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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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