Patient dose in diagnostic radiology Flashcards

1
Q

What value is typically calculated to determine an individual patient dose estimate (e.g. for an incident)? What would be calculated in an ideal situation?

A
  • Effective dose.
  • Dose to radiosensitive organs.
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2
Q

Why do patient size and technique used need to be considered when determining an individual patient dose estimate (e.g. for an incident)?

A

Standardised factors/models are typically used to determine patient dose/risks. They may need to be corrected for patient size and technique used.

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3
Q

What considerations should be taken into account when using radiography dose calculation software?

A
  • Ensuring correct organs are within primary beam.
  • Values relative to DAP generally more accurate than those relative to ESD due to the inclusion of field size.
  • Most software assumes standard size patients.
  • Consider uncertainties when interpreting results.
  • May need software amendments to adapt to ICRP103.
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4
Q

What considerations should be taken into account when using CT dose calculation software?

A
  • Checking of technique data sent (e.g. CTDI_vol for series or exam).
  • Positioning relative to organs rather than scan length.
  • Over-ranging.
  • Use of QA values.
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5
Q

How has the trend in patient doses for radiography and fluoroscopy changed over the years? Why is this? How does this differ for CT and why?

A
  • Dropped quite quickly initially but is now beginning to level off.
  • Dose awareness, technologies and optimisation techniques have been improved.
  • Doses have slightly increased over the years for CT. This is due to more complex examinations being carried.
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6
Q

What difficulties are associated with determining NDRLs for CT?

A

CT examinations for the same region can vary a lot depending on the clinical indication.

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7
Q

Why is it difficult to create DRLs for paediatric examinations?

A

Large variations in paediatric patient size make it difficult to get reasonable sample sizes.

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8
Q

How is population dose from medical exams determined?

A
  • ESD/DAP from a national survey.
  • Conversion to effective dose using standard factors.
  • Exam frequency from national statistics.
  • Above to values combined to give estimate of average dose to member of UK population.
  • Risk factors from ICRP.
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9
Q

What are the top two medical examination contributors to UK dose?

A
  • CT.
  • Interventional radiology.
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10
Q

What does risk from diagnostic radiology exams depend on? Where can risk factors be found?

A
  • Exposure.
  • Age.
  • Sex.
  • HPA and BEIR VI data.
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11
Q

When might detailed dose risk assessments be required?

A
  • Risk benefit analysis for justification.
  • Ethics submissions.
  • SAUEs.
  • Informing worried patients/relatives.
  • Choosing between alternative procedures.
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12
Q

What are some areas of focus for CT optimisation?

A
  • Iterative reconstruction techniques.
  • mA modulation (setting reference mAs for adequate image quality).
  • Highly sensitive detector.
  • Wide beam coverage.
  • Active collimation.
  • kV modulation.
  • Superficial organ dose sparing.
  • Avoiding overlapping slices/scan areas.
  • Slice width setting.
  • Changing settings for paediatric patients.
  • QA programmes.
  • Patient dose assessments.
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13
Q

What are some areas of focus for radiography/fluoroscopy optimisation?

A
  • Sensitive detector.
  • Low attenuation couch tops, grids etc.
  • AECs.
  • DAP meters.
  • Low grid factor.
  • Avoid cine fluoroscopy.
  • Screening times/radiograph numbers.
  • Collimation.
  • Last image hold.
  • Pulsed fluoroscopy.
  • Exclude unnecessary examinations.
  • QA programmes.
  • Patient dose assessments.
  • Patient compression
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14
Q

What are some general optimisation techniques?

A
  • Assess equipment doses, image quality and optimisation features prior to purchase.
  • Assess doses and compare with DRLs.
  • Assess image quality.
  • Step-wise changes in technique and re-assessment of dose.
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