This power-point presentation is very important for radiology resident radiologist and radiographers and technician. this includes principles, technique , biological effects of radiation and how to protect, whats should normal radiation dose with latest update. This slide also includes ALARA PRINCIPLE thanks.
This power-point presentation is very important for radiology resident radiologist and radiographers and technician. this includes principles, technique , biological effects of radiation and how to protect, whats should normal radiation dose with latest update. This slide also includes ALARA PRINCIPLE thanks.
Radiation Protection in Diagnostic and Interventional Radiology, MDIRT Nchanj...Nchanji Nkeh Keneth
Radiation Protection; an overview of ionising radiations. Radiation measuring instruments. Radiation Protection in Diagnostic and Interventional Radiology, credit to IAEA
Radiation protection, also known as radiological protection, is defined by the International Atomic Energy Agency (IAEA) as "The protection of people from harmful effects of exposure to ionizing radiation, and the means for achieving this". Exposure can be from a source of radiation external to the human body or due to internal irradiation caused by the ingestion of radioactive contamination.
Ionizing radiation is widely used in industry and medicine, and can present a significant health hazard by causing microscopic damage to living tissue. There are two main categories of ionizing radiation health effects. At high exposures, it can cause "tissue" effects, also called "deterministic" effects due to the certainty of them happening, conventionally indicated by the unit gray and resulting in acute radiation syndrome. For low level exposures there can be statistically elevated risks of radiation-induced cancer, called "stochastic effects" due to the uncertainty of them happening, conventionally indicated by the unit sievert.
Fundamental to radiation protection is the avoidance or reduction of dose using the simple protective measures of time, distance and shielding. The duration of exposure should be limited to that necessary, the distance from the source of radiation should be maxi mised, and the source shielded wherever possible. To measure personal dose uptake in occupational or emergency exposure, for external radiation personal dosimeters are used, and for internal dose to due to ingestion of radioactive contamination, bioassay techniques are applied.
Radiation Protection in Diagnostic and Interventional Radiology, MDIRT Nchanj...Nchanji Nkeh Keneth
Radiation Protection; an overview of ionising radiations. Radiation measuring instruments. Radiation Protection in Diagnostic and Interventional Radiology, credit to IAEA
Radiation protection, also known as radiological protection, is defined by the International Atomic Energy Agency (IAEA) as "The protection of people from harmful effects of exposure to ionizing radiation, and the means for achieving this". Exposure can be from a source of radiation external to the human body or due to internal irradiation caused by the ingestion of radioactive contamination.
Ionizing radiation is widely used in industry and medicine, and can present a significant health hazard by causing microscopic damage to living tissue. There are two main categories of ionizing radiation health effects. At high exposures, it can cause "tissue" effects, also called "deterministic" effects due to the certainty of them happening, conventionally indicated by the unit gray and resulting in acute radiation syndrome. For low level exposures there can be statistically elevated risks of radiation-induced cancer, called "stochastic effects" due to the uncertainty of them happening, conventionally indicated by the unit sievert.
Fundamental to radiation protection is the avoidance or reduction of dose using the simple protective measures of time, distance and shielding. The duration of exposure should be limited to that necessary, the distance from the source of radiation should be maxi mised, and the source shielded wherever possible. To measure personal dose uptake in occupational or emergency exposure, for external radiation personal dosimeters are used, and for internal dose to due to ingestion of radioactive contamination, bioassay techniques are applied.
Those who administer ionizing radiation must become familiar with the magnitude of exposure encountered in medicine, dentistry and every day life; the possible risks associated with such exposure; and the methods used to affect exposure.
Practitioners should remain informed about safety updates to further improve diagnostic quality of radiographs and decrease radiation exposure.
radiation control safety, role of Organization in radiation protection and environmental radiological surveillance.
