CN113658670A - Method and device for determining whether operation of therapeutic apparatus is standard or not and therapeutic apparatus - Google Patents
Method and device for determining whether operation of therapeutic apparatus is standard or not and therapeutic apparatus Download PDFInfo
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- CN113658670A CN113658670A CN202110948694.1A CN202110948694A CN113658670A CN 113658670 A CN113658670 A CN 113658670A CN 202110948694 A CN202110948694 A CN 202110948694A CN 113658670 A CN113658670 A CN 113658670A
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- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
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- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/20—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
- G16H40/63—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/60—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices
- G16H40/67—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for remote operation
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Abstract
The application discloses a method, a device and a therapeutic apparatus for determining whether the operation of the therapeutic apparatus is standard, wherein the method comprises the following steps: recording operation information corresponding to the operation executed by the user; recording the first time for starting to output the physical energy and recording the condition of the therapeutic apparatus for outputting the physical energy; recording a second time when the therapeutic apparatus stops outputting the physical energy; generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the output physical energy of the treatment instrument into the log file; and comparing the content recorded in the log file with the operation standard to determine whether the operation executed by the user meets the operation standard. By the method and the device, the problem that whether the treatment process of a doctor can be standardized or not can not be effectively evaluated due to the fact that the behavior of the doctor for adjusting the parameters cannot be acquired in the related technology is solved, and a data basis is provided for the doctor to use the treatment equipment to carry out standardized evaluation on the treatment behavior or not.
Description
Technical Field
The application relates to the field of medical instruments, in particular to a method and a device for determining whether the operation of a therapeutic apparatus is standard or not and the therapeutic apparatus.
Background
During the treatment of diseases, some treatment devices are used to treat patients, and during the treatment with the treatment devices, the treatment devices are required to be operated according to the standard of use of the treatment devices.
Currently, some operating parameters of the treatment device are pre-configured according to the patient's condition so that the physician uses the treatment device according to the parameters. However, in order to enable a doctor to flexibly treat a patient according to the condition of the patient, the parameters may be adjusted, and the behavior of adjusting the parameters by the doctor is not obtained by a method in the related art, which may result in that whether the treatment process of the doctor is standardized or not cannot be effectively evaluated.
Disclosure of Invention
The embodiment of the application provides a method and a device for determining whether the operation of a therapeutic apparatus is standard or not and the therapeutic apparatus, so as to at least solve the problem that whether the treatment process of a doctor is standardized or not cannot be effectively evaluated due to the fact that the behavior of adjusting parameters of the doctor cannot be acquired in the related technology.
According to one aspect of the application, there is provided a method of determining whether operation of an apparatus is standard, comprising: the method comprises the steps of obtaining the operation of a user on the therapeutic apparatus, and recording operation information corresponding to the operation executed by the user, wherein the operation information comprises at least one of the following: the operation process of the user and the parameter information configured by the user through the operation are the basis for outputting the physical energy by the therapeutic apparatus; under the condition that the operation starts the therapeutic apparatus to output the physical energy, recording a first time for starting the output of the physical energy and recording the condition that the therapeutic apparatus outputs the physical energy; recording a second time when the therapeutic apparatus stops outputting the physical energy after the therapeutic apparatus stops outputting the physical energy; generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the physical energy output by the treatment instrument into the log file; and comparing the content recorded in the log file with an operation standard, and determining whether the operation executed by the user meets the operation standard according to a comparison result, wherein the operation standard is preset.
Further, generating the log file includes: acquiring naming information, wherein the naming information comprises at least one of the following: identification information of the therapeutic apparatus, identification information of the user, and information of a therapeutic object of the therapeutic apparatus; naming the log file according to the naming information and the time information used by the therapeutic apparatus; and saving the named log file.
Further, saving the log file comprises: storing the log file locally on the treatment apparatus; and sending the log file to a log file storage server for storage.
