By
Altaf Qadir Khan
Computed
Tomography(CT)Scan
 Greek word
 Tomos (slice)
 Graphein (to write)
 Large series of two-dimensional X-ray
images taken around a single axis of
rotation
 Images generated are in axial or transverse
plane
 Modern scanners allow this volume of data
to be reformatted in various planes or even
as volumetric (3D)
History
 Invented by Godfrey Newbold Hounsfield
in Hayes, England using X-rays in 1972
 “The greatest legacy” of the Beatles (the
massive profits from their record sales
enabled EMI to fund scientific research)
 Allan McLeod Cormack of Tufts University
independently invented a similar process
and they shared a Nobel Prize in medicine
in 1979
Prototype
 Took 160 parallel readings through 180
angles, each 1° apart, with each scan taking
a little over five minutes
 The images from these scans took 2.5
hours to be processed
 This scanner required the use of a water-
filled Perspex tank with a pre-shaped
rubber “head-cap” at the front, which
enclosed the patient's head
 The water-tank was used to reduce the
dynamic range of the radiation reaching
the detectors
History (Cont..)
 First EMI-Scanner was installed in Atkinson
Morley's Hospital in Wimbledon, England
 First patient brain-scan was made in 1972
 In the U.S., the first installation was at the
Mayo Clinic
 The images were relatively low resolution,
being composed of a matrix of only 80 x 80
pixels
Cranial CT
CVA & Hemorrhages
 Diagnosis of cerebrovascular accidents
and intracranial hemorrhage
 Is the most frequent reason for a "head
CT" or "CT brain
 Scanning is done with or without
intravenous contrast agents
 Does not exclude infarct in the acute
stage of a stroke, but is useful to
exclude a bleed
Tumors
 Detection of tumors
 CT scanning with IV contrast is
occasionally used but is less sensitive
than magnetic resonance imaging
ed Intra-Cranial
Pressure
 Can also be used to detect increases in
intracranial pressure
 Before lumbar puncture or to evaluate
the functioning of a
ventriculoperitoneal shunt
Vascular & BB Barrier
IV contrast helps reveal vascular
anomalies like
 Arteriovenous malformations
 Aneurysms
Lesions producing abnormalities of Blood
Brain Barrier like
 Abscesses
 Certain Tumors
 Demyelinating Lesions
Neuropsychiatric
 Widely used in neuropsychiatric
research for the calculation of
“ventricular-to-brain” ratio
Other Indications
 Setting of trauma for evaluating facial and
skull fractures.
 In the head/neck/mouth area, CT scanning
is used for
 Surgical planning for craniofacial and
dentofacial deformities
 Evaluation of cysts and some tumors of the
jaws/paranasal sinuses/nasal cavity/orbits
 Diagnosis of the causes of chronic sinusitis,
and for planning of dental implant
reconstruction.
Advantages and hazards
Of CT
Advantages over
projection Radiography
 Completely eliminates the superimposition of
images of structures outside the area of interest
 Because of the inherent high-contrast resolution
of CT, differences between tissues that differ in
physical density by less than 1% can be
distinguished
 Data from a single CT imaging procedure can be
viewed as images in the axial, coronal, or
sagittal planes, depending on the diagnostic
task
Radiation exposure
 Regarded as a moderate to high
radiation diagnostic technique
 radiation dose depends on:
 Volume scanned
 Patient build
 Number and type of scan sequences
 Desired resolution and image quality
 In children, produces increases in the
probability of lifetime cancer mortality
Adverse reactions to
contrast agents
 Certain patients may experience severe
and potentially life-threatening allergic
reactions to the contrast dye
 May induce kidney damage (contrast
nephropathy)
 Contraindicated in Moderate Renal
Failure
 However can be done in severe renal
failure requiring dialysis
Contra-Indication Of CT-
Scan
Pregnancy (involve doses of ionizing
radiation and may increase the risk of
malignancy, especially in a fetus)
Limitations Of Old CT-
Scan
 Unable to visualize structures immediately
adjacent to bone because of artifacts
 Inferior surface of frontal and temporal
lobes as well as entire posterior fossa is
not best visualized
Process Of CT
Process
 X-ray slice data is generated using an X-ray
source that rotates around the object
 X-ray sensors are positioned on the
opposite side of the circle from the X-ray
source
 Many data scans are progressively taken as
the object is gradually passed through the
framework
 They are combined together by the
mathematical procedure known as
Tomographic reconstruction
Mechanism
 An X-ray tube and detector are
physically rotated
 An electron beam is produced by X-Ray
Tube and is deflected in a hollow funnel
shaped vacuum chamber
 X-rays are generated when the beam
hits the stationary target
 The detector is also stationary
Spiral CT
 Can process not only individual cross
sections but continuously changing cross
sections as the gantry, with the object to
be imaged, is slowly and smoothly slid
through the X-ray circle.
