WO2023000789A1 - 程控信息记录方法及相关装置 - Google Patents

程控信息记录方法及相关装置 Download PDF

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Publication number
WO2023000789A1
WO2023000789A1 PCT/CN2022/092817 CN2022092817W WO2023000789A1 WO 2023000789 A1 WO2023000789 A1 WO 2023000789A1 CN 2022092817 W CN2022092817 W CN 2022092817W WO 2023000789 A1 WO2023000789 A1 WO 2023000789A1
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WIPO (PCT)
Prior art keywords
patient
target
time period
program
information
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PCT/CN2022/092817
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English (en)
French (fr)
Inventor
刘鑫蕊
王倩
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苏州景昱医疗器械有限公司
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Publication of WO2023000789A1 publication Critical patent/WO2023000789A1/zh

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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
    • G16H40/20—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
    • 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
    • G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
    • G16H10/60—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
    • 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
    • G16H80/00—ICT specially adapted for facilitating communication between medical practitioners or patients, e.g. for collaborative diagnosis, therapy or health monitoring

Definitions

  • the present application relates to the technical field of data processing, and in particular to a program-controlled information recording method, device, electronic equipment, and computer-readable storage medium.
  • An implantable neurostimulation system mainly includes a stimulator implanted in the body, electrodes and a program controller outside the body.
  • the existing neuromodulation technology mainly uses stereotaxic surgery to implant electrodes in specific structures (i.e., targets) in the body, and the stimulator implanted in the patient sends electrical pulses to the targets through the electrodes to regulate the corresponding neural structures and networks. Electrical activity and its function, thereby improving symptoms and relieving pain.
  • hospitals are usually unable to record all the information of patient program control.
  • the existing program control recording method only records the information of remote program control, and does not include the information of the patient's program control in the hospital.
  • the doctor when performing program control on a patient, he would like to know all the program control records of the patient.
  • the purpose of this application is to provide a program control information recording method, device, electronic equipment and computer-readable storage medium, capable of recording all program control information of patients' remote program control and hospital program control.
  • the present application provides a method for recording program-controlled information, which is applied to electronic devices, and the method includes: for each patient in at least one patient, acquiring the program-controlled information of the program-controlled device installed outside the patient’s body, so
  • the program-controlled equipment includes one or more of an in vitro program-controlled instrument, a program-controlled device, a charger, a tablet computer, a notebook computer, a desktop computer, and a mobile phone; a program-controlled record of the patient is generated, and the program-controlled record of the patient includes the patient
  • the identification information and program control information of the patient; the program control record of the patient is stored in a storage device.
  • the patient is any one of the following: patients with Parkinson's disease; patients with depression; patients with addictive diseases; patients with obsessive-compulsive disorder;
  • the method further includes: using the program-controlled device to receive a first selection operation on a target patient, where the target patient is one of the at least one patient; Selecting an operation to obtain the identification information of the target patient; using the program-controlled device to receive an inquiry operation on at least one program-controlled record of the target patient; in response to the inquiry operation, using the identification information of the target patient to select from the Querying the storage device to obtain at least one program-controlled record of the target patient; sending the at least one program-controlled record of the target patient to the program-controlled device.
  • the method further includes: acquiring additional information of the target patient, where the additional information includes one or more of historical chief complaint information, historical appointment information, and implantation information; The additional information of the target patient is sent to the program-controlled device.
  • the method further includes: using the patient device to receive a second selection operation on the target doctor; in response to the second selection operation, acquiring the schedule information of the target doctor and sending it to the According to the patient device, the scheduling information includes at least one time period and the number of reservations available for each time period; the patient device is used to receive an appointment operation for the target doctor's target time period, and the target time period is the specified time period.
  • one of the at least one time period in response to the reservation operation, when the number of appointments available for the target doctor’s target time period is not less than 1, perform Subtract one operation; generate first prompt information and send it to the doctor device of the target doctor, and/or generate second prompt information and send it to the patient device, the first prompt information includes the target time period and The identification information of the patient corresponding to the patient device, and the second prompt information includes the target time period.
  • the method further includes: in response to the appointment operation, when the number of appointments available for the target doctor in the target time period is less than 1, from the schedule information of the target doctor Determine at least one spare time period, the at least one spare time period is a part of the at least one time period and the number of reservations for each spare time period is not less than 1; use the patient device to perform a prompt operation, the prompt The operation is used to indicate that the at least one backup time slot is reservable.
  • the determining at least one backup time period from the schedule information of the target doctor includes: determining from the schedule information of the target doctor The closest at least one time period is used as the at least one backup time period; or, at least one time period that is the same as the time period type of the target time period is determined from the schedule information of the target doctor as the at least one time period Alternate time period.
  • the present application provides a program-controlled information recording device, which is applied to electronic equipment.
  • the device includes: an information acquisition module, for each patient in at least one patient, to acquire a program-controlled information recording device set outside the patient's body.
  • the program control information of the equipment, the program control equipment includes one or more of in vitro program control instrument, program controller, charger, tablet computer, notebook computer, desktop computer and mobile phone;
  • the record generation module is used to generate the program control information of the patient record, the patient's program-controlled record includes the patient's identification information and program-controlled information;
  • a record storage module configured to store the patient's program-controlled record in a storage device.
  • the patient is any one of the following: patients with Parkinson's disease; patients with depression; patients with addictive diseases; patients with obsessive-compulsive disorder;
  • the apparatus further includes: a first selection module, configured to use the program-controlled device to receive a first selection operation on a target patient, where the target patient is one of the at least one patient An identification acquisition module, configured to acquire identification information of the target patient in response to the first selection operation; a query receiving module, configured to use the program-controlled device to receive a query operation of at least one program-controlled record of the target patient a record query module, configured to use the identification information of the target patient to obtain at least one program-controlled record of the target patient from the storage device in response to the query operation; a record sending module, configured to send the target patient At least one programmed record of the target patient is sent to the programmed device.
  • a first selection module configured to use the program-controlled device to receive a first selection operation on a target patient, where the target patient is one of the at least one patient
  • An identification acquisition module configured to acquire identification information of the target patient in response to the first selection operation
  • a query receiving module configured to use the program-controlled device to receive a query operation of at least
  • the device further includes: an additional acquisition module, configured to acquire additional information of the target patient, where the additional information includes one of historical chief complaint information, historical appointment information, and implant information or more; an additional sending module, configured to send the additional information of the target patient to the program-controlled device.
  • the apparatus further includes: a second selection module, configured to use a patient device to receive a second selection operation on the target doctor; a shift acquisition module, configured to respond to the second selection operation , acquire the schedule information of the target doctor and send it to the patient device, the schedule information includes at least one time period and the number of appointments available for each time period; an appointment receiving module is configured to use the patient device to receive An appointment operation for the target doctor's target time period, the target time period is one of the at least one time period; a quantity update module, configured to respond to the appointment operation, when the target doctor's When the number of reservations available in the target time period is not less than 1, perform an operation of subtracting one from the number of reservations available in the target time period of the target doctor; the reminder sending module is used to generate first reminder information and send it to the doctor of the target doctor device, and/or, generate second prompt information and send it to the patient device, the first prompt information includes the target time period and the identification information of the patient corresponding to the patient device, and the second prompt information
  • the device further includes: a standby determination module, configured to respond to the appointment operation, when the number of appointments available for the target doctor in the target time period is less than 1, from the Determine at least one spare time period in the schedule information of the target doctor, the at least one spare time period is a part of the at least one time period and the number of appointments for each spare time period is not less than 1; the spare prompt module is used for Using the patient device to perform a prompt operation, the prompt operation is used to indicate that the at least one spare time slot can be reserved.
  • a standby determination module configured to respond to the appointment operation, when the number of appointments available for the target doctor in the target time period is less than 1, from the Determine at least one spare time period in the schedule information of the target doctor, the at least one spare time period is a part of the at least one time period and the number of appointments for each spare time period is not less than 1
  • the spare prompt module is used for Using the patient device to perform a prompt operation, the prompt operation is used to indicate that the at least one spare time slot can be reserved
  • the standby determining module includes: a first determining unit, configured to determine at least one time period that is temporally closest to the target time period from the schedule information of the target doctor As the at least one spare time period; or, the second determining unit is configured to determine at least one time period of the same time period type as the target time period from the schedule information of the target doctor as the at least one Alternate time period.
  • the present application provides an electronic device, the electronic device includes a memory and a processor, the memory stores a computer program, and the processor implements the steps of any one of the above methods when executing the computer program.
  • the present application provides a computer-readable storage medium, where the computer-readable storage medium stores a computer program, and when the computer program is executed by a processor, the steps of any one of the above-mentioned methods are implemented.
  • FIG. 1 is a schematic flow diagram of a method for recording program-controlled information provided by an embodiment of the present application
  • Fig. 2 is a partial flow diagram of another program-controlled information recording method provided by the embodiment of the present application.
  • Fig. 3 is a partial flow diagram of another program-controlled information recording method provided by the embodiment of the present application.
  • Fig. 4 is a partial flow diagram of another program-controlled information recording method provided by the embodiment of the present application.
  • Fig. 5 is a partial flow diagram of another program-controlled information recording method provided by the embodiment of the present application.
  • FIG. 6 is a schematic flow chart of determining a backup time period provided by an embodiment of the present application.
  • Fig. 7 is a schematic structural diagram of a program-controlled information recording device provided by an embodiment of the present application.
  • Fig. 8 is a partial structural schematic diagram of another program-controlled information recording device provided by the embodiment of the present application.
  • Fig. 9 is a partial structural schematic diagram of another program-controlled information recording device provided by the embodiment of the present application.
  • Fig. 10 is a partial structural schematic diagram of another program-controlled information recording device provided by the embodiment of the present application.
  • Fig. 11 is a partial structural schematic diagram of another program-controlled information recording device provided by the embodiment of the present application.
  • FIG. 12 is a schematic structural diagram of a standby determination module provided in an embodiment of the present application.
  • FIG. 13 is a schematic structural diagram of an electronic device provided by an embodiment of the present application.
  • FIG. 14 is a schematic structural diagram of a program product for implementing a method for recording program-controlled information provided by an embodiment of the present application.
  • At least one means one or more, and “multiple” means two or more.
  • “And/or” describes the association relationship of associated objects, indicating that there may be three types of relationships, for example, A and/or B, which can mean: A exists alone, A and B exist simultaneously, and B exists alone, where A, B can be singular or plural.
  • the character “/” generally indicates that the contextual objects are an “or” relationship.
  • “At least one of the following” or similar expressions refer to any combination of these items, including any combination of single or plural items.
  • At least one item (piece) of a, b or c can represent: a, b, c, a and b, a and c, b and c or a and b and c, wherein a, b and c can be It can be single or multiple. It should be noted that "at least one item (item)” can also be interpreted as “one item (item) or multiple items (item)”.
