Professional Documents
Culture Documents
Atlas of
FACIAL IMPLANTS
L E A D EDI TO R
Michael J. Yaremchuk, MD
Clinical Professor of Surgery
Harvard Medical School
Chief of Craniofacial Surgery
Massachusetts General Hospital
Boston, MA, USA
ASSOCIATE EDITORS
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Notices
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ISBN: 978-0-323-62476-3
Printed in China
This atlas presents the use of alloplastic implants uti- refining orthognathic surgical procedures and surgically
lized for aesthetic and reconstructive applications of the treating Graves’ ophthalmopathy. These innovations are
craniofacial skeleton. In the decade since I wrote the first included in this second edition.
edition of the Atlas of Facial Implants much has transpired In addition, the 10-year clinical experience has afforded
in related technology, clinical applications and implant many new insights into this surgery providing improved
design. For example, Computer Aided Design (CAD)/ results and avoiding as well as treating complications.
Computer Aided Manufacture (CAM) of implants is This edition includes chapters arranged in five sections.
rapidly evolving not only for cranial reconstruction, but As before, the first section, Background, includes chapters
also for aesthetic applications. Cranial implants are now addressing implant fundamentals. It is followed by sec-
designed not only for protective or aesthetic indications, tions addressing implant applications for each anatomic
but also with functional components (implantable neuro- facial third - Upper, Middle and Lower Face. A fifth sec-
technology - e.g. pressure monitoring, drug delivery…). tion, Developing Applications, now includes chapters
Recent studies have shown that critical areas of the addressing implant use in facial rejuvenation, CAD/CAM
facial skeleton resorb with aging and hence, facial implants aesthetic surgery and postorthognathic surgery refine-
have shown to be an important adjunct in rejuvenative ment. Videos of the implant procedure appropriate to each
aesthetic surgery. Implants now have an accepted role in anatomic area are now included.
vii
Acknowledgments
My co-authors, Doctors Catherine Chang, Erez Dayan, Amir Mrad and Alan
Yan, were indispensable in the preparation of this book. They are all previous
trainees at the Massachusetts General Hospital and the Boston Center and are
now practitioners spread throughout the world.
Kip Carter, Chief of Medical Illustration Services at the College of Veterinary
Medicine at the University of Georgia, once again added his artistic precision
and nuance to the Atlas of Facial Implants. His illustrations are obviously key to
the visual presentation of this work.
Finally, Elsevier’s Sharon Nash, Belinda Kuhn and Julie Taylor coordinated
our efforts with great skill and professionalism.
viii
to
MARILYNN
and KAIT
as well as
CHARLES and DEUCE (CHARLES II)
Chapter 1
3
Chapter 1 Indications for facial implants
A B
4 D E
Skeletal deficiency
SKELETAL DEFICIENCY
A B
C D
Chapter 1 Indications for facial implants
C D
6
Skeletal deficiency
Fig. 1.5 shows a patient with corrected occlusion who underwent multiple
implant correction of her midface and mandibular deficiencies.
A B
Fig. 1.5 A 46-year-old woman had undergone facelift, blepharoplasty, and browlift in the past. She underwent
infraorbital rim, paranasal, malar, mandible, and chin augmentation with lengthening. The brow was lowered
and a midface lift was also performed. (A) Preoperative frontal view. (B) Postoperative frontal view.
7
Chapter 1 Indications for facial implants
CONGENITAL DEFORMITIES
A B
C D
8
Congenital deformities
9
Chapter 1 Indications for facial implants
A B
C D
10
Skeletal versus soft tissue augmentation
A B C D
Fig. 1.9 Sequential frontal views (A) preoperatively, (B) 1 year postoperatively, (C) 10 years postoperatively, and (D) 14 years postoperatively
of a woman treated for a chondromyxoid fibroma of the left zygoma. The patient was treated with radical removal of the involved facial
skeleton and immediate reconstruction with porous polyethylene implants stabilized with plates and screws. Parts A and B from Carr NJ,
Rosenberg AE, Yaremchuk MJ. Chondromyxoid fibroma of the zygoma. J Craniofac Surg. 1992;3(4):217–222, with permission. Parts C and D
courtesy Dr. Yaremchuk.
Plastic surgery’s last decade is notable for its recognition that aging is accom-
panied by facial soft tissue atrophy. Facial rejuvenation surgery is no longer
one of simple excising and tightening. The value of soft tissue reposition-
ing and augmentation have been recognized and exploited. Unfortunately, PEARL
since the ultimate expression of skeletal or soft tissue structure is reflected
Soft tissues change with time,
on the skin’s surface, some surgeons have used this as a justification for the implants don’t.
equivalence and interchangeability of soft and hard tissue augmentation. Although there is limited
For example, malar skeletal implants are used to restore cheek fullness while interchangeability between soft
fat grafts are used to create malar skeletal prominence. Up to a millimeter tissue and skeletal augmentation,
they can certainly be complementary.
or so, the visual effect of either augmentation modality may be equivalent, Many patients can benefit from both
depending on the thickness of the overlying soft tissue envelope. However, volumetric increase in their soft tissue
beyond a minimal augmentation, the visual effects of these modalities are envelope and an increase in their
markedly different. This is easily conceptualized when envisioning large skeletal projection.1,2
augmentations. A large implant placed on the malar bone will make the
cheek project more, making the face more defined and angular, therefore
making the face appear thinner and more skeletal. Large implants placed
in patients with thin soft tissue envelopes will become increasingly visible PEARL
with aging (Fig. 1.10). With implant selection, the surgeon should remember
that soft tissues change over time, while implants do not. Implanting fat Soft tissue augmentation and
into the cheeks will also make the cheeks project more; however, the face hard tissue implants are not
interchangeable. They may be
will appear increasingly round, and therefore less defined and less angular complementary.
(Fig. 1.11).3
11
Chapter 1 Indications for facial implants
A B
Fig. 1.10 A 64-year-old woman had previous Fig. 1.11 A 30-year-old woman had undergone fat grafting of the malar midface area. Fat
malar implant surgery, upper and lower lid grafting in this young woman obliterated skeletal definition and distorted cheek contour.
blepharoplasty as well as rhytidectomy as (A) Frontal and (B) oblique view.
rejuvenation procedures in the past. Over
time, the large implant created an overly
prominent skeletal contour.
REFERENCES
1. Barton Jr FE. Aesthetic surgery of the face and neck. Aesthet Surg J 2009;29(6):449–63.
2. Endara MR, Allred LJ, Han KD, Baker SB. Applications of fat grafting in facial aesthetic skeletal
surgery. Aesthet Surg J 2014;34(3):363–73.
3. Yaremchuk MJ. Commentary on: the role of microfat grafting in facial contouring. Aesthet Surg J
2015;35(7):772–3.
12
Chapter 2
A B C
Fig. 2.1 To demonstrate the asymmetry in a “normal” face, a photograph has been manipulated to create three separate images. (A) Frontal
view of 20-year-old woman presenting for rhinoplasty. (B) Composite created by joining right side of face with its mirror image. (C) Composite
created by joining left side of face with its mirror image.
RADIOLOGIC EXAMINATION
judgments. Cephalometric X-rays are most often used for planning chin and
mandibular augmentation surgery. These studies define skeletal dimensions and
asymmetries as well as the thickness of the chin pad.
While preoperative radiologic examination is uncommon for purely aes-
thetic surgery, computed tomographic (CT) evaluation is almost routine for
reconstructive procedures. CT scans provide the ability to view the skeleton
in different planes and, through computer manipulation, in three dimensions.
CT imaging provides digitized information that can be transferred to design
software. CAD/CAM implants provide an increased level of refinement in both
reconstructive and aesthetic applications. This modality has been used since
the 1990s to reconstruct cranial defects. Computer-aided design (CAD) and
computer-aided manufacture (CAM) can be used to create life-sized models for
surgical planning (Fig. 2.2) and implants customized for the needs of the patient
(Fig. 2.3).
The design process can also be conducted virtually as demonstrated in Fig. 2.4. Fig. 2.2 CT scan data was used to fabricate a
skull model in planning surgery for a patient
The CAD/CAM process is the focus of Chapters 14 and 15. with facial asymmetry.
Cone beam CT scans are available in many dental offices. They have the
advantages of less expense and less radiation exposure to the patient. They can
provide three-dimensional images of the facial skeleton and are therefore valu-
able in planning. Because their field is limited and head-positioning devices
distort the soft tissue envelope, cone beam CT has a limited role in the CAD/
CAM implant process.
Magnetic resonance imaging, invaluable for soft tissue assessment, does not
have a role in skeletal evaluation and implant surgery planning.
FACIAL MEASUREMENTS
Mathematical ideals
In his book on Leonardo da Vinci’s anatomical drawings, Martin Clayton
explains how mathematical ideals influenced classical and Renaissance art-
ists in their perception and depiction of the human body.1 The ancient Greeks
observed that musical notes created by strings whose lengths were in simple
numeric ratios were intrinsically pleasing. They extended this concept to spa-
tial intervals and established the concept that harmonic ratios were intrinsically
“right” and thus fundamental to the structure of the universe. In the 1st century
BC, Vitruvius adapted the proportional concept to the human body. He pro-
B
posed that the body should be divisible into equal parts, and that all of its units
should be expressible in terms of that unit or fractions of the whole. His treatise Fig. 2.3 (A) Skull model and (B) with
De architectura, which describes his proportional system, was one of the few custom cranial implant obtained from
classical texts that survived to the Renaissance and became highly influential in three-dimensional CT scan data.
the thinking of artists and scholars of that time, including Leonardo da Vinci.
14 Early in his career, Leonardo adopted many of Vitruvius’ ratios. Most of us
today associate Leonardo’s anatomic drawings with his rendition of Vitruvius’
Facial measurements
Max Max
projection projection
@ 9 mm @ 9 mm
Max projection
@ 6.5 mm
Max anterior
Max projection projection
@ 8.5 mm Max projection @ 6.5 mm
B
@ 5 mm
ideal proportions for the human body (c.1490–92) whereby “the body when
standing with arms stretched fits into a square and, with all limbs splayed, into
a circle centered on the navel” (Fig. 2.5).
Leonardo soon found limitations in the use of proportions to depict the
human form. By 1500 he abandoned the idea of a single canon of ideal propor-
tion to describe the human body. In the winter of 1510 he collaborated with
the Professor of Anatomy at the University of Pavia, Marcantonio della Torre.
This relationship provided Leonardo access to human material allowing him to
depict human structure with great accuracy. As Leonardo learned human anat-
omy, he realized that the use of ideal proportions thwarted its accurate depic-
tion. He used proportion as a tool to help describe its form and function rather
than as an end to itself.
When the dimensions of normal males and females were evaluated objec-
tively and compared to these artistic ideals, it was found that some theoretic
proportions are one of many variations found in healthy normal individu- 15
als, including those determined more attractive than most individuals, and
Chapter 2 Evaluation and planning for facial implant surgery
some are never found2,3 (Fig. 2.6). The neoclassical canons do not allow for
facial dimensions known to differ with sex and age. Most of these canons of
proportion, for example that the width of the upper face is equal to five eye
widths, are interesting but hold for few individuals and cannot be obtained
surgically or, if obtainable, only with extremely sophisticated craniofacial
procedures.
Researchers from various disciplines have emphasized the difficulties
with mathematically defining a beautiful face. For example, the orthodontist
Robert M. Ricketts pointed out that although the ratio phi, equal to 1.1618
and known as the divine proportion, may be seen in many biologic forms and
its approximation may characterize certain relations of the normal human
face, it does not distinguish beautiful from plain.4 The psychologist Nancy
Etcoff analyzed human beauty and its impact on society in a book that is sub-
titled The Science of Beauty. She also found that the perception of beauty could
not be defined by mathematical formulae. The summary of her analysis of
mathematical ideals to human beauty was, “For scientists in this century, the
key to understanding human beauty is in our biology not in mathematics.”5
Since neither the normal nor the beautiful face can be defined by mathemati-
cal ideals, we have found it more useful to use the averaged anthropomet- PEARL
ric measurements of selected age, sex and ethnicity, rather than neoclassical Symmetry is beneficial but does not
canons, to guide our gestalt for the selection of implants for facial skeletal define facial beauty.
augmentation.
Facial anthropometrics
The late Leslie Farkas, a medical anthropologist, accumulated large num-
bers of precise, reproducible surface measurements of various population
groups of both sexes.6 These data define normative values, as well as gender
and ethnic differences in facial measurements and proportions. The anthro-
pometric data used in this book come from measurements made in a large
group of young white North American adult men and women.6 Similar infor-
16 mation is available for Asian, African, and certain other ethnic groups.7–9
Anthropometric landmarks, measurements, and inclinations are useful for
Facial measurements
25.0%
25.0%
25.0%
25.0%
A
21.1%
24.3%
26.5%
26.9%
B
Fig. 2.6 A comparison of young male adult faces constructed from neoclassical canons and from anthropometric measurements. (A) Frontal
and lateral views of the young male adult face constructed with the help of the neoclassical canons. The head and face have five equal
vertical sections and four equal horizontal sections. The nose width equals the eye fissure width and the interocular distance. (B) Frontal
and lateral views of the average young male white North American head and face constructed with mean measurements of both sexes. In
general, these measurements are different than the idealized ones shown in (A). From Farkas et al. 1985,2 with permission.
17
Chapter 2 Evaluation and planning for facial implant surgery
planning implant and other craniofacial surgery. Table 2.1 lists anthropometric
landmarks (landmarks used in craniofacial anthropometry and radiographic
cephalometry may have the same name but not the same anatomic location),
while Table 2.2 lists measurements and inclinations.
These landmarks and measurements are diagrammed in Figs. 2.7–2.10.
Definitions of frontal and lateral anthropometric landmarks useful for evaluating the face
Table 2.1 Definitions of frontal and lateral anthropometric landmarks useful for evaluating the face
See frontal view (Fig. 2.7A); lateral view (Fig. 2.7B).
18
Facial measurements
Table 2.2 Craniofacial complex measurements useful for evaluating the face
See frontal female (Fig. 2.8A), frontal male (Fig. 2.8B); lateral female (Fig. 2.9A), lateral male (Fig. 2.9B).
Sexual dimorphism
These objective data identify the sexual dimorphism in human faces. On the
average, all facial measurements are greater in men than in women. In addi-
tion, the relationship between measurements differs in men and women. These
differences are pronounced in the lower third of the face. The bigonial dis-
tance (go–go) is the transverse facial dimension that has the greatest difference
between the sexes. In other words, the lower one-third of women’s faces tends
to be absolutely and relatively narrower than that of men. Gender-related dif-
ferences have implications for surgical planning. For example, if a normal-
dimensioned male mandible is augmented in the transverse dimension, it may
be perceived as stronger. However, if a normal-dimensioned female mandible
is augmented, it may be perceived as masculine. Fig. 2.11 shows typical male
and female skulls.
Anthropometric data aids facial evaluation and surgical planning by
describing normal facial measurements and relations. With this framework,
the status of the patient is more easily understood and the goals of surgery
defined.
19
Chapter 2 Evaluation and planning for facial implant surgery
v
v
tr tr
ft ft
g ft
g
n n
op
zy
or cdl
zy or zy
sn
ls
sn
ls sto
go go li
sto go
li pg
pg
gn
A B
gn
Fig. 2.7 Anthropometric landmarks relevant to implant surgery; see Table 2.1 for definitions. The schematic drawings show the surface
landmarks in relation to the underlying facial skeleton: (A) frontal and (B) lateral view.
v
v
46
46
tr tr
109
111
ft-ft ft-ft
63 67
111 116
n
n
zy-zy 215
zy-zy 229
130 139
70
sn 76
111 sn
125
sto
go-go 64
95 sto
go-go
43 106 73
51
gn
gn
A B
Fig. 2.8 Frontal view of female and male faces drawn from average anthropometric measurements for 21-year-old white North
Americans: (A) female and (B) male. See Table 2.1 for definitions.
20
Facial measurements
v v
47 46
tr tr
63 67
n n
cdl
70 cdl
76
sn 62
sn
68
sto
sto
go
64 43
81
73 51 go
gn 86
gn
A B
Fig. 2.9 Lateral view of female and male faces drawn from average anthropometric measurements for 21-year-old white North Americans:
(A) female and (B) male. See Table 2.1 for definitions.
tr tr
10°
6°
n
n
1°
2°
-3°
-4° 2°
2°
sn
sn
ls
ls
-11
-13° li
li
-19° -15°
pg pg
A B
Fig. 2.10 Lateral view of female and male faces drawn from average anthropometric
measurements for 21-year-old white North Americans showing profile inclinations: (A)
female and (B) male. See Table 2.1 for definitions.
21
Chapter 2 Evaluation and planning for facial implant surgery
A B
Fig. 2.11 (A) Female and (B) male skull images. From the Atkinson Skull Collection, University of the Pacific, Dugoni School of Dentistry, 155
Fifth Street, San Francisco, CA.
The small dimensions and complex configuration of the face make millime-
ter differences and changes noticeable and significant. For these reasons, it is
important to know the average or “normal” dimensions of the face and its com-
ponent features. Implants that are too large create unnatural contours that relate
poorly to other areas of the face. Inappropriate implants may therefore upset
the “balance” of the face. Facial implants must be appropriately sized, shaped,
and positioned to be effective.
REFERENCES
1. Clayton M. Leonardo Da Vinci – The divine and the grotesque. 1st ed. London: Royal
Collection Enterprises; 2002.
2. Farkas L, Hreczko TA, Kolar JC, Munro IR. Vertical and horizontal proportions of the face in
young adult North American Caucasians: revision of neoclassical canons. Plast Reconstr Surg
1985;75(3):328–38.
3. Farkas LG, Kolar JC. Anthropometrics and art in the aesthetics of women’s faces. Clin Plast
Surg 1987;14(4):599–616.
4. Ricketts RM. Divine proportions in facial esthetics. Clin Plast Surg 1982;9(4):401–22.
5. Etcoff N. Survival of the prettiest. 1st ed. New York: Anchor Books; 2000.
6. Farkas LG, Hreczko TA, Katic MJ. Appendix A: Craniofacial norms in North American
Caucasians from birth (one year) to young adulthood. In: Farkas LG, editor. Anthropometry of
the head and face. 2nd ed. New York: Raven Press; 1994.
7. Farkas LG, Ngim RCK, Lee ST. Appendix B: Craniofacial norms in 6-, 12-, and 18-year-old
Chinese subjects. In: Farkas LG, editor. Anthropometry of the head and face. 2nd ed. New York:
Raven Press; 1994.
8. Farkas LG, Venkatadri G, Gubbi AV. Appendix B: Craniofacial norms in young adult African-
Americans. In: Farkas LG, editor. Anthropometry of the head and face. 2nd ed. New York:
Raven Press; 1994.
9. Farkas LG, Katic MJ, Forrest CR. International anthropometric study of facial morphology in
various ethnic groups/races. J Craniofac Surg 2005;16:615–46.
22
Chapter 3
Implant materials
The craniofacial skeleton can be reconstructed with both autogenous bone and
alloplastic implants. Alloplastic implants are used only as onlay grafts to the
native skeleton to improve facial contour and to replace missing portions of
the non-load-bearing cranial vault and internal orbit. Autogenous bone may be
used for these purposes, but is more suited to replace segmental, load-bearing
defects of the facial skeleton. Virtually all aesthetic facial skeletal augmenta-
tion, as well as cranial vault replacement, is done with alloplastic materials.
Three basic categories of alloplastic materials are used in facial reconstruction.
Polymers and ceramics are used to replace or augment bone. Metals are used as
fixation or support devices.
AUTOGENOUS MATERIALS
Bone
Autogenous bone has long been considered the standard material to restore or
improve the craniofacial skeleton because it has the potential to become revascu-
larized and then assimilated into the facial skeleton. In time, it could be biologi-
cally indistinguishable from the adjacent native skeleton. These attributes make
it ideal and the only material available to reliably reconstruct segmental load-
bearing defects of the facial skeleton. When used as an onlay graft, these attri-
butes lead to graft resorption and unreliable augmentation of the facial skeleton.
Cortical bone
Cancellous bone
Fig. 3.1 Schematic drawing of the placement of iliac crest (left) and calvarial (right) onlay
bone grafts on the snout of the rabbit.
Fig. 3.2 Latex vascular cast injection of 6-week onlay bone graft harvested from the
calvarium and fixed to the snout of its rabbit host with a lag screw (×5). Arrow points to lag
screw. Broken line separates cortical layer (above) from cancellous layer (below). Note that
the vessels (yellow dye) penetrate only the cancellous portions of the graft.
A B
Fig. 3.3 Latex vascular cast injection of (A) 10-day calvarial graft and (B) 10-day iliac crest
graft (×10). The orientation is similar to that shown in Fig. 3.1. Arrows point to lag screws.
Note that the blood vessels (red dye) penetrate only the cancellous portions of the graft.
A B
Fig. 3.4 Tartrate-resistant acid phosphatase (TRAP) histochemical stain of the osteoclastic
activity of (A) 10-day calvarial and (B) 10-day iliac crest grafts (both ×50). There was
significant osteoclastic activity (red dye) in the cancellous areas of the grafts but minimal
activity in the cortex. Solid line separates onlay graft from snout. TRAP stain penetration
mimics that of vascular penetration shown in Fig. 3.3.
cortical bone in an onlay graft determines its volume maintenance. The impor-
tance of graft architecture, as opposed to its embryologic origin, to the volume
persistence of onlay bone grafts has been supported in later studies by Gosain.5
Rigid fixation
Chen’s study also explained the observation of others that rigid fixation
improves graft volume maintenance.4 Lag screw fixation obliterates the gap
between the graft and the recipient bed and therefore may reduce neovascu-
larization of the graft at this interface. Rigid fixation may therefore improve the
volume maintenance of onlay bone grafts by limiting, rather than facilitating,
revascularization of the graft.
Recipient site
The volume maintenance of a bone graft depends on where it is placed. Zins 25
et al. originally proposed that bone grafts placed in depository fields on the
Chapter 3 Implant materials
Cartilage
In the realm of facial skeletal augmentation, cartilage has a limited role except
for nasal onlay grafts. Advantages for using cartilage include lowest rate of
resorption (since it is not vascularized) and extrusion. Potential donor sites
include auricular, nasal septal, and costal grafts. Costal cartilage grafts provide
an ample source of cartilage for nasal dorsal augmentation. However, cartilage
grafts have a tendency to warp and their donor site is not free of morbidity.11
Cadaveric cartilage presents an alternative source of cartilage, free of donor site
morbidity, with reports of good tissue compatibility and low rate of infection.
26 However, the problem of warping remains, regardless of whether the cartilage
was irradiated or not. Graft resorption has been reported as well.12
Alloplastic materials
Fat
Autogenous fat grafting has become a valuable addition to both the recon-
structive and aesthetic procedural armamentarium. However, it is important
to emphasize that there is a difference in the resultant facial contour when it is
altered by expanding the soft tissue envelope as opposed to increasing the pro-
jection of the underlying skeleton. Small augmentation of either the underlying
skeleton or the overlying soft tissue envelope may result in changes to the facial
contour that are almost clinically imperceptible. However, when skeletal or soft
tissue deficits become more severe, their correction requires use of the appropri-
ate tissue or tissue substitute. Although both modalities result in an augmenta-
tion of facial contour, the aesthetic result obtained with fat grafting is different
from that of skeletal advancement. A progressive increase in the projection of
the facial skeleton by osteotomy and advancement or alloplastic augmentation
results in a facial contour that is increasingly skeletal and defined. On the other
hand, a progressive increase in the volume of the overlying soft tissue enve-
lope results in a facial contour that is increasingly less defined.13 An example is
shown in Fig. 3.5.
ALLOPLASTIC MATERIALS
A B C
Fig. 3.5 Example using the same individual showing the difference in facial contours resulting from skeletal as opposed to soft tissue
augmentation. (A) Appearance prior to facial surgery. (B) Appearance after skeletal augmentation with implants. (C) Appearance after 27
aggressive fat grafting.
Chapter 3 Implant materials
the implant tends to maintain its volume and shape. Likewise, the implant has a
minimal and predictable effect on the host tissue that surrounds it. This type of
relationship is an advantage over the use of autogenous bone or cartilage which,
when vascularized, will be remodeled to varying degrees, thereby changing vol-
ume and shape.
The alloplastic implants currently used for facial reconstruction have not
shown to have any toxic effects on the host.14 The host responds to these materi-
als by forming a fibrous capsule around the implant, which is the body’s way of
isolating the implant from the host. The most important implant characteristic
that determines the nature of the encapsulation is the implant’s surface. Smooth
implants result in the formation of smooth-walled capsules (Fig. 3.6). Porous
implants allow varying degrees of soft tissue ingrowth, which results in a less
dense capsule (Fig. 3.7).
Animal studies have demonstrated that implant pore sizes of more than
100 μm encourage tissue ingrowth.15 Pore sizes of less than 100 μm limit
tissue ingrowth. Materials with large pore sizes (>300 μm) have drawbacks
Implant
Implant
Implant
28 Fig. 3.7 Tissue ingrowth into a porous polyethylene implant (original magnification ×100;
hematoxylin and eosin stain). From Rubin and Yaremchuk 1997,14 with permission.
Alloplastic materials
Polysiloxane (silicone)
Polysiloxane is a polymer created from interlinking silicone and oxygen
[SiO(CH3)2] with methyl side groups, and as such is the only non-carbon chain
polymer used in medical implantation. Solid silicone or the silicone rubber used
for facial implants is a vulcanized form of polysiloxane.
Solid silicone has the following advantages: it can be sterilized by steam or
irradiation, it can be carved with either a scissors or scalpel, and it can be stabi-
lized with a screw or a suture. Because of its smooth surface, it can be removed
quite easily. Disadvantages include the tendency to cause resorption of bone
underlying it, particularly when used to augment the chin; the potential to
migrate if not fixed; and the potential for its fibrous capsule to be visible when
placed under a thin soft tissue cover. Fig. 3.8 shows examples of silicone malar
and chin implants.
