What is the role of custom made prosthesis for temporomandibular joint replacement?

Jaw joint (temporomandibular joint or TMJ) disease is estimated to affect 30 million Americans, with approximately 1 million new patients diagnosed each year (1). Although many of these patients can be managed with nonsurgical therapies, some patients require surgical intervention. The TMJ is a unique joint in that it does not function independently but works in tandem with its contralateral joint. Therefore, disease affecting 1 joint can either directly or indirectly affect the functioning and health of the contralateral joint. When surgical intervention of the TMJ is required, the joint can often be reconstructed with autogenous tissues.

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However, certain TMJ conditions and pathology require reconstruction with a total joint prosthesis for predictable treatment outcomes. Some of these conditions include &#;2 previous TMJ surgeries; previous TMJ alloplastic implants containing Proplast/ Teflon (PT), Silastic, acrylic, or bone cements; inflammatory or resorptive TMJ pathology; connective tissue or autoimmune disease (i.e., rheumatoid arthritis, psoriatic arthritis, scleroderma, Sjögren's syndrome, lupus, and ankylosing spondylitis); fibrous or bony ankylosis; absence of TMJ structures due to pathology, trauma, or congenital deformity; and tumors involving the condyle and mandibular ramus area.

Currently, the only TMJ total joint prosthesis approved by the Food and Drug Administration (FDA) is the custom-made device manufactured by TMJ Concepts, Inc. (Camarillo, Calif). The device was manufactured by the same company under the name Techmedica, Inc. from to .

HISTORICAL CONSIDERATIONS

Although the use of some form of alloplastic TMJ prosthesis dates back to the early s, it was not until the s that TMJ prostheses became popular with the introduction of the Vitek- Kent prosthesis (Vitek, Inc., Houston, Tex) (1, 2). Many other companies subsequently introduced their own TMJ prostheses. The Vitek-Kent prosthesis was the most popular prosthesis used in the s and early s, but PT was one of its main materials.

Early reports on implants with PT were very encouraging, with claims of 91% of patients having satisfactory results (3). However, continued clinical and radiographic follow-up revealed that most patients developed increasingly severe pain, condylar resorption, malocclusion, and a proliferative foreign body giant cell reaction (FBGCR) to the PT implants (4, 5). The PT implants disintegrated with fragmentation and particularization, creating the FBGCR, which results in severe destruction of local soft and hard tissues (4). This FBGCR continues despite removal of the PT implants and repeated aggressive surgical debridement (3, 4). Numerous clinical complications were reported in the literature, including perforation of the PT implants, unstable occlusion, facial disfigurement, lymphadenopathy, severe osteoarthritis, perforation into the middle cranial fossa, severe pain, headaches, and a multitude of systemic problems such as immunological dysfunction and malnutrition (2). This led the FDA to stop production of TMJ total joint prostheses in .

The only total joint prostheses that were still commercially available were the Christensen and Morgan devices. Although these devices were not FDA approved, they were still available to practitioners as &#;grandfathered&#; devices, since they fell into the FDA preamendment of . Both of these devices contained articulating surfaces that are not used in FDA-approved orthopaedic total joint devices because of poor wear properties and subsequent particularization. Another problem with these &#;off-the-shelf&#; prosthetic devices was the lack of fit for individual patients. The FDA has recently taken the mandibular components of the Christensen device off the market. The TMJ Concepts total joint prosthesis was granted FDA approval in June .

TECHNICAL CONSIDERATIONS

For a TMJ total joint prosthesis to be successful, the following structural and functional characteristics should be met: 1) biocompatible and functionally compatible materials; 2) low wear, flow, and fatigue coefficients of articulating materials; 3) close adaptability to anatomic structures and function; 4) rigidly stabilized components; 5) corrosion resistant, nonfragmenting, and nontoxic materials; 6) low incidence of hypersensitivity; 7) posterior stop in the fossa component; and 8) close tolerance of the screw and prosthesis hole diameter (6). A prosthesis that meets these criteria is extremely important in the long-term successful outcome of the reconstructive process. The TMJ Concepts custom-made total joint prosthesis was the first TMJ prosthesis that used materials that are well proven in orthopaedics for joint replacement.

The TMJ Concepts total joint prosthesis has 2 basic components: a fossa component and a mandibular component.

The fossa component is made of 2 basic materials. A custom-fitted, commercially pure wrought titanium (CPT) shell conforms to the anatomic contours of the glenoid fossa. This shell is firmly bonded on both sides with 4 layers of CPT mesh. The CPT mesh allows bone and soft tissue ingrowth for long-term stabilization to the glenoid fossa. The articulating surface of the fossa component is made of dense ultra-high-molecular-weight polyethylene (UHMWP) that is bonded to the CPT mesh.