  • words such as “exemplary” or “for example” are used to mean an example, illustration or description. Any embodiment or design described herein as “exemplary” or “for example” is not to be construed as preferred or advantageous over other embodiments or designs. Rather, the use of words such as “exemplary” or “such as” is intended to present related concepts in a concrete manner.
  • the implantable neurostimulation system mainly includes a stimulator implanted in the body and a program-controlled device outside the body.
  • the existing neuromodulation technology mainly uses stereotaxic surgery to implant electrodes in specific structures (i.e., targets) in the body, and the stimulator implanted in the patient sends electrical pulses to the targets through the electrodes to regulate the corresponding neural structures and networks. Electrical activity and its function, thereby improving symptoms and relieving pain.
  • the stimulator can be an implantable electrical nerve stimulation device, an implantable cardiac electrical stimulation system (also known as a cardiac pacemaker), an implantable drug infusion device (I mplantable Drug Delivery System, referred to as IDDS) and a wire. Any one of the switching devices.
  • Implantable electrical nerve stimulation devices are, for example, Deep Brain Stimulation (DBS), Implantable Cortical Nerve Stimulation (CNS), Implantable Spinal Cord Stimulation , referred to as SCS), implanted sacral nerve stimulation system (Sacral Nerve Stimulation, referred to as SNS), implanted vagus nerve stimulation system (Vagus Nerve Stimulation, referred to as VNS), etc.
  • DBS Deep Brain Stimulation
  • CNS Implantable Cortical Nerve Stimulation
  • SCS Implantable Spinal Cord Stimulation
  • SNS implanted sacral nerve stimulation system
  • Vagus Nerve Stimulation referred to as VNS
  • the stimulator can include IPG, extension wires and electrode wires.
  • IPG implantable pulse generator, implantable pulse generator
  • IPG is set in the patient's body, and relies on sealed batteries and circuits to provide controllable electrical stimulation energy to biological tissues.
  • the extended lead wire and electrode lead wire inserted can provide one or two controllable specific electric stimulation energy for the specific area of the biological tissue.
  • the extension lead is used in conjunction with the IPG as a transmission medium for the electrical stimulation signal, and transmits the electrical stimulation signal generated by the IPG to the electrode lead.
  • the electrode lead releases the electrical stimulation signal generated by IPG to a specific area of the biological tissue through multiple electrode contacts;
  • the implantable medical device has one or more electrode leads on one or both sides,
  • the electrode wires are provided with a plurality of electrode contacts, and the electrode contacts can be arranged uniformly or non-uniformly in the circumferential direction of the electrode wires.
  • the electrode contacts are arranged in an array of 4 rows and 3 columns (a total of 12 electrode contacts) in the circumferential direction of the electrode wire.
  • Electrode contacts may include stimulation electrode contacts and/or collection electrode contacts.
  • the electrode contacts can be in the shape of, for example, a sheet, a ring, or a dot.
  • the stimulated biological tissue may be the patient's brain tissue, and the stimulated part may be a specific part of the brain tissue.
  • the stimulated site is generally different, the number of stimulation contacts used (single source or multi-source), one or more channels (single-channel or multi-channel) specific electrical stimulation signals
  • the application and stimulus parameter data are also different. This application does not limit the applicable disease types, which may be the applicable disease types for deep brain stimulation (DBS), spinal cord stimulation (SCS), pelvic stimulation, gastric stimulation, peripheral nerve stimulation, and functional electrical stimulation.
  • DBS disorders that DBS can be used to treat or manage include, but are not limited to: spasticity disorders (e.g., epilepsy), pain, migraine, psychiatric disorders (e.g., major depressive disorder (MDD)), bipolar disorder, anxiety disorders, Post-traumatic stress disorder, hypodepression, obsessive-compulsive disorder (OCD), conduct disorder, mood disorder, memory disorder, mental status disorder, mobility disorder (eg, essential tremor or Parkinson's disease), Huntington's disease, Al Alzheimer's disease, drug addiction disorder, autism, or other neurological or psychiatric conditions and impairments.
  • spasticity disorders e.g., epilepsy
  • DMDD major depressive disorder
  • bipolar disorder e.g., anxiety disorders, Post-traumatic stress disorder, hypodepression, obsessive-compulsive disorder (OCD)
  • CCD obsessive-compulsive disorder
  • conduct disorder mood disorder, memory disorder, mental status disorder, mobility disorder (eg, essential tre
  • the stimulator in this application is described by taking the deep brain stimulator (DBS) as an example.
  • DBS deep brain stimulator
  • the program-controlled device and the stimulator establish a program-controlled connection
  • the program-controlled device can be used to adjust the stimulation parameters of the electrical stimulation signal of the stimulator, or the stimulator can sense
  • the bioelectric activity in the deep brain of the patient can be measured, and the stimulation parameters of the electrical stimulation signal of the stimulator can be adjusted continuously through the sensed bioelectric activity.
  • the programmable device can be a physician programmer or a patient programmer.
  • This application does not limit the data interaction between the doctor's programmer and the stimulator.
  • the doctor's programmer can exchange data with the stimulator through the server and the patient's programmer.
  • the doctor program controller can interact with the stimulator through the patient program controller, and the doctor program controller can also directly interact with the stimulator.
  • the patient programmer may include a host (in communication with the server) and a slave (in communication with the stimulator), the host and slave being communicably connected.
  • the doctor program controller can exchange data with the server through the 3G/4G/5G network
  • the server can exchange data with the host through the 3G/4G/5G network
  • the host can exchange data with the slave through the Bluetooth protocol/WIFI protocol/USB protocol.
  • the sub-machine can exchange data with the stimulator through the 401MHz-406MHz working frequency band/2.4GHz-2.48GHz working frequency band
  • the doctor's program controller can directly exchange data with the stimulator through the 401MHz-406MHz working frequency band/2.4GHz-2.48GHz working frequency band interact.
  • FIG. 1 is a schematic flow chart of a method for recording program-controlled information provided by an embodiment of the present application.
  • the embodiment of the present application provides a method for recording program-controlled information, which is applied to electronic devices.
  • the method includes steps S101 to S103.
  • Step S101 For each patient in at least one patient, obtain the program control information of the program control equipment installed outside the patient's body, the program control equipment includes an in vitro program control instrument, a program controller, a charger, a tablet computer, a notebook computer, a desktop computer and one or more of the mobile phones.
  • Program-controlled devices can also include smart wearable devices.
  • the patient may be any one of the following: patients with Parkinson's disease; patients with depression; patients with addictive diseases; patients with obsessive-compulsive disorder;
  • the addictive disease patients include drug addictive disease patients and/or drug addictive disease patients (ie drug addicts).
  • all the program control information of patients with Parkinson's disease, depression, addictive disease, obsessive-compulsive disorder or bipolar disorder can be recorded, especially Parkinson's patients are mostly inconvenient to move, and there is a great demand for remote program control.
  • other diseases that can be treated are within the scope of protection of the embodiments of this application, including patients with mental diseases and other addictive diseases.
  • the program-controlled device is used to receive the doctor's configuration operation on the stimulator parameters, and the program-controlled information may be the identification and parameter value of one or more stimulator parameters corresponding to the configuration operation.
  • the in vitro program control instrument is, for example, the in vitro program control instrument disclosed in patent CN105709336B, or the implantable neural stimulator program control instrument disclosed in patent CN207412517U.
  • the program controller is, for example, a program controller in an implantable nerve electrical pulse stimulation system disclosed in patent CN100469401C, or a doctor program controller with security and confidentiality functions disclosed in patent CN201894778U.
  • the parameters of the stimulator are, for example, frequency (for example, the number of electrical stimulation pulse signals per unit time 1s, in Hz), pulse width (the duration of each pulse, in ⁇ s), and amplitude (generally expressed in voltage, that is, intensity of each pulse in V).
  • frequency for example, the number of electrical stimulation pulse signals per unit time 1s, in Hz
  • pulse width the duration of each pulse, in ⁇ s
  • amplitude generally expressed in voltage, that is, intensity of each pulse in V.
  • various parameters of the stimulator can be adjusted in current mode or voltage mode.
  • the embodiment of the present application does not limit the number of stimulator parameters configured by the doctor in one configuration operation, and the doctor may configure one or more stimulator parameters at one time.
  • the purpose of the embodiment of the present application is to record the program-controlled information obtained by the program-controlled device to facilitate subsequent data query work, and the data interaction between the program-controlled device and the stimulator is not within the protection scope of the embodiment of the present application.
  • the embodiment of the present application does not include the method of using a program-controlled device to control a stimulator for treatment.
  • the program-controlled information recording method in the embodiment of the present application does not include treatment steps, nor is it aimed at treating patients, nor does it contain the nature of treating patients.
  • the purpose of this program-controlled information recording method is only for data recording, which is convenient for subsequent Doctors or hospitals conduct data queries.
  • Step S102 generating the patient's program control record, the patient's program control record including the patient's identification information and program control information.
  • the patient's identification information is generally the patient's name and/or number, and the identification information may include at least one of letters, numbers, Chinese characters, symbols, and special symbols, for example.
  • the identification information of patient Zhang San is, for example, "Zhang San", “Mr. Zhang”, “A123”, “CN0001M” and so on.
  • the stimulator parameter is amplitude
  • the parameter identifier of the amplitude is, for example, FZ
  • the parameter value of the amplitude is, for example, 4V.
  • Step S103 storing the patient's program-controlled records in a storage device.
  • the storage device is, for example, a computer or a server for storing data, and the storage device may also be integrated with the electronic device.
  • the program control information of the program control device is obtained, and then a program control record containing the program control information is generated and stored.
  • the program control uses an external program controller or a tablet computer
  • the remote program control uses a tablet computer, a notebook computer or a desktop computer. Since the program control equipment includes at least one of the external program controller, program controller, tablet computer, notebook computer, desktop computer and mobile
  • the program control equipment includes at least one of the external program controller, program controller, tablet computer, notebook computer, desktop computer and mobile
  • FIG. 2 is a partial flowchart of another method for recording program-controlled information provided by the embodiment of the present application.
  • the method may further include steps S104-S108.
  • Step S104 using the program-controlled device to receive a first selection operation of a target patient, where the target patient is one of the at least one patient.
  • At least one patient includes, for example, Zhang San, Li Si, Wang Wu, and Zhao Liu, and the target patient is, for example, Wang Wu.
  • Step S105 Acquiring identification information of the target patient in response to the first selection operation.
  • the identification information of Wang Wu is, for example, "A003".
  • Step S106 using the program-controlled device to receive an inquiry operation on at least one program-controlled record of the target patient.
  • the at least one programmed record of the target patient may be part or all of all the programmed records of the target patient.
  • Step S107 in response to the query operation, using the identification information of the target patient to query from the storage device to obtain at least one program-controlled record of the target patient.
  • Step S108 Send at least one program-controlled record of the target patient to the program-controlled device.
