CN108904923A - A kind of intelligent transfusion monitoring method and system - Google Patents

A kind of intelligent transfusion monitoring method and system Download PDF

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Publication number
CN108904923A
CN108904923A CN201810798781.1A CN201810798781A CN108904923A CN 108904923 A CN108904923 A CN 108904923A CN 201810798781 A CN201810798781 A CN 201810798781A CN 108904923 A CN108904923 A CN 108904923A
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target
infusion
unit
bottle
monitoring platform
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CN108904923B (en
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肖永辉
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GUANGZHOU HUIQUN INTELLIGENT TECHNOLOGY Co Ltd
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GUANGZHOU HUIQUN INTELLIGENT TECHNOLOGY Co Ltd
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/16804Flow controllers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/1407Infusion of two or more substances
    • A61M5/1408Infusion of two or more substances in parallel, e.g. manifolds, sequencing valves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/14Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
    • A61M5/168Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
    • A61M5/16831Monitoring, detecting, signalling or eliminating infusion flow anomalies
    • A61M5/1684Monitoring, detecting, signalling or eliminating infusion flow anomalies by detecting the amount of infusate remaining, e.g. signalling end of infusion
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/18General characteristics of the apparatus with alarm
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/33Controlling, regulating or measuring
    • A61M2205/3379Masses, volumes, levels of fluids in reservoirs, flow rates
    • A61M2205/3386Low level detectors
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/35Communication
    • A61M2205/3546Range
    • A61M2205/3561Range local, e.g. within room or hospital
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2230/00Measuring parameters of the user
    • A61M2230/04Heartbeat characteristics, e.g. ECG, blood pressure modulation
    • A61M2230/06Heartbeat rate only
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2230/00Measuring parameters of the user
    • A61M2230/30Blood pressure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2230/00Measuring parameters of the user
    • A61M2230/40Respiratory characteristics
    • A61M2230/42Rate

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  • Health & Medical Sciences (AREA)
  • Vascular Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Infusion, Injection, And Reservoir Apparatuses (AREA)

Abstract

A kind of intelligent transfusion monitoring method and system, including:Fuction monitoring device for infusion detects the current dose (for example, 50 milliliters) in first object transfusion bottle, and the first object information for including at least current dose and first object transfusion bottle corresponding target ward position is sent to monitor supervision platform;Monitor supervision platform exports the first warning information when detecting current dose lower than preset target dose (for example, 100 milliliters);Wherein, the first warning information is for prompting the current dose of medical staff's first object transfusion bottle too low, also, the first warning information includes at least first object information.Implement the embodiment of the present invention, can notify in time monitor supervision platform when the dose in transfusion bottle is too low, so that the medical staff of operation monitor supervision platform is that patient replaces transfusion bottle, and then reduces the probability that malpractice occurs when learning the too low information of dose in time.

Description

Intelligent infusion monitoring method and system
Technical Field
The invention relates to the technical field of electronic equipment, in particular to an intelligent infusion monitoring method and system.
Background
At present, medical care personnel need regularly for the remaining dose in the patient inspection transfusion bottle when the patient infuses to in time change the transfusion bottle for the patient. However, in real life, the medical staff often fails to check the residual medicine amount in the infusion bottle for the patient in time, so that the infusion bottle which is about to be infused is not replaced for the patient in time, and the probability of occurrence of medical accidents is increased.
Disclosure of Invention
The embodiment of the invention discloses an intelligent infusion monitoring method and system, which can reduce the probability of medical accidents.
The first aspect of the embodiment of the invention discloses an intelligent infusion monitoring method, which comprises the following steps:
the infusion monitoring device detects the current dosage in the first target infusion bottle;
the infusion monitoring device sends first target information to a monitoring platform; the first target information at least comprises the current medicine amount and the position of a target ward corresponding to the first target hanging bottle;
the monitoring platform judges whether the current medicine amount is lower than a preset target medicine amount, and if the current medicine amount is lower than the target medicine amount, first early warning information is output; the first early warning information is used for prompting medical personnel that the current medicine amount of the first target infusion bottle is too low, and the first early warning information at least comprises the first target information.
As an optional implementation manner, in the first aspect of the embodiment of the present invention, after the monitoring platform outputs the first warning information, the method further includes:
the monitoring platform starts timing from the moment of outputting the first early warning information and judges whether second target information sent by the infusion device is received before the timing time reaches a preset target time; wherein the second target information comprises the current medicine amount which is not less than the target medicine amount;
and if the second target information is not received before the timing duration reaches the target duration, the monitoring platform determines a mobile terminal which is connected with the monitoring platform and is closest to the monitoring platform, and sends the first early warning information to the mobile terminal.
As an optional implementation manner, in the first aspect of the embodiment of the present invention, after the monitoring platform determines that the second target information sent by the infusion apparatus is received before the timed duration reaches the target duration, the method further includes:
the monitoring platform determines a target response time length from the moment of outputting the first early warning information to the moment of receiving the second target information sent by the infusion device;
the monitoring platform determines the average response time length in a circular area range which takes the monitoring platform as the circle center and takes the preset length as the radius from cloud data, and judges whether the target response time length is lower than the average response time length;
if the average response time is shorter than the average response time, the monitoring platform outputs prompt information for prompting medical staff to increase the response speed.
As an optional implementation manner, in the first aspect of the embodiment of the present invention, after the monitoring platform outputs the first warning information, the method further includes:
the monitoring platform judges whether a transfusion bottle replacing operation is detected or not, and if the transfusion bottle replacing operation is detected, a transfusion bottle replacing instruction is sent to the transfusion monitoring device;
and after receiving the transfusion replacement instruction, the transfusion monitoring device closes a first transfusion sub-device used for inputting the liquid medicine in the first target transfusion bottle to the patient corresponding to the first target transfusion bottle, and opens a second transfusion sub-device used for inputting the liquid medicine in a second target transfusion bottle to the patient.
As an optional implementation manner, in the first aspect of this embodiment of the present invention, the method further includes:
the infusion monitoring device determines physiological parameters of a patient corresponding to the first target infusion bottle; wherein the physiological parameters at least comprise a heart rate parameter, a blood pressure parameter and a respiratory rate parameter;
the infusion monitoring device judges whether all the parameters in the physiological parameters are in a preset normal parameter range;
if not, the infusion monitoring device sends physiological early warning information comprising the physiological parameters to the monitoring platform; wherein the physiological early warning information is used for indicating that the patient has life danger;
and the monitoring platform outputs an acousto-optic alarm signal after receiving the physiological early warning information.
The second aspect of the embodiment of the invention discloses an intelligent infusion monitoring system, which comprises an infusion monitoring device and a monitoring platform, wherein the infusion monitoring device comprises a detection unit and a first sending unit, and the monitoring platform comprises a first receiving unit, a first judging unit and an output unit;
the detection unit is used for detecting the current medicine amount in the first target infusion bottle;
the first sending unit is used for sending first target information to the monitoring platform; the first target information at least comprises the current medicine amount and the position of a target ward corresponding to the first target hanging bottle;
the first receiving unit is configured to receive the first target information.
The first judging unit is used for judging whether the current medicine amount is lower than a preset target medicine amount;
the output unit is used for outputting first early warning information after the first judging unit judges that the current medicine amount is lower than the target medicine amount; the first early warning information is used for prompting medical personnel that the current medicine amount of the first target infusion bottle is too low, and the first early warning information at least comprises the first target information.
As an optional implementation manner, in the second aspect of the embodiment of the present invention, the monitoring platform further includes a timing unit and a first determining unit, wherein:
the timing unit is used for starting timing from the moment of outputting the first early warning information after the output unit outputs the first early warning information;
the first judging unit is further used for judging whether second target information sent by the infusion device is received before the timing duration reaches a preset target duration; wherein the second target information comprises the current medicine amount which is not less than the target medicine amount;
the first determining unit is configured to determine, after the first determining unit determines that the second target information is not received before the timing duration reaches the target duration, a mobile terminal that is connected to the monitoring platform and has a closest distance to the monitoring platform, and send the first warning information to the mobile terminal.
