CLINICAL EVALUATION OF PROPESS FOR CERVICAL RIPENING IN PROLONGED PREGNANCY

ObjectiveTo evaluate the efficacy and safety of the controlled release of prostaglandin suppository——propess for cervical ripening in prolonged pregnancy. MethodsA case-control study method was used,randomly selected 30 primiparas of cervical immature prolonged pregnancy as the study group ,in which propess was used,30 cases of the same conditions as the control group in which oxytocin traditional method was used for cervical ripening.The maternal cervical Bishop score and maternity informations was compared between the two groups. ResultsAfter use of propess,the cervical Bishop score of the study group was score ≥2 in 24 cases,while 5 cases whose score ≥2 in control group (P0.05); The time from administration to mobilizing labor was (11.50±7.31)h in the study group,the control group was (27.70±7.10)h (P0.05); The total stage of labor in the study group was (12.40±3.52)h,the control group was (11.80±3.60)h(P0.05); The C-sect rate of the study group was 40%,the contral group was 57%(P0.05); There was no significant difference between the two groups in fetal distress rate and neonatal asphyxia rate(P0.05). ConclusionThere were satisfactory results about clinical evaluations of propess for cervical ripening in prolonged pregnancy.