How Is The X-Ray Beam Created?
X -rays are produced when fast moving
electrons collide with a metal target. The energy carried in the
electrons is converted to x-rays and heat.
How Do You Control The Production Of The X-rays? & What
Characteristics Of The X-ray Beam Can You Control?
The Operator can control •
The Number of X-Rays produced, and
• The
Energy of the X-Ray Beam. These controls are achieved through the
exposure selections made on the x-ray machine operator console.
Knobology:
kVp Selector: kVp
stands for kilovolt peak/kilovolt potential. It affects the following:
-
Selects the voltage
differential used to accelerate the electrons.
-
Gives variable "speed" to
the electrons
-
Selects the penetrating
quality of the x-ray beam
-
Effects the efficiency of
x-ray production
-
Determines the scale of
contrast in the image
-
Determines the Scatter
radiation produced by the patient
Because x-ray production is basically the conversion of
one type of energy-Kinetic Energy-to two other types of energy - x-rays
and heat - the energy of the x-ray is dependent on the energy of the
electron at the time of conversion. The more energetic the electron, the
more energetic the x-ray. The faster an object-the electron-is moving,
the greater the kinetic energy. The electrons kinetic energy is
increased by implying an electrical potential between the cathode and
anode of the x-ray tube. The stronger this potential difference the
greater the developed kinetic energy of the electrons.
When you change the kVp you are changing the ability of
the x-rays to pass through the object. Thicker and/or Denser objects
require more energetic x-rays to pass through them. Thinner and or less
dense objects require less energetic x-rays to pass through them.
The x-ray image is formed by the differential absorption
of the x-ray beam. What you want to depict are the differences in the
body’s tissues. If there are a lot of small differences you want to
demonstrate that just as well as when there is big difference. The most
common way of referring to differences is contrast. The range of
differences is typically referred to as a scale of contrast. When there
are only one or two big differences this is referred to as a short scale
of contrast. Controversially where there are a lot of small differences
it is referred to as a Log scale of contrast. Obviously you need a kVp
that is sufficient to penetrate the body area of interest. The lower the
kVp, the more likely the x-ray is to be absorbed by most any type of
tissue. At quite high kVp, the energy is sufficient enough that just
about any tissue will be penetrated. So the objective of kVp selection
is to choose so that there is sufficient 4 penetration, but not so great
as to over-penetrate. Over-Penetration will not allow the differences or
contrast to be depicted.
mA Selector:
mA stands for milliampere: This is the measure
of the number of electrons flowing in the x-ray tube.
-
Activates a current flowing
through the filament
-
Heats the filament causing
electrons to be "boiled off"
-
Determines the number of
x-rays produced per unit time.
-
The number of x-rays
reaching the film determines the degree of blackening of the film.
Exposure Timer:
Controls the Duration of electron flow being subjected to the voltage
differential.
mAs Selector: mA
stands for milliampere-seconds It is the multiplication of mA x seconds
= mAs.
When you change the mAs you change the number of x-rays
produced. Film blackening is directly proportional to the number of
x-rays that pass through the object-Room Air or Patient Tissue.
Summary:
1) kVp controls x-ray energy and thus
penetrating ability and thus scale of contrast. 2) mA x Sec controls the
total number of x-rays produced and thus film blackening.
Choosing The Appropriate Exposure Factors:
So how do you go about choosing the appropriate
technique for the area that you want to display? The factors that need
to be considered are the type of tissue in the region of interest, the
type of x-ray machine (Specifically the type of generator), and the type
of film-screen system being used.
General Principles:
1) Rely on kVp to penetrate the area 2) Rely on
mAs to provide the film blackening.
The type of tissue in the region of interest constitutes
the subject contrast and this is what you want to display. For Example
you want to display the difference between the bone cortex, the bone
marrow cavity and the surrounding muscle; you want to display the
difference between the liver, the falciform fat, The intestinal wall and
the intestinal lumen; you want to display the difference between the air
filled region of the lung, the pulmonary vessels and the heart. The
major way to depict these is in the selection of the kVp used to image
the area of interest.
In small animals and in the distal extremity region of
the large animals where bone is the major structure of interest, a
relatively low kVp (60-70) is sufficient to penetrate the bone and soft
tissue. The low kVp will be very effectively absorbed by the bone
mineral and provide good contrast. This level of kVp will provide a
rather "contrasty" image which most find pleasing to use for bone
evaluation. To provide the film blackening needed, relatively high mAs
will be needed. As always try to use the shortest time possible to
prevent blurring from patient motion.
