76: Localized Bone Augmentation and Implant Site Development

Localized Bone Augmentation and Implant Site Development

Perry R. Klokkevold

One of the most critical aspects of creating an esthetic implant restoration is surgical placement of the implant in a “prosthetically driven” position to restore the tooth in a natural position and to emulate the natural emergence of the tooth from the soft tissues. Implants placed without regard for prosthetic position often lead to dental restorations that are functionally and esthetically compromised, and patients are left with a less-than-optimal reconstruction. Placement of dental implant(s) in an esthetically and functionally optimal position requires reconstruction of deficient alveolar ridges (or preservation of ridges when teeth are to be extracted).

Periodontal bone loss, gingival recession, tooth loss, and long-term use of removable appliances typically result in alveolar defects that prevent the placement of implants in an optimal prosthetic position. It also leads to soft-tissue deficiencies that are unacceptable. Fortunately, continuous innovations in surgical techniques and advances in the biologic understanding of bone-regenerative techniques have led to advanced implant procedures and an increased predictability in the reconstruction of alveolar ridge defects.27,38

Standard implant placement surgery, as described in Chapter 75, is based on adequate bone volume and quality in the desired implant location. The time-tested standard protocol allows for adequate remodeling and maturation of bone, with healing periods of 3 to 6 months. Recent implant procedures often challenge these original conventions by placing implants in areas with inadequate bone volume, simultaneous with bone augmentation, and restoring or loading implants after shorter healing periods. This chapter presents an overview of surgical bone augmentation procedures used to correct or to prevent alveolar ridge deficiencies for the optimal placement of dental implants.

Guided Bone Regeneration

Much of what can be achieved with implant surgery and specifically with bone augmentation procedures is directly related to the achievements and understanding of guided bone regeneration (GBR). Historically, augmentation or “regeneration” of alveolar bone that was lost following tooth removal, or from alveolar bone resorption or traumatic injury, presented a significant challenge for clinicians. Allowed to heal without the intervention of regenerative procedures, extraction site defects (especially those lacking a self-supporting bone structure) heal with fibrous connective tissue or scar formation and often did not fill completely with bone. The surrounding soft tissues collapsed into the bone defect, leaving an alveolar ridge deficiency with respect to the natural tooth position and jaw shape. Over time, the alveolar ridge continued to resorb, especially when removable prosthetic appliances are used.

Periodontal studies during the last several decades have led to new techniques and a new treatment approach referred to as guided tissue regeneration (GTR). Briefly, this concept is based on the principle that specific cells contribute to the formation of specific tissues. Exclusion of the faster-growing epithelium and connective tissue from a periodontal wound for a minimum of 6 to 8 weeks allows the slower-growing tissues to occupy the space adjacent to the tooth. Osteoblasts, cementoblasts, and periodontal ligament cells are then afforded the opportunity to regenerate a new periodontal attachment (defined by new bone and new connective tissue fibers inserted into newly formed cementum) on the previously diseased root surface. Chapter 61 includes a discussion on the concepts of GTR as related to periodontal regeneration.

The same basic principle of GTR has been applied to alveolar bone defects to regenerate new bone.13 Using a canine model, Schenk et al47 demonstrated with histology that bone regeneration in membrane-protected defects healed in a sequence of steps that simulated bone formation after tooth extraction. They found that after blood clot formation, bone regeneration was initiated by the formation of woven bone initially along new blood vasculature at the periphery of the defect. The new vascular supply emanated from the existing bone bed (recipient site). Cortical perforations surgically created in the recipient site are thought to enhance the blood supply and cellular access to the bone grafted area. The woven bone, which is formed quickly with a disorganized, immature structure, was subsequently replaced by lamellar bone with an organized, mature structure. Over time, bone remodeling continued with new, secondary osteons being formed.

This concept employed the same principles of specific tissue exclusion but was not associated with teeth. Rather, it was bone that was being isolated from the surrounding soft tissues. Thus the term applied to this technique was GBR. Because the objective of GBR is to regenerate a single tissue, namely bone, it is theoretically easier to accomplish than GTR, which strives to regenerate multiple tissues simultaneously in a complex relationship.

