ΠΑΑΝΝΕΕΠΠΙΣΤΤΗΗΜΜΙΙ...
Transcript of ΠΑΑΝΝΕΕΠΠΙΣΤΤΗΗΜΜΙΙ...
ΕΕΠΠ
ΕΕΛΛΕΕΓΓΧΧ
ΠΠΙΙΒΒΛΛΕΕΠΠΩΩΝΝ:: ΠΠΑΑ
ΚΚΑΑ
ΧΟΟΣΣ ΠΠΟΟΙΙΟΟ
ΠΠΑΑΝΝΟΟ
ΑΑΝΝΑΑΓΓΙΙΩΩΤΤΑΑΚΚΗΗΣΣ
ΑΑΘΘΗΗΓΓΗΗΤΤΗΗΣΣ ΠΠΑΑΝΝ
ΠΠΠΑΑΑΝΝΝΕΕΕΠΠΠΙΙΙ
ΤΜΗΜΑ ΙΑΤ
ΔΙΑΤΜΗΜΑ
ΜΕΤΑΠΤΥΧΙ
ΟΟΤΤΗΗΤΤΑΑΣΣ ΣΣ
ΟΟΡΡΑΑΜΜΙΙΚΚ
ΔΔΙΙΠΠΛΛΩΩΜ
ΝΝιιώώΑρ.
ΣΣ ΓΓΕΕΩΩΡΡΓΓΙΙΟΟΣΣ
ΝΝΕΕΠΠΙΙΣΣΤΤΗΗΜΜΙΙΟΟΥΥ ΠΠ
ΔΔΕΕ
ΙΙΣΣΣΤΤΤΗΗΗΜΜΜΙΙΙΟΟΟΟΟΟ
ΤΡΙΚΗΣ – ΤΜ
ΑΤΙΚΟ ΠΡΟΓΡ
ΙΑΚΩΝ ΣΠΟΥ
ΣΣΥΥΣΣΤΤΗΗΜΜΑΑ
ΗΣΗΣ ΑΑΚΚΤΤΙΙΝΝ
ΜΜΑΑΤΤΙΙΚΚΗΗ ΕΕ
ττοουυ
ώώττηη ΔΔηημμήή. Μητρώου: 1
ΠΠΑΑΤΤΡΡΩΩΝΝ
ΠΠΑΑΤΤΡΡΑΑ
ΕΕΚΚΕΕΜΜΒΒΡΡΙΙΟΟΣΣ,, 2200
ΠΠΠΑΑΑΤΤΤΡΡΡΩΩΩΝΝΝΝ
ΜΗΜΑ ΦΥΣΙΚΚΗΣ ΡΑΜΜΑ
ΥΔΩΝ ΣΤΗΝ ΙΑΤΡΙΚΗ ΦΥΥΣΙΚΗ
ΑΤΤΩΩΝΝ ΟΟΑ ΔΔ
ΝΝΟΟΓΓΡΡΑΑΦΦ
ΕΕΡΡΓΓΑΑΣΣΙΙΑΑ
ττρρηη 1287
001100
ΔΔΟΟΝΝΤΤΙΙΑΑΤΤΤΤΡΡΙΙΚΚΗΗΣΣ
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ACKNOWLEDGMENTS
I would like to thank Professor George Panayiotakis for his inspiring, encouraging and
helpful guidance and consistent supervision on my work, as also for the extensive and
sincere discussions on several subjects that we shared.
I would also like give special thanks to Medical Radiation Physicist Harry Delis for his
enormous and direct help concerning various questions and clarifications aroused on my
research as well as on the experimental procedures.
Last but not least, I would like to thank all friends, closed ones and colleagues who
showed a remarkably inexhaustible, encouraging ‐yet hopefully not inexplicable‐
patience concerning the making of this work.
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PREFACE
Over the last decades, medical x rays have remarkably expanded their necessity on
medical diagnosis, treatment planning and evaluation of therapy. In this way, the
parallel ongoing development as well as the evolution of the x ray techniques has
brought a vast range of potential usage, which needs to be fairly acknowledged for the
optimization of each technique and the overall control of the radiation dosage, not to
mention the permanently questioned necessity and high rates of the examinations.
Dental radiography represents the most frequent diagnostic x ray examination
undertaken in the industrialized countries of the world. On this basis, the relatively low
dosage of these techniques can not underestimate the questions of radioprotection
fields, as for example the overall dosage in each country from these techniques is more
than negligible.
Panoramic radiography is a simplified dental extraoral procedure which depicts the
entire maxillomandibular region on a single film. The development of the principles of
dental panoramic radiology represented a major innovation in dental imaging. Prior to
this, dental radiographic examinations were limited to intraoral and oblique lateral
projections of the jaws taken using a dental x ray set. For the first time practitioners
were able to produce an image of both jaws and their respective dentitions on a single
radiographic film by a quick and relatively simple procedure.
The simplicity of operation, the broadened scope of examination, the ability to project
anatomic structures in their normal relationship with reduced superimposition of
intervening parts, and the low radiation dosage are reasons for its widely growing
popularity. The latter has raised the necessity of the formation of a regulatory basis in
each country, according to the demographic and practitioners standards, which will
provide a safe and proper quality assurance guide, allowing each practitioner to
optimize the technique, both in terms of image quality and patient dosimetry, according
to the subjective grounds of every laboratory, rather than restricting the practice into a
single and solid mode.
Quality Control (QC) protocols, Diagnostic Reference Levels (DRLs) and guidance
programs for proper usage of the panoramic unit as well as the processing procedures
are some of the fields that need to researched and well established.
In Greece, where the number of both panoramic units and examinations follow a
remarkably yet undefined increasing curve during the last two decades, there has been
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initialized a researching and scientific debate about these fields although it is still in a
primary stage.
The following thesis, taking into consideration the difficulties and the complexity of this
technique, as well as the questions and problems that rise upon its general practice in
Greek laboratories, and trying to provide a more aggregate view of panoramic imaging,
focuses on the QC of panoramic radiography, including the determination of DRLs in this
technique, with a respective presentation of the principles of function and the necessary
radioprotection information.
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Contents
SECTION I
GENERAL PART
CHAPTER 1 : The included anatomical structures on the panoramic radiograph
Introduction 3 The Skull 3 The Mandible 4 The Maxilla (Upper Jaw) 5 The Temperomandibular Joint 5 The Foramina 6 The Salivary Glands 7The Cervical Vertebrae 8
General Overview of the Oral, Neck and Lower Face Anatomy 8The Tongue 9
Oral Anatomy Elements 9The Tooth 11
Tooth Development 12
CHAPTER 2 : Panoramic Radiography: a clinical overview
Introduction 19Diagnostic Regions in PR 19The Normal Panoramic Radiograph 21
CHAPTER 3 : Panoramic Radiography: principles of function
Introduction 30Broad Beam Linear Tomography 31Slit or Narrow Beam Linear Tomography 31Narrow Beam Rotational Tomography 32Dental Panoramic Tomography 33
Focal Trough 35 Formation of the Image Layer 38 Geometric Distortion 41
Screen Film and Intensifying Screens 43The Screen Film 43Intensifying Screens 45Digital Panoramic Tomography 48
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Solid‐state systems using CCD 50 Storage Phosphor Plates Technology 53 Interoperability 55Radiation Dosage 56
Comparison Between Film and Digital PR 56Equipment 58Patient Positioning 61Field Limitation Techniques 62
CHAPTER 4: Radiation Effects, Doses and Protection concerning Quality Controlling of panoramic radiography
Introduction 65Sources of Radiation 66Classification of Biological Effects 67
Somatic Deterministic Effects 67 Somatic Stochastic Effects 67 Genetic Stochastic Effects 68
Harmful Effects Important in Dental Radiology 69Estimating the Dose and Risk of PR 69Main Methods of Monitoring and Measuring Radiation Dose 73
Film Badges 73TLDs 74Ionization Chambers 75
Measurements using Phantoms 75Patient Dosimetry 75List of Equipment 76
Methods 76 Worksheets 83
Dose Area Product 86Diagnostic Reference Levels (DRLs) deriving from DAP measurements 87Dose Width Product 88DAP and Effective Dose 89
CHAPTER 5: Quality Control Protocols – Codes of Practice ‐ Legislation
Greek Atomic Energy Commission Protocol of Periodical Quality Control Checks on Orthopantograph
92
Requirements for Dental Panoramic and Cephalometric Examinations, by GAEC 93
Conference of Radiation Control Program Directors, Inc Quality Control Recommendations for Diagnostic Radiography
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European Commission – Radiation Protection 136 European Guidelines Radiation Protection in Dental Radiology, 2004
95
International Atomic Energy Agency – Dosimetry in Diagnostic Radiology: An International Code of Practice
96
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Health Canada – Radiation Protection in Dentistry, Recommended Safety Procedures for the Use of Dental x ray Equipment
96
Care Quality Commission – The Ionizing Radiation (Medical Exposure) Regulations 97
Greek Ministry of Health, Greek Regulations for Radiation Protection, 2001. 97
SECTION II
EXPERIMENTAL PART
CHAPTER 6:
Calculation of the Effective Dose (E), Using the DRLs of Tierris et al. (2004)
101
CHAPTER 7: Quality Control of a Panoramic Unit
A.1 LABORATORY DESCRIPTION – EQUIPMENT RECORDA.1.1 Equipment Description 104 A.1.2 Ventilation – Air Condition ‐ Illumination 106
A.2 CONTROLS A.2.1 General Apparatus Controls 107
A.2.1.1 Inspectional Control of the Unit Components 107A.2.1.3 Presence of Technical Manuals and Log Book 107
A.2.2 Radioprotection Control 108A.2.2.1 Spatial Characterization – Chamber Signage 108A.2.2.2 Verification of Radioprotection Report – Shield Control 108A.2.2.3 Record and Control of Physical Condition of Radioprotection Apparatus
109
A.2.2.4 Tube Head Escape 109A.2.3 Beam Geometry Control 110
A.2.3.1 Conjunction of Radiation Field with the Alignment Slit of the Digital Detector
110
A.2.3.2 Measurement of Minimum Distance Focus‐Examinee 110A.2.3.3 FFD Control 110
A.2.4 Beam Quality Control 111A.2.4.1 Accuracy of High Voltage Values 111A.2.4.2 Repeatability of High Voltage Values 112A.2.4.3 Half Value Layer (HVL) of the beam – Tube Total Filtering 113
A.2.5 Beam Quantity Control 114
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A.2.5.1 Timer Accuracy 114A.2.5.2 Timer Repeatability 115A.2.5.3 Tube Supply Linearity and Repeatability 115
A.2.6 Automatic Exposure Selection System 116A.2.7 Typical Patient Doses 118A.2.8 Image Quality Control 118
REFERENCES 120
Appendix I: The Diagnostic Value of the Panoramic Radiograph
The Popularity of Panoramic Imaging 128 The Quality of Panoramic Images 129Technical and Processing Faults Affecting Image Quality 130Film Fault Frequency within Panoramic Radiographs taken in General Dental Practice
134
The Questionable Necessity of the Panoramic Radiograph 138The Panoramic X‐ray Equipment and the Operating Personnel 142
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Lists of Figures
CHAPTER 1 Figure 1: http://www.3dmouth.org/4/4_1.cfm
Figure 2: http://www.3dmouth.org/4/4_2_1.cfm
Figure 3: http://www.3dmouth.org/4/4_2_2.cfm
Figure 4: http://www.3dmouth.org/4/4_2_3.cfm
Figure 5: http://www.3dmouth.org/4/4_2_4.cfm
Figure 6: http://www.3dmouth.org/4/4_3.cfm
Figure 7: http://www.en.wikipedia.org/wiki/File:Illu_vertebral_column.jpg
Figure 8: http://www.doctorspiller.com/oral%20anatomy.htm
Figure 9: http://www.med.mun.ca/anatomys/head/head.htm
Figure 10: http://www.doctorspiller.com/oral%20anatomy.htm
Figure 11: http://www6.ufrgs.br/favet/imunovet/molecular_immunology/tooth1.jpg
Figure 12: http://www.3dmouth.org/6/6_2_1.cfm
Figure 13: http://dentdoctor.tripod.com/Oral_Anatomy/index2.html
Figure 14: http://dentdoctor.tripod.com/Oral_Anatomy/index2.html
Figure 15: http://www.3dmouth.org/6/6_2_3.cfm
Figure 16: http://www.nytimes.com/imagepages/2007/08/01/health/adam/9445Dentalanatomy.html
Figure 17: http://dentdoctor.tripod.com/Oral_Anatomy/index2.html
Figure 18: Pasler A Friedrich. Color Atlas of Dental Medicine, p. 62 – Radiology, Thieme, 1993
Figure 19: http://en.wikipedia.org/wiki/File:Teeth_diagram.png
Figure 20: http://dentdoctor.tripod.com/Oral_Anatomy/index2.html
Figure 21: Pasler A Friedrich, Visser Heiko. Pocket Atlas of Dental Radiology, Panoramic Radiography, Tooth and Jaw Development as Depicted in Panoramic Radiographs, page 37, Thieme, 2007.
Figure 22: Pasler A Friedrich, Visser Heiko. Pocket Atlas of Dental Radiology, Panoramic Radiography, Tooth and Jaw Development as Depicted in Panoramic Radiographs, page 37, Thieme, 2007.
Figure 23: Pasler A Friedrich, Visser Heiko. Pocket Atlas of Dental Radiology, Panoramic Radiography, Tooth and Jaw Development as Depicted in Panoramic Radiographs, page 39, Thieme, 2007.
xiv
Figure 24: Pasler A Friedrich, Visser Heiko. Pocket Atlas of Dental Radiology, Panoramic Radiography, Tooth and Jaw Development as Depicted in Panoramic Radiographs, page 37, Thieme, 2007.
Figure 25: Pasler A Friedrich, Visser Heiko. Pocket Atlas of Dental Radiology, Panoramic Radiography, Tooth and Jaw Development as Depicted in Panoramic Radiographs, page 37, Thieme, 2007.
Figure 26: http://media‐2.web.britannica.com/eb‐media/91/74891‐004‐345232AC.jpg
CHAPTER 2
Figure 1: Pasler A Friedrich. Color Atlas of Dental Medicine, p. 5 – Radiology, Thieme, 1993
Figure 2: Pasler A Friedrich. Color Atlas of Dental Medicine, p. 5 – Radiology, Thieme, 1993
Figure 3: Pasler A Friedrich. Color Atlas of Dental Medicine, p. 5 – Radiology, Thieme, 1993
Figure 4: Pasler A Friedrich. Color Atlas of Dental Medicine, p. 5 – Radiology, Thieme, 1993
Figure 5: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 1, p. 4, Springer, 2007
Figure 6: Pasler A Friedrich. Color Atlas of Dental Medicine, p. 26 – Radiology, Thieme, 1993
Figure 7: William S. Moore. Kodak Successful Panoramic Radiography, p.2
Figure 8: Murray Diane, Whyte Andy. Dental Panoramic Tomography: What the General Radiologist Needs to Know. Clinical Radiology 57: 1‐7, 2002.
Figure 9: Murray Diane, Whyte Andy. Dental Panoramic Tomography: What the General Radiologist Needs to Know. Clinical Radiology 57: 1‐7, 2002.
CHAPTER 3 Figure 1: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p.
162. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 2: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p.
163. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 3: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p.
163. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 4: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p.
164. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 5: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p.
164. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 6: White S C, Pharoah M J. Oral Radiology: Principles and Interpretation,
Chapter 11, p. 208, 4th ed. (St.Louis: Mosby Inc.) 2000. Figure 7: Whaites, E. Essentials of Dental Radiography and Radiology, Chapter 15, p.
165. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 8: X ray Phantoms, Panoramic Dental Test Object, TO PAN, Leeds Test Objects
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Figure 9: X ray Phantoms, Panoramic Dental Test Object, TO PAN, Leeds Test Objects
Figure 10: William S. Moore. Successful Panoramic Radiography, Kodak Dental Radiography Series.
Figure 11: http://www.kodak.com/US/plugins/acrobat/en/motion/support/h1/H1_23‐27.pdf
Figure 12: http://www.medcyclopaedia.com/library/topics/volume_i/f/film_screen_radiography.aspx
Figure 13: http://www.medcyclopaedia.com/upload/medcyc/volumes/volume_i/dintensifying_screen_fig1.jpg
Figure 14: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 15: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 16: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 17: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 18: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 19: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 20: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 21: Farman G Allan. Panoramic Radiology – Seminars on Maxillofacial Imaging and Interpretation, Chapter 3, Springer, 2007
Figure 22: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p. 168. 2nd ed. (Edinburgh: Churchill Livingstone) 1996.
Figure 23: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p. 168. 2nd ed. (Edinburgh: Churchill Livingstone) 1996.
Figure 24: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p. 166. 2nd ed. (Edinburgh: Churchill Livingstone) 1996.
Figure 25: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 15, p. 167. 2nd ed. (Edinburgh: Churchill Livingstone) 1996.
CHAPTER 4 Figure 1: White S C, Pharoah M J. Oral Radiology: Principles and Interpretation,
Chapter 3, p. 44, 4th ed. (St. Louis: Mosby Inc.) 2000. Figure 2: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 4, p.
31. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 3: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 6, p.
60. 2nd ed. (Edinburgh: Churchill Livingstone) 1996. Figure 4: Whaites E. Essentials of Dental Radiography and Radiology, Chapter 6, p.
64. 2nd ed. (Edinburgh: Churchill Livingstone) 1996.
Figure 5: International Atomic Energy Agency. Dosimetry in Diagnostic Radiology: An International Code of Practice (Technical Reports Series No. 457). Vienna, 2007
Figure 6: Williams JR, Montgomery A. Measurement of dose in panoramic dental radiology. Br J Radiol;73(873):1002–6, 2000.
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Figure 7: http://www.gehealthcare.com/usen/xr/edu/products/dose.html
Figure 8: http://www.e‐radiography.net/radtech/d/Dose_ge/dose.htm
APPENDIX I
Figure 1‐6: Akarslan ZZ, Erten H, Güngör K, et. al. Common Errors on Panoramic Radiographs Taken in a Dental School. J Contemporary Dental Practice;(4)2:024‐034, May 2003
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SECTION I
GENERAL PART
1
2
CCHAPTEER 1
THE INCLUUDED ANNATOMIICAL STRUCTURRES
ON THHE PANOORAMIC RADIOGGRAPH
INNTRODUCTION
On
as
Du
co
st
in
n this sectio
s all the add
ue to this pr
onsists a ba
ructures, the
terpretation
n, a short an
ditional struc
roject’s goal
sic and very
eir surround
n of the pano
natomical re
ctures that a
s, which are
y brief anat
ding tissues a
oramic radiog
eference of t
appear or m
e not such o
tomical refe
and their rel
graphy and t
the dental re
ay appear in
of a pure me
erence. The
ations is an
the discussio
egion is pres
n a panoram
edical interes
knowledge
essential too
on of its qual
sented, as w
mic radiograp
st, this secti
of the den
ol for a prop
ity control.
well
ph.
on
tal
per
THHE SKULL
Th
th
he skull is a h
he human sp
hollow and r
pine providin
F
rigid structur
ng a protectiv
Figure 1: The Hu
3
re made of b
ve shell to t
uman Skull
bone tissue.
he brain and
all the he
enabling
head (che
expressio
The skull
1) The cra
is the top
2) The fac
of the fa
region.
It is attached
d the eyes. U
ead muscles
all the fun
ewing, air cir
ns etc.).
d on the top
Upon the sku
s are attache
nctions of t
rculation, fac
of
ull,
ed,
the
cial
is divided intto two parts:
anial part o
part that co
r “cranium”
overs the bra
”. It
ain.
cial part whi
acial bones
ich is consist
at the fro
ted
ont
THHE MANDIBBLE (LOWERR JAW)
Th
an
ea
th
he lower jaw
nd it stretche
ar. It is joine
he “temporo
w has its own
es from one
ed to the upp
‐mandibular
n separate b
ear, down to
per part of t
r joints – TM
bone which is
o the chin ar
the head aro
MJs”.
s called “the
ea and then
ound the ear
e mandible”.
back up aga
r region by t
It is U‐shap
ain to the oth
two jaw join
ped
her
nts,
Thhe mandible is divided into the followwing parts:
The b
‐
of th
suppo
ody f the m
the middle
he U‐shape
orts the lowe
mandible
section
which
er teeth.
The c
round
that fi
joint
mand
craniu
each
mand
The co
‐ tria
from t
joins o
the m
The as
jaw w
condy
condyle
ded end of
its into the m
between
ible and
um. There is
side of
ible.
oronoid proc
angular pro
the mandibl
one of the c
andible.
scending ram
which joins t
yles.
‐ the
f bone
movable
the
the
one for
f the
cess
ojection
e which
chewing mus
mus ‐ th
he body of
4
scles to the c
he flatter, st
the mandib
Fig
cranium. The
raighter part
le to the co
gure 2: The Hum
ere is one fo
t on the side
oronoid proc
man Mandible
or each side of
es of the lowwer
cesses and tthe
TH
Th
HE MAXILLA
he maxilla, o
A (UPPER JA
or the upper j
AW)
jaw, is madee up of severr
sit
ch
Th
TH
Th
pa
bo
cu
ts in front of
heeks, the no
he maxilla is
the m
of the
HE TEMPER
he temperom
art of the cra
one surfaces
ushion.
F
f and just be
ose and the r
divided into
mouth. The h
e mouth. The
ROMANDIBU
mandibular j
anium called
s are separa
igure 3: The Hu
elow the cra
roof of the m
:
ard part is c
e softer part,
ULAR JOINT
joint (TMJ) i
d the tempor
ated by a ci
uman Maxilla
5
nium. It is a
al bones stu
ttached to
ck (or fused)) together, a
and forms
nd
tthe cranium tthe
mouth.
