The document outlines procedures for radiation surveys and documentation in radiology, emphasizing the roles of qualified experts like health physicists and radiation safety officers. It details the importance of accurate record-keeping for regulatory compliance, patient safety, and quality control, as well as the types of surveys required based on radioactive materials. Additionally, it discusses personal radiation monitoring devices and their significance in ensuring safety for healthcare workers and patients.
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The document outlines procedures for radiation surveys and documentation in radiology, emphasizing the roles of qualified experts like health physicists and radiation safety officers. It details the importance of accurate record-keeping for regulatory compliance, patient safety, and quality control, as well as the types of surveys required based on radioactive materials. Additionally, it discusses personal radiation monitoring devices and their significance in ensuring safety for healthcare workers and patients.
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Radiation Surveys and Documentation in Radiology (AKORN)
1.General Survey Procedures
1.1 Qualified Experts: - Health Physicist: Specializes in the application of physics principles to protect workers, the public, and the environment from ionizing radiation. They conduct radiation surveys, develop safety programs, and ensure regulatory compliance. - Medical Physicist: Works in healthcare, applying physics knowledge to medical radiation treatments, devices, and technologies. They ensure equipment safety and effectiveness and are often involved in patient diagnosis and treatment, radiation safety, and product development. - Radiation Safety Officer (RSO): Assesses potentially hazardous situations to improve the safety and health of individuals. They handle hazardous materials to minimize radioactive exposure, manage the Radiation Protection Program (RPP), and ensure regulatory compliance. 1.2 Records: Accurate records of radiation surveys are crucial for: - Regulatory Compliance: Meeting legal requirements and demonstrating adherence to safety standards. - Trend Analysis: Identifying patterns in radiation exposure levels to assess effectiveness of protection measures. - Verification of Radiation Protection Measures: Confirming that safety practices are effective and meeting intended goals. 1.2.2 Standard Documentation Requirements in Radiology: Proper documentation is essential for: o Patient Safety: Ensuring appropriate procedures and minimizing risks. o Regulatory Compliance: Meeting legal requirements for record-keeping. o Quality Control: Maintaining standards for image quality and patient care. o Efficient Workflow Management: Streamlining processes and facilitating communication. 1.2.2.1 Patient and Exam Information: - Full patient identification, including name, date of birth, medical record number (MRN), and contact details. - Referring physician details, including name and credentials. - Clinical indications, outlining the reason for the imaging procedure. - Imaging modality, specifying the type of equipment used. - Procedure details, including date, time, and site of imaging.
1.2.2.2 Radiology Report:
- Exam findings, detailing observations based on image interpretation. - Comparisons (if applicable), mentioning previous imaging for comparison. - Impressions/Conclusions: Summarizing findings and suggesting diagnoses. - Recommendations: Follow-up imaging, additional tests, or specialist referrals. - Radiologist’s signature and credentials: Legally required authentication of the report. 1.2.2.3 Imaging and Technical Data: - Radiation dose records, tracking patient exposure levels. - Contrast agent documentation (if applicable), specifying type, volume, concentration, and route of administration. - Adverse reactions and management, documenting any complications. - Image quality and repeat exposures, including image acquisition parameters (kVp, mA, exposure time). - Reasons for repeat imaging and corrective actions taken. 1.2.2.4 Equipment and Maintenance Logs: - Daily/Weekly Quality Control (QC) Checks: Calibration and performance testing records, phantom test results for image quality assessment. - Preventive Maintenance Reports: Regular servicing logs by biomedical engineers, equipment malfunction reports, and corrective actions. 1.2.2.5 Radiation Safety and Compliance Records: - Radiation exposure monitoring, including personnel dosimetry reports, badge readings, and occupational exposure records. - Lead shielding and protective equipment checks, ensuring proper function and maintenance. - Regulatory compliance documentation (e.g., FDA), demonstrating adherence to legal standards. 1.2.2.6 Incident Reports and Adverse Event Documentation: - Contrast reaction reports, detailing mild/moderate/severe allergic reactions. - Radiation overdose incidents, documenting any deviation from standard dose levels and corrective measures. - Equipment malfunctions affecting patient care, documenting machine failures and impact on imaging quality.
