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1145

Guided Tissue Regeneration and Bone


Grafts in the Treatment of Furcation
Defects*
Raul G. Caffesse, Carlos E. Nasjleti, Anthony E. Plotzke, Gissela B. Anderson, and
Edith C. Morrison

The present study evaluated the effects of guided tissue regeneration (GTR), with
and without demineralized freeze-dried cortical bone grafts, in the treatment of furcation
defects in 4 female beagle dogs with naturally occurring periodontal disease. The root
surfaces were thoroughly debrided. Four weeks later, full thickness facial and lingual
mucoperiosteal flaps were reflected using inverse bevel incisions on both sides of the
mandible involving the 2nd, 3rd, and 4th premolar, and the 1st molar teeth. Following
debridement, notches were placed on the roots at the level of supporting bone. Test
quadrants were randomly selected and furcations were filled with reconstituted, demi-
neralized, freeze-dried human cortical bone grafts. Following bone grafting, all defects
were covered with an expanded polytetrafluoroethylene (ePTFE) membrane, which was
sutured with 4-0 sutures. Afterward, interproximal sutures were placed through the flaps,
assuring the flaps covered the membranes completely. The contralateral side, serving as
control, was treated by debridement only and application of ePTFE membrane. All
membranes were removed 6 weeks after surgery. Dogs were sacrificed at 4 months after
surgery. Both mesio-distal and bucco-lingual histologie sections were evaluated by de-
scriptive histology. Linear measurements and surface area determination of the furcal
tissues were carried out using the microscope attached to a digitizer. Twelve to 20 non-
serial sections were made of the mid-buccal aspects of each root of each treated tooth.
Half of these sections were stained with Harris' hematoxylin and eosin (H&E) and the
other half stained with Mallory's trichrome stain. Additionally, another group of 12 to
20 non-serial sections cut in the mesio-distal direction were secured for the surface area
measurements of the furcations. Mean values for each dog were obtained for test and
control teeth. ANOVA procedure for a split plot design was employed. Periodontal
healing following the use of guided tissue regeneration procedures resulted in an increase
in connective tissue and alveolar bone regeneration. Adjunctive bone grafting did not
appear to enhance regeneration. / Periodontol 1993; 64:1145-1153.

Key Words: Bone, demineralized, freeze-dried; guided tissue regeneration; grafts/sur-


furcation; surgical flaps; membranes, artificial; polytetrafluoroethylene/therapeutic
gery;
use.

The predictable regeneration of a new attachment appara- tween the gingiva


and the root surface. This membrane
tus, after the natural attachment has been destroyed by peri- serves as a barrier preventing the gingival epithelium and
odontal disease, is one of the most challenging problems in the gingival connective tissue from reaching contact with
dentistry. Several recent studies in animals1"5 and in the root during healing, and at the same time, giving pref-
humans611 have demonstrated that extensive regeneration erence to cells originating from the periodontal ligament
of the attachment apparatus (new cementum, new bone, and and bone to repopulate the wound area adjacent to a pre-
a functional periodontal ligament) occurred with the use of viously exposed root surface.
a surgical procedure termed guided tissue regeneration (GTR). Previously, Nyman et al.1 reported that regeneration of
This procedure includes the placement of a membrane be- periodontal tissues was obtained when a filter1" was inter-
posed between the gingival tissue on one side and the ex-
*Department of Periodontics, The University of Texas Health Science
Center at Houston, Houston, TX. +Millipore Corporation, Bedford, MA.
J Periodontol
1146 GTR AND BONE GRAFTS IN THE TREATMENT OF FURCATIONS November 1993 (Supplement)

