Accuracy of several maternal seric markers for predicting histological chorioamnionitis after preterm premature rupture of membranes: a prospective and multicentric study

Abstract Objective To assess and compare several maternal seric markers for the prediction of histological chorioamnionitis (HCA) after preterm premature rupture of membranes (PPROM). Study design A prospective and multicentric observational study was undertaken, including six French tertiary referr...

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Veröffentlicht in:European Journal of Obstetrics & Gynecology and Reproductive Biology 2016-10, Vol.205, p.133-140
Hauptverfasser: Caloone, Jonathan, Rabilloud, Muriel, Boutitie, Florent, Traverse-Glehen, Alexandra, Allias-Montmayeur, Fabienne, Denis, Laure, Boisson-Gaudin, Catherine, Hot, Isabelle Jaisson, Guerre, Pascale, Cortet, Marion, Huissoud, Cyril
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container_title European Journal of Obstetrics & Gynecology and Reproductive Biology
container_volume 205
creator Caloone, Jonathan
Rabilloud, Muriel
Boutitie, Florent
Traverse-Glehen, Alexandra
Allias-Montmayeur, Fabienne
Denis, Laure
Boisson-Gaudin, Catherine
Hot, Isabelle Jaisson
Guerre, Pascale
Cortet, Marion
Huissoud, Cyril
description Abstract Objective To assess and compare several maternal seric markers for the prediction of histological chorioamnionitis (HCA) after preterm premature rupture of membranes (PPROM). Study design A prospective and multicentric observational study was undertaken, including six French tertiary referral centres. Pregnant women over 18 years, with PPROM between 22 + 0 and 36 + 6 WG were enrolled. A blood sample was obtained before delivery and analysed for C-Reactive Protein (CRP), InterCellular Adhesion Molecule-1 (ICAM-1), Interleukin-6 (IL-6), Interleukin-8 (IL-8), Matrix-Metalloproteinase 8 and 9 (MMP-8, MMP-9), Triggering receptor on myeloid cells (TREM-1), and Human Neutrophile Peptides (HNP). HCA was determined by histological examination distinguishing maternal from fetal inflammatory response. Placental analyses and biological assays were performed in duplicate. Comparison of maternal seric markers levels in women with or vs. without HCA was performed, using a non-parametric Receiver Operating Characteristic. Results 295 women were kept for analysis. The prevalence of HCA was 42.7% (126/295). The concentrations of MMP-8, MMP-9, HNP and CRP were higher in HCA vs. the non-HCA group ( P < 0.05) whereas the concentrations of ICAM- 1, IL-6, IL-8 were not different ( P > 0.05). The ROC curve with the largest AUC was for CRP (AUC; 0.70; 95% CI; 0.64–0.77) and it was significantly higher than those for MMP-8, MMP-9, or HNP ( P < 0.03). Conclusion CRP was the best maternal marker for predicting HCA in women with PPROM.
