Cardiac MRI Made Easy 2008

To R and K
—My constant companions

AV
To Indigo Lucy
—May the wonder of nature always fascinate you
DJP
For Elsevier
Commissioning Editor: Laurence Hunter
Development Editor: Helen Leng
Project Manager: Elouise Ball
Design Direction: Erik Bigland
Illustration Manager: Merlyn Harvey
Illustrator: Paul Bernson
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First published 2008
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Preface
Cardiovascular magnetic resonance (CMR) describes the use of magnetic resonance
imaging (MRI) for the anatomical and functional evaluation of the heart and vascular
tree. The traditional arsenal of noninvasive imaging modalities available to the
cardiologist and cardiothoracic surgeon include echocardiography and nuclear
cardiology. CMR is a contemporary and complementary technology which is rapidly
gaining popularity in this dynamic field.
At present, there are several large reference books on CMR which provide a
comprehensive guide to the physics and clinical application of this technique. In this
book we provide a more easily digestible synopsis which is readily portable and can
be rapidly updated. The Royal Brompton Hospital has been at the vanguard of CMR
throughout its journey from a fledgling research idea to fully grown clinical ideal and
we hope this small book successfully condenses our experience in this arena.
We have targeted the text predominantly at the needs of cardiologists and
cardiothoracic surgeons wishing to acquaint themselves with CMR — what it can do
and what it cannot. The chapters therefore concentrate on the cardiac side of CMR
but also address its more established vascular uses in a later section. Before both of
these, however, we outline some of the basic principles of MRI.
Anitha Varghese
Dudley Pennell
v
Acknowledgements
Our thanks go to all the past and present members of the CMR Department, Royal
Brompton Hospital. Additionally, we express our specific gratitude to Laurence
Hunter, Helen Leng, Charles Lauder Jr and Elouise Ball at Elsevier, Ritesh Mewar,
Didier Locca, Henning Steen, Taigang He, Paul Kotwinski and Karen Symmonds for
their role in the preparation of the final manuscript.
Note to readers
Please note that the statements made in this book refer to CMR performed at a magnet
field strength of 1.5 Tesla.
Contributors
Beatriz Bouzas MD Katharina Kiss MD
Consultant Cardiologist, Servicio de Department of Cardiology, Hospital
Cardiologia, Complejo Hospitalario of Hietzing, City of Vienna and
Universitario Juan Canalejo, La Caruña, Spain Cardiovascular Imaging Unit
Rudolfinerhaus Vienna, Austria
Ping Chai MRCP
Consultant Cardiologist, Cardiac James C Moon MA MRCP MD
Department, National University Hospital, Senior Lecturer in Cardiology, The Heart
Singapore Hospital, London, UK
The Heart Institute, National Healthcare
Group, Singapore Richard Steeds MA MRCP MD
Consultant Cardiologist with Special
Ilse Crevits MD Interest in Imaging, University Hospital
General Radiologist, HHR—Site Roeselare Birmingham NHS Foundation Trust,
Hospital, Roeselare Birmingham, UK
Visiting Consultant CMR, University
Hospitals of Leuven, Belgium Marc D Tischler BA MD FACC FAHA FACP
Associate Professor of Medicine, University
George E Gentchos MD of Vermont College of Medicine
Assistant Professor of Radiology, College of Director, Cardiac Ultrasound Laboratory,
Medicine University of Vermont, Burlington, Fletcher Allen Health Care
Vermont, USA Director, Clinical Cardiac MR Unit, Fletcher
Allen Health Care, Canada
Chad A Hoyt MD FACC
Director of Cardiovascular CT and MR, Anitha Varghese BSc MRCP
Stroobants Heart Center, Centra Health Research Fellow, Royal Brompton Hospital,
Director of Noninvasive Cardiovascular London; Specialist Register in Cardiology,
Services, Bedford Memorial Hospital West Midlands Deanery, UK
Cardiologist, The Cardiovascular Group,
Centra Health, Lynchburg, Virginia, USA
vii
Abbreviations
ACHD Adult congenital heart disease IVS Interventricular septum
AFD Anderson Fabry disease kg Kilograms
AICD Automated implantable cardiac l/min Litres per minute
defibrillator LA Left atrium
AMVL Anterior mitral valve leaflet LAD Left anterior descending artery
Ao Aorta LCx Left circumflex artery
APVD Anomalous pulmonary venous LGE Late gadolinium enhancement
drainage LMS Left main stem
AR Aortic regurgitation LPA Left pulmonary artery
ARVC Arrhythmogenic right ventricular LV Left ventricle
cardiomyopathy LVEDV Left ventricular end-diastolic
AS Aortic stenosis volume
ASD Atrial septal defect LVEF Left ventricular ejection fraction
AV Aortic valve LVESV Left ventricular end-systolic
CABG Coronary artery bypass grafting volume
CAD Coronary artery disease LVH Left ventricular hypertrophy
ccTGA Congenitally corrected LVNC Left ventricular non-compaction
transposition of the great arteries LVOT Left ventricular outflow tract
CE-MRA Contrast-enhanced magnetic LVSV Left ventricular stroke volume
resonance angiography m/s Metres per second
CFR Coronary flow reserve MAPCAs Major aortopulmonary collateral
cm Centimetres arteries
CMR Cardiovascular magnetic MHz Megahertz
resonance MI Myocardial infarction
CSF Cerebrospinal fluid min Minute
CT Computed tomography MIP Maximal intensity projection
DCM Dilated cardiomyopathy mL Millilitre(s)
DSE Dobutamine stress ml/s Millilitre per second
echocardiography mm Millimetres
ECG Electrocardiogram mmHg Millimetres of mercury
EDV End-diastolic volume MPA Main pulmonary artery
EF Ejection fraction MPR Multiplanar reconstruction
EGE Early gadolinium enhancement MR Mitral regurgitation
ESV End-systolic volume MRA Magnetic resonance
FLASH Fast low-angle shot angiography
FSE Fast spin echo MRI Magnetic resonance imaging
g/m2 Grams per metre squared MRS Magnetic resonance
Gd Gadolinium spectroscopy
Gd-DTPA Gadolinium diethylenetriamine ms Milliseconds
pentaacetic acid MS Mitral stenosis
GE Gradient echo MV Mitral valve
HCM Hypertrophic cardiomyopathy MVO Microvascular obstruction
IAS Interatrial septum MVP Mitral valve prolapse
IVC Inferior vena cava PA Pulmonary artery
ix
Abbreviations
Abbreviations (continued)
PAPVD Partial anomalous pulmonary T Tesla
venous drainage T1W T1-weighted/weighting
PCI Percutaneous coronary T2W T2-weighted/weighting
intervention TGA Transposition of the great
PDA Patent ductus arteriosus arteries
PMVL Posterior mitral valve leaflet TOE Transoesophageal
PR Pulmonary regurgitation echocardiography/
PS Pulmonary stenosis echocardiogram
PV Pulmonary valve TOF Tetralogy of Fallot
RA Right atrium TR Tricuspid regurgitation
RCA Right coronary artery TS Tricuspid stenosis
RF Radiofrequency TSE Turbo spin echo
RPA Right pulmonary artery TTE Transthoracic
RV Right ventricle echocardiography/
RVH Right ventricular hypertrophy echocardiogram
RVOT Right ventricular outflow tract TV Tricuspid valve
RVSV Right ventricular stroke volume Venc Maximal encoding velocity
SE Spin echo Vmax Peak velocity
SNR Signal-to-noise ratio VSD Ventricular septal defect
SoV Sinus of Valsalva WMA Wall motion abnormality/
SSD Shaded surface display abnormalities
SSFP Steady state free precession 2D Two-dimensional
SV Stroke volume 3D Three-dimensional
SVC Superior vena cava ␮g Micrograms
x
Chapter 1
Principles of CMR
Anitha Varghese
Basic physics
MRI is based on nuclear magnetic resonance, the phenomenon of the resonance of
atomic nuclei in response to radiofrequency (RF) waves.
The hydrogen atom is the simplest and most abundant element in the body and
consists of one proton nucleus orbited by one electron. The hydrogen nucleus can
therefore also be termed a proton, and current clinical MRI techniques are based
on receiving and processing RF signals from protons. Protons have a magnetic axis
which is normally randomly orientated. When a magnetic field is applied, the protons
align in synchrony and spin around an axis in line with the main magnetic field—
this spinning is termed precession. The rate at which protons precess is measured
by the precession frequency, which changes linearly with increasing magnetic field
strengths. When protons precess in synchrony they are said to be in-phase. There is
loss of synchrony with time, and this is also termed out-of-phase.
At equilibrium within a magnetic field, overall proton alignment is in the
direction of the main magnetic field and they have net longitudinal magnetization.
This equilibrium can be disturbed by transmission of RF energy at the precession
frequency of the proton which is 63 megaHertz (MHz) for water protons at 1.5 Tesla
(T)—the strength of most commercially used magnets (Figure 1.1).
The degree of proton excitation is proportional to the amplitude and duration of
the RF pulse. After excitation, proton relaxation occurs as the energy is dissipated
and this process is defined by two parameters known as T1 and T2. T1 relaxation
times measure the time after excitation to recover the longitudinal magnetization
found in the equilibrium state. Transverse magnetization decays at a rate measured
by T2, which is faster than the rate of T1 recovery. T1 and T2 relaxation vary
according to the environment of the hydrogen atom within tissues and imaging
sequences can be designed with different preference (or weighting) to one of these
relaxation parameters for tissue characterization, known as T1-weighted (T1W) and
T2-weighted (T2W) acquisitions. The values for T2 are always below that of T1,
and T1 represents the upper limit of T2. T1 and T2 values tend to parallel each
other when proton motion is relatively random, for example in adipose tissue, which
has a short T1 and T2, and free water, which has a long T1 and T2. Tissues with
a more organized structure contain abundant bound water. In this case proton motion
is not random, there is increased transverse decay from the exchange of energy
between protons, and T2 values become shorter than those of T1.
1
1 Principles of cardiovascular magnetic resonance (CMR)
Magnet
Table
Figure 1.1 1.5T CMR Scanner. The adjustable patient table is shown within the
surrounding superconducting magnet.
Localization of anatomical position within a selected imaging slice or volume is

done with the application of frequency- and phase-encoding gradients. The corres-
ponding direction of application of these gradients is known as the frequency encode
or phase encode direction. With modifications of the phase-encoding gradients flowing
blood can be differentiated from stationary anatomy via alterations in the phase of
the MR signal. The velocity of material is proportional to the phase change or phase
shift caused by its movement during gradient application.
Transmission and reception of RF energy is via special aerials known as coils with
subsequent conversion of these raw data into images using ultrafast computers and
a process known as Fourier transformation.
Main sequences
There are two fundamental types of sequence commonly used in CMR: gradient
echo (GE) and spin echo (SE). As a general rule, with GE sequences both blood and
fat appear white and so this technique is also known as white-blood imaging
(Figure 1.2a). By contrast, in SE sequences blood is usually black but fat is white,
giving rise to the term black-blood imaging (Figure 1.2b). SE sequences are more
useful for anatomical imaging as opposed to the functional imaging performed with
GE sequences. Variations of GE sequences are fast low-angle shot (FLASH), fast
imaging with steady-state free precession (SSFP), and velocity mapping. GE imaging
also forms the basis of the inversion recovery technique.
2
Main sequences 1
LV
b
Figure 1.2 (a) CMR of mid-ventricular short-axis view using GE imaging. Blood
within the left ventricle (LV) is white as is the surrounding epicardial fat (black arrow). The
LV myocardium (white arrow) appears mid-grey. (b) CMR in the same plane using SE
imaging. Blood within the LV now appears black while the fat remains white.
Areas of focal myocardial dysfunction and abnormal flow patterns are readily
visualized with the technique of cine imaging using SSFP (or cines). Cines are obtained
by rapid repetition of a variant of the basic GE sequence to obtain a series of
cardiac images at progressively advancing points of the cardiac cycle which when
put together form a cine loop. The weighting of SSFP sequences depends on the
ratio of T2/T1, therefore most fluids and fat have a high signal and appear white.
However, muscle and many other solid tissues have a long value for T1 and a short
value for T2. This means that their signal intensity is reduced to shades of grey
3
(Figure 1.2a). In addition to cines, the SSFP sequence can also be applied
as a two-dimensional (2D) single-shot technique, as a real-time technique (not
requiring breath holding or electrocardiogram (ECG) triggering), and as a three-
dimensional (3D) volume scan.
Velocity mapping (or flow velocity mapping) techniques can determine the average
velocity within a single imaging voxel, typically 1 μ 1 μ 10 mm3. The operator selects
the required plane and sets a maximal encoding velocity (Venc; Figure 1.3). The
initial Venc used is an approximation of the velocity expected based on factors such
LV
a b
d e
4
Main sequences 1
as clinical history, the type of valve or conduit lesion, and images already acquired.
The Venc represents the practical upper limit of velocities that can be depicted
unambiguously and should ideally be set to a numerical value just greater than
the true velocity. Problems occur if it is set much higher or lower than this value—
with the former leading to less sensitivity and the latter causing misrepresentation
via the phenomenon of aliasing. Velocity aliasing is when the flow appears to be
in the opposite direction and is characterized by a sudden transition of white-to-
black or vice versa within the chosen flow region (Figure 1.3d). To eliminate or
reduce aliasing a higher Venc must be set and the velocity mapping sequence
repeated (Figure 1.3e). The maximal velocity of jets under interrogation should only
be determined from the Venc-optimized images. Aliasing is also noted with 2D
Doppler echocardiography and the technique of velocity mapping gives similar
information. Subjects are asked to suspend their breathing for measurement of peak
velocities using this method, which takes approximately 20 seconds to perform.
An example of its use is for the quantification of peak velocity in valvular stenosis.
Velocity mapping sequences are also used to calculate overall flow in a major vessel
through the cardiac cycle and so can be used for quantification of regurgitation in
valvular incompetence. For calculation of peak velocity and transvalvular flow,
the plane used must be through plane—a plane perpendicular and just distal
to the area of interest. Velocity mapping CMR is also used to confirm abnormal
chamber communication and the ratio of pulmonary to systemic flow in shunts
such as septal defects.
Compared to GE sequences, SE pulse sequences are usually more robust to system
imperfections, such as magnetic field inhomogeneities. In SE imaging, structures
need to be stationary for the delivery of two RF pulses. The T2 value of stationary
fluid is long and gives high signal. Examples are fluid-filled structures such as cysts,
which therefore appear white with SE sequences. However, flowing blood moves
out of the selected slice before receiving the second pulse and so gives no signal
and appears black (Figure 1.2b). Slower flowing blood can give persistent signal of
varying signal intensity. Important variations of SE sequences are fast (or turbo) spin
echo (FSE or TSE). FSE allows faster imaging than standard SE by acquiring more
Figure 1.3 Cine images (a, b) combined with velocity mapping imaging (c–e).
(a) Left ventricular outflow tract (LVOT) cine image of severe aortic stenosis (AS). The plane
chosen for velocity mapping is just distal and perpendicular to the valve orifice (white line)
and results in the oblique sagittal view shown in (b). (b) This shows a tricuspid aortic valve
(AV; white arrow) and is the plane used for subsequent velocity mapping. AV area can be
measured in this view. (c) Magnitude image component of the velocity mapping sequence,
which confirms reduced valve area in a tricuspid AV. (d) The velocity mapping sequence
shows systolic blood flow through the AV as black, but the Venc was set too low by the
operator and the centre of the jet has turned white, a phenomenon known as aliasing
(white arrow). (e) A second velocity mapping sequence was therefore performed using an
increased Venc. The black jet through the AV is now clearly seen (white arrow) and there
are only occasional edge pixels which are aliased. Peak systolic velocity in the centre of
the stenotic jet was 4 m/s.
5
lines of data for every RF pulse delivered and allows acquisition of an entire image
in a single heartbeat.
The inversion recovery technique uses a prepulse to create high T1 tissue contrast
which is important for infarct imaging. This sequence and contrast-enhanced magnetic
resonance angiography (CE-MRA) require use of a contrast agent. MRI contrast agents
are commonly based on chelates of gadolinium which are paramagnetic, one example
being gadolinium diethylenetriamine pentaacetic acid (Gd-DTPA). All gadolinium
chelates currently approved for clinical use are extravascular and therefore become
distributed within the interstitium following initial intravenous delivery.
CMR is performed by applying these main sequences and their variants to
evaluate cardiovascular physiology and anatomy, characterize tissue, and perform
vascular angiography. Additionally, cardiac metabolism can be determined with
magnetic resonance spectroscopy (MRS). MRS is not covered in this book and the
interested reader is referred to the further reading section.
Most CMR scans are timed with respect to the ECG (ECG-gated) to minimize
cardiac motion artefact, and subjects are asked to suspend their breathing in end
expiration (breath-hold) to minimize respiratory motion artefact. In some cases scans can
be linked to the respiratory cycle using diaphragmatic monitoring techniques (respiratory-
gated), allowing subjects to breathe normally (free breathing). High signal from fat can
be reduced by the application of a frequency-selective prepulse (fat suppression).
Patients are advised that data are being acquired during the time when the
scanner is making a noise. This noise is generated by coils within the magnet.
Headphones are worn by subjects during a CMR study and this serves to minimize
their discomfort during noisy periods, facilitate hearing instructions from scanner
operators, and allow music to be heard throughout if requested.
Hardware and software requirements

CMR is performed within a large superconducting magnet with its associated radio
wave generation and computer systems. Medical gases, physiological monitoring
telemetry, stress infusion pumps for delivery of adenosine and dobutamine, a power
injector for contrast studies, and full resuscitation equipment and drugs are also
required. As mentioned above, microphones, headphones and a music system are
important. Ear plugs are needed for people who are required to accompany certain
patient groups such as children, and those with varying degrees of claustrophobia.
Less than 2% of scans are limited by claustrophobia in the adult population and
other measures of alleviating anxiety are blindfolds and prism glasses. The latter
provide a way for the patient to look out even when enclosed by the bore of the
magnet.
Modern scanners have ultrafast applications for real-time imaging and assessment
of coronary artery disease (CAD). Additional software is important for the post-
processing of data. Manufacturers such as Siemens, Philips and General Electric
provide their own software for analysis and other third party packages are available
such as CMRtools (Cardiovascular Imaging Solutions).
6
Imaging planes and protocols 1
Imaging planes and protocols
CMR can obtain images in any plane but standard planes of reference are used to
enable normal ranges to be defined. Subjects are generally scanned in the supine
position and the most important planes in cardiac imaging are four-chamber, two-
chamber, short-axis, LVOT and right ventricular outflow tract (RVOT). Suggested
steps in obtaining these standard planes are shown sequentially in Figures 1.4–1.9,
and a protocol incorporating them into routine cardiac evaluation is shown in
Table 1.1.
LV
RV
apex
AMVL
PMVL
i
ii
iii
iv
LV
apex
b
Figure 1.4 (a) From the initial low-resolution free breathing transaxial FSE, a
perpendicular two-chamber pilot view is obtained through a perpendicular plane placed at
the mid-point of the mitral valve (MV) leaflets and the LV apex (solid white line). (b) Using
this pilot two-chamber view, four perpendicular short-axial pilot views are acquired: one at
the atrioventricular groove (slice ii; solid white line), and three either side on the atrial and
ventricular aspects (slices i, iii and iv; dashed white lines). Abbreviations: A, anterior aspect
of the image; LV, left ventricle; RV, right ventricle; AMVL, anterior mitral valve leaflet; PMVL,
posterior mitral valve leaflet.
7
LA
Ao Ao
RA
IAS
a b
LV
RV
c d
Figure 1.5 The four-chamber cine is obtained from the resulting four short-axial pilots (a–d):
the imaging slab (solid white line) is placed through the centre of the LV cavity, the acute margin
of the RV (c—white ellipse), and the interatrial septum (IAS), just below the aorta (Ao). LA, left
atrium; RA, right atrium.
8
LV
apex
v
iv
iii
i ii
Ao
i
A MPA
v
LV
apex
Figure 1.6 The four-chamber cine (a) is used along with the two-chamber pilot view to
obtain the two-chamber cine (b). From the end-diastolic frame of the four- and two-chamber
cines, the ventricular short-axis stack of cines are acquired: the initial perpendicular short-
axis slice (solid white line) is placed on the atrioventricular groove through the back of the
LV and RV, and subsequent slices (dashed white lines) are acquired incrementally towards
the LV apex. MPA, main pulmonary artery.
9
a d
b e
c f
10
Figure 1.7 Nine short-axis cines (slice

thickness 7 mm, with 3 mm interslice
gap) typically allows full coverage of the
ventricles (a–i).
i
11
LA/
basal LV slice
RV
LV
Ao
RA
a b
Ao
A
PA
Ao
LV
LV
c d
Figure 1.8 The LVOT cine is acquired using a basal short-axis pilot (a) and four-
chamber cine (b): a perpendicular slice is placed through a plane on the short-axis pilot
which transects the aortic root and the distal LA/basal LV cavity (solid white line). This slice
is then angulated to cut through the LV apex (white ellipse), giving the first LVOT view (c).
Transection through the aorta (dashed white line) results in the second, coronal LVOT view
(d). PA, pulmonary artery.
12
RV
MPA
RA LV
Ao
LPA
LA
RPA
right lower
pulmonary vein
a b
A MPA Ao
RV
c
Figure 1.9 For the RVOT cine, the transaxial FSE is recalled: a slice is placed
perpendicular to the MPA, which transects the RV (a, b—white line). (c) The resulting RVOT
view. RPA, right pulmonary artery; LPA, left pulmonary artery.
Protocols for cardiac imaging involve four stages:
Stage 1: Initial, rapid, pilot scans in the three orthogonal planes—transaxial,

coronal and sagittal;
Stage 2: Slower, low-resolution, comprehensive anatomical coverage from the
diaphragm up to the thoracic inlet in two to three orthogonal planes—
mandatory transaxial, suggested coronal, optional sagittal (mandatory in
aorta imaging);
Stage 3: Specific cardiac imaging in the standard planes with GE cines and
optional additional SE sequences;
Stage 4: Targeted CMR with additional planes and sequences such as inversion
recovery.
13
Table 1.1 A standard CMR protocol which typically takes 30 minutes to perform
Pre-contrast
Five-slice SSFP pilot
Free breathing, low-resolution transaxial FSE
Breath-hold, low-resolution coronal (+ sagittal) FSE
Two-chamber pilot
Four short-axial pilots
Four-chamber and two-chamber cines
LVOT and RVOT cines
Ventricular short-axis stack cines
Post-contrast
Early gadolinium enhancement (1–5 minutes)
(a) Rpt four-chamber
(b) Rpt two-chamber
(c) Rpt LVOT
Late gadolinium enhancement (5–15 minutes)
(a) Rpt four-chamber
(b) Rpt two-chamber
(c) Rpt ventricular short-axis stack
The initial pilot images are performed in a breath-hold and are used to optimize
subject placement within the magnetic field using the table-positioning tool—the
centre of the heart should be at the centre of the field. The pilot scan also enables
the user to check that the correct coils are activated and other system requirements
are satisfactory. Subsequent low-resolution anatomical coverage using FSE acquires
one image per cardiac cycle. This allows a ‘quick-look’ for cardiac and extracardiac
pathology at the start of the study and resulting images must be reviewed prior
to further acquisitions. A series of transaxial FSE images usually consists of 35–
40 slices, performed in free breathing over 1–2 minutes. A 12- to 15-slice series
of coronal and sagittal FSE images encompass the heart and can be performed
in a breath-hold. Breath-hold images do enable more accurate positioning of
subsequent slices, but respiratory variations are small within the transaxial plane.
Acquisition of the standard planes has been detailed in Figures 1.4–1.9. Additional
targeted planes and sequences are chosen depending on the referral request, and
presence and type of other pathology.
Normal ranges
The normal ranges for end-diastolic volumes (EDV), end-systolic volumes (ESV),
stroke volumes (SV), ejection fraction (EF) and myocardial mass indexes in males
and females are presented in Table 1.2. These values are calculated using semi-
automated software analysis tools applied to the ventricular short-axis stack of GE
cines. Calculation of LV parameters is performed in approximately 5 minutes while
14
Normal ranges 1
Table 1.2 Normal values for EDV, ESV, EF and myocardial mass indices in males and
females
EDV (ml) ESV (ml) SV (ml) EF (%) Mass index (g/m2)
Males
LV 77–195 19–72 51–133 56–78 < 113
RV 88–227 23–103 52–138 47–74 < 36
Females
LV 52–141 13–51 33–97 56–87 < 95
RV 58–154 12–68 35–98 47–80 < 33
RV parameters take longer because of the more complex anatomy. Quantification

of LV parameters is mandatory for CMR reporting and RV parameters are calculated
as required, for example in patients with congenital heart disease, arrhythmogenic
right ventricular cardiomyopathy (ARVC), dilated cardiomyopathy (DCM) and cases
of valvular regurgitation. Normal ranges are age and body surface area dependent
and normatized values are also available.
Other important cardiovascular normal ranges, including dimensions for the
aorta and pulmonary vessels, are currently based on echocardiographic data, since
CMR specific values are yet to be published (Table 1.3).
Table 1.3 Normal ranges for cardiovascular structures by echocardiography

Cardiovascular structure Range (cm)
Aorta dimensions (end-diastole)
Aortic annulus 1.4–2.6
Sinus of Valsalva 2.1–3.5
Sinotubular junction 1.7–3.4
Ascending aorta (at MPA bifurcation) 2.1–3.4
Aortic arch 2.0–3.6
Descending thoracic aorta (at MPA bifurcation) 1.4–3.0
Distal descending thoracic aorta 1.3–2.8
LVOT (diastole) 1.4–2.6

RVOT (diastole) 1.8–3.4
PA dimensions (end-diastole)
Pulmonary annulus 1.0–2.2
MPA 0.9–2.9
RPA 0.7–1.7
LPA 0.6–1.4
Venous dimensions
Pulmonary 0.7–1.6
Inferior vena cava 1.2–2.3
Superior vena cava 0.8–2.0
Hepatic 0.5–1.1
15
Indications
The European Society of Cardiology published guidelines in November 2004 on the
clinical indications for CMR (Tables 1.4–1.8) with the usefulness of this imaging
technique in specific diseases classified as follows:
Class I: Provides clinically relevant information and is usually appropriate, may

be used as the first-line imaging technique, usually supported by substantial
literature;
Class II: Provides clinically relevant information and is frequently useful,
other techniques may provide similar information, supported by limited literature;
Class III: Provides clinically relevant information but is infrequently used
because information from other imaging techniques is usually adequate;
Class Inv: Potentially useful, but still investigational.
CMR also has an important role in research and development and is being
increasingly used by the pharmaceutical industry in preclinical trials.
Tables 1.4, 1.5, 1.6, 1.7 and 1.8 used with kind permission of European Society of
Cardiology from Pennell et al Clinical Indications for Cardiovascular Magnetic Resonance
(CMR): Consensus Panel Report, European Heart Journal, 2004, 25 (21), 1940–1965.
Table 1.4 Indications for CMR in CAD

Indication Class
1. Assessment of global ventricular (left and right) function and mass I
2. Detection of CAD
Regional LV function at rest and during dobutamine stress II
Assessment of myocardial perfusion II
Coronary MRA (CAD) III
Coronary MRA (anomalies) I
Coronary MRA of bypass graft patency II
CMR flow measurements in the coronary arteries Inv
Arterial wall imaging Inv
3. Acute and chronic myocardial infarction (MI)

