Oral Radiology
Oral Radiology
Oral Radiology
I. HISTORY
- discovered by Wilhelm Conrad Roentgen 1895
- Gamma radiation has identical energy to diagnostic x-rays
II. PRODUCTION
- electrons originate at the cathode by heating a tungsten filament
- X-rays are produced when fast moving electrons are suddenly decelerated in
the tungsten target (anode) thus loosing much of their energy.
- electric field between the cathode and anode cause the electrons to accelerate
towards the anode
- < 1% of the energy formed at the anode is in the form of x-rays. Rest produces
heat .
- energy of electrons hitting the target varies because the voltage across the xray tube continually varies - the highest energy across the tube = peak kilovolt
(kVp)
- tube current (mA) controls the NUMBER of electrons produced at the cathode
- filters block low energy photons from leaving the tube resulting in fewer x-rays
leaving the tube but those that do have higher average energy
On striking the tungsten atoms, the electrons produce x-rays in two processes.
1. Characteristic radiation - where an electron is removed from the K shell and an
electron drops down from the L shell emitting exactly a 59 keV photon. This
amount of energy emitted is characteristic for tungsten.
2. Bremsstrahlung radiation - or general radiation - where an electron passes near
the positively charged nucleus and is deflected losing some of its energy. Here
the energy of the photon emitted depends on many factors; such as original
energy of the electron and how close it came to the nucleus of a tungsten atom.
Here the energy is not discrete like characteristic radiation but a whole series of
energy levels. Some low energy radiation such as heat is absorbed by the target.
Other low energy, long wavelength radiation is removed by filters in the x-ray
tube.
Intensity of the x-ray beam
1. Intensity = number of x-ray photons X energy of each photon
2. Depends on kilovoltage, tube current, target material, and filtration.
a. Kilovoltage (kVp) controls the energy field across the tube from cathode to
anode - thus, how much energy the electrons have when they strike the
anode.
b. Tube current (mA) controls the number of electron produced at the
cathode and thus the number available to strike the anode target.
c. Target material (tungsten) determines how much radiation will be produced
at a given kVp. High atomic number targets like tungsten are more efficient
in producing x-rays. The target determines the quality of x-rays produced
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anode.
b. Tube current (mA) controls the number of electron produced at the
cathode and thus the number available to strike the anode target.
c. Target material (tungsten) determines how much radiation will be produced
at a given kVp. High atomic number targets like tungsten are more efficient
in producing x-rays. The target determines the quality of x-rays produced
and the energy of the characteristic radiation produced.
d. Filters block low energy photons from leaving the x-ray tube resulting in
fewer x-rays leaving but those that do have a higher average energy level.
e. X-rays are produced by characteristic and bremsstrahlung effects and have a
continuous as well as a discrete component.
f. Nearly all the scatter that fogs diagnostic x-rays is the result of the Compton
effect
QUALITY
EXPOSURE
RADIATION TYPE
ONLY X-RAYS OR
GAMMA RAYS
MEDIA
ABSORBED
DOSE
DOSE
EQUIVALENT
ACTIVITY
ALL IONIZING
RADIATION
ALL IONIZING
RADIATION
ALL
ONLY IN AIR
ANY
BIOLOGICAL
SYSTEMS
ALL
OBSERVED UNIT
IONIZATION
ENERGY
DEPOSITION
BIOLOGIC
EFFECT
NUCLEAR
TRANSFORMATION
OLD UNIT
ROENTGEN (R)
RAD
REM
REM=RAD X
CURIE (CI)
OF
NEW UNIT
COULOMB/KG
(C/KG)
GRAY (GY)
SIEVERT (SV)
BECQUEREL (BQ)
EQUIVALENCIES
1 C/KG=3.88 X
103R
1 GRAY=100
1 SIEVERT = 100
RADS
REM
1 BEQUEREL = 3.7
X 10-10
1 RAD=1 CGY
1 REM=1 CSV
OF UNITS
COMPTON EFFECT
- MORE LIKELY WITH HIGHER ENERGY INCIDENT X-RAY PHOTONS
- ONLY PART OF ITS ENERGY IS TRANSMITTED TO OUTER ELECTRON BUT STILL CAUSING
IONIZATION
- THE RESULTANT X-RAY PHOTON (SCATTER PHOTON) HAS LESS ENERGY AND DIFFERENT
DIRECTION THAN THE INCIDENT PHOTON.
