Professional Documents
Culture Documents
Types of Gingival Grafts
Types of Gingival Grafts
Types of Gingival Grafts
By
Ahmad Mahir Tawfeeq
Periodontics Master Class 2023-2024
To achieve proficiency and mastery of intraoral soft-tissue grafting, the surgeon must
have a strong grasp in understanding the anatomy and biological processes that occur
during the maturation and modification of oral soft tissues. Oral mucosa can be
identified and classified under 3 primary entities: masticatory mucosa, oral mucous
membranes, and specialized mucosa covering the dorsum of the tongue. Implant
surgeons, in particular, are most concerned with the masticatory mucosa, which includes
the gingiva as well as the mucosal component of the hard palate. The gingival complex,
while sharing an essential esthetic responsibility, also serves a crucial protective and
structural function within the periodontium and peri-implant tissues. For these reasons,
defects of the gingiva can be particularly devastating to the status of the dentition and
endosseous implants.
During the immediate postoperative period, free grafts or the cells contained in them (in
the case of autografts) are supplied exclusively by diffusion. Apart from their limited
intracellular energy reserves, these grafts are entirely dependent on the influx of
metabolites with the extracellular fluid by means of diffusion for survival. The driving
force behind this diffusion process, also known as plasmatic circulation, is the
concentration gradient between the native and the transplanted tissues. From the third
to fourth postoperative day on, the mediator-stimulated ingrowth of capillaries from the
recipient bed into the graft and the formation of anastomoses between blood vessels of
the graft and the recipient bed begins, gradually reestablishing circulation to the graft
(revascularization). The stages of wound healing that follow are dependent on these
capillary proliferation processes. the end of which is characterized by a dense network of
blood vessels extending beyond the preexisting graft margins.
For optimal plasmatic circulation and revascularization, the graft should bn adapted to
the recipient bed as intimately as possible to minimize the diffusion distance and
capillary proliferation length to be covered and to maximize the number of transplanted
cells receiving an adequate supply of nutrients during the early post-operative period.
Intimate and extensive contact between the graft and the well-vascularized recipient
bed is crucial to graft survival. Heavy bleeding and the formation of a large blood clot
between the graft and the recipient bed impairs the nutrient supply to the transplanted
cells. The surgical techniques used to create the recipient bed and establish primary
wound closure are also crucial to the success of grafting.
In the case of free autografts, the first two requirements are directly dependent on the
selected donor site and the corresponding harvesting procedure, whereas the next three
are directly related to the biologic and bio-functional characteristics of the graft
material.
Connective tissue autografts are ideal materials for the reconstruction of soft tissue
defects. The organic extracellular connective tissue matrix can serve as a space-holder
and conductor for new ingrowing fibroblasts, ensuring smooth integration into the
surrounding tissue. Tissue-specific endogenous proteins as well as specific connective
tissue cells (fibroblasts) are transferred with the connective tissue autograft. The
majority of these cells are well nourished by the blood supply from the plasmatic
circulation in the initial period and from revascularization in the subsequent period
following transplantation. Consequently, they have a good prognosis.
Several intraoral donor sites for connective tissue autografts have been described. The
most commonly used donor site is the palate, but the maxillary tuberosity area and the
mandibular retromolar region are also used. Two types of connective tissue autografts
can be distinguished: the free subepithelial connective tissue graft and the full-thickness
free mucosal graft. The former is harvested without covering epithelium and consists
mainly of a subepithelial collagen tissue matrix, whereas the latter contains all histologic
tissue layers, including the covering epithelium.
Free gingival grafts are used to create a widened zone of attached gingiva. They were
initially described by Bjorn in 1963 and have been extensively used since that time.
The connective tissue autograft technique was originally described by Edel and is based
on the fact that the connective tissue carries the genetic message for the overlying
epithelium to become keratinized. Only connective tissue from beneath a keratinized
zone can be used as a graft.
The advantage of this technique is that the donor tissue is obtained from the
undersurface of the palatal flap, which is sutured back in primary closure. Healing is by
first intention. The patient has less discomfort postoperatively at the donor site. Another
advantage of the free connective tissue autograft is that improved aesthetics can be
achieved because of a better color match of the grafted tissue to the adjacent areas.
Successful and predictable root coverage has been reported using free gingival
autografts.
Free gingival graft. (A) Before treatment, showing minimal keratinized gingiva. (B) Recipient site
prepared for a free gingival graft. (C) The palate is the donor site. (D) Free graft. (E) Graft transferred
to the recipient site. (F) At 6 months, showing widened zone of attached gingiva.
Free connective tissue graft. (A) Lack of keratinized, attached gingiva buccal to the central incisor. (B)
Vertical incisions to prepare the recipient site. (C) Recipient site is prepared. (D) Palate from which
connective tissue is removed for donor tissue. (E) Removal of connective tissue. (F) Donor site is
sutured. (G) Connective tissue for the graft. (H) Free connective tissue is placed at the donor site. (I)
Postoperative healing at 10 days. (J) Final healing at 3 months. Notice the wide, keratinized, attached
gingiva.
