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DOI: 10.1055/s-0044-1791686
A Case Report: Regenerative Biodegradable Chin Implant—A Viable Futuristic Option
Abstract
Chin augmentation can dramatically transform a patient's appearance. Various techniques are in use, each with their specific problems and limitations. We present the first case report from the Indian subcontinent using a custom 3D-printed, bioresorbable polycaprolactone implant. We demonstrate, by appropriate imaging, the replacement of the implant at long-term (22 months) follow-up by patient's own autologous bone formation. An excellent aesthetic result was achieved. Relevant points of technique, as well as pertinent properties of the material, are discussed. This material has been used in neurosurgery and in the management of orbital fractures. Yet, worldwide, very few (3–4) cases of chin implant have been done using this material. We believe this to be a useful and sustainable material, offering several advantages, as set out in the case report.
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Keywords
customized chin augmentation - biodegradable chin implant - case report of regenerative chin implantIntroduction
The options for chin augmentation include genioplasty, bone graft, and silastic implants. Genioplasty by advancement osteotomy may not be sufficient and require the placement of hardware. Bone graft requires additional surgery, with donor site pain and deformity, along with hardware placement. Silicon implants are commonly done through the intra- or extraoral route, but they never integrate with the body. The chances of extrusion, displacement, and availability of limited size are some of their shortcomings.[1] [2] [3] We present a 2-year follow-up of a customizable biodegradable chin implant that can integrate permanently with the mandible, with new bone formation.
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Case Report
A 23-year-old man ([Figs. 1A] [2A] [3A]) presented with a request for augmentation of the chin. The patient was assessed with 3D simulation software to understand the extent of augmentation desired. The desired augmentation in the anteroposterior plane was 1.7 cm: much beyond the usual available size. The patient expressed the desire to avoid a foreign body and refused to allow a bone graft to be harvested from the iliac crest. The senior author came across a regenerative material by Osteopore, marketed in India by Myovatec. The said material is polycaprolactone, which is biodegradable in the body by hydrolysis.[4] [5] [6] [7] [8] The material was described as being light, porous with a honeycomb structure, like cancellous bone. A customized implant was 3D printed based on the patient's computed tomography (CT) scan Digital Imaging and Communications in Medicine (DICOM) images shared with the company. Necessary suture or biodegradable screw points were identified and necessary modification in shape was made ([Fig. 4]). The implant was delivered in a gamma-ray-sterilized packet. The surgery was performed under general anesthesia through the intraoral route. Standard gingivolabial sulcus incision extending from the first right premolar to the first left premolar was made. An effort was made to retain enough muscle on the alveolus for watertight closure later. The periosteum was then elevated along with the rest of the muscle bulk, sparing the mental nerve carefully. The length of the incision required was nearly as much as the length of implant. The implant ([Fig. 5A]) was soaked in about 8 mL of the patient's own platelet-rich plasma (PRP). The implant was inserted and adjusted, snugly fitting the symphysis menti and the mandibular border. The fit was perfect as it was made as per the patient's own CT images. The implant was secured to the mandibular periosteum using 4–0 PDS. A robust, watertight closure was done, approximating the periosteum, muscles, and mucosa in that order using 4–0 PDS. The standard postoperative protocol including antibiotics, anti-inflammatory agents, and antiseptic mouthwash was followed. Chin belt immobilization was continued for 30 days. [Figs. 1B] [2B], and [3B] show the result after 30 days. [Figs. 1C] [2C], and [3C] show the result of augmentation with regenerative implant after 22 months. X-ray of the skull, lateral view, done 45 days after the procedure failed to show the implant, as seen in [Fig. 5B]. However, upon soft-tissue X-ray exposure, the implant was well visible on the same day, as seen in [Fig. 5C]. Formation of cancellous-like bone was confirmed on post-op magnetic resonance imaging (MRI) done after 22 months. The implant shadow was reported as isodense with the bone ([Fig. 6]).
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Discussion
Chin augmentation is a frequently requested surgery by both men and women. A strong, projecting, shapely, and well-defined chin adds to aesthetic facial balance and enhances the confidence of the patient. Socially, a strong chin is associated with assertiveness, leadership, and confidence.
