CN113314192A - Clinical trial data processing system, method, device and storage medium - Google Patents
Clinical trial data processing system, method, device and storage medium Download PDFInfo
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Abstract
The present disclosure provides a clinical trial data processing system, method, electronic device and storage medium. The system comprises a clinical test data management system and a hospital information system, wherein the clinical test data management system is used for acquiring the project information of clinical test projects and synchronizing the project information of the clinical test projects to the hospital information system; the hospital information system is used for screening and obtaining target patients, adding the target patients as target subjects and adding prescription information of the target subjects, and synchronizing the subject information of the target subjects and the prescription information thereof to the clinical test data management system; the clinical trial data management system is used for receiving the subject information of the target subject and the prescription information thereof and distributing the medicine for the target subject according to the prescription information. The system realizes real-time synchronization of clinical test data in the clinical test management system and the hospital information system, and improves the clinical test efficiency and the accuracy of the clinical test data.
Description
Technical Field
The present disclosure relates to the field of computer technologies, and in particular, to a clinical trial data processing system, method, system, electronic device, and storage medium.
Background
The hospital information system has functions related to patient management, such as patient data recording and prescription order issuing. Clinical trial project management systems require separate records of trial-related data including medical orders, medications, laboratory examinations, illicit medications, etc. during participation of a patient as a subject in a clinical trial.
In the related art, the hospital information system and the clinical test project management system operate independently to perform daily management on patients and clinical test projects, the repeated workload can be increased when the hospital information system and the clinical test project management system operate independently, and the two systems respectively manage and record inconsistent data easily.
It is to be noted that the information disclosed in the above background section is only for enhancement of understanding of the background of the present disclosure, and thus may include information that does not constitute prior art known to those of ordinary skill in the art.
Disclosure of Invention
The system realizes real-time synchronization of clinical test data in a clinical test management system and a hospital information system, improves the clinical test efficiency and the accuracy of the clinical test data, and saves the execution time of clinical tests.
Additional features and advantages of the disclosure will be set forth in the detailed description which follows, or in part will be obvious from the description, or may be learned by practice of the disclosure.
The disclosed embodiment provides a clinical trial data processing system, including: the clinical test data processing system comprises a clinical test data management system and a hospital information system; the clinical test data management system is used for acquiring project information of clinical test projects and synchronizing the project information of the clinical test projects to the hospital information system; the hospital information system is used for receiving the project information of the clinical test project, screening a patient library according to the project information of the clinical test project to obtain a target patient, adding the target patient as a target subject corresponding to the clinical test project and adding prescription information of the target subject, and synchronizing the subject information of the target subject and the prescription information thereof to the clinical test data management system; the clinical trial data management system is used for receiving the subject information of the target subject and prescription information thereof and dispensing the medicine for the target subject according to the prescription information.
In some exemplary embodiments of the present disclosure, the clinical trial data management system is further configured to receive subject information of the target subject, and generate a clinical trial visit reminder according to the project information and the subject information. In some exemplary embodiments of the present disclosure, the clinical trial data management system is further configured to determine cost information for the target subject based on prescription information for the target subject and to synchronize the cost information to the hospital information system; the hospital information system is used for receiving the expense information of the target subject and carrying out the exemption treatment on the expense information.
In some exemplary embodiments of the present disclosure, the item information of the clinical trial item includes trial grouping conditions of the clinical trial item; the clinical test data management system is used for synchronizing the project information of the clinical test projects to a hospital information system; and the hospital information system is used for receiving the test grouping condition of the clinical test item and screening target patients meeting the test grouping condition from a patient bank according to the test grouping condition.
In some exemplary embodiments of the present disclosure, the item information of the clinical trial item includes forbidden drug information corresponding to the clinical trial item; the hospital information system is used for determining prescription information of the target subject according to forbidden medicine information corresponding to the clinical test items, and the prescription information comprises medical orders and medicine information.
In some exemplary embodiments of the present disclosure, the clinical trial data management system is configured to obtain interview information of the target subject; and analyzing the visit information of the target subject to obtain the test effect of the clinical test item.
