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TRANSCRIPT
Sudan Academy of Science (SAS)
Atomic Energy Council
Evaluation of Quality Control in X-ray
departments in Al Neelain University
Hospitals
A proposal submitted for partial fulfillment requirements of
master (M. Sc) degree in Radiation Protection and environment
By:
Hafsa Idrees MerghaniB. Sc in Radiotherapy (SUST)
Supervisor:
Dr. ABD ELRHMAN A. EL BADAWIY
Dedication
This study is dedicated to my father, my great
mother, my loved family and to my friends.
Acknowledgements
I would like to thank my supervisor
Dr. ABD ELRHMAN A. EL BADAWIY
Al Mogran University Hospital
Al Neelain University Dental Clinics
Department of Medical Physics(AL Neelain University)
List of contents
Title pages
Dedication.......................................................................................................... i
Acknowledgment.............................................................................................. ii
List of content..................................................................................................... iii
List of tables........................................................................................................iv
List of abbreviation............................................................................................ v
Abstract................................................................................................................vi
Chapter one: Introduction
V Introduction......................................................................................................
Definition of Quality Control (QC)................................................................ Y
Quality Assurance (QA)..................................................................................
M Quality Control Program.................................................................................. *
Quality Assurance Program............................................................................. °
Optimization.......................................................................................................
Criteria of quality...............................................................................................V
conventional x-ray............................................................................A
Dental radiology................................................................................................
W Intraoral Radiographic Examination............................................................
Periapical examination................................................................................
W Paralleling Technique......................................................................................
W Bisected Angle Technique...............................................................................
Bite-wing Radiography..............................................................................
Occlusal radiograph.............................................................................
V* Justification.............................................................................................
Problem of the study.............................................................................
Objectives................................................................................................
W General objective..................................................................................
Specific objectives................................................................................
Thesis outlines..........................................................................................
Chapter two: Literature review
^A Theoretical background...........................................................................
^AA Quality Control....................................................................................
^AA Quality Administration Procedure....................................................
^AA Quality control tests.............................................................................
^AA Equipment.............................................................................................
^A.° Dental x-ray machine.............................................................................
X-ray machine test..................................................................................
fJ.V X-ray film..........................................................................................................
Screens and cassettes..........................................................................................
Viewing equipment......................................................................................
Film processing............................................................................................
Darkroom lighting......................................................................................
Processing equipment..................................................................................
Processing solution......................................................................................
V.V® Developer strength..................................................................................
Fixer strength...............................................................................................
Manual and automatic film processing...................................................
Reject analysis............................................................................................
Radiation protection..................................................................................
ALARA concept........................................................................................
previous studies................................................................................................
Chapter three
Materials
materials........................................................................................................
Conventional x-ray machine....................................................................
Dental x-ray machine..................................................................................
f.\f Digital meter...................................................................................................
f.M Fresh films.........................................................................................................
f.\° View box............................................................................................................
Methods................................................................................................................
f.V Sample size........................................................................................................
f.^A Data collection.................................................................................................
f.^.f Study area........................................................................................................
f.f.* Data analysis......................................................................................................
f.f.® Ethical clearance...............................................................................................
f.'O Study period.........................................................................................................
Chapter four
Results
M Results for quality control tests..........................................................................
*.f Observed result for other tests......................................................................
*.V Results of testing darkroom integrety..........................................................
Chapter five
Discussion,...
Discussion.........................................................................................
°.f Conclusion......................................................................................................
®.f Recommendation...................................................................................
References..............................................................................................................
Title
List of tables
page
Table *. Kvp &time accuracy in dental clinic......................................
Table Kvp &time reproducibility in dental clinic.............................
Table patient dose evaluation in dental clinic....................................
Table *. * Kvp &time accuracy in ALmogran Hospital...........................
Table Relative mA & mAs Linearity .............................................
Table O mAs Consistency
Table *.V KVp & Time reproducibility and linearity test
(output)............................................................................................................
Table Half value layer (HVL) test......................................
Table Developing and fixing time in dental clinic..............................
Table Reject films analysis in dental clinic..........................................
Table Reject films analysis in AL Mogran Hospital.............................
List of abbreviations
ALARA: As low as reasonable achievable
KV: Kilovoltage
KVp: Kilovoltage power
mA: milliamper Q.C: Quality Control
Q.A: Quality Assurance
SAEC: Sudanese Atomic Energy Committee
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Abstract
The aim of radiographic quality control (QC) program is to ensure that the
diagnostic images produced by this machine are of a sufficiently high quality so
that they provide adequate diagnostic information at the lowest possible cost
and with the least possible exposure of the patient to radiation. Quality control
measures are therefore as essential in a medical practice, as they are in a
specialized radiography department. This importance of quality is
acknowledged in the ionizing radiation regulations which make quality
assurance\control in radiography department a mandatory requirement.
This study aims to assess the quality control in x-ray department in AL Neelain
University Hospitals. The study was experimental, done by testing the
operational status of the x-ray machines and assessing the radiation protection
system.
The experiments results showed that there was a noted drop in the kVp
accuracy, and there was no regular reject analysis system.
Chapter One
M Introduction:
The principle goal of quality assurance of X-ray machine is minimization of
radiation exposure and obtains high image quality. This can be assess by
performance the X-ray machine by optimum operating parameters such as
reproducibility of tube voltage, dose output, time, X-ray tube efficiency,
Accuracy of kVp , mA , time , focal spot size and half value layer (T.M. Taha
AAPM report —describes quality assurance protocol for diagnostic x-ray
equipment at the radiologic technologist level. also The World Health
Organization (WHO) defines a quality assurance (QA) program in diagnostic
radiology as an organized effort by the staff operating a facility to ensure that
the diagnostic images produced are of sufficiently high quality so that they
consistently provide adequate diagnostic information at the lowest possible cost
and with the least possible exposure of the patient to radiation (Stephen Inkoom
et al Y«U).
