NCRP PAC 4: Radiation Protection in Medicine. Overview. NCRP and PAC 4. Donald L. Miller, MD FSIR FACR Center for Devices and Radiological Health FDA

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Transcription:

NCRP PAC 4: Radiation Protection in Medicine Donald L. Miller, MD FSIR FACR Center for Devices and Radiological Health FDA 1 Overview NCRP and PAC 4 Recent PAC 4 publications Reports in preparation 2 NCRP and PAC 4 3 1

Program Area Committees (PACs) PAC 1 Basic Criteria, Epidemiology, Radiobiology, and Risk PAC 2 Operational Radiation Safety PAC 3 Nuclear/Radiological Security and Safety PAC 4 Radiation Protection in Medicine 4 Program Area Committees (PACs) PAC 5 Environmental Radiation and Radioactive Waste Issues PAC 6 Radiation Measurements and Dosimetry PAC 7 Radiation Education, Risk Communication, Outreach, and Policy 5 PAC 4 Responsibilities Radiation protection in medicine Radiation protection of patients in medical, dental, and chiropractic practice Examining and evaluating techniques and procedures to eliminate unnecessary radiation exposure to the patient Examining and evaluating training of medical personnel in radiation protection 6 2

PAC 4 25 members: Radiology Diagnostic radiology Interventional radiology, Pediatric radiology Nuclear medicine Medical physics Health physics Radiation oncology Cardiology Interventional cardiology Nuclear cardiology Dentistry Occupational and environmental medicine 7 Recent PAC 4 publications 8 9 3

Report No. 172 (2012) Reference Levels and Achievable Doses in Medical and Dental Imaging: Recommendations for the United States Defines purposes and values of Diagnostic Reference Levels (DRL) and Achievable Doses (AD) Provides numerical values for U.S. DRLs and ADs 10 Diagnostic Reference Level QA/QI tool for controlling radiation dose Designed to reduce the risk of stochastic effects DRL value = 75th percentile of survey data When doses exceed the DRL value the reasons should be investigated. 11 Diagnostic Reference Levels DRL values are not: An indicator of optimum performance Dose limits Regulatory (use of the DRL process may be) DRL values do not apply to individual patients or individual cases 12 4

Achievable Dose A dose that serves as a goal for optimization efforts and is achievable with standard techniques and technologies in widespread use, while maintaining clinical image quality adequate for the diagnostic purpose. AD value = 50th percentile of survey data (median) 13 Report No. 174 (2013) Preconception and Prenatal Radiation Exposure: Health Effects and Protective Guidance General misconception that any amount of ionizing radiation is much more detrimental to the embryo or fetus than is actually the case Diagnostic radiological procedures necessary for the care of the mother, embryo, or fetus can be performed at any time during pregnancy 14 Report No. 174 Increased risks to the embryo or fetus have not been observed below a weighted uterine dose of 0.1 Gy for mental retardation birth defects growth retardation neurobehavioral effects impaired school performance convulsive disorders embryonic or fetal death 15 5

Statement No. 11 (2014) Outline of Administrative Policies for Quality Assurance and Peer Review of Tissue Reactions Associated with Fluoroscopically- Guided Interventions Structured recommendations for QA processes for review of radiation use in fluoroscopicallyguided interventional (FGI) procedures 16 Statement No. 11 Provides Tables that summarize Model policies and processes for the management of radiation dose for FGI procedures Essential elements of a QA-peer review program Criteria for evaluation of tissue reactions relative to recognized practice parameters Outcomes and actions after QA-peer review evaluation of a clinically important tissue reaction. 17 Reports in Preparation 18 6

Scientific Committee 4-5, Chairs: Alan Lurie and Mel Kantor. Radiation Protection in Dentistry Scientific Committee 4-7, Chair: Julie Timins. Evaluating and Communicating Radiation Risks for Studies Involving Human Subjects: Guidance for Researchers and Reviewing Bodies Scientific Committee 4-8, Chair: Manudeep Kalra. Improving Patient Dose Utilization in Computed Tomography 19 Radiation Protection in Dentistry Update of NCRP Report No. 145, Radiation Protection in Dentistry (2003) Intended as comprehensive, self-contained guide for dental facilities New material: cone beam CT, digital radiography, hand-held dental radiography devices Data from 2014-2015 NEXT dental survey 20 Radiation Risks: Guidance for Researchers and IRBs Guidance for researchers and IRBs in preparing and reviewing research protocols that include radiation exposure to human subjects Cites relevant regulatory requirements Discusses estimation of radiation dose and risk in research protocols 21 7

Radiation Risks: Guidance for Researchers and IRBs Discusses the ethical considerations involved in human studies research Provides advice on presenting radiation risk information to subjects as part of the informed consent process 22 Improving Patient Dose Utilization in CT Integrated set of recommendations for CT radiation dose optimization and error prevention Intended audience: practicing physicians and other healthcare providers, physicists and technologists 23 Possible Future Topics Program Components for Error Prevention in Radiation Therapy Radiation Effects on Implantable and Other Medical Devices Radiation Protection for PET-CT and other Multimodality Imaging Systems 24 8

Summary 25 In NCRP, PAC 4 has oversight of activities in the field of radiation protection in medicine 25 members, with diverse areas of expertise, including medical physics Three recent publications of interest: Diagnostic Reference Levels and Achievable Doses Preconception and Prenatal Radiation Exposure QA and Peer Review of Tissue Reactions Associated with FGI 26 Work in progress: Radiation Protection in Dentistry Evaluating and Communicating Radiation Risks for Studies Involving Human Subjects: Guidance for Researchers and Reviewing Bodies Improving Patient Dose Utilization in Computed Tomography Several possible topics for future reports 27 9

Thank You! Questions? donald.miller@ fda.hhs.gov 28 10