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Pulsesequencesfornon
CE‐MRA
S. I. Gonçalves, PhD
Radiology Department
University Hospital Coimbra
Autumn Semester, 2011
Pulse sequences for non CE‐MRA
“MRI: Principles and Applications”, Friday, 8.30‐9.20 am
1
Magneticresonanceangiography(MRA)
• For that reason, cardiac gating and blood flow compensation are commonly used strategies to overcome these problems;
• However, imaging blood vessels has an interest on its own, and that is the goal of Magnetic Resonance Angiography (MRA);
Pulse sequences for non CE‐MRA
• In conventional MRI, one tries to visualize organ parenchyma. In this sense, blood vessels and the effects of blood flow are often confounders and a source of artifacts;
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MRAmethods
RARE
Dark Blood
MRA pulse sequences
CE MRA
Bright
Blood
TOF
Non‐CE MRA
RARE – Rapid acquisition with refocused echoes (FSE)
IR – Inversion Recovery
CE – Contrast enhanced
TOF – Time‐of‐flight
PC MRI – Phase Contrast MRI
SSFP – Steady‐state free precession
Pulse sequences for non CE‐MRA
IR
PC MRI
SSFP
3
MRAmethods
RARE
Dark Blood
MRA pulse sequences
CE MRA
Bright
Blood
TOF
Non‐CE MRA
RARE – Rapid acquisition with refocused echoes (FSE)
IR – Inversion Recovery
CE – Contrast enhanced
TOF – Time‐of‐flight
PC MRI – Phase Contrast MRI
SSFP – Steady‐state free precession
Pulse sequences for non CE‐MRA
IR
PC MRI
SSFP
4
Introduction
Or
• It can be accomplished by looking carefully into blood flow effects and take advantage of those to retrieve information about vessel morphology (e.g. measurement of blood vessel lumen) but also about flux velocities: Time‐Of‐Flight (TOF) or Phase Contrast (PC‐) MRI;
Pulse sequences for non CE‐MRA
• MRA can be accomplished by enhancing the signal from blood through the inflow of fresh (unsaturated) spins into the slice of interest via the use of an exogenous T1‐
reducing contrast agent – CE‐MRA;
5
Introduction
 CE‐MRA is the traditional method to acquire MRA images;
 It has short acquisition times and it is characterized by good SNR;
 Decreased susceptibility artifacts due to blood flow and pulsatility;
 There have been reports linking gadolinium usage to nephrogenic systemic fibrosis in patients with kidney disease or insufficiencies (http://www.nephrogenicsystemicfibrosis.org/nsf/);
 Current CE MRA using conventional Gd‐contrast agents are limited to the need of acquiring images very fast during the first pass of the contrast in the vessels of interest;  Cost;
Pulse sequences for non CE‐MRA
 Improved anatomical coverage;
6
MRAmethods
RARE
Dark Blood
MRA pulse sequences
CE MRA
Bright
Blood
TOF
Non‐CE MRA
RARE – Rapid acquisition with refocused echoes (FSE)
IR – Inversion Recovery
CE – Contrast enhanced
TOF – Time‐of‐flight
PC MRI – Phase Contrast MRI
SSFP – Steady‐state free precession
Pulse sequences for non CE‐MRA
IR
PC MRI
SSFP
7
Time‐Of‐Flight(TOF)
• With the exception of a few single‐shot methods, the magnetization must be excited several times (at least once per TR), in order to acquire an image;
• This leads to magnetization saturation and signal loss due to incomplete T1 relaxation;
Pulse sequences for non CE‐MRA
• In a conventional analysis of imaging sequences, tissues (spins) are assumed to be stationary;
8
Time‐Of‐Flight(TOF)
RF excitation
Measured signal
Pulse sequences for non CE‐MRA
Stationary tissue
9
Time‐Of‐Flight(TOF)
RF excitation
Measured signal
Pulse sequences for non CE‐MRA
Stationary tissue
10
Time‐Of‐Flight(TOF)
RF excitation
Measured signal
Pulse sequences for non CE‐MRA
Stationary tissue
Saturation
11
Time‐Of‐Flight(TOF)
RF excitation
Pulse sequences for non CE‐MRA
Blood flow (moving spins)
v
Measured signal
Imaging volume
12
Time‐Of‐Flight(TOF)
• Rapid series of slice‐selective RF excitation pulses that saturate (null) background signal;
• Signal from flowing blood results from the constant entrance of “fresh” magnetization into the imaging plane – Flow Related Enhancement (FRE) (Axel, 1984);
• FRE increases with blood flow velocity;
Pulse sequences for non CE‐MRA
• It is the most commonly used non CE MRA technique, especially for intracranial and peripheral applications;
13
Pulse sequences for non CE‐MRA
Time‐Of‐Flight(TOF)
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3D TOF MRA
Time‐Of‐Flight(TOF)
Carotid arteries
Pulse sequences for non CE‐MRA
Carotid arteries
Vertebral arteries
Native image
MIP reconstruction
2D TOF MRA
15
Hartung et al., 2011
 TOF can be 2D or 3D;
 Assumed to have velocity compensation;
 Susceptible to signal voids in regions with slow flow, tortuous vessels or in‐plane vessels;
 3D TOF most commonly used for intra‐cranial vasculature (where in‐plane flow is more frequent);
 2D more frequently used for carotid evaluation;
 Variable flip angles and MOTSA techniques to overcome signal saturation;
2D TOF MRA
Pelvis, thighs, calves
Bilateral occlusion of superficial femoral arteries, flow to runoff arteries (calves) through collateral vessels in the thighs, arising from the profunda femoris arteries.
