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Proposal for a histopathological consensus classification of the periprosthetic interface membrane

Identifieur interne : 001C30 ( Istex/Corpus ); précédent : 001C29; suivant : 001C31

Proposal for a histopathological consensus classification of the periprosthetic interface membrane

Auteurs : L. Morawietz ; R-A Classen ; J H Schröder ; C. Dynybil ; C. Perka ; A. Skwara ; J. Neidel ; T. Gehrke ; L. Frommelt ; T. Hansen ; M. Otto ; B. Barden ; T. Aigner ; P. Stiehl ; T. Schubert ; C. Meyer-Scholten ; A. König ; P. Ströbel ; C P Rader ; S. Kirschner ; F. Lintner ; W. Rüther ; I. Bos ; C. Hendrich ; J. Kriegsmann ; V. Krenn

Source :

RBID : ISTEX:2FC4A4CF2A090B2C2E196116455365D949E07FB1

English descriptors

Abstract

Aims: The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery. Methods: Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria. Results: Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%). Conclusion: The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.

Url:
DOI: 10.1136/jcp.2005.027458

Links to Exploration step

ISTEX:2FC4A4CF2A090B2C2E196116455365D949E07FB1

Le document en format XML

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<name sortKey="Meyer Scholten, C" sort="Meyer Scholten, C" uniqKey="Meyer Scholten C" first="C" last="Meyer-Scholten">C. Meyer-Scholten</name>
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<name sortKey="Rader, C P" sort="Rader, C P" uniqKey="Rader C" first="C P" last="Rader">C P Rader</name>
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<mods:affiliation>Orthopedic Hospital König-Ludwig-Haus, University Hospital, Würzburg, Germany</mods:affiliation>
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<name sortKey="Ruther, W" sort="Ruther, W" uniqKey="Ruther W" first="W" last="Rüther">W. Rüther</name>
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<mods:affiliation>Department for Orthopedic Surgery, University Hospital, Hamburg, Germany</mods:affiliation>
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<name sortKey="Bos, I" sort="Bos, I" uniqKey="Bos I" first="I" last="Bos">I. Bos</name>
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<mods:affiliation>Institute for Pathology, Medical University of Lübeck, Germany</mods:affiliation>
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<name sortKey="Hendrich, C" sort="Hendrich, C" uniqKey="Hendrich C" first="C" last="Hendrich">C. Hendrich</name>
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<mods:affiliation>Orthopädisches Krankenhaus Schloss Werneck, Germany</mods:affiliation>
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<name sortKey="Kriegsmann, J" sort="Kriegsmann, J" uniqKey="Kriegsmann J" first="J" last="Kriegsmann">J. Kriegsmann</name>
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<name sortKey="Krenn, V" sort="Krenn, V" uniqKey="Krenn V" first="V" last="Krenn">V. Krenn</name>
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<mods:affiliation>Institute für Pathologie, University Hospital Charité, Berlin, Germany</mods:affiliation>
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<title level="j">Journal of Clinical Pathology</title>
<title level="j" type="abbrev">J Clin Pathol</title>
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<publisher>BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher>
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<term>PE, polyethylene</term>
<term>PMMA, polymethyl methacrylate</term>
<term>TJA, total joint replacement</term>
<term>aseptic loosening</term>
<term>classification</term>
<term>histopathology</term>
<term>septic loosening</term>
<term>total joint replacement</term>
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<div type="abstract" xml:lang="en">Aims: The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery. Methods: Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria. Results: Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%). Conclusion: The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.</div>
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<abstract>Aims: The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery. Methods: Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria. Results: Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%). Conclusion: The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.</abstract>
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 Professor V Krenn
 Charité University Hospital, Institute for Pathology, Schumannstrasse 20/21, D-10117 Berlin, Germany; veit.krenn@charite.de</note>
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<p>Aims: The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery. Methods: Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria. Results: Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%). Conclusion: The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.</p>
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<journal-id journal-id-type="nlm-ta">J Clin Pathol</journal-id>
<journal-title>Journal of Clinical Pathology</journal-title>
<abbrev-journal-title abbrev-type="publisher">J Clin Pathol</abbrev-journal-title>
<issn pub-type="ppub">0021-9746</issn>