 Their computer systems integrate the data
of the moving individual slices to generate
three dimensional volumetric information
(3D-CT scan)
3D Reconstruction
 It is possible for a software program to
build a volume by “stacking” the individual
slices one on top of the other
 A volume is built by stacking the axial slices.
 The software then cuts slices through the
volume in a different plane
Segmentation
 Procedure that removes the unwanted
structures from the image
 For Example, The bones are whiter than
the surrounding area. Blood vessels
also show brightly when injected with
iodine-based contrast agent
 By segmentation, bone can be removed
and blood vessels can be seen in detail
 The bones are
whiter than the
surrounding
 Note the blood
vessels (arrowed)
showing bright
Bone re-
constructed
in 3D
Brain
vessels
reconstruct
ed in 3D
after bone
has been
removed by
segmentati
on
Magnetic resonance
imaging
History
 Inventor of MRI was Paul Lauterbur
 Named it – “zeugmatography”
 A Greek term meaning “that which is used
for joining”
 The term referred to the interaction
between the static and the gradient
magnetic fields necessary to create an
image
 But, this name never caught on
History (Cont..)
 Later named as Nuclear Magnetic
Resonance Imaging (NMRI)
 But, the word “nuclear” has been
associated with ionizing radiation
exposure
 So, to prevent patients from making a
negative association between MRI and
ionizing radiation, the word has been
almost universally removed
Technique
 Relies on the relaxation properties of excited
hydrogen nuclei (proton) in water and lipids.
 Patient head is placed in a magnetic field that
forces protons in the brain to align
 Series of radio frequency pulses are then applied
perpendicular to this field
 Causes protons to change their alignment briefly
 Then, emit energy as they relax back to previous
alignment
 As the high-energy nuclei relax and realign they
emit energy at rates which are recorded to
provide information about the material they are
in
Parameters of MRI
 Image is created by using a selection of
image gaining parameters which include
1.The Spin proton Density – {No Relaxation
time}
2.T1 or Spin-Lattice relaxation time
3.T2 or Spin-Spin Relaxation time
 Proton density reflects the numbers of
protons present in a tissue sample
 T1 and T2 values are tissue specific
 Imaging sequences can be varied to
highlight the T1 or T2 component of
signal
T1
 The realignment of nuclear spins with the
magnetic field is termed “longitudinal
relaxation”
 Time required for a certain percentage of the
tissue's nuclei to realign in longitudinal
fashion is termed “Time 1” or T1
 Typically about 1 second
 T1 causes the nerve connections of white
matter to appear white, neurons of gray
matter to appear gray, while CSF appears
dark
T2
 T2-weighted imaging relies upon local
dephasing of spins following the application
of the transverse energy pulse
 The transverse relaxation time is termed
"Time 2" or T2
 Typically < 100 ms for tissue
 T2 causes the nerve connections of white
matter to appear dark, and the congregations
of neurons of gray matter to appear white,
while cerebrospinal fluid appears white
Commonly Used Sequences
The two most common sequences in
clinical use are
1.Inversion recovery
2.Spin-echo
Inversion recovery
 Rely heavily on the T1 component
 Produce the best gray-white resolution
 Best for visualizing anatomical detail
 Very sensitive to differences between
normal and abnormal tissue
Spin-echo
 Sequences are usually T2 weighted
 Best for detecting small focal lesions
(e.g., multiple sclerosis plaques)
 Increased signal intensity or image
brightness is associated with
 Increased proton density (i.e., water
content)
 Decreased T1 values
 Increased T2 values
Resultant Images
 Water content tends to increase with
most brain pathology, resulting in
increased T1 and T2 signals
 High T1 signals appear black (as CSF
does on a CT scan)
 High T2 signals appear white
Resultant Images
(Cont..)