As an optional implementation manner, in the second aspect of the embodiment of the present invention, the first determining unit is further configured to determine a target response time period from a time when the first warning information is output to a time when the second target information sent by the infusion apparatus is received after the first judging unit judges that the second target information is received before the timed period reaches the target period;
the first determining unit is further configured to determine, from cloud data, an average response time length within a circular area range that takes the monitoring platform as a circle center and takes a preset length as a radius;
the first judging unit is further configured to judge whether the target response duration is lower than the average response duration;
the output unit is further configured to output prompt information for prompting the medical staff to increase the response speed after the first determination unit determines that the target response duration is shorter than the average response duration.
As an optional implementation manner, in the second aspect of the embodiment of the present invention, the infusion monitoring device further includes a second receiving unit, a closing unit, and an opening unit, and the monitoring platform further includes a second sending unit;
the first judging unit is further used for judging whether the transfusion bottle replacing operation is detected or not after the first early warning information is output by the output unit;
the second sending unit is used for sending a transfusion bottle replacing instruction to the transfusion monitoring device after the first judging unit judges that the transfusion bottle replacing operation is detected;
the second receiving unit is used for receiving the hanging bottle replacing instruction;
the closing unit is used for closing a first infusion sub-device which is used for inputting the liquid medicine in the first target infusion bottle to the patient corresponding to the first target infusion bottle;
the opening unit is used for opening a second infusion sub-device used for inputting the liquid medicine in the second target infusion bottle to the patient.
As an alternative implementation, in the second aspect of the embodiment of the present invention, the infusion monitoring device further includes a second determination unit and a second judgment unit, wherein:
the second determination unit is used for determining the physiological parameters of the patient corresponding to the first target infusion bottle; wherein the physiological parameters at least comprise a heart rate parameter, a blood pressure parameter and a respiratory rate parameter;
the second judging unit is used for judging whether all the parameters in the physiological parameters are in a preset normal parameter range;
the first sending unit is further configured to send physiological warning information including the physiological parameters to the monitoring platform when the second determining unit determines that all the parameters in the physiological parameters are not within the normal parameter range; wherein the physiological early warning information is used for indicating that the patient has life danger;
the first receiving unit is further used for receiving the physiological early warning information;
the output unit is also used for outputting sound and light alarm signals.
A third aspect of the embodiments of the present invention discloses an infusion monitoring device, including:
a memory storing executable program code;
a processor coupled with the memory;
the processor calls the executable program code stored in the memory to execute the intelligent infusion monitoring method disclosed by the first aspect of the embodiment of the invention.
A fourth aspect of the embodiments of the present invention discloses a monitoring platform, including:
a memory storing executable program code;
a processor coupled with the memory;
the processor calls the executable program code stored in the memory to execute the intelligent infusion monitoring method disclosed by the first aspect of the embodiment of the invention.
A fifth aspect of the embodiments of the present invention discloses a computer-readable storage medium storing a computer program, wherein the computer program enables a computer to execute the intelligent infusion monitoring method disclosed in the first aspect of the embodiments of the present invention.
A sixth aspect of the present invention discloses a computer program product, which, when running on a computer, causes the computer to execute the intelligent infusion monitoring method disclosed in the first aspect.
Compared with the prior art, the embodiment of the invention has the following beneficial effects:
in the embodiment of the invention, the infusion monitoring device can detect the current medicine amount (for example, 50 ml) in the first target infusion bottle and send first target information at least comprising the current medicine amount and the position of a target ward corresponding to the first target infusion bottle to the monitoring platform; the monitoring platform outputs first early warning information when detecting that the current medicine amount is lower than a preset target medicine amount (for example, 100 milliliters); the first early warning information is used for prompting that the current medicine amount of the first target infusion bottle of the medical personnel is too low, and the first early warning information at least comprises first target information. By the method, the monitoring platform can be timely informed when the medicine amount in the infusion bottle is too low, so that medical staff operating the monitoring platform can timely replace the infusion bottle for a patient when knowing that the medicine amount is too low.
Drawings
In order to more clearly illustrate the technical solutions in the embodiments of the present invention, the drawings needed to be used in the embodiments will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments of the present invention, and it is obvious for those skilled in the art that other drawings can be obtained according to these drawings without creative efforts.
FIG. 1 is a schematic flow chart of an intelligent infusion monitoring method according to an embodiment of the present invention;
FIG. 2 is a schematic flow chart diagram of another intelligent infusion monitoring method disclosed in the embodiments of the present invention;
FIG. 3 is a schematic flow chart of another intelligent infusion monitoring method according to the embodiment of the present disclosure;
FIG. 4 is a schematic structural diagram of an intelligent infusion monitoring system according to an embodiment of the present invention;
FIG. 5 is a schematic structural diagram of another intelligent infusion monitoring system disclosed in the embodiments of the present invention;
FIG. 6 is a schematic structural diagram of another intelligent infusion monitoring system disclosed in the embodiments of the present invention;
FIG. 7 is a schematic structural diagram of an infusion monitoring device according to an embodiment of the present disclosure;
fig. 8 is a schematic structural diagram of a monitoring platform disclosed in the embodiment of the present invention.
Detailed Description
The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
It is to be noted that the terms "comprises" and "comprising" and any variations thereof in the embodiments and drawings of the present invention are intended to cover non-exclusive inclusions. For example, a process, method, system, article, or apparatus that comprises a list of steps or elements is not limited to only those steps or elements listed, but may alternatively include other steps or elements not listed, or inherent to such process, method, article, or apparatus.
The embodiment of the invention discloses an intelligent infusion monitoring method and system, which can reduce the probability of medical accidents. The following are detailed below.
Example one
Referring to fig. 1, fig. 1 is a schematic flow chart of an intelligent infusion monitoring method according to an embodiment of the present invention. The intelligent infusion monitoring method as shown in fig. 1 may include the following steps:
101. the infusion monitoring device detects the current amount of the drug in the first target infusion bottle.
In the embodiment of the present invention, the current dosage detection mode may be determined according to the pressure value collected by the pressure sensor, may also be determined according to the weight value collected by the weight sensor, may also be determined according to the image captured by the camera, and may also be determined according to the weight value collected by the weight sensor and the remaining infusion time calculated according to the low speed of the liquid medicine in the infusion bottle, which is not limited in the embodiment of the present invention.
102. The infusion monitoring device sends first target information to the monitoring platform; the first target information at least comprises the current dosage and the position of a target ward corresponding to the first target infusion bottle.
In the embodiment of the present invention, the infusion monitoring device may send the first target information to the monitoring platform through the built-in communication module, where the first target information may further include a current medical record of the patient, an identifier of a ward where the patient is currently located, and details of the ward where the patient is currently located (for example, the total number of patients in the ward in the infusion state).
103. And the monitoring platform judges whether the current medicine quantity is lower than a preset target medicine quantity, if so, the step 104 is executed, and if not, the step 103 is executed.
104. The monitoring platform outputs first early warning information; the first early warning information is used for prompting that the current medicine amount of the first target infusion bottle of the medical personnel is too low, and the first early warning information at least comprises first target information.
In the embodiment of the present invention, optionally, the monitoring platform may output the first warning information through a display screen, may also output the first warning information in a form of voice output, and may also send the first warning information to the mobile terminal of the medical care personnel through an application program for performing instant messaging, which is not limited in the embodiment of the present invention.
As an alternative embodiment, after step 104, the following steps may also be performed:
the monitoring platform determines a target area corresponding to a target ward corresponding to the first target infusion bottle on the display screen, and converts the current state of an icon in the target area from a constant-brightness state to a flashing state; or,
the monitoring platform determines a target area corresponding to a target ward corresponding to the first target infusion bottle on the display screen, and converts the color of an icon in the target area from a preset safe color (e.g., green) to a preset early warning color (e.g., red); or,
the monitoring platform determines a target area corresponding to a target ward corresponding to the first target infusion bottle on a display screen, and displays a real-time image of the target ward displayed in the target area in a full screen mode, wherein the real-time images of a plurality of wards can be displayed on the display screen of the monitoring platform at the same time; or,
and the monitoring platform outputs an audible and visual alarm signal.
