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Файл:Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_5545_Библиотеки_им_академика_М_И_Перельмана.pdf
X
- •Preface
- •Contents
- •1: Structure of Matter
- •2: Radioactive Decay
- •2.1 Spontaneous Fission
- •1.1.1 Radiation
- •1.2 The Atom
- •1.2.3 Nuclear Binding Energy
- •1.3 Nuclear Nomenclature
- •1.5 Questions
- •Suggested Readings
- •2.2 Isomeric Transition
- •2.2.1 Gamma (γ)-Ray Emission
- •2.2.2 Internal Conversion
- •2.2.2.1 Problem 2.1
- •2.2.2.2 Answer
- •2.3 Alpha (α)-Decay
- •2.4 Beta (β−)-Decay
- •2.5 Positron (β+)-Decay
- •2.6 Electron Capture
- •2.7 Questions
- •Suggested Readings
- •3.1 Radioactive Decay Equation
- •3.1.1 General Equation
- •3.1.2 Half-Life
- •3.1.3 Mean Life
- •3.1.4 Effective Half-Life
- •3.2 Units of Radioactivity
- •3.3 Specific Activity
- •3.4 Calculation
- •3.5 Successive Decay Equations
- •3.5.1 General Equation
- •3.5.2 Transient Equilibrium
- •3.5.3 Secular Equilibrium
- •3.6 Questions
- •Suggested Readings
- •4.5 Poisson Distribution
- •4.6 Gaussian Distribution
- •4.7 Chi-Square Test
- •4.8 Minimum Detectable Activity
- •4.10 Questions
- •Suggested Readings
- •5.1 Cyclotron-Produced Radionuclides
- •5.2 Reactor-Produced Radionuclides
- •5.2.1 Fission or (n, f) Reaction
- •5.2.2 Neutron Capture or (n, γ) Reaction
- •5.6 Radionuclide Generators
- •5.8 Questions
- •Suggested Readings
- •6.1.1 Specific Ionization
- •6.1.2 Linear Energy Transfer
- •6.1.3 Range
- •6.1.4 Bremsstrahlung
- •6.1.5 Positron Annihilation
- •6.2.1.1 Photoelectric Effect
- •6.2.1.2 Compton Scattering
- •6.2.1.3 Pair Production
- •6.2.1.4 Raleigh Scattering
- •6.2.1.5 Photodisintegration
- •6.3.2 Half-Value Layer
- •6.5 Questions
- •Suggested Readings
- •7: Gas-Filled Detector
- •7.1 Principles of Gas-Filled Detector
- •7.2 Ionization Chamber
- •7.2.1 Ion Chamber Survey Meter
- •7.2.2 Dose Calibrator
- •7.2.2.1 Constancy
- •7.2.2.2 Accuracy
- •7.2.2.3 Linearity
- •7.2.2.4 Geometry
- •7.2.3 Pocket Dosimeter
- •7.3 Proportional Counter
- •7.4 Geiger–Müller Counter
- •7.5 Questions
- •Suggested Readings
- •8.1 Scintillation Counter
- •8.4.3 Characteristic X-Ray Peak
- •8.4.4 Backscatter Peak
- •8.4.5 Iodine Escape Peak
- •8.2 Solid Scintillation Detector
- •8.2.1 NaI (Tl) Detector
- •8.2.2 Bismuth Germanate Detector
- •8.2.3 Barium Fluoride Detector
- •8.2.4 Lutetium Oxyorthosilicate Detector
- •8.2.5 Gadolinium Oxyorthosilicate Detector
- •8.2.6 Yttrium Oxyorthosilicate Detector
- •8.2.7 Yttrium Aluminum Perovskite Detector
- •8.2.8 Lutetium Yttrium Oxyorthosilicate Detector
- •8.2.9 Lanthanum Bromide Detector
- •8.3 Solid-State Detector
- •8.3.2 Cadmium–Zinc–Tellurium Detector
- •8.3.3 Cesium Iodide (CsI(Tl)) Detector
- •8.3.4 Solid Scintillation Counter
- •8.3.4.1 NaI(Tl) Detector
- •8.3.4.2 Photomultiplier Tube
