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 />
5 MONITORING PROGRAMMES<br />
5.1 Introduction<br />
(268) The design and management <strong>of</strong> monitoring programmes is considered in this<br />
chapter. It is recommended that the emphasis in any particular monitoring programme<br />
should be on the formal assessment <strong>of</strong> doses to those workers who are considered<br />
likely to receive routinely a significant fraction <strong>of</strong> the relevant dose limit, or who<br />
work in areas where exposures could be significant in the event <strong>of</strong> an accident.<br />
(269) In general, the assignment <strong>of</strong> an internal exposure monitoring programme to<br />
an individual should be based on the likelihood that the individual could receive an<br />
intake <strong>of</strong> radioactive material exceeding a predetermined level, as a result <strong>of</strong> normal<br />
operations or in the event <strong>of</strong> an accident. The use <strong>of</strong> individual monitoring for<br />
workers whose effective doses from annual intakes could exceed 1 mSv is common<br />
practice in many organisations, although it may not be required by legislation.<br />
(270) It is important to consider both the monitoring programme design and the dose<br />
assessment process as integral parts <strong>of</strong> the overall radiation protection programme. An<br />
appropriately designed monitoring programme should provide the data necessary to<br />
enable a dose assessment to meet the specified need; even the most sophisticated dose<br />
assessment calculations cannot compensate for inadequate monitoring data.<br />
(271) Where assessed doses could be significant, there is much to be gained from<br />
using a combination <strong>of</strong> different monitoring methods (e.g. lung, urine, faecal<br />
monitoring and exposure monitoring in the workplace), since they provide<br />
complementary information. For instance, direct bioassay measurements provide<br />
information on deposition and retention in organs, urine measurements can provide a<br />
measure <strong>of</strong> systemic uptake, while workplace monitoring can provide information on<br />
airborne activity, particle size and chemical form.<br />
(272) The assessment <strong>of</strong> intakes and/or doses using those measured activities<br />
(bioassay monitoring results and measurements <strong>of</strong> the workplace) may be complex<br />
and <strong>of</strong>ten needs pr<strong>of</strong>essional judgment, on a case by case analysis. Responsibilities for<br />
dose assessment should only be assigned to pr<strong>of</strong>essionals with adequate expertise and<br />
skill, acquired through appropriate education, training and practical experience.<br />
5.2 General Principles for the Design <strong>of</strong> Individual Monitoring Programmes<br />
(273) A specification for an individual monitoring programme includes the<br />
monitoring method (or methods) to be employed (e.g. measurement <strong>of</strong> activity in the<br />
body, in excreta samples, and exposure monitoring in the workplace), the<br />
measurement technique used (e.g. photon spectrometry, alpha spectrometry, mass<br />
spectrometry), monitoring intervals for routine monitoring, and measurement or<br />
sample collection times for special monitoring.<br />
(274) Many factors need to be taken into consideration when designing an<br />
individual monitoring programme. These include the purpose <strong>of</strong> the monitoring (e.g.<br />
whether it is carried out to demonstrate compliance with regulatory requirements, or<br />
simply to confirm that doses are very low), local factors such as the number <strong>of</strong><br />
workers to be monitored and the availability <strong>of</strong> particular measurement methods, and<br />
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