静脉用药物调配残留量的控制  

Quality Control of Drug Residues in Intravenous Drug Admixture

作　　者：唐威[1] 程姣[1] 王未 李轶[1] 

机构地区：[1]苏州大学附属第一医院药学部,苏州215006

出　　处：《药学与临床研究》2018年第1期69-70,共2页Pharmaceutical and Clinical Research

摘　　要：对静脉药物调配中心的药物调配残留量进行质量控制,旨在保障输液的有效性。通过分析3年来残留量质量控制结果,发现药品调配残留量超标率为7.0%,残留量主要影响因素有:调配人员专业知识、调配手法、劳动强度、责任意识,可以此为药品调配改进提供方向。Quality control of drug residue in intravenous drug admixture is carried out by the pharmacyintravenous admixture services for the efficiency of finished product infusion. It can be seen from theanalysis of the quality control within three years that the rate of drug residues exceeding standard was7.0% and the main influence factors were professional knowledge of pharmacy, dispensing skills, labourintensity and responsibility.

关 键 词：静脉药物 调配 残留量 质量控制 

分 类 号：R969.3[医药卫生—药理学]