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Maxillofacial Prosthodontics
Table of contents
Page
Subject
Table of Contents.
Maxillofacial team.
20
31
Maxillofacial Splints.
40
Maxillofacial Stents.
58
63
71
Facial Impression.
73
Nasal Prosthesis.
76
Occular Prosthesis.
79
Cranial Prosthesis.
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Maxillofacial Prosthodontics
Introduction
Objectives of maxillofacial prosthetics :
1. Improve or restore the esthetics or cosmetic appearance of the patient which is of prime
importance for every body .
2. Improve or restore the functions that include :
a. Speech function in patients with cleft palate .
b. Nutritional function in patients with lost parts of the jaw .
c. Avoid the escape of food to the nasal cavity . In children with cleft palate trying to
overcome the feeding problem and help to maintain the child general health .
3. Protect the tissues :
To protect the adjacent tissues as in the radium protective shield , also to protect wound , stop
bleeding and carry medicaments after surgery . In contact sport mouth guards are used to
protect the teeth against possible injuries .
4- Therapeutic or healing effect :
Placement of appliances such as the radium needle , carrier stents and splints which are used to
aid and promote the healing process .
5- Psychologic therapy :
To raise the morale of the patient which is very important for such type of patient .
Maxillofacial Prosthodontics
Maxillofacial team :
Team is a group of people working to achieve certain purpose . The members of the team must
cooperate in every way to fulfill their goal :
The member the team furtria as a unit .
The maxillofacial prosthodontist serves primarily as a member of a team and must cooperate
with the other members in planning rehabilitative treatment for patients with maxillofacial
defects ( The members of the team function as a unit ) . Every member should have some
knowledge in other specialties .
Members of the maxillofacial team :
1- Plastic Surgeon :
Plays the most important part when surgical correction and rehabilitation of the deformity is the
proposed and favorable line of treatment . Correction of hare lip is usually done surgically . Also
correction of congenital palatal defects is done surgically in most cases .
2- Speech therapist :
The speech therapist plays an important role in rehabilitating patients with maxillofacial defects
. He often works closely with the prosthodontist in the design and fabrication of the appliance .
The responsibility of the speech therapist is great and is essential after surgery or prosthetic
restoration . The patient must be trained to articulate the words normally .
3- Radiotherapist :
Treating cancer of the oral regions with radiation or radio agents requires close cooperation
between the radiotherapist and the dentist . Radium source carriers are often required to control
the radiation at the site of the lesion radiation is sometimes combined with surgery .
4- Dental specialists :
A. Prosthodontist :
In inoperable cases , prosthetic appliance may be the only way to help in rehabilitation of facial
injury . When surgery is contraindicated or failed and when surgery is postponed for some time ,
prosthetic management is called for . The prosthodontist should be the most knowledgeable
member of the team charged with management of the patient , not only about the actual
mechanics and construction of the prosthetic device but also about disease under treatment . The
prosthodontist relationship with the oral surgeon must be intimate to be able to offer better
service to the patient . One of the common situations in which the oral surgeon needs the help of
the prosthodontist is in the design and fabrication of immobilization appliances for jaw
fractures.
B. Orthodontist :
Plays an important role and he is almost invariably required in management of malocclusion in
cleft lip and palatal cases . In such situations the child must be checked orthodontically especially
in the period of mixed dentition .
C. Oral surgeon :
An important of the team for treatment and also for planning the steps for rehabilitation . Also
he may be called upon for any extractions in the field of irradiation .
D. Dental technician :
For the construction of various maxillofacial and surgical prosthesis . Dental technician needs
special skill and training .
E. Other dental specialists :
1- Pathologist will be of value in the diagnosis of oral lesion particularly those involving the
odontogenic and salivary gland tissues .
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Maxillofacial Prosthodontics
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Maxillofacial Prosthodontics
Treatment plan :
Treatment should be mainly directed to :
1- To cure or control the disease and to prevent further disability . The prime consideration in
all aspects of rehabilitation procedure is to insure the patient that he remains free of
recurrence .
2- The objective of the total plan should contribute to the patient's well being and acceptance by
his society .
3- Each member of the team should know the overall objectives and the service to be rendered
should be closely coordinated . Arrangement for patient return at appropriate intervals to his
dentist for routine dental care and to his physician for regular health care must be
considered .
4- Maxillofacial prosthetic treatment is established after final evaluation of the physical and
radiographic finding , analysis of study casts full consideration of the patients needs for the
device and psychologic acceptance of it .
5- The patient should understand the limitations of the appliance and the complications that
may arise .
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Maxillofacial Prosthodontics
During the 5th to 6th week of embryonic development the primary palate is formed. The
primordial structures give rise to:
1) The upper lip.
2) The anterior portion of the maxillary alveolar process.
3) The premaxilla.
Therefore the primary palate represents portion of the embryonic fronto-nasal process and
maxillary processes.
The union of the different processes begins at the meeting point of the premaxilla and the
two maxillary processes in anterior and posterior directions to end with a (Y) shaped suture. The
union progresses anteriorly along the upper limbs of the (Y) to form the upper lip and maxillary
ridge and along the lower limb of the (Y) to form the hard and soft palate.
Etiology:
Congenital cleft palate results from lack of fusion of embryological processes which would
normally unite to form the palate during the 6th and 9th weeks of the embryonic life along the
lines of fusion. The fusion of the right and left palatal shelves and inter-maxillary process is at
about the 10th to 12th weeks.
The exact cause of the clefts is not well known. Some researchers believe that the abnormal
position of the embryo may play a role in inducing the cleft pressure of the amniotic fluid, failure
of the tongue to drop, or persistence of epithelium at the junction of the two palatal alveolar
processes could be the cause of failure of union between the palatal shelves.
Factors that influence the induction of the cleft palate:
1- Hereditary:
The incidence of clefts is greater in the children of parents with deformities.
2- Environmental:
A- Endocrine factors:
Experimentally cleft palate was induced in pregnant mice by injecting cortisone. Also hormonal
disturbance e.g.. pituitary may be an influencing factor.
B- Radiation and x- ray:
Large number of deformities including clefts occur when mothers receive therapeutic radiation
of the pelvis during the early months of pregnancy.
C- Nutritional inadequacies:
High percentage of cleft palate could be induced experimentally by controlled dietary deficiency
as vitamin A and riboflavin. Others suggested that the endocrine disturbance occurring with
dietary deficiency might be responsible for the occurrence of clefts.
D- Infection and disease:
Infectious disease of the mother as German measles was thought to induce clefts in children.
E- Stress and disturbances of fetal circulation:
Some studies indicate that anxiety associated with first trimester of pregnancy might cause cleft
since stresses agent influence cortical activity.
F- Chemical irritation:
Mothers exposed to chemical irritation e.g.. hypoxia and hypervitaminosis A.
It is more logic to consider the hereditary factor as increased by the environmental factors.
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Maxillofacial Prosthodontics
Maxillofacial Prosthodontics
pressing against the teeth or palate, or by closing of the lips. These called plosive sounds as
P,B,T,D,K and G are made by sudden breaking of the seal brought about by withdrawal of the
tongue or opening of the lips. For example the lip closure of P and B sounds, the tongue and
anterior hard palate contact in T and D sounds.
When the seal or stop is not complete but a channel through which the air stream must pass
is made extremely narrow called faricative. For example S,Z or C are soft sounds in which the
tongue separates itself from the anterior aspect of the hard palate forming a thin slit like channel
through which the air stream pass. Fricatives (from friction) the air pass out make friction as in
F,V and Ph labiodental Th, J lingudental fricatives.
Tongue and portion of the hard palate posterior to e.g. (J,CH,SH,L,R) contact of tongue
and nasopalate e.g. Hard K,G and Ng. Nasal sounds M,N and NG as in ring are produced with
the soft palate lowered allowing the air stream to escape through the nose.
2- Mastication:
This function is impaired due to escape of food through the nasal cavity. Also missing teeth
and mal occlusion frequently complicate the problem of mastication in cleft palate patients.
3- Swallowing:
If both the hard and soft palates are involved, the natural process of swallowing is
impossible and the first problem facing is nursing a child born with a cleft. Breast feeding is
quite difficult due to lack negative pressure in the oral cavity, regurgitation and escape of fluids
through the nose. The position of the baby during feeding should be changed to sitting position
rather than on the back. Special nipples for feeding bottles with flanges to close the palatal gap
should be used.
4- Appearance:
The presence of cleft lip and palate affects the shape of the face. The most common cause of
facial deformity is improper surgical repair of the hard palate. This is due to trauma to the
centers of bone growth and the contraction of scar tissue leading to reduction in the lateral
dimension and forward growth of the maxilla and hence deformity of the middle third of the
face.
In the absence of a labial cleft, maxillary and facial development will often processed
normally. Clefts involving only the soft palate will of course leave no facial deformity.
5- General Health:
The child's health may be affected due to problems of feeding inadequacy of nutrition and
mouth breathing.
6- Psychological:
Most of the children with such congenital defects have problems with adjustment to society.
They might withdraw completely taking negative attitude towards the outside world, or they
may turn aggressive and react violently to others.
Maxillofacial Prosthodontics
10
palate upwards and backwards causes the free margin of the soft palate to touch the posterior
pharyngeal wall as in swallowing or oral breathing.
Palato pharyngeal muscle:
Arising from the posterior borders of the thyroid cartilage pass upward to form posterior pillars
of fauces. They curve inward to enter the palate. Some fibers blend into lateral and posterior
1- it acts with the tensor to depress the palate against the levator palate in swallowing.
2- Raise the back of the tongue.
Pharynx:
The pharynx is a simple, funnel shaped tube wide at the head and narrow at esophageal
end. The pharynx has three muscles superior, middle and inferior constrictors. The constrictor
muscles are so arranged by inter looking fibers that a wave of constricting impulses helps the
food to pass towards the stomach. The upper part of the pharynx is formed by the superior
muscles, this part is concerned with both speech and swallowing. While its lower part is
concerned with swallowing only.
