Step by Step MRI

Step by Step
MRI
Step by Step
MRI
J Jagan Mohan Reddy

MD DMRD
Professor and Head
Department of Radiology and Imageology
Nizam’s Institute of Medical Sciences
(A University established under the State Act)
Hyderabad, Andhra Pradesh, 500082
V Prasad
BSc CRA PGDRIT
MRI Technologist
Department of Radiology and Imageology
Nizam’s Institute of Medical Sciences
(A University established under the State Act)
Hyderabad, Andhra Pradesh, 500082
JAYPEE BROTHERS
MEDICAL PUBLISHERS (P) LTD
New Delhi
Published by
Jitendar P Vij
Jaypee Brothers Medical Publishers (P) Ltd
EMCA House, 23/23B Ansari Road, Daryaganj
New Delhi 110 002, India
Phones: +91-11-23272143, +91-11-23272703,
+91-11-23282021, +91-11-23245672
Fax: +91-11-23276490, +91-11-23245683
e-mail: [email protected]
Visit our website: www.jaypeebrothers.com
Branches
• 202 Batavia Chambers, 8 Kumara Krupa Road
Kumara Park East, Bangalore 560 001
Phones: +91-80-22285971, +91-80-22382956, +91-80-30614073
Tele Fax : +91-80-22281761 e-mail: [email protected]
• 282 IIIrd Floor, Khaleel Shirazi Estate, Fountain Plaza
Pantheon Road, Chennai 600 008
Phones: +91-44-28262665, +91-44-28269897 Fax: +91-44-28262331
• 4-2-1067/1-3, 1st Floor, Balaji Building,
Ramkote Cross Road, Hyderabad 500 095
Phones: +91-40-55610020, +91-40-24758498 Fax: +91-40-24758499
• 1A Indian Mirror Street, Wellington Square
Kolkata 700 013, Phone: +91-33-22451926 Fax: +91-33-22456075
• 106 Amit Industrial Estate, 61 Dr SS Rao Road
Near MGM Hospital, Parel, Mumbai 400 012
Phones: +91-22-24124863, +91-22-24104532, +91-22-30926896
Fax: +91-22-24160828 e-mail: [email protected]
Step by Step MRI

© 2005, J Jagan Mohan Reddy, V Prasad
All rights reserved. No part of this publication and photo CD ROM should be
reproduced, stored in a retrieval system, or transmitted in any form or by any
means: electronic, mechanical, photocopying, recording, or otherwise, without the
prior written permission of the authors and the publisher.
This book has been published in good faith that the material provided by authors is
original. Every effort is made to ensure accuracy of material, but the publisher,
printer and authors will not be held responsible for any inadvertent error(s). In case
of any dispute, all legal matters to be settled under Delhi jurisdiction only.
First Edition: 2005
ISBN 81-8061-417-4
Typeset at JPBMP typesetting unit
Printed at Gopsons Papers Ltd, A-14, Sector 60, Noida 201 301, India
Dedicated to
Padmasri Prof Kakarla Subbarao
Director and Vice Chancellor, NIMS,
Hyderabad
Foreword
It is with great pride and gratification that I pen these few

words as a “Foreword” to this master piece. Dedication,
devotion, determination and a little detachment from the
family activities are essential to produce such a creative work.
As I know the authors quite intimately for almost two
decades, their impeccable loyalty and commitment to their
chosen speciality are exemplary.
Since the first application of MRI in clinical practice in
early 1980, phenominal developments have taken place. It
has emerged as the best non-radiation imaging method of
investigation. I know, quite a number of technologists, even
Radiologists and other MRI specialists cannot really follow
the basics, protocols, but operate and interpret the images.
This book really serves to present greater comprehension
and to put in the authors own words “a clear-cut understanding
of the principles underlying MRI for fruitful and effective
use”.
I am sure this book serves as a Bible to all those who are
involved in imaging sciences and I do hope that the authors
keep upgrading the latest developments in their next editions.
May the scientific world derive benefit by going through this
volume.
I do appreciate the sincerity, loyalty and generosity of the
authors for dedicating this invaluable piece to me.
Prof Kakarla Subbarao

Director
Preface
From the initial observation that dense material attenuates

X-rays, the complex field of medical imaging has developed.
With the knowledge of relative densities of various tissues,
radiologists and other physicians have used radiography to
diagnose disease in every body part and organ system. Nearly
two decades old clinical Magnetic Resonance Imaging offers
diagnostic power far beyond that of radiographic density or
any other principle of imaging. MRI utilizes several different
principles alone or in combination to address a medical
question. A clear-cut understanding of the principles
underlying MRI is essential for its fruitful and effective use.
The success of MRI in practice mainly lies in its clarity and
logicality. It is becoming increasingly difficult to keep pace
with the developments in MRI. MRI requires a multitude of
operating parameter decisions and improper choices can result
in impaired image quality leading to wrong diagnosis.
There are several books on MRI but they are all from
foreign authors. Some Indian authors also published books
on Radiology and Imageology, in which MRI is one chapter
or a part of it. Realizing the important role of MRI in the
field of Imageology without the effects of radiation, we have
made an attempt in this book exclusively on MRI to give a
comprehensive presentation of the various principles and
techniques of MRI.
While preparing this book we have taken into account
our experiences with the protocols which change from
institution to institution, consultant to consultant, company
x Step by Step MRI
to company and equipment to equipment, version to version
and technologists to technologists, while however the basic
fundamentals remain the same.
Chapter-1 is about Introduction
Chapter-2 deals with Basic Principles
Chapter-3 illustrates Components of MRI system
Chapter-4 relates to Contraindications and Patient Safety
Chapter-5 belongs to Pulse Sequences
Chapter-6 explains Tissue Characteristics
Chapter-7 handles Artifacts
The topics of Technical Factors Influencing the Image
Quality, MRI Contrast Agents, Recent Advances in Pulse
Sequences and Practical Imaging are dealt with in chapters
8, 9, 10 and 11
Suggestions, expert advice and constructive criticism are
invited to enable us to handle them in our future editions.
J Jagan Mohan Reddy

V Prasad
Acknowledgements
For an employee whose services are needed round the clock

that too in a premier institute like Nizam’s Institute of Medical
Sciences, which caters to patients from three southern states,
writing a book is an uphill task and literally impossible. But
our long cherished desire has become a reality with the kind
encouragement, co-operation and guidance of our beloved
Director, Prof K Subbarao. Our profound thanks go to our
Director who always said ‘OK’ to all our ventures.
Any book particularly scientific in nature requires the
assistance and co-operation from all the colleagues in the
Department. Our sincere and heartfelt thanks are to the
faculty, Residents and colleagues Mr Ch VVSN Murthy,
Mr D Sanjeevaiah, who extended their unstinted support in
preparing material for this book.
We express our sincere thanks to Mrs Sri Vani, Typist
and Mr G Mohd Siraj Ahmed, PG Diploma in Radiography
and Imaging Technology. We acknowledge, with thanks, the
contribution of Mr K Damodar Naidu, Radiographer who
wrote the Chapter on “Pulse sequences” and that of Mr
Ibrahim Jamal Mohammed, a Radiographer based in United
Kingdom.
We thank our family members and children who spared
us with the requisite time to prepare this book.
Last but not least, our grateful thanks are to M/s
SIEMENS, M/s Philips and M/s GE Wipro, whose MRI
machines are the basis for this booklet.
Our special and sincere thanks are to M/s Jaypee Brothers
Medical Publishers (P) Ltd., New Delhi, who have gracefully
accepted to publish this booklet.
Contents
1. Introduction 1
2. Basic Principles 4
3. Components of MRI System 18
4. Contraindications and Patient Safety 33
5. MRI—Pulse Sequences 49
6. Tissue Characteristics 68
7. Artifacts 90
8. Technical Factors Influencing
the Image Quality 105
9. MRI Contrast Agents 124
10. Recent Advances in Pulse Sequences 133
11. Practical Imaging 160
Abbreviations 273
Index 281
One
Introduction
The story of MRI is one of a long courtship between Physics

and Medicine. In 1952, Dr Bloch from Stanford University
and Dr Purcell from Harvard University were awarded the
Nobel Prize for their work on what was then known as
“Nuclear Magnetic Resonance (NMR)”. However, the turning
point came after 20 years with the advent of computers in
medical imaging. By this time, the word ‘nuclear’ is sub-
stituted and it is now known as “Magnetic Resonance Imaging
(MRI)”.
The medical world had experienced a boom in 1973 when
Lauterbur and Damadian, working independently, pronounced
the potentiality of the science of Magnetic Resonance, in
imaging the human body. Since then tremendous advances
have taken place in the design and technology of magnetic
resonance equipment, incorporating computer know-how and
sophisticated electronics to provide sectional images of the
human body with excellent delineation unparalleled in medical
arena. This new diagnostic modality gives minute structural
details of the human body utilizing the magnetic properties of
the nuclei of atoms, mainly hydrogen in human tissues.
As a tribute to this endeavors, Dr Damadian received the
National Medal of Technology from President Reagan in July
2 Step by Step MRI
Fig. 1.1: Dr Damadian receives the National Medal of Technology from

President Reagan in July15,1988; for his independent contributions in
conceiving and developing the application of magnetic resonance
technology to medical uses, including whole-body scanning and
diagnostic imaging
15, 1988. The pioneers of the newly emerged imaging modality

of the current era viz. Magnetic Resonance Imaging (MRI);
an American Scientist, Lauterbur aged 74 years and a British
scientist, Peter Mansfield aged 70 years are honoured with
Fig. 1.2: Sir Peter Mansfield Fig. 1.3: Prof C Lauterbur

Introduction 3
“Nobel Prize” on 10th December of the current year, i.e.
2003, for their outstanding contribution in the field of medicine
(Diagnostic Radiology) which paved the way for the novel
approach of the diagnosis of pathologies, disorders which
are even obscured in various parts of the body and help the
medical personnel in particular, in developing the corres-
ponding suitable remedies in order to abate the sufferings of
the mankind. Here we, on behalf of the mankind, are really
indebted to the above personalities for their enviable innovation
which proved to be quite helpful to a larger extent in mitigating
the sufferings of the people.
Two
Basic Principles
THE BASICS
Electromagnetic Radiation (Fig. 2.1)
Fig. 2.1: Spectrum of electromagnetic radiation

As seen in Fig. 2.1 the radiofrequencies of the nuclear
magnetic resonance (NMR) signals are 9 orders of magni-
tude smaller than the frequencies corresponding to the
X-rays. Transmitted X-rays have been used for years to
generate images of the human body. We will now show
how NMR signals can be used to produce a very exciting
new type of image. While X-ray images stem from
interactions between the X-rays and the electron clouds of
atoms, the NMR signals stem from the interaction of
radiowaves with the atomic nuclei themselves.
Atoms consist of a nucleus surrounded by one or more
electrons. The nucleus consists of one or more “positively
charged protons” and also contains neutral particles called
“neutrons”.
Basic Principles 5
Fig. 2.2: Protons possess a positive charge; like the earth, they are
constantly turning around on an axis and have their own magnetic field
Protons: The nucleus of the hydrogen atom has just one

proton and no neutron. It has the highest sensitivity to
magnetic resonance.
SPIN: Protons, neutrons, electrons and other particles
possess a remarkable characteristic known as ‘Spin’.
The spin of the atomic particles is depicted in Fig. 2.2.
MR Active Nuclei
Important MR active nuclei together with their atomic
number and orientation are given in Fig. 2.3, some of which
are used in MR spectroscopy.
Most abundantly available hydrogen nuclei is in the form
of water given in Fig. 2.4.
Hydrogen Atom
Hydrogen atoms are abundantly present in the body.
The hydrogen nucleus is the MR active nucleus used in
MRI. The hydrogen nucleus contains a single proton as
shown in Fig. 2.5.
6 Step by Step MRI
Fig. 2.3: Various MR active nuclei with their atomic number

with linear alignment
Fig. 2.4: The molecular structure of water (H2O)
Fig. 2.5: Hydrogen atom

Basic Principles 7
Fig. 2.6: A spinning top which
is hit, performs a wobbling
type of motion, protons in a
strong magnetic field shows
this motion, called precession
The nucleus of the hydrogen proton depicting its motion

is shown in Fig. 2.6.
Positive charge, i.e. Proton—it spins at a very high
speed.
This combination of spin and charge generates tiny
magnetic field.
The strength and direction of this field is represented
by a vector called ‘magnetic moment’.
Vectors
A vector is a symbol representing the magnitude and
direction of the magnetic field.
8 Step by Step MRI
Fig. 2.7: Alignment of vectors with varying magnitudes
A vector is commonly represented by a directed line

segment, i.e. an arrow which denotes its magnitude and its
direction (Fig. 2.7).
(The orientation of the arrow is space corresponding to
the direction of the vector quantity, the length of the arrow
corresponding to the vector magnitude. Please remember
that the arrow is merely a symbol for a real physi-
cal quantity).
Spin magnets behave like vectors. They exhibit a
magnetic field that has both magnitude and direction.
Magnetic Moments
a. A rotating particle has an electric charge. Moving
charges, as we know, are nothing more than electrical
currents. An electric current has an associated magnetic
field.
b. Where there is an electrical current, there is also a
magnetic field.
c. Classically, the magnetic effect of a rotating charge or
an electrical ring current is known as the magnetic
moment.
It is like the earth constantly rotates around an axis and
has its own magnetic field. Similarly, protons possessing a
positive charge and continuous motion have their own
magnetic field.
Basic Principles 9
PRINCIPLE
The human body is a chemical composition of several
elements, such as hydrogen, carbon, nitrogen, sodium,
phosphorus, potassium, etc. in various chemical combi-
nations. It has been observed that the atoms of some of
these elements, have odd number of protons in their nuclei,
possess magnetic properties. The magnetic properties of
the protons of these elements have been utilized to produce
magnetic resonance signals and images. The most abundant
of these present in the human body are the protons of
hydrogen atom in the form of water and various other
organic compounds such as fats, fluids, cholesterol, etc.
What is MR?
When a patient is placed in the strong magnetic field in
the MRI scanner, the hydrogen nucleus in the body, align
with the applied external magnetic field when exposed to
short burst of electromagnetic energy in the form of radio-
frequency (RF) pulses (Fig. 2.8).
Fig. 2.8: Alignment of hydrogen nucleus in the human body when

placed in strong magnetic field
10 Step by Step MRI
Fig. 2.9: Energy of the generated MR signal
The hydrogen nuclei in the patient’s body absorb its

energy and then generate MR signal. This process of
absorbing energy is known as ‘magnetic resonance’. It
forms the basics of MR imaging (Fig. 2.9).
Magnetic Resonance
If radiofrequency equals the precessional frequency, then
the phenomenon of resonance occurs.
Let us compare the resonance stimulations in MR with
oscillations created by various tuning forks (Fig. 2.10).
When the tuning fork is vibrated or perturbed, it begins to
oscillate at a specific frequency relative to sound. The pitch
corresponds to the oscillation frequency of the acoustic
wave. When you introduce a second tuning fork having
Fig. 2.10: Resonance stimulation with oscillation induced

by tuning forks of various frequencies
Basic Principles 11
the same frequency of the former, it starts oscillating in
response to the acoustic waves emitted from the former
tuning fork. At that moment, the tuning forks are said to
be in “resonance”.
Hydrogen nuclei (with single proton) in the absence of
external interference, are in random motion and their
magnetic moment cancel each other resulting in overall
‘null or zero magnetization’.
According to the Law of Quantum mechanics, in the
presence of an external magnetic field, the spinning nuclei
may align themselves in two directions viz. parallel or
antiparallel to the external magnetic field applied. Therefore,
when the patient is placed inside the magnetic field, the
hydrogen nuclei (protons) in the body get aligned in proper
orientation and this leads to the patient being magnetized
which in turn emits signals which are captured by the
receiver and after a series of processing, transformation
results in the formation of images on the screen (Fig. 2.11).
Fig. 2.11: The patient is placed in the

center of the huge, powerful magn-
etic system
12 Step by Step MRI
Fig. 2.12: Hydrogen protons in human body
These hydrogen protons in the human body are in a

random orientation pointing in different directions as
shown in Fig. 2.12A.
As shown in Fig. 2.12B under the influence of applied
external magnetic field, the patient’s tiny hydrogen proton
magnets tend to align themselves in the direction of the
external magnetic field.
Fig. 2.12C represents a bulk or net magnetization vector.
In conventional radiology or CT scan, the signal solita-
rily depends on one parameter, X-ray beam attenuation
coefficient. In MRI, image is constructed with a set of
signals. The image is generated by three factors.
Basic Principles 13
The three parameters—Proton density.
T1, T2—Relaxation times.
The tiny magnets of the human body are then subjected
to an impact of additional magnetic influences, in the form
of radiofrequency (RF) waves, magnetic gradient coils, etc.
to derive magnetic resonance signals. The MR signals
obtained have a wide range of specificities, depending on
the strength of the magnetic field, the frequency and
duration of radiofrequency waves (pulse sequence), the
magnetic gradients employed, the proton density, the
element containing the protons, the chemical combination
of elements, their molecular state, etc.
The various types of signals obtained are labeled as T1,
T2 relaxation signals. The magnetic resonance signals have
specific tissue characteristics. These are analyzed by a
computer and reconstructed mathematically by a process
known as “Fourier’s transformation” into sectional images
of the human body, accordingly, as T1 weighted image,
proton density image, T2 weighted images.
The various types of images exhibit specific tissue
characteristics, by which the tissues can be distinguished.
The behaviour of individual magnetic moments cannot
be measured.
The signal measured in MRI is produced by the sum of
all magnetic moments called “net magnetization”.
Net magnetization points in the same direction as the
scanned main magnetic field.
PRECESSION FREQUENCY
Every hydrogen nucleus which constitutes the net mag-
netization vector (NMV) spins on its own axis. The
14 Step by Step MRI
Fig. 2.13: Precession
influence of external magnetic field (Bo) produces an

additional spin or wobble of NMV around Bo. Like a
spinning top, proton shows wobbling type of motion called
“precession”. This secondary spin is known as ‘precession’
causes the magnetic moment to follow a circular path
around the magnetizing field (Bo). This path is known as
the “precessional path” and the speed with which the NMV
wobbles around Bo is known as the “precessional fre-
quency”. The unit of precessional frequency is “Mega Hertz
(MHz).
The precision frequency can be calculated by the
Larmor’s equation, and is higher in stronger magnetic
fields.
Larmor’s Equation (Table 2.1)

ω = γ * Bo
Precessional Hydrogen Magnetic field
frequency (42.6) MH2T strength
Basic Principles 15
ω (omega) = The precessional frequency in
MHz
γ (gamma) = The gyromagnetic ratio of hydro-
gen at 1T is 42.58 MHz
Bo = The magnetic field strength of
magnet (in Tesla).
Table 2.1: Gyromagnetic ratio (γγ) of various nuclei
Nucleus Gyromagnetic ratio MHz/T

1
H 42.58
C13 10.71
P31 17.12
Table 2.2: The Larmor’s frequency at various field strengths
Field strength Frequency

0.5T 22.28 MHz
1.0T 42.58 MHz
1.5T 63.9 MHz
The precessional frequency is often called the “Larmor’s

frequency” (Table 2.2). It is directly proportional to the
strength of the magnetic field.
Radiofrequency or Excitation
If radiofrequency pulse having the same frequency as that
of the precessing nuclei is applied, the precessing path of
the nuclei will be at right angles and thus it spirals away
which resembles like the wobbling of a spinning top.
Hence, radiofrequency pulse at Larmor’s frequency has
the following effects:
16 Step by Step MRI
1. The RF pulse provides sufficient energy to some of the
hydrogen nuclei to align antiparallel to main magnetic
field, they in turn cancel out the magnetic effect of
remaining parallel nuclei and thus decrease the amount
of longitudinal magnetization. The decrease in
longitudinal magnetization depends upon the strength
and duration of RF pulse.
2. With the decrease of longitudinal magnetization, there
is a corresponding gradual increase in magnetization in
transverse plane (B1). This is because the protons which
were in ‘out of phase’ are now precessing ‘in phase’.
Resonance occurs at 42 MHz when Bo = 1T
Loud Noise during MR Procedure

The continuous movement of the gradient coils during the
examination is very loud. Patients could use ear plugs
during MR examination to make it tolerable.
In the Magnetic Field

Each magnetic field exerts a force on magnetic and
magnetizable particles, including the spin magnets. The
effect of this force is depicted by magnetic field lines (a).
The strength of this force at each location in space is
known as “magnetic induction”. However, in MR Techno-
logy, the term “magnetic field strength” is commonly used.
The field strength is expressed in units of Tesla; (T:SI unit)
or Gauss (G:T = 10,000 G).
Tesla is approximately 20,000 times stronger than the
earth’s magnetic field.
A magnetic field of uniform field strength is known as a
“homogenous magnetic field” (Fig. 2.14).
Basic Principles 17
Fig. 2.14: Field lines in homogenous magnetic field
The field lines of homogenous field are drawn at

distance, straight lines running in parallel (b).
When the magnetic field does not vary with time, it is
known as “static field”.
Three
Components of
MRI System
INTRODUCTION
Open MRI units have two advantages that they can be used
for claustrophobic patients, and they provide imaging
guidance for interventional procedures.
Open units image the patient in larger-bore or c-shaped
magnets rather than the closed narrow tunnel used in
conventional units. These magnets are weaker (0.1-0.3 T)
than the closed units and their basic contrast results in some
limitation in anatomic and spatial resolution (Figs 3.1 and
3.2).
What is meant by high and low field strength MRI?
Manufactures produce magnets of varying strengths. The
most common magnetic field strengths clinically are 0.3,
0.5, 1.0, 1.5 and 3 Tesla. Magnets of 1.0 Tesla or higher
are treated high-field strength which generate higher signals
and usually more appealing images than lower-field
strength units.
Therefore, the high-field strength units generally offer
more esthetic and diagnostic images than the open units
and should preferably be used whenever possible.
It is easy to answer to the question about the ideal horse-
power for a motor bike.
Components of MRI System 19
Fig. 3.1: Open MRI unit (Courtesy of Siemens)
Fig. 3.2: A modern MRI unit (Courtesy of GE Medical Systems)

20 Step by Step MRI
Fig. 3.3: System of a superconductive MRI system
High-field strength systems have a better spatial reso-

lution and are used for spectroscopy.
The Components of the MRI System (Fig. 3.3)

1. The magnet which is a key element of the MRI system.
It is integrated into the system which also includes; (i)
the RF and (ii) Gradient system.
2. Power supplies
3. A computer system
4. A documentation system
5. Cooling system
6. Monitoring camera
Camera can be placed to monitor a patient inside the
magnet bore.
Magnet room has to be shielded with a Faraday’s cage
to prevent interferences between outside frequency waves
and those used with MR equipment.
Documentation
According to the tasks involved, computed data and recon-
structed images are stored either in:
• a fixed storage medium—Magnetic Hard Disks
• a removable storage medium—Magneto Optical Disks.
Camera
The MR Images are exposed on X-ray film with the laser
camera connected to the MRI system.
Magnet
The main component of MRI is, of course, the magnet,
available in three types—viz., the permanent magnets,
electromagnets and superconducting magnets. The homo-
geneous magnetic field required for MR Imaging is
generated by a strong magnet. This magnet is the most
important and expensive component of the MRI system.
a. Permanent magnets: Though simple and cheap to run,
they are still extremely heavy and do not generate high
fields (Fig. 3.4A).
Fig. 3.4A: Molecular structure of permanent magnet

22 Step by Step MRI
Fig. 3.4B: Resistive magnet
Fig. 3.4C: Superconductive magnet
b. Resistive systems: These are electromagnets wherein the

magnetic field is generated by an electric current flowing
through a coil (Fig. 3.4B). They have two major draw-
backs. High electric and water consumption (cooling)
and generate fields that are difficult to raise above
1.5 T.
c. Superconductive magnets (Fig. 3.4C): These are also
electromagnets, made of materials with no electric
resistance when placed at a temperature close to absolute
zero (–273oC). They consume no power and allow stable
and very high fields to be generated.
Their major drawback is running costs of cryogens
(helium and nitrogen). However, they are more and more
commonly used.
Coil
When the protons return to equilibrium, the signal is picked
up by the receiver coil. The spins are stimulated by pulsed
magnetic RF fields. These RF pulses are transmitted. The
resulting RF signal has to be received since it contains the
information necessary for image reconstruction.
The types of coils described below are the most com-
monly used (Figs 3.5A to C).
• Volume coils: Head/body coil
• Surface/local coils: (orbits, ear, wrist, shoulder, joints,
etc).
• Phased array coils (CTL, TORSO array, etc).
• Body coil is fixed inside the magnet (examination of
thorax, abdomen+pelvis, thigh, leg, body Angio).
Surface coils can be placed closed to region of interest
(circular, rectangular, extremity, wraparound) which gives
high signal to noise ratio (SNR) since being close to the
anatomy.
The correct choice of a coil gives the best signal to noise
ratio (SNR) in the region of interest.
• Volume coils both transmit and receive radiofrequency
(RF) pulses and are specially called ‘Transceivers’.
• Surface and local coils are traditionally used to improve
the signal to noise ratio (SNR) when imaging the struc-
ture near to the skin surface. They only receive only
signal.
• Phased array coils: It consists of multiple coils and
receivers. It is used for larger areas.
SHIELDING
• Magnetic shielding is required to protect the surrounding
environment from the effects of fringe fields which
surround a magnet.
To maintain magnetic field homogeneity, shielding is
necessary for the field to be protected from being distorted
by the external environment.
24 Step by Step MRI
Fig. 3.5A: Quadrature

CTL phased array coil
Fig. 3.5B: Extremity

coil
Fig. 3.5C: NV array coil

RF Shielding
The MRI signal is relatively weak. Hence, small external
RF interferences can significantly degrade the image
quality. As a result, MRI systems generally require that
the imaging room be shielded from external sources of RF
energy. For most of the systems, this involves building RF
shielding into the side walls, floor and ceiling of the MR
site. RF shielding also prevents the RF signal generated
during MR measurements from being disturbed by radio
signals outside the MR room.
1. Shimming
2. Gradient.
Shimming
Better homogeneity can be achieved by electrical and
mechanical adjustments by a process known as “shim-
ming”.
Correction of inhomogeneity of the magnetic field pro-
duced by the main magnet of MRI system is necessary due
to imperfections in the magnet or due to the presence of
external ferromagnetic objects.
The important quality for a magnet is “homogeneity”
of its main magnetic field. Inhomogeneities distort the
spatial encoding which in turn adversely affects the slice
geometry. The MR image will show distortions in the slice
plane.
In order to prevent this type of image errors, the magnet
system has to be adjusted during system installation to local
conditions or deviations in unit spread prevailing in the
unit. A process called shimming is used. We differentiate
between Active and Passive shimming.
26 Step by Step MRI
Active Shimming
Several shim coils are attached to a shim tube. Small static
currents with different amplitudes and polarity are adjusted
for the shim. The small magnetic fields which are generated
compensate for small inhomogeneities of the main field.
After the shim, the main field of a superconducting magnet
will vary by a few ppm (parts per million) only within a
measuring field having a diameter of 50 cm approximately.
Passive Shimming
Small iron plates are attached to the magnet. Their strategic
placement compensates for inhomogeneities or distortions
in the magnetic field. This may involve changing the
configuration of the magnet or the addition of shim coils
(active shimming) or small pieces of steel (passive shim-
ming).
Gradients
Special coils called gradient coils vary the strength of the
magnetic field, frequency and phase of the electromagnetic
wave in the transverse (X and Y axes) and longitudinal (Z
axis) planes.
Gating
Cardiac Triggering
In cardiac imaging, the acquisition is generally triggered
by an electrocardiogram and is tied to the RR interval. This
effectively eliminates the blurring and artifact problem
inherent in cardiac imaging, although it limits imaging
strategies (ECG, Pg (peripheral gating)).
Cardiac gating uses the programmed TR to deliver the
RF pulse and then monitors the cardiac cycle to determine
which signal it uses for reconstruction.
Cardiac gating uses the electrical signal detected by leads
placed on patient’s chest to trigger each RF excitation pulse.
Respiratory Gating
It is used to suppress breathing motion.
Acquisition takes place only during the “gate” when
the respiratory movements are minimal. It is relatively
effective at minimizing the effects of thoracic motion, but
results in substantial increase in imaging time and hence,
is not commonly employed.
Respiratory Triggering
In analogy to cardiac triggering, respiratory triggering can
also be used to generate an electric signal upon expiration
to start data acquisition.
Peripheral Gating (Pegating)

Pegating uses a photo sensor attached to either finger or
toe.
Gating and respiratory compensation are commonly
used to examine the chest and abdomen, and also used in
imaging of brain (CSF flow, spinal cord and in cine).
Breath Holding and Abdominal Compression

Both techniques are employed whenever short acquisition
sequences are employed, thereby minimizing the strain of
the patient (Figs 3.6 and 3.7).
28 Step by Step MRI
Fig. 3.6: Placement of the bellows
Fig. 3.7: Placement of the gating leads

