he temporomandibular joint (TMJ)
is a bilateral diarthrodial joint of the jaws in the
human skeleton. This unique joint can perform both hinge
and sliding functions and is the only synovial joint in
humans whose articulating surfaces are covered by
fibrocartilage. The joint is formed by the bony
articulations of the mandibular condyle and the temporal
bone (glenoid fossa and articular eminence). Interposed
between the condyle and the fossa is a piece of dense,
avascular fibrous connective tissue, the TMJ articular
disc. This disc divides the joint into superior and
inferior joint compartments, which normally do not
communicate with each other. The disc and condyle are in
a normal anatomic relationship if the posterior band of
the disc is located above the condylar head when the
mandibular condyle is centrically positioned in the fossa
(Figure 1a). The disc
is attached to the condylar neck by ligamentous soft
tissue attachments. The joint is circumferentially
surrounded by a fibrous capsule and has multiple
ligamentous attachments that provide stability,
especially in a lateral direction. TMJ dysfunction is a relatively
common condition: an estimated 12% to 87% of the US
population has at least 1 sign of TMJ dysfunction (1, 2).
TMJ dysfunction occurs more frequently in women than men
(8:1 ratio). The most common cause of TMJ dysfunction is
anterior and/or medial displacement of the articular disc
(also known as internal derangement of the TMJ) (Figure
1b).
Displacement of the TMJ articular disc can result in
decreased joint space; clicking, popping, or crepitation
during jaw function; arthritis; condylar resorption; jaw
deformities; malocclusion; inflammation; and compression
of the bilaminar tissue--all of which can cause various
degrees of pain and dysfunction (3). Chronic disc
displacement can lead to deformation of the disc, loss of
flexibility, vascularization of the disc (a normal disc
is avascular), and breakdown of the fibrocartilage
covering the condyle and fossa. The disc or, more
commonly, the bilaminar tissue posterior to the disc, can
perforate, and intracapsular adhesions can develop. These
changes can lead to progressive worsening of jaw function
and pain. Some common clinical symptoms of TMJ
dysfunction include TMJ sounds/noises, TMJ pain, facial
pain, headaches, limited range of mandibular movement,
change in occlusion, masticatory difficulty, earaches,
tinnitus, vertigo, and neck, shoulder, and back pain.
Some patients with pathological internal derangement of
the TMJ, however, are asymptomatic or have relatively
innocuous clinical symptoms.
Previously reported
clinical results of surgical TMJ disc-repositioning
procedures have been variable, with failures related to a
lack of long-term stability, indicating a need for
improved methods of disc stabilization (4, 5). Disc
displacement is often accompanied by a loss of structural
integrity of the posterior, medial, and lateral
supporting ligaments. Traditional disc-repositioning
techniques involve suturing (plication) of these inflamed
and often degenerated ligaments, contributing to the
instability of the disc after surgery. To overcome this
problem, Wolford et al (6) developed a surgical technique
that uses a bone anchor (Mitek mini anchor, Mitek
Products Inc., Westwood, Mass) to stabilize the TMJ
articular disc. This article presents some of the
clinical and research experience at Baylor University
Medical Center and Baylor College of Dentistry with the
use of the Mitek anchor in TMJ articular
disc-repositioning surgery.
REVIEW OF PUBLISHED
REPORTS
Although Annandale first
described surgical repositioning of the displaced
temporomandibular articular disc in 1887 (7), it was not
until 1978, when Wilkes used arthrography to describe the
anatomy, form, and function of the TMJ, that disc
repositioning became an accepted surgical technique (3,
8). Wilkes theorized that there was a very high
probability that the signs and symptoms of the
temporomandibular joint pain-dysfunction syndrome are
direct manifestations of internal derangement of the
joint (articular disc displacement). Before that
time, routine recommended treatment for TMJ internal
derangement was either to do nothing or to remove the
disc (diskectomy). In 1979, McCarty et al reported a 94%
success rate for disc-repositioning surgery; their
technique involved removing 3 to 4 mm of the
posterosuperior condylar surface and a posterior wedge
resection (2 mm) of the bilaminar zone with suture
reapproximation (9). Other surgeons, however, did not
experience similar success with this technique, and this
led to development of numerous new and modified
techniques for disc-repositioning surgery, which had
varying degrees of success (5, 6, 10-18). Some authors
have proposed arthroscopic suturing techniques to
reposition the disc (19, 20). However, the reliability of
an arthroscopic approach for predictably repositioning
and stabilizing the TMJ disc has not been documented.
