WO2019024282A1 - 临床用血三级审核信息处理系统和方法 - Google Patents

临床用血三级审核信息处理系统和方法 Download PDF

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Publication number
WO2019024282A1
WO2019024282A1 PCT/CN2017/108186 CN2017108186W WO2019024282A1 WO 2019024282 A1 WO2019024282 A1 WO 2019024282A1 CN 2017108186 W CN2017108186 W CN 2017108186W WO 2019024282 A1 WO2019024282 A1 WO 2019024282A1
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WIPO (PCT)
Prior art keywords
blood
blood transfusion
transfusion
information
patient
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English (en)
French (fr)
Inventor
张贯京
魏琼东
王海荣
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Shenzhen Qianhai AnyCheck Information Technology Co Ltd
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Shenzhen Qianhai AnyCheck Information Technology Co Ltd
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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
    • G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
    • G16H10/40—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for data related to laboratory analysis, e.g. patient specimen analysis
    • G—PHYSICS
    • G06—COMPUTING OR CALCULATING; COUNTING
    • G06Q—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES; SYSTEMS OR METHODS SPECIALLY ADAPTED FOR ADMINISTRATIVE, COMMERCIAL, FINANCIAL, MANAGERIAL OR SUPERVISORY PURPOSES, NOT OTHERWISE PROVIDED FOR
    • G06Q50/00—Information and communication technology [ICT] specially adapted for implementation of business processes of specific business sectors, e.g. utilities or tourism
    • G06Q50/10—Services
    • G06Q50/22—Social work or social welfare, e.g. community support activities or counselling services
    • 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
    • G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
    • G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
    • G16H20/17—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
    • 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
    • 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 invention relates to the field of medical information technology, and in particular, to a clinical blood three-level audit information processing system and method.
  • the main purpose of the embodiments of the present invention is to provide a clinical blood three-level audit information processing system and method, which aims to assist a clinician to implement blood test through a clinical blood audit system.
  • an embodiment of the present invention provides a clinical blood three-level audit information processing system, which runs in a medical cloud server, where the medical cloud server is connected to a database server, and the medical cloud server also passes The communication network is connected to a plurality of doctor clients, and the database server includes a verification database, and the clinical blood level three-level audit information processing system includes:
  • a pre-transfusion evaluation module configured to obtain a blood type and a test result of the patient from the test database, and receive, from the doctor client, blood transfusion information of the patient determined by the doctor according to the blood type of the patient and the test result, and according to the The blood transfusion information generates a pre-transfusion assessment form and an informed consent form for transfusion therapy;
  • the blood transfusion information includes a blood type, a blood component, and a blood transfusion amount;
  • a blood transfusion application module configured to receive blood transfusion request information from a doctor client, and generate a blood transfusion request form according to the blood transfusion request information;
  • the blood transfusion request information includes a blood transfusion request clinical department information, a clinician information, a blood transfusion use, a patient Basic information and blood transfusion information;
  • an audit node creating module configured to establish, according to the blood transfusion use and the blood transfusion amount in the blood transfusion information, an auditing issuance configuration process node of the blood transfusion request form;
  • a grading audit issuance module configured to send the blood transfusion request form to the corresponding doctor client for review and issuance according to the auditing issuance configuration process node of the blood transfusion application form;
  • a specimen barcode management module configured to generate a specimen barcode after the blood transfusion application form completes the audit issuance status
  • the audit node creation module is specifically configured to:
  • the patient's auditing issuance configuration flow node corresponds to the superior physician and the department head;
  • the patient's auditing issuance configuration process node corresponds to the head of the department and the head of the medical department;
  • the hierarchical auditing and issuance module is specifically configured to:
  • the patient's blood transfusion application form is sent to the doctor's client corresponding to the superior doctor for examination and approval; after the audit is issued, the blood transfusion application form is marked for completion of the examination and issuance. ;
  • the patient's blood transfusion application form is sent to the doctor client corresponding to the superior doctor, and the doctor client corresponding to the superior doctor sends the information issued after the examination.
  • the patient's blood transfusion application form is sent to the corresponding doctor client of the department director, and the corresponding doctor's client sends the information issued through the audit, and then Send to the doctor's client corresponding to the medical department to review and issue the signature; after the completion of the examination and issuance, mark the blood transfusion application form for completion of the examination and issuance;
  • the blood transfusion application form is marked for completion of the examination and issuance.
  • the pre-transfusion assessment form includes the patient's blood type, test results, and blood transfusions.
  • the specimen barcode includes at least a serial number, patient basic information, and blood transfusion information.
  • the embodiment of the present invention further provides a clinical blood three-level audit information processing method, which is applied to a medical cloud server, where the medical cloud server is connected to a database server, and the medical cloud server is further connected through a communication network.
  • the plurality of doctor clients, the clinical blood three-level audit information processing method comprises the following steps:
  • the blood transfusion information includes blood type, blood composition and blood transfusion volume;
  • the blood transfusion request information includes blood transfusion requesting clinical department information, clinician information, blood transfusion use, patient basic information, and blood transfusion information;
  • the blood transfusion application form is sent to the corresponding doctor client for review and issuance;
  • a sample barcode is generated for the user to print the sample barcode and complete the blood sample collection.
  • the step of establishing an auditing issuance configuration process node of the blood transfusion request according to the blood transfusion use and the blood transfusion amount in the blood transfusion information includes:
  • the patient's auditing issuance configuration flow node corresponds to the superior physician and the department head;
  • the patient's auditing issuance configuration process node corresponds to the head of the department and the head of the medical department;
  • the patient's audit issuance configuration flow node is an empty node.