Hartung et al., 2011
Pulse sequences for non CE‐MRA
Time‐Of‐Flight(TOF)
16
Phase‐Contrast (PC‐) MRI
• The resulting signal is proportional to flow velocity, as in TOF but also to the strength of the velocity encoding gradient (which is controlled by the parameter Venc);
• Contrary to TOF, the application of velocity encoding gradients allows the retrieval of information over blood flow velocities;
• Thus, PC‐MRI provides anatomical images of the vessels as well as information about the hemodynamics of blood flow;
Pulse sequences for non CE‐MRA
• PC‐MRI generates an image by applying an extra velocity encoding gradient;
17
Phase‐Contrast (PC‐) MRI

RF
Pulse sequences for non CE‐MRA
slice
phase
readout
signal
Echo 1,
1
18
Bipolar velocity encoding
TR
Phase‐Contrast (PC‐) MRI

RF
Pulse sequences for non CE‐MRA
slice
phase
readout
signal
Echo 2,
2
19
Bipolar velocity encoding
TR
Phase‐Contrast (PC‐) MRI
1
2
Phase Image from which velocities can be derived
 PC‐MRI can be used to identify the direction and velocity of flow;  Parameter Venc gives the maximum velocity that can be measured without aliasing;  Better background suppression than TOF;
 Limited by longer image acquisition times and higher sensitivity to changes in velocity and magnitude of blood flow during cardiac cycle;
 Sensitive to types of flow which can be important for diagnosis (e.g. signal voids in regions of turbulent flow in the vicinity of a stenosis;
 4D PC‐MRI is the new development of PC‐MRI where time resolved images are acquired with the add of acceleration techniques such as parallel imaging, 3D radial undersampling trajectories, etc;
Pulse sequences for non CE‐MRA
• Velocity information:
20
Phase‐Contrast (PC‐) MRI
3D CE MRA
3D PC‐MRI
Digital subtraction angiography
Pulse sequences for non CE‐MRA
Signal void indicates stenosis with important consequences in the hemodynamics of blood flow
21
Patient with renal artery stenosis
Hartung et al., 2011
Phase image of aortic arch and major pulmonary vessels
Color‐coded sagittal phase images of the thoracic aorta with flow quantification
Pulse sequences for non CE‐MRA
Phase‐Contrast (PC‐) MRI
22
https://www.medical.siemens.com/webapp/wcs/stores/servlet/
Steady‐StateFreePrecession(SSFP)
MRA
• Both arteries and veins have bright signal which makes these sequences very suited for thoracic MRA applications (evaluation of large vessels (arteries and veins) in congenital heart disease);
• Fast image acquisition in 3D;
• Very good SNR;
• Wide application in coronary MRA;
Pulse sequences for non CE‐MRA
• Popular because b‐SSFP sequences are weighted on T2/T1 which provides an inherent bright blood contrast that have little dependence on blood inflow;
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Pulse sequences for non CE‐MRA
SSFPMRA
Patient with a saccular aortic arch aneurysm
24
Hartung et al., 2011
SSFPMRA
Accessory renal artery
Main renal artery
SSFP MRA
Accessory renal artery
Main renal artery
Pulse sequences for non CE‐MRA
Segmental renal artery branches
CE MRA
25
Hartung et al., 2011
Renal artery stenosis Iliac artery stenosis
IR SSFP MRA
CE MRA
Nishimura et al., 1987
Digital subtraction angiography
Pulse sequences for non CE‐MRA
SSFPMRA
26
Patient with renal transplant artery stenosis
Hartung et al., 2011
Acoupleofarticlesforfurtherreading
 Chribiri et al., Progress in Cardiovascular Diseases 54 (2011) 240–252
http://www.onlinepcd.com
 Wilson and Maki, Magn Reson Imaging Clin N Am. 2009 Feb;17(1):13‐27
 Gough, J Vasc Surg. 2011 Oct;54(4):1215‐8. Epub 2011 Aug 25
 Bongartz et al., Eur J Radiol. 2008 May;66(2):213‐9.
Pulse sequences for non CE‐MRA
 Hartung et al., Journal of Cardiovascular Magnetic Resonance 2011, 13:19
http://www.jcmr‐online.com/content/13/1/19
27