Further, the operation information of the therapeutic apparatus received by the user after the therapeutic apparatus stops outputting the physical energy is recorded into a new log file, wherein each log file records the complete process from the time when the user operates the therapeutic apparatus to the time when the therapeutic apparatus stops outputting the physical energy.
Further, before comparing the content recorded in the log file with the operation standard, the method further includes: acquiring disease information corresponding to the operation executed by the user; and acquiring an operation standard corresponding to the disease information according to the disease information, wherein the operation standard at least comprises the range of the parameters which can be configured by the user.
According to another aspect of the application, there is also provided an apparatus for determining whether operation of an apparatus is standard, comprising: the acquisition module is used for acquiring the operation of a user on the therapeutic apparatus and recording operation information corresponding to the operation executed by the user, wherein the operation information comprises at least one of the following: the operation process of the user and the parameter information configured by the user through the operation are the basis for outputting the physical energy by the therapeutic apparatus; the log module is used for recording the first time for starting the output of the physical energy and the condition for recording the output of the physical energy of the therapeutic apparatus under the condition that the operation starts the therapeutic apparatus to output the physical energy; recording a second time when the therapeutic apparatus stops outputting the physical energy after the therapeutic apparatus stops outputting the physical energy; generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the physical energy output by the treatment instrument into the log file; and the comparison module is used for comparing the content recorded in the log file with an operation standard and determining whether the operation executed by the user meets the operation standard or not according to a comparison result, wherein the operation standard is established in advance.
Further, the log module is configured to obtain naming information, where the naming information includes at least one of: identification information of the therapeutic apparatus, identification information of the user, and information of a therapeutic object of the therapeutic apparatus; naming the log file according to the naming information and the time information used by the therapeutic apparatus; and saving the named log file.
Further, the log module is configured to record the operation information of the therapeutic apparatus received by the user after the therapeutic apparatus stops outputting the physical energy into a new log file, where each log file records a complete process from when the user operates the therapeutic apparatus to when the therapeutic apparatus stops outputting the physical energy.
Further, the obtaining module is further configured to obtain disease information corresponding to an operation performed by the user; and acquiring an operation standard corresponding to the disease information according to the disease information, wherein the operation standard at least comprises the range of the parameters which can be configured by the user.
According to another aspect of the application, there is also provided an apparatus comprising: an input part for receiving input information of the user; an energy output unit for outputting physical energy; software for performing the above-described method; and the storage part is used for storing the log file.
In the embodiment of the application, the method includes the steps of acquiring the operation of a user on the therapeutic apparatus, and recording operation information corresponding to the operation executed by the user, wherein the operation information includes at least one of the following: the operation process of the user and the parameter information configured by the user through the operation are the basis for outputting the physical energy by the therapeutic apparatus; under the condition that the operation starts the therapeutic apparatus to output the physical energy, recording a first time for starting the output of the physical energy and recording the condition that the therapeutic apparatus outputs the physical energy; recording a second time when the therapeutic apparatus stops outputting the physical energy after the therapeutic apparatus stops outputting the physical energy; generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the physical energy output by the treatment instrument into the log file; and comparing the content recorded in the log file with an operation standard, and determining whether the operation executed by the user meets the operation standard according to a comparison result, wherein the operation standard is preset. By the method and the device, the problem that whether the treatment process of a doctor can be standardized or not can not be effectively evaluated due to the fact that the behavior of the doctor for adjusting the parameters cannot be acquired in the related technology is solved, and a data basis is provided for the doctor to use the treatment equipment to carry out standardized evaluation on the treatment behavior or not.
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The accompanying drawings, which are incorporated in and constitute a part of this application, illustrate embodiments of the application and, together with the description, serve to explain the application and are not intended to limit the application. In the drawings:
fig. 1 is a flow chart of a method of determining whether an operation of an apparatus is standard according to an embodiment of the present application.
Detailed Description
It should be noted that the embodiments and features of the embodiments in the present application may be combined with each other without conflict. The present application will be described in detail below with reference to the embodiments with reference to the attached drawings.