Fig. 3.8 Examples of silicone malar (left) and chin (right) implants. These implants have a 29
smooth surface and are relatively flexible depending on the thickness of the implant.
Chapter 3 Implant materials
Polytetrafluoroethylene
Polytetrafluoroethylene (PTFE), Gore-Tex, has a carbon-ethylene backbone to
which are attached four fluorine molecules.
It is very chemically stable, has a non-adherent surface and, because it is not
cross-linked, it is very flexible. There is extensive experience with the use of this
material for vascular prostheses, soft tissue patches, and sutures. A variety of
preformed implants are available for both subdermal and subperiosteal place-
ment. Preformed implants are made with a pore size between 10 and 30 μm,
which allows for some soft tissue ingrowth. However, it is smooth enough to
be maneuvered easily through soft tissues. This material can be fixed to under-
lying structures with sutures or screws. It is easily sterilized. Fig. 3.9 shows
examples of PTFE implants.
Acrylic
Acrylic is used in cranioplasty procedures for reconstructing full-thickness
cranial defects, or in forehead contouring procedures. Acrylic biomaterials
are made from polymerized esters of either acrylic or methyl acrylic acids
(methyl methacrylate). Acrylic implants have smooth surfaces, are strong, and
are inflexible.
The most commonly used material for skull reconstruction is polymethyl-
methacrylate (PMMA). PMMA is radiolucent and therefore does not affect post-
operative imaging. It is unaffected by temperature and is strong. When used for
full-thickness defects, it can fill and obliterate intracranial dead space – a prob-
lem encountered with bone cranioplasty. When used as an onlay, overcorrection
can compensate for overlying soft tissue deficiencies, resulting in a smooth skin
surface contour. Since it is encapsulated by the host rather than incorporated
by surrounding soft tissues, PMMA is believed by some to be more susceptible
to late complications. Cranioplasty kits are available that contain a single dose
of 30 g of powdered polymer and 17 mL of liquid monomer. The elements are
mixed with a spatula in a bowl. Doughing time varies with temperature and is
30 about 5 minutes at 22°C (72°F). Fig. 3.10 shows the liquid monomer and pow-
dered polymer prior to mixing.
Alloplastic materials
Fig. 3.10 Example of a polymethylmethacrylate cranioplasty kit with liquid monomer on the
left and the powdered polymer on the right. The implants resulting after polymerization are
smooth, hard, and strong.
Polyethylene
Polyethylene is a simple carbon chain of ethylene monomer. The high density,
porous variety – Omnipor (Matrix Surgical, Atlanta, GA); Medpor (Stryker,
Kalamazoo, MI) – is used for facial implants because of its higher tensile
strength.
Polyethylene, although chemically similar to PTFE, has a much firmer con-
sistency, resisting material compression while still permitting some flexibility.
In addition to being firmer than PTFE, it has an intramaterial porosity between
125 and 250 μm, which allows more extensive fibrous ingrowth. The porosity of
Omnipor or Medpor has both advantages and disadvantages. The advantages
include its tendency to allow extensive soft tissue ingrowth, thereby lessen-
ing its tendency to migrate or to erode underlying bone. Its firm consistency
allows it to be easily fixed with screws and contoured with a scalpel or power
equipment without fragmenting. However, its porosity causes soft tissue to
adhere to it, making placement more difficult and requiring larger pockets to be
made than with smooth-surfaced implants. The soft tissue ingrowth also makes
implant removal more difficult than with smooth-surfaced implants.
Porous polyethylene is the senior author’s implant material of choice. An
example is shown in Fig. 3.11.
Polymethylmethacrylate–polyhydroxyethylmethacrylate
HTR, an abbreviation for “hard tissue replacement,” is a porous composite
of PMMA and polyhydroxyethylmethacrylate that allows some soft tissue
ingrowth. A calcium hydroxide coating imparts a negative surface charge to
encourage bony ingrowth and deter adhesion of bacteria to the implant.19 HTR
is not flexible. Examples of HTR implants are shown in Fig. 3.12.
Fig. 3.11 Example of a porous polyethylene (Medpor) implant. These implants are bendable,
depending on their thickness, and are adaptable to the facial skeleton. These implants have a
pore size that allows some soft tissue ingrowth.
Fig. 3.12 Examples of HTR implants. These implants are rigid. They have a pore size that
allows some soft tissue ingrowth.
Ceramics
Ceramic materials are usually heated to high temperatures (sintered) to fuse
their crystal-like components.
Hydroxyapatite
32 The ceramic material most commonly used in craniofacial surgery is hydroxy-
apatite. Hydroxyapatite is a calcium phosphate salt found as a major component
Alloplastic materials
Fig. 3.13 A customized polyether ether ketone (PEEK) implant used for cranioplasty.
All of the facial implant materials described in the above section have chemi-
cal compositions and biostability that provide appropriate biocompatibility
for clinical use. The senior author has personal experience with all of these
materials. It is the author’s preference to perform facial skeletal implant
augmentation with porous polyethylene because of its handling and sur-
face characteristics. The rationale for the use of this material is expanded
below.
Porous polyethylene (Omnipor, Medpor) is firm and flexible. It is eas-
ily carved with a scalpel or contoured with a rasp or motorized burr. It can
be immobilized with sutures or, in the author’s preference, screws. It can be
molded to the external contours of the skeleton by heating it in water, although
the author rarely takes advantage of this attribute.
The favorable biocompatibility of this implant material can also be attributed
to its porous surface. Porous polyethylene has a continuous system of inner
connecting pores approximately 100–250 μm in diameter. Clinical specimens
demonstrate rapid ingrowth of fibrous tissue after human implantation. Rather
than the dense connective tissue capsules observed with smooth-surfaced
implants, porous polyethylene implants exhibit a thin connective tissue mem-
brane that is contiguous with the ingrown tissue.21 It has been noted during
revision operations that fibrous tissue ingrowth is sufficient to result in bleed-
ing when the implants are modified in situ with a scalpel, and in certain circum-
stances ingrowth exhibits sufficient vascularity to allow skin grafts to be placed
directly over the implant.21
Fibrous tissue ingrowth improves the biocompatibility of porous implants
because it limits their movement. Movement is an essential factor in deter-
mining the host response to an implant.16,22–24 Because the host foreign body
reaction encapsulates smooth-surface implants, a smooth implant never binds
to the host bed and therefore is predisposed to movement. Encapsulation of
smooth implants and their consequent predisposition to movement are directly
or indirectly responsible for the majority of the late complications related
to smooth implants. These complications include the tendency of smooth
implants placed in the orbital floor to migrate and distort the eyelids; cause
hemorrhage; obstruct the lacrimal system; or erode into the maxillary sinus,
acting as a nidus for infection.22–24 The rapid tissue ingrowth and mucosaliza-
tion of porous polyethylene implants, as observed in animal studies designed
to stimulate orbital floor reconstruction,25 immobilizes these implants, which
explains why these complications have not been reported with the use of
porous polyethylene.
When used to augment the chin, smooth silicone implants are known to
cause bone resorption, which is attributed to implant motion caused by the
overlying mentalis muscle.26 Animal studies have demonstrated that porous
implants result in less bone resorption than do smooth implants.27 Bikhazi and
Van Antwerp, in a prospective cephalometric study of five patients undergoing
chin augmentation with porous polyethylene implants, did not observe bone
resorption beneath the implants.27 This author believes that bone resorption PEARL
beneath implants reflects the body’s attempt to abide by Wolff’s Law whereby
Porosity limits implant movement and
skeletal volume (in this case, bone and implant) responds to overlying soft tis- bone resorption.
34 sue deforming forces.
Morbidity and complications associated with alloplastic implants
General considerations
Carcinogenicity and systemic disease
The induction of malignancy or injury to organs or organ systems is a
potential concern of implanting foreign materials into the human body.
Clinical observation suggests that the risk of cancer with metal or poly-
mer implant devices is extremely low. An English language literature
review conducted in 1997 revealed only one case of a tumor associated
with a facial implant.14 The histology of this tumor showed squamous cell
cancer rather than sarcoma, making the implant–tumor connection less
clear.
Implanted metals are known to corrode and release metal ions. Accu-
mulation of metal ions have been found adjacent to metal fixation devices.
The corrosion process can result in a local fibroblastic tissue reaction,28,29
which has been implicated in implant failure in long-bone fixation
devices.28 Postmortem studies have found accumulation of metal prod-
ucts in regional lymph nodes, liver and spleen.29 Despite the documented
spread of degradable products from metal implants, no direct associa-
tion between implant corrosion products and systemic disease has been
drawn.14
There is scant data to support a connection between polymer implants and
carcinogenicity or systemic disease. Five cases of sarcoma associated with
Dacron vascular prostheses (latency 6 months to 5 years) appear in the lit-
erature.30 No cases of cancer have been reported in association with polymer
craniofacial implants.
The large clinical experience of breast augmentation provides the best infor-
mation supporting a lack of correlation between connective tissue disease and
silicone implant material. Gabriel et al. investigated the risk of connective tis-
sue disease in 749 women with breast implants followed for an average of 7.8
years.31 In another study, Sanchez- Guerrero et al. studied 1183 members of the
Nurse Health Study Cohort with breast implants followed for an average of 9.9
years.32 Both studies found no increased risk for connective tissue diseases after
silicone breast augmentation.
Hypersensitivity
An uncommon reaction to metal implants is cell-mediated (type IV) hypersen-
sitivity reaction resulting in pain, non-union of bone, and overlying dermatitis.
This has been reported with Vitallium and stainless steel, and suggested for
titanium. In maxillofacial use, hypersensitivity reactions have been noted with
the use of stainless steel wire33 and plates.34 Sensitivity is often confirmed by
patch testing, and removal of the implant results in resolution of symptoms
according to all reports.
True hypersensitivity reactions to prefabricated polymer implants are
almost unheard of. The free monomer of PMMA, however, has been noted
to cause asthmatic reactions in operating room staff during surgical proce-
dures. A high concentration of vaporized monomer during the curing pro-
cess can affect sensitized individuals, especially if the room is not properly
ventilated.35 35
Chapter 3 Implant materials
infection rate for polymeric and ceramic implants at mixed sites is 3%, based on
939 patients reviewed. These data are summarized in Table 3.1.
Clinical series and case reports can provide useful information about factors
that contribute to morbidity with implants. Implant composition is one such
factor. Given that several biomaterials are well tolerated in the human body,
the actual chemical structure of an implant is important only to the degree that
it influences the consistency and surface characteristics of the finished device.
For example, porous polyethylene and PTFE are extruded from the orbital floor
much less frequently than smooth-surfaced nylon implants. Tissue ingrowth
helps anchor the porous implant in place. Moreover, experimental data suggest
that the presence of host defenses within the implant can decrease the risk of
infection.
Implant site is clearly related to morbidity. Complication rates are lowest in
the chin and malar regions, and highest in the nose and ear, where soft tissue
coverage is thin and often under tension from the implanted device.
Implant material
Silicone Porous polyethylene Proplast Hydroxyapatite Expanded PTFE Overall
No. of studies reviewed 7 4 2 4 3 20
No. reporting follow-up time 6 3 2 4 2 17
Range of follow-up times 1 month–13 3 months–3 years 13 months–6 6 months–5 Up to 30 months –
years years years
No. reporting no implant-related 21 1 1 0 5
complications
Total number of patients 239 216 41 150 273 919
Average complication rates (%)
Infection 3.8 0.9 14.6 2.7 2.2 3.0
Exposure/extrusion 2.9 0.5 0 0 0.7 1.2
Displacement 4.6 0 0 3.3 0 1.7
Seroma 0 0.9 0 0 0 <0.5
Persistent edema 0.8 0 0 0 0 <0.5
Prominence 0 0 0 2.0 0 <0.5
Inflammatory reaction 0 0 0 0 1.8 0.5
Implants removed due to implant- 11.7 0.5 14.6 1.3 1.8 4.6
related complications
PTFE, polytetrafluoroethylene.
Data from Rubin and Yaremchuk,14 with permission.
37
Table 3.1 Complication rates for polymer and ceramic materials at mixed sites
Chapter 3 Implant materials
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Reconstr Surg 1985;76(4):510–6.
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1990;86(3):449–56.
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Plast Reconstr Surg 1994;93(4):714–22; discussion 723-714.
5. Gosain AK, Persing JA. Biomaterials in the face: benefits and risks. J Craniofac Surg
1999;10(5):404–14.
6. Zins JE, Kusiak JF, Whitaker LA, Enlow DH. The influence of the recipient site on bone grafts
to the face. Plast Reconstr Surg 1984;73(3):371–81.
7. Gosain AK, Riordan PA, Song L, et al. A 1-year study of hydroxyapatite-derived biomaterials
in an adult sheep model: III. Comparison with autogenous bone graft for facial augmentation.
Plast Reconstr Surg 2005;116(4):1044–52.
8. Santos A, Bakker AD, Klein-Nulend J. The role of osteocytes in bone mechanotransduction.
Osteoporos Int 2009;20(6):1027–31.
9. Albrektsson T. Repair of bone grafts. A vital microscopic and histological investigation in the
rabbit. Scand J Plast Reconstr Surg 1980;14(1):1–12.
10. Elsalanty ME, Genecov DG. Bone grafts in craniofacial surgery. Craniomaxillofac Trauma
Reconstr 2009;2(3):125–34.
11. Varadharajan K, Sethukumar P, Anwar M, Patel K. Complications associated with the use of
autologous costal cartilage in rhinoplasty: a systematic review. Aesthet Surg J 2015;35(6):
644–52.
12. Adams Jr WP, Rohrich RJ, Gunter JP, Clark CP, Robinson Jr JB. The rate of warping in
irradiated and nonirradiated homograft rib cartilage: a controlled comparison and clinical
implications. Plast Reconstr Surg 1999;103(1):265–70.
13. Yaremchuk MJ. Commentary on: the role of microfat grafting in facial contouring. Aesthet
Surg J 2015;35(7):772–3.
14. Rubin JP, Yaremchuk MJ. Complications and toxicities of implantable biomaterials used in
facial reconstructive and aesthetic surgery: a comprehensive review of the literature. Plast
Reconstr Surg 1997;100(5):1336–53.
15. Klawitter JJ, Bagwell JG, Weinstein AM, Sauer BW. An evaluation of bone growth into porous
high density polyethylene. J Biomed Mater Res 1976;10(2):311–23.
16. Spector M, Harmon SL, Kreutner A. Characteristics of tissue growth into Proplast and porous
polyethylene implants in bone. J Biomed Mater Res 1979;13(5):677–92.
17. Fiala TG, Paige KT, Davis TL, Campbell TA, Rosen BR, Yaremchuk MJ. Comparison of artifact
from craniomaxillofacial internal fixation devices: magnetic resonance imaging. Plast Reconstr
Surg 1994;93(4):725–31.
18. Eppley BL. Alloplastic implantation. Plast Reconstr Surg 1999;104(6):1761–83; quiz 1784-1765.
19. Eppley BL, Sadove AM, German RZ. Evaluation of HTR polymer as a craniomaxillofacial graft
material. Plast Reconstr Surg 1990;86(6):1085–92.
20. Gosain AK, Song L, Riordan P, et al. A 1-year study of osteoinduction in hydroxyapatite-
derived biomaterials in an adult sheep model: part I. Plast Reconstr Surg 2002;109(2):619–30.
21. Bikhazi HB, Van Antwerp R. Characteristics of the tissue response to Medpor porous
polyethylene implants in the human facial skeleton. J Long Term Eff Med Implants 1993;3:
223–35.
22. Wolfe SA. Correction of a persistent lower eyelid deformity caused by a displaced orbital floor
implant. Ann Plast Surg 1979;2(5):448–51.
23. Wolfe SA. Correction of a lower eyelid deformity caused by multiple extrusions of alloplastic
orbital floor implants. Plast Reconstr Surg 1981;68(3):429–32.
24. Kohn R, Romano PE, Puklin JE. Lacrimal obstruction after migration of orbital floor implant.
Am J Ophthalmol 1976;82(6):934–6.
25. Dougherty WR, Wellisz T. The natural history of alloplastic implants in orbital floor
reconstruction: an animal model. J Craniofac Surg 1994;5(1):26–32; discussion 33.
26. Friedland JA, Coccaro PJ, Converse JM. Retrospective cephalometric analysis of mandibular
bone absorption under silicone rubber chin implants. Plast Reconstr Surg 1976;57(2):
144–51.
27. Bikhazi HB, Van Antwerp R. The use of Medpor in cosmetic and reconstructive surgery:
Experimental and clinical evidence. In: Stucker FJ, editor. Plastic and reconstructive surgery of
the head and neck. St. Louis, Missouri: Mosby; 1990. p. 271–3. 39
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28. Byrne JE, Lovasko JH, Laskin DM. Corrosion of metal fracture fixation appliances. J Oral Surg
1973;31(8):639–45.
29. Case CP, Langkamer VG, James C, et al. Widespread dissemination of metal debris from
implants. J Bone Joint Surg Br 1994;76(5):701–12.
30. Burns WA, Kanhouwa S, Tillman L, Saini N, Herrmann JB. Fibrosarcoma occurring at the site
of a plastic vascular graft. Cancer 1972;29(1):66–72.
31. Gabriel SE, O’Fallon WM, Kurland LT, Beard CM, Woods JE, Melton 3rd LJ. Risk of connective
tissue diseases and other disorders after breast implantation. N Engl J Med 1994;330(24):
1697–702.
32. Sanchez-Guerrero J, Colditz GA, Karlson EW, Hunter DJ, Speizer FE, Liang MH. Silicone
breast implants and the risk of connective tissue diseases and symptoms. N Engl J Med
1995;332(25):1666–70.
33. Guyuron B, Lasa Jr CI. Reaction to stainless steel wire following orthognathic surgery. Plast
Reconstr Surg 1992;89(3):540–2.
34. Roed-Petersen B, Roed-Petersen J, Jorgensen KD. Nickel allergy and osteomyelitis in a patient
with metal osteosynthesis of a jaw fracture. Contact Dermatitis 1979;5(2):108–12.
35. Pickering CA, Bainbridge D, Birtwistle IH, Griffiths DL. Occupational asthma due to methyl
methacrylate in an orthopaedic theatre sister. Br Med J 1986;292(6532):1362–3.
36. Rubin LR. Polyethylene as a bone and cartilage substitute: a 32-year retrospective. In: Rubin L,
editor. Biomaterials in reconstructive surgery. St. Louis: Mosby; 1983. p. 474–93.
37. Davis PK, Jones SM. The complications of silastic implants. Experience with 137 consecutive
cases. Br J Plast Surg 1971;24(4):405–11.
38. Habal MB, Chalian VA. Experience with prefabricated silicone implants for reconstruction in
facially deformed patients. J Prosthet Dent 1974;32(3):292–9.
39. Lash H, Apfelberg DB, Lavey EB, Maser MR, Laub D. Custom-fabricated silicone implants for
contour restoration. Ann Plast Surg 1979;2(2):97–102.
40. Laub DR, Spohn W, Lash H, Weber J, Chase RA. Accurate reconstruction of traumatic bony
contour defects of periorbital area with prefabricated silastic. J Trauma 1970;10(6):472–80.
41. Mohler LR, Porterfield HW, Ferraro JW. Custom implants for reconstruction of craniofacial
defects. Arch Surg 1976;111(4):452–5.
42. Wilkinson TS, Iglesias J. Room temperature vulcanizing silastic in facial contour
reconstruction. J Trauma 1975;15(6):479–82.
43. Raval P, Schaaf NG. Custom-fabricated silicone rubber implants for tissue augmentation – a
review. J Prosthet Dent 1981;45(4):432–4.
44. Berghaus A. Porous polyethylene in reconstructive head and neck surgery. Arch Otolaryngol
1985;111(3):154–60.
45. Romano JJ, Iliff NT, Manson PN. Use of Medpor porous polyethylene implants in 140 patients
with facial fractures. J Craniofac Sur 1993;4(3):142–7.
46. Wellisz T, Dougherty W, Gross J. Craniofacial applications for the Medpor porous
polyethylene flexblock implant. J Craniofac Surg 1992;3(2):101–7.
47. Byrd HS, Hobar PC, Shewmake K. Augmentation of the craniofacial skeleton with porous
hydroxyapatite granules. Plast Reconstr Surg 1993;91(1):15–22; discussion 23-16.
48. Papacharalambous SK, Anastasoff KI. Natural coral skeleton used as onlay graft for contour
augmentation of the face. A preliminary report. Int J Oral Maxillofac Surg 1993;22(5):260–4.
49. Salyer KE, Hall CD. Porous hydroxyapatite as an onlay bone-graft substitute for maxillofacial
surgery. Plast Reconstr Surg 1989;84(2):236–44.
50. Rosen HM, Ackerman JL. Porous block hydroxyapatite in orthognathic surgery. The Angle
Orthodontist 1991;61(3):185–91; discussion 192.
51. Mole B. The use of Gore-Tex implants in aesthetic surgery of the face. Plast Reconstr Surg
1992;90(2):200–6.
52. Lassus C. Expanded PTFE in the treatment of facial wrinkles. Aesthetic Plast Surg
1991;15(2):167–74.
53. Cisneros JL, Singla R. Intradermal augmentation with expanded polytetrafluoroethylene
(Gore-Tex) for facial lines and wrinkles. J Dermatol Surg Oncol 1993;19(6):539–42.
54. Yaremchuk MJ. Facial skeletal reconstruction using porous polyethylene implants. Plast
Reconstr Surg 2003;111(6):1818–27.
55. Zimmerli W, Trampuz A, Ochsner PE. Prosthetic-joint infections. N Engl J Med
2004;351(16):1645–54.
56. Zimmerli W, Waldvogel FA, Vaudaux P, Nydegger UE. Pathogenesis of foreign body
infection: description and characteristics of an animal model. J Infect Dis 1982;146(4):487–97.
40
Chapter 4
This chapter presents the principles and basic steps of the senior author’s oper-
ative technique for implant augmentation of the facial skeleton.
PREPARATION
ANESTHESIA
With the exception of chin augmentation, operations are performed with the
patient under general anesthesia, preferably nasotracheal anesthesia. Since
most operations employ intraoral incisions, this approach optimizes access and
allows optimum preparation of the operative site as well as control of the air-
way (Fig. 4.1). The operative field is infiltrated with a solution containing bupi-
vacaine (Marcaine) and epinephrine (1:200,000), for immediate postoperative
pain relief and to optimize intraoperative hemostasis. Both the skin and the
oral mucosa are prepared with a povidone-iodine solution. Antibiotics, usu-
ally cephalosporins, are administered intravenously prior to the onset of sur-
gery and intraoperatively depending on the length of surgery. Oral antibiotics
are administered for the 5 days following surgery only if intraoral access for
implant placement was employed.
INCISIONS
Incisions are borrowed from craniofacial and aesthetic surgery. They are always
made through intact skin remote from implant placement. Implants positioned
directly beneath surgical incisions are at risk for exposure, contamination and
then, implant loss.
Coronal incisions are used to place implants in the frontal and temporal areas.
Transconjunctival retroseptal incisions (often with a lateral canthotomy for increased
exposure) are used to access the infraorbital rim, malar area, and internal orbit. The 41
lateral extent of the lower lid blepharoplasty incision provides access to the lateral
Chapter 4 Principles and operative technique for facial skeletal augmentation
Fig. 4.1 General anesthesia using nasotracheal intubation is ideal for midface and mandible
augmentation. Endoscopy draping of the endotracheal tube and circuit allows it to be visible
in the operative field and mobile. The airway is protected and controlled. A panoramic view
of the operative area is provided.
orbit and zygomatic arch. This small cutaneous incision leaves an inconspicuous
scar. It is used with the transconjunctival approach when a lateral canthotomy is
avoided. Blepharoplasty skin–muscle flaps provide alternative access to this area.
Intraoral incisions are used to augment the midface as well as the mandibu-
lar body and ramus. Intraoral incisions are made with a generous labial cuff to
allow watertight, reliable mucosal closure (Fig. 4.2).
Chin area augmentation is preferably performed through submental inci-
sions (Fig. 4.3). Submental approaches to the chin provide optimal exposure
of the skeletal anatomy and the mental nerves. Unlike the intraoral approach,
which avoids a cutaneous scar, the submental approach does not violate the
mentalis muscle. Mentalis dysfunction can result in lower lip descent, excessive
lower tooth show, and chin pad ptosis.
EXPOSURE
Fig. 4.2 Illustration shows surgical access to expose the posterior mandible. An intraoral
mucosal incision is made along ramus and posterior body of mandible. It is made
approximately 1 cm above the sulcus on its labial side. Intraoral incisions to expose the
midface are also made approximately 1 cm above the sulcus.
Orbicularis
oris m.
Depressor labii
inferioris m.
Mentalis m.
Fig. 4.3 Illustration shows surgical access to the chin and anterior mandibular border. A
submental skin and subcutaneous incision is telescoped over the chin. The striped area
denotes the area of subperiosteal dissection. Note that a pocket larger than the implant is
dissected to allow ease of implant insertion and to provide a panoramic view of the area to
be augmented.
43
Chapter 4 Principles and operative technique for facial skeletal augmentation
IMPLANT SELECTION
The senior author prefer porous polyethylene implants (Omnipor, Matrix Sur-
gical, Atlanta, GA; Medpor, Stryker, Kalamazoo, MI), to augment the facial
skeleton.
Porous polyethylene is firm and flexible. It is easily carved with a scal-
pel or contoured with a rasp or motorized burr. It is best immobilized and
applied to the skeleton with screws. It can be molded to the external contours
of the skeleton by heating it in hot water, an attribute that the author utilizes
infrequently.