Quality control in diagnostic radiology is essential to ensuring accurate
diagnostic information at optimal radiation doses, thereby making it possible to
reduce unnecessary radiation hazard to patients, workers and the public. Quality
assurance actions include both quality control (QC) techniques and quality
administration procedures. QC is normally part of the QA programme and
quality control techniques are those techniques used in the monitoring (or
testing) and maintenance of the technical elements or components of an X-ray
system. Certain essential quality control tests have greater effect on the final
diagnostic image quality.
The quality control techniques thus are concerned directly with the equipment
that can affect the quality of the image i.e. the part of the QA programme that
deals with instrumentation and equipment. (Stephen Inkoom et al Y*U) In
diagnostic radiology, the half-value layer (HVL) of the x-ray beam is needed in
order to judge the beam quality of the X-rays spectra.
M Definition of Quality Control (QC):These are specific actions designed to keep measurable aspects of the process
involved in manufacturing a product or providing a service within specified
limits. These actions typically involve measurement of a process variable,
checking the measured value against a limit, and performing corrective action if
the limit is exceeded. . (Stephen Inkoom et al Y*U)
Y.f Quality Assurance (QA):These are planned and systematic actions that provide adequate confidence that
a diagnostic x-ray facility will produce consistently high quality images with
minimum exposure of the patients and healing arts personnel. The
determination of what constitutes high quality will be made by the facility
producing the images. Quality assurance actions include both quality control
techniques and quality administration procedures. . (Stephen Inkoom et al Y«)1)
M Quality Control Program:Is allows a facility with limited resources and personnel to monitor the basic
components of the imaging process at a low cost through the usage of simple in
expensive tools and minimal staff time. . (Stephen Inkoom et al Y*U)
Y.® Quality Assurance Program:It is an organized entity designed to provide quality assurance for a diagnostic
radiology facility. The nature and extent of this program will vary with the size
and type of the facility, the type of examinations conducted, and other factors. .
(Stephen Inkoom et al Y«U)
Optimization:Optimization in the field of diagnostic radiology simply means any process or
procedure which ensures that doses due to appropriate medical exposure for
radiological purposes are kept as low as reasonably achievable (ALARA)
consistent with obtaining the required diagnostic information, taking into
account economic and social factors.
There are two types of x-ray machines in AL Neelain University Hospitals one
is dental machine in college of dentistry, the other is plain x-ray machine in AL
mogran Hospital. . (Stephen Inkoom et al Y.U)
'.V Criteria of quality:Every radiographic examination should produce radiographs of optimal
diagnostic quality, having the following features:
i. The radiographs should show the complete area of interest on the image.
ii. The radiographs should have the least possible amount of distortion.
iii. The radiographs should have the least optimal density and contrast (Eric
Whaites, Y««Y).
'.A Conventional x-ray:Radiography is the imaging of body structures, or parts of the body, using X-
rays. X-rays are a form of radiation (X-radiation) similar to visible light, radio
waves and microwaves. X-radiation is special because it has a very high energy
level that allows the X-ray beam to penetrate through the body and create an
image or picture. (Hakan Ilaslan,Y« ^°)
Plain film X-rays remain an important tool for the diagnosis of many disorders.
In radiography, a beam of X-rays, produced by an X-ray generator, is
transmitted through an object, e.g. the part of the body to be scanned. (Hakan
Ilaslan,Y« °)
The X-rays are absorbed by the material they pass through in differing amounts
depending on the density and composition of the material. X-rays that are not
absorbed pass through the object and are recorded on X-ray sensitive film.
While bone absorbs X-rays particularly well, soft tissue such as muscle fiber,
which has a lower density than bone, absorbs fewer X-rays. This results in the
familiar contrast seen in X-ray images, with bones shown as clearly defined
white areas and darker areas of tissue (Figure Y) Y. This makes conventional X-
rays very suitable for scans of bones and tissue dense in calcium such as in
dental images and detection of bone fractures. Other uses of radiography
include the study of the organs in the abdomen, such as the liver and bladder;
chest radiography for diseases of the lung, such as pneumonia or lung cancer
and mammography to screen for breast cancer. X-ray fluoroscopy is used to
detect a number of diseases associated with the stomach and intestine, genitals
and urinary tract. (Hakan Ilaslan,Y* °)
Traditionally, medical X-ray images were exposed onto photographic film,
which require processing before they can be viewed and take up a lot of space
in hospitals and doctors' offices. Digital X-rays, which overcome these
problems, have therefore become increasingly popular in radiography. Similar
to a digital camera, an electronic detector is used instead of film. This
“electronic image” is processed by a computer, enabling it to be stored digitally
and viewed on screen immediately without processing. (Hakan Ilaslan,Y* °)
X-ray imaging provides fast, high-resolution images and is relatively
inexpensive. The average examination for most plain film examinations takes
no more than minutes and requires no special preparation of the patient.
The operator, usually the radiographer (also known as a radiologic
technologist), selects the amount and type of X-rays to be used according to the
patient's size, the tissue or part of the body being imaged and the amount of
image contrast required. Because movement, e.g. of the lungs and diaphragm,
blurs the image, patients are usually asked to hold their breath during the
exposure. The X-ray picture is stored on a piece of film called a radiograph.
These are interpreted by a physician specially trained to interpret them, known
as a radiologist. (Hakan Ilaslan,Y °)
'.^ Dental radiology
'A' Intraoral Radiographic Examination
The intraoral radiographic examination is a radiographic inspection of teeth &
intraoral adjacent structures. It requires the use of intraoral film, which placed
inside the mouth.
There are three common types of radiographic examination that use intraoral
film:
Periapical examination.
Interproximal examination.
Occlusal examination.
'A* Periapical examination:
Main Indications:
Detection of apical infection/inflammation.
Assessment of the periodontal status.
After trauma to the teeth and associated alveolar bone.
Assessment of the presence and position of unerupted teeth.
Assessment of root morphology before extractions.
During endodontics.
Preoperative assessment and postoperative appraisal of apical surgery.
Detailed evaluation of apical cysts and other lesions within the alveolar bone.
Evaluation of implants postoperatively.
