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Volume 147, Issue 2, Pages 124-129 (December 2009)


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Accuracy of C-reactive protein determination in predicting chorioamnionitis and neonatal infection in pregnant women with premature rupture of membranes: A systematic review

Rafli van de Laara, David P. van der HamaCorresponding Author Informationemail address, S. Guid Oeib, Christine Willekesa, Carl P. Weinerc, Ben W.J. Molbd

Received 21 January 2009; received in revised form 30 June 2009; accepted 15 September 2009. published online 30 September 2009.

Abstract 

Preterm premature rupture of the fetal membranes (PPROM) is associated with intra-uterine infection. Early detection of intra-uterine infection may help prevent neonatal sepsis. C-reactive protein (CRP) is an acute phase protein often elevated when inflammation is present. The aim of this review was to assess whether CRP accurately predicts chorioamnionitis and/or neonatal sepsis in women with PPROM.

We searched Medline and Embase databases for articles reporting on CRP and chorioamnionitis and/or neonatal sepsis. Two reviewers extracted clinical and methodological study characteristics and test accuracy data. Accurate data were used to form 2×2 data tables comparing CRP and the occurrence of infection. For the selected studies, sensitivity and specificity of CRP in the prediction of histological chorioamnionitis, clinical chorioamnionitis and neonatal sepsis were calculated separately. A bivariate meta-regression model was used to calculate pooled estimates of sensitivity and specificity.

The search revealed 200 articles, of which only five met the inclusion criteria. These five articles reported on 381 patients, of which four articles (227 patients) reported on CRP as a predictor for histological chorioamnionitis and four studies (330 patients) reported on CRP as a predictor for clinical chorioamnionitis. None of the selected articles fulfilled our criteria for the use of CRP as a predictor of neonatal sepsis. CRP was moderately predictive of histological chorioamnionitis. Unfortunately, the studies of clinical chorioamnionitis were too heterogeneous to pool data.

Current literature does not support the use of CRP in women with PPROM.

a Department of Obstetrics & Gynaecology, Maastricht University Medical Centre, GROW – School for Oncology and Developmental Biology, PO Box 5800, 6202 AZ Maastricht, The Netherlands

b Department of Obstetrics and Gynaecology, Máxima Medical Centre, De Run 4600 PO Box 7777, 5500 MB Veldhoven, The Netherlands

c Department of Obstetrics and Gynecology, University of Kansas School of Medicine, 3901 Rainbow Boulevard, MS 2028 Kansas City, KS 66160-7316, USA

d Department of Obstetrics & Gynaecology, Academic Medical Centre, PO Box 22700, 1105 DE Amsterdam, The Netherlands

Corresponding Author InformationCorresponding author. Tel.: +31 0 43 3874768; fax: +31 0 43 3874765.

PII: S0301-2115(09)00555-7

doi:10.1016/j.ejogrb.2009.09.017


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