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Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes

OBJECTIVE: The main aim of this study was to determine the relationship between the maternal white blood cell (WBC) count at the time of hospital admission in pregnancies complicated by preterm prelabor rupture of membranes (PPROM) and the presence of microbial invasion of the amniotic cavity (MIAC)...

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Autores principales: Musilova, Ivana, Pliskova, Lenka, Gerychova, Romana, Janku, Petr, Simetka, Ondrej, Matlak, Petr, Jacobsson, Bo, Kacerovsky, Marian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726631/
https://www.ncbi.nlm.nih.gov/pubmed/29232399
http://dx.doi.org/10.1371/journal.pone.0189394
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author Musilova, Ivana
Pliskova, Lenka
Gerychova, Romana
Janku, Petr
Simetka, Ondrej
Matlak, Petr
Jacobsson, Bo
Kacerovsky, Marian
author_facet Musilova, Ivana
Pliskova, Lenka
Gerychova, Romana
Janku, Petr
Simetka, Ondrej
Matlak, Petr
Jacobsson, Bo
Kacerovsky, Marian
author_sort Musilova, Ivana
collection PubMed
description OBJECTIVE: The main aim of this study was to determine the relationship between the maternal white blood cell (WBC) count at the time of hospital admission in pregnancies complicated by preterm prelabor rupture of membranes (PPROM) and the presence of microbial invasion of the amniotic cavity (MIAC) and/or intra-amniotic inflammation (IAI). The second aim was to test WBC diagnostic indices with respect to the presence of MIAC and/or IAI. METHODS: Four hundred and seventy-nine women with singleton pregnancies complicated by PPROM, between February 2012 and June 2017, were included in this study. Maternal blood and amniotic fluid samples were collected at the time of admission. Maternal WBC count was assessed. Amniotic fluid interleukin-6 (IL-6) concentration was measured using a point-of-care test, and IAI was characterized by an IL-6 concentration of ≥ 745 pg/mL. MIAC was diagnosed based on a positive polymerase chain reaction result for the Ureaplasma species, Mycoplasma hominis, and/or Chlamydia trachomatis and/or for the 16S rRNA gene. RESULTS: Women with MIAC or IAI had higher WBC counts than those without (with MIAC: median, 12.8 × 10(9)/L vs. without MIAC: median, 11.9 × 10(9)/L; p = 0.0006; with IAI: median, 13.7 × 10(9)/L vs. without IAI: median, 11.9 × 10(9)/L; p < 0.0001). When the women were divided into four subgroups based on the presence of MIAC and/or IAI, the women with both MIAC and IAI had a higher WBC count than those with either IAI or MIAC alone, and those without MIAC and IAI [both MIAC and IAI: median, 14.0 × 10(9)/L; IAI alone: 12.1 × 10(9)/L (p = 0.03); MIAC alone: 12.1 × 10(9)/L (p = 0.0001); and without MIAC and IAI: median, 11.8 × 10(9)/L (p < 0.0001)]. No differences in the WBC counts were found among the women with IAI alone, MIAC alone, and without MIAC and IAI. CONCLUSION: The women with both MIAC and IAI had a higher maternal WBC count at the time of hospital admission than the remaining women with PPROM. The maternal WBC count at the time of admission showed poor diagnostic indices for the identification of the presence of both MIAC and IAI. Maternal WBC count at the time of admission cannot serve as a non-invasive screening tool for identifying these complications in women with PPROM.
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spelling pubmed-57266312017-12-22 Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes Musilova, Ivana Pliskova, Lenka Gerychova, Romana Janku, Petr Simetka, Ondrej Matlak, Petr Jacobsson, Bo Kacerovsky, Marian PLoS One Research Article OBJECTIVE: The main aim of this study was to determine the relationship between the maternal white blood cell (WBC) count at the time of hospital admission in pregnancies complicated by preterm prelabor rupture of membranes (PPROM) and the presence of microbial invasion of the amniotic cavity (MIAC) and/or intra-amniotic inflammation (IAI). The second aim was to test WBC diagnostic indices with respect to the presence of MIAC and/or IAI. METHODS: Four hundred and seventy-nine women with singleton pregnancies complicated by PPROM, between February 2012 and June 2017, were included in this study. Maternal blood and amniotic fluid samples were collected at the time of admission. Maternal WBC count was assessed. Amniotic fluid interleukin-6 (IL-6) concentration was measured using a point-of-care test, and IAI was characterized by an IL-6 concentration of ≥ 745 pg/mL. MIAC was diagnosed based on a positive polymerase chain reaction result for the Ureaplasma species, Mycoplasma hominis, and/or Chlamydia trachomatis and/or for the 16S rRNA gene. RESULTS: Women with MIAC or IAI had higher WBC counts than those without (with MIAC: median, 12.8 × 10(9)/L vs. without MIAC: median, 11.9 × 10(9)/L; p = 0.0006; with IAI: median, 13.7 × 10(9)/L vs. without IAI: median, 11.9 × 10(9)/L; p < 0.0001). When the women were divided into four subgroups based on the presence of MIAC and/or IAI, the women with both MIAC and IAI had a higher WBC count than those with either IAI or MIAC alone, and those without MIAC and IAI [both MIAC and IAI: median, 14.0 × 10(9)/L; IAI alone: 12.1 × 10(9)/L (p = 0.03); MIAC alone: 12.1 × 10(9)/L (p = 0.0001); and without MIAC and IAI: median, 11.8 × 10(9)/L (p < 0.0001)]. No differences in the WBC counts were found among the women with IAI alone, MIAC alone, and without MIAC and IAI. CONCLUSION: The women with both MIAC and IAI had a higher maternal WBC count at the time of hospital admission than the remaining women with PPROM. The maternal WBC count at the time of admission showed poor diagnostic indices for the identification of the presence of both MIAC and IAI. Maternal WBC count at the time of admission cannot serve as a non-invasive screening tool for identifying these complications in women with PPROM. Public Library of Science 2017-12-12 /pmc/articles/PMC5726631/ /pubmed/29232399 http://dx.doi.org/10.1371/journal.pone.0189394 Text en © 2017 Musilova et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Musilova, Ivana
Pliskova, Lenka
Gerychova, Romana
Janku, Petr
Simetka, Ondrej
Matlak, Petr
Jacobsson, Bo
Kacerovsky, Marian
Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes
title Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes
title_full Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes
title_fullStr Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes
title_full_unstemmed Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes
title_short Maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes
title_sort maternal white blood cell count cannot identify the presence of microbial invasion of the amniotic cavity or intra-amniotic inflammation in women with preterm prelabor rupture of membranes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726631/
https://www.ncbi.nlm.nih.gov/pubmed/29232399
http://dx.doi.org/10.1371/journal.pone.0189394
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