posed root surfaces and the surrounding alveolar bone on aP-10 universal tip and Gracey curettes.11 Teeth were sub-
the other. However, since the filter is difficult to remove sequently polished. Plaque control was maintained by top-
at the end of the treatment, it is considered impractical in ical application of a .12% solution of Chlorhexidine glu-
routine clinical practice. Recently, the case reports of Ny- conate, 5 times weekly. Surgical wounding of the animals
mn et al.,6 Becker et al.,7,8 Gottlow et al.,9 Pontonero et started 2 weeks following the scaling and plaque control
al.,10 and Caffesse et al.,11 coupled with animal studies,4,5 phase.
have generated major interest in the GTR procedure, with
the use of an expanded teflon membrane rather than filters. Surgical Procedures
These authors611 reported successful treatment of furca- Prior to surgery, each dog was sedated with ketamine given
tions and vertical defects after treatment with ex- intramuscularly (10 mg/kg body weight) and subsequently
panded polytetrafluoroethylene* (ePTFE) membranes. anesthetized with isoflurane gas. In addition, the dog was
Also, in a number of reports,1218 the flap procedure has locally infiltrated with 2% Xylocaine (1:50,000 epineph-
been combined with insertion of different kinds of bone rine) to reduce hemorrhage. Two mandibular quadrants in
grafts into the curetted bony defects in order to enhance each dog were surgically treated. Each quadrant included
new attachment. These studies showed an increased bone the 2nd, 3rd, and 4th premolar and the 1st molar. The test
fill and it was postulated that new attachment occurred where quadrant was selected by the toss of a coin. Reverse bevel,
new bone was present. Clinical parameters such as probing full thickness, mucoperiosteal flaps were raised with ver-
depth, attachment level, and radiographie bone height showed tical releasing incisions at the mesial and distal aspects of
significant improvement and were considered to represent the surgical sites. Following the elevation of the soft tissue
evidence of new attachment. Recently, in human studies, flaps, removal of granulation tissue, and complete root in-
Bowers et al.19,20 presented evidence of new attachment strumentation, reference notches were placed in the roots
apparatus following placement of decalcified freeze-dried at the level of the alveolar bone crest, using a number 1/2
bone allografts in intrabony defects, both in a submerged round bur. These notches were positioned on the buccal
and non-submerged environment. For these studies, grafted aspects of the roots and extended interproximally and into
and non-grafted sites were histometrically evaluated and the furcation areas as deep as the involvement of the Class
compared 6 months after surgery. Results indicated that II furcation permitted. Following the placement of the
significantly more new attachment, including cementum, notches, the surgical sites were thoroughly flushed with
bone, and periodontal ligament, formed in intrabony defects sterile saline, and then blotted dry with a sterile gauze sponge.
grafted with demineralized bone than in non-grafted defects. The Class II furcation defects of the teeth in 1 of the 2
The present study in beagle dogs combined the procedure mandibular quadrants (test quadrant) were filled with re-
of epithelium and gingival connective tissue exclusion via constituted DFDCB grafts. Following bone grafting, all teeth
ePTFE with demineralized freeze-dried cortical human bone involved received the ePTFE membrane. The material was
grafts (DFDCB) to enhance regeneration. The aim was to placed so that 2 to 3 mm of crestal bone was covered. Once
histologically and histometrically evaluate and compare the the periodontal material was in place, it was sutured using
effectiveness of ePTFE membranes, with and without the a suspensory suture around each tooth with a 4-0 suture.1
use of DFDCB graft, in periodontal regeneration. Afterwards, interproximal sutures were placed through the
flap assuring that it covered the membrane completely. Fol-
MATERIALS AND METHODS lowing this, the vertical releasing incisions were also su-
This animal study was approved by the Animal Welfare tured. Once suturing was completed, moderate pressure was
Committee of The University of Texas Health Science Cen- applied over the sites for 4 to 5 minutes using a sterile
ter at Houston, and was performed in accordance with the gauze moistened with sterile saline, so as to minimize clot
National Institutes of Health Guide for the Care and Use thickness and tissue gaping. On each tooth of the contra-
of Laboratory Animals. lateral side, serving as control, the same procedure was
Four purebred female beagle dogs with naturally occur- performed, but without bone graft. Therefore, a split mouth
ring periodontal disease, 4 to 6 years old, were used in this design was obtained: test, DFDCB graft plus ePTFE; and
study. They were maintained on a hard diet except for a 2- control, ePTFE only.
week period of time following surgery, when a soft diet
was used. The dogs were subjected to a thorough intra-oral Post-Surgical Procedures
examination which included periodontal probing and intra- During the 2 weeks following surgery, all dogs were fed a
oral radiographs. Removal both of bacterial plaque and su- soft diet, and during the first week, tooth brushing was
pra- and subgingival calculus plus root planing with local suspended in order to prevent unnecessary disruption of the
anesthesia was performed with an ultrasonic sealer8 using ePTFE membrane and healing flap.
Seven days after surgery, the dogs were sedated to allow
*Gore-Tex periodontal material, W.L. Gore & Associates, Inc., Flagstaff,
AZ. 'Hu-Friedy Company, Chicago, IL.
5Cavitron Corporation, Long Island, NY. 'W.L. Gore & Associates, Inc., Flagstaff, AZ.
Volume 64
Number 11 CAFFESSE, NASJLETI, PLOTZKE, ANDERSON, MORRISON 1147

