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Custom-Made Synthetic Scaffolds for Bone Reconstruction: A Retrospective, Multicenter Clinical Study on 15 Patients

Identifieur interne : 002929 ( Pmc/Curation ); précédent : 002928; suivant : 002930

Custom-Made Synthetic Scaffolds for Bone Reconstruction: A Retrospective, Multicenter Clinical Study on 15 Patients

Auteurs : Fabrizia Luongo [Italie] ; Francesco Guido Mangano [Italie] ; Aldo Macchi [Italie] ; Giuseppe Luongo [Italie] ; Carlo Mangano [Italie]

Source :

RBID : PMC:5192311

Abstract

Purpose. To present a computer-assisted-design/computer-assisted-manufacturing (CAD/CAM) technique for the design, fabrication, and clinical application of custom-made synthetic scaffolds, for alveolar ridge augmentation. Methods. The CAD/CAM procedure consisted of (1) virtual planning/design of the custom-made scaffold; (2) milling of the scaffold into the exact size/shape from a preformed synthetic bone block; (3) reconstructive surgery. The main clinical/radiographic outcomes were vertical/horizontal bone gain, any biological complication, and implant survival. Results. Fifteen patients were selected who had been treated with a custom-made synthetic scaffold for ridge augmentation. The scaffolds closely matched the shape of the defects: this reduced the operation time and contributed to good healing. A few patients experienced biological complications, such as pain/swelling (2/15: 13.3%) and exposure of the scaffold (3/15: 20.0%); one of these had infection and complete graft loss. In all other patients, 8 months after reconstruction, a well-integrated newly formed bone was clinically available, and the radiographic evaluation revealed a mean vertical and horizontal bone gain of 2.1 ± 0.9 mm and 3.0 ± 1.0 mm, respectively. Fourteen implants were placed and restored with single crowns. The implant survival rate was 100%. Conclusions. Although positive outcomes have been found with custom-made synthetic scaffolds in alveolar ridge augmentation, further studies are needed to validate this technique.