Therefore, by implementing the optional implementation mode, medical staff can be timely informed to replace the infusion bottle for the patient when the residual medicine amount of the first target infusion bottle is low, and the probability of medical accidents is reduced.
As another alternative, after step 104, the following steps may be further performed:
the monitoring platform determines a target parameter corresponding to the current drug amount, sends the target parameter to a user terminal (for example, a mobile phone of a patient) connected with the monitoring platform, and sends residual amount early warning information used for indicating that the drug amount of the first target infusion bottle is too low to the user terminal when the monitoring platform detects that the target parameter is lower than a preset residual amount parameter, so that the user terminal sends the residual amount early warning information to a mobile terminal (for example, a mobile phone of a medical worker) connected with the user terminal.
Therefore, by implementing the alternative implementation mode, when the residual medicine amount of the first target infusion bottle is lower, the patient can use the mobile phone of the patient to inform medical staff of replacing the infusion bottle for the patient in time, and the probability of medical accidents is reduced.
As a further alternative, after step 104, the following steps may also be performed:
the monitoring platform determines a target area corresponding to the first target infusion bottle from the display screen, and updates a medicine quantity parameter corresponding to the medicine quantity of the first target infusion bottle in the target area to a medicine quantity parameter corresponding to the current medicine quantity; the display screen can display a plurality of target areas, each target area corresponds to a different ward, and each target area can display the medicine quantity parameter corresponding to the medicine quantity of at least one infusion bottle;
the monitoring platform determines the total number of all the target areas and the single maximum display number of the display screen, judges whether the total number of all the target areas is more than the single maximum display number, and if so, divides the total number of all the target areas by the single maximum display number to obtain the display page number;
the monitoring platform outputs all target areas according to the displayed page number; wherein the output time length of each page in the displayed page number is a preset output time length (for example, 5 seconds).
It should be noted that, the monitoring platform outputs all the target regions according to the displayed page number, that is, the monitoring platform may output all the target regions respectively and automatically according to the displayed page number, or may output one page at a time by the monitoring platform, and then output the next page according to the detected page turning operation input by the user, which is not limited in the embodiment of the present invention.
Optionally, the monitoring platform may include at least a software platform, a server, a computer, a display, a monitor, and a broadcast device, and the infusion monitoring device may include a hanger (not shown), an infusion monitoring component (not shown), an alarm device (not shown), and at least one hanger component (not shown). Wherein, the infusion monitoring part is arranged at the top of the hanger, at least one hanging part is arranged at the lower side of the infusion monitoring part and is used for hanging a hanging bottle, and the alarm device is arranged on the infusion monitoring part. In addition, the infusion monitoring device may include an acquisition module (not shown) corresponding to the hanger device, one for each acquisition module (which may include a pressure sensor). The infusion monitoring component is used for starting an acquisition module corresponding to a certain hanging component when the infusion bottle is hung on the certain hanging component, acquiring real-time parameters (the real-time parameters can be readings of a pressure sensor) acquired by the acquisition module aiming at the infusion bottle, judging whether the real-time parameters meet preset parameter conditions, and controlling an alarm device to start if the real-time parameters meet the preset parameter conditions so as to output alarm information, wherein the alarm information is used for prompting that a patient using infusion bottle for infusion and/or corresponding medical personnel are about to finish infusion. In addition, the infusion monitoring component may further include a wireless communication module, and may be further configured to send a prompt message to a mobile terminal (e.g., a mobile phone of a medical worker) that establishes a connection relationship in advance when it is determined that the real-time parameter satisfies a preset parameter condition, so as to prompt that the infusion is to be completed. Therefore, alarm information can be sent out in time when the medicine amount in the transfusion bottle is too low, and the probability of medical accidents is reduced.
Further, the infusion monitoring device detects the current amount of the drug in the first target infusion bottle, and the method comprises the following steps:
the infusion monitoring device collects real-time parameters of a first target infusion bottle hung on the hanging frame, and determines the current dosage of the first target infusion bottle according to the real-time parameters;
the infusion monitoring device sends first target information to the monitoring platform; the first target information at least includes the current dose and the position of the target ward corresponding to the first target infusion bottle, and may include the following steps:
the infusion monitoring device judges whether the acquired real-time parameters meet preset parameter conditions or not;
when the real-time parameter is judged to meet the preset parameter condition, the infusion monitoring device sends first target information to the monitoring platform, and step 103 is executed; the first target information at least comprises the current medicine amount, the position of a target ward corresponding to the first target infusion bottle, the identity information of the patient and the current infusion condition of the patient (for example, the total number of infusion bottles).
The real-time parameter may be a pressure value acquired by the pressure sensor, a weight value acquired by the weight sensor, an image captured by the camera, or a remaining infusion time calculated according to the weight value acquired by the weight sensor and a low speed of the liquid medicine in the infusion bottle, which is not limited in the embodiment of the present invention. In addition, the first target information may also include a current medical record of the patient, an identification of a patient room in which the patient is currently located, and patient room details of the patient room in which the patient is currently located (e.g., the total number of patients in the patient room in the infusion state).
It should be noted that, when the infusion detection device determines that the real-time parameter meets a preset parameter condition (for example, less than 250 ml), the infusion monitoring device sends first target information and warning information to the monitoring platform, so that the monitoring platform determines whether the current drug amount is less than a preset target drug amount (for example, 100ml), and then outputs first warning information when the current drug amount is less than the target drug amount. Because the dosage is sufficient when the infusion is started, namely alarm information does not need to be output, the problem of insufficient dosage only exists after the infusion lasts for a period of time, the method can firstly detect the residual dosage through the infusion detection device, and then transmit the current dosage to the monitoring platform when the dosage is not high, so that the monitoring platform can output first early warning information when detecting that the current dosage is low. Therefore, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device is prolonged.
As another optional embodiment, after the infusion monitoring device detects the current amount of the drug in the first target infusion bottle, the following steps may be further performed:
the infusion monitoring device determines an early warning signal of a target grade according to the current dosage and sends the early warning signal of the target grade to a user terminal (such as a mobile phone of a patient) which establishes a connection relation with the infusion monitoring device.
Therefore, the user of the user terminal can know the infusion condition in time.
It can be seen that the method described in fig. 1 can reduce the probability of medical accidents; in addition, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device is prolonged.
Example two
Referring to fig. 2, fig. 2 is a schematic flow chart of another intelligent infusion monitoring method according to an embodiment of the present invention. As shown in fig. 2, the intelligent infusion monitoring method may include the following steps:
step 201 to step 204, please refer to the detailed description of step 101 to step 104 in the first embodiment for the description of step 201 to step 204, which is not described again in the embodiments of the present invention.
205. The monitoring platform starts timing from the moment of outputting the first early warning information and judges whether second target information sent by the infusion device is received before the timing time reaches a preset target time; wherein, the second target information comprises the current medicine amount which is not lower than the target medicine amount, if yes, step 207 is executed, and if not, step 206 is executed.
In the embodiment of the invention, if the monitoring platform determines that the second target information sent by the infusion apparatus is received before the timed duration reaches the target duration, it indicates that the first target infusion bottle is replaced by the second target infusion bottle.
206. The monitoring platform determines the mobile terminal which is connected with the monitoring platform and is closest to the monitoring platform, and sends first early warning information to the mobile terminal.
207. The monitoring platform determines a target response time from the time of outputting the first early warning information to the time of receiving the second target information sent by the infusion device.
208. The monitoring platform determines the average response time length in a circular area range which takes the monitoring platform as the circle center and takes the preset length as the radius from the cloud data, and judges whether the target response time length is lower than the average response time length, if so, step 209 is executed, and if not, the process is ended.
209. And the monitoring platform outputs prompt information for prompting medical staff to increase the response speed.
In the embodiment of the present invention, the manner of outputting the prompt information by the monitoring platform may be outputting the prompt information through a power amplifier, or sending the prompt information to the mobile terminal, which is not limited in the embodiment of the present invention.