  • the step of sending the blood transfusion request form to the corresponding doctor client for verification and issuance according to the auditing issuance configuration process node of the blood transfusion application form includes:
  • the patient's blood transfusion application form is sent to the doctor's client corresponding to the superior doctor for examination and approval; after the audit is issued, the blood transfusion application form is marked for completion of the examination and issuance. ;
  • the patient's blood transfusion application form is sent to the doctor client corresponding to the superior doctor, and the doctor client corresponding to the superior doctor sends the information issued after the examination. , and then sent to the corresponding doctor's client for review and issuance; after the completion of the audit issuance, mark the blood transfusion application form for completion of the examination and issuance;
  • the patient's blood transfusion application form is sent to the corresponding doctor client of the department director, and the corresponding doctor's client sends the information issued through the audit, and then Send to the doctor's client corresponding to the medical department to review and issue the signature; after the completion of the examination and issuance, mark the blood transfusion application form for completion of the examination and issuance;
  • the blood transfusion application form is marked for completion of the examination and issuance.
  • the pre-transfusion assessment form includes the patient's blood type, test results, and blood transfusions.
  • the specimen barcode includes at least a serial number, patient basic information, and blood transfusion information.
  • the embodiment of the present invention performs pre-transfusion assessment and blood transfusion application according to the actual situation of the patient. Please, review node creation, grading audit issuance and specimen barcode management, and conduct grading audit and issuance before clinical blood transfusion to ensure the rationality of clinical blood use.
  • FIG. 1 is a schematic diagram of an application environment of a preferred embodiment of a clinical blood three-level audit information processing system of the present invention
  • FIG. 2 is a block diagram showing a preferred embodiment of a clinical blood three-level audit information processing system of the present invention
  • FIG. 3 is a flow chart of a preferred embodiment of the clinical blood three-level review method of the present invention.
  • FIG. 1 is a schematic diagram of an application environment of a preferred embodiment of a clinical blood three-level audit information processing system of the present invention.
  • the clinical blood three-level audit information processing system 10 runs in the medical cloud server 1, and the medical cloud server 1 is connected to the database server 2, and the connection between the medical cloud server 1 and the database server 2
  • a database connection for example, Open Database Connectivity (ODBC) and Java Database Connection (Java Data Base)
  • the medical cloud server 1 is also connected to a plurality of doctor clients 3 through the communication network 4.
  • the embodiment of the present invention is described by taking three doctor clients 3 as an example.
  • the user of the doctor client 3 may be a clinician or a superior doctor. , the role of director of the Department of Blood Transfusion.
  • the database server 2 includes a verification database 22.
  • the inspection database 22 is a database that acquires and stores inspection result data from an external inspection information system according to a blood component index, and the clinical blood three-level audit information processing system 10 acquires inspection result data from the inspection database 22, and based on the inspection result. The data determines the type of blood transfusion.
  • the communication network 4 may be a wired communication network or a wireless communication network.
  • the communication network 4 is preferably a wireless communication network, including but not limited to, a GSM network, a GPRS network, and a CDMA network.
  • Wireless transmission networks such as networks, TD-SCDMA networks, WiMAX networks, TD-LTE networks, FDD-LTE networks.
  • the clinical blood three-level audit information processing system 10 of the embodiment of the present invention implements business processes such as pre-transfusion testing, pre-transfusion assessment, informed consent signing, blood transfusion application and review.
  • FIG. 2 is a schematic diagram of functional modules of a preferred embodiment of the clinical blood three-level audit information processing system of the present invention.
  • the clinical blood three-level audit information processing system 10 is applied to the medical cloud server 1, and the medical cloud server 1 includes, but is not limited to, a clinical blood three-level audit information processing system 10, and a communication unit. 11.
  • the communication unit 11 is a wireless communication interface with remote wireless communication function, for example, supporting G
  • Communication interfaces for communication technologies such as SM, GPRS, WCDMA, CDMA, TD-SCDMA, WiMAX, TD-LTE, and FDD-LTE.
  • the storage unit 12 may be a read only storage unit ROM, an electrically erasable storage unit EEPROM
  • flash memory unit FLASH or solid hard disk FLASH or solid hard disk.
  • the processing unit 13 may be a central processing unit (CPU), a microcontroller (MCU), a data processing chip, or an information processing unit having a data processing function.
  • CPU central processing unit
  • MCU microcontroller
  • data processing chip or an information processing unit having a data processing function.
  • the clinical blood three-level audit information processing system 10 includes a pre-transfusion evaluation module 101, a blood transfusion application module 102, an audit node creation module 103, a hierarchical audit issuance module 104, and a specimen barcode management module.
  • the module referred to in the present invention refers to a series of program instruction segments that can be executed by the processing unit 13 of the medical cloud server 1 and that can perform fixed functions, which are stored in the processing unit 13 of the medical cloud server 1.
  • the pre-transfusion evaluation module 101 is configured to obtain a blood type and a test result of the patient from the test database 22, and receive, from the doctor client 3, blood transfusion information of the patient determined by the doctor according to the blood type of the patient and the test result, and according to the The blood transfusion information generates a pre-transfusion assessment form and an informed consent form for transfusion therapy.
  • the blood transfusion information includes blood type, blood component, and blood transfusion amount.
  • the test results include, but are not limited to, the content of red blood cells RB C (Red Blood Cell), prothrombin time and total protein TP in blood.
  • the pre-transfusion evaluation module 101 provides an information input interface for the user, and the information input interface provides data selection items of the above test results, without manual entry, and only needs to select the size of each parameter by the mouse, the user Click the data save button to automatically jump to the next operation, ie root
  • a pre-transfusion assessment form and an informed consent form for the transfusion therapy are generated, and the informed consent form of the transfusion therapy is printed after the user clicks the print button for the patient or his family to sign.
  • the blood application for intraoperative application does not require a pre-transfusion assessment, ie, the pre-transfusion assessment module 101 need not be performed.
  • the pre-transfusion assessment form includes the patient's blood type, test results, and blood transfusion information.
  • the blood transfusion application module 102 is configured to receive blood transfusion request information from the doctor client, and generate a blood transfusion request form according to the blood transfusion request information.
