G16.4428 Practical Magnetic Resonance Imaging...
Transcript of G16.4428 Practical Magnetic Resonance Imaging...
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G16.4428 Practical Magnetic Resonance Imaging II
Part 2: Medical Image Analysis
Henry Rusinek, Artem Mikheev and Jelle Veraart
Tuesdays 2:00, Fridays 1:00
The second part introduces the basics of medical image representation
and analysis. This includes post-processing algorithms that are highly
relevant in clinical radiology: tissue/organ segmentation, coregistration
and kinetic modeling of dynamic MRI. During laboratory sessions and
homework, students will use Matlab and FireVoxel to implement and test
image reconstruction methods, perform image segmentation and
coregistration.
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Part 2 consists of six lectures and four labs:
lecture #9 Fri 10/24 HR imaging modalities
lab #7 Tue 10/28 HR image representation & formats
lecture #10 Fri 10/31 AM nonuniformity correction
lab #8 Tue 11/4 HR image processing, FireVoxel
lecture #11 Fri 11/7 AM organ/tissue segmentation
lab #9 Tue 11/11 HR segmentation at work
lecture #12 Fri 11/14 JV noise & parametric mapping
lecture #13 Tue 11/18 HR dynamic MRI & models
lecture #14 Fri 11/21 HR intro to image coregistration
lab#10 rm chnge Tue 11/25 HR coregistration at work
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Imaging plays a key role in modern medicine
Image data are found in many clinical
specialties:
orthopedics (x-ray, CT)
pulmonology (x-ray, CT)
cardiology (nuclear medicine)
cardiac intervention (fluoroscopy)
urology and gastro-intereology (ultrasound
and endoscopy)
In addition to diagnosis and therapy, imaging
methods are vital for basic biomedical research
and drug development.
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Medical imaging modalities
In addition to MRI, today the most important medical imaging modalities are: planar X-ray
CT
ultrasound
gamma cameras
PET/SPECT scanners
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Basics of CT
CT scanner consists of an array of x-ray detectors opposing an
x-ray tube. This gantry rotates around the object being
imaged.
The attenuation profile changes
depending on the object and the
rotation angle when an x-ray passes
a volume element of length ds
having an attenuation coefficient μ
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Relationship between detected & emitted x-rays flux
The exit x-ray intensity I (detected flux) is related to the emitted intensity by the
equation:
𝐼𝑑𝑒𝑡𝑒𝑐𝑡 = 𝐼𝑒𝑚𝑖𝑡 e−μds [1]
where μ is the attenuation coefficient, ds is the path length. If we divide the object in a
discrete pixels indexed with i, equ.[1] can be refined as:
𝐼𝑑𝑒𝑡𝑒𝑐𝑡 = 𝐼𝑒𝑚𝑖𝑡 e− i μi ds i [2]
After a logarithmic transformation:
ln(𝐼𝑒𝑚𝑖𝑡 /𝐼𝑑𝑒𝑡𝑒𝑐𝑡 ) = i μi dsi [3]
Thus we can capture the unknown attenuation coefficients in a LINEAR system of
equations. The system is sparse, which facilitates accurate solution.
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Reconstruction of CT image from projections
Back in 1917 an Austrian mathematician Johann Radon derived an analytic solution
for reconstructing an image from its projections. This solution, termed "filtered
backprojection" was rediscovered in 1970's and used in the first generation CT scanner
developed by a British engineer Hounsfield.
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Non-filtered vs filtered back-projection
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The first EMI CT developed by Hounsfield at
Godfrey Hounsfield (1919 – 2004) was an English engineer who shared the
1979 Nobel Prize for Physiology or Medicine with Allan Cormack for his part in
developing at EMI Ltd. the computed tomography.
His name is immortalized in the quantitative measure of attenuation coefficient μ.
The scale is defined in Hounsfield units (HU), running from air at −1000 HU,
through water at 0 HU (dense cortical bone ~1000 HU).
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CT scanner generations
1st Gen -- translate and rotate, single detector, 5 mins/slice 2nd Gen -- fan beam and multiple detectors, translations, 20 secs/slice 3rd Gen -- curved detector, no translation, tube and detector rotate 4th Gen -- 360° detector ring -- too expensive!
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Spiral (helical) CT
Earlier x-ray CT scanners imaged one slice at a
time while the patient remained static. In spiral
CT, the patient is being moved axially at a
uniform rate, the x-ray source describes a
helical trajectory relative to the patient body.