It can be seen that the method described in fig. 2 can reduce the probability of medical accidents; in addition, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device is prolonged.
EXAMPLE III
Referring to fig. 3, fig. 3 is a schematic flow chart of another intelligent infusion monitoring method according to an embodiment of the present invention. The intelligent infusion monitoring method as shown in fig. 3 may include the following steps:
step 301 to step 309, please refer to detailed descriptions of step 201 to step 209 in embodiment two for descriptions of step 301 to step 309, which is not described again in this embodiment of the present invention.
310. The monitoring platform determines whether a bottle replacement operation is detected, if so, step 311 is performed, and if not, step 310 is performed.
It should be noted that, optionally, after the monitoring platform determines that the operation of replacing the infusion bottle is not detected, the following operations may also be performed:
the monitoring platform sends a transfusion bottle to be replaced instruction to the transfusion monitoring device, and the transfusion bottle to be replaced instruction is used for indicating the transfusion monitoring device to detect whether a transfusion bottle to be replaced exists;
after receiving a transfusion bottle to be replaced instruction, the transfusion monitoring device detects whether a transfusion bottle to be replaced exists;
if the infusion bottle to be replaced exists, the infusion monitoring device feeds back a target signal for indicating that the infusion bottle to be replaced exists to the monitoring platform;
after receiving the target signal, the monitoring platform sends a manual bottle changing instruction for prompting a user to manually change a hanging bottle to the infusion monitoring device;
after receiving a manual bottle changing instruction, the infusion monitoring device outputs prompt information for prompting a user to manually change a hanging bottle; or,
the monitoring platform sends a transfusion bottle to be replaced instruction to the transfusion monitoring device, and the transfusion bottle to be replaced instruction is used for indicating the transfusion monitoring device to detect whether a transfusion bottle to be replaced exists;
after receiving a transfusion bottle to be replaced instruction, the transfusion monitoring device detects whether a transfusion bottle to be replaced exists;
if the infusion bottle to be replaced exists, the infusion monitoring device feeds back a target signal for indicating that the infusion bottle to be replaced exists to the monitoring platform;
after receiving the target signal, the monitoring platform sends advanced alarm information used for indicating that no medical staff changes the infusion bottle for the patient in the target area where the first target infusion bottle is located to the master control center.
Therefore, when the monitoring platform does not detect the operation of replacing the infusion bottle, the embodiment of the invention can inform the user of manually replacing the infusion bottle so that the user can replace the infusion bottle according to the medical advice to reduce the probability of medical accidents, and can also send advanced alarm information to the master control center so that the master control center can send medical staff to replace the infusion bottle for the patient to reduce the probability of medical accidents.
It should be noted that, optionally, after the monitoring platform determines that the operation of replacing the infusion bottle is detected, the following operations may also be performed:
the monitoring platform sends a transfusion bottle to be replaced instruction to the transfusion monitoring device, and the transfusion bottle to be replaced instruction is used for indicating the transfusion monitoring device to detect whether a transfusion bottle to be replaced exists;
after receiving a transfusion bottle to be replaced instruction, the transfusion monitoring device detects whether a transfusion bottle to be replaced exists;
if the infusion bottle to be replaced exists, the infusion monitoring device feeds back information of the infusion bottle to be replaced to the monitoring platform, and if the infusion bottle to be replaced does not exist, the infusion monitoring device feeds back target information for indicating that no infusion bottle to be replaced exists to the monitoring platform; the information of the hanging bottle to be replaced comprises the name of the liquid medicine in the hanging bottle to be replaced;
after receiving the information of the infusion bottles to be replaced, the monitoring platform outputs the information of the infusion bottles to be replaced and outputs prompt information for prompting selection of a second target infusion bottle from the infusion bottles to be replaced according to the information of the infusion bottles to be replaced;
the monitoring platform judges whether a target operation for selecting a second target infusion bottle is detected;
if a target operation is detected, step 311 is performed.
Further, the infusion monitoring device can replace the first target infusion bottle with a second target infusion bottle according to a second target infusion bottle selected by the medical staff on the monitoring platform from the to-be-replaced infusion bottles if the to-be-replaced infusion bottle has a plurality of bottles. As medical personnel can change the infusion bottle for the patient by operating the monitoring platform in the monitoring room, the embodiment of the invention not only can improve the convenience of changing the infusion bottle, but also can improve the efficiency of changing the infusion bottle.
311. And the monitoring platform sends a transfusion bottle replacing instruction to the transfusion monitoring device.
312. After receiving the infusion bottle replacement instruction, the infusion monitoring device closes a first infusion sub-device used for inputting the liquid medicine in the first target infusion bottle to the patient corresponding to the first target infusion bottle, and opens a second infusion sub-device used for inputting the liquid medicine in the second target infusion bottle to the patient.
In the embodiment of the present invention, when the infusion monitoring device turns on the second infusion sub-device for infusing the liquid medicine in the second target infusion bottle to the patient, step 301 is triggered.
Therefore, by implementing the embodiment of the invention, the infusion bottles can be replaced for the patient through the preset infusion bottle replacement sequence, namely the first infusion sub-device is closed and the second infusion sub-device is opened, so that the automation degree of the infusion monitoring device is improved.
The intelligent infusion monitoring method can also comprise the following steps:
313. the infusion monitoring device determines physiological parameters of a patient corresponding to the first target infusion bottle; the physiological parameters at least comprise a heart rate parameter, a blood pressure parameter and a respiratory rate parameter.
314. The infusion monitoring device determines whether all of the physiological parameters are within a preset normal parameter range, if so, step 314 is performed, and if not, step 315 is performed.
315. The infusion monitoring device sends physiological early warning information comprising physiological parameters to the monitoring platform; wherein, the physiological early warning information is used for indicating that the patient has life danger.
316. The monitoring platform outputs an audible and visual alarm signal after receiving the physiological early warning information.
It can be seen that the method described in fig. 3 is implemented to reduce the probability of medical accidents; in addition, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device can be prolonged; in addition, the automation degree of the infusion monitoring device can be improved.
Example four
Referring to fig. 4, fig. 4 is a schematic structural diagram of an intelligent infusion monitoring system according to an embodiment of the present invention. As shown in fig. 4, the intelligent infusion monitoring system may include an infusion monitoring device and a monitoring platform, wherein the infusion monitoring device includes a detection unit 401 and a first sending unit 402, and the monitoring platform includes a first receiving unit 403, a first judging unit 404 and an output unit 405, wherein:
the detection unit 401 is configured to detect a current amount of the drug in the first target infusion bottle.
In the embodiment of the present invention, the current dosage detection mode may be determined according to the pressure value collected by the pressure sensor, may also be determined according to the weight value collected by the weight sensor, may also be determined according to the image captured by the camera, and may also be determined according to the weight value collected by the weight sensor and the remaining infusion time calculated according to the low speed of the liquid medicine in the infusion bottle, which is not limited in the embodiment of the present invention.
In the embodiment of the invention, after the detection unit 401 detects the current amount of the medicine in the first target infusion bottle, the first sending unit 402 is triggered to start.
A first sending unit 402, configured to send first target information to the monitoring platform; the first target information at least comprises the current dosage and the position of a target ward corresponding to the first target infusion bottle.
In this embodiment of the present invention, the first sending unit 402 may send the first target information to the monitoring platform through a built-in communication module, where the first target information may further include a current medical record of the patient, an identifier of a ward where the patient is currently located, and ward details of the ward where the patient is currently located (for example, the total number of patients in an infusion state in the ward).
A first receiving unit 403, configured to receive the first target information.
In this embodiment of the present invention, after the first receiving unit 403 receives the first target information, the first determining unit 404 is triggered to start.
The first determining unit 404 is configured to determine whether the current amount of the drug is lower than a preset target amount of the drug.
The output unit 405 is configured to output first warning information after the first judging unit 404 judges that the current drug amount is lower than the target drug amount; the first early warning information is used for prompting that the current medicine amount of the first target infusion bottle of the medical personnel is too low, and the first early warning information at least comprises first target information.
