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 />
(344) It is convenient to assume that for each monitoring interval n the associated<br />
effective dose En could be equal to 0 or positive. For a given measured quantity,<br />
M(tk), obtained at the end <strong>of</strong> the last monitoring interval k, the associated effective<br />
dose Ek is:<br />
k 1 <br />
E n<br />
Ek <br />
M<br />
( tk<br />
) <br />
z(<br />
tk<br />
<br />
k )<br />
n 1 z(<br />
tk<br />
n ) <br />
<br />
<br />
<br />
<br />
(6.7)<br />
<br />
where k t<br />
is the time <strong>of</strong> measurement k (end <strong>of</strong> the last monitoring interval k);<br />
n and<br />
k are the time at mid-points <strong>of</strong> monitoring intervals n and k, respectively. If M(tk)<br />
is below the decision threshold (ISO, 2011) or the result <strong>of</strong> background subtraction<br />
is negative, then<br />
Ek<br />
0<br />
.<br />
6.4.3 Multiple Measurements<br />
(345) Usually, the bioassay data for an intake estimate will consist <strong>of</strong> results for<br />
different measurements performed at different times, and even from different<br />
monitoring techniques, e.g. direct and indirect measurements.<br />
(346) To determine the best estimate <strong>of</strong> a single intake, when the time <strong>of</strong> intake is<br />
known, it is first necessary to calculate the predicted values, m(ti), for unit intake <strong>of</strong><br />
the measured quantities. It is then required to determine the best estimate <strong>of</strong> the<br />
intake, I, such that the product I m(ti) ‘best fits’ the measurement data (ti, Mi). In cases<br />
where multiple types <strong>of</strong> bioassay data sets are available, it is recommended to assess<br />
the intake and dose by fitting predicted values to the different types <strong>of</strong> measurement<br />
data simultaneously. For example, if urine and faecal data sets are available then, the<br />
intake is assessed by fitting appropriately-weighted predicted values to both data sets<br />
simultaneously (ISO, 2011; Doerfel et al, 2006, 2007).<br />
(347) Numerous statistical methods for data fitting are available (IAEA, 2004a,b).<br />
The two methods that are most widely applicable are the maximum likelihood method<br />
(ISO, 2011; Doerfel et al, 2006) and the Bayesian approach (Miller et al, 2002;<br />
Puncher and Birchall, 2008). Other methods such as the mean <strong>of</strong> the point estimates<br />
and the least-squares fit can be justified on the basis <strong>of</strong> the maximum likelihood<br />
method for certain assumptions on the error associated with the data. For example, the<br />
least squares method can be derived from the maximum likelihood method if it is<br />
assumed that the uncertainty on the data can be characterised by a normal distribution.<br />
The assumed distribution (e.g. normal or lognormal) can have a dramatic influence on<br />
the assessed intake and dose if the model is a poor fit to the data. However, as the fit<br />
<strong>of</strong> the model to the data improves, the influence <strong>of</strong> the data uncertainties on the<br />
assessed intake and dose reduces.<br />
6.4.4 Chronic Exposures<br />
(348) The amount <strong>of</strong> activity present in the body and the amount excreted daily<br />
depend on the period <strong>of</strong> time over which the individual has been exposed. The<br />
bioassay result obtained, e.g. the amount present in the body, in body organs, or in<br />
excreta, will reflect the super-position <strong>of</strong> all the intakes. Intake retention functions for<br />
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