WO2020150924A1

WO2020150924A1 - Mobile monitoring system with distributed information prompting function and method thereof

Info

Publication number: WO2020150924A1
Application number: PCT/CN2019/072840
Authority: WO
Inventors: 刘启翎; 任健; 薛冰冰
Original assignee: 深圳迈瑞生物医疗电子股份有限公司
Priority date: 2019-01-23
Filing date: 2019-01-23
Publication date: 2020-07-30
Also published as: CN112788992B; CN112788992A

Abstract

Provided are a mobile monitoring system (100) with a distributed information prompting function, and a mobile monitoring method. The mobile monitoring system comprises an electrocardiogram/respiration lead cable (30), a defibrillation protection structure (50), and at least three electrode sheet connectors (70), wherein one end of the electrocardiogram/respiration lead cable (30) is configured to be connected to a mobile monitoring device (10); the defibrillation protection structure (50) and the at least three electrode sheet connectors (70) are sequentially arranged in series on the electrocardiogram/respiration lead cable (30) from one end, close to the mobile monitoring device (10), to one end, away from the mobile monitoring device (10); the electrode sheet connectors (70) are used for clamping electrode sheets (80); a first information prompting component (55) is provided on the defibrillation protection structure (50); and the first information prompting component (55) is used for at least indicating the physiological status of a patient. The first information prompting component (55) provided on the defibrillation protection structure (50) of the mobile monitoring system (100) can indicate the physiological status of a patient, and provides an obvious prompt to inform medical personnel of the status of the patient in a timely manner.

Description

Mobile monitoring system and method with distributed information prompt function

Technical field

This application relates to the technical field of physiological data monitoring, in particular to a mobile monitoring system and method with a distributed information prompt function.

Background technique

The existing portable monitoring equipment can be divided into two categories, one is that the device does not have an information prompt function locally, and the other is that the device has an information prompt function locally, such as a display screen or an indicator light. When the device has no information prompt function locally, after the medical staff connects the device to the patient, the inspection of the working status of the device needs to be confirmed on the remote controller. If there is a problem, the patient needs to be adjusted again. This way It will cause inconvenience to medical staff and result in low work efficiency. When the device has an information prompt function locally, it can solve the aforementioned problems of inconvenience and low efficiency of the device without information prompt function, that is, if the device is faulty or not worn correctly, the local display or indicator can prompt the medical staff to readjust , But these information are displayed on one device. If medical staff want to view the relevant physiological parameters, alarm information, etc., they need to be close to the patient to see clearly. Especially when the size of the equipment is small and the patient's wearing position is not conducive to direct observation, even if the medical staff is close to the patient's position, the physiological parameter alarms or equipment failure information displayed locally on the equipment are not easy to be observed by the medical staff in time. As a result, the patient cannot be treated in time or loses normal supervision.

Summary of the invention

The embodiment of the present application discloses a mobile monitoring system and a mobile monitoring method, and the monitoring prompt is eye-catching to solve the above technical problem.

The embodiment of the application discloses a mobile monitoring system with a distributed information prompt function, including a mobile monitoring device, an ECG/respiratory lead cable, a defibrillation protection structure and at least three electrode pad connectors. One end of the breathing lead cable is used to connect to the mobile monitoring device, and the ECG/respiration lead cable is connected in series from the end close to the mobile monitoring device to the end far away from the mobile monitoring device. The defibrillation protection structure and the at least three electrode pad connectors, the electrode pad connectors are used to clamp the electrode pads, the defibrillation protection structure is provided with a first information prompting component, and the first information prompting component Used to at least indicate the physiological state of the patient.

The embodiment of the application also discloses a mobile monitoring system with a distributed information prompt function, which includes a mobile monitoring device, an ECG/respiratory lead cable, a defibrillation protection structure and at least three electrode pad connectors. One end of the/breathing lead cable is used to connect to the mobile monitoring device, and the ECG/respiratory lead cable is serially connected from the end close to the mobile monitoring device to the end far away from the mobile monitoring device. The defibrillation protection structure and the at least three electrode pad connectors, the electrode pad connectors are used to clamp the electrode pads, the defibrillation protection structure is provided with a first information prompt component, and the mobile monitoring device A second information prompt component is provided, and each electrode sheet connector is provided with a third information prompt component. When the mobile monitoring system generates an alarm signal, the first information prompt component, the second information prompt component, and the At least one of the third information prompt components is used to issue a corresponding alarm prompt signal.

The embodiment of the present application also discloses a mobile monitoring method, which is applied to a mobile monitoring system, the mobile monitoring system includes a defibrillation protection structure, the defibrillation protection structure is provided with a first information prompt component, and the mobile monitoring system The method includes the steps of: controlling the first information prompting component to at least indicate the physiological state of the patient.

In the mobile monitoring system and mobile monitoring method disclosed in the embodiments of the present application, the defibrillation protection structure is provided with a first information prompt component, which can indicate the physiological state of the patient, the monitoring prompt is eye-catching, and the medical staff can be informed of the patient state in time.

Description of the drawings

In order to more clearly illustrate the technical solutions in the embodiments of the present application, the following will briefly introduce the drawings that need to be used in the embodiments. Obviously, the drawings in the following description are only some embodiments of the present application. A person of ordinary skill in the art can obtain other drawings based on these drawings without creative work.

Fig. 1 is a schematic structural diagram of a mobile monitoring system in an embodiment of the application.

Fig. 2 is a schematic diagram of a disassembled state of the mobile monitoring system shown in Fig. 1.

Figure 3 is a schematic structural diagram of a mobile monitoring device in an embodiment of the application.

FIG. 4 is a schematic structural diagram of the mobile monitoring device in another direction in an embodiment of the application.

Fig. 5 is a schematic structural diagram of the mobile monitoring device in an embodiment of the application in another direction after the wristband is removed.

Fig. 6 is a schematic structural diagram of a wristband module of a mobile monitoring device in an embodiment of the application.

FIG. 7 is a schematic structural diagram of a mobile monitoring device in the first direction in an embodiment of the application.

FIG. 8 is a schematic structural diagram of a mobile monitoring device in a second direction in an embodiment of the application.

FIG. 9 is a schematic diagram of the structure of the electrode pad connector in an embodiment of the application.

FIG. 10 is a schematic diagram of the structure of an electrode pad connector in an embodiment of the application.

FIG. 11 is a schematic structural diagram of a mobile monitoring system in another embodiment of the application.

FIG. 12 is a schematic flowchart of a mobile monitoring method in an embodiment of this application.

detailed description

The following will clearly and completely describe the technical solutions in the embodiments of the present application in conjunction with the drawings in the embodiments of the present application. Obviously, the described embodiments are only a part of the embodiments of the present application, rather than all the embodiments. Based on the embodiments in this application, all other embodiments obtained by those of ordinary skill in the art without creative work shall fall within the protection scope of this application.

