable 2, and the hemostat 7 is used to be worn on the patient's wrist to stop bleeding in the radial artery; the limiting mechanism 1 is used to retract and release the connecting cable 2 and adjust the spacing distance between the limiting mechanism 1 and the hemostat 7; the hemostat 7 is provided with a signal transmitter; the communicator and the controller are both arranged on the limiting mechanism 1; the controller is electrically connected to the communicator, and the communicator signal is connected to the signal transmitter, and the controller is used to control the communicator to send a start signal to the signal transmitter when the connecting cable 2 and the hemostat 7 are disconnected, so that the signal transmitter sends a position signal to the outside world; the controller is also used to obtain the position signal through the communicator, and determine the spacing distance between the hemostat 7 and the limiting mechanism 1 according to the position signal obtained by the communicator, so that when the spacing distance is greater than or equal to the warning distance, an alarm message is sent to the outside world through the communicator.

[0042] The limiting mechanism 1 is fixed to one side of the bed, and the hemostat 7 is used to stop bleeding in the radial artery of the patient. The patient's activities are initially restricted through the connecting cable 2. When the patient needs to go to the toilet, the connecting cable 2 and the hemostat 7 are separated, and the patient's position is monitored in real time through the signal transmitter, which is convenient for medical staff to quickly find the patient and reduce safety risks.

[0043] Specifically, the limiting mechanism 1 is also provided with an audio module, which is electrically connected to the controller. The audio module is used to obtain audio information within a preset range around the limiting mechanism 1 and send it to the controller; the controller is used to store preset keywords and medical advice voice packages corresponding to each keyword; the controller is also used to determine text information based on the audio information, and determine whether there are keywords in the text information. When there are keywords in the text information, the corresponding medical advice voice package is determined according to the keywords, and the medical advice voice package is played through the audio module; when there are no keywords in the text information, the step of obtaining audio information within a preset range around the limiting mechanism 1 and sending it to the controller is executed. According to the sound information of the patient's surrounding conversation, timely medical advice reminders (i.e., medical advice voice packages) can further reduce the situation of patients not following medical advice. For example, the medical advice voice package corresponding to keywords such as jumping can be: Do not exercise excessively, and excessive exercise has the risk of bleeding. Patients can be prevented from exercising during radial artery hemostasis to avoid bleeding; and the medical advice voice package corresponding to keywords such as food names and water can be: Do not eat certain food and water, and surgery cannot be performed 24 hours after eating. Avoid patients who have to undergo other subsequent operations by mistake to ensure the normal progress of subsequent operations.

[0044] Specifically, the controller is also used to set a weight ranking for each keyword; the controller is also used to determine the number of keywords in the text information when there are keywords in the text information, and when the number of keywords in the text information is equal to one, execute the steps of determining the corresponding medical order voice package according to the keywords, and playing the medical order voice package through the audio module; when the number of keywords in the text information is greater than one, determine the keyword with the highest weight ranking according to each keyword and the weight ranking, and play the medical order voice package corresponding to the keyword with the highest weight ranking.

[0045] Specifically, the controller is also used to determine whether the number of keyword triggering times within a preset time period is greater than or equal to the warning number. When the number of keyword triggering times is greater than or equal to the warning number, the controller sends a warning message to the outside world.

[0046] Specifically, the hemostat 7 includes a middle key, a left key, a right key and a side sliding switch. The middle key is used to enter the control state; the left key and the right key are used to adjust the parameters of the hemostat 7 when it is pressed; the side sliding button is used to lock the middle key, the left key and the right key when the hemostat 7 is working to avoid accidental touch; when the hemostat 7 is in standby mode, the medical staff presses the left key and the right key at the same time, and the hemostat 7 is started to pressurize. When the left key and the right key are released, it stops. In this way, the hemostat 7 can be tied to the corresponding treatment part of the patient under the preset pressure. In the standby mode, the medical staff presses the left key for more than 3 seconds to start the automatic operation mode, and the real-time pressure flashes to prompt. When the pressure value reaches the set pressure value, the pressurization stops automatically. In the automatic operation mode, press the right key for more than 3 seconds to stop the automatic operation and release the pressure (release the pressure to normal pressure).

