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Clinical courses following acute bacterial prostatitis
PURPOSE: There are few studies about clinical courses following acute bacterial prostatitis (ABP). We evaluated the progression rates of chronic bacterial prostatitis (CBP) and inflammatory chronic pelvic pain syndrome (CPPS) after ABP treatment. Also evaluated the characteristics of the patients wh...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Asian Pacific Prostate Society (APPS)
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814117/ https://www.ncbi.nlm.nih.gov/pubmed/24223408 http://dx.doi.org/10.12954/PI.12013 |
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author | Yoon, Byung Il Han, Dong-Seok Ha, U-Syn Lee, Seung-Ju Sohn, Dong Wan Kim, Hyun Woo Han, Chang-Hee Cho, Yong-Hyun |
author_facet | Yoon, Byung Il Han, Dong-Seok Ha, U-Syn Lee, Seung-Ju Sohn, Dong Wan Kim, Hyun Woo Han, Chang-Hee Cho, Yong-Hyun |
author_sort | Yoon, Byung Il |
collection | PubMed |
description | PURPOSE: There are few studies about clinical courses following acute bacterial prostatitis (ABP). We evaluated the progression rates of chronic bacterial prostatitis (CBP) and inflammatory chronic pelvic pain syndrome (CPPS) after ABP treatment. Also evaluated the characteristics of the patients who developed CBP and inflammatory CPPS after ABP treatment. METHODS: Total 437 patients compatible with a confirmed diagnosis of ABP from 5 urological centers between 2001 and 2010 were enrolled to study. We defined chronic infection (CI) as a progression to CBP and inflammatory CPPS after treatment of ABP in admission periods when followed up at 3 months or more. Results were analyzed between two groups: recovered without CI (group A, n=385) and developed to CI (group B, n=52). RESULTS: Of the 437 ABP patients, 1.3% (6/437) progressed to CBP and 10.5% (46/437) progressed to inflammatory CPPS. The progression rate of CI was 11.8% (52/437). The patients who developed to CI were higher in alcohol consumption rate, diabetes, voiding symptoms, prior manipulation rate, enlarged prostate volume, catheterization history rate and short duration of antibiotic treatment (P<0.05). CONCLUSIONS: The identification and characterization of these factors may accelerate the development of preventive, diagnostic and therapeutic strategies for the treatment of CI from ABP. |
format | Online Article Text |
id | pubmed-3814117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Asian Pacific Prostate Society (APPS) |
record_format | MEDLINE/PubMed |
spelling | pubmed-38141172013-11-12 Clinical courses following acute bacterial prostatitis Yoon, Byung Il Han, Dong-Seok Ha, U-Syn Lee, Seung-Ju Sohn, Dong Wan Kim, Hyun Woo Han, Chang-Hee Cho, Yong-Hyun Prostate Int Original Article PURPOSE: There are few studies about clinical courses following acute bacterial prostatitis (ABP). We evaluated the progression rates of chronic bacterial prostatitis (CBP) and inflammatory chronic pelvic pain syndrome (CPPS) after ABP treatment. Also evaluated the characteristics of the patients who developed CBP and inflammatory CPPS after ABP treatment. METHODS: Total 437 patients compatible with a confirmed diagnosis of ABP from 5 urological centers between 2001 and 2010 were enrolled to study. We defined chronic infection (CI) as a progression to CBP and inflammatory CPPS after treatment of ABP in admission periods when followed up at 3 months or more. Results were analyzed between two groups: recovered without CI (group A, n=385) and developed to CI (group B, n=52). RESULTS: Of the 437 ABP patients, 1.3% (6/437) progressed to CBP and 10.5% (46/437) progressed to inflammatory CPPS. The progression rate of CI was 11.8% (52/437). The patients who developed to CI were higher in alcohol consumption rate, diabetes, voiding symptoms, prior manipulation rate, enlarged prostate volume, catheterization history rate and short duration of antibiotic treatment (P<0.05). CONCLUSIONS: The identification and characterization of these factors may accelerate the development of preventive, diagnostic and therapeutic strategies for the treatment of CI from ABP. Asian Pacific Prostate Society (APPS) 2013 2013-06-30 /pmc/articles/PMC3814117/ /pubmed/24223408 http://dx.doi.org/10.12954/PI.12013 Text en Copyright © 2013 Asian Pacific Prostate Society (APPS) This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yoon, Byung Il Han, Dong-Seok Ha, U-Syn Lee, Seung-Ju Sohn, Dong Wan Kim, Hyun Woo Han, Chang-Hee Cho, Yong-Hyun Clinical courses following acute bacterial prostatitis |
title | Clinical courses following acute bacterial prostatitis |
title_full | Clinical courses following acute bacterial prostatitis |
title_fullStr | Clinical courses following acute bacterial prostatitis |
title_full_unstemmed | Clinical courses following acute bacterial prostatitis |
title_short | Clinical courses following acute bacterial prostatitis |
title_sort | clinical courses following acute bacterial prostatitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3814117/ https://www.ncbi.nlm.nih.gov/pubmed/24223408 http://dx.doi.org/10.12954/PI.12013 |
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