The terms "first", "second", etc. in the specification and claims of this application and the aforementioned drawings are used to distinguish different objects, rather than to describe a specific sequence. In addition, the term "including" and any variations of them are intended to cover non-exclusive inclusion. For example, a process, method, system, product, or device that includes a series of steps or units is not limited to the listed steps or units, but optionally includes unlisted steps or units, or optionally also includes Other steps or units inherent to these processes, methods, products or equipment.

The subsequent descriptions of the specification are preferred embodiments for implementing the application, but the foregoing description is for the purpose of explaining the general principles of the application, and is not intended to limit the scope of the application. The protection scope of this application shall be subject to those defined by the appended claims.

Please refer to FIG. 1. FIG. 1 is a schematic structural diagram of a mobile monitoring system 100 in an embodiment of the application. The mobile monitoring system 100 includes a mobile monitoring device 10, an ECG/respiratory lead cable 30, a defibrillation protection structure 50, at least three electrode pad connectors 70, a blood oxygen cable 60 and a blood oxygen probe 90. The mobile monitoring device 10 is connected to one end of the ECG/respiratory lead cable 30. The defibrillation protection structure 50 and the at least three electrode pad connectors 70 are sequentially arranged in series on the electrocardiogram/respiration lead cable 30 from the end close to the mobile monitoring device 10 to the end far away from the mobile monitoring device 10. The electrode tab connector 70 is used to clamp the electrode tab 80. In one embodiment, the aforementioned electrode sheet 80 is a disposable electrode sheet. It can be understood that, in another embodiment, the above-mentioned electrode sheet 80 is a disposable ECG electrode sheet. One end of the blood oxygen cable 60 is connected to the mobile monitoring device 10, and the other end is connected to the blood oxygen probe 90.

Specifically, in one of the embodiments, the above-mentioned mobile monitoring device 10 is used to be tied to the patient's wrist to monitor the patient's physiological data signals. In some of the modified embodiments, the above-mentioned ECG/respiratory lead cable 30 may adopt a cable structure, which is sequentially arranged in series with the above-mentioned defibrillation protection structure 50 and the above-mentioned at least three electrode pad connectors 70. /Respiratory lead cable can also be constructed with bifurcated cable structure. If the above-mentioned ECG/respiratory lead cable 30 adopts a bifurcated cable structure, the ECG/respiratory lead cable 30 includes a main part and at least three branch parts, and one end of the main part is connected to the above-mentioned mobile monitoring device 10 , The other end of the main part is connected to at least three bifurcation parts, each bifurcation part is provided with at least one electrode pad connector 70, and the above-mentioned defibrillation protection structure 50 is arranged at any position on the main part. Each electrode patch connector 70 is used to hold a piece of electrode patch 80, and each electrode patch 80 is used to attach to a certain part of the patient's body to measure the physiological data signal or impedance signal of the part. The defibrillation protection structure 50 contains a defibrillation protection circuit, and the defibrillation protection circuit is used to prevent damage to the ECG detection system when necessary to defibrillate the patient's heart to restore a normal heart beat. In the present application, the above-mentioned defibrillation protection structure 50 and the above-mentioned mobile monitoring device 10 are arranged independently, so that the volume of the above-mentioned mobile monitoring device 10 is reduced, and it is convenient to carry. The signal in the mobile monitoring device 10 causes interference.

Please refer to FIG. 2 together. In order to facilitate fixing the mobile monitoring system 100 on the patient's body, the mobile monitoring system 100 is divided into two parts that can be detachably connected. Specifically, the defibrillation protection structure 50 is divided into a first resistance. The defibrillation part 51 and the second anti-defibrillation part 53. The first anti-defibrillation portion 51 and the second anti-defibrillation portion 53 are connected to each other to form the defibrillation protection structure 50. In this embodiment, the above-mentioned first anti-defibrillation part 51 and the second anti-defibrillation part 53 are connected together in a plug-in manner. The first anti-defibrillation unit 51 is also connected to the mobile monitoring device 10 via the ECG/respiration lead cable 30. The second anti-defibrillation unit 53 is also connected to the at least three electrode pad connectors 70 through the electrocardiogram/respiratory lead cable 30. Therefore, when the mobile monitoring device 10 is installed on the patient's wrist, the ECG/respiration lead cable 30 and the first anti-defibrillation part 51 connected to the mobile monitoring device 10 are passed through the patient's sleeve to the patient's neck. When the at least three electrode strip connectors 70 clamp the electrode strips 80 and stick them on the designated part of the patient’s body, the ECG/respiration lead cables 30 and the second After the anti-defibrillation part 53 is worn from the inside of the patient’s clothes to the patient’s neck, and is connected to the first anti-defibrillation part 51, it is disposed on the first anti-defibrillation part 51 and/or the second anti-defibrillation part 51. The clip of the defibrillation part 53 clips the defibrillation protection structure 50 to the collar of the patient.

Please also refer to FIG. 3, the above-mentioned mobile monitoring device 10 includes a host 11. The mainframe 11 includes a mainframe 111 and a parameter measurement circuit board 113 arranged in the mainframe 111. It can be understood that the parameter measurement circuit board 113 shown in FIG. 3 is only for illustration. The host 11 described above further includes a connector 115. The parameter measurement circuit board 113 is connected to the electrocardiogram/respiration lead cable 30 through the connector 115. Therefore, the parameter measurement circuit board 113 can be electrically connected to the external defibrillation protection structure 50 through the ECG/respiration lead cable 30.

Specifically, the above-mentioned host 11 further includes an ear part 117. The ear 117 is provided on the side of the main casing 111. In one of the embodiments, the connector 115 is provided in the ear 117. It can be understood that, in some of the modified embodiments, the ear portion 117 is a storage bin with a hollow interior, and the connector 115 is detachably plugged into the storage bin.

Furthermore, the ear part 117 is provided at one end of the main casing 111. The parameter measurement circuit board 113 is disposed at one end of the main casing 311 adjacent to the ear portion 117. The mobile monitoring device 10 described above further includes a battery 119. The battery 119 is arranged at an end of the main casing 111 away from the ear 117. The battery 119 is electrically connected to the parameter measurement circuit board 113.

Further, the ear part 117 includes a first ear part 1171 and a second ear part 1173. The first ear portion 1171 and the second ear portion 1173 are respectively provided on both sides of the main casing 111. The aforementioned connector 115 includes a first connector 1151 and a second connector 1153. The first connector 1151 is provided in the first ear portion 1171 and connected to the parameter measurement circuit board 113. The first connector 1151 is also connected to the blood oxygen probe 90 through the blood oxygen cable 60. The second connector 1153 is arranged in the second ear part 1173 and connected to the parameter measurement circuit board 113. The second connector 1153 is also connected to the at least three electrode pad connectors 70 through the ECG/respiration lead cable 30.

Further, referring to FIG. 3 again, the first ear portion 1171 is provided with a first connection port 1175. The first connection port 1175 is connected to the first connector 1151. Therefore, the first connector 1151 is connected to the blood oxygen probe 90 through the first connection port 1175.

Further, please also refer to FIG. 4, the second ear portion 1173 is provided with a second connection port 1177. The second connection port 1177 is connected to the second connector 1153. Thus, the second connector 1153 is connected to the ECG/respiratory lead cable 30 through the second connection port 1177.