doi_str_mv 10.1016/j.ejogrb.2016.08.022
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Study design A prospective and multicentric observational study was undertaken, including six French tertiary referral centres. Pregnant women over 18 years, with PPROM between 22 + 0 and 36 + 6 WG were enrolled. A blood sample was obtained before delivery and analysed for C-Reactive Protein (CRP), InterCellular Adhesion Molecule-1 (ICAM-1), Interleukin-6 (IL-6), Interleukin-8 (IL-8), Matrix-Metalloproteinase 8 and 9 (MMP-8, MMP-9), Triggering receptor on myeloid cells (TREM-1), and Human Neutrophile Peptides (HNP). HCA was determined by histological examination distinguishing maternal from fetal inflammatory response. Placental analyses and biological assays were performed in duplicate. Comparison of maternal seric markers levels in women with or vs. without HCA was performed, using a non-parametric Receiver Operating Characteristic. Results 295 women were kept for analysis. The prevalence of HCA was 42.7% (126/295). The concentrations of MMP-8, MMP-9, HNP and CRP were higher in HCA vs. the non-HCA group ( P &lt; 0.05) whereas the concentrations of ICAM- 1, IL-6, IL-8 were not different ( P &gt; 0.05). The ROC curve with the largest AUC was for CRP (AUC; 0.70; 95% CI; 0.64–0.77) and it was significantly higher than those for MMP-8, MMP-9, or HNP ( P &lt; 0.03). Conclusion CRP was the best maternal marker for predicting HCA in women with PPROM.</description><identifier>ISSN: 0301-2115</identifier><identifier>EISSN: 1872-7654</identifier><identifier>EISSN: 2590-1613</identifier><identifier>DOI: 10.1016/j.ejogrb.2016.08.022</identifier><identifier>PMID: 27591714</identifier><language>eng</language><publisher>Ireland: Elsevier B.V</publisher><subject>Adult ; Biomarkers - blood ; C-reactive protein ; C-Reactive Protein - metabolism ; Chorioamnionitis - blood ; Chorioamnionitis - diagnosis ; Chorioamnionitis - etiology ; Female ; Fetal Membranes, Premature Rupture - blood ; Histological choriomanionitis ; Humans ; Intercellular Adhesion Molecule-1 - blood ; Interleukin-6 - blood ; Interleukin-8 - blood ; Life Sciences ; Maternal seric markers ; Matrix Metalloproteinase 8 - blood ; Matrix Metalloproteinase 9 - blood ; Membrane Glycoproteins - blood ; Obstetrics and Gynecology ; Placenta - metabolism ; Prediction ; Pregnancy ; Prospective and multicentric study ; Prospective Studies ; Receptors, Immunologic - blood ; Triggering Receptor Expressed on Myeloid Cells-1</subject><ispartof>European Journal of Obstetrics &amp; Gynecology and Reproductive Biology, 2016-10, Vol.205, p.133-140</ispartof><rights>Elsevier Ireland Ltd</rights><rights>2016 Elsevier Ireland Ltd</rights><rights>Copyright © 2016 Elsevier Ireland Ltd. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-645694dd2ab7b59225e2cb263930251e12c1e0a7ddf02261964905f87d81e5113</citedby><cites>FETCH-LOGICAL-c418t-645694dd2ab7b59225e2cb263930251e12c1e0a7ddf02261964905f87d81e5113</cites><orcidid>0000-0003-1324-0356 ; 0000-0002-2538-7219 ; 0000-0001-9216-8318</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ejogrb.2016.08.