The mandibular component of the prosthesis is also constructed from 2 basic materials. The shaft is made of wrought titanium alloy containing 90% titanium, 6% aluminum, and 4% vanadium. This alloy is extremely hard, very biocompatible, and bend resistant. The articulating surface of the mandibular component is made of a wrought chrome-cobaltmolybdenum alloy that contains approximately 64% cobalt, 28% chromium, 6% molybdenum, and 2% trace elements (nickel, iron, carbon, silicon, manganese, and nitrogen). The functioning surfaces of this prosthesis have low wear, flow, and fatigue coefficients.

PREOPERATIVE CONSIDERATIONS

Initially, a preoperative computed tomography (CT) scan of the jaws and jaw joints is obtained using a specific protocol. Using the CT data, a 3- dimensional plastic model of the TMJ and associated jaw structures is made using stereolithographic technology. The mandible is spatially repositioned on the model to correct the functional and aesthetic malalignment problems. The condyle is removed, and any necessary bony recontouring of the fossa and mandibular ramus is completed and marked on the plastic model, since all the alterations on the model must be accurately duplicated on the patient intraoperatively. A custom-made total joint prosthesis conforming to the patient's specific anatomical morphology and jaw interrelationships is then fabricated on the plastic model by the TMJ Concepts engineers working in close collaboration with the surgeon (Figure 1).

Figure 1.

A 3-dimensional plastic model of the TMJs and jaws is manufactured using stereolithographic technology. The TMJ Concepts custom-made total joint prosthesis is constructed on the model.

Many of these complex TMJ patients have associated jaw and facial deformities. Use of a custom-made joint prosthesis allows correction of the facial deformity and reconstruction of the TMJs during the same operation. The surgeon must be able to accurately reposition the mandible on the 3-dimensional plastic model based on preoperative cephalometric surgical treatment objectives (Figure 4b. In these cases, the plastic model, with the mandible placed in its new position, is used to fabricate the custom-made prosthesis as previously described. Prior to surgery, all mandibular movements performed on the plastic model are accurately duplicated on anatomically mounted dental plaster models, from which an intermediate acrylic occlusal splint is constructed for accurate intraoperative repositioning of the mandible.

Figure 4.

A tracing of the patient's presurgical lateral cephalometric radiograph demonstrates the severity of her jaw and facial deformity. Note the severely decreased oropharyngeal airway of 2 mm (normal dimension is 12 mm). (b) The surgical treatment objective demonstrates the planned surgical movements of the jaws and soft tissue structures.

SURGICAL CONSIDERATIONS

The TMJ is approached via an endaural or preauricular incision, and the mandibular ramus is approached via a submandibular incision. Condylectomy, debridement, and bone recontouring are accomplished as previously determined on the plastic model. Intermaxillary fixation (wiring of the upper and lower jaws together) with the intermediate splint in place is then performed. The fossa component of the prosthesis is inserted through the endaural/ preauricular incision and is stabilized to the zygomatic arch with three to four 2-mm-diameter screws. The mandibular component is inserted via the submandibular incision and fixated to the lateral surface of the ramus with eight to ten 2-mm-diameter screws. Autogenous fat grafts, harvested from the abdomen or buttocks, are packed around the joint prosthesis to prevent postsurgical fibrosis and reactive/heterotropic bone formation (7). Surgical repositioning of the maxilla and other indicated treatment are then performed using standard techniques. At completion of surgery, the intermaxillary fixation is removed and active jaw function is encouraged.

CASE PRESENTATION

A 15-year-old girl with juvenile rheumatoid arthritis had severe destruction of the TMJs, resulting in a facial deformity (Figure 2a, 2b), progressively worsening mandibular retrusion (Figure 3a), and severe sleep apnea symptoms secondary to airway obstruction (Figure 4a). Clinical examination also showed an accompanying excessive vertical growth of the anterior maxilla, resulting in a &#;gummy smile.&#; The patient was treated in 1 operation by using the following steps:

1. Bilateral TMJ reconstruction and mandibular advancement (28 mm) were accomplished using the TMJ Concepts total joint prostheses. Vertical height of the ramus was lengthened 30 mm (Figure 4b).

2. Multiple maxillary osteotomies were performed with bone plate stabilization and synthetic bone grafting to reposition the anterior maxilla upward (7 mm) and the posterior maxilla downward (10 mm) (Figure 4b).

3. A 14-mm porous block hydroxyapatite implant was used to augment the chin. The chin point came forward 42 mm as a result of the mandibular advancement and chin augmentation procedures (Figure 4b).

