首页> 外文会议>NATO Advanced Research Workshop on Environmental Aspects of Converting CW Facilities to Peaceful Purposes and Derivative Technologies in Modeling, Medicine and Monitoring Apr, 1999 Spiez, Switzerland >EFFECTS OF LONG-TERM EXPOSURE TO LOW LEVELS OF TOXIC MATERIALS: Considerations for the Estimation and Implementation of 'Allowable' Exposure Levels
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EFFECTS OF LONG-TERM EXPOSURE TO LOW LEVELS OF TOXIC MATERIALS: Considerations for the Estimation and Implementation of 'Allowable' Exposure Levels

机译:长期暴露于低水平的有毒物质的影响:“允许”暴露水平的估算和实施注意事项

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摘要

In the last few years, there has been considerable concern over the effects of long term exposure to low levels of toxic materials―especially chemical agents. Controlled data for such exposure paradigms are extremely limited; most studic s have been for relatively short exposures to high levels. Where long-term data exist, chemical agents were often administered by routes inappropriate to the exposure scenario for which allowable levels are required, and there was no long-term follow-up after termination of exposure. Although it is known that some agents produce long-term effects and others may, it is often not clear that long-tenn effects are produced in the absence of a symptomatic exposure. Extrapolation of such data to "safe" exposure levels is not advocated, but it is recognized that, too often, interim exposure limits must be derived from existing data. In doing the risk assessment for estimating allowable exposure levels (AELs), it is important to fully characterize the exposure scenario, and to understand the concentration-time relationship for the chemical(s) in question. Although the fundamental process of establishing exposure limits is independent of the type of available data, the quality of the data affects the confidence in the exposure limits so derived. Risk Management should be the final step in the process of implementing AELs and should be independent of the Risk Assessment.
机译:在过去的几年中,人们一直对长期暴露于低水平的有毒物质(尤其是化学制剂)的影响感到担忧。这种暴露范式的受控数据极为有限;大多数研究都是相对短时间地暴露于高水平的。在存在长期数据的情况下,化学制剂通常通过不符合需要允许水平的暴露情景的途径进行管理,并且在暴露终止后没有进行长期随访。尽管已知某些药物会产生长期作用,而其他药物可能会产生长期作用,但通常不清楚在没有症状暴露的情况下会产生长期的作用。不提倡将此类数据外推至“安全”暴露水平,但应认识到,过渡暴露限值往往必须从现有数据中得出。在进行风险评估以估算允许的暴露水平(AEL)时,重要的是充分表征暴露情况,并了解所涉及化学物质的浓度-时间关系。尽管建立暴露极限的基本过程与可用数据的类型无关,但是数据的质量会影响由此得出的暴露极限的置信度。风险管理应该是实施AEL的最后一步,并且应独立于风险评估。

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