There are two methodes for obtaining periapical radiograph:
A. Paralleling technique
B. The bisecting angle technique
Y.^.f Paralleling Technique
The film packet is placed in a holder and positioned in the mouth parallel to the
long axis of the tooth under investigation (magnification, loss of definition
target-film distance long PID).
Y. The X-ray tube head is then aimed at right angles (vertically and
horizontally) to both the tooth and the film packet.
f. A film holder must be used to hold the film parallel with the long axis of the
tooth. The patient cannot hold the film. The technique is reproducible.
This positioning has the potential to satisfy four of the five ideal requirements
of shadow cast principles.
Y.M Bisected Angle TechniqueThe film packet is placed as close to the tooth under investigation as possible
without bending the packet.
Y. The angle formed between the long axis of the tooth and the long axis of the
film packet is assessed and mentally bisected.
f. The X-ray tube head is positioned at right angles to this bisecting line with
the central ray of the X-ray beam aimed through the tooth apex.
Using the geometrical principle of similar triangles, the actual length of the
tooth in the mouth will be equal to the length of the image of the tooth on the
film.
'A® Bite-wing Radiography:
Interproximal caries.
Over-hang filling.
Level of crestal bone between the teeth.
Interproximal calculus.
Principles:
The film is placed in the mouth parallel to the crown of both upper & lower
teeth.
The film stabilized when the patient bites on the bite-wing tab or bite-wing film
holder.
The central ray of the x-ray beam is directed through the contacts of the teeth,
using a + *̂ degree vertical angulation.
'A^ Occlusal radiograph:
The maxillary anterior occlusal radiograph can be made on both adults and
children. For an adult, it is made using a size t film/phosphor plate with the
long axis anterior-posteriorly or horizontally. It is important to have a
minimum of cm of film/phosphor plate anterior to the maxillary central
incisors. (T.M. Taha Y^T).
'.'» Justification:
Radiation is a major risk in diagnostic medical imaging and therapy. The
problem is caused by incorrect use of radiography equipment and from
unnecessary radiation exposure to patients.
Y.YY Problem of the study:
In Sudan, there is lack of knowledge of the importance quality control of X-ray
machine, in the most hospitals there is no regular quality control of X-ray
machine, also majority of them no radiation protection officer (RPO) employed
to monitors the radiation protection and supervise the quality control process.
Y.YY Objectives:
Y.YY.Y General objective:
The main objective of this study is to evaluate the quality control in X-ray
departments.
Y.YY'.Y Specific objectives:
- To evaluate the quality control program in Al Neelain University
hospitals.
- To evaluate radiation protection program at X-ray departments under
study in order to reduce unnecessary radiation to the patients and
occupational.
- to identify the effect of quality control tests in reducing the radiation dose
to the patients and operators.
- to get image with high quality with minimum radiation (ALARA).
Y.Yf Thesis outlines:
This study consists of five chapters; chapter one includes introduction, problem
of the study, and objectives, chapter two highlights the literature review, chapter
three shows the methodology of the study, chapter four deals with results and
data analysis, and chapter five discusses the results, conclusion, and
recommendations. At last there are references and appendices.
Chapter Two
Literature review
Y.' Theoretical background:
Y.'.' Quality Control:
Quality control uses a plan of action to ensure radiographs of consistently high
quality and high protection from radiation and infection. This plan includes
several routine assessments of image, and protective measures. The assessment
includes the image quality; this is affected by the performance of the x-ray
machine, manual processing procedure, viewing condition, system of infection
control and radiation protection. Optimization of these conditions results in the
most accurate diagnostic images and lowest possible exposure for patient and
radiographer. The study aimed to assess the quality control system in the x-ray
departments in AL Neelain University Hospitals, and suggests a corrective
action when necessary, in order to solve the problems which may lead to errors
in the application of quality control. The study will be carried out through the
data collection and assessment of radiation protection in this department. In
previous studies a comparison done between different types of dental
radiographic techniques, said that the bisecting technique is the best in
visualizing the entire tooth and its supporting structures (Rehab et al, Y««V).
Another study said the orthopan tomography is the best in demonstrating the
surrounding bone of the teeth (Fekry et al Y««Y).
Y.'.Y Quality Administration Procedure
It is refers to the management of the quality assurance plane in x-ray office. The
basic elements of a quality administration program include the following:
i. Description of the plan
ii. Assignment of duties
iii. A monitoring schedule
iv. A maintenance schedule
v. A record-keeping log
vi. A plan for evaluation and revision
vii. In-service training
A written description of the quality assurance plan used x-ray radiography
should be on file and made available to all staff members. The staff members
must understand the standards of quality as well as the purpose of maintaining
quality control of radiographic procedures. A written monitoring schedule
detailing all quality control tests and the frequency of testing for all x-ray
equipment should be posted in the department. A record-keeping log of all
quality tests, including the specific test performed, the data performed, and the
test results, should be carefully maintained and kept on a file in the department
(Bachman et al *̂ ).
^.Y.f Quality control tests:
Are specific test that are used to maintain and monitor x-ray equipment. To
avoid excess exposure of patient and personnel to x-radiation, the radiographer
must have clear understanding of the quality control procedure used to test
specific equipment, supplies, and film processing in x-ray office. (Quality
assurance for dental facilities et al, *̂ ).
^.Y.i EquipmentQuality control test are necessary to monitor x-ray machine, x-ray film screen,
and cassettes and viewing equipment to consistently produced diagnostic high
quality radiographs, dental x-ray equipment must be functioning properly
(Quality assurance for dental facilities et al *̂)
^.Y.® Dental x-ray machine
The dental x-ray machine most be inspected and monitoring periodically and
most also be calibrated at regular interval and. Calibration of dental x-ray
equipment most be performed by qualified technique to ensure consistent x-ray
machine performance and production of diagnostic radiographs. There are many
annual tests recommended for dental x-ray machine. These tests are designed to
identify minor manufactions, including machine output variation, tube head
drift, timing errors, inaccurate Kilo voltage and mill amperage reading. Most of
the tests require some basic testing material, film and test logs to record results
(Quality assurance for dental facilities et al *̂).