Detection and assessment I
Myocardial viability I
Ventricular septal defect III
Mitral regurgitation (acute MI) III
Ventricular thrombus II
Acute coronary syndromes Inv
16
Indications 1
Table 1.5 Indications for CMR in patients with pericardial disease, cardiac tumours,
cardiomyopathies and cardiac transplants
Indication Class
1. Pericardial effusion III
2. Constrictive pericarditis II
3. Detection and characterization of cardiac and pericardiac tumours I
4. Ventricular thrombus II
5. Hypertrophic cardiomyopathy
Apical I
Non-apical II
6. DCM Inv
Differentiation from dysfunction related to coronary artery disease I
7. ARVC I
8. Restrictive cardiomyopathy II
9. Siderotic cardiomyopathy (in particular thalassaemia) I
10. Non-compaction II
11. Post-cardiac transplantation rejection Inv
Table 1.6 Indications for CMR in patients with valvular heart disease
Indication Class
1. Valve morphology
Bicuspic AV II
Other valves III
Vegetations Inv
2. Cardiac chamber anatomy and function I
3. Quantification of regurgitation I
4. Quantification of stenosis III
5. Detection of paravalvular abscess Inv
6. Assessment of prosthetic valves Inv
17
Table 1.7 Indications for CMR in congenital heart disease

Indication Class
General indications
1. Initial evaluation and follow-up of adult congenital heart disease I
Specific indications
1. Assessment of shunt size (Qp/Qs) I
2. Anomalies of the viscero-atrial situs I

Isolated situs anomalies II
Situs anomalies with complex congenital heart disease I
3. Anomalies of the atria and venous return

Atrial septal defect (secundum and primum) II
Anomalous pulmonary venous return, especially in complex anomalies
and cor triatriatum I
Anomalous systemic venous return I
Systemic or pulmonary venous obstruction following intra-atrial baffle
repair or correction of anomalous pulmonary venous return I
4. Anomalies of the atrioventricular valves

Anatomic anomalies of the mitral and tricuspid valves II
Functional valvular anomalies II
Ebstein’s anomaly II
Atrioventricular septal defect II
5. Anomalies of the ventricles

Isolated ventricular septal defect (VSD) III
VSD associated with complex anomalies I
Ventricular aneurysms and diverticula II
Supracristal VSD I
Evaluation of right and left ventricular volumes, mass and function I
6. Anomalies of the semilunar valves

Isolated valvular pulmonary stenosis and valvular dysplasia III
Supravalvular pulmonary stenosis II
Pulmonary regurgitation I
Isolated valvular AS III
Subaortic stenosis III
Supravalvular AS I
7. Anomalies of the arteries

Malpositions of the great arteries II
Post-operative follow-up of shunts I
Aortic (sinus of Valsalva) aneurysm I
Aortic coarctation I
Vascular rings I
Patent ductus arteriosus III
Aortopulmonary window I
Coronary artery anomalies in infants Inv
Anomalous origin of coronary arteries in adults and children I
Pulmonary atresia I
Central pulmonary stenosis I
Peripheral pulmonary stenosis Inv
Systemic to pulmonary collaterals I
18
Contraindications and issues of safety 1
Table 1.8 Indications for CMR in acquired diseases of the vessels

Indication Class
1. Diagnosis and follow-up of thoracic aortic aneurysm including
Marfan disease I
2. Diagnosis and planning of stent treatment for abdominal aortic

aneurysm II
3. Aortic dissection
Diagnosis of acute aortic dissection II
Diagnosis and follow-up of chronic aortic dissection I
4. Diagnosis of aortic intramural haemorrhage I
5. Diagnosis of penetrating ulcers of the aorta I
6. PA anatomy and flow I
7. Pulmonary emboli
Diagnosis of central pulmonary emboli III
Diagnosis of peripheral pulmonary emboli Inv
8. Assessment of thoracic, abdominal and pelvic veins I
9. Assessment of leg veins II
10. Assessment of renal arteries I
11. Assessment of mesenteric arteries II
12. Assessment of iliac, femoral and lower leg arteries I
13. Assessment of thoracic great vessel origins I
14. Assessment of cervical carotid arteries I
15. Assessment of atherosclerotic plaque in carotid artery/aorta III
16. Assessment of pulmonary veins I
17. Endothelial function Inv
Contraindications and issues of safety

CMR is noninvasive and uses no ionizing radiation.
Contrast agents Gadolinium have very low nephrotoxicity but some agents have been linked to
systematic fibrosis in renal failure.
Patients with prosthetic heart valves, sternal wires, joint replacements, retained epicardial pacing leads
and intracoronary stents can be safely scanned.
CMR on patients with permanent pacemakers and automated implantable cardiac defibrillators
(AICDs) should only be considered in specialist centres and remains a strong relative contraindication,
while ferromagnetic cerebrovascular aneurysm clips are currently absolute contraindications.
There are no known risks for use during pregnancy, but CMR is usually avoided in the first trimester
and used only for urgent clinical need after this time. Women who are breastfeeding must express and
discard their breast milk for 24 hours after contrast use.
19
The environment in which CMR is performed must be constantly protected

from the inadvertent introduction of ferromagnetic metallic objects and electronic
equipment near the powerful magnetic field, with safety failures possibly leading
to injury and rare cases of mortality. Potential subjects fill out a checklist as shown in
Figure 1.10, which is then reviewed by trained personnel prior to placement within
the magnet. Regular cardiorespiratory arrest scenario training in the safe and speedy
removal of subjects undergoing CMR to nearby, designated resuscitation areas are
advocated for clinical and allied MRI staff.
Checklist for subjects having a Cardiovascular Magnetic Resonance Scan

Name: Date of birth:
........................................................................... ...................................................
Hospital number: Height: Weight:
........................................................................... ................................................... ...................................................
There are no known harmful effects of this scan but we need to know about
any metallic objects or implants in the body, and some other conditions.
Yes No
Do you have a pacemaker or pacing wires in your heart?
Do you have any other implants or metal in your body?

e.g.: Hearing aid, ear or spine implant, programmable hydrocephalus shunt
Have you had any operation on your head or spine?
Have you had an injury to an eye which might have left metal in it?
Have you had cardiac surgery?
Do you have epilepsy, diabetes, asthma or allergies (if yes, please circle which)?
Do you have a history of renal failure, or are you on dialysis?
Are you wearing a nitro patch?
Are you pregnant?
Have you removed your watch, bankcards, spectacles, hearing aids, keys, coins,
jewellery and hairgrips? (Gold rings are not a problem)
Please tick
You may need to have an injection during the scan of a contrast agent or “dye” called gadolinium.
This is a very safe procedure. At the time of the injection you may feel some sensations at the site of the injection
and transient headache, nausea or a metallic taste can occur. Major side effects are very rare.
By signing below you acknowledge that the procedure has been explained to you by a qualified person, and
that you have answered the above questions correctly.
Signature: ........................................................................... Witnessed by: ............................................................................
Date: ..........................................
Figure 1.10 Subjects are asked to fill in a safety questionnaire upon arrival for their
CMR scan. The completed form is reviewed by trained personnel prior to commencement
of the study. The questions are partly designed to identify contraindications to CMR,
and partly to alert staff to important medical conditions which are not themselves
contraindications.
20
Chapter 2
Ischaemic heart
disease
Katharina Kiss
Introduction
CMR is the current gold standard for the recognition of infarcted myocardium and the
assessment of global and regional cardiac wall motion abnormalities (WMA). WMA
arise in the context of MI and ischaemia. Stress-induced WMA are early indicators of
coronary artery stenosis in the ischaemic cascade and may precede clinical symptoms
and/or ECG changes (Figure 2.1). CMR can also diagnose haemodynamically
significant coronary stenosis by measuring myocardial perfusion, although clinical
experience is less extensive currently. Clinical CMR studies should follow the cardiac
imaging protocol detailed in Chapter 1. Evaluation of global and regional ventricular
function is by means of cines which reveal global and focal WMA. The four-
chamber, two-chamber and short-axis stack cines are mandatory with subsequent
imaging planes being directed by these initial views. These planes are repeated after
gadolinium for imaging of myocardial pathology.
Myocardial infarction
Shortly after coronary artery occlusion, myocardial necrosis begins. This spreads
outwards through the myocardial layers from the subendocardium towards the
subepicardium. This progression of transmurality cannot be confidently discerned
Subendocardial perfusion defect
Transmural perfusion defect
Diastolic dysfunction
Systolic WMA
ECG change
Angina
Figure 2.1 The cascade of ischaemia shows that classic signs such as angina appear
late in the course of ischaemic heart disease.
21
2 Ischaemic heart disease
with the ECG but is readily appreciated by CMR. Accurate imaging of infarcted
territory is useful for diagnosis and in predicting outcomes such as the development
of heart failure, and planning coronary arterial revascularization by either PCI
(percutaneous coronary intervention) or CABG (coronary artery bypass grafting).
Diastole Systole
LV
a b
Diastole Systole
LV
c d
Diastole Systole
LV
e f
Figure 2.2 Pre-contrast CMR study from a 26-year-old man who presented with dyspnoea,
presyncope and palpitations. (a, b) Four-chamber view in diastole and systole. (c, d) Two-
chamber view in diastole and systole. (e, f) Mid-ventricular short-axis view in diastole and
systole. Comparison of these diastolic and systolic cine frames revealed global LV dilatation
with thinning and akinesis in the lateral wall extending into the apex (white ellipses).
22
Myocardial infarction 2
Characteristic regional thinning of myocardium with akinesia suggests MI and is

first noted on the cines (Figure 2.2). Exact delineation of damaged myocardium is
then performed using the technique of late enhancement with gadolinium, or LGE.
Gadolinium is bound to a chelate in contrast agents which limits its distribution
to the extracellular space. Gadolinium accumulates within abnormal interstitium in
the myocardium affected by acute or chronic MI. In the acute setting gadolinium
distributes into necrotic tissue, and in the chronic setting gadolinium is found in
fibrosis of the infarct scar. Gadolinium accumulation reduces T1 and therefore
increases signal on T1W images. This principle along with an ECG-gated, inversion
recovery fast GE sequence underlies the LGE technique. An important additional
feature of this technique is the inversion time delay set by the operator to optimize
contrast between normal myocardium and infarcted tissue. With optimal setting of this
inversion time, normal myocardium becomes black while infarcted myocardium is
bright white. This has led to the aphorism that in infarction ‘white is dead’ (Figure 2.3).
LV LV
a b
LV
LV
c d
Figure 2.3 LGE CMR study from the patient in Figure 2.2 which shows transmural
enhancement within the left circumflex (LCx) territory (white arrows) in the (a) four-chamber,
(b) two-chamber, (c) mid-ventricular short-axis and (d) LVOT views.
23
CMR is also used to image zones of microvascular obstruction (MVO) using early
gadolinium enhancement (EGE). MVO occurs in the first hours post-MI, predicts an
unfavourable prognosis, and corresponds to areas of no-reflow. The CMR appearances
are of a black area within the infarct zone with exclusion of gadolinium relative to the
surrounding reperfused infarcted tissue (Figure 2.4). These appearances also occur
in LV thrombus and the clinical context of the CMR study must be borne in mind
(Figure 2.5). EGE uses the same sequence as LGE but images are acquired in the
LV
Figure 2.4 Mid-ventricular short-axis view of an EGE study in an acute lateral MI

showing a small dark zone of MVO embedded within the infarcted area (white arrow).
LV
LV
a b
Figure 2.5 (a) Four- and (b) two-chamber views from a 74-year-old man who had a
history of MI in the left anterior descending artery (LAD) territory. EGE shows an LV apical
thrombus (black arrows) overlying a transmural chronic infarct.
24
Myocardial infarction 2
first 1–5 minutes following contrast injection. LGE is commenced after 5 minutes
have elapsed and imaging can continue for up to 20 minutes. The two-chamber, four-
chamber and LVOT are standard views taken in EGE studies. For LGE a full short-
axis stack and long-axis images are acquired. Additional imaging through areas of
known or suspected pathology are recommended and positive findings are reported
as early or late enhancement, respectively.
The technique takes approximately 20 minutes to perform and begins with dose
calculation of gadolinium, selection of initial views, and setting of the inversion time.
Images are acquired in late diastole when cardiac motion artefact should be minimal.
Another artefact reduction technique is the application of a saturation prepulse over
the spinal column to overcome the problem of cerebrospinal fluid (CSF) ghosting
(Figure 2.6). Gadolinium is typically given at a dose of 0.1 mmol/kg by rapid
hand injection into a peripheral vein. Inversion time for EGE imaging is set at 440
milliseconds (ms) and reduced to around 320 ms for LGE imaging to commence.
Throughout the LGE acquisition, the inversion time is gradually increased up to 440 ms
to maintain correct signal nulling of normal myocardium (Figure 2.7). Abnormal
findings should be confirmed by changing the phase encode direction of the slice to
confidently exclude artefact (Figure 2.8). This is known as phase-swapping.
So in the setting of MI, CMR can:
1. Evaluate global and regional cardiac function;

2. Demonstrate wall thickness and contractility; and
3. Highlight zones of MVO (or thrombus) and transmurality of infarction with
EGE and LGE.
RV
LV
RA
LA
LGE
Figure 2.6 Four-chamber LGE image showing CSF ghosting (white arrows) along the
phase encode axis.
25
LV
RV
LGE
a b
c
Figure 2.7 LGE mid-ventricular short-axis views of the appearance of the myocardium
when the inversion time is set (a) too short, (b) too long and (c) correctly.
RV
LV
Ao
LA
LGE
a b
Figure 2.8 LVOT view showing artefactual late enhancement within the interventricular
septum (IVS) (a; solid white arrow), which disappears upon changing the direction of the
phase encode axis (b; dashed white arrow).
26
Myocardial viability 2
The scan report should address all these issues and will be discussed in more
detail in the next section on myocardial viability.
Myocardial viability
Viable myocardium exhibits contractile dysfunction at baseline but recovery over time
either spontaneously after MI (myocardial stunning) or after physical re-establishment
of coronary blood flow (hibernating myocardium). CMR can differentiate between
viable myocardium and areas of infarction using LGE since, in the former, significant
WMA are present but late enhancement is absent or limited. Combination of CMR
findings and clinical history allows further discrimination.
Stunned myocardium is usually a transient phenomenon seen after ischaemia
often in the setting of an occluded coronary artery. With chronically impaired maximal
myocardial perfusion, such as in the presence of a severe coronary artery stenosis,
hibernation may occur with chronic WMA. Patients with hibernating myocardium
tend to have multivessel disease and impaired LV function. Regional WMA can
persist for six months or longer after successful revascularization of hibernation
without evidence of myocardial necrosis according to the severity of the baseline
myocardial cellular derangement.
CMR assessment of viability is performed as discussed in section 2.1 on MI with
cine imaging and LGE. The cine slices and equivalent LGE views must be reviewed
in parallel to correlate the following parameters:
1. Wall thickness and contractility;

2. Presence or absence of WMA; both with respect to
3. Presence or absence of LGE and degree of transmurality.
For example, significant wall thinning and impaired contractility in association

with akinesia and transmural late enhancement indicates myocardial scarring.
However, reduced contractility in association with normal thickness and no late
enhancement indicates viable hibernating myocardium (Figure 2.9). This mismatch
between cines and contrast findings is the key to reporting myocardial viability CMR
studies. LGE CMR can quantify the degree of transmural involvement in MI and as
transmurality increases the likelihood of improvement in regional contractility post-
revascularization decreases.
Dysfunctional myocardium which shows < 50% transmural gadolinium enhancement has a high
likelihood of functional recovery (Figure 2.10), while transmural infarction of
> 75% is unlikely to recover contractility (Figure 2.3).
The scan report should follow the 17-segment model (Figure 2.11) and include:
1. Qualitative and quantitative description of global and regional ventricular

function;
2. A description of the severity of WMA and percentage of transmural LGE
following the 17-segment model; and
3. Correlation of these two parameters to indicate which segments are viable.
27
Persistent WMA post-MI with successful revascularization may reflect delayed

recovery and warrants repeat CMR evaluation after 4–6 months. Perfusion CMR or
a dobutamine stress CMR can further clarify the issue of stunned versus hibernating
myocardium.
Diastole Diastole
LV LV
a d
Systole Systole
b e
LGE LGE
c f
Figure 2.9 CMR in a 51-year-old man who presented with a Troponin positive acute
coronary syndrome. X-ray coronary angiography had previously revealed a 50% stenosis
in the LAD. (a, b) Two-chamber view in diastole and systole with the equivalent slice
after gadolinium in (c). (d, e) Mid-ventricular short-axis view in diastole and systole with
the equivalent slice after gadolinium in (f). These images demonstrate wall thinning and
reduced contractility in the distal anterior wall (solid white arrows) and septum (solid black
arrows) which were associated with WMA but no late enhancement (dashed black arrows)
and good biventricular function. Such findings indicate myocardial stunning.
28
Myocardial viability 2
LV
Figure 2.10 Two-chamber view showing non-transmural LGE in the anterior wall (white
arrows) indicating subendocardial anterior MI.
A
Basal Mid Apical p
e
LV x
1
7
2 6 13
8 12 17
14 16
5 9 11
3 15
10
4
Figure 2.11 Modified schematic of the 17-segment model proposed by the American
Heart Association for describing area of LV involvement:
1 = basal anterior, 2 = basal anteroseptal, 3 = basal inferoseptal, 4 = basal inferior, 5 =
basal inferolateral, 6 = basal anterolateral; 7 = mid-anterior, 8 = mid-anteroseptal, 9 =
mid-inferoseptal, 10 = mid-inferior, 11 = mid-inferolateral, 12 = mid-anterolateral; 13 =
apical anterior, 14 = apical septal, 15 = apical inferior, 16 = apical lateral, 17 = apex.
29
Myocardial perfusion
Resting coronary blood flow increases with exercise or other stress. This increase
in coronary blood flow is the coronary flow reserve (Flowstress /Flowrest = CFR) with
a normal range of approximately 4. With significant stenosis, coronary blood flow
cannot increase adequately with stress and an inducible perfusion defect becomes
apparent in the relevant coronary artery territory (Figure 2.12). Perfusion CMR
can identify this perfusion defect and there is good correlation with myocardial
scintigraphy. However, compared to scintigraphy, CMR allows improved resolution
with no ionizing radiation. The optimal imaging sequence for perfusion CMR is
currently multislice, single-shot hybrid GE using imaging acceleration during the
first pass of a bolus of gadolinium. Good temporal (approximately 50–100 ms/image
with certain sequences) and spatial resolution (approximately 2–3 mm) is essential
in eliminating subendocardial artefacts which can mimic perfusion defects.
Pharmacological stress is usually with adenosine and contraindications are those
of the CMR itself or for use of this agent. Caution is required in patients with unstable
angina, stenotic valvular disease, reversible obstructive lung disease and sino-atrial
disease. Patients must omit caffeine-containing products (such as coffee, tea and
chocolate) for 24 hours beforehand as these are adenosine antagonists. Continuous
ECG and blood pressure monitoring is mandatory.
A perfusion CMR study incorporates functional and LGE evaluation and takes
approximately 45 minutes to perform. Standard planes are obtained as described in
the pre-contrast section outlined in Table 1.1. It is important to position the basal
short-axis so as to avoid the LVOT throughout the cardiac cycle for avoidance of
misinterpretation of abnormalities from the fibrous septum. The stress part of
the perfusion examination is then performed during an infusion of intravenous
adenosine (140 mg/kg/min for 4 minutes into the left antecubital vein) with
a bolus of intravenous Gd-DTPA (0.1 mmol/kg at a rate of 7 ml/s followed by 15 ml
of normal saline at the same rate via a large bore cannula in the right antecubital
vein) given after 2 minutes and at the commencement of the perfusion sequence.
Typically three ventricular short-axis slices are acquired in a breath-hold at
end-expiration over the first cardiac cycles of the first pass. Image acquisition
is over 60 seconds and patients are instructed to breathe gently when needed.
Rest perfusion is delayed for 20 minutes after stress perfusion in order to
reduce gadolinium levels, and is performed using the same doses and rates of
gadolinium and saline as those for stress but without the adenosine.
The perfusion CMR scan report should follow the 17-segment model (Figure 2.11)
and include:
1. Anatomical description of the perfusion defects;

2. Correlation of these defects with the pattern and percentage of LGE;
3. Description of viability; and
4. Quantitation of ventricular function.
30
Myocardial perfusion 2
LV LV
STRESS REST
a d
STRESS REST
b e
STRESS REST
c
f
Figure 2.12 Perfusion CMR in three ventricular short-axis views during adenosine stress
(a–c) and rest (d–f) in a 58-year-old man prior to CABG showing inducible ischaemia of
the inferoseptal wall in the territory of the right coronary artery (RCA) (black arrows).
31
Dobutamine stress testing

Viable myocardium that is hibernating will often improve contractility during stress.
Pharmacological stress is usually with the catecholamine dobutamine which acts
at cardiac b1 receptors to increase myocardial oxygen demand. Patients should avoid
beta-blockers for 24 hours prior to the scan. Continuous ECG monitoring with pulse
oximetry and blood pressure measurements every minute are required, along with
direct questioning of patients during the study regarding adverse events. Side effects
include nausea, dizziness, dyspnoea, chest pain and palpitations, and serious adverse
events include induction of ventricular arrhythmias or prolonged ischaemia.
Two protocols are available—a low-dose dobutamine protocol using 10 mg/kg/
min administered to assess viability, and a high-dose dobutamine protocol using
up to 40 mg/kg/min to detect ischaemia. During low-dose protocols, the focus is on
the improvement of WMA present at rest in order to differentiate between viable
and non-viable myocardium. The high-dose protocol is similar to dobutamine
stress echocardiography (DSE). Two- and four-chamber views with representative
ventricular short-axis slices are used. The initial dose with both protocols is 5 mg/kg/
min. This is increased to 10 mg/kg/min after 3 minutes. With high-dose dobutamine
stress, doses are increased every 4 minutes by 10 mg/kg/min with constant monitoring
for WMA. Dobutamine stress studies are usually terminated when the target heart
rate is achieved (target heart rate = 0.85 [220 − age]) or after peak dobutamine dose.
If the patient has a poor heart rate response to dobutamine, atropine can be given in
small repeated doses.
A dobutamine stress CMR examination takes 45 minutes to perform. Data analysis
and reporting should follow the 17-segment model (Figure 2.11) and provide
information on:
1. Resting regional WMA and EF; and

2. Improvements in contractility or identification of new WMA with stress.
Indications
CMR can:
1. Offer superior image quality to echocardiography for the detection of WMA;

2. Provide the gold standard for quantification and reproducibility of LV and
RV function;
3. Demonstrate MVO and transmurality of MI and therefore predict the
likelihood of wall motion recovery after revascularization; and
4. Provide high-resolution myocardial perfusion imaging without ionizing
radiation.
CMR cannot:
1. Be recommended for quantification of stenoses within native coronary

arteries. Coronary magnetic resonance angiography (MRA) has an 81%
negative predictive value for the exclusion of multivessel proximal CAD.
32
Indications 2
Assessment of bypass graft patency is straightforward using CMR, but

computed tomography (CT) is more commonly used. Coronary MRA is
reliable for identification of coronary artery anomalies.
33
Chapter 3
Heart failure and

cardiomyopathy
James C Moon
Introduction
Heart failure is a complex syndrome in which the heart functions inadequately
as a pump to support a physiological circulation resulting in symptoms such as
breathlessness and fatigue and signs such as fluid retention. It is associated with high
morbidity and mortality and represents a major burden for healthcare services.
The aetiology of heart failure includes CAD, hypertension, valvular pathology,
and much rarer inherited heart muscle diseases. Additionally, conditions such as
pulmonary or renal disease can mimic the symptoms and signs. The management
of heart failure rests upon accurate diagnosis and elucidation of the underlying
aetiology. This requires thorough clinical evaluation and appropriately targeted
investigations. ECG and echocardiography are the usual initial investigations and
CMR is a complementary tool that can provide important quantitative and qualitative
insights, especially with regard to the cardiomyopathies.
The cardiomyopathies are diseases of the myocardium associated with cardiac
dysfunction and are subdivided on the basis of morphology into hypertrophic,
dilated, restrictive and ARVC (Figure 3.1). Many cardiomyopathies are inherited
through a single gene abnormality. Some cardiomyopathies have an extended
phenotype with conduction disease, whilst other genetic cardiac diseases have
conduction disease (such as long/short QT and the Brugada syndrome—the
channelopathies) without ‘cardiomyopathy’. At least nine different sarcomeric genes
can cause the same phenotype of hypertrophic cardiomyopathy (HCM) and yet
different mutations in some of these nine genes can also cause DCM. Approximately
half of all HCM patients have been shown to have a genetic mutation and many
individuals carry mutations without phenotypic manifestation, and the impact of
environment, genetic modifiers and patient age are important. There are also disease
mimics known as phenocopies, such as the glycogen storage diseases, which appear
phenotypically like the genetic diseases.
CMR is the best single technique for defining the cardiomyopathy phenotype,
detecting early phenotypic changes, defining aetiology and distinguishing pheno-
copies, assessing response to treatment, and potentially aiding risk stratification.
35
3 Heart failure and cardiomyopathy
A B C
D E F
Figure 3.1 Classification of cardiomyopathies by morphology.

