Clinical courses following acute bacterial prostatitis
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 develop...
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| Format: | Article |
| Language: | English |
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Elsevier
2013-06-01
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| Series: | Prostate International |
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2287888215300301 |
| _version_ | 1797719708145811456 |
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| author | Byung Il Yoon Dong-Seok Han U-Syn Ha Seung-Ju Lee Dong Wan Sohn Hyun Woo Kim Chang-Hee Han Yong-Hyun Cho |
| author_facet | Byung Il Yoon Dong-Seok Han U-Syn Ha Seung-Ju Lee Dong Wan Sohn Hyun Woo Kim Chang-Hee Han Yong-Hyun Cho |
| author_sort | Byung Il Yoon |
| collection | DOAJ |
| description | 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. |
| first_indexed | 2024-03-12T09:08:50Z |
| format | Article |
| id | doaj.art-4b9f423a9e3849e7a1ea5e510bee5cd5 |
| institution | Directory Open Access Journal |
| issn | 2287-8882 |
| language | English |
| last_indexed | 2024-03-12T09:08:50Z |
| publishDate | 2013-06-01 |
| publisher | Elsevier |
| record_format | Article |
| series | Prostate International |
| spelling | doaj.art-4b9f423a9e3849e7a1ea5e510bee5cd52023-09-02T15:06:12ZengElsevierProstate International2287-88822013-06-0112899310.12954/PI.12013Clinical courses following acute bacterial prostatitisByung Il YoonDong-Seok HanU-Syn HaSeung-Ju LeeDong Wan SohnHyun Woo KimChang-Hee HanYong-Hyun ChoThere 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.http://www.sciencedirect.com/science/article/pii/S2287888215300301AcuteChronicBacterial prostatitisInflammatory chronic pelvic pain syndromeProgression |
| spellingShingle | Byung Il Yoon Dong-Seok Han U-Syn Ha Seung-Ju Lee Dong Wan Sohn Hyun Woo Kim Chang-Hee Han Yong-Hyun Cho Clinical courses following acute bacterial prostatitis Prostate International Acute Chronic Bacterial prostatitis Inflammatory chronic pelvic pain syndrome Progression |
| 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 | Acute Chronic Bacterial prostatitis Inflammatory chronic pelvic pain syndrome Progression |
| url | http://www.sciencedirect.com/science/article/pii/S2287888215300301 |
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