The favorable biocompatibility of this implant material can also be attributed
to its porous surface. Porous polyethylene has pores of sufficient size to allow
fibrous tissue ingrowth and relative host incorporation, as opposed to the host
encapsulation observed with smooth-surfaced implants. Porous polyethylene
has a continuous system of inner connecting pores approximately 125 to 250
μm in diameter. Animal studies have demonstrated that pore sizes of more than
100 μm encourage tissue ingrowth,1,2 whereas pore sizes of less than 100 μm
limit the extent of tissue ingrowth. Materials with pore sizes greater than 300
μm have drawbacks associated with material breakdown.3–5 Clinical specimens
have demonstrated rapid ingrowth of fibrous tissue after human implantation.
Rather than the dense connective tissue capsules observed with smooth-sur-
faced implants, porous polyethylene implants exhibit a thin connective tissue
membrane that is contiguous with the ingrown tissue.5 It has been noted dur-
ing revision operations that fibrous tissue ingrowth can be sufficient to result in
bleeding when the implants are modified in situ with a scalpel, and in certain
circumstances, ingrowth exhibits sufficient vascularity to allow skin grafts to be
placed directly over the implant.5
Fibrous tissue ingrowth improves the biocompatibility of porous implants
because it limits their movement. Movement is an essential factor in deter-
mining the host response to an implant.6 Because the host foreign body reac-
tion encapsulates smooth-surface implants, a smooth implant never binds to
the host bed and therefore is predisposed to move. Encapsulation of smooth
implants and their subsequent predisposition to movement are directly or
indirectly responsible for the majority of the late complications observed with
smooth implants.7–20 When used to augment the chin, smooth silicone implants
are known to cause significant bone resorption, which is attributed to implant
motion caused by the overlying mentalis muscle.21,22 Bone erosion is not clini-
cally significant unless an implant and the subsequent erosion overlies a tooth
root.23 Animal studies have demonstrated that porous implants result in less
bone resorption than do smooth implants.24 Bikhazi and Van Antwerp,25 in a
prospective cephalometric study of five patients undergoing chin augmentation
with porous polyethylene implants, did not observe bone resorption beneath
the implants. When this author has removed cheek implants at 6 months and
chin and mandibular implants at 1 year, the erosion was barely perceptible.
The use of porous implants has been criticized because, unlike smooth
implants, they require wider exposure for positioning and are more difficult
to remove.26 Personal preference and the “learning curve” have made both of
these problems less significant. Wider exposure has resulted in more accurate
implant positioning. Because the initial augmentation has been more satisfac-
tory for the majority of patients, revision surgical procedures have been infre-
44
quent. When porous polyethylene implants require removal, dissection directly
Screw fixation
on the implant minimizes adjacent soft tissue trauma. The absence of a thick
fibrous capsule allows the soft tissues to collapse after implant removal, per-
mitting restoration of the preimplant contour. This is not always the case after
silicone implant removal, where the fibrous capsule maintains the contour of
the implant.27
It is important to note that the manufacturer provides multiple implant
shapes and sizes intended for specific anatomical areas. It is unusual for the
senior author to use an implant without changing its contour (reducing it) to
meet the needs of the specific situation (Fig. 4.4).
C D 45
Chapter 4 Principles and operative technique for facial skeletal augmentation
46
Personal experience
A B
recipient site. This final adjustment can be performed with a scalpel, rasp, or
high-speed burr. It facilitates the custom carving of the implant in terms of
required gross contour and can allow creation of a clinically imperceptible tran-
sition between the implant and the recipient skeleton (Fig. 4.7).
HEMOSTASIS
PERSONAL EXPERIENCE
In 2003 the senior author’s personal experience with porous implants used for
aesthetic facial skeletal reconstruction was published.28 Most recently, the senior
47
author’s experience using predominantly porous polyethylene implants for
aesthetic facial skeletal augmentation was reviewed to determine the incidence
Chapter 4 Principles and operative technique for facial skeletal augmentation
Fig. 4.8 Suction drains are always placed during mandible angle implant augmentation.
They exit in the postauricular area. A mildly compressive tape dressing is applied over the
area of surgical dissection.
of infection over the 10-year period from January 2006 to December 2017. Dur-
ing that period, 1057 implants were placed in 661 patients. Eleven patients suf-
fered infections related to the implant surgery, resulting in an infection rate of
1% per implant and 1.6% per patient.
To date no patient has presented with a late infection, i.e., later than 3
months after surgery. It is presumed that infections that are delayed in their
clinical manifestation reflect a situation where implant contamination during
surgery was controlled by the perioperative antibiotic regimen and loss of
antibiotic suppression compromised the recovery in the contaminated area,
eventually unmasking the infection. Because the presence of biofilms limits
the efficacy of antibiotics to infectious suppression rather than cure, implant
removal is recommended when implant-related infection is confirmed. This
approach limits soft tissue-related morbidity and patient inconvenience.
There have been no materials-related problems during the ensuing period.
This is similar to the experience of others who have reported significant fol-
low-up for facial reconstruction using this material.29–39
REFERENCES
1. Klatwitter JJ, Bagwell JG, Weinstein AM, et al. An evaluation of bone growth into porous high-
density polyethylene. J Biomed Mater Res 1976;10(2):311–23.
2. Spector M, Flemming WR, Sauer BW. Early tissue infiltrate in porous polyethylene implants
into bone: a scanning electron microscope study. J Biomed Mater Res 1975;9(5):537–42.
3. Spector M, Harmon SL, Kreutner A. Characteristics of tissue growth into Proplast and porous
polyethylene implants in bone. J Biomed Mater Res 1979;13(5):677–92.
4. Berghaus A, Mulch G, Handrock M. Porous polyethylene and Proplast: their behavior in a
bony bed. Arch Otorhinolaryngol 1984;240(2):115–23.
5. Maas CS, Merwin GE, Wilson J, et al. Comparison of biomaterials for facial bone
augmentation. Arch Otolaryngol Head Neck Surg 1990;116(5):551–6.
6. Wellisz T, Kanel G, Anooshian RV. Characteristics of the tissues response to Medpor porous
48 polyethylene implants in the human facial skeleton. J Long Term Eff Med Implants 1993;3:223.
7. Wolfe SA. Correction of a persistent lower eyelid deformity caused by a displaced orbital floor
implant. Ann Plast Surg 1979;2(5):448–51.
References
8. Hoffman S. Loss of a silastic chin implant following a dental infection. Ann Plast Surg
1981;7(6):484–6.
9. Wolfe SA. Correction of a lower eyelid deformity caused by multiple extrusions of alloplastic
orbital floor implants. Plast Reconstr Surg 1981;68(3):429–32.
10. Brown AE, Banks P. Late extrusion of alloplastic orbital floor implants. Br J Oral Maxillofac
Surg 1981;68:429.
11. Mauriello Jr JA, Flanagan JC, Peyster RG. An unusual late complication of orbital floor
fracture repair. Ophthalmology 1984;91(1):102–7.
12. Davis RM. Late orbital implant migration. Ann Ophthalmol 1986;18(6):223–4.
13. Loftfield K, Jordan DR, Fowler J, et al. Orbital cyst formation associated with Gelfilm use.
Ophthal Plast Reconstr Surg 1987;3(3):187–91.
14. Sutula FC, Palu RN. Delayed chocolate cyst after blowout fracture. Ophthal Plast Reconstr
Surg 1991;7(4):267–8.
15. Marks MW, Yeatts RP. Hemorrhagic cysts of the orbit as a long-term complication of
prosthetic orbital floor implant. Plast Reconstr Surg 1994;93(4):856–9.
16. Kohn R, Romano PE, Puklin JE. Lacrimal obstruction after migration of orbital floor implant.
Am J Ophthalmol 1976;82(6):934–6.
17. Mauriello Jr JA, Fiore PM, Kotch M. Dacryocystitis: late complication of orbital floor fracture
repair with implant. Ophthalmology 1987;94(3):248–50.
18. Anderson MF. Sinusitis related to use of foreign materials to treat orbital floor injuries. Report
of two cases. J Oral Surg 1967;25(2):182–3.
19. Peak J, Haria S, Sleeman D. Facial pain due to a displaced orbital floor implant: report of case.
J Oral Maxillofac Surg 1992;50(11):1234–5.
20. Dougherty WR, Wellisz T. The natural history of alloplastic implants and orbital floor
reconstruction: an animal model. J Craniofac Surg 1994;5(1):26–32.
21. Robinson M. Bone resorption under plastic chin implants. Arch Otolaryngol 1972;95:30.
22. Friedland JA, Coccaro PJ, Converse JM. Retrospective cephalometric analysis of mandibular
bone absorption under silicone rubber chin implants. Plast Reconstr Surg 1976;57(2):
144–51.
23. Matarasso A, Elias AC, Elias RL. Labial incompetence: a marker for progressive bone
resorption in silastic chin augmentation. Plast Reconstr Surg 1996;98(6):1007–14.
24. Wellisz T, Lawrence M, Jazayeri MA, et al. The effects of alloplastic onlays on bone in the
rabbit mandible. Plast Reconstr Surg 1995;96(4):957–63.
25. Bikhazi HB, Van Antwerp R. The use of Medpor in cosmetic and reconstructive surgery:
experimental and clinical evidence. In: Stucker FJ, editor. Plastic and reconstructive surgery of
the head and neck. St. Louis: Mosby; 1990. p. 271–3.
26. Terino EO. Alloplastic contouring in the malar–mid-face–middle third facial aesthetic unit. In:
Terino EO, Flowers RS, editors. The art of alloplastic facial contouring. St. Louis: Mosby; 2000.
p. 79–96.
27. Cohen SR, Mardach OL, Kawamoto Jr HK. Chin disfigurement following removal of
alloplastic chin implants. Plast Reconstr Surg 1991;88(1):62–6.
28. Yaremchuk MJ. Facial skeletal reconstruction using porous polyethylene implants. Plast
Reconstr Surg 2003;111(6):1818–27.
29. Lacey M, Antonyshyn O. Use of porous high-density polyethylene implants in temporal
contour reconstruction. J Craniofac Surg 1993;4(2):74–8.
30. Wellisz T, Dougherty W. The role of alloplastic skeletal modification in the reconstruction of
facial burns. Ann Plast Surg 1993;30(6):531–6.
31. Rubin PA, Bilyk JR, Shore JW. Orbital reconstruction using porous polyethylene sheets.
Ophthalmology 1994;101(10):1697–708.
32. Couldwell WT, Chen TC, Weiss MH, et al. Cranioplasty with Medpor porous polyethylene
Flexblock implant. J Neurosurg 1994;81(3):483–6.
33. Frodel JL, Lee S. The use of high-density polyethylene implants in facial deformities. Arch
Otolaryngol Head Neck Surg 1998;124(11):1219–23.
34. Turegun M, Sengezer M, Guler M. Reconstruction of saddle nose deformity using porous
polyethylene implants. Aesthetic Plast Surg 1998;22(1):38–41.
35. Romo III T, Sclafani AP, Sabini P. Use of porous high-density polyethylene in revision
rhinoplasty and in the platyrrhine nose. Aesthetic Plast Surg 1998;22:221.
36. Choi JC, Fleming JC, Aitken PA, et al. Porous polyethylene channel implants: a modified
porous polyethylene sheet implant designed for repairs of large and complex orbital wall
fractures. Ophthal Plast Reconstr Surg 1999;15(1):56–66.
37. Niechajev I. Porous polyethylene implants for nasal reconstruction: clinical and histologic
studies. Aesthetic Plast Surg 1999;23(6):395–402.
38. Janecka IP. New reconstructive technologies in skull base surgery: role of titanium mesh and
porous polyethylene. Arch Otolaryngol Head Neck Surg 2000;126(3):396–401.
39. Ng SG, Madill SA, Inkster CF, et al. Medpor porous polyethylene implants in orbital blowout 49
fracture repair. Eye 2001;15:578–82.
Chapter 5
Cranioplasty
SKULL ANTHROPOMETRY
The position and shape of the forehead are largely responsible for the appear-
ance of the upper face. The important aesthetic variables are its inclination, its
relation to the globes, and the relative prominence of its frontal sinus. The brows
and the frontal hairline are surface landmarks that overlie the frontal area. Their
shape and location also have a powerful impact on facial appearance.
Normal values for certain dimensions of the frontal area are presented in
Figs. 5.1, 5.2, and 5.3.1–3 The bitemporal distance or width of the upper face is
similar in men and women (Fig. 5.1). Because men’s heads and their features
are, on the average, larger than women’s, this implies that the upper third of
women’s faces is relatively wide. The inclination of the forehead is more ver-
tical in women than it is in men (Fig. 5.2). More often in males, frontal sinus
development creates a prominence in the central lower forehead that is absent
or vestigial in females. In summary, when compared to men’s, the upper third
of women’s faces is relatively flat, vertical, and wide. These values and relations
should be kept in mind when reconstructing cranial defects or addressing aes-
thetic concerns in the frontal area.
The relationship of the orbital rims to the globe is a primary determinant
of the appearance of the upper one-third of the face (Fig. 5.3). On the aver-
age, the surface of the soft tissues overlying the supraorbital rim lies 10 mm 53
anterior to the cornea, while projecting 13 mm beyond the infraorbital rim.
Chapter 5 Cranioplasty
Male Female
116 + 4 111 + 5
ft-ft (116 mm) Bitemporal
ft-ft (111 mm)
Bigonial
Fig. 5.1 Normal values in millimeters for upper, middle, and lower facial width in white North American adult men (ages 19 to 25) (n = 109)
and young white North American women (n = 200).1 Bitemporal distance (ft–ft) is measured from frontotemporal (ft) to frontotemporal,
which is the point on each side of the forehead, laterally from the elevation of the linea temporalis. Bizygomatic distance (zy–zy) is measured
from zygion (zy) to zygion, which is the most lateral point of each zygomatic arch. The bigonial distance (go–go) is measured from gonion
(go) to gonion, which is the most lateral point of the mandibular angle close to the bony gonion. Because men’s heads and their features are,
on the average, larger than women’s, this implies that the upper third of women’s faces are relatively wide. Note that the male lower face is
both relatively and absolutely wider than that of the female.
A B
When the orbital rims have a greater projection beyond the anterior surface of
the cornea, the eyes appear “deep set.” When the orbital rims project less, the
eyes appear prominent. Certain craniosynostoses result in underdevelopment
of the frontal bone and midface with marked projection of the globe beyond
the orbital rims. When this disproportion is severe enough to cause symp-
54 toms due to corneal exposure or to be disfiguring, osteotomies are performed
to allow skeletal advancement and improvement of globe–rim relationships.
When globe–rim disproportions are less severe they are usually left untreated.
Cranioplasty for full-thickness defects
Fig. 5.3 Sagittal relations of the anterior surface of the cornea to the soft
tissues overlying the supraorbital and infraorbital rims. On average, in the
young adult, the supraorbital rim projects 10 mm beyond, the infraorbital
rim lies 3 mm behind, and the cheek prominence projects 2 mm beyond the
anterior surface of the cornea.1–3
10 mm
3 mm
2 mm
Indications
The most frequent indication for cranioplasty is the full-thickness skull defect
resulting from the infectious loss of a craniotomy graft after elective craniotomy.
A frequent cause of craniotomy graft (referred to as a “bone flap” by most neuro-
surgeons) loss results not from contamination at surgery but rather from wound-
closure breakdown. This is precipitated by the common practice of making the
osteotomy directly under the scalp incision. The resulting dead space directly
beneath the suture line makes the soft tissue closure tenuous. The situation is fur-
ther aggravated when plates and screws used to stabilize the replaced bone are
positioned directly beneath the suture line. Minimal trauma can result in hardware
and bone graft exposure with secondary infection (Fig. 5.4). This can be avoided
by planning the scalp flap well beyond the perimeter of the cranial osteotomy inci-
sions. This avoids scalp incisions directly overlying bone incisions, as well as the
possibility of fixation hardware being placed directly beneath the soft tissue closure.
In addition to its protective and contour-restorative functions, cranioplasty
may also improve speech problems and hemiparesis if the skull defect is large
enough to allow the scalp to exert direct pressure on the brain (“syndrome of the
trephined”).6–9 Skull defects of greater than 2 or 3 cm should be considered for
repair. However, this decision varies with location. Even small defects in the fron- PEARL
tal area can be disturbing to the patient and therefore can be considered for repair.
Scalp incisions that directly overlie
Cosmetic appearance alone can be an indication for repair such as small fixation hardware risk later wound
defects in the non-hair bearing and usually visible frontal area. On the other dehiscence.
hand, small defects of the temporal and occipital areas, which are covered by
thick muscle, are usually not reconstructed.
Timing of surgery 55
Cranioplasty is performed when the soft tissue envelope is closed and acute
infection as well as risk factors for recurrent infection are eliminated. This
Chapter 5 Cranioplasty
requires the removal of all devitalized tissues and any foreign bodies. Prepara-
tion requires the treatment of any frontal or ethmoidal sinus inflammatory dis-
ease. It also requires that any potential communications between the sinuses and
the planned cranioplasty graft be eliminated. Large communications between
the sinuses and the anterior cranial fossa, which may be the case after massive
trauma requiring frontal sinus cranialization or after tumor removal, require
placement of a vascularized barrier for effective isolation. A galea frontalis flap,
if available and adequate, or a free tissue transfer may be required. Finally, the
adequacy of the soft tissues to provide secure closure at the time of elective cra-
nioplasty must be assured. This may require a preliminary scalp expansion or
flap reconstruction before or at the time of cranioplasty.
A significant reduction in incidence of infection has been shown when 1 year
is allowed to elapse between the initial injury or infection and the subsequent
reconstruction.10–12 In the senior author’s experience, a 6-month infection-free
period has been sufficient to assure that infection has been adequately treated.
Materials
Both autogenous bone and alloplastic materials are used to reconstruct the skull.
Bone is championed by many craniofacial surgeons because it becomes
revascularized to varying extents by the host and therefore is less susceptible to
infection and late complications. It has the disadvantages of requiring a donor
site, being technically demanding and time-consuming to perform, exhibiting
variable resorption, and therefore being prone to irregular contour. When bone
is used for cranioplasty, resorption of between 25% to 40% has been demon-
strated.10 Its use alone does not address the problem of intracranial dead space.
While craniofacial surgeons traditionally advocate the use of bone for cra-
nioplasty, the vast majority of neurosurgeons use alloplasts, most often poly-
methylmethacrylate (PMMA). In reviewing the experience of 42 posttraumatic
reconstructions of frontal defects in which both bone and acrylic were used,
Manson et al.10 found that the material employed was not as important as the
timing of reconstruction and the treatment of sinus disease. In the past, the
senior author used bone when there had been recurrent infection or when over-
56 lying soft tissues were compromised (e.g., after radiation therapy). However, at
present, he uses alloplastic materials almost exclusively for cranioplasty.
Cranioplasty for full-thickness defects
The alloplastic materials used for cranioplasty include PMMA, porous poly-
ethylene, polyether ether ketone (PEEK), polymethylmethacrylate-polyhy-
droxyethylmethacrylate (HTR), titanium mesh, and hydroxyapatite.
The chemical composition and attributes of the alloplastic materials used for
cranioplasty are detailed in Chapter 3.
A B
Fig. 5.5 Acrylic cranioplasty by plastic sleeve molding technique. (A) Intraoperative view of right frontoparietal defect. (B) Molding of methyl
methacrylate to defect. (C) Postoperative result. From Yaremchuk MJ, Rubin JP. Surgical repair of major defects of the scalp and skull. In
Schmidek HH, ed: Operative Neurosurgical Techniques, 4th ed. Philadelphia, WB Saunders, 2000, with permission.
area to be augmented, leaving the head and two or three threads above the bone
surface. The acrylic is then poured over the screw so that it is incorporated in
the construct.
The implant may be perforated to allow the dura to be tented up to it. This
method lessens the potential for epidural collection. Perforations in the implant
also allow drainage and soft tissue ingrowth, which also aids in implant fixation.
Hydroxyapatite
Hydroxyapatite is available in a powdered form that, when mixed with water,
becomes a paste that is easily applied to regular surfaces. The paste sets in
approximately 20 minutes. Because of its low flexural resistance, it is recom-
mended for use as an onlay material to improve contour. It has been used with
metallic mesh to reconstruct defects. In this application, Zins reported a high
complication rate of 42.8%, with some complications occurring as late as 4 years
postoperatively. The main problems observed at reoperation were fragmenta-
tion of the hydroxyapatite cement, exudation, and severe soft tissue inflamma-
tory reaction.14 Others have cautioned about the use of this material for vault
58 reconstruction.15
Cranioplasty for full-thickness defects
Titanium mesh
Titanium mesh can be used alone to replace skull defects when precise resto-
ration of skull contour is not paramount and brain volume can expand to the
inner surface of the implant eliminating intracranial dead space. Cranioplasties
utilizing mesh alone are susceptible to contour deformation when subjected to
blunt trauma.
A B
Fig. 5.6 Acrylic cranioplasty by mesh-onlay technique. (A) Intraoperative view of titanium mesh spanning defect. (B) PMMA spread over
metallic template.
59
Chapter 5 Cranioplasty
A B
C D E
Fig. 5.7 A 60-year-old woman presented with an exposed cranial implant. By history, an asymptomatic aneurysm was treated through a left-
sided frontotemporal craniotomy. The craniotomy graft was lost to infection. A hydroxyapatite cement-and-mesh cranioplasty was performed
and was subsequently removed due to infection. Six months later, a custom HTR implant was fabricated by using three-dimensional CT data.
This became exposed. A CT scan was obtained, which showed communication between the frontal sinus and the implant. At surgery the
implant was removed and a rectus abdominis myocutaneous free flap was used to obliterate dead space in the wound, separate the frontal
sinus from the anticipated cranioplasty implant, and provide a closed soft tissue wound. Six months later, a tissue expander was placed in
the hair-bearing scalp. When the scalp was sufficiently expanded to provide hair-bearing scalp adequate to replace that lost to infection, the
expander was removed, a custom porous polyethylene implant was placed and covered with the expanded hair-bearing scalp. (A) Patient
with exposed implant. (B) Intraoperative view at time of implant removal. Arrow points to communication with frontal sinus. (C) Appearance
after rectus abdominis myocutaneous free flap wound closure. (D) Tissue expander used to expand hair-bearing scalp. (E) Skull model
obtained from three-dimensional CT scan data showing cranial defect. (F) Skull model and custom implant. (G) Appearance after custom
60 implant cranioplasty.
Functional cranioplasty
Drain
Fig. 5.8 A CAD/CAM implant immobilized with lag screws. The screw
heads are countersunk to avoid prominence above the implant surface. A
Implant channel for a drain to be placed between the dura and implant can also be
incorporated into the implant design.
Dura
Cranium
Brain
FUNCTIONAL CRANIOPLASTY
61
Chapter 5 Cranioplasty
Drug-resistant epilepsy
The NeuroPace Neuromodulation System (NeuroPace Inc., Mountain View,
CA) is a device developed to treat drug-resistant epilepsy. This device
can be incorporated into a cranial implant as shown in Fig. 5.9. CT scan
data was used to create an implant that replaced a resorbed bone flap
while incorporating the NeuroPace device within the implant contour.
Intracerebral leads are placed for control of seizure foci not amenable to
antiseizure medication. After they are placed, they are connected to the
neurostimulator and the entire complex is placed within the laser-cut por-
tion of the cranial implant. The PMMA implant is transparent allowing
visualization of the orientation of the stimulator and its leads as well as the
status of the operative field.
62
Cranioplasty for contour irregularities
A B
Shunt mechanism
A functional implant designed to house a shunt mechanism within its contours
is shown in Fig. 5.10. The ring implant is fixed to the cranium at the desired loca-
tion and functions as a cutting guide. Various housings are fixed to the guided
craniotomy defect to house the functional implant. Video 5.1 demonstrates the
operative placement.
63
Chapter 5 Cranioplasty
C D
64
Cranioplasty for contour irregularities
B C D
F G H
Fig. 5.12 A woman with Parry–Romberg syndrome underwent onlay rib frontal cranioplasty at age 21. The
grafts resorbed. At age 46 she underwent frontoorbital reconstruction with a custom porous polyethylene
implant. Her enophthalmos was corrected by implant augmentation of her internal orbit. (A) Preoperative
appearance. (B) Preoperative three-dimensional CT scan shows skeletal deficiency. (C) Skull model obtained
from three-dimensional CT data. (D) Skull model with custom implant. (E) Postoperative appearance. (F) 65
Intraoperative view. There is no remnant of previously placed onlay bone grafts. (G) Intraoperative view
shows custom implant in place. (H) Intraoperative view shows PMMA used to feather implant native skull
transition beneath extremely thin forehead skin.
Chapter 5 Cranioplasty
REFERENCES
1. Farkas LG, Hreczko TA, Katic MJ. Craniofacial norms in North American Caucasians from
birth (one year) to adulthood. Appendix A. In: Farkas LG, editor. Anthropometry of the head
and face. 2nd ed. New York: Raven Press; 1994.
2. Whitaker LA, Morales L, Farkas LG. Aesthetic surgery of the supraorbital ridge and forehead
structures. Plast Reconstr Surg 1986;78(1):23–32.
3. Bartlett SP, Wornom I, Whitaker LA. Evaluation of facial skeletal aesthetics and planning. Clin
Plast Surg 1991;18(1):1–9.
4. Pessa JE, Desvigne LD, Lambros VS, Nimerick J, Sugunan B, Zadoo VP. Changes in ocular
globe-to-orbital rim position with age: implication for aesthetic blepharoplasty of the lower
eyelids. Aesth Plast Surg 1999;23(5):337–42.
5. Marchac D. Relationship of the orbits to the upper eyelids. Clin Plast Surg 1981;8(4):717–24.
6. Grantham EG, Landis HP. Cranioplasty and posttraumatic syndrome. J Neurosurg 1948;5:19.
7. Carmichael FA. The reduction of hernia cerebri by tantalum cranioplasty. A preliminary
report. J Neurosurg 1945;2:379.
8. Tabaddor K, LaMorgese J. Complication of a large cranial defect. Case report. J Neurosurg
1976;44(4):506–8.
9. Stula D. The problem of “sinking skin-flap syndrome” in cranioplasty. J Craniomaxillofac Surg
1982;10(3):142–5.