4. Fat grafts were harvested from the abdomen and placed around the bilateral TMJ prostheses.

Figure 2.

(a, b) A 15-year-old patient is seen with an extensive facial deformity as a result of severe juvenile rheumatoid arthritis. (c, d) The patient is seen 7 years after reconstructive surgery. The TMJ Concepts total joint prosthesis was used to reconstruct the TMJs, advance the mandible (28 mm), and vertically lengthen the ramus (30 mm).

Figure 3.

(a) Presurgery, the patient had a very severe bite problem. (b) Seven years after surgery, her bite remains very stable.

Seven years postoperatively the patient demonstrates excellent long-term stability of the TMJ and jaw reconstruction (Figures 2c, 2d, 3b). She is pain free and has a jaw opening of 40 mm. The severe sleep apnea has been completely eliminated.

DISCUSSION

Although the longevity of the TMJ Concepts total joint prosthesis is yet unknown, our clinical experience over the past 10 years shows promising long-term results. Based on material selection and treatment philosophy, it is believed that these devices will provide service life comparable with or longer than that of hip stem devices.

Wolford et al in reported on 100 reconstructed TMJs in 56 patients using the TMJ Concepts (Techmedica) total joint prosthesis, with an average follow-up of 21/2 years (6). The outcomes were categorized as good, fair, or poor based on clinical and radiographic analysis of stability, function, and pain. They reported that 63% of the patients had good outcomes, 26% had fair outcomes, and 16% had poor outcomes, with irresolvable pain being the prime reason for the poor outcomes. Analyzing a subgroup of those patients who had &#;1 previous TMJ surgery showed that 84% had good outcomes, 16% had fair outcomes, and no patients had poor outcomes. Patients with &#;2 previous TMJ surgeries had relatively poorer outcomes, thereby reinforcing the fact that a greater number of TMJ surgeries results in a higher chance of poor outcomes, mainly due to an inability to reduce postoperative pain levels. Mercuri and Wolford et al in reported a multicenter study on 215 multiply operated TMJ patients (363 joints) reconstructed with the TMJ Concepts prosthesis (8). The results at 2 years postoperatively showed statistically significant favorable changes in many subjective and objective evaluations, including decrease in pain by 49%, improvement in jaw function by 43%, improvement in dietary intake by 50%, and increase in maximum jaw opening by 31%.

In , Wolford et al presented a 5-year follow-up study on 36 patients with 65 TMJs reconstructed with the TMJ Concepts total joint prosthesis (9). The overall success rate for long-term occlusal and skeletal stability after reconstruction was 90%, and pain reduction was recorded in 89% of patients. This study resulted in FDA approval of the TMJ Concepts device for use as a total joint TMJ replacement prosthesis.

In , Wolford and Karras reported on a technique they developed in which fat grafts harvested from the abdomen were packed around the total joint prosthesis (7). This technique has significantly decreased the postoperative incidence of peri-implant fibrosis, reankylosis, and heterotropic/reactive bone formation. Patients with fat grafts were shown to do better clinically with less pain and increased jaw function compared with similar patients with reconstructions without fat grafts. Prior to the use of fat grafts, approximately 35% of patients required additional surgery to remove heterotropic/reactive bone and dense fibrosis from around the prosthesis. Since developing the fat grafting technique, we have not reoperated on any patient for heterotropic/reactive bone formation in the past 71/2 years.

CONCLUSIONS

Long-term success rates for autogenous reconstruction of the TMJ drop considerably in the multiply operated complex TMJ patient (&#;2 previous surgeries), especially for patients with a history of previous alloplastic implants containing PT and Silastic. Many such patients have progressively worsening jaw function, dentofacial deformities, severe chronic pain problems, and other associated systemic, nutritional, and immunological illnesses that cause extreme disability. These patients&#;and also those with inflammatory diseases, connective tissue/autoimmune diseases, ankylosis, tumors, or absence of TMJ structures&#;may have the best opportunity of successful treatment with a total joint prosthesis. The only FDA-approved device for total joint TMJ reconstruction is the TMJ Concepts total joint prosthesis. The use of this custom-made prosthesis, made with orthopaedically proven structural materials, in combination with autogenous peri-implant fat grafting has significantly improved the predictability and success rates of treatment for the rehabilitation of complex TMJ patients.

Abstract

Introduction:

Ankylosis is a physically and psychologically distressing condition to a patient. The aim of this study was to evaluate the efficiency of custom-made temporomandibular joint (TMJ) prosthesis (fossa-condyle component) in patients with unilateral ankylosis in restoring the form and functions of the TMJ.