THE MITEK MINI ANCHOR
Mitek anchors were
originally developed for use in orthopaedic surgery
procedures, such as rotator cuff repair, medial and
lateral collateral ligament repair, biceps tendon
reattachment, and other muscle, ligament, and tendon
repairs (21, 22). Although the anchors are available in
various sizes, the Mitek mini anchor (Figure
2) is
the most adaptable for TMJ disc stabilization. The
successful use of the device for TMJ articular disc
repositioning has been previously reported in the
literature by Wolford et al (6, 17, 18, 23).
The Mitek mini anchor is
cylindrical, measuring 1.8 mm in diameter and 5.0 mm in
length. The body of the anchor is composed of titanium
alloy (titanium 90%, aluminum 6%, vanadium 4%), while its
wings are composed of a nickel-titanium (Nitinol) alloy
that uses superelastic shape memory properties. An eyelet
in the posterior aspect of the anchor allows placement of
sutures, which can function as artificial ligaments (Figure
3).
SURGICAL TECHNIQUE
A modified short endaural
incision is used by the authors to gain access to the TMJ
area. The superior and inferior joint spaces are entered,
and the disc is identified and mobilized. The anterior,
lateral, and sometimes the medial ligamentous attachments
are freed, if indicated, to permit passive repositioning
of the articular disc over the condylar head. If
necessary, discoplasty, arthroplasty, and/or eminoplasty
are performed to optimize the fit of the disc, condyle,
and fossa. Arthroplasty and eminoplasty are avoided if
possible, since these procedures can create postsurgical
adhesions of the disc to the fossa and/or condyle,
contributing to decreased joint mobility, degenerative
joint disease, and, possibly, continued pain.
A 2 x 10 mm hole is made
in the posterior head of the con-dyle, 8 to 10 mm below
the top of the condyle and just lateral to the
midsagittal plane, by using a standard Mitek drill bit (Figure
4).
The Mitek anchor, with 2 0-Ethibond braided polyester
sutures (Ethicon, Inc., Somerville, NJ) threaded through
its eyelet, is then placed into the prepared hole by
using an inserter device. The nickel-titanium wings,
which possess superelastic properties, are pressed
against the body of the anchor as they pass through the
more dense cortical bone and are reopened when they enter
the softer medullary bone (Figure
4a).
This effectively locks the anchor into place within the
condylar head. The 2 Ethibond sutures are then secured to
the disc in a horizontal mattress fashion. One suture is
placed through the medial aspect of the posterior band of
the disc, and the other is placed through the lateral
aspect of the posterior band (Figure
4b).
The remaining bilaminar tissues, capsule, subcutaneous
tissue, and skin are then closed in a routine manner. Any
orthognathic (jaw) surgical procedures indicated to
maintain the original occlusion or to correct a
coexisting dentofacial deformity are then performed.
Postsurgical physical therapy may be indicated at the
discretion of the surgeon. Postsurgical imaging
demonstrates the presence of the Mitek anchor in the
condylar head (Figure
5).
EXPERIENCE AT BAYLOR
UNIVERSITY MEDICAL CENTER
The senior author (LMW)
has used the Mitek anchor for TMJ articular disc
repositioning since 1992 with good results. Laboratory
and clinical research studies conducted at Baylor
University Medical Center and Baylor College of Dentistry
led to Food and Drug Administration approval of the Mitek
mini anchor specifically for use in TMJ surgery in 1999
(6, 17, 23-26).
Laboratory research
Fields, Cardenas, and
Wolford evaluated the pullout strength of 20 Mitek mini
anchors placed in human cadaver condyles (24). Pullout
thresholds were reached when the cortical bone overlying
the anchor gave way (18 condyles) or when the suture
broke (2 condyles). There was no breakage, deformation,
or failure of the anchors. The pullout strength averaged
16.02 lbs (range, 8.5 to 28.4 lbs), which appears to be
adequate to stabilize the anchor during osseointegration.