1.2.2.7 Billing and Administrative Documentation:
- Procedure coding and billing records, using CPT (Current Procedural Terminology) and ICD-10 codes for insurance claims. - Consent forms, documenting patient agreement for the procedure. Patient Communication Logs: Tracking follow-up calls, report delivery confirmations, and patient inquiries. 2. Dose Reporting: Conditions: Dose reporting is required when radiation exposure exceeds established thresholds or when personnel are working in high- radiation environments. 2.2 Radiographic and Fluoroscopic Equipment: - Radiation dose assessments must include evaluations of radiographic and fluoroscopic equipment to ensure that exposure levels remain within safety limits. 3. Area Survey: 3.1 Controlled/Uncontrolled Areas: o Controlled areas are designated spaces where radiation exposure is monitored and limited. o Uncontrolled areas are accessible to the general public and must have lower exposure levels. 3.2 Conditions: Surveys assess radiation levels, shielding effectiveness, and compliance with exposure limits in both controlled and uncontrolled areas. 3.3 Recommendations: Survey results lead to recommendations for improving radiation safety, including shielding adjustments, procedural modifications, and equipment maintenance. 3.4 “Radiation Area” Sign Posting: Radiation areas must be clearly marked with appropriate signage to warn personnel and the public about potential exposure risks. 3.5 Monitors: Radiation monitors, such as Geiger-Muller counters and ionization chambers, are used to assess radiation levels and ensure compliance with safety standards. Radiation Surveys and Documentation(III-Surveys) 1.What is a Survey? - A survey is a thorough evaluation of work areas, instruments, and equipment for the presence of radioactive contamination. - This includes checking surfaces like floors, sinks, faucet handles, drawer fronts, doorknobs, telephones, light switches, refrigerators, etc.
Two main types of surveys are performed:
- Radiation Field Survey: Measures radiation levels in the environment. - Contamination (Wipe) Survey: Checks for radioactive material on surfaces.
2.When to Perform Surveys?
- Surveys are required to ensure the safety of laboratory personnel and the environment. - “As used” or “daily basis”: Individuals are required to survey themselves and their work areas frequently. - After each day of radioactive material usage/experimentation. - After transfer of radioactive material from stock solutions. - After each experimental run if there is a possibility of a change in radiation levels or contamination. - After a minor radioactive spill clean up or emergency.
Survey Types Based on Radioactive Material
The type of survey performed depends on the type of radioactive material being used: o Radiation Emitting Device (e.g., X-ray machine): General Radiation Field Survey should be conducted periodically during machine operations to verify proper function. o Sealed Source: These sources are encapsulated to prevent contamination. They should be checked for radioactive material leakage semiannually by the Radiation Safety Office. Users should also perform periodic General Radiation Field Surveys. o Radioactive Material (solid, liquid, gas): Both contamination surveys and radiation field surveys are required due to potential contamination risks. Importance of Standardized Dose Reporting - Dose Reduction: Standardized dose reporting can help reduce radiation exposure for patients. - Variability Reduction: There is still a lot of variability in radiation doses for many procedures. - Information for Referring Physicians: Dictating radiation dose into radiologic reports provides referring physicians with the option of knowing a patient’s radiation dose history and whether an additional radiologic procedure is advisable.