It should be noted that the steps illustrated in the flowcharts of the figures may be performed in a computer system such as a set of computer-executable instructions and that, although a logical order is illustrated in the flowcharts, in some cases, the steps illustrated or described may be performed in an order different than presented herein.
In the present embodiment, a method for determining whether an operation of an apparatus is standard is provided, and fig. 1 is a flowchart of a method for determining whether an operation of an apparatus is standard according to an embodiment of the present application, as shown in fig. 1, the method comprising the steps of:
step S102, obtaining the operation of the therapeutic apparatus by the user, and recording operation information corresponding to the operation executed by the user, wherein the operation information comprises at least one of the following: the operation process of the user and the parameter information configured by the user through the operation are the basis for outputting the physical energy by the therapeutic apparatus;
the user in this step is the user who operates the apparatus, and the user may be a medical care provider such as a doctor. In an alternative embodiment, the user may select a condition of the patient to be treated, and after the user selects the condition, the therapeutic apparatus generates corresponding configuration information according to the condition, wherein the configuration information includes the parameter information in the above steps. If the user does not perform an operation of adjusting the parameter information, the log file may not be generated. When the user adjusts the parameter information, the following steps are continuously performed.
Step S104, recording the first time for starting to output the physical energy and the condition for recording the physical energy output of the therapeutic apparatus under the condition that the therapeutic apparatus is started to output the physical energy by the operation;
step S106, after the therapeutic apparatus stops outputting the physical energy, recording a second time when the therapeutic apparatus stops outputting the physical energy;
step S108, generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the output physical energy of the therapeutic apparatus into the log file;
step S110, comparing the content recorded in the log file with an operation standard, and determining whether the operation performed by the user meets the operation standard according to a comparison result, where the operation standard is pre-established.
For example, the range of parameters for treating Z disorder in the criteria is [ a, B ], and the log file records that the parameter entered by the user during the treatment is C, and if C is within the range of parameters, the operating criteria are met, and if C is not within the range of parameters [ a, B ], the user's operation is not met.
The standard can also comprise the step of operating the therapeutic apparatus by the user, when the comparison is carried out, the operation steps recorded in the log file are compared with the operation steps in the standard, if the operation steps are consistent, the operation standard is met, and if the operation steps are not consistent, the operation standard is not met.
The content which needs to be recorded in the whole treatment process of the user is recorded through the steps and is stored as a complete log file, so that data guarantee is provided for judging whether the operation executed by the user meets the standard.
The method for storing the log file takes the use characteristics of the therapeutic apparatus into consideration, the log file used each time is stored, which is beneficial to the reproduction and searching of problems, at the moment, the operation information of the therapeutic apparatus received by the user after the therapeutic apparatus stops outputting the physical energy is recorded into a new log file, wherein each log file records the information which needs to be recorded from the time when the user operates the therapeutic apparatus to the time when the therapeutic apparatus stops outputting the physical energy.
In order to enable the log file to store the information embodying the operation, the name of the log file may be specified. For example, naming information may be obtained first, wherein the naming information includes at least one of: identification information of the therapeutic apparatus, identification information of the user, and information of a therapeutic object of the therapeutic apparatus; then naming the log file according to the naming information and the time information used by the therapeutic apparatus; and saving the named log file. This is helpful for the lookup of log files.
The log file may be stored locally on the apparatus or may be uploaded to a server for storage, for example, to a log file storage server. All that can save log files can be referred to as log file storage servers. The log file stored on the server may be counted, for example, the number of substandard operations occurring within a predetermined time period may be counted for each treatment apparatus, and the number of substandard operations corresponding to a specific disease condition may be counted. The proportion of the user operation meeting the standard can be counted according to the user. These statistics can be used as the basis for subsequent evaluation of the user and adjustment of the criteria.
For example, the parameter range for exciting the predetermined physical energy in the standard for the treatment of the lower leg pain is [ a, B ], and it is found that 60% of the parameters used for the treatment of the lower leg pain in the log file stored in the server exceed the parameter range [ a, B ]. At this point, it may be considered whether the parameter ranges in the standard need to be adjusted.
