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Radiographic evaluation of mandibular augmentation with prefabricated hydroxylapatite/fibrin glue implants. Discussion

Identifieur interne : 000824 ( PascalFrancis/Corpus ); précédent : 000823; suivant : 000825

Radiographic evaluation of mandibular augmentation with prefabricated hydroxylapatite/fibrin glue implants. Discussion

Auteurs : H. J. A. Meijer ; W. H. A. Steen ; F. Bosman ; A. R. M. Wittkampf ; D. R. Mehlisch

Source :

RBID : Pascal:97-0210619

Descripteurs français

English descriptors

Abstract

Purpose: This study radiographically evaluated the stability of mandibular height during a 2-year follow-up after augmentation with prefabricated hydroxylapatite/fibrin glue (HA/FG) implants. Patients and Methods: Standardized, lateral oblique cephalometric radiographs were made of 22 patients 6, 12, and 24 months postoperatively and analyzed with a newly developed, computerized image analysis technique. Results: The average height of the HA/FG implants after augmentation was 9.45 mm. Average loss of total height of the augmented mandibles was 2.31 mm after 6 months, 2.90 mm after 12 months, and 3.93 mm after 24 months. Reduction of HA/FG implant height alone was 0.62 mm after 6 months, 1.24 mm after 12 months, and 2.03 mm after 24 months. Reduction occurred mainly during the first 6-month evaluation period and was probably primarily caused by adaptation of the implant to the surface of the mandible. An inferior compression of the implant or resorption of the alveolar crest and underlying basilar bone are possible reasons for loss of total mandibular height. Conclusion: The results indicate that prefabricated HA/FG implants used for augmentation of edentulous mandibles show little reduction in height, but are not completely stable during a 2-year evaluation period.

Notice en format standard (ISO 2709)

Pour connaître la documentation sur le format Inist Standard.

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A02 01      @0 JOMSDA
A03   1    @0 J. oral maxillofac. surg.
A05       @2 55
A06       @2 2
A08 01  1  ENG  @1 Radiographic evaluation of mandibular augmentation with prefabricated hydroxylapatite/fibrin glue implants. Discussion
A11 01  1    @1 MEIJER (H. J. A.)
A11 02  1    @1 STEEN (W. H. A.)
A11 03  1    @1 BOSMAN (F.)
A11 04  1    @1 WITTKAMPF (A. R. M.)
A11 05  1    @1 MEHLISCH (D. R.) @9 comment.
A14 01      @1 Department of Oral-Maxillofacial Surgery and Special Dental Care, Faculty of Medicine, University of Utrecht @2 Utrecht @3 NLD @Z 1 aut. @Z 2 aut. @Z 3 aut.
A14 02      @1 Oral Maxillofacial Surgeon, Department of Oral-Maxillofacial Surgery, University Hospital Utrecht @2 Utrecht @3 NLD @Z 4 aut.
A20       @1 138-145
A21       @1 1997
A23 01      @0 ENG
A43 01      @1 INIST @2 3005 @5 354000063465800050
A44       @0 0000 @1 © 1997 INIST-CNRS. All rights reserved.
A45       @0 34 ref.
A47 01  1    @0 97-0210619
A60       @1 P @3 AR @3 CT
A61       @0 A
A64 01  1    @0 Journal of oral and maxillofacial surgery
A66 01      @0 USA
C01 01    ENG  @0 Purpose: This study radiographically evaluated the stability of mandibular height during a 2-year follow-up after augmentation with prefabricated hydroxylapatite/fibrin glue (HA/FG) implants. Patients and Methods: Standardized, lateral oblique cephalometric radiographs were made of 22 patients 6, 12, and 24 months postoperatively and analyzed with a newly developed, computerized image analysis technique. Results: The average height of the HA/FG implants after augmentation was 9.45 mm. Average loss of total height of the augmented mandibles was 2.31 mm after 6 months, 2.90 mm after 12 months, and 3.93 mm after 24 months. Reduction of HA/FG implant height alone was 0.62 mm after 6 months, 1.24 mm after 12 months, and 2.03 mm after 24 months. Reduction occurred mainly during the first 6-month evaluation period and was probably primarily caused by adaptation of the implant to the surface of the mandible. An inferior compression of the implant or resorption of the alveolar crest and underlying basilar bone are possible reasons for loss of total mandibular height. Conclusion: The results indicate that prefabricated HA/FG implants used for augmentation of edentulous mandibles show little reduction in height, but are not completely stable during a 2-year evaluation period.
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N21       @1 104