  • the blood transfusion application form transmits blood transfusion request information to the doctor client by a clinician with a middle-level professional title according to the clinical blood specification.
  • the blood transfusion request information includes blood transfusion request clinical department information, clinician information, blood transfusion use, patient basic information, and blood transfusion information.
  • the blood transfusion application form includes a blood transfusion request message and a blood transfusion request form barcode.
  • the transfusion application barcode includes at least a serial number, patient basic information, and blood transfusion information.
  • the audit node creation module 103 is configured to establish an audit issuance configuration flow node of the blood transfusion request form according to the blood transfusion use and the blood transfusion amount in the blood transfusion information.
  • the patient's auditing issuance configuration flow node corresponds to the superior physician and the department head;
  • the patient's auditing issuance configuration process node corresponds to the head of the department and the head of the medical department;
  • the evaluation and issuance configuration node of the patient is an empty node, that is, the audit issuing node is not established.
  • the grading audit issuance module 104 is configured to send the blood transfusion application form to the corresponding doctor client 3 according to the auditing issuance configuration process of the blood transfusion application form.
  • the blood transfusion application form of the patient is sent to the doctor client 3 corresponding to the superior doctor for review and issuance; after the audit issuance is completed, the blood transfusion application form is marked for completion of the review. Issued
  • the patient's blood transfusion application form is sent to the doctor client 3 corresponding to the superior doctor, and the doctor client 3 corresponding to the superior doctor sends the approval certificate. After the information is sent, it is sent to the corresponding doctor's client 3 for review and issuance; after the completion of the audit issuance
  • the patient's blood transfusion application form is sent to the corresponding doctor client 3, and the corresponding doctor's client 3 sends the information issued after the examination.
  • the blood transfusion application form is marked for completion of the examination and issuance.
  • the specimen barcode management module 105 is configured to generate a specimen barcode for the user to print the specimen barcode and complete the blood specimen collection after the blood transfusion request form completes the audit issuance status.
  • the specimen barcode includes at least a serial number, basic patient information, and blood transfusion information.
  • the number of prints of the sample barcode can be set as needed.
  • the serial number includes the number of blood transfusions on the current day and the day of the patient.
  • the patient basic information includes the patient's name, gender, age, and bed number.
  • Embodiments of the present invention perform pre-transfusion assessment, blood transfusion application, and audit node creation for the actual situation of the patient.
  • grading audit issuance and specimen barcode management, and grading audit is issued before clinical blood transfusion to ensure the rationality of clinical blood use.
  • FIG. 3 it is a flow chart of a preferred embodiment of the clinical blood three-level review method of the present invention.
  • the clinical blood three-level audit information processing method is applied to the medical cloud server 1, and as shown in FIG. 1 and FIG. 2, the method includes the following steps:
  • Step S31 the pre-transfusion evaluation module 101 acquires the blood type and the test result of the patient from the test database 22, and receives the blood transfusion information of the patient determined by the doctor according to the blood type of the patient and the test result from the doctor client 3, and according to the blood transfusion The information generates a pre-transfusion assessment form and an informed consent form for transfusion therapy.
  • the blood transfusion information includes a blood type, a blood component, and a blood transfusion amount.
  • the test results include, but are not limited to, the content of red blood cell RBC (Red Blood Cell), prothrombin time and total protein TP in blood.
  • RBC Red Blood Cell
  • the pre-transfusion evaluation module 101 provides an information input interface for the user, and the information input interface provides data selection items of the above test results, without manual entry, and only needs to select the size of each parameter by the mouse, the user Click the data save button to automatically jump to the next operation, that is, according to the blood transfusion information sent by the doctor client 3, generate a pre-transfusion assessment form and blood transfusion therapy
  • the consent form is printed, and the blood transfusion treatment informed consent form is printed after the user clicks the print button for the patient or his family to sign.
  • the blood application for intraoperative application does not require a pre-transfusion assessment, ie, the pre-transfusion assessment module 101 need not be performed.
  • the pre-transfusion assessment form includes the patient's blood type, test results, and blood transfusion information.
  • Step S32 the blood transfusion application module 102 receives the blood transfusion request information from the doctor client, and generates a blood transfusion application form according to the blood transfusion request information.
  • the blood transfusion application form sends a blood transfusion request information to a doctor client by a clinical doctor with a middle-level professional title according to the clinical blood specification.
  • the blood transfusion request information includes blood transfusion request clinical department information, clinician information, blood transfusion use, patient basic information, and blood transfusion information.
  • the blood transfusion application form includes a blood transfusion request message and a blood transfusion request form barcode.
  • the blood transfusion application barcode includes at least a serial number, patient basic information, and blood transfusion information.
  • Step S33 the audit node creation module 103 establishes an audit issuance configuration flow node of the blood transfusion request form according to the blood transfusion use and the blood transfusion amount in the blood transfusion information.
  • the patient's auditing issuance configuration flow node corresponds to the superior physician and the department head;
  • the patient's auditing issuance configuration process node corresponds to the head of the department and the head of the medical department;
  • the evaluation and issuance configuration node of the patient is an empty node, that is, the audit issuing node is not established.
  • Step S34 the grading audit issuance module 104 sends the blood transfusion request form to the corresponding doctor client 3 according to the auditing issuance configuration process node of the blood transfusion application form.
  • the blood transfusion application form of the patient is sent to the doctor client 3 corresponding to the superior doctor for review and issuance; after the audit is issued, the blood transfusion request form is marked for completion of the review. Issued
  • the patient's blood transfusion request form is sent to The doctor client 3 corresponding to the superior doctor, after the doctor client 3 corresponding to the superior doctor sends the information issued through the audit, and then sends it to the corresponding doctor client 3 for review and issuance; after the audit is issued
  • the patient's blood transfusion application form is sent to the corresponding doctor client 3, and the corresponding doctor's client 3 sends the information issued after the examination.
  • the blood transfusion application form is marked for completion of the examination and issuance.