[0047] A connection connector 21 is provided on the side of the connection cable 2 away from the limiting mechanism 1 ; a connection mechanism 3 is provided on the outer wall of the hemostat 7 , and the connection mechanism 3 is used for detachably fixing the connection connector 21 so that the hemostat 7 and the connection cable 2 are fixedly connected.

[0048] The connection mechanism 3 includes a fixed housing 31 and a push-pull electromagnet 32. A slot 33 is provided on the side of the fixed housing 31 away from the hemostat 7. A mounting through hole 34 is provided on the slot wall of the slot 33. The push-pull electromagnet 32 ​​is arranged in the mounting through hole 34. The output end of the push-pull electromagnet 32 ​​is arranged opposite to the slot 33. A limiting through hole 22 is provided on the outer wall of the connection joint 21. The connection joint 21 is used to be inserted into the slot 33 so that the limiting through hole 22 is arranged opposite to the mounting through hole 34. The controller is electrically connected to the push-pull electromagnet 32. The controller is used to control the output end of the push-pull electromagnet 32 ​​to be inserted into the limiting through hole 22 when the limiting through hole 22 is opposite to the mounting through hole 34, so that the connection joint 21 is fixed in the slot 33. The push-pull electromagnet 32 ​​is inserted into the limiting through hole 22 to clamp the connection joint 21 in the slot 33, so as to realize the connection between the hemostat 7 and the connection cable 2.

[0049] Specifically, a flexible layer is provided on the outer wall surface of the connecting joint 21 , so as to ensure that the connecting head and the slot 33 are firmly matched.

[0050] Specifically, a marking layer is further provided on one side of the fixed housing 31 where the slot 33 is provided, and the marking layer is used for limiting the position and aligning the mounting through hole 34 .

[0051] A fixing hole 35 is provided in the side wall of the slot 33 away from the mounting through hole 34, and the fixing hole 35, the limiting through hole 22 and the mounting through hole 34 are coaxially arranged; a limiting structure 4 is provided in the limiting through hole 22, and the limiting structure 4 is used to be pushed by the output end of the push-pull electromagnet 32 ​​when the output end of the push-pull electromagnet 32 ​​is inserted into the limiting through hole 22, and inserted into the fixing hole 35 through the limiting through hole 22.

[0052] The limiting structure 4 includes a first tension spring 41, a connecting column 42, a plug column 43 and a limiting plate 44. The limiting plate 44 is arranged at one end of the limiting plate 44 away from the push-pull electromagnet 32, and a connecting through hole is opened along the plate thickness of the limiting plate 44; one end of the connecting column 42 is connected to one end of the plug column 43, and the plug column 43 is located between the limiting plate 44 and the connecting column 42; the diameter of the connecting column 42 is larger than the diameter of the plug column 43; the first tension spring 41 is sleeved on the plug column 43, one end of the first tension spring 41 abuts the connecting column 42, and the other end of the first tension spring 41 abuts the limiting plate 44; the output end of the push-pull electromagnet 32 ​​is used to insert the end of the limiting through hole 22 away from the fixing hole 35, so that the output end of the push-pull electromagnet 32 ​​pushes the connecting column 42 and the plug column 43 in turn, and drives the plug column 43 to pass through the connecting through hole and insert into the fixing hole 35. The plug post 43 and the output end of the push-pull electromagnet 32 ​​form a linkage, and the stability of the connection between the hemostat 7 and the connecting cable 2 is further improved through multi-point limiting.

[0053] The limiting mechanism 1 includes a box body 11 and a fixing structure 5, the fixing structure 5 is arranged on one side of the box body 11, and the fixing structure 5 is used to detachably fix the box body 11 to one side of the bed; a storage space 12 is opened in the box body 11, and a connecting port 13 connected to the storage space 12 is opened outside the box body 11; a servo motor 14, a wire wheel 15 and a connecting shaft 16 are arranged in the storage space 12, the output end of the servo motor 14 is connected to the connecting shaft 16, the wire wheel 15 is sleeved on the connecting shaft 16, and the end of the connecting cable 2 away from the hemostat 7 is connected to the wire wheel 15; the controller is electrically connected to the servo motor 14, and the controller is used to control the servo motor 14 to drive the wire wheel 15 to rotate, so that the wire wheel 15 retracts and releases the connecting cable 2.

