Dealing With Flow Ms 03 Ver

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    Dealing With Flow Ms 03 Ver - Presentation Transcript

    1. Dealing with Flow
    2. Difference between CT & MRI
      • In X-ray angiography a catheter is introduced and contrast injected under pressure. As it flows it displaces the blood and allows imaging of the vessel lumen, making it possible to image no matter what the natural flow dynamics of the vessel may be.
      • MRI (MRA) is a physiologic record of blood flow. If there is no flow, no blood vessels will be seen. For example a disturbance in the pattern of blood flow at a stenotic site causing turbulance may cause a reduced vascular signal or no signal at all.
    3. Flow
      • Nuclei such as that found in blood is moving, presenting a unique problem in MRI
      • The flowing nuclei have different contrast or may not show up at all if they do not produce a signal (mismapping)
      • Methods to reduce flow artefact (aka flow phenomena) exist
      • The major three types of flow phenomena are:
        • Time of flight
        • Entry slice phenomenon
        • Intra-voxel dephasing
    4. Mechanism of Flow
      • Four types of flow:
        • Laminar flow – flow is different but consistent velocity. Flow at center of vessel is faster than near walls.
        • Spiral flow – flow takes the form of a spiral
        • Vortex flow – flow starts off linear until it comes across a stricture or stenosis
        • Turbulent flow – flow at different velocities and is random in nature
    5. Flow phenomena – Time of flight
      • Stationary nuclei easily receive both the excitation RF pulse and rephasing pulses however if the nuclei is moving it can miss either one or both.
      • This phenomena is called time of flight
      • If flowing nuclei receive an excitation pulse w/o also receiving a rephasing pulse or vice versa a signal void occurs and the vessel appears dark (dark blood imaging)
    6. Flow phenomena – Time of flight
      • As velocity increases less and less nuclei will have the time to receive both the 90 0 and 180 0 RF pulses
      velocity TOF High velocity signal loss velocity TOF Flow related enhancement
    7. TE
      • The longer the TE the more chance a nuclei may receive one pulse and a signal void is created
    8. Slice thickness
      • In a thicker slice, moving nuclei have more of a chance of receiving both the 90 0 excitation and 180 0 RF pulses vs. a thinner slice .
      Excited rephased Not rephased thick thin
    9. TOF in gradient echo pulse sequences
      • In this sequence, after excitation RF, the nuclei are rephased by a gradient. The imaging volume is pulsed so rapidly that only a small portion of the tissues longitudinal magnetization can be gained between excitations. This causes an overall signal loss in the static volume of tissue. (this can be seen as a form of background suppression). Blood flow having receives less pulses will give off more signal.
      • The key here is that the gradient is applied to the whole body so it covers more than the thickness of a particular slice.
      • Therefore a flowing nuclei will be rephased and produce a signal regardless of its slice position
      • These sequences are said to be flow sensitive .
    10. Time of Flight ( TOF )
      • TOF manipulates the longitudinal magnetization of stationary spins. TOF uses coherent gradient echo sequences to enhance flow. The TR is kept below the T1 relaxation time of the stationary tissue ( T1 recovery is prevented ).
      • Inflow of protons produce siginal. Sat bands are used to in the opposite direction of the vessel you want to visualize.
    11. Disadvantages of TOF
      • If a vessel is parallel to the FOV according to the velocity it can be saturated out and the vessel can be misdiagnosed.
      • High signal from background tissue (fat has a short T1 relaxation time shows bright)
    12. TOF 2D AND 3D
      • 2D is slice by slice
        • Coverage large area
        • Sensitive to slow flow
        • Low resolution is a disadvantage
        • In-plane saturation is a disadvantage
        • Venetian blind and pulsation artifacts
      • 3D is a volume (3-6 cm) divided into 1mm sections
        • High SNR
        • Thin contiguous slices
        • Only can cover a small area is the disadvantage
        • Useful when imaging circle of willis
    13. TOF summary
    14. Entry slice phenomenon
      • This phenomenon is dependent upon the excitation history of nuclei during a TR period
      • For example nuclei having received several RF pulses within an acquisition having a short TR force the magnetic moments of the nuclei past the transverse plane where they are saturated.
      • Due to the short time longitudinal relaxation does not occur
      • Nuclei not receiving repeated RF as they enter a slice are said to be fresh
    15. Entry Slice phenomenon Nuclei not subjected to RF entering the first slice are fresh they produce a different signal compared to saturated nuclei As the nuclei moves toward the middle there is less entry slice phenomenon as the nuclei has received more excitation pulses they are “less fresh”
    16. Entry Slice phenomenon
      • The rate at which the nuclei receive excitation pulses determines the magnitude of the phenomenon.
      • This rate is influenced by the following factors:
        • TR
        • Slice thickness
        • Velocity of flow
        • Direction of flow
    17. TR
      • As a short TR increases the frequency with which RF is delivered, moving nuclei have a better chance of receiving both the excitation pulse and the rephasing pulses.
      • This in-turn decreases the magnitude of the entry slice phenomenon
