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首页> 外文期刊>International journal of medical informatics >Information on adverse drug reactions-Proof of principle for a structured database that allows customization of drug information
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Information on adverse drug reactions-Proof of principle for a structured database that allows customization of drug information

机译:有关药物不良反应的信息-允许定制药物信息的结构化数据库的原理证明

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Background: The drug information most commonly requested by patients is to learn more about potential adverse drug reactions (ADRs) of their drugs. Such information should be customizable to individual information needs. While approaches to automatically aggregate ADRs by text-mining processes and establishment of respective databases are well known, further efforts to map additional ADR information are sparse, yet crucial for customization. In a proof-of-principle (PoP) study, we developed a database format demonstrating that natural language processing can further structure ADR information in a way that facilitates customization.Methods: We developed the database in a 3-step process: (1) initial ADR extraction, (2) mapping of additional ADR information, and (3) review process. ADRs of 10 frequently prescribed active ingredients were initially extracted from their Summary of Product Characteristics (SmPC) by text-mining processes and mapped to Medical Dictionary for Regulatory Activities (MedDRA) terms. To further structure ADR information, we mapped 7 additional ADR characteristics (i.e. frequency, organ class, seriousness, lay perceptibility, onset, duration, and management strategies) to individual ADRs. In a PoP study, the process steps were assessed and tested. Initial ADR extraction was assessed by measuring precision, recall, and F-1-scores (i.e. harmonic mean of precision and recall). Mapping of additional ADR information was assessed considering pre-defined parameters (i.e. correctness, errors, and misses) regarding the mapped ADR characteristics.Results: Overall the SmPCs listed 393 ADRs with an average of 39.3 +/- 18.1 ADRs per SmPC. For initial ADR extraction precision was 97.9% and recall was 93.2% leading to an F-1-score of 95.5%. Regarding mapping of additional ADR information, the frequency information of 28.6 +/- 18.4 ADRs for each SmPC was correctly mapped (72.8%). Overall 77 ADRs (20.6%) of the correctly extracted ADRs did not have a concise frequency stated in the SmPC and were consequently mapped with 'frequency not known'. Mapping of remaining ADR characteristics did not result in noteworthy errors or misses.Conclusion: ADR information can be automatically extracted and mapped to corresponding MedDRA terms. Additionally, ADR information can be further structured considering additional ADR characteristics to facilitate customization to individual patient needs.
机译:背景:患者最常要求的药物信息是更多地了解其药物的潜在药物不良反应(ADR)。此类信息应可根据个人信息需求进行定制。虽然通过文本挖掘过程和建立相应数据库自动聚合ADR的方法是众所周知的,但映射其他ADR信息的进一步工作很少,但对于自定义至关重要。在一项原理证明(PoP)研究中,我们开发了一种数据库格式,证明了自然语言处理可以通过促进定制的方式进一步构造ADR信息。方法:我们分三步开发了数据库:(1)初始ADR提取,(2)附加ADR信息的映射,以及(3)审核过程。最初通过文本挖掘过程从其产品特征摘要(SmPC)中提取了10种常用处方活性成分的ADR,并将其映射到《管制活动医学词典》(MedDRA)术语中。为了进一步构建ADR信息,我们将7种其他ADR特征(即频率,器官类别,严重性,躺卧感,发作,持续时间和管理策略)映射到了各个ADR。在PoP研究中,对过程步骤进行了评估和测试。初始ADR提取通过测量精度,召回率和F-1分数(即精度和召回率的谐波平均值)进行评估。考虑到与映射的ADR特性有关的预定义参数(即正确性,错误和遗漏),评估了其他ADR信息的映射结果。结果:总体而言,SmPC列出了393个ADR,每个SmPC平均39.3 +/- 18.1 ADR。最初的ADR提取精度为97.9%,召回率为93.2%,导致F-1得分为95.5%。关于其他ADR信息的映射,正确映射了每个SmPC的28.6 +/- 18.4 ADR的频率信息(72.8%)。正确提取的ADR中总共有77个ADR(20.6%)没有在SmPC中说明的简洁频率,因此被映射为“未知频率”。映射其余ADR特性不会导致值得注意的错误或遗漏。结论:ADR信息可以自动提取并映射到相应的MedDRA术语。此外,可以考虑其他ADR特征来进一步构建ADR信息,以帮助定制个性化患者需求。

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