  • the doctor can select the target patient through the program-controlled device and query at least one program-controlled record of the target patient.
  • the storage device will send the program-controlled record that meets the doctor’s query conditions to the program-controlled device for easy viewing by the doctor. Therefore, the doctor can easily retrieve and view the target patient. All programmed records of patients in hospital and back home.
  • FIG. 3 is a partial flowchart of another method for recording program-controlled information provided by the embodiment of the present application.
  • the method may further include steps S109 to S110 .
  • Step S109 Obtain additional information of the target patient, the additional information includes one or more of historical chief complaint information, historical appointment information, and implantation information.
  • the historical complaint information can be used to indicate the past medical history of the patient
  • the historical appointment information can be used to indicate the number of appointments and/or the appointment time of the patient
  • the implantation information can be used to indicate the patient’s implantation time, implantation device model, implantation time, etc.
  • Step S110 sending the additional information of the target patient to the program-controlled device.
  • the historical chief complaint information can help doctors understand the patient's past medical history
  • the historical appointment information can help doctors understand the number and frequency of patient programming
  • the implantation information can help doctors understand the patient's implantation time, implanted device model and other information.
  • the method may also include:
  • the program-controlled device is used to adjust the parameters of the stimulator implanted in the target patient, so that the stimulator applies corresponding electrical stimulation energy to the target patient.
  • the training process of the parameter configuration model may include: acquiring training data of multiple sample objects, and the training data of each sample object includes additional information, program-controlled records and corresponding parameter configuration information.
  • a deep neural network is used for training to obtain a parameter configuration model.
  • the present application may use the above training process to train the parameter configuration model, and in other implementation manners, the present application may use a pre-trained parameter configuration model.
  • the present application does not limit the training process of the parameter configuration model.
  • the above-mentioned supervised learning training method, semi-supervised learning training method, or unsupervised learning training method may be used.
  • using a deep neural network for training may include:
  • the present application does not limit the preset training end conditions, for example, it can be that the number of training times reaches the preset number of times (the preset number of times is, for example, 1 time, 3 times, 10 times, 100 times, 1000 times, 10000 times, etc.), or it can be It means that all the training data in the training set have completed one or more trainings, or it can be that the total loss value obtained in this training is not greater than the preset loss value.
  • the parameter configuration information is used to determine the parameters of the stimulator, so as to adjust the electrical stimulation applied by the stimulator to the patient.
  • the parameter configuration information may be, for example: frequency 130 Hz, pulse width 60 ⁇ s, and amplitude 2-3 V.
  • using the program-controlled device to adjust the parameters of the stimulator implanted in the target patient may include:
  • an adjustment request is generated and sent to the doctor device, where the adjustment request includes the real-time status type and its corresponding parameter configuration information;
  • the feedback operation is, for example, any one of a confirmation operation, a modification operation, and a cancellation operation
  • the feedback operation is a confirmation operation
  • using the program-controlled device to adjust the parameters of the stimulator based on the parameter configuration information
  • the parameter configuration information is modified in response to the modification operation, and the parameters of the stimulator are adjusted by the program-controlled device based on the modified parameter configuration information.
  • an adjustment request can be generated and sent to the doctor’s device, and the doctor can determine whether to use the parameter configuration information to adjust the parameters of the stimulator.
  • the doctor confirms that the parameter configuration information is appropriate and does not need to be modified, it can be Use the parameter configuration information to adjust the parameters of the stimulator; on the other hand, when the doctor thinks that the parameter configuration information is inappropriate and needs to be modified, the parameter configuration information can be modified, and the stimulator parameters can be adjusted based on the modified parameter configuration information. Without the doctor's confirmation, direct application of electrical stimulation may cause harm to the patient, and may endanger life in severe cases. Therefore, the doctor's feedback operation is very necessary, which can not only protect the patient's life safety, but also allow the doctor to understand the patient's condition changes Condition.
  • FIG. 4 is a partial flowchart of another method for recording program-controlled information provided by the embodiment of the present application.
  • the method may further include steps S111-S115.
  • Step S111 Using the patient device to receive a second selection operation for the target doctor.
  • multiple doctors can be displayed on the patient device, the target doctor is one of the multiple doctors, and the multiple doctors can be displayed in a list or tiled manner.
  • Step S112 In response to the second selection operation, acquire the schedule information of the target doctor and send it to the patient device, the schedule information includes at least one time period and the number of appointments available for each time period. Wherein, each time period refers to each time period in at least one time period.
  • Xiao Liu's schedule information is, for example: "20210701: AM/1, PM/0; 20210702: AM/3, PM/2; 20210703: AM/5, PM/5" .
  • Step S113 Utilize the patient device to receive an appointment operation for the target doctor's target time period, where the target time period is one of the at least one time period.
  • the target time period of the target doctor is, for example, the morning of Xiao Liu, 20210701.
  • Step S114 In response to the appointment operation, when the number of appointments available for the target doctor in the target time period is not less than 1, perform a decrement operation on the number of appointments in the target time period of the target doctor.
  • the number of available appointments for the target doctor Xiao Liu in the morning of 20210701 is 1 and not less than 1, then the operation of reducing the number of appointments for Xiao Liu in the morning of 20210701 is performed, and the updated available number of appointments is 0.
  • Step S115 Generate first prompt information and send it to the doctor device of the target doctor, and/or generate second prompt information and send it to the patient device, the first prompt information includes the target time period and the The identification information of the patient corresponding to the patient device, and the second prompt information includes the target time period.
  • the doctor equipment is, for example, a mobile phone, a tablet computer, a notebook computer, a desktop computer, or a smart wearable device
  • the patient equipment is, for example, a mobile phone, a tablet computer, a notebook computer, a desktop computer, or a smart wearable equipment.
  • the method of sending prompt information is, for example, SMS push, email push, in-app push, phone notification, etc.
  • the prompt information includes the first prompt information and/or the second prompt information
  • the application is, for example, WeChat APP, Alipay APP, applet, etc. .
  • the schedule time can be set by the doctor, and the number of appointments available for patient registration during the schedule time can be opened.
  • the patient makes an appointment in advance with a doctor who has a schedule within a certain period of time for remote program control.
  • the SMS will remind the doctor and the patient that the appointment is successful, and the doctor will use the program-controlled equipment for remote program control on time.
  • FIG. 5 is a partial flowchart of another method for recording program-controlled information provided by the embodiment of the present application.
  • the method may further include steps S116-S117.
  • Step S116 In response to the reservation operation, when the number of available reservations for the target time period of the target doctor is less than 1, determine at least one spare time period from the schedule information of the target doctor, and the at least one The spare time period is a part of the at least one time period, and the number of reservations for each spare time period is not less than 1.
  • the target doctor’s target time period is, for example, Xiao Liu, 20210701, afternoon, and the number of appointments available for the target doctor Xiao Liu in the afternoon of 20210701 is 0, which is less than 1.
  • Step S117 using the patient device to perform a prompt operation, the prompt operation is used to indicate that the at least one backup time slot can be reserved.
  • text information can be displayed on the patient's device: "Doctor Xiao Liu 20210701 can make an appointment in the morning", or the voice can be played through voice playback: "Doctor Xiao Liu 20210701 can make an appointment in the morning", which is not limited in this embodiment of the present application.
  • the patient When the target doctor’s target time period cannot be reserved, the patient will be automatically pushed to the patient with an alternate time period that can be reserved by the same doctor, which is convenient for patients to choose an appropriate time period to make an appointment. Patients can choose any spare time slot and use the patient device to make an appointment with the target doctor.
  • An online appointment function is provided so that patients can select the target doctor and target time period for program control in advance to solve the problem. It solves the problem that the patient obtains the program control in time; in addition, the first prompt information and the second prompt information are generated and sent to the doctor and the patient respectively, so that both the doctor and the patient can know the success of the appointment in time.
  • Fig. 6 is a schematic flow chart of determining a backup time period provided by an embodiment of the present application.
  • at least one backup time is determined from the schedule information of the target doctor
  • the steps of the segment include step S201 or S202.
  • Step S201 Determine at least one time period closest to the target time period in time from the schedule information of the target doctor as the at least one backup time period.
  • At least one time period closest in time to the target time period may include the afternoon of 20210701 and the afternoon of 20210702.
  • Step S202 Determine at least one time period of the same time period type as the target time period as the at least one spare time period from the schedule information of the target doctor.
  • the time period type may include morning and afternoon.
  • at least one spare time period refers to at least one morning time period; at least one spare time period refers to at least one afternoon time period.
  • the closest time period in time is used as the backup time period, and the patient's planned schedule does not need to be greatly changed; the time period with the same type of time period is used as the backup time period, for example, the patient originally wanted to make an appointment For the morning time slot, the automatically recommended time slot is still the morning time slot, which is more in line with the patient's appointment preference.
  • the method may further include: sending the patient's programming information to a patient device of the patient. In this way, the patient can be notified of the parameter information of this program control, so that the patient can understand the situation of his own program control each time.
  • the method may further include: using the program-controlled device to receive medical order information, and sending the medical order information to a patient device of the patient. In this way, the doctor's order information can be notified to the patient, reminding the patient of matters that need attention.
  • the method may further include: using the patient device to receive evaluation information, and sending the evaluation information to a preset device.
  • the preset device may include, for example, a management device of a manager and/or a doctor device of a doctor.
  • Fig. 7 is a schematic structural diagram of a program-controlled information recording device provided by the embodiment of the present application.
  • the embodiment of the present application also provides a program-controlled information recording device, and its specific implementation method is the same as that of the above-mentioned embodiment of the program-controlled information recording method
  • the implementation mode and the achieved technical effect recorded in the document are consistent, and part of the content will not be repeated.
  • the program-controlled information recording device is applied to electronic equipment, and the device includes: an information acquisition module 101, for each patient in at least one patient, to obtain the program-controlled information of the program-controlled equipment installed outside the patient's body, the program-controlled
  • the equipment includes one or more of an in vitro program controller, a program controller, a charger, a tablet computer, a notebook computer, a desktop computer and a mobile phone;
  • a record generation module 102 is used to generate a program control record of the patient, and the program control record of the patient
  • the record includes the patient's identification information and program control information;
  • the record storage module 103 is configured to store the patient's program control record in a storage device.
  • the patient may be any one of the following: patients with Parkinson's disease; patients with depression; patients with addictive diseases; patients with obsessive-compulsive disorder; patients with bipolar disorder.
  • FIG. 8 is a partial structural schematic diagram of another program-controlled information recording device provided by an embodiment of the present application.
  • the device may further include: a first selection module 104 for using the The program-controlled device receives a first selection operation of a target patient, and the target patient is one of the at least one patient; the identification acquisition module 105 is configured to acquire identification information of the target patient in response to the first selection operation ;
  • the query receiving module 106 is used to receive the query operation of at least one program-controlled record of the target patient by using the program-controlled device;
  • the record query module 107 is used to respond to the query operation and use the identification information of the target patient Querying from the storage device to obtain at least one program-controlled record of the target patient;
  • the record sending module 108 is configured to send at least one program-controlled record of the target patient to the program-controlled device.