a rubber cup prophylaxis and intra-oral photographs. In the 3) from the root surface notch to the apical extent of the
following weeks, the surgical sites were maintained by junctional epithelium; and 4) from the free gingival margin
brushing with a .12% Chlorhexidine gluconate solution, 5 to the apical extent of the junctional epithelium.
times weekly. Surface area determination. In approximately 10 mesio-
Six weeks after surgery, the ePTFE membrane was re- distal sections per tooth, including test and control teeth,
moved. Under general anesthesia, a split thickness flap pro- surface area determinations (in mm2) relative to the furca-
cedure was performed to permit removal of the ePTFE tions were made, evaluating: 1) the whole interradicular
membrane. The flaps were then replaced and secured with space; 2) the area occupied by connective tissue plus bone;
sutures. Sutures were removed in 7 days. Tooth brushing 3) the area occupied by bone; 4) the area occupied by ep-
with Chlorhexidine solution continued as before. ithelium; and 5) the area occupied by ankylosis. Images
Four months after surgery, the dogs were anesthetized as were digitized using a microscope-image processing sys-
was done for surgery with isoflurane gas. Final radiographs, tem** attached to a microcomputer, as described previously.21
clinical measurements, and intra-oral photographs were taken.
Each dog was then given additional anesthetic and sacri- Statistical Evaluation
ficed by exsanguination. The heads of the animals were Mean values for the experimental and control teeth were
perfused with a 10% neutral formalin solution and then obtained, and both linear and surface area measurements
refrigerated for 1 to 2 days. The jaws were dissected free, were analyzed using an analysis of variance procedure for
labelled, and placed in formalin for further fixation. the split plot design. The tooth as a unit of analysis within
the dog permitted the investigation of the influence of tooth
Laboratory Procedures type on treatment outcomes.
In order to enhance the speed of demineralization, the jaws
were sectioned into one tooth blocks. Demineralization was
RESULTS
accomplished with 10% tri-fluroacetic acid (TFA), the end-
point of which was determined radiographically. Following Histologie Observations
demineralization, the blocks were washed, dehydrated, in- On the bucco-lingual histologie sections, those teeth treated
filtrated, and embedded in paraffin, and then sectioned at with GTR only and those treated with DFDCB grafts plus
6 intervals. Twelve to 20 non-serial sections were made GTR showed almost identical healing. New connective tis-
of the mid-buccal aspects of each root of each treated tooth. sue attachment was evident including cementum deposition
Half of these sections were stained with Harris' hematox- as well as bone regeneration in the area coronal to the root
ylin and eosin (H&E) and the other half stained with Mal- notch. In these sections, newly-formed connective tissue
lory's trichrome stain. Additionally, another group of 12 to fibers were oriented perpendicular or nearly perpendicular
20 non-serial sections cut in the mesio-distal direction were to the root surface and were clearly inserted into the regen-
secured for the surface area measurements of the furcations. erated bone and the highly cellular new cementum. Fibers
These microscopic slides were examined under a binocular could be seen coursing from the adjacent regenerated peri-
microscope and descriptive histologie and histometric eval- odontal ligament into the newly-formed bone. The newly-
uations were performed. formed periodontal ligament was very cellular and highly
vascularized, yet free of inflammatory cells. No signs of
Histologie Evaluation root rsorption or dentoalveolar ankylosis were seen in these
The descriptive histologieevaluation determined the pres- bucco-lingual sections. Hence, the results demonstrated that
ence or absence of root rsorption and/or dento-alveolar the reformation of a connective tissue attachment was con-
ankylosis, bone formation, the location of cementum dep- siderably favored by the placement of the ePTFE mem-
osition, the direction of the periodontal fibers, as well as branes which seemingly have prevented the gingival epi-
the degree of inflammation in the tissues. thelium and the gingival connective tissue from interfering
with healing, as shown in Figures 1A and IB.
Histometric Evaluation On the mesio-distal sections from teeth treated with GTR
Linear measurements. Under the microscope and using a only, the furcations demonstrated extensive connective tis-
micrometer eye piece,* 10 bucco-lingual tissue sections per sue and alveolar bone regeneration, as well as cemento-
tooth were measured by orienting the micrometer grid par- genesis. New cementum with inserting collagen fibers, as
allel to the shortest line which connected the apical extent well as tissue attachment uncomplicated by root rsorption
of the root notch to the landmark measured.21 The following was observed (Figs. 2A through 2D).
measurements were performed: 1) from the apical extent of However, many mesio-distal sections from teeth treated
the root notch to the coronal extent of the newly-deposited with the adjunctive bone grafts demonstrated that ankylotic
cementum; 2) from the root notch to the alveolar bone crest; manifestations did occur in the area of the implanted DFDCB.
Three patterns were evident. First, some specimens showed
#Filar micrometer eyepiece, Bausch & Lomb Optical Company, Roches-
ter, NY. **Zeiss Int., Okekochen, Germany.
) Periodontol
1148 GTR AND BONE GRAFTS IN THE TREATMENT OF FURCATIONS November 1993 (Supplement)