10. Manson PN, Crawley WA, Hoopes JE. Frontal cranioplasty: risk factors and choice of cranial
vault reconstructive material. Plast Reconstr Surg 1986;77(6):888–904.
11. Hammon WM, Kempe LG. Methyl methacrylate cranioplasty: 13 years’ experience with 417
patients. Acta Neurochir 1971;25(1):69–77.
12. Rish BL, Dillon JD, Meirowsky AM, et al. Cranioplasty: a review of 1030 cases of penetrating
head injury. Neurosurgery 1979;4(5):381–5.
13. Stelnicki EJ, Ousterhout DK. Prevention of thermal tissue injury induced by the application of
polymethylmethacrylate to the calvarium. J Craniofac Surg 1996;7(3):192–5.
14. Zins JE, Moreira-Gonzalez A, Papay FA. Use of calcium-based bone cements in the repair of
large, full-thickness cranial defects: a caution. Plast Reconstr Surg 1946;120(5):1332–42.
15. Matic D, Phillips JH. A contraindication for the use of hydroxyapatite cement in the pediatric
population. Plast Reconstr Surg 2002;110(1):1–5.
16. Wehmoller MW, Eufinge H, Kruse D, Massberg W. CAD by processing of computed
tomography data and CAM of individually designed prostheses. Int J Oral Maxillofac Surg
1995;24:90–7.
17. Eufinger H, Wehmoller MW, Machtens E, et al. Reconstruction of craniofacial bone
defects with individual alloplastic implants based on CAD/CAM manipulated CT data. J
Craniomaxillofac Surg 1995;23:175–81.
18. Bergey GK, Morrell MJ, Mizrahi EM, Goldman A, King-Stephens D, Nair D, et al. Long-
term treatment with responsive brain stimulation in adults with refractory partial seizures.
Neurology 2015;84(8):810–7.
19. Wei Z, Gordon CR, Bergey GK, Sacks JM, Anderson WS. Implant site infection and bone flap
osteomyelitis associated with the NeuroPace responsive neurostimulation system. World
Neurosurg 2016;88(687):e1–6.
20. Gordon CR, Santiago GF, Huang J, Bergey GK, Liu S, Armand M, Brem H, Anderson WS.
First in-human experience with complete integration of neuromodulation device within a
customized cranial implant. Oper Neurosurg 2018;15(1):39–45.
66
Video 5.1 InvisiShunt Implant. Courtesy of Longeviti Neuro.
66.e1
Chapter 6
Temporal augmentation
When the temporal area has not been surgically violated, concavity gradually
appears with senescence.1 It may appear in patients with low body fat, hence less
temporal fat, and after massive weight loss. It may occur as a result of HIV-asso-
ciated lipodystrophy and radiation-induced soft tissue atrophy. In other healthy
patients, prominent adjacent skeletal contour may diminish the relative projec-
tion of the temporal soft tissues. Therefore, augmenting the contours of the tem-
poral area can have a rejuvenating and/or a balancing effect on facial appearance.
Both aesthetic and reconstructive procedures that involve the temporal area
may result in temporal hollowing. Aesthetic surgeries that access the midface
via separation of the temporal fascial planes can also result in depression in the
temporal fossa. Temporal depressions also occur after neurosurgical procedures
during temporal or pterional craniotomy where detachment of the temporalis
muscle from its origin at the temporal crest or the lateral orbital rim is required.
Reattachment of temporalis muscle often yields suboptimal results, leading to
significant depressions beneath the temporal line. Moreover, the deformity is
exaggerated by the overlying soft tissues that are thinned out due to atrophy
or posttraumatic scarring. Temporal augmentation can restore the presurgical
appearance in these patients.
67
Chapter 6 Temporal augmentation
TREATMENT OPTIONS
Several procedures have been described to augment the contour of the temporal
area. These include the use of various alloplastic implants, free fat grafting, injec-
tion of various absorbable and permanent filler materials, and in some instances,
vascularized flaps.
Temporal augmentation with autologous fat grafting has been associated
with difficult irregularities.2 In fact, the temporal region is one of the subunits
with the lowest satisfaction rate after facial fat grafting.3 Patients with thick
skin generally experience the best results with fat injection; however, thick skin
is not a typical quality in patients with temporal hollowing due to senescence.
Besides skin irregularities and edema,2 other severe, but rare, complications
such as blindness and cerebral fat embolism have been reported.4–6 A thorough
knowledge of the clinical anatomy of the temporal region is crucial for the safe
performance of temporal fat grafting.7
Similarly, temporal augmentation with filler materials (e.g., hyaluronic acid)
produces similar contour irregularities. Adopting the technique of diluting
calcium-based fillers for the dorsum of the hand, Lambros described a tech-
nique for filling the temples with highly diluted hyaluronic acid.2 This dilution
method allows the filler to be distributed more evenly in the temporal area,
resulting in a more satisfactory outcome.2
Augmenting the temporal region with various alloplastic materials has
been described. Contour irregularities at the interface of the implant edge and
native anatomy are not uncommon. This chapter describes the senior author’s
use of polymethylmethacrylate (PMMA) to fill depressions in the temporal
area.8 In instances when no previous surgery has been performed or when the
temporal area has served as a dissection plane to access adjacent areas (e.g.,
subperiosteal facelift), the implant material is placed beneath the temporal
muscle through a limited incision in the hair-bearing scalp. When previous
reconstructive surgery has been performed in the temporal area, the surgi-
cal incision scars are used to access the area of depression for placement of
PMMA over the temporal muscle. The author’s techniques using PMMA to
reconstruct temporal contour depressions have been reliable, durable, and
relatively free of complications.
Access
A 5- to 6-cm vertical incision is made above the helix, within the hair-bear-
ing temporal scalp. The scalp flap is undermined anteriorly for 2 to 3 cm
before the deep temporal fascia and the underlying temporalis muscle are
incised along the direction of the vertically oriented muscle fibers. The tem-
poralis muscle is split and dissection is continued to reach the temporal
fossa (Fig. 6.2A).
68
Operative technique: aesthetic temporal augmentation
Temporalis m.
incision
Skin
incision
Pocket
A B
Fig. 6.2 Surgical incisions to access implant material beneath temporalis muscle. (A) Staggered scalp incisions and temporalis muscle
incisions to avoid suture lines overlying implant. (B) Exposure of space between temporal muscle and temporal fossa.
level as the lateral orbital rim. Any areas of overcorrection (not uncommon lat-
PEARL
erally after molding the material to be flush with the lateral orbital rim) are
revised with a contouring burr. The muscle and the temporal fascia are reap- It is better to underaugment the
proximated and the scalp incision is closed in layers after a satisfactory tempo- temporal contour – since any
ral contour has been achieved. implant undercorrection will be an
improvement, while any contour
excess is distracting.
Clinical example
A 35-year-old man presented with asymmetry and imbalance of his facial con-
tour. He was displeased with the bitemporal hollowing, which he felt was exag-
gerating the excessive width of his preauricular contour. In two procedures, he
underwent augmentation of the posterior/inferior mandible, augmentation of
the infraorbital rim, superficial parotidectomy, facelift, and temporal augmen-
tation using PMMA via the submuscular approach (Fig. 6.4).
Temporalis m.
Orbital rim
70 A B
Operative technique: postsurgical temporal muscle violation
Access
Surgical scars from the previous procedure are utilized to access the temporal
depression. A scalp flap is raised extending to the lateral orbital rim. The level
of dissection is determined by the clinical situation but the path of the frontal
branch of the facial nerve is always protected.
Attenuated temporalis m.
Fig. 6.5 Diagrammatic representation of titanium screws placed in the lateral orbital rim to function as 71
anchors for the temporal implant.
Chapter 6 Temporal augmentation
Anchor screw
Methyl methacrylate
Attenuated temporal m.
Anchor screws
allows all the deficiencies in the temporal area (bone, muscle, and scalp) to be
addressed and corrected during implant contouring. Areas of overcorrection
are revised with a contouring burr. A suction drain is placed, which exits from a
separate stab-wound incision. The scalp incision is closed in layers.
Clinical example
A 36-year-old female presented with temporal hollowing after craniotomy to
repair a cerebral aneurysm. The temporal hollowing was corrected, filling the
depression with PMMA over the temporalis muscle (Fig. 6.7).
PERSONAL EXPERIENCE
A B
REFERENCES
1. Whitaker LA. Temporal and malar-zygomatic reduction and augmentation. Clin Plast Surg
1991;18(1):55–64.
2. Lambros V. A technique for filling the temples with highly diluted hyaluronic acid: the
“dilution solution”. Aesthet Surg J 2011;31(1):89–94.
3. Mojallal A, Shipkov C, Braye F, Breton P, Foyatier JL. Influence of the recipient site on the
outcomes of fat grafting in facial reconstructive surgery. Plast Reconstr Surg 2009;124(2):471–83.
4. Hu J, Chen W, Wu Y, et al. Middle cerebral artery occlusion following autologous bitemporal
fat injection. Neurol India 2011;59(3):474–5.
5. Jiang X, Liu DL, Chen B. Middle temporal vein: a fatal hazard in injection cosmetic surgery for
temple augmentation. JAMA Facial Plast Surg 2014;16(3):227–9.
6. Lu L, Xu X, Wang Z, Ye F, Fan X. Retinal and choroidal vascular occlusion after fat injection into
the temple area. Circulation 2013;128(16):1797–8.
7. Huang RL, Xie Y, Wang W, et al. Anatomical study of temporal fat compartments and its
clinical application for temporal fat grafting. Aesthet Surg J 2017;37(8):855–62.
8. Gordon CR, Yaremchuk MJ. Temporal augmentation with methyl methacrylate. Aesthet Surg J
2011;31(7):827–33. 73
9. Ousterhout DK. Aesthetic contouring of the craniofacial skeleton. 1st ed. Boston: Little: Brown; 1991.
Chapter 7
Internal orbit
The size and shape of the internal orbit determines orbital volume and the posi
tion of the eye. An increase in orbital volume results in enophthalmos – the
recession of the ocular globe within the bony orbit. The principal mechanism in
its development is the displacement of a relatively constant volume of orbital
soft tissue into an enlarged bony orbit. Posttraumatic fat atrophy and scar con
tracture are real, but less important, factors in causing a mismatch of soft tissue
and orbital volume.1–3 Recession of the globe changes the drape of the upper lid
on the globe, tending to deepen the superior tarsal fold and cause a lowering or
pseudoptosis of the upper lid (Fig. 7.1). Two to three millimeters of enophthal
mos is clinically detectable, and more than 5 mm is disfiguring.
Enophthalmos may result from fractures involving only the orbital floor or
medial orbital wall. These are termed “pure blowout” fractures. More often,
enophthalmos is part of an orbital deformity whereby not only the internal orbit A
is disrupted, but also the adjacent facial skeleton. The internal orbit disruption
is referred to as an “impure blowout” fracture in these situations.
Because posttraumatic enophthalmos is primarily due to damage of the inter
nal orbit, the treatment strategy for restoring eye position is anatomic skeletal
reconstruction. This is best accomplished by defining the location and extent of
injury preoperatively with computed tomographic (CT) scans, widely expos
ing the injured area, retrieving displaced orbital soft tissues, and replacing the
invariably comminuted fractured skeleton.1–3
ORBITAL ANATOMY
constriction behind the globe (Fig. 7.2). Loss of this convexity transforms the
internal orbit shape from pyramidal to spherical, increasing orbital volume
and tending towards enophthalmos (Fig. 7.3). Certain injuries, usually involv
ing the lateral orbital wall or roof, may result in inward displacement of larger
fracture segments. These “blow-in” fractures decrease orbital volume, result
ing in globe proptosis.
There are nine openings within each orbit. Most important are the optic
foramen, and the superior and the inferior orbital fissures. The optic fora
men, located at the apex, transmits the optic nerve. The superior orbital fis
sure, located between the roof and the lateral wall near the apex, transmits the
oculomotor, the trochlear, the ophthalmic division of the trigeminal, and the
abducent nerves. The inferior orbital fissure separates the lateral wall from the
Fig. 7.2 Orbit with its constituent bones and communications. Note
convex shape (blue arrow) of inferomedial aspect of internal orbit.
Superior orbital fissure
Optic canal
Inferior orbital
fissure
Infraorbital foramen
Conjunctiva
Lateral rectus m.
Optic n. Optic n.
Enophthalmos
76 Fig. 7.3 Sagittal section of orbit. (A) Intact skeleton with globe position. (B) Disrupted orbital floor with globe displacement. Loss of convexity
of floor increases orbital volume and tends towards enophthalmos.
Operative technique
floor. Through this fissure the orbit communicates with the temporal, infratem
poral, and pterygopalatine fossae. It transmits the maxillary nerve, its zygo
matic branch, and the ascending branches from its sphenopalatine branch. It
also transmits the infraorbital vessels and the vein that connects the inferior
ophthalmic vein with the pterygoid venous plexus. The supraorbital foramen,
infraorbital canal, anterior and posterior ethmoidal foramina, and zygomatic
foramen transmit their respective neurovascular structures. There is also a canal
for the nasolacrimal duct.
PREOPERATIVE EVALUATION
Physical examination
The clinical diagnosis of significant internal orbital disruption is based on
globe malposition. In the uninjured state, the cornea extends approximately
16 to 17 mm anterior to the lateral orbital rim. Immediately after injury,
however, globe position may appear normal or proptotic, owing to soft
tissue swelling. Without significant edema, a difference in globe position
is most easily determined by viewing the globe from the worm’s eye. On
frontal view, a deepening of the supratarsal sulcus and a lowering of the
upper lid margin (pseudoptosis) reflects an increase in orbital volume and
subsequent recession of the globe (Fig. 7.1). When the lateral orbital rim
is intact (isolated floor or medial wall blowout fractures), the severity of
enophthalmos can be determined with a Hertel exophthalmometer, which
measures the difference between the anterior corneal surface and the lateral
orbital rim.
Radiologic imaging
CT imaging best determines the presence and extent of injury. Plain X-rays will
confirm the presence of fractures but will not define the injury or the status of
the soft tissues. The ideal preoperative evaluation consists of thin-slice axial,
coronal, and sagittal CT sections using both bone and soft tissue windows. By
adding together the consecutive CT slices where a defect appears, one can deter
mine the size of a floor or wall injury. Defects greater than 25% of the orbital
floor will result in clinically measurable enophthalmos. Those involving more PEARL
than half of the floor will result in obvious enophthalmos. Diplopia may result
The size of orbital floor defects can
from eye muscle contusion or muscle entrapment. This can be differentiated on be quantified by adding coronal and
physical exam using the forced duction test and, often, by high-resolution CT sagittal CT scan sections.
scan.
OPERATIVE TECHNIQUE
Timing
In the acute phase, CT findings coupled with forced duction testing provide the
best guide to the need for surgery.
If surgery is thought appropriate, it should be performed soon after injury,
when dissection is more straightforward, and soft tissue scarring and contrac
ture are less problematic. Late and secondary reconstructions are less successful
than appropriate reconstruction performed in the acute phase. When indica
tions for acute management are unclear, exploration is performed if enophthal
mos greater than 2 mm develops at any time within the first 6 weeks following 77
injury.4,5
Chapter 7 Internal orbit
Exposure
Proper repositioning of the globe requires exposure and anatomic reconstruc
tion of the internal orbit. A transconjunctival retroseptal incision, often with
a lateral canthotomy extension, provides excellent exposure to approach the PEARL
orbital floor and lower medial and lateral walls. The transcaruncular approach
affords added exposure to the medial wall. Skin and skin–muscle flaps that Periorbital fractures should be
reduced and fixed prior to internal
delaminate and relaminate the lower lid can result in lid malposition when orbit reconstruction.
used in the trauma setting.6 Extensive subperiosteal dissection of the lateral
orbit will detach the lateral canthus. It should be repositioned at closure.
Fig. 7.4 A thick piece of silicone sheeting is placed beneath the retrieved
orbital contents to prevent the soft tissues from prolapsing into the
maxillary antrum when the retractor is repositioned.
78
Operative technique
hence the limits of the defect. This process is complicated by the location and
extent of the injury. The bony landmark that is usually most difficult to identify
is the posterior ledge of the remaining intact orbital floor. When the orbital floor
disruption extends far posterior and intact bone cannot be visualized, it can be
located by placing the end of an elevator against the posterior wall of the maxil
lary sinus and elevating it until it meets resistance, which indicates contact with
the intact posterior remnant of the orbital floor. This structure is usually 35 to 40
mm from the infraorbital rim (Fig. 7.6).
A B
Fig. 7.5 Inferior orbitotomy simplifies retrieval of prolapsed orbital contents from the maxillary sinus and identification of intact bony
landmarks. Anatomic replacement of the osteotomized rim segment is simplified by adapting a microplate to the rim, drilling holes,
and temporarily fixing the intact rim prior to making the osteotomy. (A) Location of orbitotomy. (B) Replacement of rim segment after
reconstruction of defect.
Periosteal elevator
79
Chapter 7 Internal orbit
A B
Fig. 7.7 (A) Defect of orbital floor. (B) Orbital floor reconstructed with graft spanning the defect. Stable adjacent ledges make bone graft or
implant positioning relatively straightforward.
When reconstructing injuries to one orbital wall, the surgeon first defines
the defect by identifying intact bone edges and then spans the defect with
an implant or autogenous graft (Fig. 7.7). The size of the defect and the
normal configuration of the injured area will dictate the dimensions, thick
ness, and number of grafts. For example, a small floor defect is usually
reconstructed with a single thin implant, replicating the relatively flat shape
of the orbital floor. A similarly dimensioned inferomedially located defect
usually requires a thick implant or stacked implants to recreate the convex
shape of the orbit in this area. Failure to replicate this convexity effectively
increases the volume of the orbit from normal and tends towards enophthal
mos. Similarly, placement of an overly thick implant to reconstruct the floor
would also create an internal orbit shape different from normal. In this case,
the abnormal convexity beneath the globe would elevate it, resulting in an
ocular dystopia. For injuries involving only the floor, the senior author rou
tinely uses an alloplastic implant. Implants are immobilized with titanium
screws.
Injuries involving two or more walls of the orbit are problematic. Rigid fixa
tion techniques allow these complex injuries to be subdivided into a series of PEARL
smaller, more manageable areas for reconstruction. Implants designed to mimic
Definition of intact skeletal ledges is
the contours of the orbital floor and medial wall allow combined floor and key to placing implants.
medial wall injuries to be reconstructed with a single implant13 (Fig. 7.8).
Implant materials
Materials available for reconstruction include bone, cartilage, smooth and
porous plastics, as well as metal.
Reconstruction with autogenous bone has the conceptual advantage
that it will, in time, become vascularized and incorporated into the skel
80 eton, thereby resisting migration, extrusion, and infection. Revasculariza
tion, however, also predisposes the graft to resorb, with a concomitant
Operative technique
muscles with the possibility of ocular motility disorder. To avoid this potential
problem, polyethylene implants are now available with a smooth surface on the
inner side of the orbit and a porous surface on the other. The smooth surface
is designed to face the orbital soft tissue contents and the porous side to face
the sinuses. The smooth surface is intended to prevent soft tissue ingrowth and
possible motility problems, while the porous side allows soft tissue ingrowth
with concomitant immobilization.
Laminated implants of titanium metal and polyethylene are available (Fig.
7.9). A titanium infrastructure is sandwiched between a sheet of smooth poly
ethylene on one side and a sheet of porous polyethylene on the other. The metal
facilitates implant conformability and screw fixation. The smooth laminate is
intended to interface with the soft tissue while the porous laminate is intended
to interface with the mucosal surface.
Video 7.1 demonstrates the reconstruction of an orbital floor blowout frac
ture using a titanium mesh implant.
82
Clinical examples
CLINICAL EXAMPLES
Clinical examples of patients treated with the techniques described are pre
sented in Figs. 7.10 and 7.11).
B C
D E F
Fig. 7.10 A 30-year-old man was assaulted with a pipe. Surgery was performed through coronal, transconjunctival with lateral canthotomy,
and intraoral incisions. The internal orbit was reconstructed with titanium mesh. (A) Preoperative coronal CT scan. (B) Preoperative sagittal
CT scan. The arrow points to the intact ledge of the posterior orbital floor discussed in Fig. 7.6. (C) Postoperative coronal CT scan. (D)
Postoperative sagittal CT scan. (E) Postoperative axial CT scan. (F) Postoperative three-dimensional CT scan. (G) Postoperative worm’s eye 83
view.
Chapter 7 Internal orbit
A B
C D
E F G
Fig. 7.11 A 32-year-old woman was struck by an automobile and suffered multiple injuries including a right orbital fracture. The internal
orbit was not reconstructed acutely and the patient developed enophthalmos as well as a loss of malar prominence. The patient presented
for secondary reconstruction 9 months after her initial repair. Surgery was performed through a transconjunctival retroseptal with lateral
canthotomy and intraoral incisions. The internal orbit as well as the lateral and inferior orbital rims were reconstructed with porous
polyethylene implants immobilized with titanium screws. (A) Preoperative frontal view. (B) Postoperative frontal view. (C) Preoperative
worm’s eye view. (D) Postoperative worm’s eye view. (E) Three-dimensional CT scan showing initial reconstruction. (F) Preoperative coronal
CT scan showing enlarged, unrepaired internal orbit. (G) Intraoperative view of internal orbit reconstruction with screw-immobilized porous
polyethylene implants.
REFERENCES
1. Bite U, Jackson IT, Forbes GS, et al. Orbital measurements in enophthalmos using three-
dimensional CT imaging. Plast Reconstr Surg 1985;75:502–11.
2. Manson PN, Clifford CM, Su CT, et al. Mechanisms of global support and posttraumatic
enophthalmos. I. The anatomy of the ligament sling and its relation to intramuscular cone
orbital fat. Plast Reconstr Surg 1985;77:193–200.
3. Manson PN, Grivas A, Rosenbaum A, et al. Studies on enophthalmos. II. The measurement of
orbital injuries and their treatment by quantitative computed tomography. Plast Reconstr Surg
1985;77:201–9.
84 4. Hawes MJ, Dortzbach RK. Surgery on orbital floor fractures (influence of time and repair and
fracture size). Ophthalmology 1983;90:1066–72.
References
5. Wilkins RB, Havins WE. Current treatment of blowout fractures. Ophthalmology 1982;89:464–72.
6. Yaremchuk MJ, Kim WK. Soft tissue alterations with acute, extended open reduction and
internal fixation of orbital fractures. J Craniofac Surg 1992;3:134–40.
7. Glassman RD, Manson PN, Petty P, et al. Techniques for improved visibility and lid protection
in orbital explorations. J Craniofac Surg 1990;1:69–72.
8. Tessier P. Inferior orbitotomy. A new approach to the orbital floor. Clin Plast Surg 1982;9:569–75.
9. Romano J, Iliff N, Manson PN. Use of Medpor porous polyethylene implants in 140 patients
with facial fractures. J Craniofac Surg 1993;4:142–50.
10. Glassman RD, Manson PN, Vanderkolk CA, et al. Rigid fixation of internal orbital fractures.
Plast Reconstr Surg 1990;86:1103–10.
11. Rubin PAD, Shore JW, Yaremchuk MJ. Complex orbital fracture repair using rigid fixation of
the internal orbital skeleton. Ophthalmology 1992;99:553–61.
12. Yaremchuk MJ, Manson PN. Reconstruction of the internal orbit using rigid fixation
techniques. In: Yaremchuk MJ, Gruss JS, Manson PN, editors. Rigid fixation of the
craniomaxillofacial skeleton. Boston: Butterworth-Heinemann; 1992.
13. Gordon CR, Susarla SM, Yaremchuk MJ. Quantitative assessment of medial orbit fracture
repair using computer-designed anatomical plates. Plast Reconstr Surg 2012;130(5):698e–705e.
14. Chen NT, Glowacki J, Bucky LP, et al. The roles of revascularization and resorption on
endurance of craniofacial onlay bone grafts in the rabbit. Plast Reconstr Surg 1994;93:725–82.
15. Rubin JP, Yaremchuk MJ. Complications and toxicities of implantable biomaterials used in
facial reconstructive and aesthetic surgery: a comprehensive review of the literature. Plast
Reconstr Surg 1997;100:1336–53.
85
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Video 7.1 Orbital floor repair. This video demonstrates the reconstruction of an orbital floor
blowout fracture using a titanium mesh implant. Forced duction tests at onset and finish of
surgery demonstrate soft tissue entrapment and subsequent release, respectively.
86.e1
Chapter 8
Infraorbital rim
The upper midface skeleton has direct and indirect influences on the appear-
ance of the face and, particularly, the eyes. The relationship between the globe
and the orbital rims will determine if the eyes appear prominent or deep set.
Because the infraorbital rim and upper midface skeleton support the lower
eyelids and the cheek soft tissues, their projection impacts on lid and cheek
position. Patients with deficient skeletons are more likely to undergo prema-
ture lower lid and cheek descent with aging. This lack of skeletal support pre-
disposes to lower lid malposition after blepharoplasty and limits the efficacy
and longevity of midface lifting. This chapter demonstrates the impact that
infraorbital rim augmentation alone, or together with other soft tissue manip-
ulations, has on periorbital appearance. It includes techniques not only for
augmenting the infraorbital rim with alloplastic implants, but also for elevat-
ing the midface soft tissues as well as repositioning the lower lid and lateral
canthus.
GLOBE–RIM RELATIONS
Fig. 8.1 Sagittal relations of the anterior surface of the cornea to the soft
tissues overlying the supraorbital and infraorbital rims. On average, in the
young adult, the supraorbital rim projects 10 mm beyond, the infraorbital
rim lies 3 mm behind, and the cheek prominence projects 2 mm beyond the
anterior surface of the cornea.1–4
10 mm
3 mm
2 mm
89
Chapter 8 Infraorbital rim
soft tissues overlying the infraorbital rim lies 3 mm behind the anterior surface
of the cornea. This implies that the supraorbital rim usually projects 13 mm
beyond the infraorbital rim. When the orbital rims have a greater projection
beyond the anterior surface of the cornea, the eyes appear “deep set.” When
the orbital rims project less, the eyes appear “prominent.” In addition to being
predisposed to corneal exposure-related problems, overly prominent eyes are
usually considered less attractive.