(a) Normal; (b) hypertrophic; (c) dilated; (d) arrhythmogenic right ventricular;
(e) restrictive—the endocardial lines represent dysfunctional long-axis fibres; (f) non-
compaction—the endocardium has an open trabecular structure with relative thinning of the
compacted myocardium.
CMR protocol
A CMR heart failure and cardiomyopathy protocol typically obtains information on
cardiac morphology, cardiac function and myocardial tissue characterization. The
scan report should comment on these three areas in general terms such as:
1. Cardiac chamber size;

2. Quantitative values for cardiac function and mass with respect to the
reference ranges quoted in Chapter 1; and
3. The presence (with a description of the pattern) or absence of LGE.
Specific features for reporting are highlighted after discussion of the specific
cardiomyopathies.
Cardiac morphology
The anatomical structure of the heart can be shown using different types of sequences
and the white-blood and black-blood techniques previously described provide
complementary information. For example, black-blood imaging is extensively used
for imaging the RV in ARVC, while white-blood SSFP cines best define left ventricular
non-compaction (LVNC).
Cardiac function
CMR is the gold standard technique for the assessment of left and right ventricular
volumes and mass due to a combination of advantages (Table 3.1). CMR measurements
36
CMR protocol 3
Table 3.1 Advantages of CMR for measuring ventricular function

Precise and reproducible piloting
No problems with acoustic windows
No blind spots—image quality the same throughout
High blood–myocardial tissue contrast (even in heart failure)
True 3D assessment with no geometric assumptions
RV imaged as well as the LV
Any view or plane can be imaged as necessary
are more reproducible than echocardiography, the apex and RV are no longer blind
spots (Figure 3.2), and the technique is not window dependent (Figure 3.3). For
heart failure, the SSFP GE cine sequences have major advantages because the blood
to myocardium contrast is dependent not on blood flow but on intrinsic magnetic
differences between blood and myocardium. This means that the blood pool is more
clearly distinguished from myocardium even in slow-flow areas compared to that
using older white-blood imaging methods. The SSFP sequences can also be sped up
using parallel imaging acquisition techniques to minimize breath-holding times in
symptomatic heart failure patients.
An emerging technique for functional assessment is myocardial tagging. In this
technique, a grid of tag lines is laid over the heart magnetically in diastole and then
tracked as they distort with myocardial contraction through systole (Figure 3.4).
The tag line deformation can be analysed like tissue Doppler imaging, but rather
RV
LV
RV LV
RV
a b
Figure 3.2 Four-chamber views comparing (a) a transthoracic echocardiogram (TTE)

and (b) a CMR still of a cine loop in the same individual. CMR displays the RV (solid white
arrow), apex (dashed white arrow), and endocardial border (solid black arrows) more
clearly.
37
Right LV
lung
Left
lung
Figure 3.3 A pilot transaxial FSE CMR image from a patient with emphysema in whom
the TTE provided poor acoustic windows.
Diastole Systole
LV LV
a b
Figure 3.4 Myocardial tagging of a mid-ventricular short-axis slice in (a) diastole

and (b) systole following an acute MI. The grid of tag lines is laid down in diastole and
cardiac motion results in distortion (strain and torsion) in systole. The septum shows normal
contractile function (short white arrow), but the lateral wall tag lines are unchanged
(dashed white arrow), highlighting contractile dysfunction within this area.
38
CMR protocol 3
than being limited to strain in line with the Doppler beam, tagging can be analysed
in any direction simultaneously, including circumferentially, at any point in the
myocardium, and is able to compare epicardial and endocardial function.
Myocardial tissue characterization

Normal and abnormal myocardium can have intrinsic contrast differences in heart
failure that can be visualized by CMR. For example, fatty infiltration of the RV may
be seen in ARVC using FSE sequences with and without the addition of a specially
applied fat saturation pulse, which eliminates only fat from the images. Also, tissues
which have increased water content, such as in myocardial oedema from acute
infiltration or infarction, can be differentiated with T2W sequences (Figure 3.5).
Extrinsic contrast can be created by LGE, which uses an inversion recovery sequence
and a gadolinium contrast agent (see Chapter 2). Gadolinium highlights areas of
myocardium with expanded interstitium, such as fibrosis, necrosis or infiltration.
Different patterns of fibrosis exist in different aetiologies of heart failure and this
can be used to distinguish them (Figure 3.6). MI leads to patterns of LGE which
spread from the subendocardium outward to the subepicardium in the territory of
a coronary artery. However, changes in myocarditis are the reverse and start at the
subepicardium and can later become mid-myocardial, typically at the lateral wall. EGE
in combination with relevant cines allows identification of thrombi. This technique
has been discussed in the previous chapter and will also be covered in Chapter 5
on cardiac masses. Coronary CMR assessment of the proximal coronary arterial tree
can be combined with myocardial tissue characterization but this technique is not
robust—it is further discussed in Chapter 9.
T1W T2W
LV
a b
Figure 3.5 (a) T1W and (b) T2W four-chamber views in a case of myocardial
lymphoma showing interventricular septal infiltration. The septum is distorted by infiltration
on the T1W image, but appears similar in contrast to normal myocardium (solid white
arrows). However, subsequent T2W imaging shows high signal indicative of oedema in
both the septum and the lateral wall (dashed white arrows).
39
LV
LV
a b
Figure 3.6 Myocardium infarcted or fibrotic appears bright with LGE.
The characteristic pattern of subendocardial enhancement in a coronary artery territory is
shown post-MI (a; solid white arrow) as distinct from the pattern of contrast uptake noted
with focal fibrosis in HCM (b; dashed white arrows).
CMR in selected cardiomyopathies
Hypertrophic cardiomyopathy
HCM strictly includes the sarcomeric variants but the phenocopies are also discussed
here since the differentiation of these two groups is an important role of CMR
(Table 3.2). The HCM phenotype shows high variability and also changes throughout
Table 3.2 Phenocopies of sarcomeric HCM

Storage diseases
Anderson–Fabry disease
Glycogen storage diseases
Mucopolysaccharidoses
Mitochondrial myopathies
Syndromes (Noonan’s, Friedreich’s ataxia)
Physiological hypertrophy
Increased afterload (hypertension, AS, outflow tract obstruction)
Athlete’s heart
Afro-Caribbean
Compensatory hypertrophy (after MI)
Infiltration
Amyloid
Senile amyloid
Ageing
Sigmoid septum
40
CMR in selected cardiomyopathies 3
life. Expression of early familial disease may be with an abnormal ECG and normal
echocardiogram, fulfilling proposed familial criteria for HCM. In a proportion of
these, CMR can detect early hypertrophy overlooked at echocardiography. CMR is
especially useful in disease which is limited to the LV apex (Figure 3.7). Indicators
of apical HCM in the context of non-diagnostic echocardiography include giant
negative T waves on the ECG and subtle echocardiographic abnormalities such as
diastolic dysfunction and apical akinesis.
In established HCM, there is a need to identify patients at risk of sudden death
and this is mainly done by assessing the presence of known risk factors such as
family history of sudden death, unexplained syncope, ventricular tachycardia,
abnormal exercise test, and LV wall thickness greater than 30 mm. Adding up the
number of risk factors gives a reasonable indication of risk. In the absence of any risk
factors, the patient is considered low risk and management is with reassurance and
regular reassessment. In the presence of more than two risk factors, patients are high
risk and warrant anti-arrhythmia treatment, often with an AICD. However, a third
of patients have only one risk factor and are at intermediate risk. LGE CMR may help
further risk stratify this group into low or high risk since myocardial fibrosis may
represent the substrate for heart failure and arrhythmias (Figure 3.8). The risk of
sudden death is greater in those with greater myocardial late enhancement and in the
presence of progressive LV dilatation and thinning. This is especially true for the
younger patient population (< 40 years old). The specific pattern of LGE may also
be important and is also helpful in distinguishing HCM mimics such as Anderson–
Fabry disease (AFD). AFD is an X-linked storage disease that causes left ventricular
hypertrophy (LVH) and accounts for 1 to 3% of patients with phenotypic HCM. AFD
should be considered in middle-aged men with suspected HCM where an auto-
somal dominant family history is not present, especially if there is no evidence of
LV
apex
Diastole Systole
a b
Figure 3.7 Four-chamber SSFP cine CMR images from a 51-year-old man referred with
an abnormal resting ECG but normal TTE and X-ray coronary angiography.
There is (a) hypertrophy at the LV apex in diastole associated with (b) LV cavity obliteration
in systole, indicating a diagnosis of apical HCM.
41
LGE
LV
LV
LGE
a
Figure 3.8 Post-contrast CMR study from a 43-year-old man with a strong family history
of HCM, mildly decreased LV function on TTE, and normal coronary arteries. The (a) four-
chamber and (b) mid-ventricular short-axis views show extensive late enhancement of the
interventricular septum (white arrows), which is not subendocardial as with MI.
LVOT obstruction. Contrast enhancement in AFD occurs predominantly at the basal

inferolateral wall. Other mimics include cardiac amyloid where the heart is infiltrated
with the amyloid protein. This protein accumulates preferentially throughout the
subendocardium, the site of the longitudinal fibres, leading to reduced long-
axis function. The myocardium becomes non-compliant and exhibits a restrictive
physiology. There is symmetrical and global myocardial hypertrophy, which is
readily visualized by CMR, and there may be characteristic subendocardial contrast
enhancement and a black-blood pool due to rapid wash-out of gadolinium from the
blood (Figure 3.9).
Up to a quarter of patients with HCM have LVOT obstruction. In LVOT
obstruction, the AMVL or papillary muscles move forward into the outflow tract
in systole where they flutter and may hinder the ejection of blood. This may be
associated with a posteriorly directed jet of mitral regurgitation (MR). Treatment
is mainly with beta-blockers but surgical myomectomy or alcohol ablation can be
performed. Alcohol ablation involves injection of alcohol into the first septal
artery causing infarction of the myocardium in that territory and relieving the
obstruction. Subsequent scar formation and remodelling can be evaluated using
CMR. Rarely, a residual ridge of myocardium remains which causes further
obstruction and can be evaluated at follow-up CMR.
Specific features for reporting on are:
1. Measurements of differential septal thickness (asymmetric septal hypertrophy);

2. LVOT obstruction or systolic anterior motion of the AMVL;
42
LGE LGE
RV
LV
LV
RV
Figure 3.9 (a) Four-chamber and (b) mid-ventricular short-axis views of global late
enhancement which spares the subepicardium that is characteristic of cardiac amyloid
(white arrows). Late enhancement in this setting is due to amyloid protein deposition as
opposed to myocardial fibrosis.
3. Comments on function, morphology, and presence (and pattern) of LGE and

changes since preceding studies.
Dilated cardiomyopathy
CMR evaluation of DCM has several components. Early LV dilatation is quantified
volumetrically and can be compared with age, gender and body surface area
normalized reference ranges. The size of the heart in relation to the chest is also
immediately apparent.
CMR can distinguish DCM from cardiac chamber dilatation due to CAD using LGE, and this may
obviate the need for cardiac catheterization in some patients.
When cardiac dilatation heart due to coronary disease is advanced, myocardial

wall thinning due to infarction, remote remodelling and subendocardial infarction
can make the appearance of the heart very similar to that found in DCM. LGE CMR
studies in this situation demonstrate transmural or subendocardial MI. By contrast, in
most cases of DCM there is either no enhancement or a characteristic mid-myocardial
wall fibrosis affecting the circumferential fibres (Figure 3.10). Late enhancement in
some suspected cases of DCM may represent sequelae of previous myocarditis.
Specific comments for the CMR report in DCM are:
1. Quantification of normalized biventricular function;

2. Evidence of DCM as opposed to coronary disease; and
3. Changes in function, morphology and contrast enhancement since previous
imaging.
43
LGE
LV
Figure 3.10 Mid-ventricular short-axis view post-contrast demonstrating the characteristic

mid-myocardial wall late enhancement seen in DCM (white arrows).
Thalassaemia major
Thalassaemia is a common genetic condition worldwide which results in anaemia
secondary to defective globin synthesis. b-Thalassaemia major is the homozygous
form of defective b-globin synthesis and affected individuals are blood transfusion
dependent. Repeated transfusions contribute to iron overload and iron becomes
deposited throughout the body, especially the heart, liver, pancreas and endocrine
glands. The resulting cardiomyopathy can progress to overt cardiac failure which can
be rapidly progressive. Mortality in thalassaemia major is often from heart failure,
with many patients dying prematurely in their mid-thirties. Timely detection of
cardiac dysfunction allows targeting of aggressive iron chelation therapy in these
individuals and can reverse the cardiomyopathic process.
Currently, no echocardiographic criteria have been established for the pre-clinical
diagnosis of iron overload cardiomyopathy and haematologists have therefore relied
upon serum ferritin measurements and liver biopsy findings to act as surrogates for
quantification of cardiac iron burden. Serum ferritin is influenced by many factors
and cannot specify the organ affected and iron deposition within the liver is poorly
correlated to cardiac iron loading.
Actual myocardial iron concentration can be more directly and better quantified
using a multiecho T2* GE CMR technique which measures the myocardial relaxation
parameter known as ‘T2 star’ (Figure 3.11). Myocardial T2* measurements are
made using a mid-ventricular short-axis slice and normal values are approximately
40 ms, with a lower boundary of 20 ms. In thalassaemia, values greater than 20 ms
suggest no significant iron loading whilst values less than 10 ms indicate severe iron
loading (Table 3.3). Approximately 90% of patients presenting in heart failure have
44
LV
Liver
a b
Figure 3.11 The T2* GE CMR technique for measurement of cardiac iron status.
(a) CMR appearance in a normal subject. T2* measurements are made in a mid-ventricular
short-axis view within the area of IVS as highlighted. (b) Example of iron deposition in
a patient with thalassaemia major. The IVS now has a dark epicardial rim indicating
significant cardiac iron loading (white arrow). Iron deposition within the liver is also heavy
and the liver therefore appears black (white ellipse). This signal loss occurs because of
disturbances in the relaxation parameters of the tissues brought about by the iron causing
alterations in the local magnetic field. (c) Another case of thalassaemia major which
highlights the poor correlation between iron deposition in the heart (black arrow) and the
liver (black ellipse). This means that optimal management of myocardial iron overload to
prevent cardiac complications (arrhythmia, heart failure and death) in these patients cannot
be conducted via the surrogate marker of liver iron content.
45
Table 3.3 Guidelines for iron assessment

Iron loading Myocardial T2* (ms) Hepatic T2* (ms)
None > 20 > 6.3
Mild 14–20 2.7–6.3
Moderate 10–14 1.4–2.7
Severe < 10 < 1.4
a T2* of less than 10 ms and are at high risk of death. They require urgent increases
of iron chelation therapy, often with two drugs. Liver T2* measurements are made in
a hepatic transaxial slice avoiding hepatic blood vessels. Values greater than 6.3 ms
indicate no significant iron loading and values less than 1.4 ms indicate severe iron
loading (Table 3.3). The total study duration is approximately 15 minutes and the
technique can also be used in other iron overload conditions such as haemochromatosis
and sickle cell anaemia.
Specific elements of the CMR report are:
1. Myocardial T2* quantification;

2. Hepatic T2* quantification; and
3. Comments on changes in cardiac function and T2* parameters since previous
studies.
Arrhythmogenic right ventricular cardiomyopathy

In ARVC, ventricular tachycardia arising from the RV may cause sudden death.
The disease is usually autosomal dominant with abnormalities in genes coding for
proteins in the cell junctions known as desmosomes. Injury results from impaired
tissue integrity with fibro-fatty healing typically affecting the thinner walled RV.
Affected individuals can have associated abnormalities of RV and LV structure, and
the former are better delineated by CMR than TTE (Figure 3.12). Abnormalities
include regional RV WMA, wall thinning, fatty infiltration and LGE. In the late stages,
the RV may become poorly functioning. Early changes are difficult to detect and there
are traps for the unwary: in the normal RV, the free wall at the moderator insertion
may appear akinetic, normal RV wall motion is highly variable, and intra-myocardial
fat must be distinguished from epicardial fat. CMR in ARVC requires experience,
results must be interpreted in conjunction with the defined major and minor criteria
and with other clinical tests to generate an overall probability of disease.
The specific CMR comments here reflect the underlying suspected or known
diagnosis:
1. Quantification of biventricular function;

2. Evidence of WMA or aneurysmal changes, especially of the RV free wall,
apex and RVOT;
3. Evidence of fatty infiltration or LGE.
46
Indications 3
RV
RVOT
LV
RV
b
Figure 3.12 CMR in a patient with ARVC referred with intermittent broad complex
tachycardia maintained on amiodarone. The RV had already been noted as abnormal on
TTE. (a) Four-chamber cine CMR showing localized aneurysmal section of the RV free wall
(white arrow) which was dyskinetic. (b) RVOT cine CMR showing thinning of the RV. The
aneurysmal area is once again noted (white arrow) and there is associated dilatation of the
RV and RVOT (≥ LVOT diameter).
Other cardiomyopathies
Restrictive cardiomyopathies are well visualized with CMR and key features include reduced
long-axis function and atrial dilatation. In addition, subendocardial enhancement may
be seen. Examples of diseases that cause a restrictive pattern include cardiac amyloid
(Figure 3.9) and eosinophilic heart disease causing endomyocardial fibrosis.
Cardiac sarcoid can also cause fibrosis, visible by LGE, often with dense punched-
out lesions. Myocardial oedema may be present on T2W images in association with
active inflammation.
LVNC is a cardiomyopathy characterized by an altered structure of the LV
myocardium with very thinned, hypokinetic segments consisting of two layers: thin,
compacted myocardium on the subepicardial side, and a thicker non-compacted
subendocardial layer (Figure 3.13). RV non-compaction accompanies LVNC in a
significant proportion of patients. Clinical manifestations include heart failure,
ventricular arrhythmias and systemic embolic events. TTE and CMR are the imaging
methods of choice with the criteria for diagnosis being a ratio of non-compacted to
compacted myocardial layers of greater than 2.
Indications
CMR can:
1. Determine LV and RV cardiac morphology and function normalized to sex,

age and body surface area;
2. Reproducibly assess cardiac function and so accurately monitor response to
drug therapy;
47
LV
LV
Diastole Diastole
a b
LV
Diastole
c
Figure 3.13 (a) Four-chamber, (b) two-chamber and (c) mid-ventricular short-axis
SSFP cine CMR images from a 68-year-old man with known LVNC highlighting the
pathognomonic combination of multiple prominent ventricular trabeculations and deep
intertrabecular recesses in communication with the ventricular cavity (black arrows).
3. Detect myocardial oedema/iron/fat;

4. Visualize myocardial fibrosis and protein deposition;
5. Differentiate between DCM and cardiac dilatation due to CAD; and
6. Distinguish between the cardiomyopathies (assign the phenotype).
CMR cannot:
1. Replace comprehensive multimodality assessment—history taking, clinical

examination, chest X-ray, ECG and echocardiography;
2. Diagnose channelopathies/ARVC in the structurally normal heart;
3. Detect short temporal resolution events (premature valve opening/closure,
isovolumetric times, subtle dyssynchrony);
4. Quantify diastolic dysfunction with the temporal resolution of
echocardiography; and
5. Image patients after device therapy (MRI-compatible pacemakers are
currently being evaluated).
48
Chapter 4
Valvular heart
disease
George E Gentchos and Marc D Tischler
Introduction
Cine imaging using SSFP and velocity mapping sequences are the cornerstone of
CMR valvular assessment. Breath-hold high-resolution FSE can be useful for valve
morphology and developments such as moving slice velocity mapping and real-time
imaging will improve evaluation in the near future. CMR reporting in valvular heart
disease generally includes:
1. Comments on cardiac chamber size;

2. Quantitative values for cardiac function and mass with respect to the
reference ranges quoted in Chapter 1; and
3. Details of valve morphology where possible.
Further reporting requirements are highlighted following discussion of the specific

valvular lesions.
Aortic stenosis
AS can occur at the valvular, subvalvular or supravalvular level. Valvular AS most
commonly occurs with degeneration of a normal three-cusp aortic valve architecture.
Bicuspid valves degenerate far earlier than tricuspid valves and are the second most
common cause of AS in the adult, with rheumatic heart disease being the third.
Subvalvular AS is caused by a fibrous or fibromuscular membrane which encircles
the LVOT causing outflow tract obstruction. These patients typically present
in adulthood with recurrence of a previously resected subvalvular membrane.
Subvalvular stenosis can also be caused by asymmetric septal hypertrophy, abnormal
MV or papillary muscle insertion, or posterior displacement of the infundibular
septum. Supravalvular AS is uncommon, producing narrowing usually at the sino-
tubular junction. It occurs in patients with Williams syndrome (60%), and there are
familial forms and sporadic idiopathic cases.
AS has a long asymptomatic period after which clinical symptoms such as angina,
exertional dyspnoea and effort syncope may result. Since symptoms develop late in
the pathophysiology of AS, clinical deterioration soon follows if valve replacement
49
4 Valvular heart disease
is not undertaken. Obstruction to the LVOT leads to elevated LV pressures and

compensatory LVH which initially maintains cardiac output and reduces LV wall
stress, but ultimately decreases LV compliance and increases end-diastolic pressure.
Increased myocardial oxygen demand causes myocardial ischaemia and later LV
failure.
CMR is a robust method of calculating the severity of AS and correlates well
with continuous wave Doppler echocardiography. However, it is far superior to
echocardiography in identifying the cardiovascular functional and morphological
sequelae of AS, such as post-stenotic dilatation of the ascending aorta, degree of
LVH, and myocardial viability (Figures 4.1 and 4.2). These are important factors in
LV
Ao
LV
d
Figure 4.1 SSFP cine images
illustrating part of the CMR
b
assessment in a 66-year-old man
with mild AS. The first LVOT view
(a) shows signal loss across the AV
indicative of turbulent blood flow
(solid white arrow) and no evidence
of LVH. The second LVOT view
(b) reveals mild aortic root
dilatation at the sinuses of Valsalva
(dashed white arrow). The AV is
trileaflet (c; black arrow) and the
remainder of the ascending aorta
is mildly dilated (d; Ao). Further
quantification of LV parameters with
c a ventricular short-axis stack of cines
demonstrated mild LV dilatation with
preserved function.
50
Aortic stenosis 4
Ao
LV
LV
d
Figure 4.2 SSFP cine CMR views

from a 34-year-old man with severe
AS.
b The LVOT views (a, b) show
marked signal loss across the AV
(solid white arrows) and LVH (solid
black arrows). The AV is bileaflet (c;
dashed black arrow) and there is an
associated coarctation of the aorta
(d; dashed white arrow).
the assessment of patients prior to valve replacement surgery, which often includes
CABG and aortic root replacement. CMR also provides an excellent modality for
serial surveillance of parameters such as LV function, volumes and mass in patients
under follow-up and post operatively. This is done using the pre-contrast part of
the protocol outlined in Chapter 1. Cines can demonstrate thickening and bulging
of the aortic cusps and turbulent flow in the aorta. Imaging in an oblique sagittal
plane parallel to the valve may demonstrate restricted opening and closure of the
valve, and is frequently satisfactory for direct planimetry of the valve orifice and
evaluation of bicuspid valve morphology. Direct planimetry can be performed using
cine imaging or velocity mapping sequences (Figure 4.3).
51
Velocity mapping
Diastole
LV b
Systole
a d
Systole
c
Figure 4.3 The SSFP cine CMR LVOT view (a) allows positioning of an oblique sagittal
plane just beyond the AV (white line) which then corresponds to the cine views obtained in
diastole (b) and systole (c) showing bicuspid valve morphology with a fused commissure
(solid white arrows). Velocity mapping in this plane (d) and these latter two images allow
direct valve planimetry. However, velocity mapping is mainly used to determine the peak
AV velocity. To do this, a measurement cursor is placed at several points within the valve
orifice during systole (dashed white arrow) and the peak value recorded in Venc optimized
images.
Velocity mapping is primarily used, however, to calculate the pressure gradient

across the AV using the modified Bernoulli equation;
DP = 4 (Vmax)2
where DP (mmHg) is the pressure drop across the stenosis, and Vmax is the
peak velocity (m/s) determined by velocity mapping 1 to 1.5 cm above and
parallel to the valve plane (Figure 4.3d). The typical Venc setting for the LVOT is
2 m/s, and 2.5 to 4 m/s for the aorta. An initial Venc of 2.5 m/s is often used and
adjusted upwards if there is velocity aliasing (Figure 1.3). The velocity of blood
flow through the AV is greater than that through the MV.
Velocity mapping, SSFP cines and FSE imaging are combined to determine the
level of obstruction in AS. It is important to use information from all these sequences
since a thin subaortic shelf is not reliably excluded even with high-resolution FSE
CMR techniques. The initial planes and sequence required are the LVOT cines with
subsequent imaging targeted by the pattern of turbulence demonstrated on these
views.
52
Aortic regurgitation 4
Severity of AS is graded as: mild > 1.5 cm2, moderate 1.0–1.5 cm2, severe < 1.0 cm2,
and critical < 0.8 cm2. In severe AS, the peak transvalvular gradient is usually
> 50 mmHg.
Specific CMR reporting features for AS include:
1. Overall impression of severity (based upon peak velocity, AV area and LV

function);
2. Level of stenosis; and
3. Presence or absence of associated features, such as coarctation of the aorta or
aortic regurgitation (AR).
Aortic regurgitation
AR can be caused by valve leaflet abnormalities, dilatation of the aorta or distortion
of the aortic root. Valves that are stenotic generally also have some regurgitation.
Leaflet abnormalities include degeneration of a normal valve, bicuspid AV, infective
endocarditis, rheumatic disease, sequelae of balloon dilatation or valvotomy for
congenital AS, and thickening of the aortic cusps from the jet of subvalvular obstruc-
tion. The ascending aorta may dilate secondary to hypertension, aortitis (Reiter
syndrome, ankylosing spondylitis, giant cell arteritis, relapsing polychondritis) or
annuloaortic ectasia (Marfan syndrome, osteogenesis imperfecta, Ehlers–Danlos
syndrome and pseudoxanthoma elasticum). Additionally, there is an aortopathy
associated with bicuspid AV which causes dilatation of the ascending aorta. Distortion
of the aortic root is seen with dissection, trauma and sinus of Valsalva aneurysm.
AR results in volume overload of the LV causing increased end-diastolic pressure.
This is counteracted by compensatory ventricular dilatation and an increase in LV
compliance which accommodates the regurgitant volume and preserves cardiac
output. Patients may remain asymptomatic in this compensated phase for many years
until diastolic filling pressures continue to rise and LV dysfunction or myocardial
ischaemia ensue. Early detection of decompensation is critical to the timing of
definitive surgical repair. Factors which influence surgical timing include severity
of AR, New York Heart Association functional class, LVEF, LVESV and LVEDV,
and degree of dilatation of the aortic root. In particular, LVEF and LVESV are powerful
predictors of outcome in AR, and the reproducibility of these measurements as well
as the reproducibility of regurgitant volume with velocity mapping CMR is excellent.
Cines in the LVOT plane demonstrate the flow void due to the regurgitant jet
which can be qualitatively assessed by the size of the jet, after taking into account
the effects of echo time (Figure 4.4a). Velocity mapping is performed in a plane
perpendicular to the AV positioned just above the valve but below the coronary ostia
(Figures 4.4b–c). This plane optimally demonstrates forward and regurgitant flow
and can further characterize the morphology of the valve. The regurgitant fraction
is then calculated by graphing the flow volume curve using dedicated software
(Figures 4.4d–e). The area under the curve below zero in diastole represents the
regurgitant volume and the regurgitant fraction is calculated by dividing this
into the forward SV in systole (Figure 4.5). An alternative method is to calculate
53
LV
Systole Diastole
b c
Figure 4.4 SSFP cine CMR LVOT view (a) showing a central jet of AR (solid white
arrow) and dilated proximal aortic root (dashed white arrow). SSFP cines in the subsequent
oblique sagittal plane (b, c) show a normal trileaflet valve and confirm one central
jet (black arrows) which appears black due to turbulence. This latter plane is used for
the velocity mapping sequence, which in this case shows forward flow as black and
regurgitant flow as white (d, e). The region of interest is delineated throughout the cardiac
cycle, in this case the AV area through systole (black circle) and diastole (white circle), and
software analysis is performed to generate a curve from which the regurgitant fraction is
calculated.
54
Aortic regurgitation 4
Systole Diastole
d e
Figure 4.4 cont’d