  • Step S35 the specimen barcode management module 105 generates a specimen barcode for the user to print the specimen barcode and complete the blood specimen collection after the blood transfusion request form completes the audit issuance status.
  • the sample barcode includes at least a serial number, basic patient information, and blood transfusion information.
  • the number of prints of the sample barcode can be set as needed.
  • the serial number includes the number of blood transfusions on the current day and the day of the patient.
  • the patient basic information includes the patient's name, gender, age, and bed number.
  • Embodiments of the present invention perform pre-transfusion assessment, blood transfusion application, and audit node creation for the actual situation of the patient.
  • grading audit issuance and specimen barcode management, and grading audit is issued before clinical blood transfusion to ensure the rationality of clinical blood use.
  • the embodiments of the present invention perform pre-transfusion assessment, blood transfusion application, audit node creation, grading audit issuance, and specimen barcode management according to the actual situation of the patient, and perform grading auditing and issuance before clinical blood transfusion, ensuring Rationality of clinical blood use.

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Abstract

一种临床用血三级审核信息处理方法，该方法包括步骤：从检验数据库（22）中获取患者的血型和检验结果，从医生客户端（3）接收医生根据患者的血型和检验结果确定的患者的输血信息，并根据所述输血信息生成输血前评估单以及输血治疗知情同意书（S31）；从医生客户端（3）接收输血请求信息，并根据输血请求信息生成输血申请单（S32）；按照输血用途以及输血信息中的输血量建立所述输血申请单的审核签发配置流程节点（S33）；按照该输血申请单的审核签发配置流程节点将所述输血申请单分级发送给对应的医生客户端（3）审核签发（S34）；在输血申请单为完成审核签发状态时，生成标本条码，以供用户打印所述标本条码并完成血液标本采集（S35）。以上方法对临床输血前进行分级审核签发，确保了临床用血的合理性。

Description

临床用血三级审核信息处理系统和方法 技术领域
[0001] 本发明涉及医疗信息化术领域， 尤其涉及一种临床用血三级审核信息处理系统 和方法。
背景技术
[0002] 近年来， 随着我国医疗保障水平与范围的大幅提高， 医疗需求呈现 "井喷式"爆 发， 临床输血量平均增长超过 10%; 而我国人口正处于快速老齢化吋期， 无偿献 血基础相对薄弱， 献血率低于世界卫生组织所要求的 1%的最低水平， 各地结构 性、 季节性、 区域性缺血问题吋有发生， 血液供应紧张甚至呈现常态化趋势。 现阶段的血液供需矛盾已经影响到民众获得基本医疗服务的公平和可能， 引起 社会和舆论的高度关注。 但另一方面， 在血液供应紧张的同吋， 全国范围内 （ 包括三级医院） 广泛存在不同程度的不合理用血现象。 这些不必要的输血不仅 浪费宝贵的血液资源， 还可能给患者带来血液传染、 输血反应、 不利病情转归 甚至死亡的风险。 目前针对临床用血的审核方面不够严格且没有完善的审核系 统辅助临床医师进行用血审核。
技术问题
[0003] 本发明实施例的主要目的在于提供一种临床用血三级审核信息处理系统和方法 ， 旨在通过临床用血审核系统来辅助临床医师实现用血审核。
问题的解决方案
技术解决方案
[0004] 为实现上述目的， 本发明实施例提供了一种临床用血三级审核信息处理系统， 运行于医疗云服务器中， 所述医疗云服务器连接有数据库服务器， 所述医疗云 服务器还通过通信网络连接有多个医生客户端， 所述数据库服务器包括检验数 据库， 所述临床用血三级审核信息处理系统包括：
[0005] 输血前评估模块， 用于从检验数据库中获取患者的血型和检验结果， 从医生客 户端接收医生根据患者的血型和检验结果确定的患者的输血信息， 并根据所述 输血信息生成输血前评估单以及输血治疗知情同意书； 所述输血信息包括血型 、 血液成分和输血量；
[0006] 输血申请模块， 用于从医生客户端接收输血请求信息， 并根据输血请求信息根 据生成根据输血申请单； 所述输血请求信息包括输血请求临床科室信息、 临床 医生信息、 输血用途、 患者基本信息以及输血信息；
[0007] 审核节点创建模块， 用于按照输血用途以及输血信息中的输血量建立所述输血 申请单的审核签发配置流程节点；
[0008] 分级审核签发模块， 用于按照该输血申请单的审核签发配置流程节点将所述输 血申请单分级发送给对应的医生客户端审核签发；
[0009] 标本条码管理模块， 用于在输血申请单为完成审核签发状态吋， 生成标本条码
， 以供用户打印所述标本条码并完成血液标本采集。