Further, in order to enable the blood oxygen cable 60 to be connected to the host 11 through the shortest path without the need for cable winding, and to enable the ECG/respiratory lead cable 30 to be connected to the host 11 through the shortest path, the The first connection port 1175 is set toward the human finger, and the second connection port 1177 on the host 11 is set toward the human body; specifically, the orientation of the first connection port 1175 on the host 11 is opposite to the orientation of the second connection port 1177 on the host 11 . The first connection port 1175 is located on the side of the first ear portion 1171 close to the bottom end of the main casing 111, and the second connection port 1177 is disposed on the side of the second ear portion 1173 close to the top end of the main casing 111.

It should be noted that the above-mentioned top end refers to the front side of the main body shell 111 in the use state, specifically, when the main body 11 is worn on the wrist, it faces the human body, and the above-mentioned bottom end 117 refers to the rear side of the main body shell 111 in the use state. Specifically, the host 11 faces the fingers when worn on the wrist.

In some of the modified embodiments, the first ear portion 1171 is a first storage compartment with a hollow interior, and the first connector 1151 is detachably plugged into the first storage compartment. In some of the modified embodiments, the second ear portion 1173 is a second storage compartment with a hollow inside, and the second connector 1153 is detachably plugged into the second storage compartment. Thus, the blood oxygen accessory of the mobile monitoring system 100, for example, includes a first connector 1151, a blood oxygen cable and a blood oxygen probe 90 connected to the first connector 1151, and an ECG accessory, for example, includes a second connection The device 1153, the ECG cable 30 connected to the second connector 1153, the defibrillation protective structure 50, and the electrode connector 70 can be plugged and unplugged, so that the medical staff can select the required monitoring parameters according to the actual condition of the patient, such as , Whether to monitor blood oxygen, choose three-lead ECG monitoring or five-lead ECG monitoring, etc., so as to minimize the impact of physiological monitoring on patients’ daily life, improve monitoring comfort, and facilitate medical staff to replace monitoring accessories and extend Machine life.

Please also refer to FIG. 5, the above-mentioned mobile monitoring device 10 further includes a wristband module 13. Wherein, FIG. 5 only shows a schematic diagram of a part of the structure of the above-mentioned wristband module 13 in an embodiment. The wristband module 13 is arranged on one side of the host 11. Specifically, in this embodiment, the wristband module 13 is disposed on the back of the host 11. The wristband module 13 is used to fix the host 11 to the patient's wrist.

Please also refer to FIG. 6, which is a schematic structural diagram of the above-mentioned wristband module 13 in the first embodiment of the application. The aforementioned wristband module 13 includes a fixing frame 131 and a wristband 133. The fixing frame 131 is arranged on one side of the host 11. The fixing frame 131 fixes the battery 119 between the main casing 111 and the fixing frame 131. The wrist strap 133 is arranged on the side of the fixing frame 131 away from the host 11. The wrist strap 133 is used to fix the host 11 to the patient's wrist.

Specifically, in some embodiments, the main casing 111 has a closed cavity for accommodating the parameter measurement circuit board 113. The battery 119 is arranged on the outer wall of the main casing 111 and is located outside the closed cavity of the main casing 111; the battery 119 is held between the main body 10 and the fixing frame 131 by connecting the fixing frame 131 and the main casing 111. The battery 119 is detachably fixed on the host 11 through the fixing frame 131, which can be easily disassembled and installed, which is very convenient.

Specifically, a guide groove 1311 is provided on the side of the fixing frame 131 facing the host 11. The guide groove 1311 is used to guide the host 11 to be installed on the fixing frame 131. At least one perforation 1313 is symmetrically provided on the side of the fixing frame 131 away from the host 11. The wrist strap 133 passes through the at least one through hole 1313 to be fixed on the fixing frame 131. Preferably, the aforementioned wristband 133 is a flexible wristband. The aforementioned wristband 133 may be, but is not limited to, a silicone belt, a cloth belt, and the like.

The aforementioned wristband module 13 further includes a flexible rubber pad 135. The flexible rubber pad 135 is arranged on the side of the wrist strap 133 away from the fixing frame 131. The aforementioned flexible rubber pad 135 is used to directly contact the patient's skin to protect the patient's skin.

Please refer to FIG. 7 and FIG. 8 together, which are schematic diagrams of the above-mentioned mobile monitoring device 10a in another embodiment of the application. The difference between the wristband module 13a of the mobile monitoring device 10a and the wristband module 13 is that the wristband module 13a and the host 11 are integrated. The wristband module 13a directly extends vertically from the ear 117 of the host 11. The first connector 1151 and the second connector 1153 are respectively disposed in the wristband module 13a.

Specifically, the aforementioned wristband module 13a includes two wristbands 133a. The two wrist straps 133a respectively extend vertically from the first ear portion 1171 and the second ear portion 1173 of the main body 11, and then buckle or bond each other to form a loop-shaped strap.

Further, in this embodiment, the first connector 1151 is disposed on the wristband 133a adjacent to the first ear portion 1171. The second connector 1153 is provided on the wrist strap 133 a adjacent to the second ear portion 1173. The wristband 133a adjacent to the first ear portion 1171 is also provided with a first connection port 1331a. The first connection port 1331a is connected to the first connector 1151, so that the first connector 1151 is connected to the blood oxygen probe 90 through the first connection port 1331a. The wristband 133a adjacent to the second ear portion 1173 is also provided with a second connection port 1333a. The second connection port 1333a is connected to the second connector 1153, so that the second connector 1153 is connected to the ECG/respiratory lead cable 30 through the second connection port 1333a.

Further, the first connection port 1331a is located on the side of the wrist strap 133a close to the bottom end of the host 11, and the second connection port 1333a is located on the side of the wrist strap 133a close to the top end of the host 11.

Please also refer to FIG. 9, which is a structural diagram of the electrode pad connector 70 in an embodiment of the application. The electrode plate connector 70 includes an outer frame main body 71 and two clamping pieces 73 arranged inside the outer frame main body 71. The outer frame host 71 is used to connect with the ECG/respiratory lead cable 30. The two clamping pieces 73 are used to clamp the electrode piece 80. In one embodiment, the aforementioned electrode sheet 80 is a disposable electrode sheet. In another embodiment, the above-mentioned electrode sheet 80 is a disposable ECG electrode sheet.

Specifically, the outer frame host 71 is made of flexible material and has a mouth shape.

Further, the outer frame host 71 has a first side portion 711 and a second side portion 713 that are oppositely disposed. The two clamping pieces 73 are respectively disposed on opposite sides of the first side portion 711 and the second side portion 713. The two clamping pieces 73 are opposite to each other to form a receiving space 731. The accommodation space 731 is used to accommodate and clamp the electrode sheet 80. When the outer frame main body 71 is pinched to reduce the distance between the first side portion 711 and the second side portion 713, the receiving space 731 increases to release the electrode sheet 80.