Blood flow velocity (ml/s)
Time (milliseconds)
Figure 4.5 Flow velocity time curve from the case illustrated in Figure 4.4.
Using forward SV in systole (dark red) and the regurgitant volume in diastole (light red),
the regurgitant fraction (regurgitant volume/SV) is automatically calculated by a dedicated
software analysis tool. The value here was 20%, consistent with mild AR.
55
the aortic flow and pulmonary flow at a level just above the respective valve planes.
The difference in forward flow provides an estimate of the degree of AR in single-
valve disease, as does the quantitative difference between RV and LVSV. The degree of
ventricular dilatation also helps to qualitatively assess the severity of regurgitation. In
the presence of dilatation, LGE imaging is performed to look for myocardial fibrosis,
and this is especially useful in the preoperative setting.
Severity of AR by regurgitant fraction is graded as: mild < 30%, mild to moderate
30–39%, moderate to severe 40–49%, and severe > 50%.
Specific CMR reporting points for AR include:
1. Overall impression of severity (based upon jet appearance, LVEF, LVESV and
LVEDV, and regurgitant fraction);
2. Dimensions of the aorta at the aortic annulus, sinuses of Valsalva, sino-
tubular junction, ascending aorta (at MPA bifurcation), aortic arch, and
descending thoracic aorta (at MPA bifurcation); and
3. Possible aetiology and associated features, such as dissection of the aorta
and AS.
Mitral stenosis
Mitral stenosis (MS) is usually secondary to rheumatic heart disease. Unusual
causes of MS include congenital valvular, subvalvular or supravalvular stenosis,
leaflet deposits from amyloid or carcinoid, extensive mitral annular calcification and
left atrial myxoma. The stenotic valve leads to a pressure gradient across the MV,
causing left atrial pressures to rise. This leads to pulmonary venous hypertension
and eventually to pulmonary arterial hypertension and RV failure.
CMR complements echocardiographic evaluation of MS, especially in patients
with poor acoustic windows. Cines taken in the four-chamber, two-chamber and
LVOT views demonstrate the thickened, hypokinetic and domed MV leaflets and a
signal void arising from the MV in diastole extending into the LV (Figure 4.6). The
LA is usually enlarged in moderate to severe stenosis and this is easily visualized.
Additionally, the pulmonary trunk may be enlarged and tricuspid regurgitation (TR)
may be present in cases with pulmonary arterial hypertension. This can be assessed
in more detail by reviewing the four-chamber cine and acquiring an RVOT cine view,
while a preliminary appraisal of the pulmonary arteries is readily made with the
transaxial FSE acquisition. SSFP cines or velocity mapping performed in a plane
parallel to the MV can be performed for direct planimetry of the stenotic valve orifice,
although these can be limited by motion of the valve through the fixed imaging
plane (Figure 4.7). Calculation of the valve area by direct planimetry correlates
56
Mitral stenosis 4
LV
LV
LA LA
Diastole Diastole
a b
Figure 4.6 SSFP cine images from a patient with MS secondary to rheumatic heart
disease. The MV is thickened, there is turbulent inflow with limited valvular excursion
(a; black arrows), and a dilated LA. The AV is also thickened and there is associated AR
(b; white arrow).
LV
RV
Diastole
Figure 4.7 SSFP cine image performed in a plane parallel to the MV (white arrow) from
the case illustrated in Figure 4.6. Direct planimetry revealed a valve area of 1.8 cm3.
57
well with echocardiographic and cardiac catheterization data, but may slightly
overestimate measurements obtained by these modalities.
Velocity mapping is used to quantify the transvalvular pressure gradient using
the modified Bernoulli equation, with Vmax calculated using in-plane or preferably
through-plane velocity mapping in the LV just distal to the MV. This method can
underestimate the gradient. The Venc is set at a much lower value than in AS, for
example 1.5 m/s.
Severity of MS is graded as: mild ≥ 1.5 cm2, moderate 1.0–1.5 cm2, and severe
< 1.0 cm2.
Specific CMR reporting points for MS include:
1. Overall impression of severity (based upon MV area, Vmax);

2. Evidence of pulmonary arterial hypertension; and
3. Associated AV involvement and mitral regurgitation (MR).
Mitral regurgitation
MR can be caused by abnormalities of the MV leaflets (myxomatous degeneration
(Figure 4.8), rheumatic disease, endocarditis, parachute MV), chordae tendineae
(myxomatous or traumatic chordal rupture, endocarditis), papillary muscle (acute
infarction) or annulus (annular dilatation, periannular calcification). Chronic
MR produces LA and LV dilatation due to increased SV. Pulmonary venous
LV
Systole
Figure 4.8 Four-chamber SSFP cine CMR from a 40-year-old woman with familial MV
prolapse (MVP). MVP is thought to be caused by myxomatous degeneration of the valve
leaflets and chordae tendineae. The middle of the valve bows beyond the annulus during
systole; however, the tips of the leaflets do not pass beyond this point (black arrows). Mild
associated MR is noted in this case (white arrow) but is not always present.
58
Other valve lesions 4
hypertension may be present but is usually less severe than with MS, and pulmonary
arterial hypertension is also less common. Acute MR causes pulmonary venous
hypertension which may be asymmetrical (right upper lobe) without atrial or
ventricular enlargement.
CMR quantification of the severity of MR is useful in evaluating the signs of
decompensation, monitoring response to treatment and planning MV repair or
replacement. Important information required for preoperative assessment includes
an EF less than 50–60% and an end-systolic diameter greater than 5.0–5.5 cm, both
readily measurable with CMR. In the presence of LV dilatation or impairment,
myocardial assessment with LGE is advisable.
Cines in the four-chamber, two-chamber and LVOT views demonstrate the signal
void from the regurgitant jet. The jet may be central in annular dilatation or eccentric
in valve leaflet, chordae tendineae or papillary muscle dysfunction. Multiple or
complex jets may be present (Figure 4.9). Qualitative assessment of the severity
of regurgitation can be performed by the size of the jet (accounting for the echo
time) and the degree of LA dilatation. Quantification of regurgitant fraction can be
performed in several ways along lines similar to that already described with AR. MR
secondary to central, uncomplicated jets can be quantified by prescribing a region of
interest with velocity mapping CMR using a plane placed en-face and just distal to
the valve. This plane can also be used to measure effective regurgitant orifice area. A
method in single regurgitant lesions is via determination of the difference in LVSV
with either flow in the proximal ascending aorta or MPA, or the RVSV if no right-
sided regurgitation is present.
Severity of MR by regurgitant fraction is graded as: mild < 30%, mild to moderate
30–39%, moderate to severe 40–49%, and severe > 49%.
Additional CMR reporting points for MR are:
1. Overall impression of severity (based upon jet appearance, LVEF, LVESV and
LVEDV, and regurgitant fraction);
2. Evidence of pulmonary venous congestion or pulmonary arterial
hypertension; and
3. Comments on aetiology and additional valvular lesions.
Other valve lesions

Mixed valvular disease is often present, particular in rheumatic heart disease which
principally involves the MV and less commonly the AV. In late disease with pulmonary
arterial hypertension, TR is also present. CMR quantification of regurgitant fractions
can become complicated in this setting but is possible using velocity mapping at
the individual valve planes and generating several flow velocity time curves for
evaluation in comparison with LVSV and RVSV. Valve planimetry of the mitral and
aortic valves can also be undertaken to yield values for an effective regurgitant orifice
(Table 4.1). As with echocardiography, all available indicators of severity must be
assessed collectively prior to documenting final conclusions on the clinical report.
59
Systole
LA
LA
LV
LV
a b
Systole
Systole
LA
LV/
LA
LV
d
c
Figure 4.9 (a) Four-chamber, (b) modified two-chamber, (c) LVOT and (d) basal short-
axis cines from a 42-year-old woman with multiple, eccentric jets of MR (black arrows).
LVEF was 47% and regurgitant fraction calculated by comparison of LV and RV SV was
60%, indicating severe regurgitation. LGE demonstrated no enhancement.
60
Other valve lesions 4
Table 4.1 Grading of severity by effective regurgitant orifice (mm2)

Severity MR AR
Mild < 20 < 10
Mild to moderate 20–29 10–19
Moderate to severe 30–39 20–29
Severe > 40 > 30
CMR is also useful in quantifying the degree of TR, pulmonary regurgitation (PR)
and pulmonary stenosis (PS). Its multiplanar capability is useful in the assessment of
global RV function which may be limited using echocardiography.
Metallic prosthetic valves are safely imaged with CMR. Although assessment of
paravalvular abscesses or quantification of regurgitant lesions can be performed,
results may be markedly hindered by metal artefact and conclusions should therefore
be interpreted within this context (Figure 4.10). FSE sequences are less affected in the
presence of metal than SSFP cine or velocity mapping CMR.
Velocity mapping
Ao Ao
LV LV
a b
Figure 4.10 LVOT views by (a) SSFP cine imaging and (b) velocity mapping CMR in a
27-year-old woman who had undergone aortic root enlargement and AV replacement
(21-mm Medtronic Hall tilting disc prosthesis) 12 years previously.
Signal void from the metal valve is clearly seen using these two sequences (black arrows),
but the artefact does not preclude assessment of the valve function.
61
Indications
CMR can:
1. Image patients with poor echocardiographic windows. Although CMR

assessment can be suboptimal in subjects with cardiac arrhythmias (atrial
fibrillation is much less of a problem than ventricular bigeminy) and in the
presence of metal valves, these should not preclude referral;
2. Arbitrate between conflicting echocardiographic and cardiac catheterization
data;
3. Accurately assess the effects of valvular heart disease on cardiovascular
morphology and cardiac function, and follow up these individuals; and
4. Readily interrogate right-sided valvular lesions and RV function.
CMR cannot:
1. Replace echocardiography. Echocardiography is the principal imaging

modality for the initial evaluation of patients with valvular heart disease and
CMR is a complementary tool;
2. Exclude small valvular vegetations in endocarditis.
62
Chapter 5
Cardiac masses,
pericardial disease
and myocarditis
Anitha Varghese and Ping Chai
Introduction
Detection and characterization of cardiac and pericardial masses is a Class I indication for CMR.
Imaging in constrictive pericarditis and pericardial effusion are Class II and III
indications, respectively. CMR in myocarditis has an emerging role.
Cardiac masses
The general protocol for interrogation and subsequent reporting of masses is:
1. Anatomical evaluation—CMR can define the size, extent and anatomical

relationship of masses to neighbouring structures with high resolution, across
multiple planes, and with a wide field of view;
2. Cardiac functional assessment; and
3. Tissue characterization—available techniques are SE and GE sequences,
application of a fat saturation prepulse, EGE and LGE, and rest perfusion CMR.
Thrombus
This is by far the commonest cardiac filling defect and both atrial and ventricular
thrombi are readily visualized by SE, GE and following gadolinium (Figure 5.1).
On T1W SE imaging, thrombus has intermediate signal intensity often slightly
higher than myocardium and blood. T2W SE shows surrounding slow-flowing
blood as having higher signal intensity than the thrombus itself, thereby enhancing
differentiation from myocardium. With SSFP cine GE and velocity mapping techniques
thrombus has the lowest signal intensity in distinction to blood flow, even where it is
diminished, which has a high signal intensity. Injection of gadolinium contrast agent
increases diagnostic accuracy and characteristically demonstrates an avascular filling
defect by rest perfusion CMR and EGE. In the case of LV thrombus, subsequent LGE
images usually reveal an area of infarction which has acted as the substrate for
63
5 Cardiac masses, pericardial disease and myocarditis
LV
LV
a b
T2W T2W
c d
Figure 5.1 Large inferior LV false aneurysm lined by a thick layer of laminated thrombus
(black arrows) in a 70-year-old woman with a history of MI.
(a) Two-chamber and (b) mid-ventricular short-axis SSFP GE cines show the thrombus to
have much lower signal intensity than the intracavity blood flow above. Equivalent
(c) two-chamber and (d) short-axis views obtained using T2W SE imaging demonstrates
non-homogenous signal in the thrombus indicative of the differing stages of haemoglobin
breakdown within it.
64
Cardiac masses 5
EGE LGE
e f
Figure 5.1 cont’d (e) Two-chamber EGE confirms an avascular filling defect
surrounded inferiorly by LV transmural LGE on the ventricular short-axis view (f; dashed
white arrow).
thrombus formation. For atrial thrombi, a dilated LA and LA appendage can be

demonstrated as with transoesophageal echocardiography (TOE).
Tumours
Secondary cardiac deposits are more frequent than primary cardiac tumours, but
both are rare with a necropsy incidence of 1% and 0.05% respectively. Secondary
involvement is usually clinically silent and limited to the epicardium. Presenting
cardiac signs, when they occur, are those of a large pericardial effusion or incipient
tamponade, arrhythmias, cardiomegaly or heart failure. Locally infiltrating
malignancies include carcinoma of the lung or breast and renal cell carcinoma may
embolize to the RA (Figure 5.2). Cardiac metastases are seen with malignant
melanomas, leukaemias and lymphomas.
The majority of primary cardiac tumours are benign with the most frequent
being atrial myxomas (45%) and cardiac lipomas (20%) (Figure 5.3). Malignant
cardiac tumours make up one quarter of primary tumours and the most common are
sarcomas (95%). CMR anatomical evaluation of intra- and extracardiac involvement
has implications for staging, surgical treatment and surveillance (Figure 5.4).
CMR differentiation between malignant and benign tumours uses a combination of
general principles applied by other modalities and some more specific features. In
general terms, malignancy is more likely with larger masses having a broad-based
attachment, involving more than one cardiac chamber or great vessel, and with
associated pericardial or extracardiac extension. More specifically, T1W and T2W
images use the biochemical composition of masses to assist with diagnosis. High
signal intensity on T1W images can be due to cystic lesions with a high protein
content, fatty tumours (lipoma, liposarcoma), recent haemorrhage and melanoma.
Low signal intensity on T1W is seen in cysts with low protein content, within
vascular malformations, in calcified lesions, or if the mass contains air. Subsequent
65
RV RA
Liver Spleen
IVC
a
Left
kidney
Right
kidney Abdominal
aorta
RV
CE-MRA
RA LV c
LA
Figure 5.2 CMR study from a 63-year-old man with left renal cell carcinoma.
(a) SSFP GE cine image of the RA shows cardiac tumour invasion (white arrow) via the
inferior vena cava (IVC). (b) Transaxial SSFP GE cine confirms tumour within the RA (black
arrow). (c) Renal CE-MRA demonstrating a 5.5 μ 4.0 μ 4.5 cm3 mass in the upper half of
the left kidney (white circle).
66
Cardiac masses 5
RA Ao LV
LA
T1W
a b
RV
RA LV
LA
Perfusion
T2W CMR
c d
Figure 5.3 CMR characterization of a solitary LA myxoma (black arrows) from a
65-year-old man noted to have an LA mass on TTE and TOE. (a) Transaxial SSFP cine GE
sequence of the 4.2 μ 3.8 μ 4.0 cm3 ovoid mass within the LA. The base is attached to the
interatrial septum and the mass has a lower signal intensity than the surrounding blood pool.
(b) T1W SE imaging in an equivalent plane shows largely intermediate signal intensity but
with a central area of increased intensity consistent with haemorrhage. (c) T2W imaging
reveals the mass to have predominantly low signal intensity. (d) Four-chamber first-pass
perfusion CMR demonstrates a small central core of perfusion compatible with vascularity.
cont’d
67
EGE LGE
e f
Figure 5.3 cont’d (e) Transaxial EGE view is largely negative but with central
enhancement. (f) LGE in the same plane demonstrates significant enhancement, probably
areas of necrosis or fibrosis.
PREOPERATIVE POSTOPERATIVE POST-CHEMOTHERAPY
LV
a b c
Figure 5.4 Serial assessment two-chamber SSFP GE cine views from a 44-year-old man
with a LA sarcoma before and after treatment (a–c; solid black arrows). CMR was used to
accurately evaluate tumour size (a; white cross) and MV function (a; dashed black arrow)
at each stage.
68
Pericardial disease 5
T2W imaging demonstrates cysts as having high signal intensity, and the addition of
a fat saturation prepulse distinguishes lipid content. Rest perfusion first-pass CMR
shows contrast uptake into vascular tumours (haemangioma, angiosarcoma) and
may also identify small vessels. In malignancy, EGE typically demonstrates dark
areas with surrounding enhancement from necrotic tissue, while LGE can show
enhancement due to expanded interstitial space such as in fibrosis (Figure 5.5). Such
enhancement is absent in cystic lesions and most benign tumours, with exceptions
being haemangiomas, myxomas and fibromas (Figure 5.6).
Pericardial disease
The pericardium is a thin double-layered sac that encompasses the heart and proximal
great vessels. Its inner serosal layer adheres to the myocardium forming the visceral
pericardium or epicardium, extends up over the proximal great vessels and reflects
back on itself to become contiguous with the outer layer. This fibrous outer parietal
layer has attachments to the diaphragm, sternum, costal cartilages and the spinal
column. The two layers are separated by a space containing 15 to 35 ml of serous
fluid and total pericardial thickness is 1 to 2 mm. At the base of the heart the
pericardial reflection forms sinuses and recesses, with the reflection adjacent to the
ascending aorta potentially confused with a proximal aortic dissection by the unwary
(Figure 10.10). Since fat usually surrounds the pericardium and is also present
beneath the epicardium, the pericardium is often sandwiched between two layers
of fat. This makes it easier to visualize edge-on with CMR and gives the slightly
higher normal value of up to 4 mm for pericardial thickness. Normal pericardium
has low signal intensity by GE and SE imaging techniques (Figure 5.7). Of note, a
dark line can be present at the interface between myocardium and epicardial fat on
GE images due to artefact. This appearance is caused by the phenomenon of chemical
shift phase cancellation and should not be interpreted as pericardium (see section
10.6, Chemical Shift Edge Artefacts).
The pericardium plays an important role in protecting and restraining the heart
and has significant haemodynamic implications for atrial and ventricular filling.
Because of pericardial constraint the total volume of the four cardiac chambers is
limited and changes in the volume of one chamber are accompanied by opposite
changes in the volume of another chamber—this effect is not physiologically important.
However, when intrapericardial pressure is raised, such as in pericardial effusion, or
when the pericardial cavity becomes fixed, as with constriction, the interdependence
of filling between the ventricles becomes exaggerated. Intrapericardial pressure
is usually similar to intrapleural pressure and with inspiration there is a small
physiological increase in right heart filling and a slight decrease in left-sided filling.
With increased pericardial constraint, the respiratory alterations in filling patterns
become more marked.
Acute pericarditis and pericardial effusion

Acute pericarditis may be accompanied by symptoms and signs of heart failure
or arrhythmias if there is concomitant myocarditis. CMR findings range from no
69
Ao
Left
Right lung
lung
T1W
a
EGE
b
LGE
c
Figure 5.5 CMR study from an 82-year-old man with TTE findings of a pericardial
effusion and diastolic abnormality.
(a) Transaxial T1W FSE demonstrates a large, irregularly shaped, highly lobulated anterior
mediastinal mass (white arrow) infiltrating the sternum and chest wall anteriorly and the
pericardium posteriorly. (b) EGE shows the mass to have patchy contrast uptake. (c) Patchy
LGE was present. These appearances are highly suggestive of a malignancy such as
lymphoma, angiosarcoma or thymic carcinoma.
70
EGE
RV/ LV
RA
a b
LGE
Figure 5.6 Basal short-axis views from a 34-year-old woman referred for CMR with an
echocardiographic finding of localized basal anteroseptal hypertrophy and subsequent
normal cardiac biopsy.
Initial SSFP cine readily confirms the TTE findings (a; black arrow), while EGE showed no
enhancement within the mass (b) and LGE demonstrated homogenous contrast uptake
(c). These CMR appearances are characteristic of a fibroma.
71
RV
LV
RA
LA
T1W
Figure 5.7 Four-chamber T1W FSE image showing normal pericardial appearance in
front of the RV (black arrow).
abnormality to regional WMA, pericardial thickening and pericardial effusion. The

heart is imaged in different planes to determine the greatest extent of thickening
or effusion, especially in cases of loculation. An effusion less than 10 mm wide is
considered small whereas large effusions are greater than 20 mm. Both thickened
pericardium and effusions can show low signal intensity on T1W SE imaging while
GE techniques reveal non-haemorrhagic effusions to have high signal intensity
(Figure 5.8). The appearance of haemorrhagic effusions depends on the age of the
pericardial haematoma. Acutely, there is high signal intensity on T1W SE and lower
signal intensity on GE images, while more chronic haematomas exhibit heterogeneous
signal intensities by SE techniques. Differentiation of transudates from exudates and
chylous effusions is through T1W SE imaging. Signal intensity is low in transudates
but high in chylous collections, with an intermediate appearance in exudates.
SSFP GE cine imaging demonstrates diastolic chamber collapse and abnormal
septal motion in cardiac tamponade. In the latter, the heart can often have a swinging
motion. Other pathological findings include dilated superior and inferior vena cavae
and the presence of abnormalities within the mediastinum and lung fields which
could provide clues as to aetiology.
Following gadolinium injection, inflamed pericardium shows early enhancement
with a smooth contour suggestive of acute pericarditis in contrast to an irregular
outline after a more insidious clinical course. Such pericardial contrast enhancement
is also seen in malignant infiltration. Contrast enhancement is usually absent in
pericardial fluid.
72
RV
LV
RA
LA
T1W SE
a
Figure 5.8 Four-chamber views from a 42-year-old woman with a large global
pericardial effusion (a; white arrow) secondary to metastatic leiomyosarcoma (b; black
arrow). The effusion is seen to have intermediate signal intensity by SE imaging (a) and a
high signal intensity using the GE technique, which clearly shows the tumour (b).
With massive effusion, ECG amplitude may diminish making it difficult to trigger
cardiac imaging. CMR assessment can also be limited in patients who are significantly
symptomatic since they have a tachycardia and find it difficult to lie flat within the
magnet for prolonged periods.
73
Constrictive pericarditis
Following inflammation or bleeding into the pericardial space, fibrosis and
calcification of the pericardium may ensue and the pericardium becomes thickened
and stiff. This progressively restricts and impairs the filling of the cardiac chambers.
Diastolic pressures are elevated and equalized in all four cardiac chambers. Impaired
diastolic function leads to tachycardia and volume expansion, resulting in systemic
venous congestion. Systolic function is usually preserved unless there is associated
myocardial disease. The heart is insulated from changes in intrathoracic pressure
that occur with respiration and atrial and ventricular filling patterns vary significantly
with inspiration and expiration, resulting in ventricular interdependence. During
inspiration, right-sided filling is increased, the ventricular septum deviates to the left,
and left-sided filling correspondingly decreases. The converse occurs at expiration.
The distinction between constrictive pericarditis and restrictive cardiomyopathy
is difficult but important clinically and imaging techniques such as CMR and cardiac
CT are useful in diagnosis. The diagnostic hallmark of constrictive pericarditis is
pericardial thickening with or without calcification in the presence of suggestive
symptoms and signs of constriction (Figure 5.9). Care should be taken when evalu-
ating pericardial thickness since oblique views yield falsely high values and several
planes must be assessed and used in measurements. The absence of pericardial
thickening/calcification does not exclude the presence of constriction and a thickened
RV
RA LV
LA
Figure 5.9 Four-chamber SSFP GE cine view from an 81-year-old woman with a history
of recurrent pericardial effusions requiring surgical drainage and features of constrictive
pericarditis at recent cardiac catheterization.
There is bi-atrial dilatation and a thickened pericardium (black arrows), which measured
9 mm in this plane. No pericardial effusion is seen and LVEF was 68% (normal).
74
pericardium does not always equate to constrictive pericarditis. It is therefore crucial

to evaluate concomitant functional consequences and CMR is well-suited for this
purpose.
A thickened pericardium as well as pericardial effusions can often be identified at
the early low-resolution FSE sequence. Pericardial thickness is definitively measured
on subsequent T1W FSE views and differentiated from effusion with SSFP cines
acquired in these same planes. In the presence of effusion, pericardial thickness can
be determined by use of gadolinium which can outline the visceral and parietal
layers. Chronic fibrotic pericardium shows late enhancement, which is also seen
with associated myocardial fibrosis or infarction. Areas of calcification appear as
regions of attenuated signal intensity on CMR but CT is recommended for accurate
assessment of this feature. Other findings include typically normal-sized or small
ventricles with normal ejection fraction, dilated atria and vena cavae, pleural
effusions, plethoric hepatic veins, hepatic enlargement and ascites. The ventricles
may assume a tube-like configuration. The presence of epicardial fat separating the
epimyocardium from the thickened visceral pericardium is also a useful finding for
the surgeon when planning surgical pericardiectomy.
On high temporal resolution SSFP cines, the ventricular septum may be seen to
deviate towards the LV in early diastole. Additional real-time cines are useful in
demonstrating ventricular interdependence. The patient is instructed to inhale and
exhale throughout these cines, which are acquired over approximately 20 s and at
least three respiratory cycles. With constrictive physiology, the ventricular septum
flattens and deviates towards the LV on inspiration before resuming its normal
position on expiration—‘septal bounce’. The technique of myocardial tagging
can determine myocardial tethering to the overlying thickened pericardium with
persistent concordance of the tag lines between myocardium and pericardium
throughout systole and diastole.
In summary, a suggested CMR imaging protocol in significant pericardial effusion/
constriction is as follows:
• Multislice free breathing FSE in transaxial, coronal and sagittal planes;

• SSFP cines in the usual views, selected transaxial and sagittal planes, and
additional planes through areas of abnormal pericardium or loculated effusion;
• T1W FSE imaging of the views in which abnormalities are identified;
• Gadolinium-enhanced SE and GE imaging of the views in which the
pericardium is abnormal; and
• If constriction is suspected:
— High temporal resolution SSFP cines of the four-chamber and mid-
ventricular short-axis views;
— Real-time SSFP cines of the mid-ventricular short-axis view; and
— Myocardial tagged cine images of the views in which thickened
pericardium is identified.
75
CMR reports include:
1. Anatomical details—such as cardiac chamber size, vena cavae dilatation,

pericardial thickness, presence and characterization of effusions (especially
in terms of size, loculation and suggested sites for safe pericardiocentesis if
required) and pleural effusions;
2. Cardiac functional comments—such as evidence of cardiomyopathy and
tamponade physiology; and
3. Clues to aetiology—such as contrast enhancement patterns within the
pericardium and myocardium.
Pericardial cyst and diverticula

Pericardial cysts are uncommon remnants of defective pericardial embryologic
development. They are benign and occur as round, sharply demarcated, fluid-filled
bodies, found most commonly in the right cardiophrenic angle but also in the hilar
and mediastinal regions. They do not communicate with the pericardial space.
Using T2W SE images they typically exhibit high signal intensity, while on T1W SE
images they show intermediate or low signal intensities (Figure 5.10). There is no
enhancement with gadolinium contrast.
Pericardial diverticula are rare outpouchings of the pericardial sac and therefore
are in communication with the pericardial space.
Congenital absence of the pericardium