Interestingly, long before the current concepts of GBR were introduced, Murray and coworkers40 demonstrated that when a cavity with a source of osteoblasts and a blood supply was isolated from adjacent soft tissues, it could fill with bone, whereas if the space were not protected, it would fill with fibrous connective tissue. In addition to this observation, they suggested that a bone graft placed in the space might interfere with bone formation because the graft would need to be resorbed before bone could occupy the space.

Bone is a unique tissue that has the capacity to regenerate itself completely. Because of its rigid calcified structure, however, bone has specific requirements that must be respected to achieve regeneration. Because the calcified structure of bone is not conducive to perfusion, new bone formation is critically dependent on establishing an adequate blood supply through the ingrowth of new vasculature while maintaining rigid fixation or stabilization for bone formation. Any movement of the segments of bone relative to one another (even micromotion) during healing results in disruption of the blood supply and a change in the type of tissue formed in the site from mineralized bone to fibrous connective tissue. Table 76-1 lists the biologic requirements for bone regeneration and the associated component of GBR surgical procedures needed to accomplish bone regeneration.

TABLE 76-1

Biologic Requirements for Bone Regeneration

Requirement Surgical Procedure
Blood supply Cortical perforations
Stabilization Fixation screws, membrane tacks
Osteoblasts Autogenous bone (graft or recipient site)
Confined space Barrier membrane
Space maintenance Tenting screws, bone graft materials
Wound coverage Flap management, tension-free suturing

Barrier Membranes

Barrier membranes are biologically inert materials that serve to protect the blood clot and prevent soft-tissue cells (epithelium and connective tissue) from migrating into the bone defect, allowing osteogenic cells to be established. Membranes have been manufactured from biocompatible materials that are either nonresorbable and resorbable. The ideal properties of a barrier membrane are (a) biocompatibility, (b) space maintenance, (c) cell occlusiveness, (d) good handling properties, and (e) resorbability or ease of removal (nonresorbable). Advantages and disadvantages of the resorbable versus nonresorbable membranes are outlined next.

Nonresorbable Barrier Membranes.

Various nonresorbable materials have been used as barrier membranes, including latex and Teflon. Teflon, an expanded polytetrafluoroethylene membrane (ePTFE, Gore-Tex Periodontal and Bone Regenerative Membranes, Gore and Associates, Flagstaff, AZ), has been used extensively as a barrier membrane in both GTR and GBR procedures. A variety of shapes and sizes have been designed to be custom-fit around teeth and osseous defects. These barrier membranes are nonresorbable and thus require a subsequent surgical procedure to remove them. The advantage of a nonresorbable barrier membrane is its ability to maintain separation of tissues over an extended time. Unless the barrier is exposed, it can remain in place for several months to years. Typically, GBR membranes are removed after 6 to 12 months.

The disadvantage of a nonresorbable barrier membrane is that if it becomes exposed, it will not heal (i.e., wound will remain open) spontaneously and may become progressively more exposed. Exposed membranes become contaminated with oral bacteria, which may lead to infection of the site and result in bone loss. Therefore exposed membranes must be removed. Contamination or early removal may also result in less bone regeneration.

Space can be maintained under a barrier membrane with bone graft material or tenting screws, thereby facilitating the regeneration of increased bone volume. Stiffer or titanium-reinforced (TR) membranes (Gore and Associates, Flagstaff, AZ) with space-maintaining capabilities can regenerate bone without the need for bone grafts or tenting apparatus.36,47 Stiffer membranes are able to promote significant amounts of new bone and maintain sufficient space without the addition of supportive devices. Ridge augmentation can be enhanced with a TR membrane in conjunction with implant placement in localized bone defects.24

Resorbable Barrier Membranes.

The use of resorbable membranes continues to attract widespread interest primarily because it eliminates the need for an additional surgery to be removed. Copolymers of polylactide and polyglycolide have been used to construct biodegradable membranes. Today, collagen-based resorbable barrier membranes are used extensively. The primary advantage of a resorbable membrane is the elimination of surgical reentry for membrane removal. In the case of a subsequent implant placement procedure (or exposure surgery), this may not be a significant advantage. The other advantage is that resorbable membranes are less likely to become exposed and are less problematic if they do become exposed.