Figure IB. Higher magnification of notch area seen in Figure 1A showing


new deposited cementum, regenerated alveolar bone, and new connective
tissue attachment. (H&E stain; original magnification x 100.)

Surface Area Determinations


Table 2 shows the comparison of mean furcation fill mea-
surements in mm2 for the treatment modalities. Results
1A. GTR, with and without DFDCB grafts, successfully inhibited showed that adjunctive bone grafting did not enhance peri-
Figure
connective tissue and epithelial participation in the healing process, thus odontal tissue regeneration beyond that achieved in sites
allowing new attachment on a previously altered root surface to take treated with ePTFE membrane alone (Fig. 7).
place. (H&E stain; original magnification x 25.)
DISCUSSION
The present study was undertaken to provide histologie ob-
both newdeposited cementum and regenerated bone pen- servation on the effectiveness of DFDCB grafts in regen-
etrating an irregular manner into the periodontal ligament
in erating lost periodontal attachment when used as an adjunct
space. These projections of cementum and bone reduced to the GTR procedure. Results of the study have shown
the periodontal ligament space (Figs. 3A and 3B). A second that the graft material used was well-tolerated by the host
pattern would appear to be a somewhat later state in the tissues. Despite the fact that xenogeneic DFDCB was used,
sequence of events. Many specimens demonstrated "true" there was no evidence of any inflammatory or immunologie
bony ankylosis bridging between new deposited cementum reaction to the material. This finding is consistent with Sonis
and bone, as shown in Figure 4. Still other specimens showed et al.22 who also used xenogeneic bone grafts and demon-
a third pattern with the furcation area almost completely strated the relative biocompatibility of DFDCB. However,
filled with regenerated bone (Figs. 5A and 5B). This pattern xenogeneic material may produce an adverse immune re-
of healing was the less common among the group. It was sponse, but such grafts have also been used,23,24 in spite of
usually depicted in second premolars where the small sep- the fact that they may give a very much weaker response
aration of the roots produced a narrow furcation area. or no response at all.25
Also, the study has shown that significant amounts of
Linear Measurements new attachment may form with the use of a GTR procedure
When the linear measurements were analyzed (Table 1), no which gives preference to cells originating from the peri-
significant differences between procedures (GTR only vs. odontal ligament tissue to repopulate the wound area ad-
GTR plus DFDCB graft) were found. Nevertheless, both jacent to the periodontally-diseased root surfaces. Such
procedures gained connective tissue attachment as well as guidance of the ingrowth of the periodontal ligament tissue
new cementum and new bone deposition (Fig. 6). into the wound area was accomplished by placing the ePTFE
Volume 64
Number 11 CAFFESSE, NASJLETI, PLOTZKE, ANDERSON, MORRISON 1149

:^*i..y _' -''.^wx&' ~-.ty , .fri-- . -1 Hi I


-

Figure 2C. Higher magnification of the coronal area in Figure 2A dem-


.

onstrating newly-deposited cementum and new connective tissue attach-


ment. (H&E stain; original magnification x 100.)

Figure 2A. Photomicrograph of representative mesio-distal section show-


ing regenerative connective tissue and new alveolar bone filled completely
furcation area following application of ePTFE only. (H&E stain; original
magnification x 25.)