  • FIG. 9 is a partial structural schematic diagram of another program-controlled information recording device provided by the embodiment of the present application.
  • the device may further include: an additional acquisition module 109, configured to acquire the target Additional information of the patient, the additional information includes one or more of historical chief complaint information, historical appointment information and implantation information; an additional sending module 110, configured to send the additional information of the target patient to the program-controlled device .
  • FIG. 10 is a partial structural schematic diagram of another program-controlled information recording device provided by the embodiment of the present application.
  • the device may further include: a second selection module 111 for using patient equipment Receiving a second selection operation on the target doctor; the scheduling acquisition module 112 is configured to acquire the scheduling information of the target doctor and send it to the patient device in response to the second selection operation, the scheduling information includes At least one time period and the number of appointments available for each time period; an appointment receiving module 113, configured to use the patient device to receive an appointment operation for the target doctor's target time period, the target time period is the at least one One of the time periods; the quantity update module 114, configured to respond to the reservation operation, when the number of available appointments for the target time period of the target doctor is not less than 1, the target doctor's target time period The number of appointments can be reduced by one; the reminder sending module 115 is configured to generate first reminder information and send it to the doctor device of the target doctor, and/or generate second reminder information and send it to the patient
  • Fig. 11 is a partial structural schematic diagram of another program-controlled information recording device provided by the embodiment of the present application.
  • the device may further include: a spare determination module 116, configured to respond to the Reservation operation, when the number of available reservations for the target time period of the target doctor is less than 1, at least one spare time period is determined from the schedule information of the target doctor, and the at least one spare time period is the at least one A part of a time period and the number of appointments that can be reserved for each spare time period is not less than 1; the standby prompt module 117 is used to use the patient device to perform a prompt operation, and the prompt operation is used to indicate that the at least one spare time period can be reserve.
  • a spare determination module 116 configured to respond to the Reservation operation, when the number of available reservations for the target time period of the target doctor is less than 1, at least one spare time period is determined from the schedule information of the target doctor, and the at least one spare time period is the at least one A part of a time period and the number of appointments that can be reserved for each spare
  • FIG. 12 is a schematic structural diagram of a backup determination module provided by an embodiment of the present application.
  • the backup determination module 116 may include: a first determination unit 201 configured to Determining at least one time period closest to the target time period in the doctor's scheduling information as the at least one spare time period; At least one time period of the same time period type as the target time period is determined in the information as the at least one spare time period.
  • FIG. 13 is a schematic structural diagram of an electronic device provided by an embodiment of the present application.
  • the embodiment of the present application also provides an electronic device 200 .
  • the electronic device 200 includes at least one memory 210 , at least one processor 220 and a connection Bus 230 for different platform systems.
  • the electronic device 200 can be integrated with the program-controlled device.
  • the program-controlled device is, for example, a doctor's tablet computer, laptop computer, desktop computer, and the like.
  • Memory 210 may include readable media in the form of volatile memory, such as random access memory (RAM) 211 and/or cache memory 212 , and may further include read only memory (ROM) 213 .
  • RAM random access memory
  • ROM read only memory
  • the memory 210 also stores a computer program, and the computer program can be executed by the processor 220, so that the processor 220 executes the steps of the program-controlled information recording method in the embodiment of the present application.
  • the recorded implementation modes and achieved technical effects are consistent, and some of the contents will not be repeated.
  • Memory 210 may also include utility 214 having at least one program module 215 including, but not limited to, an operating system, one or more application programs, other program modules, and program data, examples of each or Implementations of network environments may be included in some combination.
  • program module 215 including, but not limited to, an operating system, one or more application programs, other program modules, and program data, examples of each or Implementations of network environments may be included in some combination.
  • the processor 220 can execute the above-mentioned computer program, and can execute the utility tool 214 .
  • Bus 230 may be representative of one or more of several types of bus structures, including a memory bus or memory controller, a peripheral bus, an accelerated graphics port, a processor, or a local bus using any of a variety of bus structures.
  • the electronic device 200 can also communicate with one or more external devices 240 such as keyboards, pointing devices, Bluetooth devices, etc., and can also communicate with one or more devices capable of interacting with the electronic device 200, and/or communicate with the electronic device 200 200 is capable of communicating with any device (eg, router, modem, etc.) that communicates with one or more other computing devices. Such communication may occur through input-output interface 250 .
  • the electronic device 200 can also communicate with one or more networks (such as a local area network (LAN), a wide area network (WAN) and/or a public network such as the Internet) through the network adapter 260 .
  • the network adapter 260 can communicate with other modules of the electronic device 200 through the bus 230 . It should be appreciated that although not shown, other hardware and/or software modules may be used in conjunction with electronic device 200, including but not limited to: microcode, device drivers, redundant processors, external disk drive arrays, RAID systems, tape drives And data backup storage platform, etc.
  • the embodiment of the present application also provides a computer-readable storage medium, which is used to store a computer program.
  • a computer program When the computer program is executed, the steps of the program-controlled information recording method in the embodiment of the present application are implemented.
  • the specific implementation The method is consistent with the implementation mode and the achieved technical effect described in the above-mentioned embodiment of the program-controlled information recording method, and part of the content will not be repeated.
  • Fig. 14 shows a program product 300 provided by this embodiment for realizing the above-mentioned program-controlled information recording method, which can adopt a portable compact disk read-only memory (CD-ROM) and include program codes, and can be used in terminal equipment, such as personal run on the computer.
  • the program product 300 of the present invention is not limited thereto.
  • a readable storage medium may be any tangible medium containing or storing a program, and the program may be used by or in combination with an instruction execution system, device or device.
  • Program product 300 may utilize any combination of one or more readable media.
  • the readable medium may be a readable signal medium or a readable storage medium.
  • the readable storage medium may be, for example, but not limited to, an electrical, magnetic, optical, electromagnetic, infrared, or semiconductor system, device, or device, or any combination thereof. More specific examples (non-exhaustive list) of readable storage media include: electrical connection with one or more conductors, portable disk, hard disk, random access memory (RAM), read only memory (ROM), erasable programmable read-only memory (EPROM or flash memory), optical fiber, portable compact disk read-only memory (CD-ROM), optical storage devices, magnetic storage devices, or any suitable combination of the foregoing.
  • RAM random access memory
  • ROM read only memory
  • EPROM or flash memory erasable programmable read-only memory
  • CD-ROM compact disk read-only memory
  • optical storage devices magnetic storage devices, or any suitable combination of the foregoing.
  • a computer readable storage medium may include a data signal carrying readable program code in baseband or as part of a carrier wave traveling as part of a data signal. Such propagated data signals may take many forms, including but not limited to electromagnetic signals, optical signals, or any suitable combination of the foregoing.
  • a readable storage medium may also be any readable medium that can transmit, propagate, or transport a program for use by or in connection with an instruction execution system, apparatus, or device.
  • the program code contained on the readable storage medium can be transmitted by any appropriate medium, including but not limited to wireless, cable, optical cable, RF, etc., or any suitable combination of the above.
  • the program codes for performing the operations of the present invention can be written in any combination of one or more programming languages, and the programming languages include object-oriented programming languages such as Java, C++, etc., and also include conventional procedural programming languages A programming language such as C or similar.
  • the program code may execute entirely on the user's computing device, partly on the user's device, as a stand-alone software package, partly on the user's computing device and partly on a remote computing device, or entirely on the remote computing device or server to execute.
  • the remote computing device may be connected to the user computing device through any kind of network, including a local area network (LAN) or a wide area network (WAN), or may be connected to an external computing device (e.g., using an Internet service provider). business to connect via the Internet).