 Some tissue components appear almost the
same with either T1 or T2-weighted images
 Air, calcium, and bone all have low proton
density and appear dark in either type of
image
 Fat, with its short T1 and long T2 values,
appears bright in either type of image
 What may appear at first to be skull bone
surrounding the brain on MRI is actually fat in
the bone marrow that causes a bright signal
CT Vs MRI
Advantages of CT
 Superior for detection of calcifications and
bone abnormalities (because it uses X-rays)
 Can be done rapidly to rule out
hemorrhagic conditions
 Cost is typically less than half that of MRI
 Good spatial resolution (the ability to
distinguish two structures an arbitrarily
small distance from each other as separate)
Advantages of MRI
 No ionizing radiations (Safe in pregnancy )
 Superior for detection of demyelinating
lesions, posterior fossa lesions, and small
infarctions
 Better imaging procedure in most cases to
scan for temporal-lobe lesions
 Provides comparable resolution with far
better contrast resolution (the ability to
distinguish the differences between two
arbitrarily similar but not identical tissues)
Diffusion MRI
Principal
 Diffusion MRI measures the diffusion of
water molecules in biological tissues
 Water Molecule inside the axon of a
neuron have a low probability of
crossing the myelin membrane
 Therefore the molecule will move
principally along the axis of the neural
fiber
Uses
 Enables researchers to make brain
maps of fiber directions to examine the
connectivity of different regions in the
brain
 Examine areas of neural degeneration
and demyelinaton in diseases like
Multiple Sclerosis
Uses (In Ischemic
Stroke)
 In ischemic stroke there is increase in
restriction (barriers) to water diffusion, as a
result of cytotoxic edema (cellular swelling)
 Responsible for the increase in signal
 Appears within 5-10 minutes of the onset
of stroke symptoms (as compared with CT,
which often does not detect changes of
acute infarct for up to 4-6 hours)
 Remains for up to two weeks
Uses (In Ischemic
Stroke)
 Researchers can highlight regions of
"perfusion/diffusion mismatch"
 Those regions may indicate regions
capable of salvage by reperfusion
therapy
 If available, then test of choice in
ischemic strokes
Functional MRI (fMRI)
Principal
 fMRI measures signal changes in the brain
that are due to changing neural activity
 Increased neural activity causes an
increased demand for oxygen
 Vascular system actually overcompensates
for this, increasing the amount of
oxygenated hemoglobin relative to
deoxygenated hemoglobin.
 Deoxygenated hemoglobin attenuates the
MR signal
Principal (Cont..)
 Vascular response leads to a signal
increase that is related to the neural
activity.
 This mechanism is referred to as the
BOLD (blood-oxygen-level dependent)
effect
This example of
fMRI data shows
regions of
activation including
primary visual
cortex, extrastriate
visual cortex and
lateral geniculate
body in a
comparison
between a task
involving a
complex moving
visual stimulus and
rest condition.
Contra-Indications and
side-effects of MRI
Contra-Indications
 Pacemakers – (they can cause arrhythmia)
 Other forms of medical or bio-stimulation
implants (Vagus nerve stimulators,
implanted cardio-defibrillators, insulin
pumps, cochlear implants etc.)
