Bishara Soft Tissue Grafting PDF
Bishara Soft Tissue Grafting PDF
Bishara Soft Tissue Grafting PDF
Abstract: Immediate implant placement often presents challenges in terms of predictably obtaining soft-tissue
coverage over the implant site. While delayed implant placement offers the ability for soft tissues to grow and invade
the extraction socket making their attachment around implants more predictable, immediate implant placement
poses a significant risk of bacterial invasion towards the implant surface as a result of insignificant soft-tissue
volume. Soft-tissue grafting techniques have often been proposed for use during immediate implant placement to
augment soft-tissue deficiencies, including the use of either palatal connective tissue grafts (CTGs) or collagen-
derived scaffolds. However, both of these approaches have significant drawbacks in that CTGs are harvested with
high patient morbidity and collagen scaffolds remain avascular and acelluar posing a risk of infection/implant
contamination. More recently, platelet-rich fibrin (PRF) has been proposed as an economical and biological means
to speed soft-tissue wound healing. In combination with immediate implant placement, PRF offers an easily
procurable low-cost regenerative modality that offers an efficient way to improve soft-tissue attachment around
implants. Furthermore, the supra-physiological concentration of defense-fighting leukocytes in PRF, combined
with a dense fibrin meshwork, is known to prevent early bacterial contamination of implant surfaces, and the
biological concentrations of autologous growth factors in PRF is known to increase tissue regeneration. This article
discusses soft-tissue grafting techniques associated with immediate implant placement, presents several cases
demonstrating the use of PRF in routine immediate implant placement, and further discusses the biological and
economic advantages of PRF for the management of soft-tissue grafting during immediate implant placement.
I
mplant placement often presents challenges in terms of pre- over the extraction site as primary closure is not easily achievable
dictable soft-tissue coverage. This is especially true in the without flap elevation and repositioning. Unlike types 2 through 4,
esthetic zone where a lack of supporting keratinized soft where soft tissue has formed over the socket, the practitioner is left
tissue during implant placement often compromises the final with limited methods to protect the implant site during the initial
esthetic outcomes when mucosal recession occurs around healing period. Traditionally, soft tissue is relieved (often requiring
these implants. Timing of implant placement has mainly been char- vertical releasing incisions) at the time of implant placement by un-
acterized into four categories: (1) immediate implant placement dermining the periosteum, thus allowing tissue mobilization without
(type 1) occurring when implants are placed at the same time as the tension to achieve a passive primary closure over the wound site.2
surgical extraction of teeth; (2) early implant placement (type 2) This often results in distortion of the mucogingival junction and a lack
occurring when soft-tissue healing has transpired and implants are of adequate attached gingiva on the buccal/facial aspect of the site.
placed typically within 4 to 8 weeks following extraction; (3) early Furthermore, an apical repositioning of the flap at second-stage sur-
implant placement (type 3) when partial bone healing has occurred gery (implant exposure) and/or soft-tissue grafting is often required
in the socket by typically 12 to 16 weeks after extraction; and lastly, to allow for sufficient keratinized tissue coverage around the implant
(4) late implant placement (type 4) when the extraction socket has emergence. An associated increase in swelling with associated pain
fully healed after 16 weeks.1 The principles that will be discussed while utilizing this approach due to manipulation of the periosteum
in this article may be applied with either a one-stage or two-stage related to undermining to permit flap release has also been noted.
surgical approach, depending on the practitioner’s preferences and Other techniques for wound coverage allow the site to heal by sec-
the clinical situation that presents. ondary intention and use barrier membranes to protect the implant
Type 1 immediate implant placement is deemed the most surgically site and any associated bone graft that may have been placed simul-
challenging and possesses additional risks in that soft-tissue coverage taneously during implant placement. Such techniques include the use
Fig 4. PRF clots compressed to form PRF membranes. Fig 5. PRF plugs used to fill an extraction socket without need for primary closure. Fig 6.
Radiograph of fractured central incisor with past history of root canal therapy. Fig 7. Occlusal view of fractured central incisor with past history
of root canal therapy. Fig 8. Atraumatic removal of central incisor. Fig 9. Implant placement in a palatal position. Fig 10. PRF plug used to seal the
implant site. Fig 11. Periapical radiograph taken during implant placement. Fig 12. Periapical radiograph taken at implant uncovery after 3 months
of healing, demonstrating bone fill around the implant.
turned for stage two surgery and a periapical radiograph was taken
(Figure 12). Half a carpule of 2% Xylocaine Dental with 1:100,000
epinephrine was administered into the gingiva overlaying the implant.
An incision was made with a 15c scalpel blade mesial-distally to the
palatal side of the mid-crestal line. The tissue was positioned to the
facial to preserve adequate attached gingiva and horizontal mattress
sutures with 6-0 Prolene® (Ethicon, ethicon.com) were used to se-
cure the repositioned flap. A screw-retained provisional crown was
created to develop the emergence profile of the soft tissue around
the uncovered implant. Fig 14.
Approximately 6 weeks later, the patient presented for impressions
and the screw-retained provisional crown was removed (Figure 13).
An open-tray impression coping was placed and a periapical radio-
graph was taken to ensure the impression coping was properly seated.