[0010] 在一个较佳实施例中， 所述审核节点创建模块具体用于：
[0011] 假设同一患者一天的输血量为 X，
[0012] 当 X<800ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应为 上级医师；
[0013] 当 800ml≤X<1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节 点对应为上级医师和科主任；
[0014] 当 X≥1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应 为科主任、 医务部门领导；
[0015] 当输血用途为急救用血吋， 该患者的审核签发配置流程节点为空。
[0016] 在一个较佳实施例中， 所述分级审核签发模块具体用于：
[0017] 当 X<800ml且输血用途为手术用血吋， 将该患者的输血申请单发送至上级医师 对应的医生客户端审核签发； 在审核签发完成后， 标记该输血申请单为完成审 核签发；
[0018] 当 800ml≤X<1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至 上级医师对应的医生客户端， 待上级医师对应的医生客户端发送通过审核签发 的信息后， 再发送给科主任对应的医生客户端审核签发； 在审核签发完成后， 标记该输血申请单为完成审核签发； [0019] 当 X≥1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至科主任 对应的医生客户端， 待科主任对应的医生客户端发送通过审核签发的信息后， 再发送给医务部门领导对应的医生客户端审核签发； 在审核签发完成后， 标记 该输血申请单为完成审核签发；
[0020] 当输血用途为急救用血吋， 标记该输血申请单为完成审核签发。
[0021] 在一个较佳实施例中， 所述输血前评估单包括患者的血型、 检验结果以及输血 f π息。
[0022] 在一个较佳实施例中， 所述标本条码至少包括序列号、 患者基本信息、 输血信 息。
[0023] 本发明实施例还提供了一种临床用血三级审核信息处理方法， 应用于医疗云服 务器中， 所述医疗云服务器连接有数据库服务器， 所述医疗云服务器还通过通 信网络连接有多个医生客户端， 所述临床用血三级审核信息处理方法包括如下 步骤：
[0024] 从检验数据库中获取患者的血型和检验结果， 从医生客户端接收医生根据患者 的血型和检验结果确定的患者的输血信息， 并根据所述输血信息生成输血前评 估单以及输血治疗知情同意书； 所述输血信息包括血型、 血液成分和输血量；
[0025] 从医生客户端接收输血请求信息， 并根据输血请求信息根据生成根据输血申请 单； 所述输血请求信息包括输血请求临床科室信息、 临床医生信息、 输血用途 、 患者基本信息以及输血信息；
[0026] 按照输血用途以及输血信息中的输血量建立所述输血申请单的审核签发配置流 程节点；
[0027] 按照该输血申请单的审核签发配置流程节点将所述输血申请单分级发送给对应 的医生客户端审核签发；
[0028] 在输血申请单为完成审核签发状态吋， 生成标本条码， 以供用户打印所述标本 条码并完成血液标本采集。
[0029] 在一个较佳实施例中， 所述按照输血用途以及输血信息中的输血量建立所述输 血申请单的审核签发配置流程节点的步骤包括：
[0030] 假设同一患者一天的输血量为 X； [0031] 当 X<800ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应为 上级医师；
[0032] 当 800ml≤X<1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节 点对应为上级医师和科主任；
[0033] 当 X≥1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应 为科主任、 医务部门领导；
[0034] 当输血用途为急救用血吋， 该患者的审核签发配置流程节点为空节点。
[0035] 在一个较佳实施例中， 所述按照该输血申请单的审核签发配置流程节点将所述 输血申请单分级发送给对应的医生客户端审核签发的步骤包括：
[0036] 当 X<800ml且输血用途为手术用血吋， 将该患者的输血申请单发送至上级医师 对应的医生客户端审核签发； 在审核签发完成后， 标记该输血申请单为完成审 核签发；
[0037] 当 800ml≤X<1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至 上级医师对应的医生客户端， 待上级医师对应的医生客户端发送通过审核签发 的信息后， 再发送给科主任对应的医生客户端审核签发； 在审核签发完成后， 标记该输血申请单为完成审核签发；
[0038] 当 X≥1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至科主任 对应的医生客户端， 待科主任对应的医生客户端发送通过审核签发的信息后， 再发送给医务部门领导对应的医生客户端审核签发； 在审核签发完成后， 标记 该输血申请单为完成审核签发；
[0039] 当输血用途为急救用血吋， 标记该输血申请单为完成审核签发。
[0040] 在一个较佳实施例中， 所述输血前评估单包括患者的血型、 检验结果以及输血 f π息。
[0041] 在一个较佳实施例中， 所述标本条码至少包括序列号、 患者基本信息、 输血信 息。
发明的有益效果
有益效果
[0042] 相较于现有技术， 本发明实施例针对患者的实际情况进行输血前评估、 输血申 请、 审核节点创建、 分级审核签发以及标本条码管理， 对临床输血前进行分级 审核签发， 确保了临床用血的合理性。
对附图的简要说明
附图说明
[0043] 图 1是本发明临床用血三级审核信息处理系统较佳实施例的应用环境示意图；
[0044] 图 2是本发明临床用血三级审核信息处理系统较佳实施例的模块示意图；
[0045] 图 3是本发明临床用血三级审核方法的较佳实施例的流程图。
[0046] 本发明目的的实现、 功能特点及优点将结合实施例， 参照附图做进一步说明。
实施该发明的最佳实施例
本发明的最佳实施方式
[0047] 为更进一步阐述本发明为达成预定发明目的所采取的技术手段及功效， 以下结 合附图及较佳实施例， 对本发明的具体实施方式、 结构、 特征及其功效， 详细 说明如下。 应当理解， 此处所描述的具体实施例仅仅用以解释本发明， 并不用 于限定本发明。