During speech the pharynx is contracted and causes an inward movement of the lateral
walls. In some cases passavant described a horizontal ridge or cushion " Cross roll " around the
lateral and posterior walls of the pharynx at the horizontal level of the hard palate and he called
it passavant's ridge passavant believed that the passavant's ridge is a component of the usual
mechanism of closure during speech that is visible by the presence of a cleft.
Recent studies indicated that the ridge appeared during speech in approximately 10% of
non cleft palate subjects compared with finding of about 50% of unrepaired cleft palate subjects.
Moreover evidence is lacking to suggest that the ridge is a compensatory factor associated with
cleft palate help in reducing the coronal diameter of palatopharyngeal orifice.
Palato Glossus muscle:
They originate from the sides and base of the tongue and curving outward and upwards to
enter the under surface of the soft palate forming the anterior pillars of fauces, and like palato
pharyngeal muscle, unite in the median aponeurosis of the palate to form an inverted (V).
In contraction they have three functions:
1- It acts with the tensor to depress the palate against the levator palate in swallowing.
2- Raise the back of the tongue.
Palatopharyngeal mechanism:
The palatopharyngeal valveolar or sphincter functions through the action of several muscle
groups.
At rest, the soft palate drops downward such that the oro-pharynx and naso-pharynx are
opened to allow for normal breathing through the nasal passages. When palatopharyngeal
closure is required, the middle one third of the soft palate arcs upward and backward to contact
the posterior pharyngeal wall. At the same time the lateral pharyngeal walls move medially to
contact the margins of the soft palate. The posterior pharyngeal wall may move anteriorly to
facilitate contact with the elevated soft palate.
Complete palatopharyngeal closure is required for normal deglutition and production of
some speech sounds, such as plosives. For vowels and nasal consonants the palatopharyngeal
part will be opened in varying degrees.
Function of the Palatopharyngeal mechanism:
1- Speech mechanism:
Speech mechanism is divided into five components: respiration, phonation, resonation,
articulation and neurologic integration, also audition and ability to hear sound can be added.
2- Respiration:
Speech is a process initiated by the energy inherent in the stream of air. During exhalation a
continuous stream of air is passed from the lungs (with sufficient volume and pressure) to be
modified in its course by the maxillofacial structures giving rise to the sound.
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3- Phonation:
As air leaves the lungs, it passes through the larynx, whose vocal folds modify the stream of air
by creating resistance to it, set up a sequence of laryngeal sound waves with characteristic pitch
and intensity.
4- Resonance:
The sound waves produced at the vocal folds are amplified. Amplification is by pharynx,
oral cavity and nasal cavities.
5- Articulation:
To modify the laryngeal tones and to create new sounds within the oral cavity by tongue,
teeth and lips. The tongue is the most important articulatory structure.
6- Neurologic integration:
The factor for the production of speech are highly coordinated by the central nervous
system. Speech is a learned function as adequate hearing, vision and normal nervous system are
required for its full development.
7- Phonetics:
The voice is principally produced in the larynx, whilst the tongue by constantly changing its
shape and position of contact with the lips, teeth, alveolareoli and hard and soft palates, gives the
sound form and influences its qualities. The oral cavity and the sinuses act as resonant
chambers, and the muscles of the abdomen and thorax control the volume, and rate of flow, of
the air stream passing into the speech mechanism.
The soft palate in conjunction with the pharynx controls the direction of the air stream after
it passes from the larynx. In all the vowel, and most consonant sounds, the air stream is confined
entirely to the oral cavity, but a few nasal sounds do occur, e.g.. M,N and NG, in which the air is
expelled mainly through the nose. The former are produced by raising the soft palate into close
contact with the pharynx, thus sealing off the nose and forcing the air to proceed through the
mouth.
With the nasal sounds the soft palate is pressed downwards and forwards and the dorsum of
the tongue humped up to meet it, thus sealing off the oral cavity and forcing the air stream to
proceed through the nose. The flow, the alteration in size of the mouth and the change in shape,
and size of the lip opening giving the various sounds their characteristic form.
The consonant sounds are produced by the air stream being stopped in its passage through
the mouth by the formation of complete or partial seals or stops. These are produced by the
tongue pressing against the teeth or palate, or by the closing of the lips. The sudden breaking of
the seal brought about by the withdrawal of the tongue, or the opening of the lips, produces the
sound. In many sounds there is a build up of air pressure behind the stop which when the seal is
released produces an explosive effect. Examples of these are: the lip closure of the P and B
sounds ; the tongue and anterior hard palate contact in T and D sounds.
In some cases the seal or stop is not complete, but the channel through which the air stream
must pass is made extremely narrow: an example of this is the production of an s, z,or c soft
sound, in which the tongue separates itself from he anterior aspect of the hard palate by about 1
mm., forming a thin slit- like channel through which the air stream hisses.
Speech, therefore, is largely a matter of the control of the size and shape of the mouth,
which is chiefly governed by the position of the tongue and its contact with teeth, alveolareoli
and palate.
Fortunately for the prosthetist, the tongue possesses remarkable qualities of adaptability,
and rapidly becomes accustomed to change occurring in the mouth.
The factors in denture construction affecting phonation:
The Vowel sounds:
These sounds are produced by a continuous air stream passing through the oral cavity
which is in the form of a single chamber for the (A, O, U sounds and a double chamber for the I
and E sounds), the division occurring through the dorsum of the tongue touching the soft palate
in the post dam region. The tip of the tongue, in all the vowel sounds, lies on the floor of the
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Maxillofacial Prosthodontics
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mouth either in contact with or close to the lingual surfaces of the lower anterior teeth and gums.
The application of this in prosthetic construction is that the lower anterior teeth should be set so
that they do not impede the tongue positioning for these sounds, that is, they should not be set
lingual to the alveolar ridge, since the vowels E and I necessitate contact between the tongue and
soft palate, the upper base must be kept thin, and the posterior border should merge into the soft
tissue in order to avoid irritating the dorsum of the tongue, which might occur if this surface of
the denture was allowed to remain thick and square ended.
The consonant sounds:
For convenience, these sounds may be classified thus:
a) Labials: Formed mainly by the lips (e.g.. B, P, M).
b) Labiodentals: Formed by the lips and teeth (e.g.. F, V, Ph).
c) Linguodental: Formed by the tongue and teeth (e.g.. Th).
d) Linguopalatals: Formed by the tongue and palate.
(i)
Tongue and anterior portion of the hard palate D, T, C (soft), S, z, R).
(ii)
Tongue and portion of the hard palate posterior to that of (i) (e.g.. J CH, SH, I, R).
(iii) Tongue and soft palate (e.g.. C (hard), RG, NG)
e) Nasal (e.g.. M, N, NG also belonging to the other groups).
Unless careful consideration is given to the following aspects of denture construction, speech
defects will occur varying from the almost indiscernible to the unpleasantly obvious.
Maxillofacial Prosthodontics
13
4- Neuro muscular deficient of the soft palate and pharynx. In such cases it is difficult to create
and maintain a pharyngeal flap large enough to produce a competent palato pharyngeal
sphincter without closing the airway in the presence of neurogenic deficiency of the critical
muscles. A pharyngeal flap serves best when it is surrounded by a dynamic musculature.
5- When the premaxilla has been removed.
6- Delayed surgery: When surgery is delayed for medical reasons or when the surgeon prefers to
repair the palate at late age, the cleft palate may be temporally closed with a speech aid
prosthesis.
7- Surgically risky patients.
8- Expansion prosthesis:
To creat space for the premaxilla it may also be used to stabilize the parts in normal position in
association with autogenous bone grafts.
9- Combined prosthesis and orthodontic appliance:
An orthodontic appliance may be combined with a prosthesis to move malposed teeth to a more
favorable alignment.
10- When adult patients have missing teeth and the functional closure is not sure.
Maxillofacial Prosthodontics
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2- Meatus obturator:
This prosthesis serves a space filling function. A speech pathologist and dentist team
designed the meatus obturator to reduce the resonance of the nasopharynx, particularly in the
lateral regions around the auditory meati. Molding to muscle function was not a feature in its
production.
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Maxillofacial Prosthodontics
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e. Design and construction of the prosthesis: The prosthesis is constructed in three sections:
1- Palatomaxillary section (Anterior portion):
Is similar to that of conventional partial and complete denture. In must cases the number of
retainers is increased. After delivery the patient must worn it for at least one week. The length of
the adjustment period depends on the ability of the patient to adapt to this part. Necessary
adjustments are done before the addition of the other sections.
2- Velar section or tailpiece (Middle portion):
This section varies in operated and non operated clefts:
a. In non operated clefts with the upper prosthesis in position, the extent of the tailpiece over
the margin of the cleft is marked on the posterior part of the appliance. The tailpiece extends
posteriorly to the anterior of the uvula.
b. In operated cases with short soft palate which require a prosthesis, the position of the
tailpiece is marked on the posterior margin of the prosthesis. The tailpiece extends 3 mm
behind the posterior margin of the soft palate.
Construction of velar section:
A piece of base plate of the required width and length, which acts as a tray, is securely
attached to the posterior portion of the upper prosthesis with 2 mm relief and is brought to the
mouth to a check its proper extension. The upper portion of the tray is filled with zinc oxide
impression paste and the appliance is inserted in the mouth. The patients is instructed to hold his
head in a vertical position for one minute, to prevent the escape of material into the naso
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Maxillofacial Prosthodontics
18
pharynx. After one minute, the patient is instructed to swallow some water to register soft palate
muscular movement in the impressions. After the material is set, the prosthesis removed from
the mouth and is sent to the laboratory for processing of the tailpiece.
In order to reduce the number of time the appliance has to be heat cured, self curing
acrylic is used for this procedure. I can't seems that limiting the process to two steps is more
feasible to avoid the complication arising from curing the appliance three times, the maxillary
and velar sections could be constructed at the same time a wire loop attached to the end of the
velar section.