A possible disadvantage is that many resorbable membranes degrade before bone formation is completed, and the degradation process may produce varying degrees of inflammation.61 Recent developments include cross-linking of collagen to increase resistance to biodegradation and thus increase longevity of the barrier function.17 Fortunately, the mild inflammatory reaction caused by bioresorbable membranes does not seem to interfere with osteogenesis. Another disadvantage is that resorbable barrier membranes are quite pliable. The lack of stiffness often results in collapse of the membrane into the defect area.46 Thus resorbable membranes are best suited for situations that allow the graft material or hardware (tenting screws, plates) or the adjacent alveolar bone to maintain the desired dimensions.

Human histology has demonstrated that resorbable barrier membranes support the growth of new bone when used in GBR procedures for horizontal, vertical, sinus, and extraction socket defects.18,20,37 They have also been shown to reduce bone resorption when used over a monocortical bone block to augment horizontally deficient ridges.58 Geurs et al20 demonstrated that a bioabsorbable barrier membrane, used in a GBR procedure along with an allograft, was able to facilitate new bone formation. At present, it can be stated that biodegradable membranes have the potential to support bone formation if they are supported by bone graft material to resist collapse and if they are long-lasting enough to maintain their barrier function for extended periods in small to moderate bone defects.28,29

Bone Graft Materials

Unlike other tissues, bone has the unique capacity to completely regenerate itself. The major limiting factors are maintenance of space and structure for bone formation. Bone graft materials have been used to facilitate bone formation within a given space by occupying that space and allowing the subsequent bone growth (and graft replacement) to take place on the structure. The biologic mechanisms that support the use of bone graft materials are osteoconduction, osteoinduction, and osteogenesis.

Osteoconduction is the formation of bone by osteoblasts from the margins of the defect on the bone graft material. Materials that are osteoconductive serve as a scaffold for bone growth. They neither inhibit nor induce bone formation. They simply allow the normal formation of bone by osteoblasts into the grafted defect along the surface of the graft material. Osteoconductive bone graft materials facilitate bone formation by bridging the gap between the existing bone and a distant location that otherwise would not be occupied by bone.

Osteoinduction involves new bone formation through stimulation of osteoprogenitors from the defect (or from the vasculature) to differentiate into osteoblasts and begin forming new bone. This induction of the bone-forming process by cells that would otherwise remain inactive occurs through cell mediators that “turn on” these bone-forming cells. The most widely studied of these mediators is the family of bone morphogenic proteins (BMPs). See Chapter 77 for a review of BMP use in bone augmentation.

Osteogenesis occurs when living osteoblasts are part of the bone graft, as in autogenous bone transplantation. Given an adequate blood supply and cellular viability, these transplanted osteoblasts form new centers of ossification within the graft. Thus, in addition to the bone formation from osteoblasts that already exist in the defect, osteoblasts added as part of the bone graft also form ossification centers and contribute to the total capacity for bone formation.

Numerous bone graft materials have been used to aid in the reconstruction of bone defects. These range from allografts (derived from the same species) to xenografts (derived from a different species) and alloplast or synthetic graft materials. At a minimum, bone graft materials should be osteoconductive. Bone graft materials that are also osteoinductive are believed to be more advantageous than those that are only osteoconductive. Table 76-2 lists the properties of different classes of bone graft materials.

TABLE 76-2

Biologic Properties of Various Bone Graft Materials

Source Osteoconductive Osteoinductive Osteogenic
Alloplast Yes No No
Xenograft Yes No No
Allograft Yes Yes/No? No
Autograft Yes Yes Yes


Demineralized freeze-dried bone allograft (DFDBA) is thought to have osteoinductive effects because viable BMPs within the donor tissue matrix are exposed by the decalcification process.57 In contrast to this view, more recent reports suggest that bone augmentation with DFDBA is not osteoinductive because it does not contain the BMPs necessary to induce bone formation.4,8 Schwartz et al48 reported that variations in the amount of bone formation induced by BMPs in DFDBA may be related to the source (i.e., donor tissue) of the bone and the techniques used to process it. In addition to processing variations, it has been demonstrated that young donor bone results in significantly greater quantities of BMPs retained in the bone allograft matrix compared with older donor bone.49 Therefore the source of donor bone can greatly influence its osteoinductive capacity.