  • LAN local area network
  • WAN wide area network
  • Internet service provider e.g., a wide area network

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Abstract

本申请提供了一种程控信息记录方法及相关装置，所述程控信息记录装置包括：信息获取模块，用于针对至少一个患者中的每个患者，获取设置于所述患者体外的程控设备的程控信息，所述程控设备包括体外程控仪、程控器、充电器、平板电脑、笔记本电脑、台式机和手机中的一种或多种；记录生成模块，用于生成所述患者的程控记录，所述患者的程控记录包括所述患者的标识信息和程控信息；记录存储模块，用于将所述患者的程控记录存储至存储设备。不管医生在医院程控或者远程程控时使用何种程控设备，都能够将对应的程控记录存储下来，后续医生再对患者进行程控时，可以调取并查看该患者在医院和回家后的所有程控记录。

Description

程控信息记录方法及相关装置
本申请要求于2021年7月20日提交的申请号为202110819125.7的中国专利的优先权，上述中国专利通过全文引用的形式并入。
技术领域
本申请涉及数据处理技术领域，尤其涉及程控信息记录方法、装置、电子设备及计算机可读存储介质。
背景技术
植入式神经刺激系统主要包括植入体内的刺激器、电极以及体外的程控器。现有的神经调控技术主要是通过立体定向手术在体内特定结构(即靶点)植入电极，并由植入患者体内的刺激器经电极向靶点发放电脉冲，调控相应神经结构和网络的电活动及其功能，从而改善症状、缓解病痛。
当前，医院通常无法记录患者程控的全部信息，具体来说，现有的程控记录方式仅记录了远程程控的信息，并不包含患者在医院进行程控的信息。而对医生而言，在对患者进行程控时，会希望了解到该患者的所有程控记录。
发明内容
本申请的目的在于提供一种程控信息记录方法、装置、电子设备及计算机可读存储介质，能够记录患者远程程控和在医院程控的所有程控信息。
第一方面，本申请提供了一种程控信息记录方法，应用于电子设备，所述方法包括：针对至少一个患者中的每个患者，获取设置于所述患者体外的程控设备的程控信息，所述程控设备包括体外程控仪、程控器、充电器、平板电脑、笔记本电脑、台式机和手机中的一种或多种；生成所述患者的程控记录，所述患者的程控记录包括所述患者的标识信息和程控信息；将所述患者的程控记录存储至存储设备。
在一种可能的实现方式中，所述患者是以下任意一种：帕金森病患者；抑郁症患者；成瘾性疾病患者；强迫症患者；躁郁症患者。
在一种可能的实现方式中，所述方法还包括：利用所述程控设备接收对目标患者的第一选择操作，所述目标患者是所述至少一个患者的其中一个；响应于所述第一选择操作，获取所述目标患者的标识信息；利用所述程控设备接收对所述目标患者的至少一个程控记录的查询操作；响应于所述查询操作，利用所述目标患者的标识信息，从所述存储设备中查询得到所述目标患者的至少一个程控记录；将所述目标患者的至少一个程控记录发送至所述程控设备。
在一种可能的实现方式中，所述方法还包括：获取所述目标患者的附加信息，所述附加信息包括历史主诉信息、历史预约信息和植入信息中的一种或多种；将所述目标患者的附加信息发送至所述程控设备。
在一种可能的实现方式中，所述方法还包括：利用患者设备接收对目标医生的第二选择操作；响应于所述第二选择操作，获取所述目标医生的排班信息并发送至所述患者设备，所述排班信息包括至少一个时间段和每个时间段的可预约数量；利用所述患者设备接收对所述目标医生的目标时间段的预约操作，所述目标时间段是所述至少一个时间段的其中一个；响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量不小于1时，对所述目标医生的目标时间段的可预约数量执行减一操作；生成第一提示信息并发送至所述目标医生的医生设备，和/或，生成第二提示信息并发送至所述患者设备，所述第一提示信息包括所述目标时间段和所述患者设备对应的患者的标识信息，所述第二提示信息包括所述目标时间段。
在一种可能的实现方式中，所述方法还包括：响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量小于1时，从所述目标医生的排班信息中确定至少一个备用时间段，所述至少一个备用时间段是所述至少一个时间段的一部分且每个备用时间段的可预约数量不小于1；利用所述患者设备执行提示操作，所述提示操作用于指示所述至少一个备用时间段可预约。
在一种可能的实现方式中，所述从所述目标医生的排班信息中确定至少一个备用时间段，包括：从所述目标医生的排班信息中确定与所述目标时间段在时间上最接近的至少一个时间段作为所述至少一个备用时间段；或者，从所述目标医生的排班信息中确定与所述目标时间段的时间段类型相同的至少一个时间段作 为所述至少一个备用时间段。
第二方面，本申请提供了一种程控信息记录装置，应用于电子设备，所述装置包括：信息获取模块，用于针对至少一个患者中的每个患者，获取设置于所述患者体外的程控设备的程控信息，所述程控设备包括体外程控仪、程控器、充电器、平板电脑、笔记本电脑、台式机和手机中的一种或多种；记录生成模块，用于生成所述患者的程控记录，所述患者的程控记录包括所述患者的标识信息和程控信息；记录存储模块，用于将所述患者的程控记录存储至存储设备。
在一种可能的实现方式中，所述患者是以下任意一种：帕金森病患者；抑郁症患者；成瘾性疾病患者；强迫症患者；躁郁症患者。
在一种可能的实现方式中，所述装置还包括：第一选择模块，用于利用所述程控设备接收对目标患者的第一选择操作，所述目标患者是所述至少一个患者的其中一个；标识获取模块，用于响应于所述第一选择操作，获取所述目标患者的标识信息；查询接收模块，用于利用所述程控设备接收对所述目标患者的至少一个程控记录的查询操作；记录查询模块，用于响应于所述查询操作，利用所述目标患者的标识信息，从所述存储设备中查询得到所述目标患者的至少一个程控记录；记录发送模块，用于将所述目标患者的至少一个程控记录发送至所述程控设备。
在一种可能的实现方式中，所述装置还包括：附加获取模块，用于获取所述目标患者的附加信息，所述附加信息包括历史主诉信息、历史预约信息和植入信息中的一种或多种；附加发送模块，用于将所述目标患者的附加信息发送至所述程控设备。
在一种可能的实现方式中，所述装置还包括：第二选择模块，用于利用患者设备接收对目标医生的第二选择操作；排班获取模块，用于响应于所述第二选择操作，获取所述目标医生的排班信息并发送至所述患者设备，所述排班信息包括至少一个时间段和每个时间段的可预约数量；预约接收模块，用于利用所述患者设备接收对所述目标医生的目标时间段的预约操作，所述目标时间段是所述至少一个时间段的其中一个；数量更新模块，用于响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量不小于1时，对所述目标医生的目标时间段 的可预约数量执行减一操作；提示发送模块，用于生成第一提示信息并发送至所述目标医生的医生设备，和/或，生成第二提示信息并发送至所述患者设备，所述第一提示信息包括所述目标时间段和所述患者设备对应的患者的标识信息，所述第二提示信息包括所述目标时间段。
在一种可能的实现方式中，所述装置还包括：备用确定模块，用于响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量小于1时，从所述目标医生的排班信息中确定至少一个备用时间段，所述至少一个备用时间段是所述至少一个时间段的一部分且每个备用时间段的可预约数量不小于1；备用提示模块，用于利用所述患者设备执行提示操作，所述提示操作用于指示所述至少一个备用时间段可预约。
在一种可能的实现方式中，所述备用确定模块包括：第一确定单元，用于从所述目标医生的排班信息中确定与所述目标时间段在时间上最接近的至少一个时间段作为所述至少一个备用时间段；或者，第二确定单元，用于从所述目标医生的排班信息中确定与所述目标时间段的时间段类型相同的至少一个时间段作为所述至少一个备用时间段。
第三方面，本申请提供了一种电子设备，所述电子设备包括存储器和处理器，所述存储器存储有计算机程序，所述处理器执行所述计算机程序时实现上述任一项方法的步骤。
第四方面，本申请提供了一种计算机可读存储介质，所述计算机可读存储介质存储有计算机程序，所述计算机程序被处理器执行时实现上述任一项方法的步骤。
采用本申请提供的程控信息记录方法、装置、电子设备及计算机可读存储介质，至少具有以下优点：
对于需要记录远程程控和在医院程控的程控信息的患者，针对其中每个患者，获取程控设备的程控信息，之后，生成包含程控信息的程控记录并存储，一般而言，医生在医院进行程控使用的是体外程控仪或者平板电脑，远程程控使用的是平板电脑、笔记本电脑或者台式机，由于程控设备包括体外程控仪、程控器、平板电脑、笔记本电脑、台式机和手机中的至少一种，因此，不管医生在医院程控 或者远程程控时使用何种程控设备，都能够将对应的程控记录存储下来，后续医生再对患者进行程控时，可以调取并查看该患者在医院和回家后的所有程控记录。
附图说明
下面结合附图和实施例对本申请进一步说明。
图1是本申请实施例提供的一种程控信息记录方法的流程示意图；
图2是本申请实施例提供的另一种程控信息记录方法的部分流程示意图；
图3是本申请实施例提供的又一种程控信息记录方法的部分流程示意图；
图4是本申请实施例提供的又一种程控信息记录方法的部分流程示意图；
图5是本申请实施例提供的又一种程控信息记录方法的部分流程示意图；
图6是本申请实施例提供的一种确定备用时间段的流程示意图；
图7是本申请实施例提供的一种程控信息记录装置的结构示意图；
图8是本申请实施例提供的另一种程控信息记录装置的部分结构示意图；
图9是本申请实施例提供的又一种程控信息记录装置的部分结构示意图；
图10是本申请实施例提供的又一种程控信息记录装置的部分结构示意图；
图11是本申请实施例提供的又一种程控信息记录装置的部分结构示意图；
图12是本申请实施例提供的一种备用确定模块的结构示意图；
图13是本申请实施例提供的一种电子设备的结构示意图；
图14是本申请实施例提供的一种用于实现程控信息记录方法的程序产品的结构示意图。
具体实施方式
下面，结合附图以及具体实施方式，对本申请做进一步描述。
在本申请中，“至少一个”是指一个或者多个，“多个”是指两个或两个以上。“和/或”，描述关联对象的关联关系，表示可以存在三种关系，例如，A和/或B，可以表示：单独存在A，同时存在A和B，单独存在B的情况，其中A，B可以是单数或者复数。字符“/”一般表示前后关联对象是一种“或”的关系。“以下至少一项(个)”或其类似表达，是指的这些项中的任意组合，包括单项(个)或复数项(个)的任意组合。例如，a，b或c中的至少一项(个)，可以表示：a，b，c，a和 b，a和c，b和c或a和b和c，其中a、b和c可以是单个，也可以是多个。值得注意的是，“至少一项(个)”还可以解释成“一项(个)或多项(个)”。
需要说明的是，在不相冲突的前提下，以下描述的各实施例之间或各技术特征之间可以任意组合形成新的实施例。
本申请中，“示例性的”或者“例如”等词用于表示作例子、例证或说明。本申请中被描述为“示例性的”或者“例如”的任何实施例或设计方案不应被解释为比其他实施例或设计方案更优选或更具优势。确切而言，使用“示例性的”或者“例如”等词旨在以具体方式呈现相关概念。
