Use of piezosurgery during maxillary sinus elevation: clinical results of 40 consecutive cases.
Identifieur interne : 000E51 ( PubMed/Corpus ); précédent : 000E50; suivant : 000E52Use of piezosurgery during maxillary sinus elevation: clinical results of 40 consecutive cases.
Auteurs : Michele Cassetta ; Laura Ricci ; Giovanna Iezzi ; Sabrina Calasso ; Adriano Piattelli ; Vittoria PerrottiSource :
- The International journal of periodontics & restorative dentistry [ 1945-3388 ] ; 2012.
English descriptors
- KwdEn :
- Absorbable Implants, Adult, Aged, Bone Substitutes (therapeutic use), Bone Transplantation (methods), Female, Follow-Up Studies, Humans, Intraoperative Complications, Jaw, Edentulous (surgery), Male, Maxillary Sinus (pathology), Maxillary Sinus (surgery), Membranes, Artificial, Middle Aged, Nasal Mucosa (injuries), Nasal Mucosa (surgery), Operative Time, Osteotomy (instrumentation), Piezosurgery (adverse effects), Piezosurgery (instrumentation), Radiography, Panoramic, Sinus Floor Augmentation (adverse effects), Sinus Floor Augmentation (instrumentation), Surgical Flaps (surgery), Tomography, X-Ray Computed, Treatment Outcome.
- MESH :
- chemical , therapeutic use : Bone Substitutes.
- adverse effects : Piezosurgery, Sinus Floor Augmentation.
- injuries : Nasal Mucosa.
- instrumentation : Osteotomy, Piezosurgery, Sinus Floor Augmentation.
- methods : Bone Transplantation.
- pathology : Maxillary Sinus.
- surgery : Jaw, Edentulous, Maxillary Sinus, Nasal Mucosa, Surgical Flaps.
- Absorbable Implants, Adult, Aged, Female, Follow-Up Studies, Humans, Intraoperative Complications, Male, Membranes, Artificial, Middle Aged, Operative Time, Radiography, Panoramic, Tomography, X-Ray Computed, Treatment Outcome.
Abstract
The aim of this study was to evaluate the performance of piezoelectric devices during sinus elevation to determine the percentage of sinus membrane perforation and the time required to perform the antrostomy and elevation of the membrane. A total of 35 patients and 40 grafted sinuses were included. The parameters recorded were bony window length and height, bone thickness, osteotomy area, operative time, and number of perforations. Seven (17.5%) membrane perforations were observed, which were repaired with resorbable membranes. The mean length, height, and thickness of the osteotomy were 13.8 ± 2.9 mm, 6.9 ± 1.4 mm, and 1.4 ± 0.4 mm, respectively. The mean osteotomy area was 96.8 ± 32.2 mm(2), and the mean operative time was 10.3 ± 2.1 minutes. This study demonstrated that a piezoelectric device could be an attractive alternative for successful sinus augmentation.
PubMed: 23057061
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first="Adriano" last="Piattelli">Adriano Piattelli</name></author><author><name sortKey="Perrotti, Vittoria" sort="Perrotti, Vittoria" uniqKey="Perrotti V" first="Vittoria" last="Perrotti">Vittoria Perrotti</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2012">2012</date><idno type="RBID">pubmed:23057061</idno><idno type="pmid">23057061</idno><idno type="wicri:Area/PubMed/Corpus">000E51</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000E51</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Use of piezosurgery during maxillary sinus elevation: clinical results of 40 consecutive cases.</title><author><name sortKey="Cassetta, Michele" sort="Cassetta, Michele" uniqKey="Cassetta M" first="Michele" last="Cassetta">Michele Cassetta</name><affiliation><nlm:affiliation>Department of Oral and Maxillofacial Sciences, School of Dentistry, Sapienza University of Rome, Rome, Italy.</nlm:affiliation></affiliation></author><author><name sortKey="Ricci, Laura" sort="Ricci, Laura" uniqKey="Ricci L" first="Laura" last="Ricci">Laura Ricci</name></author><author><name sortKey="Iezzi, Giovanna" sort="Iezzi, Giovanna" uniqKey="Iezzi G" first="Giovanna" last="Iezzi">Giovanna Iezzi</name></author><author><name sortKey="Calasso, Sabrina" sort="Calasso, Sabrina" uniqKey="Calasso S" first="Sabrina" last="Calasso">Sabrina Calasso</name></author><author><name sortKey="Piattelli, Adriano" sort="Piattelli, Adriano" uniqKey="Piattelli A" first="Adriano" last="Piattelli">Adriano Piattelli</name></author><author><name sortKey="Perrotti, Vittoria" sort="Perrotti, Vittoria" uniqKey="Perrotti V" first="Vittoria" last="Perrotti">Vittoria Perrotti</name></author></analytic><series><title level="j">The International journal of periodontics & restorative dentistry</title><idno type="eISSN">1945-3388</idno><imprint><date when="2012" 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(surgery)</term><term>Tomography, X-Ray Computed</term><term>Treatment Outcome</term></keywords><keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en"><term>Bone Substitutes</term></keywords><keywords scheme="MESH" qualifier="adverse effects" xml:lang="en"><term>Piezosurgery</term><term>Sinus Floor Augmentation</term></keywords><keywords scheme="MESH" qualifier="injuries" xml:lang="en"><term>Nasal Mucosa</term></keywords><keywords scheme="MESH" qualifier="instrumentation" xml:lang="en"><term>Osteotomy</term><term>Piezosurgery</term><term>Sinus Floor Augmentation</term></keywords><keywords scheme="MESH" qualifier="methods" xml:lang="en"><term>Bone Transplantation</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Maxillary Sinus</term></keywords><keywords scheme="MESH" qualifier="surgery" xml:lang="en"><term>Jaw, Edentulous</term><term>Maxillary Sinus</term><term>Nasal Mucosa</term><term>Surgical