X-ray machine test:
Generally, x-ray machines are quite stable and rarely need to be tested; the
following parameters should be measured:
. X-ray output A radiation dosimeter is used to measure the intensity of
radiation output, usually is measured in milliroentgens.
Y. Beam alignment.
T. Beam energy. The KVp or HVL of the beam should be measure to ensure
that the beam has sufficient energy to produce good quality radiograph
without excessive soft tissue dosage.
Timer. The timer should be accurate. The test can be done by using a
spinning top with notch on the edge.
mA the linearity of the mA control should be done with a dosimeter or
with step wedge.
V. Focal spot size. It may become enlarged with excessive heat generated
within the x-ray machine. (Quality assurance for dental facilities et al
m.).
X-ray film:
The x-ray film must be properly stored, protected and used before its expiration
date. For quality control purposes, each box of film should be tested for
freshness as it is opened. The following fresh film test is recommended to check
newly opened box of film:
. Prepare film. Unwrap one unexposed film from newly opened box.
Y. Process film. Use fresh chemicals to process the unexposed film.
The result of fresh film can be interpreted as follows:
a. Fresh film, if processed film appears clear with as height blue tint, the
film is fresh and has been properly stored and protected.
b. Fogged film, film that has expired, has been improperly stored, or has
been exposed to radiation appears fogged. If the film is fogged it must not
be used (Quality assurance for dental facilities et al *̂).
^.Y.A screens and cassettes:
Intensifying screen used within the cassettes holder should be examined
periodically for dirt and scratches. Screen should be cleaned be monthly
commercially available cleaners recommended by the screen manufacture.
The following film screen contact test is recommended:
. Insert one film between screens in the cassette holder.
Y. Place wire mesh test object on the top of the loaded cassette.
f. Position the position indicating device (PID) using a f* -inch target -
film distance while directing the central ray perpendicular to the cassette.
f. Expose the film using *̂ mA, V* KVp.
Process the exposed film.
V. View the film on a view box. The result of the film-screen contact test
can be interpreted as follows:
a. Adequate contact:
If the wire of mesh image seen on the film exhibits a uniform density, good
film-screen contact has taken place. Proceed with cassette and screen use.
b. Inadequate contact:
If the wire of mesh image seen on the film exhibits varying densities; poor film
screen contact has taken place. Areas of poor film-screen contact appear darker
than good contact areas.
^.'.^ Viewing equipment:
a. The view box is a light source that is used to view radiographs. A
working view box is necessary equipment for the interpretation of the
radiographs. The view box contains fluorescent light bulbs that emit light
through an opaque plastic or plexiglass front. The view box should emit a
uniform light when it is functioning properly. A photographic light meter
can be used to determine proper viewing brightness (Quality assurance
for dental facilities et al *̂).
*.'.' * Film processing:
Film processing is on the most critical areas in quality control and
requires daily monitoring, processing problem have the potential to result
in a large number of non-diagnostic radiographs. Quality control tests
must be performed routinely to determine whether or not the condition
for film processing is acceptable (Quality assurance for dental facilities et
al ^V).
^.'.'' Darkroom lighting
The darkroom must be checked for light tightness and proper safe
lighting every V months. The following light leak test is recommended for the
darkroom:
. Prepare darkroom, close the darkroom door and turn off all lights
including the safelights.
Y. Examine darkroom, once your eyes are accustomed to the darkness;
observe the areas around the door, the seams of the walls and ceiling, the
vent areas, and keyhole for light leaks.
The following safe lighting test, often referred to as the coin test is
recommended:
i. Prepare darkroom. Turn off all the lights in the darkroom including
the safelight (Quality assurance for dental facilities et al *̂).
ii. Prepare film. Unwrap one unexposed film. Place on a flat surface
at least f feet from the safelight. Place a coin on top of the film.
iii. Turn on the safelight. Allow the film and coin to be exposed to the
safelight for f to f minutes.
iv. Remove the coin and process the film.
If on visible image is seen on the processed radiograph, the safe
lighting is correct. If the image of the coin and a fogged background
appear on the processed radiograph, the safelight is not safe to use
with that type of film, to avoid safe lighting problem, the radiograph
must use the film manufactures recommended safelight filers and bulb
wattages. In addition, the film must be unwrapped at last f feet away
from the safelight. A coin test is used for safe lighting. Coin placed on
unexposed film under safelight. Developed film showing outline of
coin indicating that safelight intensity is too great and is not safe.
Safelight problem must be corrected before processing with film
processing (American Academy of Dental Radiology Quality
Assurance Committee, ^AT).
The film with seven coin on it, has been gradually uncovered every f*
second. The coin-covered part of the film remains white while the
surrounding film is blackened or fogged. The longer the film is
exposed to the safelight the darker it becomes (American Academy of
Dental Radiology Quality Assurance Committee, ^AT).
^.'.'^ processing equipment:
Processing equipment must be maintained and monitored on a daily basis.
The thermometer and timer must be checked for accuracy with manual
processing techniques. The processing time and temperature recommendations
of the film manufacturer must be followed. If automatic processing equipment
is used, the water circulation system must be checked, and the solution levels,
replenishment system, and temperatures must all be monitored. The
manufacturer's procedure and maintenance direction must be carefully
followed. Each day, two test films should be processed in the automatic
processor. Test films are recommended:
i. Prepare film. Unwrap two unexposed films, expose one to light.
ii. Process both films in the automatic processor.
The result of the automatic processor test films can be interpreted as
follows:
a. Functioning processor:
If the unexposed film appears clear and dry and if the film exposed to light
appears black and dry, the automatic processor is functioning properly.
b. Non-functioning processor:
If the unexposed film does not appear clear and dry and if the exposed
film does not completely appear black and dry, and then the
processing solution and temperature must be checked. Correction must
be made before processing with processing (American Academy of
Dental Radiology Quality Assurance Committee, ^Af).
