Lecture 6 Flashcards

(28 cards)

1
Q

What’s the purpose of reject analysis

A

Asses unnecessary dosage of departments

Establish baseline for quality assurance

Help rectify if facility is providing unnecessary exposure

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2
Q

What methods are there for rejection analysis?

A

Methods depend on the needs of individual department

Can be:

  • counting rejected images
  • analysis by room
  • analysis by reason ie. radiologist opinion
  • analysis by reason and room
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3
Q

Briefly outline the procedure of reject analysis

A

Aim and method informed to staff (radiologist, radiographer, support staff)

Length of time

Number of people supervising

Design reject sheet

All radiographers given reject sheets

Count rejected within intervals

Collect sheets

Find number of examinations done on images performed

Then use results to help rectify technique

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4
Q

What’re the reasons for reject?

A
Over exposure or under 
Positioning
Blur
Collimation
Processing equipment 
Artefact in ROI 
Miscellaneous (unknown fault)
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5
Q

What does the effective dose represent?

A

mSv

Shows the whole body dose and determines the somatic effect of radiation

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6
Q

Explain what’re DRLs

A

Measured values to be used to minimise any excessive radiation exposure to patient

Helps limit unnecessary variation in pt doses

They aren’t thresholds, so flexibility is permitted to allow higher doses for a better clinical judgment
Ie. chest DRL = 0.3 Gy but can be increased if pt is thick in order to get good image

Not to be used for individual patients or as trigger levels

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7
Q

Why’s the implementation of DRLs important?

A

Allows a comparison/standard that imaging centres can use to not allow unnecessary doses

Can help identify reasons for over exposure and determine strategies

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8
Q

How can we tell that a imaging clinic is doing an overwhelming amount of unnecessary exposing?

A

Median value is considered to be consistently exceeded when local median value > local, national, or regional DRL values

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9
Q

What’re the 2 broad groups used in the measurement of dosimetric quantities?

A

Application specific

Risk related

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10
Q

Explain what is application specific dosimetric quantity

A

Practical dosimetric quantities obtained from direct measurement tailored to specific situations of modalities
Eg. Incident air karma, entrance surface air Kerma, air kerma (area product), CT air kerma indices

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11
Q

Explain what is risk related dosimetric quantities

A

Estimates radiation detriment or risk (measure absorbed dose)

Eg. Organ dose and mean glandular dose in mammography

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12
Q

What’re DRLs quantity?

A

Application specific quantities used only (ie. incident air kerma, ESAK, AKAP)

Should be relevant to the imaging modality being evaluated specific study performed, patient size

Risk related quantity aren’t used as DRLs

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13
Q

What’re the drl quantities used in planar radiography?

A

To simplify assessment of proper use of collimation, especially paediatrics we use ESAK, IAK, AKAP&

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14
Q

When is it useful to use phantoms for measurement?

A

Do not use for drl measurement

Controlling technical parameters (the system)

Comparisons of system at different times

To optimise individual components or the whole system

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15
Q

What’re the limitations of using phantoms for measurement?

A

Doesn’t estimate average dose for a given pt population
Ie. weight, size

Therefore, doesn’t show variation in real clinics in terms of patient size and composition

No info on intra or inter operator variability in technique factor (ie. same parameters always used therefore can’t be used to find DRLs)

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16
Q

Explain what makes a patient measurements useful ?

A

Accouts for variations in equipment performance, operator technique, patient related characteristics

Increase Sample size of pts to find median and/or average calculated

Therefore allowing comparison at local, regional, national distribution, image quality might be affected negatively

17
Q

In what ways can drl quantities be collected?

A

Surveys
Registries
Or other automated data collection methods

18
Q

What exactly occurs when conducting drl surveys?

A

Calibrate all dosimeters used for patient dosimetry and traceable to primary or secondary labs

Is the drl quantity accurate from the system that was used to produce it? Medial physicists check this

Drl quantities obtained for the most frequent type of examinations

Not done for radiation therapy

Used for imaging for treatment planning, treatment rehearsal, and patient setup verification in radiotherapy

Collect data for > 20 and >30 for flurocospy and ct

Doses measured using DAP (dose area product)

19
Q

Where should the sample of DRLs be collected from for a survey?

A

Weight standardisation for adults if sample is < 50 pt.

National surveys and registries should include medium and large sized facilities

Large countries = survey Random selection of small proportion of facility

20
Q

explain how DRLs are established mathematically For routine plain X-ray examinations

A

Select dose data of 20 pt (60-70kg) or 50 pt. If weight info not provided

Measure DAP for each projection

Find median DAP of all facilities

Calculate 75th percentile of all median values which will be our DRL

21
Q

How’re DRLs obtained for CT?

A

Instead of measuring the DAP of examinations, we do CTDIvol (CT dose index volume) and DLP (dose length product)

Find median of both variables for each facility

Then calculate the 75th percentile of the median values

22
Q

Why’s there variability amongst facilities?

A

Different equipment used

Varied patient size

Differnt departmental protocols ie. methods

23
Q

How is a DRL value even set for an imaging task?

A

Value should adhere to good image quality

Data for drl values must be collected from similar procedures across all facilities

Specify views included and clinical task associated with the procedure

24
Q

What’re the types of DRLs

A

Typical values: 1 facility with several rooms or small number of facilities or single facility linked to a new technique

Local = X-ray rooms within few facilities (eg. With > 10-20 rooms) in local area

National = representative selection of facilities covering an entire country

Regional = countries within region without a relevant DRL or when national drl is higher than regional value

25
What should be done when publishing drl values?
Accompanied by a statement of local groups, national or regional With patient data (ie. size of standard pt, specific examination, date of survey)
26
How does paediatric DRLs develop?
There should be significant variation as weight in children vary by a factor of more than 100 from a premature infant to an obsess adolescent This variation in size, therefore leads to variation in dose, hence, weight bands and age bands are required
27
Do DRLs have to be changed within intervals?
National and regional DRLs must be revised every 3-5 years or more frequently if technique changes, new protocols, or post processing becomes available
28
When should you conduct an investigation?
If local or national drl is exceeded consistently Corrective action required but keep in mind flag drl values are not dose limits Action = review equipment, settings, protocols