[0054] The connecting cable 2 includes a first cable 23, a second cable 24 and a detection mechanism 6, one end of the first cable 23 is connected to the detection mechanism 6, and the other end of the first cable 23 is detachably connected to the hemostat 7; one end of the second cable 24 is connected to the detection mechanism 6, and the other end of the second cable 24 is connected to the wire wheel 15; the controller is electrically connected to the detection mechanism 6, and the detection mechanism 6 is used to detect the tension data between the first cable 23 and the second cable 24 and send it to the controller; the controller is used to control the servo motor 14 according to the tension data, so that the servo motor 14 drives the wire wheel 15 to retract and release the connecting cable 2. The detection mechanism 6 detects the tension of the patient pulling the connecting cable 2 (i.e., the tension of pulling the first cable 23), and detects the tension of the servo motor 14 pulling the connecting cable 2 (i.e., the tension of pulling the second cable 24), so as to ensure that the connecting cable 2 is pulled out of the box body 11 to a suitable length to ensure the comfort of the patient; and to prevent the connecting cable 2 from being pulled out too long from the box body 11, which affects the use of the patient.

[0055] Specifically, the controller is used to determine whether the tension data is greater than a first preset tension value according to the tension data. When the tension data is greater than or equal to the first preset tension value, the servo motor 14 rotates forward to release the second cable 24 from the box body 11; when the tension data is less than the first preset tension value, it is determined whether the tension data is greater than or equal to zero. When the tension data is equal to zero, the servo motor 14 reverses to pull the second cable 24 into the box body 11; when the tension data is greater than zero, the servo motor 14 stops rotating and executes the step of determining whether the tension data is greater than the first preset tension value after a preset time period. According to the strength of the patient pulling the first cable 23, the second cable 24 is automatically retracted and released, so as to realize automatic retraction and release and improve the comfort of the patient.

[0056] The detection mechanism 6 includes a tube body 61, a column 62, a pressure sensor 63 and a second tension spring 64, one end of the tube body 61 is a closed end, and the other end of the tube body 61 is an open end; the end of the first cable 23 away from the hemostat 7 is connected to the closed end; the pressure sensor 63 and the second tension spring 64 are both arranged in the tube body 61, the pressure sensor 63 is located in the tube body 61 close to the inner wall surface of the first cable 23, and one end of the second tension spring 64 is connected to the pressure sensor 63; one end of the column 62 is connected to the end of the second cable 24 away from the reel 15, and the other end of the column 62 is inserted into the tube body 61 from the open end and connected to the end of the second tension spring 64 away from the pressure sensor 63; the communicator signal is connected to the pressure sensor 63, and the pressure sensor 63 is used to detect tension data when the first cable 23 pulls the tube body 61 or the second cable 24 pulls the column 62, and sends it to the controller through the communicator. The tube body 61 and the column 62 are arranged to slide relative to each other via the second tension spring 64 , so that any action of the patient driving the first cable 23 can trigger the servo motor 14 , thereby ensuring timely feedback to the patient.

[0057] The fixing structure 5 includes a connecting plate 51, a bottom plate 52, a pressing plate 53, a screw 54 and a handle 55. The bottom plate 52 and the box body 11 are arranged at intervals, and the connecting plate 51 is located between the bottom plate 52 and the box body 11. The connecting plate 51 connects the bottom plate 52 and the box body 11 respectively; the pressing plate 53 is located between the bottom plate 52 and the box body 11, and a clamping gap is formed between the bottom plate 52 and the box body 11; the handle 55 is arranged on the side of the bottom plate 52 away from the pressing plate 53, and the bottom plate 52 is provided with a threaded through hole along the plate thickness; one end of the screw 54 is connected to the handle 55, and the screw 54 is threadedly connected to the threaded through hole, and the end of the screw 54 away from the handle 55 passes through the threaded through hole to connect to the pressing plate 53. The medical staff rotates the pressing plate 53 through the handle 55, and the box body 11 is clamped and fixed to one side of the bed through the pressing plate 53 and the box body 11, so as to ensure that the patient can be effectively restricted and prevented from moving during the hemostasis process.