Figure 2D. A higher power view of the right notch area seen in Figure
2A exhibiting new cementum, newly-formed alveolar bone, and repaired
periodontal space. (H&E stain; original magnification x 100.)

over the root surface which prevented granulation tissue


derived from the gingival connective tissue from reaching
contact with the root. This is also in agreement with the
findings of Gottlow et al.,3-9 Caffesse et al.,4-5-11 Becker et
al.,7'8 and Pontoriero et al.,10 who used ePTFE membranes
for the exclusion of gingival connective tissue and epithe-
lium during healing. Their results showed that the refor-
Figure 2B. Higher magnification of left notch area seen in Figure 2A mation of a connective tissue attachment was considerably
demonstrating new deposited cementum, regenerated alveolar bone, and favored by the placement of the membranes.
new connective tissue attachment. (H&E stain; original magnification x The histologie analysis of the teeth treated with GTR
100.) alone disclosed that new cementum with inserting collagen
fibers had formed on the previously periodontally-involved
root surfaces. New bone was also depicted in these speci-
J Periodontol
1150 GTR AND BONE GRAFTS IN THE TREATMENT OF FURCATIONS November 1993 (Supplement)

Figure 3A. Photomicrograph of a furcation from a tooth treated with GTR


and adjunctive DFDCB graft. Note irregular deposition of new cementum
and new bone as well as the reduced periodontal ligament space. (H&E
stain; original magnification x 25.)

Figure 5A. Other specimens from teeth also treated with the adjunctive
Figure 3B. A higher power view of the furcation fomix of Figure 3A bone grafts showed furcation areas almost completely filled with ankylotic
depicting new cementum and bone projecting into the periodontal ligament bone. (H&E stain; original magnification x 35.)
space. (H&E stain; original magnification x 100.)
Volume 64
Number 11 CAFFESSE, NASJLETI, PLOTZKE, ANDERSON, MORRISON 1151

Table 1. Linear Histometrics in Buccal-Lingual Sections from 4 Beagle Dogs After 4 months of Healing (in mm)

Cementum Bone Connective Tissue Epithelium


GTR GTR GTR GTR GTR GTR GTR GTR
Only + DFDCB Only + DFDCB Only + DFDCB Only + DFDCB
Tooth Mean SD Mean SD Mean SD Mean SD Mean SD Mean SD Mean SD Mean SD
p2 1.32 0.75 0.78 0.29 0.88 0.35 0.93 0.46 1.48 0.82 1.37 0.44 1.30 0.18 1.96 0.48
P3 1.33 0.18 1.57 0.92 0.82 0.17 0.70 0.77 1.50 0.16 1.56 0.92 1.41 0.33 1.80 0.93
P4 1.34 0.61 0.81 0.38 1.17. 0.58 1.46 0.79 1.57 0.62 1.70 0.65 1.83 0.44 1.61 0.17
M, 1.49 0.48 0.94 0.33 1.04 0.66 1.26 0.98 1.51 0.45 0.99 0.38 1.94 0.89 2.21 1.00
1.37 0.49 1.03 0.59 0.97 0.45 1.09 0.76 1.51 0.51 1.41 0.63 1.62 0.55 1.90 0.69
Source of
Variation DF* Prob* Prob Prob Prob
Dog 3 1.28 0.3271 1.00 0.4275 0.55 0.6556 1.90 0.1843
Tooth 3 1.02 0.4187 1.72 0.2160 0.69 0.5757 0.82 0.5085
Dog Tooth 9 1.18 0.3879 2.21 0.1006 1.54 0.2397 0.38 0.9248
Treatment 1 3.50 0.0861 0.32 0.5805 0.30 0.5957 1.32 0.2738
Tooth Treatment 3 1.11 0.3819 0.23 0.8739 0.55 0.6592 0.60 0.6291
Total 19 1.28 0.3372 1.53 0.2281 1.03 0.4962 0.77 0.7040

'Degrees of freedom.
*F value of test statistic.
*P value for the test.

mm
mens. Root rsorption and/or dentoalveolar ankylosis were
2.5 GTR
negligible. However, in furcation areas where ePTFE mem-
g GTR + DFDCB branes were used in combination with DFDCB grafts, vary-

MM
2.0 ing patterns of ankylosis were clearly observed.
In this study, the observation that root rsorption was
1.5 almost absent on the roots of both test and control treated
areas is not surprising. Repeatedly, ePTFE membranes ef-