In the Thorax where there is a large variation in the
types of tissue present - Thin pulmonary vessels, thick volume of the
heart, very minimally absorbing aerated portion of the lung - a
relatively high kVp (80-100) is desirable to distinguish this variety of
Subject contrast. As these x-rays will be quite energetic, not as many
are needed to establish the degree of blackening so a relatively low mAs
is used. A short exposure time is essential in the thoracic region to
stop the blur of respiration motion.
The abdomen is more like the thorax than the skeletal
regions when it comes to choosing your exposure factors. There are three
major tissue types in the abdomen, soft tissue, fat and gas. However the
individual organs vary significantly in thickness. A medium kVp (70-90)
is desirable coupled with relatively low mAs. Although respiratory
motion is not as great of a problem, it is still best to keep the
exposure time as short as possible.
Preferred Relative Exposures:
-
Skeletal - High mAs with
low kVp
-
Abdomen - Medium mAs with
medium kVp
-
Thorax - Low mAs with high
kVp
The best way to create predictably good images in
Veterinary radiography is to create and use a Technique Chart that is
particular to each body area. The technique chart is based on
standardization of as many different variables as possible and only
changing one component of the exposure factors based on the thickness of
the body area. To create this technique chart initially involves a
trial-error process. Once the ideal exposure factors have been
established for the desired area on your trial patient, there are simple
mathematical relationships that can be used to fill in the chart for any
other thickness of that body area.
To Be Standardized are:
X-Ray Tube-to-Film Focal Distance: This is a very
simple relationship. The closer the x-ray tube is to the film the
greater is the intensity of the radiation exposure to the film. So by
altering the x-ray tube to- film distance you can effectively increase
or decrease the blackening of the film. It is best to standardize this
and is easiest to standardize this with an x-ray machine that has the
tube mounted on a stand that is fixed to the table and film holder. This
is the typical use in small animal radiography. Of the tube is manually
positioned each time and several different personnel are making images
you need to use a measuring device to try to standardize the distance.
Variations in film blackening are often noted when multiple personnel
hand position the tube as everyone stands at just a little bit different
distance from the patient. The relationship of x-ray Intensity to
distance is relatively profound - Intensity (1) = 1/d 2, Where d is the
distance from the x-ray tube to the film. So you can see that if you
double the distance, you reduce the radiation intensity to 1/4th, most
small animal radiography is done at a fixed tube-film distance of 40
inches (100 cm). Large Animal Skeletal Radiography is often done with 30
inch (75 cm).
Collimator: The collimator is a device used to
restrict the x-ray exposure to a specified surface area of the body. Its
major result, relative to image quality, is that it significantly
reduces the scattered radiation produced by the patient and this
improves image contrast. It also serves 2 major radiation safety
purposes- #1 to reduce the exposure to patient; and #2 to reduce the
scattered radiation exposure to the animal holders if manual restraint
is used. Collimators are available either as various diameter
exchangeable cones or as an adjustable permanent attachment to the x-ray
tube housing the cone type collimators must be removed and exchanged
with a different diameter to achieve a change in x-ray field size. The
adjustable collimators typically have dials or slider controls that
allow you to change the field size. The adjustable collimator also
usually has a light associated with it that shows the field size on the
patient. The light field type collimator greatly improves the ability to
accurately position the x-ray beam to the area of interest on the
patient.
Use of a Grid or No Grid: A Grid is a plate that
consists of parallel spaced bars of lead. Lead is a very effective
absorber of x-rays. The interspace material does not appreciably absorb
x-rays. The purpose of the grid is to absorb scattered x-rays between
the patient and the film. The scattered x-rays are created within the
patient by an x-ray tissue interaction that results in the conversion of
the incoming x-ray to an electron and a "new" x-ray with somewhat less
energy moving in a new direction. In essence the x-ray is deflected off
its original straight-line course. If this redirected "New" x-ray
successfully exits the patient it delivers exposure to the film that is
untrue relative to the anatomical structure from which it originated. A
fundamental assumption in the formation of the xray image is that the
x-rays travel in straight lines from the origin in the x-ray tube
through the patient to the film.
Most grids are focused grids. This means that the lead
bars are angled in the same plane as the x-rays coming from the tube.
The grid is placed between the patient and the film. Most often in small
animal systems the grid is incorporated into the table positioned just
above the film tray. Grids can also be purchased that are laid on top of
or independently affixed to the cassette. Grids are quite effective in
removing the scattered x-rays from the image. Removal of the scattered
x-rays improves the contrast in the image. Grids are generally used for
area thickness greater than 10 cm. However, if you decide to use a grid
for the area in question it may be easier to use it for all thicknesses
rather than to have to remember to activate it or deactivate it.