Format Inist (serveur)

NO : PASCAL 97-0210619 INIST
ET : Radiographic evaluation of mandibular augmentation with prefabricated hydroxylapatite/fibrin glue implants. Discussion
AU : MEIJER (H. J. A.); STEEN (W. H. A.); BOSMAN (F.); WITTKAMPF (A. R. M.); MEHLISCH (D. R.)
AF : Department of Oral-Maxillofacial Surgery and Special Dental Care, Faculty of Medicine, University of Utrecht/Utrecht/Pays-Bas (1 aut., 2 aut., 3 aut.); Oral Maxillofacial Surgeon, Department of Oral-Maxillofacial Surgery, University Hospital Utrecht/Utrecht/Pays-Bas (4 aut.)
DT : Publication en série; Article; Commentaire; Niveau analytique
SO : Journal of oral and maxillofacial surgery; ISSN 0278-2391; Coden JOMSDA; Etats-Unis; Da. 1997; Vol. 55; No. 2; Pp. 138-145; Bibl. 34 ref.
LA : Anglais
EA : Purpose: This study radiographically evaluated the stability of mandibular height during a 2-year follow-up after augmentation with prefabricated hydroxylapatite/fibrin glue (HA/FG) implants. Patients and Methods: Standardized, lateral oblique cephalometric radiographs were made of 22 patients 6, 12, and 24 months postoperatively and analyzed with a newly developed, computerized image analysis technique. Results: The average height of the HA/FG implants after augmentation was 9.45 mm. Average loss of total height of the augmented mandibles was 2.31 mm after 6 months, 2.90 mm after 12 months, and 3.93 mm after 24 months. Reduction of HA/FG implant height alone was 0.62 mm after 6 months, 1.24 mm after 12 months, and 2.03 mm after 24 months. Reduction occurred mainly during the first 6-month evaluation period and was probably primarily caused by adaptation of the implant to the surface of the mandible. An inferior compression of the implant or resorption of the alveolar crest and underlying basilar bone are possible reasons for loss of total mandibular height. Conclusion: The results indicate that prefabricated HA/FG implants used for augmentation of edentulous mandibles show little reduction in height, but are not completely stable during a 2-year evaluation period.
CC : 002B25C02
FD : Implant; Préfabrication; Augmentation; Hauteur; Stabilité; Mandibule; Radiographie; Crâniométrie; Image numérique; Edentation; Etude longitudinale; Traitement; Homme; Hydroxylapatite/fibrine
FG : Chirurgie; Radiodiagnostic; Stomatologie; Dent pathologie
ED : Implant; Prefabrication; Increase; Height; Stability; Mandible; Radiography; Craniometry; Digital image; Edentulousness; Follow up study; Treatment; Human
EG : Surgery; Radiodiagnosis; Stomatology; Dental disease
GD : Hoehe; Stabilitaet; Radiographie; Aufbereiten
SD : Implante; Prefabricación; Aumentación; Altura; Estabilidad; Mandíbula; Radiografía; Craneometría; Imagen numérica; Edentación; Estudio longitudinal; Tratamiento; Hombre
LO : INIST-3005.354000063465800050
ID : 97-0210619