1.0
fectively prevented granulation tissue derived from the gin-
gival connective tissue from reaching contact with the roots.
Previous studies in dogs and monkeys by Nyman et al.,1
0.5 Gottlow et al.,3 and Karring et al.,26 have postulated that
root rsorption occurred when granulation tissue derived
from the gingival connective tissue was proliferating into
CEMENTUM BONE CONNECTIVE EPITHELIUM contact with the root surface.
TISSUE However, the observation that varying amounts of den-
Figure 6. Both procedures gained connective tissue attachment as well as toalveolar ankylosis formed in furcation defects treated with
new cementum and new bone deposition. the adjunctive DFDCB graft was unexpected. Previous au-
thors have reported20,27 29 that root rsorption and dentoal-
veolar ankylosis are not common sequelae of grafting fur-
cation defects with DFDCB. Because the real cause for the
observed ankylosis is unknown, it is only possible to spec-
ulate about it. Since the graft material used in this study
DFDCB
has been reported to be highly osteogenic, it is possible that
the osteoinductive effect triggered an early and greater bone
replacement resulting in the ankylosis observed. Previ-
ously, Urist and co-workers25,30"31 have shown that demin-
eralization of bone resulted in enhanced osteogenic activity.
This osteogenic activity has been cited in numerous
human16 20 and animal studies.32"34 According to Urist31'35
a hydrophobic glycoprotein within the bone matrix, termed
bone morphogenic protein (BMP), is responsible for the
osteoinductive effect by eliciting the differentiation of host
TOTAL FILL CONNECTIVE BONE
TISSUE mesenchymal cells into osteoblasts. Mundy and Poser36 have
Figure 7. Adjunctive bone grafting did not enhance periodontal tissue demonstrated the chemotactic effect of osteocalcin, another
regeneration beyond that achieved in sites treated with ePTFE membrane bone matrix protein. They showed that osteocalcin is a po-
alone. tent chemoattractant for cultured osteoblast-like cells and
J Periodontol
1152 GTR AND BONE GRAFTS IN THE TREATMENT OF FURCATIONS November 1993 (Supplement)
Table 2. Furcation Fill Achieved in 4 Beagle Dogs (Measured in mm2)

Total Area
EPI+ CT + Connective Tissue (CT)
GTR GTR GTR GTR
Only + DFDCB Only + DFDCB
Tooth Mean SD Mean SD Mean SD Mean SD
p2 5.93 1.60 4.44 1.71 2.33 0.78 0.94 0.21
p, 6.00 1.66 4.45 1.24 2.28 0.88 1.09 0.48
P. 6.32 1.48 9.64 4.09 1.52 0.33 5.31 4.20
M, 8.92 0.79 11.96 5.05 1.96 0.51 2.19 1.21
6.79 1.81 7.62 4.56 2.02 0.68 2.38 2.68
Source of
variation DF* Prob* Prob
Dog 3 0.11 0.9527 0.75 0.5417
Tooth 3 7.90 0.0036 2.28 0.1310
Dog tooth 9 1.47 0.2617 1.32 0.3188
Treatment 1 0.86 0.3723 0.43 0.5262
Tooth treatment 3 2.29 0.1301 4.77 0.0206
Total 19 2.37 0.0648 1.88 0.1320

'Degrees of freedom.
*F value of test statistic.
*P value for the test.