Making A Technique Chart:
Now that you have standardized as many factors as you
can you are ready to do some trial exposures, looking for the best for
the area of interest. You can make charts that are variable kVp or
variable mAs or those that are a combination. Which type you make
depends somewhat on the type of machine that you have to use. If you are
using a fixed kV, fixed mA, but variable time machine (like many of the
smaller portable machines) then your chart will by default be a variable
mA chart. If your machine has mAs and kVp selector controls or if it has
independent mA, Time, and kVp selectors then you could make either type
of a chart.
The basis for making a chart is to make several trial
exposures until you find one that works vest for that area in your trial
patient. You then apply some mathematical relations to construct the
selection factors for different sizes of that area. For an example, if
you were to make a variable kVp chart for the canine abdomen you would
make 3 trial exposures of the area with the dog lying in lateral
recumbency. Measure the thickness of the trial patient and record it in
cm. Because of the tissues within the abdomen use a fairly high kVp with
relatively low mAs. Keep exposure time short to do away with respiratory
motion effects on the cranial organs. Pick 3 exposure settings: #1 - 300
mA for 1/60 sec (5 mAs) at 70 kVp; #2 - 300 mA at 1/120 sec (2.5 mAs) at
70 kVp; and #3 - 300 mA at 1/30 sec (10 mAs) at 70 kVp. One has double
the mAs and one has half the mAs. Using good collimation for the
abdominal region, expose the three films and process them using standard
processing technique. When the images are viewed hopefully one will be
of good quality - adequate background blackness (room air space around
the patient) and good contrast scale for the abdomen. One should also be
underexposed (overall too white) and one should be overexposed (overall
too black). If none were acceptable, you would repeat the test exposure
modifying from the one that came the closest to what you want the image
to look like. If you must repeat a second set of trial exposures you
could modify any of the exposure factors, however it is preferable to
alter the mA or exposure time.
Once you have found the optimal or best set of exposure
factors for the trial dog's lateral abdomen you are ready to fill in the
working chart for other thicknesses. There is a fairly linear
relationship between kVp, area thickness, and response of the
film-screen system.
-
In the range of kVp less
than 80 a change of 2 kVp for each cm change in thickness will
maintain a quality image.
-
Between 80-100 kVp the
change is 3 kVp for each cm change in thickness.
-
For kVp greater than 100
the change must be 4 kVp for every cm change.
This allows you to make a variable kVp chart for the
abdomen. You would try this out on the same dog by taking the VD view.
Measure the abdomen, look up the kVp calculated for that thickness on
your working chart & try it out. You would then repeat this process for
every body area that you anticipate will need to be looked at
radiographically. Most small animal charts contain factors for Head;
Spine; thorax; abdomen; pelvis/hip joints; shoulder; elbow/stifle/bones
distal to elbow & stifle. Most equine charts have different settings for
a region and for a specific view within that region. For example the
equine foot requires increased exposure factors to emphasize the
navicular bone versus the thin solar margin of the 3rd phalanx.
As you repeat the trial process for each body region
some general guidelines for modifying the general chart are:
-
Low kVp settings with
concurrent high mAs settings give the best contrast for the skeletal
regions.
-
High kVp setting with
concurrent low mAs Settings give the best scale of contrast for the
thorax and abdomen.
-
Film blackening is directly
proportional to the product of the mA and the exposure time = mAs
factor.
Film blackening will also
change with a change in kVp. This is best used to change the film
blackness by a small amount. If you need a large change in film
blackening you need to change the mAs. This is preferred in that it
retains the contrast scale for the area being evaluated. However a 15%
increase in kVp will effectively double the film blackness (would have
the same effect as doubling the mAs). Controversially a 15% decrease in
kVp will effectively half the film blackness (would have the same effect
as halving the mAs) these latter two changes have then most profound
effect between 70-90 kVp.
Any technique chart when first developed is a working
chart. You may find that you need to make minor adjustments as you use
it for the first several weeks. However, it then should become quite
reliable. It is also good practice to record the exposure factors used
for each patient. Then if a re-check of that region is needed, you can
use the same exposure factors and be more likely to detect true change
in the patient. We find it easiest to record the area, exposure factors,
film-screen type on the outside of the patient’s radiographic film
filing envelope.
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Diagnostic Imaging Systems,
Inc.
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