As an optional embodiment, when the log file is generated, the log file can be generated only when the operation of the user does not meet the standard, so that the local storage space of the therapeutic apparatus can be saved. Of course, it is also possible to record that all operations of the user are generated into log files, and label each log file whether the log file meets the standard or not. And at intervals of a preset period, actively sending the log files which do not accord with the standard to a server for storage, and deleting the log files which accord with the standard, so that the log files corresponding to problematic operations can be reserved, and the local storage space of the therapeutic apparatus can be saved.
The log file can be used only by maintenance personnel, so that the log file can be encrypted and then stored. For example, the identifier of the apparatus, the first time and the second time are taken as a character sequence; carrying out Hash operation on the character sequence to obtain a Hash value; and encrypting the log file by using the hash value.
In order to keep the log file from being tampered, the log file may also be saved using blockchain techniques. Acquiring a first log file, and taking the hash value as a first verification code; acquiring a second log file, generating a hash value according to the second log file and a first verification code, taking the hash value as the second verification code, and so on to acquire an Nth log file, and taking the Nth log file and the generated hash value as an Nth verification code, wherein N is a natural number greater than 1; and respectively copying and storing all log files and verification codes on M devices, wherein M is a natural number greater than 1.
Through the implementation, the problem that the reason of the fault cannot be positioned when the fault occurs in the conventional therapeutic apparatus is solved, and the maintenance convenience and efficiency of the therapeutic apparatus are improved.
The above-mentioned method can be applied to various tools, as a typical tool, the tool can be a therapeutic pen, and the host can be a therapeutic apparatus. A typical therapeutic pen and host are described below. Or the host machine and the therapeutic pen can be considered as the therapeutic apparatus as a whole. The therapeutic apparatus may comprise: an input part for receiving input information of the user; an energy output unit for outputting physical energy; software for performing the above-described method; and the storage part is used for storing the log file.
In this embodiment, there is also provided a host for a limb pain therapy apparatus, the host comprising: the vibration prescription control system comprises a case, a touch display screen and a Central Processing Unit (CPU) main control board, wherein the case is arranged on the surface of the case, the CPU main control board is arranged in the case and electrically connected with the touch display screen, the CPU main control board is used for supplying power to a vibrator and outputting a vibration prescription signal, the touch display screen is used for a user to select a vibration prescription, and the vibration prescription signal is output to a treatment pen.
Optionally, the method further comprises: at least one intermediate frequency output interface arranged on the surface of the case; the limb pain therapeutic apparatus further comprises at least one group of electrode plates which are respectively and electrically connected with the at least one intermediate frequency output interface through cables, and the CPU main control board is also electrically connected with the at least one intermediate frequency output interface and used for outputting current prescription signals to the at least one group of electrode plates.
When the log file is recorded, the current output by the electrode slice can be recorded.
Optionally, the characteristic parameters of the vibration prescription signal include: continuous vibration of the vibrator and vibration frequency and amplitude of the continuous vibration; or the intermittent vibration of the vibrator and the duty ratio, vibration frequency and amplitude of the intermittent vibration. Optionally, the vibration prescription includes: default fixed parameters for each treatment site that have been stored and individual vibration intensity levels that are manually adjusted for the same treatment site; the touch display screen is used for selecting a corresponding vibration prescription for a treatment part by a user, generating a target characteristic parameter according to a default fixed parameter included in the selected vibration prescription and an individual vibration intensity level manually adjusted by the user on the same treatment part, and sending the target characteristic parameter generated according to the vibration prescription selected by the user to the CPU main control board; and the CPU main control board is used for generating a corresponding vibration prescription signal according to the target characteristic parameter.
These characteristic parameters may be recorded in a log file.