The
maxillary s
space tha
cheekbone
called the “h
the “soft pa
T (TMJ)
s the movab
ral bone. It is
ircular piece
the mouth.
of the face,
The
‐ a bit of bo
the maxilla
nose.
The
a curved pie
outwards fr
a part of th
The
the mouth,
ard palate”
alate”, is at th
ble joint bet
s a complica
e of softer c
e maxillary
sinus ‐
t sits just
and just abo
There is on
either side o
e anterior na
one which p
a at the low
e zygomatic
ece of bone
rom the max
e cheekbone
e palate
, separating
and it is tow
he back near
tween the m
ted joint and
cartilage wh
y antrum
‐ the air fill
t under t
or
led
the
ove the rooff of
e for each si
of the nose.
asal spine
pr
ide
otrudes froom
wer end of t
process
which exten
xilla and for
e.
‐ the roof
the nose a
wards the fro
the
‐
nds
ms
of
nd
ont
r the throat.
mandible and
d the two ha
ich acts like
d a
ard
e a
Th
an
ch
w
ro
sli
TH
A f
Th
he TMJ mov
nd forwards.
hewing, swa
hile some o
otation of th
iding movem
HE FORAMI
foramen is a
he foramina
Fig
Figu
ves up and
. It is in cons
llowing, talk
of these mov
e joint and s
ments.
INA
an opening o
are divided i
gure 4: The Hummovemen
re 5: The Huma
down, sidew
stant use du
king or laugh
vements inv
some others
or hole which
into the follo
man TMJ in actnts of the lower
an Foramina
6
ways
uring
hing,
volve
s are
h lets nerves
owing parts:
ion, causing r jaw
and blood v
Th
on the
Nerves a
travel to t
this.
Th
inferior d
the ascen
the inferio
vessels w
pass throu
Th
at the fron
Nerves ca
the blood
the palate
vessels pass tthrough bon
he mental fo
body of t
and blood
the lower lip
he mandibul
dental foram
ding ramus.
or dental ne
hich go to th
ugh this.
he incisive f
nt of the pala
alled incisiv
d which supp
e pass throug
foramen
the mandib
vessels whi
p pass throu
lar foramen
men ‐
A nerve call
erve and blo
he lower tee
foramen
e.
‐
ble.
ich
ugh
or
on
led
ood
eth
‐
ate.
ve nerves a
ply the fro
nd
n
gh this.
t f
THHE SALIVARRY GLANDS
Thhe salivary gglands produuce the cleaar liquid thaat is releasedd into the mmouth (salivva).
Thhere are threee pairs of mmajor salivarry glands andd many minoor glands. Saaliva lubricattes
thhe mouth annd start the breakdown of chewed ffood. It is mmade up of wwater, enzymme,
m
Th
ucin and pro
he salivary gl
The pa
otein.
land pairs ar
arotid
e the followiing:
gland,
saliva
called
the m
next t
is one
The s
‐ s
releas
front o
teeth.
The su
situate
releas
openi
This p
to eac
‐ salivary
the largest
, situated bbelow the ear. The
is released tthrough an oopening
the parotid
outh on the
o the upper
on each side
submandibu
situated und
ses saliva ju
d duct which
inside of the
molar teeth
e.
lar salivary
der the mand
ust
h enters
e cheek
h. There
y gland
dible. It
underneaath the
of the tongu
. There is one
ublingual sa
ed under t
se saliva f
ue, behind th
e on each sid
alivary gland
the tongue
from many
he front
de.
ds ‐
e. They
y small Figgure 6: The Human Salivary GGlands
ngs (ducts)
pair of saliva
ch other und
under the
ary glands s
er the tongu
tongue.
its next
ue.
7
THHE CERVICAAL VERTEBRRAE
Thhe cervical vvertebrae aree positionedd immediate
be readily d
ly posterior
istinguished
to the skull
from those
. They are tt
sm
an
Th
nu
th
G
Th
sa
th
st
ad
es
pr
th
th
Th
de
ai
Th
ex
ca
mallest amon
nd lumbar r
hrough each
umbered fro
he skull to the
ENERAL OV
he following
agittal sectio
he neck. Am
ructures
denoids, oro
sophagus, la
roximity bet
he tongue, t
he epiglottis
he epiglottis
etermines in
r or food flow
he pharynx i
xtends: the
avity) and the
Figure 7:
ng all verteb
regions due
h foramen
om C1 to C7,
e spine.
VERVIEW OF
figure repre
on of the fa
mong the d
(nasop
opharynx, t
arynx, trache
tween the b
he soft pala
is clear.
is the valve
to which tub
ws (trachea
s divided int
oropharynx
e laryngopha
The Cervical Ve
rae and can of the thora
he
cic
to the pres
the verteb
, which form
sence of a
ral artery
m the cervica
F THE ORAL
esents a
ace and
ifferent
harynx,
tongue,
ea) the
back of
ate and
e that
be the
or esophagu
to three par
(behind the
arynx.
ertebrae on the
8
L, NECK AN
us respective
rts according
e oral cavity
Figure 8: Sag
e Ve ebral Cort l
foramen in
passes. The
al column, w
D LOWER F
ely).
g to the anat
y), the nasop
gittal section of
lumn and a sin
each trans
ere are sev
with C1 or at
verse proce
ven vertebra
tlas connecti
ess.
ae,
ing
FACE ANATO
tomical regio
pharynx (beh
f the face and t
gle cervical ver
OMY
ons in which
hind the na
the neck
rtebra, wiki
h it
sal
THE T
The t
muscle
TONGUE
tongue is m
e. The tongu
made most
ue, much as
ly of skele
s is
etal
O
M
in
Th
ca
Th
at
Th
Th
pa
RAL ANATO
Moreover, the
the respect
he uvula is a
avity.
he labial fren
ttaches the li
he gingiva ar
he hamulii a
alate meets t
Figure 9
OMY ELEME
e following a
ive figure.
a valve whic
num is a little
ip to the gum
re what is mo
re hard little
the very bac
9: The tongue f
ENTS
anatomical st
ch keeps foo
e tag of tissu
ms.
ore common
e bumps in t
k of the tube
rom a rear view
commonnly
believeed, extends
d
from the poosterior bordder
of the iinto the oroppharynx. mouth an
The do
into tw
the m
backw
orsum, or th
wo parts: an
outh, and a
ward to the o
e upper surf
n oral, which
a pharyngea
ropharynx.
face, is divid
h lies mostly
al, which fac
ded
y in
ces
w The tw
groove
wo parts are
e, which m
e separated
arks the T
by a V‐shapped
eerminal Sulccus
(tonguue)
the oral cavtructures of iity are preseented as showw
9
od and drink
ue in the cen
nly named “g
the corners
erosities.
k from regur
nter of the up
gums”.
of the soft p
rgitating up into the na
n
sal
pper and thee lower lip thhat
palate, just wwhere the sooft
Th
sid
co
up
Th
Th
la
Th
(la
Th
fa
he maxillary
des of the
overing them
pper teeth ar
he tonsils are
he retromola
st lower mol
he vestibule
abial mucosa
he vermillion
ce.
Figgure 10: Anatoomy of the Orall Cavity
tuberosities
dental arch
m, and they
re extracted
are the toug
. These hum
are persiste
.
gh, hard pum
mps have u
ent, permane
mps behind t
nderlying bo
ent parts of
the top back
one and ha
the mouth
k teeth on bo
rd gum tiss
even if all t
oth
sue
the
e at the bordder between the mouth aand the throat.
ar pad is sim
lars, and it is
milar to the m
s not underla
maxillary tub
ain by corres
berosities, e
ponding hum
xcept that it
mp of bone.
t is behind tthe
is the curva
a) or cheeks
ature of the
(buccal muc
e tissue whe
osa) meet th
ere the lining
he gingiva.
g of the inside of the lips
n border is thhe junction oof the dry, ppink part of tthe lip with tthe skin of tthe
10
THHE TOOTH
Crrown
Th
en
(lo
he crown of
ntirely expos
ower) part of
a tooth is its
sed above th
f the ename
s portion tha
e gum line. I
l.
at is covered
In children th
d with enam
he gum may
el. It commo
partially cov
only lies nea
ver the cervi
arly
cal
Ennamel
Th
m
w
he enamen i
ost highly m
hich make u
s the substa
mineralized s
p the tooth,
ance that co
substance o
along with d
vers the cro
of the body
dentin, ceme
own of the to
and is one
entum and de
ooth. It is th
of the four
ental pulp.
he hardest a
major tissu
nd
ues
Deentin
De
bo
un
su
a
w
co
Ce
Ce
to
cr
tis
su
De
Th
tis
th
to
entin is th
one‐like
nderlie ths
urrounds the
mineralize
ith an or
d
g
ollagenous p
ementum
ementum is
ooth as en
rown. It is
ssue that c
urface in a th
ental pulp
he dental pu
ssue contain
he root, the a
ooth.
he hard, y
material
e enamel
e entire nerve
connec ive t t
ganic matr
roteins.
s the root
amel is to
a relatively
covers the
hin layer.
ulp is the ce
s blood vess
apical foram
yellow
that
nd a
e. It is
tissue
ix of
of a
o the
y soft
root
ntral part of
sels and nerv
men. The den
11
f the tooth f
ves that ente
tal pump is
F
filled with s
er the tooth
commonly c
igure 11: The H
oft connecti
from a hole
called as the
Human Tooth
ive tissue. T
at the apex
“nerve” of t
his
of
the
TOOOTH DEVEELOPMENT
Infants
sm
te
th
Th
De
th
be
De
sh
th
De
th
ha
F
maller than a
eeth come th
hrough by ab
he deciduous
eciduous Inc
he top and f
etween the 5
eciduous Can
hape. There
hey also have
eciduous Mo
han the front
ave more tha
Figure 12: The DTeeth (milk
adults’ teeth
hrough. The
bout age 2 to
s teeth are:
isors: These
four at the
5th and the 8
nines: Also k
are four alto
e a single roo
olars: These a
t teeth and h
an one root
Deciduousteeth)
s and Childre
The m
human
pushed
teeth.
should
still be
throug
erupt i
Milk o
babies
h because ch
re are 20 de
o 2.5 years.
are the fron
bottom). Tth month. Th
known as “e
ogether and
ot.
are the large
have “bumpy
and the root
Figure 13: The
12
en:
milk or decidu
ns. Between
d, extracted
By the tim
d have 28 ad
e coming th
gh after this
in late teens
uous teeth a
the ages of
and replace
me most pe
dult teeth alt
hrough. The
are the wis
.
re the first s
6 and 13, all
ed by new an
eople are te
though some
e only teeth
sdom teeth,
set of teeth
milk teeth a
nd bigger ad
eenagers, th
e of these m
h left to com
which usua
of
are
ult
hey
may
me
ally
or deciduou
s are betwe
hildren’s jaw
eciduous tee
us teeth sta
een 5 and
ws are smalle
eth altogeth
rt coming t
8 months
er. As the jaw
her and they
through wh
old. They a
ws grow, mo
y finish comi
hen
are
ore
ing
nt teeth and t
hey are usu
hey have a fla
eye teeth”, th
they come
er back teeth
y” or irregula
ts are quite s
e Primary Denti
there are 8 o
ually the firs
at biting edg
hese front t
through the
h, easy to te
ar surfaces f
splayed. The
ition Sequence
of them alto
st teeth to
e and only o
gether (four
come throu
one root.
r at
ugh
eeth have a
e age 16 to 2
more point
23 months a
ted
nd
ll because th
or chewing w
ere are 8 mo
hey look bigg
with. They a
lars altogeth
ger
lso
her
w
pr
hich come th
remolars in a
hrough betw
adults.
ween the agees of 1 to 2.55. Later on thhese teeth aare replaced by
Te
28
co
la
m
ar
th
Figure 14
eenagers and
8 Adult Tee
oming throu
rger than m
ore room fo
re 32 adult t
hrough if the
Figu
4: The Timeline
d Adults
eth: Adult
ugh at aroun
milk teeth. A
or the new
teeth altoge
jaw is not b
ure 16: The Per
e of the Primary
or permane
nd the age
As the jaw
adult teeth
ether but so
ig enough.
rmanent Dentit
13
y Dentition
ent teeth s
of 6. They
grows, ther
to erupt. Th
ometimes th
tion
start
are
re is
here
e wisdom te
The Ad
Perman
the fro
them a
and fo
are us
teeth t
disting
biting e
root th
Perman
Figu
eeth have t
dult Teeth are
nent Incisor
ont teeth and
altogether (f
our at the b
ually the fir
to come thro
uished due
edge and the
hat they have
nent Canine
ure 15: The 28 A
rouble comi
ing
e:
rs. These a
d there are 8
four at the t
bottom). Th
rst permane
ough. They a
to their f
e one and on
e.
es: Also know
Adult Teeth
are
8 of
top
hey
ent
are
flat
nly
wn
e a more poas
al
s “eye teeth”
so have one
”, these fron
root.
nt teeth hav ointed shapee. Being 4 in number, thhey
PrdeTh
Peroar
1s
m
2n
pe12
3r
wi– thprtodaca
remolars: Theciduous mohe deciduous
ermanent Mooot. They alsre first, secon
t Permanentolars and co
nd Permaneermanent m2 years.
d Permanentisdom teethif they comehere is not roperly and tooth in the famaged, or an become in
Figu
hese are theolars. The fous teeth do no
olars: These o have irregnd and third
t Molars: Theome through
ent Molarsolars come
t Molars: Co. They do noe through at enough spathey get impfront. The lathe gums anfected and q
ure 17: The Tim
e new adultur 1st premoot have prem
are the largeular or “bumpermanent
e four first page 6 to 8 y
s: The fouthrough at
ommonly knot erupt untiall, becauseace for thempacted often atter can somround the wquite painfu
14
meline of the Pe
t back teethlars erupt firmolars as bac
er back teethmpy” surfacemolars whic
permanent mears.
ur second around age
own as the il late teens sometimes m to erupt against the metimes be wisdom teetl.
ermanent Dent
h which reprst followed ck teeth, but
h and they ues with groovch come thro
molars are si
h
Figure 12agai
ition
place the firsby the four t just molars.
usually have ves called “fiough that ord
milar in size
2: A Wisdom Toinst its neighbo
st and seco2nd premola.
more than oissures”. Theder.
to the seco
ond ars.
one ere
ond
ooth erupting or tooth
Figthsuco
gure 20: A panoe primary teetccedaneous te
onsidered succe
oramic x‐ray ofh at these ageeeth because thedaneous teeth
f a 7 years old s. The develophey succeed thh.
Figure 19: D
15
child. One can ping permanentheir correspond
Deciduous and
notice the comt teeth up to tding primary te
Adult Teeth
mplex mix of thhe 2nd premoleeth. Permane
he permanent alar are also calnt molars are
and lled not
Figapincmoen
Figure
gure 22: Panorapical foramina,complete matuolars a radiogrnamel pearls.
Figure 23
e 21: Schematic
amic radiograp, especially inuration. Tooth raphic addition
3: Schematic de
c diagram of de
ph of a 9‐year‐on the maxilla, 12 is rotated an effect caused
epiction of dev
16
evelopment an
old female. All have not ye
about its axis. d by superimp
velopment and
nd eruption of t
of the permant assumed thNote in the bifosition of the
eruption of th
the primary de
nent incisors hae normal diamfurcation of throot trunks. T
e permanent d
ntition
ave erupted. Thmeter, indicate first permanThis is not due
dentition
heir ting ent e to
Figure 24: Pancomplete. Teechamber. Durithe mandible cThe neck and c
noramic radiogeth 35 and 45 ng the pubertacreated space condyle of the
graph of a 15‐have developal growth spurfor the buds omandible are n
‐year‐old femaped into taurort, dorsally andf the wisdom tnot yet fully de
ale. Root formdonts with a d cranially directeeth and theirveloped.
mation of the ecoronoapicallycted growth ofr root developm
erupted teeth y expanded puf the maxilla anment has begu
isulpndun.
Fac
Figure 25: Panoapical foramincompletely eru
oramic radiograna and the roupted but exhib
aph of a 20‐yeaoot canals exhbit a long axis t
ar‐old female. hibit normal dhat is oriented
Development diameter of ad slightly dorsal
of the dentitiodult age. The ly.
on is complete. third molars
Theare
17
Figgure 26: A commplete view of tthe Oral Anatomy
18
CHAPTER 2
PANORAMIC RADIOGRAPHY: A CLINICAL OVERVIEW
INTRODUCTION
Millions of dental panoramic radiographs are performed every year in a global basis.
Being a simple, quick and convenient technique as also as providing a respectful image
of the dentition and its related structures on a single film, with a relatively low dose in
comparison to other radiographic techniques, it is easy to understand why its popularity
has become so grown; and it is still growing.
A panoramic radiograph contains a substantial amount of diagnostic information. This
information, being sometimes difficult to be detected, finds itself upon the four basic
diagnostic regions in panoramic radiography:
1) The Dentoalveolar region
Figure 1: The Dentoalveolar region
19
2) The Maxillary region
Figure 2: The Maxillary region
3) The Mandibular region
Figure 3: The Mandibular region
20
4) The Temporomandibular joint region (abbreviated as TMJ), including the
retromaxillary and cervical regions.
Figure 4: The Temporomandibular Joint region (TMJ)
THE NORMAL PANORAMIC RADIOGRAPH
The normal panoramic radiograph contains a broad range of information that covers the
entire dentition and its surrounding structures, the facial bones and condyles and parts
of the maxillary sinus and nasal complexes.
Various interpretations of the normal panoramic radiograph exist in current literature,
so that the practitioner, the radiologist and the physician will be able to have an
appropriate comprehensive pattern of the technique and its imaging and diagnostic
potentials. However, it is crucial that each individual develops his/her own method of
interpretation according to:
a) the modality that is being used and its imaging programs and abilities, b) the clinical
cases that are taken place in general and c) the basic anatomic characteristics of the
population. The development of a consistent approach that ensures that all diagnostic
information in the panoramic radiograph is indeed read is absolutely essential.
Indicatively, four suggestions of interpreting the normal panoramic radiograph are
following:
21
A) Allan G. Farman (2007) remarks 50 distinct soft tissues, bony and dental landmarks
on a normal panoramic radiograph.
His approach on reading and evaluating the radiograph follows roughly the numerical
sequence of the figure below. It starts with the bony landmarks from the midline of the
upper jaw and nasal cavity, then back in the maxilla and zygomatic complex on each
side. The soft tissue shadows of the tongue and soft palate follow, and then the cervical
spine and its associated structures. Afterwards, the focus is on the contents of the
mandible starting from the midline and then progressing posterior on each side. Any
examination would be incomplete without a thorough evaluation of the soft tissues
anterior to the spine and inferior to the mandible. Lastly, there is the evaluation of the
area of chief complaint and the dental arches. While these regions draw the reader’s
attention automatically, the other features within the radiograph can be missed without
careful sequencing.
Figure 5: Interpreting a Normal Dental Panoramic Radiograph A
22
1. nasal septum 26. mandibular canal
2. anterior nasal spine 27. mental foramen
3. inferior turbinate 28. inferior border of mandible 4. middle turbinate 29. hyoid
5. superior turbinate 30. pharyngeal airspace 6. soft tissue shadow of the nose 31. epiglottis
7. airspace between soft tissue shadow of the upper border of tongue and hard palate
32. coronoid process of mandible
8. lateral wall of nasal passage 33. inferior orbital rim
9. maxillary sinus (antrum) 34. mastoid process
10. nasolacrimal canal orifice 35. middle cranial fossa 11. orbit 36. bite‐block for patient positioning
during panoramic radiography 12. infraorbital canal 37. chin holder (cephalostat) 13. zygomatic process of the maxilla 38. shadow of cervical spine 14. pterygomaxillary fissure 39. ethmoid sinus
15. maxillary tuberosity with developing third permanent molar tooth
40. angle of mandible
16. zygoma 41. crypt of developing mandibular third permanent molar tooth
17. zygomatico‐temporal structure 42. developing mandibular second premolar tooth
18. articular eminence of temporal bone
43. primary second molar tooth showing physiological root resorption
19. mandibular condyle 44. maxillary permanent central incisor tooth
20. external auditory meatus 45. maxillary permanent lateral incisor tooth
21. first cervical vertebra (atlas) 46. maxillary permanent canine tooth 22. second cervical vertebra (axis) 47. maxillary first premolar tooth 23. third cervical vertebra 48. maxillary permanent first molar
tooth 24. fourth cervical vertebra 49. ramus of mandible
25. mandibular foramen & lingual 50. pterygoid plates
23
B) Friedrich A. Pasler (2007) suggests the following reading of the panoramic
radiograph:
Figure 6: Interpreting a Normal Dental Panoramic Radiograph B
1. orbit 15. zygomatic arch, articular tubercle
2. intraoral canal 16. coronoid process
3. nasal cavity 17. condyle
4. nasal septum 18. external ear with external auditory meatus
5. inferior nasal concha 19. cervical vertebrae
6. incisive foramen, superiorly located anterior nasal spine, nasopalatine canal
20. temporal crest of the mandible
7. maxillary sinus 21. oblique line
8. palatal roof and floor of the nose 22. mandibular canal
9. soft palate 23. mental foramen
10. maxillary tuberosity 24. dorsum of the tongue
11. pterygoid processes (lateral and medial lamina) and the pyramidal process of the palatal bone
25. compact bone of the inferior border of the mandible
12. pterygopalatine fossa 26. hyoid bone
13. zygomatic bone 27. superimposition of the contralateral jaw 14. zygomaticotemporal suture
24
C) William S. Moore presents his landmarks of interest for the interpretation of the
normal panoramic radiography:
Figure 7: Interpreting a Normal Dental Panoramic Radiograph C
1. coronoid process 19. infraorbital canal
2. sigmoid notch 20. nasal septum
3. mandibular condyle 21. inferior turbinate
4. condylar neck 22. medial wall of maxillary sinus 5. mandibular ramus 23. inferior border of maxillary sinus 6. angle of mandible 24. posterolateral wall of max. sinus 7. inferior border of mandible 25. malar process
8. lingual 26. hyoid bone
9. mandibular canal 27. cervical vertebrae 1‐4
10. mastoid process 28. epiglottis
11. external auditory meatus 29. soft tissues of neck (look vertically for carotid artery calcifications here)
12. glenoid fossa 30. auricle
13. articular eminence 31. styloid process
14. zygomatic arch 32. oropharyngeal airspace 15. pterygoid plates 33. nasal air space
16. pterygomaxillary fissure 34. mental foramen
17. orbit 35. hard palate
18. inferior orbital rim
25
D) Having in mind the figure of a normal panoramic radiography, another suggestion for
its interpretation follows, by Eric Whaits (2006):
A. General Overview of the Entire Panoramic Film
1. Note the chronological and development age of the patient
2. Trace the outline of all normal anatomical shadows and compare their shape and
radiodensity
B. The Teeth
3. Note particularly: i) the number of teeth present, ii) stage development, iii) position,
iv) condition of the crowns (caries, restorations), v) condition of the roots (length,
fillings, resorption, crown/root ratio)
C. The Apical Tissues
4. Note particularly: i) the integrity of lamina dura, ii) any radiolucencies or opacities
associated with the apices
D. The Periodontal Tissues
5. Note particularly: i) the width of the periodontal ligament, ii) the lavel and quality of
crestal bone, iii) any vertical or horizontal bone loss, iv) any furcation involvements, v)
any calculus deposits
E. The Body and Ramus of the Mandible
6. Note: i) shape, ii) outline, iii) thickness of the lower border, iv) trabeculae pattern, v)
any radiolucent or radiopaque areas, vi) shape of the condylar heads
F. Other Structures
7. These include: i) the antra (note the outline of the floor, the anterior and posterior
walls and the radiodensity), ii) nasal cavity, iii) styloid processes.
