Modeling cumulative dose and exposure duration provided insights regarding the associations between benzodiazepines and injuries

被引:68
作者
Abrahamowicz, M [1 ]
Bartlett, G
Tamblyn, R
du Berger, R
机构
[1] McGill Univ, Dept Epidemiol & Biostat, Montreal, PQ H3A 2T5, Canada
[2] Montreal Gen Hosp, Res Inst, Div Clin Epidemiol, Montreal, PQ H3G 1A4, Canada
[3] McGill Univ, Dept Family Med, Montreal, PQ H3A 2T5, Canada
[4] McGill Univ, Dept Med, Montreal, PQ H3A 2T5, Canada
关键词
pharmacoepidemiology; benzodiazepines; Cox model; time-dependent covariates; epidemiological methods; statistical model; aged; accidental falls;
D O I
10.1016/j.jclinepi.2005.01.021
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background and Objectives: Accurate assessment of medication impact requires modeling cumulative effects of exposure duration and dose; however, postmarketing studies usually represent medication exposure by baseline or current use only. We propose new methods for modeling, various aspects of medication use history and employment of them to assess the adverse effects of selected benzodiazepines. Study Design and Setting: Time-dependent measures of cumulative dose or duration of use, with weighting of past exposures by recency, were proposed. These measures were then included in alternative versions of the multivariable Cox model to analyze the risk of fall related injuries among the elderly new users of three benzodiazepines (nitrazepam, temazepam, and flurazepam) in Quebec. Akaike's information criterion (AIC) was used to select the most predictive model for a given benzodiazepine. Results: The best-fitting model included a combination of cumulative duration and current dose for temazepam, and cumulative dose for flurazepam and nitrazepam, with different weighting functions. The window of clinically relevant exposure was shorter for flurazepam than for the two other products. Conclusion: Careful modeling of the medication exposure history may enhance our understanding of the mechanisms underlying their adverse effects. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:393 / 403
页数:11
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