Random DR/RP Flashcards
Who is responsible for implementing regulations and how is this usually done
Employer has responsibility, usually delegated to radiation protection committee
Who is RPA
Radiation protection adviser - individual or body appointed by radiation employer and meeting criteria of competence specified by HSE.
Advice on compliance that RPA might give
Radiation risk assessment
Designation of controlled and supervised areas
Handling of investigations
Contingency plans
Dose assessment and recording
What must RPAs be consulted on
Implementation of requirements for controlled and supervised areas
Plans for future installations
Calibration and use of equipment for monitoring
Periodic testing of control and safety features and systems of work
HSE graded approach
Notification (low risk) - electronic submission
Registration (includes all x-ray work) - submission, statements to agree to, small fee
Consent (licensing) - administering radionuclides, use of LINACs, more evidence and higher fee
Designated area
Work area where special procedures are needed to restrict dose (access, training, work practice). Person working here likely to receive dose over threshold.
Values for dose rate
Instantaneous dose rate
Dose rate (DR) - over 1 minute
Time-averaged dose rate (TADR) - over 8 hours
TADR2000 (same over 2000 hours)
Requirements for designated areas
Warning signs
Systems of work to restrict exposures
Environmental monitoring
Assessment of dose (personal and environmental) to ensure dose limits not exceeded
What should local rules contain
Description of area and its identification (controlled or supervised)
Name of RPS
Arrangements to restrict access
Conditions for entry for non-classified persons
Instructions for safe working
Dose investigation levels
Contingency plans
RPS
Should be appointed when local rules are needed, preferably full time and sufficiently senior.
Classified workers
Receive effective dose >20mSv or equivalent dose > a dose limit in a few minutes
Anyone likely to get an annual effective dose >6mSv or 3/10 any other dose limit
What does classification involve
Regular medical surveillance, personal monitoring performed by an approved lab and person dose record kept on CIDI
Pregnant staff
Dose to foetus should be ALARP and unlikely to exceed 1mSv - equivalent to 2mSv on abdomen
Diagnostic reference levels
A dose reference level set for a specific standard examination type and standard patient
cohort
Represents an upper level for acceptable dose
National and local
Expressed in easily measurable dose quantities (ESD, CTDI, DAP)
Should be reviewed and investigated if regularly exceeded
Stochastic vs tissue reactions
Stochastic: probability of effect occurring increases with dose, no threshold
Tissue reactions: no effect below threshold, above threshold severity increases with dose
Classified worker limits
Effective dose > 20mSv in short period of time or equivalent dose > dose limit very quickly
Likely o get annual effective dose > 6mSv or 3/10ths another dose limit
TADR2000 each area
Controlled: >3
Supervised: > 0.5
Unsupervised: <0.15
microsievert/hr
3 types of personal dosimeter
TLD (thermoluminescent dosimeter)
OSL (optically stimulated luminescence)
EPD (electronic personal dosimeter)
TLD material and details
Lithium Fluoride
1microGy - 10Gy
Reusable
OSL material and details
Aluminium oxide Al2O3:C
10microGy - 100Gy
Irradiated electrons trapped in valence band in structure
Laser light used to read results - less signal loss than TLD, can be reread
EPD
Direct read of dose and dose-rate. Audible alarms
Dose for estimating skin, eye, effective
Whole body: Hp(10)
Extremity: Hp(0.07)
Lens of eye: Hp(3)