OBJECTIVE: The aim of the study was to determine whether use of the fetal f
ibronectin assay would decrease the number of admissions to labor and deliv
ery for diagnosis and treatment of preterm labor.
STUDY DESIGN: A prospective cohort design was used to compare preterm labor
admissions during a 12-month period of fetal fibronectin assay use (study)
against a baseline period before fetal fibronectin assay was implemented a
s standard protocol. Patients coming to the physician's office or hospital
with signs and symptoms of preterm labor had a sample obtained for fetal fi
bronectin assay per labeling criteria. Comparisons were made with the Mann-
Whitney U test, independent Student t test,;chi(2) test, and Fisher exact t
est. P <.05 was considered significant.
RESULTS: There was no difference noted in the number of deliveries between
the baseline and study years. During the study year 251 of 330 patients eva
luated for preterm labor met study criteria and had the fetal fibronectin a
ssay completed. Eight patients did not have fetal fibronectin assay results
available because of specimen handling errors, leaving 243 subjects availa
ble for study. Compared with the baseline year, the study year had signific
antly fewer admissions for preterm labor, preterm labor admissions per pati
ent, and prescriptions written for tocolytic agents. In addition, the lengt
h of stay per admitted patient was significantly reduced. The study populat
ion had no differences in neonatal outcomes from the baseline population in
terms of deliveries at <35.0 weeks' gestation, number of admissions to the
neonatal intensive care unit, neonatal intensive care unit length of stay,
or days of ventilatory support per patient admitted to the neonatal intens
ive care unit.
CONCLUSIONS: Use of the fetal fibronectin assay resulted in significantly r
educed preterm labor admissions, length of stay, and prescriptions for toco
lytic agents. No negative impact on neonatal outcomes was observed. Reducti
ons in admissions for preterm labor and in charges per admission resulted i
n approximately $486,000 saved during the study period. A trend toward incr
eased corticosteroid administration (for neonates ultimately admitted to th
e neonatal intensive care unit) was noted.