Comparison of data mining methodologies using Japanese spontaneous reports

被引:73
作者
Kubota, K
Koide, D
Hirai, T
机构
[1] Univ Tokyo, Fac Med, Dept Pharmacoepidemiol, Bunkyo Ku, Tokyo 1138655, Japan
[2] Int Univ Hlth & Welf, Sch Hlth & Welf, Dept Hlth Serv Management, Tochigi, Japan
[3] MedDRA Japanese Maintenance Org, Soc Japanese Pharmacoepeia, Tokyo, Japan
关键词
pharmacovigilance; data mining; spontaneous reports; adverse reaction; adverse event;
D O I
10.1002/pds.964
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Purpose Five data mining methodologies for detecting a possible signal from spontaneous reports on adverse drug reactions (ADRs) were compared. Methods The five methodologies, the Bayesian method using the Gamma Poissson Shrinker (GPS), the method employed in the UK Medicines Control Agency (MCA), the Bayesian Confidence Propagation Neural Network (BCPNN), the method using the 95% confidence interval (CI) for the reporting odds ratio (RORCI) and that using the 95% CI of the proportional reporting ratio (PRRCI) were compared using Japanese data obtained between 1998 and 2000. Results There were all in all 38 731 drug-ADR combinations. The count of drug-ADR pairs was equal to 1 or 2 for 31230 combinations and none of them were identified as a possible signal with the MCA or BCPNN. Similarly, the GPS detected a possible signal in none of the combinations where the count was equal to I but in 7.5% of the combinations where the count was equal to 2. The RORCI and PRRCI detected a possible signal in more than half of the combinations where the count was equal to I or 2. When the pairwise agreement on whether or not a drug-ADR combination satisfied the criteria for a possible signal was assessed for the 38 731 combinations, the concordance measure kappa was greater than 0.9 between the MCA and BCPNN and between the RORCI and PRRCI. Kappa was around 0.6 between the GPS and MCA and between the GPS and BCPNN. Otherwise, kappa was smaller than 0.2. Conclusions The drug - ADR combinations detected as a possible signal vary between different methodologies. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:387 / 394
页数:8
相关论文
共 18 条
  • [1] A Bayesian neural network method for adverse drug reaction signal generation
    Bate, A
    Lindquist, M
    Edwards, IR
    Olsson, S
    Orre, R
    Lansner, A
    De Freitas, RM
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 54 (04) : 315 - 321
  • [2] DuMouchel W, 1999, AM STAT, V53, P177, DOI 10.2307/2686093
  • [3] DuMouchel W., 2001, KDD-2001. Proceedings of the Seventh ACM SIGKDD International Conference on Knowledge Discovery and Data Mining, P67, DOI 10.1145/502512.502526
  • [4] Adverse drug reactions: definitions, diagnosis, and management
    Edwards, IR
    Aronson, JK
    [J]. LANCET, 2000, 356 (9237) : 1255 - 1259
  • [5] Use of proportional reporting ratios (PRRs) for signal generation from spontaneous adverse drug reaction reports
    Evans, SJW
    Waller, PC
    Davis, S
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2001, 10 (06) : 483 - 486
  • [6] Feinstein A.R., 2002, PRINCIPLES MED STAT, P407
  • [7] SYSTEMATIC SIGNALING OF ADVERSE REACTIONS TO DRUGS
    FINNEY, DJ
    [J]. METHODS OF INFORMATION IN MEDICINE, 1974, 13 (01) : 1 - 10
  • [8] Practical pharmacovigilance analysis strategies
    Gould, AL
    [J]. PHARMACOEPIDEMIOLOGY AND DRUG SAFETY, 2003, 12 (07) : 559 - 574
  • [9] Quantitative methods in pharmacovigilance - Focus on signal detection
    Hauben, M
    Zhou, XF
    [J]. DRUG SAFETY, 2003, 26 (03) : 159 - 186
  • [10] Automated signal generation in prescription-event monitoring
    Heeley, E
    Wilton, LV
    Shakir, SAW
    [J]. DRUG SAFETY, 2002, 25 (06) : 423 - 432