Furthermore, the two clamping pieces 73 are both L-shaped hooks, and an O-shaped receiving space 731 is formed between the two clamping pieces 73.

Further, the clamping piece 73 is stepped. The electrode sheet 80 is correspondingly provided with an inverted step. Therefore, when the electrode sheet 80 is clamped by the clamping piece 73, the inverted step of the electrode sheet 80 and the step of the clamping piece 73 cooperate with each other, so that the electrode sheet 80 is stably clamped between the two clamping pieces. Between 73.

Specifically, the electrode sheet connector 70 further includes connecting posts 75 provided at both ends of the outer frame main body 71. The connecting post 75 is used to connect with the ECG/respiratory lead cable 30.

Please also refer to FIG. 10, which is a schematic diagram of the structure of the electrode tab connector 70 a in another embodiment of the application. The difference between the electrode pad connector 70 a and the electrode pad connector 70 is that the electrode pad connector 70 a has only one connecting post 75. It is understandable that if only one end of the electrode pad connector 70a needs to be connected to the ECG/respiration lead cable 30, the number of the connection posts 75 can be one.

In the mobile monitoring device 10 and the mobile monitoring system 100 of the present application, the defibrillation protection structure 50 is independent of the mobile monitoring device 10. The high current of the defibrillation protection structure 50 will not affect the function of the mobile monitoring device 10, and the mobile monitoring device 10 can do It is lighter and thinner, and more portable.

In addition, in order to facilitate the placement of the mobile monitoring system 100 on the patient's body, the mobile monitoring system 100 is divided into two parts that can be plugged together, that is, the defibrillation protection structure 50 is divided into a first anti-defibrillation part 51 and a second anti-defibrillation part 51. Defibrillation unit 53. The first anti-defibrillation part 51 and the second anti-defibrillation part 53 are connected to each other to form the aforementioned defibrillation protection structure 50. The first anti-defibrillation unit 51 is also connected to the mobile monitoring device 10 through the ECG/respiratory lead cable 30. The second anti-defibrillation part 53 is also connected to at least three electrode pad connectors 70 through an ECG/respiratory lead cable 30. The mobile monitoring device 10 has at least two different wristband modules with more options. The frame body 71 of the electrode sheet connector 70 is flexible, and the electrode sheet 80 can be clamped or released by clamping the frame body, and the operability is better.

Please also refer to FIG. 11, which is a schematic diagram of modules of a mobile monitoring system 100a with a distributed information prompt function in an embodiment of the application. The mobile monitoring system 100a is similar to the mobile monitoring system 100. The difference is that the defibrillation protection structure 50 of the mobile monitoring system 100a is further provided with a first information prompting component 55. 55 is used to at least indicate the physiological state of the patient.

It can be understood that, in one of the embodiments, the first information prompting component 55 includes a first color indicator light 551. The first color indicator light 551 is used to indicate different physiological states of the patient through different color prompt signals. In one of the embodiments, when the first color indicator light 551 displays a red prompt signal, it indicates that the patient is in poor state, when a yellow prompt signal is displayed, it indicates that the patient is in alarm, and when a green prompt signal is displayed, it indicates that the patient is in good condition. It can be understood that, in other embodiments, the first color indicator light 551 can also display different physiological states of the patient through other color prompt signals.

It can be understood that, in one of the modified embodiments, the first information prompting component 55 includes a first blinking indicator light 553. The first flashing indicator light 553 indicates different physiological states of the patient through prompt signals with different flashing frequencies. In one of the embodiments, when the first flashing indicator light 553 flashes at a flashing frequency greater than a preset value, it indicates that the patient's state is poor, and when the first flashing indicator light 553 flashes at a flashing frequency less than the preset value When the status of the patient is alarmed, when the first flashing indicator light 553 is on, it indicates that the patient is in good condition. It can be understood that, in other embodiments, the first flashing indicator light 553 may indicate different physiological states of the patient through other flashing frequencies.

It can be understood that, in one of the modified embodiments, the first information prompting component 55 includes a first display screen 555. The first display screen 555 is used to display physiological data information and/or status prompt information of the patient. Wherein, the physiological data information is at least one of numerical information and waveform information, and the state prompt information includes at least one of alarm prompt, power information, exercise data, and time information.

It can be understood that, in one of the modified embodiments, the first information prompt component 55 includes at least two of the first color indicator light 551, the first blinking indicator light 553, and the first display screen 555, for example, A color indicator light 551 and a first flashing indicator light 553 indicate different physiological states of the patient at the same time, so that the current physiological state of the patient and the patient's family and medical staff can be reminded more conspicuously.

It can be understood that, in one of the embodiments, a second information prompt component 15 is provided on the mobile monitoring device 10. The second information prompt component 15 includes a second display screen 151, which is used to display at least the patient's physiological data information and/or status prompt information, and the physiological data information is a combination of numerical information and waveform information. At least one, the status prompt information includes at least one of alarm prompt, power information, exercise data, and time information.

It is understandable that, in one of the embodiments, the content of the physiological data information of the patient displayed on the first display screen 555 is less than the content of the physiological data information displayed on the second display screen 151. Therefore, since the defibrillation protective structure 50 is fixed on the collar of the patient, it will not be blocked by the patient’s clothes and is easy to observe. Therefore, the first display screen 555 is used to display the key physiological state data of the patient and give an alarm. Eye-catching, helps the patient's family and medical staff to observe, and is more helpful for physiological data monitoring. Further, in one of the embodiments, the size of the first display screen 555 is smaller than the size of the second display screen 151, so that the defibrillation protection structure 50 is more portable.

It can be understood that, in one of the embodiments, the first display screen 555 and/or the second display screen 151 is a low-power display screen. The low-power display screen refers to a display screen with relatively low power, for example, the power is less than or equal to 5 mW. It is understandable that the low power consumption display screen may be, but is not limited to, an electronic ink screen or a monochrome LCD and other low power consumption display screens. As a result, the overall power consumption of the mobile monitoring system 100a can be reduced, the overall endurance of the mobile monitoring system 100a can be improved, and the workload of medical personnel for replacing batteries can be reduced.

It can be understood that, in one of the embodiments, a third information prompt component 71 is provided on each electrode pad connector 70. The third information prompt component 71 is used to indicate the connection quality state between the electrode sheet connector 70 and the corresponding electrode sheet 80.

It is understandable that, in one of the embodiments, the third information prompting component 71 includes a second color indicator light 711, and the second color indicator light 711 indicates the electrode sheet connector 70 through a prompt signal of a different color. Different connection quality states with the corresponding electrode sheet 80. Specifically, in one of the embodiments, when the second color indicator light 711 displays a red prompt signal, it means that the electrode sheet 80 or the electrode sheet connector 70 is not connected or the ECG lead wire is off; When the two-color indicator light 711 displays a yellow prompt signal, it indicates that the contact impedance of the electrode sheet 80 or the electrode sheet connector 70 is too large; when the second color indicator light 711 displays a green prompt signal, it indicates that the electrode The connection quality of the sheet 80 or the electrode sheet connector 70 is normal. It is understandable that, in other embodiments, the first color indicator light 551 may also indicate different connection quality states between the electrode sheet connector 70 and the corresponding electrode sheet 80 through other color prompt signals. , It is not limited here.