- •8.3.4.3 Preamplifier
- •8.3.4.4 Linear Amplifier
- •8.3.4.5 Pulse-Height Analyzer
- •8.3.4.6 Display or Storage
- •8.4 Gamma-Ray Spectrometry
- •8.4.1 Photopeak
- •8.4.6 Positron Annihilation Peak
- •8.4.7 Coincidence Peak
- •8.5 Liquid Scintillation Counter
- •8.5.1 Quenching
- •8.6.1 Energy Resolution
- •8.6.2 Detection Efficiency
- •8.6.2.1 Intrinsic Efficiency
- •8.6.2.2 Photopeak Efficiency or Photofraction
- •8.6.2.3 Geometric Efficiency
- •8.6.3 Dead Time
- •8.7 Gamma Well Counter
- •8.8 Thyroid Probe
- •8.8.1 Thyroid Uptake Measurement
- •8.9 Questions
- •Suggested Readings
- •9: Gamma Camera
- •9.1 Gamma Camera
- •9.1.2 Detector
- •9.1.3 Collimator
- •9.1.4 Photomultiplier Tube
- •9.1.5 X-, Y-Positioning Circuit
- •9.1.6 Pulse-Height Analyzer
- •9.2 Digital Camera
- •9.2.1 Solid State Digital Camera
- •9.3 Questions
- •Suggested Readings
- •10.1.1 Spatial Resolution
- •10.1.1.1 Intrinsic Resolution
- •10.1.1.2 Collimator Resolution
- •10.1.1.3 Scatter Resolution
- •10.1.2.1 Bar Phantom
- •10.1.2.2 Line-Spread Function
- •10.1.2.3 Modulation Transfer Function
- •10.1.3 Sensitivity
- •10.1.3.1 Collimator Efficiency
- •10.1.4 Uniformity
- •10.1.5 Pulse-Height Variation
- •10.1.6 Nonlinearity
- •10.1.7 Edge Packing
- •10.2 Gamma Camera Tuning
- •10.4 Contrast
- •10.4.1 Count Density
- •10.4.2 Image Noise
- •10.4.4 High Count Rate
- •10.4.6 Patient Motion
- •10.5.1 Daily Checks
- •10.5.1.2 Uniformity
- •10.5.2 Weekly Checks
- •10.5.3 Monthly Checks
- •10.5.3.1 High-Count Uniformity Calibration
- •10.5.3.2 Collimator Integrity
- •10.5.4 Annual, Semiannual, or As-Needed Checks
- •10.6 Questions
- •References and Suggested Readings
- •11.1.1 Central Processing Unit
- •11.1.2 Computer Memory
- •11.1.3 External Storage Device
- •11.1.4 Input/Output Device
- •11.1.7 Digital-to-Analog Conversion
- •11.1.8 Digital Image
- •11.2.1 Digital Data Acquisition
- •11.2.2 Static Study
- •11.2.3 Dynamic Study
- •11.2.4 Gated Study
- •11.2.7 Display
- •11.3.1 PACS
- •11.4 Questions
- •Suggested Readings
- •12: Single Photon Emission Computed Tomography
- •12.1 Tomographic Imaging
- •12.2 Single Photon Emission Computed Tomography
- •12.2.1 Data Acquisition
- •12.2.2 Image Reconstruction
- •12.2.2.1 Simple Backprojection
- •12.2.2.2 Filtered Backprojection
- •12.2.2.3 The Convolution Method
- •12.2.2.4 The Fourier Method
- •12.2.2.6 Iterative Reconstruction
- •12.3 SPECT/CT Scanner
- •12.4 Factors Affecting SPECT
- •12.4.1 Photon Attenuation
- •12.4.2 Attenuation Correction Methods
- •12.5 Partial-Volume Effect
- •12.5.2 Sampling
- •12.5.3 Scattering
- •12.6.1 Spatial Resolution
- •12.6.2 Sensitivity
- •12.6.3 Other Parameters
- •12.7.1 Daily Tests
- •12.7.2 Weekly Tests
- •12.7.2.1 Spatial Resolution
- •12.9 Questions
- •References and Suggested Readings
- •13: Positron Emission Tomography