Optionally, the CPU main control board includes: a microcomputer chip and a triode; the microcomputer chip is used for receiving the target characteristic parameters and determining a target duty ratio according to the amplitude in the target characteristic parameters and the corresponding relation between the amplitude and the duty ratio which are stored in advance; generating the vibration prescription signal according to the target duty ratio and the vibration frequency in the target characteristic parameter, and sending the vibration prescription signal to the triode; the triode is used for outputting the vibration prescription signal to the treatment pen and controlling the vibration prescription signal to drive the vibrator.
Optionally, a timer and a counter are integrated in the touch display screen, and the timer is configured to turn off the host or send an alarm when a time period during which the host outputs the vibration prescription signal to the therapeutic pen reaches a preset time period threshold; the counter is used for recording the output times of the vibration prescription signal output to the treatment pen by the host. The number of alarms sent may also be recorded in a log file.
In this embodiment, there is provided a therapeutic pen for a limb pain therapy apparatus comprising a host computer for outputting a vibration prescription signal to the therapeutic pen, the therapeutic pen comprising: penholder and detachable are connected the cap for brush of penholder distal end, the penholder can be under the dismantlement install the treatment syringe needle behind the cap for brush, just the penholder surface is provided with shift knob, the needle tubing of treatment syringe needle stretches out the distal end of cap for brush, the penholder is inside to be provided with can by shift knob control opens the vibrator that stops, the vibrator is used for when opening, will transmit to intervention focus position with the corresponding physical kinetic energy of vibration prescription signal the treatment syringe needle.
Optionally, the treatment pen satisfies at least one of the following characteristics: (a) the track of the output vibration of the vibrator is in a plane perpendicular to or parallel to the axis of the penholder, and the track of the vibration comprises: the pen holder is characterized by comprising a track which does reciprocating motion along a single direction and/or a track which does reciprocating motion circularly along a plurality of angle directions by taking the axis of the pen holder as a center; (b) the vibration amplitude of the vibrator is designed to be between 2 and 500 mu m, and the vibration frequency of the vibrator is designed to be between 5 and 500 Hz; (c) the treatment needle is a special treatment needle or a disposable syringe needle and is used for intervening in a focus part formed by the damage of soft tissues for diagnosis and/or treatment.
Optionally, the therapeutic pen further comprises: the negative pressure pump is detachably connected to the far end of the pen holder; the pen cap is made of transparent materials; the utility model discloses a treatment syringe, including pen cap, negative pressure pump, treatment syringe needle, pencil cap surface is fixed with the joint, the negative pressure pump pass through the drainage tube with articulate, the joint with the pencil cap and treatment syringe needle intercommunication, the negative pressure pump is used for providing the drawing liquid negative pressure for the hydrops in the focus position when starting, makes the hydrops follow take out in the focus position.
Optionally, the sensor is a liquid level sensor, the liquid level sensor includes two electrodes fixed on the inner wall of the communicating tube and having a gap, and a control circuit board electrically connected to the two electrodes, the control circuit board is disposed in the host, and the control circuit board is further electrically connected to the CPU main control board; when liquid is accumulated at the positions of the two electrodes in the communicating pipe, the two electrodes are conducted, and the control circuit board transmits electric signals corresponding to the conduction of the two electrodes to the CPU main control board; or when no effusion exists at the positions of the two electrodes in the communicating pipe, the two electrodes are disconnected and conducted, and the control circuit board transmits the electric signals corresponding to the disconnection and conduction of the two electrodes to the CPU main control board.
Optionally, the vibrator comprises a rotary centrifugal vibrator.
Optionally, in a case that a rotary centrifugal vibrator capable of being controlled by the switch button to start and stop is disposed inside the pen holder, the therapeutic pen further includes: and the PCB control board is electrically connected with the rotary centrifugal vibrator and used for outputting vibration prescription signals to the rotary centrifugal vibrator, and a common mode filter is further integrated on the PCB control board.
The data of the sensor in the therapeutic pen is sent to the host computer, and the data for controlling the start and stop of the switch button is also sent to obtain the host computer, the data comprises time information, and the host computer can record the time information into the same log file after receiving the time information.