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,777,781,882,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27591714$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://univ-lyon1.hal.science/hal-02016413$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Caloone, Jonathan</creatorcontrib><creatorcontrib>Rabilloud, Muriel</creatorcontrib><creatorcontrib>Boutitie, Florent</creatorcontrib><creatorcontrib>Traverse-Glehen, Alexandra</creatorcontrib><creatorcontrib>Allias-Montmayeur, Fabienne</creatorcontrib><creatorcontrib>Denis, Laure</creatorcontrib><creatorcontrib>Boisson-Gaudin, Catherine</creatorcontrib><creatorcontrib>Hot, Isabelle Jaisson</creatorcontrib><creatorcontrib>Guerre, Pascale</creatorcontrib><creatorcontrib>Cortet, Marion</creatorcontrib><creatorcontrib>Huissoud, Cyril</creatorcontrib><creatorcontrib>for the ICAMs Study Group</creatorcontrib><creatorcontrib>ICAMs Study Group</creatorcontrib><title>Accuracy of several maternal seric markers for predicting histological chorioamnionitis after preterm premature rupture of membranes: a prospective and multicentric study</title><title>European Journal of Obstetrics &amp; Gynecology and Reproductive Biology</title><addtitle>Eur J Obstet Gynecol Reprod Biol</addtitle><description>Abstract Objective To assess and compare several maternal seric markers for the prediction of histological chorioamnionitis (HCA) after preterm premature rupture of membranes (PPROM). Study design A prospective and multicentric observational study was undertaken, including six French tertiary referral centres. Pregnant women over 18 years, with PPROM between 22 + 0 and 36 + 6 WG were enrolled. A blood sample was obtained before delivery and analysed for C-Reactive Protein (CRP), InterCellular Adhesion Molecule-1 (ICAM-1), Interleukin-6 (IL-6), Interleukin-8 (IL-8), Matrix-Metalloproteinase 8 and 9 (MMP-8, MMP-9), Triggering receptor on myeloid cells (TREM-1), and Human Neutrophile Peptides (HNP). HCA was determined by histological examination distinguishing maternal from fetal inflammatory response. Placental analyses and biological assays were performed in duplicate. Comparison of maternal seric markers levels in women with or vs. without HCA was performed, using a non-parametric Receiver Operating Characteristic. Results 295 women were kept for analysis. The prevalence of HCA was 42.7% (126/295). The concentrations of MMP-8, MMP-9, HNP and CRP were higher in HCA vs. the non-HCA group ( P &lt; 0.05) whereas the concentrations of ICAM- 1, IL-6, IL-8 were not different ( P &gt; 0.05). The ROC curve with the largest AUC was for CRP (AUC; 0.70; 95% CI; 0.64–0.77) and it was significantly higher than those for MMP-8, MMP-9, or HNP ( P &lt; 0.03). Conclusion CRP was the best maternal marker for predicting HCA in women with PPROM.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>C-reactive protein</subject><subject>C-Reactive Protein - metabolism</subject><subject>Chorioamnionitis - blood</subject><subject>Chorioamnionitis - diagnosis</subject><subject>Chorioamnionitis - etiology</subject><subject>Female</subject><subject>Fetal Membranes, Premature Rupture - blood</subject><subject>Histological choriomanionitis</subject><subject>Humans</subject><subject>Intercellular Adhesion Molecule-1 - blood</subject><subject>Interleukin-6 - blood</subject><subject>Interleukin-8 - blood</subject><subject>Life Sciences</subject><subject>Maternal seric markers</subject><subject>Matrix Metalloproteinase 8 - blood</subject><subject>Matrix Metalloproteinase 9 - blood</subject><subject>Membrane Glycoproteins - blood</subject><subject>Obstetrics and Gynecology</subject><subject>Placenta - metabolism</subject><subject>Prediction</subject><subject>Pregnancy</subject><subject>Prospective and multicentric study</subject><subject>Prospective Studies</subject><subject>Receptors, Immunologic - blood</subject><subject>Triggering Receptor Expressed on Myeloid