The finished tailpiece is inserted into the mouth, and the injection of some water stimulates
the muscle movement along the lateral edge of the velar section. Lateral overextension of the
velar section usually causes undue muscle displacement and eventual tissue soreness. The velar
section should touch the remnants of the soft palate in repose and function.
3- Pharyngeal section (Posterior portion):
Construction of pharyngeal section (speech bulb):
The loop of wire is attached to the end of the velar section and adjusted to the level of
maximum activity of the pharyngeal muscles. The wire should be short 2-4mm from the
posterior wall of the pharynx. In adult patients the level of the pharyngeal activity is superior to
that in children.
Green compound is added around the wire loop to reinforce the wire. Also soft modeling
compound is added on the loop. The prosthesis is inserted with the soft compound in the
patient's mouth. The patient is instructed to move his head up and down and then from side to
side while the compound is still soft. The prosthesis is removed, cleaned, dried, reheated on an
open flame and tempered in warm water, then reinserted in the mouth and the patient is asked
to swallow and to pronounce a strong " Ah ". The patient is instructed to place his chin against
his chest and move his head from side to side. The appliance is checked and stick compound is
used to correct the impression section by the above way.
Impression wax, softened in water at 150 160 F for 4 to 5 minutes, is added over the
green compound and then inserted in the patient's mouth. The same movements are performed.
The advantage of the impression wax is that it can stay soft in the patient mouth for half an hour
to give him chance to perform the functional movements. The prosthesis is reinserted a number
of times with gradual adjustment to the speech bulb until the functional impression is made of
the involved area.
During construction of the speech bulb the speech therapist works closely with the
prosthodontist. Ideally, the size of the bulb is adjusted until the patient demonstrates good oral
air pressure for production, and until unwanted nasal resonance is eliminated. At the same time
the patient must be able to breath clearly through his nose and produce acceptable nasal sounds.
A special large flask is used for heat curing the tailpiece into clear acrylic resin.
If the lateral and posterior walls of the pharynx are sensitive enough to produce a gag
reflex, no attempt is made to obtain a functional impression for the speech bulb. The speech bulb
is constructed under extended in self curing resin at the beginning, and let the patient to use the
prosthesis for two or three weeks. After the patient is accustomed to the undersized bulb, a final
impression of the speech bulb is processed from heat curing.
The speech appliance is inserted in the patient's mouth and checked for the following:
1- Muscle adaptation of the speech bulb during swallowing and phonation.
2- Excessive pressure against the posterior and lateral walls of the pharynx.
3- Stability of the appliance during function.
4- Improvement of voice quality and articulation of speech.
Cleft palate speech aid repair:
If the speech aid bulb need repair without any alteration of the anterior part, the
conditioning material is applied to the bulb portion. The bulb portion is then duplicated into
clear acrylic resin.
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Maxillofacial Prosthodontics
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The tissue conditioning material is far superior in making the pharyngeal impression. The
patient have the opportunity to use the speech aid at home normal conditions. Whereas in the
clinic the patients tend to exaggerate the movement which leads to inaccurate impression.
- Soft palate of sufficient length but lack of sufficient mobility due to muscle paralysis.
- Lift the soft palate to contact the palato pharyngeal wall.
- Maintain some opening on the sides of the elevated palate for nasal breathing.
6- Fixed Prosthesis (Stabilize Premaxilla).
7- Snap-on Prosthesis:
Types:
a) with speech pulp.
b) without speech pulp.
8- Unconventional speech aid prosthesis:
Two sections: Nasal portion Denture.
9- Titanium self tapping implants:
Position: Alveolus Ptrygoid plates.
9- Root coping (attachments) Telescopic crown with rest.
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Disabilities:
Nearly the same as in congenital clefts.
1- Speech: Although speech is changed after surgery but ensure the patient that such a defect
will be corrected after insertion of the prosthesis.
2- Appearance: This is the big problem. Diplopia may result in resected maxilla due to lowering
of the eye to removal of the floor of the orbit.
3- Mastication: Food regurgitation through the nose is a problem.
4- Psychologic considerations:
2- Prosthetic rehabilitation:
Is indicated in the following cases:
1) Large defects that difficult to be corrected by surgery.
2) When there is likelihood of recurrence.
3) Large soft palatal defects as they are difficult to restore surgically to normal function.
Prosthetic therapy for patients with acquired surgical defects of the maxilla can be divided
into two phases of treatment:
1- Initial phase called surgical obturation entails the placement of a prosthesis at surgery or
immediately there after. This prosthesis must be modified at frequent intervals to
accommodate for the rapid soft tissue changes that occur within the defect during
organization and healing of the wound. It's objective is to restore and maintain oral functions
at reasonable levels during the postoperative period until healing is completed.
2- Second phase of prosthetic therapy. Starts 3 4 months after surgery at which time surgical
site becomes stable dimensionally permitting construction of the definitive prosthesis.
Surgical obturation:
Surgical obturation can be carried out with a variety of materials and restorations e.g.
sponges, gutta-percha and acrylic resin prosthesis. Acrylic resin prosthesis is more superior and
is our concern.
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Preoperative guidelines:
A good working relationship with the surgeon will permit ample time for patient evaluation
and treatment. Patient evaluation includes the following data:
a) Medical history: A history of the patient illness as well as the past medical history will provide
clues to potential problems in future care.
b) Dental history: the dental history can be obtained from the patient directly or in conjunction
with clinical observation. The patient's dental hygiene and previous experience with dental
prosthesis should be noted.
c) Comprehensive clinical and radiographic examination: this examination will confirm or deny
the patient's dental history and provide information useful in planning the patient's prosthetic
rehabilitation.
d) Diagnostic casts: Impressions are made in irreversible hydrocolloid to provide both diagnostic
and working casts. Inter-occlusal records and mounting the casts on a suitable articulator are
required for proper analysis.
e) Photographs: Photographs provide an excellent record of preoperative conditions.
-
Immediate surgical obturator are fabricated on maxillary casts obtained before surgery. The
patient must be seen before surgery for impression making to construct the immediate
surgical obturator. It is in the form of a simple acrylic plate with no teeth and carrying
retaining clasps. Retention of the plate in the mouth is by clasps, ligation to the teeth, wiring
to the teeth or pinned to available bone (in edentulous subjects or when the number and
distribution of the remaining teeth is not suitable for retention).It is inserted immediately
after surgery and while the patient is still in the operating room. It must not be removed
before seven to ten days post-surgically.
The prosthodontist must be informed a reasonable time before operation to give chance for
construction of the surgical obturator the surgeon and the prosthodontist should discuss the
extent of the operation and draw a diagram on the lines of surgical incision (better on the
cast if it available at this time).
Maxillofacial Prosthodontics
22
1- If it is possible persuade the surgeon to leave the posterior edge of the hard palate and
tuberosity. Otherwise the soft palate will be flabby and often drop inferiorly and will exhibit
little motion during the immediate post operative period.
2- The surgeon is encouraged to make the anterior incision through the socket of an extracted
tooth instead of between adjacent teeth. This will help to preserve the periodontal tissue of
the remaining tooth and minimize the risk of amputating its root. The surgeon should also be
informed if any of the planned incision will involve a fixed restoration. Sectioning the
restoration may be done before surgery on the dental chair to decrease operative time under
general anesthesia, but may contribute to patient apprehension and discomfort prior to
surgery.
3- The obturator should terminate short of the skin graft mucosal junction. When surgical
packing is removed extension into the defect may be accomplished with tissue conditioning
material.
4- Prosthesis should be simple and light in weight.
5- Prosthesis should be perforated at the inter-proximal extensions to help wiring to the teeth at
the time of surgery.
6- Normal palatal contours should be reproduced facilitate speech and deglutition.
7- No posterior occlusion at the defect side.
8- Old dentures if available can be used after their modification. Reduce the flange at the defect
side and remove posterior teeth. The surface should be improved for better retention by the
addition of tissue conditioning material before surgery.
9- Add a couple of wire loops at the fitting surface where the growth is going to be excised (cases
where the growth is big).
Technique of construction:
1- Tray modification: stock trays may be modified to accommodate the size of the tumor. The
tray may be extended posteriorly to record a significant part of the soft palate if affected.
2- The patient should be placed in an upright position, so that the soft palate will assume a
normal and relaxed position. To overcome the problem of gagging associated with impression
making topical anesthetics may be used and it is preferable to use rapid setting hydrocolloid.
3- Upper and lower alginate impressions are made. It is important to make accurate
impressions of the vestibular depth on the unresected side.
4- Casts are poured in stone plaster. The upper cast is duplicated for future reference. It may be
better to make more than one upper impression to give chance for selection. Mount the casts
on an articulator with the aid of a jaw relation record.
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5- After discussing the surgery, the surgeon and prosthodontist will outline the proposed
surgical margins on the upper cast. The lateral boundary is usually the labial and buccal
reflection, and the median boundary is the midline of the palate. The questionable extensions
are the anterior and posterior margins.
6- The maxillary cast is altered to conform to the proposed surgical resection. Teeth to be
included in the resection are removed from the cast, but the alveolar height maintained. The
residual alveolar ridge is trimmed moderately on the labial and buccal surface to reduce the
stress on the soft tissue closure. Any elevation on the cost denoting the swelling should be
removed to have a normal palatal contour. The cast should be modified so that an adequate
thickness (approximately 2 to 3 mm) of acrylic base will not create occlusal interferences the
cast should be reduced to the level of the palatal cusps. This will allow an adequate thickness
of acrylic resin to mimic the natural palatal contours without impinging laterally or
anteriorly on the surgical flap. The cast in the region of soft palate resection should be
reduced to the level of the hard palate. This will result in the obturator prosthesis being
posterior and superior to the natural drape of the soft palate and minimize impingement on
the tongue during speech and swallowing.
7- Wire retainers (wire clasps) are prepared on the standing teeth.