^.Y.Yf Processing solution:
The most important component of the film processing quality control
is the monitoring of the processing solution. The processing solution
must be replenished daily and changed every f to f weeks as
recommended by manufacturer. As alternative using the calendar to
determine the freshness of solution, quality control tests can be used to
monitor the strength of the developer and fixer solution. Processing
solution must be evaluated each day before any patient films are
processed (American Academy of Dental Radiology Quality
Assurance Committee, ^AT).
^.Y.Yt developer strength
When the developer solution loses strength, the time
temperature recommendation of the manufacturer is no longer
accurate.an easy way to check the strength of the developer
solution is to compare film densities to a standard. One of the
following tests can be used:
i. Reference radiograph
ii. Step wedge radiograph
iii. Normalization device
Reference radiograph:
It is one that processed under idea condition and then used to
compare the film densities of radiograph that are processed
daily.
The following step can be taken to create reference radiograph:
i. Prepare film. Use fresh film to make a reference
radiograph.
ii. Expose the film using the correct exposure factor.
iii. Process the film using fresh chemicals at recommended
time and temperature.
View the references radiograph and the daily radiographs side
by side on a view box. Compare the densities on the reference
radiograph with the densities on the daily radiographs.
Comparison of daily radiographs with the reference radiograph
can be interpreted as follows:
a. Matched densities: if the densities on the reference
radiograph match the densities on the daily radiograph, the
developer solution strength is adequate. Process with
processing.
b. Unmatched densities: if the densities on the daily
radiographs appear lighter than those seen on the reference
radiographs, the developer solution either weak or cold. If
the densities seen on the daily radiographs appear darker
than those seen on the reference radiograph, the developer
solution is either too concentrated or too worm.
Weakened or concentrated developer solution must be
replaced. If the developer solution is too cold or too worm, the
temperature must be adjusted.
Step wedge radiograph:
A step wedge is advice constructed of layered aluminum steps.
When a step wedge is placed on the top of a film and then
exposed to x-rays, the different steps absorb varying amount of
x-rays. When processed, different film densities are seen on the
dental radiograph as result of the step wedge. The following
steps can be taken to create step wedge radiographs.
i. Prepare the film: Use a total of Y. fresh films to create a
supply of films for daily testing. Place an aluminum step
wedge on top of one film.
ii. Expose the film: Repeat with remaining films using the
same step wedge and exposure factor.
iii. Using fresh chemical: Process only one of the exposed film.
This processed radiograph will exhibit different densities as the
result of step wedge and is known as standard step wedge
radiograph.
iv. Storage of the film: store of the remaining exposed films
in a cool, dry area protected from radiation.
v. films processing: each day, after the chemicals have been
replenished, process one of the exposed step wedge film.
vi. Viewing the radiographs: view the standard radiograph and
the daily radiograph side by side on a view box . Compare the
densities seen on the daily radiograph with the densities seen
on the standard radiograph. Comparison of the daily step
wedge radiograph with the standard step wedge radiograph can
be interpreted as follows.
a. Matched densities:
Use the middle densities seen on the standard step wedge
radiograph for comparison. If the density seen on the
standard radiograph matches the density seen on the
daily radiograph, the developer solution strength is
adequate. Proceed with processing.
b. Unmatched densities:
If the density on the daily radiograph differs from that on the standard
radiograph by more than two steps on the step wedge, the developer
solution is depleted. The developer solution must be changed before
proceeding with processing (American Academy of Dental Radiology
Quality Assurance Committee, ^AT).
^.Y.Y® Fixer strength:
The fixer removes the unexposed silver halide crystals on the film that result in”
clear” area on the film, when the fixer becomes weak, the film takes a longer
time to clear, and when the fixer is at full strength, a film takes minutes, to
clear without agitation(American Academy of Dental Radiology Quality
Assurance Committee, ^AT).
^.Y.Y^ Manual and automatic film processing:
Quality control of manual and automatic film processing is important because
deficiencies in this process are the most common cause of faulty radiographs.
Several steps, followed carefully, greatly increase the probability of producing
radiographs of consistently high quality. Replenish solution daily at the
beginning of the workday, check the level of processing solutions and replenish
if necessary. The developer should be Replenish with fresh developer or
preferably with developer Replenished.
The fixer should be replenished with fixer. At the beginning of the workday,
check the temperature of the processing solution. The solution must reach the
optimal temperature before use “YA F (Y*C) for manual processing and AY F (YA
C) for heated automatic processing. Regular clearing for processing equipment
is necessary for optimal operation. The replacement frequency of processing
solution depends on the rate of use of the solution and on the size of the tank
(Council dental material et al., ^Aa).
YJJV Reject analysis:
To achieve high standard level of images quality, there should be continuous
assessment for the rejected films so as to reduce the number of the retakes
radiographs. Every x-ray department must have a reject-analysis system. The
system must determine what information required, how the data can be
collected, and how correct problems arise in the department using the collected
data (Bachman et al, Yaa«).
Y.Y.YA Radiation protection:
Many of early pioneers in x-ray radiography suffered from adverse effects of
ionizing radiation. The role of the radiographer is to achieve a high protection to
the patient before, during, and after exposure to x-ray (International
Commission on Radiation Protection).
With the use of proper patient protection techniques, the amount of radiation
received by the patient can be minimized.
Y.Y.Y^ ALARA concept:
All exposure to radiation must be kept to a minimum, or as reasonably
achievable to provide both protections to the patient and operators, every
possible method should be employed to minimize risk (Alcox, ^VA).
M previous studies:
Evaluation of Diagnostic Radiology Department in Term of Quality
Control (QC) of X-Ray Units at Khartoum State Hospitals
H.A.IsmaiP, O.A.Ali\ M.A.OmerT, M.E.Garelnabii, N.S.Mustafa0
, ^Radiation & Isotopes Center -Khartoum (RICK) - Sudan
T, i, °Sudan University of Science and Technology - College of Medical,
Radiologic Science, Khartoum, Sudan
The mean objective in diagnostic radiology is to in provide high
qualitydiagnostic image while keeping the patients and workers dose in the
lower limit according toALARA principle, (Maria Lucia Nana et al ^).
