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Image Quality Test
Image Quality Test
QUALITY
IAEA
International Atomic Energy Agency
Introduction
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Overview
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IAEA Training Material on Radiation Protection in Diagnostic and Interventional Radiology
Image quality
IAEA
International Atomic Energy Agency
Imaging quality
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Factors affecting image quality
Blur or
Contrast Unsharpness
Image quality
Distortion
& artifact Noise
IAEA
IAEA Training Material on Radiation Protection in Diagnostic and Interventional Radiology
Image contrast
IAEA
International Atomic Energy Agency
Image contrast
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Some factors influencing contrast
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Technique factors (1)
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Technique factors (2)
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Technique factors (3)
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X Ray penetration in human tissues
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Receptor contrast
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Video monitor
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Contrast agents
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IAEA Training Material on Radiation Protection in Diagnostic and Interventional Radiology
IAEA
International Atomic Energy Agency
Blur or lack of sharpness
IAEA
Resolution
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Factors affecting image sharpness
Geometric Subject
Unsharpness Unsharpness
Image
Unsharpness
Motion Subject
Unsharpness Unsharpness
IAEA
Geometric blur
IAEA
Lack of sharpness due to motion (1)
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Lack of sharpness due to motion (2)
IAEA
Lack of receptor sharpness
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IAEA Training Material on Radiation Protection in Diagnostic and Interventional Radiology
IAEA
International Atomic Energy Agency
Distortion and artifacts
IAEA
Distortion and artifacts
IAEA
Distortion and artifacts
IAEA
IAEA Training Material on Radiation Protection in Diagnostic and Interventional Radiology
Image noise
IAEA
International Atomic Energy Agency
Noise
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Summary
IAEA 8
FILM SCREEN CONTACT TEST
Objective:
To test any localised distortion or blurring of the image.
Equipment
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Procedure
•The resulting image should distortion free and sharp over the
whole FOV.
•No blurring should be present.
•If blurring is present on all plates this suggests the reader fault,
whilst imperfections in individual plates may also lead to blurring.
•If blurring remains on a region of a plate after cleaning it should
not be used clinically.
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SPATIAL RESOLUTION
Objective
To test the high contrast limit of the system’s ability to resolve details
Equipment
Procedure:
•Place a cassette with the Huttner test object (line pair) positioned at its centre aligned at 45 0
to its edges.
•Set 50 kVp expose the cassette to 10 mAs.
•Adjust the window level and magnification to optimise the resolution.
•Score the number of resolvable groups of lines from the screen.
•Look up the corresponding resolution.
Criteria:
•For the 450 angled test object the resolved line pairs per mm should be > 1.2/2p where
the p is the pixel dimension in mm.
•In the scan and subscan directions the limiting resolution should be > 0.85/2p.
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CONTRAST DETAIL DETECTABILITY
Objective:
To monitor image quality by assessing the visibility of low contrast detail.
Equipment
•Leeds TOR CDR test object
Film screen casette
Procedure:
• With the tube, plate and copper, place the Leeds TOR CDR test object on the plate.
•Collimate to the size of the test object.
•Set 75 kVp and an 12.5 mAs for exposure.
•Ascertain whether clinical images are most commonly viewed soft or hardcopy.
•If hardcopy, adjust the window to optimise the visibility of the details, ensuring that background
noise is perceptible and print the image out on the largest film size.
•View image on a masked light box, and score each detail size using fixed distance viewing (< 1
m).
•If images are viewed on softcopy, score them on a reporting workstation optimising window
width and level settings for each detail size.
Criteria:
The results of this test are used to set a baseline for future QA tests.
IAEA
Where to Get More Information
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