In some exemplary embodiments of the present disclosure, the item information of the clinical trial items is synchronized to the hospital information system through an interface, and the prescription information is synchronized to the clinical trial data management system through an interface.
The embodiment of the disclosure provides a clinical test data processing method, which comprises the following steps: the method comprises the following steps that a clinical test data management system obtains project information of a clinical test project and synchronizes the project information of the clinical test project to a hospital information system; the hospital information system receives the project information of the clinical test project, screens a patient base according to the project information of the clinical test project to obtain a target patient, adds the target patient as a target subject corresponding to the clinical test project and adds prescription information of the target subject, and synchronizes the subject information of the target subject and the prescription information thereof to the clinical test data management system; and the clinical test data management system receives the subject information of the target subject and the prescription information thereof, and dispenses the medicine for the target subject according to the prescription information.
An embodiment of the present disclosure provides an electronic device, including: at least one processor; a storage means for storing at least one program which, when executed by the at least one processor, causes the at least one processor to implement the clinical trial data processing method as described above.
The disclosed embodiments provide a computer-readable storage medium having stored thereon a computer program which, when executed by a processor, implements the above-described clinical trial data processing method.
According to the clinical test data processing system provided by the embodiment of the disclosure, the project information of the clinical test projects is acquired through the clinical test project management system, and the project information of the clinical test projects is synchronized to the hospital information system, so that the hospital information system can return a target subject determined according to the project information; the clinical trial project management system may receive prescription information of the target subject synchronized by the hospital information system and dispense a drug for the target subject according to the prescription information. The method has the advantages that the clinical test management system is connected with the hospital information system in a butt joint mode, real-time synchronization of clinical test data in the clinical test management system and the hospital information system is achieved, the clinical test efficiency and the accuracy of the clinical test data are improved, the execution time of clinical tests is saved, and the workload of researchers and hospitals is greatly reduced.
It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the disclosure.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments consistent with the present disclosure and together with the description, serve to explain the principles of the disclosure. It is to be understood that the drawings in the following description are merely exemplary of the disclosure, and that other drawings may be derived from those drawings by one of ordinary skill in the art without the exercise of inventive faculty.
FIG. 1 is a schematic diagram of a clinical trial data processing system shown according to an exemplary embodiment.
FIG. 2 is a schematic diagram of a clinical trial data processing system shown according to an exemplary embodiment.
FIG. 3 is a schematic diagram illustrating a method of clinical trial data processing according to an exemplary embodiment.
FIG. 4 is a schematic diagram illustrating a method of clinical trial data processing according to an exemplary embodiment.
Fig. 5 is a schematic diagram of an electronic device according to an exemplary embodiment.
Detailed Description
Example embodiments will now be described more fully with reference to the accompanying drawings. Example embodiments may, however, be embodied in many different forms and should not be construed as limited to the examples set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the concept of example embodiments to those skilled in the art. The described features, structures, or characteristics may be combined in any suitable manner in one or more embodiments.
Furthermore, the drawings are merely schematic illustrations of the present disclosure and are not necessarily drawn to scale. The same reference numerals in the drawings denote the same or similar parts, and thus their repetitive description will be omitted. Some of the block diagrams shown in the figures are functional entities and do not necessarily correspond to physically or logically separate entities. These functional entities may be implemented in the form of software, or in one or more hardware modules or integrated circuits, or in different networks and/or processor devices and/or microcontroller devices.
FIG. 1 is a schematic diagram of a clinical trial data processing system shown according to an exemplary embodiment.
As shown in FIG. 1, the clinical trial data processing System 10 may include a clinical trial data management System 102 and a Hospital Information System 104 (HIS).
The Clinical trial data management system 102 may also be referred to as a GCP (Good Clinical Practice, drug Clinical trial management specification) system, and may provide a standardized business management and service for the whole experimental process of Clinical trials by using modern means such as computer software and hardware technology and network communication technology.