 Ferromagnetic foreign bodies (e.g. shell
fragments)
 Metallic implants (e.g. surgical prostheses,
aneurysm clips)
Side-Effects
 Hyperthermia – A powerful radio transmitter
is needed for excitation of proton spins. This
can heat the body significantly
 Twitching in extremities - The rapid
switching (on and off) of the magnetic field
is capable of causing nerve stimulation
 High acoustic noise – may reach 130 dB
(equivalent to a jet engine at take-off)
 Asphyxia – If Helium is not properly
dissipated through vents
Use in Pregnancy
 Safe in pregnancy
 However, as a precaution, pregnant
women undergo MRI only when
essential (particularly in the first
trimester )
 Contrast agents (like gadolinium
compounds) should be avoided
Claustrophobia
 Potentially unpleasant to lie in (which is
often a long, narrow tube even up to one
hour)
 Potential solutions include
 Visiting the scanner to see the room and
practice lying on the table
 Watching DVDs with a Head-mounted display
while in the machine
 The use of open MRI
 Use of sedation
 For the most severe cases, general anesthesia
Positron Emission
Tomography (PET Scan)
PET Scan
 It is a Nuclear medicine medical
imaging technique which produces a
three-dimensional image or map of
functional processes in the body
Principal of PET
 A short-lived radioactive tracer isotope – which
decays by emitting a positron – is injected
 There is a waiting period while the
metabolically active molecule becomes
concentrated in tissues of interest
 Then the patient is placed in the imaging
scanner
 The molecule most commonly used for this
purpose is fluorodeoxyglucose (FDG), a sugar,
for which the waiting period is typically an hour.
Procedure
 As the radioisotope undergoes positron
emission decay (also known as positive beta
decay), it emits a positron (the antimatter
counterpart of an electron)
 After travelling up to a few millimeters the
positron encounters and annihilates with an
electron
 Producing a pair of annihilation (gamma)
photons moving in almost opposite
directions
Procedure (Cont..)
 These are detected when they reach a
scintillator material in the scanning device
 Creating a burst of light which is detected
by photomultiplier tubes or silicon
avalanche photodiodes
 The technique depends on simultaneous or
coincident detection of the pair of photons
 Photons which do not arrive in pairs are
ignored
 This figure shows how during the
annihilation process two photons are
emitted in diametrically opposing directions.
 These photons are registered by the PET as
soon as they arrive at the detector ring
 After the registration, the data is forwarded
to a processing unit which decides if two
registrered events are selected as a so-
called coincidence event.
 All coincidences are fowarded to the image
processing unit where the final image data
is produced via image reconstruction
procedures
Radioisotopes used in
PET
 Typically isotopes with short half lives
such as
 11C (~20 min)
 13N (~10 min)
 15O (~2 min)
 18F (~110 min)
 Incorporated into compounds
normally used by the body such as
glucose, water or ammonia (these
compounds are known as radiotracers)
Uses
 Clinical oncology (medical imaging of
tumors and the search for metastases)
 Various types of dementias
 Tool to map normal human brain function
 Changing of regional blood flow in various
anatomic structures
Use in Neurology
 Brain is normally a rapid user of glucose
 Brain pathologies such as Alzheimer's
disease greatly decrease brain metabolism
of both glucose and oxygen in tandem
 Standard FDG-PET of the brain (which
measures regional glucose use) is used to
differentiate Alzheimer's disease from other
dementing processes, and also to make
early diagnosis of Alzheimer's disease
Pet Scan of Brain
Red areas show
more
accumulated
radioactivity
and blue areas
are portions
where low to
no activity was
accumulated
Use in Neuropsychology
 To examine links between specific
psychological processes or disorders
and brain activity
Use in psychiatry
 Numerous compounds that bind selectively to
neuro-receptors of interest in biological
psychiatry have been radiolabeled with 11C or
18F
 Radioligands that bind to dopamine receptors ,
serotonin receptors, opioid receptors (mu) and
other sites have been studied
 Studies have been performed examining the
state of these receptors in patients of
schizophrenia, substance abuse, mood
disorders and other psychiatric conditions
Safety
 PET scanning is non-invasive, but it
does involve exposure to ionizing
radiation
 So should be avoided in pregnancy
Single photon emission
computed tomography
(SPECT) Scan
Principal
 Imaging technique using gamma rays
 Image obtained by a gamma camera
image is a 2D view of 3D distribution of a
radionuclide.
 SPECT imaging is performed by using a
gamma camera to acquire 2D images from
multiple angles
 A computer is then used to apply a
tomographic reconstruction of the multiple
projections, yielding a 3-D dataset
Procedure
 The gamma camera is rotated around the
patient
 Projections are acquired at every degree
and full 360 degree
 The time taken to obtain each projection is
about 15 – 20 seconds
 Total scan time of 15-20 minutes
Uses
 Tumor imaging
 Infection (leukocyte) imaging
 Thyroid imaging
 Bone imaging
 Information about localized function in
internal organs
 Functional cardiac (diagnosis of ischemic
heart disease )
 Brain imaging (dementia)

Central Nervous System Recording Presentation

  • 1.