- THE EJECTED ELECTRON (COMPTON ELECTRON) PRODUCES SECONDARY IONIZATION
- THIS TYPE OF INTERACTION IS COMMON AT INTERMEDIATE DIAGNOSTIC X-RAY LEVELS AND
INTERMEDIATE TO LOW-WEIGHT ABSORBERS
- NEARLY ALL THE SCATTER RADIATION THAT FOGS DIAGNOSTIC X-RAYS IS THE RESULT OF
THE COMPTON EFFECT
- THE LITTLE X-RAY ENERGY THAT IS ABSORBED BY SOFT TISSUE IS PRIMARILY COMPTON
EFFECT. THIS IS WHY THE IMAGES OF SOFT TISSUES ARE USUALLY MORE BLURRY THAN
DENSE OBJECTS.
ATTENUATION
- IS THE REDUCTION IN INTENSITY OF THE X-RAY BEAM AS IT TRAVERSES MATTER BY EITHER
ABSORPTION (PHOTOELECTRIC EFFECT) OR DEFLECTION (COMPTON EFFECT) OF PHOTONS
IN THE BEAM
MARROW APPROXIMATE EQUIVALENT TO THAT RECEIVED FROM FOUR BITEWING FILMS. THIS
LOW DOSE RESULTS LARGELY FROM THE USE OF INTENSIFYING SCREENS. THE PATIENT
DOSE IS RELATIVELY HIGH IN THE REGION OF THE CENTERS OF ROTATION
YOUR RESPONSIBILITY IS TO KEEP RADIATION DOSES AS LOW AS REASONABLY
ACHIEVABLE (ALARA CONCEPT), DESPITE THE RELATIVE SAFETY OF DENTAL X-RAYS.
THERE IS NO ABSOLUTELY SAFE LEVEL OF X-RADIATION. ALL IONIZING RADIATION MAY
CAUSE SOME DAMAGE.
- THE LETHAL DOSE FOR 50% OF HUMANS IN 30 DAYS (LD50/30) IS APPROX 450 RADS OR 4.5
GRAYS TOTAL BODY DOSE
- CELLS THAT DIVIDE RAPIDLY AND CELLS THAT ARE RELATIVELY UNDIFFERENTIATED ARE MOST
RADIATION SENSITIVE = LAW OF BERGONIE AND TRIBONDEAU
- BIOLOGIC EFFECT OF RADIATION ARE 1) SOMATIC, EFFECTS ON ANY OF THE CELLS OF THE
INDIVIDUAL HIMSELF, OR 2) GENETIC, MUTATIONS WHICH ARE NOT EVIDENT IN THE
INDIVIDUAL BUT WHICH ARE EFFECTS ON THE GERM PLASMA THAT ARE PASSED ON TO
FUTURE GENERATIONS.
- A LISTING OF CELLS FROM THE MOST RADIOSENSITIVE TO THE LEAST RADIOSENSITIVE MIGHT
INCLUDE: 1) LYMPHOID CELLS, 2) GONADS, 3) PROLIFERATING CELLS OF THE BONE
MARROW, 4) EPITHELIAL CELLS OF THE BOWEL, 5) EPIDERMIS, 6) HEPATIC CELLS, 7)
EPITHELIUM OF THE LUNG ALVEOLI AND BILIARY PASSAGES, 8) KIDNEY EPITHELIAL CELLS, 9)
ENDOTHELIAL CELLS (PLEURA AND PERITONEUM), 10) NERVE TISSUE, 11) BONE CELLS, 12)
MUSCLE AND CONNECTIVE TISSUE. GENERALLY, THE MORE RAPID THE TURNOVER OF THE
CELL, THE GREATER THE RADIATION SENSITIVITY.