The hospital information system 104 may be an information system that comprehensively manages the human flow, physical distribution, financial flow, etc. of the hospital and its affiliated departments, collects, stores, processes, extracts, transmits, summarizes, and processes the data produced at various stages in the medical activities to form information, and provides automated management and various services for the overall operation of the hospital by using the modernization means such as computer software and hardware technology, network communication technology, etc.
In embodiments of the present disclosure, the user of the clinical trial data management system 102 may be a researcher of a clinical trial. The researcher may be the responsible person for conducting the clinical trial and for the quality of the clinical trial and the safety and benefits of the subject, and typically the researcher must go through a qualification review with the professional expertise, qualification and competence of the clinical trial, with the researcher typically being the responsibility of a hospital qualified physician. Wherein, a subject may refer to a patient involved in a clinical trial.
In an exemplary embodiment, the clinical trial data management system 102 is configured to obtain project information for the clinical trial project and synchronize the project information for the clinical trial project to the hospital information system 104.
The clinical test refers to a systematic study of the drug in human body (patient or healthy volunteer) to confirm or disclose the action, adverse reaction and/or absorption, distribution, metabolism and excretion of the test drug, so as to determine the efficacy and safety of the test drug.
In the embodiments of the present disclosure, the clinical test items may be clinical tests of cold medicines, for example, and in the following description, the clinical tests of cold medicines are all described as examples, but the present disclosure is not limited thereto.
In the embodiment of the disclosure, the user may create a clinical trial project through the clinical trial management system, and input or select project information of the clinical trial project.
The item information of the clinical trial item may include, but is not limited to, drug basic information, trial time, number of subjects of the clinical trial item.
In an exemplary embodiment, the item information of the clinical trial item may further include item information of the clinical trial item including trial grouping conditions of the clinical trial item. The test grouping condition may include, but is not limited to, height, weight, sex, age, physical indicators of the subject. Further, the item information of the clinical test item may further include forbidden drug information corresponding to the clinical test item.
The forbidden drug information corresponding to the clinical test item can be a drug which may affect the test effect of the clinical test item.
For example, the clinical trial item is a clinical trial of cold drug a, and hypertensive drug B may have an effect on the trial effect of the clinical trial of cold drug a, and hypertensive drug B may be a non-approved drug for the clinical trial of cold drug a. The user can create a cold drug test item through the clinical test management system and input cold drug information, test time, the number of testees, test group entry conditions, forbidden drugs and the like of the cold drug test item.
In the embodiment of the disclosure, the item information of the clinical test item may be synchronized to the hospital information system by way of interface docking, and the subject information of the target subject may also be synchronized to the clinical test management system by way of interface docking.
For example, a Web Service (Web Service) mode may be adopted, the hospital information system provides an interface for the server, the clinical trial project management system is the caller, and the project information of the clinical trial projects is synchronized to the hospital information system.
In an exemplary embodiment, the hospital information system 104 is configured to receive the project information of the clinical test project, screen the patient library according to the project information of the clinical test project to obtain target patients, add target patients as target subjects corresponding to the clinical test project and add prescription information of the target subjects, and synchronize the subject information of the target subjects and the prescription information thereof to the clinical test data management system.
In the disclosed embodiment, the user of the hospital information system may be a doctor.
The hospital information system can receive the item information of the clinical test items sent by the clinical test data management system, and doctors can check the item information of the clinical test items through the hospital information system.
In the embodiment of the disclosure, the hospital information system may screen a patient matched with the clinical test item from the patient library as a target patient according to the item information of the clinical test item and the patient information pre-stored in the patient library.
In the embodiment of the disclosure, the hospital information system may also display the item information of the clinical test items, the doctor may view the item information, and the doctor selects a patient matched with the clinical test items from the patient library as a target patient by judging, and inputs the target patient into the hospital information system.
Wherein the target patient may be a patient having a disease corresponding to a clinical trial project.
For example, if the clinical trial item is a clinical trial of a cold drug, the target patient may be a patient suffering from a cold.
