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欧洲立法对上市农药的影响——基于健康影响评估研究的视角

Impact of European legislation on marketed pesticides--a view from the standpoint of health impact assessment studies.

作者信息

Karabelas A J, Plakas K V, Solomou E S, Drossou V, Sarigiannis D A

机构信息

Chemical Process Engineering Research Institute, Centre for Research and Technology-Hellas, Thermi, Thessaloniki, GR 570-01, Greece.

出版信息

Environ Int. 2009 Oct;35(7):1096-107. doi: 10.1016/j.envint.2009.06.011. Epub 2009 Jul 25.

Abstract

The very significant impact of European legislation (Directive 91/414/EEC) on the authorization of plant protection products is reviewed herein, which has resulted in withdrawal of 704 active substances (AS) out of 889 assessed so far. The list of currently approved 276 AS includes 194 AS "existing" in the market before 1993 and 82 "new" AS introduced during the last 15 years. Results of toxicity characterization of the approved AS are also summarized, utilizing several well-known databases. Although significant data gaps exist for a rather large part of the approved AS, it is found that 84 AS are positive for at least one health effect (after chronic and/or acute exposure) including carcinogenicity, reproductive and neuro-developmental disorders, as well as endocrine disruption. The toxicity characterization results of this study are compared to those of recent assessments by other organizations (KemI, the Swedish Chemicals Agency, and the Pesticide Safety Directorate of the UK), where interpretation and use is made of AS "cut-off" criteria foreseen in new EU legislation. These studies report a comparatively smaller AS number with positive toxicity characterization. The possibility of some additional AS withdrawal in the near future, combined with the rather small rate of new AS introduction (approx. 5 per year) suggest that the list of approved AS over the next 10-15 years may not change very drastically. Consideration of the above trends is necessary and instructive in evaluating results of existing health impact assessment (HIA) studies, as well as in planning new ones. Due to the very drastic change in the number and type of marketed AS, that took place within the past 8-9years, it is suggested that new HIA studies (based on epidemiological data after year 2000) should focus on a rather short time frame and, therefore, on appropriate cohort groups, e.g. young children. For the same reason, results of epidemiological studies of the past (involving banned AS) should be carefully interpreted and used with caution.

摘要

本文回顾了欧洲法规(91/414/EEC号指令)对植物保护产品授权的重大影响,该法规已导致在迄今评估的889种活性物质中,有704种被撤销。目前获批的276种活性物质清单包括1993年前市场上“已有的”194种活性物质和过去15年引入的82种“新的”活性物质。还利用几个知名数据库总结了获批活性物质的毒性特征结果。尽管获批活性物质的很大一部分存在显著的数据缺口,但发现有84种活性物质至少对一种健康影响呈阳性(在慢性和/或急性接触后),包括致癌性、生殖和神经发育障碍以及内分泌干扰。本研究的毒性特征结果与其他组织(瑞典化学品管理局KemI和英国农药安全局)最近的评估结果进行了比较,这些评估对欧盟新法规中预见的活性物质“临界值”标准进行了解释和应用。这些研究报告的毒性特征呈阳性的活性物质数量相对较少。近期可能会有更多活性物质被撤销,再加上新活性物质引入速度相当缓慢(每年约5种),这表明未来10 - 15年获批活性物质清单可能不会有太大变化。考虑上述趋势对于评估现有健康影响评估(HIA)研究的结果以及规划新的研究是必要且具有指导意义的。由于过去8 - 9年市场上活性物质的数量和类型发生了巨大变化,建议新的HIA研究(基于2000年后的流行病学数据)应关注较短的时间框架,因此应关注适当的队列组,例如幼儿。出于同样的原因,过去流行病学研究(涉及已禁用活性物质)的结果应仔细解读并谨慎使用。

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