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Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease

BACKGROUND: Chlamydia infection in acute pelvic inflammatory disease (PID) is associated with serious complications including ectopic pregnancy, tubal infertility, Fitz-Hugh-Curtis syndrome and tubo-ovarian abscess (TOA). This study compared clinical and laboratory data between PID with and without...

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Autores principales: Park, Sung Taek, Lee, Suk Woo, Kim, Min Jeong, Kang, Young Mo, Moon, Hye Min, Rhim, Chae Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237214/
https://www.ncbi.nlm.nih.gov/pubmed/28086838
http://dx.doi.org/10.1186/s12905-016-0356-9
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author Park, Sung Taek
Lee, Suk Woo
Kim, Min Jeong
Kang, Young Mo
Moon, Hye Min
Rhim, Chae Chun
author_facet Park, Sung Taek
Lee, Suk Woo
Kim, Min Jeong
Kang, Young Mo
Moon, Hye Min
Rhim, Chae Chun
author_sort Park, Sung Taek
collection PubMed
description BACKGROUND: Chlamydia infection in acute pelvic inflammatory disease (PID) is associated with serious complications including ectopic pregnancy, tubal infertility, Fitz-Hugh-Curtis syndrome and tubo-ovarian abscess (TOA). This study compared clinical and laboratory data between PID with and without chlamydia infection. METHODS: The medical records of 497 women who were admitted with PID between 2002 and 2011 were reviewed. The patients were divided into two groups (PID with and without chlamydia infection), which were compared in terms of the patients’ characteristics, clinical presentation, and laboratory findings, including inflammatory markers. RESULTS: The chlamydia and non-chlamydia groups comprised 175 and 322 women, respectively. The patients in the chlamydia group were younger and had a higher rate of TOA, a longer mean hospital stay, and had undergone more surgeries than the patients in the non- chlamydia group. The erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and CA-125 level were higher in the chlamydia group than in the non-chlamydia group, but there was no significant difference in the white blood cell count between the two groups. The CA-125 level was the strongest predictor of chlamydia infection, followed by the ESR and CRP level. The area under the receiving operating curve for CA-125, ESR, and CRP was 0.804, 0.755, and 0.663, respectively. CONCLUSIONS: Chlamydia infection in acute PID is associated with increased level of inflammatory markers, such as CA-125, ESR and CRP, incidence of TOA, operation risk, and longer hospitalization.
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spelling pubmed-52372142017-01-18 Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease Park, Sung Taek Lee, Suk Woo Kim, Min Jeong Kang, Young Mo Moon, Hye Min Rhim, Chae Chun BMC Womens Health Research Article BACKGROUND: Chlamydia infection in acute pelvic inflammatory disease (PID) is associated with serious complications including ectopic pregnancy, tubal infertility, Fitz-Hugh-Curtis syndrome and tubo-ovarian abscess (TOA). This study compared clinical and laboratory data between PID with and without chlamydia infection. METHODS: The medical records of 497 women who were admitted with PID between 2002 and 2011 were reviewed. The patients were divided into two groups (PID with and without chlamydia infection), which were compared in terms of the patients’ characteristics, clinical presentation, and laboratory findings, including inflammatory markers. RESULTS: The chlamydia and non-chlamydia groups comprised 175 and 322 women, respectively. The patients in the chlamydia group were younger and had a higher rate of TOA, a longer mean hospital stay, and had undergone more surgeries than the patients in the non- chlamydia group. The erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and CA-125 level were higher in the chlamydia group than in the non-chlamydia group, but there was no significant difference in the white blood cell count between the two groups. The CA-125 level was the strongest predictor of chlamydia infection, followed by the ESR and CRP level. The area under the receiving operating curve for CA-125, ESR, and CRP was 0.804, 0.755, and 0.663, respectively. CONCLUSIONS: Chlamydia infection in acute PID is associated with increased level of inflammatory markers, such as CA-125, ESR and CRP, incidence of TOA, operation risk, and longer hospitalization. BioMed Central 2017-01-13 /pmc/articles/PMC5237214/ /pubmed/28086838 http://dx.doi.org/10.1186/s12905-016-0356-9 Text en © The Author(s). 2017 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Park, Sung Taek
Lee, Suk Woo
Kim, Min Jeong
Kang, Young Mo
Moon, Hye Min
Rhim, Chae Chun
Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease
title Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease
title_full Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease
title_fullStr Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease
title_full_unstemmed Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease
title_short Clinical characteristics of genital chlamydia infection in pelvic inflammatory disease
title_sort clinical characteristics of genital chlamydia infection in pelvic inflammatory disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237214/
https://www.ncbi.nlm.nih.gov/pubmed/28086838
http://dx.doi.org/10.1186/s12905-016-0356-9
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