In an exemplary embodiment, the hospital information system may screen the patient pool for target patients meeting the trial grouping condition according to the trial grouping condition of the clinical trial item.
For example, the test grouping condition may include an age of 20 to 30 years, and the hospital information system may obtain a patient aged 20 to 30 years from the patient pool as the target patient.
After the target patient is obtained through screening, the hospital information system may add the target patient as a target subject corresponding to the clinical trial project, and synchronize the subject information of the target subject to the clinical trial data management system.
In the embodiment of the disclosure, the hospital information system may automatically add the target patient as the target subject corresponding to the clinical test item after obtaining the consent of the target patient, and synchronize the subject information of the target subject to the clinical test item management system in an interface manner.
The subject information of the target subject may include, but is not limited to, height, weight, sex, age, physical indicators, and symptoms of the subject.
In the embodiment of the disclosure, the hospital information system can also record the case data related to the participation of the target subject in the clinical trial according to the progress of the clinical trial.
The hospital information system may also determine prescription information for the target subject based on the project information for the clinical trial project.
For example, in a cold drug clinical trial, a physician may prescribe the cold drug to a target subject via a hospital information system.
In an exemplary embodiment, prescription information of the target subject is determined according to the forbidden drug information corresponding to the clinical trial item, wherein the prescription information includes the medical order and the drug information.
For example, in clinical trials of cold drug a, if hypertension drug B is a prohibited drug, the effect of hypertension drug B on the clinical trial effect of cold drug a needs to be considered by the doctor when prescribing the drug. Generally, a doctor will not prescribe hypertension B for a target subject participating in a clinical trial of cold drug a. However, if the target subject does require hypertensive B, the doctor can prescribe hypertensive B for the target subject through the hospital information system while synchronizing the prescription information to the clinical trial project management system.
In an exemplary embodiment, the clinical trial data management system 102 is configured to receive subject information for the target subject and generate a clinical trial visit reminder based on the project information and the subject information. The clinical trial project management system can automatically generate clinical trial visit reminders for the user according to project information and subject information, the number of the clinical trial visit reminders can be one or more, and the clinical trial visit reminders can regularly remind the user to visit a clinical trial to track the progress and effect of the clinical trial.
The reminding time and the reminding content of the clinical trial visit reminder can be determined according to the project information and the subject information of the clinical trial project.
In an exemplary embodiment, the clinical trial data management system 102 is configured to receive subject information of a target subject and prescription information thereof, and to dispense drugs for the target subject according to the prescription information.
After the hospital information system synchronizes the subject information of the target subject and the prescription information thereof to the clinical trial project management system, the researcher can check and record the prescription information through the clinical trial project management system and track the progress of the clinical trial project.
After the target subject is dispensed with the medicine, the clinical trial project management system can periodically acquire the visit information of the target subject according to the visit reminding of the clinical trial. The visit information can include, but is not limited to, physical examination indexes, symptom relief degree and the like of the target subject. Physical examination may include laboratory tests for body temperature detection, hematology, hematobiochemistry, and the like. Wherein, the visit information of the target subject can be input by a researcher through a clinical test project management system, and can also be synchronously obtained through a hospital information system.
The clinical test item management system can also analyze the visit information of the target subject to obtain the test effect of the clinical test item.
For example, in a clinical trial of a hypertensive, the obtained visit information of the target subject may include blood pressure of the target subject at different time points, and the trial effect of the hypertensive may be obtained by analyzing the blood pressure of the target subject. In an exemplary embodiment, the clinical trial data management system 102 may also be configured to determine cost information for the target subject based on the prescription information for the target subject; and synchronizing cost information of the target subject to the hospital information system.
The prescription information of the target subject may include a drug name, a drug amount, or a test item, among others. The clinical trial project management system can calculate the cost information related to the participation of the target subject in the clinical trial project according to the name of the medicine, the dosage of the medicine and the unit price of the medicine or the detection project and the unit price of the detection project.
In an exemplary embodiment, the hospital information system 104 may also be used to receive cost information for the target subject and to apply a deductive process to the cost information.