26
As mentioned above, the “strategy” for the interpretation of a panoramic radiograph is
varies according to various and subjective factors. Ideally, one should create his/her own
permanent and unique method of reading a panoramic image, so that all included
diagnostic information can be detectable.
Apart from the methods of interpreting the whole normal panoramic radiograph, there
are also similar methods of interpretation specific regions, tissues or structures such as:
facial skeleton, maxillary sinus, retromaxillary space, external ear and TMJ region,
palatal bone, chin region and many others. The presentation of these methods does not
fit to the goals of this paper. However, the reference bibliography includes such
sections, for those interested in these subjects.
Errors in interpretation are commonly made in the maxillary and mandibular incisor
region. It is important to be aware of the normal appearances of the dental panoramic
image when assessing the mandibular bone density:
Lucency: Normal symmetrical lucency is common in the mandibular body inferior to the
premolar and molar apices and may be mistaken for a lytic lesion. The lucency is due to
the submandibular fossa on the lingual aspect of the mandible. The appearance is
exacerbated in middle‐aged and elderly women by reduced bone density. Artifactual
lucency over the mandibular angle is also produced by incorrect tongue positioning.
Figure 8: Coned panoramic tomograph demonstrating normalradiolucencies. The pseudolucency (air space) betw en thesoft palate and tongue (curved arrow), the normalmandibu ar lucency (straight arrows), the nasopharynx np)and oropharynx (op) are shown.
e
l (
27
Areas of increased density: The mandible may appear sclerotic in the midline owing to
superimposition of the density of cervical spine. However, intra‐oral densities may also
appear as an area of mandibular sclerosis.
Figure 9: There is an apparent area of sclerosis within the left lower mandible (arrows)
A very significant point concerning radiographic anatomy must be taken into
consideration. Representing the basis for radiographic interpretation, it follows its own
rules and demands understanding and knowledge of how x‐ray work, as well as the
normal anatomy of the irradiated spaces, depending on the radiographic technique
used. Analogous to this essential knowledge, the following basic rules must be obeyed
for every type of radiograph, including the panoramic technique:
- The tangential effect of x‐rays renders clearly visible in the irradiated space only
those hard tissues with either high density or significant thickness; thin lamella
which, at the moment of the exposure, are parallel or nearly parallel to the
central ray simulate hard tissue of significant thickness and therefore appear in
the radiograph as densely opaque. On the other hand, similar structures which,
at the moment of exposure, are perpendicular to the central ray or nearly so
may, even though they are relatively thick, appear transparent in the radiograph
because of the exposure data necessary to penetrate the tissue.
- The summation effect of x‐rays may lead to hard and soft tissue structures in the
field being exhibited more clearly, or they may disappear entirely depending
upon the selection of exposure data. For example, if soft tissues are projected
28
29
upon one section of the bone, it will appear more dense than adjacent areas
because the x‐ray beam is already ‘weakened’ when it hits the bone. On the
other hand, if an air‐containing space is projected onto a section of bone, the
situation is on in which the x‐ray beam is not weakened before it encounters the
bone, penetrates I readily and therefore eliminates the typical radiograph
features of bone. The first example is referred to as “addition effect”, and the
second example as “subtraction effect”. The situation in such cases has
absolutely nothing to do with radiographic signs of “sclerosis” or “resorption”.
Panoramic radiography is not an exception; it depicts in‐focus layers of various thickness
(but always thicker than 5mm), and thus may be classified as a type of zonography. In
the panoramic radiograph, the picture of the irradiated tissues is determined by the
tangential effect and the summation effect; however, in keeping with the principle of
tomography, all of the structures within the in‐focus layer are shown relatively distinctly
and somewhat enlarged, while all structures outside of the layer are depicted as blurred
and reduced in size or as blurred, broadened and enlarged superimpositions; such
appearance will depend upon whether the superimposed structures are between the in‐
focus layer and the film or between the in‐focus layer and the focal spot.
CHAPTER 3
PRINCIPLES OF FUNCTION
INTRODUCTION
The theory of dental panoramic tomography is complicated. Nevertheless, an
understanding is necessary of how the resultant radiographic image is produced and
which structures are in fact being imaged, so that a critical evaluation and for the
interpretation of this type of radiograph.
The difficulty in panoramic tomography arises from the need to produce a final shape of
focal trough which approximates to the shape of the dental arches.
An explanation of how this final horseshoe‐shaped focal trough is achieved is given
below. Before that, other types of tomography –which form the basis of panoramic
tomography‐ are described, showing how the result in different shapes of focal trough.
These include:
‐ Linear tomography using a wide or broad x ray beam
‐ Linear tomography using a narrow or slit x ray beam
‐ Rotational tomography using a slit x ray beam
30
Broad Beam Linear Tomography
The synchronized movement of the tubehead and film, in the vertical plane, results in a
straight linear focal trough. The broad x ray beam exposes the entire film throughout
the exposure.
Figure 1: Diagram showing the theory of broad beam linear tomography to produce a vertical coronalsection with the synchronized movement of the x ray tubehead and the film in the vertical plane. Usinga broad beam, there will be multiple centers of rotation (three are indicated), all of which will lie in theshaded zone. As all these centers of rotation will be in focus, this zone represents the focal plane orsection that will appear in focus on the resultant tomography. Note, the broad x ray beam exposes theentire film
Slit or Narrow Beam Linear Tomography
A similar straight linear tomograph can also be produced by modifying the equipment
and using a narrow or slit x ray beam. The equipment is designed so that the narrow
beam traverses the film during the tomographic movement. Only by the end of the
tomographic movement has the entire film been exposed. The following equipment
modifications are necessary:
‐ The x ray beam has to be collimated from a broad beam to a narrow beam.
‐ The film cassette has to be placed behind a protective metal shield. A narrow
opening in this shield is required to allow a small part of the film to be exposed
to the x ray beam at any one instant.
‐ A cassette carrier, incorporating the metal shield, has to be linked to the x ray
tubehead to ensure that they move in the opposite direction to one another
during the exposure. This produces the synchronized tomographic movement in
the vertical plane.
throughout the exposure.
31
‐ Within this carrier, the film cassette itself has to be moved in the same direction
as the tubehead. This ensures that a different part of the film is exposed to the x
ray beam throughout the exposure.
Figure 2: Diagram showing the theory of narrow beam linear tomography to produce a verticalcoronal section. The tomographic movement is produced by the synchronized movement of the xray tubehead and the cassette carrier, in the vertical plane. The film, placed behind the metalprotective front of the cassette carrier, also moves during the exposure, in the same direction asthe x ray tubehead. The narrow x ray beam traverses the patient and film, exposing a differentpart of the film throughout the cycle.
Narrow beam rotational tomography
In this type of tomography, narrow beam equipment is again used, but the synchronized
movement of the x ray tubehead and the cassette carrier are designed to rotate in the
horizontal plane, in a circular path around the head, with a single center of rotation. The
resultant focal trough is curved and forms the arc of a circle, as shown below. Some
important points to note are the following:
‐ The x ray tubehead orbits around the back of the head while the cassette carrier
with the film orbits around the front of the face.
‐ The x ray tubehead and the cassette carrier move in opposite directions to one
another.
‐ The film moves in the same direction as the x ray tubehead, behind the
protective metal shield of the cassette carrier.
‐ A different part of the film is exposed to the x ray beam at any one instant, as
the equipment orbits the head.
32
‐ The simple circular rotational movement with a single center of rotation
produces a curved circular focal trough.
‐ As in conventional tomography, shadows of structures not within the focal
trough will be out of focus and blurred owing to the tomographic movement.
Figure 3: Diagrams showing thetheory of narrow beam rotationaltomography. The tomographicmovement is provided by thecircular synchronized movement ofthe x ray tubehead in one directionand the cassette carrier in thehorizontal plane. The equipmenthas a single center of rotation. Thefilm also moves inside the cassettecarrier so that a different part of thefilm is exposed to the narrow beamduring the cycle, thus by the endthe entire film has been exposed.The focal plane or trough (shaded)is curved and forms the arc of acircle.
Dental Panoramic Tomography
The dental arch, though curved, is not the shape of an arc of a circle. To produce the
required elliptical, horseshoe‐shaped focal trough, panoramic tomographic equipment
employs the principle of narrow beam rotational tomography, but uses two or more
centers rotation.
There are several dental panoramic units available. They all work on the same principle
but differ in how the rotational movement is modified to mage the elliptical dental arch.
Four main methods have been used including:
33
‐ Two stationary centers of rotation, using two separate circular arcs
‐ Three stationary centers of rotation, using three separate circular arcs
‐ A continually moving center of rotation using multiple circular arcs combined to
form a final elliptical shape
‐ A combination of three stationary centers of rotation and a moving center of
rotation
Figure 4: The main methods that have been used to produce a focaltrough that approximates to the elliptical shape of the dental arch usingdifferent centers of rotation. A: 2 stationary, B: 3 stationary, C:continually moving, D: combination of 3 stationary and moving centers.
However, the focal troughs are produced, it should be remembered that they are 3‐
dimentional. The focal trough is thus sometimes described as a focal corridor. All
structures within the corridor, including the mandibular and maxillary teeth, will be in
focus on the final radiograph. The vertical height of the corridor is determined by the
shape and height of the x ray beam and the size as shown below.
34
As in other forms of narrow beam tomography, a different part of the focal trough is
imaged throughout the exposure. The final radiograph is thus built up of sections, each
created separately, as the equipment orbits around the patient’s head.
Figure 5: The figure shows how the height of the three‐dimensional focal corridor is determined. Theheight (x) of the x ray beam is collimated to just cover the height (f) of the film. The separation of thefocal trough and the film (d) coupled with the 8⁰ upward angulation of the x ray beam results in thefinal image being slightly magnified.
FOCAL TROUGH (Image Layer)
The focal trough or the image layer of a panoramic radiograph is a 3‐dimensional curved
zone. Objects inside this zone are reasonably well defined. The anatomical structures
which lie inside the image layer are depicted with the minimum of unsharpness and
distortion. Going outside this layer, unsharpness is growing. Objects outside the focal
trough are blurred, magnified or reduced in size and sometimes they are distorted to
the extent of not being visible or recognizable. As it can be easily concluded, the focal
trough and all its diagnostic information is all in all the very essence of a panoramic
radiograph.
35
The exact shape of the focal trough (horseshoe curve) varies with the brand of the
equipment used. The factors that affect its size are variables that influence image
definition:
‐ Arc path
‐ Velocity of the film and the x ray tube head
‐ Alignment of the x ray beam
‐ Collimator width
The location of the focal trough can change with extensive machine use. In this way, recalibration may be necessary if consistently suboptimal images are produced.
Figure 6 The Focal Trough. The closer to the center of the trough (dark zone) an anatomic structure is positioned. The more clearly it is imaged on the resulting radiograph.
36
Figure 7: Gradual formation of a panoramic tomograph over an 18‐second cycle, strating how a different part of the patient is imaged at different stages in the cyclillu e.
37
FORMATION OF THE IMAGE LAYER
As the x ray tube and the cassette holder are mounted at opposite ends of a gantry,
during the exposure the x ray beam and the cassette rotate around the patient. The x
ray beam is collimated both at the tube head and immediately in front of the film screen
cassette. The effect of the collimation is to create a beam that is vertically long although
horizontally narrow. Control of the rotational movement and film velocity is achieved by
computer software and mechanical gearing.
The projection technique employed in rotational panoramic radiography is unique, as
there are two foci of projection working simultaneously.
In the vertical plane the situation is analogous to conventional radiography where the x
ray tube focus acts as the focus of projection. Consequently, the magnification in the
vertical plane (MV) is as follows:
where FFD is the focus to film distance and FOD is the focus to object distance.
In the horizontal plane, the effect of the narrow collimated beam combined with its
motion creates the appearance that the point of divergence for the x rays is the rotation
centre of the beam. Therefore, this point acts as an effective focus for the x rays in the
horizontal plane and the distance between this point and the object is termed the
effective projection radius (R). The magnification in the horizontal plane (MH) is
therefore:
As the effective rotation centre is nearer the object than the conventional focus, the
effective projection distance is always smaller than the conventional focus to object
distance. Consequently, the magnification in the horizontal plane is greater than the
magnification in the vertical plane, leading to geometric distortion.
38
Figure 8: Creation of an effective focus of projection
The rotational movement of the x ray beam also means that every ray in the beam will
project the image of a discrete object point onto the film plane at a different position.
The image of a discrete object point would therefore be portrayed as a horizontal line at
the film plane if the film remained stationary during the exposure producing motion
unsharpness. However, by moving the film in the same direction as the beam and
selecting an appropriate velocity of movement, the film can be made to match the
projected path of an object plane within object. Object points within this plane are
therefore depicted with minimum motion unsharpness at the film plane.
The velocity of the film relative to the beam also affects the horizontal magnification of
points within the object. It has been shown that an object will be sharply depicted at the
film plane where the following equation is standing:
where VB is the velocity of the beam, VF is the velocity of the film, FFD is the focus to
film distance and R is the effective projection radius.
The horizontal magnification therefore depends not only on the geometric properties of
projection but also on the relative velocity of the film to the beam and consequently the
horizontal magnification is a non‐linear function with object depth.
39
The position of the focal trough within the object is not constant but depends on the
relative velocity of the film to the beam. As the FFD is generally constant, increased
acceleration of the film velocity relative to the beam shifts the position of the focal
trough away from the rotation centre and towards the film cassette, with a
corresponding increase in the effective projection radius. Decreasing the film velocity
relative to the beam moves the position of the focal trough towards the rotation centre
and away from the film cassette, thereby reducing the effective projection radius.
As the width of the focal trough is proportional to the effective projection radius, it is
possible to alter the size and position of the focal layer by adjusting the relative velocity
of the film to the beam and thereby create a focal layer that corresponds to the
idealized shape of the jaws.
In many modern systems the projection of the jaw is achieved by using an effective
rotation centre that is continuously moving throughout the exposure. In these units, the
x ray beam is always directed perpendicularly to the path of the effective rotation centre
throughout the exposure. Consequently, the effective projection radius varies
continuously throughout the exposure, being wider in the lateral aspects of the jaw than
in the anterior regions. As a result, the focal layer is narrower in the anterior region of
Figure 9: Diagram of beam projection in modern dental panoramic x ray units.
40
the jaw where the effective projection is smaller. Furthermore, as the size of the
effective projection radius also influences the horizontal magnification, the horizontal
magnification of object points outside the focal trough is more marked in the anterior
regions of the jaw compared to the lateral regions.
The path of the beam also determines the angle at which the central ray of the beam
traverses the object. Ideally, to aid interpretation and measurement, the central ray of
the beam should be projected perpendicularly to the object throughout the exposure.
However, the projection angle between the central ray and the object varies throughout
the exposure, only approaching perpendicularity in the anterior regions of the jaw.
Distortion effects are therefore produced by the oblique projection angle between the
beam and some regions of the jaw. As in conventional radiography, this effect leads to
compression of objects in the resulting image. It should be noted however, that this
effect is independent of both geometric distortion and motion unsharpness and
therefore distortion effects due to oblique projection occur even at the focal trough
position.
GEOMETRIC DISTORTION
For object points located outside the focal layer, the greatest source of distortion is the
geometric distortion caused by the discrepancy between the horizontal and vertical
magnification factors. The degree of distortion can be assessed using a relationship
termed the Distortion Index:
At the focal trough, where an object’s vertical and horizontal magnification are equal,
the DI is one and geometric distortion is minimized. A distortion index greater than one,
indicates that the horizontal magnification of the image is greater than the vertical
magnification. This effect occurs if the velocity of the film is greater than the velocity of
the beam. This occurs if the object is displaced away from the focal trough position
towards the centre of rotation (i.e. towards the beam).
41
Conversely, a distortion index less than one indicates that the vertical magnification is
larger than the horizontal one in the image and it occurs if the velocity of the beam is
greater than the velocity of the film. This occurs when the object is displaced away from
the focal trough position towards the film.
Figure 10: Magnification and x ray tube focal spot size.
Displaced towards the rotation centre
of the beam
Placed at the focal trough
Displaced towards the film
Table 1: Distortion effects. Relationship between type of distortion and displacement from the focal trough.
42
Screen Film and Intensifying Screens
A beam of x ray photons that passes through the dental arches is reduced in intensity
(attenuated) by absorption and/or scattering effects of photons out of the primary
beam. The pattern of the photons that exists the subject, the remnant beam, conveys
information about the structure and the composition of the absorber. This is why the
remnant beam has to be “written” on an image receptor, in order to be diagnostically
useful.
Dental panoramic x ray units use a combination of screen film and intensifying screens.
The advantages of this combination are the increased sensitivity and better contrast.
The screens have much higher x ray absorption efficiency (510 times) than a
photographic film and will also produce a great number of light photons per x ray
photon absorbed, thus yielding a more efficient film exposure. The x ray exposure can
often be reduced by factor of 10‐50, depending on the screen characteristics.
The sensitivity can vary depending on the screen thickness. The thicker the screen, the
higher the absorption efficiency. However, a thicker screen will also result in an
impairment o spatial resolution. The light produced in the screen will have a longer
distance before it hits the film and it will therefore be more diffused than for a thinner
screen. More sensitive screens can also be produced using larger phosphor crystals in
the screen material. This will lower the spatial resolution and will also increase the noise
level.
Due to the higher atomic number of the screen material compared to the silver halide
grains, the film‐screen combination is always relatively more sensitive to higher energy x
rays than film alone. This extends the use of film‐screen combinations to techniques
which use higher energy beams, compared to film alone.
Thus, apart from the panoramic technique, screen‐film combinations have been one of
the most important components in all modern radiology.
The Screen Film
Screen film is different than dental intraoral films in that it is designed to be particularly
sensitive to visible light rather than to x radiation because this film is placed between
two intensifying screens when an exposure is made.
The intensifying screens absorb x rays and emit visible light, which exposes the screen
film. Silver halide crystals are inherently sensitive to ultraviolet (UV) and blue light (300
to 500 nm) and thus are sensitive to screens that emit UV and blue light. When film is
43
used with screens that emit green light, the silver halide crystals are coated with
sensitizing dyes to increase absorption. Because the properties of intensifying screens
vary, the dentist should use the appropriate screen‐film combination recommended by
the screen and film manufacturer so that the emission characteristics of the screen
match the absorption characteristics of the film. In panoramic radiography fast films
that require less radiation exposure are mainly used, as fine image detail is not available
because of the movement of the x ray tube head during the exposure period.
The design of screen films changes constantly to optimize imaging characteristics. As an
example, Kodak has introduced T‐Mat films, which have tabular‐shaped (flat) grains of
silver halide. The tabular (T) grains are oriented with their relatively large, flat surfaces
facing the radiation source, providing a larger cross‐section (target) and resulting in
increased speed without loss of sharpness. In addition, green‐sensitizing dyes are added
to the surface of the tabular grains, increasing their light‐gathering capability and
reducing the crossover of light from the phosphor layer on one side of the intensifying
screen to the film emulsion on the other. Kodak’s Ektavision system also coats the film
base with an absorbing dye to prevent crossover of light from one screen to the other
emulsion. These properties increase both the speed of the film and the sharpness of the
image. Sterling uses tabular grains in its Cronex I OT film, and Imation coats its XDA+ and
XLA+ film base with an anti‐crossover agent as well.