- •13.1 Introduction
- •13.2 PET Radiopharmaceuticals
- •13.3.2 Block Detector
- •13.5 Coincidence Timing Window
- •13.6 PET/CT Scanner
- •13.7 PET/MR Scanner
- •13.7.2 MR Scanner
- •13.7.3 Commercial PET/MR Scanner
- •13.8 Mobile PET or PET/CT Scanner
- •13.9 Micro-PET Scanner
- •13.11 Data Acquisition
- •13.12 Image Reconstruction
- •13.13 Factors Affecting PET
- •13.13.1 Normalization
- •13.13.2 Photon Attenuation Correction
- •13.13.4 Random Coincidences
- •13.13.5 Scatter Coincidences
- •13.13.6 Dead Time
- •13.13.7 Radial Elongation
- •13.14.1 Spatial Resolution
- •13.14.2 Sensitivity
- •13.14.2.1 Noise Equivalent Count Rate
- •13.15.1 Daily Tests
- •13.15.1.1 Sinogram Check
- •13.15.2 Weekly Tests
- •13.15.2.1 Normalization
- •13.18 Questions
- •References and Suggested Reading
- •14.1 Background
- •14.5 Artificial Neural Network
- •14.7 Machine Learning
- •14.7.1 Decision Tree
- •14.7.2 Random Forest
- •14.7.3 Support Vector Machine
- •14.7.4 Computer Vision
- •14.8 Deep Learning
- •14.8.1 Convolutional Network
- •14.8.2 Recurrent Neural Network
- •14.8.3 Generative Adversarial Network
- •14.8.4 Transfer Learning
- •14.9 Radiomics
- •14.10 Natural Language Processing
- •14.11 Large Language Model
- •14.12 Generative Artificial Intelligence
- •14.13.1 Prompt
- •14.13.2 Token
- •14.13.3 Hallucination
- •14.13.4 Deepfake
- •14.13.5 Overfitting
- •14.15 Chatbot
- •14.18 Legal Implication
- •14.20 Questions
- •References
- •15.1 Introduction
- •15.2.1 Scheduling
- •15.2.2 Image Acquisition
- •15.2.3 Image Processing
- •15.2.4 Interpretation
- •15.2.5 Reporting
- •15.3.1 Oncology
- •15.3.2 Cardiovascular Disease
- •15.3.3 Bone Scintigraphy
- •15.3.4 Thyroid Imaging
- •15.5 Drug Development
- •15.6 Questions
- •References and Suggested Reading
- •16: Internal Radiation Dosimetry
- •16.1 Radiation Unit
- •16.1.1 Roentgen
- •16.1.2 Rad
- •16.1.3 Gray
- •16.1.4 Rem
- •16.1.5 Radiation Weighting Factor
- •16.1.6 Quality Factor
- •16.1.7 Sievert
- •16.2 Dose Calculation
- •16.2.1 Radiation Dose Rate
- •16.2.2 Cumulative Radiation Dose
- •16.2.3 Factors Affecting Ã
- •16.2.4 The S Values
- •16.4 Pediatric Dosage
- •16.5 Questions
- •References and Suggested Readings
- •17: Radiation Biology
- •17.1 The Cell
- •17.2.1 DNA Molecule
- •17.2.2 Chromosome
- •17.5 Cell Survival Curves
- •17.6 Factors Affecting Radiosensitivity
- •17.6.1 Dose Rate
- •17.6.2 Linear Energy Transfer
- •17.6.4 Chemicals
- •17.7 Radiosensitizer
- •17.7.1 Oxygen
- •17.7.2 Pyrimidine
- •17.7.3 Others
- •17.8 Radioprotector
- •17.9 Apoptosis
- •17.13.1 Hematopoietic Syndrome
- •17.13.2 Gastrointestinal Syndrome
- •17.13.3 Cerebrovascular Syndrome
- •17.14.1 Somatic Effects
- •17.14.1.1 Carcinogenesis
- •17.14.1.3 Dose–Response Relationship
- •17.14.1.5 Leukemia
- •17.14.1.6 Breast Cancer
- •17.14.1.7 Other Cancers