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Pascal:97-0210619

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<div type="abstract" xml:lang="en">Purpose: This study radiographically evaluated the stability of mandibular height during a 2-year follow-up after augmentation with prefabricated hydroxylapatite/fibrin glue (HA/FG) implants. Patients and Methods: Standardized, lateral oblique cephalometric radiographs were made of 22 patients 6, 12, and 24 months postoperatively and analyzed with a newly developed, computerized image analysis technique. Results: The average height of the HA/FG implants after augmentation was 9.45 mm. Average loss of total height of the augmented mandibles was 2.31 mm after 6 months, 2.90 mm after 12 months, and 3.93 mm after 24 months. Reduction of HA/FG implant height alone was 0.62 mm after 6 months, 1.24 mm after 12 months, and 2.03 mm after 24 months. Reduction occurred mainly during the first 6-month evaluation period and was probably primarily caused by adaptation of the implant to the surface of the mandible. An inferior compression of the implant or resorption of the alveolar crest and underlying basilar bone are possible reasons for loss of total mandibular height. Conclusion: The results indicate that prefabricated HA/FG implants used for augmentation of edentulous mandibles show little reduction in height, but are not completely stable during a 2-year evaluation period.</div>
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<s0>Hoehe</s0>
<s5>05</s5>
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<s0>Altura</s0>
<s5>05</s5>
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<s0>Stabilité</s0>
<s5>06</s5>
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<s5>07</s5>
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<s5>10</s5>
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<s5>10</s5>
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<s5>11</s5>
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<s5>11</s5>
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<s5>11</s5>
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<s0>Image numérique</s0>
<s5>12</s5>
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<s0>Digital image</s0>
<s5>12</s5>
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<s5>12</s5>
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<s0>Edentation</s0>
<s5>13</s5>
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<s0>Edentulousness</s0>
<s5>13</s5>
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<s0>Edentación</s0>
<s5>13</s5>
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<s0>Etude longitudinale</s0>
<s5>16</s5>
</fC03>
<fC03 i1="11" i2="X" l="ENG">
<s0>Follow up study</s0>
<s5>16</s5>
</fC03>
<fC03 i1="11" i2="X" l="SPA">
<s0>Estudio longitudinal</s0>
<s5>16</s5>
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<fC03 i1="12" i2="X" l="FRE">
<s0>Traitement</s0>
<s5>17</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Treatment</s0>
<s5>17</s5>
</fC03>
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<s0>Aufbereiten</s0>
<s5>17</s5>
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<s5>20</s5>
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<s5>20</s5>
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<fC03 i1="13" i2="X" l="SPA">
<s0>Hombre</s0>
<s5>20</s5>
</fC03>
<fC03 i1="14" i2="X" l="FRE">
<s0>Hydroxylapatite/fibrine</s0>
<s4>INC</s4>
<s5>86</s5>
</fC03>
<fC07 i1="01" i2="X" l="FRE">
<s0>Chirurgie</s0>
<s5>37</s5>
</fC07>
<fC07 i1="01" i2="X" l="ENG">
<s0>Surgery</s0>
<s5>37</s5>
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<fC07 i1="01" i2="X" l="SPA">
<s0>Cirugía</s0>
<s5>37</s5>
</fC07>