Cells-1</subject><issn>0301-2115</issn><issn>1872-7654</issn><issn>2590-1613</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUk2P1DAMjRCIHRb-AUK5cmiJ028OSKMVsEgjcQDOUZq6M-m2zShpR5q_xK_EobAHLuTiOHrv2fEzY69BpCCgfDekOLijb1NJWSrqVEj5hO2grmRSlUX-lO1EJiCRAMUNexHCIOhkWfOc3ciqaKCCfMd-7o1ZvTZX7noe8IJej3zSC_qZLgG9NZT6B_SB987zs8fOmsXOR36yYXGjO1pDSHNy3jo9zdbNdrGB6540IpzCFCOJrh65X8-_I5WbcGq9njG855oQLpyRlC_I9dzxaR0Xa3BeYgdhWbvrS_as12PAV3_iLfvx6eP3u_vk8PXzl7v9ITE51EtS5kXZ5F0ndVu1RSNlgdK0ssyaTMgCEKQBFLrqup4mVkJT5o0o-rrqasACILtlbzfdkx7V2Vv6_lU5bdX9_qDim4gTzyG7RGy-YQ21Hzz2jwQQKtqkBrXZpCJJiZrYkmhvNtp5bSfsHkl_fSHAhw2A9NGLRa-CsTgbGr6nIanO2f9V-FfAjHaOVj3gFcPg1mhwUKCCVEJ9i6sSNwXKTNQVrckv1NC-HA</recordid><startdate>20161001</startdate><enddate>20161001</enddate><creator>Caloone, Jonathan</creator><creator>Rabilloud, Muriel</creator><creator>Boutitie, Florent</creator><creator>Traverse-Glehen, Alexandra</creator><creator>Allias-Montmayeur, Fabienne</creator><creator>Denis, Laure</creator><creator>Boisson-Gaudin, Catherine</creator><creator>Hot, Isabelle Jaisson</creator><creator>Guerre, Pascale</creator><creator>Cortet, Marion</creator><creator>Huissoud, Cyril</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-1324-0356</orcidid><orcidid>https://orcid.org/0000-0002-2538-7219</orcidid><orcidid>https://orcid.org/0000-0001-9216-8318</orcidid></search><sort><creationdate>20161001</creationdate><title>Accuracy of several maternal seric markers for predicting histological chorioamnionitis after preterm premature rupture of membranes: a prospective and multicentric study</title><author>Caloone, Jonathan ; Rabilloud, Muriel ; Boutitie, Florent ; Traverse-Glehen, Alexandra ; Allias-Montmayeur, Fabienne ; Denis, Laure ; Boisson-Gaudin, Catherine ; Hot, Isabelle Jaisson ; Guerre, Pascale ; Cortet, Marion ; Huissoud, Cyril</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-645694dd2ab7b59225e2cb263930251e12c1e0a7ddf02261964905f87d81e5113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>C-reactive protein</topic><topic>C-Reactive Protein - metabolism</topic><topic>Chorioamnionitis - blood</topic><topic>Chorioamnionitis - diagnosis</topic><topic>Chorioamnionitis - etiology</topic><topic>Female</topic><topic>Fetal Membranes, Premature Rupture - blood</topic><topic>Histological choriomanionitis</topic><topic>Humans</topic><topic>Intercellular Adhesion Molecule-1 - blood</topic><topic>Interleukin-6 - blood</topic><topic>Interleukin-8 - blood</topic><topic>Life Sciences</topic><topic>Maternal seric markers</topic><topic>Matrix Metalloproteinase 8 - blood</topic><topic>Matrix Metalloproteinase 9 - blood</topic><topic>Membrane Glycoproteins - blood</topic><topic>Obstetrics and Gynecology</topic><topic>Placenta - metabolism</topic><topic>Prediction</topic><topic>Pregnancy</topic><topic>Prospective and multicentric study</topic><topic>Prospective Studies</topic><topic>Receptors, Immunologic - blood</topic><topic>Triggering Receptor Expressed on Myeloid Cells-1</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Caloone, Jonathan</creatorcontrib><creatorcontrib>Rabilloud, Muriel</creatorcontrib><creatorcontrib>Boutitie, Florent</creatorcontrib><creatorcontrib>Traverse-Glehen, Alexandra</creatorcontrib><creatorcontrib>Allias-Montmayeur, Fabienne</creatorcontrib><creatorcontrib>Denis, Laure</creatorcontrib><creatorcontrib>Boisson-Gaudin, Catherine</creatorcontrib><creatorcontrib>Hot, Isabelle Jaisson</creatorcontrib><creatorcontrib>Guerre, Pascale</creatorcontrib><creatorcontrib>Cortet, Marion</creatorcontrib><creatorcontrib>Huissoud, Cyril</creatorcontrib><creatorcontrib>for the ICAMs Study Group</creatorcontrib><creatorcontrib>ICAMs Study Group</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>European Journal of Obstetrics &amp; Gynecology and Reproductive Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Caloone, Jonathan</au><au>Rabilloud, Muriel</au><au>Boutitie, Florent</au><au>Traverse-Glehen, Alexandra</au><au>Allias-Montmayeur, Fabienne</au><au>Denis, Laure</au><au>Boisson-Gaudin, Catherine</au><au>Hot, Isabelle