Fields, Franco, and Wolford also demonstrated that
osseointegration of the Mitek mini anchors predictably
occurs in human mandibular condyles (25).
Clinical research
Wolford and coworkers
have published their clinical results after
disc-repositioning surgery using the Mitek anchor (6, 17,
23). Criteria for success in TMJ surgery include skeletal
and occlusal stability, significant decreases in TMJ and
myofascial pain, and a jaw opening of >35 mm. Wolford
et al reported a success rate of 91% in a group of 43
patients (78 joints) with an average postsurgical
follow-up duration of 2 1/2 years (23). Cardenas,
Wolford, and Goncalves studied 66 Mitek anchors after
placement in the TMJ for vertical and horizontal
positional changes based on standardized lateral
cephalometric tomograms and found excellent stability of
the Mitek anchors within condylar bone, with
statistically insignificant minor positional changes
(-0.01 mm with a range of -1.5 to 1.5 mm) long term (26).
We recently performed a
retrospective study evaluating 105 patients (89 women and
16 men) who underwent TMJ disc repositioning (27).
Criteria for inclusion in the study were as follows: 1)
presurgical TMJ disc displacement based on magnetic
resonance imaging (MRI) and clinical examination; 2) no
prior TMJ surgery; 3) salvageable articular disc; 4)
surgery for TMJ disc repositioning and stabilization with
the Mitek mini anchor; 5) absence of known connective
tissue/autoimmune disease; 6) absence of postsurgical
trauma; and 7) a minimum of 12 months postsurgical
follow-up. Clinical and radiographic evaluations were
done before surgery (T1), immediately after surgery (T2),
and at last follow-up (T3). Clinical evaluations were
performed by 1 clinician and included both an objective
evaluation of maximal incisal opening, lateral
excursions, and TMJ noises and a subjective evaluation
using visual analog scales for TMJ pain, facial pain, and
headaches (0 = no pain, 10 = worst pain); jaw function (0
= normal, 10 = no function); diet (0 = no restriction, 10
= liquids only); and disability (0 = no disability, 10 =
total disability). Acetate tracings of standardized
lateral cephalometric tomograms taken at T2 and T3 were
superimposed to evaluate anchor stability and assess for
condylar resorption. Student t test was used for
statistical analysis of results, and a P value
<0.01 was considered to be statistically significant.
An asterisk (*) denotes statistically significant
findings.
Mean patient age at the
time of surgery was 33 years, and the mean postsurgical
follow-up period was 46 months. A total of 188
disc-repositioning procedures were performed on the 105
patients. Simultaneous orthognathic surgery was performed
in 88 patients (83.8%) for correction of coexisting
dentofacial deformities. Mean visual analog scale scores
for the parameters assessed were as follows: TMJ pain* =
5.2 (T1) and 1.6 (T3); facial pain/headache* = 7.2 (T1)
and 2.4 (T3); jaw function* = 3.8 (T1) and 1.9 (T3);
diet* = 3.8 (T1) and 1.7 (T3); and disability* = 3.6 (T1)
and 1.1 (T3). Eighty-eight patients (83.8%) had TMJ
noises before surgery, and 6 patients (5.7%) had TMJ
noises at last follow-up. Mean maximum interincisal
opening measurements were 42.8 (T1) and 43.7 (T3). Mean
lateral excursion values were as follows: left, 5.3 mm
(T1) and 5.1 mm (T3); right, 5.1 mm (T1) and 5 mm (T3).
Fifty-eight patients (55%) reported severe TMJ pain
before surgery, while only 4 patients (3.8%) reported
severe pain at T3. Seventy-eight patients (74%) had
complete absence of TMJ pain at T3, whereas only 19
patients (18%) had no TMJ pain at T1. Only 2 patients
(1.9%) had a jaw opening of <35 mm at T3. In no
patient did TMJ pain or interincisal opening get worse
after surgery. Radiographic examination at T3
demonstrated no significant condylar resorption or
positional changes in the anchors.