Factors that affect radiation dose:
Regulations and procedures have been developed and implemented to limit radiation dose by regulating the use, storage, transport, and disposal of radioactive material by controlling time, distance and shielding
Time
The short the time spent near the source, the smaller the dose
Distance
The greater the distance the smaller the dose
Shielding
Use of materials to absorb the radiation dose
Basic Radiation Safety Awareness Training
History of Radiation
Natural and Man-Made Background Sources of Radiation
Fundamentals
Exposure Limits & Regulations
Detection of Radiation
Safe Practices with Radiation
Biological Effects of Radiation
Where to Find Further Information
Fluoroscopy ,Radiation safety and contrast agents including adverse effect an...Dr Ravi Shankar Sharma
IT includes everything related to fluoroscopy, radiation exposure, it,s effects, contrast agents , and it,s newer variants including gadolinium, anaphylaxis reactions and it,s management, images for epidural,intrathecal,subdural, intrarterial and intravenous contrast picture.
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.
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
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.
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.
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
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
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
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
2. The harmful effects of exposure to ionizing radiation
were largely unsuspected at the time of discovery of
xray.
The acceptance by society of risks associated with
radiation is conditional on the benefits to be gained
from the use of radiation.
3. RADIATION HAZARDS
RADIATION UNITS
BIOLOGICAL EFFECTS OF RADIATION
POPULATION EXPOSURES
4. DEFINITIONS
ABSORBED DOSE- radiation necessary to deposit energy of 1
joule in 1 kg of tissue.(SI unit- Gray)
ABSORBED DOSE EQUIVALENT- measure of biological
effectiveness of radiation.
ABSORBED DOSE EQUIVALENT = absorbed dose x quality
factor
Quality factor – function of particle type and energy.
X rays, β particles,ϒ rays, electrons 1
thermal neutron 5
5. The amount of energy deposited per unit length of travel
called LINEAR ENERGY TRANSFER.
Particle size α linear energy transfer α biological
damage
EFFECTIVE DOSE equivalent (hε)- purpose is to relate
exposure to risk.
.
6. NATURAL RADIATION
External and internal sources
EXTERNAL SOURCES
cosmic radiation, terrestrial gamma radiation.
Exposure varies with latitude and altitude.
INTERNAL SOURCE
Radionuclide's within the body.
K40, Rb87, C14 and members of the thorium and uranium
series.
Radon is largest contributor to avg annual effective dose
equivalent.
7. MEDICAL RADIATION
Two category – 1. diagnostic medical x-rays, CT
2. nuclear medicine
IN X RAY- 3 procedure provide > ½ of total dose (in mSv)
Barium enema - 4.0
Upper GI examination - 2.45
Lumber spine - 1.3
OTHERS-
Thoracic Spine- 1.0
Pelvis- 0.7
Chest- 0.06
10. STOCHASTIC EFFECT
Defined as an effect in which the probability of occurrence
increases with increasing absorbed dose.
severity does not depend on the magnitude of absorbed
dose.
ALL OR NONE PHENOMENON, NO DOSE THRESHOLD.
Example –cancers and genetic effects.
11. Radium watch dial workers – bone ca.
Uranium miners – lung ca
Early medical radiation workers - leukemia
Thymus gland treatment – thyroid ca
Atomic bomb survivors – leukemia/breast, lung and
bone Ca
12. NONSTOCHASTIC EFFECTS
Defined as somatic effect that increases in SEVERITY with
increasing absorbed dose.
degenerative effects such as organ atrophy and fibrosis.
Examples- lens opacification
blood changes
decreased sperm production
13. REGULATORY BODIES
ICRP – International Commission for radiation protection
is the international regulatory body.
AERB – Atomic Energy Regulatory board is Indian
regulatory body.
NCRP – National Commission for radiological protection
is the American counterpart .
.
14. FUNCTIONS
• Lay down norms for protection against radiation.
• Guidelines regarding the specification of medical x–
ray equipment, room layout of x– ray installation,
protective devices
• Responsibilities of the radiation personal, employer
and radiation safety officer
• Recommends the dose limits for radiation workers
and general public.
Approval for new models of x– ray equipment.
• Registration, inspection and ISO certification
15. DOSE LIMITING RECOMMENDATIONS
Atomic energy regulatory board (AERB) making
recommendations on limits of exposure to ionizing
radiation.