Absence of the pericardium is rare and often asymptomatic. The defect is usually
left-sided and partial but can be right-sided, diaphragmatic or complete. Associated
congenital cardiac anomalies include atrial septal defects (ASDs), patent ductus
arteriosus (PDA) and tetralogy of Fallot (TOF). The heart shifts to the left and
posteriorly, and with partial left-sided absence the left atrial appendage may be
dilated. Herniation of the left atrial appendage through a partial defect may lead
to strangulation and sudden death. CMR can reveal the defect, associated cardiac
anomalies and displacement, and herniation (Figure 5.11).
Myocarditis
Myocarditis can be caused by a wide variety of infectious agents and detected with
the technique of LGE. Patterns of enhancement do not correspond to infarction in
a coronary artery territory and are characteristically subepicardial and frequently
located in the lateral free wall (Figure 5.12). These appearances in conjunction with
the appropriate clinical setting can obviate the necessity for cardiac catheterization
and subsequent endomyocardial biopsy in selected patients. Follow-up of individuals
with significant enhancement abnormalities, with either echocardiography or CMR,
is also advisable to determine long-term ventricular function.
76
Myocarditis 5
Ao
MPA
bifurcation
T2W
a b
Figure 5.10 An incidental finding of a small 2.6 μ 1.8 μ 5 cm3 pericardial cyst (white
arrows) discovered in a 71-year-old man referred for coronary MRA showing characteristic
high signal intensity by (a) SSFP cine and (b) T2W SE imaging in a transaxial plane at the
level of the pulmonary bifurcation.
RV
RA
LV
LA
Figure 5.11 Four-chamber SSFP GE cine image from a 46-year-old patient

demonstrating herniation of both ventricles through a partially absent pericardium at the
level arrowed.
There is associated RA and RV dilatation on this image secondary to severe TR which is not
shown.
77
LGE
LV
RV
Figure 5.12 LGE in a mid-ventricular short-axis plane from a 61-year-old man with
long-standing anterolateral ST segment changes but no significant CAD at X-ray coronary
angiography. Enhancement is seen within the mid-wall of the interventricular septum
(dashed white arrows) and subepicardial aspect of the lateral wall (solid white arrows).
This pattern in association with a dilated LV and impaired LVEF (28%) was suggestive of a
myocarditis-induced cardiomyopathy.
Indications
CMR can:
1. Detect and characterize cardiac masses including atrial and ventricular thrombi;
2. Be used to stage malignant cardiac tumours;
3. Safely be used in oncology surveillance;
4. Detect and characterize pericardial effusions;
5. Detect pericardial constriction;
6. Demonstrate abnormal haemodynamics of increased intrapericardial
pressures, such as ventricular interdependence;
7. Detect and characterize pericardial masses;
8. Diagnose congenital abnormalities of the pericardium and associated cardiac
defects; and
9. Accurately diagnose myocarditis.
CMR cannot:
1. Readily image patients who have severe dyspnoea and tachycardia due to
scan positioning and duration, and imaging artefacts from respiratory and
cardiac motion; and
2. Exclude pericardial calcification.
78
Chapter 6
Diseases of the
aorta
Beatriz Bouzas
Introduction
The aorta can be evaluated by a variety of techniques (Figure 6.1). X-ray contrast
angiography was the gold standard method for many years but it is invasive and
uses ionizing radiation and nephrotoxic contrast agents. Noninvasive options are
TOE, CT and CMR (Figure 6.2). TOE is portable but relatively invasive and offers
Right common carotid artery

Left common carotid artery
Right subclavian artery Aortic arch
Brachiocephalic artery Left subclavian artery vessels
Aortic arch
Ascending aorta
Aortic root Descending aorta
Thoracic
Right coronary artery Left coronary artery aorta
Diaphragm Heart
Celiac artery
Abdominal
aorta
Renal arteries
Superior mesenteric artery
Inferior mesenteric artery
Iliac arteries
Figure 6.1 Diagrammatic representation of the normal aorta.
79
6 Diseases of the aorta
Ao
LA
RA
T1W
a b
Figure 6.2 Normal CMR study of the aorta from a 60-year-old man referred for further
investigation of hypertension with a family history of an ascending aortic aneurysm and
marfanoid features.
These images show the oblique sagittal plane (known as the ‘hockey-stick’ or ‘candy cane’
view) from which several measurements can often be made using the (a) GE or (b) SE
sequence. This aortic long-axis view is a plane obtained from the initial transaxial FSE
images by placement of three markers—at the ascending aorta, at the aortic arch and at
the descending thoracic aorta. Quoted aortic dimensions are usually intraluminal, at end-
diastole, and should state clearly the sequence used in order to facilitate serial evaluation.
incomplete coverage of the aorta with restricted visualization at the aortic arch. CT
is fast and widely available but uses ionizing radiation and nephrotoxic contrast
agents. CMR avoids these limitations and offers multiplanar imaging of the aorta
with a wide field of view and concurrent cardiac functional assessment. However,
it is less available and evaluation of critically ill patients can be hampered by MRI-
incompatible life support and monitoring equipment.
CMR reports of scans pertaining to the aorta follow the general pattern of:
(a) Anatomical details of the heart and aorta;

(b) Concurrent cardiac functional assessment, for example quantification of AR
and degree of LVH; and
(c) Likely aetiology of aortic pathology with suggestions for follow-up.
Thoracic aortic aneurysm

An aortic aneurysm is a focal dilatation of the aorta. According to the shape the
aneurysm is described as fusiform, with symmetrical dilatation of the circumference
of the aorta, or saccular where only a part of the aortic wall is dilated. Aortic aneurysms
80
Thoracic aortic aneurysm 6
can also be classified into true and false aneurysms. A true aneurysm consists of
dilatation of all the layers of the aortic wall and characteristically has a wide neck. By
contrast, in a false aneurysm perforation of the intima and media is contained by the
surrounding adventitia and peri-aortic tissue, and the neck is usually narrow.
Aortic aneurysms are usually the consequence of atherosclerotic disease and most
commonly occur at the descending aorta (Figure 6.3). Other causes are trauma,
connective tissue disorders such as Marfan and Ehlers–Danlos syndromes, congenital
abnormalities, and infections such as syphilis. Post-stenotic aneurysms are found
distal to AV stenosis and aortic coarctation or recoarctation.
CMR can readily detect aortic aneurysms and scan protocols evaluate the
following:
• Aneurysm location, shape, 3D size, and extension;

• Involvement of the AV and aortic root (including coronary arteries);
• Proximity to branch vessels (such as the left subclavian, renal and iliac
arteries);
• Presence of intraluminal flow and thrombus;
• Associated aortic dissection; and
• Pericardial effusions (Figure 6.4).
SE images acquired in the transverse and long-axis planes are useful for measuring
the diameter of the aorta at different levels and relationship of the aneurysm to
major vessels. Coronal and oblique sagittal views clearly depict the aortic root and
tortuous segments. Slow or turbulent blood flow can produce images which mimic
mural thrombus on SE imaging. SSFP cines and velocity flow mapping help to
differentiate slow flow from intraluminal thrombus. Where intraluminal thrombus
Ao
LA
RA
T2W
a b
Figure 6.3 Hockey-stick (a) SSFP cine and (b) T2W SE views from a 74-year-old man
with a 6.2 cm fusiform descending thoracic aortic aneurysm (large white arrow) containing
a large amount of mural thrombus (small white arrows).
81
Ao
Ao
LV LV
a b
Figure 6.4 LVOT SSFP GE cines from a 20-year-old man with Marfan syndrome showing
an 11.5 cm ascending aortic aneurysm (Ao) associated with severe AR (solid white
arrows), dilated LV, and a small global pericardial effusion (dashed white arrows). There
was no evidence of dissection.
is present, its thickness and extent should be determined. CMR allows characterization
of intraluminal thrombus based on signal changes caused by the paramagnetic
properties of deoxyhaemoglobin and methaemoglobin. Methaemoglobin forms
from red blood cell lysis and shortens T1 but increases T2, causing hyperintensity on
both T1W and T2W SE sequences. Thrombus with homogeneous low signal intensity
on both T1W and T2W images corresponds to macroscopic organized thrombus.
Some organized thrombi may have an internal rim of hyperintensity which
represents recent clot apposition on the luminal surface of the thrombus. Thrombi
with homogeneous high signal intensity on T1W and T2W imaging represent
unorganized thrombi, composed mainly of fresh clot. Some thrombi may appear
partially organized, with areas of high and low signal intensity (Figure 6.5).
Inflammatory aortic aneurysms may show an area of peri-aortic inflammation that
enhances following gadolinium contrast. This can be better visualized using a T1W
CMR sequence with an added fat saturation prepulse. MRA is useful for assessing
aortic flow and involvement and patency of aortic branch vessels. Images are
acquired in the aortic long-axis plane and can then be reformatted into the transaxial
plane. Post-processing techniques, such as maximum intensity projections (MIPs)
and shaded surface displays, are used for representation (Figure 6.6). CMR is useful
for follow-up evaluation of aneurysm size and serial measurements must be made
at the same level.
Percutaneous stent-graft placement has emerged in the recent years as an
effective way of treating aortic aneurysms and dissection. CMR is useful in
planning these interventions allowing customization of stent design according to
aortic anatomy, and detection of post-stent leaks. Accurate quantification of aortic
calcification prior to stenting requires CT rather than CMR.
82
Aortic dissection 6
T2W T2W
Ao Ao
Ao LA
LV RA
a b
Left
lung
Ao
Right
lung
T2W
c
Figure 6.5 Modified (a) coronal, (b) sagittal and (c) transaxial T2W SE planes from
a 70-year-old woman demonstrate a 10 μ 10 μ 6 cm3 aortic arch pseudoaneurysm on
the outer curvature of the distal aortic arch containing partially organized mural thrombus
(white arrows).
Aortic dissection
Aortic dissection consists of an intimal flap separating the true and false lumen,
and intimal tears are sites of communication between the true and false lumen.
A dissection can spread antegradely or retrogradely and may involve the whole
length of the aorta. It can lead to occlusion or obstruction of branch vessels, aortic
regurgitation and pericardial effusion. Aetiology includes hypertension (the most
common), atherosclerosis, congenital lesions, iatrogenic causes and trauma.
83
CE-MRA
Ao
Figure 6.6 MIP reconstruction of the CE-MRA data obtained from the case illustrated in
Figure 6.5.
Of note, the large outer aortic arch pseudoaneurysm (white arrow) is clearly seen to
be in communication with the aortic lumen via a 2.5 cm entry site (solid black arrow).
Additionally, a second, smaller pseudoaneurysm (3.5 μ 2.3 μ 6.0 cm3) is demonstrated on
the inner aortic arch (dashed black arrow).
Aortic dissections are classified by the De Bakey or Stanford classification system.

The De Bakey classification is based on the location of the intimal tear and the extent
of the dissection:
Type I: Intimal tear originates in the ascending aorta and extends past the origin
of the left subclavian artery.
Type II: Intimal tear originates in the ascending aorta and the dissection is limited
to the ascending aorta.
Type III: Intimal tear originates beyond the origin of the left subclavian artery
and extends distally.
The Stanford classification is based on prognosis and has implications for management.
Type A: Dissection involves the ascending thoracic aorta (Figure 6.7).

Type B: Dissection does not involve the ascending thoracic aorta (Figure 6.8).
Type A dissection carries a higher complication rate and mortality and is a surgical
emergency, while type B dissections have a better prognosis and are usually managed
medically.
CMR is the gold standard imaging technique for detecting and characterizing
aortic dissections with their associated complications in the haemodynamically
stable patient. Scan protocols evaluate the following after diagnosis:
84
Aortic dissection 6
Diastole
Aortic
graft
False lumen
of ascending
aorta
LA LV
T2W
a b
Prosthetic
valve
artefact
True
Aneurysmal lumen
native aorta
Velocity mapping Systole

c
d
Figure 6.7 CMR study from a 57-year-old man who had undergone aortic root and
valve repair the previous year, followed by AV replacement with a metal prosthetic valve.
At follow-up a dilated ascending aortic aneurysm and AR were noted. (a) LVOT SSFP cine
confirms an aneurysmal ascending aorta with false lumen between native aorta and aortic
graft. Dehiscence of the posterior suture line of the prosthetic AV resulted in a rocking
motion of the valve and severe paravalvular regurgitation (long black arrow).
(b) Comparative T2W SE image highlighting the suture line dehiscence (solid white arrow).
(c) Velocity mapping CMR in the same plane showing blood flowing freely between the LV
and false lumen (dashed white arrow). (d) Oblique sagittal SSFP GE aortic cine showing
dissection flaps in the proximal aortic arch and the descending thoracic aorta (short black
arrows).
85
Ao Ao
Liver
LA
RA Right
kidney Left
kidney
T2W
a b
Ao
CE-MRA
c
Figure 6.8 Residual type B aortic dissection from a 67-year-old man who had
undergone repair of a type A dissection one year previously.
(a) Oblique sagittal T2W SE shows the false lumen of the thoracic dissection (white arrow).
This extends from 4 cm beyond the left subclavian artery to 2 cm above the diaphragm and
is largely thrombosed with evidence of a fresh inner layer of thrombus. (b) Oblique coronal
SSFP cine demonstrates the abdominal dissection (white ellipse). (c) MIP reconstruction of
the CE-MRA data showing the two separate dissections (white arrow and white ellipse).
Both renal arteries receive flow from the true lumen.
86
Intramural haematomas and penetrating aortic ulcers 6
• Location of proximal intimal flap and involvement of the ascending aorta, AV,
and coronary arteries;
• Extension of dissection and sites of entry and re-entry (intimal tear);
• Presence of thrombus within the false lumen;
• Involvement of branch vessels with a comment on which lumen supplies
them; and
• Associated pericardial and pleural effusions.
SE imaging delineates the intimal flap as a linear structure separating the true
and false lumens. Slow flow (usually within the false lumen) or thrombus is
differentiated by SSFP cines in the same plane. Cines are useful in detecting AR,
and both sequences help in the diagnosis of pericardial effusions. Velocity mapping
CMR also distinguishes diminished flow from intraluminal thrombus and highlights
flow directionality in the false lumen (antegrade/retrograde). AR, where present, is
quantified by velocity mapping in the appropriate plane. CE–MRA shows the flap
and branch vessel involvement.
Intramural haematomas and penetrating aortic ulcers

An intramural haematoma has a similar clinical presentation and prognosis to that
of aortic dissection and is also associated with arterial hypertension. It is thought
to be caused by spontaneous rupture of the aortic vasa vasorum with subsequent
propagation of subintimal haemorrhage, and there is a high rate of progression to
aortic dissection and risk of aortic wall rupture. By contrast to dissections, there is
more frequent involvement of the descending aorta and less frequent AR, MI and
pulse deficits since they are more localized. The location of intramural haematomas
carries prognostic and management implications with those in the ascending aorta
having a higher frequency of complications and requiring surgical treatment.
Intramural haematomas are characterized by the presence of intramural blood
and/or increased arterial wall thickness which can be asymmetrical or circum-
ferential (Figure 6.9). T1W and T2W SE imaging allows some determination of the
age of the haemorrhage. Acutely (first 5–7 days) intramural haematoma appears as
increased wall thickness of intermediate signal intensity which is isodense with the
aortic wall. Subacutely (more than 8 days) there is high signal intensity similar to
fat due to the presence of methaemoglobin. Transaxial planes should be acquired in
preference to longitudinal views due to improved differentiation from mediastinal fat.
Addition of a fat saturation prepulse sequence further improves distinction between
haematoma and fat. MRA will usually not detect intramural haematomas since
there is no luminal component.
Penetrating aortic ulcers consist of an intimal erosion penetrating the aortic wall
from within the aortic lumen. There is an association with intramural haematoma
and a risk of progression to aortic dissection or perforation. MRA reveals a focal area
of contrast extravasation communicating with the aortic lumen. Penetrating ulcers
are found predominantly in the descending thoracic and abdominal aorta, with the
most frequent risk factor being aortic atherosclerosis.
87
A
Ao
T2W
b
a
Figure 6.9 (a) Oblique sagittal SSFP cine view of the aorta and (b) transaxial T2W SE
image from a 79-year-old man with chronic hypertension, aneurysm of the ascending aorta
(two-headed arrows) and extensive intramural haematoma of the distal aortic arch and
descending thoracic aorta (single-headed arrows).
Aortitis
Takayasu arteritis is a granulomatous vasculitis of unknown aetiology that commonly
affects the thoracic and abdominal aorta. Inflammation leads to thickening of the
aortic wall and the origin of the main branches, mainly in the aortic arch, with
sequelae including aortic branch thrombosis, stenosis or occlusion. The pulmonary
arteries can also be affected. SE imaging demonstrates diffuse wall thickening and
MRA provides good visualization of aneurysm formation and branch vessel stenosis
and/or occlusion.
Marfan syndrome
Marfan syndrome is an inherited connective tissue disorder with significant
cardiovascular, skeletal and ocular system complications. CMR evaluates:
• Mitral and tricuspid valve (TV) prolapse;

• Aortic root dilatation;
• Ascending and descending thoracic aortic aneurysm formation; and
• Presence of aortic dissection.
Aortic dissection and rupture account for most deaths in this condition and affected
individuals undergo regular CMR surveillance of the aorta to help plan elective aortic
root replacement. Aortic root dimension and the rate of increase are the best predictors
of those at greatest risk of aortic dissection, and prophylactic root replacement is
recommended before diameters reach 55–60 mm. In patients with family history of
88
Coarctation of the aorta 6
aortic dissection, replacement is performed when the aortic root measures 50 mm.
Progressive thoracoabdominal vasculopathy postoperatively necessitates continued
follow-up after repair of the ascending aorta. Patients with an aortic dissection or
peripheral artery aneurysms require more frequent CMR assessment.
Coarctation of the aorta

Coarctation of the aorta occurs in approximately 1 in 10 000 people and is usually
diagnosed in children or adults under 40 years old. It commonly consists of a
stenosis of the aorta just distal to the origin of the left subclavian artery. The area of
coarctation can be a localized narrowing or a long hypoplastic segment involving
the aortic arch and descending thoracic aorta. Haemodynamically significant lesions
are associated with the development of collaterals from the intercostal, internal
mammary and anterior spinal arteries which then can supply blood to the descending
aorta (Figure 6.10). Bicuspid AV is frequently seen with aortic coarctation and this
cohort can progress to AS or AR. Dilatation of the ascending aorta may precede aortic
aneurysm formation and type A aortic dissection in these patients.
CMR is the imaging modality of choice in adult aortic coarctation. The study
evaluates:
• Site, extent and degree of aortic coarctation;

• Flow across the stenosis and assessment of severity;
• Collateral blood flow;
• Associated cardiovascular complications such as bicuspid AV and dilated
ascending aorta; and
• Results of childhood and adult interventions.
Ao
Figure 6.10 MIP reconstruction of CE-MRA data in the oblique sagittal view from a 25-
year-old woman showing discrete coarctation of the aorta just distal to the left subclavian
artery pre-catheter intervention (white circle). Associated internal mammary and intercostal
artery collaterals are arrowed.
89
The oblique sagittal plane is imaged using SE and SSFP cines for assessment of
anatomy, but several other planes may be required with increased tortuosity. Blood
flow across the stenosis is recognized with cines and these are then used to position
the planes required for velocity mapping CMR. Flow velocity mapping techniques
across the coarctation measure blood flow velocity and a pressure gradient is then
estimated with the modified Bernoulli formula. Resting peak velocity of greater than
3 m/s is significant, particularly in the presence of diastolic prolongation of forward
flow—a diastolic tail. Flow velocities may normalize in significant coarctation with
extensive collateralization. The percentage of collateral blood flow is calculated from
measurements of flow just proximal to the coarctation site and within the descending
thoracic aorta at the level of the diaphragm. Collateral blood flow is significantly
increased in severe coarctation. MRA readily demonstrates tortuosity, involvement
of aortic arch vessels and presence of collaterals.
Long-term outcomes following elective intervention in coarctation are optimal
when performed at 2–5 years of age. Late complications include hypertension,
re-stenosis, residual stenosis and aneurysm formation. CMR is performed at baseline
post-intervention and then at intervals thereafter, depending on clinical and imaging
findings (Figures 6.11 and 6.12). Haemoptysis in a patient with coarctation may
indicate leakage of blood through a false aneurysm. Serial contiguous SE sequences
should be used in this situation to identify bright para-aortic haematoma.
T2W CE-MRA
Ao
a b c
Figure 6.11 One-year post-catheter intervention CMR study of the patient in Figure
6.10. Oblique sagittal views show mild residual in-stent stenosis.
(a) SSFP cine reveals metallic stent artefact at the site of previous coarctation (white
ellipse). Subsequent flow velocity mapping CMR performed distal to the stent demonstrated
increased systolic velocity without a diastolic tail. (b) T2W SE images improve the stent
artefact and allow measurement of the reduced minimum in-stent diameter (dashed white
arrow). (c) MIP reconstruction of CE-MRA data shows reduced collateralization (white arrows).
90
Indications 6
CE-MRA CE-MRA
Ao
Ao
a b
Figure 6.12 Two examples of postoperative aneurysm formation shown using MIPs
displayed in the oblique sagittal plane.
(a) CE-MRA from a 19-year-old man who had undergone repair of aortic coarctation
with a subclavian flap and Impra patch aged 3. There is a fusiform aneurysm (solid white
arrow) distal to mild recoarctation at the mid-aortic arch. (b) CE-MRA from a 51-year-old
man who had undergone aortic coarctation repair with a Gelseal graft placed between the
dilated left subclavian artery and descending thoracic aorta (dashed white arrow). There is
a small, contained false aneurysm at the distal suture line of the graft (black arrow).
Rare congenital anomalies of the aorta

A right-sided aortic arch consists of a single aortic arch located to the right of the
trachea. This congenital anomaly is associated with TOF and truncus arteriosus. A
double aortic arch refers to persistence of both the right and left aortic arch leading to
the formation of a vascular ring around the trachea and oesophagus. This ring may
compress these structures, causing dyspnoea and dysphagia. An aberrant origin of the
right subclavian artery from the descending aorta may also cause airways compromise
due to direct compression as it crosses obliquely towards the right shoulder behind
the trachea.
CMR with SE and cines permits rapid evaluation of the anatomy of aortic arch
anomalies and their relationship to surrounding structures. Associated congenital
cardiovascular anomalies must also be characterized during the study. MRA allows
easy visualization of the anomaly from different orientations and is an excellent
way of communicating these unusual findings to colleagues.
Indications
CMR can:
1. Diagnose thoracic aortic aneurysms, aortic dissection, aortic intramural haematoma and penetrating
ulcers of the aorta, coarctation (and pseudocoarctation) of the aorta, and rare congenital anomalies
of the aorta;
91
2. Readily follow-up these cases and patients with Marfan syndrome pre- and
post-intervention. Metallic artefacts will affect images but do not preclude
useful CMR evaluation;
3. Assist planning for intervention;
4. Differentiate aortic dissection from intramural haematomas and penetrating
aortic ulcers; and
5. Perform concurrent cardiac anatomical and functional evaluation.
CMR cannot:
1. Reliably detect calcification within the aortic wall; and

2. Be recommended for the assessment of acute aortic pathology in
haemodynamically unstable patients.
92
Chapter 7
Adult congenital
heart disease
Richard Steeds
Introduction
Congenital heart disease has an incidence of approximately 1% (Figure 7.1). Advances
in medical and surgical management have resulted in a growing population of
young adults who require continued care due to the predominantly palliative rather
than curative nature of their interventions. CMR provides safe serial assessment of
patients with adult congenital heart disease (ACHD).
CMR can often differentiate patients in whom cardiac catheterization can be deferred and delineate
the management required. This reduces the number of diagnostic invasive procedures and helps
optimize interventions.
RIGHT RIGHT MPA

MPA Ao
Ao
‘LV’ ‘RA’ ‘LV’

‘RV’
Liver
Liver
Gastric IVC Moderator
fundus band
a b
Figure 7.1 Two cases of dextrocardia.

(a) ‘LVOT’ SSFP cine view from a 42-year-old woman showing situs inversus with
dextrocardia. Situs inversus occurs more commonly with dextrocardia than with
levocardia. A 3–5% incidence of congenital heart disease is observed in situs inversus
with dextrocardia, usually with transposition of the great vessels, while situs inversus with
levocardia is almost always associated with congenital heart disease. (b) Coronal SSFP GE
cine view from a 40-year-old man with situs solitus and dextrocardia. There is associated
congenitally corrected transposition of the great arteries (ccTGA).
93
7 Adult congenital heart disease
CMR images and measurements complement those obtained using echocar-

diography, especially in postoperative patients. Accurate anatomical and functional
information of complex cardiac pathology can be obtained in any plane. These factors
make pre- and post-intervention CMR evaluation in ACHD invaluable.
CMR protocol
Standard CMR protocols in ACHD are centred on evaluation of cardiac morphology
and cardiac function with interrogation of stenoses, regurgitant jets, shunt patency
and chamber performance. MRA and myocardial tissue characterization are of
increasing importance. Scan reports comment on:
1. Cardiac chamber size;

2. Quantitative values for biventricular function and mass; and
3. Detailed characterization of abnormalities of flow.
Other reporting requirements are highlighted following discussion of specific

conditions.
Cardiac morphology and function

Breath-hold SE imaging with multislice transaxial FSE followed by multislice SSFP
in all three orthogonal planes (transaxial, coronal and sagittal) is useful for optimal
planning of subsequent planes. Adequate anatomical coverage is preserved despite
the temporal limitation imposed by breath-holding using staggered acquisition
of contiguous slices and allowing breathing in-between, or additional software
which speeds up the scan further at the expense of resolution. In the presence of
significant metallic artefact FSE acquisitions are degraded to a lesser degree than GE
sequences.
Subsequent cines are acquired in planes determined by the underlying diagnosis
and provide higher resolution anatomical and functional information on parameters
including biventricular size, function and mass. Assessment of the RV and
pulmonary vasculature is of particular importance in ACHD along with extensive
flow velocity mapping for measurement of peak velocities, regurgitant fractions
and shunt performance (Figure 7.2). The Venc is set to account for low velocities
in venous systems and higher velocities within shunts. Information from both the
cines and velocity mapping is crucial for interpretation of the patterns of blood
flow. Cine images also direct optimal positioning of velocity mapping sequences.
Contrast use
MRA with gadolinium is useful for the assessment of pulmonary branch artery, aortic
and major arterial anatomy. The LGE technique is being increasingly used to identify
ischaemic or post-surgical scarring of ventricular myocardium.
94
CMR in specific ACHD 7
LPA LA
Systole
b
LV at
MV level
RV
Systole
a
LA
Velocity mapping Systole
c
Figure 7.2 Preoperative CMR assessment of a 73-year-old woman with PS.
(a) Modified sagittal SSFP cine view showing the stenotic pulmonary valve (PV; black
arrow), an aneurysmal LPA (maximal diameter 4.2 cm) and right ventricular hypertrophy
(RVH). Turbulent blood flow above the valve is noted as signal loss within the otherwise
high intensity blood signal. A perpendicular imaging plane was then acquired just above
the valve, within the narrow part of the jet (black line). (b) Resulting SSFP cine showing the
PV with restricted opening (solid white arrow). (c) Subsequent velocity mapping CMR in
the same plane. Peak velocity was measured at 2.8 m/s within the area indicated (dashed
white arrow).
CMR in specific ACHD

Congenital heart disease is usually recognized in childhood and the most frequent
use of CMR is in the assessment of patients with an established diagnosis.
Ventricular septal defect

VSDs are the most common congenital heart defects. They range from small
haemodynamically insignificant and isolated lesions to large defects associated
with multiple cardiac anomalies such as in TOF. CMR is complementary to
echocardiography in the assessment of simple and complex VSDs. It allows multiplanar
visualization of the spatial relationship of the defect to surrounding structures, can
diagnose concurrent cardiac pathology and their functional sequelae, and quantify
shunt size and effect on the RV and PAs. SE imaging en-face and parallel to the VSD
95
provides anatomical information. SSFP cines show signal loss in the RV due to blood
flow through the VSD and are useful in assessing the shape and dimensions of the
defect (Figure 7.3). Shunt ratio can be calculated in two ways: firstly, comparison
of pulmonary to systemic flow (Qp:Qs) obtained by velocity mapping CMR, and
secondly, from the difference in ventricular SV obtained from the ventricular short-
axis stack of cines (Figure 7.4).
Specific reporting features in the CMR assessment of VSD are therefore:
1. Description of anatomy;
2. Quantification of shunt size; and
3. Evidence of other cardiac anomalies and consequences, such as complex
congenital heart disease and pulmonary hypertension.
Atrial septal defect

There are three types of ASDs, all of which can present initially in adulthood.
The commonest defect is the ostium secundum defect (75%) in the area of the
foramen ovale. Echocardiography is first line for the diagnosis of ASD. CMR
is used where echocardiography is suboptimal, identifying the defect through
visualization of low signal on the right side of the atrial septum on SSFP cines.
CMR quantifies shunt size, determines the anatomical and functional effects
of the shunt, and accurately identifies anomalous pulmonary venous drainage
(APVD; Figure 7.5).
RV
RA LV
LA
Diastole Systole
a b
Figure 7.3 Four-chamber SSFP GE cines from a 65-year-old man with a suspected
Gerbode defect (VSD communicating directly between LV and RA).
(a) Small, basal, probably muscular VSD is identified (dashed white arrow). (b) Flow
through this defect is into the RV (solid white arrow) and not the RA. Associated TR (black
arrow) is in fact responsible for the dilated RA. Of note, the apparent interatrial defect
seen on these images is a consequence of the imaging plane and not an ASD, and there
is RVH.
96
RA
LVOT
Ao Ao
LA
a Velocity mapping b
Ao MPA MPA
LA
RA
c d
Figure 7.4 Calculation of Qp:Qs for the VSD case presented in Figure 7.3 using
velocity mapping CMR.
(a, b) Oblique sagittal views of the ascending aorta in cross section by (a) magnitude and
(b) phase-subtracted components of velocity mapping CMR. This plane is obtained from the
SSFP cine LVOT view by imaging perpendicularly and just distal to the AV. (c, d) Oblique
transaxial views of the proximal MPA in cross section by (c) magnitude and (d) phase-
subtracted components of velocity mapping CMR. This plane is obtained from the SSFP GE
cine RVOT view by imaging perpendicularly and just distal to the PV. (b, d) Flow within the
aorta (white circle) and MPA (black circle) is calculated throughout the cardiac cycle and
was 5.0 and 9.2 L/min, respectively, giving a Qp:Qs of 1.8:1. Calculations of the Qp:Qs
by comparison of SV will be overestimated in the presence of severe TR.
Specific reporting features for ASD are:

1. Description of anatomy including suitability for device closure;
3. Evidence of other cardiac anomalies and consequences, such as APVD and
pulmonary hypertension.
Partial anomalous pulmonary venous drainage and major

aortopulmonary collateral arteries
CMR has a useful role in the detection and serial evaluation of extracardiac venous
and arterial vascular anomalies in ACHD, such as partial anomalous pulmonary
97
Velocity mapping
RV
RV
RA RA
LV
LV
LA
LA
a b
RIGHT CE-MRA
PAs
LA
Figure 7.5 Secundum ASD with Qp:Qs of 2.2:1 calculated by velocity mapping at the
aorta and MPA as described with the VSD in Figure 7.4.
(a) Atrial transaxial SSFP cine used to position the subsequent velocity map. (b) Velocity
mapping CMR shows flow from the LA to the RA as signal loss (black arrow). (c) MIP
reconstruction of CE-MRA data of the anatomy of the pulmonary vasculature showing no
evidence of APVD (white arrow)—there are two right-sided pulmonary veins and three left-
sided pulmonary veins.
venous drainage (PAPVD) and major aortopulmonary collateral arteries (MAPCAs).

