contrast enhancement and injection techniques CT

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46 Terms

1
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atomic number iodinated contrast

n=53

2
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does iodine have a higher or lower HU than blood

higher so appears radiopaque

3
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osmolarity describes

number of particles in solution

blood plasma: 290 mOsm/kg of water

4
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hyperosmolar is 

7x the value of blood plasma (290mOsm/kg)

5
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hypo-osmolar is

2x the value of blood plasma (290mOsm/kg)

6
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viscosity describes

the friction of fluid as it flows

7
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the higher concentration of iodine means what in a contrast solution

it is more viscous

8
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ionic vs non-ionic

ionic dissociates into ions when in solution

non-ionic do not but have less adverse reactions

9
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most non-ionic contrast agents have ____ osmolarity

low

10
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if the focus on the study is imaging the urinary system and we want to make sure there is no mass in the area. The patient has hematuria (typically stones or a mass), what can we do to rule out mass

give contrast to highlight masses

stones can sometimes be seen without contrast

11
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what is something we need to keep in mind when imaging the bladder

the urine will dilute the contrast so we want to use a higher osmolality option

12
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if the osmolality of contrast is close to blood what can we assume about adverse reactions

there will be less adverse reactions

13
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how does the body dispose of contrast in approx how long

through filtration in the kidneys 2 hours approx

14
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what is contrast induced nephropathy. who do we need to be concerned about

the contrast causes a temporary drop in kidney function - asymptomatic normally and recovers fast.

sometimes it does not recover quickly and there is a drop in renal function

patients at risk: diabetic, kidney transplant patients, kidney failure patients, 70+ patients, patients with 1 kidney

15
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CIN is dependent on what dose?

the dose of contrast media used

16
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what medications can make CIN worse?

NSAIDS

metformin therapy needs to be stopped - lactic acid buildup

17
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what are the different eGFR numbers associated with in terms of delivering contrast?

eGFR > 45: give contrast

30 < eGFR < 45 with no renal risk factor: give contrast

30 < eGFR < 45 + renal risk factors: written consent, hydration, give contrast

eGFR < 30: NO CONTRAST

18
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idiosyncratic reactions, how fast do they occur, do they produce antibodies

adverse reactions not related to dose

idio means we don’t know the exact reason 

typically occurs within 1 hour of injection 

no antibodies produced

19
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what is the most important factor in screening

idiosyncratic reactions 

20
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if a patient has an eGFR below 30 and has recieved dialysis within the last 24 hours can we give them contrast?

yes we can give contrast

21
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if a patient had a hives reaction last time we used contrast can we give contrast next time? what about an anaphylactic reaction?

hives: give contrast with pre-medication

anaphylactic: no contrast, not worth risking

22
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comparing the brain and lungs which has higher inherent contrast?

the lungs - air and tissue contrast

23
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do contrast agents increase or decrease sensitivity

increase sensitivity

24
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what must be the difference in HU # for us to see a difference in tissues on CT

10 HU difference between tissues

25
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do contrast agents increase or decrease specificity? what does that mean?

increase specificity

we can better see the type of tumour

26
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a patient is coming in for a brainscan with a known meningioma, what does this mean should change with our procedure?

we can image almost immediately after injecting contrast

27
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what are the phases of tissue enhancement in CT?

  1. arterial phase (bolus phase)

  2. venous phase (non-equilibrium phase)

  3. delayed phase (equilibrium phase)

28
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how is the ROI tool used?

we can use it to drop on the region of interest to know the HU number

can tell phases - place one in a artery and one in a vein then compare the HU numbers to tell if we are in an arterial or venous phase

29
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arterial phase means the AVID is what number?

AVID >- 30

30
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what can we expect to see in the venous phase? AVID?

Both artery and vein have unequal contrast but both have

10 HU < AVID < 30 HU

31
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about how long after the arterial phase do we see the delayed phase?

2 min

32
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what can we expect to see in delayed phase? AVID?

contrast is empties from arteries and greatly diluted in veins and soaked into organ parenchyma

AVID < 10 HU

33
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when can delayed phase be useful?

to assess if the metastases uptake contrast to determine if they are tumours. typically the delayed phase will be part of a series 

34
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Iodine dose is determined by:

contrast concentration and contrast volume

35
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contrast volume formula

volume = injection rate x duration of injection

mL = mL/s x s

36
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with an increase in contrast volume (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?

  1. PE increases

  2. time to PE increases - takes longer to reach

  3. duration of any given enhancement level increases

  4. duration of injection increases

37
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when we inject an increased concentration iodine (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?

  1. PE increases

  2. duration of any given enhancement level increases

  3. time to PE remains unchanged

38
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when we decrease the kVp (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?

  1. PE is higher for any given concentrations of iodine 

39
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what combination of adjustments for PE would give us the highest PE?

low kVp and high concentration would give the highest PE as the ray is being more absorbed since it has lower energy and the iodine is concentrated so it does a better job at attenuating the beam

40
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what parameters determine the phase of enhancement captured?

  1. rate of injection (ml/sec or cc/sec)

  2. scan delay

41
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what does scan delay describe? what is another name for it?

the amount of time between starting injection and imaging

another name is prep delay

42
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with an increased rate of injection (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?

  1. PE is higher

  2. time to PE is shorter

  3. duration of PE is shorter

43
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IV gauge and contrast injection rate for arterial phase

18-20G and 4-6cc/sec

44
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IV gauge and contrast injection rate for venous phase

22G and 2-3cc/sec

45
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is an aortic or venous enhancement better for showing a PE

arterial

46
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