There are 3 classes of individuals-
-occupationally exposed individuals
-the general public
-embryo-fetus
16. OCCUPATIONAL LIMITS
For stochastic effects-
ANNUAL LIMIT- 50 mSv
For lifetime dose equivalent limit(mSv) to the whole body
= 10 times of age (in yr) of individual
For nonstochastic effect:-
- lens 150 mSv
- all other organ 500 mSv
Worker exposed to x ray for their own medical diagnosis or
treatment does not count as an occupational exposure.
17. EMBRYO-FETUS
Specific dose equivalent limit applies to the conceptus
(embryo + fetus), not to the mother.
Recommended dose equivalent limit 5 mSv for entire
gestational period.
Rate not exceeding 0.5 mSv in any one month.
19. GENERAL PUBLIC
When a member of general population eg. visitor enters a
radiation area , he becomes an occasionally exposed
individual.
Annual dose limit-
- <1mSv - frequent exposure
- 5 mSv - infrequent exposure
20. ALARA CONCEPT
` As Low As Reasonably Achievable`
For any given radiation source, magnitude of
individual doses, number of people exposed, and
likelihood of incurring exposures should be kept to
as low as reasonably achievable, taking economic
and social factors into considerations.
21. .
Judicious use of investigation
These include substituting non-ionizing
methods of examination in place of ionizing
radiation methods.
Ex – Evaluation of LN status in the abdomen by
USG in place of repeated CT scan & use of colour
Doppler flow imaging in place of diagnostic
angiography.
22. PERSONNEL PROTECTION FROM EXPOSURE TO X
RAYS
RADIATION MONITORING
Devices
- pocket dosimeter
- film badge
- TLD( thermo luminescent dosimeter)
TLD(principle):-depends on the ability of certain
crystalline materials to store energy on exposure to
ionizing radiation because of the trapping of valence
electron in crystal lattice defect.
23. Crystal (lithium fluoride) heated under controlled condition
↓
electrons return to normal state
↓
stored energy released in the form of light
↓
photomultiplier device
↓
initial radiation exposure
24. PROTECTIVE MEASURES
Basic 3 principles:-
- exposure time
- distance
- lead barriers
EXPOSURE TIME :- total dose equivalent α time
DISTANCE:-
- Inverse square law applies.
- whenever possible , distance should be 2 meter from
x-ray tube.
-Distance 1 m - 400 (exposure)
-Distance 2 m - 100
25. LEAD BARRIERS :-
- efficient absorber of x rays.
- great reduction of exposure by placing it in
between source and person.
- thickness stated in HALF VALUE LAYER
(HVL) for kilo voltage x rays.
(HVL – any material thickness which reduces
exposure rate by one –half.)
Means if initial dose H 100 mSv and HVL is 1 mm Pb
for given kVp , then 1 mm Pb will reduces H to 50
mSv and second HVL of 1 mm Pb will reduce another
one- half(25 mSv).
26. PROTECTIVE BARRIERS IN RADIOGRAPHY AND
FLUOROSCOPY
RADIATION SOURCES :-
- tube must enclosed in metal housing that
reduces leakage radiation ( is radiation which penetrates
the protective housing )
WALL PROTECTION :- 4 type of radiation
- USEFUL BEAM – is radiation passing through tube
aperture (aka Iry radiation)
- LEAKAGE RADIATION
27. SCATTERED RADIATION- undergone change in
direction during passage through matter.
STRAY RADIATION – Scattered + leakage radiation
There are 2 type of wall barriers-
Iry protective barrier - protects from useful
beam(mainly).
-In radiography upto 140 kV is about 1/16 inch
lead extending 7 feet up from the floor when tube is
5-7 ft from the wall.
28. IIry protective barrier :- is about 1/32 inch lead.
- extends from the top of the 1ry barrier to ceiling.
- ordinary plaster often suffice as a 2ry barrier without
added lead.
- leaded glass observation port in the control booth should
have same lead equivalent as the adjacent wall.
- leaded glass must 4 times as thick as lead sheet.
29. Lead apron – worn in fluoroscopy room.
- Pb equivalent 0.5 mm.
Check lead protective apron periodically for cracks by
means of a radiography test.