MR COMPATIBLE CONTRAST MEDIA INJECTOR
(MED RAD)
Fig. 3.8: MR compatible contrast media injector (Med Rad)
Pulse oximeter
Fig. 3.9: MR compatible anaesthesia equipment
(Boyle’s apparatus—Excel 210)
30 Step by Step MRI
Quality Control (QC)
Quality control comprises the qualitative or quantitative
measurements or tests of performance of an instrument or
Fig. 3.10A: Phantom placed in the head coil
Fig. 3.10B: Image of DQA (daily quality assurance)

Phantom coronal view
Fig. 3.10C: Image of DQA

(daily quality assurance)
Phantom axial view Fig. 3.10D: System
performance test (SPT)
scan image for head
Fig. 3.10E: Noise scan
program and the determination of adequacy and accepta-

bility of performance. This includes the set of operation
(programming, coordinating) intend to maintain or to
improve quality (ISO definition). In other words, as applied
to diagnostic procedures, it covers monitoring, of all charac-
teristics of performance that can be defined, measured and
controlled.
Quality Assurance (QA)

The application of a service of quality control steps at
multiple stages of a procedure to verify that all aspects of
32 Step by Step MRI
the procedure are of acceptable quality. The ISO definition
is—all those planned and systematic actions necessary to
provide adequate confidence that a structure, system or
component will perform satisfactory in service.
Many of these tasks can be carried out by MR techno-
logist. More extensive quality assurance should be
performed periodically by qualified service engineer.
Quality Assurance in MRI

In order to get optimum image quality from a MRI system,
a set of tests at regular interval alongwith the preventive
maintenance measures are mandatory. The report of
acceptance testing of the system (e.g. physical inventory,
radiofrequency shielding verification, cryogenic fluid
consumption, magnetic field in homogeneity, signal to
noise ratio (SNR) or different coils, gradient coils, gradient
strength linearity, provisions of image acquisition and
image processing software, acoustic noise measurements
and functioning of hard copy camera should be taken into
account. All QA measures should be directed to get better
image quality parameters.
The daily test ensures the smooth functioning of the
system avoiding inconvenience to the patient. Daily tests
take only 20 minutes and are carried out by the technologist
every morning before the patient examination is resumed.
Four
Contraindications and
Patient Safety
MR EXAMINATION PROCEDURE
Identity
Prior to any examination being performed, the identity of
the patient must be checked by the technologist.
Patients arriving into MRI Department are often worried
or apprehensive and this may make it difficult for them to
understand the instructions or may produce an apparently
aggressive attitude. In such cases, the technologist should
convince amicably and soft tone of voice often do a great
deal of comfort and gives the patient confidence that he/
she is in an efficient hand.
The technologist should make every effort to obtain the
willing cooperation of the patient consent. Children and un-
cooperative patients should be sedated before examination.
• Before entering the equipment room, the patient must
wear a hospital gown and should remove all personal
possessions such as watch, wallet, keys, hair pins, jewels,
coils, removable dental bridge work, etc. Even credit
cards and cell phones must be secured as the scanner
will erase the information on them.
• Wheelchair and trolleys (MR noncompatible) must
always be kept outside the magnet room.
34 Step by Step MRI
The patient is made to lie down on a table. This table
then passes through a tunnel within the equipment. Inside
the tunnel, it is quite noisy when the scanning is going on.
The region of interest is positioned at the center of the
magnet. The patient can hear the voice of the radiologist or
technologist and can respond. While the patient lies within
the tunnel, images of the interested regions are taken from
different angles. These images can be seen on a computer
screen. The entire procedure takes 30 to 45 minutes
approximately depending upon the strength of the magnetic
field and the parameters set on.
It is most important that the patient should remain relaxed
and completely still during the scan. The patient can resume
the routine activities after getting the scan done.
• The patient should always be informed as to what is
going to happen and what he/she is expected to do, so
that he/she can cooperate as much as possible.
• The patient should not wear makeup because some
products may contain metallic particles.
• The patient should be covered with a lightweight blanket.
• The patient must be made comfortable as far as possible
because if the patient is in pain or in distress, it is unlikely
that he will be able to remain still for long.
• Explanation: A detailed explanation of the exam to be
performed (to be informed to the patient) to give the
patient, particularly as to how long the procedure will
take.
• The technologist from the start of examination/procedure
should make an effort to remember the name of the
patient with whom he or she is dealing and use it.
• Clear instructions regarding breathing or swallowing
should be given and rehearsed to ensure that the patient
does hold his breath or swallow when required to do so.
Contraindications and Patient Safety 35
Due to the high magnetic field strengths used during
MRI examination, certain patients are unsuitable for
imaging. These include patients who have:
• Aneurysm clips (Older Ferromagnetic types)
• Cardiac pacemakers
• Patients with otologic implants and ocular implants
• Cochlear implants
• Metallic foreign bodies, especially within the eye.
Patient Screening
The following items can interfere with MR imaging and
some can be hazardous to your safety. Please check if you
have any of the following MR incompatible objects:
• Cardiac pacemaker/pacemaker lead wires
• Brain aneurysm clips
• Aortic clips
• Implanted neurostimulators or lead wires
• Artificial heart valve
• Insulin pump
• Electrodes
• Hearing aids
• IUD (Intrauterine Device)
• Shunts
• Joint replacements
• Fractured bones treated with metal rods, metal plates,
pins, screws, nails or clips
• Harrington rod
• Bone or joint pins
• Prosthesis
• Metamesh
• Wire sutures
36 Step by Step MRI
Fig. 4.1: To mark the location of any metal inside the body
• Sharpnel
• Dentures
• Metal silvers in the eyes
• Cochlear implants
• Tattoo eyeliner
• Others
On the drawing in Fig. 4.1, please mark the location of
any metal “inside” the body.
Screening Prior to Scanning

• Glasses
• Removable dental work
• Hearing aid
• Jewellery
• Watch
• Wallet or money clip
• Pens or pencils
• Keys
• Coins
• Pocket knife
• Metal zippers or buttons
• Belt buckle
• Shoes
• Magnetic strip cards
• Credit cards, bank cards
• Hair pins or barrettes
• Metal bra hooks
• Bra and girdle underwear support
• Sanitary belt
• Safety pins
Patient Positioning
Positioning of the patient can affect the safety of the scan
procedure.
Improper positioning can result in sunburn—like burns.
Precautions to be Undertaken
In order to maintain a safer scan environment, the following
precautions are to be taken:
• MRI systems are equipped with laser alignment lights.
• Exposing eyes to the laser alignment lights may result
in eye injury.
• Do not stare directly into the laser beam.
• Instruct the patients to close their eyes during land
marking in order to avoid eye exposure to the alignment
light while the laser light is “ON”.
38 Step by Step MRI
• Do not leave the laser beam ON after you position the
patient.
• Place foams between the patient and the bore wherever
a portion of the body comes in contact with the bore.
• Ensure that the patient does not touch the magnet bore.
• Orient the patient (head first or feet first) to minimize
the length of the cable in the bore.
• For larger patients, use wide patient straps to secure the
arms, preventing them from touching the bore.
EFFECTS OF RF POWER
The RF pulses used in MR causes tissues to absorb RF
power under certain conditions. This may cause tissue
heating. The amount of heating depends on several factors
such as patient size and pulse-sequence timing.
Before the patient is being scanned, the computer
estimates the level of heating and compares it to the
predetermined exposure limits. If the scan exceeds these
limits, the system then adjusts the scan parameters before
starting the scan. The complete estimate is based partially
on patient weight. Therefore, take care to enter the patient’s
weight correctly to prevent excessive RF.
HAZARDS
Claustrophobia despite the fact that the patient lies in a
confined space is rarely a serious problem.
MRI has not been proved to have any adverse effects
on fetuses. However, some teams avoid using during the
first trimester of pregnancy.
Till date, no harmful effects have been observed from
magnetic influences.
QUENCHING
A magnet quench will result in several days of down time.
So, do not press or push the button except in a real emer-
gency. Do not test that button. It should be tested only by
qualified service personnel. Quench button is located near
the magnet.
Magnet Quench Hazards

Magnetic quench is indicated by a loud noise, warning
message, dense white vapor (with vent failure), helium
meter dropping considerably or the tilting of an image on
the image screen.
• If the patient needs medical attention, press an emergency
stop button on the console or magnet and remove the
patient from the scan room.
• Evacuate the patient and personnel from the scan room
and close the scan room door.
40 Step by Step MRI
APPENDIX
Metallic Implants and Other Objects Tested
for Deflection Forces: A Compilation of the
Literature
Highest Field
Metallic Implant or Object Deflection Strength Reference
Aneurysm and Hemostatic Clips
Drake (DR14, DR24) Yes 1.44 T 9
(Edward Weck and Co., Triangle
Park, NJ)
Drake (DR16) Yes 0.147 T 9
Park, NJ)
Drake (301 SS) Yes 1.5 T 11
Park, NJ)
Downs multipositional (17-7 PH) Yes 1.44 T 9
Gastrointestinal anastomosis clip
Autosuture SGLA, (SS) No 1.5 T 11
(United States Surgical Corp.,
Norwalk, CT)
Heifetz (17-7 PH) Yes 1.89 T 4
Park, NJ)
Heifetz (Elgiloy) No 1.89 T 4
Park, NJ)
Hemoclip #10, (316L SS) No 1.5 T 11
Park, NJ)
Hemoclip (Tantalum) No 1.5 T 11
Park, NJ)
Housepian Yes 0.147 T 9
Kapp (405 SS) Yes 1.89 T 4
(V. Mueller)
Contd...
Contd...
Highest Field
Kapp curved (404 SS) Yes 1.44 T 9
(V. Mueller)
Kapp straight (404 SS) Yes 1.44 T 9
(V. Mueller)
Ligaclip #6, (316L SS) No 1.5 T 11
(Ethicon Inc., Sommerville, NJ)
Ligaclip (Tantalum) No 1.5 T 11
(Ethicon Inc., Sommerville, NJ)
Mayfield (301 SS) Yes 1.5 T 11
(Codman, Randolph, MA)
Mayfield (304 SS) Yes 1.89 T 4
McFadden (301 SS) Yes 1.5 T 11
Olivercrona No 1.44 T 9
Pivot (17-7 PH) Yes 1.89 T 4
(V. Mueller)
Scoville (EN58J) Yes 1.89 T 4
(Downs Surgical Inc., Decatur, GA)
Stevens (50-4190, Silver alloy) No 0.15 T 2
Sugita (Elgiloy) No 1.89 T 4
Sundt-Kees (301 SS) Yes 1.5 T 11
Sundt-Kees Multi-Angle (17-7 PH) Yes 1.89 T 4
Surgiclip, Autosuture M-9.5 (SS) No 1.5 T 11
(United States Surgical Corp.,
Norwalk, CT)
Vari-Angle (17-7 PH) Yes 1.89 T 4
Vari-Angle McFadden (MP35N) No 1.89 T 4
Vari-Angle Micro (17-7PM SS) Yes 0.15 T 2
Contd...
42 Step by Step MRI
Contd...
Highest Field
Vari-Angle Spring (17-7PM SS) Yes 0.15 T 2
Yasargil (316 SS) No 1.89 T 4
(Aesculap)
Yasargil (Phynox) No 1.89 T 4
(Aesculap)
Dental Materials
Brace Band (SS) No 1.5 T 11
(American Dental, Missoula, Montana)
Brace Wire (Chrome alloy) Yes* 1.5 T 11
(Ormco Corp., San Marcos, CA)
Dental amalgam No 1.44 T 9
Silver points No 1.5 T 11
(Union Broach Co., Inc.,
New York, NY)
Permanent crown (Amalgam) No 1.5 T 11
(Ormco Corp., San Marcos, CA)
Intravascular Coils, Filters and Stents
Amplatz IVC filter No 4.7 T 13
(Cook, Bloomington, IN)
Cragg nitinol spiral filter No 4.7 T 13
Gianturco embolization coil Yes 1.5 T 13
Gianturco bird nest IVC filter Yes 1.5 T 13
Gianturco zig-zag stent Yes 1.5 T 13
Greenfield vena cava filter,
Stainless steel Yes* 1.5 T 13
(Meditech, Watertown, MA)
Greenfield vena cava filter,
Titanium alloy No 1.5 T 13
(Ormco, Glendora, CA)
Gunther IVC filter Yes 1.5 T 13
(William Cook, Europe)
Contd...
Contd...
Highest Field
Mass helical IVC filter No 4.7 T 13
(Medinvent, Lausanne, Switzerland)
Mass helical endovascular stent No 4.7 T 13
(Medinvent, Lausanne, Switzerland)
Mobin-Uddin IVC/umbrella filter No 4.7 T 13
(American Edwards, Santa Ana, CA)
New retrievable IVC filter Yes 1.5 T 13
(Thomas Jefferson University,
Philadelphia, PA)
Palmaz endovascular stent Yes 1.5 T 13
(Ethicon, Somerville, NJ)
Prosthetic Ear Implants
Cody tack No 0.6 T 8
Cochlear implant (3M/House) Yes 0.6 T 8
Cochlear implant (3M/Vienna) Yes 0.6 T 8
House-type incus prosthesis No 0.6 T 8
McGee stainless steel piston No 0.6 T 8
Reuter drain tube No 0.6 T 6
Richards House-type wire loop No 1.5 T 1
(Richard’s Company, Nashville, TN)
Richards-McGee Piston No 1.5 T 1
Richards Plasti-pore with
Armstrong-style platinum ribbon No 1.5 T 1
Richards-Schuknecht Teflon-wire No 1.5 T 1
Richard Trapeze platinum ribbon No 1.5 T 1
Shuknecht Gelfoam and wire
prosthesis, Armstrong-style No 1.5 T 6
Shea stainless steel and teflon
wire prosthesis No 1.5 T 6
Xomed stapes prosthesis
Robinson-style No 1.5 T 1
Contd...
44 Step by Step MRI
Contd...
Highest Field
Prosthetic Heart Valves
Beall Yes* 2.35 T 12
(Coratomic Inc., Indiana, PA)
Bjork-Shiley (convexo/concave) No 1.5 T 11
(Shiley Inc., Irvine CA)
Bjork-Shiley (universal/spherical) Yes* 1.5 T 11
Bjork-Shiley, Model MBC Yes* 2.35 T 5
Bjork-Shiley, Model 25 MBRC 11030 Yes* 2.35 T 5
Carpentier-Edwards, Model 2650 Yes* 2.35 T 5
(American Edwards Laboratories,
Santa Ana, CA)
Carpentier-Edwards (porcine) Yes* 2.35 T 12
Santa Ana, CA)
Hall-Kaster, Model A7700 Yes* 1.5 T 11
(Medtronic, Minneapolis, MN)
Hancock I (porcine) Yes* 1.5 T 11
(Johnson and Johnson, Anaheim, CA)
Hancock II (porcine) Yes* 1.5 T 11
Hancock extracorporeal, Model 242R Yes* 2.35 T 5
Hancock extracorporeal,
Model M 4365-33 Yes* 2.35 T 5
Hancock Vascor, Model 505 No 2.35 T 5
Ionescu-Shiley, (Universal ISM) Yes* 2.35 T 5
Lillehi-Kaster, Model 300S Yes* 2.35 T 12
(Medical Inc., Inver Grove Heights, MN)
Lillehi-Kaster, Model 5009 Yes* 2.35 T 5
Contd...
Contd...
Highest Field
Medtronic Hall Yes* 2.35 T 12
(Medtronic Inc., Minneapolis, MN)
Medtronic Hall, Model A7700-D-16 Yes* 2.35 T 5
(Medtronic Inc., Minneapolis, MN)
Omnicarbon, Model 3523T029 Yes* 2.35 T 5
Omniscience, Model 6522 Yes* 2.35 T 5
Smeloff-cutter Yes* 2.35 T 5
(Cutter Laboratories, Berkeley, CA)
Starr-Edwards, Model 1260 Yes* 2.35 T 12
Santa Ana, CA)
Santa Ana, CA)
Starr-Edwards, Model 2400 No 1.5 T 11
Santa Ana, CA)
Starr-Edwards, Model Pre 6000 Yes 1.5 T 12
Santa Ana, CA)
Santa Ana, CA)
St. Jude No 1.5 T 11
(St. Jude Medical Inc., St. Paul, MN)
St. Jude, Model A 101 Yes* 2.35 T 5
St. Jude, Model M 101 Yes* 2.35 T 5
Orthopedic Materials and Devices
AML femoral component bipolar hip
prosthesis No 1.5 T 11
(Zimmer, Warsaw, IN)
Contd...
46 Step by Step MRI
Contd...
Highest Field
Harris hip prosthesis No 1.5 T 11
Jewett nail No 1.5 T 11
Kirschner intermedullary rod No 1.5 T 11
(Kirschner Medical, Timonium, MD)
Stainless steel plate No 1.5 T 11
Stainless steel screw No 1.5 T 11
Stainless steel mesh No 1.5 T 11
Stainless steel wire No 1.5 T 11
Penile Implants
Penile implant, AMS Malleable 600 No 1.5 T 10
(American Medical Systems,
Minnetonka, MN)
Penile implant, AMS 700 CX Inflatable No 1.5 T 10
Minnetonka, MN)
Penile implant, flexi-flate No 1.5 T 10
(Surgitek Medical Engineering Corp.
Racine, WI)
Penile implant, flexi-rod (Standard) No 1.5 T 10
(Surgitek Medical Engineering Corp.
Racine, WI)
Penile implant, flexi-rod II (Firm) No 1.5 T 10
(Surgitek, Medical Engineering Corp.
Racine, WI)
Penile implant, Jonas No 1.5 T 10
(Dacomed Corp. Minneapolis, MN)
Penile implant, mentor flexible No 1.5 T 10
(Mentor Corp. Minneapolis, MN)
Contd...
Contd...
Highest Field
Penile implant, mentor inflatable No 1.5 T 10
(Mentor Corp. Minneapolis, MN)
Penile implant, Omniphase Yes 1.5 T 10
(Dacomed Corp. Minneapolis, MN)
Miscellaneous Metallic Implants
and Objects
Artificial urinary sphincter, AMS 800 No 1.5 T 11
Minnetonka, MN)
BB’s Yes 1.5 T 15
(Daisy)
BB’s Yes 1.5 T 15
(Crosman)
Cerebral ventricular shunt tube
connector,
Accu-flow, straight No 1.5 T 11
Cerebral ventricular shunt tube connector
Accu-flow, right angle No 1.5 T 11
Accu-flow, T-connector No 1.5 T 11
(type unknown) Yes 0.147 T 10
Contraceptive diaphragm, all flex Yes* 1.5 T 11
(Ortho Pharmaceutical, Raritan, NJ)
Contraceptive diaphragm, flat spring Yes* 1.5 T 11
(Ortho Pharmaceutical, Raritan, NJ)
Contraceptive diaphragm, koroflex Yes* 1.5T 11
(Young Drug Products, Piscataway, NJ)
Forceps (Titanium) No 1.44 T 10
Hakim valve and pump No 1.44 T 10
Contd...
48 Step by Step MRI
Contd...
Highest Field
Intraocular lens implant (Binkhorst,
iridocapsular lense, platinum-iridium
loop No 1.0 T 3
Intraocular lens implant (Binkhorst,
iridocapsular lens, titanium loop No 1.0 T 3
Intraocular lens implant (Worst,
platinum clip lens) No 1.0 T 3
Intrauterine Contraceptive Device,
(IUD), Copper T No 1.5 T 7
(Searle Pharmaceuticals, Chicago, IL)
Tantalum powder No 1.44 T 9
(The “highest field strength” refers to the strongest static magnetic field
that was used for the evaluation of the various metallic implant and objects.
If no deflection was observed at low to midfield strengths, it is still possible
for deflection to occur at higher static magnetic field strengths. Furthermore,
if deflection was observed at low to midfield strengths, it will be greater at
higher static megnetic fields).
*Denotes metallic implants or objects that were considered to be safe for MR imaging despite
being deflected by the static magnetic field. For example, certain prosthetic heart valves were
deflected by the static magnetic field but the actual force was considered to be less than the
force exerted on the valves in an in vivo situation by the beating heart.1, 2 Refer to indicated
reference for additional informationl. Manufacturer information provided if indicated in article
or otherwise known. Note that, besides producing movement, the elctromagnetic fields used
for MRI may produce other adverse effects in metallic bioimplants by inducing electrical
current and/or heating. Although heating has not been evaluated for most of the bioimplants
listed, data in the literature indicates that the heating of small implants and most larger ones is
negligible during MRI.3, 4 There has been no report of electrical currents induced in metallic
bioimplants. SS—stainless steel.
Courtesy from Shellock F
1. Shellock FG, Crues JV. High field strength MR imaging and metallic biomedical implants:
An ex vivo evaluation of deflection forces. AJR 1988;151:811-814.
2. Soulen RL, Budinger TF, Higgins CB. Magnetic resonance imaging of prosthetic heart
valves. Radiology 1985;154:705-707.
3. Davis PL, Crooks L, Arakawa M, McRee R, Kaufman L, Margulis AR. Potential hazards
in NMR imaging: Heating effects of changing magnetic fields and RF fields on small
metallic implants. AJR 1981;137:857-860.
4. Shellock FG, Crues JV. High field MR imaging of metallic biomedical implants: An in
vitro evaluation of deflection forces and temperature induced in large prostheses (abstr).
Radiology 1987;165:150.
Five
MRI—Pulse Sequences
INTRODUCTION
There are many different pulse sequences available, and
each is designed for a specific purpose. The image weigh-
ting, contrast and quality is determined by the type of pulse
sequence we use.
PULSE SEQUENCES
Types
1. Spin echo (SE) pulse sequences
a. Conventional spin echo (CSE) pulse sequence
b. Fast spin echo (FSE) pulse sequence
2. Inversion recovery (IR) pulse sequences
a. STIR (short inversion recovery)
b. FLAIR (fluid attenuated inversion recovery)
3. Gradient echo (GE) pulse sequences
a. Coherent gradient echo pulse sequence
b. Incoherent gradient echo pulse sequence
4. Steady state free precession (SSFP)
5. Ultrafast imaging
6. Echoplanar imaging
50 Step by Step MRI
Fig. 5.1: Schematic illustration of a spin echo pulse sequence
Spin Echo (SE) Pulse Sequences (Fig. 5.1)

Conventional Spin Echo (CSE) Pulse Sequence
In this pulse sequence, a 90° excitation RF pulse is given
followed by 180° rephasing RF pulse.
Uses
• These are the most commonly used pulse sequences
• May be used for almost every examination
• Produce optimum signal-to-noise ratio (SNR) and
contrast-to-noise ratio (CNR)
• T1, T2 and proton density weighting is possible (Figs 5.2
and 5.3).
Advantages
• Good image quality
• True T2 weighting is possible.
Disadvantages
• Scan times are relatively long
• More RF power deposition in the body.
MRI—Pulse Sequences 51
Parameters
• For T1 weighting • For T2 weighting
TE = 10-20 ms TE = 80 ms
TR = 300-600 ms TR = 2000 ms
Approx. scan time Approx. scan time
= 4-6 minutes = 7-15 minutes
• Proton density
TE = 20 ms
TR = 2000 ms
Approx. scan time = 7-15 minutes
Fast Spin Echo (FSE) Pulse Sequence

In this type of pulse sequence, 90° excitation RF pulse will
be delivered followed by several 180o rephasing RF pulses.
In conventional spin echo (CSE), only one line of K-space
is filled per TR. So the CSE takes longer scan time. But in
fast spin echo several lines of K-space will be filled per
TR. Because of this reason, the scan times are reduced in
fast spin echo. The number of lines of K-space filled per
TR is referred to as Turbo Factor (tf) (or) echo train length
(ETL). More the ETL, less the scan time (Fig. 5.4).
Uses
• Can be used as an alternative to spin echo
• Reduction in the scan time compared to conventional
spin echo.
Advantages
• Scan times are greatly reduced
• High resolution matrices and multiple NEX can be used
• Improved image quality.
Disadvantages
52 Step by Step MRI
Fig. 5.2: Spin echo T1W1

CSF appears dark
Fig. 5.3: Spin echo T2W1 CSF

appears bright
• Fat remains bright on T2 weighted images

• Image blurring may result
Parameters
Fig. 5.4: Schematic illustration of fast spin echo
• T1 weighting • T2 weighting
TE = 10-20 ms TE = 100 ms
TR = 300-600 ms TR = 5000 ms
ETL = 2-6 ETL = 8-20
Approx. scan time = 30 sec Approx. scan time
to 60 sec/acq = 2 minutes
Proton Density Weighting
TE = 20 ms
TR = 3000 ms
Approx. scan time = 3-4 minutes
Inversion Recovery (IR) Pulse Sequences

These pulse sequences use 180° inverting RF pulse followed
by 90° excitation RF pulse after certain time [Inversion
Time (IT) or Time from Inversion (TI)].
Depending on the TI value, we can classify the IR sequ-
ences into:
1. Short inversion recovery (STIR)
2. Fluid attenuated inversion recovery (FLAIR)
If we apply 180° inverting RF pulse, the NMV (net
magnetic vector) will be inverted through 180° into full
saturation. When we remove the inverting pulse, the NMV
begins to relax back to Bo (static external magnetic field)
54 Step by Step MRI
Fig. 5.5: Recovery from inversion
(Fig. 5.5).
A 90° excitation pulse is then applied at a time from the
180° inverting pulse known as the TI time (Time from
Inversion). The contrast of the image depends on the TI
value (Fig. 5.6).
These sequences are used to generate heavily T1
weighted images bringing large difference between fat and
water.
Advantages
Fig. 5.6: Schematic illustration of the inversion

recovery (IR) pulse sequence
• Produces heavily T1 weighted images
• Very good signal-to-noise ratio (SNR).
Disadvantage
• Long scan times.
STIR (Short Inversion Recovery) Pulse Sequence

This sequence is used to suppress the fat signal from the
anatomy of interest. Here we use a TI value that corres-
ponds to the time it takes fat to recover from full inversion
to the transverse plane so that there is no longitudinal
magnetization corresponding to fat. When the 90° RF
excitation pulse is applied, the fat is flipped 90o to 180°, so
there will not be any fat signal. It will suppress the fat in
STIR. Generally, a TI value of around 100-200 ms is used.
This TI value may slightly vary depending on the field
strength (Fig. 5.7, Table 5.1).
Table 5.1: Optimal inversion times for a given
Fig. 5.7: T1 determination of STIR

56 Step by Step MRI
field strength (for STIR)
Field strength (T) TI (ms)

1.5 120-150
1.0 100-230
0.5 90-115
0.2 75-90
Uses
• Used to suppress the fat signal in T1 weighted image.
Disadvantage Should not be used with contrast
enhancement.
Parameters
TE = 10-30 ms
TR = 2000 ms
TI = 150-200 ms
Average scan time = 5-15 minutes.
FLAIR (Fluid Attenuated Inversion Recovery)
It is another variation in the IR pulse sequence which uses
a TI value around 2000 ms. Usually, this sequence is used
to suppress the signal from CSF containing areas.
Fig. 5.8: FLAIR image (CSF appears

more dark since it is heavily T1 weighted
image)
Parameters
TE = Short or long depending on weighting
TR = 6000-8000 ms
TI = 2000 ms
Average scan time = 13-20 minutes
Gradient Echo (GE) Pulse Sequences

These sequences use variable flip angles and lesser repeti-
tion time (TR). The gradients are used to rephase the
protons. We can apply the gradients quickly to rephase the
protons (unlike 180° rephasing pulses in spin echo which
takes some time to apply) (Figs 5.8 and 5.9).
Because of the quicker application of gradients and
reduced repetition time and smaller flip angles, the scan
times are greatly reduced in gradient echo pulse sequences.
With this sequence, we can get T1 weighting, proton density
weighting and T2* weighting.
Fig. 5.9: Image obtained

with gradient echo pulse
sequence. Blood
vessels appear bright on
gradient echo pulse
sequences
58 Step by Step MRI
Fig. 5.10: Schematic illustration of gradient echo pulse sequence
Since the gradient does not compensate for magnetic

field inhomogeneities, we will get T2* weighting (Fig. 5.10).
Uses
• Can be used to produce T1, proton density and T2*
weighting
• Very minimal scan times
• Can be used for single slice breathhold acquisitions in
abdomen and dynamic contrast enhancement
• Since these sequences are flow sensitive, can be used
for MR angiography/MR myelography
• Less RF deposition into the body, i.e. less specific
absorption rate (SAR).
Disadvantages
• Less signal-to-noise ratio when compared to SE pulse
sequences
• True T2 weighting is not possible (T2* contrast rather
than true T2)
• More work for the gradients
• More noise to the patient.
Steady State
In this state, the selected TR will be shorter than the T1
and T2 times of the tissues. In this state, there will be coexis-
tence of both longitudinal and transverse magnetization.
Most gradient echo sequences use the steady state.
Generally, flip angles of 30° to 45° with TR of 20 to 50 ms
favours the steady state.
Depending on the residual transverse magnetization
in phase (or) out of phase GE pulse sequences are classified
into:
1. Coherent (in phase) gradient echo pulse sequence
2. Incoherent (out of phase) gradient echo pulse sequence.
Coherent (in phase) Gradient