CMR imaging protocols in PAPVD and MAPCAs incorporate MRA for optimal
detection of vessels and this often provides additional information to findings at
cardiac catheterization as well as confirming the diagnosis (Figure 7.6). Velocity
mapping quantifies shunt sizes, and SE techniques can surmount image artefact
from endovascular coils.
98
Ao
PA
RA
LV
RA
a
CE-MRA
b
Figure 7.6 Two MIP reconstructions of CE-MRA data from a 63-year-old woman showing
a CMR diagnosis of PAPVD with the left upper pulmonary vein draining via a vertical vein
into a dilated left brachiocephalic vein (white arrows).
Qp:Qs in this case was 1.4:1 and there was no evidence of RV dysfunction or pulmonary
hypertension.
CMR reports include:
1. Description of anomalous extracardiac venous or arterial drainage;

3. Evidence of other cardiac anomalies and consequences, such as ASD and
pulmonary hypertension.
Pulmonary stenosis, right ventricular outflow tract and conduit obstruction

In contrast to the assessment of ASD and VSD, the RVOT and conduits from the
RV to the PA are often poorly visualized by echocardiography. CMR provides
detailed imaging of the level and anatomy of RVOT obstruction with SE and SSFP
cine imaging in orthogonal planes. Serial, contiguous cines in the transaxial
plane are useful for functional assessment of extracardiac ventriculopulmonary
shunts, such as the Rastelli shunt. Velocity mapping quantifies severity of stenosis
or regurgitation and may be used at valve level, within the MPA, or separately
within the right and left PAs (Figure 7.7). CE-MRA is an excellent noninvasive
method of assessing branch pulmonary stenoses and identification of MAPCAs.
Patent ductus arteriosus and aortopulmonary window

PDA describes persistent arterial communication between the proximal LPA and
descending thoracic aorta distal to the origin of the left subclavian artery. It is
99
Ao MPA
Ao
Right
lung LPA Left
lung
LV
RV
b
a
Figure 7.7 SSFP cines from a 28-year-old man with an underlying diagnosis of truncus
arteriosus.
The patient had undergone the Rastelli procedure (a valved conduit from the anterior wall
of the RV to the PA with VSD closure) aged 3. The conduit had been replaced 4 years
prior to this CMR study. (a) RVOT view showing the homograft in the pulmonary position
to be functioning well without significant stenosis or regurgitation (white arrow). Metallic
artefact from sternal wiring is noted (double-headed white arrows). (b) Transaxial view of
the MPA and bifurcation into the LPA and RPA shows narrowing at the origin of the latter
with relative distal hypoplasia (solid black arrow). Signal loss within the proximal RPA
indicates turbulent blood flow and velocity mapping was therefore performed in a plane
perpendicular and just distally (dashed black line). Peak velocity was 2.4 m/s, confirming
significant proximal RPA stenosis.
usually an isolated lesion in adults. Flow through a PDA is detectable on cines,

which show turbulence in the anterior portion of the PA proximal to its bifurca-
tion (Figure 7.8). CMR can quantify shunt size and evaluate signs of pulmonary
hypertension prior to decisions regarding device closure.
Aortopulmonary window is a connection between the ascending aorta and PA
which presents in a fashion similar to that of PDA and can be differentiated by cines.
Ebstein anomaly
The diagnosis of Ebstein’s anomaly is usually made on echocardiography but CMR
has a role in defining anatomy and identifying those requiring and suitable for
surgical correction (Figure 7.9). Apical displacement of the septal and mural leaflets
of the tricuspid valve (TV) is identified on long-axis cines. Serial short-axis cines
assess enlargement of the anterior leaflet and degree of TV dysplasia, and are later
analysed to provide volumetric and functional data on the RA and RV. Velocity
mapping CMR is usually performed in order to quantify the degree of TR, but is
occasionally also used to quantify the severity of TS. Both SSFP cines and velocity
mapping are used to evaluate the presence of abnormal atrial communication.
100
Ao
PA LA
LV
Figure 7.8 Oblique sagittal SSFP cine view from a 71-year-old woman with Ehlers–
Danlos syndrome and PDA (demonstrated by marked signal loss from the aorta into the PA;
white arrow).
Tetralogy of Fallot
TOF comprises VSD, RVOT obstruction, RVH and an overriding aorta. Definitive
repair includes VSD patch closure and resection of RVOT obstruction, with
older patients often having prior palliative shunt procedures such as the
Blalock–Taussig (subclavian to PA anastomosis) shunt. Reconstruction of
the RVOT leads to important PR and serial assessments of regurgitation and
the RV are crucial following repair. Other postoperative complications, such as
aneurysm formation in the RVOT and dilatation of the aortic root, as well
as co-existing congenital anomalies, including right-sided aortic arch and
aberrant coronary anatomy, can often be identified at the initial orthogonal multi-
slice FSE sequences and are then further characterized with higher resolution
SSFP sequences.
Serial, contiguous ventricular short-axis cines enable calculation of standard
biventricular parameters and also highlight residual septal defects, confirmed using
velocity mapping CMR. Comparison of RV and LVSV or velocity mapping above
the pulmonary valve (PV) provides PV regurgitant fraction, with a value of 40%
representing free PR. Cines and velocity mapping at the RVOT, LPA and RPA evaluate
stenoses at these sites. Branch PS can arise due to distortion from palliative arterial
shunts, particularly the Pott (descending aorta to LPA) or Waterson (ascending aorta
to MPA or RPA) shunts, and may provoke worse PR. Patency of residual shunts
should be assessed due to the risk of pulmonary hypertension through augmented
pulmonary blood flow.
101
PREOPERATIVE POSTOPERATIVE
A A
RA
RA RV
RV
LA
LA LV
LV
Right
lung
Left lung
Pleural effusions
a b
Figure 7.9 Pre- and postoperative four-chamber SSFP cines from a CMR study performed
on a 16-year-old girl with severe Ebstein anomaly.
(a) There is 4 cm apical displacement of the septal leaflet of the TV (black arrow). The RA,
atrialized part of the RV, and RV are dilated. RVEF was 45% in the presence of severe
TR, regurgitant fraction 49% by comparison of LV and RVSV. (b) Satisfactory early (day
8) postoperative findings at CMR. Surgery comprised repair of the TV, plication of the RV,
cryoablation of the RA, and ASD closure with a fenestrated patch and one-way Gortex flap
to allow right-to-left shunting in the presence of elevated RA pressures. The reconstructed
TV was noted to be functioning well without TR and only mild tricuspid stenosis (TS), orifice
area 3 cm2 and peak recorded diastolic velocity of 1.2 m/s.
LGE in the RV and LV is common following TOF repair and is related to

adverse clinical markers including ventricular dysfunction. In particular, RV
enhancement predicts arrhythmia which has potential prognostic implications
(Figure 7.10).
Serial CMR assessments without contrast can be used to monitor drug treatment
and determine timing of repeat intervention to the PV.
Specific comments in TOF CMR reports include:
1. Anatomical and functional evaluation of prior interventions (surgical repair

and palliative shunts);
2. Quantification of PR (and AR if present);
3. Description of associated congenital anomalies; and
4. Presence and pattern of late enhancement.
102
LGE
Ao
Ao
RVOT RVOT
LV
LV
RV
RV
a b
Figure 7.10 (a) RVOT SSFP cine view and (b) equivalent LGE view from a 27-year-
old man with repaired TOF highlighting areas of enhancement at the free wall and septal
surface of the RV (white arrows).
Corrected transposition of the great arteries

In transposition of the great arteries (TGA) the aorta arises from the RV and the PA
arises from the LV. Almost all surviving adults with TGA have undergone operative
correction in childhood, either removal of the atrial septum and insertion of a baffle
(Mustard operation) or folding of the atrial wall (Senning operation), to redirect
atrial flow but leaving the transposed ventriculoarterial connections. The primary
aim in postoperative imaging is assessment of pulmonary and systemic venous
flow pathways (Figure 7.11). CMR readily identifies stenoses and baffle leaks with
subsequent multiplanar and multislice evaluation allowing anatomical clarification
and accurate quantification. SSFP cines are acquired to visualize each pathway in
order to identify narrowing or signal loss due to turbulence. Through-plane velocity
mapping is then used to identify flow velocities above 1 m/s, indicative of flow
obstruction at atrial level. Dilatation of the azygous and hemi-azygous veins is a
useful pointer to significant systemic venous pathway obstruction.
Cine assessment of systemic RV function is very important in these patients since
they are at risk of RV failure and TR and AR should be quantified when present.
Late enhancement of the systemic RV is also common in adults after the Mustard
or Senning procedures, and the extent correlates with ventricular dysfunction and
arrhythmia.
Patients who have undergone corrective arterial switch operations require
assessment of supravalvular PS or AS and branch PA stenoses. Such patients are also
103
Ao
SVC PA
PA
RV LV
LV
IVC
a c
LGE
RV
RV
LV LV
b d
Figure 7.11 Part of the CMR evaluation in a 30-year-old man who had undergone a
Mustard operation for TGA aged 2 months.
(a) SSFP cine views of the systemic venous pathway shows a narrowed superior vena
cava channel (SVC; dashed white arrow) and unobstructed IVC channel. Peak velocities
of the two channels were subsequently measured at 1.2 and 1 m/s respectively by velocity
mapping CMR. (b) SSFP cine view of the pulmonary venous pathways shows them to be
unobstructed (dashed black arrows). (c) SSFP cine view of the outflow tracts reveals RVH
and PR (solid black arrow). (d) LGE is noted at the RV free wall (solid white arrow).
at risk of ostial coronary artery stenoses at the site of coronary artery reimplantation,
and these can also be evaluated by CMR.
In congenitally corrected transposition of the great arteries (ccTGA), the atria have
normal position and venous return but there is atrioventricular discordance together
with TGA. CMR identifies the morphological features of each atrium and ventricle,
cardiac malposition, and associated congenital anomalies such as VSD, PS or
subvalvular PS, and Ebstein-like TV. Accurate functional assessment of the systemic
RV, which is susceptible to failure, is required prior to consideration for double
switch repairs (Senning and arterial switch).
104
Indications 7
CMR reports therefore include:
1. Anatomical and functional evaluation of pulmonary and systemic venous

flow pathways;
2. Quantification of TR (and AR if present);
3. Description of associated congenital or iatrogenic cardiac abnormalities; and
4. Presence and pattern of LGE.
Univentricular hearts and Fontan repair

In patients with one effective ventricle, the Fontan operation routes systemic venous
return directly into the PAs leaving the ventricle to pump oxygenated blood to the
systemic circulation. Pulmonary blood flow is dependent on elevated pressure within
the systemic veins and any obstruction to flow, such as with thrombus, makes the
circuit fail. Contemporary repair involves total cavopulmonary connection, usually
by an atrial tunnel or extracardiac conduit. CMR is invaluable in the assessment of
such shunts since echocardiography is often limited by the retrosternal position of
the connection. Targeted SSFP cines of the connection identify obstruction as signal
loss from turbulent blood flow. These acquisitions are also early indicators of
RA thrombus formation, which should later be confirmed or refuted using EGE
(Figure 7.12). Cine imaging is extended to the pulmonary veins to exclude post-
operative compression, with through-plane flow velocities above 1 m/s coinciding
with atrial systole being suggestive of obstruction. Serial, contiguous short-axis SSFP
cines allow determination of univentricular function and since only one SV value
is available, quantification of atrioventricular valve regurgitation requires velocity
mapping at the aorta and MPA.
Specific CMR reporting comments for the Fontan circuit are on:
1. Evaluation of the caval pathways, RA, atriopulmonary connection and PAs;

2. Active exclusion of RA thrombus;
3. Evidence of pulmonary venous compression; and
4. Quantification of atrioventricular valve regurgitation.
Indications
CMR can:
1. Diagnose, evaluate and safely follow up complex congenital cardiovascular

pathology which often spares diagnostic invasive catheterization;
2. Provide highly reproducible imaging for accurate serial assessments
including RV function;
3. Diagnose and provide additional information on PAPVD and MAPCAs;
4. Assess the PV and accurately quantify regurgitation and stenoses;
5. Evaluate the PAs and pulmonary veins; and
6. Identify extracardiac and intracardiac shunt patency.
105
SVC MPA
RA
RA LV
IVC
a b
Figure 7.12 Part of the SSFP GE cine evaluation of a 22-year-old man with a Fontan
circuit.
(a) Assessment of the caval pathways in a near sagittal plane reveals a patent SVC
and IVC. The RA is markedly dilated and contains regions of slow flow characterized
by signal loss and one area of probable thrombus (black arrow). (b) Assessment of the
atriopulmonary connection in a near coronal plane shows a patent conduit from the RA to
the MPA (white arrow). Slow flow is once again demonstrated by signal loss within the RA.
CMR cannot:
1. Be used as a screening tool due to limited availability; and

2. Be considered superior to echocardiography for evaluation of most ASDs and
simple VSDs.
106
Chapter 8
Magnetic resonance
angiography
Ilse Crevits
Introduction
Recent innovations in CMR hardware, such as stronger gradients and faster gradient
switching, and software, such as newer pulse sequences and ultrafast MRA tech-
niques, continue to ensure that it is the noninvasive imaging modality of choice in
many diseases affecting the great vessels.
Protocols for assessment of the great vessels include low- and high-resolution SE,
GE, and ultrafast MRA sequences using gadolinium contrast agent.
MRA techniques
Contrast-enhanced MRA
The basic pulse sequence for ultrafast CE-MRA is a 3D GE acquisition which is
usually designed to acquire data encoding for contrast first—centric-ordering. The
use of gadolinium contrast agent shortens the T1 value of blood so that it appears
bright irrespective of flow patterns or velocities (Figure 8.1).
Correct timing of scan acquisition is of paramount importance for optimal
imaging of the passage of contrast through the blood vessel of interest. This is usually
achieved by application of ‘bolus-track’ techniques, i.e. a real-time 2D fluoroscopic
sequence visualizing the arrival and passage of contrast in the great vessels, which
subsequently trigger the high-resolution 3D CE-MRA sequence. The time delay in
switching between these two sequences must also be taken into account. Alternative
timing methods are the use of a test bolus in order to calculate bolus arrival time, or
obtaining a series of ultrashort acquisitions so that at least one acquisition coincides
with bolus arrival time.
Time-of-flight (2D or 3D)

This is an older GE technique in which flow signal is enhanced by inflow effects.
Stationary tissue within a region of interest is saturated by rapid application of RF
pulses. This results in fresh blood flowing into this plane being non-saturated and
107
8 Magnetic resonance angiography
Ao
a
Figure 8.1 Carotid CE-MRA.
(a) MIP reconstruction of the entire CE-MRA data. The left common carotid artery (solid
white arrow) is seen to have a stenosis following its bifurcation (white square). (b) Enlarged
and rotated view of the initial MIP highlights a severe, discrete stenosis at the left internal
carotid artery (dashed white arrow).
therefore appearing bright. Unwanted venous signal can be eliminated by application

of specific saturation bands. Time-of-flight methods are sensitive to flow velocity; for
example, slow flow near the vessel wall appears less bright with this technique than
faster flow in the middle of the vessel. Importantly, the 2D time-of-flight sequence
has the disadvantage of overestimating vessel stenosis due to a phenomenon
known as phase dispersion. This effect is less pronounced using 3D time-of-flight
imaging.
Post-processing methods
Post-processing algorithms are used to create 3D images. However, they must
always be interpreted together with the source images, the ‘raw data’, to avoid
misinterpretation from post-processing induced artefacts (Figure 8.2).
108
Post-processing methods 8
Ao Ao
CE-MRA RAW DATA CE-MRA MIP

a b
Ao
CE-MRA SSD
c
Figure 8.2 CE-MRA of coarctation of the aorta (white arrows).
(a) The raw data show a severe narrowing, but this is overestimated in the subsequent
(b) MIP and (c) shaded surface display (SSD) representations. Multiple collaterals are seen
on the MIP and SSD.
109
Maximal intensity projection

In this ray tracing post-processing algorithm, the desired viewing plane is specified
first. Then the maximum intensity encountered in parallel rays along this viewing
plane is assigned to the displayed pixel. MIP reconstructions are applicable to both
time-of-flight and CE-MRA data and have the tendency to overestimate the degree of
vessel stenosis (Figure 8.2b).
Volume rendering technique and shaded surface display

This is a ray casting algorithm which selects visible voxels by tracing rays from an
instantaneous viewing position. The surfaces are identified by a threshold technique
and the resulting SSD provides 3D appreciation of the vessel. Resulting images can
also overestimate the degree of vessel stenosis (Figure 8.2c).
Curved multiplanar reconstruction

Curved multiplanar reconstruction (MPR) can be used to obtain images in views
other than that of the native acquisition (Figure 9.3). These work particularly well
on 3D data sets with isotropic voxels in which resolution is identical in any obtained
plane.
Specific Sites
Carotid arteries
The most commonly used sequences for carotid MRA are time-of-flight and CE-
MRA (Figure 8.1). For imaging of the aortic arch and cervical arteries, CE-MRA is
the only option. Both 3D TOF and CE-MRA are as accurate as conventional X-ray
angiography in the measurement of internal carotid artery stenosis, and because of
the small but significant risk of stroke with the invasive technique (0.5–1.0%), CMR
is recommended as the optimal method of evaluating carotid artery disease. Data
interpretation requires careful evaluation of the raw data to avoid overestimation
of stenosis severity. MIP projections will aggravate signal loss and cause vessels
to appear narrower because the algorithm selects brightest intensities both within
the vessel and in the background. Such overestimation with MIPs is more of a
problem in 3D time-of-flight than with CE-MRA, in which background intensities
are suppressed.
MRA is excellent for the diagnosis of carotid dissection. Dissection typically
consists of haemorrhage in the media, sometimes extending into the adventitia, and
the intimal flap is not always apparent. Angiography identifies a smooth or irregular
narrowing and high-resolution SE images with fat saturation prepulse can help to
identify the false lumen.
CE-MRA can also visualize stenoses within the vertebral artery or within the
basilar artery. Reversal of blood flow in the vertebral artery with subclavian steal
phenomenon is recognized using CE-MRA in combination with through-plane
110
Specific sites 8
velocity mapping CMR (after handgrip exercise) at the level of the vertebral arteries.
Confirmation is with 2D time-of-flight MRA acquired first with an inferior and then
a superior saturation band to confirm flow reversal.
Carotid MRA reports concentrate on:
1. Description of internal carotid artery stenoses; their location from the

bifurcation, severity and length;
2. Evaluation of concurrent vertebral disease; and
3. Assessment of the aorta arch vessel anatomy and, where relevant, atheroma
burden.
Pulmonary vessels
Pulmonary arteries
CMR is well suited for the evaluation of PA anatomy and this is widely used in
patients with ACHD where evaluation of the size, patency and anatomical relations
of the PAs is combined with RV assessment and PV status. It is also being increasingly
used in the assessment of patients with pulmonary hypertension (Figure 8.3). CT
pulmonary angiography remains the imaging modality of choice for diagnosis of
acute pulmonary embolism since MRA has longer acquisition, and thus breath-hold
times, and lower spatial resolution leading to smaller peripheral emboli potentially
going undetected.
Pulmonary veins
The use of CMR in the diagnosis and differentiation of the various forms of partial and
total APVD has already been discussed. Additionally, it has a role in the evaluation
of the pulmonary veins and LA pre-radiofrequency ablation for cardiac arrhythmias.
Subsequent assessment of pulmonary vein stenosis requires CE-MRA combined with
velocity mapping (Figure 8.4).
The pulmonary veins should also be imaged using CE-MRA in cases of cardiac
malignancy involving the LA in order to exclude extension.
MRA reports of the pulmonary vessels include:
1. Description of the anatomy;

2. Concurrent cardiac assessment, such as the RV in ACHD and pulmonary
hypertension; and
3. Measurements of pulmonary vein anatomy and orifice diameters in patients
referred for radiofrequency ablation.
Renal and mesenteric arteries

CE-MRA is a good method for assessment of the renal arteries, especially in cases of
renovascular hypertension due to atherosclerosis and, to a lesser extent, suspected
fibromuscular dysplasia.
111
Ao
MPA
CE-MRA
a
RV
Liver
RA
LV
LA
c
Figure 8.3 CMR assessment in a 59-year-old woman with pulmonary hypertension

secondary to chronic thromboembolic disease. (a) MIP reconstruction of PA CE-MRA
highlighting proximal obstruction of the right upper and middle lobe arteries (solid white
arrow). There was also evidence of multiple distal stenoses predominantly in the lower lobe
branches. (b) Concurrent serial SSFP cine cardiac assessment revealed a dilated RV with
reduced EF (34%) and moderate TR (black arrow). (c) An incidental liver cyst seen on the
pilot transaxial FSE images (dashed white arrow).
112
Specific sites 8
RIGHT CE-MRA
Ao
LA
LV
Figure 8.4 MIP reconstruction of CE-MRA data from a 47-year-old man showing
moderate stenosis (50%) of the right upper anterior pulmonary vein following
radiofrequency ablation (white arrow).
CMR screening protocols for secondary causes of hypertension conclude with angiography and are
performed during an hour-long study in the following manner:
• Cardiac assessment and later calculation of LV volumes, function and mass;

• Exclusion of coarctation of the aorta;
• Evaluation of the adrenal glands; and
• Renal CE-MRA (Figure 8.5).
CE-MRA provides reliable visualization of the major renal arteries and

accessory renal arteries along their entire length. However, spatial resolution
remains lower than with conventional X-ray angiography, so branch vessels and
small accessory vessels are less well depicted. This is of relevance, for example,
in some cases of fibromuscular dysplasia where the main renal arteries may not
be involved but smaller side branches are affected. Fibromuscular dysplasia is
a much less common cause of renal artery stenosis than atherosclerosis. It
principally affects young women who present with hypertension and biochemical
abnormalities, but rarely renal impairment. Lesions typically affect the main renal
artery, are unilateral, beaded in appearance, and may have multiple stenoses. By
comparison, atheromatous renal artery stenosis has a predilection for an older, male
population with evidence of atheroma elsewhere, treatment-resistant hypertension,
and associated renal dysfunction. Importantly, gadolinium contrast agent is not
nephrotoxic. The commonest site for atheromatous renal artery stenosis is at the
ostium of the renal artery and multiple lesions affecting different-sized vessels may
co-exist. Grading of stenosis severity is assisted by post-processing MPR reconstruction
and velocity mapping CMR.
Published data related to mesenteric CE-MRA is limited. Anecdotally, results
appear comparable to renal angiography. Most stenoses in the coeliac trunk and
superior mesenteric artery occur within the proximal segment where the diameter of
113
Ao
Right Left
kidney kidney
CE-MRA
a
RV
Ao
RA LV
LA
b c
Figure 8.5 Part of a CMR hypertension screen from a 55-year-old man.
(a) SSD reconstruction of the renal CE-MRA data showing no evidence of renal artery
stenosis. A left accessory renal artery is indicated (white arrow). (b) Prior serial SSFP
GE cine cardiac assessment was later analysed to reveal normal LV size, volume and
function, with mild LVH. (c) Oblique sagittal SSFP GE cine image showing no evidence of
coarctation of the aorta (two-headed white arrow).
High-resolution T1W SE images of the adrenal glands were normal and are not illustrated
in this figure.
114
Specific sites 8
the vessel is the greatest. The inferior mesenteric artery is often less well visualized
since it is smaller and consequently stenoses at this site are often overestimated by
CMR.
Renal MRA reports include:
1. Description of renal anatomy, such as kidney size and cortical architecture;

