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      Clinical chorioamnionitis at term X: microbiology, clinical signs, placental pathology, and neonatal bacteremia – implications for clinical care

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      Journal of Perinatal Medicine
      Walter de Gruyter GmbH

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          Abstract

          Objectives

          Clinical chorioamnionitis at term is considered the most common infection-related diagnosis in labor and delivery units worldwide. The syndrome affects 5–12% of all term pregnancies and is a leading cause of maternal morbidity and mortality as well as neonatal death and sepsis. The objectives of this study were to determine the (1) amniotic fluid microbiology using cultivation and molecular microbiologic techniques; (2) diagnostic accuracy of the clinical criteria used to identify patients with intra-amniotic infection; (3) relationship between acute inflammatory lesions of the placenta (maternal and fetal inflammatory responses) and amniotic fluid microbiology and inflammatory markers; and (4) frequency of neonatal bacteremia.

          Methods

          This retrospective cross-sectional study included 43 women with the diagnosis of clinical chorioamnionitis at term. The presence of microorganisms in the amniotic cavity was determined through the analysis of amniotic fluid samples by cultivation for aerobes, anaerobes, and genital mycoplasmas. A broad-range polymerase chain reaction coupled with electrospray ionization mass spectrometry was also used to detect bacteria, select viruses, and fungi. Intra-amniotic inflammation was defined as an elevated amniotic fluid interleukin-6 (IL-6) concentration ≥2.6 ng/mL.

          Results

          (1) Intra-amniotic infection (defined as the combination of microorganisms detected in amniotic fluid and an elevated IL-6 concentration) was present in 63% (27/43) of cases; (2) the most common microorganisms found in the amniotic fluid samples were Ureaplasma species, followed by Gardnerella vaginalis; (3) sterile intra-amniotic inflammation (elevated IL-6 in amniotic fluid but without detectable microorganisms) was present in 5% (2/43) of cases; (4) 26% of patients with the diagnosis of clinical chorioamnionitis had no evidence of intra-amniotic infection or intra-amniotic inflammation; (5) intra-amniotic infection was more common when the membranes were ruptured than when they were intact (78% [21/27] vs. 38% [6/16]; p=0.01); (6) the traditional criteria for the diagnosis of clinical chorioamnionitis had poor diagnostic performance in identifying proven intra-amniotic infection (overall accuracy, 40–58%); (7) neonatal bacteremia was diagnosed in 4.9% (2/41) of cases; and (8) a fetal inflammatory response defined as the presence of severe acute funisitis was observed in 33% (9/27) of cases.

          Conclusions

          Clinical chorioamnionitis at term, a syndrome that can result from intra-amniotic infection, was diagnosed in approximately 63% of cases and sterile intra-amniotic inflammation in 5% of cases. However, a substantial number of patients had no evidence of intra-amniotic infection or intra-amniotic inflammation. Evidence of the fetal inflammatory response syndrome was frequently present, but microorganisms were detected in only 4.9% of cases based on cultures of aerobic and anaerobic bacteria in neonatal blood.

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          Most cited references240

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          Sampling and Definitions of Placental Lesions: Amsterdam Placental Workshop Group Consensus Statement.

          -The value of placental examination in investigations of adverse pregnancy outcomes may be compromised by sampling and definition differences between laboratories.
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            Committee Opinion No 700: Methods for Estimating the Due Date.

            (2017)
            Accurate dating of pregnancy is important to improve outcomes and is a research and public health imperative. As soon as data from the last menstrual period, the first accurate ultrasound examination, or both are obtained, the gestational age and the estimated due date (EDD) should be determined, discussed with the patient, and documented clearly in the medical record. Subsequent changes to the EDD should be reserved for rare circumstances, discussed with the patient, and documented clearly in the medical record. A pregnancy without an ultrasound examination that confirms or revises the EDD before 22 0/7 weeks of gestational age should be considered suboptimally dated. When determined from the methods outlined in this document for estimating the due date, gestational age at delivery represents the best obstetric estimate for the purpose of clinical care and should be recorded on the birth certificate. For the purposes of research and surveillance, the best obstetric estimate, rather than estimates based on the last menstrual period alone, should be used as the measure for gestational age.
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              Prevalence and clinical significance of sterile intra-amniotic inflammation in patients with preterm labor and intact membranes.

