摘要
我国Direct to Patient(DTP)药房的发展可追溯到20世纪六七十年代,但由于当时的经济体制未能得到进一步的发展。进入21世纪后,由于社会疾病谱的转变、药品临床化时间过长以及新一轮医改启动等原因为DTP药房的发展带来了市场与政策的优势,但目前而言其缺乏顶层的行业规范,相关准入标准过高以及患者认知度等在一定程度上制约了DTP药房的发展。因此,从顶层设计的行业规章制度入手、加强DTP药房与第三方物流企业的合作以及增加自身的服务内容是保证DTP药房发展的关键。
The development of China’s Direct to Patient(DTP) pharmacy can be traced back to the 1960 s and 1970 s, but the economic system at that time could not be further developed. After entering the 21 st century, due to the transformation of social disease spectrum, the long time of drug clinicalization and the launch of a new round of medical reform, the market and policy advantages have been brought about by the development of DTP pharmacies. However, at present, it lacks the top-level industry norms. The excessive access standards and patient awareness have restricted the development of DTP pharmacies to some extent. Therefore, starting from the top-level design of industry rules and regulations, strengthening the cooperation between DTP pharmacies and third-party logistics companies and increasing their own service content is the key to ensuring the development of DTP pharmacies.
作者
周翔
陈超然
ZHOU Xiang;CHEN Chao-ran(College of Nursing and Health, Henan University, Kaifeng, Henan Province, 475004 China)
出处
《中国卫生产业》
2019年第19期191-193,共3页
China Health Industry
关键词
DTP药房
新医改
准入标准
DTP pharmacy
New medical reform
Access criteria