Internal dosimetric analyser to assist routine, confirmatory and special radiobioassays.
Autor: | Hunt JG; Division of Radiation, Transport and Waste Safety, International Atomic Energy Agency, Vienna International Centre, PO Box 100, 1400 Vienna, Austria., Capote-Cuellar A; Division of Radiation, Transport and Waste Safety, International Atomic Energy Agency, Vienna International Centre, PO Box 100, 1400 Vienna, Austria., Suárez RC; Division of Radiation, Transport and Waste Safety, International Atomic Energy Agency, Vienna International Centre, PO Box 100, 1400 Vienna, Austria., Kenny P; Division of Radiation, Transport and Waste Safety, International Atomic Energy Agency, Vienna International Centre, PO Box 100, 1400 Vienna, Austria., Lafranco G; Division of Radiation, Transport and Waste Safety, International Atomic Energy Agency, Vienna International Centre, PO Box 100, 1400 Vienna, Austria., Hajek M; Division of Radiation, Transport and Waste Safety, International Atomic Energy Agency, Vienna International Centre, PO Box 100, 1400 Vienna, Austria. |
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Jazyk: | angličtina |
Zdroj: | Radiation protection dosimetry [Radiat Prot Dosimetry] 2023 Oct 11; Vol. 199 (15-16), pp. 1844-1847. |
DOI: | 10.1093/rpd/ncac287 |
Abstrakt: | The IAEA Radiation Safety Technical Services Laboratory has developed and validated an Internal Dosimetric Analyser (IDA) software tool to facilitate access to dosimetric data and perform calculations related to individual monitoring for intakes of radionuclides and occupational radiation protection. IDA serves to correlate measurements from routine, confirmatory and special internal monitoring with data obtained from the Occupational Intakes of Radionuclides series of recommendations published by the International Commission on Radiological Protection. The purpose of IDA is to keep the internal dosimetry data in the background and allow the dosimetrist to make the necessary calculations to be able to decide (1) whether the bioassay method and monitoring period are appropriate for routine, confirmatory or special monitoring; (2) whether the method and period will allow the recording level to be detected; (3) whether previous intakes are contributing to the current measurement; and (4) whether measurement uncertainties affect the dose assessment. (© The Author(s) 2023. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.) |
Databáze: | MEDLINE |
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