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Draft ICRP Recommendations Peter Burns ARPANSA

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Title: Draft ICRP Recommendations Peter Burns ARPANSA


1
Draft ICRP RecommendationsPeter BurnsARPANSA
  • 15th PBNC - October 2006

2
ICRP 2006 Recommendations
  • ICRP Publication 60
  • Recommendations of the International Commission
    on Radiological Protection, 1990.
  • Widely adopted internationally - Basis for the
    IAEA BSS
  • Draft Recommendations of the International
    Commission on Radiological Protection - 02/276/06
    - 5 June 2006.

3
ICRP 2006 Recommendations
  • The ICRP has decided to issue revised
    recommendations having three primary aims in
    mind
  • To take account of new biological and physical
    information and of trends in the setting of
    radiation safety standards
  • To improve and streamline the presentation of the
    recommendations and
  • To maintain as much stability in the
    recommendations as is consistent with the new
    scientific information.

4
ICRP 2006 Recommendations
  • Foundation documents
  • Biological and Epidemiological Information on
    Health Risks Attributable to Ionising Radiation
    (C1)
  • Basis for Dosimetric Quantities Used in
    Radiological Protection (C2)
  • Building blocks
  • Low-Dose Extrapolation of Radiation-Related
    Cancer Risk (C1)
  • Radiological Protection in Medicine (C3)
  • Optimisation of Protection (C4)
  • Assessing Dose to the Representative Individual
    (C4)
  • The Scope of Radiological Protection Regulations
  • Exclusion and Exemption (MC)

5
ICRP RP 06 - Major Features
  • Maintaining the fundamental principles of
    radiological protection, and clarifying how they
    apply to sources and the individual
  • Updating the weighting factors and the radiation
    detriment
  • Maintaining the dose limits
  • Extending the concept of constraints in the
    source-related protection to all situations.

6
Why the need for change?
  • The Commission emphasises that it is not a change
    but a clarification of the existing system, which
    has its origin over 50 years ago
  • In London in 1950 ICRP recognised that the world
    of radiation protection had changing

7
Changes in radiation protection
  • Development of nuclear reactors and nuclear
    weapons in the 1940s led to
  • Atmospheric weapons tests
  • Nuclear power
  • Artificial radioisotopes for medicine and
    industry
  • These developments meant a greater potential for
    wide scale exposures of populations

8
Changes in radiation protection
  • By 1950 there was clear evidence that
  • cumulative doses from chronic exposure had caused
    leukaemia in radiologists
  • hereditary effects had been demonstrated in
    animals

9
Changes in radiation protection
  • Long term cumulative exposures were significant
    for carcinogenic and hereditary effects
  • The probability of developing these effects was
    proportional to cumulative doses
  • Previously limits had been designed to prevent
    superficial effects by keeping exposures below a
    rate of 1 R per week

10
ICRP - London 1950
  • ICRP lowered exposure rate from 1R w-1 to 0.3R
    w-1
  • "While the values proposed for the maximum
    permissible exposures are such as to involve a
    risk that is small compared to the other hazards
    of life, nevertheless in view of the
    unsatisfactory nature of much of the evidence on
    which judgements are based, coupled with
    knowledge that certain radiation effects are
    irreversible and cumulative, it is strongly
    recommended that every effort be made to reduce
    exposures to all types of ionizing radiations to
    the lowest possible level."

11
Evolution of recommendations
  • 1950 as low as possible
  • 1958 as low as practicable
  • 1966 readily achievable, economic and
    social considerations.
  • 1973 reasonably achievable
  • 1976 economic and social factors

12
ICRP 60 - 1990
  • In 1960 the Commission introduced the concept of
    Optimisation to sit with Justification and
    Limitation as the main principles for radiation
    protection
  • Dose Constraints were introduced as benchmarks
    in the Optimisation Process
  • There has been much confusion about what Dose
    Constraints are and how to apply them and the new
    recommendations are attempting to address this

13
DRAFT ICRP Recommendations
  • The General System of Radiological Protection
  • The probabilistic nature of stochastic effects
    means a clear distinction between 'safe' and
    'dangerous is impossible.
  • Fundamental principles are
  • Justification, Limitation and Optimisation.
  • Dose Constraints in the Optimisation Process are
    the primary tool in managing radiation safety.

14
Additional Radiation Dose and Risk
UNACCEPTABLE RISK
DOSE LIMIT
TOLERABLE RISK
DOSE CONSTRAINT
Optimisation
Protection optimized
ACCEPTABLE RISK
TRIVIAL RISK
15
DRAFT ICRP Recommendations
  • The General System of Radiological Protection
  • Strong radiation safety culture through a cycle
    of continuous review and assessment to optimise
    doses for practices using a single source.
  • Optimisation involves evaluating and
    incorporating measures that tend to lower doses
    to the public and workers.
  • It also entails consideration of avoidance of
    accidents and other potential exposures.

16
DRAFT ICRP Recommendations
  • Dose constraints are used as an integral part of
    the process of prospectively optimising
    radiological protection at the source.
  • If an assessment shows a relevant constraints was
    not complied with,
  • further consideration of protection options in
    an optimisation procedure is required,
  • this should not necessarily be regarded as a
    failure of protection.

