1. 16- Dec - 201416- Dec - 2014
UltrasoundUltrasound
Arsalan KhanArsalan Khan
MPhil (Clinical Medicine & Surgery)MPhil (Clinical Medicine & Surgery)
2014-ag-14512014-ag-1451
University of Agriculture, FaisalabadUniversity of Agriculture, Faisalabad
PakistanPakistan
3. UltrasoundUltrasound
The sound waves of frequency higher thanThe sound waves of frequency higher than
20KHz used for diagnostic and therapeutic20KHz used for diagnostic and therapeutic
purpose and imaging are calledpurpose and imaging are called
ultrasoundultrasound
Sound waves are measured in Hertz (Hz)Sound waves are measured in Hertz (Hz)
Diagnostic Ultrasound = 1-20 MHzDiagnostic Ultrasound = 1-20 MHz
Sound waves are produced by aSound waves are produced by a
transducertransducer
4. Principle: Pulse echo principlePrinciple: Pulse echo principle
Ultrasound waves not heard becauseUltrasound waves not heard because
human middle ear (eardrum) can’t vibratehuman middle ear (eardrum) can’t vibrate
at such frequency.at such frequency.
Frequency: 3.5 (intestines and U.Frequency: 3.5 (intestines and U.
bladder), 5 (liver, pancreas and spleen),bladder), 5 (liver, pancreas and spleen),
7.5 (Rectum and testicles) and7.5 (Rectum and testicles) and
10MHz (Superficial organs).10MHz (Superficial organs).
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5. Transducer (probe)Transducer (probe)
It consists of ; Piezoelectric crystalIt consists of ; Piezoelectric crystal
When electric charge is applied it emits soundWhen electric charge is applied it emits sound
waveswaves
Sound is reflected from patientSound is reflected from patient
Returning echo is converted to electric signalReturning echo is converted to electric signal
grayscale image on monitor is formedgrayscale image on monitor is formed
Echo may be reflected, transmitted or refractedEcho may be reflected, transmitted or refracted
This probe has dual function that is it producesThis probe has dual function that is it produces
as well as receive the sound wavesas well as receive the sound waves
The monitor converts these signals to imageThe monitor converts these signals to image
6. • As frequency increases, resolution improvesAs frequency increases, resolution improves
• As frequency increases, depth of penetrationAs frequency increases, depth of penetration
decreasesdecreases
–
Use higher frequency transducers to image moreUse higher frequency transducers to image more
superficial structuressuperficial structures
• Velocities:Velocities:
–
Soft tissues = 1400-1600m/secSoft tissues = 1400-1600m/sec
–
Bone = 4080 m/secBone = 4080 m/sec
–
Air = 330 m/secAir = 330 m/sec
7. WorkingWorking
A sound wave is produced by the vibration of PiezoA sound wave is produced by the vibration of Piezo
electric crystals in the transducer and focused by theelectric crystals in the transducer and focused by the
transducer or lens in front of transducertransducer or lens in front of transducer
Water based gel is placed between the patient body andWater based gel is placed between the patient body and
probeprobe
These waves return in the same manner and areThese waves return in the same manner and are
received by the transducerreceived by the transducer
These waves are processed and are transformed intoThese waves are processed and are transformed into
digital image on the monitordigital image on the monitor
8. Modes of SonographyModes of Sonography
A-modeA-mode: A-mode (amplitude mode) is the: A-mode (amplitude mode) is the
simplest type of ultrasound.; signals aresimplest type of ultrasound.; signals are
recorded as spikes on a graph. Therecorded as spikes on a graph. The
vertical (Y) axis of the display shows thevertical (Y) axis of the display shows the
echo amplitude, and the horizontal (X)echo amplitude, and the horizontal (X)
axis shows depth or distance into theaxis shows depth or distance into the
patient. This type of ultrasonography ispatient. This type of ultrasonography is
used for ophthalmologic scanning.used for ophthalmologic scanning.