It is understandable that, in one of the modified embodiments, the third information prompting component 71 includes a second flashing indicator light 713, and the second flashing indicator light 713 indicates that the electrode pads are connected through prompt signals with different flashing frequencies. Different connection quality states between the device 70 and the corresponding electrode sheet 80. Specifically, in one of the embodiments, when the second blinking indicator light 713 blinks at a blinking frequency greater than a preset value, it indicates that the electrode sheet 80 or the electrode sheet connector 70 is not connected or the ECG lead When the second flashing indicator light 713 flashes at a flashing frequency less than the preset value, it indicates that the contact impedance of the electrode sheet 80 or the electrode sheet connector 70 is too large; when the second flashing indicator When the light 713 is on continuously, it indicates that the connection quality of the electrode sheet 80 or the electrode sheet connector 70 is normal. It can be understood that, in other embodiments, the second blinking indicator light 713 may indicate different connection quality states between the electrode sheet connector 70 and the corresponding electrode sheet 80 through other flashing frequencies.

It is understandable that, in one of the embodiments, the connection quality status information between the electrode pad connector 70 and the corresponding electrode pad 80 can be transmitted to the defibrillation protection structure 50 and/or the mobile monitoring device 10, the first information prompt component 55 and/or the second information prompt component 15 is further used to indicate the connection quality status between the electrode sheet connector 70 and the corresponding electrode sheet 80. In other words, the connection quality status information between the electrode sheet connector 70 and the corresponding electrode sheet 80 can be passed through the first information prompting component 55, the second information prompting component 15 and/or the third information At least one of the components 71 is displayed.

It can be understood that, in one of the embodiments, the mobile monitoring system 100a further includes a call unit 20 and a controller 40. The communication unit 20 and the controller 40 are arranged on the mobile monitoring device 10 or the defibrillation protection structure 50. In this embodiment, the communication unit 20 and the controller 40 are arranged on the defibrillation protection structure 50. The controller 40 is electrically connected to the call unit 20. When the status prompt information includes an alarm prompt, the controller 40 controls the call unit 20 to establish a call with the call unit 20 of the central station equipment connection.

It is understandable that, in one of the embodiments, when it is determined that the physiological state of the patient satisfies the alarm condition, the first information prompting component 55 and/or the second information prompting component 15 issue an alarm prompt, and the The controller 40 controls the call unit 20 to establish a call connection with the call unit 20 of the central station equipment. Therefore, hospital personnel can rush to the scene for treatment in time when an alarm is issued during patient monitoring, so as to avoid delaying the best treatment opportunity.

It can be understood that, in one of the embodiments, when the connection quality state between the electrode sheet connector 70 and the electrode sheet 80 is not connected, the first information prompting component 55 and the second information prompting The component 15 and/or the third information prompting component 71 issues an alarm prompt, and the controller 40 controls the communication unit 20 to establish a communication connection with the communication unit 20 of the central station equipment. Therefore, the connection quality state between the electrode pad connector 70 that can be worn on the patient and the electrode pad 80 is not connected, and the medical staff is notified for processing in time, so that the patient's physiological data can be optimally monitored.

It is understandable that, in one of the embodiments, a motion sensor 60 is provided in the mobile monitoring device 10 and/or the defibrillation protection structure 50. In this embodiment, the motion sensor 60 is arranged on the defibrillation protection structure 50. When the motion sensor 60 senses that the patient has fallen, the first information prompting component 55 and/or the second information prompting component 15 will issue an alarm prompt, and the controller 40 controls the communication unit 20 and the central station A call connection is established between the call units 20 of the device.

It is understandable that, in one of the embodiments, after the wireless communication connection is established between the mobile monitoring device 10 and the bedside monitor, the first information prompting component 55, the second information prompting component 15 and/ Or, the content prompted by the third information prompting component 71 is simultaneously displayed on the bedside monitor for information prompting. After the bedside monitor establishes a wireless communication connection with the central station equipment or the handheld device in the hands of the medical staff, the first information prompting component 55, the second information prompting component 15 and/or the third information prompting The content prompted by the component 71 is synchronously displayed on the central station device or the handheld device for information prompting.

It is understandable that, in one of the modified embodiments, in the mobile monitoring system 100a with a distributed information prompting function, the defibrillation protection structure 50 is provided with a first information prompting component 55, and the mobile monitoring The device 10 is provided with a second information prompting component 15, and each electrode sheet connector 70 is provided with a third information prompting component 71. When the mobile monitoring system 100a generates an alarm signal, the first information prompting component 55, At least one of the second information prompt component 15 and the third information prompt component 71 is used to issue a corresponding alarm prompt signal, and the alarm manner is more flexible and diverse.

It is understandable that, in one of the embodiments, when the first information prompting component 55 includes a first color indicator light 551, the first color indicator light 551 prompts the patient's different physiology through different color prompt signals. Status: When the first color indicator light 551 displays a red prompt signal, it means that the patient is in poor condition, when a yellow prompt signal is displayed, it means that the patient is in alarm, and when a green prompt signal is displayed, it means that the patient is in good condition. It can be understood that, in other embodiments, the first color indicator light 551 can also display different physiological states of the patient through other color prompt signals.

It is understandable that, in one of the modified embodiments, when the first information prompting component 55 includes the first flashing indicator light 553, the first flashing indicator light 553 uses prompt signals with different flashing frequencies to prompt different patients. Physiological state; when the first flashing indicator light 553 flashes at a flashing frequency greater than a preset value, it indicates that the patient's state is poor, and when the first flashing indicator light 553 flashes at a flashing frequency less than the preset value, it indicates The patient status is alarmed. When the first flashing indicator light 553 is on, it indicates that the patient is in good condition. It can be understood that, in other embodiments, the first flashing indicator light 553 may indicate different physiological states of the patient through other flashing frequencies.

It is understandable that, in one of the embodiments, the first information prompting component 55 includes a first display screen 555, and the second information prompting component 15 includes a second display screen 151, the first display screen 555 and The second display screen 151 is used to display physiological data information and/or status prompt information of the patient; wherein, the physiological data information is at least one of numerical information and waveform information, and the status prompt information includes alarm prompts, At least one of power information, exercise data, and time information. Specifically, in one of the embodiments, the content of the physiological data information displayed on the first display screen 555 of the patient is less than the content of the physiological data information displayed on the second display screen 151.

It can be understood that, in one of the modified embodiments, the first information prompt component 55 includes at least two of the first color indicator light 551, the first blinking indicator light 553, and the first display screen 555, for example, A color indicator light 551 and a first flashing indicator light 553 indicate different physiological states of the patient at the same time, so that the current physiological state of the patient, his family and medical staff can be more conspicuously reminded.

