WO2020150924A1 - Système de surveillance mobile à fonction d'alerte d'informations distribuées et son procédé - Google Patents

Système de surveillance mobile à fonction d'alerte d'informations distribuées et son procédé Download PDF

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Publication number
WO2020150924A1
WO2020150924A1 PCT/CN2019/072840 CN2019072840W WO2020150924A1 WO 2020150924 A1 WO2020150924 A1 WO 2020150924A1 CN 2019072840 W CN2019072840 W CN 2019072840W WO 2020150924 A1 WO2020150924 A1 WO 2020150924A1
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WO
WIPO (PCT)
Prior art keywords
information
prompt
mobile monitoring
component
patient
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PCT/CN2019/072840
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English (en)
Chinese (zh)
Inventor
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
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Application filed by 深圳迈瑞生物医疗电子股份有限公司 filed Critical 深圳迈瑞生物医疗电子股份有限公司
Priority to PCT/CN2019/072840 priority Critical patent/WO2020150924A1/fr
Priority to CN201980064579.9A priority patent/CN112788992B/zh
Publication of WO2020150924A1 publication Critical patent/WO2020150924A1/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316—Modalities, i.e. specific diagnostic methods
    • A61B5/318—Heart-related electrical modalities, e.g. electrocardiography [ECG]

Definitions

  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • the mobile monitoring system 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • the mobile monitoring system 100 is divided into two parts that can be detachably connected.
  • the defibrillation protection structure 50 is divided into a first resistance.
  • the defibrillation part 51 and the second anti-defibrillation part 53 are connected to each other to form the defibrillation protection structure 50.
  • 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.
  • the clip of the defibrillation part 53 clips the defibrillation protection structure 50 to the collar of the patient.
  • 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.
  • 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.
  • the above-mentioned host 11 further includes an ear part 117.
  • the ear 117 is provided on the side of the main casing 111.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • the second connector 1153 is connected to the ECG/respiratory lead cable 30 through the second connection port 1177.
  • 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.
  • 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
  • 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.
  • 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.
  • 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.
  • 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
  • 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.
  • the above-mentioned mobile monitoring device 10 further includes a wristband module 13.
  • 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.
  • FIG. 6 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.
  • 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.
  • 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.
  • 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.
  • FIG. 7 and FIG. 8 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.
  • 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.
  • 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.
  • first connection port 1331a is located on the side of the wrist strap 133a close to the bottom end of the host 11
  • second connection port 1333a is located on the side of the wrist strap 133a close to the top end of the host 11.
  • FIG. 9 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.
  • the aforementioned electrode sheet 80 is a disposable electrode sheet.
  • the above-mentioned electrode sheet 80 is a disposable ECG electrode sheet.
  • the outer frame host 71 is made of flexible material and has a mouth shape.
  • 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.
  • 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.
  • 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.
  • 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.
  • FIG. 10 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.
  • 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.
  • 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.
  • FIG. 11 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.
  • 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.
  • 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.
  • 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.
  • the physiological data information is at least one of numerical information and waveform information
  • the state prompt information includes at least one of alarm prompt, power information, exercise data, and time information.
  • 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.
  • 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.
  • the status prompt information includes at least one of alarm prompt, power information, exercise data, and time information.
  • 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.
  • 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.
  • 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.
  • 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.
  • the second color indicator light 711 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.
  • 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.
  • the second blinking indicator light 713 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • the controller 40 controls the call unit 20 to establish a call with the call unit 20 of the central station equipment connection.
  • 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.
  • the connection quality state between the electrode sheet connector 70 and the electrode sheet 80 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.
  • a motion sensor 60 is provided in the mobile monitoring device 10 and/or the defibrillation protection structure 50.
  • the motion sensor 60 is arranged on the defibrillation protection structure 50.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • the first color indicator light 551 prompts the patient's different physiology through different color prompt signals.
  • the first color indicator light 551 can also display different physiological states of the patient through other color prompt signals.
  • 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.
  • the first information prompting component 55 includes a first display screen 555
  • 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.
  • 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 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • FIG. 12 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.
  • controlling the first information prompting component 55 to at least display the physiological state of the patient includes:
  • 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,
  • 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,
  • 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.
  • the status prompt information includes at least one of alarm prompt, power information, exercise data, and time information.
  • 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
  • the status prompt information includes an alarm. At least one of reminder, power information, exercise data, and time information.
  • 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.
  • 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.
  • 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.
  • 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:
  • 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 ,
  • 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.
  • 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.
  • 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.
  • 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:
  • 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,
  • 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,
  • 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.
  • 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.
  • the first information prompting component 55 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.
  • the defibrillation protection structure is provided with a first information prompting component
  • the mobile monitoring equipment is provided with a second information prompting component
  • 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.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Medical Informatics (AREA)
  • Biophysics (AREA)
  • Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Cardiology (AREA)
  • Physics & Mathematics (AREA)
  • Molecular Biology (AREA)
  • Surgery (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Electrotherapy Devices (AREA)

Abstract

La présente invention concerne un système de surveillance mobile (100) à fonction d'alerte d'informations distribuées, et un procédé de surveillance mobile. Le système de surveillance mobile comprend un fil conducteur d'électrocardiogramme/de respiration (30), une structure de protection de défibrillation (50), et au moins trois connecteurs de feuille d'électrode (70), une extrémité du fil conducteur d'électrocardiogramme/de respiration (30) étant configurée pour être reliée à un dispositif de surveillance mobile (10) ; la structure de protection de défibrillation (50) et lesdits trois connecteurs de feuille d'électrode (70) étant séquentiellement disposés en série sur le fil conducteur d'électrocardiogramme/de respiration (30) d'une extrémité, proche du dispositif de surveillance mobile (10), à une extrémité, éloignée du dispositif de surveillance mobile (10) ; les connecteurs de feuille d'électrode (70) étant utilisés pour serrer les feuilles d'électrode (80) ; un premier composant d'alerte d'informations (55) étant disposé sur la structure de protection de défibrillation (50) ; et le premier composant d'alerte d'informations (55) étant utilisé pour au moins indiquer l'état physiologique d'un·e patient·e. Le premier composant d'alerte d'informations (55) disposé sur la structure de protection de défibrillation (50) du système de surveillance mobile (100) peut indiquer l'état physiologique d'un·e patient·e, et fournir une alerte évidente pour informer à temps le personnel médical de l'état du·de la patient·e.
PCT/CN2019/072840 2019-01-23 2019-01-23 Système de surveillance mobile à fonction d'alerte d'informations distribuées et son procédé WO2020150924A1 (fr)

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PCT/CN2019/072840 WO2020150924A1 (fr) 2019-01-23 2019-01-23 Système de surveillance mobile à fonction d'alerte d'informations distribuées et son procédé
CN201980064579.9A CN112788992B (zh) 2019-01-23 2019-01-23 具有分布式信息提示功能的移动监护系统及其方法

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Publication number Priority date Publication date Assignee Title
JPH10127626A (ja) * 1996-10-31 1998-05-19 Hewlett Packard Co <Hp> Ｅｋｇデータ表示装置
CN2621603Y (zh) * 2003-05-08 2004-06-30 张伟 可视心电监测听诊器
CN107847745A (zh) * 2015-05-13 2018-03-27 阿库图森医疗有限公司 用于采集和分析心脏信息的定位系统和方法
CN106913330A (zh) * 2015-10-07 2017-07-04 株式会社K海奥斯威尔 佩戴式无线12通道心电图系统
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