2. Description of renal arteries and stenoses when present;
3. Additional comments on LV mass and function, exclusion of coarctation of the
aorta, and presence of adrenal pathology in cases of hypertension screening.
Aorta
The thoracic aorta has already been discussed in Chapter 6. Optimal visualization of
the aorta is via a combination of SE and GE techniques to ensure accurate evaluation
of the aortic wall and peri-aortic tissues, and lumen, respectively. With inflammatory
conditions, such as aortitis, contrast agents are used to further highlight aortic wall
abnormalities. CE-MRA readily depicts location, extent and exact diameter of aortic
aneurysms with measurements being made on the original images (Figure 8.6). In
cases of aortic dissection where there is continuation to the abdominal aorta it is
important to know whether side branches originate from the true or false lumen.
CT is often the modality of choice for investigating acute pathology of the aorta, for
reasons of both safety and availability, while CMR is an ideal method for patient
follow-up following surgical or medical treatment.
MRA reports on the abdominal aorta include:
1. Description of anatomy and likely aetiology of aneurysmal dilatation where

present;
2. Evidence of intramural thrombus or dissection; and
3. Proximity to and involvement of key branch vessels in any pathology, such as
the renal and iliac arteries.
Peripheral arteries
CE-MRA is the best CMR technique for evaluating arterial disease in the upper and
lower limbs. Visualization of the subclavian and brachial arteries requires a dedicated
body coil, otherwise the technique is similar to that of thoracic aorta MRA. In order
to avoid venous overlap the contrast should be injected in the contralateral arm.
Imaging of the small arteries of the hand requires high-resolution scanning, dedicated
surface coils, and precise timing of the start of imaging. An additional use of CE-
MRA is in the diagnosis of thoracic outlet syndrome where images are acquired with
the arms in abduction and in neutral position (Figure 8.7). High-resolution targeted
T1W SE sequences are required to demonstrate the cause of compression in this
condition.
For imaging of the lower limbs, the most commonly used technique is the bolus
chase technique. With this, the first step is the production of mask images of all three
stations of the leg: aortoiliac region, femoral region and lower legs. Then, during
115
Ao
Right
kidney Left
kidney
CE-MRA
a
LA LA
LV
LV
LGE
b c
Figure 8.6 CMR study from a 62-year-old man referred prior to elective CABG for
further investigation of chronic renal failure.
(a) MIP reconstruction of CE-MRA data showing a diffusely atherosclerotic abdominal
aorta with a large (6.4 μ 7.0 μ 8.7 cm3) infra-renal aneurysm (solid white arrow). The
aneurysmal segment starts 4.0 cm after the origin of the renal arteries and has a proximal
neck measuring 2.5 cm in diameter. The common iliac arteries arise from the distal
aspect of the dilatation. Multilayered mural thrombus was noted within the aneurysm on
SE imaging (images not shown). The right and left renal arteries had only mild stenoses
(dashed white arrow) and the kidneys are of comparable size. (b) Part of the prior SSFP
GE cine assessment demonstrating thinning of the mid-anterior wall on the two-chamber
view (solid black arrow). (c) This segment was associated with near transmural late
enhancement indicative of MI and non-viable myocardium (dashed black arrow).
116
Indications 8
Ao
RIGHT CE-MRA
Figure 8.7 MIP reconstruction of CE-MRA data from a 30-year-old woman with thoracic
outlet syndrome.
Images were acquired with the right arm in elevation and abduction (symptomatic position)
and show a stenosis in the proximal subclavian artery (white arrow). CE-MRA with the arm
in neutral position did not reveal any abnormalities (not shown).
constant injection of contrast, the contrast bolus is followed throughout the entire
leg using a moving table. Imaging of the tibial vessels may be compromised by
venous contamination. Steno-occlusive disease in the distal aorta is readily seen as
in Leriche’s syndrome and CE-MRA is also useful in the surveillance of extra-
anatomical bypass grafts (Figure 8.8).
Indications
MRA can:
1. Diagnose internal carotid artery stenoses as well as conventional X-ray

angiography without the small but significant risk of stroke. It has an
important role in the preoperative evaluation of carotid artery disease prior
to cardiac and vascular surgery;
2. Readily provide information on the anatomical relationships, size and
patency of pulmonary arteries and veins. This gives CMR a useful role in
ACHD, pulmonary hypertension, and pre- and post-radiofrequency ablation;
3. Evaluate the renal and mesenteric arteries;
4. Screen for secondary causes of hypertension;
5. Assess congenital and acquired aortic disease;
6. Be used at a variety of peripheral arterial sites for the assessment of suspected
atherosclerotic occlusive disease; and
7. Provide safe, serial patient follow-up.
117
MRA cannot:
1. Be considered first line in haemodynamically unstable patients; and

2. Be used in preference to CT for suspected pulmonary embolism.
A B
CE-MRA
Abdominal aorta
External iliac artery
Common femoral artery
Popliteal artery
Anterior tibial artery
Dorsalis pedis artery
Figure 8.8 Lower limb CE-MRA.

(a) Diagrammatic representation of normal lower limb arterial anatomy. (b) MIP
reconstruction of CE-MRA data from a 70-year-old man presenting with intermittent
claudication on a background of a left femoropopliteal bypass graft operation. The graft is
shown to be patent (between white arrows).
118
Chapter 9
Coronary MRA
Anitha Varghese
Introduction
Coronary MRA is technically demanding since the coronary arteries are small,
tortuous vessels embedded in epicardial fat that move with cardiac and respiratory
motion.
The current clinical utility of coronary CMR is limited to visualization of proximal coronary artery anatomy,
predominantly for the diagnosis of anomalous coronary arteries for which CMR is a class I indication.
Coronary MRA techniques

Available techniques are free breathing or breath-hold. These can provide either 2D
or 3D data sets using SE or GE sequences. For clinical imaging, we recommend using
3D free breathing or breath-hold SSFP GE techniques. In both methods, scans are
ECG-gated to commence at mid to late diastole when cardiac motion is minimal.
Optimal fat suppression is mandatory. Gadolinium contrast agent is not routinely
given.
Free breathing combined with 3D imaging provides good signal-to-noise ratio
(SNR) and anatomical coverage. GE sequences image blood within the coronaries, and
SE sequences image the vessel wall. Subjects breathe normally throughout the scan
and respiratory artefact is minimized by the prior addition of respiratory navigators.
These provide a way of monitoring respiratory motion during data collection and
correcting that data for the motion. Methods of motion assessment differ, and one
commonly used is detection of the superior–inferior movement of the dome of the
right hemidiaphragm (Figure 9.1). Following placement and navigator initiation, the
user automatically accepts data when the diaphragm–lung interface falls within a pre-
defined window and rejects data that fall outside this narrow limit. The acceptance
window is positioned at the end expiratory pause period of the respiratory cycle and
extends 2–3 mm either side of a patient-specific diaphragm–lung interface value.
Free breathing sequences acquire data over several minutes and provide
higher resolution than breath-hold techniques. Breath-hold 3D GE coronary MRA
requires subjects to suspend their respiration for 20–25 s depending on their heart
rate. Since navigators are avoided, breath-holding requires less expertise and
circumvents problems arising from suboptimal respiratory patterns. The resolution
and coverage sacrificed with the breath-hold option becomes relevant at the limits
of coronary MRA indications, such as evaluation of coronary artery stenoses, and
119
9 Coronary MRA
RVOT
RA Ao
LA
Figure 9.1 3D free breathing GE coronary MRA sequence in an oblique transaxial

plane showing characteristic signal loss from the respiratory navigator on the dome of the
right hemidiaphragm (solid white arrow) and a RCA stent (dashed white arrow).
is not of significance for delineation of proximal coronary artery origin and early
course. With free breathing SSFP GE coronary MRA a typical spatial resolution
is 1.1 μ 0.7 μ 1.5 mm3 with 30 to 48 mm through-plane coverage, as compared to
1.3 μ 1.1 μ 1.6 mm3 with 16 to 19.2 mm through-plane coverage using the breath-hold
sequence. Breath-holding permits several volumes of interest to be imaged in the same
time it takes to perform one free breathing scan. Patients do vary in their response
to the two methods with consequent compromise to image quality and diagnostic
accuracy, and both may need to be attempted (Figure 9.2). Maximal and optimal
resolution with either technique is not equivalent. Maximizing resolution will assist
accuracy but will reduce SNR and lead to grainy images, while optimal resolution
may be a little lower but produce better quality scans. Post-processing curved MPR is
an excellent way of presenting findings in coronary MRA reports (Figure 9.3).
Coronary MRA protocol

Coronary MRA protocols for evaluation of proximal coronary artery origins and
course take approximately 15 to 20 min to perform:
• Initial pilot FSE acquisitions are obtained in the three orthogonal planes:
transaxial, coronal and sagittal. This usually results in localization of at least
one of the coronary artery origins from the aortic root (Figure 9.4).
• Oblique transaxial 3D imaging volumes are then acquired around this region
either with or without the addition of a respiratory navigator depending on
user preference.
• Further acquisitions are planned from these images. Successive oblique
transaxial views tend to be the most easy to interpret, and more than one
plane is required to interrogate ostial narrowing.
120
Coronary MRA protocol 9
RVOT LAD
Ao
Great
cardiac
LA vein
LCx
a b
Figure 9.2 Raw data MRA of the left coronary system from a normal 32-year-old male
subject in an oblique transaxial plane demonstrating equivalent image quality using (a)
free breathing and (b) breath-hold techniques. With kind permission from Varghese,
Keegan and Pennell, Coronary Artery Dis, P. 2005; 16: 355–364.
MPA
Ao
Figure 9.3 Curved MPR showing the rare, interarterial left main stem (LMS) anomaly
originating from the right sinus of Valsalva (SoV; white arrow). This variant is considered
the highest risk for ischaemia and sudden death.
121
9 Coronary MRA
Ao
RA LV
a b
Figure 9.4 Two examples of pilot coronal FSE imaging showing approximate coronary
artery origins from the aortic root (white arrows). Subsequent high-resolution 3D coronary
MRA data acquisition is targeted to a volume of interest centred in an oblique transaxial
plane encompassing these origins (white rectangle).
• Poor quality images should result in:

— switching techniques (free breathing/breath-hold);
— double checking that fat suppression has been optimized; and
— reiterating relevant patient instructions. For free breathing methods
patients are asked to relax and breathe normally, while breath-holding
may need to be tried at maximal inspiration rather than expiration. End
expiratory respiratory positions are more reproducible and prone to less
diaphragmatic drift, however, end inspiration may be better tolerated.
• Functional consequences of malignant anomalies are evaluated with
perfusion CMR (Chapter 2).
Anomalous coronary arteries

Anomalous coronary arteries are rare and usually asymptomatic. Prevalence
ranges from 1% in patients with otherwise normal cardiac anatomy to 36% in
individuals with ACHD such as TOF. Their importance lies in the association of
specific variants with myocardial ischaemia or MI, syncope and sudden cardiac
death, particularly amongst young adults. This premature morbidity and mortality
typically occurs during strenuous physical exercise with coronary arteries that
traverse between the aorta and PA (Figure 9.3). Three postulated mechanisms are:
mechanical embarrassment from aortic and PA dilatation at a time of increased
122
Anomalous coronary arteries 9
coronary flow demand, kinking of an ostial or proximal segment due to a sharp turn
or bend at the origin, and a congenitally slit-like ostium which is inadequate to meet
extra requirements.
Variations of anomalies include:
• Origin of the LCx from the right SoV or RCA (Figure 9.5)—this accounts
for greater than 50% of cases, usually with a benign course behind the aorta
(retroaortic);
• Origin of the RCA from the left SoV—this accounts for 20–25% of
cases, usually with a course between the PA/proximal RVOT and aorta
(interarterial); and
• Rarely, origin of the LMS or LAD from the right SoV with an interarterial
course. Alternative proximal pathways for these vessels are retroaortic,
anterior to the PA, and intraseptal.
Coronary MRA is less helpful in the direct visualization of fistulas and coronary
origination outside the sinuses of Valsalva, such as from the PAs.
Referrals for coronary MRA are often made following X-ray coronary angiography
where there is failure to engage one of the coronary ostia, or when an anomaly is
angiographically demonstrated and delineation of the proximal course is needed.
Coronary MRA is important in patients with ACHD and as part of the work-up
in young patients with unexplained syncope or chest pain. These latter groups
invariably undergo more comprehensive CMR evaluation than coronary MRA alone.
A potential preparticipation screening role in competitive athletes has also been
A
MPA
Ao
LA
RA
Figure 9.5 Raw data coronary MRA in an oblique sagittal plane from a 63-year-old
male patient with hypertension and a positive exercise tolerance test.
X-ray coronary angiography revealed a non-dominant RCA, patent LAD and aberrant LCx
arising from the right SoV. Coronary MRA was requested in order to evaluate the course of
the LCx, which is seen to be the common retroaortic variant (white arrows).
123
9 Coronary MRA
suggested, again with a CMR protocol encompassing more than isolated exclusion of
anomalous coronary arteries.
Clinical reports comment on:
1. Presence or absence of anomalous origins and ostial appearance;

2. Subsequent coronary artery course;
3. Length of total artery adequately visualized; and
4. Perfusion CMR findings if acquired.
Coronary artery aneurysms and Kawasaki disease

Coronary artery aneurysms are rare. Causes are congenital or acquired secondary
to atherosclerosis, coronary interventions and connective tissue or inflammatory
disorders such as Kawasaki disease (Figure 9.6). Kawasaki disease is a vasculitis
affecting children. Cardiovascular complications are the leading cause of mortality
and morbidity and include myocarditis and valvular regurgitation. Coronary artery
aneurysms can lead to MI, sudden death or IHD and sites for aneurysm formation in
reducing order of frequency are:
• Proximal LAD and proximal RCA;

• LMS;
• LCx;
• Distal RCA; and the
• Junction between the RCA and posterior descending coronary artery.
The commonest sites are therefore accessible for coronary MRA, which is usually
requested following TTE diagnosis in childhood. Current management guidelines
for patients with a solitary, small to medium sized aneurysm (between 3 and 6 mm)
in one or more coronary arteries are annual ECG and TTE, and stress testing with
myocardial perfusion imaging every 2 years after the age of 10. Patients with at least
one large coronary artery aneurysm (≥ 6 mm), or segmented aneurysms without
evidence of coronary artery obstruction, and those with evidence of coronary artery
obstruction at X-ray angiography, are suggested to have biannual ECG and TTE and
annual stress tests with myocardial perfusion evaluation. Additionally, peripheral
and abdominal angiography may be required prior to the first X-ray coronary
angiography procedure since aneurysms can also occur outside the coronary arterial
system. Common sites include the subclavian, femoral and iliac arteries, with less
frequent involvement at the abdominal aorta and renal arteries. CMR is therefore an
ideal modality for follow-up in this condition.
Clinical reports on cardiac findings comprise:
1. Details on coronary artery aneurysm location and dimensions, and length of
artery adequately visualized;
2. Evidence of MR or AR on cine imaging;
3. Exclusion of myocarditis and MI using a combination of cines and LGE; and
4. Perfusion CMR results.
124
Coronary artery aneurysms and Kawasaki disease 9
RVOT
PA
Ao
Ao
LV
a b
PA
Ao
LV
Figure 9.6 3D breath-hold GE coronary MRA in a 14-year-old boy showing a giant left
coronary artery aneurysm (white arrows) secondary to previous Kawasaki disease.
(a, b) Raw data in oblique transaxial and coronal planes. The aneurysm involved the LMS
5 mm from its ostium with extension into the proximal LAD and dimensions of 33 μ 16 mm2.
(c) Curved MPR from repeat CMR evaluation performed 8 months later suggested no
change in aneurysm size.
Indications
Coronary MRA can:
1. Diagnose anomalous coronary arteries; and

2. Be used for surveillance of proximal coronary artery aneurysms.
Coronary MRA cannot:
1. Achieve the resolution of X-ray coronary angiography for the identification

and grading of coronary artery stenoses; and
2. Achieve the resolution of CT coronary angiography, nor identify coronary
artery calcification.
125
Chapter 10
Common CMR
artefacts
Chad A Hoyt
Introduction
CMR can provide excellent static and dynamic images but some knowledge of artefacts
is important when unusual findings occur or suboptimal images are obtained.
Motion artefact
Patient motion artefacts are common, and are also referred to as phase mismapping
or ghosting (Figure 10.1). Two important reasons for these artefacts are respiratory
RV
LV
Figure 10.1 SE images demonstrate ghosting of the cardiac silhouette along the phase
encode axis caused by cardiac motion artefact (arrows).
127
10 Common CMR artefacts
and cardiac motion. Other causes are flow and actual patient bodily movement on
the table. Image distortion is due to anatomical movement between the application
of the phase and frequency encoding gradients, leading to within-view errors, and
anatomical motion between each application of the phase encoding gradient, causing
view-to-view errors. Motion artefacts always occur along the direction of the phase
encoding gradient, the phase encode axis, and appear as blurring across an image.
Periodic motion will be located at regular intervals along the phase encode axis with
the shape of the ghost reflecting the moving structure. The false images usually have
increased signal intensity at the expense of the causal moving structure, from which
signal is reduced. There are several ways to reduce motion artefact. General measures
include swapping the direction of the phase and frequency encoding gradients so
that the ghosting falls outside the area of interest, and vendor-specific gradient
moment rephasing methods which can automatically correct altered phases back
to their original values. More specific measures directed at respiratory and cardiac
motion are discussed below.
Respiratory motion
Respiratory motion artefacts are usually eliminated by instructing patients to
hold their breath at end expiration throughout the duration of scanner noise
(Figure 10.2). If this is unsuccessful, then the operator should firstly reiterate
the importance of total suspension of breathing during image acquisition and
repeat the scan (Figure 10.3). Following failure of repeated instruction, breath-
holding can be tried at maximal inspiration or the scan acquisition time shortened
by the addition of parallel acquisition. These methods employ computational
techniques and arrays of coils wherein each coil independently and simultaneously
images a given volume. Parallel imaging can be used to either reduce the total
RV
RV
LV
LV
a b
Figure 10.2 GE images (a) with and (b) without breath-holding during scan acquisition
show blurring induced by movement of the anterior chest wall.
128
Motion artefact 10
LA LA
LV LV
Diastole Systole
a b
Diastole Systole
c d
Figure 10.3 Two-chamber SSFP cine images from a 71-year-old patient with dyspnoea
secondary to functional AR resulting from a dilated aortic root and proximal aorta.
(a, b) Highlight significant upward diaphragmatic motion (white arrows) at the first
attempt, which leads to loss of cardiac image clarity. (c, d) Repeat imaging after repeat
instruction result in no diaphragmatic motion (double-headed white arrow) and are
consequently much improved.
acquisition time or increase the resolution of a scan. There will be some loss of
image quality in return for reduced scan duration. Respiratory navigator techniques
can also be tried as in coronary MRA. Additionally, a prepulse RF signal can be
directed across the chest wall to reduce or eliminate signal coming from it. Such
prepulses are either spatially selective or chemically selective. Chemically selective
prepulses tend to remove signal from methylene (CH2) protons in adipose tissue and
are therefore means of fat suppression.
Cardiac motion
This is generally reduced using ECG-gating, which synchronizes data acquisition
with the phases of the cardiac cycle which are identified relative to the R-R interval.
129
R-R signal is detected using externally placed ECG electrodes as part of patient
preparation for CMR. Problems from inadequate R-R signal necessitate alternative
ECG electrode selection, placement, or further patient skin preparation to increase
electrode adhesion, while problems with varying R-R interval are more troublesome.
This occurs in arrhythmias such as atrial fibrillation, frequent ventricular ectopics,
and ventricular bigeminy (Figure 10.4). Atrial fibrillation requires the use of a
variation of the ECG-gating process known as prospective gating. This is as opposed
to retrospective gating methods, which acquire data continuously during the cardiac
cycle. Retrospective gating is suitable when the R-R interval is regular since the
same part of the data is acquired at the same point. When the R-R interval becomes
erratic then the shortest interval period is chosen and data are obtained only during
that period for each subsequent cycle until the imaging sequence is complete. With
frequent ventricular ectopy, a specific arrhythmia rejection program can be instituted
to recognize and eliminate the unwanted data. Ventricular bigeminy causes the
greatest disruption to image quality and can be counteracted by attempting to
exclusively acquire data from the ‘normal’ cardiac cycles, which will prolong scan
duration, or pharmacological methods of arrhythmia suppression such as short-
acting prior beta-blocker treatment. Parallel acquisition is also useful for reducing
cardiac motion artefacts when used to reduce scan duration.
Summary
Aetiology: Respiratory or cardiac motion, patient movement

Appearance: Ghosting or blurring
Action(s):
Respiratory—Breath-holding, adding respiratory compensation algorithm
Cardiac—Changing ECG lead placement or trying different ECG triggering
hardware, prospective versus retrospective gating, arrhythmia rejection software,
pharmacological arrhythmia control
Other—Swapping phase and frequency encode axis direction, and parallel
acquisition methods for reducing scan duration
Metallic artefact
Examples of metallic artefact, or magnetic susceptibility artefact, have been shown
throughout this book. A magnetic field is altered by tissues and other materials
placed within it. The ability of a material within this field to produce additional
magnetism is referred to as susceptibility. The susceptibility of water is defined as zero,
while air and bone have negative susceptibility since they induce magnetic fields
weaker than that of water. Ferromagnetic metals such as iron, and paramagnetic
metals such as titanium or nitinol (a titanium alloy), strengthen magnetic fields in
their vicinity and are said to have positive susceptibility. Magnetic fields become most
heterogeneous near boundaries between substances with different susceptibilities,
as in metallic objects within or adjacent to the patient. This heterogeneity alters the
precessional frequency of protons and changes their phase (phase incoherence)
resulting in artefact.
130
Metallic artefact 10
MPA
RV
Diastole Systole
a b
Figure 10.4 Blurred RVOT SSFP cine frames from a 33-year-old patient with ARVC
obtained during an episode of ventricular bigeminy.
Metallic artefacts on GE sequences appear as varying degrees of signal void

and high intensity accompanied by image distortion (Figures 10.5 and 10.6). SE
sequences rephase some of the phase incoherence and therefore allow improved
imaging (Figure 6.11). Signal void will remain unless the metallic object contains
LA
Figure 10.5 Characteristic metallic artefact (arrowed) on a pilot transaxial GE image

secondary to inadvertent imaging of a 58-year-old man with a permanent pacemaker in situ.
Permanent pacemakers remain a contraindication to CMR at most centres.
131
RA
RV
LV
LA
RA
RV
LV
LA
LGE
b
Figure 10.6 (a) Cine and (b) LGE imaging showing metallic artefact from an
Amplatzer ASD closure device (arrowed).
protons, signals from which can be imaged. Whenever possible all metallic items
are removed from patients prior to scan initiation.
Summary
Aetiology: Susceptibility differences

Appearance: Signal void, high intensity signal and image distortion
Action: Remove metal if possible, use of SE sequences
Wrap-around
This is a common artefact which occurs when the selected field-of-view of imaging
is smaller than the anatomical structure being imaged, leading to details outside the
132
Wrap-around 10
area of interest being mapped onto the final image. With modern scanners wrap-
around is usually only problematic in the phase encode axis. The appearance is
that a structure from position X is mapped into position Y or one side of the image
overlaps the other (Figure 10.7). Reduction of wrap can involve increasing the field-
of-view, or reducing signal from structures outside the original field-of-view by
placement of spatially selective prepulses. Increasing the field-of-view by alterations
RV
LV
RA
LA
b
Figure 10.7 Four-chamber SSFP cine frames demonstrating the phenomenon of wrap-
around (or wrap) in a 62-year-old patient.
(a) The posterior chest wall has been mapped onto the anterior chest wall (solid white
arrow). (b) Increased data acquisition in the phase encode axis eliminates the wrap,
lengthens scan duration, and highlights some metallic artefact on the anterior chest wall
(dashed white arrow).
133
to the frequency or phase encode axis can reduce image resolution and increase
scan duration respectively. Oversampling of data in the phase encode direction also
increases scan time. A certain amount of wrap is acceptable in most clinical imaging
as long as there is no ambiguity as to the cause of the artefact, and the area of interest
is visualized in full.
Summary
Aetiology: Insufficient data sampling

Appearance: Image wrap
Action: Increase field-of-view, oversampling in phase encode axis, foldover suppression
in the phase axis
Trade-off: Reduced resolution, prolonging scan duration (this can increase motion artefact)
Shimming artefact
Shimming effects are due to magnetic field inhomogeneities. A shim coil can be
placed within the area of inhomogeneity to create evenness, a process referred to
as shimming. Individual patient characteristics will result in bright or dark signal
inhomogeneities (Figure 10.8). Most shimming is now automated but can still be
performed manually if required in a few minutes (Figure 10.9).
RV
LV
RA
LA
Figure 10.8 Shimming artefact with bright and dark areas seen within the RA and RV
(black arrows) in a patient with liver iron overload from blood transfusions for thalassaemia.
134
Shimming artefact 10
RV
LV
RA
LA
a b
Figure 10.9 Beneficial effects of (a) pre- and (b) post-manual shimming on the clarity
and pattern of blood flow within the RV (black arrow) shown on serial four-chamber SSFP
cines.
Summary
Aetiology: Magnetic field inhomogeneities

Appearance: Bright or dark signal
Action: Passive shimming performed by magnet vendor at installation, active or manual
shimming performed by operator activating specialized coils
Anatomical mimicry
Some routine findings in CMR can appear to represent pathology if not previously
encountered, and two important appearances are that of the crista terminalis in the
RA and the superior pericardial reflection. The former can be mistaken for a RA
mass while the latter can mimic aortic dissection (Figure 10.10).
Chemical shift edge artefacts

Protons within fat and water have dissimilar chemical environments and so their
precessional frequencies vary; this difference is termed a frequency shift and is
responsible for chemical shift artefacts. Application of chemically selective prepulses
to saturate the signal from fat can improve images in cases of both chemical shift
misregistration and cancellation artefact.
135
RV
RA
LV
LA
Ao
SVC
Trachea
Ao
b
Figure 10.10 (a) Four-chamber SSFP cine frame showing a prominent crista terminalis
within the RA (black arrow). (b) Transaxial FSE demonstrating the superior pericardial
reflection adjacent to the ascending aorta (white arrow).
Chemical shift misregistration

Incorrect mapping of protons with different precessional frequencies leads to signal
dis-placement of fat and water along the frequency encode axis which can appear as
high signal bands or a signal void between these materials (Figure 10.11). Resulting
artefact is proportional to the strength of the magnetic field, with greater frequency
shift and therefore artefact noted at higher field strength. Increasing resolution along
the frequency encode axis results in the physical distance corresponding to chemical
shift artefact being reduced.
136
Chemical shift edge artefacts 10
Ao
Right Left
lung lung
Figure 10.11 SE image highlighting signal void (chemical shift artefact) along the
frequency encode axis at the boundary between subcutaneous fat and water within the left
deltoid muscle (white arrow).
Chemical shift cancellation

When protons within fat and water spin out-of-phase simultaneously, signal intensity
is reduced or lost due to signal cancellation. The out-of-phase image produces
an asymmetrical edging effect in the phase encode axis and causes a dark ring to
form around structures that contain both fat and water. SE sequences use RF
rephasing pulses which correct for phase discrepancies and therefore reduce
artefact. On GE sequences the echo time parameter can be altered to try to catch
the fat and water in-phase, this can lead to a reduction in the number of slices
obtained.
External artefact
Devices
Artefacts from externally placed devices are usually obvious since they are expected
following patient positioning in the magnet. A common example is the ECG box
required for obtaining ECG-gated images (Figure 10.12).
Radiofrequency noise
Stripe artefacts along the phase encode axis away from the point of zero frequency
encoding can result from extraneous radiofrequency noise, such as radio or television
signals (Figure 10.13).
137
A A
Ao
PA
RV
LA
RA LV LV
RV
LA
Ao
Figure 10.12 Pilot transaxial and sagittal FSE acquisitions showing external artefact
from an ECG box required for obtaining ECG-gated cardiac images (black arrows).
LA
RA LV
RV
A EGE
Figure 10.13 Four-chamber EGE sequence with a single frequency artefact (arrow)
caused by the door not being completely closed and allowing extraneous RF noise into the
scanner room during image acquisition.
138
Partial volume effects 10
Partial volume effects