In the embodiment of the disclosure, the clinical test item management system may synchronize the cost information of the target subject to the hospital information system by means of an interface, and the hospital information system may process the cost information related to the participation of the target subject in the clinical test item, so that the target subject does not need to pay, that is, the costs of medication, inspection, detection, and the like generated during the participation of the target subject in the clinical test process by the target patient do not need to be borne by the target patient, thereby realizing zero payment and zero reimbursement of the target subject.
For example, the hospital information system may set the charge information related to the participation of the target subject in the clinical trial program not to generate a bill at the time of checkout, or the hospital information system may set the charge information related to the participation of the target subject in the clinical trial program to zero at the time of checkout, or the hospital information system may transmit the charge information related to the participation of the target subject in the clinical trial program to the clinical trial program management system at the time of checkout, so that the clinical trial program management system pays the charge.
The clinical test data processing system provided by the embodiment of the disclosure can realize real-time synchronization of cost information in a clinical test project management system and a hospital information system, and saves work and burden of financial staff and testees brought by a clinical test related cost reimbursement link.
According to the clinical test data processing system provided by the embodiment of the disclosure, the project information of the clinical test projects is acquired through the clinical test project management system, and the project information of the clinical test projects is synchronized to the hospital information system, so that the hospital information system can return a target subject determined according to the project information; the clinical test project management system can generate clinical test visit reminding according to project information and subject information and automatically remind a user to carry out clinical test visit; the clinical trial project management system may receive prescription information of the target subject synchronized by the hospital information system and dispense a drug for the target subject according to the prescription information. The method has the advantages that the clinical test management system is connected with the hospital information system in a butt joint mode, real-time synchronization of clinical test data in the clinical test management system and the hospital information system is achieved, the clinical test efficiency and the accuracy of the clinical test data are improved, the execution time of clinical tests is saved, and the workload of researchers and hospitals is greatly reduced.
FIG. 2 is a schematic diagram of another clinical trial data processing system shown in accordance with an exemplary embodiment.
Referring to fig. 2, in an embodiment of the present disclosure, a clinical trial data processing system includes a clinical trial project management system and a hospital information system, where the clinical trial project management system may include: a project information acquisition module 201, a project information synchronization module 202, a subject information and prescription information receiving module 207 and a medicine dispensing module 208; the hospital information system may include: a project information receiving module 203, a target patient obtaining module 204, a target subject and prescription information adding module 205 and a target subject information and prescription information synchronizing module 206.
The project information acquisition module 201 is configured to acquire project information of a clinical test project; the project information synchronization module 202 is used for synchronizing the project information of the clinical test projects to a project information receiving module 203 of the hospital information system; the item information receiving module 203 is used for receiving the item information of the clinical test item; the target patient obtaining module 204 is used for screening and obtaining a target patient from a patient library according to the project information of the clinical test project; the target subject and prescription information adding module 205 is used for adding a target subject corresponding to a clinical trial project of a target patient and adding prescription information of the target subject; the prescription information synchronization module 206 is used for synchronizing the subject information and prescription information of the target subject to the subject information of the clinical trial data management system and the prescription information receiving module 207 thereof; the subject information and prescription information receiving module 207 is used for receiving the subject information and prescription information of the target subject; the drug dispensing module 208 is configured to dispense drugs for the target subject according to the prescription information.
The following are embodiments of the disclosed method, and for details not disclosed in the embodiments of the disclosed method, reference is made to the embodiments of the disclosed system.
FIG. 3 is a schematic diagram illustrating a method of clinical trial data processing according to an exemplary embodiment. Referring to fig. 3, the clinical trial data processing method includes:
in step S11, the clinical trial data management system acquires item information of the clinical trial item.
The item information of the clinical test item may include test grouping conditions of the clinical test item, and the item information of the clinical test item may also include forbidden drug information corresponding to the clinical test item.
After acquiring the project information of the clinical test project, the clinical test data management system can synchronize the project information to the hospital information system, and the hospital information system can receive the project information of the clinical test project.
