Literature DB >> 29727248

Quantitative fetal fibronectin and cervical length in symptomatic women: results from a prospective blinded cohort study.

Lisa D Levine1, Katheryne L Downes1, Julie A Romero2, Hope Pappas1, Michal A Elovitz1.   

Abstract

Objectives: Our objectives were to determine whether quantitative fetal fibronectin (fFN) and cervical length (CL) screening can be used alone or in combination as prognostic tests to identify symptomatic women at the highest or lowest risk for spontaneous preterm birth (sPTB).
Methods: A prospective, blinded cohort study of women presenting with a singleton gestation to our triage unit between 22-33w6d with preterm labor symptoms was performed. Women with ruptured membranes, moderate/severe bleeding, and dilation >2 cm were excluded. The primary outcome was sPTB <37 weeks. We evaluated test characteristics of quantitative fFN and CL assessment, both separately and in combination, considering traditionally reported cut-points (fFN ≥50 and CL <25), as well as cut-points above and below these measures. We found interactions between fFN >50 and CL <25 and sPTB by parity and obstetric history (p < .05) and therefore stratified results. Test characteristics are presented with positive predictive value (PPV) and negative predictive value (NPV).
Results: Five hundred eighty women were enrolled and 537 women were available for analysis. Overall sPTB rate was 11.1%. Among nulliparous women, increasing levels of fFN were associated with increasing risk of sPTB, with PPV going from 26.5% at ≥20 ng/mL to 44.4% at ≥200 ng/mL. A cut-point of 20 ng/mL had higher sensitivity (69.2%) and higher NPV (96.8%) and therefore identified a "low-risk" group. fFN was not informative for multiparous women regardless of prior obstetrical history or quantitative level chosen. For all women, a shorter CL was associated with an increased sPTB risk. Among nulliparas and multiparas without a prior sPTB, a CL <20 mm optimized test characteristics (PPV 25 and 20%, NPV 95.5, and 92.7%, respectively). For multiparas with a prior sPTB, CL <25 mm was more useful. Using fFN and CL in combination for nulliparas did not improve test characteristics over using the individual fFN (p = .74) and CL (p = .31) components separately. Conclusions: This study identifies the importance of stratifying by parity and obstetrical history when using screening modalities for risk assessment in symptomatic women. For nulliparous women, either quantitative fFN or cervical length assessment can be utilized, depending on resources available, but a lower cut-point of 20 ng/mL should be used for quantitative fFN. For multiparous women, fFN is not useful and cervical length assessment should be the main screening tool utilized when there is clinical uncertainty. Regardless of parity, the PPV of fFN and CL is low and therefore the greatest clinical utility remains in its NPV.

Entities:  

Keywords:  Cervical length; preterm birth; quantitative fetal fibronectin; symptomatic preterm labor

Year:  2018        PMID: 29727248      PMCID: PMC6237659          DOI: 10.1080/14767058.2018.1472227

Source DB:  PubMed          Journal:  J Matern Fetal Neonatal Med        ISSN: 1476-4954


  16 in total

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Authors:  Paul A Harris; Robert Taylor; Robert Thielke; Jonathon Payne; Nathaniel Gonzalez; Jose G Conde
Journal:  J Biomed Inform       Date:  2008-09-30       Impact factor: 6.317

2.  Quantitative fetal fibronectin to predict preterm birth in asymptomatic women at high risk.

Authors:  Danielle S Abbott; Natasha L Hezelgrave; Paul T Seed; Jane E Norman; Anna L David; Phillip R Bennett; Joanna C Girling; Manju Chandirimani; Sarah J Stock; Jenny Carter; Ruth Cate; James Kurtzman; Rachel M Tribe; Andrew H Shennan
Journal:  Obstet Gynecol       Date:  2015-05       Impact factor: 7.661

3.  Development and validation of a tool incorporating cervical length and quantitative fetal fibronectin to predict spontaneous preterm birth in asymptomatic high-risk women.

Authors:  K Kuhrt; E Smout; N Hezelgrave; P T Seed; J Carter; A H Shennan
Journal:  Ultrasound Obstet Gynecol       Date:  2016-01       Impact factor: 7.299

4.  The preterm prediction study: cervical lactoferrin concentration, other markers of lower genital tract infection, and preterm birth. National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network.

Authors:  R L Goldenberg; W W Andrews; R L Guerrant; M Newman; B Mercer; J Iams; P Meis; A Moawad; A Das; J P VanDorsten; S N Caritis; G Thurnau; S Bottoms; M Miodovnik; D McNellis; J M Roberts
Journal:  Am J Obstet Gynecol       Date:  2000-03       Impact factor: 8.661

5.  Clinical prediction rules for preterm birth in patients presenting with preterm labor.

Authors:  Jamie A Bastek; Mary D Sammel; Sindhu K Srinivas; Meghan A McShea; Markley N Foreman; Michal A Elovitz; Joshua P Metlay
Journal:  Obstet Gynecol       Date:  2012-06       Impact factor: 7.661

6.  Predictive Accuracy of Serial Transvaginal Cervical Lengths and Quantitative Vaginal Fetal Fibronectin Levels for Spontaneous Preterm Birth Among Nulliparous Women.

Authors:  M Sean Esplin; Michal A Elovitz; Jay D Iams; Corette B Parker; Ronald J Wapner; William A Grobman; Hyagriv N Simhan; Deborah A Wing; David M Haas; Robert M Silver; Matthew K Hoffman; Alan M Peaceman; Steve N Caritis; Samuel Parry; Pathik Wadhwa; Tatiana Foroud; Brian M Mercer; Shannon M Hunter; George R Saade; Uma M Reddy
Journal:  JAMA       Date:  2017-03-14       Impact factor: 56.272

7.  Fetal fibronectin as a predictor of preterm birth in patients with symptoms: a multicenter trial.

Authors:  A M Peaceman; W W Andrews; J M Thorp; S P Cliver; A Lukes; J D Iams; L Coultrip; N Eriksen; R H Holbrook; J Elliott; C Ingardia; M Pietrantoni
Journal:  Am J Obstet Gynecol       Date:  1997-07       Impact factor: 8.661

8.  The preterm prediction study: quantitative fetal fibronectin values and the prediction of spontaneous preterm birth. The National Institute of Child Health and Human Development Maternal-Fetal Medicine Units Network.

Authors:  A R Goepfert; R L Goldenberg; B Mercer; J Iams; P Meis; A Moawad; E Thom; J P VanDorsten; S N Caritis; G Thurnau; M Miodovnik; M Dombrowski; J M Roberts; D McNellis
Journal:  Am J Obstet Gynecol       Date:  2000-12       Impact factor: 8.661

Review 9.  Fetal fibronectin as a short-term predictor of preterm birth in symptomatic patients: a meta-analysis.

Authors:  Luis Sanchez-Ramos; Isaac Delke; Javier Zamora; Andrew M Kaunitz
Journal:  Obstet Gynecol       Date:  2009-09       Impact factor: 7.661

10.  Development and validation of a tool incorporating quantitative fetal fibronectin to predict spontaneous preterm birth in symptomatic women.

Authors:  K Kuhrt; N Hezelgrave; C Foster; P T Seed; A H Shennan
Journal:  Ultrasound Obstet Gynecol       Date:  2016-02       Impact factor: 7.299

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  2 in total

1.  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.

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Journal:  J Perinat Med       Date:  2019-04-24       Impact factor: 1.901

2.  Serum Decorin, Biglycan, and Extracellular Matrix Component Expression in Preterm Birth.

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  2 in total

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