细菌药物敏感性试验报告审核系统的设计与展现  

Design and implementation of bacterial drug sensitivity test report audit system

作　　者：杨志宁[1] 

机构地区：[1]山西省人民医院检验科,太原030012

出　　处：《中华临床实验室管理电子杂志》2017年第3期160-164,共5页Chinese Journal of Clinical Laboratory Management(Electronic Edition）

摘　　要：临床实验室面对复杂多变的耐药机制,细菌药物敏感性试验报告往往需要系统审核,但是人工操作极为繁琐,难度较大。我们通过建立一套规范的细菌名称、药敏名称,备注解释,特殊药敏数据库,在已有微生物信息系统的基础上,选用Excel+Visual Basic宏语言+应用程序编程接口(Excel+VBA+API)建立一套细菌药物敏感性试验报告审核系统,通过对微生物信息系统中已录数据的分析,实现了药物敏感性试验报告的规范化管理和微生物报告的自助审核,从而提高了工作效率,避免了疏失引起的差错,保证检验结果的准确性和完整性。The clinical laboratory is confronted with the complex drug resistance mechanism every day, and every bacterial drug sensitivity test report usually needs systematic audit, but the manual operation is very complicated and difficult. The standardized management of the drug sensitivity test was realized through the establishment of a set of standardized names of bacteria, drug sensitivity, and the interpretation of the special drug sensitivity database. On the basis of the existing microbial information system, Excel was used to make the database for audit and the working interface was developed. Through the microbial information system has been recorded in the data analysis. The VBA program and application programming interface （API） was used to analyze the bacterial drug sensitivity test. This can improve work efficiency, avoid the error, so as to ensure the accuracy and completeness of the test results.

关 键 词：药物敏感性试验 报告审核系统 多重耐药 

分 类 号：R197.3[医药卫生—卫生事业管理] TP391.13[医药卫生—公共卫生与预防医学]