Echo Pulse Sequences
These sequences use a variable flip angle excitation pulse
followed by a frequency encoding gradient rephasing to
produce a gradient echo. Here the steady state is maintained
by selecting a TR shorter than the T1 and T2 times of the
tissues. In this sequence, the tissue with long T2 values
appear with high signal intensity.
Uses
• Increased T2* Dependence
• Very fast scans
• Preserves the transverse signal
60 Step by Step MRI
• Good for angiography
• Can be acquired in a volume acquisition.
Disadvantages
• More gradient noise to the patient
• Poor SNR in 2D acquisitions compared to spin echo
• More magnetic susceptibility.
Parameters
• To maintain the steady state:
– Flip angle: 30°-45°
– TR-20-50 ms
• To maximize T2*
– TE = 15-25 ms
Incoherent (Spoiled) Gradient

Echo Pulse Sequences
These pulse sequences begin with a variable flip angle
excitation pulse and use frequency encoding gradient
rephasing to give a gradient echo. These sequences spoil
(or) dephase the residual transverse magnetization so that
its effect on image contrast is minimal.
Uses
• Increased T1 weighting
• Spoils the transverse signal
• Only the longitudinal signal contributes to the next RF
pulse
• Good SNR in volume acquisition
• Can be acquired in 2D (or) volume
• Breath holding is possible.
Disadvantages
• Decreased SNR in 2D
• Loud gradient noise.
Parameters
• To maintain the steady state
– Flip angle: 30°-45°
– TR = 20-50 ms
• To maximize T1
– TE = 5-10 ms is used.
Steady State Free Precession (SSFP)

These sequences are used to attain more T2 weighting. In
this sequence the steady state is maintained.
Parameters
—Flip angle: 30°-45°
—TR = 20-50 ms
Advantages
• True T2 weighting is achieved
• Can be acquired in volume or 2D
Disadvantages
• Loud gradient noise
• Poor image quality
Ultrafast Sequences
• These sequences use coherent (or) incoherent gradient
echo pulse sequences
• Only a portion of the RF pulse is used
• Only a portion of the echo is read
Because of the above reasons, the scan time is drastically
reduced.
62 Step by Step MRI
Echoplanar Imaging (EPI)
• The fastest scan acquisition modes in MRI are the EPI
and the gradient echo pulse sequences.
• In echoplanar imaging all the lines of K-space will be
filled in one shot. This is called single shot EPI (SS-EPI).
• If the echoes are generated by multiple 180° pulses, this
is termed as spin echo echoplanar imaging (SE-EPI).
• If the gradients are used for the purpose of rephasing in
EPI, then this sequence is called GE-EPI.
• GE-EPI and SS-EPI are faster than SE-EPI.
• SS-EPI sequences are more prone to artifacts such as
chemical shift, distortion and blurring.
• In EPI the image may contain more T2* weighting which
can be minimized by using 180° inverting pulse before
excitation pulse.
Uses
• Improved cardiac and abdominal imaging
• Used in perfusion weighted imaging
• Useful in real time and interventional MR-guided
procedures.
PERFUSION WEIGHTED IMAGING (PWI)

This is a type of dynamic MR imaging by using GRE (or)
EPI sequences with contrast enhancement to study the
uptake of contrast medium by the lesion. This technique
can be used in abnormalities of brain, pancreas, liver and
prostate.
DIFFUSION WEIGHTED IMAGING (DWI)

In this type of MR imaging either GRE (or) EPI sequences
are used to demonstrate the areas with restricted diffusion
of extracellular water such as infarcted tissue. High signal
intensity appears at the area of restricted diffusion. DWI is
mainly useful in brain to differentiate salvageable and
nonsalvageable tissue after brain stroke.
FUNCTIONAL MRI (FMRI)

It is a dynamic MR imaging Technique that acquires images
of the brain during stimulus and also at rest. Then the two
sets of images are subtracted to demonstrate functional
brain activity. This technique is called BOLD (blood
oxygenation level dependent). At the activated areas of
brain, there will be increased signal intensity. fMRI is useful
in evaluating the brain activity in the disorders of epilepsy,
stroke and behavioural problems.
MAGNETIZATION TRANSFER (MT) CONTRAST

This is a technique used to suppress the background tissue
thereby increasing the conspicuity of vessels and certain
disease processes. MT contrast is useful in diagnosing
hemorrhage, AIDS, multiple sclerosis and also to improve
contrast in TOF-MRA images by suppressing background
tissue.
MAGNETIC RESONANCE ANGIOGRAPHY

(MRA)
MRA is a technique which allows us to acquire the images
with high signal from flowing nuclei and low signal from
stationary nuclei. This technique will allow us to see the
blood vessels more clearly than surrounding. Generally, GRE
pulse sequences are used to show flowing vessels as bright.
There are two types of MRA techniques available. They
64 Step by Step MRI
are: 1) Time of flight (TOF-MRA and 2) Phase-contrast
MRA (PC-MRA).
Time of Flight MRA (TOF-MRA)

This technique commonly uses incoherent GRE pulse
sequences in conjunction with TR and flip angle combi-
nations that saturate background tissue but allowing moving
spins to show high signal intensity. This technique is used in
demonstrating arterial and venous flow in head, neck and
peripheral vessels.
Fig. 5.11: 3D TOF MRA showing intracranial vessels
Phase Contrast MRA (PC-MRA)

This technique usually uses coherent GRE sequences. It
provides excellent background suppression. But the scan
Fig. 5.12: 3D PC-MRA image
times with PC-MRA are longer than the scan times of GE

pulse sequences are flow sensitive hence used for MRA
(magnetic resonance angiography).
66 Step by Step MRI
ACRONYMS USED BY MANUFACTURERS
(Table 5.2)
Table 5.2: A comparison of the acronyms used by

manufacturers
GE Philips Siemens
Spin echo MEMP Spin echo Spin echo
VEMP
Fast spin echo FSE TSE TSE
Coherent gradient echo GRASS FFE FISP
Incoherent gradient echo
(RF spoiled) SPGR T1 FFE
Incoherent gradient echo
(gradient spoiled) MPGR FLASH
Steady state free precession SSFP T2 FFE PSIF
Inversion recovery MPIR IR IR
Short T1 inversion recovery STIR SPIR STIR
Ultrafast Fast GRASS TFE Turbo
SPGR FLASH
(IR/DE PREP) 3D
MP RAGE
Presaturation SAT REST SAT
Gradient moment rephasing Flow comp FLAG Resp.
trigger
Signal averaging NEX NSA AC
Partial averaging Fractional Half Half
NEX scan fourier
Partial echo Fractional Partial
echo echo
No phase wrap No phase Fold over Over
wrap suppression sampling
Contd..
Contd..
GE Philips Siemens
Rectangular FOV Rect FOV Rect FOV Half
Fourier
imaging
Abbreviations used in Table

AC : Number of acquisitions
FSE : Fast spin echo
FFE : Fast field echo
FLAG : Flow adjusted gradients
FISP : Fast imaging with steady precession
FLASH : Fast low angled shot
FAST : Fourier acquired steady state technique
GMR : Gradient movement rephasing
IR : Inversion recovery
MPGR : Multi planar gradient recalled acquisition in the steady
state
MPIR : Multiplanar inversion recovery
NEX : Number of excitations
NSA : Number of signal averages
PSIF : Mirrored FISP
REST : Regional saturation technique
SPGR : Spoiled gradient recalled acquisition in the steady state
STIR : Short T1 inversion recovery
SPIR : Spectrally selective inversion recovery
SAT : Saturation
TFE : Turbo field echo
TSE : Turbo spin echo
Six
Tissue Characteristics
Magnetic resonance imaging is a diagnostic modality

providing cross-sectional imaging of the entire body in any
plane with no radiation risk to the patient. There are no
known adverse effects.
ROLE OF MRI IN DISEASES

MRI has unique properties. It is a complex yet interesting
imaging technique utilized for the diagnosis of various
diseases in all parts of the body. MRI is very sensitive to
certain pathologies, demonstrating disorders not shown on
other imaging modalities, i.e. CT. The rapid advances in
MRI have resulted in many new pulse sequences providing
details about tissue characterization.
Production of Image
When the patient is placed in the scanner, the applied
external magnetic field (EMF) induces a net nuclear
magnetization (NNM) in the longitudinal axis of the patient.
This NNM is rotated through 90 degrees by the RF pulse.
When the RF pulse is discontinued, relaxation back to the
original state occurs, i.e. recovery of the magnetization in
Tissue Characteristics 69
the longitudinal plane and decay of magnetization in the
transverse plane. The recovery of longitudinal magnetization
is known as spin lattice or T1 recovery. The decay of
transverse magnetization is known as spin spin relaxation
or T2 decay. T1 is determined by how quickly the nuclei
can transfer energy to their surrounding environment
(lattice) and return to a lower energy state. T2 is determined
by how quickly the nuclei can exchange energy with
neighboring nuclei to produce random distribution of the
precessing nuclei about the magnetic field.
The sensitivity of MRI to certain substances, i.e. water
and iron compounds, is of particular importance in clinical
imaging. For example, the high sensitivity of MRI to tissue
water allows the effective demonstration of brain edema.
All types of edema namely vasogenic, cytotoxic and
interstitial, result in altered signals and are best seen on T2
weighted images as a bright signal.
The marked differences in the relaxation times of water
and brain tissue enable the differentiation of tissues. For
example, smaller structures such as cranial nerves that are
bathed in cerebrospinal fluid (CSF) are well demonstrated
on MRI. MRI is superior in the demonstration of tumors
and other abnormalities of nerves, i.e. acoustic neuromas
and lesions involving the optic chiasma.
The sensitivity of MRI to paramagnetic substances such
as iron is of great clinical importance, as lesions of increased
iron in pallideus, substantia nigra, red nucleus and dentate
nucleus demonstrate a low signal on T2 weighted images.
MRI is sensitive for the detection of cerebral ischemia,
plus has the advantage of evaluating subacute and chronic
70 Step by Step MRI
trauma cases.
Advantages of Magnetic Resonance Imaging

1. Nonionising radiation
2. No known biological hazards
3. Multiplanar imaging: images can be obtained in all planes
namely coronal, sagittal, axial or any oblique plane
4. High soft tissue resolution
5. Superior soft tissue characterization when compared to
CT as the tissue is studied in T1, T2 and other sequences
6. Blood flow imaging
7. Non-invasive imaging technique.
Disadvantages
1. High cost
2. Claustrophobia (fear of enclosed spaces). The wider
bore design associated with present equipment has
resulted in a reduction in the occurrence of MRI induced
claustrophobia
3. Longer imaging time: difficult to image critically ill and
very uncooperative patients
4. Cortical bone and calcific lesions are poorly visualized
5. High degree of technical expertise is required
6. Patients with pacemakers, surgical clips, otologic and
ocular implants, etc. are unable to undergo an MRI
examination.
MRI Image
The image represents a display of the MR signal. The signal
intensity depends on both the tissue and equipment
(operator) parameters. It is important to understand that
the gray scale on a MR image is not readily predictable
and can be dramatically altered by machine-dependent
parameters such as choice of pulse sequence, time between
pulses (TE), repetition time (TR), inversion time (TI) etc.
There are four main tissue MR parameters contributing to
the signal intensity of an image: i) proton density, ii) T1, iii)
T2 and iv) blood flow.
The MR image depends on the following four main
factors;
• T1 relaxation time
• T2 decay time
• Proton density
• Blood flow.
Proton (Spin) Density, T1W and T2W

MR imaging is related to the density of mobile protons.
Proton density is represented by the symbol (PD). The PD
image is obtained using a spin echo sequence with long TR
and short TE or a gradient echo sequence with a low flip
angle. As the PD of various tissue obtained differs only by
a few percent, this pulse sequence is not widely used.
Air contains a low density of protons; therefore sinuses
show no proton image. Trabecular bone, on the other hand,
contains many protons but still generates no signal. This is
because the protons are tightly bound and have a T2 decay
time so small that the signals vanish before conventional
MR imaging is able to detect them.
Relaxation times are affected by the chemical compo-
sition of the tissue being studied. Each normal tissue in the
body has a specific relaxation time which is either shortened
72 Step by Step MRI
or prolonged by certain pathological changes.
The choice of a short TR enhances the T1 contrast
between fats and liquids. On the T2 decay curve, each
tissue starts at a different level. Fats are characterized by
a short T2 and liquids by a long T2: there is a crossing point
between the two curves where the two substances show
an isointense signal.
INTENSITIES OF NORMAL
ANATOMICAL STRUCTURES
Normal anatomical structures are listed below according
to their signal intensity on T1 weighted images (Table 6.1).
1. High intensity
• Fat
– Orbital
– Scalp
• Mucous
• Marrow
– Cranium
Table 6.1: Typical values for normal and some abnormal tissues
at 1.0 T
Tissue type Relative proton T1 T2

density (ms) (ms)
Lipids 0.6 250 50
White matter 0.75 670 85
Gray matter 0.85 920 95
Peripheral muscle 0.8 620 45
Liver 0.70 570 45
Cerebrospinal fluid 1 2000 1000
Edema 0.90 1060 150
Brain tumor 0.90 1410 200
MS plaque 0.90 1100 150
– Sphenoid, clivus
– Vertebra
• Cartilage of nasal septum
2. Low intensity
• Venous sinuses
• Veins
– Internal jugular
– Superior ophthalmic
– Internal cerebral
– Vein of Galen
• Cortical veins
• Arteries
– Carotid
– Ophthalmic
– Anterior, middle and posterior cerebral
– Anterior inferior cerebellar artery (AICA)
– Posterior inferior cerebellar artery (PICA)
– Vertebral-basilar
• Paranasal sinuses
• Choroid plexus
• Cortical bone
• Falx cerebri
• Tentorium
• Calcified cartilage
• Calcified structures, e.g. pineal gland.
When excited protons return to equilibrium, they relax
inducing a signal. The combined signal generates the MR
image.
If the emitted signal is low, it is termed hypointense and
represented in black. If the emitted signal is high, it is termed
hyperintense and represented in white.
74 Step by Step MRI
Table 6.2: High and low MR signals
High MR signal (White) Low MR signal (Black)

Proton density High Low
T1 relaxation Short Long
T2 relaxation Long Short
Blood flow Slow/stationary Fast/turbulent
• T1 weighted images (Fig. 6.1):

Hypointense: tissue with a long T1
Hyperintense: tissue with a short T2
• T2 weighted images (Fig. 6.2):
Hypointense: tissue with a short T2
Hyperintense: tissue with a long T2
Fig. 6.1: T1 characteristics of body tissues
Liquid produces a hypointense signal on a T1 weighted

pulse sequence and a hyperintense signal on a T2 weighted
pulse sequence. Fat, on the contrary, has an opposite signal,
i.e. hyperintense on a T1 pulse sequence and hypointense
on a T2 weighted pulse sequence. Both fat and water have
the same signal (isosignal) in a mixed pulse sequence (Figs
6.3 and 6.4).
Fig. 6.2: T2 characteristics of body tissues
Causes of hypointensity (on short flip angle, long TE

gradient echo images):
• Hemorrhage
– Deoxyhemoglobin
– Ferritin/hemosiderin
– Other iron forms
• Calcification
– Diamagnetic calcium salts
– Associated paramagnetic ions
• Air containing paranasal sinuses
• Normal brain iron
• Paramagnetic contrast agents
• Ferromagnetic devices, foreign bodies
• Intravascular deoxygenated blood.
Pathological changes influencing image appearance:
Edema: Both cytotoxic edema and vasogenic edema are
hypointense on T1 and hyperintense on T2 weighted pulse
sequences. Necrosis, also appears hypointense on T1 and
hyperintense on T2 weighted pulse sequences.
Gliosis: On T2 weighted pulse sequences, gliosis appears
as distinct areas of high signal intensity.
Radiation effects: Radiation may cause a decrease in signal
76 Step by Step MRI
Fig. 6.3: Mixed sequence with short TR
Fig. 6.4: Mixed sequence with three echoes
intensity on T2 weighted pulse sequences.

Cysts: Cysts are hypointense on T1 and hyperintense on
T2 weighted pulse sequences and are similar to CSF in
intensity.
Demyelination: Areas of demyelination are visualized as
hyperintense signals on T2 weighted pulse sequences.
Fatty changes: Increased fat or lipid content as in epider-
moid tumors, result in a characteristic high intensity lesion
on T1 weighted pulse sequences.
Fibrosis: Fibrosis, seen in postoperative disk surgery,
appears hypointense on both T1 and T2 weighted pulse
sequences.
Gray-white Matter
The T2 of white matter (WM) is less than the T2 of gray
matter (GM) and the T1 of WM is less than the T1 of GM.
As WM has a shorter T1 and T2, it appears brighter on T1
weighted images whilst the short T2 makes it appear less
bright on T2 weighted images. The brightness of WM on
T1 weighted images is attributed to the membrane lipid
myelin in the brain.
Vascular Structures
If hydrogen passes through the image volume faster than
the time taken to perform an imaging sequence, there will
be no detectable signal. The signal intensity of flowing blood
is a function of the percentage of moving hydrogen nuclei,
their velocity and the temporal parameters of the imaging
technique. The normal carotid artery, basilar artery and
venous sinuses have no detectable signal, appearing black
on MR images.
Intravascular blood appears either white or black on MR
images depending on its velocity of flow or turbulence: fast
flowing blood appears black, whilst slow flowing blood
appears white.
Short T1
(White) Retro-orbital fat
78 Step by Step MRI
White matter
Internal capsule
 Thalamus
Cerebellar gray matter
Caudate nucleus
Cortical gray matter
Cerebrospinal fluid
Long T1 Ocular vitreous

(Black)
Long T2
(White) Cerebrospinal fluid
Ocular vitreous

Caudate nucleus
Orbital fat
Cortical white matter
Short T2 Internal capsule
(Black)

High proton density
(White) Fat
 Caudate
Cortical white matter
Internal capsule
CSF
Bone
Low proton density Air

(Black)
Pathological Changes and Effect

of Relaxation Time
Both the T1 and T2 recovery times can either be shortened
or prolonged by the following;
T1 Shortened
– Lipid
– Paramagnetic substance:
a. Copper
b. Iron
c. Manganese
– Mucus
– Cholesterol
– Postradiation changes (after two weeks)
– Hemorrhage (methemoglobin)
– Increased protein content
– Melanin
T2 Shortened
– Air
– Calcium
– Cortical bone
– Paramagnetic substances
– Fat
T1 Prolonged
– Air
– Calcium
– Cortical bone
– Edema
– Demyelination
– Neoplasia
– Infection
– Ischemia
80 Step by Step MRI
– Infarction
– CSF
T2 Prolonged
– Demyelination
– Infection
– CSF
– Ischemia
– Neoplasia
– Edema
Appearance of Blood on MR Images
Utilizing Various Imaging Techniques
Bright
• Gradient echo pulse sequences
• Flow compensation (slow flow)
• Short echo time
• Thin two-dimensional gradient echo section oriented
perpendicular to direction of blood flow
• MR contrast agents shorten the T1 relaxation time of
blood
• Spiral scan pulse sequence
• Segmented turbo flash pulse sequence.
Dark
• Spin echo
• Presaturation pulse
• Long echo time
• Thin two-dimensional spin echo or fast spin echo sections
oriented perpendicular to direction of flow
• Super paramagnetic iron oxide to shorten T2 relaxation
time of blood.
Thrombosis and clot formation are complex dynamic
processes. Clot retraction, cellular infiltration, fibrinolysis,
red blood cell morphology, hemoglobin desaturation and the
development of blood degradation products interact to affect
the MR appearance (Table 6.3).
Extrinsic factors such as field strength and pulse
sequences also affect the MR signal.
Table 6.3: MR appearance of hemorrhage
Hemoglobin stage MR signal RBC morphology

1. Oxyhemoglobin Center, hyperintense Normal
thin peripheral rim
surrounding edema
2. Deoxyhemoglobin Isointense Spherocytes
3. Methemoglobin Hypointense Echinocytes
4. Macrophages with Hyperintense Dehydrated
hemosiderin and Blooming of dark
ferritin signal Lysed
Hyperacute Clots and Oxyhemoglobin

Oxyhemoglobin (OxyHb) is present in hyperacute clots for
only a few minutes or up to a few hours. OxyHb contains
ferrous iron, lacks unpaired electrons and is diamagnetic.
Therefore, OxyHb does not affect T1 and T2 relaxation
times. The MR signal of hyperacute hematoma can be
attributed to its protein traces containing water content.
Hyperacute clots are typically isointense with GM on T1
weighted images and hyperintense on T2 weighted images.
Acute Clots and Deoxyhemoglobin
Hemoglobin desaturation from oxyHb to deoxyhemoglobin
(DeoxyHb) occurs within a few hours of hemoglobin. As
DeoxyHb contains ferrous iron with four unpaired electrons
in a high spin state, it is strongly paramagnetic. DeoxyHb
lacks the ability to cause proton electron dipoledipole
82 Step by Step MRI
(PEDD), proton relaxation enhancement and T1 shortening,
appearing isointense with brain parenchyma on T1 weighted
images.
If DeoxyHb is sequestrated within RBCs, as water
diffuses freely across the cell membrane, it experiences a
substantial magnetic susceptibility gradient. This results is
phase dispersion and subsequent preferential T2 proton
relaxation enhancement (T2-PRE).
The susceptibility effects seen with acute clots become
more pronounced with progressive T2 weighting. Acute
clots with DeoxyHb typically appear moderately hypointense
on balanced (long TR/short TE) pulse sequences and
profoundly hypointense on T2 weighted or gradient
refocused pulse sequences.
Subacute Clots and Methemoglobin

Methemoglobin (MetHb) is present in subacute hematoma
and can be seen from a few days to a few months following
hemorrhage. MetHb is ferric, has five unpaired electrons
and is strongly paramagnetic.
Early subacute hematomas have a bright signal on T1
weighted images. The bright signal typically begins at the
hematoma periphery and progresses inwards. Thus, the
center of early subacute clots remains relatively isointense
on T1 weighted images and the rim becomes hyperintense.
In the early subacute stage of hematoma formation, MetHb
is contained within intact RBCs and preferentially increases
T2-PRE. This T2 shortening results in low signal on long
TR/short TE, i.e. proton density weighted pulse sequences.
Early subacute clots are profoundly hypointense on T2
weighted and gradient refocused pulse sequences.
In the late subacute stage, hemolysis results in the
accumulation of extracellular MetHb within the hematoma
cavity. MetHB in a free solution is extremely hyperintense
on T1 and T2 weighted images.
Chronic Clots and Iron Storage
In the early chronic stage, a pool of dilute-free MetHb is
surrounded by the ferritin and hemosiderin containing
vascularized wall. At this stage, clots are typically homo-
geneously hyperintense on both T1 and T2 weighted images,
with a pronounced hypointense signal rim on T2 weighted
images. Edema and mass effect diminish and then disappear.
The long-term residue of late chronic hematomas
following brain hemorrhage persists as macrophages laden
with iron storage products remain around the margins old
clots for years. Two substances are present in the late phase
of resolving cerebral hematomas namely ferritin and
hemosiderin.
Hemosiderin is isointense on T1 and extremely hypo-
intense on T2 weighted images. Due to strong magnetic
susceptibility effects, ferritin and hemosiderin appear
profoundly hypointense on gradient echo pulse sequences.
CLINICAL APPLICATIONS
MRI of Brain and Spine
Brain
Tumors
Although results have proved to be disappointing, espe-
cially in the detection of small calcifications, MRI, is at
present superior to CT in its ability to detect tumor. In
comparison with CT, MRI has the advantage of detecting
84 Step by Step MRI
lesions in the posterior fossa, at the edge of calvanium and
is superior for lesions near the base of the skull and the
pituitary fossa. MRI has the added advantage of charac-
terizing tissue better in tumors with lipomatous component
and in tumors appearing as enhancing foci not distinguish-
able from vascular structures on CT.
Hemorrhage–Ischemic Stroke
Both these condition are easily detected by MRI. For
example, the detection of thrombosis/stenosis is a very
promising application of MR angiography. It is also possi-
ble to separate the hemorrhagic and edematous component
of an infarct. Using special pulse sequences, i.e. diffusion
imaging, a stroke can be detected at the onset of ischemia.
Trauma
In comparison with CT, MRI has the advantage of demons-
trating the entire extent of the extracerebral collection plus
superior evaluation of diffuse axonal injury and sequelae of
trauma. An added advantage of MRI when scanning trauma
cases is its multiplanar capabilities, i.e. the ability to scan in
different planes without moving the patient. Disadvantages
include the longer scanning times and the inability to
demonstrate the bony cranium.
Degenerative Diseases
MRI is extremely effective in diagnosing multiple sclerosis,
subcortical arteriosclerotic encephalopathy, gliosis and
syrinx. In the detection of demyelinating diseases, MRI is
clearly superior to CT.
From the above, MRI is proving to be the present method
of choice for examining the brain.
Spine
A major advantage of MRI is that the spinal cord within
the thecal sac is well-visualized without the administration
of contrast media. For example, congenital lesions such as
Arnold-Chiary malformation and intraspinal tumors are
demonstrated without the need for myelography or
intrathecal contrast media.
MRI is proving to be the gold standard in the demons-
tration of degenerative disk disease and lumbar disk
herniation: nerve roots, neural foramina and intervertebral
disk spaces are better evaluated on MRI images.
MRI of the Thorax

Because of the relatively long data acquisition time, MRI is
more applicable for static parts of the body rather than for
moving parts. This means that small lung lesions may be
missed, but large or immobile lesions near the mediastinum
are demonstrated.
Mediastinum and Hili

MRI appears to be superior to CT in the evaluation of the
mediastinum and hili due to its higher contrast resolution.
This can be attributed to the low signal (black) from flowing
blood within the vessel providing a good intrinsic contrast
to other hilar structures.
Breast, Chest Wall and Pleura

86 Step by Step MRI
There is a remarkable similarity in the morphological
appearance of MRI and mammography as both the
glandular and fibrous structures are delineated by the
stronger signal from surrounding fat.
Although primary tumors of the chest wall and pleura
are detected with MRI, there is no superiority of this
modality over CT. A disadvantage of MRI is its inability to
demonstrate small calcifications.
Cardiovascular and Flow Studies

Cardiac–gated images display impressive anatomical details
of the heart, as well as changes in the arterial lumen. MRI
is able to depict tumors and congenital anomalies. Recent
advances in MRI equipment and software, has enabled the
evaluation of coronary arteries on MR angiography.
Myocardium
Acute myocardial infarction is seen as a region of high
signal intensity on MR images.
Flow Studies
On flow studies, the vascular structures are defined with
superb anatomical detail. The administration of contrast
media is not necessary due to the intrinsic contrast between
the low/black signal of flowing blood and the vascular wall.
The sensitivity of the vascular tree is increased through the
administration of contrast media.
However, MRI is not the final answer to all cardiac
imaging as the relationship of MRI to other noninvasive
imaging techniques, i.e. ultrasonography and isotope image,
remains to be defined.
Abdominal MRI
The contours of organs, surrounded by fat, are well-dis-
played. However, the intestinal tract is not well-delineated
on MRI images as bowel motion cannot be reduced through
the application of a gating technique and a satisfactory oral
contrast medium for the intestinal tract is not yet available.
Liver
Solid regions are detected equally well on both MRI and
CT imaging. However the relationship to vascular struc-
tures is better displayed on MRI whilst the demonstration
of calcified foci in tumors is better on CT than MRI. The
hepatic, portal and biliary systems are well-delineated on
MRI with magnetic resonance pancreatography (MRCP)
a well-established procedure for the evaluation of the biliary
and pancreatic tree.
Kidneys
Tumors, cysts, hydronephrosis, calculi or abscesses are
successfully diagnosed with MRI. The renal cortex and
medulla is differentiated assisting in the diagnosis of chronic
renal failure.
Ultrasound and IVU remain the first-line standard exami-
nations for kidney disease with CT being utilized for the
diagnosis and staging of malignant renal tumors. Magnetic
resonance urography (MRU) is an alternative for
noninvasive imaging of the ureters.
Adrenals
The ability of MRI to detect adrenal disease is comparable
88 Step by Step MRI
to CT. Whilst CT demonstrates superior spatial resolution;
MRI provides superior soft tissue contrast.
Pancreas
Recent studies have established the role of MRI in the
evaluation of the pancreas. T1 and T2 weighted pulse
sequences are helpful in differentiating pancreatic islet cell
tumors from normal tissue.
MRI of the Pelvis

MRI of the pelvis is superior to CT due to minimal motion
artefact in this region and no beam hardening effect as in
CT.
Urinary Bladder
The urinary bladder is best examined when filled.
Prostatic Hypertrophy
Benign prostatic hypertrophy can be volumetrically quanti-
fied from combined multiplanar MR imaging. Prostatic
cancer can be detected at an earlier stage with MRI than
with CT. Endorectal coils for prostate imaging are utilized
for the detection of local spread from prostatic malignancy.
The Female Pelvis

On MRI images, the uterus, ovaries and follicles are clearly
displayed. The corpus uteri can be distinguished from the
cervix and the myometrium is clearly differentiated from
the endometrium. The changes of the endometrium in the
various phases of the menstrual cycle and during pregnancy
are demonstrated on MRI images.
Although MRI is currently not advocated in pregnancy,
it holds great promise in the demonstration of the fetus and
placental site. The ability of MRI to detect fetal metabolic
disorders at an early stage has yet to be tested. The
utilization of MRI for pelvimetry is possible.
The lack of known biologic hazards makes MRI an
important potential tool in the management of obstetric and
gynecologic problems.
Extremities and Musculoskeletal MRI