8- Waxing up of the obturator is carried out. An upper base palate (double thickness of base
plate wax) is adapted to the modified palate and ridges. In patients with excessive vertical
overlap, the obturator extension anteriorly must be thinned to avoid occlusal interference
with mandibular anteriors. Edentulous upper jaws can be retained by wires to the zygomatic
bone.
9- The waxed up obturator is invested, processed in clear acrylic resin finished and polished.
Clear acrylic resin is preferred because it makes it easy to see extensions and pressure areas
during surgery. Holes are drilled in the buccal flanges when it is supposed to be wired to the
zygomatic bone.
10- Wire loops (two) are fixed to the fitting surface of the obturator at the site of surgery with
self curing resin. This wires will help to retain compound in cases of big tumors.
11- Now the obturator is ready for insertion in the surgical room put the obturator in an
antiseptic solution. In most instances the immediate surgical obturator is easily fitted and
secured. Care is taken to adjust the lateral extensions of the obturator short of the skin graft
mucosal junction to avoid pressure to this area. The lateral and anterior aspects of the
prosthesis should be reduced until correct facial contours are obtained without creating
excessive tension during closure.
12- Now, this is the time for molding the compound, or tissue conditioning material to the
surgical wound. Green stick compound is softened in warm water and attached to the wire
loops. The plate is seated in position in the patients mouth after blocking the deep undercuts
with vaselinied gauze. The plate with the compound is removed and reseated in the patients
mouth several times while the compound is still soft to prevent it's anchorage to undercuts of
the surgical wound. Cheek manipulation can help in molding the material while it is still soft.
N.B. A skin graft taken from the inside of the arm may be applied to the surgical wound
(skin grafting) in this case the skin graft is spread on the surface of the compound with it's
raw surface upwards helping to maintain its contact with the walls of the surgical wound.
13- If the surgery is more extensive than planed it is preferable to add a lining material (e.g.
tissue conditioning material) to the prosthesis.
14- In dentulous patients retention can be obtained by clasping or wiring to existing teeth. A no.
8 round bur is used to create openings for every available inter-dental space. Thus, to achieve
stability and retention, many teeth can be ligated to the time of surgery. In edentulous
patients the prosthesis is wired or pinned to the alveolar ridge and/or zygomatic arches.
Ligation wire openings should be placed as high as possible on the buccal and palatal aspects
of the remaining alveolus to assure sufficient bone for placement of the ligation wire through
the alveolus. These openings should be connected by a recess into which the ligature wire will
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be placed. This recess will run mesiodistally between the inter dental wire for the dentulous
patient or labio (bucco) palatally for the edentulous patient. This will prevent the ligature
wire from irritating the patient's tongue.
15- The prosthesis and packing are removed after seven to ten days post surgically. The
prosthesis is cleaned from blood clots and nasal secretions and any necessary adjustments are
made.
e.g.:
- Adjustment of wire retainers.
- Minor occlusal discrepancies on the intact side.
- Application of tissue conditioning material to improve adaptation seal and comfort.
- Modification of the compound if present.
16- The patient is then recalled weekly for any necessary adjustment, until he has no trouble
(may be one or two months).
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Definitive Obturation
Constructed three to four months after surgery. The suitable time will vary depending on:
1- Size of the defect.
2- Progress of healing.
3- Prognosis for tumor control.
4- Presence or absence of teeth.
5- Effectiveness of the present obturator.
The defect must be engaged more aggressively for edentulous patients to maximize support,
retention and stability. Thus the recovery period is longer for these patients. Changes associated
with healing and remodeling will continue to occur in the border area of the defect for at least
one year (in edentulous patients) by this time the mental outlook of most patients will be
improved.
Treatment planning:
To suggest the line of treatment we must have information about:
1- Prognosis for tumor control.
2- General health of the patient.
3- Data from mounted diagnostic casts.
4- Radiographs for questionable teeth.
5- Desires of the patient from that treatment and his expectations.
Treatment concepts:
Several concepts will be discussed now regarding the definitive obturator:
1- Movement of the obturator:
The obturator will move during function, if the maxillary alveolar ridge and teeth are
involved in the resection. It will be displayed superiorly with the stress of mastication and will
tend to drop without occlusal contact. The degree of movement and size and configuration of the
defect. The patient must be warned about this problem.
2- Tissue changes:
Dimension change of the defect will continue to occur for at least a year secondary to scar
contracture and further organization of the wound. Also movement of the obturator during
function may contribute to tissue changes. The obturator portion should be acrylic to facilitate
the possibility of rebasing or relining.
3- Covering prosthesis:
Obturator for acquired clefts of the maxilla are basically covering prosthesis serving to
establish the oral nasal partition. The contours of the defects are relatively static during
function.
4- Extension into the defect:
The degree of extension into the defect is dependent on the requirements of retention,
stability and support. If these properties can be obtained from the remaining maxillary
structures, the extension into the defect need not to be extensive. Mostly, the defect must be used
to improve these qualities. Again extension of the prosthesis into the defect will vary according to
the configuration of the defect and the character of its lining tissue. Extension superiorly along
the nasal septum offers little mechanical advantage as the pseudo-stratified columnar epithelium
lining the nasal septum and other nasal structure will tolerate little stress. In contrast, extension
superiorly along the lateral margin of the defect will enhance retention, stability and support.
Stress is well tolerated by the skin graft and oral mucosa lining the cheek surface of the defect.
In edentulous patients the defect must be used more extensively for retention, stability and
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support. The use of the defect for dentulous patients will vary depending on the size and
configuration of the defect and the number of teeth remaining. If the prosthesis is not properly
designed and constructed, the stress on the remaining hard and soft tissues can be pathological
and can lead to premature loss of abutments and irritation of soft tissues.
5- Teeth:
Presence of teeth enhances the prosthetic prognosis.
6- Weight:
Bulky areas should be hollowed to reduce weight to avoid unnecessary stress to the teeth
and supporting tissues. There is controversy whether the supporting surface can be left open or
should be closed. If the obturator is left open, nasal secretions accumulate leading to bad odor
and added weight. On the other hand open obturator has less weight and is easier to adjust. For
drainage a small diagonal opening is made between the inferiolateral floor through to the cheek
surface for drainage. The cheek will close against the opening so the seal is not compromised.
However, sealing the top of the obturator is of advantage if the patient complains of
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The height and contour of the residual alveolar ridge and the depth of the sulci are
important considerations. A healthy well formed ridge with extensive sulci will enhance stability
and support.
The defect:
Acceptable retention can be gained by engaging key areas within the defect. The edentulous
patient should know that the prosthesis will exhibit considerable movement during function.
Engagement of the skin graft and scar band formed at the skin graft mucosal junction will
improve retention. Since, the lateral portion of the obturator exhibits the greatest degree of
movement, retention can be improved by appropriate obturator tissue contact superior
laterally.
Additional retention may be gained by extending the prosthesis along the nasal surface of
the soft palate. Flexible materials are some time used in edentulous patients but they have short
time of service, fungal contamination and poor adjustability. Engagement of key portions of the
defect can improve support and stability. Stability is enhanced by engaging the super lateral
portion of the defect and some times the medial margin (when lined with keratinized
epithelium). Support can be obtained from the oral side of the skin graft mucosal junction
from the oral surface of the soft palate.
Technique of construction:
1- Preliminary impression:
To record the remaining maxillary structures and the useful portion of the defect, an
edentulous soft metal tray is altered. The medial and anterior undercuts are blocked out as
these undercuts are not engaged by the prosthesis. Adhesive is applied to the tray. Hydrocolloid
mix is loaded in the tray, impression material is placed laterally to record the lateral
configuration of the defect. Before seating the tray, impression material is injected into the
posterior and lateral undercuts. Accurate diagnostic cast reproduces the usable undercuts, aids
in evaluating the degree of retention and stability.
2- Special tray:
Undesirable undercuts are blocked out on the diagnostic cast before constructing the
special tray (made of acrylic resin on a spacer). Extensions of the tray are verified in the mouth.
Inaccessible areas are checked with disclosing wax for possible overextension. Border molding of
the tray is carried out using modeling plastic. The palatal margins of the defect area is also
developed by border molding. Border will ensure the stability of the tray which is a key factor in
obtaining an accurate reproduction of the borders of the defect.
3- Final Impression:
Several perforations are made in the tray for escape of excess impression material that may
prevent correct of the tray. Adhesive is painted. Excess secretions are removed. The material is
injected into desirable undercut and the loaded tray is seated into position. The lips and cheeks
are manipulated and the patient is asked to do eccentric movements of the mandible. After
setting the tray is removed with a gentle teasing action.
A alternative impression technique: is suggested by making use of the surgical prosthesis.
First, do any necessary alterations if needed until the prosthesis is acceptable then apply a new
layer of tissues conditioning material.
4- Recording Jaw relation:
On the master cast construct record bases. if the defect is large and stability and support
are difficult to obtain a conventional record base, construct the permanent bas from the master
cast. if stability and support are adequate conventional self curing base is made on the master
cast (after blocking of undercuts with clay to protect the cast).
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Treatment concepts:
a) Location of the defect:
Surgical resection usually includes the distal portion of the maxilla and rarely does a distal
abutment remains. The extent of the resection anteriorly varies. Thus Kennedy class II partial
denture with extensive lever arm is that required.
b) Movement of the prosthesis:
The degree of movement of class II partial denture is dependent on the quality of the ridge
and palate and the ability to utilize the support from both the edentulous segment and teeth.
With resection of the maxilla mucosal and bony support are compromised. Hence the defect
must be used to minimize the movement trying to reduce the stress on the abutment teeth.
c) Arch form:
Square or ovoid arches posses more bearing surface perpendicular to occlusal stresses
resulting in more stable prosthesis during function. Tapering arch forms provide less palatal
shelf area and thus support is compromised.
d) Teeth:
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Preservation of the remaining teeth is important for retention. Partial denture design must
anticipate and accommodate to the movements of the prosthesis during function without
exerting pathologic stresses on teeth. Maximum retention, stability and support must be
obtained from the use of the defect.
e) Partial denture design:
Diagnostic casts are surveyed to locate undercuts, guiding planes and select the path of
insertion. Often a compound path of insertion must be employed to use the undercut in the
defect. Major connectors must be rigid, occlusal rests must direct occlusal forces along the long
axis of the teeth, and guide planes must be designed to facilitate stability and bracing.