In this embodiment of the present invention, optionally, the output unit 405 may output the first warning information through a display screen, may also output the first warning information in a form of voice output, and may also send the first warning information to a mobile terminal of a medical care worker through an application program for performing instant messaging, which is not limited in this embodiment of the present invention.
As an alternative embodiment, the output unit 405 may be further configured to, after outputting the first warning information,
determining a target area corresponding to a target ward corresponding to the first target infusion bottle on a display screen, and converting the current state of an icon in the target area from a constant-brightness state to a flashing state; or,
determining a target area corresponding to a target ward corresponding to the first target infusion bottle on the display screen, and converting the color of an icon in the target area from a preset safe color (e.g., green) to a preset early warning color (e.g., red); or,
determining a target area corresponding to a target ward corresponding to the first target infusion bottle on a display screen, and displaying a real-time image of the target ward displayed in the target area in a full screen manner, wherein the real-time images of a plurality of wards can be simultaneously displayed on the display screen of the monitoring platform; or,
and outputting an audible and visual alarm signal.
Therefore, by implementing the optional implementation mode, medical staff can be timely informed to replace the infusion bottle for the patient when the residual medicine amount of the first target infusion bottle is low, and the probability of medical accidents is reduced.
As another optional implementation, the output unit 405 may be further configured to, after the first warning information is output, determine a target parameter corresponding to the current drug amount, send the target parameter to a user terminal (for example, a mobile phone of a patient) that establishes a connection with the monitoring platform, and send remaining amount warning information indicating that the drug amount of the first target infusion bottle is too low to the user terminal when the monitoring platform detects that the target parameter is lower than a preset remaining amount parameter, so that the user terminal sends the remaining amount warning information to a mobile terminal (for example, a mobile phone of a medical staff) that establishes a connection with the user terminal.
Therefore, by implementing the alternative implementation mode, when the residual medicine amount of the first target infusion bottle is lower, the patient can use the mobile phone of the patient to inform medical staff of replacing the infusion bottle for the patient in time, and the probability of medical accidents is reduced.
As another optional implementation manner, the output unit 405 may be further configured to determine a target area corresponding to the first target infusion bottle from the display screen after the first early warning information is output, and update a drug quantity parameter corresponding to the drug quantity of the first target infusion bottle in the target area to a drug quantity parameter corresponding to the current drug quantity; the display screen can display a plurality of target areas, each target area corresponds to a different ward, and each target area can display the medicine quantity parameter corresponding to the medicine quantity of at least one infusion bottle;
determining the total number of all the target areas and the single maximum display number of the display screen, judging whether the total number of all the target areas is more than the single maximum display number, and if so, dividing the total number of all the target areas by the single maximum display number to obtain the display page number;
outputting all target areas according to the displayed page number; wherein the output time length of each page in the displayed page number is a preset output time length (for example, 5 seconds).
It should be noted that, the foregoing outputs all the target regions according to the number of displayed pages, that is, the monitoring platform may respectively and automatically output all the target regions according to the number of displayed pages, or the monitoring platform may output one page at a time, and then outputs the next page according to the detected page turning operation input by the user, which is not limited in the embodiment of the present invention.
Optionally, the monitoring platform may include at least a software platform, a server, a computer, a display, a monitor, and a broadcast device, and the infusion monitoring device may include a hanger (not shown), an infusion monitoring component (not shown), an alarm device (not shown), and at least one hanger component (not shown). Wherein, the infusion monitoring part is arranged at the top of the hanger, at least one hanging part is arranged at the lower side of the infusion monitoring part and is used for hanging a hanging bottle, and the alarm device is arranged on the infusion monitoring part. In addition, the infusion monitoring device may include an acquisition module (not shown) corresponding to the hanger device, one for each acquisition module (which may include a pressure sensor). The infusion monitoring component is used for starting an acquisition module corresponding to a certain hanging component when the infusion bottle is hung on the certain hanging component, acquiring real-time parameters (the real-time parameters can be readings of a pressure sensor) acquired by the acquisition module aiming at the infusion bottle, judging whether the real-time parameters meet preset parameter conditions, and controlling an alarm device to start if the real-time parameters meet the preset parameter conditions so as to output alarm information, wherein the alarm information is used for prompting that a patient using infusion bottle for infusion and/or corresponding medical personnel are about to finish infusion. In addition, the infusion monitoring component may further include a wireless communication module, and may be further configured to send a prompt message to a mobile terminal (e.g., a mobile phone of a medical worker) that establishes a connection relationship in advance when it is determined that the real-time parameter satisfies a preset parameter condition, so as to prompt that the infusion is to be completed. Therefore, alarm information can be sent out in time when the medicine amount in the transfusion bottle is too low, and the probability of medical accidents is reduced.
Further, the way that the detection unit 401 detects the current amount of the drug in the first target infusion bottle may specifically be:
the detection unit 401 collects real-time parameters of a first target infusion bottle hung on the hanging bracket, and determines the current dosage of the first target infusion bottle according to the real-time parameters;
the first sending unit 402 sends the first target information to the monitoring platform; the mode that the first target information at least comprises the current dose and the position of the target ward corresponding to the first target infusion bottle specifically can be as follows:
the first sending unit 402 determines whether the acquired real-time parameters meet preset parameter conditions;
when the real-time parameter is judged to meet the preset parameter condition, the first sending unit 402 sends the first target information to the monitoring platform, and triggers the first receiving unit 403 to execute the operation of receiving the first target information; the first target information at least comprises the current medicine amount, the position of a target ward corresponding to the first target infusion bottle, the identity information of the patient and the current infusion condition of the patient (for example, the total number of infusion bottles).
The real-time parameter may be a pressure value acquired by the pressure sensor, a weight value acquired by the weight sensor, an image captured by the camera, or a remaining infusion time calculated according to the weight value acquired by the weight sensor and a low speed of the liquid medicine in the infusion bottle, which is not limited in the embodiment of the present invention. In addition, the first target information may also include a current medical record of the patient, an identification of a patient room in which the patient is currently located, and patient room details of the patient room in which the patient is currently located (e.g., the total number of patients in the patient room in the infusion state).
It should be noted that, when the first sending unit 402 determines that the real-time parameter meets the preset parameter condition (for example, less than 250 ml), the first sending unit 402 sends the first target information and the warning information to the monitoring platform, so that the monitoring platform determines whether the current drug amount is lower than a preset target drug amount (for example, 100ml), and then outputs the first warning information when the current drug amount is lower than the target drug amount. Because the dosage is sufficient when the infusion is started, namely alarm information does not need to be output, the problem of insufficient dosage only exists after the infusion lasts for a period of time, the method can firstly detect the residual dosage through the infusion detection device, and then transmit the current dosage to the monitoring platform when the dosage is not high, so that the monitoring platform can output first early warning information when detecting that the current dosage is low. Therefore, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device is prolonged.
As another optional embodiment, the detecting unit 401 may be further configured to, after detecting the current amount of drug in the first target infusion bottle, determine an early warning signal of a target level according to the current amount of drug, and send the early warning signal of the target level to a user terminal (e.g., a mobile phone of a patient) that establishes a connection relationship with the infusion monitoring device.
Therefore, the user of the user terminal can know the infusion condition in time.
Therefore, the intelligent infusion monitoring system described in fig. 4 can reduce the probability of medical accidents; in addition, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device is prolonged.
EXAMPLE five
Referring to fig. 5, fig. 5 is a schematic structural diagram of another intelligent infusion monitoring system according to an embodiment of the disclosure. The intelligent infusion monitoring system shown in fig. 5 is optimized by the intelligent infusion monitoring system shown in fig. 4. Compared to the intelligent infusion monitoring system shown in fig. 4, the monitoring platform further comprises a timing unit 406 and a first determination unit 407, wherein:
a timing unit 406, configured to start timing from a time when the first warning information is output after the output unit 405 outputs the first warning information.
In the embodiment of the invention, after the timing unit 406 starts timing from the time when the first warning information is output, the first judging unit 404 is triggered to execute the operation of judging whether the second target information sent by the infusion device is received before the timing duration reaches the preset target duration.