  • 2.
    Computed Tomography(CT)Scan  Greek word Tomos (slice)  Graphein (to write)  Large series of two-dimensional X-ray images taken around a single axis of rotation  Images generated are in axial or transverse plane  Modern scanners allow this volume of data to be reformatted in various planes or even as volumetric (3D)
  • 3.
    History  Invented byGodfrey Newbold Hounsfield in Hayes, England using X-rays in 1972  “The greatest legacy” of the Beatles (the massive profits from their record sales enabled EMI to fund scientific research)  Allan McLeod Cormack of Tufts University independently invented a similar process and they shared a Nobel Prize in medicine in 1979
  • 4.
    Prototype  Took 160parallel readings through 180 angles, each 1° apart, with each scan taking a little over five minutes  The images from these scans took 2.5 hours to be processed  This scanner required the use of a water- filled Perspex tank with a pre-shaped rubber “head-cap” at the front, which enclosed the patient's head  The water-tank was used to reduce the dynamic range of the radiation reaching the detectors
  • 6.
    History (Cont..)  FirstEMI-Scanner was installed in Atkinson Morley's Hospital in Wimbledon, England  First patient brain-scan was made in 1972  In the U.S., the first installation was at the Mayo Clinic  The images were relatively low resolution, being composed of a matrix of only 80 x 80 pixels
  • 7.
  • 8.
    CVA & Hemorrhages Diagnosis of cerebrovascular accidents and intracranial hemorrhage  Is the most frequent reason for a "head CT" or "CT brain  Scanning is done with or without intravenous contrast agents  Does not exclude infarct in the acute stage of a stroke, but is useful to exclude a bleed
  • 9.
    Tumors  Detection oftumors  CT scanning with IV contrast is occasionally used but is less sensitive than magnetic resonance imaging
  • 10.
    ed Intra-Cranial Pressure  Canalso be used to detect increases in intracranial pressure  Before lumbar puncture or to evaluate the functioning of a ventriculoperitoneal shunt
  • 11.
    Vascular & BBBarrier IV contrast helps reveal vascular anomalies like  Arteriovenous malformations  Aneurysms Lesions producing abnormalities of Blood Brain Barrier like  Abscesses  Certain Tumors  Demyelinating Lesions
  • 12.
    Neuropsychiatric  Widely usedin neuropsychiatric research for the calculation of “ventricular-to-brain” ratio
  • 13.
    Other Indications  Settingof trauma for evaluating facial and skull fractures.  In the head/neck/mouth area, CT scanning is used for  Surgical planning for craniofacial and dentofacial deformities  Evaluation of cysts and some tumors of the jaws/paranasal sinuses/nasal cavity/orbits  Diagnosis of the causes of chronic sinusitis, and for planning of dental implant reconstruction.
  • 14.
  • 15.
    Advantages over projection Radiography Completely eliminates the superimposition of images of structures outside the area of interest  Because of the inherent high-contrast resolution of CT, differences between tissues that differ in physical density by less than 1% can be distinguished  Data from a single CT imaging procedure can be viewed as images in the axial, coronal, or sagittal planes, depending on the diagnostic task
  • 16.
    Radiation exposure  Regardedas a moderate to high radiation diagnostic technique  radiation dose depends on:  Volume scanned  Patient build  Number and type of scan sequences  Desired resolution and image quality  In children, produces increases in the probability of lifetime cancer mortality
  • 17.
    Adverse reactions to contrastagents  Certain patients may experience severe and potentially life-threatening allergic reactions to the contrast dye  May induce kidney damage (contrast nephropathy)  Contraindicated in Moderate Renal Failure  However can be done in severe renal failure requiring dialysis
  • 18.
    Contra-Indication Of CT- Scan Pregnancy(involve doses of ionizing radiation and may increase the risk of malignancy, especially in a fetus)
  • 19.
    Limitations Of OldCT- Scan  Unable to visualize structures immediately adjacent to bone because of artifacts  Inferior surface of frontal and temporal lobes as well as entire posterior fossa is not best visualized
  • 20.