Materials and Methods:

This retrospective study was conducted in ten patients with unilateral TMJ ankylosis who had undergone TMJ reconstruction with custom-made TMJ prosthesis. Clinical parameters assessed were maximal mouth opening, lateral movements, improvement of the pain levels, and dietary efficiency of the patient. The data were analyzed using SPSS version 20 (IBM Corporation, SPSS Inc.; Chicago, IL, USA).

Results:

The mean preoperative mouth opening was 5.70 ± 3.62 mm. After gap arthroplasty, it was 32.50 ± 3.31 mm. The postoperative mouth opening after the reconstruction of TMJ using alloplastic joint prosthesis was 34.90 ± 2.69 mm, and after a mean follow-up period of 4 years, the mean postoperative mouth opening was 34.60 ± 2.50 mm. The mean preoperative movement toward the right and left side was 0.9 ± 1.2 mm and 1.3 ± 1.25 mm, respectively. The mean right and left lateral movements of the TMJ after reconstruction were 3.5 ± 0.97 mm and 3.70 ± 1.06 mm, respectively. There was decrease in deviation of the unaffected jaw during mouth opening and closure. Functional occlusion was maintained postoperatively. There was no appreciable change in the visual analog pain scales. The dietary efficiency improved from a scale of 10 (liquids) to a scale of 0 (no restriction to diet) in eight patients and 1 in two patients. The dietary score improved significantly after alloplastic reconstruction (P = 0.000). No evidence of facial nerve paralysis or foreign body reactions was noted in the patients during the follow-up period. Radiographic assessment revealed good positioning and adaptation of the fossa component and the condylar ramal component both postoperatively and after a mean 4-year follow-up period. There was no evidence of screw loosening or prosthesis breakage during the follow-up period.

Discussion and Conclusion:

The custom-made TMJ-total joint replacement (TJR) devices provide stable, improved long-term results, thereby increasing the quality of life of the patient. The custom-made alloplastic TMJ-TJR prosthesis proves to be the optimal surgical procedure to reconstruct the TMJ in comparison to the autogenous grafts (to avoid complications) in severe degenerated and ankylosed joints. However, long-term clinical and radiological studies on a larger sample size are imperative to establish the versatility of this procedure.

Keywords: Temporomandibular joint ankylosis, temporomandibular joint custom made prosthesis, temporomandibular joint reconstruction

I

NTRODUCTION

Ankylosis is a physically and psychologically distressing condition to a patient. The temporomandibular joint (TJR) reconstruction is a very challenging procedure for a surgeon because of the integral role of the TMJ in establishing and maintaining proper form and function within the stomatognathic system. The TMJ plays a pivotal role as a secondary growth center for the growth of the mandible and is involved in functions of mastication, speech, and deglutition throughout life.

The traditional treatment modalities that are used in the management of ankylosis are the gap arthroplasty which was later replaced by the interposition gap arthroplasty.[1] The interpositional gap arthroplasty utilizes the advantages of biological tissues such as autogenous bone, myofascial flaps, cartilages, and fascia lata as well as nonbiological materials such as acrylic and silastic.[2] Autogenous bone grafts (costochondral,[3] sternoclavicular,[4] metatarsal,[5] iliac crest,[6] fibula,[7] and coronoid[8]) though have benefits of biological compatibility and growth potential in children, the unpredictable nature of growth of the grafts, the donor-site morbidity, the altered uptake of the grafts, and the chances of reankylosis led to the use of alloplasts as interpositional materials. The function in case of autografts is delayed as early mandibular mobility will result in reduced nascent blood supply to the graft interfering with incorporation of the graft into the host environment leading to graft failure which seems to be another disadvantage of the autogratfs. Marx[9] reported that capillaries can penetrate a maximum thickness of 180 μm&#;220 μm of tissue, whereas scar tissue surrounding previously operated bone averages 440 μm in thickness. Hence, the success of placing an autogenous graft in multiply operated TMJs or in case of reankylosis is always questionable, and there arose the need for an alternative treatment modality such as alloplastic TMJ prosthesis.

The advantages of the TMJ-total joint replacement (TMJ-TJR) devices are lack of donor-site morbidity, ability to maintain a stable occlusion postsurgically because of lack of dimensional change in implant, as opposed to potential resorption of autogenous graft, opportunity to manipulate prosthesis design to discourage heterotopic bone formation, potential to maintain vertical height of ramus and prevent deviation of jaw, reduced surgical time, decreased hospitalization, and immediate function.[10] There are two categories of TJR devices approved by the Food and Drug Administration for implantation in the United States.[11] They are stock (off-the-shelf) devices which the surgeon has to &#;make fit&#; at implantation and custom (patient-fitted) devices which are &#;made to fit&#; for each specific case.