              Inflammation and infection play a major role in preterm birth. The purpose of this study was to (i) determine the prevalence and clinical significance of sterile intra-amniotic inflammation and (ii) examine the relationship between amniotic fluid (AF) concentrations of high mobility group box-1 (HMGB1) and the interval from amniocentesis to delivery in patients with sterile intra-amniotic inflammation. AF samples obtained from 135 women with preterm labor and intact membranes were analyzed using cultivation techniques as well as broad-range PCR and mass spectrometry (PCR/ESI-MS). Sterile intra-amniotic inflammation was defined when patients with negative AF cultures and without evidence of microbial footprints had intra-amniotic inflammation (AF interleukin-6 ≥ 2.6 ng/mL). (i) The frequency of sterile intra-amniotic inflammation was significantly greater than that of microbial-associated intra-amniotic inflammation [26% (35/135) versus 11% (15/135); (P = 0.005)], (ii) patients with sterile intra-amniotic inflammation delivered at comparable gestational ages had similar rates of acute placental inflammation and adverse neonatal outcomes as patients with microbial-associated intra-amniotic inflammation, and (iii) patients with sterile intra-amniotic inflammation and high AF concentrations of HMGB1 (≥8.55 ng/mL) delivered earlier than those with low AF concentrations of HMGB1 (P = 0.02). (i) Sterile intra-amniotic inflammation is more frequent than microbial-associated intra-amniotic inflammation, and (ii) we propose that danger signals participate in sterile intra-amniotic inflammation in the setting of preterm labor. Published 2014. This article is a U.S. Government work and is in the public domain in the USA.
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                Author and article information

                Journal
                Journal of Perinatal Medicine
                Walter de Gruyter GmbH
                1619-3997
                0300-5577
                March 26 2021
                October 22 2020
                March 01 2021
                March 26 2021
                January 26 2021
                March 01 2021
                : 49
                : 3
                : 275-298
                Affiliations
                [1 ]Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research , Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services , Bethesda, MD, and Detroit , MI , USA
                [2 ]Department of Obstetrics and Gynecology , University of Michigan , Ann Arbor , MI , USA
                [3 ]Department of Epidemiology and Biostatistics , Michigan State University , East Lansing , MI , USA
                [4 ]Center for Molecular Medicine and Genetics , Wayne State University , Detroit , MI , USA
                [5 ]Detroit Medical Center , Detroit , MI , USA
                [6 ]Department of Obstetrics and Gynecology , Wayne State University School of Medicine , Detroit , MI , USA
                [7 ]Division of Obstetrics and Gynecology, Faculty of Medicine , Pontificia Universidad Católica de Chile , Santiago , Chile
                [8 ]Center for Research and Innovation in Maternal-Fetal Medicine (CIMAF), Department of Obstetrics and Gynecology , Sótero del Río Hospital , Santiago , Chile
                [9 ]Department of Obstetrics and Gynecology , Soroka University Medical Center, School of Medicine, Faculty of Health Sciences, Ben-Gurion University of the Negev , Beersheba , Israel
                [10 ]Department of Biochemistry, Microbiology, and Immunology , Wayne State University School of Medicine , Detroit , MI , USA
                [11 ]Perinatal Research Initiative in Maternal, Perinatal and Child Health, Wayne State University School of Medicine , Detroit , MI , USA
                [12 ]Department of Pathology , University of Ulsan College of Medicine, Asan Medical Center , Seoul , Republic of Korea
                [13 ]Department of Obstetrics and Gynecology , Seoul National University College of Medicine , Seoul , Republic of Korea
                [14 ]Office of Women’s Health, Integrative Biosciences Center , Wayne State University , Detroit , MI , USA
                [15 ]Department of Physiology , Wayne State University School of Medicine , Detroit , MI , USA
                [16 ]Department of Obstetrics and Gynecology , William Beaumont Hospital , Royal Oak , MI , USA
                [17 ]Department of Obstetrics, Gynecology, and Pediatrics , University of Salamanca , Salamanca , Spain
                [18 ]Department of Women’s and Children’s Health , University Hospital of Padua , Padua , Italy
                Article
                10.1515/jpm-2020-0297
                33544519
                9a0dda90-1e2c-490f-b2a3-a9f1f6aa30d4
                © 2021
                History

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