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 />
dose to an organ, for example, are considered to be those associated with the<br />
underlying mean absorbed dose.<br />
(394) The physical and anatomical parameters contributing to uncertainties in the<br />
mean absorbed dose for internal emitters are:<br />
Energy and intensity <strong>of</strong> the nuclear and atomic radiations emitted by the<br />
radionuclide and by any radioactive progeny;<br />
Interaction coefficients <strong>of</strong> the emitted radiations in tissues;<br />
Elemental composition <strong>of</strong> the tissues <strong>of</strong> the body;<br />
Volume, shape, density <strong>of</strong> the organs <strong>of</strong> the body; and<br />
Parameters describing the spatial relationship <strong>of</strong> the source regions (regions<br />
containing the radionuclide) and the target regions (radiosensitive organs and<br />
tissues for which dose values are desired).<br />
(395) Limitations are present in the computational model representing the anatomy<br />
and in the numerical procedures used to calculate the energy absorbed in the target<br />
tissues. The magnitudes <strong>of</strong> these uncertainties vary with radiation type, the energy <strong>of</strong><br />
the radiation, and the specific source-target pair. The adoption <strong>of</strong> computational<br />
phantoms based upon medical imaging data (<strong>of</strong>ten referred to as voxel phantoms) has<br />
reduced the uncertainties associated with cross-irradiation <strong>of</strong> tissues by photon and<br />
neutron radiations to some extent by providing more realistic spatial relationships <strong>of</strong><br />
some source and target regions (<strong>ICRP</strong>, 2009). However the absorbed dose is<br />
frequently dominated by the contributions from non-penetrating radiations. For source<br />
and target regions that cannot be resolved in the medical image data, e.g., source and<br />
target regions in the respiratory and alimentary tracts and in the skeleton, uncertainties<br />
are associated with the computational models used to represent these regions.<br />
(396) The anatomical models are static and thus do not address uncertainties in the<br />
spatial position <strong>of</strong> the organs due to breathing and posture other than reclining.<br />
Reference values for the masses and elemental composition <strong>of</strong> the organs <strong>of</strong> the body<br />
have been defined in Publication 89 (<strong>ICRP</strong>, 2002a) and used in the reference<br />
computational models <strong>of</strong> the anatomy (computational phantoms) noted above.<br />
(397) The parameters <strong>of</strong> the dosimetric model contributing to uncertainties in the<br />
absorbed dose are those physical parameters associated with the nuclear<br />
transformation processes that determine the energy and intensity <strong>of</strong> the emitted<br />
radiation and parameters which govern the transport radiations in the body. An<br />
uncertainty less than 10% has been assigned to attenuation and absorption coefficients<br />
for photons with somewhat higher uncertainties ascribed to s<strong>of</strong>t tissue stopping power<br />
values for alpha and electron particles. Improvements in the basic nuclear data have<br />
reduced the uncertainties in the physical half-lives <strong>of</strong> radionuclides and the branching<br />
fractions <strong>of</strong> decay modes. The simplified procedures used in the dosimetric<br />
calculations to address the delayed beta and gamma radiations <strong>of</strong> spontaneous fission<br />
can contribute substantial uncertainties in the mean absorbed dose in some tissues.<br />
(398) The dosimetric calculations must associate an anatomical region (source<br />
region) with each biokinetic compartment. Many biokinetic models partition the<br />
systemic activity among a few identified organs/tissues and include a compartment<br />
referred to as ‘Other tissue’ which represents the residual. The dosimetric procedure<br />
distributes the activity in the ‘Other tissue’ compartment uniformly among all tissues<br />
not explicitly noted in the model. Substantial uncertainty may be associated with the<br />
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