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atomic number iodinated contrast
n=53
does iodine have a higher or lower HU than blood
higher so appears radiopaque
osmolarity describes
number of particles in solution
blood plasma: 290 mOsm/kg of water
hyperosmolar is
7x the value of blood plasma (290mOsm/kg)
hypo-osmolar is
2x the value of blood plasma (290mOsm/kg)
viscosity describes
the friction of fluid as it flows
the higher concentration of iodine means what in a contrast solution
it is more viscous
ionic vs non-ionic
ionic dissociates into ions when in solution
non-ionic do not but have less adverse reactions
most non-ionic contrast agents have ____ osmolarity
low
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
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
if the osmolality of contrast is close to blood what can we assume about adverse reactions
there will be less adverse reactions
how does the body dispose of contrast in approx how long
through filtration in the kidneys 2 hours approx
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
CIN is dependent on what dose?
the dose of contrast media used
what medications can make CIN worse?
NSAIDS
metformin therapy needs to be stopped - lactic acid buildup
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
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
what is the most important factor in screening
idiosyncratic reactions
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
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
comparing the brain and lungs which has higher inherent contrast?
the lungs - air and tissue contrast
do contrast agents increase or decrease sensitivity
increase sensitivity
what must be the difference in HU # for us to see a difference in tissues on CT
10 HU difference between tissues
do contrast agents increase or decrease specificity? what does that mean?
increase specificity
we can better see the type of tumour
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
what are the phases of tissue enhancement in CT?
arterial phase (bolus phase)
venous phase (non-equilibrium phase)
delayed phase (equilibrium phase)
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
arterial phase means the AVID is what number?
AVID >- 30
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
about how long after the arterial phase do we see the delayed phase?
2 min
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
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
Iodine dose is determined by:
contrast concentration and contrast volume
contrast volume formula
volume = injection rate x duration of injection
mL = mL/s x s
with an increase in contrast volume (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?
PE increases
time to PE increases - takes longer to reach
duration of any given enhancement level increases
duration of injection increases
when we inject an increased concentration iodine (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?
PE increases
duration of any given enhancement level increases
time to PE remains unchanged
when we decrease the kVp (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?
PE is higher for any given concentrations of iodine
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
what parameters determine the phase of enhancement captured?
rate of injection (ml/sec or cc/sec)
scan delay
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
with an increased rate of injection (while maintaining everything else) what do we notice about PE (peak enhancement) on a graph?
PE is higher
time to PE is shorter
duration of PE is shorter
IV gauge and contrast injection rate for arterial phase
18-20G and 4-6cc/sec
IV gauge and contrast injection rate for venous phase
22G and 2-3cc/sec
is an aortic or venous enhancement better for showing a PE
arterial