- •17.14.1.10 Nonspecific Life-Shortening
- •17.14.1.11 Cataractogenesis
- •17.14.2 Genetic Effects
- •17.14.2.1 Spontaneous Mutation
- •17.14.2.2 Doubling Dose
- •17.14.2.3 Genetically Significant Dose
- •17.17 Questions
- •References and Suggested Readings
- •18.1 Introduction
- •18.2 Radiation Protection
- •18.2.3 Occupational Dose Limits
- •18.2.4 ALARA Program
- •18.2.5.1 Time
- •18.2.5.2 Distance
- •18.2.5.3 Shielding
- •18.2.5.4 Activity
- •18.2.6 Personnel Monitoring
- •18.2.6.1 Film Badge
- •18.2.6.2 Thermoluminescent Dosimeter
- •18.2.6.3 Optically Stimulated Luminescence Dosimeter
- •18.3 Radiation Regulations
- •18.3.1 License
- •18.3.1.1 General License
- •18.3.1.2 Specific License of Limited Scope
- •18.3.1.3 Specific Licenses of Broad Scope
- •18.3.2 Radiation Safety Committee
- •18.3.3 Radiation Safety Officer
- •18.3.4.3 Supervision
- •18.3.4.4 Mobile Nuclear Medicine Service
- •18.3.4.5 Written Directives
- •18.4 Bioassay
- •18.6 Radioactive Waste Disposal
- •18.6.2 Release into Sewerage Systems
- •18.6.4 Other Disposal Methods
- •18.7 Radioactive Spill
- •18.8 Recordkeeping
- •18.10 Dirty Bombs
- •18.11 Types of Accidental Radiation Exposure
- •18.12 Protective Measures in Case of Explosion of a Dirty Bomb
- •18.13 Verification Card for Radioactive Patients
- •18.14 Radiation Phobia
- •18.15 European Regulations Governing Radiation
- •18.16 Questions
- •References and Suggested Readings
- •Index

176
12 Single Photon Emission Computed Tomography
a
b
c
Fig. 12.4 An illustration of the backprojection technique using the data from an acquisition
matrix into a reconstruction matrix

=−
()
12.2 Single Photon Emission Computed Tomography
177
respectively. It is a common practice to lump several slices together to increase the
count density in the individual slices to reduce statistical uctuations.
12.2.2.2 Filtered Backprojection
The simple backprojection has the problem of “star pattern” artifacts (Fig.12.3c)
caused by “shining through” radiation from adjacent areas of increased radioactivity, resulting in the blurring of the object. Because the blurring effect decreases with
distance (r) from the object of interest, it can be described by a 1/r function
(Fig.12.3d). It can be considered as a spillover of some counts from a pixel of interest into neighboring pixels, and the spillover decreases from the nearest pixels to the
farthest pixels. This blurring effect is minimized by applying a “lter” to the acquisition data, and the ltered projections are then backprojected to produce an image
that is more representative of the original object. Such methods are called the ltered backprojection. There are in general two methods of ltered backprojection:
the convolution method in the spatial domain and the Fourier method in the frequency domain, both of which are described below.