- LOW DOSES WOULD EFFECT = RADIOSENSITIVE CELLS (PLATELETS, WBC OF LYMPH AND
BONE MARROW). YOU SEE FEVER, INFECTION, HEMORRHAGE = HEMATOPOIETIC SYNDROME
- DOSES OVER 600 RADS (6 GY) = GASTROINTESTINAL SYNDROME (FLUID LOSS, DIARRHEA,
AND GI INFECTION)
- DOSES > 10,000 RADS (100 GY) = CEREBRAL SYNDROME (RAPID DISORIENTATION AND
SHOCK IN ADDITION TO SYMPTOMS OF THE OTHER SYNDROMES)
- A TOTAL DOSE THAT WOULD BE LETHAL IF GIVEN IN A SHORT TIME, SUCH AS A FEW DAYS,
MAY RESULT IN NO DETECTABLE EFFECT IF GIVEN IN SMALL DAILY INCREMENTS OVER A
PERIOD OF SEVERAL YEARS. THIS IS DUE TO THE ABILITY OF LIVING TISSUE TO REPAIR SOME
OF THE DAMAGE DONE TO IT
VII. DENSITY
- IS THE DEGREE OF "BLACKNESS" OF THE FILM
- MA IS THE MOST IMPORTANT FACTOR CONTROLLING DENSITY
- THE DENSITY VARIES DIRECTLY WITH MA AND TIME
- MA AND EXPOSURE TIME ARE INTERCHANGEABLE AND CONSIDERED AS A SINGLE
FACTOR (MAS)
- INCREASING MAS INCREASES THE NUMBER OF X-RAYS
- INCREASED KVP ALSO INCREASES THE DENSITY
- DISTANCE IS ALSO A FACTOR IN DENSITY ( IF YOU 2X THE DISTANCE, YOU MUST 4X THE
TIME )
VIII. CONTRAST
- HIGH CONTRAST FROM LOW KVP (SHORT SCALE)
- LOW CONTRAST FROM HIGH KVP (LONG SCALE)
- HIGH KVP TECHNIQUES ALLOW A WIDER RANGE OF MA SETTINGS BUT RESULT IN LESS
CONTRAST THAN LOW KVP TECHNIQUES
REMEMBER:
KVP INFLUENCES SUBJECT CONTRAST (EXPOSURE DIFFERENCES) AND EXPOSURE LATITUDE; MA
CONTROLS FILM BLACKENING (DENSITY)
- WHEN THE KVP IS INCREASED, THE MAS MUST BE DECREASED IN ORDER TO KEEP THE
SAME RADIOGRAPHIC IMAGE
- TOO LONG
- TEMP TOO HIGH
- SOLUTION TOO STRONG
HIGH CONTRAST FILM (DARKS TOO DARK AND LIGHTS TOO LIGHT) = LOW PENETRATION (KVP TOO
LOW), OR OVER DEVELOPMENT, TOO LONG EXPOSURE
LOW CONTRAST (ALL GRAY TONES) = EXCESSIVE PENETRATION (KVP TOO HIGH), UNDER
DEVELOPMENT, EXCESSIVE SCATTER FOG, UNDER EXPOSURE
XI. GEOMETRIC FACTORS
- THE SOURCE OF THE RADIATION SHOULD BE AS SMALL AS POSSIBLE
- DISTANCE FROM THE SOURCE OF THE RADIATION TO THE OBJECT SHOULD BE AS LONG
AS POSSIBLE
- THE DISTANCE FROM THE OBJECT TO THE RECORDING SURFACE SHOULD BE AS SHORT
AS POSSIBLE
- FOR TRAUMA OR LESIONS IN THE MANDIBLE, YOU SHOULD ORDER ONE OR MORE OF THE
FOLLOWING: LOWER FACE SERIES: - TRAUMA TO MANDIBLE
1. POSTERIOR-ANTERIOR VIEW
2. LATERAL OBLIQUE
3. MODIFIED TOWNES VIEW (RAMUS AND NECK OF CONDYLE)
4. MANDIBULAR OCCLUSAL VIEW
- TMJ FILMS:
- TRANSCRANIAL VIEW (LINDBLOM VIEW)
- TRANSPHARYNGEAL VIEW (MCQUEEN VIEW)
- TRANSORBITAL VIEW (ZIMMER VIEW)
2. FOREIGN BODY
MODIFIED TOWNES VIEW
- CAN SEE SPHENOID SINUS, CONDYLAR PROCESS, NASAL SEPTUM AND VOMER, RAMUS AND
STYLOID PROCESS
WHILE IMAGES OF STRUCTURES ABOVE AND BELOW THAT LAYER ARE MADE
INVISIBLE BY BLURRING
TMJ ARTHROGRAPHY - THE RADIOGRAPHIC EXAMINATION OF A JOINT FOLLOWING THE
INJECTION OF RADIOPAQUE MEDIA INTO THE JOINT SPACE. IN TMJ
ARTHROGRAPHY, INJECTION OF THE LOWER JOINT IS MORE DIAGNOSTIC.
