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基于阳性结果错误率控制的药品不良反应信号检测方法 被引量:4

Signal Detection Methods Based on False Discovery Rate of Adverse Drug Reaction
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摘要 常用的药品不良反应信号检测方法均是基于不相称测定理论,这些方法在信号检测过程中发挥了重要的作用。然而目前的信号检测过程存在一些缺陷,如多重性问题等,导致信号检测的准确性降低。通过介绍多重性问题对信号检测准确性的影响,和目前解决该问题的常用方法,如阳性结果错误率(false discovery rate,FDR)方法等。 Conventional signal detection methods based on disproportionality analysis are playing an important role in the process of signal detection of adverse drug reaction. However, these methods have their own drawbacks and the detection results are influenced greatly by the multiple hypothesis testing. These problems should be solved through new analysis strategy. In this article, we present the impact of multiple hypothesis testing on the signal detection and introduce the false discovery rate (FDR) methods that should solve the problem.
出处 《中国药物警戒》 2014年第8期492-494,共3页 Chinese Journal of Pharmacovigilance
基金 国家自然科学基金资助项目(No.81373105 No.81202285 No.81072388) 2010年上海市领军人才计划(022) 上海市自然科学基金项目(12ZR1453700) 上海市循证公共卫生重点学科(12GWZX0602)
关键词 多重假设检验 信号检测 药品不良反应 阳性结果错误率 multiple hypothesis testing adverse drug reaction signal detection false discovery rate
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参考文献7

  • 1Amy Purrington.自发报告安全性数据库:FDA、WHO-UMC、Eudravigilance数据库[J].中国药物警戒,2009,6(6):382-384. 被引量:14
  • 2任经天,王胜锋,侯永芳,杜晓曦,李立明.常用药品不良反应信号检测方法介绍[J].中国药物警戒,2011,8(5):294-298. 被引量:72
  • 3CFDA.国家食品药品监督管理局发布2012年药品不良反应监测年度报告[EB/OL].http://www.sfda,gov.cn/WS01/CL0051/79058.html.
  • 4Evans S J,Waller P C,Davis S.Use of proportional reporting ratios(prrs)for signal generation from spontaneous adverse drug reaction reports[J].Pharmacoepidemiol Drug Saf,2001,10(6):483-486.
  • 5Bate A,Lindquist M,Edwards I R,et al.A bayesian neural net- work method for adverse drug reaction signal generation[J].Eur J Clin Pharmacol,1998,54(4):315-321.
  • 6Noren G N,Bate A,Orre R,et al.Extending the methods used to screen the who drug safety database towards analysis of complex associations and improved accuracy for rare events[J].Stat Med,2006,25(21):3740-3757.
  • 7Dumouchel W.Bayesian data mining in large frequency tables,with an application to the fda spontaneous reporting system [J].The American Statistician,1999,53(3):190-196.

二级参考文献18

  • 1Mcbride W G.Thalidomide and congenital abnormalities[J].Lancet,19611 Ⅰ,271.
  • 2Wiholm B-E,Olsson S,Moore N,et al.Spontaneous reporting systems outside the US[J].Pharmacoepidemiology(3rd ed):Strom B.John Wiley & Sons,Ltd,Chichester,2000,175-192.
  • 3Almenoff J,Tonning J M,Lawrence Gould A,et al.Perspectives on the use of data mining in Pharmacovigilance[J].Drug Safety,2005,28 (11):981-1007.
  • 4EMEA.Guideline on the use of statistical signal detection methods in the Eudravigilance DataAnalysisSystem[EB/OL].http://www.emea.europa.eu/pdfs/human/phvwp/10646406enfin.pdf,London,26June 2008.Doc.Ref.EMEA/106464/2006 rev.
  • 5Rawlins, M D. Spontaneous reporting of adverse drug reactions. I: the data[J]. Br J Clin Pharmacol, 1988,26(1): 1-5.
  • 6Rawlins, M D. Spontaneous reporting of adverse drug reactions. II: Uses[J]. Br J Clin Pharmacol, 1988,26(1): 7-11.
  • 7Finney, D J. The design and logic of a monitor of drug use [J].J Chronic Dis, 1965,18: 77-98.
  • 8Napke, E. Drug adverse reaction alerting program[J].Canad Pharm J, 1968,20:251-254.
  • 9Finney, D J Systematic signalling of adverse reactions to drugs[J]. Meth Inf Med, 1974,13: 1-10.
  • 10Napke, E. The Canadian drug adverse reaction reporting program [J]. Drug Inf J, 1975,9(2-3): 224-232.

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