Autograft harvesting is never a stand-alone procedure, but is always performed in
conjunction with other surgical procedures. These procedures are mostly gingival
augmentation techniques utilized to increase the width of the attached gingiva and for
the treatment of recession cases either in coronal direction (root coverage procedures)
where the donor graft tissue is placed covering the denuded root surface, or in apical
direction when the donor graft tissue is placed on a recipient bed apical to the recessed
gingival margin and no attempt is made to cover the denuded root surface where there
is gingival and bone recession.
Having said that, it would be clear to the reader of this paper that the protocols
demonstrated are focusing on the grafting techniques itself without detailing the
procedures performed on the recipient sites.
The FGG technique was first described by Bjorn in 1963 and was used to enhance zones
of attached gingiva. The primary indication for free gingival grafting is to prevent peri-
implantitis and facilitate oral hygiene through keratinized attached gingiva augmentation
in both tooth-borne and peri-implant sites. Keratinized tissue has been shown to form a
more stable environment around implant abutments, which would limit biofilm
development on an implant interface. However, the primary flaw of free gingival grafting
is that the harvested graft retains the tissue characteristics of the donor site. This
eliminates FGG as a treatment option in the esthetic zone. In addition, post-surgically
the donor site is left with a soft-tissue defect that must heal by secondary intention. This
increases the amount of discomfort experienced by the patient and delays healing time
at the donor site.
Strip technique for a free gingival graft: (A through D) Mucosal tissue around the implants. (E and F)
Recipient site is prepared. (G) Donor site with strips of free graft removed. (H) Donor strips of free graft.
(I and J) Strips placed side by side on the recipient site. (K) Donor area 1 week after graft removal. (L)
Healing of the recipient site after 3 months. Notice the good keratinized, attached gingiva.
Surgical Technique
5.1 Recipient Site Preparation
The recipient site is prepared by creating a horizontal incision at the existing
mucogingival junction using a #15 blade. This facilitates the blending of any surgical scar
into the existing mucogingival line. It is important not to disturb the periosteum during
the initial incision because this layer will facilitate the intimate adaptation and
immobilization of the graft. If 2 vertical incisions are to be incorporated into the
recipient site, they should be made to be 2-times the width of the intended
augmentation to allow for contracture during the healing phase.
After creating the outline, one edge of the graft is elevated with tissue forceps or with
well-placed sutures for retraction, and is gently lifted away from the site while
continuing to separate the graft with the blade. If one does opt to place retraction
sutures, they may remain in place to facilitate tissue transfer. Ideally, graft thickness
should be 1.0 to 1.5 mm, keeping in mind that thicker grafts may be more difficult to
immobilize and vascularize while a graft that is too thin may be subject to excessive
shrinkage or necrosis. After transfer and immobilization of the graft, it is essential to
cover the donor site to facilitate patient comfort. A variety of materials have been used
for this purpose, including periodontal dressing (eg, Coe-Pak), oxidized regenerated
cellulose (Surgicel), fast-drying butyl cyanoacrylate tissue adhesive (PeriAcryl), and
palatal stent.
Harvest of the free gingival graft. (A) Outline of the donor tissue harvest made with a #15 blade. (B)
Soft-tissue defect left in hard palate after harvest. (C) Donor site packed with absorbable hemostat for
hemostasis and patient comfort. (D) Measured thickness of FGG 1.5 mm. (E) Donor-site healing at 1-
week follow-up revealing proper granulation.
There are 2 primary options available for the recipient-site preparation steps for a
subepithelial connective tissue graft. Consideration should be made regarding whether
the surgeon would like to proceed with an open technique versus a closed technique
whereby no releasing incisions are necessary. Both of these techniques require the
surgeon to keep the dissection in a supra-periosteal plane. The closed technique
preserves circulation by avoiding vertical releasing incisions. However, it may be limited
in its ability in apical repositioning of the graft, and also is much more technically taxing
when trying to ensure that the graft is uniformly placed. An open technique allows for
direct visualization of the site and thus allows for ease of access for the surgeon. It has
the obvious drawback of requiring vertical incision(s) that sacrifice circulation and can be
esthetically concerning.
After adequate anesthesia has been administered, a #15 blade is used to create a 1- mm
deep, partial-thickness sulcular incision along the periphery of the soft-tissue defect. A
horizontal incision is then extended mesially and distally to the defect to facilitate supra-
periosteal dissection. It has been recommended that the area of supra-periosteal
dissection should be roughly 3-times the area of the soft tissue defect to ensure
adequate peripheral circulation is available to the region, and this plane can be created
by inserting the scalpel parallel into the pouch created, with extreme care not to
perforate buccally through the gingiva. This pouch can then be explored with the blunt
end of a periosteal elevator to ensure that a uniform recipient site was prepared.