It is understandable that, in one of the embodiments, the third information prompting component 71 includes a second color indicator light 711, and the second color indicator light 711 indicates the electrode sheet connector 70 through a prompt signal of a different color. Different connection quality status with the corresponding electrode sheet 80; when the second color indicator light 711 displays a red prompt signal, it indicates that the electrode sheet 80 or the electrode sheet connector 70 is not connected or the ECG lead wire is off; When the second color indicator light 711 displays a yellow prompt signal, it indicates that the contact impedance of the electrode sheet 80 or the electrode sheet connector 70 is too large; when the second color indicator light 711 displays a green prompt signal, it indicates The connection quality of the electrode strip 80 or the electrode strip connector 70 is normal. It is understandable that, in other embodiments, the first color indicator light 551 may also indicate different connection quality states between the electrode sheet connector 70 and the corresponding electrode sheet 80 through other color prompt signals. , It is not limited here.

It is understandable that, in one of the embodiments, the third information prompting component 71 includes a second flashing indicator light 713, and the second flashing indicator light 713 indicates the electrode sheet connector through prompt signals with different flashing frequencies. Different connection quality status between 70 and the corresponding electrode sheet 80; when the second flashing indicator light 713 flashes at a flashing frequency greater than the preset value, it means that the electrode sheet 80 or the electrode sheet connector 70 is not connected or the heart The electrical lead wire falls off; when the second flashing indicator light 713 flashes at a flashing frequency less than the preset value, it indicates that the contact impedance of the electrode strip 80 or the electrode strip connector 70 is too large; when the second When the flashing indicator 713 is on, it indicates that the connection quality of the electrode sheet 80 or the electrode sheet connector 70 is normal. It can be understood that, in other embodiments, the second blinking indicator light 713 may indicate different connection quality states between the electrode sheet connector 70 and the corresponding electrode sheet 80 through other flashing frequencies.

Please refer to FIG. 12, which is a flowchart of a mobile monitoring method applied to the mobile monitoring system 100a in an embodiment of the application. The mobile monitoring system 100a includes a defibrillation protection structure 50 on which a first information prompting component 55 is provided. The execution sequence of the mobile monitoring method is not limited to the sequence shown in FIG. 12. The mobile monitoring method includes:

Step 121: Control the first information prompting component 55 to at least indicate the physiological state of the patient.

It is understandable that, in one of the embodiments, "controlling the first information prompting component 55 to at least display the physiological state of the patient" includes:

When the first information prompting component 55 includes a first color indicator light 551, controlling the first color indicator light 551 to indicate different physiological states of the patient through different color prompt signals; and/or,

When the first information prompting component 55 includes a first flashing indicator light 553, controlling the first flashing indicator light 553 to indicate different physiological states of the patient through prompt signals with different flashing frequencies; and/or,

When the first information prompting component 55 includes the first display screen 553, the first display screen 553 is controlled to display the patient's physiological data information and/or status prompt information, and the physiological data information is a combination of numerical information and waveform information. At least one, the status prompt information includes at least one of alarm prompt, power information, exercise data, and time information.

It is understandable that, in one of the embodiments, the mobile monitoring system 100a includes a mobile monitoring device 10, and the mobile monitoring device 10 is provided with a second information prompt component 15, and the mobile monitoring method further includes:

Step 122: Control the second information prompting component 15 to display at least one of physiological data information and status prompt information. The physiological data information is at least one of numerical information and waveform information, and the status prompt information includes an alarm. At least one of reminder, power information, exercise data, and time information.

It is understandable that, in one of the embodiments, the second information prompt component 15 includes a second display screen 151, and the second display screen 151 is used to display at least the patient's physiological data information and/or status prompt information, The physiological data information is at least one of numerical information and waveform information, and the state prompt information includes at least one of alarm prompt, power information, exercise data, and time information.

Specifically, in one of the embodiments, the content of the physiological data information displayed on the first display screen 555 of the patient is less than the content of the physiological data information displayed on the second display screen 151.

The first display screen 555 and/or the second display screen 151 is a low-power display screen, for example, an electronic ink screen or a monochrome LCD.

It is understandable that, in one of the embodiments, the mobile monitoring system 100a further includes at least three electrode plate connectors 70, and each electrode plate connector 70 is used to connect a corresponding electrode plate 80; A third information prompt component 71 is provided on the device 70, and the mobile monitoring method further includes:

Step 123: Control the third information prompting component 71 to indicate different connection quality states between the electrode sheet connector 70 and the corresponding electrode sheet 80.

It is understandable that, in one of the embodiments, "controlling the third information prompting component 71 to indicate the different connection quality states between the electrode sheet connector 70 and the corresponding electrode sheet 80" includes:

When the third information prompt component 71 includes a second color indicator light 711, different color prompt signals indicate different connection quality states between the electrode sheet connector 70 and the corresponding electrode sheet 80; and/or ,

When the third information prompting component 71 includes the second flashing indicator light 713, the second flashing indicator light 713 indicates the contact between the electrode sheet connector 70 and the corresponding electrode sheet 80 through prompt signals with different flashing frequencies. Different connection quality status.

It is understandable that, in one of the embodiments, the mobile monitoring method includes:

Step 124: Transmit the connection quality status information between the electrode pad connector 70 and the corresponding electrode pad 80 to the defibrillation protection structure 50 and/or the mobile monitoring device 10, and further pass the first information The prompt component 55 and/or the second information prompt component 15 indicate the connection quality state between the electrode sheet connector 70 and the corresponding electrode sheet 80.

It is understandable that, in one of the embodiments, the mobile monitoring system 100a further includes a call unit 20 which is arranged on the mobile monitoring device 10 or the defibrillation protection structure 50, and the mobile Monitoring methods also include:

Step 125: When the status prompt information includes an alarm prompt, control the call unit 20 to establish a call connection with the call unit 20 of the central station equipment.

It is understandable that, in one of the embodiments, each electrode pad connector 70 is provided with a third information prompt component 71, "When the state prompt information includes an alarm prompt, control the communication unit 20 and the central Establishing a call connection between the call units 20 of the station equipment includes:

When it is determined that the physiological state of the patient meets the alarm condition, the first information prompting component 55 and/or the second information prompting component 15 issue an alarm prompt, and control the communication unit 20 and the communication unit 20 of the central station equipment Establish a call connection between; or,

When the connection quality state between the electrode sheet connector 70 and the electrode sheet 80 is not connected, the first information prompting component 55, the second information prompting component 15 and/or the third information prompting component 71 issues an alarm prompt and controls the call unit 20 to establish a call connection with the call unit 20 of the central station equipment; or,

When the patient falls, the first information prompting component 55 and/or the second information prompting component 15 issue an alarm prompt and control the communication unit 20 to establish a communication connection with the communication unit 20 of the central station equipment.

It is understandable that, in one of the embodiments, the mobile monitoring method further includes:

Step 126: After the wireless communication connection is established between the mobile monitoring device 10 and the bedside monitor, the first information prompting component 55, the second information prompting component 15 and/or the third information prompting component 71 The prompt content is synchronously displayed on the bedside monitor for information prompting.