The first judging unit 404 is further configured to judge whether the second target information sent by the infusion apparatus is received before the timed duration reaches the preset target duration; wherein the second target information comprises the current drug amount not less than the target drug amount.
In the embodiment of the invention, if the second target information sent by the infusion apparatus is judged to be received before the timed duration reaches the target duration, the first target infusion bottle is replaced by the second target infusion bottle.
A first determining unit 407, configured to determine, after the first determining unit 404 determines that the second target information is not received before the timed duration reaches the target duration, a mobile terminal that is connected to the monitoring platform and is closest to the monitoring platform, and send the first warning information to the mobile terminal.
The first determination unit 407 is further configured to determine a target response time period from the time when the first warning information is output to the time when the second target information sent by the infusion apparatus is received, after the first determination unit 404 determines that the second target information is received before the timed period reaches the target time period.
In the embodiment of the present invention, after the first determining unit 407 determines the target response time from the time when the first warning information is output to the time when the second target information sent by the infusion apparatus is received, the first determining unit 407 is triggered to perform an operation of determining, from the cloud data, an average response time within a circular area with a monitoring platform as a center and a preset length as a radius.
The first determining unit 407 is further configured to determine, from the cloud data, an average response time length within a circular area range with the monitoring platform as a center and a preset length as a radius.
In the embodiment of the present invention, after the first determining unit 407 determines, from the cloud data, an average response time length within a circular area range with a monitoring platform as a center and a preset length as a radius, the first determining unit 404 is triggered to perform an operation of determining whether the target response time length is lower than the average response time length.
The first determining unit 404 is further configured to determine whether the target response time length is lower than the average response time length.
The output unit 405 is further configured to output prompt information for prompting the medical staff to increase the response speed after the first judging unit 404 judges that the target response time length is lower than the average response time length.
In this embodiment of the present invention, the output unit 405 may output the prompt message through a power amplifier, or may send the prompt message to the mobile terminal.
Therefore, the intelligent infusion monitoring system described in fig. 5 can reduce the probability of medical accidents; in addition, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device is prolonged.
EXAMPLE six
Referring to fig. 6, fig. 6 is a schematic structural diagram of another intelligent infusion monitoring system disclosed in the embodiment of the present invention. The intelligent infusion monitoring system shown in fig. 6 is optimized by the intelligent infusion monitoring system shown in fig. 5. Compared with the intelligent infusion monitoring system shown in fig. 5, the infusion monitoring device further includes a second receiving unit 408, a closing unit 409, an opening unit 410, a second determining unit 411, and a second determining unit 412, and the monitoring platform further includes a second sending unit 413, where:
the first determining unit 404 is further configured to determine whether a bottle replacement operation is detected after the first warning information is output by the output unit 405.
As an alternative embodiment, the first determining unit 404 may be further configured to send a to-be-replaced infusion bottle instruction to the infusion monitoring device after determining that the infusion bottle replacement operation is not detected, where the to-be-replaced infusion bottle instruction is used to instruct the infusion monitoring device to detect whether there is an infusion bottle to be replaced;
the second receiving unit 408 may further be configured to detect whether there is a hanging bottle to be replaced after receiving the hanging bottle to be replaced instruction;
the second receiving unit 408 may further be configured to feed back a target signal indicating that the hanging bottle to be replaced exists to the monitoring platform after detecting that the hanging bottle to be replaced exists;
the first judging unit 404 is further configured to send a manual bottle changing instruction to prompt a user to manually change a hanging bottle to the infusion monitoring device after receiving the target signal;
the second receiving unit 408 may further be configured to output a prompt message for prompting a user to manually replace the infusion bottle after receiving the manual bottle replacement instruction; or,
the first judging unit 404 may be further configured to send a to-be-replaced hanging bottle instruction to the infusion monitoring device, where the to-be-replaced hanging bottle instruction is used to instruct the infusion monitoring device to detect whether a hanging bottle to be replaced exists;
the second receiving unit 408 may further be configured to detect whether there is a hanging bottle to be replaced after receiving the hanging bottle to be replaced instruction;
the second receiving unit 408 may further be configured to feed back a target signal indicating that the hanging bottle to be replaced exists to the monitoring platform after detecting that the hanging bottle to be replaced exists;
the first determining unit 404 may be further configured to send, after receiving the target signal, advanced alarm information to the master control center, where the advanced alarm information indicates that no medical staff is present in the target area where the first target infusion bottle is located, to replace the infusion bottle for the patient.
Therefore, when the monitoring platform does not detect the operation of replacing the infusion bottle, the embodiment of the invention can inform the user of manually replacing the infusion bottle so that the user can replace the infusion bottle according to the medical advice to reduce the probability of medical accidents, and can also send advanced alarm information to the master control center so that the master control center can send medical staff to replace the infusion bottle for the patient to reduce the probability of medical accidents.
It should be noted that, optionally, the first determining unit 404 may be further configured to send a to-be-replaced hanging bottle instruction to the infusion monitoring device after determining that the operation of replacing the hanging bottle is detected, where the to-be-replaced hanging bottle instruction is used to instruct the infusion monitoring device to detect whether a hanging bottle to be replaced exists;
the second receiving unit 408 may further be configured to detect whether there is a hanging bottle to be replaced after receiving the hanging bottle to be replaced instruction;
the second receiving unit 408 may further be configured to feed back information of the hanging bottle to be replaced to the monitoring platform after the hanging bottle to be replaced is detected, and feed back target information indicating that there is no hanging bottle to be replaced to the monitoring platform after the hanging bottle to be replaced is detected; the information of the hanging bottle to be replaced comprises the name of the liquid medicine in the hanging bottle to be replaced;
the first judging unit 404 may be further configured to, after receiving the information about the bottles to be replaced, output information about the bottles to be replaced and output prompt information indicating that a second target bottle is selected from the bottles to be replaced according to the information about the bottles to be replaced;
the first judging unit 404 may be further configured to judge whether a target operation for selecting a second target hanging bottle is detected;
the first determining unit 404 may be further configured to trigger the second sending unit 413 to execute an operation of sending a transfusion replacement command to the infusion monitoring device after the target operation is detected.
Further, the infusion monitoring device can replace the first target infusion bottle with a second target infusion bottle according to a second target infusion bottle selected by the medical staff on the monitoring platform from the to-be-replaced infusion bottles if the to-be-replaced infusion bottle has a plurality of bottles. As medical personnel can change the infusion bottle for the patient by operating the monitoring platform in the monitoring room, the embodiment of the invention not only can improve the convenience of changing the infusion bottle, but also can improve the efficiency of changing the infusion bottle.
And a second sending unit 413, configured to send a transfusion replacement instruction to the infusion monitoring device after the first judging unit 404 judges that the transfusion replacement operation is detected.
And a second receiving unit 408 for receiving a command for replacing the transfusion bottle.
In the embodiment of the present invention, after the second receiving unit 408 receives the command for replacing the hanging bottle, the trigger closing unit 409 is activated.
And a closing unit 409 for closing the first infusion sub-device for inputting the medical solution in the first target infusion bottle to the patient corresponding to the first target infusion bottle.
In the embodiment of the present invention, after the infusion monitoring device turns on the second infusion sub-device for inputting the liquid medicine in the second target infusion bottle to the patient, the detection unit 401 is triggered to perform the operation of detecting the current medicine amount in the first target infusion bottle.
Therefore, by implementing the embodiment of the invention, the infusion bottles can be replaced for the patient through the preset infusion bottle replacement sequence, namely the first infusion sub-device is closed and the second infusion sub-device is opened, so that the automation degree of the infusion monitoring device is improved.
And an opening unit 410 for opening the second infusion sub-set for infusing the liquid medicine in the second target infusion bottle to the patient.
In the embodiment of the present invention, after the opening unit 410 opens the second infusion sub-device for infusing the liquid medicine in the second target infusion bottle to the patient, the detection unit 401 is triggered to perform the operation of detecting the current medicine amount in the first target infusion bottle.
The second determining unit 411 is configured to determine a physiological parameter of the patient corresponding to the first target infusion bottle; the physiological parameters at least comprise a heart rate parameter, a blood pressure parameter and a respiratory rate parameter.