It is single dimension and represented inIt is single dimension and represented in
the form of spikes and peaks.the form of spikes and peaks.
9. B-mode or 2D modeB-mode or 2D mode: In B-mode: In B-mode
(brightness mode) ultrasound, a linear(brightness mode) ultrasound, a linear
array of transducers simultaneously scansarray of transducers simultaneously scans
a plane through the body that can bea plane through the body that can be
viewed as a two-dimensional image onviewed as a two-dimensional image on
screen. B-mode is commonly used toscreen. B-mode is commonly used to
evaluate the developing fetus and toevaluate the developing fetus and to
evaluate organs, including the liver,evaluate organs, including the liver,
spleen, kidneys, thyroid gland, testes,spleen, kidneys, thyroid gland, testes,
breasts, and prostate gland.breasts, and prostate gland.
Image shown by grey to bright dots.Image shown by grey to bright dots.
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10. M-modeM-mode: In M-mode (motion mode) ultrasound, pulses: In M-mode (motion mode) ultrasound, pulses
are emitted in quick succession – each time, either an A-are emitted in quick succession – each time, either an A-
mode or B-mode image is taken. It is used for movingmode or B-mode image is taken. It is used for moving
organs and image is shown as oscillations about verticalorgans and image is shown as oscillations about vertical
lines. M-mode is used primarily for assessment of fetallines. M-mode is used primarily for assessment of fetal
heartbeat and in cardiac imaging, most notably toheartbeat and in cardiac imaging, most notably to
evaluate valvular disorders ( Mitral valve regurgitation).evaluate valvular disorders ( Mitral valve regurgitation).
Doppler modeDoppler mode: This mode makes use of the Doppler: This mode makes use of the Doppler
effect in measuring and visualizing blood flow. In thiseffect in measuring and visualizing blood flow. In this
mode, the velocity and direction of blood flows aremode, the velocity and direction of blood flows are
depicted in a color map superimposed on the 2-D image.depicted in a color map superimposed on the 2-D image.
It evaluates the blood perfusion of the organs.It evaluates the blood perfusion of the organs.
11. Scanners:Scanners:
1)1)Linear array: It is rectangular. LargeLinear array: It is rectangular. Large
number of piezo electric crystals. Used fornumber of piezo electric crystals. Used for
superficial organs and rectal examination.superficial organs and rectal examination.
It has 64x256 crystals.It has 64x256 crystals.
2)2)Sector array: It is convex probe. It hasSector array: It is convex probe. It has
single piezo electric crystal.single piezo electric crystal.
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12. Types of image interpretation:Types of image interpretation:
1)1)Hyper echoic: Returning of echo is veryHyper echoic: Returning of echo is very
strong. It is reflecting from very highstrong. It is reflecting from very high
density tissue. Bright image is formed.density tissue. Bright image is formed.
2)2)Hypo echoic: Returning echo is weak. LowHypo echoic: Returning echo is weak. Low
density tissues. Grey to dark image isdensity tissues. Grey to dark image is
formed. E.g. Tumours, abcess,formed. E.g. Tumours, abcess,
Hematoma, granulation, inflammation.Hematoma, granulation, inflammation.
It is more cellular in nature.It is more cellular in nature.
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13. 3) An echoic: Complete attenuation. No3) An echoic: Complete attenuation. No
reflection. From fluid or air. Image is darkreflection. From fluid or air. Image is dark
black. E.g. Urinary bladder, lungs, odema,black. E.g. Urinary bladder, lungs, odema,
fluid or water accumulation.fluid or water accumulation.
4) Iso echoic: It is normal image. Grey color4) Iso echoic: It is normal image. Grey color
image is formed. E.g Liver, spleen,image is formed. E.g Liver, spleen,
muscles etc.muscles etc.