<issn pub-type="epub">1472-4146</issn>
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<article-id pub-id-type="other">jclinpath;59/6/591</article-id>
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<article-title>Proposal for a histopathological consensus classification of the periprosthetic interface membrane</article-title>
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<contrib-group>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Morawietz</surname>
<given-names>L</given-names>
</name>
<xref rid="AFF1">1</xref>
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<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Classen</surname>
<given-names>R-A</given-names>
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<xref rid="AFF1">1</xref>
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<name name-style="western">
<surname>Schröder</surname>
<given-names>J H</given-names>
</name>
<xref rid="AFF2">2</xref>
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<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Dynybil</surname>
<given-names>C</given-names>
</name>
<xref rid="AFF2">2</xref>
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<name name-style="western">
<surname>Perka</surname>
<given-names>C</given-names>
</name>
<xref rid="AFF2">2</xref>
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<name name-style="western">
<surname>Skwara</surname>
<given-names>A</given-names>
</name>
<xref rid="AFF3">3</xref>
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<surname>Neidel</surname>
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</name>
<xref rid="AFF4">4</xref>
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<name name-style="western">
<surname>Gehrke</surname>
<given-names>T</given-names>
</name>
<xref rid="AFF5">5</xref>
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<name name-style="western">
<surname>Frommelt</surname>
<given-names>L</given-names>
</name>
<xref rid="AFF5">5</xref>
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<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Hansen</surname>
<given-names>T</given-names>
</name>
<xref rid="AFF6">6</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Otto</surname>
<given-names>M</given-names>
</name>
<xref rid="AFF7">7</xref>
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<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Barden</surname>
<given-names>B</given-names>
</name>
<xref rid="AFF8">8</xref>
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<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Aigner</surname>
<given-names>T</given-names>
</name>
<xref rid="AFF9">9</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Stiehl</surname>
<given-names>P</given-names>
</name>
<xref rid="AFF10">10</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Schubert</surname>
<given-names>T</given-names>
</name>
<xref rid="AFF11">11</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Meyer-Scholten</surname>
<given-names>C</given-names>
</name>
<xref rid="AFF12">12</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>König</surname>
<given-names>A</given-names>
</name>
<xref rid="AFF13">13</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Ströbel</surname>
<given-names>P</given-names>
</name>
<xref rid="AFF14">14</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Rader</surname>
<given-names>C P</given-names>
</name>
<xref rid="AFF15">15</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Kirschner</surname>
<given-names>S</given-names>
</name>
<xref rid="AFF15">15</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Lintner</surname>
<given-names>F</given-names>
</name>
<xref rid="AFF16">16</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Rüther</surname>
<given-names>W</given-names>
</name>
<xref rid="AFF17">17</xref>
</contrib>
<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Bos</surname>
<given-names>I</given-names>
</name>
<xref rid="AFF18">18</xref>
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<contrib contrib-type="author" xlink:type="simple">
<name name-style="western">
<surname>Hendrich</surname>
<given-names>C</given-names>
</name>
<xref rid="AFF19">19</xref>
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<name name-style="western">
<surname>Kriegsmann</surname>
<given-names>J</given-names>
</name>
<xref rid="AFF6">6</xref>
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<name name-style="western">
<surname>Krenn</surname>
<given-names>V</given-names>
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<xref rid="AFF1">1</xref>
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<aff id="AFF1">
<label>1</label>
Institute für Pathologie, University Hospital Charité, Berlin, Germany</aff>
<aff id="AFF2">
<label>2</label>
Department for Orthopedic Surgery, University Hospital Charité, Berlin, Germany</aff>
<aff id="AFF3">
<label>3</label>
Department for Orthopedic Surgery, University Hospital, Münster, Germany</aff>
<aff id="AFF4">
<label>4</label>
Department for Orthopedic Surgery, Klinik Dr Guth, Hamburg, Germany</aff>
<aff id="AFF5">
<label>5</label>
Endo-Klinik, Hamburg, Germany</aff>
<aff id="AFF6">
<label>6</label>