[0058] To achieve the above object, the present invention further provides a monitoring method for radial artery, wherein the monitoring method for radial artery monitors a patient based on any one of the above monitoring systems for radial artery, and the method comprises:

[0059] Step S1, when the connection cable 2 and the hemostat 7 are disconnected, the signal transmitter sends position information;

[0060] Step S2, judging whether the spacing distance between the hemostat 7 and the limiting mechanism 1 is less than the warning distance according to the position information;

[0061] Step S3: When the interval distance is greater than or equal to the warning distance, an alarm message is sent to the outside world.

[0062] The above description is only a preferred embodiment of the present invention, and does not limit the patent scope of the present invention. All equivalent structural changes made by using the contents of the present invention specification and drawings under the inventive concept of the present invention, or directly / indirectly applied in other related technical fields are included in the patent protection scope of the present invention.

Claims

1. A monitoring system for radial artery, characterized in that: The invention comprises a controller, a communicator, a limiting mechanism, a connecting cable and a hemostat, wherein the limiting mechanism is driven to connect one end of the connecting cable, the hemostat is detachably connected to the other end of the connecting cable, and the hemostat is used to be worn on the patient's wrist to stop radial artery bleeding; the limiting mechanism is used to retract and release the connecting cable and adjust the spacing distance between the limiting mechanism and the hemostat; the hemostat is provided with a signal transmitter; the communicator and the controller are both arranged on the limiting mechanism; the controller is electrically connected to the communicator, and the communicator signal is connected to the signal transmitter, and the controller is used to control the communicator to send a start signal to the signal transmitter when the connecting cable and the hemostat are disconnected, so that the signal transmitter sends a position signal to the outside world; the controller is also used to obtain a position signal through the communicator, and determine the spacing distance between the hemostat and the limiting mechanism according to the position signal obtained by the communicator, so that when the spacing distance is greater than or equal to the warning distance, an alarm message is sent to the outside world through the communicator.

2. A monitoring system for radial artery according to claim 1, characterized in that: A connecting joint is arranged on a side of the connecting cable away from the limiting mechanism; a connecting mechanism is arranged on the outer wall surface of the hemostat, and the connecting mechanism is used for detachably fixing the connecting joint so that the hemostat and the connecting cable are fixedly connected.

3. A monitoring system for radial artery according to claim 2, characterized in that: The connecting mechanism includes a fixed shell and a push-pull electromagnet. A slot is provided on the side of the fixed shell away from the hemostat, and a mounting through hole is provided on the slot wall. The push-pull electromagnet is arranged in the mounting through hole, and the output end of the push-pull electromagnet is arranged opposite to the slot; a limiting through hole is provided on the outer wall surface of the connecting joint, and the connecting joint is used to be inserted into the slot so that the limiting through hole is arranged opposite to the mounting through hole; the controller is electrically connected to the push-pull electromagnet, and the controller is used to control the output end of the push-pull electromagnet to be inserted into the limiting through hole when the limiting through hole is opposite to the mounting through hole, so that the connecting joint is fixed in the slot.

4. A monitoring system for radial artery according to claim 3, characterized in that: A fixing hole is provided in the side wall of the slot away from the mounting through hole, and the fixing hole, the limiting through hole and the mounting through hole are coaxially arranged; a limiting structure is provided in the limiting through hole, and the limiting structure is used to be pushed by the output end of the push-pull electromagnet when the output end of the push-pull electromagnet is inserted into the limiting through hole, and inserted into the fixing hole through the limiting through hole.