12.2.2.3 The Convolution Method
The blurring of reconstructed images caused by simple backprojection is eliminated
by the convolution method in which a function, termed “kernel,” is convolved with
the projection data, and the resultant data are then backprojected. The application of
a kernel is a mathematical operation that essentially removes the l/r function by taking some counts from the neighboring pixels and putting them back into the central
pixel of interest. Mathematically, a convolved image f′(x, y) can be expressed as
N
fxyhfxiy j
' , ,
()
∑∑
iNNjN
=− =−
⊙
ij ij
−
(12.1)
where fij(x−i, y− j) is the pixel count density at the x− i, y−j location in the
acquired projection, the h
values are the weighting factors of the convolution ker-
ij
nel, and ⨀ indicates the convolution operation. The arrangement of hij is available
in many forms.
A familiar “nine-point smoothing” kernel (i.e., 3×3 size), also called a smoothing lter, has been widely used in nuclear medicine to decrease statistical variation.
The essence of this technique is primarily to average the counts in each pixel with
those of the neighboring pixels in the acquisition matrix. An example of the application of nine-point smoothing to a section of an image is given in Fig.12.5.
Let us assume that the thick-lined pixel with value 5in the acquisition matrix is
to be smoothed. First, we assume a 3×3 acquisition matrix (same as 3×3 kernel
matrix) centered at the pixel to be convolved. Each pixel datum of this matrix is
multiplied by the corresponding weighting factor, followed by the summation of the
products. The weighting factors are calculated by dividing the individual pixel values of the kernel matrix by the sum of all pixel values of the matrix. The result of

178
Ac
9-point
el
12 Single Photon Emission Computed Tomography
quisition matrix
6312
3050
9837
1425
3x1+1x2+2x1
+0x2+5x4+0x2
+8x1+3x2+7x1
Fig. 12.5 The smoothing technique in the spatial domain using a 9-point smoothing kernel. The
thick-lined pixel with value 5 is smoothed by rst assuming a 3×3 acquisition matrix (same size
as the smoothing matrix) centered at this pixel and multiplying each pixel value of the matrix by
the corresponding weighting factor, followed by summing the products. The weighting factor is
calculated by dividing the individual pixel value by the sum of all pixel values of the smoothing
matrix. After smoothing the value of the pixel is changed from 5 to 3. Similarly all pixel values of
the acquisition matrix are smoothed by the nine-point smoothing kernel, to give a smoothed image
smoothing filter
1
2
1
4
2
2
2
11
1+2+1+2+4+2
+1+2+1
Smoothed pix
48
==
3
16
3
this operation is that the value of the pixel has changed from 5 to 3. Similarly, all
pixels in the acquisition matrix are smoothed, and the proles are then
backprojected.
The spatial kernel described above with all positive weighting factors reduces
noise but degrades the spatial resolution of the image. Sharp edges in the original
image become blurred in the smoothed image as a result of averaging the counts of
the edge pixels with those of the neighboring pixels.
Another lter kernel commonly used in the spatial domain consists of a narrow
central peak with both positive and negative values on both sides of the peak, as
shown in Fig.12.6. When this so-called edge-sharpening lter is applied centrally
to a pixel for correction, the negative values in effect cancel or erase all neighboring
pixel count densities, thus creating a corrected central pixel value. This is repeated
for all pixels in each projection, and the corrected projections are then backprojected. This technique reproduces the original image with better spatial resolution
but with increasing noise. Note that blurring due to simple backprojection is
removed by this technique but the noise inherent in the data acquisition due to the
limitations of the spatial resolution of the imaging device is not removed, but rather
enhanced.