  • 21.
    Process  X-ray slicedata is generated using an X-ray source that rotates around the object  X-ray sensors are positioned on the opposite side of the circle from the X-ray source  Many data scans are progressively taken as the object is gradually passed through the framework  They are combined together by the mathematical procedure known as Tomographic reconstruction
  • 22.
    Mechanism  An X-raytube and detector are physically rotated  An electron beam is produced by X-Ray Tube and is deflected in a hollow funnel shaped vacuum chamber  X-rays are generated when the beam hits the stationary target  The detector is also stationary
  • 24.
    Spiral CT  Canprocess not only individual cross sections but continuously changing cross sections as the gantry, with the object to be imaged, is slowly and smoothly slid through the X-ray circle.  Their computer systems integrate the data of the moving individual slices to generate three dimensional volumetric information (3D-CT scan)
  • 26.
    3D Reconstruction  Itis possible for a software program to build a volume by “stacking” the individual slices one on top of the other  A volume is built by stacking the axial slices.  The software then cuts slices through the volume in a different plane
  • 27.
    Segmentation  Procedure thatremoves the unwanted structures from the image  For Example, The bones are whiter than the surrounding area. Blood vessels also show brightly when injected with iodine-based contrast agent  By segmentation, bone can be removed and blood vessels can be seen in detail
  • 28.
     The bonesare whiter than the surrounding  Note the blood vessels (arrowed) showing bright
  • 29.
  • 30.
    Brain vessels reconstruct ed in 3D afterbone has been removed by segmentati on
  • 31.
  • 32.
    History  Inventor ofMRI was Paul Lauterbur  Named it – “zeugmatography”  A Greek term meaning “that which is used for joining”  The term referred to the interaction between the static and the gradient magnetic fields necessary to create an image  But, this name never caught on
  • 33.
    History (Cont..)  Laternamed as Nuclear Magnetic Resonance Imaging (NMRI)  But, the word “nuclear” has been associated with ionizing radiation exposure  So, to prevent patients from making a negative association between MRI and ionizing radiation, the word has been almost universally removed
  • 34.
    Technique  Relies onthe relaxation properties of excited hydrogen nuclei (proton) in water and lipids.  Patient head is placed in a magnetic field that forces protons in the brain to align  Series of radio frequency pulses are then applied perpendicular to this field  Causes protons to change their alignment briefly  Then, emit energy as they relax back to previous alignment  As the high-energy nuclei relax and realign they emit energy at rates which are recorded to provide information about the material they are in
  • 35.
    Parameters of MRI Image is created by using a selection of image gaining parameters which include 1.The Spin proton Density – {No Relaxation time} 2.T1 or Spin-Lattice relaxation time 3.T2 or Spin-Spin Relaxation time
  • 36.
     Proton densityreflects the numbers of protons present in a tissue sample  T1 and T2 values are tissue specific  Imaging sequences can be varied to highlight the T1 or T2 component of signal
  • 37.
    T1  The realignmentof nuclear spins with the magnetic field is termed “longitudinal relaxation”  Time required for a certain percentage of the tissue's nuclei to realign in longitudinal fashion is termed “Time 1” or T1  Typically about 1 second  T1 causes the nerve connections of white matter to appear white, neurons of gray matter to appear gray, while CSF appears dark
  • 38.
    T2  T2-weighted imagingrelies upon local dephasing of spins following the application of the transverse energy pulse  The transverse relaxation time is termed "Time 2" or T2  Typically < 100 ms for tissue  T2 causes the nerve connections of white matter to appear dark, and the congregations of neurons of gray matter to appear white, while cerebrospinal fluid appears white
  • 39.
    Commonly Used Sequences Thetwo most common sequences in clinical use are 1.Inversion recovery 2.Spin-echo
  • 40.
    Inversion recovery  Relyheavily on the T1 component  Produce the best gray-white resolution  Best for visualizing anatomical detail  Very sensitive to differences between normal and abnormal tissue
  • 41.
    Spin-echo  Sequences areusually T2 weighted  Best for detecting small focal lesions (e.g., multiple sclerosis plaques)  Increased signal intensity or image brightness is associated with  Increased proton density (i.e., water content)  Decreased T1 values  Increased T2 values
  • 42.
