Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study

<p>Abstract</p> <p>Background</p> <p>Accurate prediction of infection, including maternal chorioamnionitis and early-onset neonatal infection, remains a critical challenge in cases of preterm rupture of membranes and may influence obstetrical management. The aim of our...

Full description

Bibliographic Details
Main Authors: Schmitz Thomas, Maillard Françoise, Goffinet François, Popowski Thomas, Leroy Sandrine, Kayem Gilles
Format: Article
Language:English
Published: BMC 2011-04-01
Series:BMC Pregnancy and Childbirth
Online Access:http://www.biomedcentral.com/1471-2393/11/26
id doaj-572f74d1accf4b299a51ffae6a6746e4
record_format Article
spelling doaj-572f74d1accf4b299a51ffae6a6746e42020-11-24T21:09:27ZengBMCBMC Pregnancy and Childbirth1471-23932011-04-011112610.1186/1471-2393-11-26Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective studySchmitz ThomasMaillard FrançoiseGoffinet FrançoisPopowski ThomasLeroy SandrineKayem Gilles<p>Abstract</p> <p>Background</p> <p>Accurate prediction of infection, including maternal chorioamnionitis and early-onset neonatal infection, remains a critical challenge in cases of preterm rupture of membranes and may influence obstetrical management. The aim of our study was to investigate the predictive value for early-onset neonatal infection and maternal histological and clinical chorioamnionitis of maternal biological markers in routine use at or after 34 weeks of gestation in women with premature rupture of membranes.</p> <p>Methods</p> <p>We conducted a two-center prospective study of all women admitted for premature rupture of membranes at or after 34 weeks of gestation. The association of C-reactive protein, white blood cell count, vaginal sample bacteriological results, and a prediction model at admission, for early-onset neonatal infection and maternal chorioamnionitis were analyzed by comparing areas under the receiver operating characteristic curves and specificity.</p> <p>Results</p> <p>The study included 399 women. In all, 4.3% of the newborns had an early-onset neonatal infection and 5.3% of the women had clinical chorioamnionitis. Histological chorioamnionitis was detected on 10.8% of 297 placentas tested. White blood cell counts and C-reactive protein concentrations were significantly associated with early-onset neonatal infection and included in a prediction model. The area under the receiver operating characteristic curve of this model was 0.82 (95% CI [0.72, 0.92]) and of C-reactive protein, 0.80 (95% CI [0.68, 0.92]) (p = 1.0). Specificity was significantly higher for C-reactive protein than for the prediction model (48% and 43% respectively, p < 0.05). C-reactive protein was associated with clinical and histological chorioamnionitis, with areas under the receiver operating characteristic curve of 0.61 (95% CI [0.48, 0.74]) and 0.62 (95% CI [0.47, 0.74]), respectively.</p> <p>Conclusions</p> <p>The concentration of C-reactive protein at admission for premature rupture of membranes is the most accurate infectious marker for prediction of early-onset neonatal infection in routine use with a sensitivity > 90%. A useful next step would be a randomized prospective study of management strategy comparing CRP at admission with active management to assess whether this more individualized care is a safe alternative strategy in women with premature rupture of membranes at or after 34 weeks.</p> http://www.biomedcentral.com/1471-2393/11/26
collection DOAJ
language English
format Article
sources DOAJ
author Schmitz Thomas
Maillard Françoise
Goffinet François
Popowski Thomas
Leroy Sandrine
Kayem Gilles
spellingShingle Schmitz Thomas
Maillard Françoise
Goffinet François
Popowski Thomas
Leroy Sandrine
Kayem Gilles
Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study
BMC Pregnancy and Childbirth
author_facet Schmitz Thomas
Maillard Françoise
Goffinet François
Popowski Thomas
Leroy Sandrine
Kayem Gilles
author_sort Schmitz Thomas
title Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study
title_short Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study
title_full Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study
title_fullStr Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study
title_full_unstemmed Maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study
title_sort maternal markers for detecting early-onset neonatal infection and chorioamnionitis in cases of premature rupture of membranes at or after 34 weeks of gestation: a two-center prospective study
publisher BMC
series BMC Pregnancy and Childbirth
issn 1471-2393
publishDate 2011-04-01
description <p>Abstract</p> <p>Background</p> <p>Accurate prediction of infection, including maternal chorioamnionitis and early-onset neonatal infection, remains a critical challenge in cases of preterm rupture of membranes and may influence obstetrical management. The aim of our study was to investigate the predictive value for early-onset neonatal infection and maternal histological and clinical chorioamnionitis of maternal biological markers in routine use at or after 34 weeks of gestation in women with premature rupture of membranes.</p> <p>Methods</p> <p>We conducted a two-center prospective study of all women admitted for premature rupture of membranes at or after 34 weeks of gestation. The association of C-reactive protein, white blood cell count, vaginal sample bacteriological results, and a prediction model at admission, for early-onset neonatal infection and maternal chorioamnionitis were analyzed by comparing areas under the receiver operating characteristic curves and specificity.</p> <p>Results</p> <p>The study included 399 women. In all, 4.3% of the newborns had an early-onset neonatal infection and 5.3% of the women had clinical chorioamnionitis. Histological chorioamnionitis was detected on 10.8% of 297 placentas tested. White blood cell counts and C-reactive protein concentrations were significantly associated with early-onset neonatal infection and included in a prediction model. The area under the receiver operating characteristic curve of this model was 0.82 (95% CI [0.72, 0.92]) and of C-reactive protein, 0.80 (95% CI [0.68, 0.92]) (p = 1.0). Specificity was significantly higher for C-reactive protein than for the prediction model (48% and 43% respectively, p < 0.05). C-reactive protein was associated with clinical and histological chorioamnionitis, with areas under the receiver operating characteristic curve of 0.61 (95% CI [0.48, 0.74]) and 0.62 (95% CI [0.47, 0.74]), respectively.</p> <p>Conclusions</p> <p>The concentration of C-reactive protein at admission for premature rupture of membranes is the most accurate infectious marker for prediction of early-onset neonatal infection in routine use with a sensitivity > 90%. A useful next step would be a randomized prospective study of management strategy comparing CRP at admission with active management to assess whether this more individualized care is a safe alternative strategy in women with premature rupture of membranes at or after 34 weeks.</p>
url http://www.biomedcentral.com/1471-2393/11/26
work_keys_str_mv AT schmitzthomas maternalmarkersfordetectingearlyonsetneonatalinfectionandchorioamnionitisincasesofprematureruptureofmembranesatorafter34weeksofgestationatwocenterprospectivestudy
AT maillardfrancoise maternalmarkersfordetectingearlyonsetneonatalinfectionandchorioamnionitisincasesofprematureruptureofmembranesatorafter34weeksofgestationatwocenterprospectivestudy
AT goffinetfrancois maternalmarkersfordetectingearlyonsetneonatalinfectionandchorioamnionitisincasesofprematureruptureofmembranesatorafter34weeksofgestationatwocenterprospectivestudy
AT popowskithomas maternalmarkersfordetectingearlyonsetneonatalinfectionandchorioamnionitisincasesofprematureruptureofmembranesatorafter34weeksofgestationatwocenterprospectivestudy
AT leroysandrine maternalmarkersfordetectingearlyonsetneonatalinfectionandchorioamnionitisincasesofprematureruptureofmembranesatorafter34weeksofgestationatwocenterprospectivestudy
AT kayemgilles maternalmarkersfordetectingearlyonsetneonatalinfectionandchorioamnionitisincasesofprematureruptureofmembranesatorafter34weeksofgestationatwocenterprospectivestudy
_version_ 1716758255552692224