SIALOGRAPHY - RADIOGRAPHIC VISUALIZATION OF THE DUCTAL TREE AND PARENCHYMA OF
THE MAJOR SALIVARY GLANDS BY MEANS OF INTRADUCTAL INJECTION OF A
RADIOPAQUE CONTRAST MEDIUM.
CT SCAN - OR COMPUTED TOMOGRAPHY (ALSO KNOWN A CAT - COMPUTED AXIAL
TOMOGRAPHY) PRODUCES DIGITAL DATA MEASURING THE X-RAY
DISADVANTAGES
- THE RESULTANT IMAGE IS NOT AS SHARP AS WITH ORDINARY X-RAYS
- THE RADIATION DOSE IS HIGH (FROM 2.2 TO 6.8 RADS IN A NORMAL HEAD SERIES)
- BONY LESIONS ARE BETTER VISUALIZED ON NORMAL X-RAYS
- GREAT DIFFICULTY IN IMAGING METALLIC OBJECTS
- EXPENSIVE
- ACCORDING TO LAST WRITTEN BOARD - MAJOR DISADVANTAGE IS INABILITY OF
THE PATIENT TO REMAIN STILL.
- MRI - USES THE RESONANCE OF HYDROGEN NUCLEI FOLLOWING EXCITATION BY A
RADIOWAVE TO PRODUCE A COMPUTER DERIVED PICTURE OF THE TISSUE. NO
X-RAYS ARE USED. THE TECHNIQUE IS VERY EFFECTIVE IN DETECTING
NECROTIC TISSUE, ISCHEMIA, MALIGNANCY AND DEGENERATIVE DISEASE IN
SOFT TISSUE. BUT TEETH AND BONES ARE NOT WELL IMAGED. CAN BE USED
TO EXAMINE TMJ DISK DISPLACEMENTS
REMEMBER THE ALARA CONCEPT KEEP RADIATION DOSES AS LOW AS REASONABLY ACHIEVABLE
THERE IS NO ABSOLUTELY SAFE LEVEL OF X-RADIATION.
XV. X-RAY PROTECTION
- CURRENT FEDERAL AND STATE LAWS ARE BASED ON NATIONAL COUNCIL ON RADIATION
PROTECTION (NCRP) REPORT #35.
- THE POPULATION AT LARGE (AVERAGE OF WHOLE POPULATION) - MAXIMUM PERMISSIBLE
DOSE (MPD) = 1.7 MSV/YR (0.17 REM/YR)
- DESPITE DOSE LIMITS, ALL RADIATION MAY BE DAMAGING, SO BEYOND MEETING THE MPD WE
MUST REDUCE RADIATION AS MUCH AS POSSIBLE (ALARA)
METHODS TO REDUCE RADIATION EXPOSURE
- TIME = < AND YOU WILL < EXPOSURE
- DISTANCE - INTENSITY OF THE X-RAY BEAM DECREASES AS THE SQUARE OF THE DISTANCE.