首先对本申请的应用领域进行简单说明。
植入式神经刺激系统主要包括植入体内的刺激器以及体外的程控设备。现有的神经调控技术主要是通过立体定向手术在体内特定结构(即靶点)植入电极，并由植入患者体内的刺激器经电极向靶点发放电脉冲，调控相应神经结构和网络的电活动及其功能，从而改善症状、缓解病痛。其中，刺激器可以是植入式神经电刺激装置、植入式心脏电刺激系统(又称心脏起搏器)、植入式药物输注装置(I mplantable Drug Delivery System，简称I DDS)和导线转接装置中的任意一种。植入式神经电刺激装置例如是脑深部电刺激系统(Deep Brain Stimulation，简称DBS)、植入式脑皮层刺激系统(Cortical Nerve Stimulation，简称CNS)、植入式脊髓电刺激系统(Spinal Cord Stimulation，简称SCS)、植入式骶神经电刺激系统(Sacral Nerve Stimulation，简称SNS)、植入式迷走神经电刺激系统(Vagus Nerve Stimulation，简称VNS)等。
刺激器可以包括IPG、延伸导线和电极导线，IPG(implantable pulse gener ator，植入式脉冲发生器)设置于患者体内，依靠密封电池和电路向生物体组织提供可控制的电刺激能量，通过植入的延伸导线和电极导线，为生物体组织的特定区域提供一路或两路可控制的特定电刺激能量。延伸导线配合IPG使用，作为电刺激信号的传递媒体，将IPG产生的电刺激信号，传递给电极导线。电极导线将IPG产生的电刺激信号，通过多个电极触点，向生物体组织的特定区域释放电刺激能量；所述植入式医疗设备具有单侧或双侧的一路或多路电极导线，所述电 极导线上设置有多个电极触点，所述电极触点可以均匀排列或者非均匀排列在电极导线的周向上。作为一个示例，所述电极触点以4行3列的阵列(共计12个电极触点)排列在电极导线的周向上。电极触点可以包括刺激电极触点和/或采集电极触点。电极触点例如可以采用片状、环状、点状等形状。
在一些可能的实现方式中，受刺激的生物体组织可以是患者的脑组织，受刺激的部位可以是脑组织的特定部位。当患者的疾病类型不同时，受刺激的部位一般来说是不同的，所使用的刺激触点(单源或多源)的数量、一路或多路(单通道或多通道)特定电刺激信号的运用以及刺激参数数据也是不同的。本申请对适用的疾病类型不做限定，其可以是脑深部刺激(DBS)、脊髓刺激(SCS)、骨盆刺激、胃刺激、外周神经刺激、功能性电刺激所适用的疾病类型。其中，DBS可以用于治疗或管理的疾病类型包括但不限于：痉挛疾病(例如，癫痫)、疼痛、偏头痛、精神疾病(例如，重度抑郁症(MDD))、躁郁症、焦虑症、创伤后压力心理障碍症、轻郁症、强迫症(OCD)、行为障碍、情绪障碍、记忆障碍、心理状态障碍、移动障碍(例如，特发性震颤或帕金森氏病)、亨廷顿病、阿尔茨海默症、药物成瘾症、自闭症或其他神经学或精神科疾病和损害。当DBS用于治疗药物成瘾症患者时，可以帮助吸毒人员戒毒，提升他们的幸福感和生命质量。
本申请中的刺激器以脑深部刺激器(DBS)为例进行阐述，程控设备和刺激器建立程控连接时，可以利用程控设备调整刺激器的电刺激信号的刺激参数，也可以通过刺激器感测患者脑深部的生物电活动，并可以通过所感测到的生物电活动来继续调节刺激器的电刺激信号的刺激参数。
程控设备可以是医生程控器或者患者程控器。
本申请对医生程控器和刺激器的数据交互不进行限制，当医生远程程控时，医生程控器可以通过服务器、患者程控器与刺激器进行数据交互。当医生线下和患者面对面进行程控时，医生程控器可以通过患者程控器与刺激器进行数据交互，医生程控器还可以直接与刺激器进行数据交互。
患者程控器可以包括(与服务器通信的)主机和(与刺激器通信的)子机，主机和子机可通信的连接。其中，医生程控器可以通过3G/4G/5G网络与服务器进行数据交互，服务器可以通过3G/4G/5G网络与主机进行数据交互，主机可以 通过蓝牙协议/WIFI协议/USB协议与子机进行数据交互，子机可以通过401MHz-406MHz工作频段/2.4GHz-2.48GHz工作频段与刺激器进行数据交互，医生程控器可以通过401MHz-406MHz工作频段/2.4GHz-2.48GHz工作频段与刺激器直接进行数据交互。
参见图1，图1是本申请实施例提供的一种程控信息记录方法的流程示意图，本申请实施例提供了一种程控信息记录方法，应用于电子设备，所述方法包括步骤S101～S103。
步骤S101：针对至少一个患者中的每个患者，获取设置于所述患者体外的程控设备的程控信息，所述程控设备包括体外程控仪、程控器、充电器、平板电脑、笔记本电脑、台式机和手机中的一种或多种。程控设备还可以包括智能穿戴设备。
其中，所述患者可以是以下任意一种：帕金森病患者；抑郁症患者；成瘾性疾病患者；强迫症患者；躁郁症患者。其中，成瘾性疾病患者包括药物成瘾性疾病患者和/或毒品成瘾性疾病患者(即戒毒人员)。由此，可以记录帕金森病患者、抑郁症患者、成瘾性疾病患者、强迫症患者或者躁郁症患者的所有程控信息，特别是帕金森患者大多行动不便，远程程控的需求很大。需要注意的是，除了上述列举的病症之外，其他所能治疗的病症均在本申请实施例的保护范围内，包括精神类疾病和其他成瘾性疾病患者。
本申请实施例中，程控设备用于接收医生对刺激器参数的配置操作，程控信息可以是配置操作对应的一个或多个刺激器参数的标识和参数值。体外程控仪例如是专利CN105709336B公开的体外程控仪，或者是专利CN207412517U公开的植入式神经刺激器程控仪。程控器例如是专利CN100469401C公开的一种植入式神经电脉冲刺激系统中的程控器，或者是专利CN201894778U公开的具有安全保密功能的医生程控器。
刺激器参数例如是频率(例如是单位时间1s内的电刺激脉冲信号个数，单位为Hz)、脉宽(每个脉冲的持续时间，单位为μs)和幅值(一般用电压表述，即每个脉冲的强度，单位为V)。在具体应用中，可以在电流模式或者电压模式 下对刺激器的各参数进行调节。
本申请实施例对医生一次配置操作所配置的刺激器参数的数量不做限定，医生可以一次性配置一个或多个刺激器参数。
本申请实施例的目的是对程控设备得到的程控信息进行记录，便于后续的数据查询工作，程控设备与刺激器之间的数据交互不在本申请实施例的保护范围之内。
显然，本申请实施例不包含利用程控设备控制刺激器进行治疗的方法。换句话说，本申请实施例中的程控信息记录方法既不包含治疗步骤，也不以治疗患者为目的，也不含治疗患者的性质，该程控信息记录方法的目的只是进行数据记录，便于后续医生或者医院进行数据查询。
步骤S102：生成所述患者的程控记录，所述患者的程控记录包括所述患者的标识信息和程控信息。
其中，患者的标识信息一般是患者的姓名和/或编号，标识信息例如可以包括字母、数字、中文、符号、特殊符号中的至少一种。在一实施方式中，患者张三的标识信息例如是“张三”、“张先生”、“A123”、“CN0001M”等。
在一实施方式中，刺激器参数是幅值，幅值的参数标识例如是FZ，幅值的参数值例如是4V。
步骤S103：将所述患者的程控记录存储至存储设备。
其中，存储设备例如是用于存储数据的计算机或者服务器，存储设备也可以和电子设备集成为一体。
由此，对于需要记录远程程控和在医院程控的程控信息的患者，针对其中每个患者，获取程控设备的程控信息，之后，生成包含程控信息的程控记录并存储，一般而言，医生在医院进行程控使用的是体外程控仪或者平板电脑，远程程控使用的是平板电脑、笔记本电脑或者台式机，由于程控设备包括体外程控仪、程控器、平板电脑、笔记本电脑、台式机和手机中的至少一种，因此，不管医生在医院程控或者远程程控时使用何种程控设备，都能够将对应的程控记录存储下来，后续医生再对患者进行程控时，可以调取并查看该患者在医院和回家后的所有程控记录。
参见图2，图2是本申请实施例提供的另一种程控信息记录方法的部分流程示意图，在一些可能的方式中，所述方法还可以包括步骤S104～S108。
步骤S104：利用所述程控设备接收对目标患者的第一选择操作，所述目标患者是所述至少一个患者的其中一个。至少一个患者例如包括张三、李四、王五、赵六，目标患者例如是王五。
步骤S105：响应于所述第一选择操作，获取所述目标患者的标识信息。王五的标识信息例如是“A003”。
步骤S106：利用所述程控设备接收对所述目标患者的至少一个程控记录的查询操作。目标患者的至少一个程控记录可以是目标患者的所有程控记录的部分或者全部。
步骤S107：响应于所述查询操作，利用所述目标患者的标识信息，从所述存储设备中查询得到所述目标患者的至少一个程控记录。
步骤S108：将所述目标患者的至少一个程控记录发送至所述程控设备。
医生可以通过程控设备选择目标患者，并查询目标患者的至少一个程控记录，存储设备将符合医生查询条件的程控记录发送至程控设备，便于医生查看，由此，医生可以方便地调取并查看目标患者在医院和回家后的所有程控记录。
参见图3，图3是本申请实施例提供的又一种程控信息记录方法的部分流程示意图，在一些可能的方式中，所述方法还可以包括步骤S109～S110。
步骤S109：获取所述目标患者的附加信息，所述附加信息包括历史主诉信息、历史预约信息和植入信息中的一种或多种。
其中，历史主诉信息可以用于指示患者的过往病史，历史预约信息可以用于指示患者的预约次数和/或预约时间，植入信息可以用于指示患者的植入时间、植入设备型号、植入医院和植入医生中的一种或多种。
步骤S110：将所述目标患者的附加信息发送至所述程控设备。
由此，历史主诉信息可以帮助医生了解患者过往病史，历史预约信息可以帮助医生了解患者程控次数和频率，植入信息可以帮助医生了解患者植入时间、植 入设备型号等信息。
在一些可能的方式中，所述方法还可以包括：
将所述目标患者的附加信息以及至少一个程控记录输入参数配置模型，得到所述目标患者对应的参数配置信息；
基于所述参数配置信息，利用所述程控设备调整植入所述目标患者体内的刺激器的参数，以使所述刺激器对所述目标患者施加对应的电刺激能量。
参数配置模型的训练过程可以包括：获取多个样本对象的训练数据，每个样本对象的训练数据包括附加信息、程控记录以及对应的参数配置信息。
根据所述多个样本对象的训练数据，利用深度神经网络进行训练，得到参数配置模型。
在一些实施方式中，本申请可以采用上述训练过程训练得到参数配置模型，在另一些实施方式中，本申请可以采用预先训练好的参数配置模型。
本申请对参数配置模型的训练过程不作限定，其例如可以采用上述监督学习的训练方式，或者可以采用半监督学习的训练方式，或者可以采用无监督学习的训练方式。
所述根据所述多个样本对象的训练数据，利用深度神经网络进行训练可以包括：
检测是否满足预设的训练结束条件，如果是，则停止训练，并将训练得到的所述深度神经网络作为所述参数配置模型，如果否，则利用下一个样本对象的训练数据训练所述深度神经网络。
本申请对预设的训练结束条件不作限定，其例如可以是训练次数达到预设次数(预设次数例如是1次、3次、10次、100次、1000次、10000次等)，或者可以是训练集中的训练数据都完成一次或多次训练，或者可以是本次训练得到的总损失值不大于预设损失值。
参数配置信息用于确定刺激器的参数，从而调整刺激器对患者施加的电刺激。
参数配置信息例如可以是：频率130Hz、脉宽60μs和幅值2-3V。
其中，所述基于所述参数配置信息，利用所述程控设备调整植入所述目标患者体内的刺激器的参数，可以包括：