The second determining unit 412 is configured to determine whether all the parameters in the physiological parameters are within a preset normal parameter range.
The first sending unit 402 is further configured to send physiological warning information including the physiological parameters to the monitoring platform when the second determining unit 412 determines that all the parameters in the physiological parameters are not within the normal parameter range; wherein, the physiological early warning information is used for indicating that the patient has life danger.
The first receiving unit 403 is further configured to receive physiological warning information.
In the embodiment of the present invention, after the first receiving unit 403 receives the physiological warning information, the output unit 405 is triggered to execute an operation of outputting an audible and visual alarm signal.
The output unit 405 is further configured to output an audible and visual alarm signal.
Therefore, the implementation of the intelligent infusion monitoring system described in fig. 6 can reduce the probability of medical accidents; in addition, the power consumption of the infusion detection device can be reduced, and the service life of the infusion detection device can be prolonged; in addition, the automation degree of the infusion monitoring device can be improved.
EXAMPLE seven
Referring to fig. 7, fig. 7 is a schematic structural diagram of an infusion monitoring device according to an embodiment of the disclosure. As shown in fig. 7, the infusion monitoring device may include:
a memory 701 in which executable program code is stored;
a processor 702 coupled to the memory 701;
the processor 702 calls the executable program code stored in the memory 701 to execute any one of the intelligent infusion monitoring methods shown in fig. 1 to 3.
The embodiment of the invention also discloses a computer readable storage medium which stores a computer program, wherein the computer program enables a computer to execute the steps executed by the infusion monitoring device in any one of the intelligent infusion monitoring methods disclosed in the first embodiment to the third embodiment.
The embodiment of the invention also discloses a computer program product, and when the computer program product runs on a computer, the computer executes the steps executed by the infusion monitoring device in any one of the intelligent infusion monitoring methods disclosed in the first embodiment to the third embodiment of the invention.
It will be understood by those skilled in the art that all or part of the steps in the methods of the embodiments described above may be implemented by instructions associated with a program, which may be stored in a computer-readable storage medium, where the storage medium includes Read-Only Memory (ROM), Random Access Memory (RAM), Programmable Read-Only Memory (PROM), Erasable Programmable Read-Only Memory (EPROM), One-time Programmable Read-Only Memory (OTPROM), Electrically Erasable Programmable Read-Only Memory (EEPROM), compact disc-Read-Only Memory (CD-ROM), or other Memory, magnetic disk, magnetic tape, or magnetic tape, Or any other medium which can be used to carry or store data and which can be read by a computer.
In the above embodiments, the implementation may be wholly or partially implemented by software, hardware, firmware, or any combination thereof. When implemented in software, may be implemented in whole or in part in the form of a computer program product. The computer program product includes one or more computer instructions. When loaded and executed on a computer, cause the processes or functions described in accordance with the embodiments of the application to occur, in whole or in part. The computer may be a general purpose computer, a special purpose computer, a network of computers, or other programmable device. The computer instructions may be stored in a computer readable storage medium or transmitted from one computer readable storage medium to another, for example, the computer instructions may be transmitted from one website, computer, server, or data center to another website, computer, server, or data center by wire (e.g., coaxial cable, fiber optics, digital subscriber line) or wirelessly (e.g., infrared, wireless, microwave, etc.). The computer readable medium can be any available medium that can be accessed by a computer or a data storage device, such as a server, a data center, etc., that incorporates one or more available media. The usable medium may be a magnetic medium (which may be, for example, a floppy disk, a hard disk, a magnetic tape), an optical medium (such as an optical disk), a semiconductor medium (such as a solid state disk), or the like. In the foregoing embodiments, the descriptions of the respective embodiments have respective emphasis, and for parts that are not described in detail in a certain embodiment, reference may be made to related descriptions of other embodiments.
In the embodiments provided in the present application, it should be understood that the disclosed apparatus may be implemented in other manners. For example, the above-described embodiments of the apparatus are merely illustrative, and for example, the above-described division of the units is only one type of division of logical functions, and other divisions may be realized in practice, for example, a plurality of units or components may be combined or integrated into another system, or some features may be omitted, or not executed. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be through some interfaces, indirect coupling or communication connection of devices or units, and may be in an electrical or other form.
The units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiment.
In addition, functional units in the embodiments of the present application may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit. The integrated unit can be realized in a form of hardware, and can also be realized in a form of a software functional unit.
The integrated units, if implemented as software functional units and sold or used as a stand-alone product, may be stored in a computer accessible memory. Based on such understanding, the technical solution of the present application, which is a part of or contributes to the prior art in essence, or all or part of the technical solution, may be embodied in the form of a software product, stored in a memory, including several requests for causing a computer device (which may be a personal computer, a server, a network device, or the like, and may specifically be a processor in the computer device) to execute all or part of the steps of the above-described method of the embodiments of the present application.
The above embodiments are only used for illustrating the technical solutions of the present application and not for limiting the same; although the present application has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art; the technical solutions described in the foregoing embodiments may still be modified, or some technical features may be equivalently replaced; and such modifications or substitutions do not depart from the spirit and scope of the corresponding technical solutions in the embodiments of the present application.
Example eight
Please refer to fig. 8, fig. 8 is a schematic structural diagram of a monitoring platform according to an embodiment of the present invention. As shown in fig. 8, the monitoring platform may include:
a memory 801 in which executable program code is stored;
a processor 802 coupled with the memory 801;
the processor 802 calls the executable program code stored in the memory 801 to execute any one of the intelligent infusion monitoring methods shown in fig. 1 to 3.
The embodiment of the invention also discloses a computer readable storage medium which stores a computer program, wherein the computer program enables a computer to execute the steps executed by the monitoring platform in any one of the intelligent infusion monitoring methods disclosed in the first embodiment to the third embodiment.
The embodiment of the invention also discloses a computer program product, and when the computer program product runs on a computer, the computer executes the steps executed by the monitoring platform in any one of the intelligent infusion monitoring methods disclosed in the first embodiment to the third embodiment of the invention.
It will be understood by those skilled in the art that all or part of the steps in the methods of the embodiments described above may be implemented by instructions associated with a program, which may be stored in a computer-readable storage medium, where the storage medium includes Read-Only Memory (ROM), Random Access Memory (RAM), Programmable Read-Only Memory (PROM), Erasable Programmable Read-Only Memory (EPROM), One-time Programmable Read-Only Memory (OTPROM), Electrically Erasable Programmable Read-Only Memory (EEPROM), compact disc-Read-Only Memory (CD-ROM), or other Memory, magnetic disk, magnetic tape, or magnetic tape, Or any other medium which can be used to carry or store data and which can be read by a computer.
In the above embodiments, the implementation may be wholly or partially implemented by software, hardware, firmware, or any combination thereof. When implemented in software, may be implemented in whole or in part in the form of a computer program product. The computer program product includes one or more computer instructions. When loaded and executed on a computer, cause the processes or functions described in accordance with the embodiments of the application to occur, in whole or in part. The computer may be a general purpose computer, a special purpose computer, a network of computers, or other programmable device. The computer instructions may be stored in a computer readable storage medium or transmitted from one computer readable storage medium to another, for example, the computer instructions may be transmitted from one website, computer, server, or data center to another website, computer, server, or data center by wire (e.g., coaxial cable, fiber optics, digital subscriber line) or wirelessly (e.g., infrared, wireless, microwave, etc.). The computer readable medium can be any available medium that can be accessed by a computer or a data storage device, such as a server, a data center, etc., that incorporates one or more available media. The usable medium may be a magnetic medium (which may be, for example, a floppy disk, a hard disk, a magnetic tape), an optical medium (such as an optical disk), a semiconductor medium (such as a solid state disk), or the like. In the foregoing embodiments, the descriptions of the respective embodiments have respective emphasis, and for parts that are not described in detail in a certain embodiment, reference may be made to related descriptions of other embodiments.
