Twenty-three neutrophil granulocytes in 10 high-power fields is the best histopathological threshold to differentiate between aseptic and septic endoprosthesis loosening
Identifieur interne : 001013 ( Main/Merge ); précédent : 001012; suivant : 001014Twenty-three neutrophil granulocytes in 10 high-power fields is the best histopathological threshold to differentiate between aseptic and septic endoprosthesis loosening
Auteurs : Lars Morawietz [Allemagne] ; Obbe Tiddens [Allemagne] ; Michael Mueller [Allemagne] ; Stephan Tohtz [Allemagne] ; Tserenchunt Gansukh [Mongolie] ; Joerg H. Schroeder [Allemagne] ; Carsten Perka [Allemagne] ; Veit Krenn [Allemagne]Source :
- Histopathology [ 0309-0167 ] ; 2009.
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- Pascal (Inist)
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Abstract
Aims: The histopathological diagnosis of infection in periprosthetic tissue from loose total joint endoprosthesis has been the subject of controversy. The aim was to define a histological criterion that would best differentiate between aseptic and septic endoprosthesis loosening. Methods and results: Neutrophilic granulocytes (NG) were enumerated histopathologically in 147 periprosthetic membranes obtained from aseptic and septic revision surgery, using periodic acid-Schiff (PAS) stains and CD15 immunohistochemistry. Cell numbers were correlated with the results of microbiological culture and the clinical diagnoses. Using receiver-operating characteristics, an optimized threshold was found at 23 NG in 10 high-power fields (HPF). Using this threshold, histopathological examination had a sensitivity of 73% and specificity of 95% when compared with microbiological diagnosis (area under the curve 0.881), and a sensitivity of 77% and specificity of 97% when compared with clinical diagnosis (area under the curve 0.891). Conclusions: We therefore recommend a counting algorithm with a threshold of ≥23 NG in 10 HPF (visual field diameter 0.625 mm) for the histopathological diagnosis of septic endoprosthesis loosening. If the enumeration of NG is difficult in conventional haematoxylin and eosin-stained slides, CD15 immunohistochemistry should be performed, whereas the PAS stain has not proven to be helpful.
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Anatomic pathology</term>
<term>Endoprosthesis</term>
<term>Granulocyte</term>
<term>High field</term>
<term>Histopathology</term>
<term>Immunohistochemistry</term>
<term>Infection</term>
<term>Loosening</term>
<term>Neutrophil</term>
<term>Threshold</term>
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<keywords scheme="Pascal" xml:lang="fr"><term>Infection</term>
<term>Neutrophile</term>
<term>Granulocyte</term>
<term>Champ intense</term>
<term>Anatomopathologie</term>
<term>Histopathologie</term>
<term>Seuil</term>
<term>Endoprothèse</term>
<term>Immunohistochimie</term>
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<front><div type="abstract" xml:lang="en">Aims: The histopathological diagnosis of infection in periprosthetic tissue from loose total joint endoprosthesis has been the subject of controversy. The aim was to define a histological criterion that would best differentiate between aseptic and septic endoprosthesis loosening. Methods and results: Neutrophilic granulocytes (NG) were enumerated histopathologically in 147 periprosthetic membranes obtained from aseptic and septic revision surgery, using periodic acid-Schiff (PAS) stains and CD15 immunohistochemistry. Cell numbers were correlated with the results of microbiological culture and the clinical diagnoses. Using receiver-operating characteristics, an optimized threshold was found at 23 NG in 10 high-power fields (HPF). Using this threshold, histopathological examination had a sensitivity of 73% and specificity of 95% when compared with microbiological diagnosis (area under the curve 0.881), and a sensitivity of 77% and specificity of 97% when compared with clinical diagnosis (area under the curve 0.891). Conclusions: We therefore recommend a counting algorithm with a threshold of ≥23 NG in 10 HPF (visual field diameter 0.625 mm) for the histopathological diagnosis of septic endoprosthesis loosening. If the enumeration of NG is difficult in conventional haematoxylin and eosin-stained slides, CD15 immunohistochemistry should be performed, whereas the PAS stain has not proven to be helpful.</div>
</front>
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<affiliations><list><country><li>Allemagne</li>
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<region><li>Berlin</li>
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<name sortKey="Krenn, Veit" sort="Krenn, Veit" uniqKey="Krenn V" first="Veit" last="Krenn">Veit Krenn</name>
<name sortKey="Mueller, Michael" sort="Mueller, Michael" uniqKey="Mueller M" first="Michael" last="Mueller">Michael Mueller</name>
<name sortKey="Perka, Carsten" sort="Perka, Carsten" uniqKey="Perka C" first="Carsten" last="Perka">Carsten Perka</name>
<name sortKey="Schroeder, Joerg H" sort="Schroeder, Joerg H" uniqKey="Schroeder J" first="Joerg H." last="Schroeder">Joerg H. Schroeder</name>
<name sortKey="Tiddens, Obbe" sort="Tiddens, Obbe" uniqKey="Tiddens O" first="Obbe" last="Tiddens">Obbe Tiddens</name>
<name sortKey="Tohtz, Stephan" sort="Tohtz, Stephan" uniqKey="Tohtz S" first="Stephan" last="Tohtz">Stephan Tohtz</name>
</country>
<country name="Mongolie"><noRegion><name sortKey="Gansukh, Tserenchunt" sort="Gansukh, Tserenchunt" uniqKey="Gansukh T" first="Tserenchunt" last="Gansukh">Tserenchunt Gansukh</name>
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