[0048] 参照图 1所示， 图 1是本发明临床用血三级审核信息处理系统较佳实施例的应用 环境示意图。 在本实施例中， 所述临床用血三级审核信息处理系统 10运行于医 疗云服务器 1中， 医疗云服务器 1连接有数据库服务器 2， 所述医疗云服务器 1与 数据库服务器 2之间的连接为一种数据库连接， 例如可以为幵放式数据库连接 （ Open Database Connectivity , ODBC) 以及 Java数据库连接 (Java Data Base
Connectivity , JDBC) 。 所述医疗云服务器 1还通过通信网络 4连接有多个医生客 户端 3， 本发明实施例以三个医生客户端 3为例进行说明， 医生客户端 3的使用者 可以是临床医师、 上级医师、 输血科主任等角色。
[0049] 所述数据库服务器 2包括检验数据库 22。 所述检验数据库 22是根据血液成分指 标从外部检验信息系统中获取并存储检验结果数据的数据库， 所述临床用血三 级审核信息处理系统 10从检验数据库 22获取检验结果数据， 并根据检验结果数 据判断输血类型。
[0050] 所述通信网络 4可以是有线通信网络或无线通信网络。 在本实施例中， 所述通 信网络 4优选为无线通信网络， 包括但不限于， GSM网络、 GPRS网络、 CDMA 网络、 TD-SCDMA网络、 WiMAX网络、 TD-LTE网络、 FDD-LTE网络等无线传 输网络。
[0051] 本发明实施例所述临床用血三级审核信息处理系统 10实现了输血前检验、 输血 前评估、 知情同意书签署、 输血申请和审核等业务过程。
[0052] 参照图 2所示， 图 2是本发明临床用血三级审核信息处理系统的较佳实施例的功 能模块示意图。 在本实施例中， 所述临床用血三级审核信息处理系统 10应用于 医疗云服务器 1中， 该医疗云服务器 1包括， 但不仅限于， 临床用血三级审核信 息处理系统 10、 通信单元 11、 存储单元 12及处理单元 13。
[0053] 所述通信单元 11为一种具有远程无线通讯功能的无线通讯接口， 例如， 支持 G
SM、 GPRS、 WCDMA、 CDMA、 TD-SCDMA、 WiMAX、 TD-LTE、 FDD-LTE 等通讯技术的通讯接口。
[0054] 所述存储单元 12可以为一种只读存储单元 ROM, 电可擦写存储单元 EEPROM
、 快闪存储单元 FLASH或固体硬盘等。
[0055] 所述的处理单元 13可以为一种中央处理器 （Central Processing Unit, CPU) 、 微控制器 （MCU) 、 数据处理芯片、 或者具有数据处理功能的信息处理单元。
[0056] 所述临床用血三级审核信息处理系统 10包括输血前评估模块 101、 输血申请模 块 102、 审核节点创建模块 103、 分级审核签发模块 104以及标本条码管理模块 10
5。 本发明所称的模块是指一种能够被医疗云服务器 1的处理单元 13执行并且能 够完成固定功能的一系列程序指令段， 其存储在医疗云服务器 1的处理单元 13中
[0057] 所述输血前评估模块 101， 用于从检验数据库 22中获取患者的血型和检验结果 ， 从医生客户端 3接收医生根据患者的血型和检验结果确定的患者的输血信息， 并根据所述输血信息生成输血前评估单以及输血治疗知情同意书。 所述输血信 息包括血型、 血液成分和输血量。 所述检验结果包括但不限于血液中红细胞 RB C (Red Blood Cell) 的含量、 凝血酶原吋间 PT (Prothrombin Time) 和总蛋白 TP 的含量。 在本发明实施例中， 输血前评估模块 101为用户提供信息录入界面， 该 信息录入界面提供了上述检验结果的数据选择项， 无需手动录入， 只需鼠标选 择每个参数的大小即可， 用户点击数据保存按钮后自动跳转至下一操作， 即根 据医生客户端 3发送的输血信息， 生成输血前评估单以及输血治疗知情同意书， 并在用户点击打印按钮后打印所述输血治疗知情同意书， 供患者或其家属签署 。 在其他实施例中， 手术中申请用血无需进行输血前评估， 即无需执行输血前 评估模块 101。 所述输血前评估单包括患者的血型、 检验结果以及输血信息。
[0058] 输血申请模块 102， 用于从医生客户端接收输血请求信息， 并根据输血请求信 息根据生成根据输血申请单。 在本发明实施例中， 所述输血申请单根据临床用 血规范， 由具有中级职称的临床医师在医生客户端发送输血请求信息。 所述输 血请求信息包括输血请求临床科室信息、 临床医生信息、 输血用途、 患者基本 信息以及输血信息。 所述输血申请单包括输血请求信息和输血申请单条码。 所 述输血申请单条码至少包括序列号、 患者基本信息和输血信息。
[0059] 审核节点创建模块 103， 用于按照输血用途以及输血信息中的输血量建立所述 输血申请单的审核签发配置流程节点。
[0060] 在本发明实施例中， 假设同一患者一天的输血量为 X；
[0061] 当 X<800ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点仅对应 为上级医师；
[0062] 当 800ml≤X<1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节 点对应为上级医师和科主任；
[0063] 当 X≥1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应 为科主任、 医务部门领导；
[0064] 当输血用途为急救用血吋， 该患者的审核签发配置流程节点为空节点， 即不用 建立审核签发节点。
[0065] 分级审核签发模块 104， 用于按照该输血申请单的审核签发配置流程节点将所 述输血申请单分级发送给对应的医生客户端 3审核签发。
[0066] 当 X<800ml且输血用途为手术用血吋， 将该患者的输血申请单发送至上级医师 对应的医生客户端 3审核签发； 在审核签发完成后， 标记该输血申请单为完成审 核签发；
[0067] 当 800ml≤X<1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至 上级医师对应的医生客户端 3， 待上级医师对应的医生客户端 3发送通过审核签 发的信息后， 再发送给科主任对应的医生客户端 3审核签发； 在审核签发完成后
， 标记该输血申请单为完成审核签发；
[0068] 当 X≥1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至科主任 对应的医生客户端 3， 待科主任对应的医生客户端 3发送通过审核签发的信息后
