Brief definition of Multi-modality Diagnostic facility, Teleradiology, PACS, RIS, Quality Assurance Programme
Explanation of the Quality assurance Committee
Introduction to Chest X-ray technology and CR cassette
Quality Control Tests for Chest x-ray Technology
Introduction to Fluoroscopy Technology
Quality Control test for Fluoroscopy
Quality Assurance Program Review Test
Quality Assurance Drawback
Quality Assurance Programme in Computed TomographyRamzee Small
Introduction to Computed Tomography
Basic description of the components of a CT System
Introduction to Quality Assurance
Quality Assurance and Quality Control Tests in Computed Tomography base on frequency
Objective of QA/QC Test
Quality Assurance Programme in Computed TomographyRamzee Small
Introduction to Computed Tomography
Basic description of the components of a CT System
Introduction to Quality Assurance
Quality Assurance and Quality Control Tests in Computed Tomography base on frequency
Objective of QA/QC Test
All medical personnel share same thing in common, they all serve the patients. no one of them is entirely independent of others. the patient is a reason for existence in whole organisation. hence, the duty of RADIOGRAPHER must be seen in relation to the patient in particular and hospital as a whole.
All medical personnel share same thing in common, they all serve the patients. no one of them is entirely independent of others. the patient is a reason for existence in whole organisation. hence, the duty of RADIOGRAPHER must be seen in relation to the patient in particular and hospital as a whole.
Mammography : quality control (quality assurance)Kajal Jha
Mammography quality control. This is the class presentation for the syllabus of BSC MIT at BPKIHS Dharan. It is the concise ppt dealing with the quality control of mammography and hence quality control. Mammography is an x-ray imaging
method used to examine the breast for the early detection of cancer and other breast diseases. It is used as both a diagnostic and screening tool.
- also known as Mastography
Elevating Patient Care: Medical Equipment and ServicesSando Surgical
Explore how advanced medical equipment and services empower healthcare professionals to deliver superior patient care. Dive into the transformative impact of technology on efficiency within the healthcare sector.
Clinical evaluation report cer in a more stringent regulatory- Pepgra HealthcarePEPGRA Healthcare
European regulatory framework has established rules that govern the development, manufacturing, and marketing of medical devices in the European market. Both European and non-European medical device manufacturer’s fall under the purview of the regulatory framework, which is established to
provide condence to the clinicians and the patients that the medical devices and the implantable devices used in the region have been validated for their potential benets and certied as safe for usage.
Greetings from ACS!
After the series of successful courses on PACS, ACS is closely working with two expert trainers, Mr. Andrea Poli, PACS Implementation expert from Italy, and Mr. Ronald Gilbert, senior Imaging and Informatics practitioner and Instructor from US, to organize our upcoming 05 days professional course “PACS AND IMAGING INFORMATICS”, with ASRT approved 37.50 Category A CE credits.
This course is scheduled from March 26th to March 30th, 2018 at Aloft Kuala Lumpur Sentral, Kuala Lumpur, Malaysia.
The course is great chance to prepare for CIIP exam.
In case of any inquiry, please feel free to contact Mr. Syed at training@acsmb.com
Thank you.
STANDARDS AND PRACTICE FOR INFECTION PREVENTION AND CONTROL IN SONOGRAPHY: WH...convegnonazionaleaiic
STANDARDS AND PRACTICE FOR INFECTION PREVENTION AND CONTROL IN SONOGRAPHY: WHICH CLEANING, DISINFECTION AND/OR STERILIZATION IS RIGHT FOR MY ULTRASOUND PROBE?
A brief introduction to PACS along with its pros and cons. General PACS workflow of a medical imaging department and a general PACS configuration. Guide for Integration of PACS into a department with already existing PACS and several configuration set up that can be adapted to maintained the workflow of the imaging department along with their requirement, advantages and disadvantages.
Brief explanation of what is PET, the main components for a PET system along with their basic functions. The principle behind PET inclusive of positron emission and emission detection. Acquisition and reconstruction of the collected data to produce the final image. Finally the pros and cons of Positron emission tomography.
