Occupational Intakes of Radionuclides Part 1 - ICRP
Occupational Intakes of Radionuclides Part 1 - ICRP
Occupational Intakes of Radionuclides Part 1 - ICRP
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DRAFT REPORT FOR CONSULTATION<br />
6.3 Understanding Exposure Situations<br />
(314) Workplace information should be gathered in order to understand the<br />
exposure situations, e.g. radionuclides that may have been incorporated (including<br />
equilibrium assumptions for the natural series), chemical form, presumed particle<br />
size, likely time, pattern and pathway <strong>of</strong> any intake.<br />
6.3.1 Time(s) and Pattern <strong>of</strong> Intake<br />
(315) A principal source <strong>of</strong> uncertainty in the interpretation <strong>of</strong> bioassay data is the<br />
assignment <strong>of</strong> the time(s) and pattern <strong>of</strong> intake. Since the bioassay function that gives<br />
the predicted measurement depends on the time since the intake it follows that the<br />
estimate <strong>of</strong> intake will vary, depending on when it is assumed the intake took place.<br />
Consideration should be given to different possible patterns <strong>of</strong> intake, such as a single<br />
contamination event, several individual events during the monitoring period, intakes<br />
lasting a short period <strong>of</strong> time or chronic intakes.<br />
(316) Where chronic intakes are expected, an assessment should be made as to<br />
whether the working schedule should be taken into account when selecting the time <strong>of</strong><br />
measurement (or sampling), and interpreting the results from bioassay monitoring.<br />
For elements where a fraction <strong>of</strong> the intake is rapidly excreted, the times and duration<br />
<strong>of</strong> periods when no exposure could take place such as the weekend, days <strong>of</strong>f or<br />
vacations could strongly influence the assessed intake. With the exception <strong>of</strong> short<br />
half-life radionuclides, the selection <strong>of</strong> a measurement or sampling time immediately<br />
following such a period will reduce the uncertainty in assessed intake associated with<br />
rapid excretion.<br />
(317) For routine monitoring, when chronic exposures are not expected, it is<br />
necessary to estimate an intake from a measurement made at the end <strong>of</strong> a monitoring<br />
interval, <strong>of</strong>ten without knowing the time <strong>of</strong> intake.<br />
(318) When a positive measurement appears from a routine bioassay programme, a<br />
the review <strong>of</strong> workplace monitoring data, such as airborne or surface contamination<br />
levels, can indicate a likely time for the intake to have occurred. Similarly, if other<br />
workers in the same workplace have exhibited positive routine bioassay samples, a<br />
review <strong>of</strong> the data and monitoring schedules for those individual workers will help<br />
determine the time <strong>of</strong> intake for all. Workers interviews should elucidate whether if<br />
an incident, an unusual procedure or equipment failure could have led to the intake.<br />
Follow-up bioassay should be scheduled to confirm the positive measurement. When<br />
several bioassay results are available, perhaps including different types <strong>of</strong><br />
measurement, a comparison <strong>of</strong> these results with the intake retention fractions tables<br />
may help in narrowing the choice <strong>of</strong> the time the intake occurred.<br />
(319) Another approach has been described by Miller et al (2002) in which<br />
Bayesian-based dosimetry calculations are performed using a Markov chain Monte<br />
Carlo algorithm. This method, which analyzes all available bioassay data<br />
simultaneously, determines probabilistically the number, magnitude and times for N<br />
possible intakes using a previously agreed set <strong>of</strong> biokinetic models. The Weighted<br />
Likelihood Monte Carlo Sampling (WeLMoS) method is another Bayesian technique<br />
(Puncher and Birchall, 2008). In this approach, biokinetic model parameters and times<br />
<strong>of</strong> intake are sampled from probability distributions that express the state <strong>of</strong><br />
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