monocytes. Therefore, it is possible that any single factor in dogs treated by guided tissue regeneration (GTR). / Periodontol
or any combination of factors could have contributed to the 1990; 61:45-50.
6. Nyman S, Gottlow J, Lindhe J, et al. New attachment formation by
ankylosis observed. guided tissue regeneration. / Periodont Res 1987; 22:252-254.
A close look at the histometric results depicted in Tables 1 7. Becker W, Becker BE, Berg L, et al. New attachment after treatment
and 2 clearly indicates that the adjunctive use of DFDCB graft with root isolation procedures: Report of treated class III and class II
in this study did not enhance periodontal attachment over that furcations and vertical osseous defects. Int J Periodontics Restorative
observed when ePTFE was used alone. These results seem to Dent 1988; 8(3):9-23.
8. Becker W, Becker BE, Prichard J, et al. Root isolation for new
follow Egelberg's view,37 in relationship to the use of bone
attachment procedures: A surgical and suturing method. Three Case
grafts. He stated that "there is little reason to believe that reports. J Periodontol 1987; 58:819-823.
such bone grafts would stimulate connective tissue attachment 9. Gottlow J, Nyman S, Lindhe J, et al. New attachment formation in
to root surface." Apparently, the results achieved were the the human periodontium by guided tissue regeneration. Case reports.
effect of guided tissue regeneration, independent of the pres- / Clin Periodontol 1986; 13:604-616.
10. Pontoriero R, Lindhe J, Nyman S, et al. Guided tissue regeneration
ence of the bone graft. Others have also questioned the value
in degree II furcation-involved mandibular molars. A clinical study.
of bone grafts and whether or not a graft contributes to new / Clin Periodontol 1988; 15:247-254.
connective tissue attachment.38^2 11. Caffesse RG, Smith BA, Duff B, et al. Class II furcations treated by
Probably, the function of a grafting material in associa- guided tissue regeneration in humans: Case reports. / Periodontol
tion with guided tissue regeneration would be as a scaffold 1990; 61:510-514.
12. Hiatt WH, Schallhorn EG. Intraoral transplants of cancellous bone
to provide and maintain space whenever the membrane may
and marrow in periodontal lesions. J Periodontol 1973; 44:194-208.
have the possibility to collapse, and therefore, reducing the 13. Froum SJ, Ortiz M, Witkin RT, et al. Osseous autografts. III. Com-
chances for periodontal ligament cells to repopulate the pre- parison of osseous coagulum-bone blend implants with open curett-
viously-exposed root surface. age. J Periodontol 1976; 47:287-294.
14. Ellegaard B, Nielsen IM, Karring T. Composite jaw and iliac can-
cellous bone grafts in intrabony defects in monkeys. J Periodont Res
1976; 11:299-310.
REFERENCES 15. Dragoo MR. Closed curettage. In: Dragoo MR, ed. Regeneration of
1. Nyman S, Gottlow J, Karring T, Lindhe J. The regenerative potential the Periodontal Attachment in Humans. Philadelphia: Lea & Febiger;
of the periodontal ligament. An experimental study in monkeys. / 1981:36-37.
Clin Periodontol 1982; 9:257-265. 16. Mellonig JT. Decalcified freeze-dried bone allograft as an implant
2. Aukhil I, Simpson DM, Schaberg TV. An experimental study of new material in human periodontal defects. Int J Periodontics Restorative
attachment procedure in beagle dogs. J Periodont Res 1983; 18:643- Dent 1984; 4(4):41-55.
654. 17. Bowen JA, Mellonig JT, Gray JL, Towle HJ. Comparison of decal-
3. Gottlow J, Nyman S, Karring T, Lindhe J. New attachment formation cified freeze-dried bone allograft and porous particulate hydroxyapa-
as the result of controlled tissue regeneration. / Clin Periodontol tite in human periodontal osseous defects. J Periodontol 1989; 60:647-
1984; 11:494-503. 654.
4. Caffesse RG, Smith BA, Castelli WA, Nasjleti CE. New attachment 18. Rummelhart JM, Mellonig JT, Gray JL, Towle HJ. Comparison of
achieved by guided tissue regeneration in beagle dogs. J Periodontol freeze-dried bone allograft and demineralized freeze-dried bone al-
1988; 59:589-594. lograft in human periodontal osseous defects. / Periodontol 1989;
5. Caffesse RG, Domnguez LE, Nasjleti CE, et al. Furcation defects 60:655-663.
Volume 64
Number 11 CAFFESSE, NASJLETI, PLOTZKE, ANDERSON, MORRISON 1153

Bone () Epithelium (EPI) Ankylosis


'

GTR GTR GTR GTR GTR GTR


Only + DFDCB Only + DFDCB Only + DFDCB
Mean SD Mean SD Mean SD Mean SD Mean SD Mean SD
3.44 2.04 2.76 0.96 0.0 0.0 0.0 0.0 0.15 0.17 0.75 0.90
3.72 1.39 3.06 0.69 0.10 0.13 0.0 0.0 0.0 0.0 0.30 0.52
4.64 1.25 4.33 1.39 0.0 0.0 0.0 0.0 -

0.24 0.18 0.0 0.0


6.78 0.46 8.97 4.71 0.10 0.13 0.04 0.09 0.12 0.24 0.81 1.40
4.64 1.84 4.78 3.42 0.05 0.10 0.01 0.04 0.13 0.18 0.46 0.85

F Prob F Prob F Prob


0.53 0.6713 0.64 0.6037 2.68 0.0943
10.46 0.0011 1.93 0.1781 0.91 0.4653
1.53 0.2432 1.21 0.3702 1.24 0.3564
0.04 0.8446 2.25 0.1597 2.99 0.1092
1.04 0.4116 0.87 0.4856 1.15 0.3703
2.62 0.0456 1.24 0.3612 1.49 0.2414