Definition of Side lobes and the principle behind its production during ultrasound imaging. Side lobes artifact and its result on image. Explanation of harmonic imaging, its production and the techniques use to eliminate fundamental frequency to produce optimal harmonic images.
Explanation of what splenomegaly is in relation to its dimension deviation from normal spleen.Classification of splenomegaly according to it's size in adult and pediatric. The causes of splenomegaly along with the symptom that would manifest as a result of this anomaly. Lastly, diagnosis of splenomegaly
A brief Introduction into the spleen (size, shape, location, function etc). Procedure for splenic ultrasound, Sonographic appearance of the normal spleen.
Pathologies of the Spleen (Splenic rupture , Splenic Hemangioma ,Sonographic appearance of)
Ultrasonography in Abdominal Aortic Aneurysm Diagnosis (A Literature Review)Ramzee Small
Introduction to Abdominal Aortic Aneurysm, Signs and Symptoms of AAA, possible treatment, Diagnosis of Abdominal Aortic Aneurysm. Diagnosing Abdominal Aortic Aneurysm with Ultrasonography. Appearance of AAA on a sonogram and limitation of ultrasound in diagnosing Abdominal Aortic Aneurysm.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
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Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
2. Outline
Brief Definition of Terms
Quality Assurance Program
Quality Control
Administrative Procedure
Preventive Maintenance Procedure
Training
Quality Assurance Committee
Chest X-ray Technology
Quality Control Test for Chest X-ray Equipment
Fluoroscopy Technology
Quality Control Test For Fluoroscopy Equipment
Quality Assurance Program Review Test
Integration of Quality Control Test into Multimodality System
Quality Assurance Drawback
Health and Safety
Conclusion
References
4. Diagnostic Facility
A diagnostic radiology facility is any facility in which an x-
ray system(s) is used in any procedure that involves
irradiation of any part of the human for the purpose of
diagnosis or visualization.
6. Radiology Information System
(RIS)
A RIS is an information system where;
Patients are registered,
Examinations are scheduled and
Radiologists’ reports are recorded,
Stored and distributed.
The RIS can also provide management information and
may hold information that is important for revenue
generation
7. Picture Archiving and Communication System
(PACS)
PACS is a healthcare technology use for;
The short- and long-term storage,
Retrieval,
Management,
Distribution and
Presentation of medical images.
PACS and a RIS need to work seamlessly together
9. Teleradiology
Teleradiology is considered to be the transmission of a full set
of full integrity images to a Centre distant from where the
images were generated.
Purposes of teleradiology includes;
Primary diagnostic interpretation
Expert secondary consultation
Preoperative surgical planning
10. Teleradiology
Benefits of Teleradiology
Provide access to medical image reporting for underserviced centers.
Support patient consultations and inform patient treatment decisions
Provide access to image interpretation for remote regions
Provide reporting in shifts to provide timely interpretation after
normal working hours
14. Quality Assurance Program
What is a Quality Assurance Program ?
An organized effort by the staff operating a facility to ensure that
the diagnostic images produced are of a 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.
_World Health Organization (WHO)
15. Quality Assurance Program
Objectives of QA Program
to maintain optimal quality of diagnostic images;
to reduce unnecessary radiation exposure to patient and staff; and
to be cost effective
The primary goal of a radiology QA program is to ensure the consistent
provision of prompt and accurate diagnosis of patients
16. Quality Assurance Program
This program has many facets, including,
1. Quality Control tests,
2. Administrative procedures,
3. Preventive maintenance procedures and
4. Training.
17. Quality Assurance Program
1. Quality Control
Quality control (QC) is an integral part of quality assurance
It involves specific actions designed to keep measurable aspects
of the process involved in manufacturing a product (image) or
providing a service within specified limits.
18. Quality Assurance Program
QC is summarized in four principal steps.
I. Acceptance testing to detect defects in equipment that is newly
installed or has undergone major repair
II. Establishment of baseline performance of the equipment
(commissioning test)
III. Detection and diagnosis of changes in equipment performance before
they become apparent in images
IV. Verification that the causes of deterioration in equipment performance
have been corrected
19. Quality Assurance Program
The frequency of any QC test depends on the following variables;
The inherent variability of the process or equipment
The age, reliability, and frequency of use of the equipment
The criticality of the element in the imaging chain
20. Quality Assurance Program
2. Administrative Procedure
These procedures are design to verify that QC testing is effective, i.e., the
tests are performed regularly and correctly, the results evaluated promptly
and accurately, and the necessary action taken.