Figure 11: T grains of silver halide in an emulsion of T‐Mat film (A) are larger andflatter that he smaller, thicker crystals in an emulsion of conventional film (B).Note that he flat surfaces of the T grains are oriented parallel with the filmsurface, facing the radiation source. (Courtesy Eastman Kodak, Rochester, N.Y)
44
INTENSIFYING SCREENS
Wilhelm Conrad Roentgen, along with the x rays, discovered the intensifying screens. He
was experimenting with high energy cathode ray tube and had enclosed the tube in
black cardboard. When passing a high voltage discharge through the tube, he noticed a
faint light from a piece of paper left on a work bench. The paper was covered with a thin
layer of barium platinocyanide. This first “intensifying screen” sent out fluorescent light
of inorganic salts (phosphors) which emit
fluorescent light when excited by x ray radiation. The sheets are used to intensify the
At
is
into eV
at y
is 850. Approximately, half of these will escape from the screen to
expose the emulsion. About 100 light photons may be sufficient to form one latent
: calcium
tungstate screen (CaWO4) and rare earth screens (La2O2S:Tb, Gd2O2S:Tb, Y2O2S:Tb),
38.9 lower
caused by the x rays.
An intensifying screen is a sheet of crystals
effect of x rays during exposure of x ray film.
The intensifying screen or a pair of screens is nearly always used with x ray film in
radiography. Film may be used as the only radiation detector but having a relatively low
atomic number (that of silver halide), film is relatively radiolucent. direct exposure of
film, only about 5% of the x ray photons will be absorbed by the film and react with the
emulsion. For comparison, a high speed calcium tungstate screen will absorb
approximately 40% of the x ray photons. Furthermore, each absorbed x ray photon will
be converted into many light photons. The efficacy of the screen in converting x rays
into light photons is called the intrinsic conversion efficiency. The efficiency of calcium
tungstate about 5%. A 50 keV x ray photon when absorbed by calcium tungstate (by
photoelectric absorption), will be converted about 17,000 light photons of 3
energy 100% efficiency. Since the efficiency is onl 5%, the actual number of light
photons emitted
image centre.
There are two major types of phosphors and therefore intensifying screens
where terbium (Tb) is often used as an impurity or activating substance.
During the 70’s, the principal material in intensifying screens was calcium tungstate
(CaWO4). Nowadays, the principle materials are based on gadolinium and lanthanum
substances. Calcium tungstate suffers from the drawback that the K‐edge for W in the
absorption curve is situated at 69.5 keV. This means that the CaWO4 screen is quite
insensitive to the part of the x ray spectrum with photons of energies between 50 and
69 keV when compared to gadolinium or lanthanum screens, which have their Kedges
lower at 50.2 and keV respectively, due to their atomic number. Since this
part of the x ray spectrum often contains a significant fraction of the x rays that exit
45
from the patient, the sensitivity is increased using these newer materials. This is
furthermore amplified by the fact that the new materials have a higher light conversion
efficiency, which means that more light photons are generated per x ray photon
absorbed. Compared to CaWO4, the newer screens produce about 3.5 to 4 times more
reen part of the spectrum but smaller
ones also in the blue, blue‐green and yellow regions. The term “green screen” may be
sed. It is absolutely necessary to use green sensitive film with these screens to make
sure that useful transmitted radiation is not lost.
light.
Figure 12: X ray absorption spectra for calcium tungstate (W) and gadolinium (Gd) based intensifying screens.
The spectral output of the phosphor must be matched to the response of the film.
Calcium tungstate screens emit blue light of continuous spectrum with a peak
wavelength at about 430 nm. The term “blue screen” refers both to the screen itself and
to the blue sensitive film used together with the Ca WO screen. Rare earth screens emit
light in narrow lines with strong peak(s) in the g
u
46
Figure 13: Spectrum of light emitted from calcium tungstate (CaWO) and rare earth screen (GdOS), respectively, in comparison with the light sensitivity of blue sensitive
and green sensitive film.
There are many factors affecting the speed of a screen. The phosphor type determines:
‐ The x ray radiation absorption efficiency
‐ The radiation to light conversion efficiency
‐ The thickness of the phosphor
The fraction of x rays absorbed by a pair of calcium tungstate screens is about 20‐40%
depending on the speed (determined mainly by screen thickness), while rare earth
screens absorb about 60%. The radiation to light conversion efficiency of calcium
tungstate is about 1/3 or 1/4 of that of the film‐screen cassette. The relative speed of
film‐screen combinations is normalized to 100 which corresponds the basic calcium
tungstate screen with the basic film. Speed values vary from 20 and 50 (slow screens)
through 100, 200, 400 and 800 to 1,600.
An essential basic feature of the two screen types is related to the position of the K edge
on the energy axis. Tungsten (W) being a heavy element has its K edge at 69.5 keV, while
that for rare earth elements is in the vicinity of 50 keV. Most x ray spectra used in
conventional radiography have their mean energy between 40‐50 keV, signifying that
also for this reason rare earth screens are more effective than CaWO4 in absorbing x ray
quanta.
47
Compared to film only, the contrast of the same film together with screens is always
higher. The reason for this is not precisely known.
DIGITAL PANORAMIC RADIOGRAPHY
An image is said to be a digital one when it is composed of separate (distinct) elements.
Each element is called a “picture element” or a pixel. If an image is displayed on the
computer monitor and the pixel is smaller than the smallest detail the viewer’s eye can
see, it is hard to determine that the image is indeed a digital one. If this is not the case,
that is the individual pixels can be spotted, the eye views the image as a mosaic of
pixels.
Each pixel can only take on a limited number of gray shades. The number of possible
gray shades depends on the number of bits (binary digits) that are used to store a pixel.
A 1‐bit pixel can only take two values (0 or 1 – that is black or white). An 8‐bit pixel can
take any one of 256 (28) values. A 16‐bit pixel can take more than sixty five thousand
grayscale values (216). The total number of bits that are used to store an image is the
number of pixel times the number of bits per pixel.
Most systems of digital panoramic radiographs use on the final depiction mostly 8 bits
(thus, 256 different grey levels). Newer systems deposit the image as data of 10, 12 or
16 bits (thus 1024, 4096 or 65536 different grey levels). However, these systems lay the
final image out using 8‐bit data and 256 different grey levels. It is generally accepted
that the human eye can only distinguish about 20 magnitudes of light intensity, and is
probably unable to discern all 256 gray levels that a standard computer monitor can
display. Thus, a human eye cannot distinguish totally a little more than 100 different
grey levels. Indeed, in cases where these levels of grey find themselves on the same
radiograph, then the number of the distinguished levels is limited between 30 and 40.
For example, for the panoramic system Dimax I (Planmeca Oy, Helsinki, Finland) the
functional and true size of the pixel that presents the final image is 132 μm. This pixel
size delivers a maximum theoretical resolution, which is the Nyquist frequency, of 3.78
cycles per mm.
There are three methods available to produce digital panoramic images. First, it is
possible to digitize conventional analog film radiographs through secondary capture
using transparency scanners or specialized digital cameras. Film scanners and digitals
cameras, though, can be used to produce digital images only from an analog film
radiograph.
48
In general, secondary capture is best achieved with a good quality scanner having a
radiography adaptor (i.e. scanning light in the lid to pass light through the radiograph. A
sharp black and white photograph setting is preferred. Excellent scanners for this
purpose for a sufficient high quality system have a cost varying from 600$ to 1,500$.
Scanners are preferred to digital cameras as they practically eliminate optical distortion
and the reflection from the surface of the radiograph that would otherwise reduce
image quality. Film scanners do not change the need to continue making radiographs
with x ray film. They introduce additional time‐consuming activity to scan images but
that is the price for continuing the use of analog film radiographs while digitally storing
images.
No matter the quality of the film scanner, scanned images can only be as good as the
priginal film radiographs. The advantage is that the user can scan and archive the
existing film files over time and determine if digital panoramic imaging is needed
without spending a lot of money in purchasing sophisticated equipment. While Schultz
et al. (2002) found the sensitivity for detection of low contrast simulated bone lesions
was greater with film than after digitization, the absolute differences were small.
Figure 14: Nikon CoolPix scanner withtransparency adaptor in lid sufficient forextraoral radiograph duplication.
Figure 15: Panoramic radiograph placed fordigitization in an alternative flat bedscanner, the Epson FinePix Z2 withtransparency adaptor.
The result of this method is apparently substandard in comparison to the following two
methods. However, these two technologies have the same principles of function with
those that are applied in endodentulous radiographies.
49
Solid‐state systems using the technology of Charged‐Coupled Device (CCD) or
complementary metal oxide semiconductor (CMOS) comparable to the computer chip
found in a digital photographic camera
McDavid et al. (1995) presented and evaluated the first experimental system for
panoramic radiography with the use of CCD technology. This original system was a
modification of the panoramic machine OP10 (Instrumentarium Imaging, Finland). The
rotation time around the patient’s head remained stable and the same with the
equivalent conventional system, but the combination of film and rare earth screens had
been replaced by a narrow linear sensor CCD. The height of this sensor was
approximately 15 cm and its width a few millimeters.
During the last years, different systems of digital panoramic imaging using CCD
technology have been introduced into the market. The procedure of the production of
the image remains the same. Solid‐state digital x ray detectors are based on a silicon
chip that permits the acquisition of an image. Such a chip consists of a myriad of pixels
and each pixel captures a small quantity of energy (usually light from a scintillator) and
converts this radiant energy into electricity. For panoramic radiology, this generally
involves a charged coupled device (CCD) or complementary metal oxide semiconductor
(CMOS) of sufficient dimensions to cover the secondary slit of the panoramic machine
(i.e. tall and narrow). The solid‐state chip (CCD or CMOS) converts radiant light photons
into electrons when a scintillator is used. The ability of detectors to capture radiant
energy is no longer limited to visible photon as cadmium telluride can produce electrons
directly on impact of x ray photons. Most systems, however, still use a scintillator layer,
similar to the scintillators that are used as intensifying screens in analog film panoramic
radiography. An example of one of the earliest commercialized digital panoramic
systems was that of the Trophy Digipan adaptor for the Instrumentarium OP 100.
Figure 16: The Trophy Digipan adaptor used with Instrumentarium OP 100 panoramic system in place of the film cassette. A variety of “add‐on” systems from several different vendor sources are now available for most panoramic systems.
50
Figure 17: Schematic representation of a solid‐state detector. Unlike analog x ray film radiography, the receptor is stationary and the image for each segment is read out in
appropriate sequence.
Solid state systems are available both to retrofit an existing panoramic system and as
integrated units dedicated to a specific panoramic x ray generator. A potential concern
with retrofitting a unit is that if something does go wrong, the owner may be in the
position of working together with the manufacturer of the panoramic system, the
manufacturer of the retrofit system and the installer.
As with analog film, the panoramic image is pieced together during the scan. Unlike
analog film radiography, the receptor is stationary and the image for each segment is
read out in appropriate sequence. As it was mentioned above, in conventional
panoramic imaging, the position of the image layer is determined by the velocity of the
film in relation to the x ray beam. In digital panoramic radiography using CCD
technology, it is not the film that is moving in order to form the image properly but the
charges themselves as they are read‐out. Thus, the velocity by which the pixels give their
data for the final imaging is exactly the same with the velocity of the movement, in the
scintillator’s plane, of the projections of the anatomical structures and elements inside
the focal trough. In this way, the image is formed partially and almost simultaneously
with the patient’s radiation, thus in real time.
51
A direct practical consequence of this fact is that the user can control at any time of the
radiation the quality of the final imaging. If the user sees that the patient is not properly
positioned during the radiation, he/she is able to interrupt the procedure and re‐
position the patient, so that a more correct imaging will be achieved.
Researchers report that the width of the x ray beam which scans every moment the
patient to form the image, is much more narrow in digital panoramic imaging using CCD
technology, in relation to conventional panoramic radiography. This happens due to the
high sensitivity of the CCD and to the attempt of bounding the x ray beam, using special
collimators, exactly at the width of the slit linear sensor. This offers an important
advantage, which is a significant reduce of the radiation dose of the patient. Farman et
al. (2000), as well as Dula et al. (2008), confirmed this experimentally.
Additionally, MacDavid and Dove (1995) report two direct practical consequences. The
zone in which the depiction’s sharpness is maximum is larger, thus the positioning of the
patient is not as much important as in conventional procedures and in this way some
small positioning errors may not be of such significant importance. However, many
times the over‐projection of other anatomical regions cannot be avoided, resulting in
the black‐out of elements of diagnostic interest. For example, the spine can break the
depiction of the front regions, or the depiction of the lateral regions of the mandible
being blocked by the respective regions of the other side.
Moreover, as the CCD sensor is much more sensitive to the combination of film and rare
earth screens, a reduction of the mA of the machine (less quantity of radiation) may be
achieved with the same kV, as in conventional methods, or even higher. In this way, a
reduction in the patient’s dose is possible. Higher photon energy is less harmful for the
patient. The contrast of the final image will be lower in this case, with higher voltage.
This happens due to the different absorption of the radiation, depending on the beam
energy when the beam enters through matter (an object). However, this is something
that can be overcome, as there is the possibility of editing the image, adjusting the
contrast.
The percentage of dose reduction in digital panoramic radiography using CCD
technology is not always the same. It is a fact that a reduction of the radiation dose
similar to intraoral radiography is not possible, due to the fact that in conventional
panoramic radiography the dose is already very low, as a consequence of the film‐rare
earth screen combination. The dose reduction percentage that is reported in the global
bibliography varies from 20% to up to 40% related to conventional panoramic
52
radiography. In this case, the final image will have an intense noise. However, using the
editing techniques that digital imaging systems offer even such an image may be
corrected and used for diagnostic purposes.
Units which use the technology of Storage Phosphor Plates (SPP)
In the middle of the 80’s, Kashima et al. (1985) presented the first digital panoramic
radiograph using a Storage Phosphor Plate (SPP). This technique has been improved
over the years, until it reached a widespread level of acceptance all over the world.
Today, a variety of companies use this technology.
In this technique a special plate, with the same size (30x15 cm) as in conventional
panoramic radiography, is used. Such plates contain a phosphor layer that deposits the
energy of the photon with which it interacted. Hence, the name “storage phosphor” is
used. After its irradiation, the plate is placed in a special scanner or digitizer where it is
scanned by radiation of specific wavelength. When a portion of the plate is illuminated,
it emits light that is photomultiplied and collected by a digital imaging chip. The image
appears through sophisticated electronic processes (photomultiplier, analog to digital
converters) in a monitor of a computer.
Photostimulable phosphor systems dedicated to dentistry are available from a number
of manufacturers. Each system is comprised of the phosphor plates and a laser scanner
that interfaces with a computer. The plates can be quite expensive, costing from 500
euro up to 2,000 euro each. While extraoral plates are not as sensitive to scratching as
are the intraoral ones, care must still be taken not to scratch or contaminate them. The
plates are very sensitive to ambient light which can erase much of the latent image.
Furthermore, they need extensive exposure to light in order to completely erase the
image before reuse. On the other hand, storage phosphor systems are versatile in that
they can be used with a wide range of different x ray systems.
It is of particular importance that this technique can be applied upon every conventional
panoramic system. The only modification needed, is the placement in the holder of the
panoramic machine, of the Storage Phosphor Plate, instead of the combination of film‐
rare earth screen. The only extra equipment needed, to gain the final image, is the
specialized scanner or digitizer. Many manufactures offer themselves the scanner along
with the conventional panoramic machine.
53
A basic characteristic of the plates used in this technique, is that they do not have
picture elements (pixels). The latter are formed during the procedure of the laser
scanning of the plate and their exact size depends on the degree of focalization of the
laser radiation. For example, the DenOptix system (Gendex) uses a pixel size of 170 μm,
when the resolution in the scanner is determined to be 150 dots per inch (150 dpi). This
pixel gives out a maximum theoretical resolution, the Nyquist frequency, equal to 2.95
cycles / mm.
The phosphor plates have a very high dynamic range of irradiation. Thus, with the use of
this technique the quantity of the radiation targeting the patient (mA) may be reduced,
without any loss of the diagnostic quality of the final image. The dose reduction
percentage, related to conventional techniques, is approximately at 20%. The time
period of the radiation cannot be reduced, as it is always stable for a specific unit
depending on the whole rotation movement that it makes.
Figure18: Imaging using storage phosphor plate.
54
Figure19: Loading a photostimulable phosphor plate into a soft cassette.
Interoperability
It is not unusual to review film radiographs that are decades old –especially when
demonstrating “classical” radiographic features of disease entities at a continuing
education forum. Archived film images that are decades old are usually still of high
quality and can be viewed by anyone who happens to have a view box to transmit light
through the radiographs.
One might question whether the digitized or digital versions will be as readily accessible
as the analog film versions decades into the future. The likelihood of being able to
retrieve digital images is dependent upon both hardware and software/file format
considerations.
Regarding hardware issues, one simply needs to back up all files on new media as they
become accepted. If one intends to use digital images they periodic storage hardware
upgrades must be performed. Regarding the matter of software/file format
interoperability, the digital x ray industry and practice management system vendors are
presently working together to facilitate digital image interoperability using specifications
from the DICOM (Digital Image Communication) standards that were developed initially
for medical radiology. This specification includes image format rules and associated
information for transmission of radiographs used in dentistry including intraoral surveys
and panoramic images.
55
However, no guidelines or specifications will guarantee interoperability. Interoperability
needs to be demonstrated practically. Such practical demonstrations were initiated at
the ADA Annual Congress in New Orleans in 2002, where ten companies demonstrated
that interoperability of their image files could be archived satisfactory. Similar practical
demonstrations have been made with DICOM validation at all ADA Annual Sessions,
through at least until the time of publication of this book. Each time there are more
vendors involved.
Interoperability within the DICOM Standard is important so that the dentist can
integrate data from different digital sources and read diagnostic images referred from
outside sources where different systems may have been used. Otherwise there could be
inconvenience both for the patient and for the practitioner.
Radiation Dosage
Unlike intraoral radiology, the switch to digital panoramic imaging does not generally
result in a substantial dose reduction to the patient. In fact it is sometimes necessary to
actually increase dosage to optimize image quality when using digital systems.
With intraoral x ray film radiography, the emulsion is directly sensitive to x rays, so
adding a scintillating screen can improve the efficiency with which x rays are detected.
However, for extraoral radiography, an intensifying screen is generally employed –and
this is not so very different from the scintillating layer used with solid‐state detectors.
Gijbels et al. found no difference in exposure settings or organ doses between analog x
ray film and digital panoramic radiography using Photostimulable phosphor plates.
COMPARISON BETWEEN FILM AND DIGITAL PANORAMIC IMAGING
Digital panoramic radiography includes the following essential properties:
‐ Images of diagnostic quality
‐ Radiation dose similar or reduced compared to film radiography
‐ Lossless archiving (storage of the full original radiographic image)
‐ Interoperability of image format so that the patient’s information can be
conveniently shared when professionally necessary
Below there is a summary of the advantages and disadvantages of the two categories.
56
ADVANTAGES DISADVANTAGES
FILM TECHNIQUE
• Low initial cost, especially for manual processing
• Often already in place • l No changes or additiona
training required • Known entity – proven
output • f Relatively low cost ooperation
• Excellent diagnostic clarity possible if exposed and processed optimally
• Widely accepted
• Cost of consumables such as film and processing solutions
• ent Cost of processing equipmand darkroom space
• Time consumption in film processing and processor maintenance
• Processed film images are rarely optimal
• Used processing chemicals are toxic to the environment
• d Film radiograph storage anretrieval can be problematic
• Duplicates made from film radiographs are invariably inferior to the original images
DIGITAL X RAY
IMAGING
e is Time saving as therno chemical processing
More consistent in quality for the same reason
Digital images ease communication with patients
Digital images are readily stored and retrieved
Digital radiology opens the way to electronic interchange
Consultation can be expedited
Digital images allow perfect “clone” duplication and backup
Post‐processing can help optimize the diagnostic yield
Digital radiology eliminates environmental silver contamination from spent fixer
Added initial cost for equipment if film imaging is already used
Need for additional computers, monitors, networking, backup storage
Detectors (both solid‐state and phosphor systems) can add an important cost of the panoramic system
Changes in operations, systems and procedures require an investment in time and involve a learning curve
Not all digital image formats are identical at this moment, so interoperability can be problematic both in the same office and when making outside referrals
Eventually hardware obsolescence
Table 2: Advantages and disadvantages of conventional and digital panoramic imaging (Farman, 2007).
57
Equipment
There are several different dental panoramic tomographic units. Although they vary in
design, all of them consist of three main components:
‐ An x ray tubehead and its power supply, producing a narrow fan‐shaped x ray
beam, angled upwards at approximately 8⁰ to the horizontal
‐ A cassette and cassette carriage assembly
‐ Patient positioning apparatus including light beam markers
Figure 20: A modern panoramic x ray unit.
The equipment should have a range of tube potential settings, preferably from 60 to 90
kV. The beam height at the receiving slit of cassette holder should not be greater than
the film in use (normally 125 mm or 150 mm). The width of the beam should not be
greater than 5mm. Equipment should be provided with adequate patient‐positioning
aids incorporating light beam markers. New equipment should provide facilities for field
limitation techniques.
58
Almost all modern panoramic machines have a continuous‐mode of operation and
produce a so called continuous image showing an uninterrupted image. X ray production
is continuous throughout an uninterrupted tomographic cycle, during which the centers
of rotation are adjusted automatically. However, one machine was developed which
produced a so called split‐mode image because the radiographic image is split by a
broad, vertical, white, unexposed zone, with duplication of the midline. The split mode
equipment is now only of historical interest.
