2017 AAPM Annual Meeting
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Session Title: DBT Quality Assurance: Medical Physicists Role, From Equipment Evaluation to Soft Copy Image Display
Question 1: Currently there are _______ number of FDA Approved DBT Systems:
Reference:FDA Website (https://www.fda.gov/Radiation-EmittingProducts/MammographyQualityStandardsActandProgram/FacilityCertificationandInspection/ucm114148.htm)
Choice A:2.
Choice B:3.
Choice C:5.
Choice D:None of the above.
Question 2: Which GE systems require grid line tests?
Reference:GE Quality Control Manuals
Choice A:Ge Pristina.
Choice B:Ge Senoclaire.
Choice C:GE Essential.
Choice D:None of the above.
Question 3: Which DBT systems require z-axis resolution test?
Reference:Siemens & Fuji Quality Control Manuals
Choice A:All DBT systems.
Choice B:Siemens DBT system.
Choice C:Fuji DBT system.
Choice D:B & C.
Choice E:None.
Question 4: The main item that FDA reviews for certificate extension:
Reference:FDA Website: https://www.fda.gov/radiation-emittingproducts/mammographyqualitystandardsactandprogram/facilitycertificationandinspection/ucm413117.htm and Policies Discussed during the Presentation
Choice A:Mammography Equipment Evaluation test results as per the manufacturer’s requirements.
Choice B:3D phantom image from a tomosynthesis plane.
Choice C:Lead Interpreting Physician Attestation to Staff Personnel Qualifications.
Choice D:All of the above.
Question 5: The GE Pristina unit primarily uses what Target/Filter combination for Tomosynthesis images?
Reference:GE Pristina Quality Control Manual
Choice A:Mo/Mo.
Choice B:Mo/Rh.
Choice C:Rh/Rh.
Choice D:W/Al.
Choice E:Rh/Ag.
Question 6: T/F: The FDA requires medical physicists to have training specific to the "unique features" of each manufacturer's Tomosynthesis system.  
Reference:FDA Website (https://www.fda.gov/Radiation-EmittingProducts/MammographyQualityStandardsActandProgram/FacilityCertificationandInspection/ucm447869.htm)
Choice A:True.
Choice B:False.
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