They include recommendations regarding the responsibility for quality
assurance action, staff training, equipment standards, and the selection of
the appropriate equipment for each examination
22. Quality Assurance Program
3. Preventive Maintenance Procedure
These are performed on a regularly scheduled basis with the goal of preventing
breakdowns due to equipment failing without warning signs detectable by monitoring.
These procedures includes;
Visual inspection of the mechanical and electrical characteristics of the x-ray system
Assuring cleanliness with respect to spilling of contaminants in the examination
room.
Following the manufacturer’s recommended procedures for cleaning and
maintenance of the equipment
Regular inspection and replacement of switches and parts that routinely wear out or
fail
23. Quality Assurance Program
4. Training
The QA program include the means to provide appropriate training for all
personnel with QA responsibilities (especially those directly involved with
QC testing) to ensure each meet a minimum level of competency to
perform QC test correctly and consistently.
Companies whose sole purpose is training as well as service and repair
companies and the facility’s medical physicist can provide seminars and
training courses on the how to perform Quality Control tests.
25. Quality Assurance Committee
What is the Quality Assurance Committee ?
Personnel in the QA program who are responsibility for oversight of the QA
program, setting the goals and direction, determining policies, and
assessing the effectiveness of QA activities.
They have an overall documented strategy with clearly defined work plans
to achieve the goals and objectives of the radiology department.
26. Quality Assurance Committee
QA committee members includes;
Medical Physicist
Radiologist
Biomedical engineer
Medical Imaging Technologist (MIT) and Radiographer
Information Technology (IT) Technician
27. Quality Assurance Committee
Medical Physicist
An individual who is competent to independently practice in one or more of
the subfields in medical physics.
Advising the facility on radiation protection of the patient, staff and members of the
public.
Conducting tests to ensure the safety and proper performance of imaging equipment
used.
Assignment of Bio-medical engineering service staff for corrective maintenance or
preventive actions.
Training of personnel utilized for quality control
Develop and implement a radiation protection program
28. Quality Assurance Committee
Radiologist
A medical doctor who specializes in the diagnosis and treatment of disease
and injury by using medical imaging technologies.
Determine the overall quality of the output image
Select the technologist to be the primary QC technologist, performing the prescribed
QC tests.
Ensure that appropriate test equipment and materials are available to perform the QC
tests.
Ensuring that medical physicists and radiographers have adequate training and
continuous education
29. Quality Assurance Committee
Biomedical Engineer
Biomedical engineers use their knowledge of modern biological principles
in their engineering principle to design and develop devices and
procedures that solve medical and health-related problems.
Biomedical engineer are involve in;
Corrective and preventative maintenance
Fault Reporting
30. Quality Assurance Committee
Medical Imaging Technologist (MIT) and Radiographer
Ensuring that the appropriate protocol and technique factors are used for
the requested examination.
Ensuring that the QC tests are performed, interpreted and recorded
appropriately.
Perform all the checks for the daily, monthly and quarterly QC testing of
equipment
Report faults immediately any deviation in trend of equipment
performance to QA manager
Undertaking additional continuous education courses
31. Quality Assurance Committee
Information Technology (IT) Technician
IT is a key element of any digital radiology facility that intends to store,
review and distribute images electronically or using hard copy. There
responsibility includes;
Maintenance of the integrity of system databases to ensure continuous
and accurate operation of the information systems
Planning,
Deployment,
Testing
34. Chest X-ray Technology
The technology use for chest examination is similar to that of any
other x-ray examination,
however it is perform with the patient in an upright position
against a tube stand.
35. Chest X-ray Technology
The x-ray tube emits x-rays directed towards the patient, which interacts
with the patient's anatomy.
The computed radiography (CR) image receptor records the altered x-ray
distribution to form the image.
CR system firstly converts the incoming x-ray photons
to light then converts light into an electronic signal.
The images are read by a reader device where it is scanned by a laser
beam and the final image appearing on the computer screen.