There are a number of different panoramic machines available in the market. The
machines operate on the same image formation principles and only differ in the added
features. Panoramic machines employ a single‐phase x ray robe that requires an average
cool down period of 5 minutes between exposures for maximum tube life. Machines
have an upright construction with an adjustable vertical tube height range typically of 3
feet (0.91 m) to 6 feet and 4 inches (1.92 m) from the floor. The entire machine may be
freestanding with a heavily weighted base or wall mounted. The cassette holder and x
ray tube are attached to a carrier that mechanically rotates them at a preset path and
speed around the patient’s head during each exposure. These variables stay consistent
from patient to patient unless the technologist changes the location or width of the
focal trough which is adjustable to accommodate different facial profiles.
Two types of cassettes are made for panoramic machines: hard and floppy. The type of
cassette to be used is determined by the manufacturer. The standard film sizes available
for panoramic imaging are 6’’x 12’’ and 5’’x 12’’. Sizes are also determined by the
machine manufacturer. Cassettes incorporate rare earth screens and use 400 speed
film. Specific film types may be chosen to optimize bony or soft tissue detail.
Most modern panoramic machines allow the patient to stand up for the exposure. A
chair or wheelchair can be accommodated. All panoramic machines have some type of
guides to help position and hold the patient within the focal zone. This commonly
includes a platform for the chin to rest on and a bite stick with grooves for the upper
and lower central incisors, placing the oral cavity within the focal plane. For edentulous
patients there may be a separate, specialized positioning device that is used in place of
the bite stick. Many machines use laser light guides at the infraorbitalmetal (IOM) line
and along the midsagital plane to help the technologist adjust the patient into position,
as well as guide bars that can be secured alongside the head to help the patient
maintain the correct position throughout the exposure.
Almost every panoramic machine produces standard panoramic films as well as
specialized projections of the (TMJ) such as transmaxillary projections and either single
images or multiple “cuts”. Even the least sophisticated machines typically offer multiple
59
views of the TMJ area including lateral images with the mouth open and closed,
producing all 4 images on one film. A wide array of programs specifically designed to
evaluate the TMJ are available with more advanced machines. Additional programs
allow for multilayered exposures of the area in the frontal, transmaxillary and lateral
projections to evaluate fractures, arthritic changes and abnormalities in the size, shape
and position of the condylar head. Programs can also assess the articular processes.
More sophisticated panoramic machines offer a variety of programs that produce
tomographic images of predefined areas of almost any area of the head. Using a series
of computer controlled programs that use various tube head and film motions, including
multidirectional, these machines can perform coronal, sagittal and cross‐sectional
images through a predetermined area. These programs can be helpful in the assessment
and treatment of sinusitis, neoplasm, fractures, foreign bodies, air‐fluid level detection
in the sinuses, mucosal changes of the sinuses and soft tissue calcifications. Many
panoramic machines can be fitted with a film holder that supports an 8’’ x 10’’ film used
for static skull views using the panoramic x ray tube head.
Figure 21: The Instrumentarium OP 200D (PaloDEx, Tuusula, Finland)
60
Patient Positioning
The exact positioning techniques vary from one machine to another. However, there are
some general requirements that are common to all machines and these can be
summarized as follows:
Patients should be asked to remove any earrings, jewellery, hair pins, spectacles,
dentures or orthodontic appliances.
The procedure and equipment movements should be explained, to reassure
patients.
A protective lead apron should not be used as it can interfere with the final
image.
Patients should be placed accurately within the machines using the various
head‐positioning devices and light‐beam marker positioning guides. (In some
units the patients face away from the equipment and towards the operator and
in others the patient faces the other way round.)
Patients should be instructed to place their tongue into the roof of the mouth so
that it is in contact with the hard palate and not to move during the exposure
cycle (approximately from 9 to 18 seconds).
Appropriate exposure setting should be selected, typically in the range of 70‐100
kV and 4‐12 mA.
The positioning of the patient’s head within this type of equipment is critical –it must be
positioned accurately so that the teeth lie within the focal trough. The effects of placing
the head too far forward, too far back or asymmetrically on relation to the focal trough
are quite easy to take place. The parts of the jaws outside the focal trough will be out of
focus. The fan‐shaped x ray beam causes patient malposition to be represented mainly
as distortion in the horizontal plane, i.e. teeth appear too wide or too narrow rather
than foreshortened or elongated. These and other positioning errors are shown later.
However accurately the patient’s head is positioned, the inclination of the incisor teeth,
or the underlying skeletal base pattern, may make it impossible to position both the
mandibular and maxillary teeth ideally within the focal corridor.
61
Field Limitation Techniques
In panoramic radiography, there is the ability to program the equipment to only radiate
certain parts of the jaws when specific information is required, rather than the entire
dentition. This results in a significant radiation dose reduction. A variety of these so‐
called field limitation techniques are possible.
Figure 22: Diagrams showing the position of the mandible in relation to the focal troughwhen the patient is not positioned correctly. A) The patient is too close to the film and infront of the focal trough. B) The patient is too far away from the film and behind the focaltrough. C) and D) The patient is placed asymmetrically within the machine.
62
Figure 23: Diagrams showing the vertical walls of the focal trough in the incisorregion and the relative positions of the teeth with different underlying dental orskeletal abnormalities. A) Class I, B) Gross class II division 1 malocclusion with largeoverjet. C) Angle’s class II skeletal base. D) Angle’s class III skeletal base. The shadedareas outside the focal trough will be blurred and out of focus.
The two figures below represent the relative movements of the x ray tubehead, cassette carrier and film during an exposure cycle of a continuous‐mode panoramic unit.
Figure 24: Initially the left side of the jaw is imaged (position 1). As the x ray tubehead movesbehind the patient’s head to image the anterior teeth, the cassette carrier moves in front of thepatient’s face and the centre of rotation moves forward along the dark arc (arrowed) towardsthe midline.
63
Figure 25: The x ray tubehead and cassette carrier continue to move around the patient’shead to image the opposite side and the centre of rotation moves backwards along the darkarc (arrowed) away from the midline. Throughout the cycle, the film is also continuouslymoving as illustrated, so that a different part of the film is being exposed at any one moment.
64
CHAPTER 4
RADIATION EFFECTS, DOSES AND PROTECTION CONCERNING QUALITY CONTROLLING ON
PANORAMIC RADIOGRAPHY
INTRODUCTION
X rays have taken their name due to their unknown nature, at the time of their discovery
(1895) by Roentgen. Being one of the different types of ionizing radiation and being able
to penetrate the human tissues, they are a form of high energy electromagnetic
radiation and part of the electromagnetic spectrum, which also includes lower energy
radio waves, as well as television and visible light.
Radiation Wavelength Photon Energy Radio, television and radar waves
3x104 m to 100 m 4.1x10‐11 to 1.2x10‐2 eV
Infra‐red 100 m to 700 m 1.2x10‐2 eV to 1.8 eV Visible light 700 nm to 400 nm 1.8 eV to 3.1 eV Ultra violet 400 nm to 10 nm 3.1 eV to 124 eV X and gamma rays 10 nm to 0.01 pm 124 eV to 124 MeV Table 1: The electromagnetic spectrum ranging from the low energy (long wavelength) radiowaves to the
high energy (short wavelength) x and gamma rays (White, 2000).
X rays consist of wave packets of energy, called photons. A photon is equivalent to one
quantum of energy. The x ray beam, as used in diagnostic radiology, is made up of
millions of individual photons. Although the production and interactions of x rays with
matter is an essential knowledge, in this project such a presentation is out of its interest
as such background information is presupposed.
65
SOURCES OF RADIATION
Everyone is exposed to some form of ionizing radiation from the environment. The
sources of radiation may be either natural or artificial. These include:
Natural Radiation Artificial Radiation Cosmic radiation from the earth’s atmosphere
Fallout from nuclear explosions
Gamma radiation from the rocks and soin the earth’s crust
il Radioactive waste discharged from nuclear establishments
Radiation from ingested radioisotopes, e.g. 40K, in certain foods
Medical and dental diagnostic radiation
Radon and its decay products, 222Rn is a gaseous decay product of uranium that is present naturally in granite. As a gas, radon diffuses readily from rocks through soil and can be trapped in poorly ventilated houses and then breathed into the lungs.
Radiation from occupational exposure
Table 2: Natural and artificial sources of radiation (Whaites, 1996).
Figure 1: The distribution of natural and artificial radiation. Natural radiation contributes more exposure than artificial radiation. Note that medical x ray diagnosis is the largest component of artificial radiation.
66
In the UK, an individual’s average dose from background radiation is approximately 2
mSv per year, while in the US it is estimated approximately at 3.6 mSv. Having these
numbers in mind, one can refer more safely to the numbers of doses of the medical
diagnostic radiographies.
As indicated above, medical x ray diagnosis produces the largest exposure of all artificial
sources of radiation (11%). This should not surprise anyone, as the millions of x ray
examinations that are made every year worldwide contribute to the total radiation
doses which add up through arithmetic progression. As such techniques are widespread
all over the world, it is crucial to find out whether some proportion of this exposure
could and should be avoided. The relatively very low doses that are produced from a
single x ray examination of any kind should not loosen neither the criteria by which an x
ray examination is decided nor the standards of the proper functioning of the x ray units
and their proper usage.
Classification of the biological effects
Three main categories classify the biological damaging effects of ionizing radiation:
Somatic Deterministic Effects
Somatic Stochastic Effects
Genetic Stochastic Effects
Somatic Deterministic Effects
These are the damaging effects to the body of the person that will definitely result from
a specific high dose of radiation. Examples include skin reddening and cataract
formation. The severity of the effect is proportional to the dose received and in most
cases a threshold dose exists below which there will be no effect.
Somatic Stochastic Effects
Stochastic effects are those that may develop. Their development is random and
depends on the laws of chance or probability. Examples of somatic stochastic effects
include leukemia and certain tumors.
These damaging effects may be induced when the body is exposed to ant dose of
radiation. Experimentally it has not been possible to establish a safe dose (a dose below
which stochastic effects do not develop). It is therefore assumed that there is no
67
threshold dose and that every exposure to ionizing radiation carries with it the
possibility of inducing a stochastic effect.
The lower the radiation dose, the lower the probability of cell damage. However, the
severity of the damage is not related to the size of the inducing dose. This is the
underlying philosophy behind present radiation projection recommendations.
Somatic effects are further subdivided into:
‐ Acute or immediate effects, appearing shortly after exposure, e.g. as a result of
large whole body doses
‐ Chronic or long‐term effects, becoming evident after a long period of time, the so
called latent period (20 years or more), e.g. leukemia.
DOSE WHOLE BODY EFFECT 0.25 Sv Nill
0.25 – 1.0 Sv Slight blood changes, e.g. decrease in white blood cell count 1 – 2 Sv Vomiting in 3 hours, fatigue, loss of appetite, blood changes.
Recovery in a few weeks 2 – 6 Sv Vomiting in 2 hours, severe blood changes, loss of hair within 2
weeks. Recovery in 1 month to year for 70% 6 – 10 Sv Vomiting in 1 hour, intestinal damage, and severe blood
changes. Death in 2 weeks for 80‐100% > 10 Sv Brain damage, coma, death. Table 3: Summary of the main acute effects following large whole body doses of radiation
Genetic Stochastic Effects
Mutations result from any sudden change to a gene or a chromosome. They can be caused by external factors, such as radiation or may occur spontaneously.
Radiation to the reproductive organs may damage the DNA of the sperm or egg cells. This may result in a congenital abnormality in the offspring of the person irradiated. However, there is no certainty in this, so all genetic effects are determined as stochastic.
A cause‐and‐effect relationship is difficult, if not impossible, to prove. Although ionizing radiation has the potential to cause genetic damage, there are no human data that show convincing evidence of a direct link with radiation. Risk estimates have been based mainly on experiments with mice. It is estimates that a dose to the gonads of 0.5 – 1.0 Sv would double the spontaneous mutation rate. Once again it is assumed that there is no threshold dose.
68
Harmful Effects Important in Dental Radiology
In dentistry, the sizes of the doses used routinely are relatively small and well below the
threshold doses required to produce the somatic deterministic effects. However, the
somatic and genetic deterministic effects can develop with any dose of ionizing
radiation. Dental radiology does not usually involve irradiating the reproductive organs,
thus in dentistry somatic stochastic effects are the damaging effects of most concern.
The precise mechanism of how x rays can cause damaging effects is not yet fully known
but two main mechanisms are thought to be responsible:
• Direct damage to specific targets within the cell
• Indirect damage to the cell as a result of the ionization of water or other
molecules within the cell
A photon strikes upon a molecule of water:
1. H2O H2O+ + e‐
2. The positive ion immediately breaks up: H2O H+ + OH
3. The electron (e‐) attaches to a neutral water molecule: H2O + e
‐ H2O‐
4. The resulting negatively charged molecule dissociates: H2O
‐ H + OH‐ 5. The electrically neutral H and OH are unstable and highly reactive
and called free radicals. They can combine with other free radicals, e.g: H + H H2 (hydrogen gas) OH + OH H2O2 (hydrogen peroxide)
The hydrogen peroxide can then damage the cell by breaking down large molecules like proteins or DNA.
Table 4: A diagrammatic summary of the sequence of events following ionization of water molecules
leading to indirect damage to the cell (Whaites, 1996)
Estimating the Dose and Risk of Panoramic Radiography
Quantifying the risk of somatic stochastic effects, such as radiation‐induced cancer, is
complex and controversial. Data from groups exposed to high doses of radiation (i.e.
radiotherapy, or survivors of nuclear accidents like Hiroshima or Chernobyl) are analyzes
and the results are used to provide an estimate of the risk from low doses of radiation
encountered in diagnostic radiology.
69
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fatal cancer of 1.3x10 . Other risk estimates have arrived at varying figures: Danford and
Gibbs (1980) estimated the risk to be between 2 and 7x10‐6 and Bengtsson (1978)
4.2x10‐6. Since much of this work was undertaken, several international organizations
have suggested that the risk may be greater than previously estimated. Over the same
period of time the design of panoramic machines has changed and rare earth
screen/film combinations have become more widely used, resulting in a reduction in
computed the average effective dose for a panoramic examination to be 6.7μSv; this
figure is associated with an estimated risk of fatal malignancy of 0.21x10‐6.
Despite these encouraging findings, it should be emphasized that the lower levels of risk
are associated with new equipment. Horner and Hirschmann (1990) described the
various methods of limiting patient dose in panoramic radiography. The facility for field
size reduction is associated with a reduction in absorbed dose of 85% and effective
efficients and assuming the use of rare earth screen/film combinations, White (199
of 50%, when the TMJs are excluded from the field. However, it is likely that the higher
levels of dose and risk reported by previous researchers will remain valid as long as older
equipment remains in clinical use. For example, certain types of equipment using a
circular scanning motion incorporating three centers of rotation produce doses between
3 and 16 times higher than those with an elliptical system, due to the proximity of
rotational centers to the mandible and parotid glands. A study carried out in France
showed this type of equipment to be the most widely used. Furthermore, a survey of
panoramic equipment in the UK found that a higher dose than appropriate was being
delivered during use of 70% of this equipment.
Although abdominal lead protection is clearly inappropriate in panoramic radiography,
some researchers have recommended the use of a lead thyroid collar in younger
patients because of the relatively high anatomical position of the gland. However,
because the primary beam does not strike the patie
examination, a thyroid shield must logically be placed on the back of the neck. This runs
the risk of attenuating useful parts of the primary beam and obscuring areas of the
mandible on the radiograph.
71
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uring panora
would seem
amic radiogra
reasonable t
aphy.
to suggest thhat no lead pprotection should be usedd
Figure 3:equiv
: Examples of thvalent). In the s
hyroid lead prosecond picture,
otection. In the, a hand‐held n
e first picture, aneck shield (0.5
a lead collar (0. mm Pb equiva
.5 mm Pb alent).
72
MMain Methods of Monittoring and Measuring Radiation DDose
Thhere are 3 main devices ffor monitorinng and meassuring radiation dose:
Film BBadges
Thermmoluminesceent Dosimeteers (TLDs)
‐ BBadge
‐ Extremity Moonitor
Ionization Chambeers
Film Badges
They c
and a
They
reprod
They a
Figure 4: MonitorTLD
r Devices: A. Pebadge. C. Ioniz
ersonal monitoation bleeper.
ring film badgeD. TLD extrem
e. B. Personal mity monitor.
monitoring
consist of a b
small radiog
blue plastic f
graphic film w
frame contai
which reacts
ining a varie
to radiation
nt metal filteers ty of differe
n
are worn o
ductive orga
on the outs
ns, for 1‐3 m
side of the
months befor
clothes, us
re being proc
ually at the
cessed
e level of tthe
are the mostt common foorm of personal monitoring device cuurrently in usse
73
Advantages
‐ Provides a permanent record of dose received
‐ May be checked and reassessed at a later date
‐ Can measure the type and energy of radiation encountered
‐ Simple, robust and relatively inexpensive
Disadvantages
‐ No immediate indication of exposure – all information is retrospective
‐ Processing is required which may lead to errors
‐ The badges are prone to filter loss
TLDs
They are used for personal monitoring of the whole body and/or the
extremities, as well as measuring the skin dose from particular investigations
They contain materials such as lithium fluoride (LiF) which absorb radiation and
then release the energy in the form of light when heated
The intensity of the emitted light is proportional to the radiation energy
absorbed originally
Personal monitors consist of a yellow or orange plastic holder, worn like the film
badge for 1‐3 months
Advantages
‐ The lithium fluoride is re‐usable
‐ Read‐out measurements are easily automated and rapidly produced
‐ Suitable for a wide variety of dose measurements
Disadvantages
‐ Read‐out is destructive, giving no permanent record, results cannot be checked
or reassessed.
‐ Only limited information provided on the type and energy of the radiation
‐ Dose gradients are not detectable
‐ Relatively expensive
74
Ionization Chambers
They are used for personal monitoring (thimble chamber) and by physicists
(free‐air chamber) to measure radiation exposure
Radiation produces ionization of the air molecules inside the closed chamber,
which results in a measurable discharge and hence a direct read‐out
They are available in many different sizes and forms
Advantages
‐ The most accurate method of measuring radiation dose
‐ Direct read‐out gives immediate information
Disadvantages
‐ They give no permanent record of exposure
‐ No indication of the type or energy of the radiation
‐ Personal ionization monitors are not very sensitive to low‐energy radiation
‐ They are fragile and easily damaged
Measurements using phantoms
Phantom measurements in dental radiography are usually performed on
anthropomorphic phantoms in order to derive organ doses and thereby determine the
effective dose and/or the energy imparted to the patient.
Measurements in anthropomorphic phantoms are performed using TLDs positioned in
drilled holes in the phantom. General principles for the use of TLDs should be followed.
Patient Dosimetry
For patient dose measurements in panoramic projections, the measured quantity is the
air kerma‐length product, PKL. The PKL is the integral of the free in air profile of the air
kerma across the front side of the slit of the secondary collimator. Methods using a CT
chamber or a stack of TLDs for the measurement of PKL will be described. The air kerma‐
area product, PKA, is obtained as PKA=PKLH, where H is the height of the x‐ray beam at the
secondary collimator.
75
List of Equipment
The equipment used for panoramic projection comprises:
‐ Calibrated cylindrical ionization chamber and electrometer
‐ Chamber support
‐ Thermometer and barometer
‐ TLDs and a jig for mounting the dosimeters in front of the secondary collimator
may be used as an alternative to the pencil ionization chamber. Dosimeter
thickness and their diameter should be about 1 mm or less and 3 mm,
respectively. Dosimeters should have had their individual sensitivity correction
factors established or dosimeters within a selected sensitivity range should be
chosen
‐ Film and a ruler (for screen‐film systems)
Methods
The air kerma‐length product is measured using either a calibrated cylindrical ionization
chamber or an array of TLDs. The air kerma‐length product is immediately obtained
using an ionization chamber whereas use of TLDs requires several procedures before the
result is registered. When neither a cylindrical ionization chamber not TLD is available,
direct film could be used as described by Napier. The latter method requires calibration
of the film in terms of air kerma and careful handling of film development (IAEA, 1996).
Measurement of the air kerma‐length product using a cylindrical ionization chamber and
electrometer
1. Position the cylindrical ionization chamber in front of the secondary collimator (slit),
at the centre of the slit and perpendicular to its length direction
2. Make sure that the space between the chamber and the headrest is sufficient when
the secondary collimator is rotated.
76
M
1.
tim
sig
ca
2.
3.
pe
tu
ra
F
Measurement
Select a set
mes the slit w
gnal obtaine
an be identifi
Pack the ch
Position the
erpendicular
ube, includin
ay beam.
Figure 5: Experkerma‐area
t of the air ke
t of TLDs wit
width. Keep
ed without ir
ied in calibra
ips in a tube
e tube with t
r to the leng
g insertions
rimental arrang product for a d
c
erma‐length
h the sum of
another thre
rradiation. La
ations and m
of PMMA.
the TLDs in f
gth of the sli
for intraora
gement for meadental panoramhamber
77
product usin
f the thickne
ee dosimete
abel each ind
measurement
ront of the s
t and at its
al film for me
asurements of mic unit using a
3.
th
se
tu
cy
do
an
4.
st
th
5.
an
. Expose
hree times u
ettings of
ube load
ng an array o
ess sufficient
rs for measu
dividual dos
ts.
secondary co
center. A jig
easurement
the air a CT
a
ycle d
the chamb
using standa
tube voltag
an exposd u
an
osimeter rea
record t
adings, M1,
ber
ard
ge,
ure
the
MM2
nd M . 3
. Repeat ste
tandard
ep 3 for othher
seettings used in
he clinic.