Implant
A B C
Fig. 8.2 Jelks and Jelks5 categorized globe–orbital rim relationships by placing a line or “vector” between the most anterior
projection of the globe and the soft tissues overlying the midface skeleton in the parasagittal plane. (A) Positive vector
90 relationship. (B) Negative vector relationship. (C) “Reversed” negative vector relationship resulting from increasing the sagittal
projection of the infraorbital rim with an implant. After Yaremchuk 2003.11
Altering globe–rim relations: reversing the “negative vector”
measured relative to the lateral orbital rim, men’s globes, on average, were 2
mm more prominent than women’s, and black men’s and black women’s globes
were 2 mm more prominent than those of white men and white women.
Pessa et al.3 showed that the globe–orbital rim relationship changes with
age. Retrusion of the infraorbital rim with aging makes the eyes appear more
prominent by changing globe–rim relations, and exaggerates lower lid fat
prominence, particularly in those who tend toward maxillary hypoplasia. These
findings and surgical maneuvers to rejuvenate this anatomy are described in
Chapter 14.
After blepharoplasty
Patients with prominent eyes have long been recognized to develop symp-
tomatic lower lid descent (with exaggeration of their “round eyes”) after con-
ventional lower blepharoplasty. Negative vector patients who develop lid PEARL
malposition after conventional blepharoplasty can have their lid position and
Deficient infraorbital rim projection
palpebral fissure shape improved by increasing their skeletal support by allo- predisposes to lower lid descent after
plastic augmentation of the infraorbital rim together with midface soft tissue blepharoplasty.
elevation and lateral canthopexy.12
Graves’ disease
Eye prominence results from a deficiency in sagittal skeletal projection, as has
been discussed, but may also result from excess of orbital soft tissue volume as
occurs with thyroid ophthalmopathy. Infraorbital rim augmentation together
with midface soft tissue elevation can be a useful adjunct to orbital decompres- 91
sion in patients with Graves’ disease.13
Chapter 8 Infraorbital rim
A B
Fig. 8.3 (A) Frontal and (B) lateral views of a woman with midface skeletal morphology (negative vector) predisposing to lower lid and cheek
descent resulting in a “round eye” appearance with prominent bags. On lateral view (B), the artist has drawn in the underlying deficient facial
skeleton. Reproduced from Yaremchuk 2004,12 with permission.
The infraorbital rim has lateral zygomatic bone and medial maxillary bone
contributions. The zygomaticomaxillary suture is situated approximately at
the midpupillary line. Approximately 8 mm beneath the orbital rim14 (or 3 to
6 mm in severely hypoplastic midfaces) and along the zygomaticomaxillary
suture exits the infraorbital nerve. The infraorbital nerve travels beneath
the levator superioris and above the levator anguli oris. Its branches supply
the skin of the lower lid, the side of the nose, most of the cheek, and upper
lip. The zygomaticofacial nerve exits through its small foramen located on
the lateral aspect of the zygoma, approximately 8 to 10 mm beneath the
infraorbital rim and in line with the lateral orbital rim. It supplies a small
portion of the skin of the upper cheek. Whereas the infraorbital nerve must
be protected, the zygomaticofacial nerve is routinely sacrificed during infra-
orbital rim augmentation, with the ensuing sensory loss rarely noted by the
patient.
In exposing the surface of the infraorbital rim area for implant augmenta-
tion, the origins of the upper lip elevators are detached from their skeletal
92 origins. The zygomaticus major muscle originates from the lateral surface
Surgical anatomy
Orbicularis oculi m.
Nasalis m.
Infraorbital n.
Zygomaticus major m.
Infraorbital n.
Zygomaticus minor m.
Orbicularis oris m.
Fig. 8.4 Midface skeletal anatomy with muscle origins and nerve foramina.
Fig. 8.5 Implants designed specifically for infraorbital rim sagittal augmentation (Matrix Surgical, Atlanta, GA). (A) Oblique
view. (B) Overhead view.
PREOPERATIVE EVALUATION
As depicted in Fig. 8.1, in young, healthy adults, the average projection of the
soft tissues overlying the supraorbital rim beyond the surface of the cornea is
about 10 mm, and the projection of the cornea beyond the soft tissues overlying
the infraorbital rim is 2 mm. These relations are the approximate goals of aug-
mentation of the orbital rims. A disproportion in sagittal globe–rim relations is
usually obvious and correction is made by clinical judgment.
THE IMPLANT
Implants are designed to augment the sagittal projection of the infraorbital rim.8 PEARL
Implants can provide up to 5 mm of anterior projection. They have malar com-
Infraorbital rim augmentation can
ponents of various surface areas and can be segmented for easier placement and
provide support for the resuspended
conformation to the underlying skeleton (Matrix Surgical, Atlanta, GA). They lower lid and cheek in patients with
are fixed with screws to eliminate movement and apply the implant to the skel- midface skeletal deficiency.
eton. Implants are trimmed to meet the specific needs of the patient. (Fig. 8.5).
Primary surgery
Midface skeletal augmentation and rejuvenation shown in Fig. 8.6 and Video 8.1
demonstrates both placement of an infraorbital rim implant and a subperiosteal
midface lift.
The infraorbital rim and adjacent anatomy must be exposed sufficiently to
assure ideal implant placement, smooth implant–facial skeleton transition, and
94 screw fixation. Subciliary skin–muscle flap approaches can provide this expo-
sure. A transconjunctival retroseptal incision, if used, requires lengthening with
Operative technique to augment the infraorbital rim
is tied to a drill hole placed in the lateral orbital rim. The elevated subobicu-
laris oculi fat (SOOF) and adjacent musculature now rest on the augmented
skeleton and help to support the freed and elevated lid margin. This technique
of midface elevation is adapted from the method by Phillips et al.15 for sub-
periosteal midface soft tissue repositioning used after extensive facial skeletal
degloving performed to access and treat the fractured midface. This author also
uses it to restore a youthful cheek–lid interface during rejuvenative aesthetic
surgery7 and together with lateral canthopexy8 to reposition the inferiorly dis-
placed lower lid occurring after blepharoplasty in patients with normal skeletal
anatomy. A “negative vector” patient who has undergone infraorbital rim aug-
mentation for periorbital rejuvenation is shown in Fig. 8.7.
A B
D
Fig. 8.7 Photographs of the woman shown
in Fig. 8.3 who underwent infraorbital
rim augmentation and midface lift. No
fat was removed from the lower lids. (A) C
Preoperative frontal view. (B) One-year
postoperative frontal view. Note that
without direct manipulation of lower lid
fat, the “early bags” are ameliorated but not
eliminated. (C) Fourteen-year postoperative
frontal view (a transconjunctival
blepharoplasty had been performed 2 years
after the implant surgery). (D) Preoperative
lateral view with artist’s rendition of
underlying facial skeleton. (E)
One-year postoperative lateral view with
artist’s rendition of augmented facial F
skeleton. (F) Fourteen-year postoperative
lateral view. Parts A, B, D, and E reproduced E
from Yaremchuk 2004,12 with permission.
96
Operative technique to augment the infraorbital rim
97
Chapter 8 Infraorbital rim
B
Subperiosteal
dissection to
Whitnall’s
tubercle Suture in
lateral canthal
ligament
canthal position, which should be 2 to 3 mm above the plane of the medial can-
thi. The lateral canthus is not supraplaced.
The bridge of bone canthopexy is preferred for both practical and conceptual
reasons. Drill holes placed in the lateral orbital rim can be placed after precise
measurement allowing for predictable and symmetric lateral canthus position-
ing. The bridge of bone provides a secure fixation point. The passing of the can-
thopexy stitch from inside the orbit to outside applies the lid to the globe. This
maneuver avoids the lid–globe dysjunction in the lateral commissure, which
is common when canthopexy sutures are tied to the outer surface of the lateral
orbit (Fig. 8.10). Lateral canthopexy, since it does not violate the lid margin,
maintains, or has the potential to restore, palpebral fissure shape including the
lateral canthal angle.
Lid–globe
dysjunction
A B
Fig. 8.10 The position of the lateral canthus relative to the lateral orbital rim determines the relation of the lower lid to the surface of the
globe. (A) The lateral canthopexy stitch is passed through the inner surface of the lateral orbital wall and tied on its outside surface. The lid is
applied to the globe. (B) The lateral canthopexy stitch is attached to the periosteum of the anterior surface of the lateral orbital rim. Note the 99
gap between the surface of the globe and the lateral aspect of the lower lid.
Chapter 8 Infraorbital rim
See Video 8.1 showing infraorbital rim implant augmentation and midface
PEARLS
lift.
The temporal soft tissues are elevated and redistributed to avoid the “Madam • Screw fixation prevents implant
Butterfly” look.21 When a coronal incision is used to perform the lateral cantho- migration and eliminates gaps be-
pexy, a lateral brow lift will avoid any upper lid bunching after lateral canthal tween the implant and underlying
skeleton.
elevation. When the latter extent of an upper lid blepharoplasty incision is used, • Midface tissues can be resuspended
a small ellipse of skin and underlying orbicularis oculi muscle is removed at the to the implant and lateral orbital rim
time of closure. A temporary tarsorraphy stitch is placed to limit postoperative using drill holes.
chemosis. • Periosteal-only fixation is not reli-
able in the long term.
The effect of skeletal augmentation and midface elevation is demonstrated
in Fig. 8.11. A patient who underwent infraorbital rim augmentation, midface
elevation, and lateral canthopexy is presented in Fig. 8.12. A patient treated for
Graves’ disease is presented in Fig. 8.13.
A B C
Fig. 8.11 Sagittal sections of lower lid, globe, and orbital rim taken at midpupil in (A) a “normal” patient, (B) a “deficient orbit”
(“morphologically prone”) patient with lid descent after previous blepharoplasty, and (C) a “correction” of a “morphologically
prone” patient with lid descent who has undergone infraorbital rim implant augmentation and midface elevation.
100
Operative technique to augment the infraorbital rim
A B
C D
Fig. 8.12 A 52-year-old woman had undergone previous browlift, rhytidectomy, and upper and lower lid blepharoplasty. Lower lid retraction
was previously attempted by multiple canthopexies, spacer grafts, and full-thickness skin grafts. Dry eye symptoms persisted. Infraorbital rim
augmentation, midface lift, and lateral canthopexy resolved her symptoms. Her brows and hairline were repositioned. (A) Preoperative frontal
view. (B) Postoperative frontal view. (C) Preoperative lateral view. (D) Postoperative lateral view.
101
Chapter 8 Infraorbital rim
A B
C D E
Fig. 8.13 A 30-year-old woman with Graves’ disease underwent medial and lateral orbital decompression with preservation of the lateral
orbital rim. The orbital floor was not manipulated to avoid problems with globe displacement and dystopia. Globe–rim relations were
further improved by augmenting the infraorbital rim, elevating the midface soft tissue, and performing lateral canthopexy. In this patient,
a transconjunctival incision with lateral canthotomy was used. Note the distortion in the lateral canthal appearance on the right side due
to improper lateral canthal realignment. Dry eye symptoms were relieved. (A) Preoperative frontal view. (B) Postoperative frontal view.
(C) Preoperative lateral view. (D) Postoperative lateral view. (E) Diagrammatic representation of procedure. Panels A–D reproduced from
Yaremchuk 2004,12 with permission.
102
References
REFERENCES
1. Mulliken JB, Goodwin SL, Pracharktam N, Altobelli DE. The concept of the sagittal orbital–
globe relationship in craniofacial surgery. Plast Reconstr Surg 1996;97(4):700–6.
2. Whitaker LA, Morales Jr L, Farkas LG. Aesthetic surgery of the supraorbital ridge and
forehead structures. Plast Reconstr Surg 1986;78(1):23–32.
3. Pessa JE, Desvigne LD, Lambros VS, Nimerick J, Sugunan B, ZadooVP. Changes in ocular
globe-to-orbital rim position with age: implications for aesthetic blepharoplasty of the lower
eyelids. Aesthet Plast Surg 1999;23(5):337–42.
4. Farkas LG, Hreczko TA, Katic JJ. Craniofacial norms in North American Caucasians from birth
(one year) to adulthood: appendix A. In: Farkas LG, editor. Athropometry of the head and
face. 2nd ed. New York: Raven Press; 1995.
5. Jelks GW, Jelks EB. The influence of orbital and eyelid anatomy on the palpebral aperture.
Clin Plast Surg 1991;18(1):183–95.
6. Rees TD, LaTrenta GS. The role of Schirmer’s test and orbital morphology in predicting dry-
eye syndrome after blepharoplasty. Plast Reconstr Surg 1988;82(4):619–25.
7. Migliori ME, Gladstone GJ. Determination of the normal range of exophthalmometric values
for black and white adults. Am J Ophthalmol 1984;98(4):438–42.
8. Yaremchuk MJ. Infraorbital rim augmentation. Plast Reconstr Surg 2001;107(6):1585–92.
9. Hirmand H, Codner MA, McCord CD, Hester TR, Nahai F. Prominent eye: operative
management in lower lid and midface rejuvenation the morphologic classification system.
Plast Reconstr Surg 2002;110(2):620–8.
10. Yaremchuk MJ. Subperiosteal and full-thickness skin rhytidectomy. Plast Reconstr Surg
2001;107(4):1045–58.
11. Yaremchuk MJ. Restoring palpebral fissure shape after previous lower blepharoplasty. Plast
Reconstr Surg 2003;111(1):441–50.
12. Yaremchuk MJ. Improving periorbital appearance in the “morphologically prone”. Plast
Reconstr Surg 2004;114(4):980–7.
13. Doumit G, Abouhassan W, Yaremchuk MJ. Aesthetic refinements in the treatment of graves
ophthalmopathy. Plast Reconstr Surg 2014;134(3):519–26.
14. Raschke R, Hazani R, Yaremchuk MJ. Identifying a safe zone for midface augmentation using
anatomic landmarks for the infraorbital foramen. Aesth Surg J 2013;33(1):13–8.
15. Phillips JH, Gruss JS, M.D., Wells MD, Challet A. Periosteal suspension of the lower eyelid and
cheek following subciliary exposure of facial fractures. Plast Reconstr Surg 1991;88(1):145–8.
16. McCord Jr CD. Eyelid surgery: principles and techniques. 1st ed. Philadelphia: Lippincott-
Raven; 1995. p. 95.
17. McCord Jr CD. The correction of lower lid malposition following lower blepharoplasty. Plast
Reconstr Surg 1999;103(3):1036–9.
18. Baylis HI, Goldberg RA, Groth MJ. Complications of lower blepharoplasty. In: Putterman
AM, editor. Cosmetic oculoplastic surgery: eyelid, forehead and facial techniques. 3rd ed.
Philadelphia: WB Saunders Co.; 1999. p. 446.
19. Yaremchuk MJ, Chen Y-C. Bridge of bone canthopexy. Aesth Surg J 2009;29(4):323–9.
20. Whitaker LA. Selective alterations of palpebral fissure form by lateral canthopexy. Plast
Reconstr Surg 1984;74(5):611–9.
21. Shorr N, Fallor MK. “Madam Butterfly” procedure: combined cheek and lateral canthus
suspension procedure for post-blepharoplasty: “round eye” and lower eyelid retraction.
Ophthalmic Plast Reconstr Surg 1985;1:229–33.
103
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Video 8.1 Infraorbital rim implant augmentation and midface lift.
104.e1
Chapter 9
Malar
Prominent malar bones are considered attractive.1 Hence, the malar area is fre-
quently augmented with implants. Although not documented in the literature,
personal experience with primary and secondary malar implant surgery has
shown that there is a significant incidence of patient dissatisfaction with this
surgery. Patients presenting for secondary surgery have three main complaints:
implant asymmetry; displeasing implant contours – too wide, too large, too low,
or too prominent with time; and symptoms of infraorbital nerve compression.2
Concepts and techniques presented in this chapter hope to optimize results and
avoid these problems.
PREOPERATIVE PLANNING
A dome-like shape with an absence of easily defined landmarks that are pro-
jected to the surface of the skin precludes anthropometric or cephalometric
analysis of the malar area. The resultant paucity of objective data describing the PEARL
malar area has inevitably made implant augmentation of this area more subjec-
There are no anthropometric or
tive. Because it is difficult to define what is average or normal for the malar cephalometric landmarks defining
area, selection of implant shape, implant size, and implant position for malar malar prominence.
augmentation can be problematic.
Anthropometric data
The only anthropometric landmark for analysis of the malar area is zygion (zy),
which measures the bizygomatic distance or width of the midface (Fig. 9.1).3
Several landmarks lie adjacent to or involve portions of the malar bone, but
there are none defining an area of maximum malar prominence.
Subjective analyses
Several surgeons, working without quantitative data, have suggested tech-
niques to identify the malar prominence as a guide to malar augmentation.
Their techniques use fixed relations to various anatomic landmarks to deter-
mine an ideal position of malar prominence.4–8 The availability of three-
dimensional computed tomography (CT) scans has allowed the senior author
to correlate the underlying skeletal topography with the overlying soft tissue
envelope. With this information, the senior author places the point of maxi-
mum projection just at, or slightly lateral to, the intersection of a vertical line
placed through the lateral canthus and a horizontal line traversing the infraor-
bital foramen (Fig. 9.2). This location is similar to that described by Hinderer4
and Wilkinson.6
Hinderer, one of the first to advocate the use of alloplastic implants for aes- 105
thetic surgery,4 divided the malar area into quadrants formed by two intersecting
Chapter 9 Malar
ft-ft
en-en
zy-zy
Fig. 9.3 Hinderer’s lines are two intersecting lines. One is drawn from the ala
to the tragus and the other from the oral commissure to the lateral canthus.
106 He advocated placing the implant in the upper outer quadrant formed by
these intersecting lines.4
Preoperative planning
lines. One is drawn from the ala to the tragus and the other from the oral com-
missure to the lateral canthus. He advocated placing the implant in the upper
outer quadrant formed by these intersecting lines (Fig. 9.3).
Wilkinson proposed a method for determining the point of maximum malar
projection by dropping a line vertically to the mandible border, then dividing it
into thirds. The malar prominence should lie just lateral to the point one-third
down from the canthus6 (Fig. 9.4).
Whitaker’s analysis of the malar midface9 considers three zones in the
malar–midface complex: a medial paranasal area, a central malar area, and
a lateral zygomatic arch area. It does not define an area of maximum malar
prominence. The division of the midface into anatomic zones, also advo-
cated, but divided differently by Terino,10 has been extremely helpful in
visualizing and correcting not only malar but also other areas of midface
deficiency.
As the most prominent and surgically accessible portion of the midface and
until recently the only area of the midface for which implants were available,
many patients receive malar implants when the entire midface or another mid-
face area is deficient. This may exaggerate the facial imbalance. For example,
malar augmentation, particularly when it extends far onto the zygomatic arch,
may exaggerate the appearance of prominent eyes due to midface hypoplasia.
These patients are better served with augmentation of the infraorbital rim alone
or in combination with malar augmentation and other soft tissue manipula-
tions11 (see Chapter 8).
Since full cheeks are associated with youth, malar augmentation is often
performed to provide a youthful appearance. This may provide an aesthetic
benefit if there is a relative malar hypoplasia or if the implants are of mod-
est size and projection. This skeletal augmentation is not equivalent to a
107
Chapter 9 Malar
SURGICAL ANATOMY
The anatomic structures relevant to implant augmentation of the malar area are
presented below (Fig. 9.5).
Nasalis m.
Orbicularis oculi m.
Levator labii superioris
alaeque nasi m.
Infraorbital foramen
Zygomaticus minor m.
A
108
Fig. 9.5 The midface anatomy. (A) Frontal view.
Surgical anatomy
Skeleton
The zygomatic or malar bone forms the prominence of the cheek. It also forms
part of the lateral wall and floor of the orbit, as well as parts of the temporal
and infratemporal fossae. The zygoma sends a frontal process upwards along
the lateral margin of the orbit to articulate with the frontal bone, and a temporal
process backward to form the anterior end of the zygomatic arch. The zygoma
articulates with the maxilla medially and presents malar, orbital, and temporal
surfaces. The malar surface is convex and is perforated in its midaspect by the
zygomaticofacial foramen for the passage of the zygomaticofacial neve and ves-
sels. Just below this foramen is a slight elevation of the bone from which the
zygomaticus major and the levator labii superioris arise.
Muscles
The muscles of the midface largely provide facial expression. They arise from
the bones of the face and insert into the skin. These muscles seldom remain
distinct throughout their length; rather, they tend to merge with their neighbor
where they terminate. Those that are freed from their origins during malar aug-
mentation elevate the upper lip and are described below.
Zygomaticus minor m.
Levator labii superioris
alaequae nasi m.
Nasalis m.
Depressor nasalis m.
Zygomaticus major m.
Orbicularis oris m.
Parotid duct
Buccinator m.
B
109
The zygomaticus major muscle originates from the lateral surface of the
zygoma just medial to the zygomaticotemporal suture and sometimes inter-
mingles with the orbicularis oculi. It passes obliquely downward and forward
to the corner of the mouth where it inserts into skin and mucosa.
The zygomaticus minor lies medial to the zygomaticus major. It originates
from the malar surface of the zygoma immediately lateral to the zygomatico-
maxillary suture and passes downward and medially to insert into the lip just
medial to the corner of the mouth.
The levator labii superioris originates from the lower margin of the orbit just
above the infraorbital foramen. It travels downward and medially to insert into
the orbicularis oris as well as the skin of the lip.
The levator anguli oris (caninus) lies deep to the above muscles. It arises
from the canine fossa of the maxilla immediately inferior to the infraorbital
foramen. It inserts into the angle of the mouth. The facial vessels travel across
its lower border. Branches of the infraorbital nerve travel in the connective tis-
sue between it and the overlying musculature.
Sensory nerves
The infraorbital nerve exits the maxilla through the infraorbital foramen
and travels beneath the levator superioris and above the levator anguli oris.
Its branches supply the skin of the lower lid, the side of the nose, most of
the cheek, and upper lip. This nerve must be identified and preserved. The
zygomaticofacial nerve exits through a small foramen located on the lateral
aspect of the malar bone. It supplies a small portion of the skin of the upper
cheek. It is routinely sacrificed during malar augmentation.
IMPLANT DESIGN
A malar implant should reproduce the normal contours of the facial skeleton.
Myriad implant designs of both porous polyethylene (Matrix Surgical, Atlanta,
GA; Stryker, Kalamazoo, MI) and silicone (Implantech, Ventura, CA) are avail-
able. An intraoperative photograph shows a typical shape and placement of a
malar implant (Fig. 9.6).
the surgical site. This solution reduces general anesthetic requirements and
postoperative discomfort while it aids in hemostasis.
Exposure of the area to be augmented is key. To that end, both eyelid and
intraoral approaches are employed. A transconjunctival retroseptal incision
with lateral canthotomy is the senior author’s preferred eyelid approach. A
skin–muscle approach is an alternative option. An upper gingivobuccal sul-
cus incision is made over the premolars. The incision is made at least 1 cm
above the sulcus to provide an adequate inferior cuff of mucosa for closure.
The lip elevators can be seen after the mucosa is incised. These muscles
are not divided but rather separated in their longitudinal orientation and
retracted during the exposure of the zygoma and lower maxilla.
Subperiosteal dissection exposes the area to be augmented. Laterally, the
dissection extends just beyond the zygomaticotemporal suture. Medially, at
this level, it extends to the infraorbital foramen where the infraorbital nerve
is visualized. This requires elevation of the zygomaticus major and zygomati-
cus minor muscles from their origins and the sacrifice of the zygomaticofacial
nerve. The levator anguli oris (caninus) lies deep to the above muscles. Its ori-
gins are usually separated from the canine fossa of the maxilla immediately
inferior to the infraorbital foramen. The lip elevators and the infraorbital nerve
are retracted to provide exposure.
After skeletal exposure, the implants are modified to meet the specific needs
of the reconstruction. As noted above, symmetric implant placement is chal-
112 lenging. Implants are available with registration features that aid implant
Operative technique – primary surgery
positioning (Matrix Surgical, Atlanta, GA). Fig. 9.10 depicts a malar implant
with flanges that register with the border of the infraorbital rim and the zygo-
matic arch.
Finally, the implant is fixed with titanium screws to permanently assure
the desired intraoperative position. Gaps between the surface of the skel-
eton and the undersurface of the implant can equal or exceed the thickness
of the implant. These gaps, which would result in unanticipated increases
in augmentation, are obliterated by screw fixation of the implant to the
skeleton.
Before the incisions are closed, the infraorbital nerve is identified in order to
be confident that any early postoperative complaints of decreased sensation in
the distribution of the infraorbital nerve can be attributed to the trauma of soft
tissue retraction and not implant compression.
Video 9.1 demonstrates placement of a porous polyethylene implant placed
through eyelid and intraoral incisions. The implant was modified intraopera-
tively to fit the needs of the patient. Patients who have undergone malar aug-
mentation are shown in Figs. 9.11 and 9.12.
113
Chapter 9 Malar
A B
C D
114
Operative technique – primary surgery
A D
B E
C F
Fig. 9.12 A 50-year-old woman had undergone bilateral upper and lower lid blepharoplasty,
browlift, and rhytidectomy 5 years prior to presentation. In addition to infraorbital rim and
malar augmentation, midface elevation and lateral canthopexy, the hairline and brows were
lowered and the chin was lengthened. Preoperative: (A) frontal, (B) lateral, and (C) oblique
views. Postoperative: (D) frontal, (E) lateral, and (F) oblique views.
115
Chapter 9 Malar
A B
116
Operative technique – secondary surgery
A D
B E
C F
Fig. 9.14 The patient shown in Fig. 9.7: A 64-year-old woman underwent surgery for her
submalar implant-induced midface deformity. Corrective surgery included implant removal,
subperiosteal midface elevation, and lateral canthopexy. Preoperative: (A) frontal, (B) lateral,
and (C) oblique views. Postoperative: (D) frontal, (E) lateral, and (F) oblique views.