Custom TMJ-TJR devices, by the nature of metals used, design of the prosthesis, and biomaterial composition, appear to provide stable, improved long-term outcomes over stock devices. The advantages of the custom-made devices in contrast to stock devices are that the custom-made system is virtually a perfect fit into the host bone every time, making it more predictable, thus reducing operating time. Custom-made joints also allow for a change in anteroposterior and vertical dimensions, thus enabling changes to be made in the occlusion.[12] Studies on total alloplastic TMJ replacement outcomes showed acceptable improvements in terms of both pain levels and jaw functions, thus making these interventions worthy of further evaluation.

The cost of the devices, material wear and failure, long-term stability, and their restriction in following the growth of the patient have always been a matter of concern in using alloplastic TMJ reconstruction prosthesis. Hence, the purpose of this study was to evaluate the efficiency of custom-made TMJ prosthesis (fossa-condyle component) in patients with ankylosis in terms of restoring form and function of the TMJ. Moreover, an attempt has also been made to reduce the cost factor, which seems to be the main restriction in using these devices in the developing and the underdeveloped countries of the world.

The objectives of the study were to assess the mouth opening, range of mandibular movements possible, usage of the devices in growing patients, and its effect on the growth, the dietary efficacy, and the long-term stability of the device.

M

ATERIALS AND

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M

ETHODS

Study design and setting

This study was an evaluative study of patients with unilateral TMJ ankylosis in whom TMJ ankylosis release and TMJ reconstruction with custom-made TMJ-TJR prosthesis were carried out. Patients with unilateral TMJ ankylosis who were referred to the department of oral and maxillofacial surgery from December to April were included in the study. The required data were collected from the clinical records of the patient and from the patients at consecutive follow-up period.

Inclusion criteria

• Patients within the age group of 10&#;40 years, with unilateral TMJ ankylosis

• Patients who had undergone TMJ ankylosis release and TMJ reconstruction with custom-made alloplastic TMJ prosthesis

• Patients presenting no systemic contraindication for the surgical procedure

• Those willing to cooperate for the surgery and further follow-up.

Exclusion criteria

• Medically compromised patients

• Patients allergic to metal alloys

• Patients with incomplete clinical and radiological data

• Patients who had undergone TMJ reconstruction with autogenous bone grafts.

Parameters assessed

The clinical parameters assessed were maximal mouth opening and lateral movements, the improvement of the pain levels, and the dietary efficiency of the patient. Maximal mouth opening and lateral excursions were evaluated before the release of ankylotic mass, after the release, before the reconstruction of TMJ with the alloplastic joint prosthesis, and thereafter. Radiographic evaluation included orthopantomogram (OPG) and computed tomography (CT) scans. The improvement in pain scales was evaluated by means of visual analog pain scale with a score 0 (no pain) to 10 (maximal bearable pain).[13] Visual analog scores were assessed postrelease of ankylosis, post-TMJ reconstruction, and after a 5-year follow-up period on joint movements. The diet efficiency was similarly assessed with a scale of 0 (with no restriction of diet) to 10 (liquids only).[10] Postoperative evaluation of the position of the prosthesis was done by OPG. The other clinical parameters evaluated were wound infection and evidence of any neurological deficit. Clinically facial nerve paralysis was assessed by evaluating the patient's ability to raise the eyebrows and tight closure of eyelids

Sample size

Inability in mouth opening or a limited mouth opening was the chief complaint in all patients [Figure 1a]. Twenty-one patients presented with ankylosis during the study period of which ten patients who met the inclusion criteria were included in the study.

Figure 1.

(a) Preoperative frontal view. (b) Preoperative computed tomographic scan showing ankylosis of temporomandibular joint - coronal view

Statistical analysis

The data were analyzed using SPSS version 20 (IBM Corporation, SPSS Inc.; Chicago, IL, USA). Paired t-test was used to compare the pre- and post-operative dietary score and laterotrusive movements. Repeated-measure ANOVA was used to compare the mouth opening preoperatively, after gap arthroplasty, after TMJ reconstruction, and after a 5-year follow-up period. A P < 0.05 was considered statistically significant.

The study was carried out after approval from the institutional ethical committee (Tamil Nadu Government Dental College and Hospital, /DE/ dated November 21, ) adhering to the ethical guidelines of Declaration of Helsinki, and informed consent was obtained from each patient in the regional language (Tamil) for both the surgery and the study explaining the nature of the surgical procedure and the outcome, potential risks, and benefits of participating in the study both during the first, second surgery and even during the follow-up period.

