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Dental and Craniomaxillofacial Implant Surgery
INTRODUCTION
Reconstructive dental and craniomaxillofacial implant surgery encompasses the use of implants to rehabilitate and
restore form and function to the edentulous or partially edentulous jaws and the craniomaxillofacial skeleton of patients
using fixed and removable prostheses. Implants also assist in the stabilization of prostheses that replace missing
maxillofacial parts, such as the nose, eyes, and ears. Implant reconstruction enables patients to regain normal
mastication, speech, and deglutition; resolves pain, gagging, and dysfunction from conventional removable prostheses;
and improves the symmetry and appearance of the face. Thus, it promotes self-esteem and restores both masticatory
function and a sense of well-being in patients with congenital, developmental, and acquired orofacial deficits and
deformities. The conditions are described generically and listed without any judgment regarding priority.
Advances in implant science, biomaterials, and biotechnology, together with a better understanding of the biology of
osseointegration, the bone-implant interface, and biomechanics, have resulted in improved outcomes and expanded
applications for implants. Improved methods of imaging for diagnosis, a diverse availability of implants with varied
geometry and surfaces, and refinement of augmentation and reconstructive techniques have enabled previously rejected
or inadequately rehabilitated patients to be treated. Nanotechnology manipulates biomaterials on an atomic and
molecular scale. The reconstruction techniques include guided bone regeneration, autogenous grafting from the
maxillofacial region and other sites, and use of bone substitutes, composite grafts, and bone. The techniques involve
materials using the concepts of osteogenesis, osteoinduction, osteoconduction, and osteopromotion. Soft tissue proce-
dures, in combination with implant surgery, have improved the health and aesthetics of the peri-implant tissues.
Increased understanding of biologic, biomechanical, and patient- and clinician-related risk factors, as well as a growing
consensus of biologically acceptable patient treatment protocols, has improved the safety and efficacy of dental and
craniomaxillofacial implant surgery.
The use of implants (temporary, provisional) may provide function and aesthetics during the reconstructive phase of
treatment.
The team approach, involving a restorative dentist, in the management of dental implant patients emphasizes that the
restoration is the primary factor that drives the implant placement and the requirements for adjunctive grafting
procedures. It is essential that there is proper patient selection and presurgical consultation with a restorative dentist
involved in the treatment planning using appropriate available assessment tools. Implant dentistry is a recognized
method for tooth replacement.
reason for the procedure followed. Moreover, it should be understood that adherence to the parameters does not
guarantee a favorable outcome.
PARTIAL EDENTULISM
I. Indications for Therapy for Partial Edentulism
May include one or more of the following:
A. Preservation of natural tooth by avoiding tooth preparation for a fixed and/or removable prosthesis
B. Inadequate natural teeth to support a fixed and/or removable prosthesis
C. Prevention of occlusal overloading of remaining natural dentition
D. Prevention of alveolar bone resorption and loss of osseous support
E. Clinical or imaging evidence of hard or soft tissue defect(s) in the maxillofacial region, including defects
resulting from tooth loss, oncologic therapy, and trauma (eg, mandibular, maxillary, nasal, orbital, ear)
F. Masticatory dysfunction (eg, maxillary and/or mandibular partial edentulism and/or alveolar atrophy)
G. Aesthetic deficiency and/or compromise
H. Speech impairment
I. Behavioral and/or psychological impairment
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EDENTULOUS MANDIBLE
I. Indications for Therapy for Edentulous Mandible
May include one or more of the following:
A. Absence of natural teeth to support a fixed and/or removable prosthesis
B. Prevention of alveolar bone resorption and loss of supportive bone
C. Clinical or imaging evidence of hard or soft tissue defect(s) in the mandible, including those resulting from
tooth loss, oncologic therapy, and trauma
D. Masticatory dysfunction
E. Aesthetic deficiency and/or compromise
F. Speech impairment
G. Behavioral and/or psychological impairment
H. Neurologic dysfunction
1. Nerve compression
2. Soft tissue irritation
I. Intolerance to and/or inability to accommodate to a complete denture
J. Reaction to materials used in denture construction
II. Specific Therapeutic Goals for Edentulous Mandible
The goal of therapy is to restore form and/or function. However, risk factors and potential complications may
preclude complete restoration of form and/or function.
