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A high concentration of fetal fibronectin in cervical secretions increases the risk of intra-amniotic infection and inflammation in patients with preterm labor and intact membranes.

Authors :
Oh, Kyung Joon
Romero, Roberto
Park, Jee Yoon
Kang, Jihyun
Hong, Joon-Seok
Yoon, Bo Hyun
Source :
Journal of Perinatal Medicine. Apr2019, Vol. 47 Issue 3, p288-303. 16p. 5 Charts, 2 Graphs.
Publication Year :
2019

Abstract

Objective: To determine whether the risk of intra-amniotic infection/inflammation and spontaneous preterm delivery (SPTD) varies as a function of the concentration of cervical fetal fibronectin (fFN) in patients with preterm labor and intact membranes. Methods: This prospective study included 180 patients with preterm labor and intact membranes who had a sample collected for quantitative fFN measurement and underwent amniocentesis. Amniotic fluid was cultured for aerobic and anaerobic bacteria and genital mycoplasmas. Intra-amniotic inflammation was defined as an amniotic fluid matrix metalloproteinase-8 concentration >23 ng/mL. Results: (1) The prevalence of intra-amniotic infection/inflammation and SPTD within 7 days was 32.2% (58/180) and 33.9% (61/178), respectively; (2) The higher the fFN concentration, the greater the risk of intra-amniotic infection/inflammation and SPTD within 7 days (P<0.001, respectively); (3) An fFN concentration 150 ng/mL had a better diagnostic performance than an fFN 50 ng/mL in the identification of intra-amniotic infection/inflammation and SPTD within 7 days; (4) Among the patients with an fFN <50 ng/mL, intra-amniotic infection/inflammation was identified in 7.6% (6/79) of patients and 66.7% (4/6) delivered within 7 days. Conclusion: The higher the concentration of fFN, the greater the risk of intra-amniotic infection/inflammation and SPTD in patients with preterm labor and intact membranes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03005577
Volume :
47
Issue :
3
Database :
Academic Search Index
Journal :
Journal of Perinatal Medicine
Publication Type :
Academic Journal
Accession number :
135798354
Full Text :
https://doi.org/10.1515/jpm-2018-0351