After eliciting a detailed history, a thorough clinical examination was carried out. A two-stage surgery was planned; the first was the release of ankylotic mass and the second was the reconstruction of the TMJ using an alloplastic joint prosthesis. The second stage of the surgery was done after a month of gap arthroplasty.

CT scans were taken preoperatively to assess the extent of ankylosis [Figure 1b]. The fabrication of a custom-made alloplastic joint prosthesis obviates the use of the stereolithographic model. Hence, for each patient, CT scans were taken in axial, coronal, and sagittal sections (0.5 mm thickness) with a three-dimensional (3D) reconstruction after the ankylosis release, and a patient-specific 3D model was then developed using these CT data. The use of the stereolithographic model offers an accurate fabrication of the prosthesis conforming to patient's &#;specific anatomical morphology and jaw interrelationships.&#; The joint prosthesis essentially consists of two components, the glenoid fossa component and condylar ramal component, and both the glenoid fossa component and the ramal condylar component were made of cast cobalt-chromium-molybdenum (Co&#;Cr&#;Mb) alloy. The glenoid fossa and condylar ramal component had screw holes drilled in it to accommodate screws of 2 and 2.5 mm diameter, respectively.

Surgical procedure

The surgical procedure was done in two stages. Both the procedures were done under general anesthesia with blind nasal intubation in two patients and fiber-optic-assisted nasoendotracheal intubation in eight patients, for Stage 1 (gap arthroplasty) procedure. For Stage 2 procedure in which the reconstruction of the TMJ was done using alloplastic joint prosthesis, all ten patients were intubated nasoendotracheally. The incision used in all cases was the preauricular incision with a temporal extension, the Al-Kayat&#;Bramley modification[14] for the purpose of greater access [Figure 2a]. At the root of the zygoma, an inverted L-shaped incision was made just 2 mm above the zygomatic arch, through both the superficial layer of temporalis fascia and periosteum of the zygomatic arch to expose the ankylotic mass [Figure 2b]. The ankylosed segment was removed in increments by upper and lower osteotomy cuts, and a gap of about 1.5 cm was achieved [Figure 2c]. The mouth opening achieved was 31&#;34 mm after gap arthroplasty. In all the cases, coronoid hypertrophy was observed, and ipsilateral coronoidectomy was performed as an adjuvant therapy to improve the mouth opening.[15] Postoperatively, patients were administered antibiotics and analgesics for 5 days. Active mouth opening exercises were initiated from the third postoperative day. Sutures were removed on the 10th postoperative day. Heister jaw opener was applied thereafter to improve and maintain mouth opening. Patients were followed up every week postoperatively. Patients were taken up for second-stage surgery 1 month later. CT scans were taken before the surgery for the purpose of stereolithographic model [Figure 3a&#;c] and prosthesis fabrication [Figure 4a and b]. The approach to the field of surgery was through the existing scar. The gap created earlier was cleared of all soft tissue adherence for the insertion of the glenoid fossa component. The glenoid fossa component was then placed to check for its fit and adaptation over the zygomatic arch and temporarily secured to the position using 2 mm × 6 mm screws [Figure 5a]. For the insertion of condylar ramal component, a submandibular incision was planned. Layer-wise dissection was carried out, pterygomasseteric sling was incised, and exposure to bone was made submasseterically. Condylar ramal component was then positioned and checked for its adaptation and fit [Figure 5b]. Intraorally intermaxillary fixation (IMF) was done. After accomplishing it, condylar ramal component was fixed using 2.5 mm × 8 mm screws. IMF was then released and the condylar movements are performed. Then, the screws were finally tightened over the glenoid fossa and condylar ramal component [Figure 5c]. Copious amount of povidone iodine and saline irrigation was done, and closure was accomplished layer-wise using 3-0 vicryl and 3-0 ethilon. Patients were administered antibiotics and analgesics for 5 days. Patients were kept in IMF for 7 days and active physiotherapy was started thereafter. The skin sutures were removed on the 10th day. The patients were followed up periodically monthly once during the immediate postoperative period, and thereafter, yearly follow-up was done.

Figure 2.

(a) Al-Kayat&#;Bramley incision. (b) Exposure of ankylotic mass. (c) Gap arthroplasty

Figure 3.

(a) Postoperative computed tomographic showing gap arthroplasty - coronal view. (b) Postoperative computed tomographic showing gap arthroplasty - three-dimensional reconstruction image. (c) Stereolithographic model after gap arthroplasty

Figure 4.