The primary goal of implant reconstruction is to provide long-term, stable anchorage for a prosthesis. The
implant, in combination with a prosthesis, may then provide one or more of the following:
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EDENTULOUS MAXILLA
I. Indications for Therapy for Edentulous Maxilla
May include one or more of the following:
A. Absence of natural teeth to support a fixed and/or removable prosthesis
B. Prevention of alveolar bone resorption and loss of supportive bone
C. Clinical or imaging evidence of hard or soft tissue defect(s) in the maxilla, including those resulting from tooth
loss, oncologic therapy, and trauma
D. Masticatory dysfunction
E. Aesthetic deficiency and/or compromise
F. Speech impairment
G. Behavioral and/or psychological impairment
H. Neurologic dysfunction
1. Nerve compression
2. Soft tissue irritation
I. Intolerance to and/or inability to accommodate to a complete denture
J. Reaction to materials used in denture construction
K. Combination syndrome (anterior maxillary resorption, maxillary hyperplasia, bulbous tuberosities)
L. Maxillary and/or mandibular vertical, transverse, and anterior-posterior skeletal discrepancies
II. Specific Therapeutic Goals for Edentulous Maxilla
The goal of therapy is to restore form and/or function. However, risk factors and potential complications may
preclude complete restoration of form and/or function.
The primary goal of implant reconstruction is to provide long-term, stable anchorage for a prosthesis. The
implant, in combination with prosthesis, may then provide one or more of the following:
A. Presence of a general therapeutic goal, as listed in the section entitled General Criteria, Parameters, and
Considerations for Dental and Craniomaxillofacial Implant Surgery
B. Improved mastication
C. Prevention of alveolar atrophy and loss of supportive bone
D. Improved deglutition
E. Improved nutrition
F. Improved speech
G. Prevention of gagging
H. Enhancement of aesthetics
III. Specific Factors Affecting Risk for Edentulous Maxilla
Severity factors that increase risk and the potential for known complications:
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IRRADIATED BONE
I. Indications for Therapy for Irradiated Bone
May include one or more of the following:
A. Preservation of natural tooth by avoiding tooth preparation for fixed and/or removable prosthesis
B. Inadequate or absence of natural teeth to support a fixed and/or removable prosthesis
C. Prevention of occlusal overloading of remaining natural dentition
D. Prevention of alveolar bone resorption and loss of supportive bone
E. Clinical or imaging evidence of hard or soft tissue defect(s) in the maxillofacial region, including those
resulting from tooth loss, oncologic therapy, and trauma (eg, mandibular, maxillary, nasal, orbital, ear)
F. Masticatory dysfunction (eg, maxillary and/or mandibular partial or total edentulism and/or alveolar atrophy)
G. Aesthetic deficiency and/or compromise
H. Speech impairment
I. Behavioral and/or psychological impairment
J. Neurologic dysfunction
1. Nerve compression
2. Soft tissue irritation
K. Intolerance to and/or inability to accommodate to tooth/soft tissue– borne prosthesis
L. Reaction to materials used in tooth/soft tissue– borne prosthetic reconstruction
M. Unstable obturator
N. Provision of a stable prosthesis in the irradiated jaw with low tolerance to soft and hard tissue irritation or
trauma
O. Provision of retention and anchorage for maxillofacial, nasal, orbital, and ear prosthesis in irradiated tissue
P. Provision of retention and support of a prosthesis in a xerostomic patient
II. Specific Therapeutic Goals for Irradiated Bone
The goal of therapy is to restore form and/or function. However, risk factors and potential complications may
preclude complete restoration of form and/or function.
The primary goal of implant reconstruction is to provide long-term, stable anchorage for a prosthesis. The
implant, in combination with prosthesis, may then provide one or more of the following:
A. Presence of a general therapeutic goal, as listed in the section entitled General Criteria, Parameters, and
Considerations for Dental and Craniomaxillofacial Implant Surgery
B. Prevention of loss of soft tissue integrity to minimize contribution to osteoradionecrosis
C. Improved mastication
D. Improved deglutition
E. Improved nutrition
F. Improved speech
G. Prevention of gagging
H. Enhanced aesthetics
I. Preservation of remaining natural dentition
J. Improved stability of obturators
K. Provision of anchorage of maxillofacial, nasal, orbital, and ear prosthesis
L. Diminished risk of osteoradionecrosis secondary to trauma from conventional removable prosthesis
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III. Specific Factors Affecting Risk for Developmental or Acquired Craniofacial Deformities
Severity factors that increase risk and the potential for known complications:
A. Presence of a general factor affecting risk, as listed in the section entitled General Criteria, Parameters, and
Considerations for Dental and Craniomaxillofacial Implant Surgery
B. Quantity and quality of remaining hard and soft tissues
C. Unfavorable access
D. Relative position of vital structures (eg, nerves, cranial contents, vasculature)
E. Relative position of craniofacial sinus
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