30. DOSE REDUCTION IN RADIOGRAPHY
BEAM FILTRATION –
- exposure greatly reduced by ALUMINIUM filter.
- removes lower energy photons.
- recommendations:-
operating kVp Minimum HVL
Al (mm)
< 50 0.3
50-70 1.2
> 70 2.3
31. COLLIMATION( BEAM LIMITATION) :-
- decrease in cross sectional area of the beam avoids
unnecessary exposure of tissues outside the area of
interest.
- also reduces amount of scattered radiation.
- modern equipment have automatic variable beam
limiting device with manual override.
32. GONADAL ,THYROID SHIELDING :-
- beam should be so restricted that direct
exposure of gonads does not occur.
- thyroid ,testes shield must have lead equivalent
0.5 mm.
- ovaries should be shielded whenever possible.
33. MODIFIED PROJECTION :-
- In radiography of girls for scoliosis should be use PA view.
- Reduces breast dose at least 98 % without loss of
radiographic quality.
34. HIGH KILOVOLTAGE :-
- high kVp with low mAs delivers smaller absorbed
dose to the patient.
CAREFUL TECHNIQUE :-
- to minimize repeat examination.
Radiographic examination in fertile women preferably
performed during 1st 10 days following onset of menstrual
period.
Ovulation and pregnancy are much less apt during this
time than later menstrual cycle.
35. PROTECTION IN MAMMOGRAPHY
Skillful technique minimizes breast dose.
Goal achieved by molybdenum targets and filters in
mammographic tubes.
Low dose screens and films, with/ without grid having
ratios of 3:1 or 4:1.
Efficient breast compression device :- reduces breast
thickness and make more uniform.
36. ADVANTAGE :-
1. decreases exposure factors with reduction of dose.
2. diminished amount of scattered thereby improving
contrast.
3. improved recorded details by bringing breast closer to the
image receptor.
37. CT SCANNING
Dose in CT scanning , by measuring absorbed dose at
the centre of one “slice” with small dosimeter in water
phantom.
Scanning this slice and 3 adjoining slices on both side.
Dosimeter record dose from direct beam through the
centre slice, as well as scattered radiation from adjoining
slices.
Collimator should also checked periodically to assure its
proper function.
38. PATIENT PROTECTION IN FLUOROSCOPY
Intermittent fluoroscopy – decreases exposure and
prolong tube life.
Restriction of field size – must be limited by suitably
lead shutters placed between tube and patient.
Correct operating factors – exposure decreases as kVp
increases and mA is lowered.
Recommended factors are 90-100 kVp, 2-3 mA and 2.
mm aluminium filter
39. The source-skin distance must be at least 15 inch with
stationary and 12 inch with mobile fluoroscopic
equipment.
Filtration :-
– increase in hardness of x ray beam by filter.
– Filter removed relatively more soft than hard
xrays.
40. PROTECTION IN NUCLEAR MEDICINE
Medical compounds containing radionuclide's are called
radiopharmaceuticals.
Types of radiation
– alpha particles
– beta particles
– gamma rays
radiopharmaceuticals emits beta and gamma rays.
41. Gamma rays are electromagnetic wave and have much
greater penetrability than beta particle.
Beta particles consist of high-speed electrons.
Beta particles are much less penetrating ,their effect
limited to the skin (external source) immediate
vicinity(internal source).
43. DISTANCE: -
- In case of gamma rays inverse square law applies
for the purpose of protection in storage and handling.
- long forceps should be used.
- avoid spillage of liquids
- container should be as remote as possible.
44. SHIELDING:-
- shield may be incorporated in the container itself
or it may be placed as a barrier around sources.
- γ emitting radiopharmaceuticals should be stored in their
container and surrounded with lead bricks (5 cm) on all
sides.
LEAD-SHIELDED SYRINGES – always be used for i.v.
injection.
- Disposable gloves should be worn to protect against
contamination by radionuclide's and by infection as well.
45. Low energy β particles are absorbed by container ,
cornified layer of skin.
Medical radionuclide P32 requires plastic such as
polystyrene.
LENGTH OF EXPOSURE-
- faster procedure → less exposure