    Resultant Images  Watercontent tends to increase with most brain pathology, resulting in increased T1 and T2 signals  High T1 signals appear black (as CSF does on a CT scan)  High T2 signals appear white
  • 43.
    Resultant Images (Cont..)  Sometissue components appear almost the same with either T1 or T2-weighted images  Air, calcium, and bone all have low proton density and appear dark in either type of image  Fat, with its short T1 and long T2 values, appears bright in either type of image  What may appear at first to be skull bone surrounding the brain on MRI is actually fat in the bone marrow that causes a bright signal
  • 44.
  • 45.
    Advantages of CT Superior for detection of calcifications and bone abnormalities (because it uses X-rays)  Can be done rapidly to rule out hemorrhagic conditions  Cost is typically less than half that of MRI  Good spatial resolution (the ability to distinguish two structures an arbitrarily small distance from each other as separate)
  • 46.
    Advantages of MRI No ionizing radiations (Safe in pregnancy )  Superior for detection of demyelinating lesions, posterior fossa lesions, and small infarctions  Better imaging procedure in most cases to scan for temporal-lobe lesions  Provides comparable resolution with far better contrast resolution (the ability to distinguish the differences between two arbitrarily similar but not identical tissues)
  • 47.
  • 48.
    Principal  Diffusion MRImeasures the diffusion of water molecules in biological tissues  Water Molecule inside the axon of a neuron have a low probability of crossing the myelin membrane  Therefore the molecule will move principally along the axis of the neural fiber
  • 49.
    Uses  Enables researchersto make brain maps of fiber directions to examine the connectivity of different regions in the brain  Examine areas of neural degeneration and demyelinaton in diseases like Multiple Sclerosis
  • 50.
    Uses (In Ischemic Stroke) In ischemic stroke there is increase in restriction (barriers) to water diffusion, as a result of cytotoxic edema (cellular swelling)  Responsible for the increase in signal  Appears within 5-10 minutes of the onset of stroke symptoms (as compared with CT, which often does not detect changes of acute infarct for up to 4-6 hours)  Remains for up to two weeks
  • 51.
    Uses (In Ischemic Stroke) Researchers can highlight regions of "perfusion/diffusion mismatch"  Those regions may indicate regions capable of salvage by reperfusion therapy  If available, then test of choice in ischemic strokes
  • 52.
  • 53.
    Principal  fMRI measuressignal changes in the brain that are due to changing neural activity  Increased neural activity causes an increased demand for oxygen  Vascular system actually overcompensates for this, increasing the amount of oxygenated hemoglobin relative to deoxygenated hemoglobin.  Deoxygenated hemoglobin attenuates the MR signal
  • 54.
    Principal (Cont..)  Vascularresponse leads to a signal increase that is related to the neural activity.  This mechanism is referred to as the BOLD (blood-oxygen-level dependent) effect
  • 55.
    This example of fMRIdata shows regions of activation including primary visual cortex, extrastriate visual cortex and lateral geniculate body in a comparison between a task involving a complex moving visual stimulus and rest condition.
  • 56.
  • 57.
    Contra-Indications  Pacemakers –(they can cause arrhythmia)  Other forms of medical or bio-stimulation implants (Vagus nerve stimulators, implanted cardio-defibrillators, insulin pumps, cochlear implants etc.)  Ferromagnetic foreign bodies (e.g. shell fragments)  Metallic implants (e.g. surgical prostheses, aneurysm clips)
  • 58.
    Side-Effects  Hyperthermia –A powerful radio transmitter is needed for excitation of proton spins. This can heat the body significantly  Twitching in extremities - The rapid switching (on and off) of the magnetic field is capable of causing nerve stimulation  High acoustic noise – may reach 130 dB (equivalent to a jet engine at take-off)  Asphyxia – If Helium is not properly dissipated through vents
  • 59.
    Use in Pregnancy Safe in pregnancy  However, as a precaution, pregnant women undergo MRI only when essential (particularly in the first trimester )  Contrast agents (like gadolinium compounds) should be avoided
  • 60.