. Record thee temperatuure
nd pressure.
of TLDs
t to cover a l
urement of th
length of thr
he backgrou
ree
nd
imeter so thhat its readinngs
ollimator wit
g may be us
h the tube a
ed to hold t
xis
the
hht, H, of thee x‐of the heig
4.
Re
Expose TLD
ecord the set
s using stand
ttings.
dard settingss of tube volltage, tube looading and eexposure cyccle.
5. Arrange forr the dosimeeters to be reead. Record the readings, M1, M2, ……, Mn, from tthe
exxposed dosimmeters and the readings,
6.
M
1.
th
0.
2.
sc
Repeat mea
Measurement
Position the
he ionization
5.
Develop the
canner.
Figure 6slit of receivinover ththe soldthe outpointinWilliam
asurements f
t of the heigh
e film in fro
chamber wa
e film and m
6: Schematic oa panoramic xng slit is facilite slit. Beam leder markers. Tter markers by g upwards, as s
ms and Montgo
for other sta
M01, M02 an
ndard setti
d M03, for thhe unexposedd dosimeterss.
nngs used in thhe clinic.
of the jig used tx‐ray unit usinated by the trngth is
to measure theng TLDs. Positiangular windo
e dose profile tioning of the ows in the jig,
across the recejig in front owhich are cen
eivingof thentered
measurred from the ddeveloped filmss using the imaage ofThe inner markkers are separaated by a distance of 120 mmm and150 mm. The jig is mountedd with the diagonal solder maarkers
(afteshown, to indicmery)
cate the orienttation of the deeveloped films r
ht of the x‐raay beam at thhe secondaryy collimator sslit
nt of the collimator slit,, at about thhe same locaation as wheere
as located annd expose thhe film to an optical denssity of less thhan
easure the hheight of the on the film uusing a rulerx‐ray beam or
78
HVL measurement
1. Set up the x‐ray equipment for the chosen examination. Suppress the tube movement
2. Select the tube voltage that would be used for a routine clinical examination.
as to avoid the effect of scattered radiation.
ifficult for the panoramic equipment unless
the width
e a detector with a smaller volume and try
to cover the maximum area of the detector.
5. Select a tube loading so that the dosimeter readings with and without the attenuator
values M1, M2 and M3.
s without any attenuator. The thickness of attenuators is selected so
that their value encloses the expected HVL of the beam.
8. Expose the detector again without any attenuator (steps 5 and 6) and record the
easured value.
Calculations
red signal for various
attenuator thicknesses. The HVL value measured during a quality assurance program can
, of the dosimeter readings.
if possible.
3. Centre the dosimeter in the x‐ray beam. The detector should be mounted free in air in
such a way
4. Collimate the beam to achieve conditions for narrow beam geometry. The beam
should just cover the detector. This may be d
of the beam can be increased. In this case, us
are within the rated range of the instrument.
6. Expose the detector three times and record measured
7. Repeat step 6 for a set of three Al attenuators and the same tube loading as that used
for measurement
m
Measurements of the air kerma‐length product using a cylindrical ionization chamber
and electrometer
1. Calculate the HVL of the beam by interpolating in measu
be also used.
2. Calculate the mean value,
79
3. Calculate the air kemra‐length product, PKL, from the mean dosimeter reading, ,
using the following equation:
ion quality Q used during measurement. It is
the dosimeter can be neglected and that no
correction has been applied for this effect.
The correction factor, kTP, given by:
273.2273.2
,
kTP is the correction factor for temperature and pressure, , is the calibration
coefficient for the radiation quality Q0 obtained at the temperature T0 and pressure P0
and kQ is the correction factor for the radiat
assumed that the leakage signal of
is
Measurement of the air kerma‐length product using an array of TLDs
1. Calculate the mean value of the background reading, , from background dosimeter
n), calculate the background corrected dosimeter reading,
Mi, from the exposed dosimeter, , and the mean background dosimeter reading, ,
using the following equation:
r the individual sensitivity of the i‐th dosimeter. This
factor is a constant for dosimeters grouped so that the sensitivity of dosimeters in the
3. For i‐th dosimeter (i = 1, …, n), calculate the air kerma, K , from the background
between irradiation of the dosimeter and its readout. The
Q ends on HVL of the beam that should be established using the
diagnostic dosimeter:
readings, M01, M02 and M03 ( 3⁄ ).
2. For i‐th dosimeter (i = 1, …,
,
where factor fs,i is used to correct fo
group lies within a selected range.
i
corrected dosimeter reading, , using the TLD calibration coefficient, , , for the
reference radiation quality, Q0, the correction factor, kQ, for the radiation quality used
and the correction factor, kf, that corrects for the effect of fading of the
thermoluminescence signal
correction factor, k , dep
,
80
4. Calculate the air kerma‐length product, PKL, using the following equation, in which Δd
is the thickness of a single TLD:
equation. In this
equation, PK is the air kerma‐length product obtained through the above equation and
H is the height of the x‐ray beam at the secondary collimator slit:
e relative standard
have to be included in the overall
is about 10.5%.
he user should establish the actual measurement uncertainty using the principles
described in the relative bibliography.
Establishment of the air kerma‐area product
Calculate the air kerma‐area product using through the following
L
Estimation of uncertainties
The uncertainty in the measurement of the air kerma can be estimated with a cylindrical
ionization chamber during panoramic projections. The value of relative expanded
uncertainty for measurements of the air kerma‐length product is again 6‐13%,
depending on the measurement scenario selected. Assuming that the maximum
difference of a measured slit height from the actual height is 2%, th
uncertainty for this effect is 1.2%. The expanded uncertainty for the measurement of
the air kerma‐area product using a cylindrical chamber is 6.4‐13.2%.
The uncertainty in measurements made with TLDs is discussed above. The relative
expanded uncertainty (k=2) of 10% was adopted. Additional contributions from
positioning of the dosimeters and measured slit height
uncertainty. The value of the relative expanded uncertainty (k=2) in measurements of
the air kerma‐area product using TLDs
T
81
Example
A panoramic dental unit is typically operated at 70 kV and 15 mA for a period of 15 s.
The air kerma‐length product was measured at a secondary collimator using a calibrated
dosimete s
mGy∙cm/reading and 0.98, respectively. The correction factor, kTP, for temperature and
pressure was 1.002. The measured air kerma‐length product is:
llimator slit was measured as 12.5 cm.
The air kerma‐area product is thus calculated as:
ncertainty (k=2) in the measurement is 6.4%.The air kerma‐area product is
written as:
114 7 ·
CT chamber. The reading of the r wa 0.923.
The calibration coefficients, , and kQ, for the dosimeter were 10.02
0.923 10.02 · 0.98 1.002 9.082 ·
The height of the x‐ray beam at the secondary co
9.082 · 12.5 113.53 ·
For scenario 3 (reference type detector and all corrections applied), the relative
expanded u
82
Worksheets
Determination of the air kerma‐length product and the air kerma‐area product for
e:___________________________________________________
No.:__________
_____ mm X ray beam height (H): _________ mm
_____ /N: ________ e of calib: _______
ressure P0 (kPa): __________ Temperature T0 (oC): _______
4. Dosimeter reading and calculation of air kerma‐length product and air kerma‐area
Mean dosimeter rea
o .
panoramic projection using a cylindrical diagnostic dosimeter
User:_________________________________ Date:____________________
Hospital or clinic nam
1. X ray equipment
X ray unit and model: __________________________________ Room
Slit width: ___
2. Dosimeter
Dosimeter model: _____ _____________ S __ Dat
Calibration coefficient ( , )*: ______ · / · /
Reference conditions: HVL (mm Al): _______________ Field size: _______________
P
3. Exposure conditions
Starting tube voltage (kV): _______ Tube current: ________ mA Time: ______s
Ambient conditions: Pressure P (kPa): ______ Temperature T (oC): ____ kTP = _______
product**
Dosimeter reading (M1, M2, M3): _______________ ding : ______
Pressure P (kPa): ___ Temperature T ( C): ____ .
= _______***
kQ = ______________
Calculated value of air kerma‐length product , ·
Calculated value of air kerma‐area product /10 __________ ·
_______________
_________
HVL (from 5 below) = ___________ mm Al
e overall calibration coefficient is calculated as a product of the two separate calibration coefficients.
an example for one setting. The measurements should be repeated for all settings used in clinical practice
*** For dosimeters with a semiconductor detector, kTP = 1
* This is the calibration coefficient for the whole dosimeter, including the detector and the measurement assembly. For systems with separate calibration coefficients for the detector and the measurement assembly, th
** This is
83
5. Determination of HVL
Dosimeter readings should be obtained for filter thicknesses that bracket the HVL. The ing
Filter ness (mm Al)
Dosimeter ading (M) (mGy)
verage dosimeter reading, , at zero thickness
____________ )
Interpolated HVL: _____ mm Al
first and last read s, M01 and M02 are made at zero filter thickness.
thick re A
0.00
0.00
84
Determination of the air kerma‐area product using an array of TLDs
User: ______________________________ Date: __________________
Hospital or clinic name: ____________________________________________________
__ Room No.:_________
h: ________ mm Slit height (H): _________ mm
TL
Al kQ for measurement set‐up: ________
): __________ cm
s (M1, M2, M3): _____________ _
n un
1. X ray equipment
X ray unit and model: _________________________________
Slit widt
2. TLDs
Identification markings on D sachet (if any): __________________________________
Calibration coefficient ( , ) for TLDs: ___________________________ mGy / reading
Reference beam quality (HVL): ______ mm
Dosimeter thickness (Δd
3. Exposure conditions
Tube voltage (kV): _____________
4. Dosimeter readings and calculation of the air kerma‐area product
Background reading ____________ ____________
Mea backgro d ⁄ _ Fa e __
No. Dosimetereading
Corrected a ing
Individual nsitivity
Air erma
No. Dosimetereading
Corrected ading
Individual nsitivity
Air erma
3 _____ ding corr ction (kf) = _
r re d se k r re se k
, Air Kerma, ,
ir kerma‐length product, ∑ ______________A ·
Air kerma‐area product, /10 ___________ ·
85
Doose Area Prroduct
Th
pa
sid
in
in
th
th
ca
an
he dose area
atient absorb
de of the pat
from of the
dependent o
he further aw
he device inc
alculated by
nd the patien
a product –
bs. It is usua
tient where
e x ray tube a
of the distan
way from th
creases, and
DAP, the siz
nt.
DAP is a m
ally measure
the radiation
and passing
nce between
e x ray tube
d the dose
ze of the me
measurement
ed behind th
n enters the
a beam thro
n the x ray tu
e this measu
itself decrea
easuring dev
t of the amo
he multi‐leaf
body, by att
ough it. The d
ube and the
urement is ta
ases. The do
vice and the
ount of radi
collimator,
taching a me
dose area pr
measuring d
aken, the mo
ose to the p
distance to
iation that t
that is, on t
easuring dev
roduct (DAP)
device becau
ore the size
patient can
the x ray tu
the
the
ice
) is
use
of
be
ube
=
Th
DA
ch
x
he
do
ad
pe
m
in
DAP
here are seve
AP meter ca
haracteristic
ray tube and
ead. This cha
ose measur
dvantage of
erf
eter
or
is rel
med in
a
terfere with
Figure 7: measurindecreasessize of the
P
eral DAP me
an eliminate
of panoram
d detect all
aracteristic m
rements in
this method
real time pa
atively trans
the x ray ex
X ray tube is ng device incres with greater e measuring de
ters availabl
problems a
ic units, sinc
radiation in
makes DAP
panoramic
d is that DAP
atient exami
sparent and
amination.
as great as doeases with gredistance to thevice enables it
86
le globally. T
rising from t
e it be moun
cident on th
meter very e
c radiology
P measureme
inations, sinc
d therefore
ose area for 10eater distance he tube. Thus, t to detect all o
The use of a
this special
nted on the
he patient’s
effective in
y. Another
ents can be
ce the DAP
does not
(Gy* m2) cc
00cm or 200cmto the x ray DAP is the samof the radiation
Figu
m, because thetube. But theme at each pon.
ure 8: Real time
e size of thee dose itselfosition if the
e DAP measureement.
Diagnostic Reference Levels (DRLs) deriving from DAP measurements
are defined as dose levels in groups of standard sized patients or standard
hantoms, for typical examinations and for broadly defined typed of equipment. These
levels should not be exceeded for standard procedures when good and normal practice
levels for panoramic
radiography. In Greece, for this technique, the report of such levels has already started
alo
the adoption of the 75 percentile as an
appropriate DRL value.
DRLs
p
is applied with regard to diagnostic and technical performance.
In this way, DRLs can play an important role in clinical practice to guarantee the
performance of diagnostic equipment and as a support to improve techniques and
procedures. Many countries have reported diagnostic reference
to take place by several publications.
The European Commission Radiation Protection Report No 109 (2004), ng with the
majority of the studies published, considers the frequency curve of a number of
examinations and their doses, and proposes th
Below, there are some indicative values from the European Commission.
COUNTRY/DATE OF RESULTS OF SURVEY PROPOSED/SET DRLs
PUBLICATION Occipital ESD: Occipital ESD:
‐ 0.7 mGy ‐ Mean 0.53 mGy ‐ Range 0.25‐0.87
Gy
Spain mGy
‐ Third Quartile 0.66 m
2001
F inland2000
DAP: ‐ Mean 94 mGy
cm2 ‐ Range 34‐254
mGy cm2
87
COUNTRY/DATE OF RESULTS OF SURVEY PROPOSED/SET DRLs
PUBLICATION
UK 1999
ose‐Width Product:D
ose Width Product
he Dose Area Product (DAP) is directly correlated to the Dose Width Product (DWP),
t of DWP and slit length.
ture of the imaging process and the
narrow width of the x ray beam. The dose quantity used is the product of the absorbed
oduct of the peak dose at the
centre of the x ray beam and the width of the beam, or from an incremental summation
D
T
since DAP is the produc
As it has been already mentioned, the assessment of patient dose in panoramic
radiography is difficult because of the dynamic na
dose in air and the horizontal width of the beam, both measured at the front side of the
secondary collimator slit and integrated over a standard exposure cycle. This is referred
to as Dose Width Product (DWP) with units of mGy mm.
The DWP provides a measurement related to the total amount of radiation to which the
patient is exposed. It can be derived either from the pr
of the dose across the beam. According to P. Doyle’s et al report in 2006, the main dos
measurement techniques, in terms of DWP, are:
‐ Mean 57.4 mGy
mm ‐ Range 1.7‐328
mGy mm
66.7 MGy mm
Dose‐Width Product: ‐ 65mGy mm
‐ Third Quartile
UK 2000
DAP: ‐ Mean 11.3 cGy
cm2 Dose‐Width Product:
‐ Mean 65.2 mGy mm
‐ Third Quartile 75.8 mGy mm
Table 6: European Commission’s Radiation Protection Guidelines in Dental Radiology No
136 (2004), indicative dose values and DRLs, for four European countries.
88
1) “In Beam” Detector and Film
2) Partial Volume Detector (proposed by the authors)
3) TLD Array
When a panoramic x ray unit is installed, radiological parameters (tube potential and
are adjusted so that the density on the resultant film is optimized. This
adjustment is dependent on the sensitivity or speed of the film‐screen combination and
DAP and Effective Dose
In medical radiology, including panoramic x ray imaging, DAP can be converted to
te‐Carlo‐generated conversion factors. DAP can also be used
in dental radiology for the assessment of E without the need for extensive phantom
rmined conversion factor. Poppe et al. (2006) calculated the effective doses E
from the DAP and consequent DRLs’ (by the 75th percentile) results of their survey, using
from a research based in Athens, Greece in
order to create a background of DAP reference levels for future studies, in Greece.
tube current)
the effect of such an adjustment will be reflected in changes in DWP. This parameter is
therefore a useful quality control tool but is not directly related to patient risk. A more
useful parameter for this is the dose area product.
effective dose E using Mon
studies.
The calculation of the effective dose can be carried out by multiplying the DAP with a
pre‐dete
three conversion factors, found in literature.
The same calculations of effective doses E will take place in the 2nd part of this thesis,
according to the results of Tierris et al (2004)
89
J. – S. Lee et al (2010) have summarized the DAP and DWP reference levels from a
number of well established surveys globally, including their own results. A very
tive table is demonstrated below, taken from this survey.
Survey Number of x ray units
Gender/ Age/ Size
DWP (mGy mm) DAP (mGy cm2)
indica
Mean 3rd Quartile Mean 3rd Quartile
Napier (UK) 387 57 67
16 Wi dlliams an Montgomery
(UK) 65 76 113 139
Isoardi and Ropolo (Italy) 5 Adult 74 84
Tierris et al. (Greece)
101 117 Male 62 Female 85 97
Child 68 77
H2175 (DWP) 1910 (DAP)
Ad d 60 art and Wall
(UK)
ult anChild
82
Doyle e a . t l(UK) 20 65 67 89 90
Poppe e al. Lar lt 8 101.4
t (Germany) 50
ge Adu 5.7Male 76.4 87 Female 7 8 1.6 4.4Child 59.3 75.4
Kim et l. 36 72.1 106.7 a (Korea) Adult
Lee et al. 44 Adult 47.7 60.1
(Korea)
Table 6: DR DAP in pan radiol et al 2010).
Ls (from and DWP) oramic ogy (Lee
90
91
lthough the differences between the values of the same parameters may seem quite
large, it should be mentioned that despite the fact that the parameters are the same
, DWP), the methods used for their calculation, as well as the number of panoramic
A
(DAP
x ray units used in each survey, differ from one report to another. This table is indicative
of the range of these values, but if a long‐term study from different authors is to be
made in order to achieve some useful DRLs, this should be executed in one country (or
more but without significant or determining variations in populations’ characteristics)
with some standard and commonly recognized methods and a minimum number of
panoramic x ray units needed for each survey.
CHAPTER 5
QUALITY CONTROL PROTOCOLS
CODES OF PRACTICE – LEGISLATION
INTRODUCTION
In this chapter a short presentation of Quality Control references will be presented,
concerning dental x ray panoramic imaging.
1) Greek Atomic Energy Commission – Protocol of Periodical Quality Control Checks on
Orthopantograph, October 2006
The protocol of the Greek Atomic Energy Commission focuses on the proper
functionality of the panoramic unit exclusively. On these terms it supplies a typical yet
substantial quality control upon the modalities.
While it is mentioned that all supply, HVL and repeatability checks (including time) are
the same as the basic QC checks of conventional radiographic systems, the protocol
determines the quality controlling of movement, image quality, field size, radiation
dose, FSD and correspondence of radiation field with the alignment slit of the cassette.
Taking into consideration the complexity and the difficulty of the technique, the
frequency of QC checks could be considered as an expanded one.
92
PROTOCOL OF PERIODICAL QUALITY CONTROL CHECKS FOR ORTHOPANTOMOGRAPHS
Parameter Parameter procedure Test Objects
Test Voltage
Accepted Limits
Frequency of Quality Control Check
KVp accuracy and repeatability checks (*), supply, HVL and exposure time repeatability checks are the same with t cks of entional radiographic systems. he basic quality control che conv
Correspondence of radiation field
with the alignment slit of the radiographic
cassette
Check of correspondence of radiation field with the alignment slit of the radiographic cassette
Film
Annually
Movement
Rotation of the tubecassette
system
Check and confirmation
of proper movement/rotation of tube‐cassette system
Annually
Image Quality Check of the quality of received images
Film Annually
Field Size
Measurement of the field diameter on the outer extremity of the beam
applier
Film and Led
Markers
≤ 150x10 mm in t he slot
Annually
Radiation Supply
Measurement of the radiation supply
Proper Dosimeter
50‐70 KVp with 1 m
distance from the radiant
30‐80 mGy/ mAs
Annually
Focal to Skin Distance (FSD)
Tapeline ≥ 30 cm
*The supply in panoramic systems is measured with DAP or with pencil beam dosimeters.
Requirements for Dental Panoramic and Cephalometric Examinations, by the GAEC.
‐ All units must satisfy the requirements of the regulations that are mentioned at
the department of medical radio‐diagnostic machines. Moreover the following
must be effective:
‐ The units must function with high voltage of at least 60 – 90 kVp, while the
minimum filter that interferes to the used beam must be 2.5mm Al.
‐ Specialized systems and equipment of head holding and immobilizing must be
present.
93
‐ During panoramic examinations, the dimensions of the radiation field upon the
film holder must not exceed the 10 mm x 150 mm.
‐ The use of endodentulous tubes for panoramic or simple radiographs is
prohibited.
2) Conference of Radiation Control Program Directors, Inc – Quality Control
Recommendations for Diagnostic Radiography, Volume 1, Dental Facilities, July 2001
This general and integrated Quality Control Program concerns all facilities using dental
intraoral, panoramic or cephalometric x ray units. Although it corresponds mainly to the
employees of such facilities and secondly to QA experts, this Protocol succeeds in
introducing a well based overall quality check of the whole laboratory, including the x
ray panoramic unit. The frequency of the tests is well established according to the
needs. The following table is indicative of the information contained in this Program.
