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Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas
PURPOSE: Cellulitis is normally treated without knowledge of the responsible pathogen. Blood cultures are positive in about 2–4 %, and superficial swabs are of no value. Needle aspiration has been proposed with identifying the likely pathogen in up to 29 %, but these studies are of older date and th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025406/ https://www.ncbi.nlm.nih.gov/pubmed/27652151 http://dx.doi.org/10.1186/s40064-016-3293-z |
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author | Piso, Rein Jan Pop, R. Wieland, M. Griesshammer, I. Urfer, M. Schibli, U. Bassetti, S. |
author_facet | Piso, Rein Jan Pop, R. Wieland, M. Griesshammer, I. Urfer, M. Schibli, U. Bassetti, S. |
author_sort | Piso, Rein Jan |
collection | PubMed |
description | PURPOSE: Cellulitis is normally treated without knowledge of the responsible pathogen. Blood cultures are positive in about 2–4 %, and superficial swabs are of no value. Needle aspiration has been proposed with identifying the likely pathogen in up to 29 %, but these studies are of older date and the technique is not widely used. METHODS: We prospectively evaluated the sensitivity of needle aspiration cultures in all patients with erysipelas/cellulitis. Diagnosis was made clinically by the treating physician. Needle aspiration was done with a 1 ml syringe and a 26G needle. The needle was removed and the syringe brought to the microbiological laboratory and analysed according to standard procedures. RESULTS: 95 Patients were seen during a period of 22 month. 4 Patients were excluded, as diagnosis was not confirmed. Cellulitis was present in 10/91 and erysipelas in 81/91 patients. In the first 25 patients with needle aspiration from the margin, none was positive. In 8/66 (12 %) patients where needle aspiration was done at the site of maximum inflammation, the pathogen was identified. 4/8 Cultures were positive for S. aureus, 2/8 for streptococci and 2/8 for other bacteria. In 11/66 (16.6 %) patients, skin colonisation flora was detected. In the subgroup of patients without prior antibiotic treatment and needle aspiration from the site of maximum inflammation, sensitivity was slightly better 8/55 (14.5 %; 95 % CI 7.5–25.8 %). CONCLUSIONS: Needle aspiration culture had a low sensitivity for detecting responsible pathogen in patients with cellulitis/erysipelas. No impact in antibiotic treatment could be observed. |
format | Online Article Text |
id | pubmed-5025406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-50254062016-09-20 Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas Piso, Rein Jan Pop, R. Wieland, M. Griesshammer, I. Urfer, M. Schibli, U. Bassetti, S. Springerplus Research PURPOSE: Cellulitis is normally treated without knowledge of the responsible pathogen. Blood cultures are positive in about 2–4 %, and superficial swabs are of no value. Needle aspiration has been proposed with identifying the likely pathogen in up to 29 %, but these studies are of older date and the technique is not widely used. METHODS: We prospectively evaluated the sensitivity of needle aspiration cultures in all patients with erysipelas/cellulitis. Diagnosis was made clinically by the treating physician. Needle aspiration was done with a 1 ml syringe and a 26G needle. The needle was removed and the syringe brought to the microbiological laboratory and analysed according to standard procedures. RESULTS: 95 Patients were seen during a period of 22 month. 4 Patients were excluded, as diagnosis was not confirmed. Cellulitis was present in 10/91 and erysipelas in 81/91 patients. In the first 25 patients with needle aspiration from the margin, none was positive. In 8/66 (12 %) patients where needle aspiration was done at the site of maximum inflammation, the pathogen was identified. 4/8 Cultures were positive for S. aureus, 2/8 for streptococci and 2/8 for other bacteria. In 11/66 (16.6 %) patients, skin colonisation flora was detected. In the subgroup of patients without prior antibiotic treatment and needle aspiration from the site of maximum inflammation, sensitivity was slightly better 8/55 (14.5 %; 95 % CI 7.5–25.8 %). CONCLUSIONS: Needle aspiration culture had a low sensitivity for detecting responsible pathogen in patients with cellulitis/erysipelas. No impact in antibiotic treatment could be observed. Springer International Publishing 2016-09-15 /pmc/articles/PMC5025406/ /pubmed/27652151 http://dx.doi.org/10.1186/s40064-016-3293-z Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Piso, Rein Jan Pop, R. Wieland, M. Griesshammer, I. Urfer, M. Schibli, U. Bassetti, S. Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas |
title | Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas |
title_full | Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas |
title_fullStr | Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas |
title_full_unstemmed | Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas |
title_short | Low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas |
title_sort | low sensitivity of needle aspiration cultures in patients with cellulitis/erysipelas |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025406/ https://www.ncbi.nlm.nih.gov/pubmed/27652151 http://dx.doi.org/10.1186/s40064-016-3293-z |
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