Cortical bone and epiphyseal plates appear as signal free
areas, whilst normal bone marrow is seen as high signal
intensity on MRI images. Conventional radiographic techni-
ques are still superior for the demonstration of bone lesions
and fractures. However fat suppressed MRI pulse
sequences are highly sensitive in the detection of fractures.
The advantage of musculoskeletal examination by MRI
is the superior soft tissue contrast. Fat, muscle, tendons,
ligaments, nerves and blood vessels have different MRI
characteristics and are separately displayed.
In joints, MRI differentiates between fluid collections of
different etiologies. For example, infection, blood, serous
fluid, osteomyelitis and bone marrow tumors are better
characterized with MRI. Whilst the normal bone marrow
gives high MRI signals, the intensity of metastatic infiltrated
bone marrow is low.
Seven
Artifacts
Artifacts may be defined as the false features in the image

produced during the imaging process. The random
fluctuation of intensity due to noise can be considered
separately from artifacts. Artifacts can be rectified easily
when the causes are known. It is necessary to be familiar
with specific artifacts since they can conceal pathological
elements or simulate pathology that does not exists.
Artifacts can be classified into different categories, viz.
• Aliasing
• Chemical shift
• Gibbs/truncation
• Magic angle
• Motion
• Point
• Slice overlap
• Susceptibility
• Zipper
• Array processing
• Coil selection
Wrap Around/Aliasing
Wrap around or aliasing appears when the diameter of the
scanned area is greater than the dimensions of the field of
view used a part of the image is ‘folded’ on it self.
Artifacts 91
Fold over artifacts also known as :
i. Back folding
ii. Aliasing
iii. Wrap around artifact
Phase of the signal just out side of the field of view,
increase FOV, changes preparation direction increased
phase encoding.
Fig. 7.1: FOV: 18 cm Aliasing of the Fig. 7.2: FOV: 32 cm

back of the head onto the forehead in
the phase direction is seen
Fig. 7.3: Back folding artifact Fig. 7.4: Fold over artifact
92 Step by Step MRI
Remedies
1. Increase FOV
2. Filtering the frequency encoded direction
3. Oversampling in the phase encoded direction
Figs 7.5A and B: Tissues outside the FOV are folded back and
appear other side of the image (zebra type)
Chemical Shift Artifacts

Chemical shift artifacts appear at the interfaces between
water and fat because the precessional frequency of protons
is slightly different in these two substances. This leads to
misregistration of the signals. They are displayed by the
equipment as dark region of signal void on one side of
water containing tissue and a region of bright signal at the
other end of the water fat interface due to super imposition
of fat and water signals on the frequency encoding
direction.
The chemical shift artifacts is commonly noticed in the
abdomen, spine and orbits where fat and other tissues from
boarders.
Artifacts 93
This artifact is greater at higher field strengths and can
be reduced by increasing the bandwidth.
Fig. 7.6: Chemical shift mis-

registration artifact water in
the kidneys is misregistered
along the frequency axis. This
causes black signal (arrow)
voids at the kidneys left
margins and white lines at
their right margin (arrow)
The only way to eliminate this artifact is to use a fat

suppression technique.
Gibbs or Truncation Artifacts

Gibbs or Truncation artifacts are bright and dark lines that
are seen parallel and adjacent to boarders of abrupt intensity
Figs 7.7A and B: Low intensity lines appearing near the boundaries of
the brain/skull interface, are characteristic of a 160 phase encoding
acquisition
94 Step by Step MRI
change, as many be seen at CSF, spinal cord, fat and
muscle.
These artifacts are commonly seen in phase encoding
direction. They can be reduced by
a. Increasing the matrix
b. Using a filter
c. Change the direction of phase and frequency.
Magic Angle Artifacts

Magic angle artifact is seen mostly in tendons and ligaments
of knee-joint that are oriented at a magic angle, i.e. 55° to
the main magnetic field. This artifact is seen commonly in
the rotator cuff and occasionally in the patellar tendon
region and elsewhere.
Fig. 7.8: Magic angle artifacts
Motion Artifact
Motion artifacts appear as repeating densities oriented in
the phase direction occurring as the results of motion during
acquisition of a sequence. These artifacts may be seen from
Artifacts 95
arterial pulsations, swallowing, breathing, peristalsis and
physical movement of a patient.
This type of artifact is caused by the motion of the
patient voluntarily on involuntarily during the scanning.
The various types of motion artifacts are as follows:
Patient motion Since all the images in one sequence
are taken at the same time, it is important not to use
excessively long sequences, as movement for a brief period
spoils all the images.
Fig. 7.9: Patient moving head. Axial Fig. 7.10: Patient lying still
section of the brain caused by motion
of the head
Remedy: Make patient lie comfortably, stabilize, with straps

and cushions.
Cardiac motion This type of artifact is caused by the
contraction and relaxation of heart (chest) while the
scanning is going on.
Remedy: To avoid this type of artifact, cardiac gating is
mandatory during the procedure.
96 Step by Step MRI
Fig. 7.11: Motion of the heart has Fig. 7.12: With cardiac
produced ghost images without synchronization
cardiac synchronization, (ECG)
Respiratory motion This type of artifact is caused by

respiration during the scanning.
No breath hold Breath hold

Figs 7.13A and B: Respiration-induced artifact on axial section of the
abdomen. (This can be corrected by breath holding)
Remedy: This can be avoided by respiratory gating and

respiratory compensation. It can be avoided by placing
bellows (pressure transducers) around the patient’s chest
or abdomen.
Blood flow motion This type of artifact is caused by the
flow of blood throughout the cardiac cycle. The artifact
are prominent in axial images.
Artifacts 97
Fig. 7.14: On spoiled gradient

echo images, the distance
between aorta and ghost
artifacts (without triggering)
Remedy: An effective remedy for blood flow motion

artifact is ‘Spatial Presaturation (SAT)’.
CSF pulsation The remedy for CSF pulsation ghosting
is ‘Gating’ to the cardiac cycle, e.g. plethysmograph (peri-
pheral gating). However, combination of ‘Gating’ and flow
compensation (flow comp) is optimal for cervical and
thoracic imaging.
Figs 7.15A and B: Transversal image of the

T spine showing flow voids in CSF
98 Step by Step MRI
Fig. 7.16: Image showing step Fig. 7.17: Postcontrast smart

artifact due to MOTSA (3D TOF) prep.
3D TOF MOTSA Three dimensional TOF and multiple

overlapping thin slab acquisitions (MOTSA) images of the
neck. Patient motion and vascular pulsations during
acquisition resulted in a stair-step pattern in the 3D TOF
of MIP. The MOTSA images have higher SNR but greater
background signal.
Aperiodic motion This type of artifact is caused by the
involuntary motion of the patient like peristalsis,
swallowing and blinking of the eye.
Fig. 7.18: Without respiratory Fig. 7.19: With respiratory

compensation compensation
Arrow shows motion of the abdomen has produced several curved lines
Artifacts 99
Remedy: Except for peristalsis, the patient motion is best
controlled by cooperation and suitable education.
In order to reduce the motion artifacts caused by bowel
movement administration of Glucagon (IV) or Buscopan
(IM). Preprocedural is advisable.
Point Artifact
Point artifact is seen as a bright spot of increased signal
intensity in the center of the image. This is caused due to
constant offset of DC voltage in the receiver coil which
after Fourier transformation appear as a bright spot in the
center of the image.
Fig. 7.20: This is an axial image of the cardiac

showing a central point artifact
Slice Overlap Artifact

The slice overlap artifact is a name given to the loss of
signal seen in an image from a multiangle, multislice
acquisitions, as is obtained commonly in the lumbar spine.
If the slices obtained at different disk spaces are not
parallel, then the slices may overlap.
100 Step by Step MRI
Figs 7.21A and B: Para-axials (oblique) T2 weighted images through

optic nerves from a multiangle. This causes a band of signal loss crossing
vertically in sagittal image
Arrow shows signal loss from overlap

Figs 7.22A and B: This is a para-axial T2 weighted image through L5/
S1 from a multiangle, multislice acquisition, as is obtained commonly in
the lumbar spine
If two levels are done at the same time, e.g. L4/L5 and
L5/S1 then the level acquired second will include spins
that have already been saturated. This causes a band of
signal loss crossing horizontally or vertically in our image,
usually prominent posteriorly.
Artifacts 101
Susceptibility Artifacts
The susceptibility of a tissue fells us how easily it can be
magnetized. Normally most of the tissues have suscepti-
bility values which fall in a fairly narrow range. However,
presence of paramagnetic material like hemoglobin
degradation products or tissue-air interphases lead to local
A Make up eyeliner
B Magnetic field distortion C Harrington rod

due to hair pin
Figs 7.23A to C: Arrows indicate distortion due to susceptibility
differences between metal and body tissue. Artifacts caused by metallic
objects, causing severe signal loss and geometric distortion
variations in the susceptibility. This is turn results in
reduction in the quality of the local field.
Tissue air interphases related artifacts are commonly
seen around the para nasal sinuses and the lungs. These
susceptibility artifacts can be removed by using spin echo-
sequences.
Zipper Artifacts
This artifact is caused by external RF entering the room at
a certain frequency and interfering with inherently weak
signal coming from the patient.
There are various causes for zipper artifacts in images.
Most of them are related to hardware or software problems.
The zipper artifacts that can be controlled easily are those
due to RF entering the scanning room when the door is
open during acquisition of images.
RF from radio transmitters will cause zipper artifacts
that are oriented perpendicular to the frequency axis of
the image.
Frequently there is more than one artifact line on an
image from this cause.
Figs 7.24A and B: Effect of right interface causing streak artifacts. This
can be caused by a leaking RF, causing pick-up of external RF signals
Artifacts 103
Remedy: System generated artifacts should be reported
service engineer.
IMPROPER COIL SELECTION

Select a proper suitable coil, if you do not enter correct
one, the system will create noise on image. Structured noise
caused due to coil selection.
Select a coil from the coil name window.
The coil selected should match the one that is connected.
Arrows show artifact Without artifact

(Improper selection of coil) (Proper selection of coil)
A. CTL — Bottom coil B. CTL — 456 coil
Figs 7.25A and B: An example of lumbar spine
sagittal image is shown in Fig (a)
Array Processing Artifact

The array processor (AP) is part of the computation system.
It is a very fast parallel processor for execution of simul-
taneous tasks. The array processor is involved in the signal
averaging process during data acquisition and recons-
truction.
Fig. 7.26: Coronal T2 weighted spin echo

image of the head. Grid-like artifacts super-
imposed on the image are characteristic of
a faulty array processor
Eight
Technical Factors
Influencing the
Image Quality
INTRODUCTION
There are many factors available to the technologist when
setting up a sequence. The appropriate selection of the
parameters determines the weighting, improved quality of
images and sensitivity to pathology. Therefore, the techno-
logist should be aware of these factors and their
interrelation so that optimal quality of the images can be
obtained. The following are the factors discussed below
which affect the quality of the image.
Performing an MR examination demands multiple
choices:
i. The acquisition parameters
ii. The imaging plane orientation,
Type of coil, slice thickness, matrix size, number of
excitations, etc.
FACTORS AFFECTING THE SNR

Field of View (FOV)
FOV is one of the important factors affecting the SNR.
An image consists of a FOV that relates to the region of
interest (anatomy) covered.
Fig. 8.1: Field of view (FOV)
The field of view ranges from 10 to 50 cm for most of

the equipment. Therefore, if the entire spinal cord is to be
imaged in the sagittal plane, its upper and lower parts need
complementary series of pulse sequences.
FOV controls spatial resolution and SNR.
Small FOV produces ↑ (high) resolution ↓ (low) SNR
and increases the minimum TE value = SAT pulses
decreases the number of slices in an acquisition.
At a given matrix size (i.e. number of pixels on the two
image coordinates), the FOV determines pixel size, e.g. at
a FOV of 24 cm and a matrix size of 256 × 256 pixels, the
pixel size is 0.9 mm × 0.9 mm (240 mm/256).
FOV = 175 mm FOV = 325 mm
High resolution Low resolution
SNR = 100 percent SNR = 345 percent
It is critical that the technologist should understand the
relationship between signal-to-noise and FOV. SNR is
proportional to square of the FOV.
Technical Factors 107
FOV: 12 cm FOV: 24 cm
Figs 8.2A and B: SNR ~ FOV2
For example, Having a FOV reduced from 24 to 12 cm

results in, a signal-to-noise reduction of 75 percent.
In practice, the reduction in FOV requires some change
that results in increased SNR.
Spatial Resolution
Spatial resolution is defined as the ability to separate closely
spaced anatomical details.
Slice Thickness
To give each slice a thickness, a band of nuclei must be
excited by the excitation pulse.
Increase of slice thickness, increases SNR, coverage of
anatomy and partial volume whereas spatial resolution is
decreased.
As slice thickness ↑ (increases), resolution ↓ (decre-
ases) and SNR ↑ (increases).
Decrease of slice thickness, reduces SNR, coverage of
anatomy and partial volume whereas spatial resolution is
increased.
Figs 8.3A and B: SNR ~ slice thickness
The basic values of slice thickness ranges from 3 to 15

mm.
Slice thickness controls resolution and SNR.
The technologist should be aware that as the slice
thickness is increased or decreased, there will be a
corresponding change in the S/N ratio for the image.
If one slice is acquired at a 6 mm thickness, and another
slice is acquired at a 3 mm thickness (with all other factors
equal), the second slice will have one-half the signal of the
first slice. Since the noise is essentially unchanged, the effect
is that the S/N ratio will be cut in half for the second slice.
SNR ~ SLICE THICKNESS

Thickness = 3 mm Thickness = 10 mm
Scan time = 1.28 sec Scan time = 1.28 sec
Ideally, we would like to obtain images from, infinitely
thin sections. The thicker the slice, the more partial volume,
Figs 8.4A and B: SNR ~ slice thickness
which implies that certain structures may be hidden by

overlying tissues.
On the other hand, SNR and CNR are improved for
larger slice thickness.
Spacing
Spacing is the gap between two slices. When acquiring a
multiplanar, single acquisition, spacing controls cross-talk.
As spacing ↑ (increases), cross-talk ↓ (decreases)
Typically, a spacing that is 20 percent of the slice
thickness is sufficient to minimize cross-talk.
Fig. 8.5A: Contiguous slices Fig. 8.5B: Overlapping slices

As no.of slices ↑ (increases), scan time also ↑ (increases)
Ideally, we would like to obtain our images from
completely contiguous slices. In practice, there is always
some excitation outside the slice boundaries. This means
that when exciting a particular slice with a RF pulse, partial
excitation of neighboring slices will cause an alteration in
image contrast, or the effective TR for every slice is less
than determined by TR.
Matrix Size
The matrix size is represented by two figures. The first
figure usually relates to the number of frequency samples
taken, whereas the second relates to the number of phase
encodings performed. For example 256 × 128 indicates
that 256 frequency samples are taken during readout and
128 phase encodings are performed. A course matrix
corresponds to less number of pixels and fine matrix
corresponds to more number of pixels.
In all digital imaging methods, and therefore in MR too,
the image is divided into small picture elements called
pixels. Each individual pixel corresponds to the intensity
and amplitude of MR signal represented on gray scale.
The dimensions of the matrix can be changed. The most
commonly used matrix is 256 × 256. Some systems offer
low-resolution (128 × 128) and or/high-resolution (512 ×
512) matrixes.
At a given FOV, matrix size determines pixel size and
thus spatial resolution.
Therefore, an image obtained with 128 × 256 pixels is
typically less well resolved in the Y dimension than one
obtained with 256 × 256 pixels. However, all other para-
Fig. 8.6
Fig. 8.7
Fig. 8.8
Fig. 8.9
meters being equal, the 256 × 256 image has a factor of 2
less SNR, while it requires twice the scan time.
Pixel: Acronym for a picture element, the smallest discrete
part of a digital image display.
Voxel: Volume element, the element of the three-dimensional
space (3D-space) corresponding to a pixel, for a given slice
thickness.
Scan Time ∼ Matrix Size
Fig. 8.10 Fig. 8.11

Scan time ∼ matrix size
Matrix size = 256 mm Matrix size = 512 mm
Good resolution High resolution
Time: 2 min Time: 4 min
Prescan
Prescanning is a method of calibration to be performed
prior to every data acquisition. The following are the three
main tasks involved in prescanning viz.
i. Finding out the center frequency at which RF is to be
transmitted.
ii. Finding the exact magnitude of radiofrequency ought
to be transmitted in order to generate maximum signal
in the coil.
iii. Adjustment of the magnitude of the received signal.
Prescan allows for the adjustment of the transmit and
receive gain and the setting of the center frequency for a
specific body part to be imaged.
Number of Excitations or Number of

Signal Averages (NEX/NSA)
Every individual signal which contributes to form a MR
image, can be received once or collected several times
using repeated excitations. Hence, the average signal value
is used to generate the image. When the number of
excitations are increased, the error (the noise) doubt and
the measurements are more precise.
Fig. 8.12 Fig. 8.13

Nex = 2 Nex = 4
Scan time = 1.28 min Scan time = 2.48 min
In practice, the number of excitations ranges from 1 to 6.
The number of excitations (Nex) implies the number of
times a particular line in sampled in K space. K space refers
to the raw data of an image.
A line in K space corresponds to the spin echo obtained
at a particular setting of the phase encoding gradient. Scan
time is proportional to Nex.
By increasing the number of excitations, the SNR is
improved and vice versa.
Image Acquisition Time (Examination Time)

The longer the scan time, the more chances that the patient
moves and generates, more artifacts that prevent the
interpretation of the images. Hence, optimum scanning time
is to be maintained so that appreciable quality of images
can be obtained which are free of artifacts (motion artifacts).
For a given patient, the duration of an MR examination
depends on several factors.
• Getting the patient settled and centering the area to be
studied.
• The number of areas to be examined.
• The number and characteristics of the pulse sequences
used.
• The acquisition time (T) of a sequence is given by the
following formula:
Acquisition Time (T) = TR × N × Nex
Where, TR is the repetition time,
N is the number of phase encodings in the matrix
Nex is the number of excitations
Acquisition Time = TR × N × Nex
= 400 × 160 × 2
= 128 sec
= 2.14 minutes
Image (Data) Acquisition Time

The time required to gather a complete set of image data.
The total time for performing a scan must be taken into
consideration. The additional image reconstruction time
when determining how quickly the image(s) may be
viewed.
Increase of TR increases the scan time and similarly
increasing the number of phase encodings in a matrix
increases the scan time and vice versa.
Improving the SNR by increasing Nex also increases
the imaging time and vice versa.
Frequency
Frequency axis of the acquisiton matrix.
The number of cycles or separations of a periodic
process per unit time. In electromagnetic radiation, it is
usually expressed in units of Hertz (Hz), where 1 Hz = 1
cycle.
Increase the frequency matrix to produce (high)
resolution, ↓ (low) SNR and ↓ less number of slices.
Phase
In a periodic function (such as rotational or sinusoidal
motion), the position relative to a particular part of the
cycle.
Phase controls scan time for most pulse sequence data
base and may control resolution.
Nex: Select a Nex value that produces sufficient SNR.
Phase FOV
PFOV shortens scan time by scaling down the FOV size
in the phase direction.
Select 0.75 or 0.5 to reduce phase steps and thus
↓ (less) Scan time
↓ (less) FOV in the Phase direction
↓ (decreases) SNR slightly.
Freq DIR: S/I (superior to inferior), A/P (anterior to
posterior), R/L (right to left).
The scanning direction associated with the frequency
gradient.
The direction displayed is the default frequency direction
which is typically the long axis of the image.
To swap phase and frequency, select the other direction.
Auto Shim
Auto shim is typically selected when the FOV center is not
at isocenter.
A preparation phase is performed in which small gradient
amplitudes are determined which optimize the main
magnetic field homogeneity. The small gradients remain
present during the scan.
Contrast
Select only contrast if contrast is injected. Enter amount of
contrast injected and the type of contrast used in the
designated fields.
Phase Correction
A process that mathematically corrects for phase errors in
FSE and (EP) sequences. Phase correction is selected for
EPI and FSE, FSE-IR and FLAIR protocols.
1. Corrective processing of the spectrum so that spectral
lines at different frequencies all have the decorption—
mode phase.
2. In imaging, adjustment of the signal in different parts of
the image to have a consistent phase.
Auto Center Frequency

Select the CF peak that should be set during prescan.
A prescan procedure to fine-tune the system’s RF
transmit/receive frequency to the precessional frequency
of the protons under study, providing optimal sampling of a
patient’s anatomy.
Unlike other imaging modalities, magnetic resonance
(MR) imaging requires a multitude of operating parameter
decisions. Improper choices can result in impaired image
quality, cause artifacts and reduce a study’s diagnostic
efficacy. Therefore, it is important that the technologist
should understand both intrinsic tissue parameters, extrinsic
equipment parameters as well as how they interact.
Noise is always superimposed on the images. This noise
causes a fluctuation of pixel values.
Signal-to-Noise Ratio (SNR)

It is defined as the ratio of the amplitude of the signal
generated to the average amplitude of the noise. Quality
of image is mainly characterized by its SNR. Increase of
signal increases the SNR and vice versa. The following
are the factors that affect the SNR:
• Coil type
• Volume of the voxel
SNR
Fig. 8.14: Various factors which contributes to change of SNR
• Proton density of the region of interest under exami-

nation
• TR, TE and Flip angle
• Nex
• Receive bandwidth
• FOV
Scan time, spatial resolution, SNR are mathematically
related.
Contrast-to-Noise Ratio (CNR)

It is defined as the difference in the SNR of two adjacent
areas. The factors that affect CNR are the same as that of
SNR.
Bandwidth (BW)
A general term referring to a range of frequencies (e.g.
contained in a signal or passed by a signal processing
system).
A. Large bandwidth
B. Small bandwidth
Figs 8.15A and B: Selecting slice

thickness
This is the range of frequencies that are acquired by the

readout gradient. As bandwidth is decreased, noise is
reduced thereby increasing the SNR. If the bandwidth is
reduced to half, SNR is increased by 40 percent but
increases the sampling time.
Bandwidth defines the number of frequencies. We can
change the bandwidth with RF pulses.
Frequency can be swapped with phase direction by
champing the entry in (Freq DIR), following the table sum.
The default directions of phase freq. and slice select by
coil selection.
Two-Dimensional Fourier Transform (2DFT)

In order to reconstruct the image, each gradient cycle (slice-
selection, phase-encoding, readout) must be repeated for
each level of the phase-encoding axis. For example, a matrix
of 256 × 256 would require 256 cycles. Each of the 256
resulting signals (k-space data) is then converted from its
time domain into its frequency domain by a Fourier
Transform. Each signal produced along the horizontal axis
is the sum of all the magnetization vectors for that level of
the phase encoding gradient. After all 256 signals have
been transformed into their frequency domain (shown
below), a Fourier Transform is performed at each frequency
utilizing the data at all phase encoding levels to decode
the spatial information along the vertical axis. The second
Fourier Transform is performed on each corresponding
point along x and y, where y = the sum of all 256 signals
collected at each level of the y-axis.
Figs 8.16A and B: Fourier transformation

Table 8.1: The default directions for phase,

frequency, and slice, select by coil selection
Coil Plane Frequency Phase Slice Select
Head coil Axial A/P R/L S/I
Sagittal S/I A/P R/L
Coronal S/I R/L A/P
Body, Axial R/L A/P S/I
extremity, NV Sagittal S/I A/P R/L
Array coil, Coronal S/I R/L A/P
Surface coil
Receive only
Frequency can be swapped with phase direction by

changing the entry in (Frequency Direction).
Image Reconstruction
The mathematical process of converting the composite
signals obtained during the data acquisition phase into an
image.
GRADIENTS
In order to spatially encode the NMR signal, a gradient
magnetic field is superimposed on the static magnetic field.
The gradients place the nuclei in a slightly different magnetic
field depending on their location.
SLICE-SELECT
In order to confine excitation to a single slice only, an RF
pulse containing a narrow band of frequencies is applied,
in conjunction with the gradient located in the plane
perpendicular to the imaging plane. In an axial image in
the x-y plane, for example, the slice-selection gradient is
Gz. The gradient is applied only during the RF excitation
pulse. Only that plane of nuclei located with its z position
such that its Larmor Frequency matches that of the applied
RF will be excited to produce a signal.
Slice Orientation
Superior Inferior (axial plane)
Right Left (sagittal plane)
Anterior Posterior (coronal plane).
Fig. 8.17: A gradient is applied along the z-axis in conjunction with a

narrow band RF pulse to confine excitation to a single slice only
Fig. 8.18A: The orientation of simple

oblique slices can be specified by rotating
a slice
Fig. 8.18B: A plan of planes. The diagram

shows the slice plane in the patient trans-
verse, sagittal and coronal
Nine
MRI Contrast Agents
CONTRAST AGENTS
MRI provides excellent soft tissue contrast. However,
enhancement with contrast agents substantially improves
the sensitivity and specificity of lesions. Contrast agents
are pharmaceuticals that enhance the contrast between
the lesions and normal structures. Enhancement of the image
contrast between normal and diseased tissue increases the
diagnostic accuracy. Contrast agents are commonly used
in clinical practice for a broad range of indications.
IDEAL CONTRAST
The ideal contrast agent should have the following proper-
ties:
1. The contrast agent must be efficient at low concentrations
2. The contrast agent should possesses tissue specificity
to enable higher concentration in specific tissue
3. The contrast agent must be substantially chased from
the targeted tissue.
4. It must have low viscosity
5. The contrast agent must possesses a suitable shelf life
for storage purposes
6. It should be nontoxic.
MRI Contrast Agents 125
There is no ideal contrast to date. However there are
many MR contrast agents that are safe, highly effective
and widely used in routine clinical practice.
HISTORY
Nearly all MR contrast agents constitute paramagnetic
compounds. The most commonly used paramagnetic ion is
the gadolinium (Gd) ion. This ion attaches with various
ligands (chemical compounds) such as diethylenetriamine
penta acetic acid (DTPA) that act as chelating agents. The
reaction of Gd ions with DTPA forms a stable chelate
complex. The presence of unpaired electrons in the para-
magnetic ion is a mandatory component to affect changes
in the T1 and T2 relaxation times of protons. The utilization
of a paramagnetic ion with highest spin quantum number is
desirable. The Gd ion of the lanthanide metal group has a
high spin quantum number (7/2), making this ion a desirable
contrast agent.
The first and foremost MRI contrast agent on the world
market was Schering Magnevist, the dimeglumine salt of
gadolinium–diethylenetriamine penta acetic acid (Gd-
DTPA).
Presently three gadolinium based contrast agents are
approved by the US Food and Drug Administration (FDA).
These are nonionic Gd-DTPA-BMA (Gadodiamide or
omniscan), ionic Gd-DTPA(gadopentetate dimeglumine or
magnevist) and nonionic Gd-HP-DO3A (gadoteridol or
prohance). The osmolarity and viscosity of each of these
three contrast agents are given in Table 9.1.
Mechanism of Action
MR contrast agents alter tissue contrast. Signal will increase
when hydrogen proton increases, T1 decreases and T2
Table 9.1: The osmolarity and viscosity of

commonly used MR contrast agents
Trade name Osmolarity Viscosity (cp)

Osm/kg
Gadodiamide 783 1.4
Gadopentetate dimeglumine 1960 2.9
Gadoteridol 630 1.3
increases. Signal will be decreased when hydrogen protons

decrease, T1 increases or T2 decreases. CO2, perfluoro-
carbons and deuterated water decrease protons as they
possess no hydrogen nuclei. Paramagnetic materials like
Gd, Fe and Mn decrease both T1 and T2 thereby altering
the signal. Super paramagnetic particles reduceT2 thereby
decreasing the signal. Diamagnetic substances have
negative induced magnetization and are used in situations
where they can displace or mix with normal tissue. Water,
fat, perfluorocarbon and CO2 are used as gastrointestinal
contrast agents by the displacement of normal bowel
contrast.
Contrast agents have been broadly classified as positive
relaxation agents (T1 contrast agents) and negative
relaxation agents (T2 contrast agents).
Positive Relaxation Agents

The contrast agent that affects T1 relaxation is referred as
positive relaxation agent. These contrast agents reduce T1
relaxation times and shows increased signal intensity on
T1 weighted images. The gadolinium chelates, namely
paramagnetic agents, are examples of positive relaxation
agents and have wide clinical application.
Negative Relaxation Agent
The contrast agent that affects T2 relaxation is referred to
as negative relaxation agent. These contrast agents
reduceT2 relaxation times resulting in decreased signal
intensity on T2 weighted images. Examples of these
contrast agents are ferromagnetic and supermagnetic
metals. Gd chelates in high concentration can also be used
as negative relaxation agents, provided fast imaging
sequences are used. Perfusion imaging with high dose of
contrast and associated EPI pulse technique reduces T2
with relative loss of signal.
Negative relaxation agents have a limited role in clinical
practice.
Table: 9.2: Classification of contrast agents