12.2.2.4 The Fourier Method
Nuclear medicine data obtained in the spatial domain (Fig.12.7a) can be expressed
in terms of a Fourier series in the frequency domain as the sum of a series of

f(x,y)
Spatial domain
Amplitude
Distance (cm) Distance (cm)
Frequency (cm
)
Sinusoidal waves
Frequency domain
12.2 Single Photon Emission Computed Tomography
Fig. 12.6 A lter in the
spatial domain. The
negative side-lobes in the
spatial domain cancel out
the unwanted contributions
that lead to blurring in the
reconstructed image
y
x
ab c
179
Amplitude
Fig. 12.7 Representation of an object in the spatial and frequency domains. A prole in the spatial domain can be expressed as an innite sum of sinusoidal functions (the Fourier series). For
example, the activity distribution as a function of distance in an organ (a) can be composed of the
sum of the four sine functions (b). The Fourier transform of this activity distribution is represented
in (c), in which the amplitude of each sine wave is plotted at the corresponding frequency of the
sine wave
Amplitude
-1
sinusoidal waves of different amplitudes, spatial frequencies, and phase shifts running across the image (Fig.12.7b). This is equivalent to sound waves that are composed of many sound frequencies. Thus, the data for each row and column of the
acquisition matrix can be considered as composed of sinusoidal waves of varying
amplitudes and frequencies in the frequency domain. The process of determining
the amplitudes of sinusoidal waves is called the Fourier transformation (Fig.12.7c)

180
F
()
=
()
F HFvvv
()=() ()
·
and the method of changing from the frequency domain to the spatial domain is
called the inverse Fourier transformation.
The Fourier method of reconstruction can be applied in two ways: either directly
or by using lters. In the direct Fourier method, the Fourier transforms of individual
acquisition projections are taken in polar coordinates in the frequency domain,
which are then used to calculate the values in rectangular coordinates. Inverse
Fourier transforms of these proles are taken to compute the image. The method is
not a true backprojection and is rarely used in the reconstruction of images in
nuclear medicine because of the time-consuming computation.
A more convenient method of reconstruction is the ltered backprojection (FBP)
using the Fourier technique. In this method, lters are used to eliminate the blurring
function l/r that arises from simple backprojection of the projection data. These
lters are analogous to tone controls or equalizers in radios or CD players that act
as lters to vary the amplitudes of different frequencies, bass for low-frequency
amplitudes and treble for high-frequency amplitudes. In image reconstruction, lters do the same thing, modulating the amplitudes of different frequencies, preserving the broad structures (the image) represented by low frequencies and removing
the ne structures (noise) represented by high frequencies.
The Fourier method of ltering the projection data is based on the initial transformation of these data from the spatial domain to the frequency domain, which is
symbolically expressed as
12 Single Photon Emission Computed Tomography
,F,vv fxy
where F(vx, vy) is the Fourier transform of f(x, y) and F denotes the Fourier transformation. Next a Fourier lter, H(v) is applied in the frequency domain; that is,
where F′(v) is the ltered projection in the frequency domain, which is obtained as
the multiplication product of H(v) and F(v). Finally, the inverse Fourier transformation is performed to obtain the ltered projections, which are then backprojected.
The results obtained by the Fourier method are identical to those obtained by the
convolution method. Although the Fourier method appears to be somewhat cumbersome and difcult to understand, the use of modern computers has made it much
easier and faster to compute the reconstruction of images than the convolution method.
xy
(12.2)
(12.3)
12.2.2.5 Types ofFilters
A number of Fourier lters have been designed and used in the reconstruction of
images in nuclear medicine. All of them are characterized by a maximum frequency,
called the Nyquist frequency that gives an upper limit to the number of frequencies
necessary to describe the sine or cosine curves representing an image projection.
Because the acquisition data are discrete, the maximum number of peaks possible
in a projection would be in a situation in which peaks and valleys occur in every

ec
=
12.2 Single Photon Emission Computed Tomography
181
alternate pixel (i.e., one cycle per two pixels or 0.5 cycle/pixel), which is the Nyquist
frequency. If the pixel size is known for a given matrix, then the Nyquist frequency
can be determined. For example, if the pixel size in a 64×64 matrix is 4.5mm for
a given detector, then the Nyquist frequency will be
Nyquist frequencycycle pixel
05
./
cycl
=
05 045
./.