36. Quality Control Test
Acceptance Test
Equipment Visual Check Test
Control Panel
Collimator/Indicator/Locks
Upright Bucky
General
Commissioning Test
System assembly evaluation
Collimation assessment
kVp accuracy and reproducibility
Exposure reproducibility and beam quantity (mR/mAs)
Radiographic AEC system performance assessment
Focal Spot Size
Beam quality assessment (HVL)
Equipment warm-up test
View boxes and viewing conditions
Phantom image quality evaluation
Laser Film Printer Quality Control Test
Protective Shielding Test
38. Quality Control Test
Focal Spot test
Objective
To determine effective focal spot size, the magnification factor must be known (image
size/object size)
Frequency
Initially and after tube replacement
Equipment required
Star test Pattern- e.g. 9 - 2,0°; 9 - 1, 5°-360 (A disk with radiating bars is used to produce
a radiographic image).
Cassette 35cm×35cm
39. Quality Control Test
Procedure
1. Mount the star test plate so that the radiographic central ray is perpendicular to the star pattern and
passes through the center of the star.
2. Place a image plate at about the same distance from the test plate as the plate is from the focal spot,
and align it so that the central ray strikes the center of the film.
3. If the blur pattern is too small, magnification can be increased by moving the film further from the
test plate. If the blur pattern is too large, magnification can be decreased by moving the film closer to
the tube.
4. The kV and mA should be comparable to that used clinically, to get the true focal size which is
somewhat dependent upon the electrical factors. Recommended technique should be one half the
maximum mA at 75 kVp. The density of the image should be about 1.5.
40. Quality Control Test
5. Process the CR cassette. Determine the magnification (M) by dividing the diameter
of the radiographic image of the star pattern by the true star test pattern diameter
(45 mm).
6. Scan the star pattern on the radiograph inward from the periphery to find the
outermost region in which the image of the sectors disappears. This is the region of
zero contrast. Measure the diameter of this region across its greatest extent and also
in the perpendicular dimension. Let these diameters be called D1 and D2.
7. The focal spot size corresponding to the individual diameter dimensions can be
determined by the following formula:
𝑭 =
𝑵
𝟓𝟕. 𝟑
×
𝑫
(𝑴 − 𝟏)
Where:
F - Focal spot size in mm
N - Angle of the star pattern line
D- Diameter of the zero contrast region in mm
M- Magnification
41. Quality Control Test
8. Several regions of zero contrast may be found on a single film. It is extremely
important that the largest one be used.
Analysis
Measurements of the radiographic image of the star are taken lengthwise and
crosswise. Along with the magnification factor, the measurements are put into the
formula.
𝑭 =
𝑵
𝟓𝟕. 𝟑
×
𝑫
(𝑴 − 𝟏)
𝑴 =
𝟓𝟑𝒎𝒎
𝟒𝟑𝒎𝒎
= 𝟏. 𝟏𝟖𝒎𝒎
N=2
Magnification (M - 1) = 0.18
42. Quality Control Test
For the Anode-Cathode Diameter:
D u- d =2 mm
𝑭𝒖 − 𝒅 =
𝟐
𝟓𝟕. 𝟑
×
𝟐𝟖
𝟎. 𝟏𝟖
=
𝑭𝒖 − 𝒅 = 𝟓. 𝟒 𝒎𝒎
For the Transverse Diameter:
D a- c = 28 mm
𝑭𝒂 − 𝒄 =
𝟐
𝟓𝟕. 𝟑
×
𝟑𝟒
𝟎. 𝟏𝟖
=
𝑭𝒂 − 𝒄 = 𝟔. 𝟔 𝒎𝒎
Therefore
The focal spot is 5.4 mm x 6.6 mm at the kVp and mA setting used.
44. Fluoroscopy Technology
Fluoroscopy refers to the continuous acquisition of a sequence of
x-ray images over time.
A standard fluoroscopic imaging system contains an x-ray tube,
filters, and collimation similar to the technologies used in
radiography
The principal component of the imaging system that
distinguishes fluoroscopy from radiography is the image
intensifier
45. Fluoroscopy Technology
An x-ray beam is passed through the patient body
The antiscatter grid removes contrast degrading
scattered radiation from the x ray beam
The intensifying screen converts the low intensity x
ray photon fluence exiting the patient into a high
fluence of visible photons by using multiple
conversion layers and a series of electrodes inside a
vacuum container.