After the bedside monitor establishes a wireless communication connection with the central station equipment or the handheld device in the hands of the medical staff, the first information prompting component 55, the second information prompting component 15 and/or the third information prompting component The content prompted by 71 is synchronously displayed on the central station device or the handheld device for information prompting.

In the mobile monitoring system and mobile monitoring method thereof of the present application, the defibrillation protection structure is provided with a first information prompting component, the mobile monitoring equipment is provided with a second information prompting component, and each electrode pad connector is provided with a third information prompting component. Information prompting component, when the mobile monitoring system generates an alarm signal, at least one of the first information prompting component, the second information prompting component, and the third information prompting component is used to issue a corresponding alarm prompting signal , The prompt is obvious and eye-catching.

The embodiments of the application are described in detail above, and specific examples are used in this article to illustrate the principles and embodiments of the application. The descriptions of the above embodiments are only used to help understand the methods and core ideas of the application; A person of ordinary skill in the art, based on the idea of the present application, will have changes in the specific embodiments and scope of application. In summary, the content of this specification should not be construed as limiting the application.

Claims

A mobile monitoring system with a distributed information prompt function, characterized in that, the mobile monitoring system includes a mobile monitoring device, an ECG/respiratory lead cable, a defibrillation protection structure and at least three electrode pad connectors, and One end of the ECG/respiration lead cable is used to connect to the mobile monitoring device, and the ECG/respiration lead cable runs from the end close to the mobile monitoring device to the end far away from the mobile monitoring device. The defibrillation protection structure and the at least three electrode pad connectors are arranged in series, the electrode pad connectors are used to clamp the electrode pads, the defibrillation protection structure is provided with a first information prompting component, and the An information prompt component is used to at least indicate the physiological state of the patient.
The mobile monitoring system according to claim 1, wherein the defibrillation protection structure comprises a first anti-defibrillation part and a second anti-defibrillation part, the first anti-defibrillation part and the second anti-defibrillation part The first anti-defibrillation part is detachably connected to the mobile monitoring device through the ECG/respiratory lead cable, and the second anti-defibrillation part is connected through the ECG/respiratory lead The connecting cable is connected to the at least three electrode pad connectors; and/or, the defibrillation protection structure is used to fasten the patient's collar with a clip; and/or, the ECG/respiratory lead wire The cable is a one-wire ECG/respiratory lead cable.
The mobile monitoring system according to claim 1, wherein the first information prompt component comprises a first color indicator light, and the first color indicator light indicates different physiological states of the patient through different color prompt signals.
The mobile monitoring system according to claim 1, wherein the first information prompt component includes a first flashing indicator light, and the first flashing indicator light indicates different physiological states of the patient through prompt signals with different flashing frequencies .
The mobile monitoring system according to any one of claims 1 to 4, wherein the first information prompting component comprises a first display screen, and the first display screen is used to display the patient's physiological data information and/or State prompt information, the physiological data information is at least one of numerical information and waveform information, and the state prompt information includes at least one of alarm prompt, power information, exercise data, and time information.
The mobile monitoring system of claim 5, wherein a second information prompting component is provided on the mobile monitoring device, the second information prompting component includes a second display screen, and the second display screen is used for At least the patient’s physiological data information and/or state prompt information is displayed, the physiological data information is at least one of numerical information and waveform information, and the state prompt information includes at least one of alarm prompt, power information, exercise data, and time information One kind.
The mobile monitoring system according to claim 6, wherein the content of the physiological data information of the patient displayed on the first display screen is less than the content of the physiological data information displayed on the second display screen; the first display The display screen and/or the second display screen is a low power consumption display screen.
The mobile monitoring system of claim 6, wherein a third information prompt component is provided on each electrode pad connector, and the third information prompt component is used to indicate that the electrode pad connector is connected to the corresponding electrode pad. The connection quality status between.
The mobile monitoring system according to claim 8, wherein the third information prompt component includes a second color indicator light, and the second color indicator light indicates that the electrode pad connector is connected to the Different connection quality states between corresponding electrode pieces.
The mobile monitoring system according to claim 8, wherein the third information prompt component includes a second flashing indicator light, and the second flashing indicator light indicates the electrode sheet connector through prompt signals with different flashing frequencies Different connection quality status with the corresponding electrode sheet.
The mobile monitoring system according to any one of claims 8 to 10, wherein the connection quality status information between the electrode pad connector and the corresponding electrode pad is transmitted to the defibrillation protection structure and/or On the mobile monitoring device, the first information prompting component and/or the second information prompting component are further used to indicate the connection quality status between the electrode sheet connector and the corresponding electrode sheet.
The mobile monitoring system according to claim 8, wherein the mobile monitoring system further comprises a call unit and a controller, and the call unit and the controller are provided in the mobile monitoring device or the defibrillation protection Structurally, the controller is electrically connected to the call unit, and when the status prompt information includes an alarm prompt, the controller controls the call unit to establish a call connection with the call unit of the central station equipment.
The mobile monitoring system according to claim 12, wherein when it is determined that the physiological state of the patient satisfies the alarm condition, the first information prompting component and/or the second information prompting component issue an alarm prompt, and The controller controls the call unit to establish a call connection with the call unit of the central station equipment.
The mobile monitoring system according to claim 12, wherein when the connection quality state between the electrode sheet connector and the electrode sheet is not connected, the first information prompting component and the second information prompt The component and/or the third information prompt component issues an alarm prompt, and the controller controls the call unit to establish a call connection with the call unit of the central station equipment.
The mobile monitoring system according to claim 12, wherein the mobile monitoring device and/or the defibrillation protection structure is provided with a motion sensor, and when the motion sensor senses that the patient falls, the first An information prompt component and/or a second information prompt component issue an alarm prompt, and the controller controls the call unit to establish a call connection with the call unit of the central station equipment.
The mobile monitoring system according to any one of claims 8 to 15, wherein after a wireless communication connection is established between the mobile monitoring device and the bedside monitor, the first information prompting component, the second The information prompting component and/or the content prompted by the third information prompting component are simultaneously displayed on the bedside monitor for information prompting, and the bedside monitor establishes a wireless connection with the central station equipment or the handheld device in the hands of the medical staff. After the communication connection, the content prompted by the first information prompt component, the second information prompt component, and/or the third information prompt component are simultaneously displayed on the central station device or the handheld device for information prompting .
A mobile monitoring system with a distributed information prompt function, characterized in that, the mobile monitoring system includes a mobile monitoring device, an ECG/respiratory lead cable, a defibrillation protection structure and at least three electrode pad connectors, and One end of the ECG/respiration lead cable is used to connect to the mobile monitoring device, and the ECG/respiration lead cable runs from the end close to the mobile monitoring device to the end far away from the mobile monitoring device. The defibrillation protection structure and the at least three electrode pad connectors are arranged in series, the electrode pad connectors are used to clamp the electrode pads, the defibrillation protection structure is provided with a first information prompting component, and the moving The monitoring equipment is provided with a second information prompting component, and each electrode pad connector is provided with a third information prompting component. When the mobile monitoring system generates an alarm signal, the first information prompting component and the second information At least one of the prompt component and the third information prompt component is used to issue a corresponding alarm prompt signal.
The mobile monitoring system of claim 17, wherein when the first information prompting component includes a first color indicator light, the first color indicator light prompts the patient's different physiology through different color prompt signals. Status: When the first color indicator shows a red prompt signal, it means that the patient is in poor condition, when a yellow prompt signal is displayed, it means that the patient is in alarm, and when a green prompt signal is displayed, it means that the patient is in good condition.
The mobile monitoring system according to claim 17, wherein when the first information prompting component includes a second flashing indicator light, the second flashing indicator light prompts the patient's different status through prompt signals with different flashing frequencies. Physiological state; when the second flashing indicator light flashes at a flashing frequency greater than the preset value, it indicates that the patient is in poor state, and when the second flashing indicator light flashes at a flashing frequency less than the preset value, it indicates that the patient state is alarmed When the second flashing indicator light is on, it indicates that the patient is in good condition.
The mobile monitoring system according to any one of claims 17 to 19, wherein the first information prompt component includes a first display screen, the second information prompt component includes a second display screen, and the first information prompt component includes a second display screen. The display screen and the second display screen are respectively used to display the patient's physiological data information and/or status prompt information; and the content of the patient's physiological data information displayed on the first display screen is less than that displayed on the second display screen The content of the physiological data information.
The mobile monitoring system according to claim 17, wherein the third information prompt component comprises a second color indicator light, and the second color indicator light indicates that the electrode sheet connector is connected to the Different connection quality status between the corresponding electrode pads; when the second color indicator shows a red prompt signal, it means that the electrode pads or the electrode pad connectors are not connected or the ECG lead wire is off; when the second color When the indicator light shows a yellow prompt signal, it means that the contact impedance of the electrode strip or the electrode strip connector is too large; when the second color indicator shows a green prompt signal, it means the electrode strip or the electrode strip connector is connected The quality status is normal.
The mobile monitoring system according to any one of claims 17 or 21, wherein the third information prompting component includes a second flashing indicator light, and the second flashing indicator light indicates the status of Different connection quality states between the electrode strip connector and the corresponding electrode strip; when the second flashing indicator light flashes at a flashing frequency greater than the preset value, it indicates that the electrode strip or the electrode strip connector is not connected or the heart The electrical lead wire falls off; when the second flashing indicator light flashes at a flashing frequency less than the preset value, it means that the contact impedance of the electrode sheet or the electrode sheet connector is too large; when the second flashing indicator light When it stays on, it indicates that the connection quality of the electrode sheet or the electrode sheet connector is normal.
A mobile monitoring method is applied to a mobile monitoring system, the mobile monitoring system includes a defibrillation protection structure, the defibrillation protection structure is provided with a first information prompt component, characterized in that the mobile monitoring method includes step:

