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    Allogenic tissue, such as demineralized

    freeze-dried bone allograft (DFDBA), can also

    be used in combination with CS as a bone-

    filling binder.15,16 A CS or synthetic mem-

    brane barrier is then added to prevent

    ingrowth of cells. Nonresorbable synthetic

    membranes, such as expanded polytetraflu-

    oroethylene, are far more invasive and time-

    consuming than is a resorbable CS mem-

    brane.17 Calcium sulfate, a material that has

    been used as a bone-filling material for

    more than 110 years,18 has been shown to

    be completely bioabsorbable,19 to be os-

    teoconductive,14 to allow fibroblast migra-

    tion,20 to not cause an inflammatory re-

    sponse,21 and to not elevate serum calcium

    levels.22 Recently, it has been shown that CS

    can be manufactured into a granular

    composite of CS and poly-L-lactic acid to

    decrease the degradation rate if the appli-

    cation calls for a slower dissolution.23

    Strocchi et al observed significantly more

    blood vessel growth in defects filled with

    CS than those filled with autograft, proving

    its angiogenic properties.24

    Blood vesselsprovide nutrition for growing bone and

    accelerate bone growth. Two parallel series

    of mechanisms are triggered by the degra-

    dation of CS into deep bone defect

    (Figure 1). The first mechanism involves

    the release of calcium and sulfur ions in

    the biological environment, which results in

    carbonate apatite formation and calcium

    ion stimulation of cellular activity.25 The

    second mechanism is the precipitation of

    calcium phosphate, which leads to a

    transient, local drop in pH. This causes

    surface demineralization of existing bone

    resulting in exposure of bioactive molecules

    and the release of growth factors such as

    transforming growth factors and bone

    morphogenetic proteins, which stimulates

    the growth of bone in defects filled with

    CS.2528 Calcium sulfate has been used as a

    bone graft by itself, in combination with

    other bone grafts, and also as a barrier to

    treat extraction sockets.

    CASE REPORT

    A 37-year-old male patient presented with

    advanced periodontal disease around an

    upper canine. A deep bone defect of 8 mm

    was found in the distal aspect of the tooth,

    as seen grossly and by radiograph in

    Figure 2a and b.

    The deep bone defect was accessed by

    elevating the full mucoperiosteal plate. The

    defect was debrided of all granulation tissue,

    and the root surface was carefully planed.

    DFDBA was mixed with medical grade CS

    (trade name DentoGen, Orthogen, LLC,

    Springfield, NJ) at a ratio of 75:25 (DFDBA:

    DentoGen; Figure 3a). Fast-setting solution

    was added to this mixture to form the bone

    graft composite. The composite was grafted

    into the deep bone defect using a spatula, as

    shown in Figure 3b. It was tightly compressed

    to thoroughly fill the defect. The defect was

    closed with a pure CS (DentoGen) barrier to

    prevent the ingrowth of soft tissue. Fast-setting solution was added to CS to form the

    putty, which was implanted as a barrier

    (Figure 3c). Nonresorbable suture was placed

    to reposition the flap (Figure 3d). Preopera-

    tive digital radiographs of the deep bone

    defect were taken to facilitate comparison

    with future time points. Digital radiographs of

    the grafted site were taken at 1- and 5-month

    FIGURE 1. Calcium sulfate degradation mechanismin a deep bone defect.

    Bone Repair in Periodontal Defect

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    postoperative time points. A standard bite

    holder was placed while taking a radiograph.

    The patient was followed every month for up

    to 6 months.

    When observed grossly, the site was

    healing well at the 1-month time point,

    and radiographs showed the grafted mate-

    rial was slowly resorbing (Figure 4a). At the

    5-month postoperative time point, the site

    was grossly observed to have healed well,

    and the deep bone defect observed in the

    preoperative radiograph was now replaced

    with bone, as evidenced by radiographs

    (Figure 4b).

    FIGURE 3. (a) Mixture of allograft and DentoGen. (b) Allograft and DentoGen composite implanted inperiodontal deep bone defect. (c) Defect closed with DentoGen membrane barrier. (d) Sutures placedover the top.

    FIGURE 2. (a) Preoperative periodontal deep bone defect around upper canine. (b) Preoperativeradiograph of periodontal deep bone defect around upper canine.

    Mazor et al

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    DISCUSSION

    A severe form of periodontal disease has

    been surgically treated using a 75% DFDBA/

    25% CS composite graft and a pure CS

    membrane barrier. Because CS has signifi-

    cant bone regeneration properties of its own

    as a bone graft, it not only acts as a binder

    that prevents DFDBA from migrating out of

    the deep bone defect but also further aids in

    bone growth by depositing a calcium

    phosphate trellis, preventing ingrowth of

    soft tissues, stimulating blood vessel forma-

    tion, and affecting the release of growth

    factors.

    When comparing the gross initial bonedefect to the 5-month time point, a com-

    plete healing of the bone with no gingival

    recession was noted. At both the 1- and 5-

    month time points, the patient showed no

    signs of discomfort, and no infection was

    observed. Analysis of the radiographs veri-

    fied the gross observations as the bone

    showed signs of remodeling at the 1-month

    time point and complete bone growth at the

    5-month time point. As DFDBA underwent

    remodeling, CS degraded and slowly re-

    sorbed, leading to the formation of a calcium

    phosphate trellis, which further stimulatedbone growth. This resulted in the deep bone

    defects being filled with regenerated bone

    at the 5-month postoperative time point.

    These results were similar to previous

    clinical studies on 19 patients with chronic

    periodontitis, which indicate that CS, used as

    a binder and barrier in combination with

    DFDBA, supports significant clinical improve-

    ment in intrabony defects.29 The authors

    observed that after 6 months, there was areduction in probe depth, gains in clinical

    attachment level, and defect fill and resolu-

    tion. A similar study by Harris and colleagues

    evaluated a CS porous hydroxyapatite and

    tetracycline binder combined with DFDBA

    and a CS barrier in 100 patients.30 Their

    technique also found a decrease in probe

    depth and an increase in clinical attachment

    FIGURE 4. (a) Radiograph obtained 1 month postoperatively. (b) Radiograph obtained after 5 monthsshows degradation of grafted material and bone growth in the original defect.

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    level after 6 months. A long-term, 6-year

    study of 12 patients by Orsini et al also

    yielded similar results.31 They used a combi-

    nation of autogenous bone grafting plus CS

    as a binder and barrier and compared it to a

    defect treated with a bioabsorbable mem-

    brane.31 After 6 years, there was no signifi-

    cant difference found between the two

    techniques. There was also a decrease in

    probe depth and an increase in clinical

    attachment level. It was also observed that

    there was no statistically significant differ-

    ence when comparing the long-term, 6-year

    results to their short-term, 6-month data.

    CONCLUSION

    In this surgical case report, medical-grade CS

    mixed with DFDBA was found to be a

    biocompatible composite graft with the

    ability to provide radiographic evidence of

    hard-tissue repair of a periodontal intrabony

    defect. The incorporation of CS improves the

    handling characteristics of DFDBA as well as

    the cost-effectiveness of the procedure.

    ABBREVIATIONS

    CS: calcium sulfate

    DFDBA: demineralized freeze-dried bone

    allograft

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