STAY AS FAR FROM THE X-RAY SOURCE AS POSSIBLE
- BARRIERS - EVEN NORMAL BUILDING MATERIALS ARE OFTEN EFFECTIVE BARRIERS
- LEAD LINED WALLS ARE EXPENSIVE AND SELDOM NEEDED WITH DENTAL X-RAY
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UNITS
- OTHER PROCEDURES THAT DONT REDUCE OCCUPATIONAL EXPOSURE BUT MONITOR IT, SUCH
AS THE USE OF PERSONAL AND ENVIRONMENTAL RADIATION DOSIMETERS, ARE OF LIMITED
VALUE IN FACILITIES USING LOW DOSE RADIATION AND ARE NO LONGER REQUIRED IN NAVY
DENTISTRY.
- THERE IS NO MPD FOR THE PATIENT
- SINCE THE X-RAY IS PRIMARILY FOR THE PATIENTS BENEFIT, IT IS ASSUMED THAT THE
ADVANTAGES OF THE INFORMATION GAINED OUTWEIGH THE POTENTIAL RISKS
- NO MATTER HOW MUCH PREVIOUS EXPOSURE THE PATIENT HAS HAD, IF YOU DECIDE THAT A
DIAGNOSTIC X-RAY IS NEEDED - THEN TAKE IT
- DIAGNOSTIC X-RAYS DO NOT COUNT AGAINST THE MPD DOSE.
- HOWEVER, DO NOT TAKE UNNECESSARY Z-RAYS
- EACH X-RAY SHOULD BE ORDERED ON AN INDIVIDUAL BASIS - NO ADMINISTRATIVELY
REQUIRED X-RAYS ARE NOW PERMITTED
- GENERALLY, IT IS RECOMMENDED THAT A FULL SERIES BE TAKEN ON THE INITIAL EXAM, THEN
FOLLOWED UP WITH BITEWINGS EVERY 24 TO 36 MONTHS IN AN ADULT AND EVERY 12 TO 24
MONTHS IN CHILDREN
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LIGHT BY INTENSIFYING SCREENS, AND THIS LIGHT IN TURN USED TO EXPOSE THE FILM.
THE METHOD USED IN EXTRAORAL RADIOGRAPHY.
THIS IS
- THE DELICATE EMULSION IS PROTECTED FROM MECHANICAL DAMAGE BY A THIN LAYER KNOWN
AS THE SUPERCOATING.
FILM BASE
- BASICALLY PROVIDES SUPPORT FOR THE FRAGILE EMULSION
- USED TO BE CELLULOSE TRIACETATE
- NOW POLYESTER IS 1ST CHOICE BECAUSE IT IS MORE RESISTANT TO WARPING WITH AGE, IT IS
STRONGER AND HAS GREATER DIMENSIONAL STABILITY
THE
PROCESSING CHEMICALS TO PENETRATE IT TO GAIN ACCESS TO SILVER HALIDE CRYSTALS
RAPIDLY WITHOUT DESTROYING ITS STRENGTH OR PERFORMANCE.
GELATIN IS MADE FROM BONE
FILMS HAVE PHOTOSENSITIVE EMULSIONS COATED ON BOTH SIDES OF THE FILM BASE FOR:
1. THE FILM WOULD MOST LIKELY CURL IF THE EMULSION WAS APPLIED TO ONLY ONE SIDE,
BECAUSE, AFTER APPLICATION THE EMULSION DRIES AND SHRINKS TO 1/10TH ITS ORIGINAL
VOLUME.
2. LIGHT PHOTONS ARE ABSORBED ONLY IN THE OUTER LAYERS OF THE EMULSION,
THEREFORE, IT IS IMPORTANT TO HAVE TWO THIN LAYERS INSTEAD OF ONE THICK LAYER.
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LATENT IMAGE
- THE LATENT IMAGE IS DEFINED AS THE INVISIBLE IMAGE PRODUCED IN THE FILM EMULSION BY
LIGHT OR X-RAYS THAT IS CONVERTED TO A VISIBLE IMAGE UPON DEVELOPING.
- AN X-RAY OR LIGHT PHOTON INTERACTS WITH AN AGIBR CRYSTAL TO ALLOW AN ELECTRON
TO ESCAPE FROM A BR- OR I- ION
- THE BR-, OR I- ION, WHICH BECOMES NEUTRAL BY LOSS OF AN ELECTRON, MIGRATES FROM
THE CRYSTAL AND IS TAKEN UP BY THE GELATIN OF THE EMULSION.
