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[个人剂量测定服务的质量评估]

[Quality evaluation of a personal dosimetry service].

作者信息

Mondini L, Piccagli V, Ferretti P P, Borasi G

机构信息

Servizio di Fisica Sanitaria, Arcispedale S. Maria Nuova, Azienda Ospedaliera, Reggio Emilia.

出版信息

Radiol Med. 1997 Mar;93(3):278-83.

PMID:9221423
Abstract

In a hospital environment high quality personal dosimetry is demanded by two different considerations: first, the marked reduction in the radiation exposure levels of hospital workers during the last 10 years and second, the recent decrease in the allowed absorbed dose thresholds for the different categories of workers and for the general population. In fact, according to the new Italian Radioprotection Law (D.L. vo 230/95), the dose equivalent limit for the general population has been decreased to 1 mSv per year. This means that a dosimetric system should be able to measure, with acceptable precision and accuracy, dose levels as low as 0.1 mSv per observation period (generally 1 month or 45 days). This is quite a stringent requirement for this kind of dosimetry. During a tender, the performances of the whole body personal dosimetry systems by four Italian service providers were analyzed by irradiating more than 60 test samples for each provider with four different energies in a wide dose interval (0.01-100 mSv). The results show that all systems perform quite well in the 0.2-100 mSv dose range; on the contrary, in the 0.01-0.2 mSv dose range, significant differences appear between the services and TLD based systems perform better than film based ones. In particular, one of the two TLD based systems measured doses as low as 0.01 mSv. To conclude this very high sensitivity level really opens a new "observation window" on the low doses world. The use of higher quality (and, of course, more expensive) materials by this provider seems to be the key of its success.

摘要

在医院环境中,高质量的个人剂量测定受到两方面不同因素的要求:其一,过去十年医院工作人员辐射暴露水平显著降低;其二,近期不同类别工作人员以及普通公众的允许吸收剂量阈值有所降低。事实上,根据意大利新的辐射防护法(第230/95号法律令),普通公众的剂量当量限值已降至每年1毫希沃特。这意味着剂量测定系统应能够以可接受的精度和准确度测量低至每个观察期(通常为1个月或45天)0.1毫希沃特的剂量水平。对于这种剂量测定而言,这是一项相当严格的要求。在一次招标过程中,通过在较宽剂量区间(0.01 - 100毫希沃特)用四种不同能量对每个供应商的60多个测试样品进行辐照,分析了四家意大利服务提供商的全身个人剂量测定系统的性能。结果表明,所有系统在0.2 - 100毫希沃特剂量范围内表现都相当出色;相反,在0.01 - 0.2毫希沃特剂量范围内,各服务之间出现了显著差异,基于热释光剂量计(TLD)的系统比基于胶片的系统表现更好。特别是,两个基于TLD的系统之一能够测量低至0.01毫希沃特的剂量。总而言之,这种非常高的灵敏度水平确实为低剂量领域打开了一扇新的“观察窗口”。该供应商使用更高质量(当然也更昂贵)的材料似乎是其成功的关键。

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