Positive relaxation agents:
Parenteral (systemic):
Gd-DTPA:Gadopentetatedimeglumine(magnevist)
Gd-DTPA-BMA Gadodiamide(omniscan)
Gd-HP-DO3A-Gadoteridol (prohance)
Gd-BOPTA –Gadobenate dimeglumine
Gastrointestinal (oral):
Gd-DTPA
Ferric ammonium citrate(geritol)
Vegetable oils, fats, etc.
Negative relaxation agents:

Parenteral (systemic):
SPIO—Superparamagnetic iron oxide
USPIO—Ultrasmall superparamagnetic iron oxide
MION—Monocrystalline iron oxide
Gastrointestinal (oral):
OMP—oral magnetic particles
PFOB—Perfluoro octyl bromide
In post contrast images, the contrast enhancement is
increased by various imaging parameters other than contrast
media. Such parameters include magnetization transfer, fat
suppression techniques, etc.
Magnetization Transfer (MT)

The application of magnetization transfer (MT) in spin echo
imaging can improve the enhancement effect produced by
a gadolinium chelate in the brain. MT pulses preferentially
suppress the signal from background tissue, usually
improving the conspicuity of gadolinium-enhanced regions.
This can lead to improvement in the visualization of contrast
enhancement at standard dose. Hence MT is advisable in
all post contrast sequences in brain.
Fat Suppression
In areas of the body with abundant fat, T1 weighting with
fat suppression (short T1 inversion recovery–STIR) provide
improved depiction of contrast enhancement. Fat
suppression is indicated in all fat rich areas like breast, retro-
orbital and bone marrow, etc.
Perfusion Imaging
For perfusion imaging, the contrast medium is injected as a
bolus using MRI compatible power injector. Images are
acquired very rapidly during and immediately post injection.
This helps to study the first pass of the contrast agent through
the brain. In brain perfusion imaging studies T2 weighted
scans are used. These scans provide the required high
temporal resolution and are also quite sensitive to the
vascular bed. On T2 weighted scans, the gadolinium chelates
cause a reduction in signal intensity as opposed to the
increase in signal intensity seen on T1 weighted scans. After
acquisitions with the help of software relative cerebral blood
volume (rCBV) and relative mean transit time (rMTT) of
a given area is calculated. Perfusion imaging can detect
brain ischemia far sooner than standard T2 weighted scans.
It also detects the tissue at risk.
Administration of Contrast Agent

Administration of a gadolinium chelate can substantially
improve lesion identification and characterization. After
injection the MR contrast agent is distributed into the blood
pool and extracellular fluid compartment of the body. In
the brain lesion, enhancement occurs as a result of disrup-
tion of the blood brain barrier (BBB): MR contrast agents
do not cross the normal blood brain barrier. The standard
dose of gadolinium is 0.1 mmol/kg, which is equivalent to
0.2 ml/kg. The contrast is generally available in 10 or 20 ml
vials. It is injected through the intravenous route and is
rapidly excreted by glomerular filtration through the kidneys.
Contrast agents have half-lives between 1 and 2 hours.
Adverse Reactions
There may be occasionally pain at the injection site. Nausea
and vomiting are the two most common mild reactions
encountered. Headache, paresthesia, dizziness, focal
convulsions, skin reaction, flush are other adverse effects
noted. There is no major change of incidence in various
contrast agents regarding severe anaphylactoid reaction.
Patients with asthma, multiple allergies, or known drug
sensitivity (including to iodinated contrast media) are at
increased risk. The incidence of patients with adverse
effects after IV injection of Gd-DTPA was found to be
approximately 1 to 2%. In a post marketing survey of 5
million applications of Gd-DTPA, possible drug related death
was reported in one patient. Gd contrast media are safe to
be administered in children. During pregnancy use of
contrast is not recommended as it crosses the placental
barrier. Lactating mothers should stop breastfeeding their
babies, as contrast is excreted in breast milk.
All emergency drugs should be made available while
injecting contrast.
Hepatobiliary Agents
Gd-Benzyloxy propiomic tetraacetic acid (Gd-BOPTA)
Multihance (Gadobenate dimeglumine) is used both in CNS
and body. Multihance is excreted principally by the kidneys
and to a small extent by the liver. The latter feature markedly
improves the performance of this agent in the liver.
Multihance binds to protein improving its relativity
regardless of location in the body. Delayed scans are
particularly useful for the detection of small liver meta-
stases.
Feridex (fevumoxides, berlex laboratories) is a super
paramagnetic iron oxide containing dextran, formulated for
intravenous administration. This contrast agent is taken up
by cells of the reticuloendothelial system (RES) and is
sequestered by the RES, producing profound signal loss
from normal background tissue. On T2 weighted images
focal lesions like metastasis can be seen better. Its principal
use is as a liver agent.
Tesla scan (Mn DPDP, Nycomed) agent was designed
to be incorporated into hepatocytes. Post contrast moderate
enhancement of normal liver parenchyma is seen improving
lesion conspicuity.
Oral Contrast Agents

Complete bowel opacification is difficult and side effects
are high due to the rapid transit of the agent through the
bowel. The majority of the agents are eliminated rectally
within the first few hours’ administration and are not
absorbed by the bowel. Either positive or negative relaxa-
tion agents can be used in bowel imaging. Positive contrast
agents, increasing the signal intensity of the bowel are Gd-
DTPA with a volume expander or ferric ammonium citrate
(geritol). Examples of negative contrast agents, causing a
reduction in signal intensity of the intestinal lumen, are small
particles of iron oxide (SPIO-AMI-25) and ultrasmall
particles of iron oxide (USPIO-AMI-227).
Magnetic resonance angiography can be performed with
Gd contrast. After bolus injection of intravenous contrast a
10 to 20 fold reduction in blood T1 occurs during the first
pass, producing a large signal between vessels and
background tissue.
Tissue specific agents of MR contrast are yet to be
standardized.
Conclusion
The gadolinium chelates play a major role as contrast agents
in the evaluation of the patients by MRI. They improve
sensitivity and specificity of the lesion detection. Lesion
delineation, assessment of lesion activity, and narrowing of
differential diagnosis are improved with contrast study.
The MR contrast agents play an important role in routine
practice. They are already stabilized in intracranial pathology
and have improved the resolution in imaging of the vascular
tree. Currently, new contrast agents are under development
with the most promising being for liver imaging. Other
contrast agents for bowel, lymph nodes and selective
vascular imaging are yet to be standardized.
Ten
Recent Advances in
Pulse Sequences
Magnetic resonance imaging (MRI) has created a new era

in diagnosis and management of various diseases. Contrast
in MRI is dependent on T1 relaxation, T2 relaxation and
proton density. Depending on the predominant component,
the image is called T1 weighted image, T2 weighted image
or proton density (PD) image. The contrast is achieved by
the basic pulse sequence namely, spin echo (SE), gradient
recalled echo (GRE), and inversion recovery (IR). All the
new pulse sequences have their origin in them.
The hydrogen protons present in the body act like tiny
magnets. When the body is exposed to magnetic field the
hydrogen protons align and precess. The precession fre-
quency is proportional to the strength of the magnetic field.
External energy in the form of Radiofrequency (RF) is
applied to the precessing protons. There is disturbance in
the magnetic equilibrium of the protons. Discontinuation
of RF pulse causes the magnetic equilibrium of body to
return to normal. While magnetic equilibrium is returning
to normal it emits energy which is recorded as signal. It is
the detected signal which forms the MR image.
Routine Sequences used in MRI
There are essentially three pulse sequences which are
routinely used.
1. Spin echo (SE)
2. Inversion recovery (IR)
3. Gradient recalled echo (GRE) technique.
SPIN ECHO IMAGING

A spin echo sequence is the most commonly used technique
in MRI.
A slice selection 90° RF pulse is applied in conjunction
with a slice selection gradient. After a time of TE/2 a 180°
slice selection gradient is applied. A phase encoding gradient
is applied between the 90° and 180° pulses. The frequency
encoding gradient is applied after the 180° pulse, during the
time the signal is collected. The recorded signal is the echo
(Fig. 10.1).
Repetition time (TR) is the time between successive
excitation pulses for a given slice. Echo time (TE) is the
time from the excitation pulse to the maximum echo.
Fig. 10.1: Spin echo pulse sequence diagram

Recent Advances in Pulse Sequences 135
The contrast between white matter and edema is
maximized in two distinct situations. A short repetition time
(TR) and Echo time (TE) situation where white matter is
brighter than edema and a long TR and TE situation where
edema is brighter than white matter.
Gradients
The imaging plane or point is determined by applying
magnetic field gradients. There are basically three types of
gradient coils. One gradient is required in each of the x, y,
and z direction. A gradient is simply a magnetic field that
changes from point to point. Depending on their orientation
axis they are called Gx, Gy, Gz, and used for slice select,
frequency (read out), or phase encoding.
1. Slice selection gradient: It is turned on only during
application of RF pulse. If we make the magnetic field
change from point to point, then each position will have
its own resonance frequency. We can make the magnetic
field slightly weaker in strength at the feet and gradually
increase in strength at the head. This effect is achieved
by using slice selecting gradient coil. It helps to select
the point of the slice.
2. Phase encoding gradient: The gradient is applied in
one direction of the slice. Protons precess at slightly
different speeds (according to the intensity of the gradi-
ent) and thus have different phase angles which make it
possible to differentiate them. This operation is called
phase encoding. Phase encoding gradient is usually
applied between the 90° and the 180° RF pulses or
between the 180° pulse and the echo. For every slice,
each TR interval contains one phase encoding step. This
process completes one line in K-space corresponding
to the selected gradient strength. This process is repeated
to fill the entire K-space.
3. Frequency encoding gradient (read out gradient). This
is applied perpendicular to the phase encoding. It gives
rise to phase angle differences in each band of protons
which previously had the same phase angle. The new
phase angle provides spatial information. This operation
is called frequency encoding. The frequency encoding
gradient is applied during the time the echo is received,
i.e. during read out. Each TR interval contains one read
out per slice.
T1 and T2
T1 and T2 refer to physical properties of tissues after expo-
sure to a series of pulses at predetermined time intervals.
Different tissues have different T1 and T2 properties based
on the response of their hydrogen nuclei to radiofrequency
pulses imposed by the magnetic field. MRI exploits these
different tissue properties by selecting equipment para-
meters (TE and TR) producing images based on either the
T1 or T2 properties of the tissues. TE is the time interval
between applying the pulse and receiving the signal. TR is
interval between two radiofrequency pulses. TE and TR
are both expressed in milliseconds (ms). A relatively low
TE is about 20 ms, and high TE is above 100 ms. Low TR
is about 50 ms and long TR is above 1500 ms T1 weighted
images have a low TE and low TR (Fig. 10.2). Whereas
both are high for T2 weighted images. Proton density images
have a low TE and high TR (Fig. 10.3).
Fig. 10.2: Conventional spin echo T1 weighted image
Fig. 10.3: Conventional spin echo T2 weighted image

CONTRAST
Contrast agent currently in use are paramagnetic sub-
stances. Molecules of paramagnetic contrast material create
varying magnetic fields in tissues dependent on their
vibration/tumbling velocities and concentration. These
movements accelerate the relaxation process of the hydro-
gen nuclei in the tissues, shortening both T1 and T2. At
certain tissue concentrations these substances produce a
much shorter T1 effect and if image acquisition is T1
weighted certain tissues demonstrate contrast enhancement.
The most promising contrast material developed to date
is Gd-DTPA (Gadolinium diethylenetriamine pentaacetic
acid). It has a similar effect in MR as that of iodine in CT.
However the action of gadolinium DTPA is to shorten T1
relaxation time and the area appears brighter on T1
weighted image (Fig. 10.4). In contrary the action of iodine
in CT is to increase the density of area of the tissue and
hence appears brighter.
INVERSION RECOVERY (IR)

The RF pulses are 180°–90°–180°. A slice selection 180°
RF pulse is applied in conjunction with a slice selection
Plain Contrast
Fig. 10.4: Plain and contrast of calf showing
enhancement of abscess
gradient. A period of time equal to inversion time (TI)
elapses and a spin echo sequence is applied. The remainder
of the sequence is equivalent to a spin echo sequence.
Inversion time (TI) is between the initial 180° pulse and
90° pulse. The inversion recovery sequence is generally
used in a highly T1 dependent medium. Inversion recovery
images are strongly T1 dependent providing excellent image
contrast and anatomical details when the correct pulse
parameters are used. Areas of short T1 appear bright
(white) and areas of long T1 appear dark (black). Areas of
low proton density such as cortical bone and air appear
dark in IR sequence. Hence lesion adjacent to bone, e.g.
Acoustic neuroma, chordoma, etc. cannot be easily distin-
guished (Fig. 10.5).
Short Inversion Time Inversion Recovery (STIR)

The T1 relaxation time of fat is 150 ms. By selection of
inversion time (TI) equal to 150 ms, the fat in the images
Fig. 10.5: Inversion recovery pulse sequence diagram

gets suppressed and it is termed as fat suppression images.
This is useful technique in fatty tissues like retroorbital
fat, musculoskeletal system and to differentiate between
lipoma and subacute hematoma (methemoglobin stage) as
both are hyperintense on T1 weighted images .Lipoma is a
fatty lesion and is therefore suppressed on STIR sequences.
The inversion time of 2000 ms suppresses CSF and it is
known as FLAIR (Fluid attenuated inversion recovery).
FLAIR
Fluid attenuated inversion recovery (FLAIR) MR imaging
techniques were first described by Hajnal et al.
In a IR sequence if the inversion time (TI) is increased
to 1500 – 2000 msec the longitudinal magnetization of the
brain is almost fully recovered. The signal from CSF can
be nulled.
The FLAIR sequence has been used in the brain in cases
of infarction and multiple sclerosis. The FLAIR sequence
is used in heavily T2 weighted form in the brain where
most lesions are highlighted . It also can be used to improve
the accuracy of detecting T2 prolongation in the hippo-
campus in mesial temporal sclerosis. The CSF signal is
decreased and this helps in detecting acute subarachnoid
hemorrhage (Fig. 10.6).
One of the main disadvantages of FLAIR MR imaging
was long acquisition times, however newer techniques
combining FLAIR like sequences with fast spin echo
techniques have greatly shortened acquisition times.
FLAIR technique is currently used in a variety of brain
diseases including ischaemic stroke, demyelinating disorders,
subarachnoid hemorrhage, meningitis, trauma (diffuse
Fig. 10.6: FLAIR image
axonal injury), cystic lesions, tumors ( pilocystic astrocy-

toma and glioblastoma multiforme) and vascular
malformation.
Gradient Recalled Echo (GRE) Technique

Gradient echoes achieve their speed by using a low flip
angle and gradient reversal resulting in a short TR. In GRE
imaging sequence a slice selection RF pulse is applied to
the imaged object. This RF pulse typically produces a
rotation angle between 10 and 90 called flip angle. A
refocusing gradient (read out direction) is employed that
eliminates the original 180° pulse of SE and later recalls it
at the echo time TE (hence the name gradient recalled
echo or GRE (Fig. 10.7).
Gradient reversal echo
Fig. 10.7: Gradient reversal echo pulse diagram
Fast low angle shot (FLASH) and gradient recalled

acquisition study state (GRASS) are examples of gradient
echo technique. The shortening of TR values from seconds
in conventional SE or IR sequences to tens of milliseconds
in gradient echo sequences greatly reduces scan times.
The table below contains important acronyms used by
major manufacturers.
Table 10.1: Important acronyms
GE SIEMENS
GRASS FISP
SPGR FLASH
SSFP PSIF
FSPGR turbo-FLASH
GRASS : Gradient recalled acquisition in the
steady state
SPGR : Spoiled GRASS
SSFP : Steady state free precession
FSPGR : Fast SPGR
FISP : Fast imaging with steady state pre-
cession
FLASH : Fast low angle shot
PSIF : Fast imaging with steady state preces-
sion (opposite of FISP)
Turbo-FLASH : (Turbo is used in place of Fast)
GRASS yields more T2* weighting images.
In SPGR, a long TR and a large a yield T1 weighting
image. The disadvantages of SPGR include increased
dephasing caused by inhomogeneity, increased magnetic
susceptibility and chemical shift artifacts.
SSFP images yield heavily T2 (not T2*) weighted images
with increased scan speed without the use of dedicated
excitation and rephasing pulses. The advantages include
decreased dephasing caused by inhomogeneity, decreased
magnetic susceptibility and chemical shift artifacts. The
disadvantages are decreased SNR and increased sensitivity
to nonstationary tissue.
Multiplanar Techniques: The GRASS and SPGR sequen-
ces can be performed using a multiplanar technique by
selecting a long TR. These are called MPGR (multiplanar
gradient recalled, MPSPGR. A small α yields PD weighted
while a large α yields T1 weighting. Advantages of multi-
planar technique include increased SNR, mutiplanar scan-
ning, multiecho imaging and reduces saturation effects.
Fast Gradient Echo Technique: The GRE techniques are
generally faster than SE techniques. There are additional
methods to increase the speed of scanning. These methods
are called Fast GRASS, Fast SPGR Fast multiplanar
GRASS, Fast multiplanar spoiled GRASS, etc. Ultrafast
TRs and TEs are employed to reduce the sequence time.
This is achieved by fractional echo, fractional RF, fractional
NEX, and reduction in the sampling time (increasing the
band width).
Advantages of Fast GRE Techniques

1. Single breath hold techniques in the abdomen.
2. Imaging a joint in motion.
3. Cine imaging of the heart.
4. Temporal scanning of the same slices after contrast
administration.
5. Perfusion imaging.
Disadvantages of Fast GRE

1. Decreased SNR
2. Increased chemical shift artifacts.
FLOW IMAGING
GRE scanning performs one slice at a time except in multi-
planar imaging. Each slice is an entry slice. Consequently,
flow related enhancement (FRE) applies to every single
slice, and vessels appear bright on GRE images. No
saturated flowing protons enter the slice, so that flipping
these protons yields maximum signal. This is the basic
concept behind 2D or 3D Time of Flight (TOF) MR
angiography.
RAPID SCAN TECHNIQUES
As a result of ongoing technical developments rapid scan
techniques have established themselves as indispensable
for state of the art clinical magnetic resonance imaging. A
ten minute scan protocol is becoming popular for most of
the routine imaging. Rapid MR techniques are based on
either gradient recalled or RF refocusing.
Radiofrequency Refocussed Technique

This achieves speed by sampling multiple lines of K space
per TR. Fast spin echo (FSE), Turbo spin echo (TSE) and
Half Fourier Single Shot Turbo Spin Echo (HASTE) are
the examples of this technique.
FAST SPIN ECHO

In fast spin echo (FSE) long train of RF focusing pulses
can be applied to create multiple SE’s after an initial RF
excitation pulse, then the individual echoes may be differ-
ently phase encoded to produce a data set for image
reconstruction. This principle underlines the RARE (rapid
acquisition with relaxation enhancement) imaging techni-
que.
Fast spin echo (FSE) is one of the most important recent
advances in MRI. It was originally called RARE. The
primary advantages of FSE is speed without the usual
concomitant loss of signal to noise ratio (Fig. 10.8).
The essential difference between convential spin echo
(CSE) and FSE is that in CSE all echoes in a train are
preceded by a single value of phase encoding gradient
whereas in FSE each echo in a train is preceded by different
value of the phase encoding gradient (Fig. 10.9).
Fig. 10.8: Fast spin echo pulse sequence diagram
Fig. 10.9: Fast spin echo T2 weighted image

For an eight echo train length the scan time is reduced
by a factor of 8. FSE can use a higher TR, larger matrix
and is more advantageous than CSE and still do it in much
reduced times (Fig. 10.10).
Fast spin echo advantages include acquisition of true T2
weighted images and the possibility of thin section T2
weighted three-dimensional imaging. FSE is relatively
insensitive to magnetic susceptibility effects hence artifacts
produced by metallic objects are reduced. However, small
hemorrhagic or calcified lesions may be missed. Fat is bright
on proton density and T2 weighted images on FSE
compared to CSE.
Subtle differences between FSE and CSE imaging include
failure to detect small objects with T2 values close to
background, minor changes in the size of small objects, and
decreased signal in some stationary tissues related to
increased magnetization tranfer and saturation effects in
fast SE images. The protein bound water is relatively
suppressed on FSE images compared with CSE images.
Fig. 10.10: Fast spin echo T2 weighted image

This effect is most noticeable in the spine where normally
hydrated disks are bright on T2 weighted CSE images but
some what darker on FSE images.
In general FSE sequences have replaced CSE sequences
for many clinical applications because they provide a
comparable signal to noise ratio (SNR) and image contrast
at significantly shorter scan times.
Half Fourier imaging uses only about half the number
of phase encoding steps of conventional image matrix. For
example, a K-space consists of 256 horizontal lines with
256 data samples with a spatial resolution of 256 * 256
pixels. Imaging times may be cut by a factor of 2 if only
half of the data in K-space is acquired saving 50 percent in
imaging time.
ECHOPLANAR IMAGING
Echoplanar imaging fills K-space after a single RF pulse
in a single measurement or shot.
A magnetic resonance image is referred to as image
space. Its Fourier transform is referred to as K-space. In
magnetic resonance imaging K-space is equivalent to the
space defined by the frequency and phase encoding
directions. Conventional imaging sequences record one line
of K-space in each encoding step. Since one phase encoding
step occurs with each TR time, the time required to produce
an image is determined by the product of TR and the number
of phase encoding steps. Echoplanar imaging measures all
lines of K-space in a single TR period.
There is a 90° slice selection RF pulse which is applied
in conjunction with a slice selection gradient. There is an
initial phase encoding gradient pulse. Next there is 180°
pulse. There are 128 or 256 phase and frequency encoding
gradients when the echo is recorded. The rate at which K-
space is reversed is rapid (Fig. 10.11).
The greatest application of echoplanar imaging appears
to be in the area of functional MRI of the brain. During
brain activity there is a rapid momentary increase in the
blood flow to the specific thought center in the brain.
Similarly, movement of index finger causes rapid momen-
tary increase in the circulation of the specific part of the
brain controlling the movement of the finger. The increase
in oxygen (which is paramagnetic) affects the T1 and T2
of the local brain tissues. The difference in T1 and T2
relative to surrounding tissue causes a contrast between
the tissues. This is known as BOLD (blood oxygen level
detection) technique (Fig. 10.12).
Fig. 10.11: Spin echo- EPI pulse sequence diagram

Fig. 10.12: GRE-EPI pulse sequence diagram
ECHOPLANAR DIFFUSION IMAGING

Diffusion imaging is accomplished by adding diffusion
sensitizing gradient pulses on either side of the 180° of a
SE sequence either CSE or SE-EPI.
Diffusion is the process of random thermal motion of
molecules (Brownian motion). These motions occur at
microscopic scale (i.e. on the order of tenths or hundredths
of millimeter per second). To enable MR acquisition to
detect these small motions, gradients applied across the
imaging field gradients, experience a phase change. These
phase changes either combine to retain signal, or combine
to reduce signal. Signal loss is related to the product of the
apparent diffusion coefficient of the tissue and b value of
the sequence, which is determined by the amplitude, duration
and spacing of the additional gradient pulses (Fig. 10.13).
Fig. 10.13: Spin echo EPI diffusion
In echoplanar diffusion imaging of the brain two or more

acquisitions must be made. First a base line SE-EPI image
is made with the diffusion sensitizing gradient off (b=0)
establishing a reference image. Next a diffusion sensitized
image is taken using a b value in the range of 1000 sec/
mm2. Typically the following four sequences are required:
b=0 baseline image and then b=1000 images sensitizing
along each of the three (x, y and z) axes. In each diffusion
image white matter tracts running parallel to the gradients
appear dark and white matter tracts running perpendicular
to the gradients appear bright reflecting the preferred
diffusion direction of water along the axons (Fig. 10.14).
Because this bright signal can potentially simulate
pathology (i.e. ischemic lesion), lesions must be assessed
in all three diffusion images to accurately diagnose patho-
logy. Alternatively a trace image can be acquired showing
the average diffusion changes along the three axes.
Fig. 10.14: Diffusion image
ECHOPLANAR PERFUSION IMAGING

Perfusion or blood flow of the brain can be assessed with
EPI by monitoring the first pass effect of gadolinium
contrast. T2 weighted EPI sequences can be used to
measure susceptibility changes caused by the passage of
the paramagnetic contrast agent. Large macromolecules
of gadolinium do not cross the blood brain barrier. As this
bolus traverses vascular bed it changes the intravascular
signal and dephases spins outside the lumen in the nearby
tissues. This long range intravascular phenomenon has the
beneficial effect of increasing the potential volume of tissue
signal changes.
The transient drop in the signal intensity caused by the
passage of the gadolinium bolus provides indirect evidence
of the state of perfusion of the tissue. From these data,
relative cerebral blood volume (rCBV) and mean transit
time (MTT) maps can be generated. The sensitivity to
perfusion in vessels of a particular site depends on the
specific EPI sequence used. Performing echoplanar
perfusion imaging with a spin echo (SE-EPI) provides
sensitivity to the microcirculation alone and a GRE-EPI
sequence provides sensitivity to both the microcirculation
and the capillary circulation (Fig. 10.15).
MAGNETIZATION TRANSFER
CONTRAST (MTC)
The main use of MTC is to extract more information from
relaxation of biological tissues. In most biological tissue,
there is cross relaxation between the free proton pool in
protons in moving water (Hf) and the restricted proton pool
in protons in stationary water or tissues such as macro-
molecues (Hr).
Only protons that have a sufficiently long T2 time (Hf)
can be imaged. Typically, these protons are found in moving
water. Other protons (Hr) lose their transverse magneti-
zation decay before their signal is collected.
Fig. 10.15: Echoplanar perfusion graph

Magnetization is constantly being transferred between
Hf and Hr and this will result in a change to the T1 values
of Hf. If the Hr pool is saturated by off resonance irradiation,
this will reduce its magnetization to zero. This causes loss
of signal intensity from the Hf pool at the interface between
the two pools. Due to the very short T2 value of the Hr
pool, the behavior of the magnetization during the RF pulse
is dominated by relaxation. Hr makes up only around 10
percent of the total proton pool in muscle tissue and
therefore continuous or repeated saturation is needed to
create sufficient MTC in the Hf pool. MTC is particularly
good at increasing the T1 contrast between normal and
diseased tissue and is noted as being particularly useful in
MR angiography.
MTC is proposed by most MRI manufacturers as a
standard push button technique. It has been widely applied
in clinical routines. Main applications are the suppression
of background tissue in MR angiography, and synergetic
enhancement of contrast in the T2 weighted or contrast
agent enhanced scans.
However, only recently has the value of MTC for
assessing tissue diseases by quantitative indexes started to
emerge.
MAGNETIC RESONANCE OF
ANGIOGRAPHY (MRA)
Magnetic resonance angiography is a noninvasive method
of study of blood vessels. Fast imaging techniques like
gradient echo are used for MRA. There are two major ways
of performing MRA (i) Time of Flight (TOF), (ii) Phase
Contrast (PC).
TIME OF FLIGHT
In TOF angiography low flip angle is used and 180° pulse
is eliminated. Stationary tissue is exposed to multiple RF
pulses and is fully saturated. Unsaturated blood entering
this slice gives high signal. Obviously, maximum enhance-
ment will be obtained when the imaging plane is at right
angles to the direction of blood flow (Figs 10.16 and 10.17).
Fig. 10.16: MR angiography

TOF technique. Circle of
Willis
Fig. 10.17: MR angiography TOF

technique extracranial vessels
PHASE CONTRAST
PC MRA is based on the principle that flow of blood along

a magnetic field gradient causes a phase shift in the MR
signal. Pairs of images are obtained using different gradient
polarities. One image of a pair will be obtained with a
gradient of positive polarity to induce positive flow related
phase shift, whilst for the other image a gradient of negative
polarity is used to induce a negative flow related phase
shift. These images are subtracted to delete stationary tissue
so that only blood vessels are seen. Phase contrast sequen-
ces have to be encoded for specific peak velocities. Unlike
multiple projection images on TOF MRA, in PC MRA a
single collapsed image available from the subtracted
phase,forms the source image (Fig. 10.18).
Fig. 10.18: MR venography PC technique dural sinuses

Table 10.2: TOF versus phase contrast
TOF PC
Images Multiple projection Usually single collapsed