Bone graft materials help maintain space under a barrier membrane to facilitate the formation of bone within a confined space. Perhaps more importantly, bone graft materials should facilitate neovascularization and the migration of osteoprogenitors. Because the size of the bone graft particles determines the resultant space available (between particles) for osseous formation, particle size has been carefully selected according to this concept. The typical size of bone graft particles ranges from 100 to 1000 µm, which is conducive to neovascularization and the ingrowth of bone. Bone forms in cones called osteons with a central blood supply. The dimension of these cones (100-µm radius) is determined by the distance that the central vasculature supply can provide nutrients to cells at the edges of the osteon.

Autogenous Bone

Compared with other bone graft materials, autogenous bone is thought to be the best bone graft material because, in addition to being osteoconductive, it is osteoinductive and osteogenic. Furthermore, barring contamination, there is no risk of rejection or adverse reaction to the autogenous graft material. Intraoral sources of autogenous bone include edentulous spaces, maxillary tuberosity, mandibular ramus, mandibular symphysis, and extraction sites. Bone harvested from a recent extraction site (e.g., approximately 6 to 12 weeks healing) may have the advantage of increased osteogenic activity compared with other sites, which are more static and undergoing little or no osteogenesis. The maxillary tuberosity provides a more cellular source of autogenous bone compared with other sites. However, the trabecular nature of this site provides a lesser quantity of mineralized matrix, and the resultant total volume of bone available for grafting is often inadequate. For greater amounts of bone, it is more desirable to harvest bone from the mandibular ramus or symphysis. This bone, which is typically more cortical, can be harvested and used as a monocortical block graft or it can be ground or shaved into small fragments and used as a particulate graft.

Although the mandibular ramus and symphysis offer good sources of bone for grafting, clinicians are sometimes reluctant to harvest bone from these sites because of an increased risk of morbidity from the surgical procedure. Risks of surgery in the mandibular symphysis region include postoperative bleeding, bruising, wound dehiscence, damage to lower incisors, disfigurement, and injury to nerves. Nerve injury may be the most significant concern because it can be a long-term (possibly permanent), annoying alteration in sensation of the lower lip, chin, anterior teeth, and gingiva for the patient. A more serious risk is the alteration of facial appearance, particularly when the facial muscles are completely elevated from the bone beyond the inferior border of the mandible. A condition referred to as “witch’s chin” can occur when the facial muscles and overlying skin of the chin fall, causing a disfiguring sag of facial tissues after surgery.

A retrospective analysis of 48 chin graft–harvesting procedures, suggests that maintaining a 5-mm margin of safety between graft harvest sites and vital structures (e.g., lower incisors, the inferior border of the chin, and the mental foramen) will minimize postoperative complications.21 In the 48 procedures, postoperative sequelae included bruising of the lower face (48/48), bruising of the upper neck (6/48), and paresthesia of the lower lip and incisors (6/48). No patient experienced facial disfigurement or muscle prolapse (chin droop). Three of the six patients with paresthesia experienced transient symptoms and recovered completely within 2 months, whereas symptoms persisted longer than 6 months in the other three patients. Not surprisingly, the larger harvest defects (trephined six-ring sites) resulted in a higher incidence of paresthesia, which was longer lasting than that of the smaller defects (trephined four-ring sites). Harvesting bone in a custom-shaped “block” did not result in paresthesia, presumably because these harvest sites were smaller than the four-ring and six-ring trephine-harvested sites.

Observation of the following basic principles can minimize the risk of postoperative morbidity:

1. Carefully evaluate the harvest site for potential risks. A critical radiographic evaluation before surgery can identify individuals with inferior alveolar nerve branches that extend anterior beyond the mental foramen.

2. Use extreme care in making incisions laterally toward the mental nerve, and dissect the area with blunt instruments to locate the foramen.

3. Do not elevate and reflect muscle attachments beyond the inferior border of the mandible.

4. Limit bone cuts to an area at least 5 mm away from the tooth apices, the inferior border of the mandible, and the mental foramen. Do not extend cuts or harvest bone deeper than 6 mm, and do not include both labial and lingual cortical plates.