- THE FREE ELECTRON IS CAPTURED AND TEMPORARILY HELD AT THE SENSITIVITY SPECK IN THE
CRYSTAL
- THE TRAPPED ELECTRON ATTRACTS A MOBILE INTERSTITIAL AG+ ION TO THE SENSITIVITY
SPECK, FORMING A NEUTRAL AG ATOM.
- THE REPEATED ATTRACTION AND NEUTRALIZATION OF INTERSTITIAL SILVER IONS BUILDS UP A
CLUMP OF SILVER ATOMS, CALLED THE LATENT IMAGE CENTER IN THE CRYSTAL, WHICH MUST
-
BE PRESENT BEFORE THE DEVELOPING PROCESS WILL CAUSE VISUAL AMOUNTS OF METALLIC
AG TO BE DEPOSITED.
THE MORE SILVER ATOMS WHICH EXIST AT A LATENT IMAGE CENTER, THE GREATER IS THE
PROBABILITY THAT THE CRYSTAL WILL BE DEVELOPED
FILM PROCESSING
- THE PRIMARY ACTIONS OF THE PROCESSING SOLUTIONS ARE TO CONVERT THE CRYSTALS
WITH LATENT IMAGES INTO BLACK METALLIC SILVER GRAINS THAT CAN BE VISUALIZED AND TO
REMOVE THE UNEXPOSED SILVER BROMIDE CRYSTALS.
DEVELOPMENT
- A CHEMICAL PROCESS WHICH AMPLIFIES THE LATENT IMAGE BY A FACTOR OF 100,000,000
TO FORM A VISIBLE PATTERN OF METALLIC SILVER
EMULSION
2. A PRESERVATIVE (SODIUM SULFITE) HAS A NATURAL AFFINITY FOR O2
- EXTENDS THE USEFUL LIFE OF THE DEVELOPER BY PROTECTING IT FROM ATMOSPHERIC
OXIDATION
- COMBINES WITH BROWN, OXIDIZED DEVELOPER TO PRODUCE A COLORLESS, SOLUBLE
COMPOUND
3. A RESTRAINER (POTASSIUM BROMIDE) ANTIFOG AGENT
- DECREASES THE RATE OF DEVELOPMENT OF UNEXPOSED CRYSTALS (FOG)
RINSING
- ELIMINATES ALKALI (ACTIVATOR) WHICH WOULD CONTAMINATE THE FIXER
- DILUTES THE DEVELOPER IN THE EMULSION AND STOPS THE DEVELOPMENT PROCESS
FIXING SOLUTIONS
- REMOVES THE UNDERDEVELOPED SILVER HALIDE CRYSTALS FROM THE EMULSION
- HARDENS THE GELATIN EMULSION
- CONTAINS FOUR COMPONENTS
1. CLEARING AGENT (SODIUM OR AMMONIA THIOSULFATE)
- REMOVES UNDEVELOPED SILVER IONS FROM SOLUTION BY FORMING STABLE, WATER
SOLUBLE COMPLEXES
2. ACIDIFIER (ACETIC ACID)
- NEUTRALIZES DEVELOPER, THEREBY, STOPS DEVELOPMENT THUS REDUCES POTENTIAL
FOR FOG
- PREVENTS CONTAMINATION OF THE FIXER
3. PRESERVATIVE (SODIUM SULFITE)
- PREVENTS OXIDATION OF ANY DEVELOPER WHICH MAY HAVE CONTAMINATED THE FIXER
- COMPLEXED WITH THE COLORED OXIDIZED DEVELOPER AND REMOVES IT FROM THE FIXER
BEFORE IT CAN STAIN THE FILM.
- INHIBITS THE DECOMPOSITION OF THE THIOSULFATE CLEARING AGENT
4. HARDENER (POTASSIUM ALUM)
- INCORPORATES WITH THE GELATIN TO BECOME MORE RESISTANT TO ABRASION
- DECREASES THE SWELLING OF THE GELATIN
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