The distribution of the visible photons are capture by
the video camera to form the image seen on the
monitor.
46. Quality Control Test
Acceptance Test
Equipment Visual Checklist
Table
Fluoroscopy Image Intensifier Assembly
Monitor
General
Commissioning Test
System assembly evaluation
Fluoroscopy System high and low contrast resolution test
Laser Film Printer Test
Fluoroscopy Collimation field size Test
kVp accuracy and reproducibility
mAs Linearity Test
Spot film AEC system performance
Entrance skin air kerma and air kerma rate
Maximum air kerma (exposure) rate
Beam quality assessment (HVL)
Equipment warm-up test
Artifact evaluation
Phantom image quality evaluation
CR Cassette Integrity Check
View Box
Protective Shielding integrity check
48. Quality Control Test
kVp Reproducibility Test
Objective
To measures the ability of the x-ray generator to faithfully deliver the same output when the
same exposure factors are used.
Suggested performance criteria
Limit (±5%)
Frequency
Initially, annually
Equipment required
Multifunction meter
49. Quality Control Test
Procedure
1. Take 5 consecutive measurements at the same SID (~150cm for the
chest detector and 110cm for the table detector)
2. Use any combination of operating loading factors (kVp and mAs), while
kVp is kept fixed.
3. From the recorded output readings, the maximum and minimum
readings are plugged into the following formula;
𝑹𝒆𝒑𝒓𝒐𝒅𝒖𝒄𝒊𝒃𝒊𝒍𝒊𝒕𝒚 𝑽𝒂𝒓𝒊𝒂𝒏𝒄𝒆 =
𝒎𝑹 𝐦𝐚𝐱 − 𝒎𝑹 𝒎𝒊𝒏
𝒎𝑹 𝒎𝒂𝒙 + 𝒎𝑹 𝒎𝒊𝒏
× 𝟏𝟎𝟎
50. Quality Control Test
Example
A test of reproducibility using 70kVp, 100 mA and 0.10 seconds resulted in the
following readings;
𝑹𝒆𝒑𝒓𝒐𝒅𝒖𝒄𝒊𝒃𝒊𝒍𝒊𝒕𝒚 𝑽𝒂𝒓𝒊𝒂𝒏𝒄𝒆 =
𝒎𝑹 𝒎𝒂𝒙 − 𝒎𝑹 𝒎𝒊𝒏
𝒎𝑹 𝒎𝒂𝒙 + 𝒎𝑹 𝒎𝒊𝒏
× 𝟏𝟎𝟎
=
𝟎. 𝟒𝟓 − 𝟎. 𝟑𝟖
𝟎. 𝟒𝟓 + 𝟎. 𝟑𝟖
𝒙 𝟏𝟎𝟎
= 𝟖. 𝟒𝟑%
The control limit for reproducibility is no more than 5%. In this case, a variance of 8.4%
is clearly unacceptable and corrective action is needed.
Exposure 1 Exposure 2 Exposure 3 Exposure 4 Exposure 5
0.45 0.38 0.45 0.44 0.40
51. Quality Assurance Program Review Test
Objective
The Quality Assurance Program must be reviewed in its entirety to ensure that all information is current
and accurate.
Frequency
Annually, After any equipment or personnel change
Procedure
1. Review and update as necessary the following information
QA personnel
QC measures
Policies and procedure
Corrective action
Record keeping
52. QA Program Drawback
Costly
The QA program is based on, planning, delegating responsibility, training and purchasing the proper
equipment, then establishing a high standard of quality and maintaining it.
Personnel
Unclear responsibility
Lack of qualification
Lack of commitment to perform QC test
Any program lacking genuine interest from its staff and initiated only to satisfy a regulatory requirement
is unlikely to produce optimal results.