Personal Radiation Monitoring: History, Devices, and Safety
1. Radiation Protection History: - Ionizing Radiation: Ionizing radiation causes neutral atoms or molecules to acquire an electrical charge. It includes alpha, beta, gamma, X, and neutron rays. - Direct vs. Indirect Ionization: Charged particles (alpha, beta) directly ionize, while neutral radiation (X, gamma, neutron) indirectly ionizes by creating charged particles. - Early Detection: Tools like the gold leaf electroscope, photography, and the cloud chamber helped in detecting radiation, but the discovery of X-rays by Roentgen and uranium radiation by Becquerel in the late 19th century revolutionized the field. - The International Commission on Radiological Protection (ICRP): Founded in 1928, the ICRP is a leading body in establishing radiation safety principles. Its recommendations are adopted by national regulatory bodies to protect workers and the public. - Post-War Evolution: The increased use of radioactive substances in military and civil nuclear programs led to the expansion of radiation protection efforts. The ICRP has continued to evolve its recommendations and committee structure to address new challenges. 2. Personal Radiation Monitoring Devices: Features and Safety Issues - National Regulations: Regulations determine whether healthcare providers require radiation monitoring. In some countries, it’s mandatory for all radiation-exposed personnel to wear dose-monitoring badges. - Pregnant Workers: Special precautions are necessary for pregnant workers to minimize fetal exposure to radiation. 2.1 Film Badges: - Purpose: Keep a detailed record of quarterly, annual, and lifetime radiation doses received. - How It Works: Film badges contain radiation-sensitive film that is exposed and developed to measure exposure. - Advantages: Provides a permanent record and is relatively inexpensive. - Disadvantages: Requires a processor for development, results are not instant, and may give inaccurate results at high temperatures. - Accuracy: Film badges must be worn properly, stored away from radiation sources, and investigated if overexposure is detected.
2.2 Thermoluminescent Dosimeters (TLDs):
- How It Works: TLDs consist of a phosphor-containing crystal structure. The phosphor interacts with ionizing radiation, releasing light proportional to the exposure. - Advantages: More accurate than film badges, higher low-dose sensitivity, reusable. - Disadvantages: Results are not instant, cannot store permanent records, and are not re-readable. - Applications: Monitoring both personal and environmental radiation exposure. 2.3 Optically Stimulated Luminescence Dosimeter (OSLD): - How It Works: OSLDs use pre-irradiated aluminum oxide, which emits light when stimulated with specific wavelengths. The light intensity is proportional to the absorbed dose. - Advantages: Very sensitive, can determine radiation type and energy. - Disadvantages: Must be worn with the dosimeter facing the radiation source. - Luxel Dosimeter: A common type of OSLD considered the most sensitive. 2.3 Pocket Dosimeter: - How It Works: Provides an immediate reading of radiation exposure. Types: - Direct Read Pocket Dosimeter: Reusable and provides instant readings. - Digital Electronic Dosimeter: Uses Geiger-Müller counters to detect dose rate. - Advantages: Provides immediate readings. - Disadvantages: Cannot store permanent records, limited range, prone to data loss. 3.International Commission on Radiation Units and Measurements (ICRU): - Purpose: Develops concepts, definitions, and recommendations for ionizing radiation units and measurements. - Relationship to ICRP: The ICRU defines the units, while the ICRP recommends their application in radiation protection. 4.Radiation Quantities: - Units: The ICRU has defined various radiation quantities using SI and non-SI units.
5.Total Effective Dose Equivalent (TEDE):
- Definition: A radiation dosimetry quantity used to monitor and control human exposure to ionizing radiation. - Components: Sum of effective dose equivalent from external exposure and committed effective dose equivalent from internal exposure. - Regulatory Limits: TEDE limits are imposed on occupationally exposed individuals and the general public. 6.Fetal Effects of Radiation Dosage: - Stochastic Effects: Radiation-induced cancer and heritable effects. - Deterministic Effects: Tissue reactions following high doses. - Fetal Sensitivity: Fetuses are more vulnerable to radiation due to cell growth and longer lifespan for cancer development. - Intellectual Deficit: Estimated to be about 25 IQ-points per 1,000 mGy at 10 to 17 weeks of gestation.
Absorbed Dose Determination in External Beam Radiotherapy: An International Code of Practice for Dosimetry Based on Standards of Absorbed Dose To Water