Url:
DOI: 10.1155/2016/5862586
PubMed: 28070512
PubMed Central: 5192311

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PMC:5192311

Le document en format XML

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<italic>Purpose</italic>
. To present a computer-assisted-design/computer-assisted-manufacturing (CAD/CAM) technique for the design, fabrication, and clinical application of custom-made synthetic scaffolds, for alveolar ridge augmentation.
<italic> Methods</italic>
. The CAD/CAM procedure consisted of (1) virtual planning/design of the custom-made scaffold; (2) milling of the scaffold into the exact size/shape from a preformed synthetic bone block; (3) reconstructive surgery. The main clinical/radiographic outcomes were vertical/horizontal bone gain, any biological complication, and implant survival.
<italic> Results</italic>
. Fifteen patients were selected who had been treated with a custom-made synthetic scaffold for ridge augmentation. The scaffolds closely matched the shape of the defects: this reduced the operation time and contributed to good healing. A few patients experienced biological complications, such as pain/swelling (2/15: 13.3%) and exposure of the scaffold (3/15: 20.0%); one of these had infection and complete graft loss. In all other patients, 8 months after reconstruction, a well-integrated newly formed bone was clinically available, and the radiographic evaluation revealed a mean vertical and horizontal bone gain of 2.1 ± 0.9 mm and 3.0 ± 1.0 mm, respectively. Fourteen implants were placed and restored with single crowns. The implant survival rate was 100%.
<italic> Conclusions</italic>
. Although positive outcomes have been found with custom-made synthetic scaffolds in alveolar ridge augmentation, further studies are needed to validate this technique. </p>
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<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Biomed Res Int</journal-id>
<journal-id journal-id-type="iso-abbrev">Biomed Res Int</journal-id>
<journal-id journal-id-type="publisher-id">BMRI</journal-id>
<journal-title-group>
<journal-title>BioMed Research International</journal-title>
</journal-title-group>
<issn pub-type="ppub">2314-6133</issn>
<issn pub-type="epub">2314-6141</issn>
<publisher>
<publisher-name>Hindawi Publishing Corporation</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">28070512</article-id>
<article-id pub-id-type="pmc">5192311</article-id>
<article-id pub-id-type="doi">10.1155/2016/5862586</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Clinical Study</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Custom-Made Synthetic Scaffolds for Bone Reconstruction: A Retrospective, Multicenter Clinical Study on 15 Patients</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0001-7998-613X</contrib-id>
<name>
<surname>Luongo</surname>
<given-names>Fabrizia</given-names>
</name>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0001-5488-4268</contrib-id>
<name>
<surname>Mangano</surname>
<given-names>Francesco Guido</given-names>
</name>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
<xref ref-type="corresp" rid="cor1">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Macchi</surname>
<given-names>Aldo</given-names>
</name>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Luongo</surname>
<given-names>Giuseppe</given-names>
</name>
<xref ref-type="aff" rid="I3">
<sup>3</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid" authenticated="false">http://orcid.org/0000-0002-4419-4674</contrib-id>
<name>
<surname>Mangano</surname>
<given-names>Carlo</given-names>
</name>
<xref ref-type="aff" rid="I4">
<sup>4</sup>
</xref>
</contrib>
</contrib-group>
<aff id="I1">
<sup>1</sup>
Private Practice, 00193 Rome, Italy</aff>
<aff id="I2">
<sup>2</sup>
Department of Surgical and Morphological Science, Dental School, Insubria University, 21100 Varese, Italy</aff>
<aff id="I3">
<sup>3</sup>
Department of Oral and Maxillofacial Surgery, Federico II University, 80131 Naples, Italy</aff>
<aff id="I4">
<sup>4</sup>
Department of Dental Sciences, Vita Salute San Raffaele University, 20132 Milan, Italy</aff>
<author-notes>
<corresp id="cor1">*Francesco Guido Mangano:
<email>francescomangano1@mclink.net</email>
</corresp>
<fn fn-type="other">
<p>Academic Editor: Sérgio Alexandre Gehrke</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>14</day>
<month>12</month>
<year>2016</year>
</pub-date>
<volume>2016</volume>
<elocation-id>5862586</elocation-id>
<history>
<date date-type="received">
<day>31</day>
<month>10</month>
<year>2016</year>
</date>
<date date-type="accepted">
<day>23</day>
<month>11</month>
<year>2016</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2016 Fabrizia Luongo et al.</copyright-statement>
<copyright-year>2016</copyright-year>
<license xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p>
</license>
</permissions>
<abstract>
<p>
<italic>Purpose</italic>
. To present a computer-assisted-design/computer-assisted-manufacturing (CAD/CAM) technique for the design, fabrication, and clinical application of custom-made synthetic scaffolds, for alveolar ridge augmentation.
<italic> Methods</italic>
. The CAD/CAM procedure consisted of (1) virtual planning/design of the custom-made scaffold; (2) milling of the scaffold into the exact size/shape from a preformed synthetic bone block; (3) reconstructive surgery. The main clinical/radiographic outcomes were vertical/horizontal bone gain, any biological complication, and implant survival.
<italic> Results</italic>