(a) Fabrication of custom-made temporomandibular joint prosthesis. (b) Custom-made temporomandibular joint prosthesis made using cobalt-chromium-molybdenum

Figure 5.

(a) Fixation of glenoid fossa component of the temporomandibular joint prosthesis. (b) Fixation of condylar-ramal component of the temporomandibular joint prosthesis. (c) Custom-made temporomandibular joint prosthesis fixation

D

ISCUSSION

The multiple disadvantages of an autogenous graft have led the surgeons to consider alloplastic replacement of TMJ as a better and viable option. A review of literature reveals that an alloplastic TMJ replacement could produce a favorable and successful outcome, especially in patients with reankylosis.

Mercuri et al.[16] in their study reported decrease in pain by 49%, improvement in jaw function by 43%, improvement in dietary intake by 50%, and increase in maximum jaw opening by 31%. Garrett et al.[17] reported an average decrease in pain of 65%, a 71% increase in diet, and a 66% increase in Maximum Incisal Opening (MIO) when using a metal-on-metal TMJ reconstruction system. Fernandes[18] reported in his study that 75% of patients had improvement in mastication. In the present study, subjective evaluation of pain and efficiency of diet was done. All the patients had ankylosed joints and restriction of mouth opening as their primary complaint with no history of pain in the joints. Hence, postoperative improvements in pain showed no appreciable changes. There was 100% improvement in efficiency of the diet, which could be attributed to the improved jaw function following the reconstruction of the TMJ.

Mercuri and Giobbie-Hurder[19] showed a 30% improvement in the mandibular range of motion and Wolford et al.[20] using the Techmedica patient-fitted TMJ-TJR device published a statistically significant improvement in incisal opening. In a study on simultaneous treatment of TMJ ankylosis with severe mandibular deficiency by standard TMJ prosthesis by Hu et al.,[21] the mean postoperative mouth opening achieved was 31.5 mm. Fernandes[18] reported a postoperative mouth opening of 31.5 ± 3.41 mm. The postoperative mouth opening after the reconstruction of TMJ using alloplastic joint prosthesis was 34.90 ± 2.69 mm, and after a 4-year follow-up, the mean postoperative mouth opening was 34.60 ± 2.50 mm in the current study which is very similar to the above-mentioned studies.

Hu et al.[21] suggested that their previous studies on autogenous bone grafts, including rib grafts and coronoid process grafts for the treatment of ankylosis, showed that there were no significant differences of mouth opening among rib grafts, coronoid process grafts, and alloplastic TMJ prostheses. However, both rib grafts and coronoid process grafts reported bone resorption and recurrence of TMJ ankylosis. In contrast to this, in our previous study using sternoclavicular graft, the mean postoperative mouth opening after a follow-up period of 4 years was 26.7 ± 7.57 mm and there were two cases of reankylosis.[22]

There was no evidence of reankylosis or significant decrease in mouth opening in any of the cases in the current study. This is one of the greatest advantages of alloplastic TMJ reconstruction. The reasons for the low recurrence of ankylosis after alloplastic TMJ prostheses are that the fossa prosthesis covers the exposure of the bone and prevents downward bone formation by acting as a barrier; second, the stability of the osteotomy gap is maintained by the mandibular prosthesis.[23]

The results of the lateral excursive movements in this study showed sufficient improvements in the lateral movements to the unaffected side following the reconstruction of the TMJ after gap arthroplasty. In a study of long-term follow-up of the CAD/CAM patient fitted with total TMJ reconstruction system by Mercuri and Giobbie-Hurder,19 the multiple regression analysis confirmed what is seen clinically with unilateral alloplastic reconstructions. The unilaterally reconstructed patient will exhibit greater lateral excursion to the reconstructed side than to the nonreconstructed side. This is attributable not only to the loss of lateral pterygoid function on the implanted side but also to the formation of periarticular scar tissue. This was evident in our study also. Fernandes[18] published a postoperative lateralization movement of (3.1 ± 1.71 mm). The mean right and left lateral movements of the TMJ after reconstruction were 3.5 ± 0.97 mm and 3.70 ± 1.06 mm in the current study. The improved mandibular function is due to the fact that the center of rotation of the condylar prosthesis is placed much more inferior than that of the natural condyle.

Another advantage of the TMJ-TJR prosthesis is that they can bear more stress than the autogenous bone grafts without resorption. The longevity of prosthesis for any joint is dependent on materials, design, stability, and functional loading. For the average adult, the biting forces generated at the molars are approximately 60 pounds and that for the incisors are 35 pounds.[24] There were no issues of wear of the prosthesis even after a mean follow-up period of 4 years. The lower functional loads by the patients as well as the stability of the device could explain the longevity of these TMJ prostheses.