cycle
=
111
.sscm/
m
A common and well-known lter is the ramp lter (name derived from its shape
in the frequency domain) shown in Fig.12.8 in the frequency domain. An undesirable characteristic of the ramp lter is that it amplies the noise associated with
high frequencies in the image, even though it removes the blurring effect of simple
backprojection. To eliminate the high-frequency noise, a window is applied to the
ramp lter. A window is a function that is designed to eliminate high-frequency
noises and retain the low-frequency patient data. Typical lters that are commonly
used in reconstruction are basically the products of a ramp lter that has a sharp
cut-off at the Nyquist frequency (0.5cycle/pixel) and a window with amplitude 1.0
at low frequencies but gradually decreasing at higher frequencies. A few of these
windows (named after those who introduced them) are illustrated in Fig.12.9, and
the corresponding lters (more correctly, lter-window combinations) are shown in
Fig.12.10.
Fig. 12.8 The ramp lter
in the frequency domain

182
Fig. 12.9 Different
windows for reconstruction
lters in SPECT.Different
windows suppress the
higher spatial frequencies
to a variable degree with a
cutoff Nyquist frequency
of 0.5cycle/pixel
Fig. 12.10 Different
lters for SPECT that are
obtained by multiplying
the respective windows by
the ramp lter with cutoff
at Nyquist frequency of
0.5cycle/pixel
12 Single Photon Emission Computed Tomography
The effect of a decreasing window at higher frequencies is to eliminate the noise
associated with them. The frequency above which the noise is eliminated is called
the cut-off frequency. As the cut-off frequency is increased, spatial resolution,
improves and more image detail can be seen up to a certain frequency. At a too high
cut-off value, image detail may be lost due to the inclusion of inherent noise. Thus,
a lter with an appropriate cut-off value should be chosen so that primarily noise is
removed, and image detail is preserved. Note that the Nyquist frequency is the highest cut-off frequency for a reconstruction lter and typical cut-off frequencies vary

Frequency (cycles/pixel)
1.00
5
5
5
5
5
5
12.2 Single Photon Emission Computed Tomography
183
from 0.2 to 1.0 times the Nyquist frequency. Filters are selected based on the amplitude and frequency of noise in the data. Normally, a lter with a lower cut-off value
is chosen for noisier data, as in the case of obese patients and in
201
Tl myocardial
perfusion studies or other studies with poor count density.
Hann, Hamming, Parzen, and Shepp–Logan lters are all low-pass lters because
they preserve low-frequency structures, while eliminating high-frequency noise. All
of them are dened by a xed formula with a user-selected cut-off frequency. It is
clear from Fig.12.10 that most smoothing is provided by the Parzen lter and the
Shepp–Logan lter produces the least smoothing.
An important low-pass lter that is most commonly used in nuclear medicine is
the Butterworth lter (Fig.12.11). This lter has two parameters: the critical frequency (vc) and the order or power (n). The critical frequency is the frequency at
which the lter attenuates the amplitude by 0.707, but not the frequency at which it
is reduced to zero, as with other lters. The parameter, order or power n, determines
how rapidly the attenuation of amplitudes occurs with increasing frequencies. The
higher the order, the sharper the fall. Lowering the critical frequency, while maintaining the order, results in more smoothing of the image.
Another class of lters, the Weiner and Metz lters, enhances a specic frequency response.
Many commercial software packages are available, offering a variety of choices
for lters and cut-off values. The selection of a cut-off value is important such that
noise is reduced and image detail is preserved. Reducing a cut-off value will increase
smoothing but will curtail low-frequency patient data and thus degrade image contrast, particularly in smaller lesions. No lter is perfect, and, therefore, the design,
acceptanc3e, and implementation of a lter are normally done by trial and error
with the ultimate result of clinical utility.
As already mentioned, ltered backprojection was originally applied only to
transverse slices from which vertical and horizontal long-axis slices are constructed.