N.B: Image of ultrasound is cross sectionalN.B: Image of ultrasound is cross sectional
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14. ArtifactsArtifacts
Artifacts lead to the improper display of the structures toArtifacts lead to the improper display of the structures to
be imagedbe imaged
1) Acoustic shadowing:1) Acoustic shadowing:
–
Ultrasound beam does not pass through an object because ofUltrasound beam does not pass through an object because of
reflection or absorption.reflection or absorption.
–
When the reflecting tissue is situated behind the strong reflectingWhen the reflecting tissue is situated behind the strong reflecting
tissue. E.g kidney muscles behind the stone. Weak echoes aretissue. E.g kidney muscles behind the stone. Weak echoes are
received and the image can misguide for the presence of fluid.received and the image can misguide for the presence of fluid.
–
Black area beyond the surface of the reflectorBlack area beyond the surface of the reflector
–
Examples: cystic calculi, bonesExamples: cystic calculi, bones
• Acoustic enhancementAcoustic enhancement
–
Hyperintense (bright) regions below objects of lowHyperintense (bright) regions below objects of low
Ultrasound beam attenuation. High echo. E.g odemaUltrasound beam attenuation. High echo. E.g odema
or fluid behind the muscles.or fluid behind the muscles.
15. 3)Refraction:3)Refraction:
Occurs when the sound wave reaches two tissues ofOccurs when the sound wave reaches two tissues of
differing acoustic impedancesdiffering acoustic impedances
Ultrasound beam reaching the second tissue changesUltrasound beam reaching the second tissue changes
directiondirection
May cause an organ to be improperly displayedMay cause an organ to be improperly displayed
4) Reverberation: It is the back and forth motion of4) Reverberation: It is the back and forth motion of
ultrasound waves. E.g due to the presence of air theultrasound waves. E.g due to the presence of air the
waves cannot be processed.waves cannot be processed.
5) Mirror imaging: Double image is seen. It is due to the5) Mirror imaging: Double image is seen. It is due to the
production of large number of waves from theproduction of large number of waves from the
transducer.transducer.
16. AdvantagesAdvantages
It imagesIt images musclemuscle,, soft tissuesoft tissue, and bone surfaces very, and bone surfaces very
well & interfaces between solid and fluid-filled spaces.well & interfaces between solid and fluid-filled spaces.
It renders "live" images, where the operator canIt renders "live" images, where the operator can
dynamically select the most useful section for diagnosingdynamically select the most useful section for diagnosing
Live images also allow for ultrasound-guided biopsiesLive images also allow for ultrasound-guided biopsies
It shows the structure of organs.It shows the structure of organs.
It has no known long-term side effects and rarely causesIt has no known long-term side effects and rarely causes
any discomfort to the patient.any discomfort to the patient.
Equipment is widely available and comparatively flexible.Equipment is widely available and comparatively flexible.
Small, easily carried scanners are available;Small, easily carried scanners are available;
Relatively inexpensive compared to other modes ofRelatively inexpensive compared to other modes of
investigation, such asinvestigation, such as computed X-ray tomographycomputed X-ray tomography,or,or
magnetic resonance imagingmagnetic resonance imaging..
17. DisadvantagesDisadvantages
Sonography performs very poorly when there is a gasSonography performs very poorly when there is a gas
between the transducer and the organ of interestbetween the transducer and the organ of interest
Sonographic devices have trouble penetratingSonographic devices have trouble penetrating bonebone
Even in the absence of bone or air, the depth penetrationEven in the absence of bone or air, the depth penetration
of ultrasound may be limited depending on the frequencyof ultrasound may be limited depending on the frequency
of imagingof imaging
A high level of skill and experience is needed to acquireA high level of skill and experience is needed to acquire
good-quality images and make accurate diagnosesgood-quality images and make accurate diagnoses
There is no scout image as there is with CT and MRI.There is no scout image as there is with CT and MRI.
Once an image has been acquired there is no exact wayOnce an image has been acquired there is no exact way
to tell which part of the body was imagedto tell which part of the body was imaged
19. Bioluminescence imagingBioluminescence imaging
Bioluminescence, the biochemical generation ofBioluminescence, the biochemical generation of
light by a living organism, is a naturally occurringlight by a living organism, is a naturally occurring
phenomenon.phenomenon.
