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Forensic science meets clinical pharmacology: pharmacokinetic model based estimation of alcohol concentration of a defendant as requested by a local prosecutors office

机译:法医学符合临床药理学:根据当地检察官办公室的要求基于药代动力学模型估算被告的酒精浓度

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摘要

Drunk driving is a serious social problem. We estimated the blood alcohol concentration of a defendant on the request of local prosecutor's office in Korea. Based on the defendant's history, and a previously constructed pharmacokinetic model for alcohol, we estimated the possible alcohol concentration over time during his driving using a Bayesian method implemented in NONMEM®. To ensure generalizability and to take the parameter uncertainty of the alcohol pharmacokinetic models into account, a non-parametric bootstrap with 1,000 replicates was applied to the Bayesian estimations. The current analysis enabled the prediction of the defendant's possible blood alcohol concentrations over time with a 95% prediction interval. The results showed a high probability that the alcohol concentration was ≥ 0.05% during driving. The current estimation of the alcohol concentration during driving by the Bayesian method could be used as scientific evidence during court trials.
机译:酒后驾驶是一个严重的社会问题。我们应韩国当地检察院的要求估算了被告的血液酒精浓度。根据被告的历史以及先前建立的酒精药代动力学模型,我们使用NONMEM®中实现的贝叶斯方法估算了他开车期间随时间推移可能出现的酒精浓度。为确保通用性并考虑酒精药代动力学模型的参数不确定性,将具有1,000个重复的非参数自举应用于贝叶斯估计。当前的分析能够以95%的预测间隔预测被告随时间的可能血液酒精浓度。结果表明,驾驶过程中酒精浓度≥0.05%的可能性很高。通过贝叶斯方法对驾驶过程中酒精浓度的当前估算可以用作法庭审判期间的科学证据。

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