OBJECTIVE: To study the safe use of Dilaparn at term for ripening the unfav
ourable cervix in an outpatient setting.
STUDY DESIGN: Prospective review of cervical ripening with Dilapan in women
at term gestation. Such women were assigned to either outpatient or inpati
ent cervical ripening with Dilapan.
RESULTS: Twenty-one patients were assigned to each group. The length of ind
uction was similar between women who had ambulatory cervical ripening and h
ospitalized patients (11+/-7 vs. 14+/-7 hours, respectively), and the rates
of chorioamnionitis, endometritis and nonreassuring fetal heart rate traci
ngs were also similar. However, the average length of hospitalization was s
ignificantly shorter for those who had ambulatory ripening as compared to t
hose who were hospitalized (51+/-27 vs. 70+/-20 hours, respectively; P<.000
7).
CONCLUSION: The use of Dilapan for cervical ripening at term in an ambulato
ry setting is safe and effective and may decrease the overall hospitalizati
on time and cost.