Editorial Type:
Article Category: Research Article
 | 
Online Publication Date: 01 Feb 2011

Part III: Crystalline Fluorapatite-Coated Hydroxyapatite; Potential Use as a Bacteriostatic Agent for Both Pre-Implant Cases and Retreatment of Infected Implant Sites: A Report of 4 Cases

DMD, MS and
DDS, MS
Page Range: 43 – 51
DOI: 10.1563/AAID-JOI-D-10-00165
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Abstract

Four cases of peri-implant bone loss associated with undiagnosed necrotic pulps of adjacent teeth are reported. In two cases, bone was obliterated along sinus tracts (fistulas) that coursed between the implant and adjacent tooth. Endodontic treatment was completed on the adjacent teeth concurrent with periapical surgery to seal the tooth apex. The sinus tract (fistula) was excised, and the implant plus tooth surfaces were treated with a combination of concentrated citric acid and 4.3% sodium fluoride solutions. The third case involved peri-implant surgery with endodontic treatment on the adjacent tooth. A fourth case represented an infected socket augmentation which was surgically treated, augmented with microcrystalline fluorapatite in the range of a 300 µm to 400 µm cluster, and allowed to heal for 4 months followed by a trephine bone biopsy and subsequent analysis for bone growth around the fluoridated nonceramic microcrystalline hydroxyapatite (HA). An augmentation procedure employing fluoridated of resorbable HA was then completed. Histologic analysis showed healthy bone regeneration suggesting that therapeutic fluoride treatment and resultant fluorapatite were helpful in inhibiting reinfection following surgical treatment. All 4 infected implant sites were successfully managed and retained using the aforementioned treatment schemes, and there was no evidence of posttreatment infection in any of the 4 cases. It is proposed that fluoride treatment, through the use of 4.3% sodium fluoride and/or fluoridated hydroxyapatite (fluorapatite), shows promise as an adjunctive treatment component in inhibiting peri-implant infection and reinfection when managing ailing or failing implants.

Copyright: by the American College of Veterinary Internal Medicine
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1–5.
F igures 1–5.

Figure 1. Implant completed. Figure 2. The sinus tract between implant and tooth No. 9. Figure 3. Augmentation. Figure 4. The tissue is approximated and sutured to complete the procedure. Figure 5. The tissue is healed.


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6–11.
F igures 6–11.

Figure 6. The bone has filled in between the implant and adjacent tooth. Figure 7. Mirror image shows the bone loss associated with adjacent periapical lesion on tooth No. 26. Figure 8. The endodontic treatment is completed and the area is augmented. Figure 9. One year later showing the bone fill-in. Figure 10. The bone before implant placement. Figure 11. The bone loss around the apical portion of the implants.


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12–16.
F igures 12–16.

Figure 12. The trimmed portion of the implants plus the augmentation material 6 months after the procedure. Figure 13. The large abscessed failure root canal treated tooth held in place with a plain gut multiple crisscrossing suture stitched across the extraction socket. Figure 14. The finished augmentation using fluoridated HA immediately into the infected extraction site. Notice the cytoplast nonresorbable barrier member held in place with a plain gut multiple crisscrosses the socket suture. Figure 15. The augmentation site 6 months post surgery just prior to harvesting the trephine bone biopsy. Figure 16. At ×200 the engulfment of the augmented fluoridated hydroxylapatite crystals in the immediate grafting subsequent to extraction in an infected extraction socket.


Contributor Notes

*Corresponding author, e-mail: wnordquist@yahoo.com
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