Bright Met Hb Simulates flow Image subtracted
Slice thickness 1-2 mm 3-5 mm
Resolution Good Fair
Flow sensitivity Fair Good
Time 3-4 min 7-8 min
Table 10.3: MR angiography clinical application
Method Anatomy
1. 2 D TOF (Conventional carotid artery overview,

venous flow gradient echo)
2. 3 D TOF with MOTSA Carotid artery overview with optimal
visualization of stenosis. Combined
with contrast for intracranial aneurysm
3. 3 D TOF with MOTSA Cerebral arteries
and MTC dural sinus
(< 20 cm/s)
4. 2 D PCA Vertebral basilar system (30 cm/s)
5. 3 D PCA Carotid arteries (30-60 cm/s)
MR SPECTROSCOPY
MR Spectroscopy (MRS) relies on information provided
by chemical shifts. The magnetic field around nuclei in a
chemically complex environment is altered due to shielding
currents that are associated with the electron distribution
around adjacent atoms. These alterations in the magnetic
field cause small changes in the resonance frequency which
are known as chemical shifts and these allow a distinction
to be made between the small nuclei in different chemical
environment.
MR spectroscopy may be obtained with many clinical
1.5 T MR units. Adequate MR spectra may be obtained in
periods of time as short as 10 to 15 minutes. Therefore,
they may be added to routine MR imaging studies. MR
spectroscopy provides greater information concerning tissue
characterization than what is possible with MR imaging
studies alone.
31P MR spectroscopy can be utilized to measure the
concentration of ATP, phosphocreatine and inorganic
phosphate as well as the intracellular pH in muscle. The
metabolites of interest in brain include N-acetyle aspartate
(NAA), choline containing compounds (Cho) as well as
creatine and phosphocreatine (Cr). The NAA serves as a
marker of neurons. In a variety of disorders it may be
decreased where there is little or no change on the MR
image (Fig. 10.19).
Proton spectroscopy appears complementary to MR
imaging which generally of value in acute and subacute
disease. Proton MR spectroscopy readily distinguishes
normal brain from tissues from astrocytoma. However,
TE 35 TE 288
Fig. 10.19: MR spectroscopy
proton MR spectroscopy may not be able to distinguish
between different histologic grades of malignancy in
astrocytoma. MR spectroscopy may be useful in difficult
cases to differentiate tumors. Proton MR spectroscopy
shows elevation of lactate in patients who have received
40 Gy or more to the brain. It also demonstrates marked
metabolic alterations in patients with mild AIDS related
dementia. Spectroscopy is also helpful in degenerative
disorders like Alzheimer and Parkinson disease, hepatic
encephalopathy, cerebral ischaemia, etc. some innovative
applications include measurment of psychoactive drugs,
neurofibromatosis type 1, cerebral heterotopias, multiple
sclerosis, etc.
CONCLUSIONS
Rapid scanning techniques have established themselves as
indispensable for state-of art clinical magnetic resonance
imaging. A major breakthrough came with introduction of
low flip angle gradient echo imaging which is the basis for
most recent advances. Now we have magnets with
high field strengths (1.5T – 3T) high gradient strength
25-40 mt/m which enables far better contrast functional
imaging. MR spectroscopy is a new development and its
application in metabolic and functional imaging is rapidly
evolving. Recent advances in MRI include new pulse
sequences, rapid scanning, functional imaging, angio-
graphy and spectroscopy.
Eleven
Practical Imaging
IMAGE PRESENTATION
Each displayed image will have two orientation labels, one
at the top, and the other at the left of the image. Images
from the three standard orthogonal planes are displayed in
the following manner in the absence of a scout:
S Sagittal Images: These are dis-
played with the patient’s anterior
to the left (marked A), and the
A
superior portion of the image
(marked S) at the top of the screen.
Slices are numbered and displayed
sequentially, beginning on the
Fig. 11.1 patient’s right and proceeding
leftward.
S
Coronal Images: These are dis-
S
played with the patient’s right side
(marked R) on the left side of the
R
screen. The superior portion of the
image is at the top of the screen
(marked S). The slices are num-
Fig. 11.2 bered and displayed sequentially
from posterior to anterior.
Practical Imaging 161
A
Fig. 11.3
Axial Images: These are displayed with the patient’s right

side (marked R) on the left side of the screen and the
anterior portion of the image at the top of the screen
(marked A). Slices are numbered and displayed from
inferior to superior.
SCOUT SLICE PLACEMENT AND ANGLES
Using an Allows only a Allows only a Allows obliquing

axial scout sagittal image coronal image for rotation
Using an Allows only Allows obliquing Allows only

sagittal scout an axial image for rotation coronal image
Using a coronal Allows only a Allows obliquing Allows only an

scout sagittal image for rotation axial image
IMAGE REVIEW
Identifying Image Labels
Fig. 11.16
Right NP : No phase wrap

VB : Variable bandwidth
Signa 1.5 T : Equipment name
Se : Series number
Im : Image Nnmber Left
OAX : Plane sequence NIMS : Institution name and
ET : Echo train length Hyderabad place
R/L : Side orientation marks
S/I : Top orientation marks
: Patient name
TR : Repetition time
: Gender, age and IP
TE : Echo time number
31.2 : Band width : Date
Head : Coil name : Time
FOV : Field of view Mag : Magnification
: Thickness and spacing FL : Filter
: No. of slice and ROT : Rotation
acquisition time W : Window width
: Frequency and phase L : Window level
encoding matrix ν : Frequency encoding
N ex : Number of excitations : Measurement scale in
F Cf : Flow compensation mm
ANATOMICAL REFERENCE POINTS
The following anatomical reference points are provided
as a general guideline for patient positioning. Internal
structures of the body may be located at different positions
depending on patient size. When you are not sure of the
exact location of the area of interest, use the standard
protocols provided at your site, and perform a scout scan.
Head protocol—align red cross with orbital/meatal line
Breast protocol—align red cross with nipple line
Chest protocol—align red cross with mid-sternum
Abdomen protocol—align red cross with twelfth rib
Pelvic scan—align red cross with anterior superior iliac
spine (ASIS)
The chart below provides reference points for common
anatomical structures.
Anatomical level Reference points

C-1 Mastoid Tip (most inferior level of skull).
Coincides with foramen magnum
C-3 Hyoid Bone
C-5, C-6 Thyroid Cartilage
C-7 Level of Shoulder, Vertebral Prominence
T-1 1.5 Inches(3.8 cm) superior to supra-
sternal notch
T-2, T-3 Suprasternal Notch
T-4, T-5 Sternal Angle, Second Costal Cartilage
T-7 3 inches (7.6 cm) inferior to Sternal Angle
T-9, T-10 Xiphoid Tip
L-3 Bottom of Ribs
L-3, L-4 Iliac Crest, Umbilicus
L-5, S-1 Midway between iliac crest and Anterior

Superior Iliac Supine
S-2 Anterior Superior Iliac Supine
Skull Base Mastoid Tip
Pituitary(Sella Turcica) 1.5 inches (3.8 cm) Anterior and Superior
to External Auditory Meatus
Orbits Orbital-Meatal (OM) Line
Heart(Superior Border) T-4, T-5, Sternal Angle
Heart [Inferior (Apex)] Fifth or Sixth Rib
Kidneys T-12 through L-3 (Right Kidney is higher.)
Gallbladder T-9-Xiphoid Tip
Pancreas Xiphoid Tip
Bladder Symphysis Pubis
MRI EXAMINATIONS BY
ANATOMICAL REGION
HEAD AND NECK
1. Brain
2. Temporal Lobes
3. Posterior Fossa and IAM
4. Pituitary
5. Orbits
6. T-M Joint
7. Diffusion
8. Perfusion
9. Spectroscopy
10. Functional
11. MRA-Head
12. MRV
13. MRI in Steriotaxy
14. D.B.S
15. CSF-Flow
16. CSF-Rhinorrhea
17. MRA Neck
SPINE
18. C-Spine
19. D-Spine
20. L-Spine
21. Whole Spine
CHEST AND ABDOMEN

22. Chest
23. Heart and great vessels
24. Breast
25. Brachial Plexus
26. Abdominal Angio
27. MRCP
28. MRU
29. Pelvis
30. Endorectal
UPPER EXTREMITY
31. Shoulder
32. Humerus
33. Elbow
34. Forearm
35. Wrist and Hand
LOWER EXTREMITY
36. Hips
37. Thigh
38. Knee Joint
39. Tibia and Fibula
40. Ankle
41. Vascular Imaging
HEAD AND NECK
BRAIN
Patient Position-Head coil
Patient Position-Head coil:

• Set-up the head coil
• Place the patient in the head coil
• Immobilize the patient using sponges and straps
Sagittal localizer to Sagittal localizer to Axial localizer to

obtain axial slices obtain coronal slices obtain sagittal slices
BRAIN
Indication
• Evaluation of infarction , AIDS
• Multiple sclerosis(MS), Primary tumor assessment and metastatic disease
• Unexplained neurological symptoms or deficit
Sequences
Pulse Sequence Axial T2 Axial T1 Axial T1 Sag T2 Cor T2 Axial Flair

FSE FSE SE FSE FSE
TR 4900 525 600 3650 4000 9000

TE/IR 85 Min. Min. 85 85 120/2000
ETL 16 2 — 15 15 —
Bandwidth 20.83 20.83 20.83 20.83 20.83 15.63
Nex 2 1 2 2 2 1
Slice 5 5 5 5 5 5
Gap 1.5 1.5 1.5 1 1.5 1.5
No. of Slices 20 20 20 20 20 20
Matrix Freq/Phase 256 / 256 256 / 256 512/256 256 / 256 256 / 256 256/192
Practical Imaging
FOV 24 24 24 24 24 24
SNR 100 100 100 100 100 100
Scan Time 2.02 1.44 3.54 2.18 2.00 4.12
Frequency
Direction A/P A/P A/P S/I S/I A/P
Auto Center Frequency Water Water Water Water Water Water
Flow Compensation Direction Slice — — Freq Freq Slice
Saturation I I I I I I
169
Contrast Usage: Inject Gadolinium (10 ml), if pathological conditions seen. Acquire post-contrast T1W Images in all 3 planes
TEMPORAL LOBES

Sagittal localizer to obtain coronal slices

of the hippocampus
PROTOCOL: TEMPORAL LOBES
Indication
• Diagnosis and evaluation of a lesion specifically in the temporal lobes (tumours, vascular malformation, leukodystrophies and atrophic
processes).
• Evaluation of signal change in the hippocampus and the temporal lobe.
• Measurements of the hippocampal volume (hippocampal atrophy is presently considered the most sensitive indicator of hippocampal disease).
Sequences
Pulse Sequence Axial T2 Oblique Oblique Oblique Cor

Cor T1 Cor T2 Cor-FLAIR 3DSPGR
TR 4900 400 4000 4200 30

TE/IR 85 Min 85 50/350 Min
ETL 16 2 16 12 FA-45 Deg.
Bandwidth 20.83 20.83 15.63 20.83 15.63
Nex 2 4 4 2 2
Slice 5 4 4 4 1.5
Gap 1.5 1 1 1 No. of scan locs: 28
No. of Slices 20 16 16 16 Slab 1
Practical Imaging
Matrix Freq/Phase 256/256 256/192 320/256 320/192 256/192

FOV 24 16 16 16 20
SNR 100 65 100 94 100
Scan Time 2.02 5.12 4.24 4.37 6.12
Frequency
Direction A/P S/I S/I S/I S/I
Auto Center Frequency Water Water Water Water Water
Flow Compensation Direction Slice ——- Freq Freq ——-
171
Saturation I I I I I
INTERNAL AUDITORY MEATUS
Patient Position-Head Coil

Axial localizer for coronal slices Coronal localizer for axial slices
PROTOCOL: POSTERIOR FOSSA AND INTERNAL AUDITORY MEATUS
Indication
• Symptoms that require the exclusion of an acoustic neuroma (vertigo, unilateral sensory hearing loss, tinnitus )
• Facial palsy / numbness, • Diagnosis of a posterior fossa lesion
• Hemifacial spasm, • Trigeminal neuralgia
Sequences
Pulse Sequence Axial T2 Axial T1 *Axial COR T1 Axial 3DT2 AX-T1

T1+C-FS FS-FSE
TR 4000 450 600 650 4000 450

TE/IR 85 Min Min Min 130 Min
ETL 20 —— —— 2 64 2
Bandwidth 15.63 15.63 15.63 20.83 15.63 20.83
Nex 5 3 2 4 1 4
Slice 3 3 3 3 0.8 3
Gap 0 0 0 0 LOCS per slab;30 0
No. of Slices 12 12 12 11 No. of slab 1 12
Matrix Freq/Phase 320/256 256/256 256/224 320/256 256/256 320/256
Practical Imaging
FOV 18 18 18 18 18 18
SNR 100 100 100 100 100 100
Scan Time 4.37 5.45 4.32 5.30 8.01 7.34
Frequency Direction R/L R/L A/P S/I R/L R/L
Flow Compensation Direction Slice —— —— —— Slice Slice
Saturation A,P,S,I S,I S,I FAT S,I A,P,S,I S,I FAT
Contrast Usage: Inject Gadolinium (10 ml) if pathological condition seen. Acquire post-contrast T1W images in all 3 planes
173
PITUITARY

Sagittal localizer for axial Sagittal localizer for coronal

slices slices
Coronal localizer for sagittal slices

PROTOCOL: PITUITARY
Indication
Investigation of diseases related to pituitary function (hyperprolactinaemia, Cunhing’s disease, acromegaly, hypopituitarism, diabetes insipidus,
amenorrhea)
• Hypothalamic disorders, • Visual field defect, • Pre- and postoperative assessment of pituitary adenomas
Sequences
Pulse Sequence AxialT2 COR T1 COR T2 Sag T1 Sag T1+C-fs Cor T1+C-dyn-FSE
TR 4900 450 4000 450 650 400

TE/IR 85 Min 85 Min Min-full Min
ETL 16 —- 24 —— —— 4
Bandwidth 20.83 10.42 20.83 10.42 12.50 20.83
Nex 2 3 4 3 3 1
Slice 5 3 3 3 3 3
Gap 1.5 0.3 0.3 0.3 0.3 0
No. of Slices 20 11 12 11 12 6
FOV/Phase FOV 24/ .75 18 18 18 18 20/ .75
Practical Imaging
SNR 100 100 100 100 100 100

Scan Time 2.02 4.20 3.20 4.20 6.17 0.14
Frequency Direction A/P S/I S/I S/I S/I S/I
Flow Compensation Direction Slice —— Freq —— —— ——
Saturation I I I I I,FAT S,I
Contrast Usage: Inject Gadolinium (10 ml), if pathological condition seen

Remarks: Dynamic scans should be taken after IV contrast/Coronal images should be taken first/Acquire postcontrast T1W images in all 3 planes
175
ORBITS
Patient Position-Surface Coils
• Before you bring the patient into the scan room, have the patient
remove all eye make-up.
• Position the patient supine with the head in the positioner.
• Place the chin up with the Orbital-meatal line +15 to the table top. This
position places the optic nerve perpendicular to the table
• Turn on the alignment lights. Place the sagittal light on the mid-sagittal
line of the patient’s head and the axial line to pass through both outer
canthus of the eyes.
• Place the coils parallel to the anatomy and as close as possible to the
eye without touching the patient.
Sagittal image of
the orbit and optic
nerve showing
the correct
placement of axial
oblique slices
parallel to the
optic nerve
Sagittal image Axial oblique image of the

showing orbits clearly demonstrat-
correct ing the lens of eye, the
placement of globe, the optic nerves
coronal slices and the optic chiasma
PROTOCOL: ORBITS
Indication:
• Visual disturbance
• Proptosis
• Evaluation of orbital or ocular mass lesions
Sequences
Pulse Sequence Ax T2 Ax T1 COR T2 Sag T1 Sag T2-fs Sag FATSAT T1
TR 4000 450 4000 400 4050 400

TE/IR 85 Min full 85 Min 85 Min
ETL 16 —— 16 —— 24 ——
Bandwidth 20.83 15.63 12.50 15.63 20.83 15.63
Nex 2 2 4.00 2.00 3 2
Slice 5 3 3 3 3 3
Gap 1.5 0 0 0 0 0
No. of Slices 20 12 1 12 12 12
Practical Imaging
FOV 24 16 16 16 16 16
SNR 115 100 55 100 100 100
Scan Time 2.16 3.20 3.52 3.02 1.41 6.04
Frequency
Direction A/P A/P S/I R/L S/I S/I
Flow Compensation Direction Slice —— Freq —— Freq ——
Saturation I S,I —— S,I S,I FAT S,I FAT
177
Contrast Usage: Inject Gadolinium(10 ml) ,if pathological conditions seen. Acquire post-contrast TI WI images in all 3 planes
TEMPOROMANDIBULAR JOINT
Patient Position- dual 3 inch Coil
Closed Mouth
Open Mouth (Mouth Opening Device)

Patient Position-dual 3 inch coil
perform both closed and open mouth sagittal views
R L R L
Right TM Joint Left TM Joint

Axial localizer through the TM joint showing correct placement of sagittal
oblique slices perpendicular to the Mandibular Condyles
PROTOCOL: TEMPOROMANDIBULAR JOINT
Indication
• Suspected internal meniscal derangement
Sequences
Pulse Sequence Sag T1 Sag T2 Sag T2* CorT2* Cor Sag 3D

FSE FSE GRE GRE T1 SE T2*GRE
TR 450 2600 300 350 400 29.0

TE/IR Min 85 15.0 15 Min 12.0
ETL 3 16 FA-20Deg FA-20Deg —- FA-20Deg
Bandwidth 20.83 20.83 8.93 8.93 8.93 8.93
Nex 4 4 3 3 3 2
Slice 2 2 2 2 2 1.2
Gap 0 0 0 0 0 Overlap locs;2
No. of Slices 9 9 11 11 12 Locs per slab:24
Practical Imaging
FOV 12 12 12 16 16 12
SNR 100 100 100 100 100 100
Scan Time 2.13 2.31 2.56 3.19 3.56 3.01
Frequency Direction S/I S/I S/I S/I S/I S/I
Flow Compensation Direction —- — —- —- —- —-
Saturation —- —- —- —- —- —-
179
Remarks: Inject Gadolinium (10 ml), if pathological conditions seen acquire post-contrast T1 WI images in all 3 planes
DIFFUSION

Sagittal localizer for axial slices

PROTOCOL: DIFFUSION
Indication
• Early detection of cerebral infarction
• Differentiating between arachnoid cysts versus epidermoid
• To differentiate cerebral abscess from necrotic tumor
• In the evaluation of patients with multiple sclerosis
Sequences
Pulse Sequence O-Axial T2 O-Axial FLAIR

DW-EPI DW-EPI
TR 10,000 10,000
TE/IR Minimum Minimum
ETL —- Inv.Time:2500
Bandwidth —- —-
Nex 1 1.00
Slice 5 5
Gap 0 0
No. of Slices 25 25
Matrix Freq/Phase 96/128 128/128
FOV/Phase FOV 36/0.60 36/0.60
SNR 100 100
Scan Time 0.40 2.00
Frequency Direction A/P R/L
Auto Center Frequency Water Water
Flow Compensation —- —-
Direction
Saturation I —-
Remarks: B-Value 1000

Diffusion direction: ALL
PERFUSION


PROTOCOL: PERFUSION
Indication
• For the evaluation of hyper acute stroke
• For the evaluation of brain tumors ( for tumor grading, sterotactic biopsy guidance,
distinguishing radiation necrosis from recurrent glioma and determining prognosis
and response to treatment)
• For the evaluation of epilepsy and Alzheimer’s type dementia.
Sequences
No. of Shots
Pulse Sequence O-Ax dyn EPI SE-EPI
TR 2000
TE/IR 60
ETL FA-90 Degrees
Bandwidth 62.50
Nex 1
Slice 10
Gap 0
No. of Slices 12
Matrix
Freq/Phase 96/64
FOV 30
SNR 100
Scan Time 1.20
Frequency Direction R/L
Auto Center Frequency Water
Flow Compensation Direction —-
Saturation —-
Contrast Usage: Contrast -20 ml

Remarks: All image data has to be transferred to work station for further evaluation.
4
mΙ2(4.06)
mΙ2(4.06)
Gla(3.γ)
α-Glx(3.65-3.8)
mlI1(3.56)
Gl,(3-43)
SI,(3-3.6)
cho (3.22)
3
(γ,(3.03)
NAP2(2.6)
NAA3(2.5)
βγ,a-Glx (2.05-2.5)
2
1
Chemical shifts of metabolite resonance in MR spectra of human brain
Step by Step MRI 184
N-acetylaspartate 2.02
(first peak, NAA1)
β-γ-Glutamine and glutamate 2.05-2.5
(β, γ-Glx)
(second peak, NAA2)
(third peak, NAA3)
Total creatine (Cr) 3.03
Total choline (Cho) 3.22
Scyllo-inositol (SI) 3.30
Glucose 3.43
Myo-inositol (mI) 3.5
α-Glutamine and Glutamate (α-Glx) 3.65
Practical Imaging
Second peak of glucose 3.8

Second peak of Cr 3.9
Second peak of mI 4.06
185
SPECTROSCOPY

Axial localizer for spectroscopy Spectroscopic image

PROTOCOL: SPECTROSCOPY
Indication
• In the evaluation of brain tumors, • Radiation injury, • For the evaluation of hyper acute stroke, • In cases of mesial temporal sclerosis
• In the evaluation of pediatric degenerative and metabolic disorders, • Alzheimer’s disease,
• To differentiate pyogenic abscesses from brain tumors
Sequences
Pulse Sequence Localizer for Ax probe Ax probe Ax probe AX-Probe-SV- Multi voxel
Spectroscopy SV-Press SV-Press SV-Press STEAM Axial Probe
35 TE 144TE 288TE 30TE SI Press-144TE
TR 3000 1500 1500 1500 2000 1000

TE/IR 85.0 35.0 144 288 30.0 144.0
ETL 24 —- —- —- —-
Bandwidth 20.83 —- —- —- —-
Nex 0.50 8 8 8 8 1.00
Slice/Voxel Thickness 20 20 20 20 20 10
Gap 0 —- —- —- —-
No. of Slices 9 1 1 1 1 1
Practical Imaging
Matrix Freq/Phase 256/192 1/1 1/1 1/1 —- 16/16

FOV 24 24 24 24 24 24
SNR 100 100 100 100 100 100
Scan Time 0.24 2.12 3.48 3.48 5.04 4.20
Frequency Direction A/P A/P A/P A/P A/P A/P
Flow Compensation Direction Slice —- —- —- —- —-
Saturation —— —- —- —- —- —-
187
Remarks: The study takes approximately six minutes and can be add-on to a routine brain MRI. MRS provides a brain map of chemical spectra
and biochemical information about the tissues.
FUNCTIONAL


PROTOCOL: FUNCTIONAL
Indication:
• To map sensorimotor functions in patients with a variety of brain pathology such as
tumors, arteriovenous and cavernous malformations and cortical dysplasias
• For the detection of language areas
• To map primary auditory cortex and visual cortex
Sequences
Pulse Sequence O-Axial tc-EPI Axial

GR-EPI 4 locs SE:T1
TR 3000 440
TE/IR 60 15
ETL Flip Angle:90 Deg —-
Bandwidth 62.50 15.6
Nex 1.00 2
Slice 10 10
Gap 2 0
No. of Slices 4 4
Matrix
Freq/Phase 64/64 256/224
FOV 40 40
SNR 100 100
Scan Time 6.26 3.20
Frequency
Direction } R/L A/P

Flow Compensation Direction —- —-
Saturation —- —-
Remarks: Functional imaging maps out specific regions of brain corresponding to

various functions such as motor, sensory, visual and language. This technique has an
important role to play in patients with neoplasms opting for surgery, as well as
psychiatric disorders.
MRA-HEAD

MRA 3D TOF single slab

PROTOCOL: MRA-HEAD
Indication
• Circle of Willis (stroke or TIA)
Sequences
Pulse Sequence AX 3D TOF: 1 slab AX3D TOF:4 slab
TR 36 36
TE 6.9 6.9
Flip Angle 20 Deg. 20 Deg.
Nex 1 1
Slice Thickness 1.2 1.2
Overlap Locations 12 2
Locations per slab 64 20
Matrix
Freq/Phase 256/192 256/192
FOV 20 20
SNR 100 100
Scan Time 7.25 7.05
Frequency
Direction } A/P A/P

Saturation S S
MRV

MRV 2D TOF
MRV 2D -PC (Sagittal)

Protocol: MRV-Head
Indication
• Deep venous and superficial sinus thrombosis
Sequences
Pulse Sequence Sag Cor Axial PC Cor

2D PC 2D PC 2D TOF
TR 33 33 33.0 Minimum
TE/IR — — — Minimum
Flip Angle 20 Deg. 20 Deg. 20 Deg. 15 Deg.
Bandwidth — — — 15.63
Nex 4 4 4.00 1.00
Slice Thickness 40 40 15.0 1.5
Gap 0 0 0 —
No. of Slices 1 1 5 120
Matrix Freq/Phase 256/256 256/256 256/160 256/128
FOV 24 24 22 22
SNR 100 100 100 100
Scan Time 2.15 2.15 5.19 4.54
Frequency Direction S/I S/I A/P S/I
Auto Center Water Water Water Water
Frequency }
Flow Compensation — — — —
Direction
Saturation — — — Inferior
Velocity Encoding 15.0 15.0 60.0
STERIOTACTIC BIOPSY PROCEDURE
Patient with Steriotactic Frame

• Place the patient in the head coil with stereotactic frame
Sagittal localizer for axial slices Post-contrast T1W axial image

for biopsy site
PROTOCOL: STEREOTACTIC BIOPSY
Indication
• Deep seated , small, eloquent-location of the lesion

• Diagnosis in doubt?
• When lesions are multiple and small
Sequences
Pulse Sequence AX SET1 AX SE T1

Post-contrast Post BX
TR 400 400
TE/IR 9.0 9.0
ETL —- —-
Nex 2 2
Slice 6 6
Gap 1.5 1.5
No. of Slices 16 16
FOV 26 26
SNR 105 105
Scan Time 2.40 2.40
Frequency
Direction A/P A/P
Saturation I I
Remarks:
• MR Compatible Stereotactic frame is fixed to the patients head by a surgeon.
- The biopsy site will be selected on post-contrast T1W axial image
- Post-procedure plain axial T1W image should be taken to know weather biopsy
was taken from the target side or not
• To see any postoperative hematoma formation or injury to the eloquent areas
DEEP BRAIN STIMULATION(DBS)

• Place the patient in the head coil with stereotaxy frame
Patient fixed with stereotaxy frame
Sagittal localizer for axial slices Post DBS T1 W axial

PROTOCOL: D.B.S (DEEP BRAIN STIMULATION)
Indication:
Identification of Anterior Commisure, Posterior Commisure, Sub-thalamic nucleus, palladium

and thalamic nuclei
Usually done for movement disorder (i.e., Parkinson’s disease, essential tremor, dystonia)
Sequences
Pulse Sequence Sag T1 Axial T1 Cor T2 Axial T1 FSE

SE SE SE (Post DBS)
TR 500 500 2500 525

TE/IR 10 10 90 Min
ETL —- —- —- 2
Bandwidth 15.63 20.83 15.63 20.83
Nex 2 2 1 1
Slice 3 2 3 5
Gap 1 1 0 1.5
FOV 26 26 26 24
SNR 103 105 112 100
Scan Time 4.20 3.16 16.10 1.44
Frequency Direction S/I A/P S/I A/P
Auto Center Frequency Water Water Water Water
Flow Compensation —- —- —- —-
Direction
Saturation I I I I
Remarks: -Obtain Post-procedure axial and coronal T1W images to see the correct position
of the electrodes and to detect any complication.
CSF FLOW
Patient Position-Head Coil with Peripheral Gating

Coronal localizer for sagittal slices

PROTOCOL: CSF-FLOW
Indication
• For the evaluation of normal pressure hydrocephalus (NPH)

• Evaluation of third ventriculostomy
• Evaluation of intracranial cystic or other cisternal lesions
• Evaluation of chiari 1 malformation
• Evaluation of spinal canal
(Causes of syringomyelia like arachnoiditis, intradural scarring, arachnoid cysts)
Sequences
Pulse Sequence O-Sag Cine PC Quantitative Axial

CSF Flow flow analysis T2 FSE
TR 33.0 40 4900
TE/IR —- —- 85
ETL FA:20 Deg FA:15 Deg 16
Bandwidth —- —- 20.83
Nex 2.00 1.00 2
Slice 5.00 4.00 5
Gap 0 0 1.5
No. of Slices 1 1 20
Matrix Freq/Phase 256/192 256/256 256 / 256
FOV 24 16 24
SNR 100 100 100
Scan Time 3.54 2.35 2.02
Frequency Direction S/I A/P A/P
Auto Center Frequency Water Water Water
Flow Compensation —- —- Slice
Direction
Saturation —— —— I
Remarks:
I. Retrospectively cardiac gate to 32 cine phase
II. Angle perpendicular to aqueduct (for R/O Shunt malfunction: venc=2 cm/sec)
III. Peripheral gating
PROTOCOL:
CSF-RHINORRHOEA/OTORRHOEA
Patient Position- Prone

• Place the patient prone in the head coil
Coronal localizer for sagittal Sagittal localizer to obtain coronal

slices images
(Patient prone )
PROTOCOL: CSF-RHINORRHOEA/OTORRHOEA
Indication
Post-traumatic watery discharge from nose and ears

Sequences
Heavily WI Heavily WI Heavily WI

Pulse Sequence Cor-T2 Sag-T2 Axial-T2
TR 6000 6000 6000

TE/IR 250 250 250
ETL 20 20 20
Bandwidth 15.63 15.63 15.63
Nex 3 3 3
Slice 2 2 2
Gap Interleave Interleave Interleave
Matrix Freq/Phase 256/256 256/256 256/256
FOV 30 30 30
SNR 100 100 100
Scan Time 6.12 6.12 6.12
Frequency Direction S/I S/I S/I
Flow Compensation Frequency Frequency Frequency
Direction
Saturation
MRA-NECK
Patient Position-Vascular Neck
Patient Position:
• Position the patient supine, head first .use sponges or the head
holder to support the patient’s head. Elevate the head slightly for the
best coil fit.
• Place the coil to cover the head and neck.
• Turn on the alignment lights and center the patient’s midline (nose
and sternal notch) to the sagittal light.
• Move the coil as close to the patient’s jaw as possible.
• Use sponges or cushions as needed for patient comfort.
• Landmark at the centre of the coil.
• Instruct the patient to breath evenly and minimize swallowing.
Coronal localizer for axial slices Axial slab to obtain axial slices
PROTOCOL: MRA-NECK
Indication:
• Cervical Carotid Arteries-T1A ‘S, Strokes, Dissections, Occlusions

Sequences
Pulse Sequence AX AX Coronal

2D TOF 3D TOF vasc. TOF
SPGR, pg 6 Slabs SPGR
TR Minimum 26.0 —-
TE Minimum 6.9 Minimum
ETL/Flip Angle FA-45 Deg. 20 FA-45 Deg.
Bandwidth 31.25 15.63 31.25
Nex 1.00 1.00 1.00
Slice 2.0 2.4 1.4
Gap/Overlap Locations 0 5/20 No. of
Slabs:1
No. of Slices/Slabs 101 6 Locations
per slab:44
FOV 20 20 24
SNR 100 100 100
Scan Time 20.14 5.45 0.49
Frequency Direction R/L R/L S/I
Flow Compensation —- —- —-
Direction
Saturation S S —-
> Smart Prep.