117
Chapter 9 Malar
A D
B E
C F G
Fig. 9.15 The patient shown in Fig. 9.8 underwent revision surgery to correct her facial imbalance. Her brow was repositioned, her submalar
implants were removed, a subperiosteal midface lift was performed, the depressions at the chin osteotomy sites were bridged with porous
polyethylene implants, and her chin pad was resuspended. Preoperative: (A) frontal, (B) lateral, and (C) oblique views. Postoperative: (D)
frontal, (E) lateral, and (F) oblique views. (G) Intraoperative view during revision surgery shows submalar position of implant responsible for
undesired midface contour.
118
References
REFERENCES
1. Perrett DI, May KA, Yoshokawa S. Facial shape and judgment of female attractiveness. Nature
1994;368:239–42.
2. Yaremchuk MJ. Secondary malar implant surgery. Plast Reconstr Surg 2008;121(2):620–8.
3. Farkas LG, Hreczko TA, Katic MJ. Craniofacial norms in North American Caucasians from
birth (one year) to adulthood. In: Farkas LG, editor. Anthropometry of the head and face. 2nd
ed. New York: Raven Press; 1994, Appendix A.
4. Hinderer UT. Malar implants for the improvement of facial appearance. Plast Reconstr Surg
1975;56:157–65.
5. Silver WE. The use of alloplastic material in contouring the face. Facial Plast Surg 1986;3:81–
98.
6. Wilkinson TS. Complications in aesthetic malar augmentation. Plast Reconstr Surg
1983;71(5):643–9.
7. Powell NB, Riley RW, Lamb DR. A new approach to evaluation and surgery of the malar
complex. Ann Plast Surg 1988;20:206–14.
8. Prendergast M, Schoenrock LD. Malar augmentation. Arch Otolaryngol Head Neck Surg
1989;115:964–9.
9. Whitaker LA. Aesthetic augmentation of the malar-midface structures. Plast Reconstr Surg
1987;80(3):337–46.
10. Terino EO. Alloplastic contouring by zonal principles of skeletal anatomy. Clin Plast Surg
1992;19(2):487–510.
11. Yaremchuk MJ. Making concave faces convex. Aesth Plast Surg 2005;29(3):141–7.
12. Binder WJ. Submalar augmentation. An alternative to face-lift surgery. Arch Otolaryngol Head
Neck Surg 1989;115:797–801.
119
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Video 9.1 Malar implant. This video demonstrates placement of a porous polyethylene
implant placed through eyelid and intraoral incisions. The implant was modified
intraoperatively to fit the needs of the patient.
120.e1
Chapter 10
Pyriform aperture
The surface of the maxilla is very irregular. Inferiorly, this is due to a series of
eminences and corresponding depressions reflecting the apices of the teeth.
The incisive fossa is the depression above the prominent incisors. This depres-
sion gives rise to the origin of the depressor septi. The canine tooth forms a
vertical ridge that separates the incisive fossa from the canine fossa, which
is deeper and larger than the incisive fossa. The canine fossa gives rise to the
levator anguli oris. The infraorbital foramen is located just above the canine
fossa. It allows exit of the infraorbital nerve and vessels. They travel beneath
the levator superioris and above the levator anguli oris. The infraorbital nerve
supplies the skin of the lower lid, the side of the nose, most of the cheek and
upper lip. Medial to the infraorbital foramen is the nasal notch, which is a
concavity whose margin gives rise to the dilator naris as it ends below as the
anterior nasal spine. 121
Chapter 10 Pyriform aperture
g g
Is
Is
0° 0°
Fig. 10.1 The inclination of the midface, i.e., glabella (g) to upper lip (ls), in men and women. (A) In men g–ls is 1.3 ± 3.5 degrees. (B) In
women g–ls is 1.6 ± 2.5. Data from Farkas et al. 1994,1 with permission.
99.8° mean
(+ 11.8°)
104.2° mean
(+ 9.8°)
0°
0°
–3.1° mean
(+ 3.5°) 1.6° mean
A B (+ 2.5°)
Fig. 10.2 The nasolabial angle in men and women. (A) In men the nasolabial angle is 99.8 ± 11.8 degrees. (B) In women the nasolabial angle
is 104.2 ± 9.8 degrees. Data from Farkas et al. 1994,1 with permission.
122
The implant
Nasalis m.
Orbicularis oculi m.
Levator labii superioris
alaeque nasi m.
Infraorbital foramen
Zygomaticus minor m.
THE IMPLANT
Pyriform aperture (or paranasal) implants are available from Matrix Surgical
Inc. (Atlanta, GA) as Omnipor and from Stryker (Kalamazoo, MI) as Medpor.
They are designed as right and left crescents and come in two sizes. The smaller
implant is 27 mm long by 25 mm high and provides 4.5 mm of projection. The
larger implant, which is 30 mm long by 28 mm high, provides 7 mm of projec-
tion. These implants are designed to be tailored to the patient’s particular aes-
thetic needs. The implant is positioned to sit flush on the bone. Patient anatomy
will determine whether the entire crescent or just the horizontal or vertical limb
of the crescent are used (Fig. 10.4).
123
Chapter 10 Pyriform aperture
A B
Fig. 10.4 Porous polyethylene paranasal implants are designed to augment both the lateral and inferior aspects of the
pyriform aperture. Implants can be carved to allow selective augmentation. Screw fixation prevents movement of the
implant and allows in-place contouring. (A) Implant augments pyriform aperture skeleton (maxilla lateral to the pyriform
aperture and alveolus). (B) Implant contoured and positioned to selectively augment alveolus. (C) Implant contoured and
positioned to selectively augment maxilla lateral to the pyriform aperture.
identified during surgery. Defining the bony edges of the pyriform aper-
ture provides bony landmarks facilitating precise and symmetric implant
placement. The implant may compromise the nasal airway if positioned
beyond the bony edge of the aperture. Identification of the nerve avoids
inadvertent retractor or implant damage to the structure. The root of the
canine tooth will be visible as a distinct bulge just lateral to the pyriform
aperture. The implant will, in part, lie directly over it. The surgeon must
avoid damaging these structures if screw fixation is used to immobilize the
implant.
The deeply located levator anguli oris (caninus), dilator naris, and depres-
sor septi, as well as portions of the maxillary origins of the buccinators, are
separated from the maxilla during implant placement. The lip elevators and
the infraorbital nerve are retracted to provide exposure. As a result of these
manipulations there is usually temporary dysfunction of these structures post-
operatively. The incision is closed in layers. Because of the relatively small area
of dissection, no drains are used.
CLINICAL EXAMPLES
A B
A B
126 C D
Clinical examples
Patients who have been treated for extensive midface or panfacial fractures
may present with relative midface deficiency but normal occlusion. This “dish
face” deformity occurs when the pre-injury maxillary anatomy is not restored
or not maintained. Retrusion of the lower midface may occur when upper
and lower jaw fractures are reduced with respect to occlusion only, and not
to pre-injury three-dimensional skeletal anatomy above the occlusal level. It
may also occur after comminuted maxillary fracture reduction and fixation if
the surgery is inadequate to resist soft tissue deformity forces accompanying
massive edema. As seen in Fig. 10.8, paranasal augmentation can help restore
the pre-injury lower face convexity.
A B
C D 127
Chapter 10 Pyriform aperture
Another major group of patients is made up of people who were born with
relative midface lower deficiency. These facial skeletal characteristics are noted
more commonly in certain ethnic groups, including Asians and black people,
in whom relative maxillary hypoplasia can result in a concave midface pro-
file.15,16 Pyriform aperture augmentation often benefits those patients during
rhinoplasty where, depending on implant placement, it can increase the pro-
jection of the nasal base, efface the acute nasolabial angle, and straighten the
vertical plane of the lip (Figs. 10.9 and 10.10). The patient in Fig. 10.11 had nasal
aesthetics improved with pyriform aperture augmentation without rhinoplasty.
A B
C D
128
Clinical Examples
A B
Fig. 10.10 A 30-year-old Asian woman underwent paranasal augmentation only to correct lower midface concavity. (A) Preoperative lateral
view. (B) Postoperative lateral view.
A B C
129
D E F
Fig. 10.11 A 20-year-old woman underwent rhinoplasty and paranasal augmentation. (A–C) Preoperative frontal, lateral, and oblique views.
(D–F) Postoperative frontal, lateral, and oblique views.
Chapter 10 Pyriform aperture
NASAL IMPLANTS
A B
Fig. 10.12 Intraoperative view of a sheet of porous polyethylene used to support a fractured caudal nasal septum in a professional wrestler.
(A) Fractured displaced caudal septum. (B) Porous polyethylene batten supporting repositioned septum.
130
References
REFERENCES
1. Farkas LG, Hreczko TA, Katic MJ. Craniofacial norms in North American Caucasians from
birth (one year) to adulthood. In: Farkas LG, editor. Anthropometry of the head and face.
2nd ed. New York: Raven Press; 1994. Appendix A.
2. Yaremchuk MJ, Israeli D. Paranasal implants for correction of midface concavity. Plast
Reconstr Surg 1998;102(5):1676–84.
3. Yen CI, Chen RF, Zelken J, et al. The influence of paranasal augmentation on the measurement
of the nose for the treatment of midfacial concavity. Aesthet Surg J 2018;38(3):241–51.
4. Yaremchuk MJ, Chang CS. Commentary on: the influence of paranasal augmentation
on the measurement of the nose for the treatment of midfacial concavity. Aesthet Surg J
2018;38(3):252–3.
5. Converse JM. Techniques of bone grafting for contour restoration of the face. Plast Reconstr
Surg 1954;14(5):332–46.
6. Converse JM, Horowitz SL, Valauri AJ, Montandon D. Treatment of nasomaxillary hypoplasia.
Plast Reconstr Surg 1970;45(6):527–35.
7. Jackson IT, Moos KF, Sharpe DT. Total surgical management of Binder’s syndrome. Ann Plast
Surg 1981;7(1):25–34.
8. Obwegeser HL. Surgical correction of small or retrodisplaced maxillae. Plast Reconstr Surg
1969;43(4):351–65.
9. Ortiz-Monasterio F, Molina F, McClintock JS. Nasal correction in Binder’s syndrome: the
evolution of a treatment plan. Aesthet Plast Surg 1997;21(5):299–308.
10. Psillakis JM, Lapa F, Spina V. Surgical correction of mid-facial retrusion (nasomaxillary
hypoplasia) in the presence of normal dental occlusion. Plast Reconstr Surg 1973;51(1):67–70.
11. Ragnell A. A simple method of reconstruction in some cases of dish-face deformity. Plast
Reconstr Surg 1952;10(4):227–37.
12. Caronni E. A new method to correct the nasolabial angle in rhinoplasty. Plast Reconstr Surg
1972;50(4):338–40.
13. Guerrerosantos J. Nose and paranasal augmentation: autogenous fascia and cartilage. Clin
Plast Surg 1991;18(1):65–86.
14. Hinderer UT. Nasal base, maxillary, and infraorbital implants––alloplastic. Clin Plast Surg
1991;18(1):87–105.
15. Tham C, Lai YL, Went CJ, Chen YR. Silicone augmentation rhinoplasty in an oriental
population. Ann Plast Surg 2005;54(1):1–5.
16. Chao JW, Lee JC, Chang MM, Kwan E. Alloplastic augmentation of the Asian face: a review of
215 patients. Aesthet Surg J 2016;36(8):861–8.
131
Chapter 11
Chin
Physical examination
Physical examination must include analysis of both the skeleton and its soft tis-
sue envelope. The lower one-third of the face must relate appropriately to the
upper two-thirds. Within the lower one-third, the position of the lips and depth
of the labiomental sulcus are impacted by the projection of the chin.
X-rays
Unlike orthognathic surgery, where cephalometric X-ray studies are intrinsic to
the preoperative plan, for implant surgery, preoperative X-rays can be helpful
but are not mandatory. Plain X-rays may be particularly helpful during revision
surgery after previous osteotomies.
Three-dimensional computed tomography (CT) scans and the models
that can be generated from their data can be useful for planning surgery to
ameliorate facial skeletal asymmetries. Custom implants can be made using
these data (see Chapters 14 and 15).
Anthropometric data
Normative data are helpful in analyzing the chin, not only in its sagittal but
also in its vertical and horizontal projections. These dimensions and their 135
potential change with chin augmentation should all be considered in the
Chapter 11 Chin
g
g
pg pg
0°
0°
–3.0° mean
A (+ 3.4°) B –4.1° mean
(+ 3.0°)
Fig. 11.1 The inclination of the facial profile as defined by a line from the glabella (g) to the pogonion (pg). The broken line is drawn
perpendicular to the Frankfort horizontal at the inclination of 0 degrees. The solid red line represents the mean inclination of the study group.
The shaded area encompasses 1 standard deviation (SD). (A) The mean inclination in 100 young North American white men was −3 ± 3.4
degrees. (B) The mean inclination in 100 young North American white women was −4.1 ± 3 degrees. In both men and women, note that
the chin rests slightly posterior to the lower lip and the lower lip lies slightly posterior to the upper lip. Data from Farkas et al. 1994,7 with
permission.
context of lip projection and the depth of the labiomental angle. Although
these data derive from large numbers reflecting a heterogeneous population,
and cannot be applied to every individual, average values of the normal face
should not be discounted and should be used in the evaluation process.
Lip–chin relations
Suggested ideal relationships between the chin and the lips based on norma-
tive cephalometric data by different authors8–12 are in consensus that the chin
should rest slightly posterior to the lower lip and the lower lip posterior to the
upper lip (Fig. 11.1).
136
Evaluation and planning
Labiomental angle
The inclination of labiomental angle must be evaluated when considering an
increase in the sagittal projection of the chin. There is a considerable variability
in this inclination. In general, the inclination is more acute in men (113 ± 21
degrees) than it is in women (121 ± 14 degrees) (Fig. 11.2).
A B
Fig. 11.2 Labiomental angle has considerable variability. The mean inclination is more acute in men
at 113 ± 21 degrees (A), than it is in women at 121 ± 14 degrees (B). Data from Farkas et al. 1994,7
with permission.
When the angle is already acute, chin augmentation will make it more
acute, thereby deepening the labiomental angle. Such deepening is usually
dysaesthetic. Certain patients with retrognathia have their upper central inci-
sors abutting on their lower lip, thrusting it forward, and creating a deep sul-
cus (Fig. 11.3). Depending on the occlusal status, these patients may be better
served with repositioning of the entire mandible by sagittal split osteotomy.3,13
A B
Fig. 11.3 In patients with severe mandibular deficiency and overbite, the upper incisors may thrust 137
the lower lip forward resulting in an acute labiomental angle.13 Chin augmentation in such patients
will further increase the labiomental angle. (A) Artist’s depiction. (B) Lateral X-ray. After Flowers
1991.13
Chapter 11 Chin
Subjective criteria
Subjective criteria for an ideal profile are at variance from those obtained by
objective analyses. When McCarthy and Ruff14 and Farkas et al.15 compared
the profile of young North American white adults to classic art and medical
illustrations, they found that artists usually portray a larger chin than nor-
mally exists in reality. A frequently cited ideal chin projection is adapted from
Gonzalez-Ulloa.16,17 His ideal facial plane was a vertical line that extended
downward from the nasion to meet the Frankfort horizontal (which extends
from the upper margin of the external auditory meatus to the lower orbital
ridge). This was determined from his analysis of “contemporary beautiful faces
and faces known as beautiful through history.”16 It is redrawn in Fig. 11.4. PEARL
This ideal is beyond the upper limit of normal for women as determined by A large chin implant in a woman may
the data of Farkas et al.,7 does not take into account sexual dimorphism, and is masculinize her lower face.
at variance with ideal lip–chin relations derived from cephalometric studies.8–12
Frankfort plane
138
Evaluation and planning
Increasing the vertical height of the chin with implants can be accomplished
in three ways. An illusion of increased length can be obtained by moving the
most projecting part of the chin inferiorly by implant positioning (Fig. 11.6).
However, real increases in vertical projection require CAD/CAM implants or
horizontal osteotomy with a spacer of desired height between the proximal and
distal chin segments.
The senior author’s preference is to place a porous polyethylene block
between the segments. Because the entire lower jaw is small and to eliminate
a step-off between the intact mandible body and lengthened chin, a mandible
implant is placed to create a smooth mandibular border as well as increase the
overall size of the lower jaw.
Fig. 11.5 Average dimensions of both male and female faces. The
distance from the base of the nose (subnasale; sn) to the mouth
opening (stomion; sto) is half of the distance from the subnasale
to the gnathion (gn). In other words, the height of the mandible in
the midline (sto–gn) should account for two-thirds of the lower face
height (sn–gn).
sn
sto
gn
A B 139
Fig. 11.6 A 7-mm, in projection, implant was repositioned at the inferior border of the chin to visually increase the vertical height of the chin.
(A) Preoperative. (B) Postoperative.
Chapter 11 Chin
A B
Fig. 11.7 (A) Male and (B) female skulls demonstrate the difference in chin and overall lower facial width. From the Atkinson Skull Collection,
University of the Pacific, Dugoni School of Dentistry, San Francisco, CA.
SURGICAL ANATOMY
Inferior alveolar n.
Orbicularis
Mentalis m.
Platysma m. Mentalis
Mental n.
Depressor anguli oris m. Levator labii inferioris m. Mental n.
(origin) Inferior alveolar n.
Levator labii inferioris m.
Levator labii inferioris m. Depressor anguli oris m.
(origin) (origin)
Platysma m. Depressor anguli
Mentalis
A B Platysma m.
Fig. 11.8 Shows the anatomy of the lower lip elevators and retractors as well as the path of the mental nerve relative to the mandible. These
structures are susceptible to injury during chin augmentation. (A) Frontal view with facial musculature and position of infraorbital and mental
nerves. (B) Lateral view with facial musculature origins and path of inferior alveolar nerve.
Mental nerve
The inferior alveolar nerve is a branch of the mandibular nerve (V3). It enters
the mandibular canal with the inferior alveolar vessels through the mandibu-
lar foramen, which is located in the inner aspect of the ramus of the mandible.
The nerve, together with vessels, courses obliquely from the ramus to the body
where it exits as the mental nerve through the mental foramen, which is located
at the level of the first or second premolar. Hwang et al. documented the course
of the inferior alveolar nerve in Korean cadavers.23 They found that the foramen
was located below the second premolar tooth in approximately two-thirds of
the cadavers studied. Vertically, the mental foramen was located almost half-
way from the tip of the alveolar process to the lower border of the mandible.
They also found that the terminal mandibular canal is an average of 4.5 mm
under the mental foramen, advances 5 mm anteriorly, loops, and ends at the
foramen. The potential location of this nerve is important to recognize when
placing screws or performing horizontal osteotomies of the mandible. Any cuts PEARL
or holes made in the bone should be placed at least 6 mm beneath the foramen.
The inferior alveolar nerve courses at
After exiting the foramen, the mental nerve divides into two or three branches a level inferior to the mental foramen.
to supply sensation to the mucosa and the skin of the lower lip and chin.
Mentalis muscle
Zide has defined the anatomy of the mentalis muscle and the repercussions of
iatrogenic injury to this structure.24,25 The mentalis muscle is an elevator of the
central lower lip. It arises from the mandible at the level of the root of the lower 141
lateral incisor and therefore defines the inferior limits of the sulcus intraorally. It
Chapter 11 Chin
fans inferiorly as a truncated cone whose base inserts on the skin and therefore PEARL
dimples the skin when elevating and protruding the lower lip (Fig. 11.9).
The mentalis muscle is the most
This is the most frequently damaged muscle during chin surgery. If it is frequently damaged structure during
divided and improperly repaired, or stripped from its origin and allowed to chin surgery. A submental surgical
descend to a more inferior position, the result is inferior malposition of the approach and extended subperiosteal
lower lip with increased lower incisor show, deepening of the sulcus, and dissection avoid damage to the
mentalis muscle.
inferior displacement of the chin pad20 (Fig. 11.10).
A B
Fig. 11.10 Lower lip descent and a deep labiodental sulcus in a patient whose mentalis muscle is divided or stripped and
not attached to the mandible during the intraoral approach for chin implant placement. (A) Frontal intraoral view lower lip
posture at rest. (B) Intraoral view of deep sulcus reflecting descent of mentalis muscle origin.
The depressor anguli oris (triangularis), the depressor labii inferioris (quadra-
tus), and platysma are all depressors of the lower lip. The depressor labii infe-
rioris and depressor anguli oris arise from the oblique line of the mandible to
merge with orbicularis oris and skin of the lower lip. The platysma muscle sends
fibers that originate from the mandible beneath the oblique line and merge with
the lip depressors. Subperiosteal dissection separates these muscles as a contin-
uum from the bone. Failure to stay in the subperiosteal plane may cause damage,
usually short lived, to these muscles. Clinically this injury mimics that of mar-
142 ginal mandibular branch palsy since the marginal branch innervates the lower
lip depressors. Temporary palsy to this musculature may last 1 to 2 weeks after
primary surgery and 2 to 3 months after revision surgery (Fig. 11.11).
The implant
A B
Fig. 11.11 Temporary palsy of lower lip depressors after chin implant surgery. (A) Two weeks after tertiary chin implant surgery.
(B) Resolution of palsy 10 weeks postoperatively.
THE IMPLANT
Fig. 11.14 The arc, the inclination of its limbs, and the contour of its posterior surface of an
extended one-piece implant may all be inappropriate for the shape of a mandible. A three-
dimensional CT scan demonstrating a clinical example.
144
The implant
A B
Implants that augment only the chin point produce an abrupt, protruding
PEARL
chin13,26 (Fig. 11.16). There should be an imperceptible transition between the
mandible and the implant. Implants that augment only the chin
point produce an abrupt, protruding
chin rather than a jaw–chin
continuum.
Button implant
A B
Fig. 11.16 Illustration (A) and clinical example (B) of a large button chin implant resulting in a poor implant–mandible transition with a stuck-
on appearance.
145
Chapter 11 Chin
Anesthesia
Chin augmentation with implants may be performed under local or general
anesthesia.
Submental incision
The chin and the anterior mandible are accessed through a submental incision
(Fig. 11.17). The midline of the chin is marked on the pogonion as a reference
point. Wide subperiosteal dissection is performed. The upper limit of the dis-
section is the origin of the mentalis muscle. Laterally, the mental foramen with
its exiting nerve and the inferior border of the mandible body are exposed. Lat-
eral dissection extends approximately 1 cm beyond the area of augmentation.
The submental approach and extended dissection avoid damage to the mentalis
muscle, allow visualization of the mental nerve, and provide a panoramic view of
the complex and varying contours of the mandible to allow precise implant place-
ment. The technique of intraoral placement of chin implants avoids a cutaneous
scar but provides limited exposure to the menton while compromising the men-
talis muscle. As a result, the intraoral approach is often associated with implant
malposition and lower lip dysfunction resulting from mentalis muscle division
PEARL
or detachment24 (Fig. 11.10). After reviewing his series of more than 100 cases of Many chin implant problems are
postoperative chin problems, Zide noted that almost all chin implant problems caused by transoral placement.
that he experienced were caused by implants that were placed transorally.3
Depressor labii
inferioris m.
Mentalis m.
146
Preferred operative technique
Implant positioning
Marking the midline of the pogonion aids symmetric implant placement. The
midline can be marked with a marker, drill hole, or temporary screw (Fig. 11.18).
This is useful for implants of any design or material. It may be beneficial to con-
tour prominences on the native mandible to allow better congruence between the
posterior surface of the implant and the mandible surface. The author’s prefer-
ence is a two-piece porous polyethylene implant with registration tabs incorpo-
rated at the inferior border of the implant. Right and left portions of the implant
are placed and then positioned. The registration tab dictates lateral positioning.
The connecting tab joins the two implant segments in the midline and also acts
as a hinge to allow the implant to adjust to the unique inclination of the man- PEARL
dible border. The connecting bar also allows the width of the implant to be varied
Mark the midline of the chin for
as dictated by the space between the right and left implant segments. In most orientation.
instances, there will be a gap between the medial aspects of the implant halves.
Screw fixation
The implant is fixed to the skeleton with screws for several reasons. It allows
precise, stable positioning of the implant. It adapts the posterior surface of
the implant to the anterior surface of the mandible, thereby obliterating gaps
between the implant and the mandible. Gaps between the implant and the
mandible result in an undesirable increase in augmentation in the gap area.
Immobilizing the implant with screws allows final in-place contouring of the
implant to ensure proper implant projection and an imperceptible transition
between the implant and the mandible (Figs. 11.19 and 11.20). The wound is
closed in layers. A mildly compressive dressing is placed and then removed
in 48 to 72 hours.
Submental lipectomy
Many patients benefit from defatting the submental area. Precise defatting
improves neck contour and improves mandibular border definition. The
author’s preference is to use the submental incision to create a full-thickness
skin and subcutaneous flap by dissecting directly on the platysma. The fat is
trimmed from the full-thickness flap with scissors. The wound is closed in lay-
ers and a mildly compressive dressing applied.
Defatting could also be done with liposuction. I prefer excision under direct 147
observation because it avoids irregularities and possible overresection that, in
the author’s experience, is more possible with liposuction.
Chapter 11 Chin
2 piece implant
Gap before
fixation
B C
148
Preferred operative technique
Clinical examples
Patients who have undergone primary chin augmentation using the above-
described techniques are shown in Figs. 11.21–11.24.
A B
C D E
Fig. 11.21 A 50-year-old woman underwent chin augmentation with a 3-mm two-piece, porous polyethylene implant at the time of
rhytidectomy. It was placed to lower the most projecting point of the chin. (A) Preoperative frontal view. (B) Preoperative lateral view.
(C) Postoperative frontal view. (D) Postoperative lateral view. (E) Postoperative oblique view. From Yaremchuk 2003,4 with permission.
