Literature DB >> 18843732

Fetal fibronectin testing for reducing the risk of preterm birth.

Vincenzo Berghella1, Edward Hayes, John Visintine, Jason K Baxter.   

Abstract

BACKGROUND: Fetal fibronectin (FFN) is an extracellular matrix glycoprotein localized at the maternal-fetal interface of the amniotic membranes, between chorion and decidua, where it is concentrated in this area between decidua and trophoblast. In normal conditions, FFN is found at very low levels in cervico-vaginal secretions. Levels greater than or equal to 50 ng/mL at or after 22 weeks have been associated with an increased risk of spontaneous preterm birth. In fact, FFN is one of the best predictors of preterm birth in all populations studied so far, and can help selecting which women are at significant risk for preterm birth.
OBJECTIVES: To assess the effectiveness of management based on knowledge of FFN testing results for preventing preterm birth. SEARCH STRATEGY: We searched the Cochrane Pregnancy and Childbirth Group's Trials Register (January 2008), MEDLINE (1966 to December 2007) and all references in identified articles. SELECTION CRITERIA: Randomized controlled trials of pregnant women between the gestational ages of 22 and 34 weeks screened with FFN for risk of preterm birth. Studies included are based exclusively on knowledge of FFN results versus no such knowledge, and we have excluded studies including women with only positive or only negative FFN results. DATA COLLECTION AND ANALYSIS: All four authors assessed studies for inclusion and quality and extracted data. MAIN
RESULTS: We identified 13 trials, of which five were eligible for inclusion. The five included studies randomized 474 women, of which 235 were randomized to knowledge and 249 to no knowledge of FFN.Preterm birth less than 37 weeks was significantly decreased with management based on knowledge of FFN results (15.6%) versus controls without such knowledge (28.6%; risk ratio 0.54; 95% confidence interval 0.34 to 0.87). All other outcomes for which there were available data (preterm birth at less than 34, 32, or 28 weeks; gestational age at delivery; birthweight less than 2500 grams; perinatal death; maternal hospitalization; tocolysis; steroids for fetal lung maturity; and time to evaluate) were similar in the two groups. No other maternal or neonatal outcome was available for meaningful analysis. AUTHORS'
CONCLUSIONS: Although FFN is commonly used in labor and delivery units to help in the management of women with symptoms of preterm labor, currently there is not sufficient evidence to recommend its use. Since this review found an association between knowledge of FFN results and a lower incidence of preterm birth before 37 weeks, further research should be encouraged.

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Year:  2008        PMID: 18843732      PMCID: PMC6492504          DOI: 10.1002/14651858.CD006843.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  20 in total

1.  The utility of fetal fibronectin in asymptomatic singleton and twin pregnancies with a cervical length ≤ 10 mm.

Authors:  Noelia Zork; Moti Gulersen; Anne Mardy; Caroline Pessel; Sara Brubaker; Joy Vink; Cynthia Gyamfi-Bannerman; Cande V Ananth
Journal:  J Matern Fetal Neonatal Med       Date:  2019-01-13

2.  Fetal fibronectin testing for reducing the risk of preterm birth.

Authors:  Vincenzo Berghella; Gabriele Saccone
Journal:  Cochrane Database Syst Rev       Date:  2019-07-29

Review 3.  Screening for spontaneous preterm birth and resultant therapies to reduce neonatal morbidity and mortality: A review.

Authors:  Angelica V Glover; Tracy A Manuck
Journal:  Semin Fetal Neonatal Med       Date:  2017-12-09       Impact factor: 3.926

4.  Adipokinins in pregnancies at risk of preterm delivery.

Authors:  Michelle A Kominiarek; Cecilia T Gambala; Monique Sutherland; Krista Varady
Journal:  Gynecol Endocrinol       Date:  2015-10-01       Impact factor: 2.260

Review 5.  Home uterine monitoring for detecting preterm labour.

Authors:  Christine Urquhart; Rosemary Currell; Francoise Harlow; Liz Callow
Journal:  Cochrane Database Syst Rev       Date:  2017-02-15

Review 6.  Cervicovaginal fetal fibronectin for the prediction of spontaneous preterm birth in multiple pregnancies: a systematic review and meta-analysis.

Authors:  Agustín Conde-Agudelo; Roberto Romero
Journal:  J Matern Fetal Neonatal Med       Date:  2010-12

7.  Critical appraisal and clinical utility of atosiban in the management of preterm labor.

Authors:  Olaleye Sanu; Ronald F Lamont
Journal:  Ther Clin Risk Manag       Date:  2010-04-26       Impact factor: 2.423

8.  Quantitative fetal fibronectin to predict spontaneous preterm birth: a review.

Authors:  Natasha L Hezelgrave; Andrew H Shennan
Journal:  Womens Health (Lond)       Date:  2015-12-11

9.  Cost-effectiveness of fibronectin testing in a triage in women with threatened preterm labor: alleviation of pregnancy outcome by suspending tocolysis in early labor (APOSTEL-I trial).

Authors:  Jolande Y Vis; Femke F Wilms; Martijn A Oudijk; Martina M Porath; Hubertina C J Scheepers; Kitty W M Bloemenkamp; Annemiek C Bolte; Jérôme Cornette; Jan B Derks; Johannes J Duvekot; Jim van Eyck; Anneke Kwee; Brent C Opmeer; Maria G van Pampus; Fred K Lotgering; Sicco A Scherjon; Krystyna M Sollie; Marc E A Spaanderman; Christine Willekes; Joris A M van der Post; Ben Willem J Mol
Journal:  BMC Pregnancy Childbirth       Date:  2009-09-01       Impact factor: 3.007

10.  Assessment of perinatal outcome after sustained tocolysis in early labour (APOSTEL-II trial).

Authors:  Carolien Roos; Liesbeth Hcj Scheepers; Kitty Wm Bloemenkamp; Annemiek Bolte; Jerome Cornette; Jan B Derks; Hans Jj Duvekot; Jim van Eyck; Joke H Kok; Anneke Kwee; Ashley Merién; Brent C Opmeer; Mariëlle G van Pampus; Dimitri Nm Papatsonis; Martina M Porath; Joris Am van der Post; Sicco A Scherjon; Krystyne Sollie; Marc Ea Spaanderman; Sylvia Mc Vijgen; Christine Willekes; Ben Willem J Mol; Fred K Lotgering
Journal:  BMC Pregnancy Childbirth       Date:  2009-09-09       Impact factor: 3.007

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