And step S12, the hospital information system screens the patient base according to the item information of the clinical test items to obtain target patients, and the target patients are added as target subjects corresponding to the clinical test items.
The hospital information system can screen and obtain target patients meeting the test grouping conditions from the patient library according to the test grouping conditions in the project information, and add the target patients as target subjects.
After adding the target subject, the hospital information system feeds back the subject information to the clinical trial management system.
And step S13, the clinical trial data management system generates a clinical trial visit reminder according to the project information and the subject information.
And step S14, the hospital information system determines the prescription information of the target subject according to the project information and sends the prescription information to the clinical trial data management system.
The prescription information may include medical orders and drug information.
In the embodiment of the present disclosure, the hospital information system may determine the prescription information of the target subject according to the forbidden drug information corresponding to the clinical trial item.
Step S15, the clinical trial data management system issues the drug for the target subject according to the prescription information, and determines the cost information of the target subject. After determining the cost information for the target subject, the clinical trial data management system synchronizes the cost information to the hospital information system.
Step S16, the hospital information system records and reimburses the cost information.
The hospital information system may receive cost information for the target subject and perform a deduction process on the cost information.
The method for processing clinical trial data provided by the embodiment of the disclosure may further include: the clinical test data management system acquires the visit information of a target subject; and analyzing the visit information of the target subject to obtain the test effect of the clinical test item.
According to the clinical test data processing method provided by the embodiment of the disclosure, the project information of the clinical test projects is acquired through the clinical test project management system, and the project information of the clinical test projects is synchronized to the hospital information system, so that the hospital information system can return a target subject determined according to the project information; the clinical test project management system can generate clinical test visit reminding according to project information and subject information and automatically remind a user to carry out clinical test visit; the clinical trial project management system may receive prescription information of the target subject synchronized by the hospital information system and dispense a drug for the target subject according to the prescription information. The method has the advantages that the clinical test management system is connected with the hospital information system in a butt joint mode, real-time synchronization of clinical test data in the clinical test management system and the hospital information system is achieved, the clinical test efficiency and the accuracy of the clinical test data are improved, the execution time of clinical tests is saved, and the workload of researchers and hospitals is greatly reduced.
FIG. 4 is a schematic diagram illustrating a method of clinical trial data processing according to an exemplary embodiment.
In the disclosed embodiment, referring to fig. 4, a researcher may create a clinical trial project in the clinical trial data management system 102 and fill in information related to the clinical trial project.
The clinical trial data management system 102 may obtain the item information of the clinical trial items, and synchronize the item information of the clinical trial items to the hospital information system 102 in an interface manner.
The hospital information system 104 may receive the item information of the clinical test item, screen out a suitable target patient from the patient library according to the item information of the clinical test item, add the target patient as a target subject corresponding to the clinical test item, and synchronize the subject information of the target subject to the clinical test data management system 102 in an interface manner.
The clinical trial data management system 102 may receive subject information of a target subject and generate a clinical trial visit reminder according to the project information and the subject information, where the clinical trial visit reminder may periodically remind a user of a subject visit for a clinical trial.
The hospital information system 104 may determine prescription information for the target subject, which may include visit related prescriptions for drugs, test exams, etc., based on the project information and synchronize the prescription information to the clinical trial data management system 102.
The clinical trial data management system 102 may receive prescription information for a target subject and dispense a drug for the target subject based on the prescription information.
The clinical trial data management system 102 may determine cost information for the target subject based on the prescription information for the target subject and synchronize the cost information for the target subject to the hospital information system 104.
The hospital information system 104 can receive the cost information of the target subject sent by the hospital information system; and recording and reimbursing the target subject's fee information so that the target subject does not have to pay a fee.
When a clinical trial is completed, or when the subjects complete all clinical trial visits, the hospital information system 104 can group the target subjects and synchronize the grouped target subject information to the clinical trial data management system 102, and the clinical trial data management system 102 can end the clinical trial.