Retention should be within the physiologic limits of the periodontal ligament and maximum
support must be gained from the residual soft tissues. A tooth closely adjacent to the anterior
margin of the defect must have a rest and a retainer, if adequate retention is to achieved. the
anterior occlusal rest and retainer ensures oriention of the prosthesis.
If this concept is not employed the prosthesis will tend to rotate out of the retentive area is
not employed the prosthesis will tend to rotate out of the retentive area posteriorly. Often the
bony support for the tooth adjacent to the defect is questionable and does not permit its use as
abutment. Other adjacent tooth will have to be used.
The fulcrum line is determined by the position of the occlusal, incisal or cingulum rests.
Since there is no cross arch reciprocation of either buccal or lingual retention, this partial
denture may be viewed as a unilateral partial denture. For this reason both buccal and lingual
retentive arms may be considered to obtain cross tooth retention and reciprocation.
Prosthetic procedures:
1234-
Treatment plane.
Required restorative procedures.
Mouth preparation.
Master impression to construct the partial denture frame work.
Prior to impression making, the medial palatal undercut in the defect is blocked out with
gauze, however, the lateral portion of the defect should be recorded with the impression as these
contours will be necessary to fabricate the tray for the altered cast impression. The master cast is
made and the metal frame work fabricated. The obturator portion should be of acrylic resin to
allow for adjustment and rebasing. Retention for the obturator portion should extend laterally
into the defect and should be located 2mm. Superior to the normal palatal contour. Frame work
is adjusted to the abutment teeth in the patient's mouth using disclosing wax.
When the framework seats properly, the undesirable undercuts within the defect are
blocked out on the cast with wax. Self curing acrylic resin is molded to the frame work and the
defect in preparation for the altered cast impression (to make the form of the tray for the
defective area).
The prosthesis is then placed in the mouth and the tray is examined for extension and
proximity to the tissues. Modeling plastic (green stick compound) is added to the tray material
until desired extensions are achieved. Retention, stability and seal of the prosthesis are checked
and if inadequate, further extension into the undercut area may be indicated. Adhesive is applied
to the obturator part and an elastic impression material is used to complete the altered cast
impression. When the frame work is stead in the mouth, the patient is directed to make
eccentric mandibular movements. After setting, the impression attached to the frame work is
removed and examined for tissue adaptation, proper extension and excessive displacement of
tissues. The master cast is segmented. Then the framework with the altered cast impression are
seated on the tooth segment. The impression is boxed and poured in dental stone.
In the finished obturator, slight pressure against the cheek is desirable to ensure maximum
retention, stability and support.
Record the jaw relation try in, processing in the usual manner then finish and polish.
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Maxillofacial Splints
Definition:
Appliance used for immobilization of the fractured jaw guided by centric occlusion into
their original position until repair occurs.
Uses:
In the treatment of fractured jaws: immobilize fractured segment till healing occurs.
In surgical orthodontics of malposed jaws: ex: mandibular prognathism after segmental
osteotomy to splint bone segments together.
In conjunction with bone graft.
In treatment of periodontally mobile teeth (periodontal splint).
Advantages:
Requirements
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Types of splints
a)
b)
c)
d)
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Construction:
Impression of both arches with alginate is made with short tray flange as occlusal surface of
the teeth is only needed.
If displacement occurs, cast sectioned at line of fracture, casts are hand articulated,
reassembled and mounted on simple hinge articulator guided by the occlusion of opposing
teeth.
Cast is surveyed, path of insertion is selected, undercuts were blocked out.
Sheet of wax is warmed and adapted on the occlusal surface of the teeth on the cast and the
articulator is closed to carry the imprints of opposing teeth. Wax should be thin and not
interfere with free way space and the periphery of the wax should be square (not knife edge).
Cusps of teeth may perforate the wax and project through the splint to decrease jaw
separation and help in escapement of the cement through the vents.
Tags (underplates) are embedded in the wax pattern which hold wire loop (overplates), it also
help in intermaxillary fixation.
a) Tags (underplates): it is the female element, waxed in the wax pattern or soldered later.
b) Wire loops (overplates): screwed to the tags with screw.
Wax pattern is invested and casted with direct or indirect casting system:
Direct system of casting: done directly over the cast, stone cast under cuts were blocked
out on the surveyor, then the cast is duplicated into refractory cast on which the wax
pattern is made
Indirect system of casting: wax pattern is removed from the cast (to verify that
undercut is blocked to avoid interference during insertion), invested and casted.
Cement the splints on the corresponding teeth, apply careful directed traction force to the
bone segments till assume proper reduction.
Wire loops screwed to the tags, use quick setting plaster to hold the position of the wire loop
in reduced state of fracture, after plaster setting wire loops unscrewed and removed while it
is attached to the plaster and the jaws are allowed to return temporarily to the displaced
position.
Wire loops invested in the laboratory and connected together by soldering metal bar to them.
Reduce the fractured part again, the wire loops with connecting bar screwed to the tags.
Other method used to connect the 2 pieces metal cap splint using metal rode and metal tube:
the anterior portion contain metal rode (male part) and posterior portion have metal tube
(female part) that contain channel for rode and inserted before anterior portion, after
reduction the metal rode inserted into metal tube to immobilize fractured segments.
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Advantages:
Not need intermaxillary fixation.
Not interfere with opposing occlusion.
Clear acrylic resin allow observation of tissue undercuts under the splint.
Easily constructed, easily adjusted and easily repaired.
Provide good oral hygiene (removable).
Retention from proximal embrassres and not need fully erupted crown.
Radiolucent: allow monitoring of fracture union by x-ray.
Removed easily to test union of the 2 fractured part.
Can incorporate undercut in soft and hard tissues.
Disadvantages:
Easily fractured as it not resist force of muscles in case of displacement of fractured segments
leading to misalignment of fractured segments.
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3. Fenestrated splint:
Indications:
Deciduous teeth with no clinical crown badly decayed teeth post radiation carries.
Construction:
Resemble labiolingual splint without button.
retention mechanically by friction into interproximal spaces.
fit the dentition of one arch through the fenestration of the occlusal surfaces, wire tags or
holes may be incorporated to the buccal flange to facilitate immobilization.
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9. Lingual splint:
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Maxillofacial Stents
Def: removable appliance used to perform specific function as:
Control bleeding.
Protect the tissue from radiation, maintain tissue in position, carry radium in the
treatment of malignancy.
Carry medications.
Promote healing and decrease wound infection.
Protect teeth.
Protect skin graft and preserve the depth of vestibule after vestibuloplasty.
Materials:
1. Hard acrylic materials: heat cure, self cure acrylic resin, may be lined with soft liner
or tissue conditioner.
2. Soft materials: silicone vinyl rubber-poly vinyl vaccuform.
Types:
A. Intra-oral stents:
1. Anti-hemorrhagic stent.
2. Medication carrier.
3. Fluoride carrier.
4. Radiation stents (prosthesis for radiotherapy):
a. Radium applicator (carrier).
b. Positioning peri-oral cone (Docking device).
c. Displacement (positional) stent.
d. Intra oral radiation protective stent ( tongue protector).
e. Positioning dosemetric device stent.
f. Stent for recontouring tissue to simplify dosemetery.
g. Positioning radioactive source.
h. Positioning radioactive source after loading.
i. Stent used in direct implantation.
j. Stent used to prevent tongue and check biting.
5. Pedodontic stent.
6. Periodontic stent (labio-lingual stent- cosmetic stent).
7. Paraplegic stent.
8. Drainage stent.
9. Cyst plug.
10. Occlusal stent.
11. Mouth guard.
12. Oral screen.
13. Trismus stents:
a. T.M.J exerciser (dynamic bite opener).
b. Inflatable bite opener.
c. Intra oral prosthesis with inter arch spring.
14. Stent for vestibuloplasty.
15. Palatal stent.
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A. Intra-oral stents
2. Anti-haemorrhagic stent:
Function:
Control bleeding in hemophilic patient after extraction if other measures used to control
bleeding (gentile pressure-haemostatic dressing as thrombin) failed.
Construction:
Primary alginate impression is made before extraction and diagnostic casts are mounted at
centric occlusion, increase vertical dimension of occlusion by 1mm.
Tooth to be extracted are removed from the cast, apply layer of wax on the ridge and
buccal and lingual to the ridge and make wax rim over extraction site, close the articulator
to make the opposing teeth touch the rim.
Process the wax in clear acrylic resin (RPD), then lined with soft liner and inserted
immediately after extraction, patient bite on it to control bleeding.
3. Medication carrier:
Function:
Carry medical paste (palliative paste) to contact oral mucosa in case of chemotherapy and
osteoradionecrosis.
Construction:
Acrylic base plate made on the diagnostic caste with relief space in the area of the lesion in
which palliative paste will be applied.
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4. Fluoride carrier:
Function:
Used in fluoride gel application to the teeth to protect it from carries (ex: osteoradionecrosis
after mouth preparation for RPD)
Construction:
Made of resilient material (vaccum machine) on the occlusal, buccal and lingual surfaces of
the teeth after covering these surfaces with tin foil to allow a space (reservoir) for fluoride
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Advantages:
Simple, economic, efficient in irradiation of persistent superficial carcinoma.
Easy to control dose to various parts of lesion, if large does required, simply remove some
seeds
Construction:
Primary alginate impression cast outline surface to be irradiated with a pencil adapt
layer of base plate wax to outline. A line is drawn 1 cm beyond periphery lesion, strip of
beading wax attached to cast at this line, self lure acrylic resin extend 1cm beyond periphery
lesion in all directions. While the wax is soft hooks attached to it for retention of
prosthesis.
