Protection Physic lecture 6
RADIATION PROTECTION PHYSICS RIT 302 RADIATION SAFETY
Advisory Agencies
Analyze existing data to develop recommendations for dose limits.
Recommendations can be acted on by Congress or state governments and made into law.
Major Advisory Agencies include:
NCRP (National Council on Radiation Protection and Measurement)
Established in the U.S.
Primary standard setter for radiation protection.
ICRP (International Commission on Radiation Protection)
Set the first radiation protection standards globally.
UNSCEAR (United Nations Scientific Committee on the Effects of Atomic Radiation)
Regulatory Agencies
Responsibilities include licensing users of radioactive materials and radiation-producing equipment.
Conduct inspections and enforce laws.
NRC (Nuclear Regulatory Commission)
A U.S. agency overseeing reactor-produced isotopes and naturally occurring radioactive material.
Regulates both medical and nonmedical practices.
Many states have agreements concerning licensing, inspection, and enforcement with the NRC, referred to as “agreement” states.
Other Agencies
DOT (Department of Transportation)
Manages the transportation of radioactive materials.
FDA (Food and Drug Administration)
Regulates machines producing ionizing radiation.
EPA (Environmental Protection Agency)
Regulates the design and manufacture of electronic products (e.g., medical x-ray equipment, linear accelerators).
Establishes operational standards for these devices.
Regulation of Medical Events
Radiation therapy is highly regulated.
Majority of reported medical events relate to:
Wrong dose of radiation delivered.
Administration to wrong patient.
Wrong location targeted.
Incorrect side treated.
Wrong setup applied during therapy.
Most medical events stem from human error.
Reporting Events
New conditions for reporting therapy medical events have been in effect since May 2012.
Facilities must report if:
The total delivered dose differs from the prescribed dose by 20% or more.
Any single fraction of a fractionated treatment exceeds the prescribed dose by 50% or more.
Event involves the wrong patient, treatment modality, or treatment site.
A written report must be submitted to the department within 30 days.
The report should include a summary of the event, root cause, and corrective actions taken, along with the effect on the patient.
Radiation Safety Program
Establishes standards and rules for the safe handling and usage of radiation.
Involves a Radiation Safety Committee.
Should include members from each department:
Surgery
Radiation Oncology
Diagnostic Radiology
Nuclear Medicine
Radiation Safety Program - RSO
The Radiation Safety Officer (RSO) must be a qualified Medical Physicist.
Main responsibilities include:
Overseeing a comprehensive radiation safety program.
Overseeing activities related to:
Receipt of radioactive material.
Conducting radiation surveys.
Monitoring personnel and areas.
Conducting leak tests.
Designing shielding.
Managing emergency response procedures.
Decontaminating radioactive spills.
Restricted Access
Restricted areas limit access to protect individuals from undue radiation exposure.
Unrestricted areas have radiation levels at background levels; do not require monitoring, posting, or control measures.
Three Categories of Restricted Areas
Radiation Area
Could result in an exposure of more than 5 mrem but less than 100 mrem in 1 hour at a distance of 30 cm from the radiation source.
Access control is required.
Warning sign must be purple, magenta, or black on a yellow background stating: “Caution- Radiation Area” with a three-blade radiation symbol.
High-Radiation Area
Could result in an exposure of more than 100 mrem in 1 hour at a distance of 30 cm from the radiation source.
Access must be controlled with features such as door interlocks to prevent unauthorized entry.
Warning sign: purple, magenta, or black on a yellow background stating: “Caution- High Radiation Area” with a three-blade radiation symbol.
Very High Radiation Area
Could result in an exposure of more than 500 cGy in 1 hour at a distance of 30 cm from the radiation source.
Access control must include features to prevent unauthorized entry.
Warning sign: purple, magenta, or black on a yellow background stating: “Grave Danger, Very High Radiation Area” with a three-blade radiation symbol.
Personnel Monitoring Program
The RSO must monitor exposure records for all individuals assigned film badges.
Mandatory monitoring for any individual who:
Receives or is likely to receive 10% of the applicable radiation dose limit.
Enters high radiation areas.
Operates portable x-ray equipment.
Operates photo-fluoroscopic equipment.
Services x-ray equipment.
Dose Equivalent Limits
Annual occupational exposure limit is set at per year.
General public limit is per year.
Embryo Fetus Exposure limits:
Total:
Per month:
From NCRP Report No. 116, Limitation of Exposure to Ionizing Radiation:
Occupational exposures (annual): Effective dose equivalent limit (stochastic effects) (or )
Public exposures (annual): Effective dose equivalent limit, continuous or frequent exposure (or )
Embryo-fetus exposures:
Total Dose equivalent limit (or )
Dose equivalent in a month (or )
Pregnant Employee
May choose to declare or not declare a pregnancy at any time to the RSO.
If declared, must advise the RSO voluntarily and in writing; the employer then takes responsibility for fetal dose monitoring.
The RSO provides instructions and evaluates the radiation work environment of the employee.
Restrictions may be applied to certain duties, such as caring for brachytherapy patients.
Embryo Fetus Exposure limits remain: total of (or ), and (or ) per month.
The pregnant employee will have 2 radiation monitor badges:
Fetal dose monitor worn at the waist.
Mother’s monitor worn at the collar/chest.
Protecting the Worker
ALARA Principle: As Low As Reasonably Achievable; exposure levels set lower than regulatory limits.
At GVSU (Grand Valley State University), if a radiation exposure reading exceeds on any report, the program director is notified and an investigation is conducted.
If a student exceeds the trigger dose limit () on any personal monitoring report, they must be removed from clinical settings immediately and counseled by the university RSO, Program Director, and Clinical Coordinator on how to avoid further exposure.
During fluoroscopy procedures, personal monitoring devices should be worn outside of the lead shielding.