chap 8 Flashcards

1
Q

MRA techniques include

A
  • PC- MRA
  • TOF - MRA
  • CE - MRA
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2
Q

what is the equation for available imaging time ?

A

= R-R interval - (trigger window + trigger delay)

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3
Q

the parameters used in gating for T1 weighting

A

1 R-R interval, short TE

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4
Q

the parameters used in gating for PD weighting

A

2-3 R-R intervals, short TE

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5
Q

parameters used in gating for T2 weighting

A

2-3 R-R intervals, long TE

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6
Q

the vascular signal, produced on PC-MRA, relies on

A

velocity - induced phase shifts

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7
Q

remedy for Moire artifact

A

keep arms/shoulders or other anatomy within the FOV, use SE

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8
Q

remedy for Magic angle artifact

A

move the body part or change the TE

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9
Q

remedy for aliasing or “wrap” artifact

A

use “no phase wrap” software or increase the FOV

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10
Q

remedy for chemical misregistration artifact

A

select a TE that matches the periodicity of fat and water, & use an SE rather than a GRE

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11
Q

remedy for zipper artifact

A

check for RF leak, call an engineer

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12
Q

remedy for cross excitation artifact

A

gap between the slices, alternate slices

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13
Q

remedy for chemical shift

A

use lower field strengths, smaller FOV, & lower rBW

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14
Q

remedy for truncation artifact

A

increase the number of phase encoding steps and not undersampling of data. Square matrix will also avoid

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15
Q

remedy for Magnetic susceptibility

A

remove metal, use SE, decrease TE, lower field strengths

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16
Q

remedy for ghosting artifact

A

swap phase & frequency, pre sat, respiratory compensation, concise patient directions

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17
Q

technique for black blood imaging

A

SE with pre sats, inversion recovery

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18
Q

technique for bright blood imaging

A

GRE, GMN, contrast enhancement

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19
Q

how much do patients heart rate vary during the scan?

A

10-20%

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20
Q

what causes ghosting artifact

A

anatomy moving along the phase direction during the pulse sequence

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21
Q

what causes aliasing artifact

A

anatomy outside the FOV is mapped inside the FOV

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22
Q

what causes chemical shift artifact

A

different chemical environments of fat & water

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23
Q

what causes truncation artifact

A

under sampling of data

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24
Q

what causes cross excitation artifact

A

RF pulse not square, adjacent slices get energy pulse from neighbors

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25
Q

what causes a zipper artifact

A

leak in the RF shielding

26
Q

what causes magic angle artifact

A

collagen or other tightly bound structure of fibers is 55 degree angle to Bo

27
Q

what causes shading artifact

A

inhomogeneities in the main magnetic field

28
Q

MRA techniques: 2 T2 data sets, one during systolic and one during diastolic (fresh blood imaging)

A

digital subtraction MRA

29
Q

MRA techniques: Enhancement related to the flow of blood

30
Q

MRA techniques: Signal relies on velocity induced phase shifts , takes advantage that flowing nuclei moving along a bipolar gradient have a higher signal than stationary nuclei

31
Q

MRA techniques: T1 3D gradient echo following gadolinium and dynamic imaging

A

contrast enhanced MRA

32
Q

when using MRA to evaluate extracranial vascular flow, such as that within common carotid arteries, a recommended technique is

A

2D time of flight MRA

33
Q

lead wires on the patients chest, used when imaging the chest, heart, & great vessels

34
Q

light sensor attached to patients finger to detect pulses through capillaries, not as accurate

A

peripheral gating

35
Q

bellows around the chest, signal corresponds to max and min motion of the chest, TR may be reduced

A

respiratory compensation

36
Q

the signal from flowing blood within the vessels in MRI and MRA relies on

A

first order motion

37
Q

scan is triggered from beats of the heart, uses R-R, signal during diastole

A

prospective gating

38
Q

post process after the scan is completed, continuously throughout all the cardiac phases

A

retrospective gating

39
Q

waiting time before each R-R wave

A

trigger window

40
Q

waiting period after each R-R

A

trigger delay

41
Q

MOTSA

A

maintain signal & improve coverage with large volume

42
Q

projects maximum intensity

43
Q

surface is presented on the reformatted data as though illuminated by a directional light source

44
Q

the direction in which ghosting & truncation artifacts happen in

A

phase only

45
Q

the direction in which aliasing, magnetic susceptibility, & magic angle artifacts happen in

A

both phase & frequency

46
Q

the direction in which chemical shift & zipper artifacts happen in

A

frequency only

47
Q

first small wave on ekg

A

p wave , atrial systole

48
Q

last wave on ekg

A

T-wave , ventricular diastole, may be elevated due to magnetohemodynamic effect

49
Q

chemical shift occurs in what direction

A

frequency only

50
Q

the appearance of phase mismapping artifact (ghosting)

A

produces replications of moving anatomy across the image

51
Q

the appearance of chemical shift artifact

A

dark edges at edge between fat & water

52
Q

appearance of magnetic susceptibility artifact

A

large signal voids , worse on 3T than 1.5T

53
Q

appearance of cross excitation & cross talk artifact

A

black line over cord, adjacent slices in different image contrasts

54
Q

appearance of zipper artifact

A

dense line across the image

55
Q

in tissues that contain collagen at high signal intensity

A

magic angle artifact

56
Q

aka wrap, anatomy outside FOV is folded on top of anatomy inside FOV

57
Q

black & white bending at the edge of the FOV

A

Moire artifact

58
Q

aka gibbs , from under sampling, banding at the interfaces of high & low signal, low intensity band running through high intensity area

A

truncation artifact

59
Q

optimizes scan time - the operator witnesses the arrival of the contrast

A

fluoro triggering

60
Q

optimizes scan time - tracker pulse measures signal from the lumen

A

bolus tracking

61
Q

optimizes scan time - small injection made to determine the exact time to begin scanning

A

test bolus