17
DRAFT ICRP Recommendations
  • It is the process of prospectively optimising
    radiological protection that is important
  • Constraints should be set according to well
    managed practices and should be monitored and
    modified if necessary
  • Reference or Action Levels - Level of Ambition
  • It is not about compliance with a number

18
Application of Dose Constraints
  • The optimisation of protection is a forward
    looking iterative process aimed at preventing
    exposures before they occur.
  • Operators and the appropriate national
    authorities have responsibilities for applying
    the optimisation principle.
  • Optimisation of protection is the responsibility
    of the operating management, subject to the
    requirements of the authority.
  • An active safety culture supports the successful
    application of optimisation by both the
    operational management and by the authority.

19
Application of Dose Constraints
  • All aspects of optimisation cannot be codified
    optimisation is more an obligation of means than
    of results.
  • The authority should focus on processes,
    procedures and judgements rather than specific
    outcomes.
  • An open dialogue must be established between the
    authority and the operating management to ensure
    a successful optimisation process.

20
DRAFT ICRP Recommendations
  • Three exposure situations are identified
  • Planned Situations are everyday situations
    involving the planned operation of practices.
  • Emergency Situations are unexpected situations
    that occur during the operation of a practice
    requiring urgent action.
  • Existing Situations are exposure situations that
    already exist when a decision on control has to
    be taken, including natural background radiation
    and residues from past practices.

21
DRAFT ICRP Recommendations
  • For planned situations
  • constraints represent a basic level of
    protection
  • In emergency or existing controllable exposure
    situations
  • constraints represent a level of dose or risk
    where action to reduce that dose or risk is
    almost always warranted.

22
Band of Projected Effective Dose0.01 - 1 mSv -
Acute or Annual

23
Band of Projected Effective Dose1 to 20 mSv -
Acute or Annual

24
Band of Projected Effective Dose20 to 100 mSv -
Acute or Annual

25
ICRP Radiation Protection 06
  • Minor changes to
  • Radiation weighting factors
  • Tissue weighting factors
  • Risk coefficients
  • Caution on the use of
  • Effective Dose
  • Collective dose

26
Main Conclusions on Biology
  • Dose-response for stochastic effects A simple
    proportionate relationship between dose and risk
    at low doses.
  • DDREF 2.
  • Genomic instability, bystander effects, adaptive
    response Still insufficient knowledge for
    protection purposes.
  • Genetic susceptibility Known disorders too rare
    to distort risk estimates impact of weak genetic
    determinants cannot be judged.
  • In-utero cancer risk Life time risk similar to
    that of young children (a few times higher than
    that of the whole population).

27
Main Conclusions on Biology
  • Nominal probability coefficients for cancer
    Based on incidence and not mortality.
  • Nominal probability coefficients for heritable
    diseases Based on UNSCEAR 2001
  • - up to 2nd generation
  • Tissue reactions in adults Revised judgements
    but no major changes.
  • Risks of non-cancer diseases (A-bomb LSS) Great
    uncertainty on dose response below 1 Sv no
    judgement on low dose risk possible.

28
Radiation Weighting Factors, wR
29
Tissue Weighting Factors
  • Determine lifetime cancer incidence risk for
    radiation associated cancers.
  • Apply DDREF.
  • Transfer risk estimates across populations
    (ERREAR weights).
  • Apply weighted risk estimates to and average
    across seven Western and Asian populations to
    provide nominal risk coefficients.
  • Adjust for lethality, quality of life and for
    years of life lost to obtain the radiation
    detriment for each type of cancer.
  • Normalize to unity and obtain the relative
    radiation detriments.
  • Group into four categories broadly reflecting the
    relative detriments, i.e. the tissue weighting
    factors.

30
Tissue Weighting Factors, wT
1 Nominal wT divided equally between 14 tissues.
31
Nominal Risk Coefficients for Stochastic Effects
( Sv-1)
32
Use of Effective Dose (E)
  • E is calculated by using reference values for a
    reference person or group. Weighting factors are
    averaged over age and gender.
  • E should be used only for compliance of
    constraints and dose limits to control stochastic
    effects.
  • E should mainly be used for planning in
    prospective situations.
  • E should not be used for more detailed
    retrospective dose and risk assessments on
    exposure of individuals.
  • E should not be used for epidemiological studies.

33
Use of Collective Dose
  • Is an instrument for optimisation, for comparing
    radiological technologies and protection
    procedures.
  • Is not intended as a tool for epidemiologic risk
    assessment. It is therefore inappropriate to use
    it in risk projections based on epidemiological
    studies.
  • The computation of cancer deaths based on
    collective doses involving trivial exposures to
    large populations is not reasonable and should be
    avoided. Such a use was never intended and is an
    incorrect use of the collective dose.

34
UNSCEAR 2006 Report
  • United Nations Scientific Committee on the
    Effects of Atomic Radiation
  • 2006 Report to be submitted to the General
    Assembly on 25 October

35
UNSCEAR 2006
  • 5 Annexes on biological effects of radiation
  • Sources-to-effects assessment for radon in homes
    and workplaces
  • Epidemiological studies of radiation and cancer
  • Epidemiological evaluation of cardiovascular
    disease and other non-cancer diseases following
    radiation exposure
  • Effects of ionizing radiation on the immune
    system
  • Non-targeted and delayed effects of exposure to
    ionizing radiation
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