The helical scan method reduces the x-ray dose
to the patient required for a given resolution
and scan is faster. There is however greater
complexity in the reconstruction of the image.
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Multi-detector CT
Since its invention by Kalender in the 1980s, spiral CTs have increased the number of
rows of detectors. The prototype 16-slice scanner was introduced in 2001. In 2004, 64-
scanners became available, that can produce a chest volume image in a few sec. This is
important for imaging the heart and coronary vessels.
512 x 512 x 340
(1/2 mm)3
in 3 sec
cardiac vessel imaging
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CT image artifacts
CT is prone to artifacts, as it depends on consistency of millions of measurements:
Streaking
Shading – defect in a group of channels
Ring – detector failure
Beam hardening -- x-ray physics
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Nuclear medicine imaging
fundamental difference from CT: radiation source is introduced to patient
instruments: gamma camera, SPECT, PET
radioactivity: unstable elements 99m-TC or 123-I emit gamma radiation
radiochemistry: science of binding radioactive elements with important
molecules that are taken up by tumors or body organs due to their chemical
properties
radioactive quantity is tiny: "tracer" method
nuclear medicine images show body function, unlike CT that show structure.
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Half-life of common radioactive isotopes
Half-life ( h ) is the time required for a quantity to fall to half its value:
𝑁 𝑡 = 𝑁0 1
2
𝑡
ℎ or 𝑁 𝑡 = 𝑁0𝑒
−𝑡𝜌 where ℎ =ln(2)
𝜌
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Conventional 2D gamma camera – Anger camera
Invented by Hal Anger (1920-2005)
a large area crystal made of NaI(Tl)
collimator placed in front of the crystal
behind the collimator – a 2D array of photo multiplier tubes (PM)
signal from PM used to resolve gamma incidence -- event locator
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SPECT camera
SPECT imaging is performed by using a several
gamma cameras to acquire 2-D images
(projections) at defined points during the
rotation, typically every 3–6 degrees. Typical
time taken to obtain each projection is ~20
seconds, yielding a total scan time of ~20 min.
A tomographic reconstruction algorithm, similar
to CT reconstruction, yields a 3-D image.
Typical spatial resolution is ~8mm. Camera cost
= $200,000, exam cost ~$200.
Multi-headed gamma cameras can provide
accelerated acquisition. For example, a
dualheaded camera can be used with heads
spaced 180 degrees apart, allowing 2 projections
to be acquired simultaneously, with each head
requiring 180 degrees of rotation. Triplehead
cameras with 120-degree spacing are also used.
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Example of a cardiac SPECT study
The SPECT cardiac stress images are
standard heart exams. Patient is imaged
at rest and after exercise (causing dilated
the coronary arteries). The most
common tracers are Thallium-201 or
Technetium Sestamibi.
SPECT camera detects significant
coronary artery blockages that result in
lower perfusion to a segment of the
heart. If both the resting and stress
images show defects, the tissue is dead
(the patient had a heart attack).
Images are generally displayed in three
different projections, with stress images
directly next to resting images.
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Solid state gamma camera technology
Research is being done on solid state detector
technology, mostly based on cadmium
telluride (CdTe) and cadmium zinc telluride
(CdZnTe) crystals. Compared to Anger
cameras based on NaI crystals, these solid state
detectors provide better photon energy
discrimination. They may be also more sensitive
(faster acquisition) and since they
don’t require photomultiplier tubes, they are more
compact.
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Positron (β+) emitters for PET imaging
atoms with excess # of protons used as tracers
Release of a β+ and a neutrino
2 gamma in exactly opposite directions, 511 keV each
coincidence time window: ~ 5 nsec
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PET camera
PET is similar to SPECT in its use of
radioactive tracer material and detection
of gamma rays. In contrast with
SPECT, PET tracers emits two gamma
photons to be emitted in opposite
directions. A PET scanner detects these
emissions coincident in time, which
provides better localization and higher
resolution than SPECT. Typical spatial
resolution is ~5mm. PET cameras are
significantly more expensive
(~1,500,000$) than SPECT. The cost of
each exam is high, ~$2,000. PET camera uses shorter-lived and
less easily-obtained radioisotopes than SPECT. PET/CT are common. PET/MR are now
becoming available.