Institute for Pathology, University Hospital, Mainz, Germany</aff>
<aff id="AFF7">
<label>7</label>
Group Practice for Pathology, Trier, Germany</aff>
<aff id="AFF8">
<label>8</label>
Department for Orthopedic Surgery, St-Augustinus Hospital, Düren, Germany</aff>
<aff id="AFF9">
<label>9</label>
Institute for Pathology, University Hospital, Erlangen, Germany</aff>
<aff id="AFF10">
<label>10</label>
Institute for Pathology, University Hospital, Leipzig, Germany</aff>
<aff id="AFF11">
<label>11</label>
Institute for Pathology, University Hospital, Regensburg, Germany</aff>
<aff id="AFF12">
<label>12</label>
Center for Rheumapathology, Johannes-Gutenberg-University, Mainz, Germany</aff>
<aff id="AFF13">
<label>13</label>
Orthopedic Hospital, Göppingen, Germany</aff>
<aff id="AFF14">
<label>14</label>
Institute für Pathology, University Hospital, Würzburg, Germany</aff>
<aff id="AFF15">
<label>15</label>
Orthopedic Hospital König-Ludwig-Haus, University Hospital, Würzburg, Germany</aff>
<aff id="AFF16">
<label>16</label>
Pathological-bakteriological Institute, SMZ Otto-Wagner-Spital, Wien, Austria</aff>
<aff id="AFF17">
<label>17</label>
Department for Orthopedic Surgery, University Hospital, Hamburg, Germany</aff>
<aff id="AFF18">
<label>18</label>
Institute for Pathology, Medical University of Lübeck, Germany</aff>
<aff id="AFF19">
<label>19</label>
Orthopädisches Krankenhaus Schloss Werneck, Germany</aff>
</contrib-group>
<author-notes>
<corresp>Correspondence to:
 Professor V Krenn
 Charité University Hospital, Institute for Pathology, Schumannstrasse 20/21, D-10117 Berlin, Germany;
<ext-link xlink:href="veit.krenn@charite.de" ext-link-type="email" xlink:type="simple">veit.krenn@charite.de</ext-link>
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<pub-date pub-type="ppub">
<month>6</month>
<year>2006</year>
</pub-date>
<pub-date pub-type="epub">
<day>26</day>
<month>5</month>
<year>2006</year>
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<volume>59</volume>
<volume-id pub-id-type="other">59</volume-id>
<volume-id pub-id-type="other">59</volume-id>
<issue>6</issue>
<issue-id pub-id-type="other">jclinpath;59/6</issue-id>
<issue-id pub-id-type="other">6</issue-id>
<issue-id pub-id-type="other">59/6</issue-id>
<fpage>591</fpage>
<history>
<date date-type="accepted">
<day>09</day>
<month>06</month>
<year>2005</year>
</date>
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<copyright-statement>Copyright 2006 Journal of Clinical Pathology</copyright-statement>
<copyright-year>2006</copyright-year>
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<abstract xml:lang="en">
<p>
<bold>Aims:</bold>
The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery.</p>
<p>
<bold>Methods:</bold>
Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria.</p>
<p>
<bold>Results:</bold>
Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%).</p>
<p>
<bold>Conclusion:</bold>
The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.</p>
</abstract>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
<languageTerm type="code" authority="rfc3066">en</languageTerm>
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<abstract lang="en">Aims: The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery. Methods: Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria. Results: Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%). Conclusion: The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.</abstract>
<note type="author-notes">Correspondence to:
 Professor V Krenn
 Charité University Hospital, Institute for Pathology, Schumannstrasse 20/21, D-10117 Berlin, Germany; veit.krenn@charite.de</note>
<subject lang="en">
<genre>ABR</genre>
<topic>PE, polyethylene</topic>
<topic>PMMA, polymethyl methacrylate</topic>
<topic>TJA, total joint replacement</topic>
</subject>
<subject lang="en">
<genre>KWD</genre>
<topic>total joint replacement</topic>
<topic>aseptic loosening</topic>
<topic>septic loosening</topic>
<topic>classification</topic>
<topic>histopathology</topic>
</subject>
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<title>Journal of Clinical Pathology</title>
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<titleInfo type="abbreviated">
<title>J Clin Pathol</title>
</titleInfo>
<genre type="journal">journal</genre>
<identifier type="ISSN">0021-9746</identifier>
<identifier type="eISSN">1472-4146</identifier>
<identifier type="PublisherID-hwp">jclinpath</identifier>
<identifier type="PublisherID-nlm-ta">J Clin Pathol</identifier>
<part>
<date>2006</date>
<detail type="volume">
<caption>vol.</caption>
<number>59</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>6</number>
</detail>
<extent unit="pages">
<start>591</start>
</extent>
</part>
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<identifier type="istex">2FC4A4CF2A090B2C2E196116455365D949E07FB1</identifier>
<identifier type="DOI">10.1136/jcp.2005.027458</identifier>
<identifier type="href">jclinpath-59-591.pdf</identifier>
<identifier type="PMID">16731601</identifier>
<identifier type="local">0590591</identifier>
<accessCondition type="use and reproduction" contentType="copyright">Copyright 2006 Journal of Clinical Pathology</accessCondition>
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