The first information prompt component is controlled to at least indicate the physiological state of the patient.
The mobile monitoring method according to claim 23, wherein "controlling the first information prompting component to at least display the physiological state of the patient" comprises:

When the first information prompting component includes a first color indicator light, controlling the first color indicator light to indicate different physiological states of the patient through different color prompt signals; and/or,

When the first information prompting component includes a first flashing indicator light, controlling the first flashing indicator light to indicate different physiological states of the patient through prompt signals with different flashing frequencies; and/or,

When the first information prompting component includes a first display screen, the first display screen is controlled to display physiological data information and/or status prompt information of the patient, and the physiological data information is at least one of numerical information and waveform information , The status prompt information includes at least one of alarm prompt, power information, exercise data, and time information.
The mobile monitoring method according to claim 24, wherein the mobile monitoring system comprises a mobile monitoring device, the mobile monitoring device is provided with a second information prompt component, and the mobile monitoring method further comprises the steps:

Control the second information prompting component to display at least one of physiological data information and status prompt information, the physiological data information being at least one of numerical information and waveform information, and the status prompt information including alarm prompts and power information , At least one of exercise data and time information.
The mobile monitoring method according to claim 25, wherein the second information prompting component comprises a second display screen, and the content of the physiological data information of the patient displayed on the first display screen is less than that of the second display screen. The content of the displayed physiological data information; the first display screen and/or the second display screen are low power consumption display screens.
The mobile monitoring method of claim 25, wherein the mobile monitoring system further comprises at least three electrode pad connectors, and each electrode pad connector is used to connect a corresponding electrode pad; A third information prompt component is provided, and the mobile monitoring method further includes the steps:

The third information prompting component is controlled to indicate different connection quality states between the electrode sheet connector and the corresponding electrode sheet.
The mobile monitoring method according to claim 27, wherein "controlling the third information prompting component to indicate different connection quality states between the electrode sheet connector and the corresponding electrode sheet" comprises:

When the third information prompt component includes a second color indicator light, different color prompt signals indicate different connection quality states between the electrode sheet connector and the corresponding electrode sheet; and/or,

When the third information prompting component includes the second flashing indicator light, the prompt signals with different flashing frequencies indicate different connection quality states between the electrode sheet connector and the corresponding electrode sheet.
The mobile monitoring method of claim 27, wherein the mobile monitoring method comprises the steps:

The connection quality status information between the electrode pad connector and the corresponding electrode pad is transmitted to the defibrillation protection structure and/or the mobile monitoring device, and the first information prompt component and/or the The second information prompt component indicates the connection quality status between the electrode sheet connector and the corresponding electrode sheet.
The mobile monitoring method according to claim 27, wherein the mobile monitoring system further comprises a call unit, and the call unit is arranged on the mobile monitoring device or the defibrillation protection structure, and the mobile monitoring method It also includes steps:

When the status prompt information includes an alarm prompt, the call unit is controlled to establish a call connection with the call unit of the central station equipment.
The mobile monitoring method of claim 30, wherein each electrode pad connector is provided with a third information prompt component, "When the state prompt information includes an alarm prompt, control the communication unit and the central The establishment of a call connection between the call units of the station equipment includes:

When it is determined that the physiological state of the patient satisfies the alarm condition, the first information prompting component and/or the second information prompting component issue an alarm prompt, and control the call unit to establish a call connection with the call unit of the central station equipment ;or,

When the connection quality state between the electrode sheet connector and the electrode sheet is not connected, the first information prompting component, the second information prompting component and/or the third information prompting component issue an alarm prompt, And controlling the call unit to establish a call connection between the call unit of the central station equipment; or,

When the patient falls, the first information prompting component and/or the second information prompting component issue an alarm prompt, and control the call unit to establish a call connection with the call unit of the central station equipment.
The mobile monitoring method of claim 27, wherein the mobile monitoring method further comprises the steps:

After the wireless communication connection is established between the mobile monitoring device and the bedside monitor, the content prompted by the first information prompting component, the second information prompting component, and/or the third information prompting component are simultaneously displayed on Information prompt on the bedside monitor;

After the bedside monitor establishes a wireless communication connection with the central station equipment or the handheld device in the hands of medical staff, the first information prompt component, the second information prompt component and/or the third information prompt component prompt The content of is synchronously displayed on the central station device or the handheld device for information prompting.