5. A monitoring system for radial artery according to claim 4, characterized in that: The limiting structure includes a first tension spring, a connecting column, an insertion column and a limiting plate, wherein the limiting plate is arranged at one end of the limiting plate away from the push-pull electromagnet, and the limiting plate has a connecting through hole along the thickness of the plate; one end of the connecting column is connected to one end of the insertion column, and the insertion column is located between the limiting plate and the connecting column; the diameter of the connecting column is larger than the diameter of the insertion column; the first tension spring is sleeved on the insertion column, one end of the first tension spring abuts against the connecting column, and the other end of the first tension spring abuts against the limiting plate; the output end of the push-pull electromagnet is used to insert into the end of the limiting through hole away from the fixing hole, so that the output end of the push-pull electromagnet pushes the connecting column and the insertion column in turn, and drives the insertion column to pass through the connecting through hole and insert into the fixing hole.

6. A radial artery monitoring system according to any one of claims 1 to 5, characterized in that: The limiting mechanism includes a box body and a fixing structure, wherein the fixing structure is arranged on one side of the box body, and the fixing structure is used to detachably fix the box body to one side of the bed; a storage space is provided in the box body, and a connecting port connected to the storage space is provided outside the box body; a servo motor, a wire wheel and a connecting shaft are arranged in the storage space, the output end of the servo motor is connected to the connecting shaft, the wire wheel is sleeved on the connecting shaft, and the end of the connecting cable away from the hemostat is connected to the wire wheel; the controller is electrically connected to the servo motor, and the controller is used to control the servo motor to drive the wire wheel to rotate so that the wire wheel can retract and release the connecting cable.

7. A monitoring system for radial artery according to claim 6, characterized in that: The connecting cable comprises a first cable, a second cable and a detection mechanism, one end of the first cable is connected to the detection mechanism, and the other end of the first cable is detachably connected to the hemostat; one end of the second cable is connected to the detection mechanism, and the other end of the second cable is connected to the wire wheel; The controller is electrically connected to the detection mechanism, and the detection mechanism is used to detect the tension data between the first cable and the second cable and send it to the controller; The controller is used to control the servo motor according to the tension data, so that the servo motor drives the wire wheel to retract and release the connecting cable.

8. A monitoring system for radial artery according to claim 7, characterized in that: The detection mechanism includes a tube body, a column, a pressure sensor and a second tension spring, one end of the tube body is a closed end, and the other end of the tube body is an open end; the end of the first cable away from the hemostat is connected to the closed end; the pressure sensor and the second tension spring are both arranged in the tube body, the pressure sensor is located on the inner wall surface of the tube body close to the first cable, and one end of the second tension spring is connected to the pressure sensor; one end of the column is connected to the end of the second cable away from the reel, and the other end of the column is inserted into the tube body from the open end and connected to the end of the second tension spring away from the pressure sensor; the communicator signal is connected to the pressure sensor, and the pressure sensor is used to detect tension data when the first cable pulls the tube body or the second cable pulls the column, and send it to the controller through the communicator.

9. A monitoring system for radial artery according to claim 6, characterized in that: The fixing structure includes a connecting plate, a bottom plate, a pressing plate, a screw and a handle, the bottom plate and the box body are spaced apart, the connecting plate is located between the bottom plate and the box body, and the connecting plate connects the bottom plate and the box body respectively; the pressing plate is located between the bottom plate and the box body, and a clamping gap is formed between the bottom plate and the box body; the handle is arranged on the side of the bottom plate away from the pressing plate, and the bottom plate has a threaded through hole along the thickness of the plate; one end of the screw is connected to the handle, the screw is threadedly connected to the threaded through hole, and the end of the screw away from the handle passes through the threaded through hole to connect to the pressing plate.

10. A method for monitoring radial artery, characterized in that: The radial artery monitoring method is based on a radial artery monitoring system according to any one of claims 1 to 9 to monitor a patient, and the method comprises: When the connecting cable and the hemostat are disconnected, the signal transmitter sends position information; determining, according to the position information, whether the spacing distance between the hemostat and the limiting mechanism is less than a warning distance; When the interval distance is greater than or equal to the warning distance, an alarm message is sent to the outside world.

Citation Information

Patent Citations

  • Induction alarm device for unplanned extubation

    CN113662731A

  • Off-bed detection alarm system and device

    CN116158759A