Grooves placed along inner surface of prosthesis in which nylon tubes embedded to average
depth 5 mm from inner surface in depth of each groove, tubes are parallel to each other at
interval of 1cm, extend 3-5mm out of the prosthesis.
Nylon ribbon contains radioactive seeds fit within hollow tube, prosthesis attached by hooks
(3 wire hooks) to modified orthodontic head gear maintained in stable position to
deliver desired amount of radiation.
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B. Stent used to protect the tongue (tongue protector): in treatment of buccal mucosa,
posterolateral border of tongue, alveolar ridge protect tongue and opposite side of
mandible.
Construction:
Patient is asked to bite on soft compound ball push check, tongue aside (made during
impression of mandible).
Mandibular and maxillary cast mounted on articulator at centric occlusion with incisal pin
opened 2-3mm 3-4 sheets of wax softened, placed between teeth form occlusal index.
Wax strip fit into lingual surface (concavity) created by compound lingual wax extension
is covered to create 1cm concavity then packed into acrylic resin.
Low fusing metal (lead-cerrobend) is melted and poured in cavity of acrylic resin
prosthesis, covered by acrylic resin or wax to decrease scattered radiation (2-3min
thickness lead if low voltage radiation, 5mm thickness lead if high voltage radiation used).
If patient is edentulous it is made on duplicate upper, lower denture.
Needle invested in acrylic resin of affected side to irradiate ridge growth.
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This stent used in radiation of skin of upper and lower lip, as in this site radiation at
corner of mouth is less than mid line of lip due to curvature of lip stent
is used to
flatten lip, corner of mouth entire lip at the same plane.
Made from modeling plastic, processed to acrylic resin.
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6. Pedodontic stent:
Function:
Used when unerupted tooth surgically uncovered to stimulate eruption to prevent closure of
uncovered tissue over the tooth.
Construction:
Make impression of the surgical site, poured, wax adapted over the cast and extend to the
surgical site to prevent its closure.
Disadvantages:
Sudden fall or accident which may lead to sub-luxation or damage to the tooth.
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8. Paraplegic stent:
Function:
Used as a mouth controlled device for handicapped patient in: feeding holding things dial
telephone tying painting pushing buttons).
Construction:
Upper and lower primary impression alginate is taken and the upper cast mounted with
face bow transfer and the lower cast mounted with centric inter occlusal record at proper
vertical dimension of occlusion (VDO).
Wax protrusive record is build up between opposing teeth to increase VDO by 2mm and
poly ethylene tube (10-12 inch) is waxed in a hole between 2 central incisors and the wax is
processed into acrylic resin, tested intra-orally and adjusted to harmonize condylar
guidance of the patient.
Entire thickness of intraoral prosthesis should not exceed 3mm to avoid interference of free
way space.
Arch shape metal frame may be embedded in the resin of the oral part to hold extra oral
aluminum tube. Active friction grip connector that accepts various attachments may be
attached to the stent. These attachments held in various devises which patient needs thus
the patient can change these devices himself.
To decrease lever forces on the stent: the stent should have maximum teeth coverage
(extend 2mm into the labial surface) to maximize distribution of forces over large number
of teeth.
9. Drainage stent:
Function:
Drain fluid and blood from periapical infection in endodontic therapy.
Construction:
Primary impression used to produce stone casts, fistula enlarged to form a hole on the cast.
15mm gauge poly ethylene tube is inserted in the hole, and labial surface of the cast is
covered with base plate wax around the tube, the wax is processed into acrylic resin as
apart of RPD.
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Construction:
Alginate impression including the reflection of the buccal sulcus of both jaws are made,
casts are mounted on the articulator at correct centric occlusion or centric relation.
2 layers of wax are adapted to the labial surface upper and lower teeth and extended to the
depth of the sulcus , processed into clear acrylic resin, it should not interfere with labial
frenum or muscle attachment and all pressure areas on attached gingival and movable
tissues are relieved.
b. Tongue depressor:
Painted with petroleum jelly and placed between the 2 arches to exert a unilateral force by
the patient.
c. Inflatable bite opener:
Pediatric blood pressure bag inserted and inflated between maxillary and mandibular stents
to force stents apart.
Pressure maintained for 10 seconds followed by 1 minute rest and the procedure repeated
for 10 minutes / 3 times per day.
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After surgery, the stent is lined with tissue conditioner and placed on the palate , left in mouth
for 24 hours till healing occurs.
If upper complete denture is present it is used as a palatal stent.
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B. Extra-oral Stents:
1. Extra oral radiation protective stent:
Function
Protect extra-oral organs from effect of radiation ex; basal cell
carcinoma of eye lid- seqamous cell carcinoma of lip.
Construction:
Lead mask cover most of the face, fenestrated for passage of
radiation beam. At least 3-4mm thickness lead covered with
acrylic to prevent scattered radiation which is harm full to
adjacent tissue.
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4. Nasal stent:
Function:
Support nasal cartilage transplant during healing of normal nasal deformity in cleft lip.
Decrease scar contraction following skin graft to the nostril.
Widen nostril in burned patient prior to graft procedure.
Restore nasal air way passage if obstruction occurs.
Construction:
Impression with green stick compound is taken to the nostril and poured to produce a cast,
wax pattern is made then processed into clear acrylic resin.
The acrylic resin stent is hollowed to maintain air way and tinted with intrinsic stain as skin
color to be less noted by eye.
In case of enlarging nasal air way use series of stents of increasing size or use expandable
nasal stent (have orthodontic expansion screw in the lumen of sectioned stent).
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5. Auditory stent:
Indications:
In surgical reconstruction of external auditory meatus.
mastoid surgery in patients wearing hearing aids.
protect swimmer from chronic ear infections.
Allow anasethiologist to prolong monitor the patient during extensive surgery.
Construction:
It is made from acrylic resin, polyvinyl-silicone.
Cotton wrapped around dental floss and inserted in external auditory meatus leaving 3mm of
floss exposed.
Free flowing alginate impression is loaded into a syringe and injected into the meatus and ear
pinna. The impression is poured, floss removed.
Mold splitted into 2 halves, lubricated with petroleum jelly and filled with acryl or silicone,
extend beyond ear pinna to facilitate orientation and tinted with the color of skin.
6. Oro-facial plug:
Indication:
To plug skin fistula resulted from infection or done dehiscence which lead to opening on the
outer akin and dribbling of saliva.
Construction:
Impression alginate is taken to the opening, cast is scrapped at the site of the fistula, wax
applied to the defect and flanges made for retention, wax processed into silicone rubber, tinted,
flushed with adjacent tissues for esthetics until corrective surgery is made.
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Types of Radiation:
Factors affecting rate of damage:
General tissue effects of radiation:
[ I ] Immediate effects:
[ II ] Delayed effects:
Radiotherapy Prosthesis:
Def.:
Objectives:
Requirements:
Types:
1- Carrier applicator.
2- Director appliance.
3- Maintaining the structure of the tissues to be treated.
4- Tongue protector (shielding).
5- Prevention of tongue and cheek biting.
6- Positioning of the radioactive source (Dosimentric device).
7- Recontouring tissues to simplify dosimetry.
Dental management of irradiated patient:
- Treatment procedures will be divided to:
a) Pre-irradiation treatment.
b) Post-irradiation treatment.
c) Prosthodontic treatment.
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[ II ] Delayed effects:
1- Salivary glands:
a) Decreased amount of saliva.
b) Increased viscosity of saliva.
c) Decreased the PH of saliva.
d) Difficulty in swallowing.
- Prosthetic effects: the patient can't tolerate his prosthesis due to more friction during
function as saliva acts as an effective lubricant. Retention is compromised, as the
peripheral seal may be difficult to obtain.
2- Eyes: Damage to eye lenses Cataract.
3- Teeth and Periodontal ligaments:
a) Decalcification.
b) Sensitivity.
c) Destruction of tooth bud.
d) Arrest teeth growth.
4- Tongue and mucosa: partial and complete loss of taste.
5- Diet: loss of appetite, nausea and pain.
6- Skin: Erythema, ulceration and pigmentation.
7- Bone: maxillary bone effects is more than the mandibular due to more radiation
absorption osteoradionecrosis.
8- Trismus: when the T.M.J and muscles of mastications are in field 3-6 months after
therapy fibrosis of muscle fibers, impaired mastication and limited mandibular
movements 10 to 15 mm. Treatment: includes exercising and the use of dynamic bite
opener.
9- Edema.
Radiotherapy Prosthesis:
Def.: Stents used to help the radiotherapist in the treatment of oral malignances by radiation.
Objectives:
1- Reduce the side effects of treatment.
2- Protects the tissue not important for exposure.
3- Enable lowering the field of radiation (protect the parotid gland).
4- Safer for radiotherapist in treatment.
5- Increase the accuracy of radiation source (ensure that area of exposure is the same each
time).
6- Decrease patient discomfort and injuries (increase patient cooperation).
Requirements:
1- Comfortable to the patient.
2- Minimal weight more tolerated by patient.
3- High retention and stability this prevent displacement of radiation source during
therapy.
4- High accuracy.
5- High strength to resist breakage (acrylic resin).
6- Easy to clean and repair (smooth) soft brush, soap and water are sufficient to clean the
prosthesis.
7- Allow the patient to breath easily perforation performed through the prosthesis.
8- Allow visualization of tissues clear acrylic resin allow for tissue observation during
procedures.
9- Easy to be inserted and removed by patient.
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Types:
1- Carrier applicator.
2- Director appliance.
3- Maintaining the structure of the tissues to be treated.
4- Tongue protector (shielding).
5- Prevention of tongue and cheek biting.
6- Positioning of the radioactive source (Dosimentric device).
7- Recontouring tissues to simplify dosimetry.
Dental management of irradiated patient:
- Treatment procedures will be divided to:
a) Pre-irradiation treatment.
b) Post-irradiation treatment.
c) Prosthodontic treatment.
a) Pre-irradiation treatment:
- The following must be removed:
1- Teeth in the field of radiation must be extracted prior to therapy to avoid
osteoradionecrosis.