6.1.2 Recipient Site Preparation: Open Technique
The open technique for recipient-site preparation is a standard elevation of a buccal flap
in a supraperiosteal plane, incorporating vertical releasing incisions similar to those
previously discussed in for FGGs.
Subepithelial connective tissue graft. (A) A 4-mm Class I Miller defect at the mesial root of tooth #14.
(B) Donor site. (C) Closed tunneling technique used for preparation of recipient site. (D) Harvest of
subepithelial connective tissue graft via L-shaped incision with an anterior vertical release. (E) Primary
closure of the donor site. (F) Harvested donor tissue (measured 1.5 mm in thickness, not shown). (G)
Application and immobilization of the harvested graft into recipient site. (H) An 8-week follow-up with
100% root coverage. (I) Donor-site healing at 8 weeks.
6.2 Donor Site Graft Harvest: Overview
The most common location for harvest of a subepithelial connective tissue graft is from
the masticatory mucosa located on the patient’s hard palate between the mesial line
angle of palatal root of the first molar and the distal line angle of the canine, as this is
where the thickest tissue can be found. Care must be taken not to injure the greater
palatine artery, which arises from the greater palatine foramen. This is located at the
junction of the horizontal and vertical shelves of the palatine bone, often apical to the
third molar.
Clinical situation before harvesting of a free subepithelial connective tissue graft from the palate
The donor site is closed with a crossed periosteal suture of Gore-Tex CV-5. The first suture is placed externally, slightly
coronal to the mucogingival junction, through the buccal flap. First, the needle enters slightly mesial to the distal surface
of the last molar, passes obliquely through the flap in an apico-coronal direction, and emerges in the coronal portion of
the buccal flap, slightly distal to the last molar. Next, the needle enters the palatal flap distal to the donor site, passes
through it horizontally, from distal to mesial, and emerges on the buccal side, where the suture knot tied. Anchorage of
the suture in this manner (by the periosteum buccally and by the masticatory mucosa palatally) serves two purposes:
apical flap repositioning and wound compression. Interrupted sutures can be used to close the remaining wound areas
in the distal region, but it is acceptable to leave these small areas open to heal by secondary intention because the
periosteum has been left on the bone.
8. References
1. Dale BA. Periodontal epithelium: a newly recognized role in health and disease. Periodontol
2000 2002;30:70–8.
2. Bral MM, Stahl SS. Keratinizing potential of human crevicular epithelium. Periodontol 2000
1977;48:381.
3. Caffesse RG, Nasjleti CE, Castelli WA. The role of sulcular environment in controlling
epithelial keratinization. Periodontol 2000 1979;50:1.
4. Listgarten MA. Electron microscopic study of the gingivo-dental junction of man. Am J Anat
1966;119(1):147–77.
5. Pollanen MT, Salonen JI, Uitto J. Structure and function of the tooth-epithelial interface in
health and disease. Periodontol 2000 2003;31:12.
6. Eggert ME, Levin L. Biology of teeth and implants: the external environment, biology of
structures, and clinical aspects. Quintessence Int 2018;49(4):301–12.
7. Fowler C, Garrett S, Crigger M, et al. Histologic probe position in treated and untreated
human periodontal tissues. J Clin Periodontol 1982;9:373–85.
8. Skougaard M. Turnover of the gingival epithelium in marmosets. Acta Odontol Scand
1965;23:623–43.
9. Oliver R. Lac H, Karring T. Microscopic evaluation of the healing and revascularization of free
gingival grafts. J Periodontal Res 1968:3:84-95.
10. Pallesen L. Schou S. Aaboe M. Hjorling-Hansen E. A. Melson F. Influence of particle size of
autogenous bone grafts on the early healing stages of bone regeneration: A histologic and
serologic study in rabbit calvarium. lnt. J Oral Maxillofac Implants. 2002; 17:498-506.
11. Wessel J. Tatakis D. Patient outcomes following subepithelial connective tissue graft and free
gingival graft procedures. J Periodontol. 2008;79:425-430.
12. Bjorn H. Free transplantation of gingiva propria. Swed Dent J 1963;22:684–9.
13. Karring T, Ostergaard E, Lo¨e H. Conservation of tissue specificity after heterotopic
transplantation of gingiva and alveolar mucosa. J Periodontal Res 1971;6: 282–93.
14. Nabers JM. Free gingival grafts. Periodontics 1966;4:243.
15. Mormann W, Schaer F, Firestone AC. The relationship between success of free gingival grafts
and transplant thickness. Periodontol 1981;52:74.
16. Langer B, Calagna L. The subepithelial connective tissue graft. J Prosthet Dent
1980;44(4):363–7.
17. Reiser GM, Bruno JF, Mahan PE, et al. The subepithelial connective tissue graft palatal donor
site: anatomic considerations for surgeons. Int J Periodontics
Restorative Dent 1996;16(2):130–7.