149
Chapter 11 Chin
A B
C D
150
Skeletal asymmetries
A B
C D E
Fig. 11.23 A 31-year-old man underwent chin augmentation with a 7-mm projection two-piece porous polyethylene implant. A submental
lipectomy was performed. (A) Preoperative frontal view. (B) Preoperative lateral view. (C) Postoperative frontal view. (D) Postoperative lateral
view. (E) Postoperative oblique view. From Yaremchuk 2003,4 with permission.
SKELETAL ASYMMETRIES
Congenital asymmetries of the facial skeleton are usually more complex than
localized areas of volume excess or deficiency. Rather they resemble a warp-
ing or twisting of the facial skeleton. This is difficult to discern on physical
examination or plain X-rays but becomes obvious with three-dimensional
CT imaging. CT data also allows fabrication of hard or virtual models for
planning. Computer-aided design and manufacture (CAD/CAM) of implants
provides added sophistication when addressing significant asymmetries (see 151
Chapters 14 and 15).
Chapter 11 Chin
A D
B E
C F
SECONDARY SURGERY
A B C
D E F
Fig. 11.25 A patient exhibiting deformity due to mentalis muscle damage including chin ptosis, lip descent and a deepened intraoral sulcus.
(A) Chin pad ptosis. (B) Lower lip descent. (C) Deep sulcus due to loss of mentalis continuity or detachment. (D) Corrected chin ptosis. (E)
Restored lip posture. (F) Restored sulcus.
A B
153
Chapter 11 Chin
Implant-related deformity
Dissatisfaction with previous chin implant surgery most often includes implant
asymmetry (particularly with extended implants), implant malposition, and
poor implant-to-native mandible transition (Figs. 11.14 and 11.16).
Revision surgery requires implant removal and replacement with an
appropriately sized, shaped, and positioned implant (Fig. 11.27). Removal
A B
C D E
Fig. 11.27 A 36-year-old woman presented 17 years after previous smooth silicone chin implant placement. She was displeased with the
asymmetry and unnatural appearance of her chin. Through a submental approach, the silicone implant was removed. It was replaced
154 with a two-piece porous polyethylene implant fixed with screws. A submental lipectomy was performed. (A) Preoperative frontal view.
(B) Preoperative lateral view. (C) Postoperative frontal view. (D) Postoperative lateral view. (E) Postoperative oblique view. Despite the
replacement with a symmetrically positioned and immobilized implant, asymmetry, although less, persists. This is due to the soft tissue
distortion caused by the contraction process encapsulating the malpostioned original implant.
Sliding genioplasty
Fig. 11.28 CT scan showing implant over tooth root. Bone erosion
resulted in root exposure and symptoms necessitating implant
removal and root canal surgery.
SLIDING GENIOPLASTY
155
Chapter 11 Chin
A B
Fig. 11.29 Advancement osteotomy of chin results in tightening of the suprahyoid muscles and may decrease submental fullness. (A) Before
osteotomy. (B) After osteotomy and advancement. Note indentation at osteotomy site.
156
Sliding genioplasty
A B
Fig. 11.32 Implants are available that span the gap in inferior border contour after horizontal or sagittal osteotomy (Matrix Surgical, Atlanta,
GA). These implants may be placed at the time of osteotomy surgery or during secondary surgery. (A) Model with osteotomy gap. (B) Implant
spans osteotomy gap resulting in regular mandible border.
C D
REFERENCES
1. Millard DR. Adjuncts in augmentation mentoplasty and corrective rhinoplasty. Plast Reconstr
Surg 1965;36:48–61.
2. Spear SL, Kassan M. Genioplasty. Clin Plast Surg 1989;16(4):695–706.
3. Zide BM, Pfeifer TM, Longaker MT. Chin surgery: I. Augmentation – the allures and the alerts.
Plast Reconstr Surg 1999;104(6):1843–53.
4. Yaremchuk MJ. Improving aesthetic outcomes after alloplastic chin augmentation. Plast
Reconstr Surg 2003;112:1422–32.
5. Newman J, Dolsky RL, Mai ST. Submental liposuction extraction with hard chin
augmentation. Arch Otolaryngol 1984;110(7):454–7.
6. Courtiss EH. Suction lipectomy of the neck. Plast Reconstr Surg 1985;76(6):882–9.
7. Farkas LG, Hreczko TA, Katic MJ. Craniofacial norms in North American Caucasians from
birth (one year) to adulthood. In: Farkas LG, editor. Anthropometry of the head and face. 2nd
ed. New York: Raven Press; 1994. Appendix A.
8. Steiner CC. Cephalometrics in clinical practice. Angle Orthod 1959;29:8–29.
9. Hambleton RS. Tissue covering of the skeletal face as related to orthodontic problems. Am J
Orthod 1964;50(6):405–20.
10. Burstone CJ. Lip posture and its significance in treatment planning. Am J Orthod
158 1967;53(4):262–84.
References
11. Ricketts RM. Esthetics, environment and the law of lip relation. Am J Orthod 1968;54(4):
272–89.
12. Legan HL, Burstone CJ. Soft tissue cephalometric analysis for orthognathic surgery. J Oral
Surg 1980;38(1):744–51.
13. Flowers RS. Alloplastic augmentation of the anterior mandible. Clin Plast Surg 1991;18(1):
107–38.
14. McCarthy JG, Ruff GL. The chin. Clin Plast Surg 1988;15(1):125–37.
15. Farkas LG, Sohm P, Kolar JC, Katic MJ, Munro IR. Inclinations of the facial profile: art versus
reality. Plast Reconstr Surg 1985;75(4):509–19.
16. Gonzalez-Ulloa M. Quantitative principles in cosmetic surgery of the face (profileplasty). Plast
Reconstr Surg 1962;29:186–98.
17. Gonzalez-Ulloa M, Stevens E. The role of chin correction in profileplasty. Plast Reconstr Surg
1968;41(5):477–86.
18. Yaremchuk MJ. Mandibular augmentation. Plast Reconstr Surg 2000;106:697–706.
19. Dann JJ, Epker BM. Proplast genioplasty: a retrospective study with treatment
recommendations. Angle Orthod 1977;47(3):173–85.
20. Moenning JE, Wolford LM. Chin augmentation with various alloplastic materials: a
comparative study. Int J Adult Orthodon Orthognath Surg 1989;4(3):175–87.
21. Karras SC, Wolford LM. Augmentation genioplasty with hard tissues replacement implants. J
Oral Maxillofac Surg 1998;56(5):549–52.
22. Michelow BJ, Guyuron B. The chin: skeletal and soft tissue components. Plast Reconstr Surg
1995;95(3):473–8.
23. Hwang K, Jin S, Park JH, Kim DJ, Chung IH. Relation of mental nerve with mandibular
branch of the facial nerve. J Craniofac Surg 2007;18(1):165–8.
24. Zide BM. The mentalis muscle: an essential component of chin and lower lip position. Plast
Reconstr Surg 1989;83(3):413–20.
25. Zide BM. Discussion of Yaremchuk MJ. Improving aesthetic outcomes after alloplastic chin
augmentation. Plast Reconstr Surg 2003;112:1422–32; discussion 1433–1434.
26. Terino EO. Alloplastic contouring in the malar-mid-face-middle third facial aesthetic unit. In:
Terino EO, Flowers RS, editors. The art of alloplastic facial contouring. St. Louis: Mosby; 2000.
159
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Video 11.1 Chin implant. This video demonstrates the placement of a two-piece porous
polyethylene implant using a submental approach.
160.e1
Chapter 12
Mandible
INDICATIONS
Normal dimensions
Most patients who desire mandible augmentation have lower face horizontal
dimensions that relate to the upper and middle thirds of the face within a nor-
mal range (Figs. 12.1 and 12.2).1 These patients, usually males, perceive a wider
lower face as desirable. This group benefits from implants designed to augment
the ramus and posterior body of the mandible and, in so doing, increase the
bigonial distance. Other patients desire more definition and angularly to the
mandibular border. Implants that augment the anterior mandible back to the
ramus can achieve this goal.
Male Female
116 + 4 111 + 5
ft-ft (116 mm) Bitemporal ft-ft (111 mm)
Bigonial
Fig. 12.1 Normal values in millimeters for upper, middle, and lower facial width in white North American adult men (ages
19 to 25) (n = 109) and young white adult women (n = 200).1 The bigonial distance (go–go) is measured from gonion (go) to
gonion, which is the most lateral point of the mandibular angle close to the bony gonion. Note that the male lower face is both
relatively and absolutely wider than that of the female.
161
Chapter 12 Mandible
cdl cdl
68 mm 62 mm
go go
gn 87 mm gn 82 mm
78º 84º
Mentocervical angle Mentocervical angle
A B
Fig. 12.2 Normal values for mentocervical angle (in degrees), height of the mandible ramus (in millimeters; go–cdl),
and depth of the lower face (in millimeters; go–gn) in white North Americans: (A) young adult men and (B) young
adult women.1 The menton (or gnathion; gn) is the lowest median landmark on the lower border of the mandible. It is
identified by palpation and is identical to the bony gnathion. The gonion (go) is the most lateral point of the mandibular
angle close to the bony gonion. The mentocervical angle is formed by the upper contour of the chin and the surface
beneath the mandible.
Skeletal deficiency
Another group of patients who benefit from mandible augmentation are those
with skeletal mandibular deficiency (Fig. 12.3).2 It has been estimated that
approximately 5% of the total US population has skeletal mandibular deficiency
resulting in a class II occlusal problem. The majority of these patients (approxi-
mately 80%) can have their dental relationships normalized through orthodon-
tic tooth movement. The remaining 20%, or 1% of the total population, have
mandibular deficiency that is so severe that surgical mandibular advancement
would be needed to correct it.2
The classic method of correcting class II dental malocclusion in patients with
significant mandibular deficiency, in addition to preoperative and postopera-
tive orthodontic treatment, includes sagittal split ramus osteotomy and sliding
advancement genioplasty, with possible Le Fort I maxillary impaction. This
combination of procedures can provide a class I dental relationship while nor-
malizing the skeletal contour. In patients with mandibular deficiency who have
had their malocclusion corrected through orthodontics alone, mandibular oste-
otomy would disturb these dental relationships, requiring extensive periopera-
tive orthodontic treatment. This type of treatment is both costly and time
consuming. Alloplastic augmentation of the mandible can provide a visual
effect similar to and, in my opinion, superior to that of sagittal osteotomy with
advancement. Implant augmentation involves a less surgical procedure that
avoids any further dental manipulation. Mandible implants can address the
obtuse mandible angle with steep mentocervical angle, as well as the decreased
162 vertical (go–cdl) and transverse ramus (go –gn) dimensions. An extended chin
implant will camouflage the poorly projecting chin.
Indications
Fig. 12.3 Soft tissue contour and skeletal configuration of a patient with
mandibular deficiency and corrected occlusion. Note the obtuse mandibular
and mentocervical angles with steep mandibular plane.
A C
Fig. 12.4 Illustration (A) showing skeletal contour after sagittal split osteotomy and advancement of the distal
segment, as well as sliding advancement genioplasty of the deficient mandible. Note that there is an indentation along
the mandibular border at the sites of osteotomy and advancement. Acrylic models (B, C) obtained from CT scan data of
a patient who had undergone sagittal split and horizontal maxillary osteotomies. Note the contour irregularities along
the mandibular border at the sites of mandibular osteotomies. Note also the asymmetries in the posterior segment
position. These will lead to discrepancies in lower face width and height.
Physical examination
Physical examination is the most important element in preoperative assessment
and planning. Reviewing life-size posteroanterior and lateral photographs with
the patient can be helpful when discussing aesthetic concerns and goals. To
allow the patient to understand the scale and scope of augmentation, it is useful
to have sample implants available to demonstrate on a model skull and to apply
164
these implants to the relevant area of the patient’s face.
Surgical anatomy
X-rays
Posterior–anterior and lateral cephalograms provide data that help the surgeon
determine how the dimension of the implant might be altered to best suit the
patient. Three-dimensional computed tomographic (CT) scans and the models
obtained from their data can be invaluable when attempting to correct asym-
metries associated with congenital, posttraumatic, or postsurgical deformities.
In general, however, the size and position of the implant are largely aesthetic
judgments. An approximately 1:1 ratio of augmentation to resultant projection
is anticipated where soft tissue coverage is relatively thin, such as the inferior
border of the mandible. Masseter muscle coverage over the ramus decreases the
amount of projection provided by the implant.
Skeleton
The mandible consists of the tooth-bearing body and the ramus that extends
upward from the angle. The ramus, including the angle, is covered on its
external surface by the masseter muscle. The gonion is the tip of the outer
surface of the angle. The outer surface of the angle may be embellished by a
masseteric tuberosity denoting the insertion of the masseter muscle. (Its inner
surface may be raised by a pterygoid tuberosity where the medial pterygoid
muscle inserts.) The upper aspect of the ramus ends posteriorly in a condylar
process and anteriorly in a coronoid process separated by the mandibular
notch. The oblique line runs forward and downward from the anterior border
of the ramus. It affords attachment for the depressor labii inferioris and
depressor anguli oris. The platysma is attached near the inferior border of the
mandible. The buccinator muscle is attached to the outer lip of the superior
border of the mandible as far forward as the first molar tooth. The mental
foramen lies approximately at the interspace between the two premolars and
about midway in the height of the dentulous adult mandible. As the body
proceeds anteriorly toward the midline, it swells out to form the mental
protuberance.
Musculature
There are four muscles predominantly responsible for the movement of the
mandible: the masseter, the temporal, the medial pterygoid, and the lateral
pterygoid. Only the masseter and, indirectly, the medial pterygoid, as part of
the mandibular sling, are encountered during mandibular augmentation. The
masseter muscle consists of superficial and deep portions. The larger superficial
portion arises from the zygomatic process of the maxilla and from the anterior
two-thirds of the inferior border of the zygomatic arch. Its fibers pass inferiorly
and posteriorly to insert into the angle and inferior half of the lateral surface of
the ramus of the mandible. The masseter and the medial pterygoid muscle are
so positioned that they form a sling around the inferior border of the mandible
and therefore suspend the angle of the mandible. When placing a mandibular
angle implant it is necessary to separate the superficial portion of the masseter
and its sling component from the mandible in a subperiosteal plane. Tearing the
periosteum at the inferior border may disrupt the sling mechanism and allow
the freed masseter to ride up, causing a depression in the soft tissues overlying
the angle. This depression is exaggerated when the muscle is contracted. The 165
smaller deep portion of the masseter arises from the posterior third of the
Chapter 12 Mandible
Coronoid process
Mandibular notch
Condylar process
Mandibular foramen
Oblique line
Ramus
Mental
foramen
Angle
Mental
protuberance Body
Temporalis m.
Inferior alveolar n.
Lateral pterygoid m.
Medial pterygoid m.
Masseter m.
Mentalis m.
Oblique line
Mental n.
Buccinator m.
Platysma m.
Depressor anguli oris m.
B Depressor labii inferioris m.
inferior border and from the whole of the medial surface of the zygomatic arch.
This portion of the muscle passes anteriorly and inferiorly to insert into the
superior half of the ramus and the lateral surface of the coronoid process.
The buccinator is another muscle that is encountered during exposure of the
mandible during mandibular augmentation. The buccinator is the principal
muscle of the cheek. It forms the lateral wall of the oral cavity. It occupies the
area between the mandible and the maxilla and originates in part from both
structures. It originates from the outer surface of the alveolar processes of the
maxilla above and the mandible below, adjacent to their three molar teeth. The
other origin of this quadrilateral muscle is the pterygomandibular raphe, which
stretches from the medial pterygoid process to the inner surface of the mandi-
166
ble. Its fibers pass forward to become continuous with the orbicularis oris.
Implant design
IMPLANT DESIGN
Ramus and body implants are capable of changing the shape of the mandible in
three dimensions: bigonial width (go–go), ramus height (go–cdl), and body length
(go–gn). Fig. 12.6 depicts a basic implant design. The implant usually extends from
the posterior vertical border of the mandible to the oblique line. The flange at the
implant’s inferior border allows the implant to register to the mandible border.
Fig. 12.7 demonstrates a mandibular body and angle implant used with a
chin implant to augment all dimensions of the congenitally deficient mandible.
These implant designs and concepts are developed from the work of Terino,4,5
Whitaker,6 Aiche,7 Taylor and Teenier,8 Ramirez,9 as well as this author.10
OPERATIVE TECHNIQUE
Anesthesia
It is the senior author’s preference to perform chin and mandibular augmenta-
tion under general anesthesia (nasotracheal intubation is ideal). This provides a
panoramic view of the operative field. The airway is protected while the oral
cavity can be optimally prepared. The face and oral cavity are prepared with an
iodine solution after placement of a throat pack. The operative site is infiltrated
with 1:200,000 epinephrine solution to provide hemostasis.
Incisions
A generous intraoral mucosal incision is made to expose the ramus and body
of the mandible. It is made at least 1 cm above the sulcus on its labial side
(Fig. 12.8). The anterior ramus and body of the mandible are freed from their
soft tissues. It is important to free both the inferior and posterior borders of
the mandible of soft tissue attachments to allow implant placement (Fig. 12.9).
Freeing of the inferior border inevitably violates the pterygomasseteric sling.
Care should be taken not to divide the sling, which results in postoperative
elevation of the muscle and mid-ramus bulging with masseter muscle contrac-
tion. As determined by preoperative assessment, the implant is trimmed with a
scalpel or mechanical burr before its placement on the mandible.
The intraoral incision should be made at least 1 cm above the lower intraoral
sulcus on the labial side. This location provides adequate soft tissue for two-
layer closure and avoids saliva pooling over the suture line in the early post
operative period.
168
Operative technique
169
Chapter 12 Mandible
A B
Fig. 12.10 Screw fixation of an implant to the mandible through an intraoral approach. (A) Artist’s depiction.
(B) Clinical photograph during mandibular augmentation. The lower lip is being retracted. The portion of the
implant augmenting the mandibular body is being exposed. Note screw fixation.
to the mandible (Fig. 12.11). Screws are used to obliterate any gaps between the
mandible and the implant (Fig. 12.12). Screws are placed to avoid the antici-
pated path of the inferior alveolar nerve before its exit from the mental foramen.
Gaps may also arise when there are significant prominences on the surface of
the mandible. This is often the case at the angle of the mandible as well as at the
oblique line of the mandible body. Reduction of these prominences allows the
170
Operative technique
posterior surface of the implant to be congruent with the anterior surface of the
implant thereby avoiding gaps. Fig. 12.13 shows a mandible implant that was
improperly positioned or perhaps dislocated due to lack of fixation.
It is crucial to soften any transitions between the implant and the mandible,
particularly where the implant extends beyond the anterior mandibular bor-
der’s inferior edge. Any step-offs between the implant and the mandible in this
area may be visible in thin patients. Screw fixation of the implants allows scalpel
or mechanical burr final contouring with the implants in place. After hemostasis
as appropriate, the wound is irrigated (antibiotic irrigation is a rational adjunct
to decrease bacterial contamination in this operation performed through intra-
oral access). A suction drain with trocar travels through the skin and exits in the
postauricular area. The incision is closed in two layers with absorbable sutures.
Care is taken to evert the mucosal edges. An elastic tape dressing is used to help
apply the soft tissues to the implant and avoid hematoma formation. The suc-
tion drain usually remains until the next morning unless drainage persists.
A B C
A liquid diet is prescribed for the first 3 days postoperatively and a soft diet
for the next 5 days. Frequent mouth washes are advised as well as very careful
tooth brushing.
Medial
pterygoid
Contracted
Masseter masseter
Mandibular
Periosteal implant
tear
Periosteum
A B C
Fig. 12.14 Artist’s rendition of disruption of pterygomasseteric sling. (A) Sling intact. (B) Sling disrupted and mandible border exposed. (C)
Contraction of masseter results in bulge at mid-aspect of ramus.
Fig. 12.15 The inferior border of the ramus and retracted edge of
the masseter has been identified through a facelift approach. The
retracted edge has been purchased with figure-of-eight sutures and
will be sewn to drill holes located at the border of the mandible.
172
Clinical examples
CLINICAL EXAMPLES
A B C
D E F
Fig. 12.16 A 30-year-old male actor with normal facial dimensions and class I dental occlusion desired more “strength” to his jaw and
requested chin augmentation. After evaluation, a mandible ramus and posterior body augmentation with the implants described in Fig. 12.6
was performed as well as a tertiary rhinoplasty. (A) Preoperative frontal view. (B) Postoperative frontal view. (C) Artist’s simulation of implant
surgery – frontal view. (D) Preoperative lateral view. (E) Postoperative lateral view. (F) Artist’s simulation of implant surgery – lateral view.
173
Chapter 12 Mandible
A B C
D E F
Fig. 12.17 A 21-year-old woman who had undergone orthodontic correction of her class II malocclusion desired improved nasal and
mandibular contour. Rhinoplasty and mandibular augmentation with mandibular ramus and body implants as well as an extended chin
implant were undertaken. (A) Preoperative frontal view. (B) Postoperative frontal view. (C) Artist’s simulation of implant surgery – frontal view.
(D) Preoperative lateral view. (E) Postoperative lateral view. (F) Artist’s simulation of implant surgery – lateral view.
174
Clinical examples
A B C
D E F
Fig. 12.18 A 35-year-old male had five previous chin operations. He desired a very strong mandible. A silicone chin implant was removed.
A 9-mm porous polyethylene chin implant and a mandibular angle implant were placed. The chin pad was resuspended. (A) Preoperative
frontal view. (B) Preoperative lateral view. (C) Preoperative oblique view. (D) Postoperative frontal view. (E) Postoperative lateral view. (F)
Postoperative oblique view.
175
Chapter 12 Mandible
A D
B E
C F
176
References
A B
C D
Fig. 12.20 A 24-year-old woman underwent chin and mandible augmentation. (A) Preoperative frontal view. (B) Postoperative frontal view.
(C) Preoperative oblique view. (D) Postoperative oblique view.
REFERENCES
1. Farkas LG, Hreczko TA, Katic MJ. Craniofacial norms in North American Caucasians from
birth (one year) to young adulthood. In: Farkas LG, editor. Anthropometry of the head and
face. 2nd ed. New York: Raven Press; 1994.
2. Bell WH, Proffit WR, Chase DL, Wickwire NA, Poultom DR. Mandibular deficiency. In: Bell
WH, Proffit WR, White RP, editors. Surgical correction of dentofacial deformities, vol. 1.
Philadelphia: Saunders; 1980.
3. Semergidis TG, Migliore SA, Sotereanos GC. Alloplatic augmentation of the mandibular angle.
J Oral Maxillofac Surg 1996;54(12):1417–23.
4. Terino EO. Alloplastic facial contouring: surgery of the fourth plane. Aesthetic Plast Surg
1992;16(3):195–212.
5. Terino EO. Unique mandibular implants, including lateral and posterior angle implants. Facial
Plast Surg Clin North Am 1994;2:311–28.
6. Whitaker LA. Aesthetic augmentation of the posterior mandible. Plast Reconstr Surg
1991;87(2):268–75.
7. Aiche AE. Mandibular angle implants. Aesthetic Plast Surg 1992;16(4):349–54.
8. Taylor CO, Teenier TJ. Evaluation and augmentation of the mandibular angle region. Facial
Plast Surg Clin North Am 1994;2(3):329–37.
9. Ramirez OM. Mandibular matrix implant system: a method to restore skeletal support to the
lower face. Plast Reconstr Surg 2000;106(1):176–89.
10. Yaremchuk MJ. Mandibular augmentation. Plast Reconstr Surg 2000;106(3):697–706.
11. Thomas MA, Yaremchuk MJ. Masseter muscle reattachment after mandibular angle surgery.
Aesthet Surg J 2009;29(6):473–6.
177
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Video 12.1 Mandible angle augmentation. This video demonstrates the placement of a
porous polyethylene mandible angle implant immobilized with titanium screws.
178.e1
Chapter 13
Soft tissue ptosis secondary to gravity has long been considered the major
mechanism responsible for facial aging. There is no doubt that gravity and
ptosis are the main factors leading to facial aging.2 Lambros and others have
concluded that changes in volume of cheek fat, both loss and gain, rather than
ptosis account for an aged appearance.3,4 Numerous anatomical studies, how-
ever, show that there are also many changes to the craniofacial skeleton as
patients age that contribute to the aging process.
The aging face typically shows the following changes: descent of the brow,
changes in contour of the upper eyelid, medialization of the lateral canthus,
lower eyelid descent, deflated infraorbital skin envelope, increased visibility of
the lid–cheek junction and nasojugal crease, increased prominence and depth
of the nasolabial fold, and increased prominence of the labiomandibular crease.
These signs of aging have been related to changes in skin and soft tissue.
In addressing soft tissue ptosis and volume changes, many facelifting tech-
niques involve the removal of excess skin and also fat grafting and sculptur-
ing. The main purpose of this chapter is to address the skeletal changes in the
face that contribute to aging. Other chapters discuss the techniques available to
address and reconstruct the facial skeleton for a more youthful appearance as a
sole procedure or in addition to other techniques.
In addition to soft tissue changes, it has been demonstrated that there is remod-
eling of the craniofacial skeleton with age,5–7 for example, bony remodeling in
the orbit.8,9 These will be discussed separately in the remainder of this chapter.
One of the theories behind the skeletal changes is mechanotransduction,
which is the process of skeletal remodeling due to mechanical forces of soft tis-
sue on bone.10
The functional matrix hypothesis states that “epigenetic, extra skeletal
factors and processes are the prior, proximate, extrinsic, and primary cause 181
of all adaptive, secondary responses of skeletal tissues and organs.”10 This
Chapter 13 Rejuvenation of the aging face and skeleton with implants
The notion of orbital aging has been the focus of several strands of research.