In this embodiment, an electronic device is provided, comprising a memory in which a computer program is stored and a processor configured to run the computer program to perform the method in the above embodiments.
The programs described above may be run on a processor or may also be stored in memory (or referred to as computer-readable media), which includes both non-transitory and non-transitory, removable and non-removable media, that implement information storage by any method or technology. The information may be computer readable instructions, data structures, modules of a program, or other data. Examples of computer storage media include, but are not limited to, phase change memory (PRAM), Static Random Access Memory (SRAM), Dynamic Random Access Memory (DRAM), other types of Random Access Memory (RAM), Read Only Memory (ROM), Electrically Erasable Programmable Read Only Memory (EEPROM), flash memory or other memory technology, compact disc read only memory (CD-ROM), Digital Versatile Discs (DVD) or other optical storage, magnetic cassettes, magnetic tape magnetic disk storage or other magnetic storage devices, or any other non-transmission medium that can be used to store information that can be accessed by a computing device. As defined herein, a computer readable medium does not include a transitory computer readable medium such as a modulated data signal and a carrier wave.
These computer programs may also be loaded onto a computer or other programmable data processing apparatus to cause a series of operational steps to be performed on the computer or other programmable apparatus to produce a computer implemented process such that the instructions which execute on the computer or other programmable apparatus provide steps for implementing the functions specified in the flowchart flow or flows and/or block diagram block or blocks, and corresponding steps may be implemented by different modules. In this embodiment, there is provided a device, referred to as a device for determining whether the operation of the apparatus is standard, comprising: the acquisition module is used for acquiring the operation of a user on the therapeutic apparatus and recording operation information corresponding to the operation executed by the user, wherein the operation information comprises at least one of the following: the operation process of the user and the parameter information configured by the user through the operation are the basis for outputting the physical energy by the therapeutic apparatus; the log module is used for recording the first time for starting the output of the physical energy and the condition for recording the output of the physical energy of the therapeutic apparatus under the condition that the operation starts the therapeutic apparatus to output the physical energy; recording a second time when the therapeutic apparatus stops outputting the physical energy after the therapeutic apparatus stops outputting the physical energy; generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the physical energy output by the treatment instrument into the log file; and the comparison module is used for comparing the content recorded in the log file with an operation standard and determining whether the operation executed by the user meets the operation standard or not according to a comparison result, wherein the operation standard is established in advance. The apparatus includes one or more modules that perform the steps of the above-described method.
For example, the log module is configured to obtain naming information, where the naming information includes at least one of: identification information of the therapeutic apparatus, identification information of the user, and information of a therapeutic object of the therapeutic apparatus; naming the log file according to the naming information and the time information used by the therapeutic apparatus; and saving the named log file.
For another example, the log module is configured to record the operation information of the therapeutic apparatus received by the user after the therapeutic apparatus stops outputting the physical energy into a new log file, where each log file records a complete process from when the user operates the therapeutic apparatus to when the therapeutic apparatus stops outputting the physical energy.
For another example, the obtaining module is further configured to obtain disease information corresponding to an operation performed by the user; and acquiring an operation standard corresponding to the disease information according to the disease information, wherein the operation standard at least comprises the range of the parameters which can be configured by the user.
The embodiment solves the problem that the behavior of adjusting the parameters of the doctor cannot be acquired effectively in the related technology, which results in the fact that the treatment process of the doctor cannot be standardized, and provides a data basis for the standardized evaluation of the treatment behavior of the doctor using the treatment equipment
The above are merely examples of the present application and are not intended to limit the present application. Various modifications and changes may occur to those skilled in the art. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present application should be included in the scope of the claims of the present application.
