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Nine‐ to fourteen‐year follow‐up of implant treatment. Part II: presence of peri‐implant lesions

Identifieur interne : 006360 ( Istex/Corpus ); précédent : 006359; suivant : 006361

Nine‐ to fourteen‐year follow‐up of implant treatment. Part II: presence of peri‐implant lesions

Auteurs : Ann-Marie Roos-Jans Ker ; Christel Lindahl ; Helena Renvert ; Stefan Renvert

Source :

RBID : ISTEX:C8449F40897CFA6C8FA8605603EEFCEE58A2F6A5

English descriptors

Abstract

Objectives: The aim of this study was to analyse the proportions of peri‐implant lesions at implants after 9–14 years of function.

Url:
DOI: 10.1111/j.1600-051X.2006.00906.x

Links to Exploration step

ISTEX:C8449F40897CFA6C8FA8605603EEFCEE58A2F6A5

Le document en format XML

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<hi rend="bold">Objectives: </hi>
The aim of this study was to analyse the proportions of peri‐implant lesions at implants after 9–14 years of function.</p>
<p>
<hi rend="bold">Material and Methods: </hi>
Two hundred and ninety‐four patients underwent implant therapy during the years 1988–1992 in Kristianstad County. These individuals were recalled to the speciality clinic 1 and 5 years after placement of the suprastructure. Between 2000 and 2002, 218 patients with 999 implants were examined clinically and radiographically.</p>
<p>
<hi rend="bold">Results: </hi>
Forty‐eight per cent of the implants had probing depth
<graphic url="ges.gif" rend="geqslant R: gt-or-equal, slanted"></graphic>
4 mm and bleeding on probing (peri‐implant mucositis). In 20.4% of the implants, the bone level was located 3.1 mm apical to the implant shoulder. Progressive bone loss (
<graphic url="ges.gif" rend="geqslant R: gt-or-equal, slanted"></graphic>
1.8 mm) during the observation period was found in 7.7% of the implants. Peri‐implantitis defined as bone loss
<graphic url="ges.gif" rend="geqslant R: gt-or-equal, slanted"></graphic>
1.8 mm compared with 1‐year data (the apical border of the bony defect located at or apical to the third thread, i.e. a minimum of 3.1 mm apical to the implant shoulder), combined with bleeding on probing and or pus, were diagnosed among 16% of the patients and 6.6% of the implants.</p>
<p>
<hi rend="bold">Conclusion: </hi>
After 10 years in use without systematic supportive treatment, peri‐implant lesions is a common clinical entity adjacent to titanium implants.</p>
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<correspondenceTo>Address: 

<i>Stefan Renvert</i>
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E‐mail:
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Roos-Jansåker A-M, Lindahl C, Renvert H, Renvert S. Nine-to fourteen-year follow-up of implant treatment. Part II: presence of peri-implant lesions. J Clin Periodontol 2006; 33: 290–295. doi: 10.1111/j.1600-051X.2006.00906.x. © Blackwell Munksgaard, 2006.

-->
<title type="main">Abstract</title>
<p>
<b>Objectives: </b>
The aim of this study was to analyse the proportions of peri‐implant lesions at implants after 9–14 years of function.</p>
<p>
<b>Material and Methods: </b>
Two hundred and ninety‐four patients underwent implant therapy during the years 1988–1992 in Kristianstad County. These individuals were recalled to the speciality clinic 1 and 5 years after placement of the suprastructure. Between 2000 and 2002, 218 patients with 999 implants were examined clinically and radiographically.</p>
<p>
<b>Results: </b>
Forty‐eight per cent of the implants had probing depth
<inlineGraphic alt="geqslant R: gt-or-equal, slanted" extraInfo="nonStandardEntity" location="ges.gif" href=""></inlineGraphic>
4 mm and bleeding on probing (peri‐implant mucositis). In 20.4% of the implants, the bone level was located 3.1 mm apical to the implant shoulder. Progressive bone loss (
<inlineGraphic alt="geqslant R: gt-or-equal, slanted" extraInfo="nonStandardEntity" location="ges.gif" href=""></inlineGraphic>
1.8 mm) during the observation period was found in 7.7% of the implants. Peri‐implantitis defined as bone loss
<inlineGraphic alt="geqslant R: gt-or-equal, slanted" extraInfo="nonStandardEntity" location="ges.gif" href=""></inlineGraphic>
1.8 mm compared with 1‐year data (the apical border of the bony defect located at or apical to the third thread, i.e. a minimum of 3.1 mm apical to the implant shoulder), combined with bleeding on probing and or pus, were diagnosed among 16% of the patients and 6.6% of the implants.</p>
<p>
<b>Conclusion: </b>
After 10 years in use without systematic supportive treatment, peri‐implant lesions is a common clinical entity adjacent to titanium implants.</p>
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<abstract>Objectives: The aim of this study was to analyse the proportions of peri‐implant lesions at implants after 9–14 years of function.</abstract>
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