基于所述参数配置信息，生成调整请求并发送至所述医生设备，所述调整请求包括所述实时状态类型及其对应的参数配置信息；
接收所述医生设备的反馈操作，其中，反馈操作例如是确认操作、修改操作、取消操作中的任意一种；
当所述反馈操作是确认操作时，响应于所述确认操作，基于所述参数配置信息，利用所述程控设备调整所述刺激器的参数；
当所述反馈操作是修改操作时，响应于所述修改操作，修改所述参数配置信息，基于修改后的参数配置信息，利用所述程控设备调整所述刺激器的参数。
由此，可以基于参数配置信息，生成调整请求并发送至医生设备，由医生确定是否采用该参数配置信息调整刺激器的参数，一方面，当医生确认该参数配置信息合适，无需修改时，可以采用该参数配置信息调整刺激器的参数；另一方面，当医生认为该参数配置信息不合适，需要修改时，可以对参数配置信息进行修改，基于修改后的参数配置信息调整刺激器的参数。若不经医生确认，直接施加电刺激可能会对患者造成伤害，严重时可能危害生命，因此医生的反馈操作是十分必要的，既可以保障患者的生命安全，还可以让医生了解患者的病情变化情况。
参见图4，图4是本申请实施例提供的又一种程控信息记录方法的部分流程示意图，在一些可能的方式中，所述方法还可以包括步骤S111～S115。
步骤S111：利用患者设备接收对目标医生的第二选择操作。例如可以在患者设备上显示多个医生，目标医生是多个医生的其中一个，多个医生可以以列表或者平铺的方式显示。
步骤S112：响应于所述第二选择操作，获取所述目标医生的排班信息并发送至所述患者设备，所述排班信息包括至少一个时间段和每个时间段的可预约数量。其中，每个时间段是指至少一个时间段中的每个时间段。
举例说明，目标医生例如是小刘，小刘的排班信息例如是：“20210701：上午/1，下午/0；20210702：上午/3，下午/2；20210703：上午/5，下午/5”。
步骤S113：利用所述患者设备接收对所述目标医生的目标时间段的预约操作，所述目标时间段是所述至少一个时间段的其中一个。目标医生的目标时间段例如是小刘，20210701，上午。
步骤S114：响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量不小于1时，对所述目标医生的目标时间段的可预约数量执行减一操作。目标医生小刘在20210701上午的可预约数量是1，不小于1，则对小刘在20210701上午的可预约数量执行减一操作，更新后的可预约数量是0。
步骤S115：生成第一提示信息并发送至所述目标医生的医生设备，和/或，生成第二提示信息并发送至所述患者设备，所述第一提示信息包括所述目标时间段和所述患者设备对应的患者的标识信息，所述第二提示信息包括所述目标时间段。
其中，医生设备例如是手机、平板电脑、笔记本电脑、台式计算机或者智能穿戴设备等，患者设备例如是手机、平板电脑、笔记本电脑、台式计算机或者智能穿戴设备等。发送提示信息的方式例如是短信推送、邮件推送、应用内推送、电话通知等，此处提示信息包括第一提示信息和/或第二提示信息，应用例如是微信APP、支付宝APP、小程序等。
在一个远程程控的具体应用中，可以由医生设置排班时间，开放排班时间内可供患者挂号的可预约数量。患者根据排班的情况，提前预约某时间段内有排班的医生进行远程程控。预约成功后，短信提醒医生和患者预约成功，医生按时使用程控设备进行远程程控。
参见图5，图5是本申请实施例提供的又一种程控信息记录方法的部分流程示意图，在一些可能的方式中，所述方法还可以包括步骤S116～S117。
步骤S116：响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量小于1时，从所述目标医生的排班信息中确定至少一个备用时间段，所述至少一个备用时间段是所述至少一个时间段的一部分且每个备用时间段的可 预约数量不小于1。目标医生的目标时间段例如是小刘，20210701，下午，目标医生小刘在20210701下午的可预约数量是0，小于1，则从小刘的排班信息中确定一个备用时间段，例如是20210701上午或者20210702下午。
步骤S117：利用所述患者设备执行提示操作，所述提示操作用于指示所述至少一个备用时间段可预约。例如可以在患者设备上显示文字信息：“医生小刘20210701上午可预约”，也可以通过语音播放的方式播放语音：“医生小刘20210701上午可预约”，本申请实施例对此不做限定。
当目标医生的目标时间段不可预约时，自动向患者推送同一医生可以预约的备用时间段，便于患者选择合适的时间段预约程控，智能化程度高，患者体验好。患者可以选择任意一个备用时间段，利用患者设备对目标医生进行预约。
由此，当前存在患者需要进行程控时被医生因无排班被拒绝的情况，耽误了患者的治疗时间，提供线上预约功能，使患者可以提前选择进行程控的目标医生以及目标时间段，解决了患者及时得到程控的问题；另外，生成第一提示信息和第二提示信息分别发送给医生和患者，使医生和患者都能及时了解到预约成功的情况。
参见图6，图6是本申请实施例提供的一种确定备用时间段的流程示意图，在一些可能的方式中，所述步骤S116中从所述目标医生的排班信息中确定至少一个备用时间段的步骤，包括步骤S201或者S202。
步骤S201：从所述目标医生的排班信息中确定与所述目标时间段在时间上最接近的至少一个时间段作为所述至少一个备用时间段。
以一天中的上午或者下午作为一个时间段，当目标时间段为20210702的上午时，与目标时间段在时间上最接近的至少一个时间段可以包括20210701的下午和20210702的下午。
步骤S202：从所述目标医生的排班信息中确定与所述目标时间段的时间段类型相同的至少一个时间段作为所述至少一个备用时间段。
时间段类型可以包括上午和下午，当目标时间段的时间段类型为上午时，至少一个备用时间段是指至少一个上午时间段；至少一个备用时间段是指至少一个 下午时间段。
由此，以时间上最接近的时间段作为备用时间段，患者计划好的时间安排不需要做较大变动；以时间段类型相同的时间段作为备用时间段，例如患者本来想要预约的是上午时间段，自动推荐的时间段仍是上午时间段，更符合患者的预约偏好，这两种确定备用时间段的方式进一步提高了患者体验，且智能化程度更高。
在一些可能的方式中，所述方法还可以包括：将所述患者的程控信息发送至所述患者的患者设备。由此可以通知患者此次程控的参数信息，使患者了解自身每次程控的情况。
在一些可能的方式中，所述方法还可以包括：利用所述程控设备接收医嘱信息，并将所述医嘱信息发送至所述患者的患者设备。由此可以将医生的医嘱信息通知到患者，提醒患者需要注意的事项。
在一些可能的方式中，所述方法还可以包括：利用患者设备接收评价信息，并将所述评价信息发送至预设设备。其中，预设设备例如可以包括管理人员的管理设备和/或医生的医生设备。由此，患者可以对本次的程控效果进行评价，管理人员可以督查医生的程控情况，避免医生利用程控的机会报复特定患者或者无差别报复社会，而对医生来说，效果不好的患者医生可以对其进行回访。
参见图7，图7是本申请实施例提供的一种程控信息记录装置的结构示意图，本申请实施例还提供了一种程控信息记录装置，其具体实现方式与上述程控信息记录方法的实施例中记载的实施方式、所达到的技术效果一致，部分内容不再赘述。
所述程控信息记录装置应用于电子设备，所述装置包括：信息获取模块101，用于针对至少一个患者中的每个患者，获取设置于所述患者体外的程控设备的程控信息，所述程控设备包括体外程控仪、程控器、充电器、平板电脑、笔记本电脑、台式机和手机中的一种或多种；记录生成模块102，用于生成所述患者的程 控记录，所述患者的程控记录包括所述患者的标识信息和程控信息；记录存储模块103，用于将所述患者的程控记录存储至存储设备。
在一些可能的方式中，所述患者可以是以下任意一种：帕金森病患者；抑郁症患者；成瘾性疾病患者；强迫症患者；躁郁症患者。
参见图8，图8是本申请实施例提供的另一种程控信息记录装置的部分结构示意图，在一些可能的方式中，所述装置还可以包括：第一选择模块104，用于利用所述程控设备接收对目标患者的第一选择操作，所述目标患者是所述至少一个患者的其中一个；标识获取模块105，用于响应于所述第一选择操作，获取所述目标患者的标识信息；查询接收模块106，用于利用所述程控设备接收对所述目标患者的至少一个程控记录的查询操作；记录查询模块107，用于响应于所述查询操作，利用所述目标患者的标识信息，从所述存储设备中查询得到所述目标患者的至少一个程控记录；记录发送模块108，用于将所述目标患者的至少一个程控记录发送至所述程控设备。
参见图9，图9是本申请实施例提供的又一种程控信息记录装置的部分结构示意图，在一些可能的方式中，所述装置还可以包括：附加获取模块109，用于获取所述目标患者的附加信息，所述附加信息包括历史主诉信息、历史预约信息和植入信息中的一种或多种；附加发送模块110，用于将所述目标患者的附加信息发送至所述程控设备。
参见图10，图10是本申请实施例提供的又一种程控信息记录装置的部分结构示意图，在一些可能的方式中，所述装置还可以包括：第二选择模块111，用于利用患者设备接收对目标医生的第二选择操作；排班获取模块112，用于响应于所述第二选择操作，获取所述目标医生的排班信息并发送至所述患者设备，所述排班信息包括至少一个时间段和每个时间段的可预约数量；预约接收模块113，用于利用所述患者设备接收对所述目标医生的目标时间段的预约操作，所述目标时间段是所述至少一个时间段的其中一个；数量更新模块114，用于响应于所述 预约操作，当所述目标医生的所述目标时间段的可预约数量不小于1时，对所述目标医生的目标时间段的可预约数量执行减一操作；提示发送模块115，用于生成第一提示信息并发送至所述目标医生的医生设备，和/或，生成第二提示信息并发送至所述患者设备，所述第一提示信息包括所述目标时间段和所述患者设备对应的患者的标识信息，所述第二提示信息包括所述目标时间段。
参见图11，图11是本申请实施例提供的又一种程控信息记录装置的部分结构示意图，在一些可能的方式中，所述装置还可以包括：备用确定模块116，用于响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量小于1时，从所述目标医生的排班信息中确定至少一个备用时间段，所述至少一个备用时间段是所述至少一个时间段的一部分且每个备用时间段的可预约数量不小于1；备用提示模块117，用于利用所述患者设备执行提示操作，所述提示操作用于指示所述至少一个备用时间段可预约。
参见图12，图12是本申请实施例提供的一种备用确定模块的结构示意图，在一些可能的方式中，所述备用确定模块116可以包括：第一确定单元201，用于从所述目标医生的排班信息中确定与所述目标时间段在时间上最接近的至少一个时间段作为所述至少一个备用时间段；或者，第二确定单元202，用于从所述目标医生的排班信息中确定与所述目标时间段的时间段类型相同的至少一个时间段作为所述至少一个备用时间段。
参见图13，图13是本申请实施例提供的一种电子设备的结构示意图，本申请实施例还提供了一种电子设备200，电子设备200包括至少一个存储器210、至少一个处理器220以及连接不同平台系统的总线230。
在一些可能的方式中，该电子设备200可以与程控设备集成为一体。
程控设备例如是医生的平板电脑、笔记本电脑、台式计算机等。
存储器210可以包括易失性存储器形式的可读介质，例如随机存取存储器(RAM)211和/或高速缓存存储器212，还可以进一步包括只读存储器(ROM)213。