2- Periodontal involved, badly decayed or questionable teeth should be removed before
therapy.
3- Sharp bony specules.
- The following must not be removed:
Teeth within tumor to avoid dissemination of tumor cells.
- The following could be left:
Teeth of unaffected side if radiotherapist allow that.
b)
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Post-irradiation treatment:
Conservative, strict oral hygiene rinses with H2O2 or warm saline.
Antibiotics and analgesics in case of infection or pain.
Any surgical intervention is contraindicated massive tissue loss.
Prophylaxis against tooth decay ( treatment by 10% stannous fluoride application ).
c) Prosthodontic treatment:
- Placement of Dentures (Timing):
Denture construction for irradiated patients should made if 12 14 months had
elapsed for mucosal healing. Some patient may wait 2 3 years before mucosa has recovered
sufficiently to tolerated denture.
- Two groups to consider:
1Patients edentulous prior to radiation therapy and having denture
experience new denture can be made after mucositis has resolved.
Denture bearing area should be checked with PIP before insertion.
2Patients undergoing pre-radiation or post-radiation extraction with denture
after completion of radiation denture bearing should be examined
contour, irregularity and scar before denture fabrication.
- Success of prosthodontic treatment depends on:
1- Pre-operative data.
2- Through oral examination.
3- Prosthodontic treatment (Non traumatic and non irritating denture).
4- Effective follow up system.
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[ I ] Preoperative data:
1- Type and size of tumor.
2- Mode of therapy.
3- Total dose.
4- Data of treatment.
5- Radiation fields.
6- Tumor response.
7- Prognosis of tumor.
[ II ] Oral examination:
1- Routine examination for denture:
- The entire oral cavity should be examined visually and palpated for any soreness.
- Appearance of oral mucosa.
- Scarring and fibrosis at tumor site.
- Degree of trismus.
- Salivary function.
- Tori.
- High tissue attachments.
- Enlarged maxillary tuberosity.
- Flabby tissue.
- Abnormal jaw relation.
2- Undercuts are undesirable to engaged, if they are present in field of radiation.
3- Surgery is contraindicated.
4- Post-irradiation symptoms. e.g. pain, Xerostomia and trismus.
5- Patient warned of possibility of osteoradionecrosis.
[ III ] Prosthodontic procedures:
1- Impression:
- 1ry impression: should be made with alginate and not compound.
- Xerostomia: should be treated by using petroleum jelly.
- Border molding: Done by using low fusing wax or heavy rubber base. The lingual flange
shouldn't used to gain more retention and only for stability.
- 2ry impression: should be made with rubber base.
2- Jaw relation:
- Low vertical dimension of occlusion offers low forces and less trismus.
- Centric relation record should be achieved with no trauma.
3- Try-in:
- Modified anatomical or flat teeth should be used to decrease the horizontal forces.
- Denture base should cut away to minimize irritation.
4- Insertion:
- Any roughness or sharp angles should be removed.
- Silicone soft liners may be used to minimize mucosal trauma.
[ IV ] Follow-up:
- The patient follow-up performed daily for about 2 weeks.
- Then patient follow-up performed once every 3 months.
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Etiology:
1- Neoplasm
2- Trauma
3- Congenital defect.
4- Osteoradionecrosis.
Classification of mandibular defects:
a) Marginal Resection ( Continuity defects)
1- Anterior marginal resection.
2- Lateral marginal resection.
b) Segmental resection ( Discontinuity defects)
- Complications.
- Treatment.
- Prosthetic rehabilitation:
o Intermaxillary fixation.
o Resection guidance restoration. (Types Technique of fabrication)
o Speech aid appliances. (Types Technique of fabrication)
Prosthetic rehabilitation of dentulous patient:
1- with lateral discontinuity defects:
a) Partial denture design.
b) Altered cast impression.
c) Clinical procedures.
2- with mandibular continuity defects:
a) Anterior defects.
b) Lateral defects.
Prosthetic rehabilitation of edentulous patient:
- Factors compromise use of complete denture.
- Factors determining prognosis of complete denture.
- Procedures:
a) Impression.
b) Centric relation.
c) Determining vertical dimension of occlusion (V.D.O.)
d) Determining centric occluding relation (C.O.R.)
e) Occlusion.
f) Processing, delivery and follow up.
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Complications:
1- Deviation of the mandible towards the resected side:
- Determinants of normal mandibular movements are:
a) T.M.J.
b) Neuromascular complex.
c) Dentition.
- So, when continuity of the mandible disrupts causes: mandibular imbalance and discontinuity
deviation due to scar contraction and muscle adhesion.
2- Traumatic occlusion.
3- Pain and discomfort.
4- Tension to T.M.J., ligaments and muscles.
5- Improper speech.
6- Improper mastication and swallowing.
Treatment:
a) Surgical reconstruction: Alloplastic implant with or without bone graft.
b) Prosthetic rehabilitation:
1- Intermaxillary fixation.
2- Resection guidance restoration.
3- Speech aid appliances.
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1- Intermaxillary fixation:
- Immediate fixation in order to:
a- Preventing or minimizing deviation post-surgically.
b- It helps the patient to preserve the proprioceptive sense of occlusion.
- Technique:
1- Maxillary & mandibular cast from post-surgical impression are essential for
intermaxillary fixation.
2- Arch bars or labiolingual splints Dentulous patient.
3- Gunning splint Edentulous patient.
2- Resection guidance appliances:
- About 2 weeks post-surgically, the patient should practice an exercise program:
a) Maximum opening.
b) Moving the mandible to the unaffected side.
- These movements tends to:
a) Loosen scar contraction.
b) Reduce trismus.
c) Improve maxillo-mandibular relationship.
- Increase severity of resection as in classical radial neck dissection or in radiation therapy
or increase time after surgical procedure increase the difficulty of guidance procedure
and increase occlusal problems.
- If the teeth aren't present guidance isn't effective.
- If only mandibular teeth are present guidance is possible.
- If mandibular and maxillary teeth are present guidance is effective.
- Guidance prosthesis is used as interim prosthesis until acceptable occlusal relationships
and proper proprioception are reestablished it will discarded or reinforce the
proprioceptive mechanism.
Types of resection appliances:
a) Mandibular resection appliance (Mandibular guiding flange):
- It's R.P.D. framework with a metal flange extend 7-10 mm lateral and superior on the
buccal aspect of the bicuspids and molars on non-defect side.
- This flange engages the maxillary teeth during mandibular closure direct the mandible
to proper intercuspal position.
- R.P.D. framework must be suitably stable and retained to counteract lateral forces
generated during closure.
- It may be constructed from:1) Cast Chrome-Cobalt metal: Mandible can position comfortably to acceptable position.
2) Acrylic resin: Some resistance is encountered in positioning of the mandible.
- Fabrication:
1) Construction of suitable mandibular and maxillary casts.
2) Wax interocclusal record to mount diagnostic casts.
3) Surveying of the diagnostic cast of the mandible.
4) Design of R.P.D. framework is outlined framework design should positively engage
most of the remaining dentition to prevent teeth movement.
5) The guidance ramp is usually designed to extend from a continuous clasp along the buccal
surfaces of the bicuspids and molars.
6) If autopolymerized resin is to be used to form the guidance ramp a retentive
meshwork is extended from the continuous buccal clasp of non-defect side.
7) The R.P.D. framework is formed as conventional R.P.D.
8) The waxed up framework should be viewed by clinician before casting.
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d) Determining C.O.R. :
- Recorded with wax or plaster.
- The mandible should be manipulated by the operator in most advantageous position.
e)
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Occlusion:
The non-anatomic teeth is preferred due to:
Deviation of the mandible.
Lack of definite closing position.
Loss of proprioception.
Increase lateral stresses.
Setting of anterior mandibular teeth in neutral zone.
Advisable to place maxillary anterior teeth lingual and the mandibular anterior teeth
labial to custom position.
Mandibular posterior teeth on the unresected side buccal to crest of the ridge (
Increase stability ).
Mandibular posterior teeth on the surgical side lingual to crest of the ridge ( Increase
stability ).
Thickening of denture flange below crest of the ridge proper support of lip and angle
of the mouth.
Occlusal palatal ramp should be added in the resected side to give simulations contact
during deviation.
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Facial Impression
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Introduction:
- The facial impression require much time and energy in preparing the patient and
materials and carrying out this technique.
- Selection of the material according to:
1- Great accuracy is needed, (use reversible hydrocolloid or plaster of Paris).
2- Good details quickly, (irreversible hydrocolloid or silicone).
3- Contour but not very much details, (impression compound or orthopedic plaster bands).
Patient preparation before facial impression:
a) Position of the patient:
- Patient should lying on the table with head slightly elevated. This position is achieved by:
1- Relaxed muscle tone of the face.
2- Easier material application.
3- Gravity helps to stabilize the material.
b) Preparation of the patient:
1- The hair is boxed out by using cloth towels.
2- The face should be free from make up and eye glasses.
3- The facial hair should be isolated by a means of separating medium.
4- Undercuts of defect should be blocked out with gauze.
5- Tie string to block out material, this prevent un expected swallowing, aspiration or other
problem occur during application of material.
6- The face or external borders of defect should be boxed out of wax.
7- If the impression entered to the mouth or nose, care must be taken in order to provide
breathing and prevent the anxiety in patient.
8- The airway is maintained by straws into the nostrils or mouth.
Impression materials and procedures:
a) Reversible hydrocolloid:
1- Thinner reversible hydrocolloid is applied to the face, using 1.5 inch paint brush.
2- Building up uniform layer of impression and embedded L-shaped clips.
3- Whole area is poured with a suitable layer of plaster of Paris which is connected to
improve faster set as one piece with the L-shape clips.
4- Boxed out area is removed in one piece with the impression.
5- Check the impression for any errors.
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6- Impression is placed under cold water, to prevent cracking of the impression material by
the exothermal setting reaction of dental stone.
