1. Clinical Application of Quantitative Foetal Fibronectin for the Prediction of Preterm Birth in Symptomatic Women.
- Author
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Radford SK, Da Silva Costa F, Araujo Júnior E, and Sheehan PM
- Subjects
- Adult, Biomarkers blood, Female, Gestational Age, Humans, Infant, Newborn, Obstetric Labor, Premature etiology, Predictive Value of Tests, Pregnancy, Premature Birth blood, Premature Birth etiology, Prospective Studies, Risk Factors, Sensitivity and Specificity, Fetal Blood metabolism, Fibronectins blood, Obstetric Labor, Premature blood, Obstetric Labor, Premature diagnosis, Pregnancy Trimester, Second blood, Pregnancy Trimester, Third blood
- Abstract
Aim: To evaluate the clinical application of the new Hologic quantitative foetal fibronectin (qfFN) bedside test for the prediction of spontaneous preterm birth (sPTB) in patients with symptoms suggestive of spontaneous threatened preterm labour (sPTL)., Methods: A prospective observational study with 154 pregnant women presenting signs and symptoms of sPTL was conducted. These women were subjected to a qfFN test between 22 and 35 weeks of gestation For each cut-off threshold, the ability to predict sPTB at within 14 days of conducting the test and <37 weeks was assessed by calculating the positive predictive value (PPV), negative predictive value (NPV), likelihood ratios, odds ratios, sensitivity, and specificity., Results: For the outcome of delivery within 14 days of the test, qfFN <10 ng/mL had a 100% NPV and >200 ng/mL produced a 50.0% PPV; thus, qfFN added enhanced discrimination between high- and low-risk patients. The overall rate of sPTB (<37) was 13.3% (16/120), which increased progressively with increasing levels of fFN, with rates of 9.8% (8/81), 11.5% (3/26), 14.2% (1/7), 50% (3/6) within the 4 categories (fFN 0-9, 10-49, 50-200, 200+) respectively., Conclusions: The use of the qfFN testing in symptomatic patients allowed for more accurate identification of women at risk of sPTB and thus more directed management., (© 2017 S. Karger AG, Basel.)
- Published
- 2018
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