The commonest material used to augment the chin is silicon, which is flexible and can be customized. Silicone implants never integrate and remain encapsulated. They are vulnerable to displacement and deviation with even minor trauma.[1] [2] [3] They are fixed to the symphysis menti with nonabsorbable sutures or even a screw. This amounts to putting a permanent foreign body, which is not desirable in a young patient if the option of an integrable material is available. The main advantage of silicone implant is that it can be inserted through a small incision, which can be intra- or extraoral. The surgery can be done under local anesthesia.
Autologous bone usually integrates well with local bone, yet it needs screws and plates for fixation. An additional surgery, leaving a painful donor area with residual defect, and painful walking in the postoperative period for a long time are the major disadvantages of using iliac bone, the commonest donor site.
Medpor polyethylene implants also have a porous structure, allowing vascular ingrowth and tissue integration, but they are not biodegradable.[9]
Both autologous bone and polycaprolactone need long incisions for insertion. These must be intraoral. Surgery is essentially done under general anesthesia.
The Osteopore technology relies upon in situ tissue engineering to regenerate and rebuild host tissue. The implant has a honeycomb structure. This allows vascular ingrowth and bone deposition into the depth of the implant. The new bone is adequately stiff and has a structure similar to cancellous bone.[4] [5] [6] [7] [8] The implant is completely disintegrated by hydrolysis over 18 to 24 months, by which time bone formation occurs. The shape can be customized as the implant is designed using patient's own images and software-generated wish images and then 3D printed. In our patient, the central dimple was specifically requested, and the implant was shaped according to this. It is important to note that intraoperative adjustment and customization, as can be done with silicon or bone implants, is NOT easily possible in Osteopore implants. The implant can be carved to some extent by chipping with a blade. The material has a melting point of 55 °C. Hence, using a water bath at high temperature may simply melt the implant.[10] Postoperative photographs ([Figs. 1B, C] [2B, C], and [3B, C]) clearly show a square jaw shape with a central dimple, matching the preaugmentation shape. Only the size and projection have increased. This would not be possible with any other material. The follow-up X-ray taken 45 days postsurgery revealed only a soft-tissue shadow, whereas the MRI done after 22 months showed good bone formation. This is in accordance with the properties of the material, as described in the literature by Young et al.[11] The skin over the implant is totally free and can be animated. The aesthetic result was very satisfactory.
An issue we faced was the need for prolonged immobilization using a chin strap. This required the patient to be off work for a good 15 to 20 days. Another issue was discharge of serous fluid on day 7, which necessitated reopening a small part of the incision, followed by drainage of collected 4- to 5-mL serosanguinous fluid and performing meticulous everting reclosure. Otherwise, there were no problems such as bruising, hematoma, infection, and displacement.
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Conclusion
This is a case report of the first regenerative chin implant ever done in the Indian subcontinent. Before this, only three to four cases have been done worldwide. Hence, the senior author was keen to present a fairly long-term follow-up, with demonstration of actual bone formation. This material has been used in neurosurgery and spine surgery, successfully. We should look at this as an effective option for autologous bone. We should also establish a proper, regular follow-up community of those who have successfully used this material. Although it is currently considered expensive, this is definitely a futuristic material that allows local bone formation while the material itself undergoes complete hydrolysis.
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Conflict of Interest
None declared.
Note
This manuscript was initially presented with a short follow-up during the APSICON 2021 Online Meeting.