7- Impression is then poured to provide the master cast.
b)
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Irreversible hydrocolloid:
The material applied and the L-shaped clips is inserted.
Plaster of Paris is applied till cover the all clips.
When the plaster harden, ask the patient wrinkle his skin. The whole impression is
removed in one piece with straws and the cotton plugs.
c)
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Plaster of Paris:
A mix creamy and thin is poured and brushed carefully onto the face.
Brushing is done to build up the plaster by layers. No paper clips is used.
After initial setting, it should be removed before exothermic changes. (Glycerin is used as
separating medium).
4- After application of the separating medium, the impression is poured with dental stone.
d)
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Orthopedic plaster band material: (Used for fabrication of radiation protection shields)
Cut bands into narrow strips.
Dipped into cold water.
Applied to the face and smoothed to facial contours (no need for boxing).
Additional layers build up.
The material is allowed to harden.
Glycerin or petroleum gel may be used as separating medium.
The impression is then poured with dental stone.
e)
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Impression compound:
Compound is warmed, flattened and applied to the face.
Care should be taken not to distort facial contours.
Reproduction of gross structures should be obtained.
f) Silicone:
1- Material is applied directly from jar with spatula and starts to build up with gauze
reinforcement.
2- Then more silicone is added.
3- 5 min are needed to setting before removal.
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Nasal Prosthesis
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Physical properties:
Strong enough.
Sufficient flexibility (used on movable tissue bed).
Dimensional stable.
Light in weight.
Suitable edge strength (permit thinning or fathering margins).
Low thermal conductivity.
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4- A facial cast is made, then master special tray is fabricated and confined to the defect
area.
5- Using a syringe we inject the flowable material in the undercut areas. But, take into
consideration not to compress the soft tissue bed.
6- Load the special tray with impression material in position. The excess material should be
removed periodically by index finger.
7- When the impression is set it will be removed and poured by dental stone to fabricate the
master cast.
- Wax pattern carving:
1- It is important in carving to produce the same contour, texture and proper placement of
the line of junction.
2- If presurgical cast is not available, the wax is adapted to cast and basic contour is done.
3- Patient should have multiple presurgical photographs for reference.
4- It is preferred to have a family member during carving for better perception of contours
than the patient.
5- Ala of the nose should be in a proper location in relation to nasolabial fold.
6- Care must be taken not to make the nose wide in Alar region (equal to inter-canine
distance).
7- Nares should be symmetrical and resemble the presurgical contours.
8- Junction between Columella and skin should be right angle or acute angle, in order to be
difficult to seen under the tip of the nose.
9- Tip and Dorsum of the nose should be resemble presurgical contour.
10- The bridge area shouldn't be wide and this is verified by wearing of eye glasses.
11- Eye glasses frames may improve appearance, if possible margins of the prosthesis extend
to mask the superior and lateral margins beneath it.
12- If we can't mask the margins for any reason, care should be taken to feather the margin
of the nasal prosthesis. i.e. (smooth transition between the skin and the prosthesis).
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Processing:
Wax pattern is invested in suitable mold material.
Basic shade of the prosthesis should match the lightest color in area.
If the basic shade is darker, it will be impossible to have esthetic match.
Extrinsic coloration done under presence of the patient and under good light.
Evaluation of coloration under varied (different) light sources.
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Delivery:
Hollowing the inner surface as much as possible decrease the weight of the prosthesis.
Retention is achieved by using medical grade skin adhesive.
The patient must be followed up periodically.
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Occular Prosthesis
Materials of construction:
a) Plastic acrylic eye:
b) Glass eye:
Examination of eye socket:
Technique of fabrication of the plastic eye prosthesis:
Clinical Procedures:
a) Scleral pattern from stainless steal ball bearing:
b) Registration of socket using alginate impression:
1- Making Impression: preparation of the patient impression procedures.
2- Making stone cast:
3- Selecting the eye:
4- Carving clay pattern:
Materials of construction:
a) Plastic acrylic eye:
Advantages:
1- Not fragile as glass and don't cause etching sensation.
2- It is custom made easy to adjust size, form and contours.
3- Easily adapted to individual esthetic requirements.
4- Actual 3 dimensional effect in Iris construction.
5- Perforated Iris buttons can be socketed.
6- Permits elimination of time consuming steps as multiple mold construction.
7- Method is easy to teach.
b) Glass eye:
Disadvantages:
1- Extremely fragile may explode in eye socket.
2- Glass interact with fluid of the socket.
3- Difficult to fit properly in relation to defect.
4- Giving the wearer the appearance of Exophthalmoses.
Examination of eye socket:
1- Knowledge of the anatomic features of the eye is essential.
2- Existing muscle movements should be studied.
3- Type of operation by the surgeon: enucleation evisceration.
4- If there is implant sphere was embedded at the time of surgery or not and what the type
of its material (gold glass).
5- The amount of orbital adipose tissue present.
6- Extent of muscle atrophy.
7- Contour and tonus of the eye lids.
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1) Making Impression:
Preparation of the patient:
9- The hair is boxed out by using cloth towels.
10- The face should be free from make up and eye glasses.
11- The facial hair should be isolated by a means of separating medium.
12- The eye brow and supra-orbital tissue of the defective eye are retracted.
13- Full width of the face (1 inch above eye brow and to upper lip) is boxed.
14- Patient instructed to close his remaining eye and breath through his mouth.
Impression procedure:
1- Using reversible hydrocolloid (50% water : 50% impression).
2- When material are heated to proper temperature, consistency and ready to be used the
operator tests the material with little finger for proper temperature before applying over
patient skin.
3- The impression material is painted on patient face with camel's hair brush starting
from undercuts and point of the greatest depth then the entire box area building up
at least 3 mm layer of material.
4- Pre bend L-shaped clips is inserted for reinforcement.
5- Wait for 5 minutes for setting of impression and proper reinforcement of clips.
6- Sufficient thickness of Plaster of Paris is poured removed after initial setting by asking
the patient to wrinkle his face and put in cold water to prevent cracking of impression
under exothermal setting of Plaster.
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Advantages:
1. Excellent cosmetic results and easy to achieve.
2. Have same density and strength as bone.
3. Transparent to x-rays.
4. The material is inert and lacks the physical effects of metal plates as temperature change
and electric phenomena.
b) Split rip graft cranioplasty:
- Indicated for larger defects.
- Portions of the 9th or 10th ribs are generally used.
- After proper length of rib has been resected, the piece is split longitudinally with a sharp
thin chisel.
- The technique of exposing the skull defect and dura is the same as previous technique.
- Part of the outer table is removed from the defect margins to form a ledge into which the
ends of the rib are inserted.
- Fixation is obtained with wire inserted through small holes drilled into the rib.
- The wound is closed in the usual manner.
- Head protection is recommended for several weeks until stabilization occurs.
Disadvantages:
1. The necessity of a separate incision.
2. Incomplete coverage of the defect.
3. There is a period required for stabilization.
c) Technique of Polyethylene Cranial Implant:
Advantages:
1. High density and high impact strength.
2. It is available in sheets and with proper compression molding.
3. Very strong and stress free product.
4. Inert.
5. Light in weight.
6. Radiolucent.
7. Easily trimmed at the time of surgery.
8. Cover large skull defects with good cosmetic results.
Steps of obtaining prostheses:
1. Impression taking with alginate impression material.
2. Modeling in stone.
3. Patterning with wax.
4. Flasking.
5. Compression molding at approximately 300 F.
6. Finishing.
7. Cold sterilization.
d) Technique of Tantalum Cranial Implant:
- To obtain the natural shape of the skull, it is important that the head be shaved before the
impression is made.
- The defect is palpated and the peripheral border is marked with indelible pencil at a
margin of approximately 1 to 2 cm from the penciled lines.
- The area is boxed in with boxing wax.
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- The impression is made by applying irreversible hydrocolloid to the entire surface of the
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boxed-in area.
Pre-bent paper clips opened to an L shape are inserted in the impression material for
reinforcement.
After setting of the irreversible hydrocolloid, quick setting plaster of Paris is added for
backing.
When the plaster has set, the impression is gently removed from the skull and the pencil
line is reoutlined with indelible pencil.
Dental stone is then poured slowly into the impression.
Once the stone has set, the impression is separated from the moulage.
At this stage, the prosthodontist study the moulage to determine whether an inlay or
onlay implant should be used.
With an Inlay implant, a shoulder rest is prepared around the defect at the periphery line
1mm deep to compensate for the tissue overlying the defect.
The depressed area of the moulage is filled in with modeling clay or plaster to bring the
contour out to normal.
One baseplate thickness of wax is applied to the pencil line as a pattern to cutout the
tantalum metal.
The moulage is used as a die and after using separating medium, a counter die is poured
using a thick mix of stone.
After setting, the 2 halves of the mold are separated and the tantalum pattern is placed
between the dies and the dies are inserted under press.
After molding of the tantalum, it is peforated by the use of round burs size 5 : 8 to allow
the connective tissue to penetrate the implant and neutralize its physical property.
After making perforations, the implant is finished by rubber points, polished, scrubbed,
and immersed in nitric acid to eliminate contamination.
The tissue bed is prepared in the same manner as described for methyl methacrylate.
The sterilized perforated tantalum implant is then seated over the cranial defect and fixed
with 4 to 6 stainless steel wires to the surrounding skull.
The wound is closed in layers as usual manner.
Complications of cranioplasty:
1. Infection.
2. Instability of the prosthesis.
3. Erosion of the overlying skin.
4. C.S.F. leakage through dural laceration.
5. Epidural granuloma.
6. Hematoma.
7. Pneumothorax following rib removal.
8. Thermal damage to the surround tissue from the heat of polymerization of methyl
methacrylate.
Perforated Tantalum Implants for Reconstruction of Facial Bones:
- Used for reconstructing other defected facial bones, such as the infraorbital bone, the
zygomatic orbital malar bone, the symphysis and associated mandibular defects.
- Used in case of T.M.J. ankylosis after accident.
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