19. Bowers GM, Chadroff , Carnevale R, et al. Histologie evaluation materials. Part II. New bone formation with autografts and allografts:
of new attachment apparatus formation in humans. Part II. / Perio- A histological evaluation. / Periodontol 1981; 52:297-302.
dontol 1989; 60:675-682. 33. Mellonig JT, Bowers GM, Baily RC. Comparison of bone graft ma-
20. Bowers GM, Chadroff B, Carnevale R, et al. Histologie evaluation terials. Part I. New bone formation with autografts and allografts
of new attachment apparatus formation in humans. Part III. J Per- determined by strontium-85. / Periodontol 1981; 52:291-296.
iodontol 1989; 60:683-693. 34. Koskinen EV, Ryoppy SA, Lindholm TS. Osteoinduction and Osteo-
21. Smith B, Caffesse R, Nasjleti C, et al. Effects of citric acid and genesis in implants of allogeneic bone matrix. Clin Orthop 1972;
fibronectin and laminin application in treating Periodontitis. / Clin 87:116-121.
Periodontol 1987; 14:396-402. 35. Urist MR, Lietze A, Mitzuni H, et al. A bovine low molecular weight
22. Sonis ST, Williams RC, Jeffcoat MK, et al. Healing of spontaneous bone morphogenic protein (BMP) fraction. Clin Orthop 1982; 162:219-
defects in dogs treated with xenogeneic demineralized bone. / Per- 232.
iodontol 1985; 56:470^179. 36. Mundy GR, Poser JW. Chemotactic activity of the carboxyglutamic
23. Thieleman FW, Veihelmann D, Schmidt K. The induction of new acid containing protein in bone. Calcif Tissue Int 1983; 35:164-168.
bone formation after transplantation. Arch Orthop Trauma Surg 1978; 37. Egelberg J. Regeneration and repair of periodontal tissues. J Perio-
91:3-9. dont Res 1987; 22:233-242.
24. Thieleman FW, Schmidt K, Koslowski L. Osteoinduction. II. Puri- 38. Caton J, Nyman S, Zander H. Histometric evaluation of periodontal
fication of the osteoinductive activities of bone matrix. Arch Orthop surgery. II. Connective tissue attachment levels after four regenerative
Trauma Surg 1982; 100:73-78. procedures. / Clin Periodontol 1980; 7:224-231.
25. Urist MR, Silverman BF, Bring , et al. The bone induction prin- 39. Listgarten MA, Rosenberg MM. Histological study of repair follow-
ciple. Clin Orthop 1967; 53:243-250. ing new attachment procedures in human periodontal lesions. / Per-
26. Karring , Nyman S, Lindhe J, Sirirat M. Potentials for root rsorp- iodontol 1979; 50:333-344.
tion during periodontal wound healing. J Clin Periodontol 1984; 11:41- 40. Steiner SR, Crigger M, Egelberg J. Connective tissue regeneration to
52. periodontally diseased teeth. II. Histologie observations. / Periodont
27. Perlus JD. Histological evaluation of the osteogenic potential of de- Res 1981; 16:109-116.
calcified lyophilized bone and dentin. J Periodontol 1975; 46:628- 41. Martin M, Gantes B, Garrett S, Egelberg J. Treatment of periodontal
633. furcation defects. I. Review of the literature and description of a
28. Pearson GE, Rosen S, Dporter DA. Preliminary observations on the regenerative surgical technique. J Clin Periodontol 1988; 15:227-
usefulness of a decalcified, freeze-dried cancellous bone allograft ma- 231.
terial in periodontal surgery. J Periodontol 1981; 52:55-59. 42. Gantes , Martin M, Garrett S, Egelberg J. Treatment of furcation
29. Quintero G. Evaluation of decalcified freeze-dried bone allografts in defects. II. Bone regeneration in mandibular class II defects. / Clin
periodontal osseous defects. J Periodontol 1985; 56:250-252. Periodontol 1988; 15:232-239.
30. Urist MR. Bone formation by autoinduction. Science 1965; 150:893-
899.
31. Urist MR, Strates BS. Bone morphogenetic protein. / Dent Res 1971 ; Send reprint requests to: Dr. Raul G. Caffesse, Department of Perio-
50:1392-1398. dontics, Dental Branch, The University of Texas at Houston, 6516 John
32. Mellonig JT, Bowers GM, Cotton WR. Comparison of bone graft Freeman Avenue, Houston, TX 77030.

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