>Contrast
Remarks: Peripheral Gating

SPINE
CERVICAL SPINE
Patient position-CTL-Top
Patient Position:
• Place the coil on the magnet table and plug it in
• Place patient supine, head first. Rest the head and neck in the coil
• Position the superior end of the coil at the base of the skull. This
position should include C1 on a sagittal image so that you can count
vertebra for localization purpose.
Coronal localizer for Sagittal C-spine showing axial-

sagittal slices oblique slice positions parallel to
each disc spaces
PROTOCOL: CERVICAL SPINE
Indication
• Cervical myelopathy
• Cervical cord compression or trauma
• Assessment of extent of spinal infection or tumor
• Diagnosis of chiari malformation and cervical syrinx (total extent of syrinx must be determined. Whole spine imaging may be necessary).
• Visualization of MS plaques within the cord.
Sequences
Pulse Sequence Sag T2 Sag T1 Sag ST1R Axial T2 Axial T1 Cor T1
TR 3000 475 2700 3000 500 575

TE/IR 102 15 50/150 102 Min 13
ETL 18 2 6 16 2 2
Band width 31.25 13.89 15.63 31.25 11.36 20.83
Nex 4 3 2 4 3 2
Slice 3 3 3 4 4 3
Gap 1 1 1 3 3 1
Practical Imaging
No. of slices 11 11 11 11 11 9
FOV 24 24 24 22 22 26
SNR 100 100 85 100 100 100
Scan Time 2.18 2.14 2.58 2.30 2.26 2.25
Frequency Direction A/P S/I A/P A/P A/P S/I
Flow Compensation Direction —— —— Slice Slice —— ——
Saturation —— —— —— —— —— a
205
THORACIC SPINE
Patient Position-Phased Array Coil-CTL Mid

• Place the phased array coil on the magnet table and plug the phased
array coil port.
• Position patient supine, and either head or feet first. A feet first
position may be preferred by claustrophobic patients.
• Place arms at the sides or above the head, whichever is most
comfortable for the patient. If you’re using the gating option, place
the arms by the sides to keep good blood flow to the fingers. Attach
the P-gating device.
• Use accessories such as the knee bolster and blankets to make the
patient as comfortable as possible.
• Locate T1 through T12 on the patient and determine which coils will
best cover the whole spine (ex. CTL mid and CTL Bottom)
• Place the axial alignment light 2 cm above the xiphoid which is
approximately T7. Press landmark
• Explicitly instruct the patient not to move during the scan, e.g: don’t
shift hips or move legs.
Coronal localizer for sagittal slices Sagittal image of the dorsal spine
showing axial oblique slice posi-
tions parallel to each disk space
PROTOCOL: THORACIC SPINE
Indication
• Thoracic disc disease
• Thoracic cord compression
• Visualisation of an MS plaques in the thoracic cord
• Thoracic cord tumor
• To visualize the inferior extent of cervical syrinx
Sequences
Pulse Sequence Sag - T2 Sag T1 Sag STIR Axial-T2 Axial-T1 COR-T1
TR 3500 400‘ 3000 3000 350 500

TE/IR 102 Min 85/150 102 Min 13.0
ETL 16 —— 8 32 2 2
Bandwidth 31.25 31.25 15.63 20.83 20.83 ——
Nex 4 3 3 4 4 3
Slice 4 4 4 4 4 3
Gap 1 1 1 1 1 1
Practical Imaging
No. of Slices 11 11 10 11 11 9
FOV 36 36 36 22 22 36
SNR 100 100 100 100 100 100
Scan Time 3.51 4.35 3.42 3.24 2.34 3.14
Frequency Direction A/P A/P S/I A/P Un swap S/I
Flow Compensation Direction Freq —— —— Slice —— ——
Saturation a,p —— a,p S,I a
207
LUMBAR SPINE
Patient Position-Phased Array Coil-CTL Bottom
array coil port.
• Position patient supine and either head first.
the P-gating device. CTLBOT). Adjust the patient so that the anatomy
of interest is center over the selected coil.
• Use accessories such as the knee bolster, to flatten the lumbar
curve and bring it closer to the coil, and blankets to make the patient
as comfortable as possible.
Coronal localizer for Sagittal image of the Sagittal localizer for

sagittal slices lumbar spine showing coronal slices
axial oblique slice
prescription
PROTOCOL: LUMBAR SPINE
Indication
• Disc prolapse with cord or nerve root compression
• Spinal dysraphism to assess cord termination, syrinx, diastematomyelia
• Discitis
• Evaluation of the conus in patients with appropriate symptoms
• Arachnoiditis
• Arrange the form pads under the knees to elevate
Sequences
Pulse Sequence Sag T2 Sag T1 Sag –STIR Axial T2 Axial T1 Coronal T1
TR 3600 400 3000 3000 350 500

TE/IR 102 Min 50/150 102 Min 13
ETL 16 —— 8 12 —— 2
Bandwidth 20.83 31.25 15.63 20.83 31.25 ——
Nex 4 3 3 3 3 3
Slice thickness 4 4 4 4 4 3
Gap 1 1 1 1 1 1
Practical Imaging
No. of Slices 11 11 11 11 11 9
FOV 28 28 28 20 20 36
SNR 100 87 100 93 88 100
Scan Time 3.29 3.28 4.18 2.57 3.22 3.14
Flow Compensation Direction Slice —— —— Slice —— ——
Saturation L L —— S,I S,I a
209
WHOLE SPINE IMAGING
Patient Position-Phased Array Coil-CTL Mid
array coil port.
• Position patient supine, and either head or feet first. A feet first position
may be preferred by claustrophobic patients.
the P-gating device.
• Use accessories such as the knee bolster and blankets to make the
patient as comfortable as possible.
• Locate C1-S1 on the patient and determine which coils will best cover
the Whole spine (e.g. CTL mid and CTL Bottom)
• Explicitly instruct the patient not to move during the scan. e.g: don’t
shift hips or move legs.
Coronal localizer Sagittal spine showing axial oblique slice

for sagittal slices positions parallel to each disc spaces
PROTOCOL: WHOLE SPINE IMAGING
Indication
• Cord compression (level unknown) , due to metalistic disease or primary cord tumor
• Bone marrow screening
• Congenital abnormalities of spinal curvature (scoliosis and kyphosis)
• Evaluation of the extent of syrinx
• Heptomeningeal disease
Sequences
Pulse Sequence Sag - T2 Sag T1 Sag STIR Axial-T2 Axial-T1 COR-T1
TR 3500 400‘ 3000 3000 350 500

TE/IR 102 Min 85/150 102 Min 13.0
ETL 16 —— 8 32 2 2
Bandwidth 31.25 -31.25 15.63 20.83 20.83 ——
Nex 4 3 3 4 4 3
Slice 4 4 4 4 4 3
Gap 1 1 1 1 1 1
Practical Imaging
No. of Slices 11 11 10 11 11 9
FOV 48 48 48 22 22 36
SNR 100 100 100 100 100 100
Scan Time 3.51 4.35 3.42 3.24 2.34 3.14
Frequency Direction A/P A/P S/I A/P Un swap S/I
Flow Compensation Direction Freq —— —— Slice —— ——
Saturation a,p —— a,p S,I a
211
CHEST
CHEST
Placement of the gating leads
Patient position: Torso array coil

Place the patient supine, feet first on the table.
Coronal localizer for axial slices Coronal localizer for sagittal slices
Axial image through the ascending and

descending Aorta showing correct
placement of the first and last oblique
slices for examining the arch of aorta
PROTOCOL: CHEST
Indication
• Mediastinal mass, adenopathy

Sequences
Pulse Sequence Axial SE AXIAL FSE Oblique Oblique

Cine Coronal
T1 SE
TR —- —- 18 —-
TE/IR Minimum 14.0 Min Minimum
ETL —- 12 FA30 Deg —-
Bandwidth 15.00 20.83 15.63 15.63
Nex 4.00 4.00 2.00 4.00
Slice 10 10 10 10
Gap 2 2 2 2
FOV 32 32 32 32
SNR 100 100 100 100
Scan Time 8.54 4.54 2.36 8.54
Frequency Direction R/L R/L Unswap Unswap
Flow Compensation —- —- —- —-
Direction
Saturation S,I S,I —- —-
Remarks:
· All sequences are cardiac gated.
· Set TR to 80% of R-R Interval for T1 weighted image, trigger every second or third
R wave for T2 weighting
HEART AND GREAT VESSELS
Placement of the gating leads bellows
• Patient position-Torso array coil
• Place the patient supine, feet first on the table.
Sagittal localizer to obtain

coronal images Coronal localizer for sagittal
slices
PROTOCOL: HEART AND GREAT VESSELS
Indication
• Diagnosis and evaluation of thoracic aortic aneurysm, dissection and coarctation

• Assessment of complex congenital abnormalities of the heart and great vessels
• Diagnosis of atrial or ventricular septal defect
• Assessment of ventricular function
• Assessment of ventricular muscle mass
• Evaluation of vessel patency and thrombus
• Evaluation of valvular dysfunction
Sequences
Pulse Sequence Vasc, TOF SPGR Axial T1 Sagittal T2

FSE FSE
TR —- —- —-
TE/IR Minimum Minimum Minimum
ETL FA-45deg 18 16
Bandwidth 31.25 20.83 20.83
Nex 1 3.00 3.00
Slice 2..8 4 4
Gap 30 5 5
FOV 38 32 32
SNR 100 100 100
Scan Time 0.29 3.50 2.30
Frequency
Direction A/P R/L S/I
Flow Compensation —- —- —-
Direction
Saturation —- —- —-
Contrast Usage: 20 ml Bolus

Remarks:
• Select tracker button
• Save the series with tracker
• Smart prep
• Breath hold
• Placement of the gating leads (ECG)
BREAST
Patient Position: Breast coil
• Place the patient prone head first on the table.

• Place breast coil, cushions, and body pad with ankle pad on the
table. Position the coil with the cable end pointing towards the magnet.
• Insert the appropriate pads into the coil wells.
• Lower the patient transport to its lowest position to help the patient
position herself.
• Seat the patient on the table between the body pad and ankle support.
Patient Preparation Instructions

• Deodorant and nipple earrings may cause artifacts: have the patient
remove both if necessary.
• Have the patient change into a gown with the opening in the front.
• Apply nipple markers if requested by the Radiologist Incorrect
positioning compresses the nipple and distorts the overall breast
shape
Axial localizer for coronal slices
Axial localizer for sagittal slices

PROTOCOL: BREAST
Indication:
• Characterization of abnormalities seen on a mammogram especially , but not exclusively , in patients with previous disease
• Characterization of abnormalities in patients with very fatty breasts
• Characterization of abnormalities in patients with breast implants
Sequences
Pulse Sequence Sag FSE T2 Sag FAST STIR Sag FAST Axial-FSE T2 Axial T1 Axial T1
Water SAT STIR-FAT SAT FSE FAT SAT
TR 4200 4600 4600 4700 400 400

TE/IR 85.0 50/150 50/150 85.0 8.0 8.0
ETL 16 6 6 16 3 3
Bandwidth 20.83 15.63 15.63 20.83 31.25 31.25
Nex 4 2 2 4 4 4
Slice 5 5 5 5 4 4
Gap 1 1 1 1 1 1
Practical Imaging
No. of Slices 18 18 18 20 16 16
FOV 20 20 20 36 18 18
SNR 100 100 100 100 100 100
Scan Time 4.33 5.02 4.57 5.05 2.58 4.27
Auto Center Frequency Water Fat Fat Water Water Water
Flow Compensation Direction —- —- —- —- —- —-
Saturation S,I S,I, Water S,I S,I S,I S,I, FAT
217
BRACHIAL PLEXUS
Patient Position-CTL top
• Place the coil on the magnet table and plug it in.

• Place patient supine, head first. Rest the head and neck in the coil.
• Position the superior end of the coil at the base of the skull. This
position should include C1 on a sagittal image so that you can count
vertebra for localization purpose.
Axial localizer for Brachial

Plexus showing correct Place-
ment of the first and last slices Sagittal localizer for
of the coronal series axial slices
PROTOCOL: BRACHIAL PLEXUS
Indication
• Diagnosis and characterization of brachial plexus lesions, especially those secondary to carcinoma of the breast and the bronchus
• Thoracic outlet syndrome
• evaluation of the brachial plexus following trauma
Sequences
Pulse Sequence Cor T2 Cor T1 Cor-STR Sag T2-FSE Sag-STIR Axial T2
TR 3500 600 2700 3500 2700 3000

TE/IR 102 Min 50/150 102 50/150 102
ETL 16 2 6 16 6 16
Bandwidth 31.25 20.83 15.63 31.25 15.63 31.25
Nex 4 3 2 4 2 4
Slice 4 4 4 3 3 4
Gap 1 1 1 1 1 3
No. of Slices 14 11 10 15 11 12
Practical Imaging

FOV 32 32 32 34 24 22
SNR 100 100 106 100 100 100
Scan Time 3.51 3.53 3.57 3.51 2.58 2.30
Frequency Direction Unswap Unswap R/L Swap R/L S/I
Flow Compensation Direction Freq —- —- —- —- Slice
Saturation A,p A,P —- A,P —- —-
219
ABDOMINAL ANGIO
Placement of the respiratory compensation (RC) bellows
Patient Position- Torso array coil
• Position the patient supine, feet first

• Place the arms at the sides or overhead.
• Position comfort cushions at any pressure points, e.g. under elbows.
Coronal localizer for Sagittal localizer to obtain

axial slices coronal slices
PROTOCOL: ABDOMEN- VASCULAR IMAGING
Indication
• Preoperative assessment of abdominal aortic aneurysyms

• Demonstration of major vascular anatomy
• Evaluation of hepatic vascular anatomy prior to tumor resection
• Assessment of renal vein thrombosis
• Assessment of vasculature prior to renal transplant
Sequences
Pulse Sequence Vasc. ToF, SpGR Axial T1 Sagittal T1

FSE FSE
TR — — —
TE/IR Minimum Minimum Minimum
ETL FA-45Deg 18 16
Bandwidth 31.25 20.83 20.83
Nex 1 3 3
Slice 2.6 4 4
Gap 36 5 5
FOV/Phase FOV 48/.80 32 32
SNR 100 100 100
Scan Time 0.29 3.50 2.30
Frequency Direction A/P R/L S/I
Flow Compensation — — —
Direction
Saturation — — —
Contrast Usage: 20 ml Bolus

Remarks:
• Select tracker button
• Save the series with tracker
• Smart prep
• Breath hold
MRCP
Placement of the respiratory compensation (RC) bellows
Patient Position: Torso phased array coil
• Position the patient supine, feet first on the table.

• Place the arms at the sides or under the head.
SSFSE- single shot breath hold technique

PROTOCOL: MRCP
Indication
• For the evaluation of biliary system in cases of obstructive jaundice

• Pancreas divisum
• For the evaluation of intrahepatic biliary ducts in the postoperative conditions
• For the evaluation of pancreatic duct abnormalities
Sequences
Pulse Sequence Axial Axial Thick Slab Thin Slab Thinner Slices
SPGR T1 SSFSE T2
TR 140 1069 2045 2045 2045

TE/IR Minimum 90 Maximum Maximum Maximum
ETL 90 —- —- —- —-
Bandwidth 31.25 62.50 31.25 31.25 31.25
Nex 1 —- —- —- —-
Slice 10 8 70 40 4.0
Gap 2.0 2 0 0 0
Practical Imaging
No. of Slices 16 20 1 1 12
FOV 40 40 36 40 40
SNR 100 100 100 100 100
Scan Time 0.21 0.20 0.01 0.01 0.23
Frequency Direction R/L R/L Unswap A/P S/I
Flow Compensation Direction —- —- —- —- —-
Saturation —- —- —- —- —-
223
MRU
Placement of the RC bellows
Patient Position: Torso array coil

• Place the arms at the sides or under the head.
Axial localizer to obtain

Coronal localizer for axial slices
MRU slab
PROTOCOL: MRU
Indication
• For the evaluation of urinary tract in patients with renal failure
• For the evaluation of non-excreting kidneys in IVU
• For the evaluation of urinary obstruction
Sequences
Pulse Sequence MRU MRU MRU Axial

Thick Slab Thin Slab Thinner Slab SSFSE T2
TR 2045 2045 2045 1069

TE/IR 883 883 883 90
ETL — — — —-
Bandwidth 31.25 31.25 31.25 62.50
Nex — — — —-
Slice 70 40 4 8
Gap 0 0 0 2
Practical Imaging

FOV 40 40 40 40
SNR 100 100 100 100
Scan Time 0.01 0.01 0.39 0.20
Frequency Direction S/I Unswap S/I R/L
Flow Compensation Direction — — — —-
Saturation — — — —-
225
PELVIS
Patient Position- Pelvic Array Coil
Patient Preparation:
• An empty bladder can minimize motion artifacts from urine. However,
a full bladder can aid visualization of bladder wall anatomy and
pathology by improving definition between anatomy, (e.g. differen-
tiating prostate from bladder wall).
Patient Position:
• Position the patient supine, feet first. Place an angle sponge under
the knee for comfort.
• Place the arms at the or overhead.
• Position comfort cushions at any pressure points (e.g. under elbow)
Axial localizer for Coronal localizer for Coronal localizer for

coronal slices axial slices sagittal slices
PROTOCOL: PELVIS
Indication
• Assessment of congenital abnormalities of the urogenital tract
• Diagnosis and staging of carcinoma of the cervix
• Diagnosis of carcinoma of the uterus
• Assessment of benign uterine tumours, e.g: Leiomyoma and fibroids
• Diagnosis of carcinoma of the bladder rectum
• Evaluation of rectal fistulae especially in patients with Crohn’s disease
• Evaluation of sacral lesions.
Sequences
Pulse Sequence Sag FSE T2 Axial FSE T2 Axial SE T1 Cor FSE T2 Cor FSE IR Cor FSE T2 fat sat
TR 5000 4500 675 4650 4775 5000

TE/IR 102.0 80 Min 80 50/150 102
ETL 12 21 —- 21 6 10
Bandwidth 15.63 31.25 20.83 31.25 20.83 15.63
Nex 3 3 2 3 2 3
Slice 5 8 8 5 5 4
Gap 1 2 2 1 1 1
Practical Imaging
No. of Slices 20 20 20 20 20 20
FOV 24 38 38 38 38 24
SNR 100 100 100 100 100 100
Scan Time 5.35 3.13 4.17 3.05 5.09 5.35
Frequency Direction A/P R/L R/L S/I S/I S/I
Flow Compensation Direction —- —- —- —- Freq —
227
Saturation S,I S,I S,I S,I S,I S,I , FAT

ENDORECTAL
Patient Position- Endorectal coil

• Place the arms at the side or under the head.
• Position comfort cushions at any pressure point, e.g. under elbows.

PROTOCOL: ENDORECTAL
Indication
• Prostatic inflammation, benign hyperplasia and neoplasm
Sequences
Pulse Sequence Sag FSE T2 Axial FSE T2 Axial SE T1 Axial STIR Axial FSPGR
T1 fat sat
TR 3525 3500 500 3000 175

TE/IR 102 102 Minimum 68/150 In phase
ETL 12 12 —- 8 FA-60deg
Bandwidth 62.50 62.50 15.63 15.63 15.63
Nex 4 3 2 2 2
Slice 4 4 4 4 3
Gap 1 1 1 1 0.5
No. of Slices 20 20 19 10 30
Practical Imaging

FOV 16 16 16 16 16
SNR 100 100 100 100 100
Scan Time 5.17 3.58 3.20 2.30 4.39
Frequency Direction S/I R/L R/L A/P R/L
Flow Compensation Direction —- Slice —- —- —-
Saturation —- S,I S,I —- S,I fat
229
UPPER EXTREMITY
SHOULDER
Patient Position-Flex coil
• Position the patient supine, head first. Offset the patient left or right
and bring the shoulder as close as possible to magnet isocenter. To
help minimize motion, oblique the patient, shoulder of interest down.
• Recheck the straps to make sure they are secure, now that the patient
is lying down. Position the straps as far superior as possible to
minimize respiratory motion.
Coronal localizer for Coronal localizer for Axial localizer to obtain

sagittal slices axial slices oblique coronal slices
PROTOCOL: SHOULDER
Indication
• Diagnosis and evaluation of impingement syndrome and instability
• Sometimes useful in the evaluation of frozen shoulder syndrome
Sequences
Pulse Sequence Cor T1 Cor T2 Cor STIR-FSE Sag T1 FSE AX T1 AX T2* GRE
TR 500 3600 2600 500 500 500

TE/IR Min 85.0 42/150 Min Min 22.0
ETL —- 18 4 —- —- FA-20Dge.
Bandwidth 15.63 20.83 15.63 15.63 12.50 10.42
Nex 3 4 2 2 3 3
Slice 4 4 4 4 4 4
Gap 0 0 0 0 0 0
No. of Slices 16 14 12 12 12 12
Practical Imaging
FOV 14 14 14 14 14 12
SNR 100 100 100 100 100 100
Scan Time 6.32 3.43 4.15 3.52 6.32 5.40
Frequency Direction Unswap Uswap Unswap Unswap R/L R/L
Saturation R,I R,I R,I R,I R
Remarks: Both shoulders should be scanned for evaluation of symmetry.

231
HUMERUS
Patient Position: Extremity coil (Swimmer position)
• Position the patient prone, head first, arms at the sides

• Wrap the coil around the affected forearm with the cable end towards
the magnet
• Turn on the alignment lights and landmark to centre of coil

PROTOCOL: HUMERUS
Indication
• Visualisation of bony and soft tissue abnormalities
Sequences
Pulse Sequence O-CorT2 O-Axial T1 Cor T2* O-Cor T1 O-Axial O-Axial

FSE SE GRE SE STIR T2 FSE
TR 4000 550 550 450 2700 5075

TE/IR 85 Minimum 15 Minimum 85/150 85
ETL 16 —- FA-20Deg —- 6 16
Bandwidth 20.83 15.63 31.25 20.83 15.63 20.83
Nex 2 2 3 3.00 2 3
Slice 4 4 4 4 4 4
Gap 0 1 1 1 1 1
Practical Imaging
No. of Slices 16 16 16 16 10 16
FOV 16 16 16 16 12 16
SNR 100 100 100 100 100 100
Scan Time 1.28 4.09 6.28 5.45 2.58 4.08
Frequency Direction A/P S/I Unswap Unswap Unswap Unswap
Saturation a,p —- —- —- —- —-
233
ELBOW
• Position the patient prone, head first, arms at the sides.

the magnet.
• Do not overlap the coil, if the elbow is small, place the cushions
around the forearm to keep the elbow centered in the flex coil.
• Turn on the alignment lights and landmark to centre of coil.

PROTOCOL: ELBOW
Indication
• Visualisation of joint abnormalities
• Adjoining soft tissues(including bursa)
Sequences
Pulse Sequence Cor T2 Cor STIR CorT2* Sag T1 Sag STIR Sag T2
GRE
TR 5075 2700 500 550 2700 5075

TE/IR 85 85.0/150 15 Min 85.0/150 85
ETL 85/16 6 FA-20Deg —- 6 16
Bandwidth 20.83 15.63 31.25 15.63 15.63 20.83
Nex 3 2 3 2 2 3
Slice 4 4 4 4 4 4
Gap 1 1 1 1 1 1
No. of Slices 20 20 20 20 10 10
Practical Imaging

FOV 16 12 16 16 12 16
SNR 100 100 100 100 100 100
Scan Time 4.08 2.58 628 4.09 2.58 4.08
Frequency Direction A/P S/I Unswap S/I S/I S/I
Flow Compensation Direction —- —— —- —- —- —-
Saturation —- —- —- —- —- —-
235
FOREARM
Patient Position-Flex coils
• Position the patient supine, head first, arms at the sides.

the magnet.
• Do not overlap the coil, if the forearm is small, place the cushions
around the forearm to keep the forearm centered in the flex coil
• Turn on the alignment lights and landmark to centre of coil

PROTOCOL: FOREARM
Indication
• Visualization of bony and soft tissue abnormalities
Sequences
Pulse Sequence O-CorT2 Cor T1 O-Axial O-Axial O-Cor T2 O-Axial T2

FSE SE GRE SE STIR FSE
TR 4000 550 550 450 2700 5075

TE/IR 85 Minimum 15 Minimum 85/150 85
ETL 16 —- FA-20Deg — 6 16
Bandwidth 20.83 15.63 31.25 20.83 15.63 20.83
Nex 2 2 3 3.00 2 3
Slice 4 4 4 4 4 4
Gap 0 1 1 1 1 1
No. of Slices 16 16 16 16 10 16
Practical Imaging

FOV 16 16 16 16 12 16
SNR 100 100 100 100 100 100
Scan Time 1.28 4.09 6.28 5.45 2.58 4.08
Frequency Direction A/P S/I Unswap Unswap Unswap Unswap
Saturation a,p —- —- —- —- —-
237
WRIST AND HAND
Patient Position: Flex coil
• Place the coil on the table and plug it into the surface coil port
• Position the patient supine, arm at the side with the wrist either prone
(palm down) or lateral (thumb up).
Patient Position: 3’’ coils in a dual
• Place the wrist prone, with the carpal bones positioned in the coil
center of one coil. Place the other coil on top of the wrist and secure
it with straps.
• Do not place the two coils facing one another, rather, position them
back-to-back.
Coronal localizer for axial Axial localizer for coronal slices

slices
PROTOCOL: WRIST AND HAND
Indication
• Assessment of wrist pain of unknown origin, (tears of the triangular cartilage) osteronecrosis of the lunate, occult ganglia
• Assessment of avascular necrosis (AVN) of the scaphoid following trauma
• Diagnosis of carpal tunnel syndrome/ tenosynovitis
• Possibly valuable in early evaluation of rheumatoid arthritis
• Assessment of the scapholunate and scaphotriquetral ligament when wrist instability is suspected.
Sequences
Pulse Sequence COR T1SE O-COR T2 FSE O-COR T2*GRE Oblique STIR O-Axial T1 SE Oblique PD
TR 550 5075.0 500 3000 450 3000

TE/IR Minimum 85.0 15.0 150/50 Minimum 30.0
ETL —- 16 Flip Ang-20 deg 8 —- 7
Bandwidth 15.63 20.83 31.25 15.63 20.83 25
Nex 2 3 3 2 3 3
Slice 4 4 4 3 4 2
Gap 1.0 1 1 0 1 0.2
No. of Slices 16 20 20 11 20 20
Practical Imaging

FOV 16 16 16 12 16 10
SNR 100 100 100 100 100 100
Scan Time 4.09 4.08 6.28 2.30 5.45 4.18
Frequency Direction A/P A/P Unswap Unswap Unswap A/P
Auto Center
Frequency Water Water Water Water Water Water
Saturation I —- —- S,I —- —-
239
Remarks: Both wrists should be scanned for evaluation of symmetry.

LOWER EXTREMITY
HIPS
Patient Position-Pelvic array coil
• Place the pelvic array coil on the table.

• Place the patient supine, feet first, with the legs extended and straight.
• Place the patient’s arms at the sides or resting on the abdomen, but
not on the pelvis.
• Position comfort cushions at any pressure points.
• If necessary, use patient straps to immobilize the patient and provide
support for the arms. Tape the feet together so the legs and hips are
immobilized.
Axial localizer for Axial localizer for Coronal localizer for

coronal slices sagittal slices axial slices
PROTOCOL: HIPS
Indication
• Evaluation of unexplained hip pain mainly caused by avascular necrosis(AVN) of the femoral head
• Possibly useful in the diagnosis of labral tears
Sequences
Pulse Sequence O/Cor O/Cor O/Cor O/Cor O/AX-SET1 Axail FSE T2

FSE T2 SE T1 FAST STIR GRE T2*
TR 4825.0 525 3000 500 525 5000

TE/IR 85 Min. Full 50/150 20.0 Min. Full 102.0
ETL 16 —- 6 FA-20 deg —- 12
Bandwidth 20.83 31.25 15.63 15.63 31.25 15.63
Nex 4 3 2 3 3 3
Slice 4 4 4 4 4 5
Gap 1 1 1 1 1 1
No. of Slices 16 16 12 16 16 20
Practical Imaging

FOV 32 32 32 32 36 24
SNR 100 100 100 100 100 100
Scan Time 4.34 5.06 3.18 4.52 3.51 5.35
Frequency Direction Unswap Unswap Unswap A/P Unswap A/P
Saturation I S,I —- S,I S,I ——
241
Remarks: Both hips should be scanned for evaluation of symmetry.