Flaps</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Absorbable Implants</term><term>Adult</term><term>Aged</term><term>Female</term><term>Follow-Up Studies</term><term>Humans</term><term>Intraoperative Complications</term><term>Male</term><term>Membranes, Artificial</term><term>Middle Aged</term><term>Operative Time</term><term>Radiography, Panoramic</term><term>Tomography, X-Ray Computed</term><term>Treatment Outcome</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The aim of this study was to evaluate the performance of piezoelectric devices during sinus elevation to determine the percentage of sinus membrane perforation and the time required to perform the antrostomy and elevation of the membrane. A total of 35 patients and 40 grafted sinuses were included. The parameters recorded were bony window length and height, bone thickness, osteotomy area, operative time, and number of perforations. Seven (17.5%) membrane perforations were observed, which were repaired with resorbable membranes. The mean length, height, and thickness of the osteotomy were 13.8 ± 2.9 mm, 6.9 ± 1.4 mm, and 1.4 ± 0.4 mm, respectively. The mean osteotomy area was 96.8 ± 32.2 mm(2), and the mean operative time was 10.3 ± 2.1 minutes. This study demonstrated that a piezoelectric device could be an attractive alternative for successful sinus augmentation.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">23057061</PMID><DateCompleted><Year>2013</Year><Month>12</Month><Day>11</Day></DateCompleted><DateRevised><Year>2012</Year><Month>10</Month><Day>11</Day></DateRevised><Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1945-3388</ISSN><JournalIssue CitedMedium="Internet"><Volume>32</Volume><Issue>6</Issue><PubDate><Year>2012</Year><Month>Dec</Month></PubDate></JournalIssue><Title>The International journal of periodontics & restorative dentistry</Title><ISOAbbreviation>Int J Periodontics Restorative Dent</ISOAbbreviation></Journal><ArticleTitle>Use of piezosurgery during maxillary sinus elevation: clinical results of 40 consecutive cases.</ArticleTitle><Pagination><MedlinePgn>e182-8</MedlinePgn></Pagination><Abstract><AbstractText>The aim of this study was to evaluate the performance of piezoelectric devices during sinus elevation to determine the percentage of sinus membrane perforation and the time required to perform the antrostomy and elevation of the membrane. A total of 35 patients and 40 grafted sinuses were included. The parameters recorded were bony window length and height, bone thickness, osteotomy area, operative time, and number of perforations. Seven (17.5%) membrane perforations were observed, which were repaired with resorbable membranes. The mean length, height, and thickness of the osteotomy were 13.8 ± 2.9 mm, 6.9 ± 1.4 mm, and 1.4 ± 0.4 mm, respectively. The mean osteotomy area was 96.8 ± 32.2 mm(2), and the mean operative time was 10.3 ± 2.1 minutes. This study demonstrated that a piezoelectric device could be an attractive alternative for successful sinus augmentation.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Cassetta</LastName><ForeName>Michele</ForeName><Initials>M</Initials><AffiliationInfo><Affiliation>Department of Oral and Maxillofacial Sciences, School of Dentistry, Sapienza University of Rome, Rome, Italy.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ricci</LastName><ForeName>Laura</ForeName><Initials>L</Initials></Author><Author ValidYN="Y"><LastName>Iezzi</LastName><ForeName>Giovanna</ForeName><Initials>G</Initials></Author><Author ValidYN="Y"><LastName>Calasso</LastName><ForeName>Sabrina</ForeName><Initials>S</Initials></Author><Author ValidYN="Y"><LastName>Piattelli</LastName><ForeName>Adriano</ForeName><Initials>A</Initials></Author><Author ValidYN="Y"><LastName>Perrotti</LastName><ForeName>Vittoria</ForeName><Initials>V</Initials></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType></PublicationTypeList></Article><MedlineJournalInfo><Country>United States</Country><MedlineTA>Int J Periodontics Restorative Dent</MedlineTA><NlmUniqueID>8200894</NlmUniqueID><ISSNLinking>0198-7569</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D018786">Bone Substitutes</NameOfSubstance></Chemical><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D008567">Membranes, Artificial</NameOfSubstance></Chemical></ChemicalList><CitationSubset>D</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D020341" MajorTopicYN="N">Absorbable Implants</DescriptorName></MeshHeading><MeshHeading><DescriptorName 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Time</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D010027" MajorTopicYN="N">Osteotomy</DescriptorName><QualifierName UI="Q000295" MajorTopicYN="N">instrumentation</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D059745" MajorTopicYN="N">Piezosurgery</DescriptorName><QualifierName UI="Q000009" MajorTopicYN="N">adverse effects</QualifierName><QualifierName UI="Q000295" MajorTopicYN="Y">instrumentation</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D011862" MajorTopicYN="N">Radiography, Panoramic</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D059546" MajorTopicYN="N">Sinus Floor Augmentation</DescriptorName><QualifierName UI="Q000009" MajorTopicYN="N">adverse effects</QualifierName><QualifierName UI="Q000295" MajorTopicYN="Y">instrumentation</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D013524" MajorTopicYN="N">Surgical Flaps</DescriptorName><QualifierName UI="Q000601" 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