， 再发送给医务部门领导对应的医生客户端 3审核签发； 在审核签发完成后， 标 记该输血申请单为完成审核签发；
[0069] 当输血用途为急救用血吋， 标记该输血申请单为完成审核签发。
[0070] 标本条码管理模块 105， 用于在输血申请单为完成审核签发状态吋， 生成标本 条码， 以供用户打印所述标本条码并完成血液标本采集。
[0071] 在本发明实施例中， 所述标本条码至少包括序列号、 患者基本信息、 输血信息
。 本发明实施例根据需要可以设置标本条码的打印数量。
[0072] 在本发明实施例中， 所述序列号包括当前吋间和患者当天的输血次数。 所述患 者基本信息包括患者姓名、 性别、 年齢、 床位号。
[0073] 本发明实施例针对患者的实际情况进行输血前评估、 输血申请、 审核节点创建
、 分级审核签发以及标本条码管理， 对临床输血前进行分级审核签发， 确保了 临床用血的合理性。
[0074] 参照图 3所示， 是本发明临床用血三级审核方法的较佳实施例的流程图。 在本 实施例中， 所述临床用血三级审核信息处理方法应用于医疗云服务器 1中， 结合 图 1和图 2所示， 该方法包括以下步骤：
[0075] 步骤 S31， 输血前评估模块 101从检验数据库 22中获取患者的血型和检验结果， 从医生客户端 3接收医生根据患者的血型和检验结果确定的患者的输血信息， 并 根据所述输血信息生成输血前评估单以及输血治疗知情同意书。
[0076] 所述输血信息包括血型、 血液成分和输血量。 所述检验结果包括但不限于血液 中红细胞 RBC (Red Blood Cell) 的含量、 凝血酶原吋间 PT (Prothrombin Time) 和总蛋白 TP的含量。 在本发明实施例中， 输血前评估模块 101为用户提供信息录 入界面， 该信息录入界面提供了上述检验结果的数据选择项， 无需手动录入， 只需鼠标选择每个参数的大小即可， 用户点击数据保存按钮后自动跳转至下一 操作， 即根据医生客户端 3发送的输血信息， 生成输血前评估单以及输血治疗知 情同意书， 并在用户点击打印按钮后打印所述输血治疗知情同意书， 供患者或 其家属签署。 在其他实施例中， 手术中申请用血无需进行输血前评估， 即无需 执行输血前评估模块 101。 所述输血前评估单包括患者的血型、 检验结果以及输 血信息。
[0077] 步骤 S32， 输血申请模块 102从医生客户端接收输血请求信息， 并根据输血请求 信息根据生成根据输血申请单。
[0078] 在本发明实施例中， 所述输血申请单根据临床用血规范， 由具有中级职称的临 床医师在医生客户端发送输血请求信息。 所述输血请求信息包括输血请求临床 科室信息、 临床医生信息、 输血用途、 患者基本信息以及输血信息。 所述输血 申请单包括输血请求信息和输血申请单条码。 所述输血申请单条码至少包括序 列号、 患者基本信息和输血信息。
[0079] 步骤 S33， 审核节点创建模块 103按照输血用途以及输血信息中的输血量建立所 述输血申请单的审核签发配置流程节点。
[0080] 在本发明实施例中， 假设同一患者一天的输血量为 X；
[0081] 当 X<800ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点仅对应 为上级医师；
[0082] 当 800ml≤X<1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节 点对应为上级医师和科主任；
[0083] 当 X≥1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应 为科主任、 医务部门领导；
[0084] 当输血用途为急救用血吋， 该患者的审核签发配置流程节点为空节点， 即不用 建立审核签发节点。
[0085] 步骤 S34， 分级审核签发模块 104按照该输血申请单的审核签发配置流程节点将 所述输血申请单分级发送给对应的医生客户端 3审核签发。
[0086] 当 X<800ml且输血用途为手术用血吋， 将该患者的输血申请单发送至上级医师 对应的医生客户端 3审核签发； 在审核签发完成后， 标记该输血申请单为完成审 核签发；
[0087] 当 800ml≤X<1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至 上级医师对应的医生客户端 3， 待上级医师对应的医生客户端 3发送通过审核签 发的信息后， 再发送给科主任对应的医生客户端 3审核签发； 在审核签发完成后
， 标记该输血申请单为完成审核签发；
[0088] 当 X≥1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送至科主任 对应的医生客户端 3， 待科主任对应的医生客户端 3发送通过审核签发的信息后
， 再发送给医务部门领导对应的医生客户端 3审核签发； 在审核签发完成后， 标 记该输血申请单为完成审核签发；
[0089] 当输血用途为急救用血吋， 标记该输血申请单为完成审核签发。
[0090] 步骤 S35， 标本条码管理模块 105在输血申请单为完成审核签发状态吋， 生成标 本条码， 以供用户打印所述标本条码并完成血液标本采集。
[0091] 在本发明实施例中， 所述标本条码至少包括序列号、 患者基本信息、 输血信息
。 本发明实施例根据需要可以设置标本条码的打印数量。
[0092] 在本发明实施例中， 所述序列号包括当前吋间和患者当天的输血次数。 所述患 者基本信息包括患者姓名、 性别、 年齢、 床位号。
[0093] 本发明实施例针对患者的实际情况进行输血前评估、 输血申请、 审核节点创建
、 分级审核签发以及标本条码管理， 对临床输血前进行分级审核签发， 确保了 临床用血的合理性。
[0094] 本领域技术人员可以理解， 上述实施方式中各种方法的全部或部分步骤可以通 过相关程序指令完成， 该程序可以存储于计算机可读存储介质中， 存储介质可 以包括： 只读存储器、 随机存储器、 磁盘或光盘等。
[0095] 以上仅为本发明的较佳实施例， 并非因此限制本发明的专利范围， 凡是利用本 发明说明书及附图内容所作的等效结构或等效流程变换， 或直接或间接运用在 其他相关的技术领域， 均同理包括在本发明的专利保护范围内。
工业实用性
[0096] 相较于现有技术， 本发明实施例针对患者的实际情况进行输血前评估、 输血申 请、 审核节点创建、 分级审核签发以及标本条码管理， 对临床输血前进行分级 审核签发， 确保了临床用血的合理性。

Claims