THIGH
Patient Position- Body coil
• Place the patient supine, feet first.

• Place the thigh in the coil as close as possible to isocenter.
• Immobilize the thigh by sliding the small, long cushions.

PROTOCOL: THIGH
Indication
• Visualisation of joint abnormalities

• Visualisation of soft tissue abnormalities
Sequences
Pulse Sequence Cor T2 Sag T2 Sag STR O-Axial O-Axial

STIR T2 FSE
TR 4750 5075 5250 4000 5075.0

TE/IR 85 85.0 50/150 80/150 85
ETL 16 16 8 6 16
Bandwidth 20.83 20.83 15.63 15.63 20.83
Nex 3 3 2 3 3
Slice 4 4 4 4 4
Gap 1 1 1 1 1
No. of Slices 20 20 20 16 20
Practical Imaging

FOV 16 16 16 20 16
SNR 100 100 100 100 100
Scan Time 3.52 4.08 3.35 6.32 4.08
Frequency Direction S/I A/P A/P Unswap A/P
Flow Compensation Direction —— —— —— —- —-
Saturation S,I S,I S,I —- —-
243
Remarks: Both thighs should be scanned for evaluation of symmetry.

KNEE JOINT
Patient Position-Extremity coil

• Place the knee in the bottom half of the coil. Slide the coil bottom
along its base until you have the knee as close as possible to isocenter.
• Position comfort cushions at any pressure points with the opposite
knee.
• Place cushions under both feet, but don’t hyperextend the knee in
the coil.
• If you’re examining the anterior cruciate ligament, externally rotate
the knee per the radiologist’s instruction.
• Attach the top half of the coil and lock it in place. Do not pinch any
skin between the coil halves.
• Immobilize the knee by sliding the small, long cushions between the
knee and the coil.
Coronal localizer for Sagittal localizer for Coronal localizer for

sagittal slices coronal slices axial slices
PROTOCOL: KNEE
Indication
• Assessment of internal derangement of the joint (meniscal tears, cruciate ligament tears, post repair cruciate ligament tears,bursae)
• Evaluation of chondromalacia, patella and patella tracking
• Diagnosis of bone tumors and bony damage within the knee joint
• Almost all other knee disorders can also be visualized
Sequences
Pulse Sequence Sag T2 Sag T1 Sag STR Cor T2 Sag T2* GRE O.COR STIR
TR 5075 550 5250 4750 500 3000

TE/IR 85.0 Min 50/150 85 15.0 68./150
ETL 16 —— 8 16 FA:20Degrees 8
Bandwidth 20.83 15.63 15.63 20.83 31.25 15.63
Nex 3 2 2 3 3 2
Slice 4 4 4 4 4 4
Gap 1 1 1 1 1 1.5
No. of Slices 20 20 20 20 20 20
Practical Imaging
FOV 16 16 16 16 16 16
SNR 100 100 100 100 100 100
Scan Time 4.08 2.25 3.35 3.52 6.28 5.00
Frequency Direction A/P R/L A/P S/I S/I R/L
Auto Center
Frequency Water Water Water Water Water Water
Flow Compensation Direction —— —— —— —— —— ——
Saturation S,I S,I S,I S,I S,I ——
245
Remarks: Both knees should be scanned for evaluation of symmetry.

TIBIA AND FIBULA
Patient Position- Body coil

• Place the leg in the coil as close as possible to isocenter.

PROTOCOL: TIBIA AND FIBULA
Indication
• Assessment of suspected or unknown pathology of soft tissue and bone (tumours, infection)
Sequences
Pulse Sequence O-Cor T1 Cor T2 O-Ax T1 O-AxT2 O-Axial O-Axial T2*

SE FSE SE FSE STIR GRE
TR 550 4750 650 5575 5325 675

TE/IR Minimum 85.0 Minimum 85.0 50/150 15.0
ETL —- 16 —- 16 8 Flip Angle:20 Deg
Bandwidth 15.63 20.83 20.83 20.83 31.25 31.25
Nex 2 3 3 3 3 3
Slice 4 4 4 4 4 4
Gap 1 1 1 1 1 1
No. of Slices 19 20 20 20 20 20
Practical Imaging

FOV 16 16 16 16 16 16
SNR 100 100 100 100 100 100
Scan Time 4.05 3.52 5.33 4.32 8.36 8.30
Frequency Direction S/I S/I A/P A/P A/P A/P
Flow Compensation Direction —- —— —— —- —- —-
Saturation —- —- S,I S,I S,I S,I
247
Remarks: Both limbs should be scanned for evaluation of symmetry.

ANKLE
Patient Position- Extremity coil

• Place the patient supine, feet first, with both feet in the coil if possible.
If both feet don’t fit, place the opposite limb outside the coil and use
pads for comfort.
• Centre the anatomy of interest to the coil center.
• Use sponges to elevate the anatomy to isocenter and immobilize
with cushions and tape.
• Place cushions at any pressure points to increase comfort and
decrease motion.
Coronal localizer for Sagittal localizer for Sagittal localizer for

sagittal slices coronal slices axial slices
PROTOCOL: ANKLE
Indication
• Assessment of ankle pain of unknown cause • Assessment of tendonitis (especially posterior tibial)
• Exclusion of osteochondritis dessicans • Evaluation of achilles tendon rupture or tear
• Avascular necrosis of the talus • Evaluation of the ankle joint following trauma
• Visualisation of soft tissue abnormalities • Possibly useful for evaluation of lateral ligament complex
Sequences
Pulse Sequence Cor T1 Cor T2 Cor T2* Oblique Oblique Oblique

SE FSE GRE Sag T2 STIR PD
TR 550 5075 500 4300 3000 2400

TE/IR Minimum 85 15.0 100 50/150 30.0
ETL —- 16 FA-20 Deg 17 8 9
Bandwidth 15.63 20.83 31.25 20.83 15.63 25
Nex 2 3 3 4 2 4
Slice 4 4 4 3 3 3
Gap 1 1 1 0.5 0.5 0.5
Practical Imaging
No. of Slices 20 20 16 20 20 20
FOV 16 16 16 12 12 12
SNR 102 100 100 100 100 100
Scan Time 4.09 4.08 6.28 3.30 5.00 4.43
Frequency Direction S/I A/P S/I S/I S/I S/I
Saturation —- a,p —- —- —- —-
249
VASCULAR IMAGING
Patient Position: Body coil

• Place the leg in the coil as close as possible to isocenter.
• Immobilize the leg by sliding the small, long cushions.

PROTOCOL: LEG-VASCULAR IMAGING
Indication
• Evaluation of peripheral vascular disease

• Evaluation of normal vasculature (prior to coronary artery by pass surgery to
determine the optimal graft site)
Sequences
Pulse Sequence Gated TOF Gated TOF

Angiography Venography
Axial Axial
TR Minimum Minimum
TE/IR Minimum Minimum
ETL FA-60 Deg FA-60 Deg
Nex 1 1
Slice 3 3
Gap 0.5 0.5
No. of Slices 124 124
FOV 40 40/.75
SNR 100 100
Scan Time 9.19 9.19
Frequency Direction R/L R/L
Flow Compensation Direction
Saturation I S
MR IMAGES BY
ANATOMICAL REGION
ROUTINE IMAGING
• Neuro Imaging
• Neck and spine imaging
• Cardiac imaging
• Abdominal imaging
• Musculoskeletal imaging
VASCULAR IMAGING
SPECIALIZED IMAGING
• Diffusion imaging
• Perfusion imaging
• Functional imaging
• Spectroscopic imaging
• CSF flow
• Steriotactic biopsy
Routine Imaging
Fast SE T2WI Sagittal-Brain Fast SE T2WI Coronal-Brain
FSE T2WI Sagittal-Brain FSE T2W Axial-Brain
FSE T1WI Axial-Brain FLAIR Axial-Brain

Postoperative case of pilocytic astrocytoma of brainstem

extending into left thalamus with b/l subdural haemorrhage
FSE T2WI coronal-orbit

FSE T2 WI axial orbit
STIR coronal -orbit Heavily FSE T2 WI sagittal

prone-CSF rhinorrhea
3D reconstruction
Neck and Spine Imaging
FSE T2WI coronal neck FSE T2WI axial -lumbar disc

plexiform neurofibroma
FSE T2WI sagittal -cervical spine

FSE T1W I FSE T2WI STIR

Lumbar spine-sagittal images
Myelograms of DL spine Myelogram of L-spine

Cardiac Imaging
SE T1W axial -heart with SE T1W axial -heart

ECG gating Dissection of descending aorta
Axial SE T1WI-chest
Cornal SE T1WI -chest
Axial FSE T2W I-breast
Sagittal SE T1WI -chest

Abdominal Imaging
Axial SE T1WI- abdomen
Coronal fast SPGR -abdomen
Ca cervix along with fibroid uterus

sagittal FSE T2WI-pelvis
Axial STIR -abdomen
Coronal FSE T2WI -pelvis

fibroid uterus
ERCP- lower CBD stone
MRCP-postcholecystectomy CBD calculus
MR urography
Musculoskeletal Imaging
O-axial gradient shoulder O-coronal FSE T2WI -

shoulder
Coronal stir -both hip joints

juvenile chronic arthritis with
Gradient coronal -hand involvement of b/l hip joints
Gradient sagittal -ankle joint

FSE T2WI sagittal -knee joint diabetic foot
VASCULAR IMAGING
TOF acquisition of circle of Willis 3D PC intracranial angio
2D TOF-MRV SAG-2D PC-MRV

Normal MRV
SSD-MRV 2DTof-motsa (6 slab) acquisition

MRA extracranial vessels with
spinal AVM
Contrast enhanced MRA Contrast enhanced angiography

of neck vessels of aorta and its branches
Post-traumatic aortic aneurysm

39 years/male, H/O RTA 10-yr back. Incidentally detected aortic
aneurysm in 1999 at UGI endoscopy
RT. Renal artery stenosis
Contrast enhanced abdominal angiogram

AVM Thigh
30 Y/M, follow-up case of AVM RT thigh—post-embolisation
TOF acquisition with ECG gating of

ARM -without contrast
SPECIALIZED IMAGING
Diffusion Imaging
T2WI
DWI
Acute PCA territory stroke
42 M, with suspected posterior circulation stroke
Perfusion Imaging
Normal
Abnormal
Functional Imaging
Localisation of speech cortex

young adult with glioma. lt parietal cortex
functional MRI-preop
Localisation of speech cortex

functional MR - postop
Spectroscopic Imaging
Cor FSEIR MRS

Mesial temporal sclerosis
22 M, H/O seizures since 5-yr on antiepileptic medication
CEMR-T1WI MRS
Tuberculoma
Multi voxel-spectroscopy
CSF Flow
CSF flow
Steriotactic Biopsy
Steriotaxic biopsy
Deep brain stimulation (DBS)

Abbreviations
2DFT : Two-Dimensional Fourier Transformation

3-D : Three Dimensional
A : Anterior
AAA : Abdominal Aortic Aneurysm
ACA : Anterior Cerebral Artery
ACM : Arnold-Chiari Malformation
ACQ : Acquisition
A/P : Anterior/Posterior
AP : Anterioposterior
AP : Array Processor
AVM : Arteriovenous Malformation
AVN : Avascular Necrosis
BOLD : Blood Oxygenation Level Dependent
CAD : Coronary Artery Disease
CBD : Common Bile Duct
CBF : Cerebral Blood Flow
CDJ : Cervico Dorsal Spine Junction
CF : Center Frequency
CHA : Common Hepatic Artery
Chem Sat : Chemical Shift Saturation
CHO : Choline
CM : Contrast Medium
CN Ratio : Contrast to Noise Ratio
CNS : Central Nervous System
COPD : Chronic Obstructive Pulmonary Disease
CR : Creatinine
CSE : Conventional Spin Echo
CSF : Cerebro Spinal Fluid
CSVT : Cortical Sinus Venous Thrombosis
CVA : Cerebro Vascular Accident
CVJ : Cranio Vertebral Junction
CXR : Chest X-Ray
Db : Decibels
DICOM : Digital Imaging and Communications in
Medicine
DLJ : Dorso Lumbar Junction
DM : Diabetes Mellitus
DSA : Digital Subtraction Angiography
DVT : Deep Vein Thrombosis
EAM : External Auditory Meatus
ECG : Electro Cardiogram Gating
EDH : Extra Dural Hematoma
EHBO : Extra Hepatic Biliary Obstruction
EPI : Echo Planar Imaging
ETL : Echo Train Length
FA : Flip Angle
Abbreviations 275
FAT : Fat
FC : Flow Compensation
FDD : Floppy Disk Drive
F/F : Feet First
FFE : Fast Field Echo
FID : Free Induction Decay
FOV : Field of View
FSE : Fast Spin Echo
GA : General Anaesthesia
GB : Gall Bladder
gd : gadolinium
GIT : Genito Intestinal Tract
GRASS : Gradient Recalled Acquisition the
Steady State
GRE : Gradient Recalled Echo
HASTE : Half Fourier Acquisition Single Shot
Turbo Spin Echo
HDD : Hard Disk Drive
H/F : Head First
HNR : Head and Neck Region
HTN : Hyper Tension
I : Inferior
IAC : Internal Auditory Canal
IAM : Internal Auditory Meatus
ICA : Internal Carotid Artery
IHBC : Intra Hepatic Biliary Canaliculi
IHBD : Intra Hepatic Biliary Dilatation
IHBO : Intra Hepatic Biliary Obstruction
IOML : Infra Orbito Meatal Line
IRFSE : Inversion Recovery Fast Spin Echo
IV : Intravenous
IVC : Inferior Vena Cava
IVD : Inter Vertebral Disc
IVU : Intra Venous Urogram
L : Left
LAT : Lateral
LN : Lymph Node
LSJ : Lumbo Sacral Spine Junction
MCA : Middle Cerebral Artery
ME : Multi Echo
Min- : Minimum
Min-IP : Minimum Intensity Projection
MIP : Maximal Intensity Projection
mm : millimeter
MOD : Magneto Optical Disc
MOTSA : Multiple Overlapping Thin Section
Angiography
MPR : Multi Planar Reconstruction
MR : Magnetic Resonance
MRCP : Magnetic Resonance Cholangio
Pancreotography
MRI : Magnetic Resonance Imaging
MRS : MR Spectroscopy
MRU : Magnetic Resonance Urography
Abbreviations 277
MS : Milli Seconds
MS : Multiple Sclerosis
MSK : Musculo Skeletal
MTC : Magnetization Transfer Contrast
MV : Multi Voxel
NAA : N-Acetylaspartate
Nex : Number of Excitations
NMR : Nuclear Magnetic Resonance
NMV : Net Magnetization Vector
NP : Number of Phase Encodings
NPW : No. Phase Wrap
NS : Number of Slice Encodings
NSA : Number of Signal Averaged
OC : Operators Console
OML : Orbito Meatal Line
OPLL : Ossification of Posterior Longitudinal
Ligament
P : Posterior
PC : Phase Contrast
PCA : Phase Contrast Angiography
PCA : Posterior Cerebral Artery
PCA : Posterior Communicating Artery
PD : Proton Density
PE : Pulmonary Embolism
Pe-gating : Peripheral Gating
PIVD : Protruded Inter Vertebral Disk
PNS : Para Nasal Sinus
PO : Postoperative
PPM : Parts Per Million
Pr Inj. : Pressure Injector
PRESS : Point Resolved Spectroscopy
Probe : Proton Brain Examination
PS : Partial-Saturation
PS : Pulse Sequence
PSD : Phase Sensitive Detection
PUJ : Pelvi Ureteric Junction
R : Right
RAT : Renal Artery Thrombosis
RC : Respiratory Compensation
RCBV : Regional Cerebral Blood Volume
RCC : Renal Cell Carcinoma
Reconstr : Reconstruction
Ref : Reference
REST : Regional Saturation Technique
RF : Radio Frequency
R/L : Right/Left
R/O : Rule Out
ROI : Region of Interest
RR : R to R Interval
RT : Rectangular Field of View
RVT : Renal Vein Thrombosis
S : Superior
SAH : Subarachnoid Hemorrhage
SAR : Specific Absorption Rate
Abbreviations 279
SAT : Pre Saturation Pulse
SCJ : Sterno Clavicular Joint
SCM : System Control Module
SDH : Sub Dural Hematoma
SE : Spin-Echo Pulse Sequence
Sec. : Second
S/I : Superior/Inferior
SL No. : Slice Number
SL Thick : Slice Thickness
SNR : Signal-to-Noise Ratio
SOL : Space Occupying Lesion
SP : Spine
SPGR : Spoiled GRASS
SR : Saturation-Recovery Pulse Sequence
SS FP : Steady State Free Precession
SS FSE : Signal Shot Fast Spin Echo
SSD : Shaded Surface Display
STIR : Short TI Inversion Recovery Pulse
Sequence
SV : Single Voxel
SVC : Superior Vena Cava
T1 : Longitudinal Relaxation Time
T2 : Transverse Relaxation Time
T2* : The Time Constant of the FID Signal
TB : Temporal Bone
TBM : Tuberculous Meningitis
TD : Delay Time
TE : Time Echo
TI : Inversion Time
TIA : Transient Ischemic Attack
TMJ : Temporomandibular Joint
TOF : Time of Flight
TOPO : Topogram, Scanogram, Scout View,
Pilot, Localizer
TPA : Tissue Plasminogen Activator
TR : Repetition Time
TS : Time Sequence
TW : Trigger Window
VB : Variable Bandwidth
VENC : Velocity Encoding
VR : Volume Rendering
W/L : Window Level
W/W : Window Width
WI : Weighted
XYZ : The Coordinate Axes of the rotating
coordinate system
Index
A Axial oblique image 176

Axial-brain 253
Abdominal angiogram 264 Axial-lumbar disc 256
Abdominal compression 27
Abdominal MRI 87 B
adrenals 88
kidneys 87 Breath holding 27
liver 87
pancreas 88
Acute clots 81
C
Administration of contrast agent 129 Cardiac triggering 26
Adverse reactions 129 Chronic clots 83
Anatomical reference points 164 Circle of Willis 262
Appearance of blood on MR images Claustrophobia 38, 70
80
Coil 22
bright 80
Contrast agent 124, 138
dark 80
classification of 127
Artifacts 90
negative relaxation agents 127
categories 90
aliasing positive relaxation agents 127
array processing 90 history 125
chemical shift 90 ideal contrast 124
coil selection 90 mechanism of action 125
gibbs/truncation 90 Contrast enhanced angiography 263
magic angle 90 Coronal neck plexiform neurofib-
motion 90 roma 256
point 90 Coronal-brain 253
slice overlap 90 CSF pulsation 97
susceptibility 90 CSF rhinorrhea 255
zipper 90 Cysts 76
Atomic number 6
Atoms 4 D
electrons 4
neutrons 4 Deep brain stimulation 271
protons 4 Deflection forces 40
spin 5 Deoxyhemoglobin 75
Diabetic foot 261 spacing 109
Diffusion weighted imaging (DWI) two-dimensional fourier trans-
62 forms 120
Fast gradient echo technique 143
E Fast spin echo 145
Fat suppression 128
ECG gating 258 Fibroid uterus 259
Echoplanar imaging 62, 148 Flight MRA 64
echoplanar diffusion imaging 150 Flow imaging 144
echoplanar perfusion imaging 152 Functional MRI 63
Effect of relaxation time 79
T1 prolonged 79
G
T1 shortened 79
Effects of RF power 38 Gadolinium chelates 131
Electromagnetic radiation 4 Gating 26
spectrum of 4 Gliosis 76
Extracranial vessels 262 Gradient coronal hand 261
Extremities and musculoskeletal Gradients 26, 121
MRI 89 Gray-white matter 77
F H
Factors affecting the SNR 105 Hemoglobin desaturation 81
auto center frequency 117 Hepatobiliary agents 130
auto shim 116 Hydrogen atom 5
bandwidth 118
Hyperacute clots 81
contrast 116
Hypointensity 75
contrast-to-noise ratio 118
field of view 105
spatial resolution 107 I
frequency 115
image acquisition time 114 Image presentation 160
image reconstruction 121 axial images 161
matrix size 110 coronal images 160
number of signal averages 113 sagittal images 160
phase 115 Image review 163
phase correction 116 identifying image labels 163
prescan 112 Imaging process 90
scan time 112 Intensities of normal anatomical
signal-to-noise ratio 117 structures 72
slice thickness 107 high intensity 72
SNR-slice thickness 108 low intensity 73
Index 283
Intracranial angio 262 cardiac imaging 258
Inversion recovery 138 musculoskeletal imaging 261
FLAIR 140 neck and spine imaging 256
GRE technique 141 specialized imaging 266
short inversion time inversion CSF flow 270
recovery 139 diffusion imaging 266
Iron storage 83 functional imaging 268
perfusion imaging 267
L spectroscopic imaging 269
steriotactic biopsy 271
Larmor’s equation 14 vascular imaging 262
Law of quantum mechanics 11 MR signals 74
MR spectra of human brain 184
MR spectroscopy 157
M
MR urography 260
Magnetic field 16 MR venography 156
Magnetic moment 7, 8 MRCP-postcholecystectomy 260
Magnetic resonance angiography MRI examinations by anatomical
63, 131, 154 region 166
Magnetic resonance imaging 1, 70 abdominal angio 220
advantages 70 protocol 221
disadvantages 70 ankle 248
Magnetization 154 protocol 249
Magnetization transfer (MT) 128 brachial plexus 218
Magnetization transfer contrast protocol 219
63, 153 brain 169
Mesial temporal sclerosis 269 indication 169
Metabolite resonance 184 breast 216
Metallic implants 40 protocol 217
Methemoglobin 82 cervical spine 204
MR 9 protocol 205
MR active nuclei 5 chest 212
MR appearance of hemorrhage 81 protocol 213
MR examination procedure 33 CSF flow 198
identity 33 protocol 199
patient positioning 37 CSF-rhinorrhoea/otorrhoea 200
patient screening 35 protocol 201
screening prior to scanning 36 deep brain stimulation (DBS) 196
MR images by anatomical region 252 protocol 197
routine imaging 253 diffusion 180
abdominal imaging 259 protocol 181
elbow 234 steriotactic biopsy procedure 194
protocol 235 protocol 195
endorectal 228 temporal lobes 170
forearm 236 temporomandibular joint 178
head and neck 168 thigh 242
heart and great vessels 214 protocol 243
protocol 215 thoracic spine 206
hips 240 protocol 207
protocol 241 tibia and fibula 246
humerus 232 protocol 247
protocol 233 vascular imaging 250
internal auditory meatus 172 protocol 251
protocol 173 whole spine imaging 210
knee joint 244 protocol 211
protocol 245 wrist and hand 238
lumbar spine 208 protocol 239
protocol 209 MRI image 71
MRA-head 190 blood flow 71
protocol 191 blood flow 71
MRA-neck 202 proton density 71
protocol 203 T1 relaxation time 71
MRCP 222 T2 decay time 71
protocol 223 MRI of brain and spine 83
MRU 224 brain 83
protocol 225 degenerative diseases 84
MRV 192 hemorrhage-ischemic stroke
protocol 193 84
orbits 176 trauma 84
protocol 177 tumors 83
pelvis 226 spine 85
protocol 227 MRI of the pelvis 88
perfusion 182 prostatic hypertrophy 88
protocol 183 the female pelvis 88
pituitary 174 urinary bladder 88
protocol 175 MRI of the thorax 85
shoulder 230 breast, chest wall and pleura 86
protocol 231 cardiovascular and flow studies
spectroscopy 186 86
protocol 187 flow studies 86
Index 285
mediastinum and Hili 85 Pulse sequences 133
myocardium 86 gradients 135
MRI system 18 frequency encoding gradient
components of 20 136
computer system 20 phase encoding gradient 135
cooling system 20 selection gradient 135
documentation system 20 spin echo imaging 134
magnet 20 Pulse sequences 49
monitoring camera 20 gradient echo 57
power supplies 20 coherent (in phase) gradient
Multi voxel-spectroscopy 270 59
Multiplanar techniques 143 incoherent (spoiled) gradient
Myelograms 257 echo 60
inversion recovery (IR) pulse
N sequences 53
FLAIR 56
Nuclear magnetic resonance (NMR) STIR 55
1 spin echo (SE) pulse sequences
50
conventional spin echo 50
O
fast spin echo 51
Oral contrast agents 131 steady state free precession 61
Oxyhemoglobin 81 types 49
P Q
PC technique 156 Quality assurance in MRI 32
Pegating 27 Quenching 39
Perfusion imaging 128 magnet quench hazards 39
Perfusion weighted imaging (PWI) 62
Phantom 30 R
Phase contrast 156
Phase contrast MRA 64 Radiation effects 76
Phosphocreatine 158 Radiofrequency 15
Post-embolisation 265 Radiofrequency refocussed
Post-traumatic aortic aneurysm 263 technique 145
Practical imaging 160 Rapid scan techniques 145
Precession frequency 13 Renal artery stenosis 264
Production of image 68 Respiratory triggering 27
Proton spectroscopy 158 RF pulses 38
Role of MRI in diseases 68 Steriotaxic biopsy 271
Routine sequences 133 Story of MRI 1
Subacute clots 82
Swimmer position 224
S
Sagittal localizer 174, 180 T
T2 prolonged 80
Thrombosis 81
T2 shortened 79
Time of flight 155
Sagittal slices 174
Tuberculoma 269
Sagittal-brain 253
Sensitivity of MRI 69
Shielding 23 U
RF shielding 25 Ultrafast sequences 61
Shimming 25
active shimming 26
passive shimming 26 V
Slice-select 121 Vascular neck 202
Spectroscopic image 186 Vascular structures 77
Static field 17 Vectors 7

Step by Step MRI

Uploaded by

Copyright:

Available Formats

Step by Step MRI

Uploaded by

Document Information

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Step by Step MRI

Uploaded by

Copyright:

Available Formats

Step by Step

J Jagan Mohan Reddy

Step by Step MRI

It is with great pride and gratification that I pen these few

Prof Kakarla Subbarao

From the initial observation that dense material attenuates

J Jagan Mohan Reddy

For an employee whose services are needed round the clock

The story of MRI is one of a long courtship between Physics

Fig. 1.1: Dr Damadian receives the National Medal of Technology from

15, 1988. The pioneers of the newly emerged imaging modality

Fig. 1.2: Sir Peter Mansfield Fig. 1.3: Prof C Lauterbur

Fig. 2.1: Spectrum of electromagnetic radiation

Protons: The nucleus of the hydrogen atom has just one

Fig. 2.3: Various MR active nuclei with their atomic number

Fig. 2.4: The molecular structure of water (H2O)

Fig. 2.5: Hydrogen atom

The nucleus of the hydrogen proton depicting its motion

Fig. 2.7: Alignment of vectors with varying magnitudes

A vector is commonly represented by a directed line

Fig. 2.8: Alignment of hydrogen nucleus in the human body when

Fig. 2.9: Energy of the generated MR signal

The hydrogen nuclei in the patient’s body absorb its

Fig. 2.10: Resonance stimulation with oscillation induced

Fig. 2.11: The patient is placed in the

Fig. 2.12: Hydrogen protons in human body

These hydrogen protons in the human body are in a

Fig. 2.13: Precession

influence of external magnetic field (Bo) produces an

Larmor’s Equation (Table 2.1)

Table 2.1: Gyromagnetic ratio (γγ) of various nuclei

Nucleus Gyromagnetic ratio MHz/T

Table 2.2: The Larmor’s frequency at various field strengths

Field strength Frequency

The precessional frequency is often called the “Larmor’s

Loud Noise during MR Procedure

In the Magnetic Field

Fig. 2.14: Field lines in homogenous magnetic field

The field lines of homogenous field are drawn at

Fig. 3.1: Open MRI unit (Courtesy of Siemens)

Fig. 3.2: A modern MRI unit (Courtesy of GE Medical Systems)

Fig. 3.3: System of a superconductive MRI system

High-field strength systems have a better spatial reso-

The Components of the MRI System (Fig. 3.3)

Fig. 3.4A: Molecular structure of permanent magnet

Fig. 3.4B: Resistive magnet

Fig. 3.4C: Superconductive magnet

b. Resistive systems: These are electromagnets wherein the

Fig. 3.5A: Quadrature

Fig. 3.5B: Extremity

Fig. 3.5C: NV array coil

Peripheral Gating (Pegating)

Breath Holding and Abdominal Compression

Fig. 3.6: Placement of the bellows

Fig. 3.7: Placement of the gating leads

Fig. 3.8: MR compatible contrast media injector (Med Rad)

Fig. 3.10A: Phantom placed in the head coil

Fig. 3.10B: Image of DQA (daily quality assurance)

Fig. 3.10C: Image of DQA

Fig. 3.10E: Noise scan