Jaisson</au><au>Guerre, Pascale</au><au>Cortet, Marion</au><au>Huissoud, Cyril</au><aucorp>for the ICAMs Study Group</aucorp><aucorp>ICAMs Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Accuracy of several maternal seric markers for predicting histological chorioamnionitis after preterm premature rupture of membranes: a prospective and multicentric study</atitle><jtitle>European Journal of Obstetrics &amp; Gynecology and Reproductive Biology</jtitle><addtitle>Eur J Obstet Gynecol Reprod Biol</addtitle><date>2016-10-01</date><risdate>2016</risdate><volume>205</volume><spage>133</spage><epage>140</epage><pages>133-140</pages><issn>0301-2115</issn><eissn>1872-7654</eissn><eissn>2590-1613</eissn><abstract>Abstract Objective To assess and compare several maternal seric markers for the prediction of histological chorioamnionitis (HCA) after preterm premature rupture of membranes (PPROM). Study design A prospective and multicentric observational study was undertaken, including six French tertiary referral centres. Pregnant women over 18 years, with PPROM between 22 + 0 and 36 + 6 WG were enrolled. A blood sample was obtained before delivery and analysed for C-Reactive Protein (CRP), InterCellular Adhesion Molecule-1 (ICAM-1), Interleukin-6 (IL-6), Interleukin-8 (IL-8), Matrix-Metalloproteinase 8 and 9 (MMP-8, MMP-9), Triggering receptor on myeloid cells (TREM-1), and Human Neutrophile Peptides (HNP). HCA was determined by histological examination distinguishing maternal from fetal inflammatory response. Placental analyses and biological assays were performed in duplicate. Comparison of maternal seric markers levels in women with or vs. without HCA was performed, using a non-parametric Receiver Operating Characteristic. Results 295 women were kept for analysis. The prevalence of HCA was 42.7% (126/295). The concentrations of MMP-8, MMP-9, HNP and CRP were higher in HCA vs. the non-HCA group ( P &lt; 0.05) whereas the concentrations of ICAM- 1, IL-6, IL-8 were not different ( P &gt; 0.05). The ROC curve with the largest AUC was for CRP (AUC; 0.70; 95% CI; 0.64–0.77) and it was significantly higher than those for MMP-8, MMP-9, or HNP ( P &lt; 0.03). Conclusion CRP was the best maternal marker for predicting HCA in women with PPROM.</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>27591714</pmid><doi>10.1016/j.ejogrb.2016.08.022</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1324-0356</orcidid><orcidid>https://orcid.org/0000-0002-2538-7219</orcidid><orcidid>https://orcid.org/0000-0001-9216-8318</orcidid></addata></record>
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subjects Adult
Biomarkers - blood
C-reactive protein
C-Reactive Protein - metabolism
Chorioamnionitis - blood
Chorioamnionitis - diagnosis
Chorioamnionitis - etiology
Female
Fetal Membranes, Premature Rupture - blood
Histological choriomanionitis
Humans
Intercellular Adhesion Molecule-1 - blood
Interleukin-6 - blood
Interleukin-8 - blood
Life Sciences
Maternal seric markers
Matrix Metalloproteinase 8 - blood
Matrix Metalloproteinase 9 - blood
Membrane Glycoproteins - blood
Obstetrics and Gynecology
Placenta - metabolism
Prediction
Pregnancy
Prospective and multicentric study
Prospective Studies
Receptors, Immunologic - blood
Triggering Receptor Expressed on Myeloid Cells-1
title Accuracy of several maternal seric markers for predicting histological chorioamnionitis after preterm premature rupture of membranes: a prospective and multicentric study
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