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Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability

INTRODUCTION: The objective of this study was to identify prenatal markers of histological chorioamnionitis (HC) during pPROM using fetal computerized cardiotocography (cCTG). MATERIALS AND METHODS: Retrospective review of medical records from pregnant women referred for pPROM between 26 and 34 week...

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Autores principales: Vandenbroucke, Laurent, Doyen, Matthieu, Le Lous, Maëla, Beuchée, Alain, Loget, Philippe, Carrault, Guy, Pladys, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612643/
https://www.ncbi.nlm.nih.gov/pubmed/28945767
http://dx.doi.org/10.1371/journal.pone.0184924
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author Vandenbroucke, Laurent
Doyen, Matthieu
Le Lous, Maëla
Beuchée, Alain
Loget, Philippe
Carrault, Guy
Pladys, Patrick
author_facet Vandenbroucke, Laurent
Doyen, Matthieu
Le Lous, Maëla
Beuchée, Alain
Loget, Philippe
Carrault, Guy
Pladys, Patrick
author_sort Vandenbroucke, Laurent
collection PubMed
description INTRODUCTION: The objective of this study was to identify prenatal markers of histological chorioamnionitis (HC) during pPROM using fetal computerized cardiotocography (cCTG). MATERIALS AND METHODS: Retrospective review of medical records from pregnant women referred for pPROM between 26 and 34 weeks, in whom placental histology was available, in a tertiary level obstetric service over a 5-year period. Fetal heart rate variability was assessed using cCTG. Patients were included if they were monitored at least six times in the 72 hours preceding delivery. Clinical and biological cCTG parameters during the pPROM latency period were compared between cases with or without HC. RESULTS: In total, 222 pPROM cases were observed, but cCTG data was available in only 23 of these cases (10 with and 13 without HC) after exclusion of co-morbidities which may potentially perturb fetal heart rate variability measures. Groups were comparable for maternal age, parity, gestational age at pPROM, pPROM duration and neonatal characteristics (p>0.1). Baseline fetal heart rate was higher in the HC group [median 147.3 bpm IQR (144.2–149.2) vs. 141.3 bpm (137.1–145.4) in no HC group; p = 0.02]. The number of low variation episodes [6.4, (3.5–15.3) vs. 2.3 (1–5.2); p = 0.04] was also higher in the HC group, whereas short term variations were lower in the HC group [7.1 ms (6–7.4) vs. 8.1 ms (7.4–9); p = 0.01] within 72 hours before delivery. Differences were especially discriminant within 24 hours before delivery, with less short-term variation [5 ms (3.7–5.9) vs. 7.8 ms (5.4–8.7); p = 0.007] and high variation episodes [3.9 (4.9–3.2) vs. 0.8 (1.5–0.2); p < 0.001] in the HC group. CONCLUSION: These results show differences in fetal heart rate variability, suggesting that cCTG could be used clinically to diagnoses chorioamnionitis during the pPROM latency period.
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spelling pubmed-56126432017-10-09 Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability Vandenbroucke, Laurent Doyen, Matthieu Le Lous, Maëla Beuchée, Alain Loget, Philippe Carrault, Guy Pladys, Patrick PLoS One Research Article INTRODUCTION: The objective of this study was to identify prenatal markers of histological chorioamnionitis (HC) during pPROM using fetal computerized cardiotocography (cCTG). MATERIALS AND METHODS: Retrospective review of medical records from pregnant women referred for pPROM between 26 and 34 weeks, in whom placental histology was available, in a tertiary level obstetric service over a 5-year period. Fetal heart rate variability was assessed using cCTG. Patients were included if they were monitored at least six times in the 72 hours preceding delivery. Clinical and biological cCTG parameters during the pPROM latency period were compared between cases with or without HC. RESULTS: In total, 222 pPROM cases were observed, but cCTG data was available in only 23 of these cases (10 with and 13 without HC) after exclusion of co-morbidities which may potentially perturb fetal heart rate variability measures. Groups were comparable for maternal age, parity, gestational age at pPROM, pPROM duration and neonatal characteristics (p>0.1). Baseline fetal heart rate was higher in the HC group [median 147.3 bpm IQR (144.2–149.2) vs. 141.3 bpm (137.1–145.4) in no HC group; p = 0.02]. The number of low variation episodes [6.4, (3.5–15.3) vs. 2.3 (1–5.2); p = 0.04] was also higher in the HC group, whereas short term variations were lower in the HC group [7.1 ms (6–7.4) vs. 8.1 ms (7.4–9); p = 0.01] within 72 hours before delivery. Differences were especially discriminant within 24 hours before delivery, with less short-term variation [5 ms (3.7–5.9) vs. 7.8 ms (5.4–8.7); p = 0.007] and high variation episodes [3.9 (4.9–3.2) vs. 0.8 (1.5–0.2); p < 0.001] in the HC group. CONCLUSION: These results show differences in fetal heart rate variability, suggesting that cCTG could be used clinically to diagnoses chorioamnionitis during the pPROM latency period. Public Library of Science 2017-09-25 /pmc/articles/PMC5612643/ /pubmed/28945767 http://dx.doi.org/10.1371/journal.pone.0184924 Text en © 2017 Vandenbroucke 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
Vandenbroucke, Laurent
Doyen, Matthieu
Le Lous, Maëla
Beuchée, Alain
Loget, Philippe
Carrault, Guy
Pladys, Patrick
Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability
title Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability
title_full Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability
title_fullStr Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability
title_full_unstemmed Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability
title_short Chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability
title_sort chorioamnionitis following preterm premature rupture of membranes and fetal heart rate variability
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612643/
https://www.ncbi.nlm.nih.gov/pubmed/28945767
http://dx.doi.org/10.1371/journal.pone.0184924
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