    18. Slice Thickness
      • Nuclei traveling through thick slices will have the time to receive more RF pulses than nuclei moving through a thin slice
      • Entry slice phenomenon therefore increases in thick slices compared with thin slices.
    19. Velocity of flow
      • The faster nuclei move, the less chance they have of receiving both the excitation and rephasing RF pulses.
      • Thus if blood velocity is slow entry slice phenomenon is decreased as velocity lowers
    20. Direction of flow
        • Co-current flow in which nuclei travel in the same direction as slice selection. This scenario is best as nuclei has more chance to receive repeated RF excitations, reducing the entry slice phenomenon.
        • Counter –current in which nuclei travel in the opposite direction to slice selection. Nuclei moving opposite to slice excitation when entering slices are less likely to have received excitation pulses and stay (fresh).
    21. Intra voxel dephasing
      • Each voxel in a MR image contributes signal. If the contents within any one voxel are out of phase with each other, the overall average signal amplitude from the voxel will decrease.
      • This can occur when a moving nuclei interact with a stationary nucleus.
      • Depending on the nuclei motion and how the gradient is applied, it may either lose (slower) or gain phase (faster)
    22. Flow phenomena compensation
      • All flow phenomena are detrimental to image quality and when possible should be compensated for.
      • There are several methods to accomplish this:
        • Even echo rephasing
        • Gradient moment nulling
        • Spatial pre-saturation
    23. Even echo rephasing
    24. Gradient moment rephasing (nulling)
      • This method of dealing with intra-voxel dephasing from flowing nuclei utilizes the slice select gradient and/or the readout (fq) gradients to bring the nuclei back into phase.
      • When in phase both stationary and moving nuclei contribute to the signal and flowing nuclei give a bright signal.
      • STEPS
        • nuclei traveling along a gradient will be of varying speeds ( phases)
        • The slice select/readout gradient alters its polarity from positive to double negative and then back to positive again
      • For GMR to work well flow must be of constant velocity and direction
    25.  
    26. Spatial pre-saturation
      • The prefix pre is the major aspect of this flow compensation method as nuclei in a volume outside the FOV receive 90 0 RF pulses to presaturate it prior to it entering the slices.
      • After entering the stack it is hit again with an excitation pulse.
      • If the two add to 180 0 the nuclei will be fully saturated and will not have any transverse component magnetization and thus no signal.
    27. Fat saturation
      • As we have learned to satruate fat a 90 0 pre-saturaton pulse will need to be applied at the precessional frequency of fat.
      • This is followed by the excitation RF pluse (total of 180 0 ) which will push the fat nuclei into saturation producing a signal void.
      • The time interval between the pre-saturation pulses is called SAT TR
      SAT TR = Scan TR / # of slices
    28. FatSat
    29. Water saturation
    30. Spatial pre-saturation
    31. Spatial inversion recovery (SPIR)
      • SPIR selectively inverts and thus nulls the signal from fat.
      • STEPS
        • RF pulse at precessional frequency of fat is applied (180 0 ) twice as much as chemical pre-saturation technique.
        • The magnetic moments of the nuclei are now in the -Z direction.
        • After a time interval (TI) corresponding to the null point an excitation pulse is applied. Fat signal is nulled as there is no transverse magnetization.
    32. SPIR advantage
      • As mentioned chemical fat suppression relies on the precessional fq. of fat and for optium results the precessional frequency of a volume should be the same but this is unrealistic.
      • SPIR is not dependent (like chemical fat suppression) on magnetic field homogeneity and utilizes null point of fat much like STIR
    33. STIR better but
      • STIR shows more uniform nulling of fat than SPIR but gadolinium may also be nulled along with fat.
      • Thus SPIR should be used to null signal from fat if gadolinium is to be given
    34. Out of phase imaging (Dixon technique)
      • This technique is utilized in gradient echo sequences.
      • This technique will null any signal arising from voxels which contain both fat and water.
      • By utilizing a TE when fat and water are out of phase with each other they will not yield a signal
    35. summary
      • Fat is nulled with the following techniques:
        • Fat saturation
        • STIR
        • SPIR
        • Out of phase imaging (Dixon technique)
      • Even echo rephasing
        • Balanced echoes where even echoes demononstrate less dephasing than odd echoes
        • Reduces intra voxel dephasing
        • Used in T2 weighted sequences
    36. summary
      • Gradient moment rephasing:
        • Additional gradients to correct altered phase values
        • Reduces artefact from intra-voxel dephasing
        • Gives flowing nuclei bright signal
        • Used with T2 or T2*
        • Best with slow, laminar flow within the slice
      • Chemical pre-saturation:
        • Extra RF used to null signal from flowing nuclei
        • Reduces artefact from TOF and entry slice phenomenon
        • Creates a signal void from flow
        • Used with T1
        • Best on both fast or slow flow
        • Increases RF to pt.
        • Used to null signal from fat or water to reduce aliasing.

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