Fig. 5 is a schematic diagram of an electronic device according to an exemplary embodiment. It should be noted that the electronic device shown in fig. 5 is only an example, and should not bring any limitation to the functions and the scope of use of the embodiment of the present invention.
As shown in fig. 5, the electronic apparatus 900 includes a Central Processing Unit (CPU)901 that can perform various appropriate actions and processes in accordance with a program stored in a Read Only Memory (ROM)902 or a program loaded from a storage section 908 into a Random Access Memory (RAM) 903. In the RAM 903, various programs and data necessary for the operation of the system 900 are also stored. The CPU 901, ROM 902, and RAM 903 are connected to each other via a bus 904. An input/output (I/O) interface 905 is also connected to bus 904.
The following components are connected to the I/O interface 905: an input portion 906 including a keyboard, a mouse, and the like; an output section 907 including components such as a Cathode Ray Tube (CRT), a Liquid Crystal Display (LCD), and the like, and a speaker; a storage portion 908 including a hard disk and the like; and a communication section 909 including a network interface card such as a LAN card, a modem, or the like. The communication section 909 performs communication processing via a network such as the internet. The drive 910 is also connected to the I/O interface 905 as necessary. A removable medium 911 such as a magnetic disk, an optical disk, a magneto-optical disk, a semiconductor memory, or the like is mounted on the drive 910 as necessary, so that a computer program read out therefrom is mounted into the storage section 908 as necessary.
In particular, according to an embodiment of the present invention, the processes described above with reference to the flowcharts may be implemented as computer software programs. For example, embodiments of the invention include a computer program product comprising a computer program embodied on a computer-readable medium, the computer program comprising program code for performing the method illustrated in the flow chart. In such an embodiment, the computer program may be downloaded and installed from a network through the communication section 909, and/or installed from the removable medium 911. The above-described functions defined in the system of the present invention are executed when the computer program is executed by a Central Processing Unit (CPU) 901.
It should be noted that the computer readable medium shown in the present invention can be a computer readable signal medium or a computer readable storage medium or any combination of the two. A computer readable storage medium may be, for example, but not limited to, an electronic, magnetic, optical, electromagnetic, infrared, or semiconductor system, apparatus, or device, or any combination of the foregoing. More specific examples of the computer readable storage medium may include, but are not limited to: an electrical connection having one or more wires, a portable computer diskette, a hard disk, a Random Access Memory (RAM), a read-only memory (ROM), an erasable programmable read-only memory (EPROM or flash memory), an optical fiber, a portable compact disc read-only memory (CD-ROM), an optical storage device, a magnetic storage device, or any suitable combination of the foregoing. In the present invention, a computer readable storage medium may be any tangible medium that can contain, or store a program for use by or in connection with an instruction execution system, apparatus, or device. In the present invention, however, a computer readable signal medium may include a propagated data signal with computer readable program code embodied therein, for example, in baseband or as part of a carrier wave. Such a propagated data signal may take many forms, including, but not limited to, electro-magnetic, optical, or any suitable combination thereof. A computer readable signal medium may also be any computer readable medium that is not a computer readable storage medium and that can communicate, propagate, or transport a program for use by or in connection with an instruction execution system, apparatus, or device. Program code embodied on a computer readable medium may be transmitted using any appropriate medium, including but not limited to: wireless, wire, fiber optic cable, RF, etc., or any suitable combination of the foregoing.
The flowchart and block diagrams in the figures illustrate the architecture, functionality, and operation of possible implementations of systems, methods and computer program products according to various embodiments of the present invention. In this regard, each block in the flowchart or block diagrams may represent a module, segment, or portion of code, which comprises one or more executable instructions for implementing the specified logical function(s). It should also be noted that, in some alternative implementations, the functions noted in the block may occur out of the order noted in the figures. For example, two blocks shown in succession may, in fact, be executed substantially concurrently, or the blocks may sometimes be executed in the reverse order, depending upon the functionality involved. It will also be noted that each block of the block diagrams or flowchart illustration, and combinations of blocks in the block diagrams or flowchart illustration, can be implemented by special purpose hardware-based systems which perform the specified functions or acts, or combinations of special purpose hardware and computer instructions.