. Fifteen patients were selected who had been treated with a custom-made synthetic scaffold for ridge augmentation. The scaffolds closely matched the shape of the defects: this reduced the operation time and contributed to good healing. A few patients experienced biological complications, such as pain/swelling (2/15: 13.3%) and exposure of the scaffold (3/15: 20.0%); one of these had infection and complete graft loss. In all other patients, 8 months after reconstruction, a well-integrated newly formed bone was clinically available, and the radiographic evaluation revealed a mean vertical and horizontal bone gain of 2.1 ± 0.9 mm and 3.0 ± 1.0 mm, respectively. Fourteen implants were placed and restored with single crowns. The implant survival rate was 100%.
<italic> Conclusions</italic>
. Although positive outcomes have been found with custom-made synthetic scaffolds in alveolar ridge augmentation, further studies are needed to validate this technique. </p>
</abstract>
</article-meta>
</front>
<floats-group>
<fig id="fig1" orientation="portrait" position="float">
<label>Figure 1</label>
<caption>
<p>Virtual 3D model of the deficient ridge and first drawing of the customized scaffold (Mimics®, Materialise. Leuven, Belgium): (a) frontal view of the ridge without the customized scaffold; (b) frontal view of the ridge with the customized scaffold; (c) occlusal view of the ridge without the customized scaffold; (d) occlusal view of the ridge with the customized scaffold.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.001"></graphic>
</fig>
<fig id="fig2" orientation="portrait" position="float">
<label>Figure 2</label>
<caption>
<p>The customized synthetic scaffold was designed with a hole in its centre to allow the placement of a fixation screw (Rhino®, Robert McNeel & Associates, Seattle, WA, USA): (a-b-c-d) different views of the scaffold design.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.002"></graphic>
</fig>
<fig id="fig3" orientation="portrait" position="float">
<label>Figure 3</label>
<caption>
<p>The proper size/shape of the customized scaffold was verified and the adaptation to the bone defect and the congruence with the bony walls was perfectioned (Mimics®, Materialise. Leuven, Belgium): (a) frontal view; (b) axial view; (c) lateral view; (d) 3D reconstruction.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.003"></graphic>
</fig>
<fig id="fig4" orientation="portrait" position="float">
<label>Figure 4</label>
<caption>
<p>A block of synthetic micromacroporous biphasic calcium-phosphate (BCP), consisting of 70% beta-tricalcium-phosphate and 30% hydroxyapatite (BTK®, Dueville, Vicenza, Italy), was placed into the CNC milling machine (DWX-51®, Roland DG Mid Europe, Acquaviva Picena, AP, Italy) and milled into the size/shape of the 3D virtual model, so that a customised synthetic BCP scaffold was fabricated: (a) buccal aspect of the scaffold design; (b) lingual aspect of the scaffold design; (c) the milled customized scaffold ready for clinical use.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.004"></graphic>
</fig>
<fig id="fig5" orientation="portrait" position="float">
<label>Figure 5</label>
<caption>
<p>Bone reconstruction: (a) a full-thickness flap was elevated in order to fully expose the bone defect, and a series of little perforations, 1-2 mm deep, were made on the defect walls, in order to increase the amount of bleeding at the surgical site; (b) the customized synthetic scaffold was placed in position; (c) the scaffold was fixed to the remaining wall by means of a titanium mini-screw, positioned through the predetermined hole; (d) an absorbable collagen membrane was placed, in order to protect the scaffold.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.005"></graphic>
</fig>
<fig id="fig6" orientation="portrait" position="float">
<label>Figure 6</label>
<caption>
<p>After 8 months from the regenerative surgery, the implant was placed: (a) after the elevation of a full-thickness flap, the regenerated site showed an increased bone thickness with a considerable amount of new, clinically well-integrated bone; (b) the mini-screw used for fixation was removed; (c) the preparation of the surgical site was performed with drills of increasing diameter; (d) a 3.5 diameter × 13 mm length implant (NobelActive®, Nobel Biocare, Kloten, Switzerland) was placed in the regenerated site.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.006"></graphic>
</fig>
<fig id="fig7" orientation="portrait" position="float">
<label>Figure 7</label>
<caption>
<p>The implant was located in the perfect 3D position: (a) it was placed in a clinically well-integrated, regenerated bone; (b) as confirmed by the CBCT control examination.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.007"></graphic>
</fig>
<fig id="fig8" orientation="portrait" position="float">
<label>Figure 8</label>
<caption>
<p>After being submerged for a period of 2-3 months, the implant was uncovered and a prosthetic restoration was placed: (a) a full-thickness surgical flap was raised; (b) the implant was uncovered; (c) the cover cap was replaced by a transmucosal healing abutment and interrupted sutures were performed; (d) two weeks later, the provisional crown was placed.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.008"></graphic>
</fig>
<fig id="fig9" orientation="portrait" position="float">
<label>Figure 9</label>
<caption>
<p>Radiographic history of the case: (a) periapical rx taken immediately after the reconstructive procedure; (b) periapical rx taken immediately after implant placement; (c) the implant during the provisional phase, 4 months after placement of the fixture; (d) final rx control of the definitive crown, 3 years after implant placement.</p>
</caption>
<graphic xlink:href="BMRI2016-5862586.009"></graphic>
</fig>
</floats-group>
</pmc>
</record>

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