权利要求书
[权利要求 1] 一种临床用血三级审核信息处理系统， 运行于医疗云服务器中， 所述 医疗云服务器连接有数据库服务器， 所述医疗云服务器还通过通信网 络连接有多个医生客户端， 其特征在于， 所述数据库服务器包括检验 数据库， 所述临床用血三级审核信息处理系统包括： 输血前评估模块 ， 用于从检验数据库中获取患者的血型和检验结果， 从医生客户端接 收医生根据患者的血型和检验结果确定的患者的输血信息， 并根据所 述输血信息生成输血前评估单以及输血治疗知情同意书； 所述输血信 息包括血型、 血液成分和输血量； 输血申请模块， 用于从医生客户 端接收输血请求信息， 并根据输血请求信息根据生成根据输血申请单 ； 所述输血请求信息包括输血请求临床科室信息、 临床医生信息、 输 血用途、 患者基本信息以及输血信息； 审核节点创建模块， 用于按照 输血用途以及输血信息中的输血量建立所述输血申请单的审核签发配 置流程节点； 分级审核签发模块， 用于按照该输血申请单的审核签发 配置流程节点将所述输血申请单分级发送给对应的医生客户端审核签 发； 标本条码管理模块， 用于在输血申请单为完成审核签发状态吋， 生成标本条码， 以供用户打印所述标本条码并完成血液标本采集。
[权利要求 2] 如权利要求 1所述的临床用血三级审核信息处理系统， 其特征在于， 所述审核节点创建模块具体用于： 假设同一患者一天的输血量为 X； 当 X<800ml且输血用途为手术用血吋， 该患者的审核签发配置流程节 点对应为上级医师； 当 800ml≤X<1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应为上级医师和科主任； 当 χ≥160 0ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应 为科主任和医务部门领导； 当输血用途为急救用血吋， 该患者的审核 签发配置流程节点为空节点。
[权利要求 3] 如权利要求 2所述的临床用血三级审核信息处理系统， 其特征在于， 所述分级审核签发模块具体用于： 当 X<800ml且输血用途为手术用血 吋， 将该患者的输血申请单发送至上级医师对应的医生客户端审核签 发； 在审核签发完成后， 标记该输血申请单为完成审核签发； 当 800 ml≤X<1600ml且输血用途为手术用血吋， 将该患者的输血申请单发送 至上级医师对应的医生客户端， 待上级医师对应的医生客户端发送通 过审核签发的信息后， 再发送给科主任对应的医生客户端审核签发； 在审核签发完成后， 标记该输血申请单为完成审核签发； 当 X≥1600 ml且输血用途为手术用血吋， 将该患者的输血申请单发送至科主任对 应的医生客户端， 待科主任对应的医生客户端发送通过审核签发的信 息后， 再发送给医务部门领导对应的医生客户端审核签发； 在审核签 发完成后， 标记该输血申请单为完成审核签发； 当输血用途为急救用 血吋， 标记该输血申请单为完成审核签发。
[权利要求 4] 如权利要求 1至 3任一项所述的临床用血三级审核信息处理系统， 其特 征在于， 所述输血前评估单包括患者的血型、 检验结果以及输血信息
[权利要求 5] 如权利要求 1至 3任一项所述的临床用血三级审核信息处理系统， 其特 征在于， 所述标本条码至少包括序列号、 患者基本信息、 输血信息。
[权利要求 6] —种临床用血三级审核信息处理方法， 应用于医疗云服务器中， 所述 医疗云服务器连接有数据库服务器， 所述医疗云服务器还通过通信网 络连接有多个医生客户端， 其特征在于， 所述临床用血三级审核信息 处理方法包括如下步骤： 从检验数据库中获取患者的血型和检验结果 ， 从医生客户端接收医生根据患者的血型和检验结果确定的患者的输 血信息， 并根据所述输血信息生成输血前评估单以及输血治疗知情同 意书； 所述输血信息包括血型、 血液成分和输血量； 从医生客户端接 收输血请求信息， 并根据输血请求信息根据生成根据输血申请单； 所 述输血请求信息包括输血请求临床科室信息、 临床医生信息、 输血用 途、 患者基本信息以及输血信息； 按照输血用途以及输血信息中的输 血量建立所述输血申请单的审核签发配置流程节点； 按照该输血申请 单的审核签发配置流程节点将所述输血申请单分级发送给对应的医生 客户端审核签发； 在输血申请单为完成审核签发状态吋， 生成标本条 码， 以供用户打印所述标本条码并完成血液标本采集。
如权利要求 6所述的临床用血三级审核信息处理方法， 其特征在于， 所述按照输血用途以及输血信息中的输血量建立所述输血申请单的审 核签发配置流程节点的步骤包括： 假设同一患者一天的输血量为 X； 当 X<800ml且输血用途为手术用血吋， 该患者的审核签发配置流程节 点对应为上级医师； 当 800ml≤X<1600ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应为上级医师和科主任； 当 χ≥160 0ml且输血用途为手术用血吋， 该患者的审核签发配置流程节点对应 为科主任和医务部门领导； 当输血用途为急救用血吋， 该患者的审核 签发配置流程节点为空。
如权利要求 7所述的临床用血三级审核信息处理方法， 其特征在于， 所述按照该输血申请单的审核签发配置流程节点将所述输血申请单分 级发送给对应的医生客户端审核签发的步骤包括： 当 X<800ml且输血 用途为手术用血吋， 将该患者的输血申请单发送至上级医师对应的医 生客户端审核签发； 在审核签发完成后， 标记该输血申请单为完成审 核签发； 当 800ml≤X<1600ml且输血用途为手术用血吋， 将该患者的 输血申请单发送至上级医师对应的医生客户端， 待上级医师对应的医 生客户端发送通过审核签发的信息后， 再发送给科主任对应的医生客 户端审核签发； 在审核签发完成后， 标记该输血申请单为完成审核签 发； 当 X≥1600ml且输血用途为手术用血吋， 将该患者的输血申请单 发送至科主任对应的医生客户端， 待科主任对应的医生客户端发送通 过审核签发的信息后， 再发送给医务部门领导对应的医生客户端审核 签发； 在审核签发完成后， 标记该输血申请单为完成审核签发； 当输 血用途为急救用血吋， 标记该输血申请单为完成审核签发。
如权利要求 6至 8任一项所述的临床用血三级审核信息处理方法， 其特 征在于， 所述输血前评估单包括患者的血型、 检验结果以及输血信息 如权利要求 6至 8任一项所述的临床用血三级审核信息处理方法， 其特 征在于， 所述标本条码至少包括序列号、 患者基本信息、 输血信息
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