The units described in the embodiments of the present invention may be implemented by software or hardware. The described units may also be provided in a processor, and may be described as: a processor includes a transmitting unit, an obtaining unit, a determining unit, and a first processing unit. The names of these units do not in some cases constitute a limitation to the unit itself, and for example, the sending unit may also be described as a "unit sending a picture acquisition request to a connected server".
Exemplary embodiments of the present invention are specifically illustrated and described above. It is to be understood that the invention is not limited to the precise construction, arrangements, or instrumentalities described herein; on the contrary, the invention is intended to cover various modifications and equivalent arrangements included within the spirit and scope of the appended claims.
Claims (10)
1. A clinical trial data processing system, wherein the clinical trial data processing system comprises a clinical trial data management system and a hospital information system; wherein,
the clinical test data management system is used for acquiring the project information of clinical test projects and synchronizing the project information of the clinical test projects to the hospital information system;
the hospital information system is used for receiving the project information of the clinical test project, screening a patient library according to the project information of the clinical test project to obtain a target patient, adding the target patient as a target subject corresponding to the clinical test project and adding prescription information of the target subject, and synchronizing the subject information of the target subject and the prescription information thereof to the clinical test data management system;
the clinical trial data management system is used for receiving the subject information of the target subject and prescription information thereof and dispensing the medicine for the target subject according to the prescription information.
2. The clinical trial data processing system of claim 1, wherein the clinical trial data management system is further configured to receive subject information for the target subject and generate a clinical trial visit reminder based on the project information and the subject information.
3. The clinical trial data processing system of claim 1,
the clinical trial data management system is further used for determining the cost information of the target subject according to the prescription information of the target subject and synchronizing the cost information to the hospital information system;
the hospital information system is used for receiving the expense information of the target subject and carrying out the exemption treatment on the expense information.
4. The clinical trial data processing system according to claim 1 or 2, wherein the item information of the clinical trial item includes trial grouping conditions of the clinical trial item;
the clinical test data management system is specifically used for synchronizing the test grouping conditions of the clinical test items to the hospital information system;
the hospital information system is specifically used for receiving the test grouping conditions of the clinical test items, and screening target patients meeting the test grouping conditions from a patient bank according to the test grouping conditions.
5. The clinical trial data processing system according to claim 1 or 2, wherein the item information of the clinical trial item includes forbidden drug information corresponding to the clinical trial item;
the hospital information system is used for determining prescription information of the target subject according to forbidden medicine information corresponding to the clinical test items, and the prescription information comprises medical orders and medicine information.
6. The clinical trial data processing system of claim 2, wherein the clinical trial data management system is configured to obtain interview information of the target subject; and analyzing the visit information of the target subject to obtain the test effect of the clinical test item.
7. The clinical trial data processing system of claim 1, wherein the item information for the clinical trial items is synchronized to the hospital information system via an interface, and the prescription information is synchronized to the clinical trial data management system via an interface.
8. A method of processing clinical trial data, comprising:
the method comprises the following steps that a clinical test data management system obtains project information of a clinical test project and synchronizes the project information of the clinical test project to a hospital information system;
the hospital information system receives the project information of the clinical test project, screens a patient base according to the project information of the clinical test project to obtain a target patient, adds the target patient as a target subject corresponding to the clinical test project and adds prescription information of the target subject, and synchronizes the subject information of the target subject and the prescription information thereof to the clinical test data management system;
and the clinical test data management system receives the subject information of the target subject and the prescription information thereof, and dispenses the medicine for the target subject according to the prescription information.
9. An electronic device, comprising:
at least one processor;
storage means for storing at least one program which, when executed by the at least one processor, causes the at least one processor to carry out the method of claim 8.
10. A computer-readable storage medium having computer-executable instructions stored thereon, wherein the executable instructions, when executed by a processor, implement the method of claim 8.
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