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References
- 1 Meyer DR. Alloplastic materials for orbital surgery. Curr Opin Ophthalmol 1995; 6 (05) 43-52
- 2 Chowdhury K, Krause GE. Selection of materials for orbital floor reconstruction. Arch Otolaryngol Head Neck Surg 1998; 124 (12) 1398-1401
- 3 Brown AE, Banks P. Late extrusion of alloplastic orbital floor implants. Br J Oral Maxillofac Surg 1993; 31 (03) 154-157
- 4 Al-Sukhun J, Törnwall J, Lindqvist C, Kontio R. Bioresorbable poly-L/DL-lactide (P[L/DL]LA 70/30) plates are reliable for repairing large inferior orbital wall bony defects: a pilot study. J Oral Maxillofac Surg 2006; 64 (01) 47-55
- 5 Kontio R, Suuronen R, Salonen O, Paukku P, Konttinen YT, Lindqvist C. Effectiveness of operative treatment of internal orbital wall fracture with polydioxanone implant. Int J Oral Maxillofac Surg 2001; 30 (04) 278-285
- 6 Lieger O, Schaller B, Zix J, Kellner F, Iizuka T. Repair of orbital floor fractures using bioresorbable poly-L/DL-lactide plates. Arch Facial Plast Surg 2010; 12 (06) 399-404
- 7 Dietz A, Ziegler CM, Dacho A. et al. Effectiveness of a new perforated 0.15 mm poly-p-dioxanon-foil versus titanium-dynamic mesh in reconstruction of the orbital floor. J Maxillofac Surg 2001; 29 (02) 82-88
- 8 Teo L, Teoh SH, Liu Y. et al. A novel bioresorbable implant for repair of orbital floor fractures. Orbit 2015; 34 (04) 192-200
- 9 Rubin PA, Bilyk JR, Shore JW. Orbital reconstruction using porous polyethylene sheets. Ophthalmology 1994; 101 (10) 1697-1708
- 10 Hwang K, Kim DH. Comparison of the supporting strength of a poly-L-lactic acid sheet and porous polyethylene (Medpor) for the reconstruction of orbital floor fractures. J Craniofac Surg 2010; 21 (03) 847-853
- 11 Young SM, Sundar G, Lim TC, Lang SS, Thomas G, Amrith S. Use of bioresorbable implants for orbital fracture reconstruction. Br J Ophthalmol 2017; 101 (08) 1080-1085
Address for correspondence
Publication History
Article published online:
03 October 2024
© 2024. Association of Plastic Surgeons of India. This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)
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References
- 1 Meyer DR. Alloplastic materials for orbital surgery. Curr Opin Ophthalmol 1995; 6 (05) 43-52
- 2 Chowdhury K, Krause GE. Selection of materials for orbital floor reconstruction. Arch Otolaryngol Head Neck Surg 1998; 124 (12) 1398-1401
- 3 Brown AE, Banks P. Late extrusion of alloplastic orbital floor implants. Br J Oral Maxillofac Surg 1993; 31 (03) 154-157
- 4 Al-Sukhun J, Törnwall J, Lindqvist C, Kontio R. Bioresorbable poly-L/DL-lactide (P[L/DL]LA 70/30) plates are reliable for repairing large inferior orbital wall bony defects: a pilot study. J Oral Maxillofac Surg 2006; 64 (01) 47-55
- 5 Kontio R, Suuronen R, Salonen O, Paukku P, Konttinen YT, Lindqvist C. Effectiveness of operative treatment of internal orbital wall fracture with polydioxanone implant. Int J Oral Maxillofac Surg 2001; 30 (04) 278-285
- 6 Lieger O, Schaller B, Zix J, Kellner F, Iizuka T. Repair of orbital floor fractures using bioresorbable poly-L/DL-lactide plates. Arch Facial Plast Surg 2010; 12 (06) 399-404
- 7 Dietz A, Ziegler CM, Dacho A. et al. Effectiveness of a new perforated 0.15 mm poly-p-dioxanon-foil versus titanium-dynamic mesh in reconstruction of the orbital floor. J Maxillofac Surg 2001; 29 (02) 82-88
- 8 Teo L, Teoh SH, Liu Y. et al. A novel bioresorbable implant for repair of orbital floor fractures. Orbit 2015; 34 (04) 192-200
- 9 Rubin PA, Bilyk JR, Shore JW. Orbital reconstruction using porous polyethylene sheets. Ophthalmology 1994; 101 (10) 1697-1708
- 10 Hwang K, Kim DH. Comparison of the supporting strength of a poly-L-lactic acid sheet and porous polyethylene (Medpor) for the reconstruction of orbital floor fractures. J Craniofac Surg 2010; 21 (03) 847-853
- 11 Young SM, Sundar G, Lim TC, Lang SS, Thomas G, Amrith S. Use of bioresorbable implants for orbital fracture reconstruction. Br J Ophthalmol 2017; 101 (08) 1080-1085