<fC07 i1="02" i2="X" l="FRE">
<s0>Radiodiagnostic</s0>
<s5>61</s5>
</fC07>
<fC07 i1="02" i2="X" l="ENG">
<s0>Radiodiagnosis</s0>
<s5>61</s5>
</fC07>
<fC07 i1="02" i2="X" l="SPA">
<s0>Radiodiagnóstico</s0>
<s5>61</s5>
</fC07>
<fC07 i1="03" i2="X" l="FRE">
<s0>Stomatologie</s0>
<s5>69</s5>
</fC07>
<fC07 i1="03" i2="X" l="ENG">
<s0>Stomatology</s0>
<s5>69</s5>
</fC07>
<fC07 i1="03" i2="X" l="SPA">
<s0>Estomatología</s0>
<s5>69</s5>
</fC07>
<fC07 i1="04" i2="X" l="FRE">
<s0>Dent pathologie</s0>
<s5>70</s5>
</fC07>
<fC07 i1="04" i2="X" l="ENG">
<s0>Dental disease</s0>
<s5>70</s5>
</fC07>
<fC07 i1="04" i2="X" l="SPA">
<s0>Diente patología</s0>
<s5>70</s5>
</fC07>
<fN21>
<s1>104</s1>
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<server>
<NO>PASCAL 97-0210619 INIST</NO>
<ET>Radiographic evaluation of mandibular augmentation with prefabricated hydroxylapatite/fibrin glue implants. Discussion</ET>
<AU>MEIJER (H. J. A.); STEEN (W. H. A.); BOSMAN (F.); WITTKAMPF (A. R. M.); MEHLISCH (D. R.)</AU>
<AF>Department of Oral-Maxillofacial Surgery and Special Dental Care, Faculty of Medicine, University of Utrecht/Utrecht/Pays-Bas (1 aut., 2 aut., 3 aut.); Oral Maxillofacial Surgeon, Department of Oral-Maxillofacial Surgery, University Hospital Utrecht/Utrecht/Pays-Bas (4 aut.)</AF>
<DT>Publication en série; Article; Commentaire; Niveau analytique</DT>
<SO>Journal of oral and maxillofacial surgery; ISSN 0278-2391; Coden JOMSDA; Etats-Unis; Da. 1997; Vol. 55; No. 2; Pp. 138-145; Bibl. 34 ref.</SO>
<LA>Anglais</LA>
<EA>Purpose: This study radiographically evaluated the stability of mandibular height during a 2-year follow-up after augmentation with prefabricated hydroxylapatite/fibrin glue (HA/FG) implants. Patients and Methods: Standardized, lateral oblique cephalometric radiographs were made of 22 patients 6, 12, and 24 months postoperatively and analyzed with a newly developed, computerized image analysis technique. Results: The average height of the HA/FG implants after augmentation was 9.45 mm. Average loss of total height of the augmented mandibles was 2.31 mm after 6 months, 2.90 mm after 12 months, and 3.93 mm after 24 months. Reduction of HA/FG implant height alone was 0.62 mm after 6 months, 1.24 mm after 12 months, and 2.03 mm after 24 months. Reduction occurred mainly during the first 6-month evaluation period and was probably primarily caused by adaptation of the implant to the surface of the mandible. An inferior compression of the implant or resorption of the alveolar crest and underlying basilar bone are possible reasons for loss of total mandibular height. Conclusion: The results indicate that prefabricated HA/FG implants used for augmentation of edentulous mandibles show little reduction in height, but are not completely stable during a 2-year evaluation period.</EA>
<CC>002B25C02</CC>
<FD>Implant; Préfabrication; Augmentation; Hauteur; Stabilité; Mandibule; Radiographie; Crâniométrie; Image numérique; Edentation; Etude longitudinale; Traitement; Homme; Hydroxylapatite/fibrine</FD>
<FG>Chirurgie; Radiodiagnostic; Stomatologie; Dent pathologie</FG>
<ED>Implant; Prefabrication; Increase; Height; Stability; Mandible; Radiography; Craniometry; Digital image; Edentulousness; Follow up study; Treatment; Human</ED>
<EG>Surgery; Radiodiagnosis; Stomatology; Dental disease</EG>
<GD>Hoehe; Stabilitaet; Radiographie; Aufbereiten</GD>
<SD>Implante; Prefabricación; Aumentación; Altura; Estabilidad; Mandíbula; Radiografía; Craneometría; Imagen numérica; Edentación; Estudio longitudinal; Tratamiento; Hombre</SD>
<LO>INIST-3005.354000063465800050</LO>
<ID>97-0210619</ID>
</server>
</inist>
</record>

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