5. Suture the wound in layers (muscle and overlying mucosa separately) to prevent postoperative wound separation.

When harvesting autogenous bone, regardless of site or method used, it is important to use techniques that prevent overheating and maintain viability of the bone cells. Exceeding 47° C (116.6° F) is known to cause bone necrosis.16 Thus the use of drills, trephines, or saws to cut bone should always be done with profuse irrigation to keep instruments and bone cooled. Precision of osseous cuts can be facilitated with new technologies such as piezoelectric bone surgery (see Chapter 80).

Localized Ridge Augmentation

Patients often present for implant planning after tooth loss and alveolar ridge resorption. In these cases, the clinician is obligated to perform augmentation procedures to reconstruct lost bone and place implants in a prosthetically driven position.

Surgical reconstructive procedures for the preparation and placement of dental implants have become more numerous and complex. Depending on the size and morphology of the defect, various augmentation procedures can be used. These procedures have been categorized according to the deficient dimension: horizontal or vertical. Methods used to augment horizontal, as well as vertical, bone deficiencies include particulate bone grafts and monocortical block grafts. Barrier membranes can be used with bone grafts to reconstruct all types of alveolar bone defects. See Chapter 77 for a review of procedures used to achieve vertical augmentation. All the proven principles of GBR and flap management must be followed to achieve good results. These include an adequate blood supply; maintaining a stable, protected space for bone growth; and achieving tension-free flap wound closure.

Flap Management

Soft-tissue management is a critical aspect of bone augmentation procedures. Incisions, reflection, and manipulation should be designed to optimize blood supply and wound closure. The design and management of mucoperiosteal flaps must consider the increased dimensions of the ridge after augmentation as well as esthetics and approximation of the wound margins. The surgical procedure must be executed with the utmost of care in order to preserve the vascularity of the flap and to minimize tissue injury.1

Several flap techniques maintain a “submerged” position of bone grafts and barrier membranes during the entire healing process, including a remote or displaced incision.9,25 The advantage of a remote incision is that the wound opening is positioned away from the graft. A conventional crestal incision can be used, even in large supracrestal defects, as long as a periosteal releasing incision and coronal advancement of the flap achieve a tension-free closure.30 Most reports suggest removing sutures approximately 10 to 14 days after surgery. It is also suggested that no prosthesis be inserted for 2 to 3 weeks after surgery to avoid pressure over the wound during the early healing phase.

General concepts for flap management associated with ridge augmentation include the following:

1. It is desirable to make incisions remote relative to the placement of barrier membranes (e.g., vertical releasing incisions at least one tooth away from the site to be grafted). In the anterior maxilla, keeping vertical incisions remote is also an esthetic advantage.

2. Full mucoperiosteal flap elevation at least 5 mm beyond the edge of the bone defect is desirable.

3. The use of vertical incisions, although often required for surgical access, should be minimized.

4. Use of a periosteal releasing incision to give the flap elasticity and permit tension-free suturing is essential. This permits complete closure without stress on the wound margins.

5. Removable appliance should not be inserted over the wound for 2 weeks or more to avoid postoperative trauma to the surgical site.

6. Wound closure should incorporate a combination of mattress sutures to approximate connective tissues and interrupted sutures to adapt wound edges.

Horizontal Bone Augmentation

A deficiency in the horizontal dimension of bone may be minimal, such as a dehiscence or fenestration of an implant surface, or it may be more significant, such that the implant would have more than one axial surface exposed while having some bone along the entire vertical length. Dehiscence defects can usually be managed during implant placement because most of the implant is covered and stabilized by native bone. If the horizontal deficiency is large and the implant placement would result in significant exposure (i.e., implant body is significantly outside the alveolar bone), it may be better to reconstruct the bone first, in a staged approach, with a subsequent surgery for implant placement.

Although reconstruction of deficient ridges with bone grafts alone (i.e., without barrier membrane) has proved to be effective, variable resorption of the grafted bone has been reported. Preliminary results in a 1- to 3-year study using autografts harvested from the maxillary tuberosity showed an increased ridge width, but resorption of 50% of the graft volume was also />

Jan 15, 2015 | Posted by in Periodontics | Comments Off on 76: Localized Bone Augmentation and Implant Site Development
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