Bioluminescence imaging detects light produced byBioluminescence imaging detects light produced by
the reaction of luciferase enzymes with a definedthe reaction of luciferase enzymes with a defined
substrate. Luciferase enzymes catalyze thesubstrate. Luciferase enzymes catalyze the
oxidation of a substrate (luciferin), and photons ofoxidation of a substrate (luciferin), and photons of
light are a product of the reaction.light are a product of the reaction.
Optical imaging by bioluminescence allows a low-Optical imaging by bioluminescence allows a low-
cost, noninvasive, and real-time analysis of diseasecost, noninvasive, and real-time analysis of disease
processes at the molecular level in living organisms.processes at the molecular level in living organisms.
Bioluminescence has been used to track tumorBioluminescence has been used to track tumor
cells, bacterial and viral infections, gene expression,cells, bacterial and viral infections, gene expression,
and treatment response.and treatment response.
20. TechniqueTechnique
Instruments for BLI use a very sensitive charge-Instruments for BLI use a very sensitive charge-
coupled device (CCD) camera to detect the lowcoupled device (CCD) camera to detect the low
levels of light emitted from luciferase reporterslevels of light emitted from luciferase reporters inin
vivovivo..
Bioluminescence can be measured byBioluminescence can be measured by
computer analysis of emitted photons, allowingcomputer analysis of emitted photons, allowing
relative quantification of data.relative quantification of data.
21. Bioluminescence imaging utilizes native light emissionBioluminescence imaging utilizes native light emission
from one of several organisms which bioluminesce. Thefrom one of several organisms which bioluminesce. The
three main sources are the North Americanthree main sources are the North American fireflyfirefly, the, the
sea pansysea pansy (and related marine organisms), and bacteria(and related marine organisms), and bacteria
likelike Photorhabdus luminescensPhotorhabdus luminescens andand Vibrio fischeriVibrio fischeri. The. The
DNADNAencoding the luminescent protein is incorporatedencoding the luminescent protein is incorporated
into the laboratory animal either via ainto the laboratory animal either via a viral vectorviral vector or byor by
creating acreating a transgenic animaltransgenic animal..
Systems derived from the three groups above differ inSystems derived from the three groups above differ in
key ways;key ways;
1)1) Firefly luciferase requires D-luciferin to be injected intoFirefly luciferase requires D-luciferin to be injected into
the subject prior to imaging. The peak emissionthe subject prior to imaging. The peak emission
wavelength is about 560 nm.wavelength is about 560 nm.
2)2) Renilla luciferase (from theRenilla luciferase (from the Sea pansySea pansy) requires its) requires its
substrate, coelenterazine, to be injected as well.substrate, coelenterazine, to be injected as well.
24. Diffuse Optical ImagingDiffuse Optical Imaging
Diffuse optical imagingDiffuse optical imaging (DOI) is a method of imaging (DOI) is a method of imaging
using using Near Infrared SpectroscopicNear Infrared Spectroscopic (NIRS) or (NIRS) or
Fluorescence based methodsFluorescence based methods
InfraredInfrared ( (IRIR) is invisible radiant energy, ) is invisible radiant energy,
electromagnetic radiationelectromagnetic radiation with longer with longer wavelengthswavelengths than than
those of those of visible lightvisible light, extending from the nominal , extending from the nominal redred
edge of the edge of the visible spectrumvisible spectrum at 700 at 700 nanometersnanometers to to
1 mm1 mm
When used to create 3D volumetric models of the When used to create 3D volumetric models of the
imaged material DOI is referred to as imaged material DOI is referred to as diffuse opticaldiffuse optical
tomographytomography, whereas 2D imaging methods are , whereas 2D imaging methods are
classified as classified as diffuse optical topographydiffuse optical topography
