What is fetal fibronectin (FN) and when is it indicated?

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From the Guidelines

Fetal fibronectin testing is indicated in pregnant women between 24 and 34 weeks gestation who present with symptoms of preterm labor, as it has a high negative predictive value, allowing clinicians to avoid unnecessary interventions. Fetal fibronectin (fFN) is a glycoprotein produced by the fetal membranes that acts as a biological glue, helping to secure the placental membranes to the uterine lining. The test is most valuable when the result is negative, as it has a high negative predictive value (>99%), meaning that women with a negative result have less than a 1% chance of delivering within the next 7-14 days, as noted in studies such as 1.

Key Points to Consider

  • The test should not be performed if there is rupture of membranes, cervical dilation >3 cm, or recent sexual intercourse or cervical examination (within 24 hours), as these can cause false positive results.
  • A positive result (>50 ng/mL) indicates an increased risk of preterm birth but is less predictive.
  • The test involves collecting cervicovaginal secretions during a speculum examination and can provide results within an hour, making it useful for immediate clinical decision-making in the management of threatened preterm labor, as supported by guidelines and recommendations from organizations such as those discussed in 1.

Clinical Decision Making

When deciding whether to order a fetal fibronectin test, clinicians should consider the patient's symptoms and medical history, as well as the potential benefits and limitations of the test. The test can help identify women at low risk of preterm birth, allowing for more targeted interventions and reducing unnecessary hospitalizations and treatments. However, it is essential to interpret the results in the context of the patient's overall clinical presentation, as noted in 1.

From the Research

Definition and Purpose of Fetal Fibronectin

  • Fetal fibronectin (FFN) is an extracellular matrix glycoprotein localized at the maternal-fetal interface of the amniotic membranes, between chorion and decidua 2.
  • It is used to predict the risk of preterm birth in pregnant women, with levels greater than or equal to 50 ng/mL at or after 22 weeks indicating an increased risk 2.

Indications for Fetal Fibronectin Testing

  • FFN testing is indicated for pregnant women between 22 and 34 weeks of gestation who are at risk of preterm birth 2.
  • It can help identify women who are at significant risk of preterm birth and guide management decisions 2.
  • A negative FFN result has a high negative predictive value for delivery within 7 days, making it a useful tool for ruling out preterm labor in women with symptoms 3, 4, 5, 6.

Interpretation of Fetal Fibronectin Results

  • A positive FFN result is associated with an increased risk of preterm birth, while a negative result indicates a low risk of preterm birth within 7-14 days 4, 6.
  • The presence of FFN in vaginal secretions is a strong predictor of preterm birth, with a relative risk of 25.9 for delivery within 7 days 4.
  • The absence of FFN in vaginal secretions has a high negative predictive value, making it a useful tool for avoiding unnecessary interventions in women with symptoms of preterm labor 3, 5.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Fetal fibronectin testing for reducing the risk of preterm birth.

The Cochrane database of systematic reviews, 2008

Research

Rapid fetal fibronectin swab-test in preterm labor patients treated by betamimetics.

European journal of obstetrics, gynecology, and reproductive biology, 1997

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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