QAQC (PRELIM L1 - L3) Flashcards
Possible cause of low density and high contrast that appears on film is due to ________ ?
A. Decreased Immersion Time
B. Low Developer Temperature
C. Under Replenishment
D. AOTA
D. AOTA
Overall decrease in density is due to _______
A. Wrong Control Film
B. Unseasoned Developer
C. Under replenishment
D. NOTA
A. Wrong Control Film
Possible cause of overall increase in density are the following except:
A. Fogged Film
B. Wrong Control Film
C. Contaminated Developer
D. AOTA
D. AOTA
Contaminated developer and unseasoned developer appears overall increased density to the film. Indicator deviation should be ?
A. Increase Base + Fog
B. Decrease Base + Fog
C. Decrease mid density
D. Increase Density Difference
A. Increase Base + Fog
Wrong control film and low developer temperature appears overall decrease in density, indicator deviation should be ?
A. Decreased Mid Density
B. Increased Density Difference
C. Decrease Base + Fog
D. Increase Base + Fog
C. Decreased Base + Fog
Decreased density difference appears low contrast with high density in lighter areas. Possible causes includes the following except ?
A. Increased Immersion Time
B. Contaminated Fixer
C. Contaminated Developer
D. Over replenishment
B. Contaminated Fixer
Decrease in immersion time, low developer temperature, and improperly mixed developer appears high contrast in the film this indicates deviation with _____ ?
A. Increased Density
B. Decreased Density
C. Increased Density Difference
D. NOTA
C. Increased Density Difference
The processor QC Chart should be maintained for _____ ?
A. 5 Years
B. 3 Years
C. 1 Year
D. 10 Years
C. 1 Year
Records of corrective action must be kept for how many years ?
A. 4 Years
B. 2 Years
C. 3 Years
D. 5 Years
B. 2 Years
Sensitometric strip should be maintained for ______ ?
A. 4 Weeks
B. 5 Weeks
C. 6 Weeks
D. 1 Year
C. 6 Weeks
The densitometer must be zeroed before each use. This is actually done by holding down the optical sensory arm and pressing the _______ button until 0.00 is displayed
A. ON Button
B. HOLD Button
C. NULL Button
D. START Button
C. NULL Button
MD and DD values that exceed ± ________ should be investigated immediately before the limit of 0.15 OD is exceeded.
A. 0.10
B. 0.1
C. 0.15
D. 0.05
A. 0.10
Tanks should be covered when not in use to prevent evaporation and ______ of solutions
A. Contamination
B. Oxidation
C. Contagion
D. Pollution
B. Oxidation
For single-sided emulsion film, the emulsion side of the film must be placed ______ in the sensitometer
A. Down
B. Up
C. In
D. Out
A. Down
Running a sheet of clear film through the processor will help clear the _____ of debris
A. Gears
B. Chemical
C. Roller
D. Film
C. Roller
The regulations require that processor quality control be performed each workday when radiographs are to be processed, before processing any patient films, the following are the equipment required except ?
A. Sensitometer
B. Densitometer
C. Fresh Box of Control Film
D. Glass thermometer accurate of at least 0.5 F
D. Glass thermometer accurate of at least 0.5 F
(Rationale: DIGITAL Thermometer accurate of at least 0.5 F)
For automatic film processors, the temperature must be within the film manufacturer’s specifications (usually ± ____ degrees F).
A. 0.5
B. 1.5
C. 2.5
D. 3.5
A. 0.5
Changing the chemistry, as part of routine preventative processor maintenance, is not justification for re-establishing processor operating _____ ?
A. Limits
B. Levels
C. Time
D. AOTA
B. Levels
Re-establishing processor control limits are the following, except ?
A. A change in film brand or speed
B. A change in film brand or type of chemistry
C. A change in replenishment rate
D. A change of processor
D. A change of processor
The Mid-density (MD) step is the step where the average density is closest to but not less than _______ ?
A. 1.10
B. 1.20
C. 2.20
D. 0.45
B. 1.20
The High Density (HD) step is the step where the average density is closest to _____ ?
A. 1.10
B. 1.20
C. 2.20
D. 0.45
C. 2.20
The Low Density (LD) step is the step where the density is closet to but not less than _____ ?
A. 1.10
B. 1.20
C. 2.20
D. 0.45
D. 0.45
To determine the average density for each step by adding the five readings for that step and dividing by ______ ?
A. 2
B. 5
C. 3
D. 7
B. 5
With the densitometer, we must read the density of each of the 21 steps for all five sensitometric control strips. If the densitometer has several aperture sizes, we must use the _____ mm aperture
A. 5 mm
B. 4 mm
C. 2 mm
D. 6 mm
C. 2 mm
Prior to establishing processor operating levels and control limits, the processor must be cleaned and filled with fresh ______
A. Water
B. Developer
C. Chemistry
D. Solution
C. Chemistry
Using the densitometer, determine the Base + Fog for all five sensitometric control strips. Base + Fog readings can be taken over any ______ areas of the film
A. Unexposed
B. Exposed
C. Blank
D. Uneven
A. Unexposed
TRUE OR FALSE
Polaroid Instant Film System operates with a darkroom, with the standard processor and with separate processing
FALSE
TRUE OR FALSE
New Jersey Administrative Code 7:28-22.5 requires Processor QC of all processors. For Daylight systems, Rapido systems, or other “non-standard” processing systems, it will be necessary to feed the sensitometric film through the MANUAL method
TRUE
TRUE OR FALSE
You can widen the control limits since the data indicates that the processor is out of control and corrective action is essential. These limits are set by NJ State regulation.
FALSE
When establishing a processor quality control program. It is necessary to determine the operating levels and control limits. The control limits are the extreme ranges of _____ operation.
A. Exceeded
B. Acceptable
C. Unacceptable
D. Maximum Limit
B. Acceptable
If the result is still out of limits, corrective action may include changing the ______ except ?
A. Temperature
B. Developer
C. Chemistry
D. Processor
D. Processor
The cause of trends should be _______ before the control limits are reached or exceeded
A. Repeated
B. Monitored
C. Investigated
D. Determined
C. Investigated
TRUE OR FALSE
Notes regarding changes in operating conditions (such as a change in the developer temperature or replenishment rate) should be recorded on the control chart
TRUE
It is recommended that all facilities dedicate a ______ of film for QC testing. However, facilities with very small volume may use film from the clinical batch for QC testing also
A. Box
B. 8x10
C. 10x12
D. 5 Sheets
A. Box
It is inappropriate, and _____, to process clinical films and then determine, hours or days later, that the film processor was not operating optimally.
A. Wrong
B. Unprofessional
C. Improper
D. Illegal
D. Illegal
Sensitometric strips that are pre-exposed (_______in advance) will suffer from latent image effect and will not be as sensitive as freshly exposed strips to changes in the processor function
A. Months
B. Years
C. Hours or Days
D. Weeks
C. Hours or Days
The control film need not be the same size as the clinical film. In other words, the QC film can be _______ even if all clinical images are produced on 14 x 17 film
A. 8x10
B. 10x12
C. 11x14
D. 14x14
A. 8x10
The sensitometric control strips must be read with a densitometer. It is appropriate to visually compare sensitometric control strips
FALSE
(Rationale: Must be read with a SENSITOMETER)
TRUE OR FALSE
For monitoring the temperature of the film processor , it is recommended that only a thermometer containing mercury to be used
FALSE
EF stands for _______
Evaporative Fraction