    Claustrophobia  Potentially unpleasantto lie in (which is often a long, narrow tube even up to one hour)  Potential solutions include  Visiting the scanner to see the room and practice lying on the table  Watching DVDs with a Head-mounted display while in the machine  The use of open MRI  Use of sedation  For the most severe cases, general anesthesia
  • 61.
  • 62.
    PET Scan  Itis a Nuclear medicine medical imaging technique which produces a three-dimensional image or map of functional processes in the body
  • 64.
    Principal of PET A short-lived radioactive tracer isotope – which decays by emitting a positron – is injected  There is a waiting period while the metabolically active molecule becomes concentrated in tissues of interest  Then the patient is placed in the imaging scanner  The molecule most commonly used for this purpose is fluorodeoxyglucose (FDG), a sugar, for which the waiting period is typically an hour.
  • 65.
    Procedure  As theradioisotope undergoes positron emission decay (also known as positive beta decay), it emits a positron (the antimatter counterpart of an electron)  After travelling up to a few millimeters the positron encounters and annihilates with an electron  Producing a pair of annihilation (gamma) photons moving in almost opposite directions
  • 66.
    Procedure (Cont..)  Theseare detected when they reach a scintillator material in the scanning device  Creating a burst of light which is detected by photomultiplier tubes or silicon avalanche photodiodes  The technique depends on simultaneous or coincident detection of the pair of photons  Photons which do not arrive in pairs are ignored
  • 68.
     This figureshows how during the annihilation process two photons are emitted in diametrically opposing directions.  These photons are registered by the PET as soon as they arrive at the detector ring  After the registration, the data is forwarded to a processing unit which decides if two registrered events are selected as a so- called coincidence event.  All coincidences are fowarded to the image processing unit where the final image data is produced via image reconstruction procedures
  • 69.
    Radioisotopes used in PET Typically isotopes with short half lives such as  11C (~20 min)  13N (~10 min)  15O (~2 min)  18F (~110 min)  Incorporated into compounds normally used by the body such as glucose, water or ammonia (these compounds are known as radiotracers)
  • 70.
    Uses  Clinical oncology(medical imaging of tumors and the search for metastases)  Various types of dementias  Tool to map normal human brain function  Changing of regional blood flow in various anatomic structures
  • 71.
    Use in Neurology Brain is normally a rapid user of glucose  Brain pathologies such as Alzheimer's disease greatly decrease brain metabolism of both glucose and oxygen in tandem  Standard FDG-PET of the brain (which measures regional glucose use) is used to differentiate Alzheimer's disease from other dementing processes, and also to make early diagnosis of Alzheimer's disease
  • 72.
    Pet Scan ofBrain Red areas show more accumulated radioactivity and blue areas are portions where low to no activity was accumulated
  • 73.
    Use in Neuropsychology To examine links between specific psychological processes or disorders and brain activity
  • 74.
    Use in psychiatry Numerous compounds that bind selectively to neuro-receptors of interest in biological psychiatry have been radiolabeled with 11C or 18F  Radioligands that bind to dopamine receptors , serotonin receptors, opioid receptors (mu) and other sites have been studied  Studies have been performed examining the state of these receptors in patients of schizophrenia, substance abuse, mood disorders and other psychiatric conditions
  • 75.
    Safety  PET scanningis non-invasive, but it does involve exposure to ionizing radiation  So should be avoided in pregnancy
  • 76.
    Single photon emission computedtomography (SPECT) Scan
  • 77.
    Principal  Imaging techniqueusing gamma rays  Image obtained by a gamma camera image is a 2D view of 3D distribution of a radionuclide.  SPECT imaging is performed by using a gamma camera to acquire 2D images from multiple angles  A computer is then used to apply a tomographic reconstruction of the multiple projections, yielding a 3-D dataset
  • 79.
    Procedure  The gammacamera is rotated around the patient  Projections are acquired at every degree and full 360 degree  The time taken to obtain each projection is about 15 – 20 seconds  Total scan time of 15-20 minutes
  • 80.
    Uses  Tumor imaging Infection (leukocyte) imaging  Thyroid imaging  Bone imaging  Information about localized function in internal organs  Functional cardiac (diagnosis of ischemic heart disease )  Brain imaging (dementia)