Recommended Quality Control Tests for Dental Facilities
TEST FREQUENCY PROCEDURE Dental System Constancy Test (Intraoral Only)
Daily, Prior to Developing Films and After Service
1
Processor QC (Extraoral) Daily, Prior to Developing Films 2, Appendix B Darkroom QC Daily and Weekly 3 View boxes Monthly 4 Visual Checklist Quarterly and After Service 5 Repeat Analysis Quarterly 6 Tube Head – Boom Stability
Quarterly 7
Film and Chemical Storage Quarterly 8 Cassettes and Screens Quarterly or Semiannually(as
needed) 9
Darkroom Fog Semiannually* 10A or 10B Lead Apron Check Annually 11 Panoramic Field Alignment Annually 12 Program Review Annually Form 6 Radiation Safety Survey Every Two Year Form 4 * Darkroom fog should beevaluated every time you change the filter, bulb or ilm type and at least every 6 months.
94
3) European Commission – Radiation Protection 136‐ European Guidelines Radiation
Protection in Dental Radiology, 2004
The European Commission Guidelines mainly concern the users of the modalities. On
these terms the x ray unit Quality Controlling lacks of detailed guideline and
information. However, this Quality Assurance Protocol gives a well established general
idea concerning the appropriate procedures that all practitioners should consider. The
following table demonstrates some quality assurance information considering
panoramic radiography.
Quality Standards for Panoramic Radiography
Patient preparation / instruction adequate ‐ Edge to edge incisor
‐
s ‐ bodies (e.g. earrings, spectacles, dentures) No removable metallic foreign
‐ No motion artefacts Tongue against roof of mouth
‐ Minimisation of spine shadow
No patient positioning errors ‐ No antero‐posterior positioning errors (equal vertical and horizontal
magnification) ‐ ors (symmetrical magnification) No mid sagittal plane positioning err‐ No occlusal plane positioning errors ‐ Correct positioning of spinal column
Correct anatomical coverage
‐ Appropriate coverage depending upon the clinical application. Field size limitation should have been used (if available) to exclude structures irrelevant to clinical needs (e.g. limitation of field to teeth and alveolar bone for everyday dental use)
Good density and contrast
‐ There should be good density and adequate contrast between the enamel and the dentine
No cassette / screen problems
‐ No lights leaksGood film / sc
‐ Clean screens
‐ reen contact
Adequate processing and darkroom techniques
‐ atches No pressure marks on film, mo emulsion scr‐ No roller marks (automatic processing only ‐ No evidence of film fog ‐ n No chemical streaks / splashes / contaminatio‐ g No evidence of inadequate fixation / washin‐ Name / date / left or right marker all legible
95
4) International Atomic Energy Agency – Dosimetry in Diagnostic Radiology: An
International Code of Practice (Technical Reports Series No. 457), Vienna, 2007
As entitled, this fully detailed protocol concerns dosimetric procedures for all medical x
ray techniques. On this basis, the dosimetric one, this scientific code of practice contains
integrated and important theoretical and practical information about dosimetric quality
control. In the previous chapter the methods and the worksheets of this protocol
concerning panoramic imaging were demonstrated.
5) Health Canada – Radiation Protection in Dentistry, Recommended Safety
Procedures for the Use of Dental x ray Equipment, Safety Code30, 2000
This Code of Practice, published by the Canadian Health Ministry, contains a full
guideline of Quality Control Assurance of the whole dental x ray laboratory. Personnel
guidelines, facilities requirements, equipment specifications, film and processing
handling, Quality Assurance Program, Radiation Reduce and proper shielding are some
of the main contents of this well based protocol. The following table demonstrates the
Quality Control Program for Dental Radiography, including panoramic imaging.
Essential Dental Radiography Quality Control
Test Performance Criteria Minimum Frequency Test Film and Film
Processing ± 1 step (stepwedge) < ± 0.1 optical density
Daily
Test Radiogram Visual Daily Retake Record Visual Daily
Operation of Darkroom Visual Quarterly Cassettes and Screens Visual Annually
Filtration (Reference) Annually and After Service Controlling Timer (Reference) Annually and After Service
X ray Tube Shielding (Reference) Annually ad After X ray Tube Housing Service
X ray Tube Voltage (Reference) Annually and After Service Irradiation Switch (Reference) Annually and After Service
Focal Spot to Skin Distance (Reference) Annually and After Service Beam Alignment and
Collimation (Reference) Annually and After Service
Patient Radiation Dose (Reference) Annually and After Service
96
6) Care Quality Commission ‐ The Ionizing Radiation (Medical Exposure) Regulations,
Great Britain, 2006
This Protocol stands mostly for the determination of the legitimacy code concerning
medial exposures. On this basis, it information is general and representative rather than
mainly scientific and technically. However, this Protocol clarifies a clear spectrum of the
medical x ray techniques, so that a responsible application can be made. This protocol
creates an appropriate basis for well established Quality Control Programs.
7) Greek Ministry of Health, Greek Regulations for Radiation Protection, 2001.
The Greek Radiation Protection Regulation clarifies the legitimate basis, on the grounds
of which Quality Assurance Programs can be developed.
97
98
SECTION II
EXPERIMENTAL PART
99
100
CHAPTER 6
CALCULATION OF THE EFFECTIVE DOSE (E), USING THE DRLs of TIERRIS ET AL. (2004)
INTRODUCTION
In this section, a calculation of the effective dose E will be carried out, from the results
of the research of Tierris et al (2004). Effective dose E can be calculated by multiplying
the DAP with a pre‐determined conversion factor.
,
METHOD
Three conversion factors will be used from literature according to the survey of Poppe et
al (2006). This survey used these 3 factors for the determination of effective dose E
according to the DAP results of a research on 50 panoramic units of different vendors.
The conversion factors are:
1) Williams and Montgomery‘s (2000) conversion factor of 0.06 mSv Gy‐1 cm‐2
(calculated using the effective dose obtained from literature by White).
2) Helmrot and Alm Carlsson (2002) published a conversion factor including
salivary glands of 0.08 mSv Gy‐1 cm‐2, for panoramic examinations, using a multi‐
material compound hard tissue phantom.
3) Visser (2000) made an extensive study with a specially designed for x ray
energies anthropomorphic tissue‐equivalent phantom and found a conversion
factor of 0.21 mSv Gy‐1 cm‐2.
Compared with the E,DAP conversion factors by Williams and Montgomery, and Helmrot
and Carlsson, Visser’s factor differs by a factor of 3.5 and 2.6 respectively. The
discrepancy of the conversion factors may result from the different measuring
techniques used and different calculation schemes adopted when calculating effective
doses. Lecomber et al (2000) have shown that the salivary gland is exposed to high doses
101
in dental panoramic radiology and its inclusion in the list of remainder organs when
calculating effective dose has been questioned. Poppe et al. (2006) mark that the
effective dose calculated using the conversion factor from Visser (2000) shows that the
risk associated with a panoramic radiography is equivalent to a chest examination.
Therefore, the suggestion is to take the values derived by Visser (2000) as an upper dose
limit as his study has been carried out under extensive consideration in order to most
closely resemble the realistic conditions of application in dental procedures.
Tierris et al (2004), measured ‐in real time patient examinations‐ DAP values in 62
panoramic x ray units of the private and public sector in Athens, Greece, with the use of
a DAP meter, in order to determine corresponding DRLs. The results are shown on the
following table:
Exposure Mean (kV)
Mean (mA)
Mean Exposure Time (s)
Mean DAP (mGy cm2)
DAP Reference Levels (3rd Quartile) (mGy cm2)
Male 72.4 10.5 15.2 101 117 Female 68.3 10.1 14.9 85 97 Child 64.3 9.7 14.8 68 77 Table 1: Mean exposures parameters for 3 different exposure types, mean measured DAP and DAP
reference levels in 62 panoramic x ray units, by Tierris et al (2004).
CALCULATION
The calculation of the effective dose E now will take place, multiplying the DAP
Reference Levels of Tierris et al. (2004) with each conversion factor shown above. The
results are demo llowing table. nstrated in the fo
Exposure
DAP Reference Levels (mGy cm2) Effe (μSctive Dose E v)
Williams and Montgomery
Helmrot and Carlsson
Visser
Male 117 7.02 9.36 24.57 Female 97 5.82 7.76 20.37 Child 77 4.62 6.16 16.17
Table 2: Calculation of Effective Dose (E), using DRLs from Tierris et al, multiplied by three different conversion factors found in literature (Poppe et al., 2006)
102
103
CONCLUSION
The values in the table above are remarkably higher than the respective values of Poppe
et al. (2006). Indeed, their higher than most results on the surveys mentioned on
Chapter 4. This may be a result from the fact that 8 x ray units from the survey of Tierris
et al. (2004) gave significantly high DAP values compared to the high DAP values of other
researchers. Excluding the 8 highest DAP doses from each research, it is noticeable that
the values lie in the same range. According to Poppe et al.(2006) it would be appropriate
to consider the values derived from Visser (2000) as an upper dose limit.
CHAPTER 7
QUALITY CONTROL OF
A PANORAMIC – CEPHALOMETRIC UNIT
(INSTRUMENTARIUM OC/OD-200D)
A.1 LABORATORY DESCRIPTION – EQUIPMENT RECORD
A.1.1 Equipment Description
The type of the machine as well as its apparatus along with the specifications of its
partial segments, have been recorded. Particularly:
Generator
The power supply generator of the tube is made by TOSHIBA Company.
Generator
Voltage : 57‐85 kVp
Current : 20 – 16 mA
Time : 2.7 – 17.6 s (panoramic), 5 – 20 s (cephalometric)
Filter : 2.5 mm Al
Focal Spot Size : 0.5 x 0.5 mm
CE Mark : OK Table 1: Generator Specifications.
Digital Detector
Type : Charged Coupled Device (CCD)
Sensor Pixel Size : 48 x 48 μm
Image Pixel Size : 96 x 96 μm
Image Field Height : 147 mm – 221 mm
Resolution : 5.5 lp/mm
CE Mark : OK Table 2: Digital Detector Specifications.
104
Bo
sy
im
45
oth modes o
ystem uses d
mages are p
500M).
f the unit, pa
igital detect
rinted in fil
anoramic an
ors (CCD) it
ms by a dig
d cephalome
is connected
gital thermo
etric, functio
d with a wor
o‐printer (Dic
on in fan bea
kstation com
com Printer
Picture 1: Panoramic – COC/O
Picture 2: W
105
Cephalometric OD‐200D, Tosh
Workstation an
Unit, Instrumehiba
am field. As t
mputer and t
r, Agfa Dryst
the
the
tar
entarium
nd Digital Printeer.
A.1.2 Ventilation – Air Condition – Illumination
nd air‐condition of the laboratory were
FUNCTIONALITY
The details concerning illumination, ventilation a
recorded. Their appropriateness was evaluated so that the optimal functional conditions
of the units, as well as the personnel working conditions and the comfort of the
examinees, are ensured.
SYSTEM Ventilation Excellent Air‐condition Excellent Illumination Excellent Notes: The illumination and the ventilation of tory are mainly artificial. the labora
Table 3: Ventilation, Air‐conditio ation Conditions.
n and Illumin
106
A.2. CONTROLS
A.2.1. General Apparatus Controls
A.2.1.1. Inspectional Control of the Unit Components
The task of this control is the contribution to the assurance of the mechanical and
electrical function of the x ray system. For this reason the motion of the tube was
checked (visually and acoustically). The movements and the mechanical condition of all
the partial systems were checked. The function of the illuminating display signs on the
console was checked. Finally, the physical condition of the cables was checked.
CONTROL RESULT Tube Motion Excellent Movement/Rotation of tube‐detector system Excellent Physical Condition of cables Excellent
Table 4: Inspectional Control of the Unit Components.
A.2.1.2. Optical and Acoustic Communication between Examiner‐Examinee
Concerning the confirmation of the optimal inspection upon the examinee, the
appropriate acoustic communication, as well as the appropriate optical contact between
the examiner and the examinee, were checked.
CONTROL RESULT Audio Communication System No intercom present Optical contact examiner‐examinee Excellent (by lead‐glass window)
Table 5: Audio‐Optical Control.
A.2.1.3. Presence of Technical Manuals and Maintenace/Functioning Log‐Book
CONTROL RESULT User Manuals Present Reference Manuals Present
Table 6: Documentation Control.
107
A.2.2. Radioprotection Control
A.2.2.1. Spatial Characterization – Chamber Signage
Control Result Controlled Areas Record System Chamber Superintended Areas Record Controlling (Consoling) Space Non‐controlled (Public) Areas Record Patient Lounge Chamber,
Dentistry Space, Doctor’s Office Presence of Warning Signs Yes Presence of Optical and Audio Sign during Exposures
Yes
Notes: Table 7: Spatial‐Chamber Control.
A.2.2.2. Verification of Radioprotection Report – Shield Control
For the transaction of the control measurements an x ray dose rate meter was used
(Survey‐Meter, Inovision 451P) with a minimum measurement capability of 0.001 μSv/h.
The shielding for the primary as well as the secondary (scattered) radiation was checked.
It was also checked whether the shielding is constant, sufficiently covering the door
frames and whether a lead incrustation is present in the monitoring (consoling) window.
Moreover, a dose rate measurement was taken upon the interfaces of the space.
Control Result Presence of Radioprotection Report Yes (by Radiophysicists H. Delis – S.
Skiadopoulos, April 2007 Workload (mAmin/week) According to the Radioprotection
Report, 210 mAmin/week Control of Shielding Constancy Acceptable (No inconstancies from the
measurements on the shielded interfaces)
Control of lead‐glass in the monitoring window
Physical Condition: Excellent
Table 8: Radioprotection Report‐ Shield Control.
108
Dose Rate Measurements in Neighboring Spaces Measurement
High Voltage (kVp): 57 Tube Current (mA): 2
Time (s): 17.6
Dose Rate (μSv/mAh) Spatial Characterization
Console Chamber Door Mount Superintended Areas (1 μSv/hr for 1mA tube
current) Monitoring Window 0.23
Toilet (WC) 0.05 Public Areas (0.1 μSv/hr for 1mA tube current) Waiting Room Mount
Table 9: Dose Rate Measurements in Neighboring Spaces.
The system functions in fan beam field (both for panoramic and cephalometric modes),
approximately 147 x 3 mm for panoramic mode and 221 x 3 mm for cephalometric
mode.
A.2.2.3. Record and Control of Physical Condition of Radioprotection Apparatus
Concerning the protection of the laboratory personnel, the public and the examinees
from causeless exposure on x ray, the laboratory has been supplied with the following
radioprotection apparatus for the personnel and examinees:
‐ One (1) full‐body protective apron of equivalent thickness 0.30 mm Pb.
‐ One (1) full‐body protective apron with a protective thyroid collar of equivalent
thickness 0.30 mm Pb.
A.2.2.4. Tube Head Escape
Measurements of exposure rate were made, in 1m distance, with an appropriate x ray
dosimeter, calibrated at energies 20‐150 keV, with minimum measurement capability
0.01 μSv/h. The maximum exposure rate measured was 0.08 mSv/h in 1m distance
(acceptance limit: 1 mSv/h in 1m distance).
109
A.2.3. Beam Geometry Control
A.2.3.1. Conjunction of Radiation Field with the Alignment Slit of the Digital Detector
For this control, a radiotherapy film was used, positioned in front of alignment slit. Upon
the film the position of the slit was marked. The total conjunction between the radiation
field and alignment slit of the digital detector was confirmed.
The system functions in fan beam field (both for panoramic and cephalometric modes),
approximately 147 x 3 mm for panoramic mode and 221 x 3 mm for cephalometric
mode.
A.2.3.2. Measurement of Minimum Distance Focus‐Examinee
With a direct measurement the distance Focus‐Examinee was determined
(approximately 18cm for panoramic mode and more than 1 m (approximately 1.4 m) for
cephalometric mode.
A.2.3.3. FFD Control
The FFD (Focus‐to‐Detector Distance), as mentioned in the technical manuals of the
unit, is 487 mm for panoramic mode and 1600 mm for cephalometric.
110
A.2.4. Beam Quality Control
A.2.4.1. Accuracy of High Voltage Values
For this specific control an electronic meter was used (Victoreen, x ray test device,
Model 4000M+ ‐ SI). Five (5) high voltage values were measured for various options of
charge (cephalometric mode). The results are listed in the following table.
Nominal High Voltage Value (kVp)
Charge (mAs)
Measured High Voltage Value (kVp)
Deflection (%)
60 12.0 58.92 1.80 60 16.0 58.76 2.07 60 20.0 58.12 3.13 66 12.0 65.07 1.41 66 16.0 64.80 1.82 66 20.0 64.64 2.06 70 12.0 70.03 ‐0.04 70 16.0 69.81 0.27 70 20.0 69.84 0.23 76 12.0 76.67 ‐0.88 76 16.0 76.64 ‐0.84 76 20.0 76.21 ‐0.28 80 19.2 80.15 ‐0.19 80 19.2 80.22 ‐0.27 80 19.2 79.91 0.11 80 9.6 80.24 ‐0.30 80 4.8 80.23 ‐0.29 80 36.0 80.45 ‐0.56 80 24.0 80.01 ‐0.01 80 8.0 80.11 ‐0.14 80 12.0 80.63 ‐0.79 80 16.0 80.63 ‐0.79 80 20.0 80.32 ‐0.40
Table 10: Accuracy of High Voltage Values Control.
The deflections listed above are acceptable, as the maximum acceptance limit 10% of
the nominal high voltage values. The maximum deflection of the measured high voltage
values is 3.13%.
±
111
A.2.4.2. Repeatability of High Voltage Values
For nominal high voltage value 80 kVp and charge 19.2 mAs, five (5) high voltage values
were measured (cephalometric mode). The results of the measurements are listed in the
table below:
Nominal High Voltage Value
(kVp)
Charge (mAs)
Measured High Voltage Value (kVp)
Repeatability (%)
80 19.2
80.15
0.17 80.22 79.91 80.24 80.23
Note: For repeatability the coefficient of variation is used. Table 11: Repeatability of High Voltrage Values Control.
From the analysis, the repeatability of the high voltage values is 0.17%. This value is
acceptable, as the maximum limit of acceptance is ± 5%.
112
A.2.4.3. Half Value Layer (HVL) of the beam – Tube Total Filtering
For this control a pencil shaped dosimeter was used along with a multimeter
(Victoreen). The dosimeter was placed in parallel with the slit.
For the calculation of the HVL different aluminum pieces of increasing thicknesses were
used. The measurements are shown in the table below.
Table 12: Half Value Layer Estimation.
The HVL that comes from the measurements above is HVL=3.0 mm Al. From the
following curve it comes that the total filtering of the tube is approximately 3.1 mm Al,
with a minimum acceptance limit of 2.5 mm Al. Thus, the total filtering of the tube is
inside the acceptance limits.
Thickness Al (mm)
0.00 0.33 1.00 2.30 3.30
Dose (%) 100.0 90.59 77.73 59.47 46.47
113
A.2.5. Beam Quantity Control
A.2.5.1. Timer Accuracy
For this specific control an electronic meter was used (Victoreen, x ray device, Model
4000M+ ‐ SI). Six (6) time values were measured (in cephalometric mode) for various
current options. The results of the measurements are listed in the following table.
Nominal Time Value (s) Measured Time Value (s) Deflection (%) 1.0 0.9967 0.33 1.6 1.5970 0.19 2.0 1.9980 0.10 1.0 0.9991 0.09 1.6 1.6010 ‐0.06 2.0 2.0020 ‐0.10 1.0 0.9998 ‐.02 1.6 1.6020 ‐0.13 2.0 2.0030 ‐0.15 1.0 0.9995 0.05 1.0 1.6030 ‐0.19 2.0 2.0020 ‐0.10 1.6 1.6030 ‐0.19 1.6 1.6030 ‐0.19 1.6 1.6030 ‐0.19 0.8 0.7999 0.01 0.4 0.3987 0.33 3.0 3.0070 ‐0.23 2.0 2.0040 ‐0.20 2.0 2.0030 ‐0.15 2.0 2.0030 ‐0.15 2.0 2.0030 ‐0.15 2.0 2.0030 ‐0.15
Table 13: Timer Accuracy Control.
From the analysis it comes that for all the used current options the highest deflection of
the measured value of the exposure time compared to its nominal value is 0.33%. The
above deflections are acceptable as the maximum limit of acceptance is 10% of the
nominal value of the exposure time for time values >0.1s.
±±
114
A.2.5.2. Timer Repeatability
The table below includes the results of the timer repeatability control for two (2) values
of the exposure time (cephalometric mode).
Nominal Time Value (s) Measured Time Value (s) Repeatability (%)
1.6
1.5970
0.146
1.6010 1.6020 1.6030 1.6030 1.6030
2.0
1.9980
0.092
2.0020 2.0030 2.0040 2.0030 2.0030 2.0030 2.0030
Table 14: Timer Repeatability Control.
The minimum repeatability is 0.146%, which is included in the acceptance limits
(acceptance limit: ± 5%).
A.2.5.3. Tube Supply Linearity and Repeatability
For this control a pencil shaped dosimeter was used along with a multimeter
(Victoreen). The dosimeter was placed in parallel with the slit and the necessary
corrections were made concerning the calibration coefficient of the dosimeter and the
active magnitude of the dosimeter in relation to the radiation field, while a reduction of
the values was made for 100 cm distance.
For most used current values (mA) and for high voltage 80 kVp, the absorbed dose
(mGy) in the panoramic system was measured for functional time 17.6 s. For the
nominal values of kVp and mAs the supply was calculated in μGy/mAs in 1 m distance.
The linearity was calculated according to the equation:
115
The measurements are listed in the following table:
High Voltage (kVp) Current (mA) Supply (μGy/mAs) Linearity (%)
80
4 42.33
8.6 5 41.95 8 40.03 10 44.02 13 47.61
Table 15: Tube Supply Linearity Control.