Filtering between the adjacent slices is not performed, and this results in distortion
Fig. 12.11 Butterworth
lter with different orders
and cutoff frequencies
0.75
0.50
0.25
n= 2.0
=0.3
n= 2.0
0
0.125 0.250 0.375 0.500
0
n= 4.0
n= 2.0
n= 4.0
n= 4.0
=0.2
=0.3
=0.1
=0.2
=0.1

184
12 Single Photon Emission Computed Tomography
of the image in planes other than the transverse plane. With algorithms available in
current SPECT systems, ltering can be applied to slices perpendicular to transverse planes or in any plane through the 3-D volume of an object. This process is
called volume smoothing. However, because of the increased popularity of iterative
methods described below, the 3-D volume smoothing is not widely applied.
12.2.2.6 Iterative Reconstruction
The basic principle of iterative reconstruction involves a comparison between the
measured image and an estimated image that is repeated until a satisfactory agreement is achieved. In practice, an initial estimate is made of individual pixels in a
projection of a reconstruction matrix of the same size as that of the acquisition
matrix, and the projection is then compared with that of the measured image. If the
estimated pixel values in the projection differ from the measured values, a correction is calculated from the ratio or difference between the two values for each projection, which is applied to each pixel in the projection to obtain an updated
estimated projection for the next comparison with the measured projection. This
process is repeated until a satisfactory agreement is obtained between the estimated
and actual images. The schematic concept of iterative reconstruction is illustrated in
Fig.12.12. The method makes many iterations requiring long computation time and
with the availability of faster computers nowadays, the method is routinely used in
image reconstruction in PET, SPECT, CT and MR imaging.
Consider a radioactive source of 5×5 pixel cross-sectional matrix containing a
varied amount of activity in each pixel as illustrated in Fig.12.13a. Only three mea-
sured projections A, B, and C, obtained at different angles are shown with ve bins
each, which are basically the pixels in a row of the acquisition matrix in line with
Backproject projections to
create a new
estimated image
Estimated
Initia
l
image
guess
Unfold
projections
Calculated
projections
of estimated
image
Correct for
differences
Fig. 12.12 Conceptual scheme of iterative reconstruction
Discrepancy
Compare A&
Reconstructed
image
B
Maximum
agreement
ba
Measured
projections

pa
j
m
=∑1
q
q
ap
k
i
j
∑
∑
12.2 Single Photon Emission Computed Tomography
185
a
Fig. 12.13 (a) Three projections A, B, and C, each with 5 bins, taken of a 5×5 cross-sectional
matrix. Counts p
tion matrix, as given by Eq. (12.4). (b) Concept of weighting factor, a
is the weighted sum of counts contributed by each pixel in a row of the acquisi-
i
b
ij
the source matrix. Since not all pixels contribute equally, a weighted sum of the
contributions from each pixel makes up the measured activity pi in the ith bin, that is,
=
i
.
ij j
q
(12.4)
where qj is the counts (activity) in the jth pixel and aij is the probability that an emission from pixel j is recorded in the ith bin. The concept of aij is illustrated in
Fig.12.13b, which is given by the shaded area of the pixel j along the ith bin.
In Eq. (12.4), the measured values of pi are known, whereas those of qj in the true
image are not known and need to be determined by the iterative method. Initially,
some arbitrary positive estimates of qj (0, 1, and so on) are assumed in each pixel of
the image matrix. Then the values of qi are calculated by adding the values of qj for
the ith bin at an angular projection. q
is compared with pi, and if there is no accept-
i
able agreement, corrections based on their ratio (pi/qi) or difference (pi−qi), are
applied to each pixel along the ith projection (backprojection) to obtain an updated
estimate of the image. This is repeated for each bin of each projection (A, B, and C,
etc.) to complete one iteration. Many iterations are performed until an acceptable
agreement between the measured and estimated images is achieved. The ratio technique is called the maximum likelihood-expectation maximization (MLEM) method
and the difference method is called the additive simultaneous iterative reconstruc-
tion technique (ASIRT). Mathematically, they are expressed as follows:
For MLEM:
n
j
n
a
ij
j
1
k
+
=
∑
ij i
m
i
aq
ij j
k
(12.5)
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