In the embodiments provided in the present application, it should be understood that the disclosed apparatus may be implemented in other manners. For example, the above-described embodiments of the apparatus are merely illustrative, and for example, the above-described division of the units is only one type of division of logical functions, and other divisions may be realized in practice, for example, a plurality of units or components may be combined or integrated into another system, or some features may be omitted, or not executed. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be through some interfaces, indirect coupling or communication connection of devices or units, and may be in an electrical or other form.
The units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiment.
In addition, functional units in the embodiments of the present application may be integrated into one processing unit, or each unit may exist alone physically, or two or more units are integrated into one unit. The integrated unit can be realized in a form of hardware, and can also be realized in a form of a software functional unit.
The integrated units, if implemented as software functional units and sold or used as a stand-alone product, may be stored in a computer accessible memory. Based on such understanding, the technical solution of the present application, which is a part of or contributes to the prior art in essence, or all or part of the technical solution, may be embodied in the form of a software product, stored in a memory, including several requests for causing a computer device (which may be a personal computer, a server, a network device, or the like, and may specifically be a processor in the computer device) to execute all or part of the steps of the above-described method of the embodiments of the present application.
The above embodiments are only used for illustrating the technical solutions of the present application and not for limiting the same; although the present application has been described in detail with reference to the foregoing embodiments, it will be understood by those of ordinary skill in the art; the technical solutions described in the foregoing embodiments may still be modified, or some technical features may be equivalently replaced; and such modifications or substitutions do not depart from the spirit and scope of the corresponding technical solutions in the embodiments of the present application.

Claims (10)

1. An intelligent infusion monitoring method, characterized in that the method comprises:
the infusion monitoring device detects the current dosage in the first target infusion bottle;
the infusion monitoring device sends first target information to a monitoring platform; the first target information at least comprises the current medicine amount and the position of a target ward corresponding to the first target hanging bottle;
the monitoring platform judges whether the current medicine amount is lower than a preset target medicine amount, and if the current medicine amount is lower than the target medicine amount, first early warning information is output; the first early warning information is used for prompting medical personnel that the current medicine amount of the first target infusion bottle is too low, and the first early warning information at least comprises the first target information.
2. The method of claim 1, wherein after the monitoring platform outputs the first pre-alarm information, the method further comprises:
the monitoring platform starts timing from the moment of outputting the first early warning information and judges whether second target information sent by the infusion device is received before the timing time reaches a preset target time; wherein the second target information comprises the current medicine amount which is not less than the target medicine amount;
and if the second target information is not received before the timing duration reaches the target duration, the monitoring platform determines a mobile terminal which is connected with the monitoring platform and is closest to the monitoring platform, and sends the first early warning information to the mobile terminal.
3. The method of claim 2, wherein after the monitoring platform determines that the second target information sent by the infusion device is received before the timed length reaches the target length, the method further comprises:
the monitoring platform determines a target response time length from the moment of outputting the first early warning information to the moment of receiving the second target information sent by the infusion device;
the monitoring platform determines the average response time length in a circular area range which takes the monitoring platform as the circle center and takes the preset length as the radius from cloud data, and judges whether the target response time length is lower than the average response time length;
if the average response time is shorter than the average response time, the monitoring platform outputs prompt information for prompting medical staff to increase the response speed.
4. The method of claim 1, wherein after the monitoring platform outputs the first pre-alarm information, the method further comprises:
the monitoring platform judges whether a transfusion bottle replacing operation is detected or not, and if the transfusion bottle replacing operation is detected, a transfusion bottle replacing instruction is sent to the transfusion monitoring device;
and after receiving the transfusion replacement instruction, the transfusion monitoring device closes a first transfusion sub-device used for inputting the liquid medicine in the first target transfusion bottle to the patient corresponding to the first target transfusion bottle, and opens a second transfusion sub-device used for inputting the liquid medicine in a second target transfusion bottle to the patient.
5. The method according to any one of claims 1 to 4, further comprising:
the infusion monitoring device determines physiological parameters of a patient corresponding to the first target infusion bottle; wherein the physiological parameters at least comprise a heart rate parameter, a blood pressure parameter and a respiratory rate parameter;
the infusion monitoring device judges whether all the parameters in the physiological parameters are in a preset normal parameter range;
if not, the infusion monitoring device sends physiological early warning information comprising the physiological parameters to the monitoring platform; wherein the physiological early warning information is used for indicating that the patient has life danger;
and the monitoring platform outputs an acousto-optic alarm signal after receiving the physiological early warning information.
6. An intelligent infusion monitoring system is characterized by comprising an infusion monitoring device and a monitoring platform, wherein the infusion monitoring device comprises a detection unit and a first sending unit, and the monitoring platform comprises a first receiving unit, a first judging unit and an output unit;
the detection unit is used for detecting the current medicine amount in the first target infusion bottle;
the first sending unit is used for sending first target information to the monitoring platform; the first target information at least comprises the current medicine amount and the position of a target ward corresponding to the first target hanging bottle;
the first receiving unit is configured to receive the first target information.
The first judging unit is used for judging whether the current medicine amount is lower than a preset target medicine amount;
the output unit is used for outputting first early warning information after the first judging unit judges that the current medicine amount is lower than the target medicine amount; the first early warning information is used for prompting medical personnel that the current medicine amount of the first target infusion bottle is too low, and the first early warning information at least comprises the first target information.
7. The intelligent infusion monitoring system of claim 6, wherein the monitoring platform further comprises a timing unit and a first determination unit, wherein:
the timing unit is used for starting timing from the moment of outputting the first early warning information after the output unit outputs the first early warning information;
the first judging unit is further used for judging whether second target information sent by the infusion device is received before the timing duration reaches a preset target duration; wherein the second target information comprises the current medicine amount which is not less than the target medicine amount;
the first determining unit is configured to determine, after the first determining unit determines that the second target information is not received before the timing duration reaches the target duration, a mobile terminal that is connected to the monitoring platform and has a closest distance to the monitoring platform, and send the first warning information to the mobile terminal.
8. The intelligent infusion monitoring system according to claim 7, wherein the first determination unit is further configured to determine a target response time period from a time when the first warning information is output to a time when the second target information transmitted by the infusion device is received, after the first judgment unit judges that the second target information is received before the timed period reaches the target time period;
the first determining unit is further configured to determine, from cloud data, an average response time length within a circular area range that takes the monitoring platform as a circle center and takes a preset length as a radius;
the first judging unit is further configured to judge whether the target response duration is lower than the average response duration;
the output unit is further configured to output prompt information for prompting the medical staff to increase the response speed after the first determination unit determines that the target response duration is shorter than the average response duration.
9. The intelligent infusion monitoring system of claim 6, wherein the infusion monitoring device further comprises a second receiving unit, a closing unit, and an opening unit, the monitoring platform further comprises a second sending unit;
the first judging unit is further used for judging whether the transfusion bottle replacing operation is detected or not after the first early warning information is output by the output unit;
the second sending unit is used for sending a transfusion bottle replacing instruction to the transfusion monitoring device after the first judging unit judges that the transfusion bottle replacing operation is detected;
the second receiving unit is used for receiving the hanging bottle replacing instruction;
the closing unit is used for closing a first infusion sub-device which is used for inputting the liquid medicine in the first target infusion bottle to the patient corresponding to the first target infusion bottle;
the opening unit is used for opening a second infusion sub-device used for inputting the liquid medicine in the second target infusion bottle to the patient.
10. The intelligent infusion monitoring system according to any one of claims 6-9, further comprising a second determination unit and a second judgment unit, wherein:
the second determination unit is used for determining the physiological parameters of the patient corresponding to the first target infusion bottle; wherein the physiological parameters at least comprise a heart rate parameter, a blood pressure parameter and a respiratory rate parameter;
the second judging unit is used for judging whether all the parameters in the physiological parameters are in a preset normal parameter range;
the first sending unit is further configured to send physiological warning information including the physiological parameters to the monitoring platform when the second determining unit determines that all the parameters in the physiological parameters are not within the normal parameter range; wherein the physiological early warning information is used for indicating that the patient has life danger;
the first receiving unit is further used for receiving the physiological early warning information;
the output unit is also used for outputting sound and light alarm signals.
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