According to Lindqvist et al.,[25] the alloplastic replacement of the condyle alone had the disadvantage of causing resorption of the fossa. In , Christensen et al.[26] added a TMJ condylar prosthesis to the TMJ fossa eminence prosthesis, to form a TMJ total joint replacement. Since then, a number of modifications have been made in the TMJ replacement devices. The custom TMJ-TJR devices published in the literature[27] are manufactured using commercially pure titanium as the fossa backing for ultrahigh molecular weight polyethylene articulating surface; wrought alloyed titanium for the ramus component and wrought Co&#;Cr&#;Mb for the articulating condylar head. However, taking the cost into consideration, in this study, a custom-made TMJ-TJR prosthesis having both fossa and condylar component made of Co&#;Cr&#;Mb alloy was used.

The absence of a posterior stop in the stock and metal on metal custom TMJ-TJR devices leads to posterior dislocation of the condylar head. If the condylar head is not perfectly aligned in the center of the fossa component in both the mediolateral and anteroposterior position, the condylar head may get displaced and impinge on the external auditory canal resulting in pain, malocclusion, or even infection in case of pressure-related perforation of the cartilaginous portion of the auditory canal.[21] This is of particular concern where the condyle needs to be placed in the centric position in case of orthognathic mandibular surgeries, especially in combination with counterclockwise mandibular rotation procedures. Hence, in the custom-made TMJ-TJR prosthesis used in the present study, even though it is a metal on metal, a posterior stop was placed.

Mercuri et al.[28] reviewed the outcomes of total alloplastic replacement with periarticular autogenous fat graft harvested from the abdomen and grafted around the articulating portion of their prosthesis, and Hu et al.[21] also placed free fat grafts harvested from submandibular incision around the TMJ prostheses as they felt that this prevents blood clot formation and osteogenesis, thereby preventing ectopic bone formation or reankylosis. However, in the current study, even though no autogenous tissue was interposed, there were no cases of heterotrophic bone formation or reankylosis.

Pearce et al.[29] and Malis et al.[30] reported a single-stage technique for the replacement of ankylosed joint using a custom-made prosthesis. The concern for a single-stage surgery is the exact replication of the presurgical plan during surgery. Any excessive trimming of the bone may jeopardize the fit of the components resulting in instability of the prosthesis. In the current study, a two-stage procedure was planned for all the patients. The advantages of the two-stage surgical procedure were that the glenoid fossa and ramal area were adequately prepared during the stage of ankylotic mass removal. This enabled easier fabrication as well as accurate fit of the prosthesis during the second stage eliminating any need for surgical template. There was no major postoperative complication in the study, except for scar in the submandibular region which was acceptable.

There is a controversy regarding alloplastic reconstruction of TMJ in growing patients; however, patients with a history of recent ankylosis with no evident facial asymmetry and a history of reankylosis were included even when the patient was in the growth period and one of the major advantages of the custom-made prosthesis was by using the stereolithographic model, the height of the ramus could be established, and there were no incidence of reankylosis which seemed to be the major issue with autogenous reconstruction in case of growing patients. Hence, TMJ-TJR custom-made prosthesis could be a viable alternative even in growing patients with no obvious facial asymmetry and in case of reankylosis.

The limitations of the study are a small sample size and a short-term follow-up period. The future research should be directed toward addressing the main drawbacks of the alloplastic TMJ reconstruction such as reducing the cost of TMJ-TJR devices and substantial evidence for usage in growing patients, and since TMJ-TJR is a biomechanical rather than a biological solution, there may arise the need for revision surgery to remove scar tissue from the articulating components of the implant or even replacement of the implant over time due to material wear and/or failure. In this regard, studies are needed on the use of proper biomaterials and design configurations to decrease material wear and increase device longevity under functional loading.

C

ONCLUSION

The reconstruction of TMJ with custom-made TMJ prosthesis has been proved to be successful in this study, as it has been mentioned in various literature, by many authors. The custom-made TMJ-TJR devices provide stable, improved long-term results, thereby increasing the quality of life of the patient. The postoperative outcomes such as mouth opening, lateral movements, masticatory efficiency, and prevention of lateral deviation and restoration of functional occlusion were satisfactory for all the patients, during the entire follow-up period. The custom-made alloplastic TMJ-TJR prosthesis proves to be the optimal surgical procedure to reconstruct the TMJ in comparison to the autogenous grafts (to avoid complications) in severe degenerated and ankylosed joints. However, long-term clinical and radiological studies on a larger sample size are imperative to establish the versatility of this procedure.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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