DISCUSSION
TMJ dysfunction is a
relatively common condition, with a 12% to 87% reported
incidence in the population (1). Clinical symptoms of TMJ
dysfunction can mimic many other medical disease
processes, as patients can present with 1 or more of the
following symptoms: TMJ pain; headaches; myofascial pain;
neck, shoulder, and back pain; decreased jaw function;
clicking or popping of the jaw joint(s); earaches;
tinnitus; and vertigo. It is recommended that patients
with such symptoms be screened for TMJ pathology along
with other appropriate medical diagnostic tests. Clinical
and radiographic examination are essential parts of the
initial screening appointment for patients with possible
TMJ dysfunction. Specialized imaging techniques,
including MRI, computed tomographic scans, and tomograms
of the TMJ, may be required to confirm clinically
suspected TMJ articular disc displacement or other TMJ
pathology.
Factors that can
predispose to or cause TMJ disc displacement and
dysfunction include trauma, parafunctional habits,
gender, malocclusion, hormones, bacterial and viral
infections, and systemic or local disease. Discs become
displaced because of rupture, tearing, herniation,
stretching, or degeneration of the ligaments that
normally support the disc in position. Any of these
conditions can create significant loss of integrity to
the supportive ligaments of the disc, rendering the
ligaments unsuitable for disc stabilization. Functional
loading of the joint following attempted ligament repair
may cause subsequent failure of the procedure and
recurrent displacement of the disc with continued
degeneration within the joint. Thus, the concept of using
a bone anchor and artificial ligaments for disc
stabilization seems attractive, as it does not depend on
the structural integrity of soft tissues for maintaining
postsurgical disc stabilization.
Osseointegration of the
Mitek anchor to the human condylar bone is a unique
feature, as it ensures stability of the anchor after
placement in the TMJ. Fields et al showed that
osseointegration of the Mitek anchor was noted as early
as 3 months after placement in the TMJ, despite probable
intermittent application of low-magnitude forces to the
anchor (25). While the magnitude of functional loading in
a healthy TMJ is a subject of considerable debate, the
force applied to a newly placed Mitek mini anchor in the
mandibular condyle is difficult to estimate in terms of
both magnitude and vector. Our present technique involves
placing a pair of number 0 Ethibond sutures through the
anchor eyelet for 2-point stabilization of the articular
disc. One suture is placed through the posteromedial
aspect of the articular disc, while the second suture is
placed more laterally (Figure
4).
Wolford et al found that
the length of time from the onset of TMJ symptoms to the
performance of the disc-repositioning surgery had a
significant influence on the success of the procedure
(17, 18). They found that surgeries performed within 4
years of the onset of symptoms had a success rate in the
90th percentile range; after 4 years following the onset
of TMJ symptoms, the success rate dropped significantly,
to approximately 68%. These results support the concept
that early identification of disc displacement and prompt
surgical repositioning may stop further progression of
osteoarthritis and disc degeneration, provided there are
no other predisposing factors such as connective tissue
or autoimmune diseases or infective agents affecting the
joints.
Most patients with
displaced articular discs will have decreased joint space
between the condyle and fossa. In addition, once discs
get displaced, they tend to shorten in length and become
thicker with time. In patients with normal occlusions,
repositioning such deformed discs will usually shift the
mandible and chin in a downward and forward direction,
resulting in a malocclusion. Surgical repositioning of
the mandible with sagittal split ramus osteotomies will
maintain the original occlusion and create space within
the joint to accommodate the disc. In patients with
coexisting jaw or facial deformities, we prefer to
reposition the displaced discs and correct the jaw or
facial deformities at the same operation because a
simultaneous procedure 1) exposes patients to only 1
general anesthetic and surgery; 2) balances jaw
structures, occlusion, TMJ, and muscles at 1 time; and 3)
decreases overall treatment time. If the surgeon prefers,
the orthognathic surgery can be delayed and performed at
a later time, but in that case the occlusion must be
carefully controlled so that the TMJs are not overloaded
between the surgical stages.
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In press.
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