53. Health And Safety
Health and safety issues in any work environment are very important
All heads of department are responsible for ensuring that injury or sickness, due to
working conditions, is kept to a minimum
To make the environment as safe as possible, make certain the following;
Regular maintenance inspections are carried out
Safety procedures are followed
Adequate staff instruction is given
Safety equipment is readily available
54. Conclusion
QA promote the effective use of radiation for a diagnostic outcome
through achieving and maintaining appropriate image quality and
reduction of patient dose.
An established QA program monitor the imaging process from start to
finish and reveal potential problems that may otherwise go unrecognized,
through a sequences of QC tests
QA in medical imaging is a rapidly evolving concept and each facility is
encouraged to continually pursue ways to improve and expand its
program.
55. References
Quality Assurance Programme for Computed Tomography; Diagnostic and Therapy Application, International Atomic Energy Agency IAEA,
Human Health Series No. 19, 2012, ISBN 978–92–0–128910–0
Worldwide Implementation of Digital Imaging in Radiology, Atomic Energy Agency IAEA, Human Health Series 28, 2015, ISBN 978–92–0–
102114–4
Radiation Protection in Diagnostic and Interventional Radiology, International Atomic Energy Agency, Part 15.1: Optimization of
protection in radiography Practical exercise
Quality Assurance Programme for Digital Mammography, Atomic Energy Agency IAEA, Human Health Series 17, 2011, ISBN 978–92–0–
111410–5
Quality assurance workbook for radiographers & radiological technologists, World Health Organization, 2001, ISBN 9241546425
X-ray equipment maintenance and repairs workbook for radiographers & radiologic technologists, World Health Organization, 2004, ISBN
9241591633
Quality Control Recommendations for Diagnostic Radiography Conference of Radiation Control Program Directors Inc. CRCPD, Volume 2,
2001
Quality Control Recommendations for Diagnostic Radiography, Volume 3: Radiographic or Fluoroscopic Machines, Conference of
Radiation Control Program Director Inc. CRCPD Publication 01-6 (July 2001)..
Quality Control in Diagnostic Radiology, American Association of Physicist in Medicine AAPM, Report No. 74. ISBN 1-888340-33-9
Basic Quality Control in Diagnostic Radiology, American Association of Physicist in Medicine AAPM, Report No. 4, 1981
Compliance Guidance for Fluoroscopic Quality Control, New Jersey Department of Environmental Protection, Bureau of Radiological
Health
56. References
Quality Control Program Department of Radiology, X-Ray Equipment Procedure manual, Mary Hitchcock Memorial Hospital Dartmouth-
Hitchcock Medical Center Lebanon, new Hampshire, June 2009
A. Dimov, J. Vassileva, Quality Control Of The X-Ray Fluoroscopy Equipment In The Period Of Their Clinical Use - Methods And First Results,
National Centre of Radiobiology and Radiation Protection, Sofia, Bulgaria
Charles R. Wilson, Ph.D., F.A.C.R., American College of Radiology ACR Radiography and Fluoroscopy Accreditation.
https://www.inlandimaging.com/what-is-a-radiologist
M.A. Périard and P. Chaloner, Diagnostic X-Ray Imaging Quality Assurance: An Overview, X-Ray Section, Consumer And Clinical Radiation
Hazards Division Radiation Protection Bureau, Environmental Health Directorate Health Protection Branch, Health Canada
Quality Control Programme for Radiodiagnostic Equipment: Acceptance tests, the radiation protection and nuclear safety authorities in
Denmark, 1999 ISSN: 0804-5038
https://www.acr.org/Quality-Safety/Radiology-Safety/Patient-Resources/About-Radiology
Phillip W. Ballinger, Eugene D. Frank, volume 3: Merrill's Atlas of Radiographic Positions and Radiologic Procedures, Edition 10, ISBN (Set)
0-323-01604-9
Jerrold T. Bushberg, J. Anthony Seibert, Edwin M. Leidholdt Jr., John N. Boone, The Essential Physic of Medical Imaging, second edition,
ISBN 0-683-30118-7
Magnetic Resonance Imaging, Quality Control manual, American College of Radiology ACR
Manual on quality assurance in diagnostic radiology - Part1 Radiographic equipment July 2001
Kamarul Aminbin Abdullah, QC Test For Fluoroscopic Equipment chapter 6 Abu Bakar School of Medical Imaging KLMUC.