期刊文献+

抗肿瘤药物处方专项点评实践的体会 被引量:6

Experience of Antineoplastic Prescription Special Review
原文传递
导出
摘要 目的:为提高医院抗肿瘤药物处方专项点评质量提供参考。方法:用回顾与对比法,就《北京市医疗机构处方专项点评指南(试行)》(以下简称《指南》)的工作表与自拟工作表对比分析,同时对抗肿瘤药物门诊处方点评工作中存在的问题进行讨论。结果:《指南》工作表1、表2和自拟工作表1、表2用药指标存在差异,前者是药品品种数统计指标,后者是合理用药国际调研处方指标;存在问题有药品说明书[包括同种药品不同厂家说明书不一致、药品说明书与美国国立综合癌症网络(NCCN)指南不一致、药品说明书与《新编药物学》(16版)不一致],处方前记项目设置缺失,人为分解处方。结论:专项处方点评质量的提升亟待药品说明书和指导性规范的完善,以及医院信息系统的有力支撑。 OBJECTIVE: To provide reference for the quality improvement of antineoplastic drugs prescription special review. METHODS: By review and comparison method, the worksheet of Prescription Special Review Guide in Beijing Medical Institutions (trial) (hereinafter referred to as the Guidelines) was compared with self-made one. The problems about outpatient prescription review for antineoplastic drugs were also discussed. RESULTS: The worksheet 1 and worksheet 2 of Guidelines were different from self-made worksheet 1 and worksheet 2; the former was drug type statistics index, and the latter was international research prescription indicators of rational drug use. The problems included: the package inserts of the same kinds of drugs from different manufacturers were different from one another; the package inserts were inconsistent with NCCN guidelines; the package inserts were inconsistent with 16 version of New Pharmacology; item record setting before prescribing missed; the prescription was decomposed artificially. CONCLUSIONS: The quality improvement of special prescription review requires promoting package inserts and guide specifications urgently, and needs strong HIS support.
出处 《中国药房》 CAS CSCD 2014年第42期4012-4015,共4页 China Pharmacy
关键词 抗肿瘤药物 处方 点评 Antineoplastic drugs Prescription Review
  • 相关文献

参考文献8

二级参考文献23

  • 1金宜纫,黄天木,杨一昆,熊惠周,刘伟平.卡铂的稳定性研究[J].中国医药工业杂志,1994,25(2):69-72. 被引量:14
  • 2胡夕春,蔡扬,杨新苗,李进.肿瘤化疗用药方法的研究进展[J].世界临床药物,2005,26(11):646-649. 被引量:19
  • 3李佩文.关于西医应用抗癌中成药的几点建议[J].中华肿瘤杂志,2006,28(12):949-950. 被引量:11
  • 4蔡卫民,袁克俭.静脉药物配制中心使用手册[M].北京:中国医药科技出版社,北京,2005:96.
  • 5高强.处方管理办法[S].卫生部第53号部长令.2007-02-14.
  • 6戴明,罗荣城.时间生物学在肿瘤学的研究进展[J].癌症进展,2007,5(4):338-345. 被引量:12
  • 7国家食品药品监督管理局.《药品注册管理办法》[EB/OL].http://www.sfda.gov.cn/WS01/CLD053/24529.html,2007-07-10.
  • 8Food and Drug Administration, HHS. Requirements on content and format of labeling for human prescription drug and biological products. Final rule[ J]. Fed Regist,2006 ;71:3921 - 3997.
  • 9国家食品药品监督管理局.《化学药品和治疗用生物制品说明书规范细则》[EB/OL].http://www.sfda.gov.cn/WS01/CL0844/10528.html.2006-05-10.
  • 10陈新谦,金有豫,汤光-寺斤编药物学[M].第16版.北京:人民卫生出版社,2007:14.

共引文献85

同被引文献40

引证文献6

二级引证文献38

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部