High Voltage (kVp) Current (mA) Supply (μGy/mAs) Repeatability (%)
80 8
40.03
1.2 40.06 39.42 39.98
Table 16: Tube Supply Repeatability Control.
The minimum radiation supply is 39.42 μGy/mAs in 100 cm distance and 80 kVp voltage.
The current linearity of the tube is 8.6% (for various mA, 15% limit) while the
repeatability of the supply is 1.2% (with constant mA) with 5% limit. Thus, the current
linearity and the repeatability of the supply are within the acceptance limits.
A.2.6. Automatic Exposure Selection System
The density scale calibration was checked depending on the tube current and the Dose‐
Area‐Product (DAP). The results are shown in the following curves for high voltage 66
kVp.
The relation between the density scale and the charge, as well as the equivalent
between the density scale and the DAP are depicted in the following graphs.
116
Graph 1: Density scale and charge relation.
Graph 2: Density Scale and DAP relation.
117
A.2.7. Typical Patient Doses
According to the manufacturing company and as the unit functions in fan beam field, the
doses of the patients during the exposures of the examinations are relatively low.
Indicative dose values for panoramic examinations are demonstrated in the following
table.
High Voltage (kV) Current (mA) Dose (μSv) 57 2 1.90 63 10 10.9 66 13 16.8 70 13 20.4 73 8 15.5 77 8 18.7 81 13 31.3 85 13 36.0
Table 17: Typical Patient Doses Estimation.
For cephalometric examinations with high voltage 85 kV and current 13 mA, as the
manufacturing company proposes, the dose values in relation to the time for profile and
anteroposterior projection are demonstrated in the following table.
Time (s) 8 10 16 20 Dose (μSv) 2.7 3.4 5.4 6.8
Table 18: Dose Values in relation to Exposure Time.
A.2.8. Image Quality Control
Using the auto‐control quality system of the unit, which radiates a field with 15 levels of
increasing density, with voltage 57 kV and current 2 mA, the attached film was produced
and the presence of 15 density levels was confirmed, as indicated by the system
manuals.
118
119
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APPENDIX I
THE DIAGNOSTIC VALUE OF
THE PANORAMIC RADIOGRAPH
A CRITICAL VIEW
THE POPULARITY OF PANORAMIC IMAGING
The use of radiographic systems has become an inextricable procedure of the western
medicine. If in the second half of the 20th century the radiographic units were rising their
popularity, becoming a must tool on the various diagnostic fields of the modern medical
practice, in the beginning of the 21st century their presence has been coincided with the
term of diagnosis itself.
Yet, the question of whether this use is following an appropriate handling is a
fundamental issue of the scientific debate. Along with the uprising of the use of x‐ray
imaging comes the increase of the radiation doses, concerning not only the patient, but
also the professionals involved in these procedures, as well as the general public. More
than ever, the issue of using x‐ray techniques as an inevitable and necessary diagnostic
tool among the others is becoming of the highest importance.
While the dental radiographic techniques import relative doses of the lowest levels,
their extensive use is positioning them very high in hierarchy of the most frequent
radiographic techniques in general. Thus, the high radiation doses which are induced by
dental radiographic systems are indicating that a potential misuse is a fact. A misuse
that concerns the correct use of such units by the professional stuff, a proper form of
selection criteria and the quality of the existing and functioning dental radiographic
units.
Panoramic radiographic units meet a high popularity in dental medicine. Various
scientific estimations report that every year, in the developed countries, millions of
panoramic radiographies are taking place and thousands of panoramic units are installed
and functioning.
(see rushton biblio)Older researches have estimated the numbers of panoramic units
and radiographies in western countries. In the middle of the 90’s, in the UK, there were
128
approximately 3250 panoramic x‐ray units and around 1.5 million of panoramic
radiographies were taken annually. In France, while the proportion of dental
radiography made up by panoramic examinations is less than in the UK, the number of
panoramic films taken exceeds that of the UK, reaching a number of 1.7 million. This
means a greater use of radiography of all kinds, as in France most of the panoramic
exposures are carries out by radiologists. In the US, during the 80’s more than 25000
panoramic x‐ray units were used with an extensive rate of usage. In Australia, in 1988,
6% of practitioners used panoramic radiography.
In Greece, the Greek Atomic Energy Commission (GAEC) ‐instituted as the national
competent authority responsible for nuclear safety and radiation protection issues‐
reports that there are 10.000 dental radiographic units installed, authorized and
licensed for use. Among them the number of panoramic units is respectfully high.
These figures obviously underestimate the true scale of use of panoramic radiology, as
films produced in private practice, hospitals and within the community dental services
are not included.
THE QUALITY OF THE PANORAMIC IMAGES
Consequently, the crucial question of whether this extended use of panoramic imaging
is properly justified remains. Although a panoramic radiograph includes an important
substance of information, it is important to realize whether this information itself is
essential for oral diagnose and treatment.
A combination of factors in panoramic radiology which reduce its diagnostic quality
should be taken into consideration by all physicians. These factors are:
‐ The limitations imposed by the film/screen/cassette combination
‐ Tomographic blur
‐ Super‐imposed tissue and “ghost” shadows
‐ The overlap of adjacent teeth
‐ Variations in magnification
Panoramic radiology, being a modified form of tomography, blurs the images of
anatomical structures above and below the “in‐focus” layer, which ranges from 4.5 to 12
mm in the anterior regions and is two or three times greater in the molar regions. In this
129
way, the transfer of information from the attenuated x‐ray beam to intensifying screens
and then to the film, inevitably degrades this information.
This degradation is increasing to a variable degree by shadows of soft tissues and
surrounding air. “Ghost” images of the spine and the mandible reduce the diagnostic
quality and the presence of air between the dorsum and the hard palate leads to a band
of relative overexposure of the roots of the maxillary teeth and alveolar bone. Variations
in the horizontal angle of the slit x‐ray beam and the line of the dental arches result in
some amount of overlap of contact points of teeth, particularly in the premolar regions.
To continue with, in panoramic radiography there is a magnification factor from 10% to
30%. However, the degree of horizontal magnification varies considerably, depending
upon the relationship of the structure to the image layer. Thus, inaccuracies in patient
positioning lead to discrepancies between vertical and horizontal magnification of teeth,
with consequent distortion of shape.
As a conclusion, the quality of any radiograph is dependent upon accurate technique
(including the quality of the x‐ray unit) and careful processing. Panoramic radiography
poses particular challenges in both of these aspects of image production. Accurate
positioning and preparation of patients is needed to ensure the image is not distorted or
affected by ghost images, while quality control is critical when screen film is processed.
TECHNICAL AND PROCESSING FAULTS AFFECTING THE IMAGE QUALITY
In 1999, Rushton, Horner and Worthington concluded that the quality of panoramic
radiographs was considerably lower than standards recently set back then for primary
dental care. However, the quality of panoramic radiography could be improved by
careful attention to radiographic technique and processing.
In a study, including 41 dentists and a total of 1,813 panoramic radiographs, only 0.8% o
radiographs were free of faults, while 66.2% were diagnostically acceptable (containing
errors which did not detract from the diagnostic utility and 33.0% were unacceptable.
When all 1,813 radiographs were considered, the mean number of technical faults per
radiograph was 2.75 (SD=1.48). The mean number of processing faults per radiograph
was 2.96 (SD=1.55).
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Faults n % Tongue not in contact with palate 1,298 71.6 Antero‐posterior positioning errors 1,066 58.8 Absence of orientation (left/right) markers 642 35.4 Occlusal plane errors 568 3.3 Incorrect sagittal plane 508 28.0 Slumped position 267 14.7 Foreign objects/ghost shadows 164 9.0 Lower border of mandible off film 164 9.0 Poor film/screen contact 60 3.3 Overlap of upper and lower teeth 56 3.1 Movement artifact 35 2.0
Table 1: Ranking of technical faults observed on the 1,813 radiographs examined in thestudy. n=number of radiographs; %=percentage of radiographs showing the fault. Thepercentages add up more than 100% because most radiographs exhibited more than onetechnical fault (Rushton et al, 1999).
Faults n % Screen artifacts 1,284 70.8 Automatic processors roller marks 752 41.5 Localized film fog 719 39.7 Faults in contrast (too low) 715 39.4 Faults in density (too pale) 659 36.3 Pressure artifacts 377 20.8 Chemical streaks/contamination 271 14.9 Emulsion scratches 248 13.7 Faults in density (too dark) 101 5.6 Generalized film fog 47 2.6 Inadequate fixation/washing 46 2.6 Developer/fixer splashes 16 0.9 Faults in contrast (too high) 6 0.3
Table 2: Ranking of processing faults observed on 1,813 radiographs examined in the study. n = number of radiographs; %=percentage of radiographs showing the fault. The percentages add up to more than 100% as most radiographs exhibit more than one processing fault (Rushton et al, 1999)
131
When the 599 (33.0%) unacceptable radiographs were considered in isolation, the mean
number of technical faults per radiograph was 3.54 (SD=147), while the mean number of
processing faults was 3.63 (SD=1.48). The most frequent faults were antero‐posterior
positioning errors and faults in film density and contrast.
Faults n % Antero‐posterior positioning errors
T 324 54.1
Faults in density (too pale) P 241 40.2 Faults in contrast (too low) P 227 37.9 Incorrect sagittal plane T 144 24.0 Occlusal plane errors T 131 21.9 Slumped position T 54 9.0 Screen artifacts P 31 5.2 Generalized film fog P 23 3.8 Foreign objects/ghost shadows T 21 3.5 Localized film fog P 20 3.3 Automatic processor roller marks P 12 2.0 Poor film/screen contact T 9 1.5 Tongue not in contact with palate T 5 0.8 Patient movement T 5 0.8 Chemical streaks/contamination P 4 0.7 Developer/fixer splashes P 3 0.5 Inadequate fixation/washing P 3 0.5
Table 3: Ranking of technical (T) and processing (P) faults observed on the 599 inadequate radiographs and which directly contributed to their inadequacy. n=number of radiographs; %=percentage of radiographs showing the fault. The percentage adds up to more than 100% because inadequacy was frequently due to more than one fault (Rushton et al, 1999)
Analysis of variance identified highly significant differences in the numbers of technical
(F=13.72, two degrees of freedom); P < 0.001) and processing (F=12.40, two degrees of
freedom; P < 0.001) faults between the dentists. Similarly, the proportion of
“unacceptable” radiographs varied markedly from dentist to dentist, from 10% to 72%.
The highest proportion of “excellent” radiographs recorded was 11.1% with no other
dentist achieving a figure exceeding 4%.
132
On the following table, there are the results of the repeatability assessment by the
observers. Values of k exceeding 0.75 indicate excellent agreement beyond chance,
values between 0.4 and 0.75 indicate fair to good agreement beyond chance, while
values below 0.4 indicate poor agreement.
Fault assessment % Agreement
k
Overall acceptability 91.2 0.79 (0.67 , 0.91) Tongue not in contact with palate 88.0 0.69 (0.55 , 0.84) Antero‐posterior positioning errors 83.2 0.73 (0.63 , 0.83) Absence of orientation (left/right) markers 95.2 0.87 (0.77 , 0.97) Occlusal plane errors 80.8 0.60 (0.46 , 0.74) Incorrect sagittal plane 76.8 0.50 (0.35 , 0.66) Slumped position 87.2 0.57 (0.39 , 0.76) Foreign objects/ghost shadows 99.2 0.93 (0.79 , 1.00) Lower border of mandible off film 100.0 1.00 (1.00 , 1.00) Screen artifacts 79.2 0.56 (0.42 , 0.71) Automatic processor roller marks 70.4 0.41 (0.26 , 0.57) Localized film fog 94.4 0.88 (0.80 , 0.97) Faults in contrast 84.4 0.66 (0.52 , 0.80) Faults in density 81.6 0.64 (0.51 , 0.77) Pressure artifacts 90.4 0.72 (0.58 , 0.87) Chemical streaks/contamination 88.8 0.40 (0.14 , 0.66) Emulsion scratches 99.2 0.97 (0.91 , 1.00)
Table 4: Repeatability of assessments. Percentage agreement between first and second assessments and the kappa statistic (k) are shown. For k values, 95% confidence intervals are shown in brackets (Rushton et al, 1999).
133
FILM FAULT FREQUENCY WITHIN PANORAMIC RADIOGRAPHS
TAKEN IN GENERAL DENTAL PRACTICE.
In a sample of 2,641 panoramic films that were assessed within published studies, the
proportion of unacceptable films and range of faults was 18.2% and 33.0%.
Anterior/Posterior positioning errors 54.1% Faults in density and contrast 13.0% and 40.2% Incorrect sagittal plane 24.0% Occlusal plan errors 21.9% Slumped patient position 9.0% Screen artifacts 5.2% Film fog 3.8% and 7.0% Foreign objects/Ghost Shadows 3.5% Poor film/screen contact 1.5%
TABLE 5: Film fault frequency within panoramic radiographs taken in general practice
(European Commission, 2004)
In another study, performed in Turkey (Akarslan et al, 2003), through a sample of 460
panoramic radiographs, 173 of them, composing a percentage of 37.61%, were found to
have no errors according to the criteria set.
The most common positioning error was found to be a radiolucent area palatoglossal
airspace over the roots of the maxillary teeth (46.3%) due to the patient’s tongue not
being raised against the palate during exposure time (see fig. 1). Superimposition of the
hyoid bone with the body of the mandible (23.6%) and superimposition of the vertebral
column on to the anterior teeth (22.17%) were the next most common errors (see fig. 2
and 3). The least seen positioning errors were the widening of the anterior teeth due to
the patient biting the bite‐block too far back (1.3%) and the vertical overlap of the
anterior teeth due to the patient’s not biting the bite‐block, or not using a bite‐block
during the exposure (2.39%).
134
On the evaluated radiographs, the most frequent technical errors were too high density
(16.52%) and too low density (15.65%), respectively (see fig. 4 and 5). The least common
error was found to be the presence of dirty or bent films (0.21%) (see fig. 6)
Error n (number) %
Shadow of airway above tongue 213 46.30
Superimposition of hyoid bone 121 26.30
Vertebral column superimposed on anterior teeth
102 22.17
Density too high 76 16.52
Density too low 72 15.65
Occlusal plane tipped down 62 13.47
Asymmetrical placement of teeth 53 11.52
Other miscellaneous errors 45 9.78
Occlusal plane tipped up 43 9.34
Film fogged 34 7.39
Blurring of anterior teeth 32 6.95
Stains on film 29 6.30
Superimposition of spine on other structures 26 5.65
Narrowed anterior teeth 26 5.65
Radiopaque artifact 24 5.21
Patient movement 15 3.26
Vertical overlap of anterior teeth 11 2.39
Marks on film 7 1.52
Widening of anterior teeth 6 1.30
Films dirty or bent 1 0.21
Table 6: Frequency of errors at the evaluated panoramic radiographs. Some films had more than one error so the percentages add up to more than 100 percent (Akarslan et al, 2003).
135
Figure 1: Palatoglossal airspace over the roots of the maxillary teeth.
Figure 2: Superimposition of the hyoid bone on the body of the mandible.
Figure 3: Vertebral column superimposed over the anterior teeth.
136
Figure 4: Film density too high.
Figure 5: Film density too low.
Figure 6: Bent film.
137
THE QUESTIONABLE NECESSITY OF THE PANORAMIC RADIOGRAPH
The same scientific team (Rushton et al, 1999) ran a study based on the same samples.
1,818 panoramic radiographs of consecutive patients along with basic patient
information, radiological reports and treatment plans were recruited. 41 general dental
practitioners who routinely took panoramic radiographs of all new adult patients
participated ad were asked to evaluate the radiographic information. The radiographs
were also reported by “experts”) consensus of two dental radiologist).
Radiological findings were recorded from general dental practitioners assessments
(dentist RY), the experts (expert RY), after exclusion of findings that would have been
seen on posterior bitewing radiographs (MRY) and after exclusion of findings of no
relevance to treatment (MRYT). The results were quite indicative of the questionable
use or abuse of the panoramic x‐ray imaging technique that is being reported.
The majority of patients were dentate (61.2%), with 38.3% being partially dentate and
only 0.5% being edentulous patients. There was no significant difference in age profile
between the study sample and the DPB population figures (P = 0.26). Males made up
1.5% of the patients.
The radiological findings between the dentists and the experts varied greatly, as the
following table shows. For some findings the agreement was higher than 90%, but for
the majority of findings the agreement was poor below 70.5% until 37.1%.
138
Dentist Assessment Number (%)
Expert Assessment Number (%)
% Agreement
P
Presence of calculus deposits
849 (46.7) 961 (52.9) 70.5 <0.001
Periodontal bone loss None Early Moderate Advanced
530 (29.2) 673 (37.0) 436 (24.0) 179 (9.8)
785 (43.2) 682 (37.5) 297 (16.3) 53 (3.0)
52.0
<0.001
Total with bone loss 1288 (70.8) 1032 (56.8) Number of carious lesions None 1 2 3 4 5 or more
783 (43.1) 386 (21.2) 219 (12.1) 151 (8.3) 100 (5.5) 179 (9.8)
560 (30.8) 359 (19.7) 290 (16.0) 182 (10.0) 127 (7.0) 299 (16.5)
37.1
<0.001
Total with any lesions 1035 (56.9) 1257 (69.2) Number of periapical lesions None 1 2 3 4 or more
1261 (69.3) 367 (20.2) 130 (7.1) 30 (1.7) 30 (1.7)
1087 (59.8) 420 (23.1) 162 (8.9) 78 (4.3) 70 (3.9)
69.9
<0.001
Total with any lesions 557 (30.7) 730 (40.2) Number of retained roots None 1 2 3 or more
1586 (87.2) 169 (9.3) 33 (1.8) 30 (1.8)
1503 (82.7) 230 (12.7) 45 (2.5) 39 (2.1)
91.3
<0.001
Total with any retained roots
232 (12.8) 314 (17.3)
Presence of unerupted teeth
623 (34.3) 647 (35.6) 95.1 0.01
Pathology of maxillary antra
11 (0.6) 255 (14.0) 86.7 <0.001
Other abnormalities 64 (3.5) 366 (20.1) 80.0 <0.001
Table 6: Radiological findings of the dentists and the experts obtained from the panoramic radiographic of the study patients (n=1,818 for dentists; n=1,817 for experts). Agreement between the two assessments is shown as a percentage. ‘P’ values relate to McNemar X2 tests comparing proportions of cases with findings present or absent for the two assessments (Rushton et al, 1999).
139
The radiological findings after the exclusion of the findings that would have been seen
on posterior bitewing radiographs are demonstrated in the next table. No radiological
findings were recorded on the radiographs of 17.2% of patients.
N )umber (% Number of carious lesions None 1 2 3 4 5 or more
1 ) 401 (77.1 243 (13.4) 96 (5.3) 38 (2.1) 20 (1.1) 19 (1.0)
Total with any lesions 406 (22.9) Number of periapical lesions None 1 2 3 4 or more
1 ) 087 (59.8 420 (23.1)162 (8.9) 78 (4.3) 70 (3.9)
Total with any lesions 730 (40.2) Number of retained roots None 1 2 3 or more
1 503 (82.7) 230 (12.7) 45 (2.5) 39 (2.1)
Total with any retained roots 314 (17.3) Presence of unerupted teeth None 1 or more
1170 ( 4.4) 6 647 (35.6)
Pathology of maxillary antra None Either or both antra
1562 86) ( 255 (14)
Other abnormalities None 1 or more
1451 (80) 366 (20)
Table 7: Radiological findings on the 1,817 panoramic radiographs after exclusion of information that would have been identified on posterior bitewing radiographs (Rushton et al, 1999)
140
After the exclusion of findings of no relevance to treatment the results were impressing.
The majority of the radiographs (56.3%) had no radiological findings of relevance to
treatment.
Number (%) of radiographs Number of carious lesions None 1 2 3 4 5 or more
1 567 (86.2)147 (8.1) 53 (2.9) 23 (1.3) 11 (0.6) 15 (0.8)
Total with any lesions 249 (13.8) Number of periapical lesions None 1 2 3 4 or more
1 ) 406 (77.4 2 ) 91 (16.0 85 (4.7) 15 (0.8) 19 (1.1)
Total with any lesions 410 (22.6) Number of retained roots None 1 2 3 or more
1 ) 681 (92.6 94 (5.2) 15 (0.8) 26 (1.4)
Total with any retained roots 135 (7.4) Presence of unerupted teeth 156 (8.6) Pathology of maxillary antra 5 (0.3) Other abnormalities 69 (3.8) Preextraction information 1 ) 89 (10.4Significant negative finding 2 (0.1)
Table 8: Radiological findings of significance to treatment on the 1,816 panoramic radiographic. This excluded information that would have been identified on posterior bitewing radiographs and findings which did not contribute to patient management (Rushton et al, 1999).
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THE PANORAMIC X‐RAY EQUIPMENT AND THE OPERATING PERSONNEL
Moreover, the status of the panoramic x‐ray units plays a crucial role in the diagnostic
value of the radiography. Much of the equipment used is greater than 10 year old.
Taking into consideration the latest 3‐D panoramic technique, there can be a substantial
recession of the panoramic units according to the available technologies, mostly due to
economical reasons, as the financial differences of the latest technologies are very high.
Also, the proper maintenance of the existing units is another crucial point as many of
them lack of proper maintenance also mostly to economical reasons.
Additionally, another factor that reduces the diagnostic value of the panoramic
radiograph is the operation of inexperienced and uneducated stuff. This is reported in
high frequencies in most countries, and especially in those in which the legislation is
looser. Panoramic imaging techniques as mentioned before needs an exacting handling
and the operation by non professionals increases the possibility of positioning errors,
technical or processing faults.