To optimize the practice of diagnostic radiology, adequatequality assurance
(QA) program should be in place. A hospitals with ^A x-ray units
distributed in Khartoum state were evaluated inthis study.Each x-ray unit
was tested for Kvp andtimeReproducibility , accuracy of Kvp and time ,
mAs linearity, and coincidence between light beam and radiation beam.
The dark rooms were alsoevaluated to assess the fog level.CONNY II QC
Dosimeter made by PTW company were use to for this study. The analysis
of the results showed that two out of eighteenunit had a problem in mAs
linearity, also two out of eighteen unit had a problem in kVp accuracy and
one had a problem inkVp reproducibility. three devices have defects
concerning adaptation with optical fieldand radiation field. More than ° * %
of the darkrooms had a problem in fog level; time accuracy and time
reproducibility were in the acceptable limit.The quality control of the
radiologicaldevices should be performed periodically and regularly and the
defects of the devices should be removed in order to beassured of the
appropriate function of the devices. many of these machines need service
because of lack ofimplementing the quality control program regularly,
which indicates that the quality control programs should be
extendedregularly.because the dark rooms is very important place specially
in conventional radiology departmentlike in Sudan so it need to periodic
review to monitor the fog.
- Ibrahim Idris Suliman B.Sc. (Physics), M.Sc. (Nuclear Physics)August
(Y**V* Patient Dosimetry and Quality Control in Diagnostic Radiology
X-ray tube voltage and generator requirements are generally fulfilled,
except for x-ray tube output at low mAs values. The use of an AEC
unit for different phantom thicknesses for various types of
examinations does not yield constant image receptor entrance dose.
The requirements for the correspondence of the x-ray filed and the
light field, as well as those for the display station and the hard copy
device are fulfilled. However, the image on the monitor is smaller than
the corresponding x-ray field. The x-ray field is completely visualised
on the hard copy. • The image quality assessed by the various methods
indicates that the results for the paediatric unit are worse than for the
chest x-ray unit. For the chest x-ray unit image quality is similar to the
results obtained in a recent survey of PA chest radiography
- RadyAzzoz, Khalid M. ElShahat , Rezk Abdel MonemRezk(Sep.-Oct.
Y*̂ ^Evaluation of Quality control systems for X-Ray machines at
different Hospitals using patient's radiological dose assessment
technology
The study showed variations in technique, exposure factors, film-screen
combinations, and radiation dose for the same type of examination, both
within and between rooms, which strongly supports the idea that further
optimization is possible. Eighty hospitals recorded lower ESD values
below EC/IAEA recommended diagnostic reference levels * mGy), and
of the hospitals exceeded the UK national reference value (* mGy).
Radiographic practices in Ghana are not fully optimized and this,
therefore, calls for robust implementation of an appropriate and realistic
QAprogram, which currently is not in existence in all the facilities
surveyed. The variations in the data obtained also demonstrate the
importance of creating awareness for the radiographic staff about regular
quality control testing of the equipment and standardization of protocols
Chapter three
Materials and methods
?.' Materials:
?.'.' X-ray machine:
Model x-ray tube assembly *.V/\^P^ADE-A o. MAX/FOCUS KV/*.V/1.V
mm. Production class . Manufactured V«^T august made in Japan
V^ABBZX**^V....
Dental x-ray machine:
Tube housing assembly model: A£V£.V< ^.manufactured: July Italy.
Output max: V.KVp -AmA-T.Vs VT.v...A IEC TTV.total filtrationVmmAL.
Preheating time: ms.
x-ray tube model
The x-ray machine was tested by the quality control team of the department of
radiation protection.
?.'.? Digital meter:
All tests of this machine were done by using:
digital meter (RAD-CHECK Plus model «V-°YV)-(KV meter RMI V£°); RMI
.SN ° *A made in USA gammex RMI.
Vi*A Multi-function meterserial no A««T^-YVVA.made in USA.gammex RMI.
which can give a reading for different tests of the x-ray machine by applying a
single exposure.
V.M Fresh films:
The x-ray films were tested by using fresh film test to check newly opened box
of films.
PRIMAX RDX-®AE soft.exp V*Y*.1.
^.Y.® View box:
The view box was examined weekly for dirt and discoloration of the plexiglass
surface.
Methods:
Sample size:
-f® periapical film
- '® A size film
- YYB size film
- YV C size film
Data collection:
V.V.V Study area:
AL Neelain university hospitals (Al Mogran Hospital and dental clinics).
Method:
The research based on performing all control test of X-ray machine and
evaluating radiation program in these departments.
Data analysis:
By using Excel program to analyze the data.
?J.® Study period:
f months
Chapter four
Result
M results for quality control tests in dental clinic showed by tables below was
performed using a digital meters .The result showed a noted variation in
Kvp&time accuracy,Kvp&time reproducibility ,HVL,patient dose evaluation .
Table *?: Kvp & time accuracy
KVp & TIME ACCURACY (Put dosemeter in beam at cm from focus)
No KVp
KVpMeasure
d Difference
CorrectedKVp
KVp Error%
Accepte d*
Time (ms)
TimeMeasured
TimeError
(%)Accepted*
*
5 V. V\o .J.A V1VA -Y.5 £ Yes v . o£o -V No
Y V. vvv .,YH VHH -Y.tr Yes ..o ..tYo .^o No
r V. VV VY.YYt -Y.V5 Yes ..o ..tYo -^o No
£ V. VY.f *.®f VY.U -r.tr Yes *.ty *.yv® -1V.Y No
®
* *>° • kV and error <±®% S > • % error for I/O units
< % error for all other units
Table f.Y Kvp &time reproducibility
< KVp & TIME REPRODUCIBILITY
KVp V. t ms
No KVp Time
V\^ *.fYf
Y V^.A *.fYf
T VY.* *.fYf
Average yyn ..nt
Coefficient of variation coefficient of variation < ®% = •.••YYH
f. Patient Dose Evaluation
■ place cone tip * mm from dosemeter
■ set maxillary molar/ bitewing setting
Standard I/O units kVp Dose
(V-V. kVp): < V.o mGy for molar view or < i mGy for 0* - kV unit
Should be kVp):
—mGy for molar view
< 0mGy for any view
0> kV: <0.* mGyV. kV: <V.° mGy
(E speed film)
Slit dose from OPG units Dose
Should be < mGycmV
Dose-width product for panoramic film: <V° mGy mm
Table i.T patient dose evaluation
D' ‘.M mAsV (V* mAs^ ) DY ..V
D,( mR ) DV (mR )
VTT
^Y Yff
YfY
...XT
Resultsfor quality control tests in conventional x-ray unit showed by tables
below was performed using a digital meters .The result showed a noted
variation Kvp&time accuracy,relative mA&mAs linearity,mAs consistency,Kvp
and linearity test and HVL test.