Claims (10)
1. A method of determining whether an operation of an apparatus is standard, comprising:
the method comprises the steps of obtaining the operation of a user on the therapeutic apparatus, and recording operation information corresponding to the operation executed by the user, wherein the operation information comprises at least one of the following: the operation process of the user and the parameter information configured by the user through the operation are the basis for outputting the physical energy by the therapeutic apparatus;
under the condition that the operation starts the therapeutic apparatus to output the physical energy, recording a first time for starting the output of the physical energy and recording the condition that the therapeutic apparatus outputs the physical energy;
recording a second time when the therapeutic apparatus stops outputting the physical energy after the therapeutic apparatus stops outputting the physical energy;
generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the physical energy output by the treatment instrument into the log file;
and comparing the content recorded in the log file with an operation standard, and determining whether the operation executed by the user meets the operation standard according to a comparison result, wherein the operation standard is preset.
2. The method of claim 1, wherein generating the log file comprises:
acquiring naming information, wherein the naming information comprises at least one of the following: identification information of the therapeutic apparatus, identification information of the user, and information of a therapeutic object of the therapeutic apparatus;
naming the log file according to the naming information and the time information used by the therapeutic apparatus;
and saving the named log file.
3. The method of claim 2, wherein saving the log file comprises:
storing the log file locally on the treatment apparatus;
and sending the log file to a log file storage server for storage.
4. The method of claim 1, wherein the information about the operation of the apparatus by the user after the apparatus stops outputting the physical energy is recorded in a new log file, wherein each log file records the complete process from the operation of the apparatus by the user to the stop of outputting the physical energy by the apparatus.
5. The method according to any one of claims 1 to 4, wherein before comparing the content recorded in the log file with the operation standard, further comprising:
acquiring disease information corresponding to the operation executed by the user;
and acquiring an operation standard corresponding to the disease information according to the disease information, wherein the operation standard at least comprises the range of the parameters which can be configured by the user.
6. An apparatus for determining whether a standard operation of an apparatus is being performed, comprising:
the acquisition module is used for acquiring the operation of a user on the therapeutic apparatus and recording operation information corresponding to the operation executed by the user, wherein the operation information comprises at least one of the following: the operation process of the user and the parameter information configured by the user through the operation are the basis for outputting the physical energy by the therapeutic apparatus;
the log module is used for recording the first time for starting the output of the physical energy and the condition for recording the output of the physical energy of the therapeutic apparatus under the condition that the operation starts the therapeutic apparatus to output the physical energy; recording a second time when the therapeutic apparatus stops outputting the physical energy after the therapeutic apparatus stops outputting the physical energy; generating a log file corresponding to the treatment process, and writing the recorded operation information, the first time, the second time and the condition of the physical energy output by the treatment instrument into the log file;
and the comparison module is used for comparing the content recorded in the log file with an operation standard and determining whether the operation executed by the user meets the operation standard or not according to a comparison result, wherein the operation standard is established in advance.
7. The apparatus of claim 6, wherein the log module is configured to obtain naming information, wherein the naming information comprises at least one of: identification information of the therapeutic apparatus, identification information of the user, and information of a therapeutic object of the therapeutic apparatus; naming the log file according to the naming information and the time information used by the therapeutic apparatus; and saving the named log file.
8. The apparatus of claim 6, wherein the log module is configured to record the operation information of the therapeutic apparatus received again from the user after the therapeutic apparatus stops outputting the physical energy into a new log file, wherein each log file records a complete process from the operation of the therapeutic apparatus by the user to the stop of outputting the physical energy by the therapeutic apparatus.
9. The device according to any one of claims 6 to 8, wherein the obtaining module is further configured to obtain disease information corresponding to an operation performed by the user; and acquiring an operation standard corresponding to the disease information according to the disease information, wherein the operation standard at least comprises the range of the parameters which can be configured by the user.
10. An apparatus, comprising:
an input part for receiving input information of the user;
an energy output unit for outputting physical energy;
software for performing the method of any one of claims 1 to 5;
and the storage part is used for storing the log file.
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN117524441A (en) * | 2024-01-03 | 2024-02-06 | 杭州海康慧影科技有限公司 | Method and device for detecting surgical quality |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN117524441A (en) * | 2024-01-03 | 2024-02-06 | 杭州海康慧影科技有限公司 | Method and device for detecting surgical quality |
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