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PET coincidence circuitry
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Positron emitters in medical imaging
Isotope Half-life
(min)
Spec.
activity
106 Ci/mmol
Max energy
(MeV)
Range
(mm)
Product
F-18 110 1.71 0.63 2.4 Oxygen-18
C-11 20.4 9.22 0.96 4.1 Boron-18
O-15 2.1 90.8 1.72 8.2 Nitrog-15
N-13 9.96 18.9 1.19 5.4 Carbon-13
These four isotopes are used more than any others.
The development of labeled 2-fluorodeoxy-D-glucose (2FDG) by the
Brookhaven group under the direction of Al Wolf and Joanna Fowler
was a major factor in popularizing PET imaging. FDG has
broadest utility, 90% of PET procedures use FDG.
18F NaF PET -- bone cancer
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Review: SPECT versus PET
SPECT PET
single gamma tracer positron emitter
50-250 keV 512 keV
collimation coincidence circuitry
Attenuation correction + Attenuation correction -
Scatter correction + Scatter correction -
Low cost scanner Expensive scanner
Low cost tracer Expensive tracer
Poor image resolution Moderate resolution
Note: CT, SPECT and PET expose patients to ionizing radiation
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Medical Ultrasound Imaging
A sound wave is typically produced by a piezoelectric transducer
made of ceramic that emits strong, short pulses at frequencies 2-18
MHz. The sound is focused to produces an arc-shaped sound wave
from the face of the transducer. The wave travels into the body and
comes into focus at a desired depth.
Newer transducers use phased array techniques to change the
direction and depth of focus. The face of the transducer has a
rubbery coating to let the sound to be transmitted efficiently into
the body. A water-based gel is placed between the patient's skin
and the probe.
The sound wave is partially reflected from the layers between
different tissues. Specifically, sound is reflected anywhere there
are density changes in the body: e.g. blood cells in blood plasma, small structures in
organs, etc. Some of the reflections return to the transducer.
The return of the sound wave to the transducer results in the same process that it took to
send the sound wave, except in reverse. The return sound wave vibrates the transducer,
the transducer turns the vibrations into electrical pulses that travel to the ultrasonic
scanner where they are processed and transformed into a digital image.
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Forming an ultrasound image
The sonographic scanner determines three things from
each received echo:
1. How long it took the echo to be received from
when the sound was transmitted. From this the
focal length for the phased array is deduced,
enabling a sharp image of that echo at that depth.
2. How strong the echo was. Noted that sound wave
is not a click, but a pulse with a specific carrier
frequency.
3. Moving objects inside the body will change the carrier frequency on reflection &
receiver’ electronics can measure the frequency of the echo sound. This is called
Doppler (or color) sonography.
From 1. and 2. the ultrasonic scanner locate which pixel in the image to light up,
corresponding pixel intensity (and at what hue, if frequency 3. is processed).
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Ultrasound Noise and Artifacts
Enhancement artifact: fluid structures (as the cyst on the
right) allow sound to pass easily, absorbing only a
minimal amount of energy. The region that lies behind
will receive more sound than expected for that depth &
will appear brighter.
Shadowing artifact: some tissues will absorb
relatively more of the sound, causing the area
behind to appear darker. In theis gallbladder
image, with a (dense) gallstone casting a shadow.
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Ionizing radiation (Xray CT SPECT PET)
Major impact of ionizing radiation: generation of free radicals
DNA molecules get damaged
most of DNA damage can be repaired, but some cells lose their
capacity and are destroyed
high radiation sensitivity: ovule, sperm, mucose cells,
lymphocytes
low sensitivity: liver, muscle
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Examples of radiation exposure
Exposure Dose [mSv]
USA-Europe round-trip air flight 0.1
Annual cosmic background radiation 1.0
Annual average natural and human-caused 3.6
Nuclear weapon test, effect over 50 years 1.5
Single radiation sterilization procedure 30,000
Local cancer therapy 60,000
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Examples of medical radiation exposure
Exposure Dose [mSv]
Chest x-ray 0.1
Dental x-ray 0.01
mammography 2
Head CT 3
Standard chest CT 20
Local cancer therapy 60,000
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Damage after exposure to acute radiation
Time after 1 Sv
Critical dose
4 Sv
Lethal dose
7 Sv
1st week low white blood cells low white blood
cells Heavy diarrhea,
vomiting, fever
2nd week no symptoms no symptoms
3rd week hair loss, diarrhea hair loss, diarrhea,
internal bleeding
4th week recovery 50% fatality 100% fatal