An open-tray fixture level impression was taken using Maxill® Light
and Heavy Body PVS (Maxill Dental, maxill.com) in a stock tray
(Master Tray®, Waterpik Oral Health, waterpik.com) and was sent
to the lab for fabrication of a screw-retained crown.
The laboratory returned the restoration for insertion. The patient
Fig 15.
presented and the provisional restoration was removed. The final
screw-retained crown was inserted and the screw was tightened with
finger pressure on a hex wrench. A radiograph was taken to verify
complete mating of the parts. A torque wrench was used to tighten
the fixation screw to the manufacturer’s recommendation of 30 Ncm.
A ball of PTFE tape was placed into the screw channel and sealed
with Filtek™ Flow composite (3M ESPE, 3m.com). Occlusion was
checked and the patient dismissed (Figure 14). Follow-up with the
patient at a post-insertion appointment demonstrated healthy non-
inflamed gingival tissue surrounding the implant restoration with a
natural emergence profile (Figure 15).
Case 2
A 38-year-old healthy woman presented to the clinic with issues
pertaining to a previously endodontically treated and restored maxil-
lary left central incisor. Radiographically the tooth appeared normal
(Figure 16). Clinically, a vertical root fracture was noted as evidenced
by an isolated probing depth on the facial of the tooth. Treatment op-
Fig 16.
tions were presented to the patient, which included: extraction with
placement of a fixed bridge using the adjacent teeth as abutments, in place using a figure 8 suture utilizing 3-0 silk on a reverse cutting
or extraction and implant placement with a single-crown restoration. C6 needle (Figure 21).
She decided to pursue the dental implant option. The patient returned a week later for postoperative evaluation and
After a thorough medical history was collected, consent for treat- suture removal. Three months post implant placement the patient
ment was provided. Two carpules of 1.8-ml 2% Xylocaine Dental returned for stage two surgery demonstrating healthy non-inflamed
with 1:100,000 epinephrine was administered as infiltration and an soft tissue overlaying the implant (Figure 22). A periapical radiograph
incisive nerve block. Blood was collected at the antecubital fossa was taken to assess implant healing (Figure 23). Half a carpule of
as previously described in Case 1. A Woodson elevator was used to 2% Xylocaine Dental with 1:100,000 epinephrine was administered
circumferentially dissect the gingiva around the central incisor. The locally and the implant cover screw was exposed. An open-tray im-
tooth was atraumatically extracted using a #76S forcep in a rotation/ pression coping was placed and a periapical radiograph was taken
counter-rotation manner (Figure 17). The extraction socket was then to verify that the impression coping was fully seated. An open-tray
debrided using a curette and irrigated with saline solution. A precision fixture level impression was taken and sent to the lab for fabrication
drill was then used to engage the dense palatal cortical bone to guide of a screw-retained crown. A healing abutment was placed and the
the pilot drill for the osteotomy. The 2.3-mm pilot drill was used to patient was dismissed after modification of the removable provisional
align the angulation to allow a screw-retained crown implant position. prosthesis. The crown was returned from the lab and inserted onto
The drilling sequence was then completed. the implant (Figure 24).
A UNC 15 periodontal probe was used to assess the osteotomy site
to ensure no fenestrations in the buccal plate were present. An MIS Discussion
SEVEN 5-mm x 13-mm implant (MIS Implants) was placed into the The present case reports highlight the use of autologous blood con-
osteotomy with primary stability as evidenced by a 30-Ncm inser- centrates (ie, PRF) for everyday dental use. While PRF has gained
tion torque (Figure 18). Again, the lateral stability was questionable much attention as a regenerative agent capable of further speeding
as a result of the gap/jump junction that was observed between the tissue regeneration across many fields of medicine, the authors fo-
buccal plate and implant. A cover screw was placed into the implant. cused the present article on its use in immediate implant dentistry.
Because this case had a larger gap/jump junction then the previ- Currently, the trend in implant placement has slowly shifted from a
ous case discussed, 0.25 cc cortical/cancellous bone allograft with a delayed approach toward immediate/early placement as patients con-
particle size ranging from 250 µm to 1000 µm (OraGRAFT®, LifeNet tinue to seek more rapid treatment protocols and final restorations.
Heath, lifenethealth.org) was mixed with an injectable PRF (i-PRF, As a result, immediate implant placement has received considerable
centrifuged at 700 rpm for 3 minutes) to create a putty-like graft, attention in recent years.
which was placed into the buccal gap (Figure 19). The fibrin clots One of the main limitations of immediate implant placements is
were removed from the centrifuged vials to produce A-PRF mem- that, unlike with early implant placement, soft tissue has not fully
branes as previously described in Case 1, and an A-PRF membrane matured over the extraction socket. This makes immediate implant
was then used to cover the extraction site (Figure 20). This was fixed placement somewhat more biologically demanding as it is now known
Fig 14.
Fig 17. Atraumatic removal of affected tooth. Fig 18. Implant placement in a palatal position relative to facial plate. Fig 19. Freeze-dried bone
allograft used to fill gap between implant and buccal wall. Fig 20. PRF membrane placed over immediate implant and tucked under buccal and
lingual gingival margins. Fig 21. A figure 8 suture was used to secure PRF membrane placed over the immediate placed implant. Fig 22. Final
healing after 3 months.
6
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CASE REPORT | IMMEDIATE IMPLANT PLACEMENT
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