其中，存储器210还存储有计算机程序，计算机程序可以被处理器220执行，使得处理器220执行本申请实施例中程控信息记录方法的步骤，其具体实现方式与上述程控信息记录方法的实施例中记载的实施方式、所达到的技术效果一致，部分内容不再赘述。
存储器210还可以包括具有至少一个程序模块215的实用工具214，这样的程序模块215包括但不限于：操作系统、一个或者多个应用程序、其它程序模块以及程序数据，这些示例中的每一个或某种组合中可能包括网络环境的实现。
相应的，处理器220可以执行上述计算机程序，以及可以执行实用工具214。
总线230可以为表示几类总线结构中的一种或多种，包括存储器总线或者存储器控制器、外围总线、图形加速端口、处理器或者使用多种总线结构中的任意总线结构的局域总线。
电子设备200也可以与一个或多个外部设备240例如键盘、指向设备、蓝牙设备等通信，还可与一个或者多个能够与该电子设备200交互的设备通信，和/或与使得该电子设备200能与一个或多个其它计算设备进行通信的任何设备(例如路由器、调制解调器等)通信。这种通信可以通过输入输出接口250进行。并且，电子设备200还可以通过网络适配器260与一个或者多个网络(例如局域网(LAN)，广域网(WAN)和/或公共网络，例如因特网)通信。网络适配器260可以通过总线230与电子设备200的其它模块通信。应当明白，尽管图中未示出，可以结合电子设备200使用其它硬件和/或软件模块，包括但不限于：微代码、设备驱动器、冗余处理器、外部磁盘驱动阵列、RAID系统、磁带驱动器以及数据备份存储平台等。
本申请实施例还提供了一种计算机可读存储介质，该计算机可读存储介质用于存储计算机程序，所述计算机程序被执行时实现本申请实施例中程控信息记录方法的步骤，其具体实现方式与上述程控信息记录方法的实施例中记载的实施方式、所达到的技术效果一致，部分内容不再赘述。
图14示出了本实施例提供的用于实现上述程控信息记录方法的程序产品300，其可以采用便携式紧凑盘只读存储器(CD-ROM)并包括程序代码，并可以在 终端设备，例如个人电脑上运行。然而，本发明的程序产品300不限于此，在本申请中，可读存储介质可以是任何包含或存储程序的有形介质，该程序可以被指令执行系统、装置或者器件使用或者与其结合使用。程序产品300可以采用一个或多个可读介质的任意组合。可读介质可以是可读信号介质或者可读存储介质。可读存储介质例如可以为但不限于电、磁、光、电磁、红外线、或半导体的系统、装置或器件，或者任意以上的组合。可读存储介质的更具体的例子(非穷举的列表)包括：具有一个或多个导线的电连接、便携式盘、硬盘、随机存取存储器(RAM)、只读存储器(ROM)、可擦式可编程只读存储器(EPROM或闪存)、光纤、便携式紧凑盘只读存储器(CD-ROM)、光存储器件、磁存储器件、或者上述的任意合适的组合。
计算机可读存储介质可以包括在基带中或者作为载波一部分传播的数据信号，其中承载了可读程序代码。这种传播的数据信号可以采用多种形式，包括但不限于电磁信号、光信号或上述的任意合适的组合。可读存储介质还可以是任何可读介质，该可读介质可以发送、传播或者传输用于由指令执行系统、装置或者器件使用或者与其结合使用的程序。可读存储介质上包含的程序代码可以用任何适当的介质传输，包括但不限于无线、有线、光缆、RF等，或者上述的任意合适的组合。可以以一种或多种程序设计语言的任意组合来编写用于执行本发明操作的程序代码，程序设计语言包括面向对象的程序设计语言诸如Java、C++等，还包括常规的过程式程序设计语言诸如C语言或类似的程序设计语言。程序代码可以完全地在用户计算设备上执行、部分地在用户设备上执行、作为一个独立的软件包执行、部分在用户计算设备上部分在远程计算设备上执行、或者完全在远程计算设备或服务器上执行。在涉及远程计算设备的情形中，远程计算设备可以通过任意种类的网络，包括局域网(LAN)或广域网(WAN)，连接到用户计算设备，或者，可以连接到外部计算设备(例如利用因特网服务提供商来通过因特网连接)。
本申请从使用目的上，效能上，进步及新颖性等观点进行阐述，本申请以上的说明书及说明书附图，仅为本申请的较佳实施例而已，并非以此局限本申请，因此，凡一切与本申请构造，装置，特征等近似、雷同的，即凡依本申请专利申 请范围所作的等同替换或修饰等，皆应属本申请的专利申请保护的范围之内。

Claims (16)

  1. 一种程控信息记录装置，应用于电子设备，所述装置包括：
    信息获取模块，用于针对至少一个患者中的每个患者，获取设置于所述患者体外的程控设备的程控信息，所述程控设备包括体外程控仪、程控器、充电器、平板电脑、笔记本电脑、台式机和手机中的一种或多种；
    记录生成模块，用于生成所述患者的程控记录，所述患者的程控记录包括所述患者的标识信息和程控信息；
    记录存储模块，用于将所述患者的程控记录存储至存储设备。
  2. 根据权利要求1所述的装置，其中，所述患者是以下任意一种：帕金森病患者；抑郁症患者；成瘾性疾病患者；强迫症患者；躁郁症患者。
  3. 根据权利要求1所述的装置，其中，所述装置还包括：
    第一选择模块，用于利用所述程控设备接收对目标患者的第一选择操作，所述目标患者是所述至少一个患者的其中一个；
    标识获取模块，用于响应于所述第一选择操作，获取所述目标患者的标识信息；
    查询接收模块，用于利用所述程控设备接收对所述目标患者的至少一个程控记录的查询操作；
    记录查询模块，用于响应于所述查询操作，利用所述目标患者的标识信息，从所述存储设备中查询得到所述目标患者的至少一个程控记录；
    记录发送模块，用于将所述目标患者的至少一个程控记录发送至所述程控设备。
  4. 根据权利要求3所述的装置，其中，所述装置还包括：
    附加获取模块，用于获取所述目标患者的附加信息，所述附加信息包括历史主诉信息、历史预约信息和植入信息中的一种或多种；
    附加发送模块，用于将所述目标患者的附加信息发送至所述程控设备。
  5. 根据权利要求1所述的装置，其中，所述装置还包括：
    第二选择模块，用于利用患者设备接收对目标医生的第二选择操作；
    排班获取模块，用于响应于所述第二选择操作，获取所述目标医生的排班信息并发送至所述患者设备，所述排班信息包括至少一个时间段和每个时间段的可预约数量；
    预约接收模块，用于利用所述患者设备接收对所述目标医生的目标时间段的预约操作，所述目标时间段是所述至少一个时间段的其中一个；
    数量更新模块，用于响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量不小于1时，对所述目标医生的目标时间段的可预约数量执行减一操作；
    提示发送模块，用于生成第一提示信息并发送至所述目标医生的医生设备，和/或，生成第二提示信息并发送至所述患者设备，所述第一提示信息包括所述目标时间段和所述患者设备对应的患者的标识信息，所述第二提示信息包括所述目标时间段。
  6. 根据权利要求5所述的装置，其中，所述装置还包括：
    备用确定模块，用于响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量小于1时，从所述目标医生的排班信息中确定至少一个备用时间段，所述至少一个备用时间段是所述至少一个时间段的一部分且每个备用时间段的可预约数量不小于1；
    备用提示模块，用于利用所述患者设备执行提示操作，所述提示操作用于指示所述至少一个备用时间段可预约。
  7. 根据权利要求6所述的装置，其中，所述备用确定模块包括：
    第一确定单元，用于从所述目标医生的排班信息中确定与所述目标时间段在时间上最接近的至少一个时间段作为所述至少一个备用时间段；或者，
    第二确定单元，用于从所述目标医生的排班信息中确定与所述目标时间段的时间段类型相同的至少一个时间段作为所述至少一个备用时间段。
  8. 一种程控信息记录方法，应用于电子设备，所述方法包括：
    针对至少一个患者中的每个患者，获取设置于所述患者体外的程控设备的程控信息，所述程控设备包括体外程控仪、程控器、充电器、平板电脑、笔记本电 脑、台式机和手机中的一种或多种；
    生成所述患者的程控记录，所述患者的程控记录包括所述患者的标识信息和程控信息；
    将所述患者的程控记录存储至存储设备。
  9. 根据权利要求8所述的方法，其中，所述患者是以下任意一种：帕金森病患者；抑郁症患者；成瘾性疾病患者；强迫症患者；躁郁症患者。
  10. 根据权利要求8所述的方法，其中，所述方法还包括：
    利用所述程控设备接收对目标患者的第一选择操作，所述目标患者是所述至少一个患者的其中一个；
    响应于所述第一选择操作，获取所述目标患者的标识信息；
    利用所述程控设备接收对所述目标患者的至少一个程控记录的查询操作；响应于所述查询操作，利用所述目标患者的标识信息，从所述存储设备中查询得到所述目标患者的至少一个程控记录；
    将所述目标患者的至少一个程控记录发送至所述程控设备。
  11. 根据权利要求10所述的方法，其中，所述方法还包括：
    获取所述目标患者的附加信息，所述附加信息包括历史主诉信息、历史预约信息和植入信息中的一种或多种；
    将所述目标患者的附加信息发送至所述程控设备。
  12. 根据权利要求8所述的方法，其中，所述方法还包括：
    利用患者设备接收对目标医生的第二选择操作；
    响应于所述第二选择操作，获取所述目标医生的排班信息并发送至所述患者设备，所述排班信息包括至少一个时间段和每个时间段的可预约数量；
    利用所述患者设备接收对所述目标医生的目标时间段的预约操作，所述目标时间段是所述至少一个时间段的其中一个；
    响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量不小于1时，对所述目标医生的目标时间段的可预约数量执行减一操作；
    生成第一提示信息并发送至所述目标医生的医生设备，和/或，生成第二提示信息并发送至所述患者设备，所述第一提示信息包括所述目标时间段和所述患 者设备对应的患者的标识信息，所述第二提示信息包括所述目标时间段。
  13. 根据权利要求12所述的方法，其中，所述方法还包括：
    响应于所述预约操作，当所述目标医生的所述目标时间段的可预约数量小于1时，从所述目标医生的排班信息中确定至少一个备用时间段，所述至少一个备用时间段是所述至少一个时间段的一部分且每个备用时间段的可预约数量不小于1；
    利用所述患者设备执行提示操作，所述提示操作用于指示所述至少一个备用时间段可预约。
  14. 根据权利要求13所述的方法，其中，所述从所述目标医生的排班信息中确定至少一个备用时间段，包括：
    从所述目标医生的排班信息中确定与所述目标时间段在时间上最接近的至少一个时间段作为所述至少一个备用时间段；或者，
    从所述目标医生的排班信息中确定与所述目标时间段的时间段类型相同的至少一个时间段作为所述至少一个备用时间段。
  15. 一种电子设备，所述电子设备包括存储器和处理器，所述存储器存储有计算机程序，所述处理器执行所述计算机程序时实现权利要求8至14任一项所述方法的步骤。
  16. 一种计算机可读存储介质，所述计算机可读存储介质存储有计算机程序，所述计算机程序被处理器执行时实现权利要求8至14任一项所述方法的步骤。
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