Pessa analyzed the changes to the orbital rims in 30 male skulls in three age
categories at the Smithsonian Institute. It was found that there was no change
in orbit width or height with increasing age. However, there was curve distor-
tion of the superomedial upper orbit and inferolateral orbit, which led Pessa to
believe that the orbital rims receded in only these regions, without an overall
change in orbit height or length.8
In a more comprehensive study by Kahn and Shaw, 60 white patients (30
female, 30 male), underwent facial bone computed tomography (CT) scans to
demonstrate how specific bony aspects of the orbit change with age. The study
population included 10 male and 10 female patients from each of the three age
categories: young (25–44 years), middle (45–64 years), and old (65+ years). CT
scans underwent three-dimensional reconstruction with volume rendering.9
182 The results, illustrated in Fig. 13.1, concluded that, with age, bony changes and
soft tissue consequences occur. These include the following:
The aging orbital skeleton
Youth Age Fig. 13.1 Upper panel: Illustrations showing the typical appearance
of orbital tissues in youth (left) and old age (right). Lower panel:
Three-dimensional CT scans showing typical contours of the orbital
skeleton in a young female (left) and old female (right). These
illustrations and images correlate the aging changes that take place
in periorbital appearance with changes to the underlying skeleton as
described in detail in the body of this chapter.
A B C
Fig. 13.2 Alloplastic augmentation of the infraorbital rim can restore youthful contour in an aged skeleton. (A) Youthful orbit. (B) Aged orbit.
(C) Implant augmenting aged orbit to simulate contour of youthful orbit.
A B
Fig. 13.3 Clinical example of a 45-year-old man who underwent infraorbital rim skeletal augmentation together with subperiosteal
midface elevation to rejuvenate the aged orbit. Note postoperative elevation of lower lid and cheek, lengthening and narrowing of
palpebral fissure, as well as lateralization of lateral canthus. (A) Preoperative appearance. (B) Postoperative appearance at 1 year after
surgery.
The midfacial skeleton, consisting of the inferior orbital rim, the maxilla
(including the pyriform aperture), and the zygoma, are also subject to the
process of facial aging and bony changes. Literature by Pessa,16,17 Shaw,18,19
and others10,11,20,21 has shown a number of changes that occur to the bones
of the midface as the aging process unfolds (Fig. 13.4). These changes can be
defined as:
• retrusion of the lower maxilla, resulting in the development of nasolabial
folds18;
• retrusion of the orbital rim and anterior cheek mass in relation to the cor-
neal surface17 (Fig. 13.5).
The above bony changes may result in the appearance of a midface concavity,
which gives the appearance of being tired due to the presence of long lower
eyelids, loss of cheek prominence, rounding of the lateral canthal angle, and
184 increased vertical height of the palpebral fissure.22
The aging midfacial skeleton
A B
Fig. 13.4 Images showing retrusion of the midface skeleton with age as demonstrated by the difference in glabella, maxilla, and pyriform
angles. (A) Young female skeleton. (B) Aged female skeleton. From Shaw and Kahn,18 with permission.
A Cornea B Cornea
It is believed that the decrease in bony projection that occurs with aging
speeds the effect of gravity on the descent of an unsupported soft tissue enve-
lope.22 An alternate hypothesis is put forward by Levine, who suggests that soft
tissue descent is the “engine” driving the aging process, with bone relocation
and reshaping determined by the pull of surrounding tissues.20 Regardless of
the pathophysiologic mechanism, skeletal augmentation provides an effective
method to restore facial convexity and to rebuild a platform that supports the
soft tissues of the face.23
185
Chapter 13 Rejuvenation of the aging face and skeleton with implants
A B
C D E
Fig. 13.6 The potential for implants to restore youthful midface contours is illustrated. (A) Young skeleton. (B) Aged skeleton. Illustrations
186 demonstrating the potential of implants to restore a youthful (more projecting and convex) midface skeletal contour. (C) Infraorbital rim
implant, (D) malar implant, and (E) pyriform aperture implant.
The aging lower facial skeleton
A B
Fig. 13.7 An example of the projecting and rejuvenating effect of pyriform aperture augmentation on the lower midface: (A)
preoperative and (B) postoperative appearance.
The mandible is the foundation of the lower face. Normal mandibular propor-
tions, including ramus height and length of the mandibular body, provide excel-
lent support for the soft tissue repositioning that occurs with aging. However,
patients with a short ramus, rounded mandibular angle, and decreased man-
dibular projection are less skeletally equipped to gracefully support middle and
lower face soft tissue repositioning with age.21
What exactly happens to the mandible as it ages? Which proportions are affected
by the aging process? In a study by Shaw et al.,21 facial bone CT scans were obtained
from 120 white subjects, of which 60 were female and 60 were male. The population
was further organized into three different age groups (20–40 years, 41–64 years, 65+
years), with 20 females and 20 males in each age category. The patients were mea-
sured for: bigonial width, ramus breadth, ramus height, mandibular body height,
mandibular body length, and mandibular angle. Fig. 13.8 demonstrates the mor-
phology of a young and aged female mandible. The results revealed the following:
• Mandibular width did not significantly change with increasing age, which
implies that skeletal width of the lower face does not impact the aged ap-
pearance of the lower face.
• Mandibular angle increased with age and became more blunted, which
results in less jawline definition and a softer, more oval appearance of the
lower face.
• Mandibular height and mandibular length (projection) significantly de-
creased with age. Interestingly, the mandible projection decreases before
there is a decrease in mandible length. These changes may cause the ap-
pearance of a receding chin, and the overall loss of mandibular volume
187
Chapter 13 Rejuvenation of the aging face and skeleton with implants
A B
Fig. 13.8 Morphologic changes that occur with age in the mandible. (A) Young skeleton. (B) Aged skeleton.
may weaken the support of the buccal fat pad, allowing it to descend and
cause the appearance of jowls. Loss of mandibular volume also affects
the aging process of the neck by contributing to the increased laxity of the
platysma and soft tissues of the neck.
• The male study subjects had greater values for ramus height and mandibu-
lar body length as compared to the female subjects.
• The only measurement that was larger for female subjects compared to
male subjects was the mandibular angle. This explains why males tend to
exhibit stronger, more prominent jawlines than females, as the male man-
dibular angle is more acute.
The mandible changes dramatically with age, and the bony aging process is
primarily that of contraction and morphologic change. Effective rejuvenation of
the mandibular area should thereby account for both soft tissue treatments and
bony loss compensation. This approach is demonstrated in Fig. 13.9 where a
53-year-old woman underwent chin and mandible augmentation together with
rhytidectomy.
A limitation in the above-referenced human studies is that they are cohort
studies, not longitudinal, meaning they involved different groups of patients
at different age intervals, rather than observing the same patients over time. In
2017, the first longitudinal study of human facial skeletal aging was published
by Paskhover et al.24 It documents patterns of change in the facial skeleton
of 14 patients who underwent CT scans at least 8 years apart, with the initial
CT measurements documented between 40–55 years. The study revealed that,
with aging, the maxillary and piriform angles significantly decrease, as do PEARL
the glabellar and maxillary angles, whereas the piriform width significantly Facial skeletal convexity and
increases. The study also notes some differences in these patterns between projection identify facial youth.
188 sexes.24
References
A B
Shaw et al.25 have suggested that skeletal bone mineral density of the face
changes with age similar to the axial skeleton. Their pilot study attempts to
pinpoint the time when these skeletal changes occur, which can allow objective
testing of specific treatments aimed at slowing or reversing these bony aging
changes. Pharmaceuticals and mechanical devices may delay, treat, or even
prevent these facial skeletal changes from occurring, opening up a whole new
paradigm in facial aging prevention.24 In the meantime, the aging process can
be masked and rejuvenated using facial implants in combination with soft tis-
sue manipulations.
REFERENCES
1. Zimbler MS, Kokoska MS, Thomas JR. Anatomy and pathophysiology of facial aging. Facial
Plast Surg Clin North Am 2001;9(2):179–87, vii.
2. Tonnard PL, Verpaele A, Gaia S. Optimising results from minimal access cranial suspension
lifting (MACS-lift). Aesthetic Plast Surg 2005;29(4):213–20; discussion 221.
3. Lambros V. Observations on periorbital and midface aging. Plast Reconstr Surg
2007;120(5):1367–76; discussion 1377.
4. Coleman SR. Facial recontouring with lipostructure. Clin Plast Surg 1997;24(2):347–67.
5. Israel H. Recent knowledge concerning craniofacial aging. Angle Orthod 1973;43(2):176–84.
6. Behrents RG. Growth in the aging craniofacial skeleton. Monograph 17. Craniofacial Growth
Series. Ann Arbor: Center for Human Growth and Development, University of Michigan;
1985.
7. Bartlett SP, Grossman R, Whitaker LA. Age-related changes of the craniofacial skeleton: an
anthropometric and histologic analysis. Plast Reconstr Surg 1992;90(4):592–600.
8. Pessa JE, Chen Y. Curve analysis of the aging orbital aperture. Plast Reconstr Surg
2002;109(2):751–5; discussion 756–760.
9. Kahn DM, Shaw RB. Aging of the bony orbit: a three-dimensional computed tomography
study. Aesthetic Surg J 2008;28(3):258–64.
10. Moss ML. The functional matrix hypothesis revisited. 1. The role of mechanotransduction. Am
J Orthod Dentofac Orthop 1997;112(1):8–11.
189
Chapter 13 Rejuvenation of the aging face and skeleton with implants
11. Sinsel NK, Opdebeeck H, Guelinckx PJ. The effect of unilateral partial facial paralysis and
muscle ablation on craniofacial growth and development: an experimental study in the rabbit.
Plast Reconstr Surg 1998;102(6):1894–912.
12. Matic DB, Yazdani A, Wells RG, Lee TY, Gan BS. The effects of masseter muscle paralysis on
facial bone growth. J Surg Res 2007;139(2):243–52.
13. Instrum SM. Cephalometric comparison of the craniofacial skeletal morphology between
Mobius syndrome and non-syndromic controls. Dissertation University of Toronto, 1999.
National Library of Canada; 1999.
14. Staley RN, Bishara SE, Hanson JW, Nowak AJ. Craniofacial development in myotonic
dystrophy. Cleft Palate Craniofac J 1992;29(5):456–62.
15. Van den Bosch WA, Leenders I, Mulder P. Topographic anatomy of the eyelids, and the effects
of sex and age. Br J Ophthalmol 1999;83(3):347–52.
16. Pessa JE, Zadoo VP, Mutimer KL, et al. Relative maxillary recursion as a natural consequence
of aging: combining skeletal and soft-tissue changes into an integrated model of midfacial
aging. Plast Reconstr Surg 1998;102(1):205–12.
17. Pessa JE, Desvigne LD, Lambros VS, et al. Changes in ocular globe-to-orbital rim position
with age: implications for aesthetic blepharoplasty of the lower eyelids. Aesthetic Plast Surg
1999;23(5):337–42.
18. Shaw Jr RB, Kahn DM. Aging of the midface bony elements: a three dimensional CT study.
Plast Reconstr Surg 2007;119(2):675–81; discussion 682–683.
19. Shaw Jr RB, Katzel EB, Koltz PF, Yaremchuk MJ, Girotto JA, Kahn DM, Langstein HN. Aging
of the facial skeleton: aesthetic implications and rejuvenation strategies. Plast Reconstr Surg
2011;127(1):374–83.
20. Levine RA, Garza JR, Wang PT, Hurst CL, Dev VR. Adult facial growth: applications to
aesthetic surgery. Aesthetic Plast Surg 2003;27(4):265–8.
21. Shaw Jr RB, Katzel EB, Koltz PF, et al. Aging of the mandible and its aesthetic implications.
Plast Reconstr Surg 2010;125(1):332–42.
22. Sharabi SE, Hatef DA, Koshy JC, Hollier Jr LH, Yaremchuk MJ. Mechanotransduction: the
missing link in the facial aging puzzle? Aesthetic Plast Surg 2010;34(5):603–11.
23. Matros E, Momoh A, Yaremchuk MJ. The aging midfacial skeleton: implications for
rejuvenation and reconstruction using implants. Facial Plast Surg 2009;25(4):252–9.
24. Paskhover B, Durand D, Kamen E, Gordon NA. Patterns of change in facial skeletal aging.
JAMA Facial Plast Surg 2017;19(5):413–7.
25. Shaw Jr RB, Katzel EB, Koltz PF, Kahn DM, Puzas EJ, Langstein HN. Facial bone density:
effects of aging and impact on facial rejuvenation. Aesthet Surg J 2012;32(8):937–42.
190
Chapter 14
191
Chapter 14 Designer faces: CAD/CAM facial implants
A B
Fig. 14.2 CAD/CAM implant allows desired width, vertical elongation, and sagittal projection of the chin as well as correcting body
asymmetry. (A) Frontal view. (B) Lateral view.
A B C
Fig. 14.3 CT scan examples of off-the-shelf and CAD/CAM implants. (A) Frontal view of a three-dimensional CT scan revealing asymmetric
192 position of malar implants. (B) Frontal view of CAD/CAM malar implants. Note symmetric placement. (C) Worm’s eye view of CAD/CAM
implants that allow symmetry of implant position, as well as symmetry of combined implant plus underlying skeleton projection.
Implant development
A B
Fig. 14.5 Implant design using model format. (A) Model obtained from CT DICOM data. (B) Model with implant prototypes fashioned by the
treating surgeon.
IMPLANT DEVELOPMENT
Computed tomography (CT) scans are obtained to provide digital imaging and
communication in medicine (DICOM) data. DICOM is a standard for handling,
storing, printing, and transmitting information in medical imaging. This data
is used to create a three-dimensional model of the facial skeleton or a three-
dimensional image. The three-dimensional model allows the surgeon to craft
with clay the desired implant configuration. The clay is then used as a proto-
type for the implant design (Fig. 14.5). DICOM data can also be used to create
a three-dimensional image for use in virtual design sessions between surgeon
and software engineer to create an implant (Fig. 14. 6). This technique is pre-
ferred by the authors because it allows millimeter precision of design. The com-
193
puterized design is then used to computer manufacture an implant.
Chapter 14 Designer faces: CAD/CAM facial implants
A B
Fig. 14.6 Image created using DICOM data to design an implant. (A) Image of facial skeleton. (B) Virtually designed implant.
Critical to the design process is to recognize the patient’s goals. The patient
may desire to create angularity, provide symmetry, improve facial balance,
or correct irregularities. It is useful for the patient to provide photographs
of people who have the desired look. Digital manipulation of patient images
can be helpful. The patient should understand that these images are used
as guides in the design process and not predictions of the surgical outcome.
There is no algorithm that can translate a digitally created change in soft tis-
sue to an implant design that will result in the outer contour change. Effec-
tive communication between surgeon and patient is invaluable to the design
process.
Because the native facial skeleton is not symmetric, implant augmen-
tation will provide a “relative symmetry.” Chin implants should create
symmetry relative to the midline structures – nasal radix, nasal septum,
central incisors, and central lip elements. This symmetry should extend
from mental foramen to mental foramen. Lateral to the mental foramen,
mandible implants should relate to the width of the upper face. For exam-
ple, the extent of lateral augmentation of the mandible angles should
relate to the lateral orbital rims in the same way (Fig. 14.7). Designing
an implant for one side of the face and mirroring it to create an implant
for the opposite side will create mandible symmetry only if the mandible
and midface are symmetric prior to augmentation. When augmenting the
midface, the goal is to achieve similar implant-plus-skeleton projection
(Fig. 14.8). Because the contours of the midface will vary from one side
to the other, mirroring one side to the other is unlikely to result in similar
contours.
194
Personal design technique
195
Chapter 14 Designer faces: CAD/CAM facial implants
Clinical experience has taught the senior author to control the design process.
PEARL
After voicing their goals and preferences, patient participation in the step-by-
step design process has proved unrewarding. The design process is inevitably Limit patient involvement in the
protracted and therefore more expensive when the patient is involved. More ongoing design process. It is often
importantly, heavily patient-influenced designs have been almost routinely unrewarding for both patient and
surgeon.
disappointing to the patient.
Clinical examples are presented in Figs. 14.9–14.12.
A B
C D
Fig. 14.9 Preoperative and postoperative clinical appearance and three-dimensional CT images of a patient who underwent CAD/CAM
implant midface and mandible augmentation. (A) Preoperative appearance. (B) Postoperative appearance. (C) Image of native skeleton. (D)
Image of designed implants.
196
Personal design technique
C D
E F
G H
197
Chapter 14 Designer faces: CAD/CAM facial implants
C D
E F
198
G H
Personal design technique
A B
C D
E F
199
G H
Chapter 14 Designer faces: CAD/CAM facial implants
ACKNOWLEDGMENT
Presented by Dr. Yaremchuk at the 22nd Annual Hans R. Wilhelmsen MD, DDS
Lectureship in the Craniofacial Sciences, May 17, 2018, at the Johns Hopkins
Hospital in Baltimore, MD.
200
Chapter 15
Implant refinement of
postorthognathic surgery
facial contour
Le Fort I maxillary and sagittal split mandibular osteotomies are performed
to correct dental malocclusion and improve facial harmony. Skeletal move-
ments of large magnitude, particularly those for correction of preexisting facial
asymmetries, may create new contour irregularities and disharmony. Both the
midface and lower face can manifest characteristic postorthognathic contour
irregularities that are amenable to alloplastic implant improvement.
A B
Fig. 15.1 Typical facial contour sequelae after orthognathic surgery. (A) Lateral appearance of patient after Le 201
Fort I advancement osteotomy, sagittal split, and horizontal chin osteotomies. (B) Artist’s rendition showing
skeletal movements responsible for facial contour disharmonies and irregularities.
Chapter 15 Implant refinement of postorthognathic surgery facial contour
Sagittal split osteotomy of the deficient mandible with advancement in the sag-
ittal plane may result in ramus asymmetry and border irregularities (Figs. 15.1
and 15.2). Ramus asymmetry immediately after surgery occurs when the sur-
geon fails to create similar osteotomies and maintain similar osteotomy gaps
(with rigid fixation) on both sides. The surgeon loses control over the relation
of the proximal and distal fragments because the condyle must be positioned in
its fossa and the body must be positioned to correct the occlusion. The position-
ing of these two areas dictates ramus and angle position. In the orthognathic
literature, the concern for the improper positioning of the proximal segments
and condyle relates to its potential for condylar resorption and postoperative
relapse.6,7 In the pre-rigid fixation era this was almost always due to counter-
clockwise rotation of the ramus of the mandible because wire osteosynthesis
did not provide enough stability. Rigid fixation has virtually eliminated these
problems related to inadequate fixation.8,9
However, contour abnormalities may still occur due to incorrect positioning
with resultant counterclockwise rotation or after very large movements. Clini-
cal experience has revealed that this is due to not only the positional restraints
of condylar positioning and osteotomy variability as described above, but also
202 Fig. 15.2 Acrylic model of mandible resulting after sagittal split and horizontal chin osteotomies. (A) Frontal view. Note differences in
posterior mandible width and height. (B) Lateral view. Note border irregularities.
Implant refinement
ramus shape changes resulting from bone atrophy (Fig. 15.3). Depending on the
circumstance, this atrophy may result from devascularization and/or remodel-
ing from altered mechanotransduction forces in accordance with Wolff’s Law.
Gaps at the osteotomy sites after sagittal osteotomy of the mandible or horizon-
tal osteotomies of the chin with advancement can result in border irregularities.
Correction of contour irregularities after skeletal rearrangement have focused on
border defects at the sliding genioplasty osteotomy site, prompting some sur-
geons to fill the defect with hydroxyapatite.10 Surgical technique and the native
mandible anatomy determine the presence and severity of these irregularities.
Patients with “high-angle” mandibular deficiency, which is seen in associa-
tion with antegonial notching and vertically deficient rami, are predisposed to
visible notching after bilateral sagittal split osteotomy (BSSO). In patients with
“low-angle” mandibular deficiency, where the ramus height is adequate and
there is no antegonial notching, post-BSSO border irregularities reflect technical
deficiencies in creating and maintaining (assuming rigid fixation) the correct
osteotomy gap geometry of the buccal cortical plates. This geometry should be
the same on both sides.
The extent of parasymphyseal notching after horizontal osteotomy of the
chin with advancement is also influenced by surgical technique. By making the
osteotomy oblique, as the artist has depicted in Fig. 15.1, the distal segment is
shortened as it is advanced, which not only accentuates border irregularities
but also causes the bone cut to exit the inferior mandibular border where the
soft tissue coverage is more tenuous and exposes the notching. By lowering
the bone cut anteriorly, one can eliminate or minimize the obliquity of the oste-
otomy and, therefore, any shortening with a more proximal inferior border exit.
IMPLANT REFINEMENT
CAD/CAM IMPLANTS
Implant design
Two options are available for the design process: From the CT data, a three-
dimensional model is manufactured of the patient’s facial skeleton. The surgeon
augments the deficient areas on the model with clay. The implant company uses
the clay prototypes to manufacture implants. The alternative technique, which
is preferred, involves a Web-based meeting between the surgeon and the manu-
facturer’s engineer, at which time implants are designed virtually. This method
allows millimeter precision in design and measurable relations between the
upper and lower face (Fig. 15.4). Yu Wang et al.13 use CT data of the postortho
gnathic image to create a template that is used during the contour-modifying
procedure to modify an off-the-shelf implant.
Upper face
The midface disharmony after Le Fort I osteotomy and advancement is a defi-
ciency in the maxilla above the level of the osteotomy. Its custom implant correction
always includes the infraorbital rim and the medial aspect of the malar prominence.
The amount of its sagittal projection is an aesthetic judgment determined by the
amount of lower midface advancement and by the amount of globe prominence.
A B
204
Fig. 15.4 CAD and CAM to correct postorthognathic mandible contour irregularities and facial imbalance. (A)
CAD plan document. (B) CAD/CAM porous polyethylene implants.
Surgical technique
Lower face
The lower face disharmonies after BSSO include possible asymmetry
in lower face height and width as well as border irregularities. If a slid-
ing genioplasty has been performed, border irregularity at the osteotomy
sites and chin asymmetry may be present. A grid pattern placed over the
image is used to design the implant addressing the central and lateral por-
tions of the mandible separately. Centrally, that is from the midline to the
mental foramen, the implant is designed to be symmetric to the midline
as determined by the position of the columella and the central incisors.
Laterally, gonial angle position is determined by its relation to its respec-
tive upper face skeleton rather than the midline. The central and lateral
designs are then coordinated to provide a regular inferior mandible border
(Fig. 15.4).
SURGICAL TECHNIQUE
Upper face
The upper face is accessed through an intraoral sulcus incision and a
transconjunctival retroseptal incision with lateral canthotomy. Skin–mus-
cle lower lid flaps are an alternative approach. The midface is elevated
in a subperiosteal plane. The infraorbital nerve is identified and pre-
served. Large, rigid implants are often segmented to allow their place-
ment through limited exposure. The custom design dictates appropriate
placement, which is secured with screw fixation. The midface soft tissue
envelope is resuspended with sutures tied to the implant or drill holes in
the bone.
Lower face
The posterior mandible is accessed through intraoral sulcus incisions and a
submental incision is used to access the chin. The entire anterior face of the
mandible is elevated in the subperiosteal plane. The mental nerves are identi-
fied and preserved. Care is taken to minimize disruption of the masseteric sling
during implant placement. Implants are immobilized with titanium screws.
The wounds are closed in layers after a suction drain is placed, which exits in
the postauricular area. The drain is usually removed the morning after surgery.
Video 15.1 demonstrates the surgical placement of CAD/CAM porous poly
ethylene implants designed to correct irregularities and imbalances resulting
after sagittal split osteotomy.
205
Chapter 15 Implant refinement of postorthognathic surgery facial contour
PATIENT EXAMPLES
A B
C D
Fig. 15.5 A 35-year-old male had undergone Le Fort I impaction, sagittal split mandibular osteotomy, and horizontal chin osteotomy
with lengthening. The surgery had been redone on two occasions. Surgical refinement included CAD/CAM chin and mandible
implants to provide angle definition, correction of contour irregularities, and increase chin projection. The native chin was shortened
to allow lip resuspension. (A) Preoperative appearance. (B) CT image. (C) Postoperative frontal appearance at 18 months. (D) Frontal
implant design.
206
Patient examples
A B
C D
Fig. 15.6 A 26-year-old woman had undergone Le Fort I advancement, sagittal split
osteotomy, and horizontal osteotomy with advancement at age 20. Midface and mandible
implant surgery, chin lengthening, and rhinoplasty were performed 6 years later. (A)
Preoperative frontal view. (B) Postoperative frontal view. (C) Preoperative lateral view. (D)
Postoperative lateral view.
207
Chapter 15 Implant refinement of postorthognathic surgery facial contour
C E
Fig. 15.7 Clinical example of CAD/CAM implants to refine midface and skeletal contours previously performed to address congenital facial
skeletal asymmetry. (A) Preoperative frontal and worm’s eye views of 15-year-old female. (B) Views after midface and mandibular osteotomies
with residual lower face asymmetry 6 years postoperatively. (C) One year later after CAD/CAM porous polyethylene implant to augment
208 deficient left mandible. An osseous genioplasty was also performed. (D) Intraoperative view of genioplasty and left-sided implant. (E) Model
shows postorthognathic mandible with CAD/CAM implant. From Lee et al. 2018,12 with permission.
References
REFERENCES
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management of midface and maxillary deficiency. J Oral Maxillofac Surg 1994;52(3):327–31.
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basis, and surgical technique. J Oral Maxillofac Surg 1991;49(10):1089–97.
3. Nocini PF, Boccieri A, Bertossi D. Gridplan midfacial analysis for alloplastic implants at the
time of jaw surgery. Plast Reconstr Surg 2009;123(2):670–9.
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polyethylene implants and orthognathic surgery for correction of malar deficiency. J Oral
Maxillofac Surg 1998;56(6):734–41; discussion 742.
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discussion 1593–1595.
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cases. J Oral Surg 1980;38(4):265–82.
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2012;114(5):567–76.
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Video 15.1 CT-designed implants to correct postorthognathic irregularities.
This video demonstrates the surgical placement of CAD/CAM porous polyethylene implants
designed to correct irregularities and imbalances resulting after sagittal split osteotomy.
210.e1