Table t.t Kvp&time accuracy
KVp & TIME ACCURACY (Using the KV meter)
First Exposure Factors KVp (a.-^. • ) A. mA (Y..-i. •) x.. t (v.-y..) ms .. mAs x.
FDD vo cm Wave Form CP
No KVp
KVpMeasure
dCorrected
KVp KVp Error% Accepted*Tim
eTime
Measured
TimeError
(%)Accepted*
*
0. 0. o.J.A .... Yes o. iV.V ..TV Yes
V V. oA.A 0V..U v. .. Yes oV oV.T ^T.Yi Yes
T V. VA.V VV.YYi W Yes VT VT.i ..oV Yes
i A. VA.A VV.Ti \o. Yes V^ V\T ..i Yes
0 V. AV . AV.. iA \VA Yes A. A..T i.o Yes
* *± ^.% **
Table f.® RELATIVE mA & mAs LINEARITY
Y RELATIVE mA & mAs LINEARITY (Using the KV meter)
KVp V* t Y**
i mA R Acceptable* mAs R Acceptable**
Y ^T Y** v Y*
Y YY® Yn* NO YY.® Yn. * NO
T Y* * T*T NO Y* T*.T NO
f Y®* TVY NO Y® TV.Y NO
* |Ri - (mAsi *R ! / mAs!) |/ (mAs *R! / mAs^ ) < !«% ** |Ri - (mAi *r! / mA!) |/ (mAi *R ! / mA! ) < !«%
Table O mAs CONSISTENCY
r mAs CONSISTENCY (Using the KV meter)
mAs (Using the KV meter) YY.o
No KVp Y. KVp V. KVp A.
Y mA t Ry mA t RY mA t Rr
Y Yr Y.. Yt. ‘ Yr Y.. Yt.o Yr Y.. Y..Y
r YYo Y.. YA.A YYo Y.. Yt.Y YYo Y.. YA.A
t Yo. o. YA.Y Yo. o. Yt.Y Yo. o. Yt.r
Average t.trr Average o.r. Average o.trr
Acceptable YES Acceptable YES Acceptable YES
* {Sqrt(S(R- Ra v)*/(n->))/ Ra v ) < *.*° } =
Table t.V KVp AND TIME REPRODUCIBILITY AND LINEARITY TEST (output)
i KVp AND TIME REPRODUCIBILITY AND LINEARITY TEST (output), Radcheck
KVp V. t msec Y.. mAsY Y. mAsY (Y* mAsY ) Y.
No KVp Time Dy( mR ) Dy (mR )
Y Yt.. Y...t ot Y Y Y
Y YA.t Y...o oA Y Y Y
T ^A.n Y* *.f ®n Y Y Y
Average nv.Y ! . •.V vi.mnv UV.mV
Coefficient of variation{sqrt(E(D- Dav)7(n-!))/ dav = •.••* Acceptable YES
KVp Reproducibility {sqrt(E(KVp- KVpav)Y/(n-!))/ KVpav <•.•» = •.••xovv Acceptable YES
Time Reproducibility {sqrt(E(t-tav)7(n-!))/ tav <.,.°} = •.• Acceptable YES
X!= D!a v / mAs! XY= DYa v / mAsY
|xy- xy 1 = xY+ xY = *.Y*(xy+ xy) = Acceptable*:
* 1 X!_ Xy l< ..!*(X !+ Xy)
Table f.A HALF VALUE LAYER (HVL) TEST
0 HALF VALUE LAYER (HVL) TEST
KVp Field Size X cm'
No Added filter(t)(mm) Iy (mR) Iy (R) lav (R)
Y ... Y Y Y
Y Y.. AV
r Y.. V.
t Y.o Yr
HVL XmmAL
RECOMMENDED MINIMUM HVLS AT VARIOUS KVPS
Measured KVp Minimum HVL(mmAl)
MeasuredKVp
Minimum HVL(mmAl)
Measured KVp Minimum HVL(mmAl)
r. ..r V. Y.o YY. r
t. ..t VY Y.Y YY. r.Y
tt ..o A. Y.r Yr. r.o
o. Y.Y t. Y.o Yt. r.A
Y. Y.r Y. . Y.V Yo. t.Y
1 RADIATION FIELD
A COLLIMATOR
Working □ YES V □ NO
Light working □ YES V □ NO
Light edge clear □ YES V □ NO
Cross indication □ YES V □ NO
Cross centered □ YES V □ NO
B BEAM ALIGNMENT TEST
I PERPENDICULARITY TEST
F-table top Y** cm
KVp ®* mA Y** t Y* msec mAs ®
Balls Images overlap
(perpendicularity within ..°o)
Ball Image in the Ystcircle
(misalignment is o)
Ball Image in the Ynd circle
(misalignment is r.. o)
Ball Image out of circles
Acceptable
Yes
V
II COINCIDING TEST
FFD mAs Measured Variance
Long Axis Short Axis
% Variance
Long Axis Short Axis
Acceptable*
Y** cm Y*
* < Y% of FFD (Ycm)
Table t.t film developing and fixing time (Dental Clinic)
Date Developing time
In sec
Fixing time
In sec
o\YY\Y.YV Yo A.
