提高中药注射剂不良反应/不良事件文献报告质量

Translated title of the contribution: Improving the quality of reporting of adverse events and adverse drug reactions to Chinese medicine injections

卞兆祥*, 田皓瑶, 高琳, 商洪才, 吴泰相, 李幼平, 张伯礼, 宋丽

*Corresponding author for this work

Research output: Contribution to journalJournal articlepeer-review

Abstract

目的: 中药注射剂(CMI)的不良反应(ADR)/ 不良事件(AE)屡有发生,临床报告本身的质量直接影响读者对ADR/AE 的充分了解。
方法: 计算机检索中国期刊全文数据库(CJN,1994 ~ 2009)和中文科技期刊数据库(VIP,1989 ~ 2009),获取有关鱼腥草注射剂的ADR/AE 报告,用自行设计的中药注射剂ADR/AE 报告质量评价表进行质量评价。
结果: 经文献检索共获得与鱼腥草注射液相关的210 篇ADR/AE 文献,其中ADR/AE 病例报告175 篇,来自ADR 监测中心的报告7 篇,医疗单位的综合报告28 篇。评价结果发现:针对ADR/AE 病例基本项目的报告很不全面,有很多与ADR/AE 发生相关的关键数据缺失。
结论:  应尽快建立中药注射剂ADR/AE 报告规范;建立ADR/AE 的汇报注册制度,为每一例严重中药注射剂ADR/AE 独立编号注册,做到有案可查。同时,国家药监部门及期刊杂志应大力宣传ADR/AE 发表规范,促进其充分使用,这样才能真正提高ADR/AE 文献的质量,避免临床ADR/AE 格式不规范、关键信息数据缺失等突出问题。

Translated title of the contributionImproving the quality of reporting of adverse events and adverse drug reactions to Chinese medicine injections
Original languageChinese (Simplified)
Pages (from-to)176-181
Number of pages6
Journal中国循证医学杂志
Volume10
Issue number2
DOIs
Publication statusPublished - Feb 2010

Scopus Subject Areas

  • Medicine(all)

User-Defined Keywords

  • Adverse drug reaction
  • Adverse event
  • Reporting quality
  • Yuxingcao injection

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