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ORIGINAL RESEARCH |
From the Departments of Obstetrics and Gynecology, 1Drexel University College of Medicine, Philadelphia, Pennsylvania; and 2Christiana Care Health System, Newark, Delaware.
OBJECTIVE: We sought to evaluate whether the presence of a positive fetal fibronectin (
50 ng/mL) in nulliparous women undergoing preinduction cervical ripening with the intracervical Foley catheter predicted vaginal birth.
METHODS: This was a prospective blinded observational trial of nulliparous women undergoing preinduction cervical ripening. We excluded women who had a contraindication to vaginal birth. Cervical and vaginal fetal fibronectin specimens were obtained before preinduction cervical ripening with an intracervical Foley catheter. The managing obstetrician was blinded to these results.
RESULTS: A total of 241 women met the inclusion criteria, of which 54.4% delivered vaginally. There was no difference in the rate of vaginal delivery among women with either a positive cervical fetal fibronectin (positive fetal fibronectin 55.8% compared with negative fetal fibronectin 53.3%, P = .70) or positive vaginal fetal fibronectin (positive fetal fibronectin 57.6% compared with negative fetal fibronectin 53.3%, P = .56). Women with a positive cervical fetal fibronectin did have a shorter duration of cervical ripening (fetal fibronectinpositive 229 ± 220 minutes compared with fetal fibronectinnegative 379 ± 193 minutes, P < .05), duration of oxytocin (fetal fibronectinpositive 655 ± 555 minutes compared with fetal fibronectinnegative 731.5 ± 342 minutes, P < .025) and required lower maximal doses of oxytocin (fetal fibronectinpositive 18.4 mIU/min compared with fetal fibronectinnegative 21.8 mIU/min, P = .005). Women with a positive vaginal fetal fibronectin demonstrated only a shorter duration of cervical ripening compared with their fetal fibronectin negative counterparts (fetal fibronectinpositive 300 ± 216 minutes compared with fetal fibronectinnegative 345 ± 201 minutes, P < .05).
CONCLUSION: Fetal fibronectin does not predict vaginal delivery in nulliparous women requiring preinduction cervical ripening.
LEVEL OF EVIDENCE: II-2
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