V\YY\Y.YV Yo Ao
t\YY\Y.YV r. to
YY\YY\Y.YV rr to
Yt\YY\Y.YV to tt
Table t.Y. rejects film analysis (Dental Clinic)
Investigation a b c D e f G h i J
Upper anterior
Y . . . Y . . Y . r
Upper premolar
Y . . . Y . Y . Y o
Upper molar . Y . . t Y Y r . YY
Loweranterior
Y . . . Y Y . . . t
Lower premolar
. Y . . . Y Y r Y A
Lower molar Y Y . . t Y Y r Y Yt
*key points:
Films total r r ♦ ♦ Y 1 1 A r £o
(a) Overdeveloped, (b) underdeveloped, (c) overexposed, (d) underexposed, (e)
film position error, (f) horizontal angulation error, (g) vertical angulation error,
(h) con-cut, (i) machine failure, (j) films total.
Table £.A rejects film analysis (Al Mogran Hospital)
Investigation a b C d E F
Chest x-ray £ 1 ♦ ^Y
Shoulder r ♦ 1
Cervical 0 r Y ♦ ♦ A
Hand forearm
♦ Y ♦ r 1
Arm-wrist Y Y ♦ 1
Pelvis-hip 0 ♦ Y ♦ A
Femur-knee £ ♦ ♦ ♦ Y 1
Leg-ankle ♦ ♦ r
Films total V V 0 V oV
*key points:
(a) Patient position, (b) angulation, (c) overexposed, (d) underexposed, (e) light
beam diaphragm, (f) films total.
M observed results for other tests:
M.Y Results of testing darkroom integrity:
The result of this test in dental clinic showed a light leakage in the area near to
the roof and the darkroom door but it did not cause film fog, but there is no
darkroom in AL Mogan Hospital because they use CR processing system.
Chapter five
Discussion, conclusion and recommendations
®.Y Discussion
In dental clinic the test showed by tables f.Y,f.Y,f.Twere performed using a
digital meter. The result shows a noted variation in kVp,TIME ACCURACY,mA &
mAs and output. The kVp of this machine was fixed at V* kv, there was
increasing in the kv(Y*%) and decreasing in time measured(Y*%),Kvp &time
reproducipility were acceptable(*.*®),also patient dose evaluation was
acceptable .
In ALMogran Hospital in tables f.f,f.®,f.\f.V,f.A, the results show variance
reading of digital meter but were acceptable (Kvp&time accuracy
Y *%),( RELATIVE mA & mAs LINEARITY !.%),(mAs CONSISTENCY—0)
),(KVp AND TIME REPRODUCIBILITY AND LINEARITY TEST (output) — 0). HVL is
Ymm.
Table f.n showed results regarding the assessment of the developing fixing
time, a timer was used to evaluate the activity of the processing solution. There
was no thermometer to check the solution temperature, and there was a mild
difference in developing and fixing time, because the processing solutions were
change continuously every two weeks.
The table f.Y* and f.YY showed that there was no regular reject analysis in the
departments under study. A number of f® films in dental department and ®V
films in conventional department were collected over the period of three
months.
Figure f.Y showed the distribution of the reject films in dental department
according to their causes and the investigation region. The highest number of
reject films (t) was in the lower and upper molar region due to patient
movement.
The study within the departments showed that there was a good radiation
protection system, therefore there was no radiation detected behind the
protective shield.
The co-patients did are not usually allowed to stay in the departments during the
exposure.
Moreover, the radiographer keeps attention to the application of the ten-day rule
to protect the pregnant ladies and their fetuses. Regarding a viability of the
protective devices, there was a lead apron beside the protective shield, but there
was no thyroid collar.
The study also showed that there was no quality control officer, and no quality
control tests programmed at all.
In AL Mogran Hospital the reject of films due to processing was very rare that
because they are use CR (computerize radiography processing system).
Conclusion
From the results in chapter four, and from discussion in chapter five, the tests
were done for the x-ray machines by using a digital meter and showed a noted
variation in kV, which degrades the image quality. The evaluation of the quality
control system revealed that the absence of regular reject analysis resulted in the
repetition of the same errors. The study also showed that the mentioned
departments should have a quality control officer to observe the quality control
program, and the departments should also provide quality control test tools.
®.V Recommendation
. The x-ray machines of AL Neelain Hospital need to be calibrated in such a
way as to be close to the standard.
Y. The dental department should be provided by thyroid collar.
r. Establishment of a written quality control programme with quality control
officer.
£. Correction of high rate of the retakes cardiographs by establishing regular
o. Providing the department staff with personnel radiation dose monitoring
devices.
1. The x-ray machines should undergo regular routine tests to ensure that
radiation protection, for both staff and patients, has not significantly
deteriorated.
V. All those involved in radiography should have received adequate theoretical
and practical training for the purpose of radiological practices and relevant
competence in radiation protection.
References
T.M. Taha.Study the Quality Assurance of Conventional X-Ray Machine using
Non-Invasive KV Meter.International Journal of Science and Research (IJSR)
ISSN (Online): YrYt-V.Yt Y.Yr).
Stephen Inkoom. Radiation Protection Institute, Ghana Atomic Energy
Commission, Wide Spectra of Quality Control Legon, Accra, Ghana.Y.YY
American academy of Dental Radiology Quality Assurance Committee:
Recommendation for quality assurance in dental radiology Oral Surg Oral Med
Oral Pathol oo:tYY, YtAr.
International commission on radiation protection: radiation protection, ICRP Publ. Y., Oxford, Ytt., Author. Blackwell Scientific, Oxford.
Armstrong P, Wastie ML, YtAr: Diagnostic Imaging. tth edn.
Glass BJ, Yttt: Infection Control in Dental Radiology, NY state Dent j Y.:tY.
H.A.IsmailY, O.A.AliY, M.A.Omerr, M.E.Garelnabit, N.S.Mustafao
MSD MANUAL professional version January Y.Yo Hakan Ilaslan,MD.