首页> 外国专利> THREE-LEVEL INFORMATION CHECK PROCESSING SYSTEM AND METHOD FOR BLOOD FOR CLINICAL USE

THREE-LEVEL INFORMATION CHECK PROCESSING SYSTEM AND METHOD FOR BLOOD FOR CLINICAL USE

机译:临床用血液三级信息检查处理系统及方法

摘要

A three-level information check processing method for blood for clinical use. The method comprises the steps of: acquiring, from a test database (22), a blood type and a test result of a patient, receiving, from a doctor's client (3), transfusion information about the patient determined by a doctor according to the blood type and the test result of the patient, and generating, according to the transfusion information, a pre-transfusion evaluation form and a transfusion treatment informed consent form (S31); receiving transfusion request information from the doctor's client (3), and generating a transfusion application form according to transfusion request information (S32); according to the transfusion purpose and a blood transfusion volume in the transfusion information, establishing a checking, signing and issuing configuration process node of the transfusion application form (S33); according to the checking, signing and issuing configuration process node of the transfusion application form, hierarchically sending the transfusion application form to a corresponding doctor's client (3) for checking, signing and issuing (S34); and when the transfusion application form is in a checking, signing and issuing completion state, generating a specimen barcode, so that a user prints the specimen barcode and completes blood specimen collection (S35). By means of the method, hierarchical checking, signing and issuing are carried out before clinical transfusion, thereby ensuring the reasonability of clinical blood use.
机译:用于临床的血液的三级信息检查处理方法。该方法包括以下步骤:从测试数据库(22)获取患者的血型和测试结果,从医生的客户(3)接收由医生根据患者确定的关于患者的输血信息。根据患者的血型和检查结果,根据输血信息生成输血前评价表和输血治疗知情同意书(S31);从医生的客户端接收输血请求信息(3),并根据输血请求信息生成输血申请表(S32);根据输血目的和输血信息中的输血量,建立输血申请表的核对,签发和下发配置过程节点(S33);根据所述输液申请表的签核签发配置过程节点,将所述输血申请表分级发送给相应的医生客户端(3)进行签核签发(S34);然后,当输液申请表处于检查,签字和签发完成状态时,生成标本条形码,以便用户打印标本条形码并完成血液标本采集(S35)。通过这种方法,在临床输血之前进行了分级检查,签名和签发,从而确保了临床血液使用的合理性。

著录项

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号