Partial volume effects occur due to the finite limits of image resolution. Image
resolution is determined by the size of image voxels. Within a voxel signals cannot
be resolved and an average signal intensity is produced. An increase in resolution
is required to obtain smaller voxels, at the expense of SNR. Small or thin structures
entirely contained within a voxel may disappear following averaging. This can lead
to missing stenosis within coronary arteries by coronary MRA, and poor visualization
of thin structures such as valves in certain planes (Figure 10.14).
a b
Figure 10.14 SSFP GE cine frames in the (a) two-chamber and (b) basal ventricular
short-axis views showing the effect of partial voluming on the appearance of the MV (black
arrows). Slice thickness is 7 mm for these cines and RF signal solely from the thin MV cannot
be differentiated in the latter plane.
Summary
Aetiology: Structure is entirely contained within a slice

Appearance: Image becomes a combination of structures
Action: Take thinner slices (giving smaller voxels)
Trade-off: Decreased SNR
139
Others
Cross talk
Cross talk occurs as a consequence of interference among adjacent slices. Slice
selection profiles are not perfectly rectangular and there is overlap at the edges if
they are closely spaced. RF pulses for one slice can then stimulate protons in adjacent
slices. Such cross talk often happens in multislice, multiangle acquisitions and gives
the appearance of dark bands of signal loss across an image. Insertion of adequate
spacing between slices (interslice gap) and obtaining slices in a non-contiguous
manner (slice interleaving) both reduce this artefact.
Summary
Aetiology: Slice excitation overlap

Appearance: Dark bands of signal loss
Action: Insertion of interslice gap (minimum 10%), or slice interleaving
Truncation artefacts
Truncation artefacts are also known as ringing, or Gibbs artefacts. CMR images are
normally the result of image approximation by Fourier transformation. Artefacts
arise as a fundamental consequence of the Fourier representation of an image when
signal intensity is abrupt and not gradual (gets truncated). Truncation artefacts can
be in the frequency or phase encode direction. Truncation can give the appearance of
multiple, parallel lines adjacent to high contrast interfaces looking like edge ringing
or a syrinx-like stripe (Figure 10.15). False widening of the high contrast interface
edges is commonly seen and edge enhancement of the interface with adjacent tissue
distortion can also occur. Truncation artefacts can be reduced by increasing the
spatial resolution or decreasing the interface contrast. The former can be achieved
by sampling for a greater time in the phase encode direction and obtaining a greater
number of phase encode steps, while an example of the latter is application of fat
suppression for truncation artefact adjacent to adipose tissue.
140
Others 10
air
water
a b
Figure 10.15 Phantom experiments demonstrating reduction of truncation artefact

(black arrow) by increased spatial resolution, in this case doubling the number of phase
encode steps obtained from (a) 128 to (b) 256.
Summary
Aetiology: Abrupt change in image signal intensity

Appearance: Edge ringing
Action: Increase spatial resolution, reduce interface contrast
Trade-off: Increased scan time and prolonged breath-hold
Central point artefact

This artefact appears as a focal dot of increased signal within the centre of an image.
Typically the scanner vendor will have installed software to prevent this and a call
to the service representative is required if this artefact is noted.
Summary
Aetiology: Failure of DC correction software

Appearance: Focal dot of increased signal in centre of image
Action: Call scanner service representative
141
Conclusion
CMR can:
1. Provide invaluable anatomical and functional cardiovascular
assessment in a safe, noninvasive manner free from ionizing radiation,
and using contrast agents with low nephrotoxicity;
2. Be used in patients with prosthetic heart valves, sternal wires, joint
replacements, retained epicardial pacing leads, and intracoronary stents.
CMR cannot:
Replace echocardiography.
143
Further reading
Short breaks Longer haul
Physics Physics
Schild HH. MRI made easy (...well Mitchell DG. MRI principles. USA: WB
almost). Germany: Heenemann, 1990. Saunders, 1999.
Sponsored by Schering AG. Combination
Clinical Manning WJ, Pennell DJ (eds).
Pennell DJ, Sechtem UP, Higgins Cardiovascular magnetic resonance.
CB, Manning WJ, Pohost GM, USA: Churchill Livingstone, 2002.
Rademakers FE, et al. Clinical
indications for cardiovascular
magnetic resonance (CMR):
Consensus Panel report. Eur Heart J
2004;25:1940–65.
Combination
Mohiaddin RH. Introduction to
cardiovascular magnetic resonance. UK:
Current Medical Literature, 2002.
Sponsored by Servier.
This book is highly recommended
for the clinician.
145
Index
Aberrant origin of right subclavian artery, Aortic stenosis, 49–53, 50, 51
91 level of obstruction determination, 52
Adenosine stress testing, 6 pressure gradient calculation, 52, 52
contraindications, 30 severity grading, 53
perfusion CMR, 30, 31 Aortic ulcer, penetrating, 87
Adult congenital heart disease, 15, 93–106 Aortitis, 53, 88, 115
CMR Aortopulmonary window, 100
indications, 18, 105–106 Arrhythmogenic right ventricular
protocol, 94 cardiomyopathy, 15, 35, 36, 39,
Aliasing, 5 46, 47
Amyloid, 42, 43 Artefacts, 127–142
Anatomical mimicry, 136, 136 Arterial switch operation, 103, 104
Anderson–Fabry disease, 41, 42 Atrial fibrillation, 130
Annuloaortic ectasia, 53 Atrial myxoma, 65
Anomalous coronary arteries, 121, Atrial septal defect, adults, 96–97, 98
122–124, 123 Automated implantable cardiac
Anomalous pulmonary venous drainage, defibrillators, 19
96, 97
partial, 97–98, 99, 99 Bicuspid aortic valve, 49, 51, 53, 89
Aorta, 79, 80 Black-blood imaging, 2, 3, 36
dimensions, normal range, 15, 15 Blalock-Taussig shunt, 101
imaging modalities, 79–80 Brachial arteries, 115
magnetic resonance angiography, 115 Breastfeeding, 19
Aortic aneurysm, 84, 115, 116 Breath-hold images, 6, 128, 129
fusiform, 80
inflammatory, 82 Cardiac arrhythmias, 130
intraluminal thrombus, 81, 82, 84 Cardiac masses, 63–69
Marfan syndrome, 81, 88 thrombus, 63–65, 64, 65
saccular, 80 tumours, 65–69, 66, 67, 68, 70, 71
thoracic, 80–82, 81, 82 Cardiac motion, 129–130, 131
true/false, 80–81 Cardiac tamponade, 72
Aortic arch, 110, 111 Cardiomyopathy, 35–48
anomalies, 91 cardiac morphology, 36
Aortic coarctation, 89, 89–90, 109 classification, 35, 36
aortic aneurysms, 81 CMR
collateral blood flow calculation, 90 advantages, 37
pressure gradient estimation, 90 indications, 17, 47–48
Aortic disease, 79–91 late gadolinium enhancement, 39
indications for CMR, 91–92 protocol, 36–39
Aortic dissection, 81, 83–87, 85, 86, 115 genetic aspects, 35
classification, 84 myocardial tissue characterization, 39,
Aortic intramural haematoma, 87–88, 88 39
Aortic regurgitation, 53–56, 59, 61 ventricular function evaluation, 36–37,
regurgitant fraction calculation, 53, 37, 38
55, 56 myocardial tagging, 37, 38, 39
regurgitant jet assessment, 53, 54, 56 Carotid arteries, 108, 110–111
Aortic root, dilatation, Marfan syndrome, Carotid artery stenosis, 108, 110–111
88 Carotid dissection, 110
147
Index
Central point artefact, 142 protocol, 120, 122, 122

Cerebrospinal fluid ghosting reduction, techniques, 119–120
25, 25 Cross talk, 139, 141
Cerebrovascular aneurysm clips, 19 Curved multiplanar reconstruction, 110
Checklist for patients, 20 coronary magnetic resonance
Chemical shift edge artefacts, 69, 137 angiography, 120, 121
cancellation, 137 Cystic lesions, 65, 69
misregistration, 137, 137
Claustrophobia, 6 Dextrocardia, 93
CMR, 1–19 Dilated cardiomyopathy, 15, 43, 44
basic physics, 1–2 Dobutamine stress testing, 6
contraindications, 19 myocardial viability, 32
hardware, 6 protocols, 32
imaging planes, 7–13, 7–13 Double aortic arch, 91
imaging protocols, 13–14, 14
indications, 16, 16 Early gadolinium enhancement
main sequence, 2–3 myocardial infarction, 24, 24–25
normal ranges, 14–15, 15 thrombus identification, 39, 63
patient comfort, 6 tumours, 69
safety, 19–20 Ebstein anomaly, adults, 100, 102
software, 6 Ehler-Danlos syndrome, 81
Coils, 2 Ejection fraction, normal range, 14, 15
Congenital heart disease, adults see Adult Electrocardiographic gating, 6, 129
congenital heart disease End-diastolic volume, normal range, 14,
Constrictive pericarditis, 74, 74–76 15
imaging protocol, 75 End-systolic volume, normal range,
Contraindications, 19 14, 15
Contrast External artefact, 138, 138, 139
agents, 6
safety, 19 Fast low-angle shot (FLASH) imaging, 2
Contrast-enhanced magnetic resonance Fast (turbo) spin echo sequences, 6
angiography, 6, 107, 108, 109 cardiomyopathy, 39
adult congenital heart disease, 94 constrictive pericarditis, 75
aortic aneurysms, 82, 86, 87, 115, 116 metallic prosthetic heart valves, 61
aortic coarctation, 90 Fat saturation prepulse, 6, 137
carotid arteries, 108, 110–111 coronary magnetic resonance
major aortopulmonary collateral angiography, 119
arteries, 98 Fibroma, 69, 71
partial anomalous pulmonary venous Fibromuscular dysplasia, 111, 113
drainage, 98, 99 Flow velocity mapping see Velocity
peripheral arteries, 115, 117, 118 mapping
pulmonary stenosis, 111, 113 Fontan operation, 105, 106
Coronary artery aneurysms, 124, 125 Four-chamber views, 7, 8, 9
Coronary artery disease see Ischaemic Free-breathing, 6
heart disease coronary magnetic resonance
Coronary flow reserve, 30 angiography, 119, 120, 121
Coronary magnetic resonance Frequency-encoding gradients, 2
angiography, 119–126
anomalous coronary arteries, 121, Gadolinium contrast, 6, 113
122–124, 123 acute pericarditis, 72
coronary artery aneurysms, 124, 125 magnetic resonance angiography see
indications, 126 Contrast-enhanced magnetic
post-processing, 120, 121 resonance angiography
148
Index
myocardial infarction see Myocardial myocarditis, 78

infarction pericardial disease, 17, 78
see also Early gadolinium enhancement; valvular heart disease, 17, 62
Late gadolinium enhancement Infective endocarditis, 53, 58
Gadolinium diethylenetriamine Inversion recovery sequences, 2, 6
pentaacetic acid (Gd-DTPA), 6, myocardial infarction, 23
19, 30 Iron overload cardiomyopathy, 44–46, 45
Ghosting, 127, 127 iron loading assessment, 44, 46, 46
cerebrospinal fluid, 25, 25 Ischaemic heart disease, 21–33, 119
Gibbs artefacts, 141 adenosine stress testing, 30, 31
Gradient-echo sequences, 2, 3, 5 dobutamine stress testing, 32
acute pericarditis, 71 indications for CMR, 16, 32–33
magnetic resonance angiography myocardial perfusion, 30, 31
contrast-enhanced, 107 myocardial viability, 27–29, 28, 29
coronary arteries, 119 17-segment model, 27, 29
time-of-flight, 107–108 see also Myocardial infarction
perfusion CMR, 30
pericardium, 69 Kawasaki disease, 124, 125
T2* imaging, myocardial iron
quantification, 44, 45, 46 Late gadolinium enhancement
thrombus visualization, 63 adult congenital heart disease, 94
cardiac amyloid, 42, 43
Haemochromatosis, iron loading cardiomyopathy, 39
assessment, 46 arrhythmogenic right ventricular, 46
Hand arteries, 115 dilated, 43
Hardware, 6 hypertrophic, risk stratification, 41
Headphones, 6 myocardial infarction, 23, 23, 25, 26
Heart failure see Cardiomyopathy myocardial tissue characterization, 39
Hibernating myocardium, 27, 28 myocardial viability evaluation, 27, 28
dobutamine stress testing, 32 myocarditis, 76, 78
Hypertension, secondary, CMR screening, perfusion CMR, 30, 31
113, 114 tetralogy of Fallot, 102, 103
Hypertrophic cardiomyopathy, 35, 40–42, thrombus visualization, 63
41, 42 tumours, 69
left ventricular outflow tract Left ventricular non-compaction, 36
obstruction, 42 Left ventricular outflow tract obstruction
phenocopies, 40, 40–41 aortic stenosis, 49, 52
sudden death risk stratification, 41 hypertrophic cardiomyopathy, 42
Left ventricular outflow tract views, 7, 12
Image resolution, 139 Leriche’s syndrome, 117
Imaging planes, 7–13, 7–13 Lipoma, 65
Imaging protocols, 13–14, 14 Lower limb arteries, 115, 117, 118
Indications, 16
acquired vessel disease, 19, 117–118 Magnetic field inhomogeneities, 5, 134
adult congenital heart disease, 18, Magnetic resonance angiography, 107–117
105–106 aorta, 115, 116
aortic disease, 91–92 carotid arteries, 110–111
cardiac tumours, 17, 78 contrast-enhanced see Contrast-
cardiomyopathies, 17, 47–48 enhanced magnetic resonance
classification, 16 angiography
coronary artery disease, 16, 32–33 coronary arteries, 119–126
coronary magnetic resonance indications, 117–118
angiography, 126 mesenteric arteries, 113, 115
149
Index
Magnetic resonance angiography, 107–117 Myocardial ischaemia, 21, 21

(Continued) anomalous coronary arteries, 123
peripheral arteries, 115 Myocardial mass, normal range, 14, 15
post-processing methods, 108–110 Myocardial oedema, 39, 39
pulmonary vessels, 111, 112, 113 Myocardial perfusion, 30, 31
renal arteries, 111–115 Myocardial stunning, 27, 28
time-of-flight technique, 107–108 Myocardial tagging, 37, 38, 39
Magnetic susceptibility, 130 constrictive pericarditis, 75
Major aortopulmonary collateral arteries, Myocardial viability, 27–28
97–98, 99 adenosine stress testing, 30, 31
Marfan syndrome, 81, 88–89 dobutamine stress testing, 32
Maximal encoding velocity (Venc), 4–5 myocardial perfusion, 30, 31
Maximum intensity projections (MIPs), 17-segment model, 27, 29
108, 109 Myocarditis, 39, 69, 76, 77, 78, 78
Mesenteric arteries, 113, 115
Metallic artefacts, 130–132, 131, 132 Normal ranges, 14–15, 15
Metastatic tumours, 65 Nuclear magnetic resonance, 1–2
Methaemoglobin, 82
Mitral regurgitation, 58, 58–59, 60, 61 Ostium secundum defect, adults, 96, 98
regurgitant jet assessment, 59
severity grading, 59 Pacemakers, 19
Mitral stenosis, 56–58, 57 Parallel acquisition, 128–129
transvalvular pressure gradient Partial anomalous pulmonary venous
quantification, 58 drainage, adults, 97–98, 99, 99
valve orifice planimetry, 56, 57 Partial volume effects, 139, 140
Mitral valve prolapse, Marfan syndrome, Patent ductus arteriosus, adults, 99–100,
88 101
Mixed valvular disease, 59 Patients
effective regurgitant orifice (severity comfort, 6
grading), 59, 61 safety questionnaire, 20
Motion artefacts, 6, 127, 127–130 Perfusion CMR, 30, 31
Multiplanar reconstruction, 110 Pericardial cyst, 76, 77
coronary magnetic resonance Pericardial disease, 69–76
angiography, 120, 121 indications for CMR, 17, 78
Mustard operation, 103, 104 Pericardial diverticula, 76
Myocardial fibrosis, 39, 40 Pericardial effusion, 69, 72, 73, 81
hypertrophic cardiomyopathy, 41 imaging protocol, 75
sarcoid, 47 Pericarditis, acute, 69, 72
Myocardial infarction, 21–27 Pericarditis, constrictive, 74, 74–76
damaged myocardium delineation, 23, imaging protocol, 75
23 Pericardium, 69, 72
gadolinium enhancement, 25 congenital absence, 76, 77
early, 24, 24–25 Peripheral arteries, 115
inversion time optimization, 23, 25 Phase-encoding gradients, 2
late, 23, 23, 25, 26, 27, 28, 29 Phase-swapping, myocardial infarction
myocardial viability evaluation, 27, imaging, 25, 26
28, 29 Pott shunt, 101
microvascular obstruction visualization, Pregnancy, 19
24, 24 Pressure gradient quantification
scan procedure, 25 aortic coarctation, 90
phase-swapping for artefact aortic stenosis, 52, 52
exclusion, 25, 26 mitral stenosis, 58
150
Index
Prospective gating, 130 Sarcoid, 47

Prosthetic heart valves, metallic, 61, 61 Sarcoma, 65, 68
Pulmonary arterial hypertension, 111, 112 Scanner, 2
mitral regurgitation, 59 Senning operation, 103, 104
mitral stenosis, 56 Shaded surface display, 109, 110
mixed valvular disease, 59 Shimming, 134, 134, 135
Pulmonary arteries Short-axis plane, 7, 8, 9, 10, 11
dimensions, normal range, 15, 15 Shunt assessment, 5, 94
magnetic resonance angiography, 111 atrial septal defect, 96, 97, 98
Pulmonary embolism, 111 partial anomalous pulmonary venous
Pulmonary regurgitation, 61 drainage, 98, 99
tetralogy of Fallot, 101 patent ductus arteriosus, 100
Pulmonary stenosis, 61, 95, 99, 112, 113 ventricular septal defect, 96, 97
Pulmonary veins, 111 Shunt ratio calculation, 96
Pulmonary venous hypertension, mitral Sickle cell anaemia, 46
regurgitation, 58–59 Software, 6
Spin-echo sequences, 2, 3, 5–6
Radiofrequency ablation for cardiac acute pericarditis, 72
arrhythmias, 111 adult congenital heart disease, 94
Radiofrequency noise, 138, 139 aortic aneurysms, 81
Rastelli shunt, 99, 100 aortic arch anomalies, 91
Real-time imaging, 6, 49 aortic coarctation, 90
Regurgitant fraction, 53, 55, 56 aortic dissection, 87
mitral regurgitation grading, 59 carotid dissection, 110
mixed valvular disease, 59 pericardium, 69
tetralogy of Fallot, 101 pilot scans, 14
Regurgitant jet assessment, 53, 54, 56 right ventricular outflow tract
mitral regurgitation, 59 obstruction, 99
velocity mapping, 5, 53, 54, 55 thrombus visualization, 63
Renal arteries, 111–115 ventricular septal defect, 96
Renal artery stenosis, 113 Steady-state free precession (SSFP), 2
Renovascular hypertension, 111 real-time technique, 4
Respiratory gating, 6 three-dimensional volume scan, 4
Respiratory motion, 119, 128, 128–129, two-dimensional single-shot technique,
129 4
Respiratory navigators, 129 Steady-state free precession (SSFP) cine
coronary magnetic resonance imaging, 3
angiography, 119, 120 acute pericarditis, 72
Restrictive cardiomyopathy, 35, 47, 74 adult congenital heart disease, 94
Retrospective gating, 130 aortic aneurysms, 81
Rheumatic heart disease, 49, 53, 56, 58, 59 aortic arch anomalies, 91
Right ventricular outflow tract aortic coarctation, 90
obstruction, adult congenital heart aortic dissection, 87
disease, 99 aortic regurgitation, 53
tetralogy of Fallot, 101 aortic stenosis, 50, 51, 51, 52, 52
Right ventricular outflow tract views, 7, aortopulmonary window, 100
13 atrial septal defect, 96
mitral stenosis, 56 constrictive pericarditis, 75
Right-sided aortic arch, 91 corrected transposition of great arteries,
103
Safety, 19–20 Ebstein anomaly, 100
checklist for patients, 20 ischaemic heart disease, 21
151
Index
Steady-state free precession (SSFP) cine Time-of-flight magnetic resonance

imaging, 3 (Continued) angiography, 107–108
left ventricular non-compaction, 36 Transposition of great arteries
metallic prosthetic heart valves, 61, 61 congenitally corrected, 104–105
mitral regurgitation, 59, 60 surgically corrected, 103–105, 104
mitral stenosis, 56, 57 Tricuspid regurgitation, 59
patent ductus arteriosus, 100, 101 Ebstein anomaly, 100
right ventricular outflow tract Tricuspid stenosis, Ebstein anomaly, 100
obstruction, 99 Truncation artefacts, 141, 141
tetralogy of Fallot, 101 Truncus arteriosus, 91, 100
thrombus visualization, 39, 63 Tumours, 65–69, 66, 67, 68, 70, 71, 111
univentricular heart, 105 indications for CMR, 17, 78
valvular heart disease, 49 Turbo spin echo sequences see Fast spin
ventricular septal defect, 96 echo sequences
Stroke volume, normal range, 14, 15 Two-chamber views, 7, 9
Subclavian arteries, 115
Subclavian steal phenomenon, 110 Univentricular heart, adults, 105, 106
Subvalvular aortic stenosis, 49 Upper limb arteries, 115, 117
Supravalvular aortic stenosis, 49
Valvular heart disease, 5, 15, 49–62
T1 relaxation, 1 indications for CMR, 17, 62
T1-weighted images, 1 Vascular ring, 91
acute pericarditis, 72 Vascular tumours, 69
aortic intramural haematoma, 87 Velocity aliasing, 5
myocardial infarction, 23 Velocity mapping, 2, 4, 4–5
pericardial cyst, 76 adult congenital heart disease, 94
thoracic outlet syndrome, 115 aortic aneurysms, 81
thrombus, 63, 82 aortic coarctation, 90
tumours, 65 aortic dissection, 87
T2* imaging, myocardial iron aortic regurgitation, 53, 54, 55, 56
quantification, 44, 45 aortic stenosis, 52, 52
T2 relaxation, 1 atrial septal defect, 98
T2-weighted images, 1 corrected transposition of great arteries,
aortic intramural haematoma, 87 103
myocardial oedema, 39, 39 Ebstein anomaly, 100
pericardial cyst, 76 maximal encoding velocity (Venc), 4–5
thrombus, 63, 82 metallic prosthetic heart valves, 61, 61
tumours, 65, 69 mitral regurgitation, 59
Takayasu arteritis, 88 mitral stenosis, 58
Tetralogy of Fallot, adults, 91, 101–102, partial anomalous pulmonary venous
103, 122 drainage, 98
Thalassaemia major, 44–46 pulmonary stenosis, 99, 111
iron loading assessment, 44, 46, 46 renal artery stenosis, 113
iron overload cardiomyopathy, 44–46 right ventricular outflow tract
Thoracic outlet syndrome, 115, 117 obstruction, 99
Thrombus, 63–65, 64, 65 tetralogy of Fallot, 101
aortic aneurysms association, 81, 82, thrombus, 63
84 ventricular septal defect shunt ratio
identification, early gadolinium assessment, 96, 97
enhancement, 39, 63 Venous dimensions, normal ranges, 15
univentricular heart with Fontan Ventricular bigeminy, 130
circuit, 105 Ventricular ectopics, 130
152
Index
Ventricular septal defect, adults, 95–96, 96 dobutamine stress testing, 32

shunt evaluation, 96, 97 hibernating myocardium, 27
tetralogy of Fallot, 101 myocardial viability evaluation, 27
Vertebral artery stenosis, 110 Waterson shunt, 101
Vessel disease, acquired, indications for White-blood imaging, 2, 3, 36
CMR, 19, 117–118 Williams syndrome, 49
Volume rendering technique, 110 Wrap-around artefact, 132–134, 133
Voxels, 139
Wall motion abnormalities, 21

acute pericarditis, 72
arrhythmogenic right ventricular
cardiomyopathy, 46
153

Cardiac MRI Made Easy 2008

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To R and K

—My constant companions

© 2008, Elsevier Limited. All rights reserved.

First published 2008

British Library Cataloguing in Publication Data

Library of Congress Cataloging in Publication Data

Localization of anatomical position within a selected imaging slice or volume is

Hardware and software requirements

Figure 1.7 Nine short-axis cines (slice

Protocols for cardiac imaging involve four stages:

Stage 1: Initial, rapid, pilot scans in the three orthogonal planes—transaxial,

RV parameters take longer because of the more complex anatomy. Quantiﬁcation

Table 1.3 Normal ranges for cardiovascular structures by echocardiography

LVOT (diastole) 1.4–2.6

Class I: Provides clinically relevant information and is usually appropriate, may

Table 1.4 Indications for CMR in CAD

3. Acute and chronic myocardial infarction (MI)

3. Detection and characterization of cardiac and pericardiac tumours I

9. Siderotic cardiomyopathy (in particular thalassaemia) I

11. Post-cardiac transplantation rejection Inv

2. Cardiac chamber anatomy and function I

4. Quantiﬁcation of stenosis III

5. Detection of paravalvular abscess Inv

6. Assessment of prosthetic valves Inv

Table 1.7 Indications for CMR in congenital heart disease

2. Anomalies of the viscero-atrial situs I

3. Anomalies of the atria and venous return

4. Anomalies of the atrioventricular valves

5. Anomalies of the ventricles

6. Anomalies of the semilunar valves

7. Anomalies of the arteries

Table 1.8 Indications for CMR in acquired diseases of the vessels

2. Diagnosis and planning of stent treatment for abdominal aortic

4. Diagnosis of aortic intramural haemorrhage I

5. Diagnosis of penetrating ulcers of the aorta I

6. PA anatomy and ﬂow I

8. Assessment of thoracic, abdominal and pelvic veins I

9. Assessment of leg veins II

10. Assessment of renal arteries I

11. Assessment of mesenteric arteries II

12. Assessment of iliac, femoral and lower leg arteries I

13. Assessment of thoracic great vessel origins I

14. Assessment of cervical carotid arteries I

15. Assessment of atherosclerotic plaque in carotid artery/aorta III

16. Assessment of pulmonary veins I

17. Endothelial function Inv

Contraindications and issues of safety

The environment in which CMR is performed must be constantly protected

Checklist for subjects having a Cardiovascular Magnetic Resonance Scan

Do you have any other implants or metal in your body?

Have you had any operation on your head or spine?

Have you had cardiac surgery?

Do you have a history of renal failure, or are you on dialysis?

Are you wearing a nitro patch?

Are you pregnant?

Signature: ........................................................................... Witnessed by: ............................................................................

Subendocardial perfusion defect

Transmural perfusion defect

Characteristic regional thinning of myocardium with akinesia suggests MI and is